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مداخلات حرفه‌ای برای پزشکان عمومی به منظور مدیریت بالینی بیماری‌های عضلانی‌اسکلتی

Appendices

Appendix 1. Search strategies

MEDLINE OVID

Search date: October 24, 2013

1 exp musculoskeletal diseases/ or rheumatology/ or exp orthopedics/ or orthopedic procedures/ (857643)
2 (musculoskeletal or arthriti$ or orthop?edic? or osteo$ or polymyalg$ or periarthrit$).ti. (249636)
3 (arthritis or back pain or chondrocalcinosis or dermatomyositis or dupuytren? contracture or fibromyal$ or Fibrositis or Fibrositides or gout or hyperostos$ or low$ back or lupus or osteitis or osteoarthrit$ or osteoarthrop$ or osteochondr$ or Osteonecros$ or osteoporos$ or periarthriti$ or polymyalgia? or raynaud disease? or rheumatism or rheumatic disease? or sciatica or scleroderma$ or Spondylarthrit$).ti,ab. (352214)
4 (((cartiledge or connective tissue? or joint? or ligament? or muscula$ or myofascial or neck or soft tissue? or spine or spinal) adj2 (damage? or disease? or disorder? or injury or injuries or pain? or strain?)) and (care or treatment)).ti. (2884)
5 ((caplan? or felty's or Sjogren's or still's or wissler's) adj (disease? or syndrome?)).ti,ab. (11736)
6 ((elbow or hand? or knee or knees or leg or muscle or muscular$ or orthop?edic? or shoulder? or wrist?) adj2 (care or treatment? or injury or injuries or pain? or strain?)).ti,ab. (38503)
7 (athletic? adj2 (strain? or injury or injuries)).ti. (451)
8 Dermatomyositis/ or Dupuytren's Contracture/ or Lupus Erythematosus, Cutaneous/ or Lupus Erythematosus, Systemic/ or exp back pain/ or neck pain/ or sciatica/ or exp Raynaud Disease/ or exp Scleroderma, Systemic/ or exp arm injuries/ or athletic injuries/ or exp back injuries/ or exp dislocations/ or exp fractures bone/ or fractures cartilage/ or exp hand injuries/ or exp hip injuries/ or exp leg injuries/ or multiple trauma/ or exp neck injuries/ or soft tissue injuries/ or exp spinal cord injuries/ or exp spinal injuries/ or exp "sprains and strains"/ or exp tendon injuries/ or exp musculoskeletal system/ (1447111)
9 or/1‐8 [MSK Rev] (2072899)
10 general practice/ or physicians, primary care/ [Terms added August 2012] (4535)
11 family practice/ or physicians, family/ or primary health care/ (122879)
12 ((family or general) adj2 (doctor? or medicine or medical practitioner? or medical practice? or practice? or practitioner? or physician$)).ti,ab. [Increased adj Aug 2012] (101849)
13 (primary adj2 (care or health care or healthcare or medical care or patient care)).ti,ab. (89077)
14 or/10‐13 [Primary Care Rev ML] (217520)
15 (randomized controlled trial or controlled clinical trial).pt. or randomized.ab. or placebo.ab. or clinical trials as topic.sh. or randomly.ab. or trial.ti. (930250)
16 exp animals/ not humans.sh. (4051829)
17 15 not 16 [Cochrane RCT Filter 6.4.d Sens/Precision Maximizing] (859939)
18 intervention?.ti. or (intervention? adj6 (clinician? or collaborat$ or community or complex or DESIGN$ or doctor? or educational or family doctor? or family physician? or family practitioner? or financial or GP or general practice? or hospital? or impact? or improv$ or individuali?e? or individuali?ing or interdisciplin$ or multicomponent or multi‐component or multidisciplin$ or multi‐disciplin$ or multifacet$ or multi‐facet$ or multimodal$ or multi‐modal$ or personali?e? or personali?ing or pharmacies or pharmacist? or pharmacy or physician? or practitioner? or prescrib$ or prescription? or primary care or professional$ or provider? or regulatory or regulatory or tailor$ or target$ or team$ or usual care)).ab. (165998)
19 (pre‐intervention? or preintervention? or "pre intervention?" or post‐intervention? or postintervention? or "post intervention?").ti,ab. [added 2.4] (10262)
20 (hospital$ or patient?).hw. and (study or studies or care or health$ or practitioner? or provider? or physician? or nurse? or nursing or doctor?).ti,hw. (720981)
21 demonstration project?.ti,ab. (1984)
22 (pre‐post or "pre test$" or pretest$ or posttest$ or "post test$" or (pre adj5 post)).ti,ab. (65680)
23 (pre‐workshop or post‐workshop or (before adj3 workshop) or (after adj3 workshop)).ti,ab. (610)
24 trial.ti. or ((study adj3 aim?) or "our study").ab. (632839)
25 (before adj10 (after or during)).ti,ab. (362830)
26 ("quasi‐experiment$" or quasiexperiment$ or "quasi random$" or quasirandom$ or "quasi control$" or quasicontrol$ or ((quasi$ or experimental) adj3 (method$ or study or trial or design$))).ti,ab,hw. [ML] (104437)
27 ("time series" adj2 interrupt$).ti,ab,hw. [ML] (1184)
28 (time points adj3 (over or multiple or three or four or five or six or seven or eight or nine or ten or eleven or twelve or month$ or hour? or day? or "more than")).ab. (9391)
29 pilot.ti. (39876)
30 Pilot projects/ [ML] (84019)
31 (clinical trial or controlled clinical trial or multicenter study).pt. [ML] (649874)
32 (multicentre or multicenter or multi‐centre or multi‐center).ti. (29829)
33 random$.ti,ab. or controlled.ti. (779263)
34 (control adj3 (area or cohort? or compare? or condition or design or group? or intervention? or participant? or study)).ab. not (controlled clinical trial or randomized controlled trial).pt. [ML] (412256)
35 "comment on".cm. or review.ti,pt. or randomized controlled trial.pt. [ML] (2959592)
36 review.ti. [EM] (255522)
37 (rat or rats or cow or cows or chicken? or horse or horses or mice or mouse or bovine or animal?).ti. (1368734)
38 exp animals/ not humans.sh. [ML] (4051829)
39 (animal$ not human$).sh,hw. [EM] (3956028)
40 *experimental design/ or *pilot study/ or quasi experimental study/ [EM] (24261)
41 ("quasi‐experiment$" or quasiexperiment$ or "quasi random$" or quasirandom$ or "quasi control$" or quasicontrol$ or ((quasi$ or experimental) adj3 (method$ or study or trial or design$))).ti,ab. [EM] (104437)
42 ("time series" adj2 interrupt$).ti,ab. [EM] (1184)
43 (or/18‐29,32‐34) or experimental design/ or between groups design/ or quantitative methods/ or quasi experimental methods/ [PsycInfo] (2839256)
44 exp animals/ or animal?.ti,id,hw. [PsycInfo] (17706941)
45 (or/18‐34) not (or/35,37‐38) [EPOC Methods Filter 2.4 Medline] (2151565)
46 (or/18‐25,28‐29,32‐33,40‐42) not (or/36,39) [EPOC Methods Filter 2.4 EMBASE] (2199704)
47 43 not (or/36‐37,44) [EPOC Methods Filter 2.4 PsycInfo] (339055)
48 9 and 14 [MSK & PC] (11460)
49 9 and 14 and 17 [MSK & PC & RCT FILTER] (1584)
50 (9 and 14 and 45) not 49 [MSK & PC & EPOC FILTER 2.4] (2810)
51 (201208$ or 201209$ or 201210$ or 201211$ or 201212$ or 2013$).ed,ep,yr. (1796601)
52 49 and 51 [rct] (167)
53 remove duplicates from 52 [RCT to export Oct 24‐2013] (129)
54 50 and 51 [EPOC] (292)
55 remove duplicates from 54 [EPOC to export Oct 2013]

EMBASE OVID

Embase Classic+Embase <1947 to 2013 October 23>

1 exp *musculoskeletal disease/ or rheumatology/ or *orthopedics/ or *orthopedic surgery/ (1190591)
2 (arthrit$ or back pain or fibromyalg$ or gout or low$ back or musculoskeletal or orthop?edic? or lupus or osteitis or osteoarthrit$ or osteoarthrop$ or osteochondr$ or Osteonecros$ or osteoporos$ or periarthriti$ or polymyalgia? or rheumatism or rheumatic disease? or sciatica or scleroderma$ or Spondylarthrit$).ti. (311875)
3 ((arthritis or back pain or chondrocalcinosis or dermatomyositis or dupuytren? contracture or fibromyal$ or Fibrositis or Fibrositides or gout or hyperostos$ or low$ back or lupus or osteitis or osteoarthrit$ or osteoarthrop$ or osteochondr$ or Osteonecros$ or osteoporos$ or periarthriti$ or polymyalgia? or raynaud disease? or rheumatism or rheumatic disease? or sciatica or scleroderma$ or Spondylarthrit$) adj3 (care or treatment?)).ab. (24640)
4 (((cartiledge or connective tissue? or joint? or ligament? or muscula$ or myofascial or neck or soft tissue? or spine or spinal) adj2 (damage? or disease? or disorder? or injury or injuries or pain? or strain?)) and (care or treatment)).ti. (3734)
5 ((caplan? or felty's or Sjogren's or still's or wissler's) adj (disease? or syndrome?)).ti,ab. (15557)
6 ((elbow or hand? or knee or knees or leg or muscle or muscular$ or orthop?edic? or shoulder? or sprain$ or wrist?) adj4 (care or treatment)).ti,ab. (32341)
7 (athletic? adj2 (strain? or injury or injuries)).ti. (491)
8 (bone adj2 (fracture? or fractured)).ti. (2759)
9 ((bone? or cartiledge or connective tissue? or joint? or ligament? or muscula$ or myofascial or neck or soft tissue? or spine or spinal) adj2 (damage? or disease? or disorder? or injury or injuries or pain? or strain?)).ti. (49287)
10 *dermatomyositis/ or *Dupuytren contracture/ or *skin lupus erythematosus/ or *systemic lupus erythematosus/ or exp *backache/ or exp *leg pain/ or exp *musculoskeletal pain/ or *neck pain/ or *ischialgia/ or *Raynaud phenomenon/ or *scleroderma/ or exp *ARM INJURY/ or exp *TENDON INJURY/ or exp *SOFT TISSUE INJURY/ or exp *NECK INJURY/ or exp *HAND INJURY/ or exp *LEG INJURY/ or exp *SPINE INJURY/ or exp *SPINAL CORD INJURY/ or exp *HIP INJURY/ or *sport injury/ or *dislocation/ or exp *fracture/ or exp *sprain/ or muscle strain/ or exp *tendon injury/ (367353)
11 or/1‐10 [MSK conditions] (1404842)
12 *general practitioner/ (15844)
13 *general practice/ (39859)
14 exp *primary health care/ (40728)
15 ((family or general) adj2 (doctor? or medical practitioner? or medical practice? or practice? or practitioner? or physician$)).ti,ab. (117580)
16 (primary adj2 (care or health care or healthcare or medical care or patient care)).ti,ab. (104088)
17 or/12‐16 [Primary care] (231098)
18 controlled clinical trial/ or controlled study/ or randomized controlled trial/ [EM] (4244044)
19 (book or conference paper or editorial or letter or review).pt. not randomized controlled trial/ [Per BMJ Clinical Evidence filter] (4034696)
20 (random sampl$ or random digit$ or random effect$ or random survey or random regression).ti,ab. not randomized controlled trial/ [Per BMJ Clinical Evidence filter] (54247)
21 (animal$ not human$).sh,hw. (3913735)
22 18 not (or/19‐21) [Trial filter per BMJ CLinical Evidence] (2801374)
23 intervention?.ti. or (intervention? adj6 (clinician? or collaborat$ or community or complex or DESIGN$ or doctor? or educational or family doctor? or family physician? or family practitioner? or financial or GP or general practice? or hospital? or impact? or improv$ or individuali?e? or individuali?ing or interdisciplin$ or multicomponent or multi‐component or multidisciplin$ or multi‐disciplin$ or multifacet$ or multi‐facet$ or multimodal$ or multi‐modal$ or personali?e? or personali?ing or pharmacies or pharmacist? or pharmacy or physician? or practitioner? or prescrib$ or prescription? or primary care or professional$ or provider? or regulatory or regulatory or tailor$ or target$ or team$ or usual care)).ab. (201463)
24 (pre‐intervention? or preintervention? or "pre intervention?" or post‐intervention? or postintervention? or "post intervention?").ti,ab. [added 2.4] (12626)
25 (hospital$ or patient?).hw. and (study or studies or care or health$ or practitioner? or provider? or physician? or nurse? or nursing or doctor?).ti,hw. (1623934)
26 demonstration project?.ti,ab. (2357)
27 (pre‐post or "pre test$" or pretest$ or posttest$ or "post test$" or (pre adj5 post)).ti,ab. (93420)
28 (pre‐workshop or post‐workshop or (before adj3 workshop) or (after adj3 workshop)).ti,ab. (809)
29 trial.ti. or ((study adj3 aim?) or "our study").ab. (838686)
30 (before adj10 (after or during)).ti,ab. (474031)
31 deleted line; no impact on strategy
32 deleted line; no impact on strategy
33 (time points adj3 (over or multiple or three or four or five or six or seven or eight or nine or ten or eleven or twelve or month$ or hour? or day? or "more than")).ab. (11728)
34 pilot.ti. (49794)
35 deleted line; no impact on strategy
36 deleted line; no impact on strategy
37 (multicentre or multicenter or multi‐centre or multi‐center).ti. (39211)
38 random$.ti,ab. or controlled.ti. (932656)
39 (control adj3 (area or cohort? or compare? or condition or design or group? or intervention? or participant? or study)).ab. not (controlled clinical trial or randomized controlled trial).pt. [ML] (615626)
40 deleted line; no impact on strategy
41 review.ti. [EM] (312835)
42 (rat or rats or cow or cows or chicken? or horse or horses or mice or mouse or bovine or animal?).ti. (1654258)
43deleted line; no impact on strategy
44 (animal$ not human$).sh,hw. [EM] (3913735)
45 *experimental design/ or *pilot study/ or quasi experimental study/ [EM] (6990)
46 ("quasi‐experiment$" or quasiexperiment$ or "quasi random$" or quasirandom$ or "quasi control$" or quasicontrol$ or ((quasi$ or experimental) adj3 (method$ or study or trial or design$))).ti,ab. [EM] (128680)
47 ("time series" adj2 interrupt$).ti,ab. [EM] (1124)
48‐50 deleted lines; no impact on strategy
51 (or/23‐30,33‐34,37‐38,45‐47) not (or/41,44) [EPOC Methods Filter 2.4 EMBASE] (3323291)
52 48 not (or/41‐42,49) [EPOC Methods Filter 2.4 PsycInfo] (715574)
53 11 and 17 [MSK & Primary Care] (10572)
54 11 and 17 and 22 [MSK & PC & RCT] (2143)
55 (11 and 17 and 51) not 54 [MSK & PC & EPOC Filter] (3595)

Cochrane Library via OVID EBM Collection

Search date: October 2013

EBM Reviews ‐ Cochrane Database of Systematic Reviews <2005 to September 2013>, EBM Reviews ‐ ACP Journal Club <1991 to October 2013>, EBM Reviews ‐ Database of Abstracts of Reviews of Effects <3rd Quarter 2013>, EBM Reviews ‐ Cochrane Central Register of Controlled Trials <September 2013>, EBM Reviews ‐ Cochrane Methodology Register <3rd Quarter 2012>, EBM Reviews ‐ Health Technology Assessment <3rd Quarter 2013>, EBM Reviews ‐ NHS Economic Evaluation Database <3rd Quarter 2013>

1 exp musculoskeletal diseases/ or rheumatology/ or exp orthopedics/ or orthopedic procedures/ (20864)
2 (musculoskeletal or arthrit$ or orthop?edic? or osteo$ or polymyalg$ or periarthrit$).ti. (13266)
3 (arthritis or back pain or chondrocalcinosis or dermatomyositis or dupuytren? contracture or fibromyal$ or Fibrositis or Fibrositides or gout or hyperostos$ or low$ back or lupus or osteitis or osteoarthrit$ or osteoarthrop$ or osteochondr$ or Osteonecros$ or osteoporos$ or periarthriti$ or polymyalgia? or raynaud disease? or rheumatism or rheumatic disease? or sciatica or scleroderma$ or Spondylarthrit$).ti,ab. (19487)
4 (((cartiledge or connective tissue? or joint? or ligament? or muscula$ or myofascial or neck or soft tissue? or spine or spinal) adj2 (damage? or disease? or disorder? or injury or injuries or pain? or strain?)) and (care or treatment)).ti. (472)
5 ((caplan? or felty's or Sjogren's or still's or wissler's) adj (disease? or syndrome?)).ti,ab. (247)
6 ((elbow or hand? or knee or knees or leg or muscle or muscular$ or orthop?edic? or shoulder? or wrist?) adj2 (care or treatment? or injury or injuries or pain? or strain?)).ti,ab. (5343)
7 (athletic? adj2 (strain? or injury or injuries)).ti. (14)
8 Dermatomyositis/ or Dupuytren's Contracture/ or Lupus Erythematosus, Cutaneous/ or Lupus Erythematosus, Systemic/ or exp back pain/ or neck pain/ or sciatica/ or exp Raynaud Disease/ or exp Scleroderma, Systemic/ or exp arm injuries/ or athletic injuries/ or exp back injuries/ or exp dislocations/ or exp fractures bone/ or fractures cartilage/ or exp hand injuries/ or exp hip injuries/ or exp leg injuries/ or multiple trauma/ or exp neck injuries/ or soft tissue injuries/ or exp spinal cord injuries/ or exp spinal injuries/ or exp "sprains and strains"/ or exp tendon injuries/ or exp musculoskeletal system/ (28264)
9 or/1‐8 [MSK Rev] (53389
10 general practice/ or physicians, primary care/ [Terms added August 2012] (145)
11 family practice/ or physicians, family/ or primary health care/ (4521)
12 ((family or general) adj2 (doctor? or medicine or medical practitioner? or medical practice? or practice? or practitioner? or physician$)).ti,ab. [Increased adj Aug 2012] (6968)
13 (primary adj2 (care or health care or healthcare or medical care or patient care)).ti,ab. (7493)
14 or/10‐13 [Primary Care Rev ML] (13418)
15 9 and 14 (1090)
16 limit 15 to yr="2012 ‐ 2014" [Limit not valid in DARE; records were retained] (68)
17 from 16 keep 1‐3 [CDSR] (3)
18 from 16 keep 4‐7 [ACP] (4)
19 from 16 keep 8‐9 [DARE] (2)
20 from 16 keep 10‐53 [Central] (44)
21 from 16 keep 45‐53 [HTA] (9)
22 from 16 keep 63‐68 [EED] (6)

Cochrane Library, Issue 2, 2010 [Wiley]

Search Date: 2010‐08‐23 15:34:51.33

#1MeSH descriptor Musculoskeletal Diseases explode all trees
#2MeSH descriptor Rheumatology, this term only
#3MeSH descriptor Orthopedics explode all trees
#4MeSH descriptor Orthopedic Procedures, this term only
#5(musculoskeletal or arthritis or osteoarthritis):ab
#6(arthrit*):ti
#7((bone near/2 fracture*) or (bone near/2 fractured)):ti
#8(Chondrocalcinosis or dermatomyositis or dupuytren* contracture or fibromyalgia* or Fibrositis or Fibrositides or gout or hyperostos* or lupus or Musculoskeletal or orthopedic* or orthopaedic* or osteitis or osteoarthrit* or osteoarthrop* or osteochondr* or Osteonecros* or osteoporos* or periarthriti* or polymyalgia* or raynaud disease* or rheumati* or sciatica or scleroderma* or Spondylarthrit* or sprain*):ti
#9((caplan* or felty's or Sjogren's or still's or wissler's) near/ disease*):ti
#10((caplan* or felty's or Sjogren's or still's or wissler's) near/ syndrome*):ti
#11((bone* or cartiledge or connective tissue* or joint* or ligament* or muscula* or myofascial or neck or soft tissue* or spine or spinal) near/2 strain*):ti
#12((bone* or cartiledge or connective tissue* or joint* or ligament* or muscula* or myofascial or neck or soft tissue* or spine or spinal) near/2 damage*):ti
#13((bone* or cartiledge or connective tissue* or joint* or ligament* or muscula* or myofascial or neck or soft tissue* or spine or spinal) near/2 disease*):ti
#14((bone* or cartiledge or connective tissue* or joint* or ligament* or muscula* or myofascial or neck or soft tissue* or spine or spinal) near/2 disorder*):ti
#15((bone* or cartiledge or connective tissue* or joint* or ligament* or muscula* or myofascial or neck or soft tissue* or spine or spinal) near/2 injury):ti
#16((bone* or cartiledge or connective tissue* or joint* or ligament* or muscula* or myofascial or neck or soft tissue* or spine or spinal) near/2 pain*):ti
#17((bone* or cartiledge or connective tissue* or joint* or ligament* or muscula* or myofascial or neck or soft tissue* or spine or spinal) near/2 injuries):ti
#18((elbow) near/2 (injury or injuries or pain* or strain*)):ti
#19((shoulder) near/2 (injury or injuries or pain* or strain*)):ti
#20((hand*) near/2 (injury or injuries or pain* or strain*)):ti
#21(knee near/2 (injury or injuries or pain* or strain*)):ti
#22(athletic* near/2 (strain* or injury or injuries)):ti
#23MeSH descriptor Dermatomyositis, this term only
#24MeSH descriptor Dupuytren Contracture, this term only
#25MeSH descriptor Lupus Erythematosus, Cutaneous, this term only
#26MeSH descriptor Lupus Erythematosus, Systemic explode all trees
#27MeSH descriptor Back Pain explode all trees
#28MeSH descriptor Sciatica, this term only
#29MeSH descriptor Raynaud Disease, this term only
#30MeSH descriptor Scleroderma, Systemic explode all trees
#31MeSH descriptor Arm Injuries explode all trees
#32MeSH descriptor Neck Pain explode all trees
#33MeSH descriptor Athletic Injuries, this term only
#34MeSH descriptor Back Injuries explode all trees
#35MeSH descriptor Dislocations explode all trees
#36MeSH descriptor Fractures, Bone explode all trees
#37MeSH descriptor Fractures, Cartilage, this term only
#38MeSH descriptor Hand Injuries explode all trees
#39MeSH descriptor Hip Injuries explode all trees
#40MeSH descriptor Leg Injuries explode all trees
#41MeSH descriptor Multiple Trauma, this term only
#42MeSH descriptor Neck Injuries explode all trees
#43MeSH descriptor Soft Tissue Injuries, this term only
#44MeSH descriptor Spinal Cord Injuries explode all trees
#45MeSH descriptor Sprains and Strains explode all trees
#46MeSH descriptor Tendon Injuries explode all trees
#47MeSH descriptor Musculoskeletal System explode all trees
#48(#1 OR #2 OR #3 OR #4 OR #5 OR #6 OR #7 OR #8 OR #9 OR #10 OR #11 OR #12 OR #13 OR #14 OR #15 OR #16 OR #17 OR #18 OR #19 OR #20 OR #21 OR #22 OR #23 OR #24 OR #25 OR #26 OR #27 OR #28 OR #29 OR #30 OR #31 OR #32 OR #33 OR #34 OR #35 OR #36 OR #37 OR #38 OR #39 OR #40 OR #41 OR #42 OR #43 OR #44 OR #45 OR #46 OR #47)
#49MeSH descriptor Family Practice, this term only
#50MeSH descriptor Physicians, Family, this term only
#51MeSH descriptor Primary Health Care, this term only
#52(general near/ (doctor* or medicine or medical practitioner* or medical practice* or practice* or practitioner* or physician*)):ti,ab
#53(family near/ (doctor* or medicine or medical practitioner* or medical practice* or practice* or practitioner* or physician*)):ti,ab
#54(primary near/2 (care or health care or healthcare or medical care or patient care)):ti,ab
#55(#49 OR #50 OR #51 OR #52 OR #53 OR #54)
#56intervention*:ti
#57(intervention* near/6 (clinician* or collaborat* or community or complex or doctor* or educational or family doctor* or family physician* or family practitioner* or financial or GP or general practice* or hospital* or impact* or improv* or individuali*e* or individuali*ing or interdisciplin* or multicomponent or multi‐component or
multidisciplin* or multi‐disciplin* or multifacet* or multi‐facet* or multimodal* or multi‐modal* or personali*e* or personali*ing or pharmacies or pharmacist* or pharmacy or
physician* or practitioner* or prescrib* or prescription* or primary care or professional* or provider* or regulatory or regulatory or tailor* or target* or team* or usual care)):ab
#58((evidence near/4 intervention) or (evidence‐based near/4 intervention) or (evidence‐driven)):ti,ab
#59"practice‐based":ti,ab
#60(improv* near/3 (decision* or implement* or health care or healthcare or initiative* or management or multifacet* or multi‐facet* or multi‐component or practi*e* or practitioner* or prescrib* or prescription* or professional* or program* or programme* or provider*)):ti

#61(improv* near/2 (patient‐care or family practice or ((family or general) near/2 (practi*e or practitioner* or doctor*)) or primary care)):ab
#62recommended practice*:ti,ab
#63((information or evidence) near/2 uptake):ti,ab
#64(knowledge near/2 (application or broke* or creation or diffus* or disseminat* or exchang* or implement* or management or mobili* or translat* or transfer* or uptake or utili*)):ti,ab
#65(evidence* near/2 (exchang* or translat* or transfer*)):ti,ab
#66(KT near/2 (application or broke* or diffus* or disseminat* or decision* or exchang* or implement* or intervent* or mobili* or plan* or policy or policies or strateg* or translat* or transfer* or uptake or utili*)):ti,ab
#67((computer‐tailored or individuali*ing or individuali*ed or personali*e* or personali*ing or tailor*) near/2 (feedback or intervention* or information or plan*)):ti,ab
#68((conventional or evidence‐based or pattern or regular or routine or standard or traditional or usual) near/2 (care or healthcare or patient care or practice)):ti,ab #69(collaborative* or interdisciplin* or inter‐disciplin* or multidisciplin* or multi‐ disciplin* or team* or team‐based or skill‐ mix):ti
#70(skill* near/2 (mix or mixes)):ti,ab
#71((collaborative) near/2 (care or patient care or healthcare)):ab
#72((multidisciplinary) near/2 (care or patient care or healthcare)):ab
#73((interdisciplinary) near/2 (care or patient care or healthcare)):ab
#74(doctor‐driven or doctor‐led or GP‐LED or nurse‐led or nurse‐driven or pharmacist‐led or pharmacist‐driven or physician‐led or physician‐ driven):ti,ab
#75physician directed:ti,ab
#76(leaflet* or pamphlet* or "written information"):ti
#77((leaflet*) near/5 (intervention* or care or healthcare or physician* or practitioner* or provider*)):ab
#78((pamphlet*) near/5 (intervention* or care or healthcare or physician* or practitioner* or provider*)):ab
#79(("written information") near/5 (intervention* or care or healthcare or physician* or practitioner* or provider*)):ab
#80((academic detailing or e‐detailing) or (opinion* near/2 leader*)):ti,ab
#81("audit and feedback"):ti,ab
#82((physician* or doctor* or practitioner* or nurse* or provider*) near/ feedback):ti,ab
#83(clinician* near/2 (prompt or prompts or prompting)):ti,ab or (physician* near/2 (prompt or prompts or prompting)):ti,ab or (remind* near/2 (prompt or prompts or prompting)):ti,ab
#84(reminder* near/2 (clinician* or physician* or practitioner* or nurse* or doctor* or provider*)):ti,ab
#85MeSH descriptor Reminder Systems, this term only

#86((doctor* or nurse* or pharmacist* or physician* or practitioner*) near/2 behavio*r*):ti,ab
#87(nurse* near/4 substitut*):ti,ab
#88(practice pattern*):ti,ab or ((change* or changing) near/2 practice):ti,ab
#89MeSH descriptor Physician's Practice Patterns, this term only
#90(nurse‐practitioner* or physician* assistant*):ti
#91((doctor* or pharmacist* or physician*) near/2 role*):ab
#92MeSH descriptor Referral and Consultation, this term only
#93(Referral* and (primary care or specialist* or general practitioner* or change* or changing or improv* or impact or effect* or reduce* or reducing or increase* or increasing or optimi* or optimal or quality or healthcare or patient care or intensive care or emergency or chronic or management or administration)):ti,ab
#94(Referral* and (primary care or specialist* or general practitioner* or optimi*e* or optimal)):ti or (Referral* near/3 (primary care or specialist* or general practitioner* or optimi*e* or optimal)):ab
#95((nurse* or physician* or pharmacist* or provider*) near/2 initiative*):ti,ab
#96(virtual reality or VR Training or VR simulat* or (simulat* near/2 skill*)):ti,ab
#97(blog* or wiki* or PDA or "palm pilot* " or blackberr* or Twitter or tweet or tweeting or facebook or social networking or social marketing or youtube):ti,ab or blogging or (health 20 or healthcare 20 or health care 20 or web 20):ti,ab
#98(guideline adherence or (guideline* near/3 (adherence or compliance or concordance or implement* or UPTAKE))):ti,ab
#99((individuali* near/2 (care or healthcare or medical care)) or (integrated near/2 (care or healthcare or medical care)) or (patient‐centred or patient‐centered or patient‐control*)):ti,ab
#100quality improvement:ti,ab
#101(Patient satisfaction or algorithm*):ti,ab
#102MeSH descriptor Education, Pharmacy, Continuing, this term only
#103MeSH descriptor Education, Medical, Continuing, this term only
#104MeSH descriptor Education, Nursing, Continuing, this term only
#105MeSH descriptor Education, Professional, this term only
#106(continuing near/2 education near/3 (physician* or nurse* or nursing or practitioner* or doctor* or family physician* or general practitioner* or family doctor* or primary care or primary healthcare)):ab
#107(continuing near/3 education):ti
#108((continuing or "on the job" or "off the job" or postgrad* or post‐grad* or resident* or intern* or internship* or workplace) near/2 training):ti,ab
#109(((continuing or "on the job" or "off the job" or postgrad* or post‐grad* or resident* or intern* or internship* or workplace) near/2 education*) or (skill* near/ (education or training))):ti,ab
#110(#56 OR #57 OR #58 OR #59 OR #60 OR #61 OR #62 OR #63 OR #64 OR #65 OR #66 OR #67 OR #68 OR #69 OR #70 OR #71 OR #72 OR #73 OR #74 OR #75 OR #76 OR #77 OR #78 OR #79 OR #80 OR #81 OR #82 OR #83 OR #84 OR #85 OR #86 OR #87 OR #88 OR #89 OR #90 OR #91 OR #92 OR #93 OR #94 OR #95 OR #96 OR #97 OR #98 OR #99 OR #100 OR #101 OR #102 OR #103 OR #104 OR #105 OR #106 OR #107 OR #108 OR #109)

#111(#48 AND #55)
#112(#48 AND #55 AND #110)
#113(#111 OR #112)

CINAHL, EbscoHost 1980‐

Search dates: August 24, 2010 AND november 20, 2013

Date: 20100101‐20131231 NOVEMBER 20, 2013

288

S52

S51 or S50 [All Results] AUGUST 24, 2010

608

S51

S49 and S46  (Results with EPOC 1.7 Filter)

485

 

 

 

S50

S49 and S45  (Results with RCT filter)

302

S49

S47 and S48 and S17  (S17= primary Care terms)

1681

S48

S18 or S19 or S20 or S21 or S22 or S23  (Education/Collaboration Intervention terms)

76261

S47

S1 or S2 or S3 or S4 or S5 or S6 or S7 or S8 or S9 or S10 or S11 or S12 or S13 or S14 or S15 or S16  (MSK terms)

404871

S46

S24 or S25 or S26 or S27 or S28 or S29 or S30 or S31 or S32 or S34 or S35 or S36 or S37 or S38  (EPOC Filter 1.7)

187032

S45

S39 or S40 or S41 or S42 or S43 or S44  (RCT filter)

126098

S44

TI ( “control* N1 clinical” or “control* N1 group*” or “control* N1 trial*” or “control* N1 study” or “control* N1 studies” or “control* N1 design*” or “control* N1 method*” ) or AB ( “control* N1 clinical” or “control* N1 group*” or “control* N1 trial*” or “control* N1 study” or “control* N1 studies” or “control* N1 design*” or “control* N1 method*” )

57555

S43

TI controlled or AB controlled

44233

S42

TI random* or AB random*

77414

S41

TI ( “clinical study” or “clinical studies” ) or AB ( “clinical study” or “clinical studies” )

11229

S40

(MM "Clinical Trials+")

6045

S39

TI ( (multicent* n2 design*) or (multicent* n2 study) or (multicent* n2 studies) or (multicent* n2 trial*) ) or AB ( (multicent* n2 design*) or (multicent* n2 study) or (multicent* n2 studies) or (multicent* n2 trial*) )

5282

S38

TI pilot

7878

S37

(MH "Pilot Studies")

20827

S36

AB "before‐and‐after"

12207

S35

AB time series

1089

S34

TI time series

141

S33

AB ( before* n7 during or before n3 after ) or AU ( before* n7 during or before n3 after )

19048

S32

TI ( (time point*) or (period* n4 interrupted) or (period* n4 multiple) or (period* n4 time) or (period* n4 various) or (period* n4 varying) or (period* n4 week*) or (period* n4 month*) or (period* n4 year*) ) or AB ( (time point*) or (period* n4 interrupted) or (period* n4 multiple) or (period* n4 time) or (period* n4 various) or (period* n4 varying) or (period* n4 week*) or (period* n4 month*) or (period* n4 year*) )

34841

S31

TI ( ( quasi‐experiment* or quasiexperiment* or quasi‐random* or quasirandom* or quasi control* or quasicontrol* or “quasi* W3 method*” or “quasi* W3 study” or “quasi* W3 studies” or “quasi* W3 trial” or “quasi* W3 design*” or “experimental W3 method*” or “experimental W3 study” or “experimental W3 studies” or “experimental W3 trial” or “experimental W3 design*” ) ) or AB ( ( quasi‐experiment* or quasiexperiment* or quasi‐random* or quasirandom* or quasi control* or quasicontrol* or “quasi* W3 method*” or “quasi* W3 study” or “quasi* W3 studies” or “quasi* W3 trial” or “quasi* W3 design*” or “experimental W3 method*” or “experimental W3 study” or “experimental W3 studies” or “experimental W3 trial” or “experimental W3 design*” ) )

8591

S30

TI pre w7 post or AB pre w7 post

6142

S29

MH "Multiple Time Series" or MH "Time Series"

922

S28

TI ( (comparative N2 study) or (comparative N2 studies) or “evaluation study” or "evaluation studies" ) or AB ( (comparative N2 study) or (comparative N2 studies) or “evaluation study” or "evaluation studies" )

5677

S27

MH Experimental Studies or Community Trials or Community Trials or Pretest‐Posttest Design + or Quasi‐Experimental Studies + Pilot Studies or Policy Studies + Multicenter Studies

24708

S26

TI ( "pre test*" or pretest* or posttest* or "post test*" ) or AB ( "pre test*" or pretest* or posttest* or "post test*" )

5942

S25

TI ( intervention* or multiintervention* or multi‐intervention* or postintervention* or post‐intervention* or preintervention* or pre‐intervention* ) or AB ( intervention* or multiintervention* or multi‐intervention* or postintervention* or post‐intervention* or preintervention* or pre‐intervention* )

105013

S24

(MH "Quasi‐Experimental Studies")

4258

S23

(MH "Professional Development")

10105

S22

(MH "Practice Patterns") OR (MH "Prescribing Patterns")

3110

S21

AB ( (multifacet* or multi‐facet* or multimodal* or multi‐modal* or multidisciplin* or interdisciplin* or collaborat* or shared or team‐based or team or skill‐mix or inter‐disciplin* or multi‐disciplin*) ) and AB ( (care or practice or decsion* or refer* or consult*) )

32079

S20

(MH "Education, Medical, Continuing") OR (MH "Education, Nursing, Continuing")

10047

S19

(MH "Multidisciplinary Care Team")

15543

S18

(MH "Referral and Consultation") OR (MH "Group Practice")

12699

S17

(MH "Family Practice") OR (MH "Physicians, Family") OR (MH "Primary Health Care") OR AB ("primary care" or "family physician*" or "family doctor*" or "primary health")

41203

S16

TI (caplan* or felty's or Sjogren's or still's or wissler's) N disease*

266964

S15

TI (Chondrocalcinosis or dermatomyositis or dupuytren* contracture or fibromyalgia* or Fibrositis or Fibrositides or gout or hyperostos* or lupus or Musculoskeletal or orthopedic* or orthopaedic* or osteitis or osteoarthrit* or osteoarthrop* or osteochondr* or Osteonecros* or osteoporos* or periarthriti* or polymyalgia* or raynaud disease* or rheumati* or sciatica or scleroderma* or Spondylarthrit* or sprain*)

19656

S14

(MH "Dermatomyositis") OR (MH "Musculoskeletal System+")

64039

S13

(MH "Back Pain+") OR (MH "Neck Pain")

13141

S12

(MH "Sciatica")

443

S11

(MH "Tendon Injuries+") OR (MH "Soft Tissue Injuries") OR (MH "Spinal Cord Injuries+") OR (MH "Dislocations+")

14157

S10

(MH "Multiple Trauma")

1104

S9

(MH "Dupuytren's Contracture") OR (MH "Scleroderma, Systemic+")

1057

S8

(MH "Raynaud's Disease")

299

S7

(MH "Back Injuries+") OR (MH "Arm Injuries+") OR (MH "Athletic Injuries+") OR (MH "Fractures+") OR (MH "Hand Injuries+") OR (MH "Leg Injuries+") OR (MH "Neck Injuries+") OR (MH "Sprains and Strains+")

38128

S6

(MH "Arthritis+")

19407

S5

(MH "Orthopedic Care") OR (MH "Orthopedic Surgery")

5307

S4

(MH "Orthopedics")

4192

S3

(MH "Rheumatology")

676

S2

(MH "Lupus Erythematosus, Systemic+")

2417

S1

(MH "Musculoskeletal Diseases+")

72861

Prisma study flow diagram.
Figuras y tablas -
Figure 1

Prisma study flow diagram.

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.
Figuras y tablas -
Figure 2

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.

Risk of bias summary for ITS study design: review authors' judgements about each risk of bias item for each included study.
Figuras y tablas -
Figure 3

Risk of bias summary for ITS study design: review authors' judgements about each risk of bias item for each included study.

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
Figuras y tablas -
Figure 4

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.

Risk of bias graph for ITS study design: review authors' judgements about each risk of bias item presented as percentages across all included studies.
Figuras y tablas -
Figure 5

Risk of bias graph for ITS study design: review authors' judgements about each risk of bias item presented as percentages across all included studies.

Comparison 1 Meta‐analysis of osteoporosis studies evaluating physician and patient interventions versus usual care, Outcome 1 Bone Mineral Density.
Figuras y tablas -
Analysis 1.1

Comparison 1 Meta‐analysis of osteoporosis studies evaluating physician and patient interventions versus usual care, Outcome 1 Bone Mineral Density.

Comparison 1 Meta‐analysis of osteoporosis studies evaluating physician and patient interventions versus usual care, Outcome 2 Osteoporosis medication.
Figuras y tablas -
Analysis 1.2

Comparison 1 Meta‐analysis of osteoporosis studies evaluating physician and patient interventions versus usual care, Outcome 2 Osteoporosis medication.

Comparison 2 Meta‐analysis of osteoporosis studies evaluating physician‐only interventions versus usual care, Outcome 1 Bone mineral density.
Figuras y tablas -
Analysis 2.1

Comparison 2 Meta‐analysis of osteoporosis studies evaluating physician‐only interventions versus usual care, Outcome 1 Bone mineral density.

Comparison 2 Meta‐analysis of osteoporosis studies evaluating physician‐only interventions versus usual care, Outcome 2 Osteoporosis medication.
Figuras y tablas -
Analysis 2.2

Comparison 2 Meta‐analysis of osteoporosis studies evaluating physician‐only interventions versus usual care, Outcome 2 Osteoporosis medication.

Comparison 3 Meta‐analysis of osteoporosis studies evaluating physician only interventions versus physician and patient interventions, Outcome 1 Bone mineral density.
Figuras y tablas -
Analysis 3.1

Comparison 3 Meta‐analysis of osteoporosis studies evaluating physician only interventions versus physician and patient interventions, Outcome 1 Bone mineral density.

Comparison 3 Meta‐analysis of osteoporosis studies evaluating physician only interventions versus physician and patient interventions, Outcome 2 Medication.
Figuras y tablas -
Analysis 3.2

Comparison 3 Meta‐analysis of osteoporosis studies evaluating physician only interventions versus physician and patient interventions, Outcome 2 Medication.

Summary of findings for the main comparison. Primary care physician alerting system and a patient‐directed intervention (education and reminder to see their primary care physician) compared to standard care for osteoporosis management

Primary care physician alerting system and a patient‐directed intervention (education and reminder to see their primary care physician) compared to usual care for osteoporosis management

Patient or population: General practitioners/family doctors involved in the management of patients with osteoporosis
Settings: Primary care
Intervention: Primary care physician alerting system and a patient‐directed intervention (education and reminder to see their primary care physician)
Comparison: Usual care

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of Participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Usual care

A physician alerting system and a patient‐directed intervention (education and reminder to see their primary care physician)

Bone Mineral Density 1
Follow‐up: 6‐12 months

Study population

RR 4.44
(3.54 to 5.55)

3386
(3 studies)

⊕⊕⊕⊕
high3

49 per 1000

220 per 1000
(124 to 390)

Moderate

39 per 1000

176 per 1000
(99 to 311)

Osteoporosis medication 2
Follow‐up: 6‐12 months

Study population

RR 1.71
(1.50 to 1.94)

4223
(5 studies)

⊕⊕⊕⊕
high3

131 per 1000

241 per 1000 3
(193 to 301)

Moderate

106 per 1000

195 per 1000 3
(156 to 244)

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: Confidence interval; RR: Risk ratio;

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1 Bone mineral density (BMD) testing is an important outcome for osteoporosis because it leads to the diagnosis of the condition. This is one of the GP behaviour‐related outcomes (primary outcome)

2 Osteoporosis medication prescribing is an important outcome for osteoporosis management as it is the main aspect of treatment. This is one of the GP behaviour‐related outcomes (primary outcome)

3 One of the five studies (Roux 2013) had two intervention comparison groups which were combined to create a single pair‐wise comparison as recommended in chapter 16.5.4 of the Cochrane Handbook.

Figuras y tablas -
Summary of findings for the main comparison. Primary care physician alerting system and a patient‐directed intervention (education and reminder to see their primary care physician) compared to standard care for osteoporosis management
Summary of findings 2. Primary care physician alerting system compared to usual care for osteoporosis management

Primary care physician alerting system compared to usual care for osteoporosis management

Patient or population: General practitioners/family doctors involved in the management of patients with osteoporosis
Settings: Primary care
Intervention: Primary care physician alerting system
Comparison: Usual care

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of Participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Usual care

Primary care physician alerting system

Bone mineral density1
Follow‐up: 6‐12 months

Study population

RR 4.75
(3.62 to 6.24)

3047
(2 studies)

⊕⊕⊕⊖
Moderate3

38 per 1000

302 per 1000
(64 to 1000)

Moderate

29 per 1000

231 per 1000
(49 to 1000)

Osteoporosis medication2
Follow‐up: 6‐12 months

Study population

RR 1.52
(1.26 to 1.84)

3047
(2 studies)

⊕⊕⊕⊖
Moderate3

102 per 1000

268 per 1000
(67 to 1000)

Moderate

77 per 1000

202 per 1000
(50 to 809)

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: Confidence interval; RR: Risk ratio;

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1 Bone mineral density (BMD) testing is an important outcome for osteoporosis because it leads to the diagnosis of the condition. This is one of the GP behaviour‐related outcomes (primary outcome)

2 Osteoporosis medication prescribing is an important outcome for osteoporosis management as it is the main aspect of treatment. This is one of the GP behaviour‐related outcomes (primary outcome)

3 The quality of evidence was downgraded because only two studies were included, one of which had a small number of participants and events, and in view of the considerable statistical heterogeneity observed.

Figuras y tablas -
Summary of findings 2. Primary care physician alerting system compared to usual care for osteoporosis management
Summary of findings 3. Primary care physician alerting system compared to primary care physician alerting system and a patient‐directed intervention (education and reminder to see their primary care physician) for osteoporosis management

Primary care physician alerting system compared to Primary care physician alerting system and a patient‐directed intervention (education and reminder to see their primary care physician) for osteoporosis management

Patient or population: General practitioners/family doctors involved in the management of patients with osteoporosis
Settings: Primary care
Intervention: Primary care physician alerting system
Comparison: Primary care physician alerting system and a patient‐directed intervention (education and reminder to see their primary care physician)

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of Participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Primary care physician alerting system and a patient‐directed intervention (education and reminder to see their primary care physician)

Primary care physician alerting system

Bone mineral density1
Follow‐up: 6‐12 months

Study population

RR 0.94

(0.81 to 1.09)

2995
(2 studies)

⊕⊕⊕⊖
moderate3

192 per 1000

194 per 1000
(123 to 261)

Moderate

254 per 1000

257 per 1000
(163 to 345)

Medication2

Follow‐up: 6‐12 months

Study population

RR 0.93
(0.79 to 1.10)

2995
(2 studies)

⊕⊕⊕⊖

moderate3

167 per 1000

176 per 1000
(115 to 264)

Moderate

182 per 1000

191 per 1000
(126 to 288)

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: Confidence interval; RR: Risk ratio;

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1 Bone mineral density (BMD) testing is an important outcome for osteoporosis because it leads to the diagnosis of the condition. This is one of the GP behaviour‐related outcomes (primary outcome)

2 Osteoporosis medication prescribing is an important outcome for osteoporosis management as it is the main aspect of treatment. This is one of the GP behaviour‐related outcomes (primary outcome)

3 The quality of evidence was downgraded because only two studies were included, one of which had a small number of participants and events.

Figuras y tablas -
Summary of findings 3. Primary care physician alerting system compared to primary care physician alerting system and a patient‐directed intervention (education and reminder to see their primary care physician) for osteoporosis management
Summary of findings 4. Osteoporosis studies: Summary of findings

Professional interventions for GPs on the management of osteoporosis compared to usual care

Patient or population: General practitioners/family doctors involved in the management of patients with osteoporosis

Settings: Primary care

Intervention: Professional interventions (targeting physician‐only)

Comparison: Usual care

Outcomes

Impact (including effect sizes wherever available)

Number of Participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Health professional (GP) behaviour‐related outcomes

  • Bone Mineral Density (BMD) testing

  • Osteoporosis medication (appropriate prescribing)

  • BMD RR 4.75 (95% CI 3.62 to 6.24)

  • Osteoporosis medication RR 1.52 (95% CI 1.26 to 1.84)

  • BMD 3047 (2 studies)

  • Osteoporosis medication 3047 (2 studies)

  • BMD ⊕⊕⊕⊖ moderate1

  • Osteoporosis ⊕⊕⊕⊖ moderate1

Patient outcomes

  • Fragility fractures

  • Hospitalisation

None of the included studies assessed these outcomes

Economic outcomes

  • Health service costs (including prescribing costs)

  • Cost effectiveness

Majumdar 2007, assessed the cost effectiveness of the study Majumdar 2008, and concluded that the intervention led to a per patient cost saving of CAD 13 (USD 9) and a gain of 0.012 quality‐adjusted life years.

272 participants (1 study)

⊕⊕⊖⊖ low2

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: Confidence Interval; RR: Risk Ratio

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1The quality of evidence was downgraded because only two studies were included, one of which had a small number of participants and events, and in view of the considerable statistical heterogeneity observed.

2 The quality of evidence was downgraded because only one study was included which had some risk of bias.

Figuras y tablas -
Summary of findings 4. Osteoporosis studies: Summary of findings
Summary of findings 5. Low back pain studies: Summary of findings

Professional interventions for GPs on the management of low back pain compared to usual care

Patient or population: General practitioners/family doctors involved in the management of patients with low back pain

Settings: Primary care

Intervention: Professional interventions (targeting physician‐only)

Comparison: Usual care

Outcomes

Impact (including effect sizes wherever available)

No of studies

Certainty of the evidence
(GRADE)

Comments

H ealth professional (GP) behaviour‐related outcomes

Guideline‐consistent advice during consultation

Bishop 2006 showed that the intervention may result in little or no improvements (RD < 10%) with regard to guideline‐consistent advice about exercise, return to work and education and reassurance.

Dey 2004 showed that the intervention probably results in a small reduction of sickness certification (RD 1.3).

Engers 2005 showed that the intervention may lead to no improvement of GP behaviour with regards to patient education and advice during the consultation (RD range (‐1.3 to 12.8), authors reported OR ranging between 0.4 and 2.9).

3

⊕⊕⊖⊖ low1

Guideline‐consistent prescribing of medication

Bishop 2006 showed that the intervention may lead to little improvements (RD < 10%) with regards to guideline‐consistent medication prescribing.

Dey 2004 showed that the intervention probably results in no difference on prescribing rates of opioids (RD ‐1.3).

Engers 2005 showed that the intervention may result in no improvement of GP behaviour with regard to prescribing (RD=2.8, OR=1, 95% CI (0.3 to 3), reported as not statistically significant).

3

⊕⊕⊖⊖ low1

Guideline‐consistent referrals for investigations (e.g.. x‐rays)

Schectman 2003 showed that the intervention may result in little or no change in GP behaviour with regards to the number of guideline‐consistent referrals for lumbar spine x‐rays and CT scans (RD <5%).

1

⊕⊕⊖⊖ low2

Guideline‐consistent referrals to other services

Bishop 2006 showed that the intervention may lead to little or no improvements (RD < 5%) with regards to guideline‐consistent referral to other services (such as physiotherapy).

Schectman 2003 showed that the intervention may result in little or no difference with regards to the number of guideline‐consistent specialist or physiotherapy referrals (RD <5%).

2

⊕⊕⊖⊖ low3

Number of investigations

Dey 2004 showed that the intervention probably results in a small increase in the ordering of x‐rays (RD 1.4).

French 2013 showed that the intervention may lead to little or no difference in the number of x‐ray and CT requests (RD ‐0.2% and 0.0% respectively).

Kerry 2000 showed that the intervention probably results in a cluster‐adjusted reduction of spinal x‐ray requests of 20% between the intervention and control groups (95% CI 4 to 36, P<0.05).

Schectman 2003 showed that the intervention may result in little or no change in GP behaviour with regards to referrals for lumbar spine x‐rays and CT scans (RD <5%).

4

⊕⊕⊖⊖low4

Number of referrals to other services

Dey 2004 showed that the intervention probably results in increased referrals to fast‐track physiotherapy and a back‐pain triage service (RD 12.6%).

Engers 2005 showed that the intervention may lead to little reduction of onward referrals to a therapist (RD 4.6, 23% in the intervention group versus 28% in the control group, clustered adjusted OR 0.8, 95% CI (0.5 to 1.4)).

Schectman 2003 showed that the intervention may result in little or no difference with regards to the number of specialist or physiotherapy referrals (RD <5%).

3

⊕⊕⊖⊖ low4

Patient outcomes

Functional capacity/activity scores

0

None of the included studies assessed this outcome

Pain control

0

None of the included studies assessed this outcome

Work absence

Hazard 1997 showed that the intervention may result in no improvement with respect to days of sick leave compared to the control group (RD ‐4.6%).

1

⊕⊕⊖⊖ low2

The study by Hazard 1997 was very small (just 53 participants)

Quality of life

0

None of the included studies assessed this outcome

Economic outcomes

  • Health service costs (including prescribing costs)

  • Cost effectiveness

0

None of the included studies assessed these outcomes

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
RD: Risk Difference SMD: Standardised Mean Difference CI: Confidence Interval; RR: Risk Ratio

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1 The quality of evidence was downgraded because the studies have a high risk of bias and high heterogeneity in terms of the types of interventions evaluated. Additionally the effect sizes are small.

2 The quality of evidence was downgraded because the results are based only on one study with high risk of bias.

3 The quality of evidence was downgraded because the results are based on just two studies with high risk of bias.

4 The quality of evidence was downgraded because the studies have a high risk of bias and high heterogeneity in terms of the types of interventions evaluated. Additionally there is high inconsistency in the direction of effects across the studies.

Figuras y tablas -
Summary of findings 5. Low back pain studies: Summary of findings
Summary of findings 6. Osteoarthritis studies: Summary of findings

Professional interventions for GPs on the management of osteoarthritis compared to usual care

Patient or population: General practitioners/family doctors involved in the management of patients with osteoarthritis

Settings: Primary care

Intervention: Professional interventions (targeting physician‐only)

Comparison: Usual care

Outcomes

Impact (including effect sizes wherever available)

No of studies

Certainty of the evidence
(GRADE)

Comments

Health professional (GP) behaviour‐related outcomes

Guideline‐consistent advice during consultation

Stross 1985 showed that the intervention may increase the use of intra‐articular corticosteroids (RD large at 29%).

⊕⊕⊖⊖ low1

Guideline‐consistent prescribing of medication

Rahme 2005 showed that the intervention may result in a slight improvement in osteoarthritis guideline‐consistent GP prescribing of medication (acetaminophen, NSAIDs and COX‐2 inhibitors) 5 months afterwards (RD 5% after dissemination of educational material, RD 7% after a workshop and RD 13% for the combined intervention)

Rosemann 2007 showed that prescriptions for painkillers may slightly increase following the intervention (RDs between ‐2.2% and 11.1%).

Stross 1985 showed that the intervention may reduce the use of systemic corticosteroids according to the guidelines (RD moderate at 19%).

⊕⊕⊖⊖ low1

Guideline‐consistent referrals for investigations (e.g.. x‐rays)

None of the included studies assessed this outcome

Guideline‐consistent referrals to other services

Stross 1985 showed that the intervention may increase the utilisation of physical therapy pre‐operatively (RD large at 57%).

⊕⊕⊖⊖ low1

Number of investigations

Rosemann 2007 showed that the intervention may result in some small reduction in the number of GP referrals for radiographs (SMD 0.2‐0.4).

⊕⊕⊖⊖low3

Number of referrals to other services

Rosemann 2007 showed that the intervention may result in a reduction in the number of GP referrals to orthopaedics (SMD 0.8 for the educational intervention and 0.2 for the combined intervention after adding nurse case management).

⊕⊕⊖⊖ low4

Patient outcomes

Functional capacity/activity scores

Chassany 2006 showed that the intervention may result in small improvements with regard to physical function scores (WOMAC index physical function score) (SMD 0.3, P<0.05).

⊕⊕⊖⊖ low5

Results were assessed within two weeks of the Chassany 2006 trial, so it is unclear whether the positive patient outcomes persisted.

Pain control

Chassany 2006 showed that the intervention may result in small improvements with regard to pain scores (VAS score, Pain relief (SPID), WOMAC index pain score) (SMD 0.2, P<0.05 across all outcomes).

⊕⊕⊖⊖ low5

Results were assessed within two weeks of the Chassany 2006 trial, so it is unclear whether the positive patient outcomes persisted.

Work absence

None of the included studies assessed this outcome

Quality of life

Rosemann 2007 showed that the intervention may result in small or no improvement with regard to patient related outcomes (SMD <0.40).

⊕⊕⊖⊖ low3

Economic outcomes

  • Health service costs (including prescribing costs)

  • Cost effectiveness

None of the included studies assessed these outcomes

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
RD: Risk Difference SMD: Standardised Mean Difference CI: Confidence Interval; RR: Risk Ratio

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1 The quality of evidence was downgraded because the results are based on one study only with high risk of bias and a small number of participants (114).

2 The quality of evidence was downgraded because the studies have high heterogeneity in terms of the types of interventions and the types of medications prescribed.

3 The quality of evidence was downgraded because the results are based on just one study and the effect size was small.

4 The quality of evidence was downgraded because the results are based on just one study and the effect size varies considerably between the two intervention groups.

5 The quality of evidence was downgraded because the results are based on just one study and were assessed just 2 weeks following the intervention.

NSAIDs: Non steroidal anti‐inflammatory drugs, COX‐2 inhibitors: Cyclo‐oxygenase 2 inhibitors, WOMAC: Western Ontario and McMaster Universities Osteoarthritis Index, VAS: Visual analogue scale, SPID: sum of pain intensity differences.

Figuras y tablas -
Summary of findings 6. Osteoarthritis studies: Summary of findings
Summary of findings 7. Shoulder pain studies: Summary of findings

Professional interventions for GPs on the management of shoulder pain compared to usual care

Patient or population: General practitioners/family doctors involved in the management of patients with shoulder pain

Settings: Primary care

Intervention: Professional interventions (targeting physician‐only)

Comparison: Usual care

Outcomes

Impact (including effect sizes wherever available)

Number of studies

Certainty of the evidence
(GRADE)

Comments

Health professional (GP) behaviour‐related outcomes

Guideline‐consistent advice during consultation

None of the included studies assessed this outcome

Guideline‐consistent prescribing of medication

None of the included studies assessed this outcome

Guideline‐consistent referrals for investigations (e.g.. x‐rays)

None of the included studies assessed this outcome

Guideline‐consistent referrals to other services

None of the included studies assessed this outcome

Number of investigations

Broadhurst 2007 showed that the intervention may result in a temporary, slight reduction in ultrasound requests, but little or no change in the x‐ray requests.

⊕⊕⊖⊖ low1

Number of referrals to other services

None of the included studies assessed this outcome

Patient outcomes

Functional capacity/activity scores

Watson 2008 showed that the intervention may result in little or no improvement in function a year later (BSDQ SMD 0.2, SF‐36 for physical component SMD 0 and SF‐36 mental component SMD 0.1)

⊕⊕⊖⊖ low2

Pain control

None of the included studies assessed this outcome

Work absence

None of the included studies assessed this outcome

Quality of life

None of the included studies assessed this outcome

Economic outcomes

  • Health service costs (including prescribing costs)

  • Cost effectiveness

McKenna 2009 assessed the cost effectiveness of providing practical training to GPs in the SAPPHIRE study by Watson 2008. It reported an incremental cost‐effectiveness ratio of GBP 2,813 per QALY gained for trained GPs.

⊕⊕⊖⊖ low2

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
RD: Risk Difference SMD: Standardised Mean Difference CI: Confidence Interval; RR: Risk Ratio

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1 The quality of evidence was downgraded because the results are based on just one study (CBA) with high risk of bias.

2 The quality of evidence was downgraded because the results are based on just one study and the effect size was small.

BSDQ: British Shoulder Disability questionnaire, SF‐36: Short‐form 36 item Health Survey, GBP: Great Britain Pound

Figuras y tablas -
Summary of findings 7. Shoulder pain studies: Summary of findings
Summary of findings 8. Studies on other musculoskeletal conditions: Summary of findings

Professional interventions for GPs on the management of shoulder pain compared to usual care

Patient or population: General practitioners/family doctors involved in the management of patients with other musculoskeletal conditions

Settings: Primary care

Intervention: Professional interventions (targeting physician‐only)

Comparison: Usual care

Outcomes

Impact (including effect sizes wherever available)

No of studies

Certainty of the evidence
(GRADE)

Comments

Health professional (GP) behaviour‐related outcomes

Guideline‐consistent advice during consultation

None of the included studies assessed this outcome

Guideline‐consistent prescribing of medication

Huas 2006 showed that the intervention may result in increased level 3 (WHO classification) analgesic prescribing (SMD 1.2, P=0.02)

⊕⊕⊖⊖ low1

Guideline‐consistent referrals for investigations (e.g.. x‐rays)

None of the included studies assessed this outcome

Guideline‐consistent referrals to other services

None of the included studies assessed this outcome

Number of investigations

Kerry 2000 showed that the intervention may result in little or no reduction in GP knee radiology requests (relative change 10%, not statistically significant).

⊕⊕⊖⊖ low2

Number of referrals to other services

None of the included studies assessed this outcome

Patient outcomes

Functional capacity/activity scores

None of the included studies assessed this outcome

Pain control

Huas 2006 showed that the intervention may result in worse patient‐related outcomes: pain relief scores (SMD 2, P=0.0004)

⊕⊕⊖⊖ low1

Work absence

None of the included studies assessed this outcome

Quality of life

None of the included studies assessed this outcome

Economic outcomes

  • Health service costs (including prescribing costs)

  • Cost effectiveness

None of the included studies assessed these outcomes

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
RD: Risk Difference SMD: Standardised Mean Difference CI: Confidence Interval; RR: Risk Ratio

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1 The quality of evidence was downgraded because the results are based on just one study with high risk of bias.

2 The quality of evidence was downgraded because the results are based on just one study and the effect size was small.

Figuras y tablas -
Summary of findings 8. Studies on other musculoskeletal conditions: Summary of findings
Table 1. Classification of relevant interventions from EPOC taxonomy

Table 1: Classification of relevant interventions from EPOC taxonomy

Intervention

Description

Distribution of educational materials

Distribution of published or printed recommendations for clinical care, including clinical practice guidelines, audio‐visual materials and electronic publications.  The materials may have been delivered personally or through mass mailings.

Educational meetings 

Healthcare providers who have participated in conferences, lectures, workshops or traineeships

Local consensus processes

Inclusion of participating providers in discussion to ensure that they agreed that the chosen clinical problem was important and the approach to managing the problem was appropriate

Educational outreach visits 

Use of a trained person who met with providers in their practice settings to give information with the intent of changing the provider’s practice.  The information given may have included feedback on the performance of the provider(s)

Local opinion leaders

Use of providers nominated by their colleagues as ‘educationally influential’.  The investigators must have explicitly stated that their colleagues identified the opinion leaders

Patient‐mediated

New clinical information (not previously available) collected directly from patients and given to the provider e.g. depression scores from an instrument

Audit and feedback 

Any summary of clinical performance of health care over a specified period of time. The summary may also have included recommendations for clinical action. The information may have been obtained from medical records, computerised databases, or observations from patients

Reminders 

Patient or encounter specific information, provided verbally, on paper or on a computer screen, which is designed or intended to prompt a health professional to recall information.  This would usually be encountered through their general education; in the medical records or through interactions with peers, and so remind them to perform or avoid some action to aid individual patient care.  Computer aided decision support and drugs dosage are included.

Marketing

Use of personal interviewing, group discussion (‘focus groups’), or a survey of targeted providers to identify barriers to change and subsequent design of an intervention that addresses identified barriers

Mass media

(i) Varied use of communication that reached great numbers of people including television, radio, newspapers, posters, leaflets, and booklets, alone or in conjunction with other interventions;  (ii) Targeted at the population level

Other

Patient‐directed (education and reminders to see their primary care physician)

Figuras y tablas -
Table 1. Classification of relevant interventions from EPOC taxonomy
Table 2. Intervention types used in each study (N.B. All interventions evaluated were professional)

Table 2. Intervention types used in each study (N.B. All interventions evaluated were professional)

Intervention methods 1,2 

No. of Studies 

Studies 3

Distribution of educational materials

27

Becker 2008; Bessette 2011; Bishop 2006; Boyd 2002; Broadhurst 2007; Chassany 2006; Ciaschini 2010; Cranney 2008; Dey 2004; Eccles 2001; Engers 2005; Feldstein 2006; French 2013; Hazard 1997; Hollingworth 2002; Kerry 2000; Leslie 2012; Majumdar 2008; Rahme 2005; Robling 2002; Rosemann 2007; Roux 2013; Rozental 2008; Schectman 2003; Solomon 2007a; Stross 1985; Watson 2008

Educational meetings 

10

Becker 2008; Chassany 2006; Engers 2005; French 2013; Gormley 2003; Huas 2006; Rahme 2005; Rosemann 2007; Schectman 2003, Watson 2008

Local consensus processes

0

Educational outreach visits 

6

Becker 2008; Broadhurst 2007; Dey 2004; Robling 2002; Schectman 2003; Solomon 2007a

Local opinion leaders

3

Majumdar 2008; Stross 1985; Schectman 2003

Patient‐mediated

6

Boyd 2002; Ciaschini 2010; Cranney 2008; Huas 2006; Roux 2013; Rozental 2008

Audit and feedback 

4

Eccles 2001; Kerry 2000; Robling 2002; Schectman 2003

Reminders 

11

Bishop 2006; Ciaschini 2010; Cranney 2008; Eccles 2001; Feldstein 2006; Hazard 1997; Lafata 2007; Leslie 2012; Majumdar 2008; Roux 2013; Rozental 2008

Marketing

0

Mass media

0

Patient‐directed4

12

Becker 2008; Bessette 2011; Bishop 2006; Leslie 2012; Ciaschini 2010; Cranney 2008; Feldstein 2006; Lafata 2007; Majumdar 2008; Rosemann 2007; Roux 2013; Solomon 2007a

1. Category of intervention as classified by the EPOC taxonomy EPOC 2007 [9]

2. See Table 1 for definition of each intervention

3. Some studies used more than one intervention type and these are listed against their corresponding category

4. Patient‐directed interventions targeted patients and included patient education and reminders to see their primary‐care physician. These were included in the review only if they were a component of a professional intervention targeting primary‐care physicians

Figuras y tablas -
Table 2. Intervention types used in each study (N.B. All interventions evaluated were professional)
Table 3. Intervention combinations compared to a no‐intervention control group

Table 3. Intervention combinations compared to a no‐intervention control group

Intervention combinations 

No. of comparisons

Study ID

Single component interventions:

Distribution of educational materials

1

Rahme 2005

Patient‐directed

3

Lafata 2007; Leslie 2012; Solomon 2007a

Educational meetings, workshops  

1

Rahme 2005

Multifaceted interventions: Two intervention components

Distribution of educational material + reminders

4

Bishop 2006; Feldstein 2006; Hazard 1997; Leslie 2012

Distribution of educational material + educational outreach visits

4

Broadhurst 2007; Chassany 2006; Dey 2004; Solomon 2007a

Distribution of educational material + educational meeting/workshop

6

Chassany 2006; Engers 2005; French 2013; Rahme 2005; Rosemann 2007; Watson 2008

Distribution of educational material + local opinion leaders

1

Stross 1985

Distribution of educational material + audit/feedback

1

Kerry 2000

Patient‐mediated + educational meeting/workshop

1

Huas 2006

Patient‐directed +reminder

1

Lafata 2007

Patient‐directed + educational material

1

Bessette 2011

Multifaceted interventions: Three intervention components

Patient‐directed + educational material + reminder

3

Bishop 2006; Feldstein 2006, Leslie 2012

Patient‐directed + educational material + educational meeting/workshop

1

Rosemann 2007

Patient‐directed + educational material + educational outreach visit

1

Solomon 2007a

Multifaceted interventions: Four intervention components

Patient‐directed + distribution of educational material + reminder + local opinion leaders

1

Majumdar 2008

Patient‐mediated + distribution of educational material + reminders + patient‐directed (education and reminders)

3

Ciaschini 2010; Cranney 2008; Roux 2013

Multifaceted interventions: Five intervention components

Distribution of educational material + educational meetings/workshops + audit + educational outreach visit + local opinion leaders

1

Schectman 2003

Figuras y tablas -
Table 3. Intervention combinations compared to a no‐intervention control group
Table 4. Intervention combinations compared to a different intervention

Table 4. Intervention combinations compared to a different intervention

Intervention combinations 

No. of comparisons

Study ID

Single component interventions:

Educational meetings/workshops vs distribution of educational material

1

Rahme 2005

Educational meetings/workshops vs a different educational meeting/workshop

1

Gormley 2003

Multifaceted interventions: Two intervention components

Distribution of educational material + patient‐mediated vs the same intervention but less intensive

1

Boyd 2002

Distribution of educational material + educational outreach visit vs distribution of educational material

1

Robling 2002

Distribution of educational material + audit vs distribution of educational material

2

Robling 2002; Eccles 2001

Distribution of educational material + audit vs distribution of educational material + reminder

1

Eccles 2001

Distribution of educational material + outreach vs distribution of educational material + audit

1

Robling 2002

Distribution of educational material + educational outreach visit vs patient‐directed

1

Solomon 2007a

Distribution of educational material + patient‐directed vs the same (more intensive)

1

Bessette 2011

Patient‐directed + reminder vs patient‐directed

1

Lafata 2007

Distribution of educational material + reminder vs distribution of educational material

1

Eccles 2001

Distribution of educational material + reminder vs patient‐mediated

1

Rozental 2008

Distribution of educational material + educational meeting/workshop vs educational meeting/workshop

1

Rahme 2005

Distribution of educational material + educational meeting/workshop vs distribution of educational material

1

Rahme 2005

Multifaceted interventions: Three intervention components

Distribution of educational material + reminders + patient‐directed vs distribution of educational material + reminders

2

Bishop 2006; Feldstein 2006

Distribution of educational material + reminder + patient‐directed vs patient‐directed

1

Leslie 2012

Distribution of educational material + audit + reminders vs distribution of educational material

1

Eccles 2001

Distribution of educational material + audit + reminders vs distribution of educational material + audit

1

Eccles 2001

Distribution of educational material + audit + reminders vs distribution of educational material + reminders

Eccles 2001

Distribution of educational material + audit + outreach vs distribution of educational material + outreach

1

Robling 2002

Distribution of educational material + audit + outreach vs distribution of educational material + audit

1

Robling 2002

Distribution of educational material + audit + outreach vs distribution of educational material

1

Robling 2002

Distribution of educational material + educational meetings/workshops + educational outreach visits vs distribution of educational material

1

Becker 2008

Distribution of educational material + educational outreach visit + patient‐directed vs patient‐directed

1

Solomon 2007a

Distribution of educational material + educational outreach visit + patient‐directed vs distribution of educational material + educational outreach visit

1

Solomon 2007a

Distribution of educational material + educational meeting/workshop + patient‐directed vs distribution of educational material + educational meeting/workshop

1

Rosemann 2007

Multifaceted interventions: Four intervention components

Distribution of educational material + educational meetings/workshops + educational outreach visits + patient‐directed vs distribution of educational material

1

Becker 2008

Distribution of educational material + educational meetings/workshops +educational outreach visits + patient directed vs distribution of educational material + educational meetings/workshops + educational outreach visits

1

Becker 2008

Patient‐mediated + distribution of education material + reminders + patient‐directed (education and reminders) vs patient‐mediated + distribution of education material + reminders + patient‐directed (education and reminders)

1

Roux 2013

Figuras y tablas -
Table 4. Intervention combinations compared to a different intervention
Table 5. Osteoporosis studies: intervention versus no intervention (control), outcome: BMD, dichotomous data

(Study)

Intervention

Int pre (%) 1

C pre (%)2

Int post (%)3

C post (%)4

ARD 5

Risk difference 6

(P value if reported by authors)

Relative % change post 7

Risk ratio 8

(Bessette 2011)*

Patient education and reminder to see their physician (patient directed), education of physician via the patient (distribution of educational material)

14.72%

11.96%

2.8%

23%

1.2

(Bessette 2011)*

Patient education (including video on osteoporosis) and reminder to see their physician, education of physician via the patient (distribution of educational material)

15.81%

11.96%

3.9%

32%

1.3

(Cranney 2008)**

Patient‐specific mailed letter to primary are physician (including guidelines) and patient education and reminder

64/125 (51%)

36/145 (25%)

26.4%

(P< 0.0001)

106%

2.1

(Feldstein 2006)

Patient‐specific Electronic Medical Record (EMR) reminders to primary‐care provider informing them of patient increased risk and guidelines. Sent twice.

40/101 (39.6%)

2/103 (1.9%)

37.7%

(P< 0.01)

1940%

20.4

(Feldstein 2006)

EMR reminder plus patient‐directed intervention: education and reminder

36/110 (32.7%)

2/103 (1.9%)

30.8%

(P< 0.01)

1585%

16.9

(Lafata 2007)**

Patient‐directed: 2 mailings (educational and reminders)

720/3367 (21.4%)

313/2901 (10.8%)

10.6%

(P< 0.001)

98%

2

(Lafata 2007)**

Physician prompt: Electronic Medical Record (EMR) reminder to physician and biweekly mailing plus patient‐directed: 2 mailings (educational and reminders)

1181/4086 (28.9%)

313/2901 (10.8%)

18.1%

(P< 0.001)

168%

2.7

(Leslie 2012)

Physician reminder plus educational material

224/1363 (16.4%)

58/1480 (3.9%)

12.5%

319%

4.2

(Leslie 2012)

Physician reminder plus educational material plus patient‐directed intervention (reminder to see their physician)

258/1421 (18.2%)

58/1480 (3.9%)

14.2%

363%

4.6

(Majumdar 2008)

Patient education, physician patient‐specific reminders by mail/fax, physician guidelines endorsed by opinion leaders

71/137 (51.8%)

24/135 (17.8%)

34%

(P< 0.001)

192%

2.9

(Solomon 2007a)**

Patient directed (3 mailed letters educational)

249/3274 (7.6%)

224/3268 (6.9%)

0.8%

(NS)

11%

1.1

(Solomon 2007a)**

Physician education following an academic‐detailing approach

183/3574 (5.1%)

224/3268 (6.9%)

‐1.7%

(NS)

‐25%

0.7

(Solomon 2007b)**

Combination of both physician and patient education

223/3339 (6.7%)

224/3268 (6.9%)

‐0.2%

(NS)

‐3%

1

1. Intervention group pre‐intervention proportion

2. Control group pre‐intervention proportion

3. Intervention group post‐intervention proportion

4. Control group post‐intervention proportion

5. ARD = [Int post (%) minus C post (%)] minus [Int pre (%) minus C pre (%)]. The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

6. Risk Difference (RD) is the absolute % change post‐intervention = Int post (%) minus C post (%). This is considered to be "small" if ≤ 5%, "modest" if > 5% and ≤10%,"moderate" if > 10% but ≤ 20%, and "large" if > 20%.The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

7. Relative % change post = absolute % change post divided by C post (%). The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

8. Risk ratio (RR) = Int post (%) divided by C post (%)

BMD: bone mineral density; C: control group; Int: intervention group; ARD: adjusted risk difference; NS: not significant

* In the study by Bessette 2011, the outcomes reported above include the participants with a diagnosis following the intervention. The women were considered "diagnosed" if they received a BMD test, if they were informed by their physician that they were suffering from osteoporosis and/or if they were initiated on osteoporosis medication. Therefore, the above percentages do not necessarily mean that the women received a BMD test.

** The data reported above for the studies by Cranney 2008, Lafata 2007 and Solomon 2007b does not account for clustering. We did not have access to sufficient information to adjust the data for clustering.

Figuras y tablas -
Table 5. Osteoporosis studies: intervention versus no intervention (control), outcome: BMD, dichotomous data
Table 6. Osteoporosis studies, intervention versus no intervention (control), outcome:osteoporosis medication, dichotomous data

(Study)

Intervention

Int pre (%) 1

C pre (%)2

Int post (%)3

C post (%)4

ARD 5

Risk difference 6

(P value if reported by authors)

Relative % change post 7

Risk ratio 8

(Bessette 2011)

Patient education (patient directed), education of physician via the patient (for group of patients without diagnosis or treatment at randomisation)

11.79%

7.78%

4%

52%

1.5

(Bessette 2011)

Patient education (including video on osteoporosis), education of physician via the patient (for group of patients without diagnosis or treatment at randomisation)

10.64%

7.78%

2.9%

37%

1.4

(Bessette 2011)

Patient education (patient directed), education of physician via the patient (for group of patients without treatment at randomisation)

13.49%

10.31%

3.2%

31%

1.3

(Bessette 2011)

Patient education (including video on osteoporosis), education of physician via the patient (for group of patients without treatment at randomisation)

12.71%

10.31%

2.4%

23%

1.2

(Bessette 2011)

Patient education, education of physician via the patient where the patient did pass the information on to the physician (for group of patients without treatment at randomisation)

15%

10%

5%

50%

1.5

(Ciaschini 2010)

Patient‐specific evidence‐based recommendations targeted to improve osteoporosis treatment to both the patients and their primary‐care providers

29/52 (55.8%)

16/60 (26.7%)

29.1%

109%

2.1

(Cranney 2008)*

Patient‐specific mailed letter to primary are physician (including guidelines) and patient education and reminder

35/125 (28%)

15/145 (10.3%)

17.7%

(P=0.0002)

171%

2.7

(Feldstein 2006)

Patient‐specific Electronic Medical Record (EMR) reminders to primary‐care provider informing them of patient increased risk and guidelines. Sent twice.

28/101 (27.7%)

5/103 (5%)

22.9%

(P< 0.01)

471%

5.7

(Feldstein 2006)

EMR reminder plus patient‐directed intervention: education and reminder

22/110 (20.2%)

5/103 (5%)

15.1%

(P< 0.01)

312%

4.1

(Lafata 2007)*

Patient‐directed: x2 mailings (educational and reminders)

11/128 (8.6%)

3/51 (5.9%)

2.7%

46%

1.5

(Lafata 2007)*

Physician prompt: Electronic Medical Record (EMR) reminder to physician and biweekly mailing plus Patient‐directed: 2 mailings (educational and reminders)

15/162 (9.3%)

3/51 (5.9%)

3.4%

57%

1.6

(Leslie 2012)

Physician reminder plus educational material

200/1363 (14.7%)

157/1480 (10.6%)

4.1%

38%

1.4

(Leslie 2012)

Physician reminder plus educational material plus patient‐directed intervention (reminder to see their physician)

234/1421 (16.5%)

157/1480 (10.6%)

5.9%

55%

1.6

(Majumdar 2008)

Patient education, physician patient‐specific reminders by mail/fax, physician guidelines endorsed by opinion leaders

30/137 (21.9%)

10/135 (7.4%)

14.5%

(P<0.001)

196%

3

(Roux 2013)

Verbal and written information on osteoporosis to patient and letter with specific management plan sent to their treating physician. Patient reminders at 6 and 12 months. Reminder to physician if patient untreated at 6 months

82/275 (29.8%)

45/199 (22.6%)

151/275 (54.9%)

71/199 (35.7%)

12%

19.2%

(P< 0.005)

54%

1.5

(Roux 2013)

Verbal and written information on osteoporosis to patient and letter with specific management plan sent to their treating physician. Blood tests and BMD test ordered for patient and results sent to the physician. Patient reminders at 4,8 and 12 months and physician reminders at 4 and 8 months if patient remained untreated

65/251 (25.9%)

45/199 (22.6%)

156/251

(62.2%)

71/199 (35.7%)

23.2%

26.5%

(P< 0.005)

74%

1.7

(Solomon 2007a)*

Patient directed (x3 mailed letters educational)

208/3274 (6.4%)

231/3268 (7.1%)

‐0.7%

‐10%

0.9

(Solomon 2007a)*

Physician education following an academic detailing approach

197/3574 (5.5%)

231/3268 (7.1%)

‐1.6%

‐22%

0.8

(Solomon 2007a)*

Combination of both physician and patient education

236/3339 (7.1%)

231/3268 (7.1%)

0

0

1

1. Intervention group pre‐intervention proportion

2. Control group pre‐intervention proportion

3. Intervention group post‐intervention proportion

4. Control group post‐intervention proportion

5. ARD = [Int post (%) minus C post (%)] minus [Int pre (%) minus C pre (%)]. The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

6. Risk Difference (RD) is the absolute % change post‐intervention = Int post (%) minus C post (%). This is considered to be "small" if ≤ 5%, "modest" if > 5% and ≤10%,"moderate" if > 10% but ≤ 20%, and "large" if > 20%.The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

7. Relative % change post = absolute % change post divided by C post (%). The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

8. Risk ratio (RR) = Int post (%) divided by C post (%)

BMD: bone mineral density; C: control group; Int: intervention group; ARD: adjusted risk difference; NS: not significant

* The data reported above for the studies by Cranney 2008, Lafata 2007 and Solomon 2007b does not account for clustering. We did not have access to sufficient information to adjust the data for clustering.

Figuras y tablas -
Table 6. Osteoporosis studies, intervention versus no intervention (control), outcome:osteoporosis medication, dichotomous data
Table 7. Osteoporosis studies intervention versus another intervention, outcome: BMD, dichotomous data

(Study)

Interventions

Int 1 pre (%) 1

Int 2 pre (%)2

Int 1 post (%)3

Int 2 post (%)4

ARD 5

Risk difference6

(P value if reported by authors)

Relative % change post 7

Risk ratio 8

(Bessette 2011)*

Patient education, education of physician via the patient, reminder to family physician versus Patient education (including video on osteoporosis), education of physician via the patient, reminder to family physician

14.72%

15.81%

‐1.1%

‐7%

0.9

(Boyd 2002)

Patient‐specific letter to primary care physician containing information on results and recommendations: standard versus extended letter

25/83 (30.1%)

29/78 (37.2%)

‐7.1%

‐19%

0.8

(Feldstein 2007)

Patient‐specific Electronic Medical Record (EMR) reminders to primary‐care provider informing them of patient increased risk and guidelines (sent twice) versus EMR plus patient‐directed intervention (education and reminder)

40/101 (39.6%)

36/110

(32.7%)

6.9%

21%

1.2

(Lafata 2007)**

Patient‐directed: 2 mailings (educational and reminders) versus physician prompt: Electronic Medical Record (EMR) reminder to physician and biweekly mailing plus patient‐directed: 2 mailings (educational and reminders)

720/3367 (21.4%)

1181/4086 (28.9%)

‐7.5%

‐26%

0.7

(Leslie 2012)

Physician reminder plus educational material versus physician reminder plus educational material plus patient‐directed intervention (reminder to see their physician)

224/1363 (16.4%)

258/1421 (18.2%)

‐1.7%

(NS)

‐9%

0.9

(Rozental 2008)

Patient‐specific letter to primary‐care physician outlining guidelines versus orthopaedic surgeon ordering BMD and forwarding results to primary‐care physician

7/23 (30.4%)

25/27(92.6%)

‐62.2%

‐67%

0.3

(Solomon 2007a)**

Patient‐directed (3 mailed letters educational) versus physician education following an academic‐detailing approach

249/3274 (7.6%)

183/3574 (5.1%)

2.5%

49%

1.5

(Solomon 2007a)**

Patient‐directed (3 mailed letters educational) versus combination of both physician and patient education

249/3274 (7.6%)

223/3339 (6.7%)

0.9%

14%

1.1

(Solomon 2007a)**

Physician education following an academic‐detailing approach versus combination of both physician and patient education

183/3574 (5.1%)

223/3339 (6.7%)

‐1.6%

‐23%

0.8

1. Intervention 1 group pre‐intervention proportion

2. Intervention 2 group pre‐intervention proportion

3. Intervention 1 group post‐intervention proportion

4. Intervention 2 group post‐intervention proportion

5. ARD = [Int 1 post (%) minus Int 2 post (%)] minus [Int 1 pre (%) minus Int 2 pre (%)]. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

6. Risk Difference (RD) is the absolute % change post‐intervention = Int 1 post (%) minus Int 2 post (%). This is considered to be "small" if ≤ 5%, "modest" if > 5% and ≤10%,"moderate" if > 10% but ≤ 20%, and "large" if > 20%.The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome.

7. Relative % change post = absolute % change post divided by Int 2 post (%). The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

8. Risk ratio (RR) = Int 1 post (%) divided by Int 2 post (%)

BMD: bone mineral density; Int 1: intervention 1 group; Int 2: Intervention 2 group; ARD: adjusted risk difference; NS: not significant

* In the study by Bessette 2011, the outcomes reported above include the participants with a diagnosis following the intervention. The women were considered "diagnosed" if they received a BMD test, if they were informed by their physician that they were suffering from osteoporosis and/or if they were initiated on osteoporosis medication. Therefore, the above percentages do not necessarily mean that the women received a BMD test.

**The data reported above for the studies by Lafata 2007 and Solomon 2007b does not account for clustering. We did not have access to sufficient information to adjust the data for clustering.

Figuras y tablas -
Table 7. Osteoporosis studies intervention versus another intervention, outcome: BMD, dichotomous data
Table 8. Osteoporosis studies, intervention versus another intervention, outcome: osteoporosis medication, dichotomous data

(Study)

Interventions

Int 1 pre (%) 1

Int 2 pre (%)2

Int 1 post (%)3

Int 2 post (%)4

ARD 5

Risk difference 6

(P value if reported by authors)

Relative % change post 7

Risk ratio 8

(Bessette 2011)

Patient education, education of physician via the patient, reminder to family physician (for group of patients without diagnosis or treatment at randomisation) versus Patient education (including video on osteoporosis), education of physician via the patient, reminder to family physician (for group of patients without diagnosis and treatment at randomisation)

11.79%

10.64%

1.2%

11%

1.1

(Bessette 2011)

Patient education, education of physician via the patient, reminder to family physician (for group of patients without diagnosis or treatment at randomisation) versus Patient education (including video on osteoporosis), education of physician via the patient, reminder to family physician (for group of patients without treatment at randomisation)

13.49%

12.71%

0.8%

6%

1.1

(Boyd 2002)

Patient‐specific letter to primary care physician containing information on results and recommendations: standard versus extended letter

11/104 (10.6%)

14/93 (15.1%)

‐4.5%

‐30%

0.7

(Feldstein 2007)

Patient specific Electronic Medical Record (EMR) reminders to primary care provider informing them of patient increased risk and guidelines (sent twice) versus EMR plus patient‐directed intervention (education and reminder).

28/101 (27.7%)

22/110 (20%)

7.7%

39%

1.4

(Lafata 2007)*

Patient‐directed: 2 mailings (educational and reminders) versus physician prompt: Electronic Medical Record (EMR) reminder to physician and biweekly mailing plus patient‐directed: 2 mailings (educational and reminders)

11/128 (8.6%)

15/162 (9.3%)

‐0.7%

‐7%

0.9

(Leslie 2012)

Physician reminder plus educational material versus physician reminder plus educational material plus patient‐directed intervention (reminder to see their physician)

200/1363 (14.7%)

234/1421 (16.5%)

‐1.8%

(NS)

‐11%

0.9

(Roux 2013)

Verbal and written information on osteoporosis to patient and letter with specific management plan sent to their treating physician. Patient reminders at 6 and 12 months. Reminder to physician if patient untreated at 6 months versus verbal and written information on osteoporosis to patient and letter with specific management plan sent to their treating physician. Blood tests and BMD test ordered for patient and results sent to the physician. Patient reminders at 4,8 and 12 months and physician reminders at 4 and 8 months if patient remained untreated

82/275 (29.8%)

65/251 (25.9%)

151/275 (54.9%)

156/251

(62.2%)

‐11.2%

‐7.2%

(P<0.001)

‐12%

0.9

(Rozental 2008)

Patient specific letter to primary care physician outlining guidelines versus orthopaedic surgeon ordering BMD and forwarding results to primary‐care physician

6/23 (26.1%)

20/27(74.1%)

‐48%

‐65%

0.4

(Solomon 2007a)*

Patient directed (x3 mailed letters educational) versus physician education following an academic detailing approach

208/3274 (6.4%)

197/3574 (5.5%)

0.8%

15%

1.2

(Solomon 2007a)*

Patient directed (x3 mailed letters educational) versus combination of both physician and patient education

208/3274 (6.4%)

236/3339 (7.1%)

‐0.7%

‐10%

0.9

(Solomon 2007a)*

Physician education following an academic detailing approach versus combination of both physician and patient education

197/3574 (5.5%)

236/3339 (7.1%)

‐1.6%

‐22%

0.8

1. Intervention 1 group pre‐intervention proportion

2. Intervention 2 group pre‐intervention proportion

3. Intervention 1 group post‐intervention proportion

4. Intervention 2 group post‐intervention proportion

5. ARD = [Int 1 post (%) minus Int 2 post (%)] minus [Int 1 pre (%) minus Int 2 pre (%)]. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

6. Risk Difference (RD) is the absolute % change post‐intervention = Int 1 post (%) minus Int 2 post (%). This is considered to be "small" if ≤ 5%, "modest" if > 5% and ≤10%,"moderate" if > 10% but ≤ 20%, and "large" if > 20%.The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome.

7. Relative % change post = absolute % change post divided by Int 2 post (%). The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

8. Risk ratio (RR) = Int 1 post (%) divided by Int 2 post (%)

BMD: bone mineral density; Int 1: intervention 1 group; Int 2: Intervention 2 group; ARD: Adjusted risk difference; NS: not significant

* The data reported above for the studies by Lafata 2007 and Solomon 2007b does not account for clustering. We did not have access to sufficient information to adjust the data for clustering.

Figuras y tablas -
Table 8. Osteoporosis studies, intervention versus another intervention, outcome: osteoporosis medication, dichotomous data
Table 9. Low back pain studies, intervention versus control, dichotomous data

(Study)

Intervention

Outcome

Int pre (%) 1

C pre (%)2

Int post (%)3

C post (%)4

ARD 5

Risk difference 6

(P value if reported by authors)

Relative % change post 7

Risk ratio 8

(Bishop 2006)

Physician education (guidelines) and 3 patient‐specific reminder letters

Education and reassurance according to guideline 0 ‐ 4 weeks post‐onset

10% (16/162)

7% (10/149)

3.2%

47%

1.5

Exercise according to guideline 0 ‐ 4 weeks post‐onset

38% (62/162)

43% (64/149)

‐4.7%

‐11%

0.9

Appropriate medication according to guideline 0 ‐ 4 weeks post‐onset

85% (138/162)

77% (115/149)

8%

(P=0.14)

10%

1.1

Spinal manipulation according to guideline 0 ‐ 4 weeks post‐onset

2.5% (4/162)

6% (9/149)

‐3.6%

‐59%

0.4

Guideline‐discordant physician recommended treatment 0 ‐ 4 weeks post‐onset

10% (16/162)

17% (25/149)

6.9%

(P=0.05)

41%

0.6

Supervised exercise programme (recommended treatment 5 ‐ 12 weeks post‐onset)

19% (29/154)

14% (21/149)

4.7%

(P=0.11)

34%

1.3

Return to work (recommended treatment 5 ‐ 12 weeks post‐onset)

24% (37/154)

17% (25/149)

7.2%

(P=0.18)

43%

1.4

Refer to interdisciplinary programme (recommended treatment 5 ‐ 12 weeks post‐onset)

4% (6/154)

2% (3/149)

1.9%

94%

1.9

Physiotherapy > 4 weeks (guideline‐discordant)

41% (63/154)

43% (64/149)

2%

5%

1

Continued use of spinal manipulation therapy (guideline‐discordant)

‐(no data available)

33% (49/149)

(P=0.04)

(Bishop 2006)

Physician education, reminders and also patient education and 3 reminders

Education and reassurance according to guideline 0 ‐ 4 weeks post‐onset

6% (9/151)

7% (10/149)

‐0.8%

‐11%

0.9

Exercise according to guideline 0 ‐ 4 weeks post‐onset

53% (80/151)

43% (64/149)

10%

(P=0.05)

23%

1.2

Appropriate medication according to guideline 0 ‐ 4 weeks post‐onset

81% (122/151)

77% (115/149)

3.6%

(P=0.08)

5%

1

Spinal manipulation according to guideline 0 ‐ 4 weeks post‐onset

5% (8/151)

6% (9/149)

‐0.7%

‐12%

0.9

Guideline‐discordant physician recommended treatment 0 ‐ 4 weeks post‐onset

18% (27/151)

17% (25/149)

‐1.1%

‐7%

1.1

Supervised exercise programme (recommended treatment 5 ‐ 12 weeks post‐onset)

18% (26/145)

14% (21/149)

3.8%

(P=0.07)

27%

1.3

Return to work (recommended treatment 5 ‐ 12 weeks post‐onset)

23% (33/145)

17% (25/149)

6%

(P=0.14)

36%

1.4

Refer to interdisciplinary programme (recommended treatment 5 ‐ 12 weeks post‐onset)

0

2% (3/149)

‐2%

‐100%

0

Physiotherapy > 4 weeks (guideline‐discordant)

42% (61/145)

43% (64/149)

0.9%

2%

1

Continued use of spinal manipulation therapy (guideline‐discordant)

3% (4/145)

33% (49/149)

30.1%

(P=0.05)

92%

0.1

(Dey 2004)*

Intervention (aimed at general practitioners): guidelines discussion (educational component), patient information leaflets, access to fast‐track physiotherapy and triage services for patients with persistent symptoms (organisational component) versus usual care (control)*

X‐ray referrals

15.1% (43/284)

13.7% (42/308)

‐1.4%

(P=0.62)

‐10%

1.1

Sickness certificates

17.9 % (34/190)

19.2% (40/206)

1.3%

(P=0.74)

7%

0.9

Prescriptions for opioids or muscle relaxants

18.6% (84/452)

18.7% (92/491)

0.1

(P=0.99)

1

1

Referrals to secondary care

3.4% (33/962)

2.3% (24/1044)

‐1.1%

(P=0.12)

‐49%

1.5

Referrals to physiotherapy or educational programme

26.3% (44/167)

13.8% (25/181)

‐12.6%

(P=0.01)

‐91%

1.9

(Engers 2005)**

Intervention (aimed at general practitioners): guidelines on low back pain, 2‐hour workshop, 2 scientific articles, guidelines on low back pain for occupational physicians, tool for patient education and management‐decision tool. Control group: usual care

Referral to a therapist

22.9% (75/328)

27.4% (79/288)

4.6%

17%

0.8

Prescription of pain medication on a time‐contingent basis

70% (139/328)

69% (130/288)

2.8%

6%

0.9

Handed patient information leaflet

36.9% (121/328)

38.2% (110/288)

‐1.3%

‐3%

1

Advised patient to stay active

95.1% (312/328)

89.2% (257/288)

5.9%

7%

1.1

Advised patient to gradually increase activity

78% (256/328)

65.3% (188/288)

12.8%

20%

1.2

Advised patient which activities to increase at what moment

18% (58/328)

9% (26/288)

8.7%

96%

2

(French 2013)***

Intervention (aimed at general practitioners): Interactive, educational workshops plus educational material disseminated (via DVDs); Control group: usual care**

Number of x‐ray requests out of total number of patients seen

0.83% (67/8,085)

1.02% (80/7,826)

0.2%

(P=0.2)

19%

0.8

Number of CT requests out of total number of patients seen

0.61% (64/10,419)

0.66% (66/10,085)

0.0%

(P=0.6)

7%

0.9

(Hazard 1997)

Intervention (aimed at physicians): notification that patient was at a high risk of disability and guidelines on management. Control group: usual care

3‐month work absence rates

28.6% (8/28)

24% (6/25)

‐4.6%

(NS)

‐19%

1.2

(Schectman 2003)

Intervention (aimed at physicians): guideline on low back pain, 90‐minute educational session on guideline implementation delivered by local opinion leaders and audit report summarising performance against the guideline plus outreach visit. Control group: usual care plus/minus patient education (pamphlet and video)

Lumbosacral X‐ray total utilisation (% of patients based on episode of care)

31%

21%

19%

18%

9%

‐1%

‐6%

1.1

Lumbosacral X‐ray not consistent with guideline

14.5%

8.2%

8.1%

8.6%

6.8%

0.5%

6%

0.9

Lumbosacral CT/MRI total utilisation (% of patients based on episode of care)

7.6%

5.6%

5.6%

7.1%

3.5%

1.5%

21%

0.8

Lumbosacral CT/MRI not consistent with guideline

5.7%

3.5%

3.5%

5.4%

4.1%

1.9%

35%

0.6

Physical therapy referral total utilisation (% of patients based on episode of care)

12%

13%

10%

13%

2%

3%

23%

0.8

Physical therapy referral not consistent with guideline

10%

10.9%

9.2%

12%

1.9%

2.8%

23%

0.8

Specialty referral total utilisation (% of patients based on episode of care)

12%

5.9%

8.6%

7.1%

4.6%

‐1.5%

‐21%

1.2

Specialty referral not consistent with guideline

9.5%

4%

7.1%

5.6%

4%

‐1.5%

‐27%

1.3

1. Intervention group pre‐intervention proportion

2. Control group pre‐intervention proportion

3. Intervention group post‐intervention proportion

4. Control group post‐intervention proportion

5. ARD = [Int post (%) minus C post (%)] minus [Int pre (%) minus C pre (%)]. The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

6. Risk Difference (RD) is the absolute % change post‐intervention = Int post (%) minus C post (%). This is considered to be "small" if ≤ 5%, "modest" if > 5% and ≤10%,"moderate" if > 10% but ≤ 20%, and "large" if > 20%.The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

7. Relative % change post = absolute % change post divided by C post (%). The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

8. Risk ratio (RR) = Int post (%) divided by C post (%)

C: control group; Int: intervention group; ARD: adjusted risk difference; NS: not significant

CT/MRI: computed tomography/magnetic resonance imaging

* Dey 2004 reported the Intercluster Correlation (ICC) for the results (mean cluster size=95.1) and this was used to calculate the above effective sample sizes according to chapter 16.3.4 of the Cochrane Handbook, Higgins 2011a.

** The data reported above for the study by Engers 2005 does not account for clustering. We did not have access to sufficient information to adjust the data for clustering.

***French 2013 reported Intercluster Correlation (ICC for x‐rays 0.004 and for CTs 0.003, mean cluster size=2,154) and this was used to calculate the above effective sample sizes according to chapter 16.3.4 of the Cochrane Handbook, Higgins 2011a

Figuras y tablas -
Table 9. Low back pain studies, intervention versus control, dichotomous data
Table 10. Low back pain studies, intervention 1 versus intervention 2, dichotomous data

(Study)

Intervention 1 versus intervention 2

Outcome

Int 1 pre (%) 1

Int 2 pre (%)2

Int 1 post (%)3

Int 2 post (%)4

ARD 5

Risk difference 6

(P value if reported by authors)

Relative % change post 7

Risk ratio 8

(Bishop 2006)

Physician education (guidelines) and 3 patient‐specific reminder letters versus physician education, reminders and also patient education and 3 reminders

Education and reassurance according to guideline 0 ‐ 4 weeks post‐onset

10% (16/162)

6% (9/151)

3.9%

(NS)

66%

1.7

Exercise according to guideline 0 ‐ 4 weeks post‐onset

38% (62/162)

53% (80/151)

‐14.7%

(P=0.0083)

‐28%

0.7

Appropriate medication according to guideline 0 ‐ 4 weeks post‐onset

85% (138/162)

81% (122/151)

4.4%

(NS)

5%

1.1

Spinal manipulation according to guideline 0 ‐ 4 weeks post‐onset

2.5% (4/162)

5% (13/151)

‐6.1%

(P=0.018)

‐71%

0.3

Guideline‐discordant physician‐recommended treatment 0 ‐ 4 weeks post‐onset

10% (16/162)

18% (27/151)

8%

(P=0.04)

45%

0.6

Supervised exercise programme (recommended treatment 5 ‐ 12 weeks post‐onset)

19% (29/154)

18% (26/145)

0.9%

(NS)

5%

1.1

Return to work (recommended treatment 5 ‐ 12 weeks post‐onset)

24% (37/154)

23% (33/145)

1.3%

(NS)

6%

1.1

Refer to interdisciplinary programme (recommended treatment 5 ‐ 12 weeks post‐onset)

4% (6/154)

0

3.9%

(P=0.02)

Physiotherapy > 4 weeks (guideline‐discordant)

41% (63/154)

42% (61/145)

1.2%

(NS)

3%

1

Continued use of spinal manipulation therapy (guideline‐discordant)

‐ (no data available)

3% (4/145)

(Eccles 2001)*

Feedback on number of spinal radiographs 6 months before and 6 months after the intervention plus guideline dissemination versus guideline dissemination

Lumbar spine radiographs concordant with guidelines

35.4% (64/181)

43.6% (120/275)

‐8.3%

‐19%

0.8

(Eccles 2001)*

Reminder messages on radiograph reports plus guideline dissemination versus guideline dissemination

Lumbar spine radiographs concordant with guidelines

41.2% (35/85)

43.6% (120/275)

‐2.5%

‐6%

0.9

(Eccles 2001)*

Feedback on number of spinal radiographs 6 months before and 6 months after the intervention plus guideline dissemination plus reminder messages on radiograph reports versus guideline dissemination

Lumbar spine radiographs concordant with guidelines

36% (89/247)

43.6% (120/275)

‐7.6%

‐17%

0.8

(Eccles 2001)*

Feedback on number of spinal radiographs 6 months before and 6 months after the intervention plus guideline dissemination versus reminder messages on radiograph reports plus guideline dissemination

Lumbar spine radiographs concordant with guidelines

35.4% (64/181)

41.2% (35/85)

‐5.8%

‐14%

0.9

1. Intervention 1 group pre‐intervention proportion

2. Intervention 2 group pre‐intervention proportion

3. Intervention 1 group post‐intervention proportion

4. Intervention 2 group post‐intervention proportion

5. ARD = [Int 1 post (%) minus Int 2 post (%)] minus [Int 1 pre (%) minus Int 2 pre (%)]. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

6. Risk Difference (RD) is the absolute % change post‐intervention = Int 1 post (%) minus Int 2 post (%). This is considered to be "small" if ≤ 5%, "modest" if > 5% and ≤10%,"moderate" if > 10% but ≤ 20%, and "large" if > 20%.The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome.

7. Relative % change post = absolute % change post divided by Int 2 post (%). The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

8. Risk ratio (RR) = Int 1 post (%) divided by Int 2 post (%)

Int 1: intervention 1 group; Int 2: Intervention 2 group; ARD: Adjusted risk difference; NS: not significant

*The data reported above for the study by Eccles 2001 does not account for clustering. We did not have access to sufficient information to adjust the data for clustering.

Figuras y tablas -
Table 10. Low back pain studies, intervention 1 versus intervention 2, dichotomous data
Table 11. Low back pain studies intervention 1 versus intervention 2, continuous data

(Study)

Intervention 1 versus Intervention 2

Outcome

Int 1 pre mean (SD)1

Int 2 pre mean (SD)2

Int 1 post mean (SD)3

Int 2 post mean (SD)4

MD 5

Relative % change 6

Adjusted relative % change7

SMD8

(P value)9

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing versus guideline dissemination

Functional capacity measured by Hannover Functional Ability Questionnaire at 6 months

72.9

70.3

2.7

4%

0.1

(P=0.12)

(Becker 2008*)

Physician education (as above) plus practice nurse training in motivational counselling versus guideline dissemination

Functional capacity measured by Hannover Functional Ability Questionnaire at 6 months

73.9

70.3

3.6

5%

0.2

(P=0.032)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing versus guideline dissemination

Days in pain at 6 months

63.3

80.8

17.4

22%

0.2

(P=0.002)

(Becker 2008*)

Physician education (as above) plus practice nurse training in motivational counselling versus guideline dissemination

Days in pain at 6 months

62.9

80.8

17.9

22%

0.2

(P=0.001)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing versus guideline dissemination

Overall activity at 6 months

36.5

33.5

3

9%

0.1

(P=0.203)

(Becker 2008*)

Physician education (as above) plus practice nurse training in motivational counselling versus guideline dissemination

Overall activity at 6 months

36.3

33.5

2.8

8%

0.1

(P=0.230)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing versus guideline dissemination

Days of sick leave at 6 months

13

14.3

1.3

9%

0

(P=0.569)

(Becker 2008*)

Physician education (as above) plus practice nurse training in motivational counselling versus guideline dissemination

Days of sick leave at 6 months

13

14.3

1.3

9%

0

(P=0.584)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing versus guideline dissemination

Quality of life at 6 months

66.6

66.8

‐0.3

0%

0

(P=0.847)

(Becker 2008*)

Physician education (as above) plus practice nurse training in motivational counselling versus guideline dissemination

Quality of life at 6 months

67.5

66.8

0.7

1%

‐‐

0

(P=0.602)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing versus guideline dissemination

Functional capacity measured by Hannover Functional Ability Questionnaire at 12 months

73

71.6

1.4

2%

0.1

(P=0.446)

(Becker 2008*)

Physician education (as above) plus practice nurse training in motivational counselling versus guideline dissemination

Functional capacity measured by Hannover Functional Ability Questionnaire at 12 months

74.6

71.6

3.1

4%

0.1

(P=0.088)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing versus guideline dissemination

Days in pain at 12 months

58.5

71.3

12.8

18%

0.2

(P=0.018)

(Becker 2008*)

Physician education (as above) plus practice nurse training in motivational counselling versus guideline dissemination

Days in pain at 12 months

61.6

71.3

9.8

14%

0.1

(P=0.067)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing versus guideline dissemination

Overall activity at 12 months

46.4

42.9

3.5

8%

0.1

(P=0.202)

(Becker 2008*)

Physician education (as above) plus practice nurse training in motivational counselling versus guideline dissemination

Overall activity at 12 months

45.4

42.9

2.5

6%

0.1

(P=0.396)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing versus guideline dissemination

Days of sick leave at 12 months

6.2

9.3

3.1

34%

0.1

(P=0.256)

(Becker 2008*)

Physician education (as above) plus practice nurse training in motivational counselling versus guideline dissemination

Days of sick leave at 12 months

6.5

9.3

2.8

30%

0.1

(P=0.320)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing versus guideline dissemination

Quality of life at 12 months

68.5

67.7

0.8

1%

0

(P=0.535)

(Becker 2008*)

Physician education (as above) plus practice nurse training in motivational counselling versus guideline dissemination

Quality of life at 12 months

70.4

67.7

2.7

4%

0.1

(P=0.036)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing vs physician education plus practice nurse training in motivational counselling

Functional capacity measured by Hannover Functional Ability Questionnaire at 6 months

72.9

73.9

‐1

‐1%

0

(NR)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing vs physician education plus practice nurse training in motivational counselling

Days in pain at 6 months

63.3

62.9

‐0.4

‐1%

0

(NR)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing vs physician education plus practice nurse training in motivational counselling

Overall activity at 6 months

36.5

36.3

0.2

0%

0

(NR)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing vs Physician education plus practice nurse training in motivational counselling

Days of sick leave at 6 months

13

13.1

0.1

0%

0

(NR)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing vs Physician education plus practice nurse training in motivational counselling

Quality of life at 6 months

66.6

67.5

‐0.9

‐1%

0

(NR)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing vs Physician education plus practice nurse training in motivational counselling

Functional capacity measured by Hannover Functional Ability Questionnaire at 12 months

73

74.6

‐1.7

‐2%

‐0.1

(NR)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing vs Physician education plus practice nurse training in motivational counselling

Days in pain at 12 months

58.5

61.6

3.1

5%

0

(NR)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing vs Physician education plus practice nurse training in motivational counselling

Overall activity at 12 months

46.4

45.4

1

2%

0

(NR)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing vs Physician education plus practice nurse training in motivational counselling

Days of sick leave at 12 months

6.2

6.458

0.3

5%

0

(NR)

(Becker 2008*)

Physician education: Guideline (in 4 versions including patient leaflet), 3 seminars and academic detailing vs Physician education plus practice nurse training in motivational counselling

Quality of life at 12 months

68.5

70.4

‐1.9

‐3%

‐0.1

(NR)

(Eccles 2001)*

Feedback on number of spinal radiographs 6 months before and 6 months after the intervention plus guideline dissemination versus guideline dissemination

Number of lumbar spine radiographs per 1000 patients

7.24 (4.8)

7.53 (4.1)

5.97 (4.2)

6.80 (4.3)

0.83

12%

8%

0.2

(NR)

(Eccles 2001)*

Reminder messages on radiograph reports plus guideline dissemination versus guideline dissemination

Number of lumbar spine radiographs per 1000 patients

7.31 (5.2)

7.53 (4.1)

5.14 (3.7)

6.80 (4.3)

1.66

24%

21%

0.4

(P=0.05)

(Eccles 2001)*

Feedback on number of spinal radiographs 6 months before and 6 months after the intervention plus guideline dissemination plus reminder messages on radiograph reports versus guideline dissemination

Number of lumbar spine radiographs per 1000 patients

8.30 (5.1)

7.53 (4.1)

5.23 (3.7)

6.80 (4.3)

1.57

23%

34%

0.4

(NR)

(Eccles 2001)*

Feedback on number of spinal radiographs 6 months before and 6 months after the intervention plus guideline dissemination versus reminder messages on radiograph reports plus guideline dissemination

Number of lumbar spine radiographs per 1000 patients

7.24 (4.8)

7.31 (5.2)

5.97 (4.2)

5.14 (3.7)

‐0.83

‐16%

‐18%

‐0.2

(NR)

1. Intervention 1 group pre‐intervention mean (standard deviation)

2. Intervention 2 group pre‐intervention mean (standard deviation)

3. Intervention 1 group post‐intervention mean (standard deviation)

4. Intervention 2 group postintervention mean (standard deviation)

5. Mean Difference (MD)=Difference between post‐intervention means. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

6. Relative percentage change post‐intervention = (Int1 post mean ‐ Int2 post mean)/Int2 post mean. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

7. Adjusted relative percentage change= (Int1 post mean‐Int2 post mean)‐(Int1 pre mean ‐ Int2 pre mean)/Int2 post mean. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome.

8. SMD=Standardised Mean Difference=(Int1 post mean‐Int2 post mean)/SD pooled. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

9. P value reported by study authors

Int 1: intervention 1 group; Int 2: Intervention 2 group; NR: not reported; SD: standard deviation

*The data reported above for Becker 2008 and Eccles 2001 was adjusted for clustering by the authors

Figuras y tablas -
Table 11. Low back pain studies intervention 1 versus intervention 2, continuous data
Table 12. Low back pain, interrupted time series studies, imaging outcomes

Study

Intervention

Outcome

Mean pre (SD)

Mean post (SD)

Mean post minus mean pre

Relative % change pre to post

SMD pre to post

Mean change in level (p value)

Mean change in slope (p value)

Hollingworth 2002

Educational material

Back x‐rays ordered

1133 (50)

1208.7 (111.5)

‐75.7

‐6.7

‐1.51

‐121.5 (P = 0.167)

6.8 (P = 0.776)

Figuras y tablas -
Table 12. Low back pain, interrupted time series studies, imaging outcomes
Table 13. Osteoarthritis studies: Intervention versus control (continuous data)

(Study)

Intervention

Outcome

Int pre mean (SD)1

C pre mean (SD)2

Int post mean (SD)3

C post mean (SD)4

MD 5

Relative % change 6

Adjusted relative % change7

SMD8

(P value)9

(Chassany 2006)*

GP training on relationships and communication, pain evaluation, prescription and negotiation of a patient contract delivered in a 4‐hour interactive session plus 8 reminders on recommendations

Pain relief (SPID)

315.6 (289.5)

264.7 (242.9)

50.9

19%

19%

0.2

(P< 0.0001)

Intensity of pain in motion on VAS

63.7 (13.8)

62.8 (13.5)

‐29 (23.1)

‐24.8 (21.1)

4.2

17%

‐21%

0.2

(P=0.01)

Lequesne Index

9.2 (2.9)

9.8 (3.2)

‐2.5 (2.5)

‐2.0 (2.4)

0.5

25%

5%

0.2

(P< 0.0001)

WOMAC index pain

9.3 (3.0)

9.6 (2.8)

‐2.9 (3.4)

‐2.2 (2.9)

0.7

32%

‐18%

0.2

(P< 0.0001)

WOMAC index stiffness

4.1 (1.4)

4.0 (1.4)

‐1.2 (1.6)

‐0.8 (1.4)

0.4

50%

‐62%

0.3

(P=0.0004)

WOMAC index physical function

31.2 (10.9)

32.8 (9.5)

‐8.7 (10.7)

‐6.1 (8.8)

2.6

43%

‐16%

0.3

(P< 0.0001)

WOMAC index global score

44.6 (14.4)

46.4 (12.5)

‐12.9 (14.8)

‐9.2 (12.2)

3.7

40%

‐21%

0.3

(P< 0.0001)

Acetaminophen consumption

3400 (800)

2900 (900)

‐500

‐17%

‐17%

‐0.6

(P< 0.0001)

(Rosemann 2007)*

Intervention (aimed at GPs): 2 interactive 8‐hour meetings focusing on arthritis self management, guideline dissemination and patient information material versus control (usual care)

Quality of life (AIMS2‐SF scores) Lower body

2.67 (1.88)

2.65 (1.85)

2.48

2.62

‐0.14

‐5%

‐6%

‐0.1

(P=0.349)

Quality of life (AIMS2‐SF scores) Upper body

1.47 (2.25)

1.33 (2.09)

1.43

1.34

0.09

7%

‐4%

0.1

P=0.694)

Quality of life (AIMS2‐SF scores) Symptom

4.87 (2.13)

4.81 (2.18)

4.51

4.72

‐0.21

‐4%

‐6%

‐0.2

(P=0.119)

Quality of life (AIMS2‐SF scores) Affect

2.89 (1.35)

2.88 (1.33)

2.92

2.83

0.09

3%

3%

0.1

(P=0.610)

Quality of life (AIMS2‐SF scores) Social

4.52 (1.88)

4.69 (1.80)

4.43

4.62

‐0.19

‐4%

0%

‐0.3

P=0.776

GP contacts

4.56 (6.13)

4.82 (6.00)

4.44

4.6

0.16

3%

‐2%

0.1

(P=0.339)

Referrals to orthopaedics

1.58 (3.43)

1.76 (3.52)

1.49

1.75

0.26

15%

5%

0.8

(P=0.153)

Radiographs

0.82 (3.12)

0.79 (2.78)

0.75

0.85

0.1

12%

15%

0.2

(P=0.05)

Non‐medical practitioners

0.11 (3.01)

0.36 (3.28)

0.09

0.32

0.23

72%

‐6%

0.6

(P=0.687)

Physiotherapy

4.70 (9.10)

5.81 (11.10)

4.63

5.77

1.14

20%

1%

2

(P=0.242)

Acupuncture

0.83 (3.45)

0.97 (3.80)

0.8

0.97

0.17

18%

3%

0.2

(P=0.821)

(Rosemann 2007)*

Intervention (aimed at GPs) as above plus patient case management via telephone by practice nurses versus control (usual care)

Quality of life (AIMS2‐SF scores) Lower body

3.01 (2.11)

2.65 (1.85)

2.61

2.62

‐0.01

0%

‐14%

0

(P=0.049)

Quality of life (AIMS2‐SF scores) Upper body

1.68 (2.44)

1.33 (2.09)

1.62

1.34

0.28

21%

‐5%

0.2

(P=0.621)

Quality of life (AIMS2‐SF scores) Symptom

5.02 (2.29)

4.81 (2.18)

4.42

4.72

‐0.3

‐6%

‐11%

‐0.2

(P=0.048)

Quality of life (AIMS2‐SF scores) Affect

3.04 (1.39)

2.88 (1.33)

2.98

2.83

0.15

5%

0%

0.2

(P=0.691)

Quality of life (AIMS2‐SF scores) Social

4.79 (1.80)

4.69 (1.80)

4.736

4.62

0.116

3%

0%

0.1

(P< 0.001)

GP contacts

5.01 (5.78)

4.82 (6.00)

4.9

4.6

‐0.3

‐7%

‐2%

‐0.2

(P=0.823)

Referrals to orthopaedics

1.76 (3.52)

1.76 (3.52)

1.52

1.75

0.23

13%

13%

0.2

(P=0.044)

Radiographs

0.80 (3.01)

0.79 (2.78)

0.71

0.85

0.14

16%

18%

0.4

(P=0.031)

Non‐medical practitioners

0.50 (4.20)

0.36 (3.28)

0.47

0.32

‐0.15

‐47%

‐3%

‐0.4

(P=0.225)

Physiotherapy

5.22 (10.03)

5.81 (11.10)

5.08

5.77

0.69

12%

2%

1.3

(P=0.129)

Acupuncture

0.77 (3.99)

0.97 (3.80)

0.72

1.09

0.37

34%

16%

0.4

(P=0.769)

(Stross 1985)**

Intervention: Educationally‐influential physicians (EIs) led education of primary‐care physicians: self‐study programme including textbook, audiovisual materials and recent articles on osteoarthritis versus control (usual care)

Length of stay for OA patients

8.8

8.4

8.4

8.6

0.2

2%

7%

NR

Length of stay for total hip arthroplasty (THA) patients

17.2

16.6

15.2

16.0

0.8

5%

9%

NR

1. Intervention group pre‐intervention mean (standard deviation)

2. Control group pre‐intervention mean (standard deviation)

3. Intervention group post‐intervention mean (standard deviation)

4. Control group pos‐tintervention mean (standard deviation)

5. Mean Difference (MD)=Difference between post‐intervention means. The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

6. Relative percentage change post‐intervention = (Int post mean ‐ Control post mean)/Control post mean

7. Adjusted relative percentage change= (Int post mean‐Control post mean)‐(Int pre mean ‐ Control pre mean)/Control post mean. The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome.

8. SMD=Standardised Mean Difference=(Int post mean‐Control post mean)/SD pooled. The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

9. P value reported by study authors

AIMS2‐SF: Arthritis Impact Measurement Scales Short Form
WOMAC: Western Ontario and McMaster Universities Osteoarthritis Index

* There are potential unit of analysis errors in the reported results as the study did not account for clustering and did not provide sufficient data to allow an approximate analysis according to chapter 16.3.4 of the Cochrane Handbook, Higgins 2011a.

**The study did not report standard deviations and therefore we were unable to calculate the SMD. There are potential unit of analysis errors in the reported results as the study did not account for clustering and did not provide sufficient data to allow an approximate analysis according to chapter 16.3.4 of the Cochrane Handbook, Higgins 2011a.

Figuras y tablas -
Table 13. Osteoarthritis studies: Intervention versus control (continuous data)
Table 14. Osteoarthritis studies: intervention versus control (dichotomous data)

(Study)

Intervention

Outcome

Int pre (%) 1

C pre (%)2

Int post (%)3

C post (%)4

ARD 5

Risk difference 6

(P Value if reported by authors)

Relative % change post 7

Risk ratio 8

(Rahme 2005)*

Intervention (aimed at GPs): 90‐minute workshop on management of osteoarthritis versus control group (usual care)

Number of adequate prescription, according to the guidelines

51% (273/536)

47% (675/1437)

56% (251/450)

49% (593/1209)

3%

7%

14%

1.1

(Rahme 2005)*

Intervention (aimed at GPs): decision tree on treatment choices for osteoarthritis patients versus control (usual care)

Number of adequate prescription, according to the guidelines

51% (799/1569)

47% (675/1437)

54% (712/1317)

49% (593/1209)

1%

5%

10%

1.1

(Rahme 2005)*

Intervention (aimed at GPs): 90‐minute workshop and decision tree as above versus control (usual care)

Number of adequate prescription, according to the guidelines

58% (1022/1776)

47% (675/1437)

62% (1008/1634)

49% (593/1209)

2%

13%

26%

1.3

(Rosemann 2007)*

Intervention (aimed at GPs): 2 interactive 8‐hour meetings focusing on arthritis self management, guideline dissemination and patient information material versus control (usual care)

Paracetamol prescriptions

8.9% (31/345)

6.6% (22/332)

16.4%

5.3%

8.7%

11.1%

(<0.001)

209%

3.1

Opioids

5.8% (20/345)

6.9% (23/332)

10.1%

7.9%

3.4%

2.2%

(NS)

28%

1.3

NSAID

40% (138/345)

41.9% (139/332)

44.3%

44.2%

2.0%

0.1%

(NS)

23%

1.0

Homeopathics

6.1% (21/345)

8.1% (27/332)

7.7%

9.8%

‐0.1%

‐2.2%

(NS)

‐22%

0.8

(Rosemann 2007)*

Intervention (aimed at GPs) as above plus patient case management via telephone by practice nurses versus control (usual care)

Paracetamol prescriptions

7.3% (25/345)

6.6% (22/332)

14.1%

5.3%

8.2%

8.8%

(<0.01)

166%

2.7

Opioids

7.3% (25/345)

6.9% (23/332)

16.0%

7.9%

7.8%

8.1%

(< 0.01)

102%

2.0

NSAID

43.3% (149/345)

41.9% (139/332)

49.7%

44.2%

4.3%

5.6%

(0.019)

13%

1.1

Homeopathics

6.7% (23/345)

8.1% (27/332)

9.6%

9.8%

1.2%

‐0.2%

(NS)

‐2%

1.0

(Stross 1985)*

Intervention: Educationally‐influential physicians (EIs) led education of primary‐care physicians: self‐study programme including textbook, audiovisual materials and recent articles on osteoarthritis versus control (usual care)

Management of OA patients with aspirin

39% (9/23)

50% (9/18)

20% (6/30)

28% (5/18)

3%

‐8%

‐28%

0.7

Management of OA patients with NSAIDs

83% (19/23)

78% (14/18)

87% (26/30)

94% (17/18)

‐13%

‐8%

‐8%

0.9

Management of OA patients with systemic corticosteroids

13% (3/23)

17% (3/18)

3% (1/30)

22% (4/18)

15%

19%

(< 0.05)

85%

0.2

Management of OA patients with intra‐articular corticosteroids

17% (4/23)

11% (2/18)

40% (12/30)

11% (2/18)

23%

29%

(<0.05)

260%

3.6

Management of OA patients with physical therapy

87% (20/23)

83% (15/18)

93% (28/30)

83% (15/18)

6%

10%

12%

1.1

Referral of OA patients

39% (9/23)

39% (7/18)

30% (9/30)

33% (6/18)

‐4%

3%

10%

0.9

Pre‐op physical therapy of THA patients

56% (10/18)

46% (12/26)

97% (35/36)

40% (12/30)

48%

57%

(< 0.05)

143%

2.4

Post‐op narcotics of THA patients

72% (13/18)

77% (20/26)

89% (32/36)

93% (28/30)

0%

4%

5%

1.0

Post‐op physical therapy of THA patients

100% (18/18)

100% (26/26)

100% (36/36)

100% (30/30)

0%

0%

0%

1.0

Post‐op complications of THA patients

11% (2/18)

15% (4/26)

6% (2/36)

13% (4/30)

4%

8%

58%

0.4

1. Intervention group pre‐intervention proportion

2. Control group pre‐intervention proportion

3. Intervention group post‐intervention proportion

4. Control group post‐intervention proportion

5. ARD = [Int post (%) minus C post (%)] minus [Int pre (%) minus C pre (%)]. The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

6. Risk Difference (RD) is the absolute % change post‐intervention = Int post (%) minus C post (%). This is considered to be "small" if ≤ 5%, "modest" if > 5% and ≤10%,"moderate" if > 10% but ≤ 20%, and "large" if > 20%.The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

7. Relative % change post = absolute % change post divided by C post (%). The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

8. Risk ratio (RR) = Int post (%) divided by C post (%)

C: control group; Int: intervention group; ARD: Adjusted risk difference; NS: not significant

NSAID: non‐steroidal anti‐inflammatory drug, THA: total hip arthroplasty

* There are unit of analysis errors in the reported results because the available data did not account for the effect of clustering.

Figuras y tablas -
Table 14. Osteoarthritis studies: intervention versus control (dichotomous data)
Table 15. Osteoarthritis studies: intervention 1 versus intervention 2, dichotomous data

(Study)

Intervention 1 versus intervention 2

Outcome

Int 1 pre (%) 1

Int 2 pre (%)2

Int 1 post (%)3

Int 2 post (%)4

ARD 5

Risk difference 6

(P value if reported by authors)

Relative % change post 7

Risk ratio 8

(Rahme 2005)*

Intervention 1 (aimed at GPs): 90‐minute workshop on management of osteoarthritis versus Intervention 2 (aimed at GPs): decision tree on treatment choices for osteoarthritis patients

Number of adequate prescription, according to the guidelines

51% (273/536)

51% (799/1569)

56% (251/450)

54% (712/1317)

1.7%

1.7%

3%

1

(Rahme 2005)*

Intervention 1 (aimed at GPs): 90‐minute workshop on management of osteoarthritis versus Intervention 2 (aimed at GPs): 90‐minute workshop and decision tree

Number of adequate prescription, according to the guidelines

51% (273/536)

58% (1022/1776)

56% (251/450)

62% (1008/1634)

0.7%

‐5.9%

‐10%

0.9

(Rahme 2005)*

Intervention 1 (aimed at GPs):decision tree on treatment choices for osteoarthritis patients versus Intervention 2 (aimed at GPs): 90‐minute workshop and decision tree

Number of adequate prescription, according to the guidelines

51% (799/1569)

58% (1022/1776)

54% (712/1317)

62% (1008/1634)

‐1%

‐7.6%

‐12%

0.9

(Rosemann 2007)*

Intervention (aimed at GPs): 2 interactive 8‐hour meetings focusing on arthritis self management, guideline dissemination and patient information material versus Intervention (aimed at GPs) as above plus patient case management via telephone by practice nurses

Paracetamol prescriptions

8.9% (31/345)

7.3% (25/345)

16.4%

14.1%

0.5%

2.3%

16%

1.2

Opioids

5.8% (20/345)

7.3% (25/345)

10.1%

16.0%

‐4.5%

‐5.9%

‐37%

1.2

NSAID

40% (138/345)

43.3% (149/345)

44.3%

49.7%

‐2.2%

‐5.4%

‐11%

1.2

Homeopathics

6.1% (21/345)

6.7% (23/345)

7.7%

9.6%

‐1.4%

‐1.9%

‐20%

1.2

1. Intervention 1 group pre‐intervention proportion

2. Intervention 2 group pre‐intervention proportion

3. Intervention 1 group post‐intervention proportion

4. Intervention 2 group post‐intervention proportion

5. ARD = [Int 1 post (%) minus Int 2 post (%)] minus [Int 1 pre (%) minus Int 2 pre (%)]. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

6. Risk Difference (RD) is the absolute % change post‐intervention = Int 1 post (%) minus Int 2 post (%). This is considered to be "small" if ≤ 5%, "modest" if > 5% and ≤10%,"moderate" if > 10% but ≤ 20%, and "large" if > 20%.The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome.

7. Relative % change post = absolute % change post divided by Int 2 post (%). The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

8. Risk ratio (RR) = Int 1 post (%) divided by Int 2 post (%)

Int 1: intervention 1 group; Int 2: Intervention 2 group; ARD: adjusted risk difference; NS: not significant, NSAID: non‐steroidal anti‐inflammatory drug

* There are unit of analysis errors in the reported results because the available data did not account for the effect of clustering.

Figuras y tablas -
Table 15. Osteoarthritis studies: intervention 1 versus intervention 2, dichotomous data
Table 16. Osteoarthritis studies: intervention 1 versus intervention 2 continuous data

(Study)

Intervention 1 versus Intervention 2

Outcome

Int 1 pre mean (SD)1

Int 2 pre mean (SD)2

Int 1 post mean (SD)3

Int 2 post mean (SD)4

MD 5

Relative % change 6

Adjusted relative % change7

SMD8

(P value)9

(Rosemann 2007)*

Intervention (aimed at GPs): 2 interactive 8‐hour meetings focusing on arthritis self management, guideline dissemination and patient information material versus Intervention (aimed at GPs) as above plus patient case management via telephone by practice nurses

Quality of life (AIMS2‐SF scores) Lower body

2.67 (1.88)

3.01 (2.11)

2.48 (1.1)

2.61 (1.4)

‐0.13

‐5%

0%

‐0.1

Quality of life (AIMS2‐SF scores) Upper body

1.47 (2.25)

1.68 (2.44)

1.43 (1.5)

1.62 (1.3)

‐0.19

‐12%

‐6%

‐0.1

Quality of life (AIMS2‐SF scores) Symptom

4.87 (2.13)

5.02 (2.29)

4.51 (1.0)

4.42 (1.8)

0.09

2%

12%

0.1

Quality of life (AIMS2‐SF scores) Affect

2.89 (1.35)

3.04 (1.39)

2.92 (0.8)

2.98 (0.9)

‐0.06

‐2%

‐1%

‐0.1

Quality of life (AIMS2‐SF scores) Social

4.52 (1.88)

4.79 (1.80)

4.43 (0.6)

4.736 (1.2)

‐0.31

‐6%

‐25%

‐0.3

GP contacts

4.56 (6.13)

5.01 (5.78)

4.44 (1.7)

4.9 (1.6)

0.46

9%

37%

0.3

Referrals to orthopaedics

1.58 (3.43)

1.76 (3.52)

1.49 (0.4)

1.52 (1.3)

0.03

2%

‐9%

0.0

Radiographs

0.82 (3.12)

0.80 (3.01)

0.75 (0.6)

0.71 (0.4)

‐0.04

‐6%

‐1%

‐0.1

Non‐medical practitioners

0.11 (3.01)

0.50 (4.20)

0.09 (0.4)

0.47 (0.4)

0.38

81%

‐45%

0.9

Physiotherapy

4.70 (9.10)

5.22 (10.03)

4.63 (0.6)

5.08 (0.6)

0.45

9%

35%

0.7

Acupuncture

0.83 (3.45)

0.77 (3.99)

0.8 (1.3)

0.72 (1.3)

‐0.08

‐11%

0%

‐0.1

1. Intervention 1 group pre‐intervention mean (standard deviation)

2. Intervention 2 group pre‐intervention mean (standard deviation)

3. Intervention 1 group post‐intervention mean (standard deviation)

4. Intervention 2 group postintervention mean (standard deviation)

5. Mean Difference (MD)=Difference between post‐intervention means. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

6. Relative percentage change post‐intervention = (Int1 post mean ‐ Int2 post mean)/Int2 post mean. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

7. Adjusted relative percentage change= (Int1 post mean‐Int2 post mean)‐(Int1 pre mean ‐ Int2 pre mean)/Int2 post mean. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome.

8. SMD=Standardised Mean Difference=(Int1 post mean‐Int2 post mean)/SD pooled. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

9. P value reported by study authors

AIMS2‐SF: Arthritis Impact Measurement Scales Short Form

* There are unit of analysis errors in the reported results because the available data did not account for the effect of clustering.

Figuras y tablas -
Table 16. Osteoarthritis studies: intervention 1 versus intervention 2 continuous data
Table 17. Shoulder studies: intervention versus control, continuous data

(Study)

Intervention

Outcome

Int pre mean (SD)1

C pre mean (SD)2

Int post mean (SD)3

C post mean (SD)4

MD 5

Relative % change 6

Adjusted relative % change7

SMD8

(P value)9

(Watson 2008)

Intervention: 60‐minute lecture on shoulder disorders, handouts, training in injection techniques versus control group (usual care)

British Shoulder Disability Questionnaire (BSDQ)

12.22 (4.21)

13.11 (4.43)

8.51 (0.60)

9.46 (0.82)

0.95

10%

1%

0.2

(P=0.36)

Short form 36 item (SF‐36) Health Survey ‐ physical component score

37.78 (8.69)

35.96 (8.93)

40.55 (0.60)

40.80 (0.90)

‐0.25

‐1%

‐5%

0.0

(P=0.82)

Short form 36 item (SF‐36) Health Survey ‐ mental component score

45.42 (13.33)

44.64 (13.09)

46.81 (0.93)

45.64 (1.28)

1.17

3%

1%

0.1

(P=0.47)

1. Intervention group pre‐intervention mean (standard deviation)

2. Control group pre‐intervention mean (standard deviation)

3. Intervention group post‐intervention mean (standard deviation)

4. Control group pos‐tintervention mean (standard deviation)

5. Mean Difference (MD)=Difference between post‐intervention means. The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

6. Relative percentage change post‐intervention = (Int post mean ‐ Control post mean)/Control post mean

7. Adjusted relative percentage change= (Int post mean‐Control post mean)‐(Int pre mean ‐ Control pre mean)/Control post mean. The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome.

8. SMD=Standardised Mean Difference=(Int post mean‐Control post mean)/SD pooled. The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

9. P value reported by study authors

Figuras y tablas -
Table 17. Shoulder studies: intervention versus control, continuous data
Table 18. Shoulder studies: intervention 1 versus intervention 2, continuous data

(Study)

Intervention 1 versus Intervention 2

Outcome

Int 1 pre mean (SD)1

Int 2 pre mean (SD)2

Int 1 post mean (SD)3

Int 2 post mean (SD)4

MD 5

Relative % change 6

Adjusted relative % change7

SMD8

(P value)9

(Gormley 2003*)

Shoulder injection training on mannequins versus shoulder injection training on mannequins and real patients

Shoulder injections performed by general practitioner

3.5

3.4

4.5

7.8

‐3.3

‐42%

‐44%

(P=0.02)

Referrals to shoulder injection clinics

2.3

2.0

1.5

0.6

‐0.9

‐150%

‐100%

(P=0.36)

Referrals to physiotherapy

5.9

5.6

4.7

3.2

‐1.5

‐47%

‐38%

(P=0.20)

1. Intervention 1 group pre‐intervention mean (standard deviation)

2. Intervention 2 group pre‐intervention mean (standard deviation)

3. Intervention 1 group post‐intervention mean (standard deviation)

4. Intervention 2 group postintervention mean (standard deviation)

5. Mean Difference (MD)=Difference between post‐intervention means. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

6. Relative percentage change post‐intervention = (Int1 post mean ‐ Int2 post mean)/Int2 post mean. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

7. Adjusted relative percentage change= (Int1 post mean‐Int2 post mean)‐(Int1 pre mean ‐ Int2 pre mean)/Int2 post mean. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome.

8. SMD=Standardised Mean Difference=(Int1 post mean‐Int2 post mean)/SD pooled. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

9. P value reported by study authors

* The study does not report SD and therefore we were not able to calculate the SMD

Figuras y tablas -
Table 18. Shoulder studies: intervention 1 versus intervention 2, continuous data
Table 19. Other musculoskeletal conditions studies: Intervention versus control, continuous data

(Study)

Intervention

Outcome

Int pre mean (SD)1

C pre mean (SD)2

Int post mean (SD)3

C post mean (SD)4

MD 5

Relative % change 6

Adjusted relative % change7

SMD8

(P value)9

(Huas 2006)

Training of general practitioners on the use of 2 validated assessment instruments for pain versus control group (usual care)

Pain relief a week after last consultation with general practitioner

41.1 (4.6)

50.7 (4.8)

‐9.6

‐19%

‐2

(P=0.0004)

Pain relief a week after last consultation with general practitioner not including patients on Level 3 analgesics

40.8 (4.0)

50.7 (4.2)

‐9.9

‐20%

‐2.4

(P=0.0001)

Level 1 analgesic treatment (as defined by WHO classification system)

34.7 (10.6)

42.9 (18.4)

29.6 (9.9)

34.2 (12.4)

‐4.6

‐13%

11%

‐0.3

(P=0.38)

Level 2 analgesic treatment (as defined by WHO classification system)

42.2 (5.9)

44.1 (19.6)

35.4 (6.3)

47.7 (8.8)

‐12.3

‐26%

‐22%

‐0.9

(P=0.003)

Level 3 analgesic treatment (as defined by WHO classification system)

7.5 (5.6)

2.5 (2.1)

7.2 (4.7)

1.8 (2.5)

5.4

300%

22%

1.2

(P=0.007)

Co‐analgesics (antidepressants, anxiolytics, anti‐epileptics)

46.0 (7.6)

38.7 (7.5)

38.4 (11.4)

33.0 (15.1)

5.4

16%

‐6%

0.7

(P=0.38)

Other drugs (non‐psychotropic muscle relaxants)

21.6 (7.1)

27.3 (13.5)

19.0 (5.3)

22.9 (11.5)

‐3.9

‐17%

8%

‐0.4

(P=0.34)

Non‐medicinal treatment (physiotherapy, homeopathy, acupuncture, compression bandages, etc)

44.3 (10.2)

44.9 (11.1)

33.8 (11.8)

39.3 (12.5)

‐5.5

‐14%

‐12%

‐0.5

(P=0.30)

1. Intervention group pre‐intervention mean (standard deviation)

2. Control group pre‐intervention mean (standard deviation)

3. Intervention group post‐intervention mean (standard deviation)

4. Control group pos‐tintervention mean (standard deviation)

5. Mean Difference (MD)=Difference between post‐intervention means. The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

6. Relative percentage change post‐intervention = (Int post mean ‐ Control post mean)/Control post mean

7. Adjusted relative percentage change= (Int post mean‐Control post mean)‐(Int pre mean ‐ Control pre mean)/Control post mean. The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome.

8. SMD=Standardised Mean Difference=(Int post mean‐Control post mean)/SD pooled. The direction of effect has been adjusted so that a positive result represents a beneficial intervention outcome, according to Grimshaw 2004.

9. P value reported by study authors

Figuras y tablas -
Table 19. Other musculoskeletal conditions studies: Intervention versus control, continuous data
Table 20. Other musculoskeletal studies: Intervention versus a different intervention, dichotomous data

(Study)

Intervention 1 versus intervention 2

Outcome

Int 1 pre (%) 1

Int 2 pre (%)2

Int 1 post (%)3

Int 2 post (%)4

ARD 5

Risk difference 6

(P value if reported by authors)

Relative % change post 7

Risk ratio 8

(Robling 2002)*

Guidelines and seminar versus guideline dissemination by post*

Concordant requests

79% (23/29)

79% (32/41)

0%

0%

1

(Robling 2002)*

Guidelines and feedback versus guideline dissemination by post*

Concordant requests

67% (21/32)

79% (32/41)

‐12.1%

‐15%

0.8

(Robling 2002)*

Guidelines, seminar and feedback versus guideline dissemination by post*

Concordant requests

71% (27/37)

79% (32/41)

‐7.6%

‐10%

0.9

(Robling 2002)*

Guidelines and seminar versus guidelines and feedback*

Concordant requests

79% (23/29

67% (21/32)

12.1%

18%

1.2

(Robling 2002)*

Guidelines and seminar versus guidelines, seminar and feedback*

Concordant requests

79% (23/29)

71% (27/37)

7.6%

11%

1.1

(Robling 2002)*

Guidelines and feedback versus guidelines, seminar and feedback*

Concordant requests

67% (21/32)

71% (27/37)

‐4.5%

‐6%

0.9

(Eccles 2001)**

Feedback on number of knee radiographs 6 months before and 6 months after the intervention plus guideline dissemination versus guideline dissemination

Knee radiographs concordant with guidelines

22% (52/240)

25% (83/328)

‐3.6%

‐14%

0.9

(Eccles 2001)**

Reminder messages on radiograph reports plus guideline dissemination versus guideline dissemination

Knee radiographs concordant with guidelines

31% (26/85)

25% (83/328)

5.3%

21%

1.2

(Eccles 2001)**

Feedback on number of knee radiographs 6 months before and 6 months after the intervention plus guideline dissemination plus reminder messages on radiograph reports versus guideline dissemination

Knee radiographs concordant with guidelines

28% (70/252)

25% (83/328)

2.5%

10%

1.1

(Eccles 2001)**

Feedback on number of knee radiographs 6 months before and 6 months after the intervention plus guideline dissemination versus reminder messages on radiograph reports plus guideline dissemination

Knee radiographs concordant with guidelines

22% (52/240)

31% (26/85)

‐8.9%

‐29%

0.7

1. Intervention 1 group pre‐intervention proportion

2. Intervention 2 group pre‐intervention proportion

3. Intervention 1 group post‐intervention proportion

4. Intervention 2 group post‐intervention proportion

5. ARD = [Int 1 post (%) minus Int 2 post (%)] minus [Int 1 pre (%) minus Int 2 pre (%)]. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

6. Risk Difference (RD) is the absolute % change post‐intervention = Int 1 post (%) minus Int 2 post (%). This is considered to be "small" if ≤ 5%, "modest" if > 5% and ≤10%,"moderate" if > 10% but ≤ 20%, and "large" if > 20%.The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome.

7. Relative % change post = absolute % change post divided by Int 2 post (%). The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

8. Risk ratio (RR) = Int 1 post (%) divided by Int 2 post (%)

Int 1: intervention 1 group; Int 2: Intervention 2 group; ARD: adjusted risk difference; NS: not significant

*The results have been re‐calculated taking into account the reported Intercluster Correlation (ICC=0.0269) and average cluster size 12.5 according to chapter 16.3.4 of the Cochrane Handbook, Higgins 2011a.

** The data reported above for the study by Eccles 2001 does not account for clustering. We did not have access to sufficient information to adjust the data for clustering.

Figuras y tablas -
Table 20. Other musculoskeletal studies: Intervention versus a different intervention, dichotomous data
Table 21. Other musculoskeletal studies: Intervention versus a different intervention, continuous data

(Study)

Intervention 1 versus Intervention 2

Outcome

Int 1 pre mean (SD)1

Int 2 pre mean (SD)2

Int 1 post mean (SD)3

Int 2 post mean (SD)4

MD 5

Relative % change 6

Adjusted relative % change7

SMD8

(P value)9

(Eccles 2001)*

Feedback on number of knee radiographs 6 months before and 6 months after the intervention plus guideline dissemination versus guideline dissemination

Number of knee radiographs per 1000 patients

7.03 (5.1)

6.67 (3.9)

6.32 (4.0)

7.02 (3.6)

0.7

10%

15%

0.2

(NR)

(Eccles 2001)*

Reminder messages on radiograph reports plus guideline dissemination versus guideline dissemination

Number of knee radiographs per 1000 patients

7.18 (5.0)

6.67 (3.9)

5.22 (3.6)

7.02 (3.6)

1.8

26%

33%

0.5

(P< 0.05)

(Eccles 2001)*

Feedback on number of knee radiographs 6 months before and 6 months after the intervention plus guideline dissemination plus reminder messages on radiograph reports versus guideline dissemination

Number of knee radiographs per 1000 patients

9.34 (6.1)

6.67 (3.9)

5.21 (3.7)

7.02 (3.6)

1.8

26%

64%

0.5

(NR)

(Eccles 2001)*

Feedback on number of knee radiographs 6 months before and 6 months after the intervention plus guideline dissemination versus reminder messages on radiograph reports plus guideline dissemination

Number of knee radiographs per 1000 patients

7.03 (5.1)

7.18 (5.0)

6.32 (4.0)

5.22 (3.6)

‐1.1

‐21%

‐24%

‐0.3

(NR)

1. Intervention 1 group pre‐intervention mean (standard deviation)

2. Intervention 2 group pre‐intervention mean (standard deviation)

3. Intervention 1 group post‐intervention mean (standard deviation)

4. Intervention 2 group postintervention mean (standard deviation)

5. Mean Difference (MD)=Difference between post‐intervention means. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

6. Relative percentage change post‐intervention = (Int1 post mean ‐ Int2 post mean)/Int2 post mean. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

7. Adjusted relative percentage change= (Int1 post mean‐Int2 post mean)‐(Int1 pre mean ‐ Int2 pre mean)/Int2 post mean. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome.

8. SMD=Standardised Mean Difference=(Int1 post mean‐Int2 post mean)/SD pooled. The direction of effect has been adjusted so that a positive result represents a beneficial intervention 1 outcome, according to Grimshaw 2004.

9. P value reported by study authors

*The above data reported above for Eccles 2001 was adjusted for clustering by the authors

Figuras y tablas -
Table 21. Other musculoskeletal studies: Intervention versus a different intervention, continuous data
Table 22. Summary of median absolute effect sizes (risk difference) of dichotomous outcomes for interventions aiming to increase or decrease a clinical behaviour

Table 23: Summary of median absolute effect sizes (risk difference) of dichotomous outcomes for interventions aiming to increase or decrease a clinical behaviour

Study characteristic: behaviour targeted

Number of comparisons (n studies)

Median absolute effect size

Interquartile range

Range

Increase an existing clinical behaviour according to guidelines

68 (14)

5%

0.6% to 12.6%

‐7.8% to 57.2%

Decrease an existing clinical behaviour according to guidelines

26 (7)

1.1%

‐1.1% to 3%

‐12.6% to 30.1%

Figuras y tablas -
Table 22. Summary of median absolute effect sizes (risk difference) of dichotomous outcomes for interventions aiming to increase or decrease a clinical behaviour
Table 23. Summary of median effect sizes (risk difference) of dichotomous outcomes for interventions aiming to increase or decrease a clinical behaviour (including only comparisons from Low Back Pain studies)

Table 24: Summary of median effect sizes (risk difference) of dichotomous outcomes for interventions aiming to increase or decrease a clinical behaviour (including only comparisons from Low Back Pain studies)

Study characteristic: behaviour targeted

Number of comparisons (n studies)

Median absolute effect size

Interquartile range

Range

Increase an existing clinical behaviour according to guidelines

18 (2)

3.7%

‐0.8% to 6.9%

‐4.7% to 12.8%

Decrease an existing clinical behaviour according to guidelines

23 (6)

0.5%

‐1.1% to 2.4%

‐12.6% to 30.1%

Figuras y tablas -
Table 23. Summary of median effect sizes (risk difference) of dichotomous outcomes for interventions aiming to increase or decrease a clinical behaviour (including only comparisons from Low Back Pain studies)
Table 24. Summary of median effect sizes (risk difference) of dichotomous outcomes for interventions aiming to increase or decrease a clinical behaviour (including only comparisons from Osteoarthritis studies)

Table 25: Summary of median effect sizes (risk difference) of dichotomous outcomes for interventions aiming to increase or decrease a clinical behaviour (including only comparisons from Osteoarthritis studies)

Study characteristic: behaviour targeted

Number of comparisons (n studies)

Median absolute effect size

Interquartile range

Range

Increase an existing clinical behaviour according to guidelines

18 (3)

6.3%

‐0.2% to 10%

‐7.8% to 57.2%

Decrease an existing clinical behaviour according to guidelines

3 (1)

7.8%

6.1% to 13.4%

4.4% to 18.9%

Figuras y tablas -
Table 24. Summary of median effect sizes (risk difference) of dichotomous outcomes for interventions aiming to increase or decrease a clinical behaviour (including only comparisons from Osteoarthritis studies)
Comparison 1. Meta‐analysis of osteoporosis studies evaluating physician and patient interventions versus usual care

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Bone Mineral Density Show forest plot

3

3386

Risk Ratio (M‐H, Fixed, 95% CI)

4.44 [3.54, 5.55]

2 Osteoporosis medication Show forest plot

5

4223

Risk Ratio (M‐H, Fixed, 95% CI)

1.71 [1.50, 1.94]

Figuras y tablas -
Comparison 1. Meta‐analysis of osteoporosis studies evaluating physician and patient interventions versus usual care
Comparison 2. Meta‐analysis of osteoporosis studies evaluating physician‐only interventions versus usual care

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Bone mineral density Show forest plot

2

3047

Risk Ratio (M‐H, Fixed, 95% CI)

4.75 [3.62, 6.24]

2 Osteoporosis medication Show forest plot

2

3047

Risk Ratio (M‐H, Fixed, 95% CI)

1.52 [1.26, 1.84]

Figuras y tablas -
Comparison 2. Meta‐analysis of osteoporosis studies evaluating physician‐only interventions versus usual care
Comparison 3. Meta‐analysis of osteoporosis studies evaluating physician only interventions versus physician and patient interventions

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Bone mineral density Show forest plot

2

2995

Odds Ratio (M‐H, Fixed, 95% CI)

0.93 [0.77, 1.12]

2 Medication Show forest plot

2

2995

Risk Ratio (M‐H, Fixed, 95% CI)

0.93 [0.79, 1.10]

Figuras y tablas -
Comparison 3. Meta‐analysis of osteoporosis studies evaluating physician only interventions versus physician and patient interventions