Scolaris Content Display Scolaris Content Display

Cochrane Database of Systematic Reviews

Herramientas creadas y distribuidas por los realizadores de guías para promover la adopción de las mismas

Information

DOI:
https://doi.org/10.1002/14651858.CD010669.pub2Copy DOI
Database:
  1. Cochrane Database of Systematic Reviews
Version published:
  1. 22 August 2016see what's new
Type:
  1. Intervention
Stage:
  1. Review
Cochrane Editorial Group:
  1. Cochrane Effective Practice and Organisation of Care Group

Copyright:
  1. Copyright © 2016 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

Article metrics

Altmetric:

Cited by:

Cited 0 times via Crossref Cited-by Linking

Collapse

Authors

  • Gerd Flodgren

    The Norwegian Knowledge Centre for the Health Services, Norwegian Institute of Public Health, Oslo, Norway

  • Amanda M Hall

    Nuffield Department of Population Health, The George Institute for Global Health, Oxford, UK

  • Lucy Goulding

    King's Improvement Science, King's College London, London, UK

  • Martin P Eccles

    Institute of Health and Society, Newcastle University, Newcastle upon Tyne, UK

  • Jeremy M Grimshaw

    Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Canada

  • Gillian C Leng

    National Institute for Health and Care Excellence, London, UK

  • Sasha Shepperd

    Correspondence to: Nuffield Department of Population Health, University of Oxford, Oxford, UK

    [email protected]

Contributions of authors

GF contributed to the writing of the protocol, led the screening of the studies for inclusion and data extraction, and drafted the review.

AH assisted with screening studies for inclusion and data extraction, and commented on drafts of the review.

LG assisted with screening studies for inclusion and data extraction, and commented on drafts of the review.

ME contributed to the writing of the protocol.

JG commented on the final version of the review prior to peer review.

GL suggested the topic of the review, and commented on drafts of the review.

SS contributed to the writing of the protocol, assisted with screening studies for inclusion, and commented on drafts of the review.

Sources of support

Internal sources

  • Nuffield Department of Population Health, University of Oxford., UK.

External sources

  • NIHR Cochrane EPOC programme grant, UK.

Declarations of interest

GF None known.

AH None known.

LG None known.

ME None known.

JG holds the Canada Research Chair in Health Knowledge Transfer and Uptake.

GL is Deputy Chief Executive and Director of Health and Social Care at the National Institute for Health and Care Excellence (NICE), and has responsibility for the implementation programme that includes the development of implementation tools.

SS None known.

Acknowledgements

We wish to thank senior information scientist Nia Roberts at the Bodleian library (Oxford, UK), for developing the search strategy and for running the electronic searches. We would also like to acknowledge Hannah Parke (from King's improvement Science) for assistance with the sifting.

Lucy Goulding and Hannah Parke are staff members at King's Improvement Science, and they wish to acknowledge their funders: King’s Improvement Science is part of the NIHR CLAHRC South London and comprises a specialist team of improvement scientists and senior researchers based at King’s College London. Its work is funded by King’s Health Partners (Guy’s and St Thomas’ NHS Foundation Trust, King’s College Hospital NHS Foundation Trust, King’s College London and South London and Maudsley NHS Foundation Trust), Guy’s and St Thomas’ Charity, the Maudsley Charity and the Health Foundation.

This project was supported by the National Institute for Health Research, via Cochrane Infrastructure funding and a Cochrane programme grant to the EPOC Group. The views and opinions expressed therein are those of the authors and do not necessarily reflect those of the Systematic Reviews Programme, NIHR, NHS or the Department of Health.

Version history

Published

Title

Stage

Authors

Version

2016 Aug 22

Tools developed and disseminated by guideline producers to promote the uptake of their guidelines

Review

Gerd Flodgren, Amanda M Hall, Lucy Goulding, Martin P Eccles, Jeremy M Grimshaw, Gillian C Leng, Sasha Shepperd

https://doi.org/10.1002/14651858.CD010669.pub2

2013 Aug 09

Tools developed and disseminated by guideline producers to promote the uptake of their guidelines

Protocol

Gerd Flodgren, Martin P Eccles, Jeremy Grimshaw, Gillian C Leng, Sasha Shepperd

https://doi.org/10.1002/14651858.CD010669

Differences between protocol and review

Two new review authors (AH and LG), who were not involved at the protocol stage, are included in the review team.

Keywords

MeSH

PICOs

Population
Intervention
Comparison
Outcome

The PICO model is widely used and taught in evidence-based health care as a strategy for formulating questions and search strategies and for characterizing clinical studies or meta-analyses. PICO stands for four different potential components of a clinical question: Patient, Population or Problem; Intervention; Comparison; Outcome.

See more on using PICO in the Cochrane Handbook.

Study flow diagram.
Figures and Tables -
Figure 1

Study flow diagram.

Risk of bias summary: review authors' judgements about each risk of bias item for each included study. White space indicate studies not reporting non‐objective outcomes and for which risk of bias could not be assessed.
Figures and Tables -
Figure 2

Risk of bias summary: review authors' judgements about each risk of bias item for each included study. White space indicate studies not reporting non‐objective outcomes and for which risk of bias could not be assessed.

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies. White spcace indicate studies not reporting non‐objective outcomes and for which risk of bias could not be assessed.
Figures and Tables -
Figure 3

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies. White spcace indicate studies not reporting non‐objective outcomes and for which risk of bias could not be assessed.

Clinical practice guideline (CPG) + implementation tool compared with CPG only for adherence to guidelines

Patient or population: Healthcare professionals (physiotherapists, hospital physicians) providing care for people with different clinical conditions (patients with non specific low back pain, patients with symptoms indicating a need for a thyroid function test)

Setting: Private physiotherapy clinics in the Netherlands, general hospitals in France

Intervention: CPG + guideline implementation tool (e.g. training workshops, paper‐based materials and order forms, reminders, web‐based tools)
Comparison: CPG only

Outcomes

Median ARD

(Absolute risk difference)
(IQR)

No of Participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Adherence to guidelines

Guideline tools provided to healthcare professionals as an aid to improve the use of a CPG probably lead to improved adherence with the CPG, as compared to guidelines only. Median ARD: 0.135 (0.115 to 0.15.9) at mean 4 weeks follow‐up

68 physio‐ therapy

practices; and 6 hospitals

(2 C‐RCTs)

⊕⊕⊕⊝
moderate1

2 of the 4 included studies reported a proxy measure for adherence to guidelines, and results from these studies could therefore not be included in the ARD calculation

Costs

Guideline tools aimed at improving the use of guidelines may lead to little or no difference in healthcare costs

68 physio‐ therapy clinics

(1 C‐RCT)

⊕⊕⊝⊝

low2

1 trial reported no difference in mean direct annual cost* per patient between intervention and control groups. 1 French paper belonging to 1 of the included trials (6 hospitals) and reporting on costs awaits translation

* Direct costs included costs of the dissemination of the guideline and healthcare resource use by the patient

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

1We downgraded the certainty of the evidence one step due to high risk of bias.

2We downgraded the certainty of the evidence two steps due to imprecision.

Figures and Tables -
Table 1. Guideline development process

Author Year

Targeted behaviour

Guideline

developers

Literature review

Critical appraisal

Consensus processes

Key stakeholder involvement

Barriers/facilitator assessment

Bekkering 2005

Targeted behaviour:

management of non‐specific low back pain

Number of recommendations: 4 main recommendations

The Royal Dutch Physiotherapy Association.

CPGs2 were constructed on the basis of the phases of the physiotherapy process, using the Dutch method of developing physiotherapy guidelines, and evidence from systematic reviews were identified through searching electronic databases

Not mentioned but probably included in the Dutch method of developing CPGs

Based on scientific evidence.

If no evidence was available, consensus between experts was obtained

The CPGs were pilot‐tested among 100 physiotherapists and reviewed by an external multidisciplinary panel

Barriers to change were assessed through a survey as part of the CPG development process

Daucourt 2003

Targeted behaviour: appropriate thyroid function testing

Number of recommendations: not reported

The Committee for Co‐ordinating Clinical Evaluation and Quality in
Aquitaine (CCECQA) developed guidelines in collaboration with a regional working group and a national review group

The CPG developers

conducted

a comprehensive

review of the literature

CPG3 development involved an expert consensus process.

Fine 2003

Targeted behaviour: appropriate duration of intravenous antibiotic therapy for treatment of pneumonia

Number of recommendations: a 2‐step recommendation

Researchers who were part of the Pneumonia Patient Outcomes Research Team (PORT)

The CPG was based on a review of the medical literature, and empiric evidence on time to reach clinical stability

The CPG development process involved the consensus of an 8‐member national guideline panel

The guideline was reviewed by clinical opinion leaders at each study site, and was approved for local use by the relevant utilisation management department.

Shah 2014

Targeted behaviour: management of cardiovascular risk
factors and outcomes of cardiovascular disease in people with
diabetes

Number of recommendations:

no information

Canadian Diabetes Association (and Expert Committee members)

Expert Committee members evaluated the relevant literature, and guidelines were developed and initially reviewed
by the Expert Committee

After formulating new recommendations or modifying existing
ones based on new evidence, each recommendation was
assigned a grade from A through D

Based on scientific evidence/review of the literature

A draft document was circulated nationally and
internationally for review by numerous stakeholders and
experts in relevant fields.
Subsequently, a panel of 6 methodologists,
who were not directly involved with the initial review and
assessment of the evidence, independently reviewed each
recommendation, its assigned grade and supportive citations

1Khunti 1998. Development of evidence‐based review criteria for the management of patients with depression in general practice. No published version of the guideline found.
2Bekkering 2003. Dutch physiotherapy guidelines for low back pain.
3Saillour Glénisson 2001. Guidelines for thyroid function tests in adults.
4Shah 2014. Canadian Diabetes Association Clinical Practice Guidelines Expert Committee: Canadian Diabetes Association 2008 clinical practice guidelines for the prevention and management of diabetes in Canada.

Figures and Tables -
Table 1. Guideline development process
Table 2. Guideline tool development and delivery

Author Year

Delivery of the intervention

Theoretical models/ frameworks used

Evidence base

Targeted to barriers

Key stakeholder involvement

Bekkering 2005

Type of intervention:

simple, but multicomponent; active only

Intervention target: the healthcare professional

Targeted behaviour:

management of nonspecific low back pain

Mode: face‐to‐face

Provider: The primary investigator and 1 of 2 additional trainers with adequate clinical experience in the management of low back pain supervised the training sessions

"The sessions were based on interventions that have all been shown to be effective, such as interactive education and discussion, feedback, and reminders".1,2,3,4,5

The content of the strategy was determined on the basis of information about the expected barriers for implementation gathered during the development of the CPGs

2 experts gave advice on the content of the strategy

Daucourt 2003

Type of intervention:

multicomponent; passive only

Intervention target: the healthcare professional

Targeted behaviour: appropriate thyroid function testing

Mode: Paper‐based materials

Provider: none

"Among the clinical guideline diffusion strategies, the most effective are feedback, reminders, academic detailing and financial incentives1,2,4,5 Administrative procedures such as the implementation of test request forms have also proved effective."

Fine 2003

Type of intervention:

single; active + passive

Intervention target: the healthcare professional

Targeted behaviour: appropriate duration of intravenous antibiotic therapy for treatment of pneumonia

Mode: Paper‐based material (detail sheets/treatment recommendations in patient records) and telephone reminder

Provider: nurse delivered telephone reminder

"The multifaceted guideline dissemination strategy consisted of interventions of proven benefit, including real‐time physician reminders" 1,6,7,8

Shah 2014

Type of intervention:

passive

Intervention target:

family physicians (and diabetes patients at high risk of cardiovascular disease)

Targeted behaviour: management of cardiovascular risk factors and outcomes of cardiovascular disease in people with diabetes

Mode: printed educational materials

Targeting the family physician:

The cardiovascular disease toolkit was a collection of printed educational materials, packaged in a brightly‐coloured box with CDA branding, sent to Canadian family physicians. The contents included an introductory letter from the Chair of the practice
guidelines’ Dissemination and Implementation Committee; an
8‐page summary of selected sections of the practice guidelines
targeted towards family physicians; a 4‐page synopsis of the key guideline elements pertaining to cardiovascular disease risk; a small double‐sided laminated card with a simplified algorithm for cardiovascular risk assessment, vascular protection strategies, and
screening for cardiovascular disease, and a pad of tear‐off sheets for patients with a cardiovascular risk self‐assessment tool and a list
of recommended risk reduction strategies

Provider: NA13

The implicit theory behind its
development was that the guidelines were too long and complex to be easily incorporated into clinical practice, so the toolkit aimed to simplify the information, tailor it towards clinical practice, and
provide explicit actionable recommendations

"The literature has demonstrated that the benefits of printed educational interventions are, at best, modest. A systematic review of methods to improve practice guideline adherence demonstrated an absolute improvement of 8% for educational materials. A more recent Cochrane review found that printed educational materials led to a median absolute improvement in performance of only 2% (25). Studies of printed materials specifically tied to clinical practice guidelines also showed modest benefits. A small English study randomised 42 family physicians to receive an algorithm for monitoring and treatment of hypertension of diabetic patients based on practice guidelines, but found no difference in blood pressure control between the intervention and control groups. However, some processes of care were slightly improved: patients in the intervention group were prescribed higher doses of antihypertensive medications, and had more physician visits to monitor blood pressure. In a larger Canadian study, family physicians were randomised to receive a 1‐page summary of a 3‐year‐old practice guideline on anti‐anginal therapy from the local medical governing body. No differences were noted in prescription of β‐blockers, antiplatelet agents, or lipid‐lowering drugs between groups in the 7000 patients reviewed" 9,10,11,12

The toolkit was
created for the CDA by clinical experts including family
physicians, endocrinologists, and other healthcare professionals,
with guidance from clinicians with expertise in knowledge
translation and implementation

1Bero 1998 Closing the gap between research and practice: an overview of systematic reviews of interventions to promote the implementation of research findings.
2Davis 1995 Changing physician performance. A systematic review of the effect of continuing medical education strategies.
3Wensing 1998 Implementing guidelines and innovations in general practice: which interventions are effective?
4Grimshaw 1995 Developing and implementing clinical practice guidelines.
5Davis 1997. Translating guidelines into practice. A systematic review of theoretic concepts, practical experience and research evidence in the adoption of clinical practice guidelines.
6Murrey 1992 Implementing clinical guidelines: a quality management approach to reminder systems.
7Grimshaw 1993. Effect of clinical guidelines on medical practice: a systematic review of rigorous evaluations.
8Weingarten 2000. Translating practice guidelines into patient care: guidelines at the bedside.
9Grimshaw 2006. Towards evidence‐based quality improvement: evidence (and its limitation) of the effectiveness of guideline dissemination and implementation strategies 1966–1998.
10Giguère 2012. Printed educational materials: effects on professional practice and healthcare outcomes.
11Bebb 2007. A cluster randomised controlled trial of the effect of a treatment algorithm for hypertension in patients with type 2 diabetes.
12Beaulieu 2004. Drug treatment of stable angina pectoris and mass dissemination of therapeutic guidelines: a randomized controlled trial.
13Not applicable

Figures and Tables -
Table 2. Guideline tool development and delivery
Table 3. Intervention components

Author Year

Tailoring

Feedback

Educational outreach/ Academic detailing/ Small group discussions

Reminders (paper, electronic, telephone)

Decision support tools

Other

(test order forms, supportive materials etc.)

Bekkering 2005

The content of the strategy was determined on the basis of information about the expected barriers for implementation gathered during the development of the clinical guidelines.

2 interactive training sessions, each lasting 2½ hours, for groups of 8 – 12 physiotherapists (including feedback on current management and reminders). For each session a preparation time of 2 hours was recommended.

Daucourt 2003

Pocket memorandum card.

Test request form.

Fine 2003

Paper‐based detail sheet/ treatment recommendations put into the patient's record + real‐time nurse telephone reminder

Shah 2014

Printed educational materials

Figures and Tables -
Table 3. Intervention components
Table 4. Results: Other outcomes

Author Year

Clinical outcomes;

Medical complications

Quality of life

Satisfaction with care

Mortality

Healthcare resource use (including medications prescribed)

Costs

Bekkering 2005

Quality of Life

(assessed with the EQ‐5D1), mean (SD):

BL:

Intervention: 0.6730 (0.2042); Control: 0.6134 (0.2661),

P = 0.006.

At 6 weeks:

Intervention: 0.7778 (0.1978); Control: 0.7497 (0.2316)

At 12 weeks:

Intervention: 0.8141 (0.1988); Control: 0.7873 (0.2210)

Note: results for 26 and 52 weeks reported graphically

Mean annual cost (Euros) per patient (SD):

Direct cost2:

Intervention: 374 (437).

Control: 449 (572).

The costs (Euro) of releasing a new guideline for low back pain to 18,000

physiotherapists:

Intervention (active strategy): 87,416

Control (passive strategy): 63,101

Daucourt 2003

Cost paper awaits translation

Fine 2003

In‐hospital medical complications, number (%):

Intervention:157 (55); Control: 206 (63), P = 0.04

Functional status3

SF‐12 physical health composite score: Intervention:45 ± 7, n = 181;
Control: 45 ± 7, n = 223; P = 0.71

SF‐12 mental health composite score: Intervention: 45 ± 6; Control: 45 ± 7, P = 0.71

Patient satisfaction with care4 , number (%):

Not satisfied with overall care: Intervention: 12 (5.3), n = 228; Control: 11 (4.0), n = 273, P = 0.67

Believed length of stay was too short: Intervention: 59 (26.1); Control: 54 (20.2), P = 0.16

Return to usual activities5,Hazard ratio (95% CI):

Nonworkers: 1.09 (0.83 to 1.43), P = 0.55

Workers: 0.85 (0.54 to 1.35); P = 0.49

Return to work (workers) 0.99 (0.63 to 1.58),

P = 0.98

Mortality6

all‐cause, number (%): Intervention: 22 (8), n = 283; Control: 29 (9), n = 325, P = 0.70

Pneumonia‐related mortality, number (%): Intervention: 15 (5); Control: 23 (7), P = 0.44

Length of index hospital (days) stay, median (IQR): Intervention: 5.0 (3.0 to 7.0); Control: 5.0 (3.0 to 8.0); Hazard ratio (95% CI): 1.16 (0.97 to 1.38), P = 0.11

Rehospitalisation7 number (%): Intervention:37 (14); Control:33 (11), P = 0.42

Duration (days) of intravenous antibiotic therapy, median (IQR): Intervention: 3.0 (2.0 to 5.0),n = 283; Control: 4.0 (2.6 to 6.0), n = 325; Hazard ratio (95% CI): 1.23 (1.00 to 1.52), P = 0.06

Shah 2014

Clinical data study:

Intervention: n = 40 practices/795 patients; Control: n = 40 practices/797 patients

Cardiovascular risk reduction (secondary outcomes):

Proportion of participants reaching glycaemic control targets (HbA1c < 7.0%): Intervention: 58.5%; Control: 58.8%; OR 0.93 (0.71 to 1.21), P = 0.58

Proportion of participants reaching blood pressure control targets (< 130/80): Intervention: 52.8%; Control: 63.5%, OR 0.72 (0.53 to 0.98), P = 0.04

Proportion of participants reaching LDL‐cholesterol control targets (< 2.0 mmol/L): Intervention: 59.2%; Control: 61.7% , OR 0.90 (0.68 to 1.18), P = 0.43

Proportion of participants reaching Total to HDL‐cholesterol ratio (< 4.0): Intervention: 74.2%; Control: 76.8%, OR 0.85 (0.63 to1.14), P = 0.27

Clinical (secondary outcomes):

When HbA1c > 8.0%: Intervention: 11.8%; Control: 13.0%, OR 0.98 (0.48 to 1.98), P = 0.95

When blood pressure > 140/90: Intervention: 5.6%; Control: 7.2%, OR 0.67 (0.25 to 1.82), P = 0.43

When LDL cholesterol > 3.0 mmol/L: Intervention: 43.5%; Control: 45.2%, OR 0.94 (0.53 to 1.67), P = 0.83

Administrative data study : Intervention: 2008 practices (467,713 participants); Control: 1999 practices (466, 076 participants)

Secondary outcomes:
Clinical events (all‐cause death, MI, MI or unstable angina, stroke, stroke or TIA, and combined outcomes): OR: from 0.98 to 1.04, P values from 0.21 to 0.96

Administrative data study : Intervention: 2008 practices (467,713 participants); Control: 1999 practices (466,076 participants)

Primary outcome: Death or non‐fatal myocardial infarction: Intervention: 2.5%; Control: 2.5%; OR 1.00 (0.96 to 1.03), P = 0.77

Secondary outcomes: Medication initiation (ACEI/ARB > 1 antihypertensive class, or > 2, or > 3, statin, glucose‐lowering drugs, insulin, nitrate): OR, range: from 0.96 to 1.02, P values from 0.03 to 0.94

Clinical data study:

Primary outcome: Proportion of participants prescribed statins (new or renewed prescription): Intervention: 700 (88.1%); Control: 725 (90.1%); OR 0.73, 95% CI 0.42 to 1.26, P = 0.26

Proportion of participants prescribed an ACEI/ARB: Intervention: Control: Secondary outcome.

Administrative data study :

Secondary outcomes: CAD assessment (electrocardiogram, cardiac stress test, nuclear imaging, coronary angiography, coronary revascularisation, cardiology or internal medicine visit): OR, range: from 0.96 to 1.00, P values from 0.02 to 0.83

1EQ‐5D: a standardised instrument for use as a measure of health outcome.The EQ‐5D has five dimensions: mobility, self‐care, usual activity,pain/discomfort and anxiety/depression. Each dimension has three levels, no problems, some problems and serious problems. Hence, EQ‐5D has 243 possible health states. Utility values of the general public for these health states as measured with the time tradeoff technique on a random sample of the adult population of the United Kingdom, the MVH‐A1 tariff, were applied in this study. The scores range from −0.594 (worst situation) to 1.0 (perfect health).
2The direct costs consisted of costs of the dissemination of the guideline and the costs of the healthcare utilisation of the patients. Prices for the year 2002.
3SF‐12 health scores were assessed in all patients able to provide reliable self‐report data during the 30‐day interview, excluding 6 intervention‐arm and 6 control‐arm patients with missing data.
4Patient satisfaction with care was assessed for all patients with a 30‐day interview that was not completed by a paid caregiver, excluding four intervention‐arm and two control‐arm patients with missing data. An additional two patients in the intervention arm and six patients in the control arm were hospitalised for the full 30 days and were not asked about length of hospital stay. SF‐12, 12‐Item Short Form was used.
5Return to usual activities among non‐workers was assessed for 183 intervention arm and 219 control arm patients not employed at baseline who completed a 30‐day interview. Return to usual activities among workers was assessed in 59 intervention‐arm and 59 control‐arm patients employed at baseline. Return to work was assessed among 54 intervention‐arm and 53 control‐arm patients employed at baseline.
6Mortality, medical complications, and return to work and usual activities were adjusted for pneumonia severity risk class.
7Rehospitalisation within 30 days of the index admission was assessed for all patients who were discharged alive from either the index hospitalisation or another acute‐care facility (if transferred to an acute‐care facility from the index hospitalisation).
8Fluid fasting times assessed by local investigator asking the patient about the fasting time, and checking this information against medical notes.
9Cost for designing, editing, reproducing, and posting need when applied to 170 acute trusts.
10Cost of providing 170 acute trusts with implementation support through a web‐based resource championed through opinion leadership. This includes development costs for the tool (which for this project were in‐house costs, in other cases external agencies may have to be used which are likely to be three times higher), publicity materials, training materials and opinion leader time and activity.

Figures and Tables -
Table 4. Results: Other outcomes
Table 5. Results: Adherence outcomes

Author Year

Adherence Outcomes

Participants (Settings)

Control Adherence

Intervention Adherence

Median ARD

Bekkering 2005

(Hoijenboos 2005)

Targeted behaviour: management of non specific low back pain

GL tool used: interactive training workshop X2

Adherence to 4 guideline recommendations:

i) Limit number of sessions in normal course back pain

ii) Set functional treatment goals

iii) Use mainly active interventions

iv) Give adequate information

Note: an increase was desirable for all outcomes

113 physiotherapists

(68 private physiotherapy practices)

i) Post:

14 (13), n = 253

ii) Post:

180 (71)

iii) Post:

154 (60)

iv) Post:

221 (87)

i) Post:

32 (27), n = 247

ii) Post: 188 (79)

iii) Post: 183 (77)

iv) Post: 229 (96)

+0.115

11.5% higher adherence in the intervention group

i) 0.14%

ii) 0.08%

iii) 0.17%

iv) 0.09%

Daucourt 2003

Targeted behaviour: appropriate thyroid function testing

Guideline tool used:
1) Dual intervention (2 + 3);
2) Order request form;
3) Pocket memorandum card

Global Guideline Conformity Rate

1412 physicians

(6 general hospitals)

Pre: 62.0%

(95% CI 47.7 to 76.4)

Dual intervention group: Post: 77.9% (95% CI 68.9 to 87.0)

Note: only results for the dual intervention presented here

+0.159%

Fine 2003

Targeted behaviour: appropriate duration of intravenous antibiotic therapy for treatment of pneumonia

GL tool used: detail sheet/ treatment recommendations+ telephone reminder

No adherence outcomes reported, only proxies

545 physicians

(7 not‐for‐profit hospitals)

Shah 2014

Targeted behaviour: improved cardiovascular risk factor management in people with diabetes

Guideline tool used: printed educational material

No adherence outcomes reported, only proxies

2 separate studies:

Administrative data study: n = 4007 practices: Intervention: 2008; Control: 1999

Clinical data study. n = 80 practices (1592 patients); Intervention: 40 practices (8795 patients); Control: 40 practices (8797 patients)

Figures and Tables -
Table 5. Results: Adherence outcomes