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Эфавиренз или невирапин в составе трехкомпонентной комбинированной терапии с двумя нуклеозидными ингибиторами обратной транскриптазы для стартовой терапии ВИЧ‐инфекции у пациентов, ранее не получавших антиретровирусную терапию

Appendices

Appendix 1. MEDLINE search strategies

Search

Most recent queries

Result

#11

Search #8 AND #9 Limits: Publication Date from 1996 to 2009

645

#10

Search #8 AND #9

656

#9

Search NNRTI OR (NON‐NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR) OR (NON NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR) OR (NONNUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR) OR (NON‐NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS) OR (NON NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS) OR (NONNUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS) OR (PI SPARING) OR (PROTEASE INHIBITOR SPARING) OR (PROTEASE‐INHIBITOR SPARING) OR (NON‐PROTEASE INHIBITOR CONTAINING) OR (NON‐PI CONTAINING) OR (NON PROTEASE INHIBITOR CONTAINING)

13943

#8

Search #3 AND #4 AND #7

1744

#7

Search #5 OR #6

4073

#6

Search NEVIRAPINE OR NVP OR VIRAMUNE OR NEVIMUNE

2872

#5

Search EFAVIRENZ OR SUSTIVA OR STOCRIN OR EFV OR EFZ

1794

#4

Search randomised controlled trial [pt] OR controlled clinical trial [pt] OR randomised controlled trials [mh] OR random allocation [mh] OR double‐blind method [mh] OR single‐blind method [mh] OR clinical trial [pt] OR clinical trials [mh] OR ("clinical trial" [tw]) OR ((singl* [tw] OR doubl* [tw] OR trebl* [tw] OR tripl* [tw]) AND (mask* [tw] OR blind* [tw])) OR ( placebos [mh] OR placebo* [tw] OR random* [tw] OR research design [mh:noexp] OR comparative study [mh] OR evaluation studies [mh] OR follow‐up studies [mh] OR prospective studies [mh] OR control* [tw] OR prospectiv* [tw] OR volunteer* [tw]) NOT (animals [mh] NOT human [mh])

3082417

#3

Search #1 OR #2

283409

#2

Search Antiretroviral Therapy, Highly Active[MeSH] OR Anti‐Retroviral Agents[MeSH] OR Antiviral Agents[MeSH:NoExp] OR ((anti) AND (hiv[tw])) OR antiretroviral*[tw] OR ((anti) AND (retroviral*[tw])) OR HAART[tw] OR ((anti) AND (acquired immunodeficiency[tw])) OR ((anti) AND (acquired immunedeficiency[tw])) OR ((anti) AND (acquired immuno‐deficiency[tw])) OR ((anti) AND (acquired immune‐deficiency[tw])) OR ((anti) AND (acquired immun*) AND (deficiency[tw]))

97848

#1

Search HIV Infections[MeSH] OR HIV[MeSH] OR hiv[tw] OR hiv‐1*[tw] OR hiv‐2*[tw] OR hiv1[tw] OR hiv2[tw] OR hiv infect*[tw] OR human immunodeficiency virus[tw] OR human immunedeficiency virus[tw] OR human immuno‐deficiency virus[tw] OR human immune‐deficiency virus[tw] OR ((human immun*) AND (deficiency virus[tw])) OR acquired immunodeficiency syndrome[tw] OR acquired immunedeficiency syndrome[tw] OR acquired immuno‐deficiency syndrome[tw] OR acquired immune‐deficiency syndrome[tw] OR ((acquired immun*) AND (deficiency syndrome[tw])) OR "sexually transmitted diseases, viral"[MH]

250716

Search

Query

Items found

#9

Search ((#3 AND #4 AND #7)) AND ("2009/05/01"[Date ‐ Publication] : "2014/02/07"[Date ‐ Publication])

236

#8

Search (#3 AND #4 AND #7)

607

#7

Search (#5 AND #6)

893

#6

Search (nevirapine[mh] OR nevirapine[tiab] OR viramune[tiab] OR nevimune[tiab] OR NVP[tiab])

4505

#5

Search (efavirenz[tiab] OR sustiva[tiab] OR stocrin[tiab] OR EFV[tiab])

2763

#4

Search (randomized controlled trial [pt] OR controlled clinical trial [pt] OR randomized [tiab] OR placebo [tiab] OR drug therapy [sh] OR randomly [tiab] OR trial [tiab] OR groups [tiab]) NOT (animals [mh] NOT humans [mh])

2838401

#3

Search (#1 AND #2)

85427

#2

Search (antiretroviral therapy, highly active[MeSH] OR anti‐retroviral agents[MeSH] OR antiviral agents[MeSH:NoExp] OR ((anti[tiab]) AND (hiv[tiab])) OR antiretroviral*[tiab] OR ((anti[tiab]) AND (retroviral*[tiab])) OR HAART[tiab] OR ((anti[tiab]) AND (acquired immunodeficiency[tiab])) OR ((anti[tiab]) AND (acquired immuno‐deficiency[tiab])) OR ((anti[tiab]) AND (acquired immune‐deficiency[tiab])) OR ((anti[tiab]) AND (acquired immun*[tiab]) AND (deficiency[tiab])))

135207

#1

Search (HIV Infections[MeSH] OR HIV[MeSH] OR hiv[tiab] OR hiv‐1*[tiab] OR hiv‐2*[tiab] OR hiv1[tiab] OR hiv2[tiab] OR hiv infect*[tiab] OR human immunodeficiency virus[tiab] OR human immunedeficiency virus[tiab] OR human immuno‐deficiency virus[tiab] OR human immune‐deficiency virus[tiab] OR ((human immun*[tiab]) AND (deficiency virus[tiab])) OR acquired immunodeficiency syndrome[tiab] OR acquired immunedeficiency syndrome[tiab] OR acquired immuno‐deficiency syndrome[tiab] OR acquired immune‐deficiency syndrome[tiab] OR ((acquired immun*[tiab]) AND (deficiency syndrome[tiab])) OR "sexually transmitted diseases, Viral"[MeSH:NoExp]))

307747

Search

Query

Items found

#9

Search (((#3 AND #4 AND #7))) AND ("2014/02/07"[Date ‐ Publication] : "2015/03/13"[Date ‐ Publication])

33

#8

Search (#3 AND #4 AND #7)

675

#7

Search (#5 AND #6)

997

#6

Search (nevirapine[mh] OR nevirapine[tiab] OR viramune[tiab] OR nevimune[tiab] OR NVP[tiab])

4901

#5

Search (efavirenz[tiab] OR sustiva[tiab] OR stocrin[tiab] OR EFV[tiab])

3120

#4

Search (randomized controlled trial [pt] OR controlled clinical trial [pt] OR randomized [tiab] OR placebo [tiab] OR drug therapy [sh] OR randomly [tiab] OR trial [tiab] OR groups [tiab]) NOT (animals [mh] NOT humans [mh])

3038686

#3

Search (#1 AND #2)

91917

#2

Search (antiretroviral therapy, highly active[MeSH] OR anti‐retroviral agents[MeSH] OR antiviral agents[MeSH:NoExp] OR ((anti[tiab]) AND (hiv[tiab])) OR antiretroviral*[tiab] OR ((anti[tiab]) AND (retroviral*[tiab])) OR HAART[tiab] OR ((anti[tiab]) AND (acquired immunodeficiency[tiab])) OR ((anti[tiab]) AND (acquired immuno‐deficiency[tiab])) OR ((anti[tiab]) AND (acquired immune‐deficiency[tiab])) OR ((anti[tiab]) AND (acquired immun*[tiab]) AND (deficiency[tiab]))

145438

#1

Search (HIV Infections[MeSH] OR HIV[MeSH] OR hiv[tiab] OR hiv‐1*[tiab] OR hiv‐2*[tiab] OR hiv1[tiab] OR hiv2[tiab] OR hiv infect*[tiab] OR human immunodeficiency virus[tiab] OR human immunedeficiency virus[tiab] OR human immuno‐deficiency virus[tiab] OR human immune‐deficiency virus[tiab] OR ((human immun*[tiab]) AND (deficiency virus[tiab])) OR acquired immunodeficiency syndrome[tiab] OR acquired immunedeficiency syndrome[tiab] OR acquired immuno‐deficiency syndrome[tiab] OR acquired immune‐deficiency syndrome[tiab] OR ((acquired immun*[tiab]) AND (deficiency syndrome[tiab])) OR "sexually transmitted diseases, Viral"[MeSH:NoExp])

324200

Search

Query

Items found

#9

Search (((#3 AND #4 AND #7))) AND ("2015/03/13"[Date ‐ Publication] : "2016/08/12"[Date ‐ Publication])

54

#8

Search (#3 AND #4 AND #7)

767

#7

Search (#5 AND #6)

1101

#6

Search (nevirapine[mh] OR nevirapine[tiab] OR viramune[tiab] OR nevimune[tiab] OR NVP[tiab])

5337

#5

Search (efavirenz[tiab] OR sustiva[tiab] OR stocrin[tiab] OR EFV[tiab])

3552

#4

Search (randomized controlled trial [pt] OR controlled clinical trial [pt] OR randomized [tiab] OR placebo [tiab] OR drug therapy [sh] OR randomly [tiab] OR trial [tiab] OR groups [tiab]) NOT (animals [mh] NOT humans [mh])

3326892

#3

Search (#1 AND #2)

100806

#2

Search (antiretroviral therapy, highly active[MeSH] OR anti‐retroviral agents[MeSH] OR antiviral agents[MeSH:NoExp] OR ((anti[tiab]) AND (hiv[tiab])) OR antiretroviral*[tiab] OR ((anti[tiab]) AND (retroviral*[tiab])) OR HAART[tiab] OR ((anti[tiab]) AND (acquired immunodeficiency[tiab])) OR ((anti[tiab]) AND (acquired immuno‐deficiency[tiab])) OR ((anti[tiab]) AND (acquired immune‐deficiency[tiab])) OR ((anti[tiab]) AND (acquired immun*[tiab]) AND (deficiency[tiab]))

159959

#1

Search (HIV Infections[MeSH] OR HIV[MeSH] OR hiv[tiab] OR hiv‐1*[tiab] OR hiv‐2*[tiab] OR hiv1[tiab] OR hiv2[tiab] OR hiv infect*[tiab] OR human immunodeficiency virus[tiab] OR human immunedeficiency virus[tiab] OR human immuno‐deficiency virus[tiab] OR human immune‐deficiency virus[tiab] OR ((human immun*[tiab]) AND (deficiency virus[tiab])) OR acquired immunodeficiency syndrome[tiab] OR acquired immunedeficiency syndrome[tiab] OR acquired immuno‐deficiency syndrome[tiab] OR acquired immune‐deficiency syndrome[tiab] OR ((acquired immun*[tiab]) AND (deficiency syndrome[tiab])) OR "sexually transmitted diseases, Viral"[MeSH:NoExp])

348268

Appendix 2. Embase search strategies

No.

Query

Results

Date

#1

(('human immunodeficiency virus infection'/exp OR 'human immunodeficiency virus infection') OR ('human immunodeficiency virus infection'/de OR 'human immunodeficiency virus infection')) OR (('human immunodeficiency virus'/exp OR 'human immunodeficiency virus') OR ('human immunodeficiency virus'/de OR 'human immunodeficiency virus')) OR (hiv:ti OR hiv:ab) OR ('hiv‐1':ti OR 'hiv‐1':ab) OR ('hiv‐2':ti OR 'hiv‐2':ab) OR ('human immunodeficiency virus':ti OR 'human immunodeficiency virus':ab) OR ('human immuno‐deficiency virus':ti OR 'human immuno‐deficiency virus':ab) OR ('human immunedeficiency virus':ti OR 'human immunedeficiency virus':ab) OR ('human immune‐deficiency virus':ti OR 'human immune‐deficiency virus':ab) OR ('acquired immune‐deficiency syndrome':ti OR 'acquired immune‐deficiency syndrome':ab) OR ('acquired immunedeficiency syndrome':ti OR 'acquired immunedeficiency syndrome':ab) OR ('acquired immunodeficiency syndrome':ti OR 'acquired immunodeficiency syndrome':ab) OR ('acquired immuno‐deficiency syndrome':ti OR 'acquired immuno‐deficiency syndrome':ab)

292,932

22 May 2009

#2

('human immunodeficiency virus vaccine'/de OR 'human immunodeficiency virus vaccine') OR ('anti human immunedeficiency':ti OR 'anti human immunedeficiency':ab) OR ('anti human immunodeficiency':ti OR 'anti human immunodeficiency':ab) OR ('anti human immuno‐deficiency':ti OR 'anti human immuno‐deficiency':ab) OR ('anti human immune‐deficiency':ti OR 'anti human immune‐deficiency':ab) OR ('anti acquired immune‐deficiency':ti OR 'anti acquired immune‐deficiency':ab) OR ('anti acquired immunedeficiency':ti OR 'anti acquired immunedeficiency':ab) OR ('anti acquired immunodeficiency':ti OR 'anti acquired immunodeficiency':ab) OR ('anti acquired immuno‐deficiency':ti OR 'anti acquired immuno‐deficiency':ab) OR ('anti hiv':ti OR 'anti hiv':ab) OR (antiretrovir*:ti OR antiretrovir*:ab) OR ('anti retroviral':ti OR 'anti retroviral':ab OR 'anti retrovirals':ti OR 'anti retrovirals':ab OR 'anti retrovirus':ti OR 'anti retrovirus':ab) OR (haart:ti OR haart:ab) OR ('aids vaccine':ti OR 'aids vaccine':ab OR 'aids vaccines':ti OR 'aids vaccines':ab) OR (('anti human immunodeficiency virus agent'/de OR 'anti human immunodeficiency virus agent')) OR (('antiretrovirus agent'/de OR 'antiretrovirus agent')) OR (('antivirus agent'/de OR 'antivirus agent')) OR (('highly active antiretroviral therapy'/de OR 'highly active antiretroviral therapy'))

92,810

22 May 2009

#3

((random*:ti OR random*:ab) OR (factorial*:ti OR factorial*:ab) OR (cross?over*:ti OR cross?over*:ab OR crossover*:ti OR crossover*:ab) OR (placebo*:ti OR placebo*:ab) OR ((doubl*:ti AND blind*:ti) OR (doubl*:ab AND blind*:ab)) OR ((singl*:ti AND blind*:ti) OR (singl*:ab AND blind*:ab)) OR (assign*:ti OR assign*:ab) OR (allocat*:ti OR allocat*:ab) OR (volunteer*:ti OR volunteer*:ab) OR (((('crossover procedure'/exp OR 'crossover procedure') OR ('crossover procedure'/de OR 'crossover procedure')) OR (('crossover procedure'/exp OR 'crossover procedure') OR ('crossover procedure'/de OR 'crossover procedure')))) OR (((('double‐blind procedure'/exp OR 'double‐blind procedure') OR ('double‐blind procedure'/de OR 'double‐blind procedure')) OR (('double‐blind procedure'/exp OR 'double‐blind procedure') OR ('double‐blind procedure'/de OR 'double‐blind procedure')))) OR (((('single‐blind procedure'/exp OR 'single‐blind procedure') OR ('single‐blind procedure'/de OR 'single‐blind procedure')) OR (('single‐blind procedure'/exp OR 'single‐blind procedure') OR ('single‐blind procedure'/de OR 'single‐blind procedure')))) OR (((('randomised controlled trial'/exp OR 'randomised controlled trial') OR ('randomised controlled trial'/de OR 'randomised controlled trial')) OR (('randomised controlled trial'/exp OR 'randomised controlled trial') OR ('randomised controlled trial'/de OR 'randomised controlled trial')))))

865,259

22 May 2009

#4

#1 OR #2

321,839

22 May 2009

#5

('efavirenz'/de OR 'efavirenz') OR ('sustiva'/de OR 'sustiva') OR ('stocrin'/de OR 'stocrin') OR efv OR efz

7,680

22 May 2009

#6

('nevirapine'/de OR 'nevirapine') OR nvp OR ('viramune'/de OR 'viramune') OR nevimune

9,696

22 May 2009

#7

#5 OR #6

12,972

22 May 2009

#8

#3 AND #4 AND #7

1,088

22 May 2009

#9

('nnrti'/de OR 'nnrti') OR 'non‐nucleoside reverse transcriptase inhibitor' OR 'non nucleoside reverse transcriptase inhibitor' OR ('nonnucleoside reverse transcriptase inhibitor'/de OR 'nonnucleoside reverse transcriptase inhibitor') OR 'non‐nucleoside reverse transcriptase inhibitors' OR 'non nucleoside reverse transcriptase inhibitors' OR 'nonnucleoside reverse transcriptase inhibitors' OR 'pi sparing' OR 'protease inhibitor sparing' OR 'protease‐inhibitor sparing' OR 'non‐protease inhibitor containing' OR 'non‐pi containing' OR 'non protease inhibitor containing'

13,324

22 May 2009

#10

#8 AND #9 AND [1996‐2009]/py

523

22 May 2009

No.

Query

Results

#14

#3 AND #9 AND #12 AND [embase]/lim AND [1‐5‐2009]/sd NOT [7‐2‐2014]/sd

554

#13

#3 AND #9 AND #12

1115

#12

#10 AND #11

7336

#11

'nevirapine'/de OR nevirapine OR 'viramune'/de OR viramune OR 'nevimune'/de OR nevimune OR nvp

16047

#10

'efavirenz'/de OR efavirenz OR 'sustiva'/de OR sustiva OR 'stocrin'/de OR stocrin OR efv

13719

#9

#4 NOT #8

1551893

#8

#5 NOT #7

4886059

#7

#5 AND #6

1247730

#6

'human'/de OR 'normal human'/de OR 'human cell'/de

14535586

#5

'animal'/de OR 'animal experiment'/de OR 'invertebrate'/de OR 'animal tissue'/de OR 'animal cell'/de OR 'nonhuman'/de

6133789

#4

'randomized controlled trial'/de OR 'randomized controlled trial' OR random*:ab,ti OR trial:ti OR allocat*:ab,ti OR factorial*:ab,ti OR placebo*:ab,ti OR assign*:ab,ti OR volunteer*:ab,ti OR 'crossover procedure'/de OR 'crossover procedure' OR 'double‐blind procedure'/de OR 'double‐blind procedure' OR 'single‐blind procedure'/de OR 'single‐blind procedure' OR (doubl* NEAR/3 blind*):ab,ti OR (singl*:ab,ti AND blind*:ab,ti) OR crossover*:ab,ti OR cross+over*:ab,ti OR (cross NEXT/1 over*):ab,ti

1782714

#3

#1 AND #2

116833

#2

'human immunodeficiency virus vaccine'/exp OR 'human immunodeficiency virus vaccine':ab,ti OR 'anti human immunedeficiency':ab,ti OR 'anti human immunodeficiency':ab,ti OR 'anti human immuno‐deficiency':ab,ti OR 'anti human immune‐deficiency':ab,ti OR 'anti acquired immune‐deficiency':ab,ti OR 'anti acquired immunedeficiency':ab,ti OR 'anti acquired immunodeficiency':ab,ti OR 'anti acquired immuno‐deficiency':ab,ti OR 'anti hiv':ab,ti OR antiretrovir*:ab,ti OR 'anti retroviral':ab,ti OR 'anti retrovirals':ab,ti OR 'anti retrovirus':ab,ti OR haart:ab,ti OR 'aids vaccine':ab,ti OR 'aids vaccines':ab,ti OR 'anti human immunodeficiency virus agent'/exp OR 'anti human immunodeficiency virus agent':ab,ti OR 'antiretrovirus agent'/exp OR 'antiretrovirus agent':ab,ti OR 'highly active antiretroviral therapy'/exp OR 'highly active antiretroviral therapy':ab,ti

165003

#1

'human immunodeficiency virus infection'/exp OR 'human immunodeficiency virus'/exp OR 'human immunodeficiency virus':ab,ti OR 'human immuno+deficiency virus':ab,ti OR 'human immunedeficiency virus':ab,ti OR 'human immune+deficiency virus':ab,ti OR hiv:ab,ti OR 'hiv‐1':ab,ti OR 'hiv‐2':ab,ti OR 'acquired immunodeficiency syndrome':ab,ti OR 'acquired immuno+deficiency syndrome':ab,ti OR 'acquired immunedeficiency syndrome':ab,ti OR 'acquired immune+deficiency syndrome':ab,ti

384563

No.

Query

Results

#14

#3 AND #9 AND #12 AND [7‐2‐2014]/sd NOT [13‐3‐2015]/sd

85

#13

#3 AND #9 AND #12

796

#12

#10 AND #11

7647

#11

'nevirapine'/de OR nevirapine:ab,ti OR 'viramune'/de OR viramune:ab,ti OR 'nevimune'/de OR nevimune:ab,ti OR nvp:ab,ti

16066

#10

'efavirenz'/de OR efavirenz:ab,ti OR 'sustiva'/de OR sustiva:ab,ti OR 'stocrin'/de OR stocrin:ab,ti OR efv:ab,ti

14587

#9

#4 NOT #8

1438290

#8

#5 NOT #7

5079643

#7

#5 AND #6

1341085

#6

'human'/de OR 'normal human'/de OR 'human cell'/de

15656505

#5

'animal'/de OR 'animal experiment'/de OR 'invertebrate'/de OR 'animal tissue'/de OR 'animal cell'/de OR 'nonhuman'/de

6420728

#4

'randomized controlled trial'/de OR 'randomized controlled trial' OR random*:ab,ti OR trial:ti OR allocat*:ab,ti OR factorial*:ab,ti OR placebo*:ab,ti OR assign*:ab,ti OR volunteer*:ab,ti OR 'crossover procedure'/de OR 'crossover procedure' OR 'double‐blind procedure'/de OR 'double‐blind procedure' OR 'single‐blind procedure'/de OR 'single‐blind procedure' OR (doubl* NEAR/3 blind*):ab,ti OR (singl*:ab,ti AND blind*:ab,ti) OR crossover*:ab,ti OR cross+over*:ab,ti OR (cross NEXT/1 over*):ab,ti

1617084

#3

#1 AND #2

126453

#2

'human immunodeficiency virus vaccine'/exp OR 'human immunodeficiency virus vaccine' OR 'human immunodeficiency virus vaccine':ab,ti OR 'anti human immunedeficiency':ab,ti OR 'anti human immunodeficiency':ab,ti OR 'anti human immuno‐deficiency':ab,ti OR 'anti human immune‐deficiency':ab,ti OR 'anti acquired immune‐deficiency':ab,ti OR 'anti acquired immunedeficiency':ab,ti OR 'anti acquired immunodeficiency':ab,ti OR 'anti acquired immuno‐deficiency':ab,ti OR 'anti hiv':ab,ti OR antiretrovir*:ab,ti OR 'anti retroviral':ab,ti OR 'anti retrovirals':ab,ti OR 'anti retrovirus':ab,ti OR haart:ab,ti OR 'aids vaccine':ab,ti OR 'aids vaccines':ab,ti OR 'anti human immunodeficiency virus agent'/exp OR 'anti human immunodeficiency virus agent' OR 'anti human immunodeficiency virus agent':ab,ti OR 'antiretrovirus agent'/exp OR 'antiretrovirus agent' OR 'antiretrovirus agent':ab,ti OR 'highly active antiretroviral therapy'/exp OR 'highly active antiretroviral therapy' OR 'highly active antiretroviral therapy':ab,ti

178964

#1

'human immunodeficiency virus infection'/exp OR 'human immunodeficiency virus'/exp OR 'human immunodeficiency virus':ab,ti OR 'human immuno+deficiency virus':ab,ti OR 'human immunedeficiency virus':ab,ti OR 'human immune+deficiency virus':ab,ti OR hiv:ab,ti OR 'hiv‐1':ab,ti OR 'hiv‐2':ab,ti OR 'acquired immunodeficiency syndrome':ab,ti OR 'acquired immuno+deficiency syndrome':ab,ti OR 'acquired immunedeficiency syndrome':ab,ti OR 'acquired immune+deficiency syndrome':ab,ti

410883

No.

Query

Results

#14

#3 AND #9 AND #12 AND [13‐3‐2015]/sd NOT [12‐8‐2016]/sd

113

#13

#3 AND #9 AND #12

907

#12

#10 AND #11

8277

#11

'nevirapine'/de OR nevirapine:ab,ti OR 'viramune'/de OR viramune:ab,ti OR 'nevimune'/de OR nevimune:ab,ti OR nvp:ab,ti

17485

#10

'efavirenz'/de OR efavirenz:ab,ti OR 'sustiva'/de OR sustiva:ab,ti OR 'stocrin'/de OR stocrin:ab,ti OR efv:ab,ti

16217

#9

#4 NOT #8

1648816

#8

#5 NOT #7

5394456

#7

#5 AND #6

1491807

#6

'human'/de OR 'normal human'/de OR 'human cell'/de

17407367

#5

'animal'/de OR 'animal experiment'/de OR 'invertebrate'/de OR 'animal tissue'/de OR 'animal cell'/de OR 'nonhuman'/de

6886263

#4

'randomized controlled trial'/de OR 'randomized controlled trial' OR random*:ab,ti OR trial:ti OR allocat*:ab,ti OR factorial*:ab,ti OR placebo*:ab,ti OR assign*:ab,ti OR volunteer*:ab,ti OR 'crossover procedure'/de OR 'crossover procedure' OR 'double‐blind procedure'/de OR 'double‐blind procedure' OR 'single‐blind procedure'/de OR 'single‐blind procedure' OR (doubl* NEAR/3 blind*):ab,ti OR (singl*:ab,ti AND blind*:ab,ti) OR crossover*:ab,ti OR cross+over*:ab,ti OR (cross NEXT/1 over*):ab,ti

1847056

#3

#1 AND #2

140484

#2

'human immunodeficiency virus vaccine'/exp OR 'human immunodeficiency virus vaccine':ab,ti OR 'anti human immunedeficiency':ab,ti OR 'anti human immunodeficiency':ab,ti OR 'anti human immuno‐deficiency':ab,ti OR 'anti human immune‐deficiency':ab,ti OR 'anti acquired immune‐deficiency':ab,ti OR 'anti acquired immunedeficiency':ab,ti OR 'anti acquired immunodeficiency':ab,ti OR 'anti acquired immuno‐deficiency':ab,ti OR 'anti hiv':ab,ti OR antiretrovir*:ab,ti OR 'anti retroviral':ab,ti OR 'anti retrovirals':ab,ti OR 'anti retrovirus':ab,ti OR haart:ab,ti OR 'aids vaccine':ab,ti OR 'aids vaccines':ab,ti OR 'anti human immunodeficiency virus agent'/exp OR 'anti human immunodeficiency virus agent':ab,ti OR 'antiretrovirus agent'/exp OR 'antiretrovirus agent':ab,ti OR 'highly active antiretroviral therapy'/exp OR 'highly active antiretroviral therapy':ab,ti

198729

#1

'human immunodeficiency virus infection'/exp OR 'human immunodeficiency virus'/exp OR 'human immunodeficiency virus':ab,ti OR 'human immuno+deficiency virus':ab,ti OR 'human immunedeficiency virus':ab,ti OR 'human immune+deficiency virus':ab,ti OR hiv:ab,ti OR 'hiv‐1':ab,ti OR 'hiv‐2':ab,ti OR 'acquired immunodeficiency syndrome':ab,ti OR 'acquired immuno+deficiency syndrome':ab,ti OR 'acquired immunedeficiency syndrome':ab,ti OR 'acquired immune+deficiency syndrome':ab,ti

448264

Appendix 3. CENTRAL search strategies

ID

Search

Hits

#1

HIV INFECTIONS explode all trees (MESH) OR HIV explode all trees (MeSH) OR hiv OR hiv‐1* OR hiv‐2* OR hiv1 OR hiv2 OR HIV INFECT* OR HUMAN IMMUNODEFICIENCY VIRUS OR HUMAN IMMUNEDEFICIENCY VIRUS OR HUMAN IMMUNE‐DEFICIENCY VIRUS OR HUMAN IMMUNO‐DEFICIENCY VIRUS OR HUMAN IMMUN* DEFICIENCY VIRUS OR ACQUIRED IMMUNODEFICIENCY SYNDROME OR ACQUIRED IMMUNEDEFICIENCY SYNDROME OR ACQUIRED IMMUNO‐DEFICIENCY SYNDROME OR ACQUIRED IMMUNE‐DEFICIENCY SYNDROME OR ACQUIRED IMMUN* DEFICIENCY SYNDROME OR LYMPHOMA AIDS‐RELATED single term (MeSH) OR SEXUALLY TRANSMITTED DISEASES VIRAL single term (MeSH)

8223

#2

ANTIRETROVIRAL THERAPY HIGHLY ACTIVE single term (MeSH) OR ANTI‐HIV AGENTS explode all trees (MeSH) OR ANTIVIRAL AGENTS single term (MeSH) OR AIDS VACCINES single term (MeSH) OR ANTI HIV OR ANTIRETROVIRAL* OR ANTI RETROVIRAL* OR AIDS VACCIN*

3577

#3

(#1 OR #2)

8432

#4

NEVIRAPINE OR NVP OR VIRAMUNE OR NEVIMUNE

315

#5

EFAVIRENZ OR SUSTIVA OR STOCRIN OR EFV OR EFZ

227

#6

(#4 OR #5)

487

#7

NNRTI OR (NON‐NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR) OR (NON NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR) OR (NONNUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR) OR (NON‐NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS) OR (NON NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS) OR (NONNUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS) OR (PI SPARING) OR (PROTEASE INHIBITOR SPARING) OR (PROTEASE‐INHIBITOR SPARING) OR (NON‐PROTEASE INHIBITOR CONTAINING) OR (NON‐PI CONTAINING) OR (NON PROTEASE INHIBITOR CONTAINING)

493

#8

(#3 AND #6 AND #7), from 1996 to 2009

146

ID

Search

Hits

#1

MeSH descriptor: [HIV Infections] explode all trees

7543

#2

MeSH descriptor: [HIV] explode all trees

2495

#3

hiv or hiv‐1* or hiv‐2* or hiv1 or hiv2 or (hiv near infect*) or (human immunodeficiency virus) or (human immunedeficiency virus) or (human immune‐deficiency virus) or (human immuno‐deficiency virus) or (human immune deficiency virus) or (human immuno deficiency virus) or (acquired immunodeficiency syndrome) or (acquired immunedeficiency syndrome) or (acquired immuno‐deficiency syndrome) or (acquired immune‐deficiency syndrome) or (acquired immun* deficiency syndrome) (Word variations have been searched)

12832

#4

MeSH descriptor: [Lymphoma, AIDS‐Related] this term only

21

#5

MeSH descriptor: [Sexually Transmitted Diseases, Viral] this term only

20

#6

#1 or #2 or #3 or #4 or #5

12913

#7

MeSH descriptor: [Antiretroviral Therapy, Highly Active] this term only

961

#8

MeSH descriptor: [Anti‐HIV Agents] explode all trees

2570

#9

MeSH descriptor: [Antiviral Agents] this term only

3288

#10

MeSH descriptor: [AIDS Vaccines] this term only

312

#11

(anti hiv) or antiretroviral* or (anti near retroviral*) or (aids near vaccin*) (Word variations have been searched)

5678

#12

#7 or #8 or #9 or #10 or #11

8955

#13

#6 and #12 from 1980 to 2014, in Trials (Word variations have been searched)

4943

#14

nevirapine:ti,ab,kw or viramune:ti,ab,kw or nevimune:ti,ab,kw or NVP:ti,ab,kw

562

#15

efavirenz:ti,ab,kw or sustiva:ti,ab,kw or efv:ti,ab,kw or stocrin:ti,ab,kw

523

#16

#14 and #15

121

#17

#13 and #16 from2009 to 2014, in Trials

61

ID

Search

Hits

#1

MeSH descriptor: [HIV Infections] explode all trees

8172

#2

MeSH descriptor: [HIV] explode all trees

2638

#3

hiv or hiv‐1* or hiv‐2* or hiv1 or hiv2 or (hiv near infect*) or (human immunodeficiency virus) or (human immunedeficiency virus) or (human immune‐deficiency virus) or (human immuno‐deficiency virus) or (human immune deficiency virus) or (human immuno deficiency virus) or (acquired immunodeficiency syndrome) or (acquired immunedeficiency syndrome) or (acquired immuno‐deficiency syndrome) or (acquired immune‐deficiency syndrome) or (acquired immun* deficiency syndrome) (Word variations have been searched)

14285

#4

MeSH descriptor: [Lymphoma, AIDS‐Related] this term only

21

#5

MeSH descriptor: [Sexually Transmitted Diseases, Viral] this term only

23

#6

#1 or #2 or #3 or #4 or #5

14369

#7

MeSH descriptor: [Antiretroviral Therapy, Highly Active] this term only

1056

#8

MeSH descriptor: [Anti‐HIV Agents] explode all trees

2753

#9

MeSH descriptor: [Antiviral Agents] this term only

3434

#10

MeSH descriptor: [AIDS Vaccines] this term only

336

#11

(anti hiv) or antiretroviral* or (anti near retroviral*) or (aids near vaccin*) (Word variations have been searched)

6380

#12

#7 or #8 or #9 or #10 or #11

9803

#13

#6 and #12 in Trials (Word variations have been searched)

5538

#14

nevirapine:ti,ab,kw or viramune:ti,ab,kw or nevimune:ti,ab,kw or NVP:ti,ab,kw

633

#15

efavirenz:ti,ab,kw or sustiva:ti,ab,kw or efv:ti,ab,kw or stocrin:ti,ab,kw

634

#16

#14 and #15

148

#17

#13 and #16 Publication Year from 2014 to 2015, in Trials

16

ID

Search

Hits

#1

MeSH descriptor: [HIV Infections] explode all trees

8983

#2

MeSH descriptor: [HIV] explode all trees

2834

#3

hiv or hiv‐1* or hiv‐2* or hiv1 or hiv2 or (hiv near infect*) or (human immunodeficiency virus) or (human immunedeficiency virus) or (human immune‐deficiency virus) or (human immuno‐deficiency virus) or (human immune deficiency virus) or (human immuno deficiency virus) or (acquired immunodeficiency syndrome) or (acquired immunedeficiency syndrome) or (acquired immuno‐deficiency syndrome) or (acquired immune‐deficiency syndrome) or (acquired immun* deficiency syndrome) (Word variations have been searched)

16377

#4

MeSH descriptor: [Lymphoma, AIDS‐Related] this term only

23

#5

MeSH descriptor: [Sexually Transmitted Diseases, Viral] this term only

25

#6

#1 or #2 or #3 or #4 or #5

16462

#7

MeSH descriptor: [Antiretroviral Therapy, Highly Active] this term only

1164

#8

MeSH descriptor: [Anti‐HIV Agents] explode all trees

3041

#9

MeSH descriptor: [Antiviral Agents] this term only

3784

#10

MeSH descriptor: [AIDS Vaccines] this term only

375

#11

(anti hiv) or antiretroviral* or (anti near retroviral*) or (aids near vaccin*) (Word variations have been searched)

7445

#12

#7 or #8 or #9 or #10 or #11

11216

#13

#6 and #12 in Trials (Word variations have been searched)

6006

#14

nevirapine:ti,ab,kw or viramune:ti,ab,kw or nevimune:ti,ab,kw or NVP:ti,ab,kw

767

#15

efavirenz:ti,ab,kw or sustiva:ti,ab,kw or efv:ti,ab,kw or stocrin:ti,ab,kw

859

#16

#14 and #15

226

#17

#13 and #16 Publication Year from 2015 to 2016, in Trials

0

Appendix 4. NLM Gateway search strategy

Search
Number

Search

Items
Found

#8

 Search: ((((((HIV INFECTIONS) OR HIV OR HIV OR HIV‐1* OR HIV‐2* OR HIV1 OR HIV2 OR (HIV INFECT*) OR (HUMAN IMMUNODEFICIENCY VIRUS) OR (HUMAN IMMUNEDEFICIENCY VIRUS) OR (HUMAN IMMUNO‐DEFICIENCY VIRUS) OR (HUMAN IMMUNE‐DEFICIENCY VIRUS) OR ((HUMAN IMMUN*) AND (DEFICIENCY VIRUS)) OR (ACQUIRED IMMUNODEFICIENCY SYNDROME))) OR (((ACQUIRED IMMUNEDEFICIENCY SYNDROME) OR (ACQUIRED IMMUNO‐DEFICIENCY SYNDROME) OR (ACQUIRED IMMUNE‐DEFICIENCY SYNDROME) OR ((ACQUIRED IMMUN*) AND (DEFICIENCY SYNDROME)) OR (SEXUALLY TRANSMITTED DISEASES, VIRAL)))) OR ((("Antiretroviral Therapy, Highly Active"[MeSH] OR "Anti‐Retroviral Agents"[MeSH] OR "Antiviral Agents"[MeSH:noexp] OR ((anti) AND (hiv[tw])) OR antiretroviral*[tw] OR ((anti) AND (retroviral*[tw])) OR HAART[tw] OR ((anti) AND (acquired immunodeficiency[tw])))) OR ((((anti) AND (acquired immunedeficiency[tw])) OR ((anti) AND (acquired immuno‐deficiency[tw])) OR ((anti) AND (acquired immune‐deficiency[tw])) OR ((anti) AND (acquired immun*) AND (deficiency[tw])))))) AND ((((RANDOMIZED CONTROLLED TRIAL) OR (CONTROLLED CLINICAL TRIAL) OR (RANDOMIZED CONTROLLED TRIALS) OR (RANDOM ALLOCATION) OR (DOUBLE‐BLIND METHOD) OR (SINGLE‐BLIND METHOD) OR (CLINICAL TRIAL) OR (CLINICAL TRIALS) OR (CLINICAL TRIAL) OR ((SINGL* OR DOUBL* OR TREBL* OR TRIPL*) AND (MASK* OR BLIND* )))) OR ((PLACEBOS OR PLACEBO* OR RANDOM* OR (COMPARATIVE STUDY) OR (EVALUATION STUDIES) OR (FOLLOW‐UP STUDIES) OR (PROSPECTIVE STUDIES) OR CONTROL* OR PROSPECTIV* OR VOLUNTEER*))) AND ((EFAVIRENZ OR SUSTIVA OR STOCRIN OR EFV OR EFZ) OR (NEVIRAPINE OR NVP OR VIRAMUNE OR NEVIMUNE))) AND ((NNRTI OR (NON‐NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR) OR (NON NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR) OR (NONNUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR) OR (NON‐NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS) OR (NON NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS)) OR ((NONNUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS) OR (PI SPARING) OR (PROTEASE INHIBITOR SPARING) OR (PROTEASE‐INHIBITOR SPARING) OR (NON‐PROTEASE INHIBITOR CONTAINING) OR (NON‐PI CONTAINING) OR (NON PROTEASE INHIBITOR CONTAINING))) Limit: 1996:2009

260 

#7

 Search: (NNRTI OR (NON‐NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR) OR (NON NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR) OR (NONNUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR) OR (NON‐NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS) OR (NON NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS)) OR ((NONNUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS) OR (PI SPARING) OR (PROTEASE INHIBITOR SPARING) OR (PROTEASE‐INHIBITOR SPARING) OR (NON‐PROTEASE INHIBITOR CONTAINING) OR (NON‐PI CONTAINING) OR (NON PROTEASE INHIBITOR CONTAINING))

16334 

#6

 Search: (((((HIV INFECTIONS) OR HIV OR HIV OR HIV‐1* OR HIV‐2* OR HIV1 OR HIV2 OR (HIV INFECT*) OR (HUMAN IMMUNODEFICIENCY VIRUS) OR (HUMAN IMMUNEDEFICIENCY VIRUS) OR (HUMAN IMMUNO‐DEFICIENCY VIRUS) OR (HUMAN IMMUNE‐DEFICIENCY VIRUS) OR ((HUMAN IMMUN*) AND (DEFICIENCY VIRUS)) OR (ACQUIRED IMMUNODEFICIENCY SYNDROME))) OR (((ACQUIRED IMMUNEDEFICIENCY SYNDROME) OR (ACQUIRED IMMUNO‐DEFICIENCY SYNDROME) OR (ACQUIRED IMMUNE‐DEFICIENCY SYNDROME) OR ((ACQUIRED IMMUN*) AND (DEFICIENCY SYNDROME)) OR (SEXUALLY TRANSMITTED DISEASES, VIRAL)))) OR ((("Antiretroviral Therapy, Highly Active"[MeSH] OR "Anti‐Retroviral Agents"[MeSH] OR "Antiviral Agents"[MeSH:noexp] OR ((anti) AND (hiv[tw])) OR antiretroviral*[tw] OR ((anti) AND (retroviral*[tw])) OR HAART[tw] OR ((anti) AND (acquired immunodeficiency[tw])))) OR ((((anti) AND (acquired immunedeficiency[tw])) OR ((anti) AND (acquired immuno‐deficiency[tw])) OR ((anti) AND (acquired immune‐deficiency[tw])) OR ((anti) AND (acquired immun*) AND (deficiency[tw])))))) AND ((((RANDOMIZED CONTROLLED TRIAL) OR (CONTROLLED CLINICAL TRIAL) OR (RANDOMIZED CONTROLLED TRIALS) OR (RANDOM ALLOCATION) OR (DOUBLE‐BLIND METHOD) OR (SINGLE‐BLIND METHOD) OR (CLINICAL TRIAL) OR (CLINICAL TRIALS) OR (CLINICAL TRIAL) OR ((SINGL* OR DOUBL* OR TREBL* OR TRIPL*) AND (MASK* OR BLIND* )))) OR ((PLACEBOS OR PLACEBO* OR RANDOM* OR (COMPARATIVE STUDY) OR (EVALUATION STUDIES) OR (FOLLOW‐UP STUDIES) OR (PROSPECTIVE STUDIES) OR CONTROL* OR PROSPECTIV* OR VOLUNTEER*))) AND ((EFAVIRENZ OR SUSTIVA OR STOCRIN OR EFV OR EFZ) OR (NEVIRAPINE OR NVP OR VIRAMUNE OR NEVIMUNE))

756 

#5

 Search: (EFAVIRENZ OR SUSTIVA OR STOCRIN OR EFV OR EFZ) OR (NEVIRAPINE OR NVP OR VIRAMUNE OR NEVIMUNE)

6894 

#4

 Search: (((RANDOMIZED CONTROLLED TRIAL) OR (CONTROLLED CLINICAL TRIAL) OR (RANDOMIZED CONTROLLED TRIALS) OR (RANDOM ALLOCATION) OR (DOUBLE‐BLIND METHOD) OR (SINGLE‐BLIND METHOD) OR (CLINICAL TRIAL) OR (CLINICAL TRIALS) OR (CLINICAL TRIAL) OR ((SINGL* OR DOUBL* OR TREBL* OR TRIPL*) AND (MASK* OR BLIND* )))) OR ((PLACEBOS OR PLACEBO* OR RANDOM* OR (COMPARATIVE STUDY) OR (EVALUATION STUDIES) OR (FOLLOW‐UP STUDIES) OR (PROSPECTIVE STUDIES) OR CONTROL* OR PROSPECTIV* OR VOLUNTEER*))

5030795 

#3

 Search: ((((HIV INFECTIONS) OR HIV OR HIV OR HIV‐1* OR HIV‐2* OR HIV1 OR HIV2 OR (HIV INFECT*) OR (HUMAN IMMUNODEFICIENCY VIRUS) OR (HUMAN IMMUNEDEFICIENCY VIRUS) OR (HUMAN IMMUNO‐DEFICIENCY VIRUS) OR (HUMAN IMMUNE‐DEFICIENCY VIRUS) OR ((HUMAN IMMUN*) AND (DEFICIENCY VIRUS)) OR (ACQUIRED IMMUNODEFICIENCY SYNDROME))) OR (((ACQUIRED IMMUNEDEFICIENCY SYNDROME) OR (ACQUIRED IMMUNO‐DEFICIENCY SYNDROME) OR (ACQUIRED IMMUNE‐DEFICIENCY SYNDROME) OR ((ACQUIRED IMMUN*) AND (DEFICIENCY SYNDROME)) OR (SEXUALLY TRANSMITTED DISEASES, VIRAL)))) OR ((("Antiretroviral Therapy, Highly Active"[MeSH] OR "Anti‐Retroviral Agents"[MeSH] OR "Antiviral Agents"[MeSH:noexp] OR ((anti) AND (hiv[tw])) OR antiretroviral*[tw] OR ((anti) AND (retroviral*[tw])) OR HAART[tw] OR ((anti) AND (acquired immunodeficiency[tw])))) OR ((((anti) AND (acquired immunedeficiency[tw])) OR ((anti) AND (acquired immuno‐deficiency[tw])) OR ((anti) AND (acquired immune‐deficiency[tw])) OR ((anti) AND (acquired immun*) AND (deficiency[tw])))))

390683 

#2

 Search: (("Antiretroviral Therapy, Highly Active"[MeSH] OR "Anti‐Retroviral Agents"[MeSH] OR "Antiviral Agents"[MeSH:noexp] OR ((anti) AND (hiv[tw])) OR antiretroviral*[tw] OR ((anti) AND (retroviral*[tw])) OR HAART[tw] OR ((anti) AND (acquired immunodeficiency[tw])))) OR ((((anti) AND (acquired immunedeficiency[tw])) OR ((anti) AND (acquired immuno‐deficiency[tw])) OR ((anti) AND (acquired immune‐deficiency[tw])) OR ((anti) AND (acquired immun*) AND (deficiency[tw]))))

122073 

#1

 Search: (((HIV INFECTIONS) OR HIV OR HIV OR HIV‐1* OR HIV‐2* OR HIV1 OR HIV2 OR (HIV INFECT*) OR (HUMAN IMMUNODEFICIENCY VIRUS) OR (HUMAN IMMUNEDEFICIENCY VIRUS) OR (HUMAN IMMUNO‐DEFICIENCY VIRUS) OR (HUMAN IMMUNE‐DEFICIENCY VIRUS) OR ((HUMAN IMMUN*) AND (DEFICIENCY VIRUS)) OR (ACQUIRED IMMUNODEFICIENCY SYNDROME))) OR (((ACQUIRED IMMUNEDEFICIENCY SYNDROME) OR (ACQUIRED IMMUNO‐DEFICIENCY SYNDROME) OR (ACQUIRED IMMUNE‐DEFICIENCY SYNDROME) OR ((ACQUIRED IMMUN*) AND (DEFICIENCY SYNDROME)) OR (SEXUALLY TRANSMITTED DISEASES, VIRAL)))

366953 

Appendix 5. Cochrane 'Risk of bias' assessment tool

Domain

Support for judgement

Review authors’ judgement

Selection bias.

Random sequence generation.

Describe the method used to generate the allocation sequence in sufficient detail to allow an assessment of whether it should produce comparable groups.

Selection bias (biased allocation to interventions) due to inadequate generation of a randomised sequence.

Allocation concealment.

Describe the method used to conceal the allocation sequence in sufficient detail to determine whether intervention allocations could have been foreseen in advance of, or during, enrolment.

Selection bias (biased allocation to interventions) due to inadequate concealment of allocations prior to assignment.

Performance bias.

Blinding of participants and personnelAssessments should be made for each main outcome (or class of outcomes).

Describe all measures used, if any, to blind study participants and personnel from knowledge of which intervention a participant received. Provide any information relating to whether the intended blinding was effective.

Performance bias due to knowledge of the allocated interventions by participants and personnel during the study.

Detection bias.

Blinding of outcome assessmentAssessments should be made for each main outcome (or class of outcomes).

Describe all measures used, if any, to blind outcome assessors from knowledge of which intervention a participant received. Provide any information relating to whether the intended blinding was effective.

Detection bias due to knowledge of the allocated interventions by outcome assessors.

Attrition bias.

Incomplete outcome dataAssessments should be made for each main outcome (or class of outcomes).

Describe the completeness of outcome data for each main outcome, including attrition and exclusions from the analysis. State whether attrition and exclusions were reported, the numbers in each intervention group (compared with total randomized participants), reasons for attrition/exclusions where reported, and any re‐inclusions in analyses performed by the review authors.

Attrition bias due to amount, nature or handling of incomplete outcome data.

Reporting bias.

Selective reporting.

State how the possibility of selective outcome reporting was examined by the review authors, and what was found.

Reporting bias due to selective outcome reporting.

Other bias.

Other sources of bias.

State any important concerns about bias not addressed in the other domains in the tool.

If particular questions/entries were pre‐specified in the review’s protocol, responses should be provided for each question/entry.

Bias due to problems not covered elsewhere in the table.

Flow diagram of study screening and selection
Figuras y tablas -
Figure 1

Flow diagram of study screening and selection

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

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

'Risk of bias' graph: review authors' judgements about each 'Risk of bias' item presented as percentages across all included studies.
Figuras y tablas -
Figure 3

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

Funnel plot of comparison: 1 Efavirenz 600 mg versus Nevirapine all doses, outcome: 1.1 Virological success.
Figuras y tablas -
Figure 4

Funnel plot of comparison: 1 Efavirenz 600 mg versus Nevirapine all doses, outcome: 1.1 Virological success.

Comparison 1 Efavirenz 600 mg versus nevirapine all doses, Outcome 1 Virological success.
Figuras y tablas -
Analysis 1.1

Comparison 1 Efavirenz 600 mg versus nevirapine all doses, Outcome 1 Virological success.

Comparison 1 Efavirenz 600 mg versus nevirapine all doses, Outcome 2 Mortality.
Figuras y tablas -
Analysis 1.2

Comparison 1 Efavirenz 600 mg versus nevirapine all doses, Outcome 2 Mortality.

Comparison 1 Efavirenz 600 mg versus nevirapine all doses, Outcome 3 Progression to AIDS.
Figuras y tablas -
Analysis 1.3

Comparison 1 Efavirenz 600 mg versus nevirapine all doses, Outcome 3 Progression to AIDS.

Comparison 1 Efavirenz 600 mg versus nevirapine all doses, Outcome 4 All severe adverse events.
Figuras y tablas -
Analysis 1.4

Comparison 1 Efavirenz 600 mg versus nevirapine all doses, Outcome 4 All severe adverse events.

Comparison 1 Efavirenz 600 mg versus nevirapine all doses, Outcome 5 Discontinuation rate.
Figuras y tablas -
Analysis 1.5

Comparison 1 Efavirenz 600 mg versus nevirapine all doses, Outcome 5 Discontinuation rate.

Comparison 1 Efavirenz 600 mg versus nevirapine all doses, Outcome 6 Change in CD4 count.
Figuras y tablas -
Analysis 1.6

Comparison 1 Efavirenz 600 mg versus nevirapine all doses, Outcome 6 Change in CD4 count.

Comparison 1 Efavirenz 600 mg versus nevirapine all doses, Outcome 7 Treatment failure.
Figuras y tablas -
Analysis 1.7

Comparison 1 Efavirenz 600 mg versus nevirapine all doses, Outcome 7 Treatment failure.

Comparison 1 Efavirenz 600 mg versus nevirapine all doses, Outcome 8 Development of drug resistance.
Figuras y tablas -
Analysis 1.8

Comparison 1 Efavirenz 600 mg versus nevirapine all doses, Outcome 8 Development of drug resistance.

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 1 Severe adverse events: central nervous system.
Figuras y tablas -
Analysis 2.1

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 1 Severe adverse events: central nervous system.

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 2 Severe adverse events: gastrointestinal tract.
Figuras y tablas -
Analysis 2.2

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 2 Severe adverse events: gastrointestinal tract.

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 3 Severe adverse events: pyrexia.
Figuras y tablas -
Analysis 2.3

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 3 Severe adverse events: pyrexia.

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 4 Severe adverse events: elevated transaminases.
Figuras y tablas -
Analysis 2.4

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 4 Severe adverse events: elevated transaminases.

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 5 Severe adverse events: elevated alkaline phosphatase.
Figuras y tablas -
Analysis 2.5

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 5 Severe adverse events: elevated alkaline phosphatase.

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 6 Severe adverse events: elevated amylase.
Figuras y tablas -
Analysis 2.6

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 6 Severe adverse events: elevated amylase.

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 7 Severe adverse events: elevated triglycerides.
Figuras y tablas -
Analysis 2.7

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 7 Severe adverse events: elevated triglycerides.

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 8 Severe adverse events: neutropenia.
Figuras y tablas -
Analysis 2.8

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 8 Severe adverse events: neutropenia.

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 9 Severe adverse events: rash.
Figuras y tablas -
Analysis 2.9

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 9 Severe adverse events: rash.

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 10 Severe adverse events: elevated SGOT.
Figuras y tablas -
Analysis 2.10

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 10 Severe adverse events: elevated SGOT.

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 11 Severe adverse events: elevated SGPT.
Figuras y tablas -
Analysis 2.11

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 11 Severe adverse events: elevated SGPT.

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 12 Severe adverse events: elevated cholesterol.
Figuras y tablas -
Analysis 2.12

Comparison 2 Efavirenz 600 mg versus nevirapine all doses: adverse events, Outcome 12 Severe adverse events: elevated cholesterol.

Comparison 3 Efavirenz versus nevirapine: subgroup analyses for concurrent TB treatments, Outcome 1 Virological success.
Figuras y tablas -
Analysis 3.1

Comparison 3 Efavirenz versus nevirapine: subgroup analyses for concurrent TB treatments, Outcome 1 Virological success.

Comparison 3 Efavirenz versus nevirapine: subgroup analyses for concurrent TB treatments, Outcome 2 Mortality.
Figuras y tablas -
Analysis 3.2

Comparison 3 Efavirenz versus nevirapine: subgroup analyses for concurrent TB treatments, Outcome 2 Mortality.

Comparison 3 Efavirenz versus nevirapine: subgroup analyses for concurrent TB treatments, Outcome 3 Progression to AIDS.
Figuras y tablas -
Analysis 3.3

Comparison 3 Efavirenz versus nevirapine: subgroup analyses for concurrent TB treatments, Outcome 3 Progression to AIDS.

Comparison 3 Efavirenz versus nevirapine: subgroup analyses for concurrent TB treatments, Outcome 4 Discontinuation rate.
Figuras y tablas -
Analysis 3.4

Comparison 3 Efavirenz versus nevirapine: subgroup analyses for concurrent TB treatments, Outcome 4 Discontinuation rate.

Comparison 4 Efavirenz 600 mg versus nevirapine: subgroup analyses for dosage, Outcome 1 Virological success.
Figuras y tablas -
Analysis 4.1

Comparison 4 Efavirenz 600 mg versus nevirapine: subgroup analyses for dosage, Outcome 1 Virological success.

Comparison 4 Efavirenz 600 mg versus nevirapine: subgroup analyses for dosage, Outcome 2 Mortality.
Figuras y tablas -
Analysis 4.2

Comparison 4 Efavirenz 600 mg versus nevirapine: subgroup analyses for dosage, Outcome 2 Mortality.

Comparison 4 Efavirenz 600 mg versus nevirapine: subgroup analyses for dosage, Outcome 3 Progression to AIDS.
Figuras y tablas -
Analysis 4.3

Comparison 4 Efavirenz 600 mg versus nevirapine: subgroup analyses for dosage, Outcome 3 Progression to AIDS.

Comparison 4 Efavirenz 600 mg versus nevirapine: subgroup analyses for dosage, Outcome 4 Discontinuation rate.
Figuras y tablas -
Analysis 4.4

Comparison 4 Efavirenz 600 mg versus nevirapine: subgroup analyses for dosage, Outcome 4 Discontinuation rate.

Summary of findings for the main comparison. 'Summary of findings' table 1

Efavirenz (600 mg) versus nevirapine (all doses) for three‐drug combination therapy with two nucleoside‐reverse transcriptase inhibitors for initial treatment of HIV infection in antiretroviral‐naïveindividuals

Patient or population: antiretroviral‐naïve individuals
Setting: all settings
Intervention: efavirenz 600 mg
Comparison: nevirapine all doses (400 mg once daily and 400 mg twice daily) as part of a three‐drug combination therapy with two NRTIs

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

Number of participants
(RCTs)

Quality of the evidence
(GRADE)

Risk with nevirapine all doses

Risk with efavirenz 600 mg

Virological success

688 per 1000

715 per 1000
(681 to 750)

RR 1.04
(0.99 to 1.09)

2438
(10 RCTs)

⊕⊕⊕⊕
high1,2,3

Mortality

64 per 1000

54 per 1000
(38 to 76)

RR 0.84
(0.59 to 1.19)

2317
(8 RCTs)

⊕⊕⊕⊝
moderate4,5

Progression to AIDS

41 per 1000

50 per 1000
(29 to 86)

RR 1.23
(0.72 to 2.11)

2005
(5 RCTs)

⊕⊕⊕⊝
moderate5,6

All severe adverse events

192 per 1000

216 per 1000
(162 to 285)

RR 0.91
(0.71 to 1.18)

2329
(8 RCTs)

⊕⊝⊝⊝
very low5,7,8

Discontinuation rate

176 per 1000

164 per 1000
(122 to 220)

RR 0.93
(0.69 to 1.25)

2384
(9 RCTs)

⊕⊕⊕⊝
moderate5

Change in CD4 count

The mean change in CD4 count was 0

MD 3.03 lower
(17.41 lower to 11.35 higher)

1829
(9 RCTs)

⊕⊕⊕⊝
moderate5,9,10,11

Treatment failure

249 per 1000

242 per 1000
(189 to 309)

RR 0.97
(0.76 to 1.24)

737
(5 RCTs)

⊕⊕⊝⊝
low12,13

*The risk in the intervention group (and its 95% CI) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
Abbreviations: CI: confidence interval; RR: risk ratio; OR: odds ratio; RCT: randomized controlled trial; GRADE: Grading of Recommendations Assessment, Development and Evaluation; MD: mean difference.

GRADE Working Group grades of evidence
High quality: we are very confident that the true effect lies close to that of the estimate of the effect
Moderate quality: we are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different
Low quality: our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect
Very low quality: we have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect

1Three trials used a cut‐off point of 400 copies/mL (Ayala Gaytán 2004; Swaminathan 2011; Sinha 2013), but we did not downgrade for this.
2Nine trials were open‐label (Ayala Gaytán 2004; Bonnet 2013a; Landman 2014; Manosuthi 2009a; Mateelli 2013; Núñez 2002; Sinha 2013; Swaminathan 2011; van Leth 2004), but we did not downgrade for this.
3Two trials were industry‐funded (Landman 2014; van Leth 2004), but we did not downgrade for this.
4Seven trials were open‐label but we did not downgrade for this (Ayala Gaytán 2004; Bonnet 2013a; Landman 2014; Manosuthi 2009a; Sinha 2013; Swaminathan 2011; van Leth 2004).
5We downgraded by 1 for imprecision due to wide CIs including appreciable harm or benefit.
6Four trials were open‐labelled but we did not downgrade for this (Ayala Gaytán 2004; Bonnet 2013a; Manosuthi 2009a; van Leth 2004)
7Six trials were open‐label (Ayala Gaytán 2004; Bonnet 2013a; Manosuthi 2009a; Núñez 2002; Swaminathan 2011; van Leth 2004). We downgraded by 1 for this.
8Trials did not report the same adverse events and used different severity scales. We downgraded by 1 for this.
9Seven of the trials were open‐label but we did not downgrade for this (Ayala Gaytán 2004; Bonnet 2013a; Manosuthi 2009a; Mateelli 2013; Núñez 2002; Swaminathan 2011; van Leth 2004).
10In one trial, the risk of bias was unclear (Sow 2006).
11One trial had industry funding (van Leth 2004), but we did not downgrade for this.
12All trials were open‐labelled but we did not downgrade for this.
13Each included trial that reported this outcome defined treatment failure differently. We downgraded by 2.

Figuras y tablas -
Summary of findings for the main comparison. 'Summary of findings' table 1
Summary of findings 2. 'Summary of findings' table 2

Efavirenz (600 mg) versus nevirapine (all doses): adverse events for three‐drug combination therapy with two nucleoside‐reverse transcriptase inhibitors for initial treatment of HIV infection in antiretroviral‐naïveindividuals

Patient or population: antiretroviral‐naïve individuals
Setting: all settings
Intervention: efavirenz 600 mg
Comparison: nevirapine all doses (400 mg once daily and 400 mg twice daily) as part of a three‐drug combination therapy with two NRTIs

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

Number of participants
(RCTs)

Quality of the evidence
(GRADE)

Risk with nevirapine all doses: adverse events

Risk with efavirenz 600 mg

Severe adverse events: central nervous system

2 per 1000

7 per 1000
(2 to 18)

RR 4.46
(1.65 to 12.03)

2049
(6 RCTs)

⊕⊕⊕⊝
moderate1

Severe adverse events: gastrointestinal

18 per 1000

14 per 1000
(9 to 22)

RR 0.76
(0.48 to 1.21)

2049
(6 RCTs)

⊕⊕⊝⊝
low1,2

Severe adverse events: pyrexia

0 per 1000

0 per 1000
(0 to 0)

RR 0.65
(0.15 to 2.73)

1799
(3 RCTs)

⊕⊕⊝⊝
low2,3

Severe adverse events: raised transaminases

257 per 1000

134 per 1000
(90 to 201)

RR 0.52
(0.35 to 0.78)

1299
(3 RCTs)

⊕⊕⊕⊕
high4

Severe adverse events: raised alkaline phosphatase

12 per 1000

7 per 1000
(2 to 29)

RR 0.65
(0.17 to 2.50)

1007
(1 RCT)

⊕⊕⊝⊝
low2,5

Severe adverse events: raised amylase

14 per 1000

20 per 1000
(10 to 38)

RR 1.40
(0.72 to 2.73)

1071
(2 RCTs)

⊕⊕⊝⊝
low2,6,7

Severe adverse events: raised triglycerides

7 per 1000

7 per 1000
(3 to 21)

RR 1.10
(0.39 to 3.13)

1071
(2 RCTs)

⊕⊕⊝⊝
low2,6,7

Severe adverse events: neutropenia

38 per 1000

18 per 1000
(11 to 31)

RR 0.48
(0.28 to 0.82)

1799
(3 RCTs)

⊕⊕⊕⊕
high3,8

Severe adverse events: rash

229 per 1000

133 per 1000
(78 to 229)

RR 0.58
(0.34 to 1.00)

2277
(7 RCTs)

⊕⊕⊕⊝
moderate2,9

Severe adverse events: serum glutamic oxaloacetic transaminase (SGOT)

The mean severe adverse events: SGOT was 0

MD 3.3 higher
(2.06 lower to 8.66 higher)

135
(1 RCT)

⊕⊕⊕⊝
moderate2

Severe adverse events: serum glutamic‐ pyruvic transaminase (SGPT)

The mean severe adverse events: SGPT was 0

MD 5.7 higher
(4.23 lower to 15.63 higher)

135
(1 RCT)

⊕⊕⊕⊝
moderate2

Raised cholesterol

29 per 1000

172 per 1000
(21 to 1000)

RR 6.03
(0.75 to 48.78)

64
(1 RCT)

⊕⊕⊕⊝
moderate2

*The risk in the intervention group (and its 95% CI) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
Abbreviations: CI: confidence interval; RR: risk ratio; OR: odds ratio; RCT: randomized controlled trial; GRADE: Grading of Recommendations Assessment, Development and Evaluation; MD: mean difference; SGOT: glutamic oxaloacetic transaminase; SGPT: serum glutamic‐ pyruvic transaminase

GRADE Working Group grades of evidence
High quality: we are very confident that the true effect lies close to that of the estimate of the effect
Moderate quality: we are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different
Low quality: our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect
Very low quality: we have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect

1Five trials (Manosuthi 2009a; Núñez 2002; Swaminathan 2011; van Leth 2004; Wester 2010) were open‐label. One trial did not report blinding (Sow 2006). We downgraded by 1 for this.
2We downgraded by 1 for very wide CIs.
3All trials were open‐label.
4Two trials (Núñez 2002; van Leth 2004) were open label. van Leth 2004 was industry‐funded. We did not downgrade for this.
5Data from one open‐label industry‐funded study (van Leth 2004). We downgraded by 1 for this.
6Both trials were open‐label (Núñez 2002; van Leth 2004), but we did not downgrade for this.
7Most data came from one industry‐funded trial (van Leth 2004). We downgraded one point for this.
8We upgraded by 1 due to the large effect.
9Six studies were open‐label (Manosuthi 2009a; Núñez 2002; Sow 2006; Swaminathan 2011; van Leth 2004; Wester 2010). We did not downgrade for this.

Figuras y tablas -
Summary of findings 2. 'Summary of findings' table 2
Table 1. Additional characteristics of included studies

Trial ID

Location

NVP dosage

NRTI combination drugs

Co‐infection with tuberculosis

Virological success cut‐off point

Ayala Gaytán 2004

Mexico

200 mg twice daily

AZT 300 mg and 3TC 150 mg

No

< 400 copies/mL

Bonnet 2013a

Mozambique

200 mg twice daily

3TC and d4T/AZT1

No

< 50 copies/mL

Landman 2014

Cameroon and Senegal

200 mg twice daily

TDF 300 mg and FTC 200 mg

No

< 50 copies/mL

Manosuthi 2009a

Thailand

400 mg once daily

3TC 150 mg and D4T 30 or 40 mg

Yes

< 50 copies/mL

Mateelli 2013

Burkina Faso

200 mg twice daily

D4T and 3TC1

Yes

Not reported

Núñez 2002

Spain

400 mg once daily

D4T 40 mg and DDI 400 mg

No

< 50 copies/mL

Sinha 2013

India

200 mg twice daily

AZT, d4T, 3TC1

Yes

< 400 copies/mL

Sow 2006

Senegal

200 mg twice daily

AZT 300 mg and 3TC 150 mg

No

Not reported

Swaminathan 2011

India

400 mg once daily

DDI 250 mg or 400 mg and 3TC 300 mg

Yes

Not reported

van den Berg‐Wolf 2008

USA

200 mg twice daily

ABC/3TC, DDI/d4T, AZT/3TC, d4T/3TC1

No

< 50 copies/mL

van Leth 2004

North/South America, Australia, Europe, South Africa, and Thailand

200 mg twice daily and 400 mg twice daily

D4T 40 mg and 3TC 150 mg

No

< 50 copies/mL

Wester 2010

Botswana

Not reported

AZT or d4T/3TC or DDI1

No

Not reported

1Dosage not specified.
Abbreviations: NRTI: Nucleoside Reverse Transcriptase Inhibitor; ART: antiretroviral therapy; AZT: zidovudine; d4T: stavudine; 3TC: lamivudine; NVP: nevirapine; DDI: didanosine; ABC: abacavir; FTC: Emtricitabine; TDF: Tenofovir.

Figuras y tablas -
Table 1. Additional characteristics of included studies
Comparison 1. Efavirenz 600 mg versus nevirapine all doses

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Virological success Show forest plot

10

2438

Risk Ratio (M‐H, Random, 95% CI)

1.04 [0.99, 1.09]

2 Mortality Show forest plot

8

2317

Risk Ratio (M‐H, Random, 95% CI)

0.84 [0.59, 1.19]

3 Progression to AIDS Show forest plot

5

2005

Risk Ratio (M‐H, Random, 95% CI)

1.23 [0.72, 2.11]

4 All severe adverse events Show forest plot

8

2329

Risk Ratio (M‐H, Random, 95% CI)

0.91 [0.71, 1.18]

5 Discontinuation rate Show forest plot

9

2384

Risk Ratio (M‐H, Random, 95% CI)

0.93 [0.69, 1.25]

6 Change in CD4 count Show forest plot

9

1829

Mean Difference (IV, Random, 95% CI)

‐3.03 [‐17.41, 11.35]

7 Treatment failure Show forest plot

5

737

Risk Ratio (M‐H, Random, 95% CI)

0.97 [0.76, 1.24]

8 Development of drug resistance Show forest plot

4

988

Risk Ratio (M‐H, Random, 95% CI)

0.76 [0.60, 0.95]

Figuras y tablas -
Comparison 1. Efavirenz 600 mg versus nevirapine all doses
Comparison 2. Efavirenz 600 mg versus nevirapine all doses: adverse events

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Severe adverse events: central nervous system Show forest plot

6

2049

Risk Ratio (M‐H, Random, 95% CI)

4.46 [1.65, 12.03]

2 Severe adverse events: gastrointestinal tract Show forest plot

6

2049

Risk Ratio (M‐H, Random, 95% CI)

0.76 [0.48, 1.21]

3 Severe adverse events: pyrexia Show forest plot

3

1799

Risk Ratio (M‐H, Random, 95% CI)

0.65 [0.15, 2.73]

4 Severe adverse events: elevated transaminases Show forest plot

3

1299

Risk Ratio (M‐H, Random, 95% CI)

0.52 [0.35, 0.78]

5 Severe adverse events: elevated alkaline phosphatase Show forest plot

1

1007

Risk Ratio (M‐H, Random, 95% CI)

0.65 [0.17, 2.50]

6 Severe adverse events: elevated amylase Show forest plot

2

1071

Risk Ratio (M‐H, Random, 95% CI)

1.40 [0.72, 2.73]

7 Severe adverse events: elevated triglycerides Show forest plot

2

1071

Risk Ratio (M‐H, Random, 95% CI)

1.10 [0.39, 3.13]

8 Severe adverse events: neutropenia Show forest plot

3

1799

Risk Ratio (M‐H, Random, 95% CI)

0.48 [0.28, 0.82]

9 Severe adverse events: rash Show forest plot

7

2277

Risk Ratio (M‐H, Random, 95% CI)

0.58 [0.34, 1.00]

10 Severe adverse events: elevated SGOT Show forest plot

1

135

Mean Difference (IV, Random, 95% CI)

3.30 [‐2.06, 8.66]

11 Severe adverse events: elevated SGPT Show forest plot

1

135

Mean Difference (IV, Random, 95% CI)

5.70 [‐4.23, 15.63]

12 Severe adverse events: elevated cholesterol Show forest plot

1

64

Risk Ratio (M‐H, Random, 95% CI)

6.03 [0.75, 48.78]

Figuras y tablas -
Comparison 2. Efavirenz 600 mg versus nevirapine all doses: adverse events
Comparison 3. Efavirenz versus nevirapine: subgroup analyses for concurrent TB treatments

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Virological success Show forest plot

9

2369

Risk Ratio (M‐H, Random, 95% CI)

1.04 [0.99, 1.10]

1.1 Concurrent treatment for TB

4

963

Risk Ratio (M‐H, Random, 95% CI)

1.08 [0.99, 1.18]

1.2 No treatment for TB

5

1406

Risk Ratio (M‐H, Random, 95% CI)

1.01 [0.95, 1.08]

2 Mortality Show forest plot

8

2317

Risk Ratio (M‐H, Random, 95% CI)

0.84 [0.59, 1.19]

2.1 Concurrent treatment for TB

4

963

Risk Ratio (M‐H, Random, 95% CI)

0.69 [0.40, 1.19]

2.2 No treatment for TB

4

1354

Risk Ratio (M‐H, Random, 95% CI)

1.01 [0.62, 1.64]

3 Progression to AIDS Show forest plot

5

2005

Risk Ratio (M‐H, Random, 95% CI)

1.23 [0.72, 2.11]

3.1 Concurrent treatment for TB

2

712

Risk Ratio (M‐H, Random, 95% CI)

1.09 [0.62, 1.92]

3.2 No treatment for TB

3

1293

Risk Ratio (M‐H, Random, 95% CI)

1.51 [0.44, 5.16]

4 Discontinuation rate Show forest plot

9

2384

Risk Ratio (M‐H, Random, 95% CI)

0.93 [0.69, 1.25]

4.1 Concurrent treatment for TB

4

963

Risk Ratio (M‐H, Random, 95% CI)

0.92 [0.59, 1.42]

4.2 No treatment for TB

5

1421

Risk Ratio (M‐H, Random, 95% CI)

0.99 [0.63, 1.55]

Figuras y tablas -
Comparison 3. Efavirenz versus nevirapine: subgroup analyses for concurrent TB treatments
Comparison 4. Efavirenz 600 mg versus nevirapine: subgroup analyses for dosage

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Virological success Show forest plot

9

2369

Risk Ratio (M‐H, Random, 95% CI)

1.04 [0.99, 1.09]

1.1 Nevirapine 200 mg twice daily

7

1766

Risk Ratio (M‐H, Random, 95% CI)

1.03 [0.97, 1.09]

1.2 Nevirapine 400 mg once daily

3

603

Risk Ratio (M‐H, Random, 95% CI)

1.12 [0.94, 1.35]

2 Mortality Show forest plot

8

2459

Risk Ratio (M‐H, Random, 95% CI)

0.80 [0.57, 1.12]

2.1 Nevirapine 200 mg twice daily

7

1781

Risk Ratio (M‐H, Random, 95% CI)

0.90 [0.64, 1.28]

2.2 Nevirapine 400 mg once daily

3

678

Risk Ratio (M‐H, Random, 95% CI)

0.34 [0.13, 0.90]

3 Progression to AIDS Show forest plot

5

2005

Risk Ratio (M‐H, Random, 95% CI)

1.20 [0.76, 1.89]

3.1 Nevirapine 200 mg twice daily

5

1585

Risk Ratio (M‐H, Random, 95% CI)

1.29 [0.75, 2.23]

3.2 Nevirapine 400 mg once daily

1

420

Risk Ratio (M‐H, Random, 95% CI)

0.79 [0.25, 2.44]

4 Discontinuation rate Show forest plot

9

2384

Risk Ratio (M‐H, Random, 95% CI)

0.87 [0.66, 1.14]

4.1 Nevirapine 200 mg twice daily

7

1781

Risk Ratio (M‐H, Random, 95% CI)

0.92 [0.71, 1.21]

4.2 Nevirapine 400 mg once daily

3

603

Risk Ratio (M‐H, Random, 95% CI)

0.79 [0.40, 1.57]

Figuras y tablas -
Comparison 4. Efavirenz 600 mg versus nevirapine: subgroup analyses for dosage