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. Author manuscript; available in PMC: 2014 Jul 7.
Published in final edited form as: AIDS Behav. 2006 May;10(3):227–245. doi: 10.1007/s10461-006-9078-6

Table 1.

Studies reporting the association of self-reported antiretroviral adherence with adherence as measured by other indirect measures or with clinical indicators

Source Study Self-report measure Recall
period
Association with other
indirect adherence measures
Association with clinical indicators
Setting; location; sample size Source/items/(nonadherence
  operationalization) (CO:
  continuous, CT: categorical,
  DI: dichotomous)
electronic data monitoring;
  pharmacy refills (PR); pill
  count (PC); other
HIV-1 RNA viral load (VL); CD4; other
  (adherent vs. nonadherent)
Alcoba et al. (2003) 2 HIV clinics; Spain;
  N=106
N/R; N/R; DI: <90% of
  prescribed doses for at least
  one drug
4 days VL detectable (NS); plasma indinavir levels
  (NS)
Aloisi et al. (2002) 57 ID hospital units; Italy;
  N = 366
N/R; 3 items; DI: “Yes” to all
  three items vs. <3
6 months VL undetectable*** 68% vs. 40% @ 12 mo
Altice, Mostashari, and Friedland (2001) 4 prison HIV clinics; CT,
  US;N=164
Ickovics ‘97; N/R; DI: 80%
  of pills taken/prescribed
7 days PR r = 0.82 (significance N/R) CD4 count (NS)
Ammassari et al. (2004) 11 clinical centers; Italy;
  N=135
Murri ‘00; 1 forced-choice
  item on timing of last
  missed dose; DI: missed
  ≥ 1 dose over last 7 days
7 days CD4 higher mean (SD)* 637 (341) vs. 509
  (362)
Antinori et al. (2004) Study cohort; Italy; N = 238 Murri ‘00; N/R; DI: missed
  ≥ 1 dose over last 7 days
7 days VL rebound > 500 copies/mL (NS)
Arnsten et al. (2001) Hospital study cohort;
  Bronx, NY, US; N = 67
N/R; N/R; CO: % of
  prescribed doses taken
1 day; 7
  days
EDM; 1-day r = 0.49***;
  7-day r = 0.46***
VL <500; 1-day r = 0.43***; 7 day
  r = 0.52***
Bangsberg et al. (2000) Community cohort; San
  Francisco, US; N = 34
N/R; 3 items; CO: Mean
  value of 3 measures of %
  prescribed doses
3 days VL r= −0.60***
Bangsberg et al. (2001) Community cohort; San
  Francisco, US; N = 45
N/R; Day-by-day review of
  doses; CO: % prescribed
  doses, DI: >80%
3 days PC r = 0.85***; PC
  κ = 0.65***; provider
  estimate (NS)
Bangsberg et al. (2002) Private clinic and county
  hospital; San Francisco,
  US;N=110
AACTG (Chesney ‘00);
  Day-by-day review of doses
  on computer; DI: 90 and
  80%
3 days Provider estimate*** (test
  statistic NR)
VL detectable ≥ 500; <80% OR 3.0 (95%
  CI 1.1–8.1)
Barroso et al. (2003) HIV reference center; Rio de
  Janeiro, Brazil; N= 64
N/R; 1 item; DI: taking as
  prescribed >80% days
30 days VL<400; OR 7.2 (95% CI 1.6–31.9) in
  semen; ORA 8.2 (95% CI 1.2–56.7) in
  plasma
Brigido et al. (2001) Public AIDS clinic; Sao
  Paulo, Brazil; N= 168
N/R; 5 items; CT: Reg: all
  doses taken, qReg: miss up
  to 4 doses or 1 full day/mo,
  Ireg: all other irregular
30 days VL median log10*; Reg 2.0 (1.6–5.6); qReg
  2.0 (1.6–5.5); Ireg 3.6 (1.6–6.2); CD4
  median gain*; (test statistic N/R); AIDS
  development or death* (test statistic N/R)
Carrieri et al. (2001) Routine clinical sites;
  France; N = 436
AACTG; 5 items for each
  drug; CT: 100%, 80–99%,
  <80%
4 days VL undetectable at 4**; 12**, and 20
  months** (test statistic N/R)
Carrieri et al., 2003 Routine clinical sites;
  France; N = 360
AACTG; 5 items for each
  drug; CT: 100%, 80–99%,
  <80%
4 days VL suppression at 3 years: Highly adherent OR 3.4 (95% CI 1.4–7.9); Mod adherent NS; CD4 increase >200 by 3 years: highly adherent OR 2.4 (95% CI 1.0–5.5); Mod adherent NS
Catz, Kelly, Bogart, Benotsch, and McAuliffe (2000) Outpatient ID clinic;
  Milwaukee, US; N = 72
N/R; 2 items; CT: missed
  doses daily, weekly,
  monthly, or never
3 months VL <400* (test statistic N/R)
Cederfjall, Langius-Eklof, Lidman, and Wredling (2002) Outpatient HIV clinic;
  Stockholm, Sweden; N = 99
N/R; 1,7, 30 days =%
  missed in 1 month; DI: 959%
1 month VL <50 71% vs. 45%*; CD4 <200 8% vs.
  32%***
Cingolani et al. (2002) Tertiary care ID department;
  Italy; N =127
Murri ‘00; 1 item, timing of
  last missed dose; DI:
  missed before 2–4 weeks
  (adherent) vs. yesterday,
  last week
N/A VL <500 at 3 mo* (test statistic NR); nonadherent OR 0.37 (95% CI 0.1–0.95)*; CD4 change; 3 mo + 50 vs. — 12**; 6 mo
  + 62 vs. −13**
Cohn, Kammann, Williams, Currier, and Chesney (2002) AACTG sites; 29 sites in US;
  N = 643
AACTG; 2 items; DI: 100% 48 hr VL>500 nonadherence over 56 weeks; OR 2.3 (95% CI N/R); 70% vs. 50%***
Dorz et al. (2003) 2 ID departments; Padua and
  Verona, Italy; N= 109
N/R; l item; CO: # pills/#
  prescribed, DI: 80%
7 days VL mean 10,854 vs. 34,149*; CD4 mean 6899 vs. 379***
Duong et al. (2001) AIDS outpatient clinic;
  Dijon, France; N= 149
PMAQ (Paterson ‘99); 4
  items; DI: 100%
  (nonadherent score<4)
Combined:
  4 days and
  4 weeks
VL reduction; ORA 2.9 (95% CI 1.2–7.1); Did not miss any PI last 4 days r = . 18*
Duran et al. (2001) Study cohort; France;
  N = 277
AACTG; 5 items; DI:100% Combined:
  4 days and
  weekend
VL undetectable 4 months after ART
   initiation 59.4% vs. 41.6%**
Duran et al. (2001) Study cohort; France; N= 57 N/R; 1 item; CT: 100%,
  99%-80%, <80%
1 week VL median log10** 100%: 2.3 (2.3–3.5); 80%–99%: 2.3 (2.3–3.6); <80%: 3.8 (2.6–5.04); VL undetectable** 100%: 73.1%; 80%–99%: 69.2%; <80%: 22.2%; CD4 (NS, p = 0.06); drug level***
Duran et al. (2003) 47 hospitals; France; N = 642 N/R; 5 items; CT: 100%,
  99%-80%, <80%
4 days VL detectable; 100%: OR 1.0; 99%–80%: OR 1.5 (95% CI 1.0–2.3); <80%: OR 2.3 (95% CI 1.3–4.1)
Eldred, Wu, Chaisson, and Moore (1998) Hospital HIV clinic;
  Baltimore, MD, USA;
  N = 244
N/R; 1 item for each time
  frame; DI: 80%
7 days; 14
  days
Medical record kappa 71%; 7
  day: 60% vs. 56% (NS); 14
  day: 74% vs. 67%**
Fong et al. (2003) HIV clinic; Hong Kong;
  N=161
N/R; Number missed doses;
  DI: 100%
Since last visit VL<500; ORA 4.2 (95% CI 1.8–12.3)
Gao et al. (2000) 3 clinics; West Virginia, US;
  N = 72
Samet ‘92; N/R, assessed
  doses; CO: prescribed –
  missed/prescribed
2 days Disease severity*
Garcia de Olalla et al. (2002) HIV hospital unit;
  Barcelona, Spain; N= 1219
N/R; N/R; DI: 90% 1 month Mortality: Non adherent; Relative hazard
  1.5 (95% CI 1.2–1.99)
Gifford et al. (2000) Community practices; San Diego CA, US; N= 133 CASQ (Berry ‘00) 4 items
  per drug taken; CT: 100%,
  80–99%, <80%
7 days VL log10 Each increase in adherence
  category associated with 1.3 log10
  decrease**
Giordano, Guzman, Clark, Charlebois, and Bangsberg (2004) Participants’ usual place of
  residence; San Francisco,
  CA,US; N=84
AACTG and Visual Analog
  Scale - VAS (Walsh ‘98); 4
  items/drug (3 day), VAS-1;
  CO: Mean adherence over
  three visits
3 days
  (AACTG)
  3 or 4
  weeks
  (VAS)
Unannounced PC and VAS:
  r = 0.76(95%CI
  0.65–0.84); 3-day r = 0.71
  (95% CI 0.59–0.80); (sig.
  N/R; NS diff betw VAS and
  3 day)
VL; VAS: r= − .49 (95% CI − .0.64–0.31);
  3-day r= –.34 (95% CI −0.51–0.13);
  (sig. N/R; NS diff betw VAS and 3 day)
Godin, Gagne, and Naccache (2003) 4 HIV clinics; Montreal,
  Quebec City; N = 256
Researcher-created; 9 items,
  # pills missed/# prescribed;
  DI: 95%
1,2,7,30
  days
VL increase over 6 months; Nonadherent 1,
  2, 30 day (NS); 7 days OR 1.9 (95% CI
  1.0–3.6)
Golin et al. (2002) 3 public HIV clinics; N/R;
  N=117
Composite score with EDM,
  PC, SR interview (Liu’01)
  1 item CO: #doses taken/#
  prescribed
7 days EDM r = 0.38 (sig. N/R); PC r = 0.62 (sig. N/R)
Gordillo, del Amo, Soriano, and Gonzalez-Lahoz (1999) HIV reference center;
  Madrid, Spain; N = 366
N/R; N/R; DI: 90% Last week CD4 at enrollment and good adherence;
  >500 ORA 2.4 (95% CI 1.3–4.4);
  200–499 ORA 2.8 (95% CI 1.4–5.5)
Goujard et al. (2003) Hospital centers; France;
  N = 326
AACTG, PMAQ, and 3
  items re: instructions
  (Metcalf ‘98) 13 items; CO:
  Nonadherence score 0–26
N/R VL lower (test statistics N/R)*** CD4
  higher (test statistics N/R)*
Guaraldi et al. (2003) 8 tertiary centers; Northern,
  Central Italy; N= 175
MOS-HIV Health Survey
  N/R; 85% (>1 dose in 7
  days)
7 days Morphologic alterations; ORA 2.36 (95% CI 1.1–5.0)
Haubrich et al. (1999) 5 university HIV clinics; CA,
  US; N = 164 @ 2 months,
  119 @ 6 months
N/R 24 items; assessed %
  prescribed doses taken; CT:
  100%, 99-95%, <95-80%,
  <80%
4 weeks Provider estimate
  kappa = 0.02 (NS)
VL log10 reduction (SD) @ 2 months*
  100%, 99-95%, <95-80%, <80%; 0.95
  (2.2); 0.79 (2.0); 0.57 (1.8); 0.04 (2.0); VL
  log10 increase (SD) @ 6 months* 100%:
  − 1.1 (2.2); <80%: 0.2 (1.2); CD4 cells @
  6 months** 100%, 99-95%, <95-80%,
  <80% 72 (162); + 87 (154); + 54 (162);
  − 19 (74)
Ho et al. (2002) Clinic; Hong Kong; N= 161 Doung ‘01 1 item, %
  prescribed doses taken CT:
  100%, 99–95%, 94-90%,
  <90%
4–6 weeks VL detectable** ≤ 99% vs. 100% OR 4.2
  (95% CI 1.8–12.3) Disease progression**
Horne et al. (2004) Outpatient clinic; Brighton,
  UK; N=109
VAS 1 item, correct dose
  timing; DI: 7 pt scale 0–6:
  cutoff ≥ 5
N/R VL>400; 18% vs. 26% (NS); CD4 (NS)
Hugen et al. (2002) University centre; Nijmegen
  and Arnhem Netherlands;
  N = 26
N/R; VAS; Multiple items;
  CT: 3 groups and range
  1–10
N/R EDM % taken on time***
  ρ = .73; % taken** ρ = .55
N/R
Ickovics et al. (2002) 21 AACTG sites; Multisites,
  US; N = 93
AACTG 1 item for each drug
  DI: 95%
4 days VL>50 @ 24 weeks <95% adherent OR
  2.6 (95% CI 1.1–6.1) CD4 change (NS)
Ingersoll (2004) University ID clinic;
  Virginia; N= 120
Medication Adherence Form
  (Ingersoll ‘99) Multiple
  items; DI: 95% PIs taken;
  DI: Adherence score 1–3,
  cutoff >2
1 week VL undetectable 77% vs. 23%* CD4 <200
  54% vs. 46%*
Kimmerling et al. (2003) Clinics, community; Los
  Angeles, US; N= 58
N/R # doses taken q.d. of last
  3; CO: score
3 days EDM: r = 0.47*** Subset
  reporting missed doses (NS)
Kleeberger et al. (2001) Research cohort; Baltimore,
  Chicago, Pittsburgh, LA,
  US;N = 393
Modified AACTG; multiple
  items; DI: 100%
4 days VL undetectable <50 copies; 53.3% vs.
  37.4%** CD4 ≥ 400 (NS); 64.4% vs.
  58.3%
Knobel et al. (2001) University HIV clinic;
  Barcelona, Spain; N = 679
N/R; N/R; DI: 90% 1 month VL <500; Adherent OR 3.1 (95% CI
  2.2–4.2)***; nonadherent ORA 0.4 (95%
  CI 0.2–0.7)**; CD4 mean increase 171 vs.
  107**
Knobel et al. (2001) 69 hospitals; Spain;
  N = 2528@3,2127@6,
  and 1797 @ 12 months
SMAQ (from Morisky ‘86);
  6 items; DI: 95% (missed
  >2days in 3 mos; 2 doses 7
  days or yes to 1/4 items)
Combined
  1
  weekend;
  1 week; 3
  months
EDM: sensitivity 72%;
  specificity 91%; PPV 91%;
  NPV 80%
VL <500; @ 3 months OR 2.2 (95% CI
  1.8–2.6)***; @ 6 months OR 2.6 (95% CI
  2.2–3.1)***; @ 12 months OR 2.5 (95% CI
  2.0–3.1)***; VL >500; Nonadherent ORA
  1.7 (95% CI 1.4–2.1)
Knobel et al. (2004) 2 hospitals; Barcelona,
  Spain; N= 85
SMAQ (from Morisky ‘86);
  6 items; DI: 90%
1 weekend;
  1 week; 3
  months
VL >500 @ first year: Nonadherent OR 5.2
  (95% CI 2.1–13.3); ORA 4.4 (95% CI
  1.6–12.3)
Laniece et al. (2003) 3 health clinics; Dakar,
  Senegal; N =158
N/R; N/R; # taken:
  #prescribed; DI: 90%
30 days VL mean difference nonadherent; Month
  18: 1.7 log10 copies*; Month 24: 1.8 log10
  copies*
Le Moing et al. (2001) 47 clinical centers;
  Paris/France; N=750
N/R; N/R; DI: 100% 4 days VL <500: 84% vs. 73%***; OR 2.0 (95%
  CI 1.3–3.0)
Le Moing et al. (2002) 47 clinical centers; France;
  N=1129
N/R; 5 items;
  categorical: 100%, 80–99%,
  <80%
4 days VL rebound = VL>500; 27% high adher.
  HR = 0.4 (95% CI 0.3–0.6)***; 34%
  moderate adher. HR = 0.6 (95% CI
  0.4–0.8)**; 53% low adher. HR= 1.0
Liu et al. (2001) Public HIV clinic; N/R;
  N=108
N/R; 2 items, composite
  adherence score; CO: mean
1 week EDM r = 0.38***; PR:
  r = 0.62***
VL <400 vs. VL>400 mean adherence 8
  week (NS), 24 week* 0.97 (0.85–0.96) vs.
  0.90(0.85 −0.96)
Lopez-Suarez,
  Fernandez-Gutierrez del
  Almo, Perez-Guzman, and
  Giron-Gonzalez (1998)
N/R; Cadiz, Spain; N = 65 N/R; N/R; DI: 80% N/R VL log10, 2 drug/3 drug regimen; 3 months:
  2.9 vs. 4.4***/3.6 vs. 4.9*; 6 months: 3.1
  vs. 4.5***/3.3 vs. 4.8*; CD4, 2 drug/3 drug
  regimen; 3 months: 550 vs. 356***/405 vs.
  333*; 6 months: 567 vs. 416***/540 vs.
  400*
Lucas, Cheever, Chaisson,
  and Moore (2001)
Johns Hopkins AIDS
  Service; Baltimore, MD,
  US; N = 533
N/R; N/R; DI: missed >2
  doses in 2 weeks
2 weeks VL log10 difference 0.4 (0.2–0.7); CD4 cell
  difference − .12 (−40-15) (sig. N/R)
Maggiolo et al. (2002) Outpatient clinic; Bergamo,
  Italy; N= 597
Modified AACTG (Chesney
  ‘00); N/R; DI: 100%
90 days VL<50; 75.6 vs. 55.3%***
Mannheimer et al. (2002) 18 CPCRA Sites; US;
  N=1095
CPCRA (Form 646, ‘02);
  N/R; CT: 100%, 80–99%,
  <80%
7 days VL log10 decrease***; 100%: 2.8, 80–99:
  2.3, <80%: 0.7; CD4 increase***; 100%:
  179, 80–99: 159, <80%: 53
Martin et al. (2001) Hospital HIV unit; Madrid,
  Spain; N =242
N/R; 4 items, # of pills
  delivered/prescribed
6 days SR vs. PR; 80% adherence
  cutoff: sens = 25%,
  spec = 86%, PPV = 49%,
  positive likelihood ratio
  (LR) = 1.8; 90% adherence:
  sens = 19%, spec = 84%,
  PPV = 58%, positive
  LR = 1.2
Martin-Fernandez et al.(2001) HIV unit; Madrid, Spain;
  N = 283
Tuldra ‘99; 2 items: Capable
  (1–5, cutoff <4); Effort
  (100 pt scale, cutoff
  < = 36); Pharmacy
  refill = gold standard; DI:
  95%
N/R Area under curve of
  measure; Capable 0.61
  (0.54–0.67); Effort 0.64
  (0.57–0.70). Concordance
  between negative response
  on 2 SR to PR kappa 0.25
  (0.13–0.36)
Mathews et al. (2002) University HIV Clinic; San
  Diego, CA, US; N= 175
Modified AACTG (Chesney
  ‘00); 5 items; DI: Score
  0–33 cutoff 5
30 days EDM ρ= −0.40 (sig. N/R) VL log10 difference*; 1 month: .04, 3
  month: 1.1, 6 month: 1.3; VL
  undetectable*; CD4*; plasma level
  ρ= − .0.48 (sig. N/R)
Melbourne et al. (1999) Physician offices;
  Providence, RI, US; N = 44
N/R; N/R; CO: mean % 1 month SR (SD) vs. EDM (SD); 1
  month: 98% (3.6) vs. 90%
  (14)*; 2 month: 96% (5) vs.
  90% (12.6)*
Moatti et al. (2000) Hospitals; Marseilles,
  Avigon, Nice, Paris, France;
  N=164
N/R; N/R; DI: 80% 7 days VL median log10 (range)**; 2.7 (2.3–5.6) vs.
  3.9 (2.3–5.8); VL undetectable or decrease
  >1 log10 57% vs. 40.3%*; CD4 median
  increase (NS); disease progression (NS)
Murri et al. (2001) University HIV clinic;
  Rome, Italy; N= 140
Researcher-created; 16
  items; DI: forgot 1 dose vs.
  >1 dose in 3 days
1 day; 3
  days
VL detectable; nonadherent 3 days; OR 2.2
  (95% CI 1.0–4.7); Plasma level PI 1 day:
  OR 15.9 (95% CI 4.9–50.7), 3 day: OR 4.4
  (95% CI 1.7–11.9)
Nieuwkerk et al. (2001) 14 hospitals; The
  Netherlands, Belgium;
  N=160
Researcher-created 3 items;
  DI: 100%
7 days PC measure for saquinavir*;
  PC measure for ritonavir
  (NS)
VL>400 @ 48 weeks; nonadherent 40%,
  adherent 15%*
Nieuwkerk et al. (2001) 22 hospitals; The
  Netherlands; N= 224
Researcher-created 4 items;
  DI: 100%
7 days VL>500; nonadherent OR 2.1 (95% CI
  0.9–1.9); nonadherent ORA 4.0 (95% CI
  1.4–11.6); drug level median concentration
  (range) 1.1 (0.6–1.4) vs. 0.8 (0.51.1)***
Oyugi et al. (2004) Research-affiliated clinics
  and hospitals; Kampala,
  Uganda; N= 34
AACTG (Chesney ‘00) and
  Visual Analogue Scale
  (VAS); N/R; CO: Mean
3 days
  (AACTG):
  30 day
  (VAS)
EDM 3 day r = 0.87***;VAS
  0.77***; PC 3 day
  r = 0.89***; VAS 0.86***; 3
  day and VAS r = 0.82***
VL < 400 @ 12 weeks; 3-day
  r=- 0.42**; 30-day VAS r= − .036*
Palepu, Horton, Tibbetts,
  Meli, and Samet (2004)
Medical and methadone
  clinics, respite facility;
  Boston, MA, US; N= 194
N/R; N/R; DI: 95%; CO:
  Mean
30 days VL log10 mean (SD); 1.8 (1.8) vs. 2.7
  (1.9)***; CD4 mean (SD); 414 (254) vs.
  375 (216) (NS)
Pinheiro et al. (2002) Public clinic; Pelotas, Brazil;
  N=195
Researcher-created; N/R; DI:
  95%
2 days VL <500; 67.5% vs. 31.5%***; CDC
  disease stage (NS)
Pradier et al. (2001) Research cohort: 12 outpatient hospitals in Marseilles, Avigon, Nice, and Paris, France; N = 119 N/R; 1 item for each medication; DI: 100% 3 groups: (1) no VL change or <0.5 decrease, (2) > 0.5 decrease but still detectable, (3) undetectable 7 days VL log10; G3 vs. G2 = ORA 5.8 (95% CI
  1.5–22.1); G3 vs. Gl = ORA 5.6 (95% CI
  1.3–24.7)
Raboud et al. (2002) N/R; Italy, The Netherlands, Canada, and Australia;
  N = 311
INC AS, AVANTI 2 and 3 studies; N/R; DI: Adherence from 3 different studies which each dichotomized differently 92.3, 75, 75% 28 days PC (N/R) Virologic failure; RR 3.0 (95% CI 1.4–6.1);
  Test statistics NR for the following:
  Virologic suppression**; Triple drug**,
  double drug (NS); VL undetectable *
Schuman et al. (2001) Research cohort; Baltimore, Chicago, Detroit, New York, LA, Wash. DC, US;
  N = 371
N/R; 1 item; DI: 75% 2 weeks VL undetectable; OR 3.9 (95% CI 1.8–8.5);
  CD4 ≥ 200; OR 2.1 (95% CI 1.0–4.3)*
Silveira et al. (2002) HIV/AIDS service; Pelotas, Brazil; N = 244 N/R; 1 item (# tablets taken); CT: ≥ 95%, 94-80%, 79-60%, <60% 48 hr VL <80 across groups OR ≥ 95%: OR 5.5
  (95% CI 2.6–11.9); 60–79%: OR 4.2 (95%
  CI 1.3–.3); 80%–%: OR 5.6 (95% CI
  2.2–.1); <60%: 1.0
Spire et al. (2002) Research cohort, 47
  hospitals, France; N = 445
N/R; 3 items; DI: 100% 4 days VL log10 median decrease @ 4 months; 1.7
  vs. 1.3***; VL ≤ 500 77% vs. 60%***
Trotta et al. (2003) Research cohorts; Rome and
  other sites, Italy; N= 596
Murri ‘00; 16 items; DI: 86%
  (missed ≥ 1 dose last 7
  days)
7 days
  
VL ≤ 500; nonadherent OR 0.7 (95% CI
  0.5–.9); CD4 <200/mm; OR 0.6 (95% CI
  0.3–.0,p = .06)
Vincke and Bolton (2002) N/R; Belgium; N= 86 PI attitude scale (Weiss N/R)
  3 items Ordinal: scale (1–,
  5: excellent)
4 weeks Clinician: r= −0.25 (NS);
  Significant other:
  r= −0.42**
VL; R = 0.30 (sig. N/R)
Wagner et al. (2001) 3 VA Medical Centers;
  Cleveland, OH, Houston,
  TX, Manhattan, NY, US; N
  = 793
N/R; 4 items; CT: 0 (poor),
  1, 2 (perfect)
4 days SR and provider agreement;
  kappa -.03, (-.09,.03)
  (NS)
VL <400; 55% vs. 36% vs. 22%***; ORA
  0.9 (95% CI 0.8–.3); VL median 141 vs.
  393 vs. 1679***; ORA 0.04 (95% CI
  −0.2-0.1)
Wagner, 2002 CBOs, clinics; Los Angeles,
  USA; N= 180
Modified AACTG (Chesney ‘00) N/R; CO: Mean 3 days 4-week EDM: r = 0.34**
Wagner et al, 2003 Mental health community;
  LA,CA, US; N = 47
N/R; N/R; CO: Means 3 days; 2
  weeks
EDM 3 days*** r = 0.61;2 weeks*** r = 0.63 VL log10 r = − .0.39* (recall period N/R);
  VL log10 mean (SD); 3 day: 2.3 log10 (1.0)
  vs. 3.5 log10 (1.2)**; CD4 3 days (NS); 14
  days (NS)
Walsh etal. (2001) Publicly funded clinic; N/R;
  N=178
Researcher-created; N/R;
  CO: Median
30 day and
  VAS (30
  days)
PR ρ = 0.19**; Nurse rating
  ρ = 0.51**; MD rating
  ρ = 0.33**¶
Walsh et al. (2002) Public HIV clinic; London,
  England; N= 78
AACTG (Chesney ‘00),
  Hecht ‘98, Fletcher ‘79; 6
  items: 3 −3day; 1–2 week, 1
  last missed; VAS 30 day
  (0–%); CO: Mean
3 day; 2
  weeks; 30
  day (VAS)
EDM: Univariate linear
  regression; 3 day r = 0.32;
  0.68 (95% CI 0.23–1.13)**;
  2 week r = 0.62; 1.21(95%
  CI 0.86–.56)***; VAS
  r = 63; 1.09 (95% CI
  0.78–1.39)***
VL<50; 3 day (NS); 14 day ρ = − .0.30**;
  VAS ρ = −0.28**
Weiser et al. (2003) 3 private clinics; Gaborone,
  Francistown, Botswana;
  N = 93–109
Modified AACTG (Chesney
  ‘00); N/R; DI: 95%
1 year SR and provider agreement;
  Kappa = .35,x2 =11.13***
Wutoh et al. (2001) 2 large HIV clinics;
  Washington DC, US;
  N=100
N/R; N/R; CO: Mean 7 days VL mean; ρ =.−312**

Notes. N/R: Not reported, NS: Non-significant, ID: Infectious disease, SD: Standard deviation, PI: Protease inhibitor.

a

Odds ratios, hazard ratios, and relative risks are unadjusted unless denoted by subscript “A”; 95% confidence intervals denote significance unless only a p-value is given.

b

Correlation statistics are Pearson’s r or Spearman’s ρ.

c

Significance level was calculated from data provided in the article using a 1 sample test of proportion.

d

Significance level was calculated from data provided in the article using a 1 sample t-test.***