Table 1.
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.
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.
Correlation statistics are Pearson’s r or Spearman’s ρ.
Significance level was calculated from data provided in the article using a 1 sample test of proportion.
Significance level was calculated from data provided in the article using a 1 sample t-test.***