European Study Group [20], 1992 9 European countries Commission of the European Communities |
Cohort |
10 women with HIV using IUDs 86 women with HIV using no contraceptive |
IUD (type not specified) |
Most stage II or III with CD4 count >200×106/L 36 women stage IV or CD4 count <200×106/L |
Seroconversion of male partner |
Male partners of IUD users: 10% (n=1/10) seroconverted Male partners ofwomen using no method: 12% (n=10/86) seroconverted Not significant (exact p value not reported but not identified as significant) |
Multiple countries |
Small sample size for comparison of interest Index cases primarily drug users (may limit generalizability) Length of follow up not stated Response rates and follow-up rates not reported IUD type not specified Unclear if reported IUD use was at baseline or at time of transmission Analysis not adjusted |
II-2, poor |
Mostad [22], 1997 Kenya NIH, Clinical Nutrition Research Unit |
Cross-sectional |
6 women with HIV using IUDs 182 women with HIV using no contraceptive |
IUD (type not specified) |
Mean CD4 count 452; 17% < 200; no information for IUD users |
Cervical HIV-1 DNA (swab) Vaginal HIV-1 DNA (swab) |
Odds of cervical HIV-1 DNA among IUD users versus no method: OR 0.2 (95% CI=0.0–2.2) No vaginal HIV-1 DNA in IUD users |
|
Small sample size of IUD users IUD type not specified Large percentage of sex workers (may limit generalizability) No information on ART use |
II-3, Poor |
Richardson [11], 1999 (follow up to Sinei [12], 1998) Kenya USAID |
Prospective follow-up without comparison group |
98 women with HIV initiating IUDs Follow up for 4 months |
Copper IUD (copper T 380 A) |
At 1 month follow-up, 7% had CD4 counts <200 |
Cervical HIV-1 DNA (endocervical swab) |
No significant difference in prevalence of cervical shedding at 4 months (43%) compared with baseline (50%): adjusted OR 0.6 (95% CI=0.3–1.1) |
Physicians performing exams were blinded to woman's HIV status Timing of IUD insertion known Cervical shedding analysis controlled for confounders 76% follow-up at 4 months Study powered to detect clinically relevant change in cervical HIV-1 DNA |
Small sample size Short follow up for changes in disease status No comparison group No information on ART use during study |
II-3, fair |
Kovacs [21], 2001 United States NIH, Agency for Health Care Policy and Research, CDC |
Cross-sectional |
Women with HIV using IUDs (N not stated) |
IUD (type not specified) |
32% CD4 count >500 cells/mm3 50% CD4 count 200–499 cells/mm3 18% CD4 count <200 cells/mm3 All on stable ART for 1 month |
Genital HIV shedding (endocervical swab and cervicovaginal lavage) |
No association of IUD use with genital HIV shedding (data not shown) |
Included women with severe disease |
Sample size using IUDs not stated IUD types not stated OR for comparison of IUD versus non-IUD users not shown |
II-3, poor |
Heikinheimo [8], 2006 Finland Helsinki University |
Prospective follow-up without comparison group |
12 women with HIV initiating IUDs Follow up for 12 months |
LNG-IUD |
CD4 count ≥0.35×109 cells/mL 10 women using ART 2 women not using ART |
Genital HIV RNA (cervicovaginal lavage) |
Women usingART (N=10): Nodifference in genitalHIV RNA (6 women undetectable) Women not using ART (N=2): genital HIV RNA present in half of samples, level decreased in 1 woman and increased in 1 woman after IUD initiation |
100% follow up at 12 months Timing of IUD insertion known |
Small sample size No comparison group No information on women with severe disease |
II-3, poor |
Coleman [15], 2013 Kenya Puget Sound Partners for Global Health, American College of Obstetricians and Gynecologists, University of Washington |
Prospective follow-up without comparison group |
30 women with HIV initiating LNG-IUDs Follow up for 6 months |
LNG-IUD |
CD4 count >250 cells/μL No ART within 90 days of study entry |
Genital HIV-1 RNA (endocervical secretions and cervical vaginal lavage) |
No statistically significant change in genital HIV-1 RNA (p=.55) |
25/30 (83%)with evaluable specimens at 6 months Timing of IUD insertion known |
Small sample size Short follow up for changes in disease status No information on women with severe disease No comparison group No information on ART use during study |
II-3, poor |