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. 2013 Nov 11;11(12):1303–1332. doi: 10.1586/14787210.2013.851601

Table 8.

Treatment efficacy studies of 1 g azithromycin for the treatment of Chlamydia trachomatis in pregnant women.

Study (year) Country Year(s) Number cured of evaluated Percent cured 95% CI Diagnostic method Birth outcomes Additional details Ref.
Kacmar et al. (2001) USA 1998–2000 18/19 94.7% 84.4–105.1% Ligase chain reaction; TOC 28–42 days NR 52.6% (n = 19; 95% CI: 31.5–72.8%) had side effects; passive or active solicitation not reported; 13.6 weeks (±8.0 SD) mean gestational age at enrolment [73]
Jacobson et al. (2001) USA 1998–2000 35/55 63.6% 47.7–79.6% DNA LCx STD assay; TOC 28 days 13.3% (6/45) preterm 10.1% (n = 55; 95% CI: 5.2–21.9%) had side effects; passive or active solicitation not reported; 20.6 weeks (±8.8 SD) mean gestational age at enrolment [74]
Wehbeh et al. (1998) USA NR 26/27 96.3% 89.0–103.6% Culture NR 100% (n = 27) of partners treated [75]
Adair et al. (1998) USA 1995–1997 37/42 88.1% 77.7–98.5% DNA assay; TOC 28 days NR 11.9% (n = 5; 95% CI: 5.3–25.1%) had side effects; passive or active solicitation not reported; 21.6 weeks (±9.5 SD) mean gestational age at enrolment; 54.8% (n = 23) of partners treated [76]
Edwards et al. (1996) USA 1993–1994 61/65 93.8% 87.8–99.9% DNA assay; TOC 14 days 9.2% (6/65) preterm, 3 due to PROM; mean birth age 38.8 weeks ±1.6 20.4 weeks mean gestational age at enrolment [78]
Rosenn et al. (1995) USA 1994–1995 21/23 91.3% 79.3–103.4% PCR (Amplicor); TOC 21 days NR 19.3 weeks (±3.5 SD) mean gestational age at enrolment [79]
Gunter et al. (1996) USA NR 22/22 100% NA DNA assay; TOC 14 days NR 13.6% (n = 3; 95% CI: 5.0–33.6%) had gastrointestinal side effects; passive or active solicitation not reported [77]
Bush & Rosa (1994) USA NR 15/15 100% NA DNA assay; TOC 14 days NR 0% of women experienced side effects; 100% (n = 15) of partners treated [80]
Rahangdale et al. (2006) USA 1999–2000 137/141 97.2% 94.4–99.9% DNA assay; TOC days 7–20; 21–34; 35–55; >56 7.5% (16/221 'any' preterm azithromycin) 13.1% (n = 191; 95% CI: 9.0–18.6%) also had BV
14.1 weeks (±6.3 SD) mean gestational age at enrolment
[185]
Miller et al. (1995) USA 1993–1994 132/138 95.6% 92.2– 99.1% DNA assay; TOC 10–14 days 15.2% (19/125) preterm 5.5% (n = 146; 95% CI: 2.8–10.4%) had side effects; 23.9% (n = 138; 17.6–31.7%) women also had NG; 17.4% (4/17) reported side effects (all GI); mean gestational age at enrolment not reported [186]

NR: Not reported; TOC: Test of cure.