Chico R Matthew, Chaponda Enesia Banda, Ariti Cono, Chandramohan Daniel
Department of Disease Control, London School of Hygiene & Tropical Medicine, United Kingdom.
Department of Biological Sciences, University of Zambia, Lusaka, Zambia.
Clin Infect Dis. 2017 Apr 15;64(8):1043-1051. doi: 10.1093/cid/cix026.
We conducted a prospective cohort study in Zambia among pregnant women who received intermittent preventive treatment using sulfadoxine-pyrimethamine (IPTp-SP).
We calculated the odds ratios (ORs) of adverse birth outcomes by IPTp-SP exposure, 0-1 dose (n = 126) vs ≥2 doses (n = 590) and ≥2 doses (n = 310) vs ≥3 doses (n = 280) in 7 categories of malaria infection and sexually transmitted and reproductive tract infections (STIs/RTIs).
We found no significant differences in baseline prevalence of infection across IPTp-SP exposure groups. However, among women given 2 doses compared to 0-1 dose, the odds of any adverse birth outcome were reduced 45% (OR, 0.55; 95% confidence interval [CI], 0.36, 0.86) and 13% further with ≥3 doses (OR, 0.43; 95% CI, 0.27, 0.68). Two or more doses compared to 0-1 dose reduced preterm delivery by 58% (OR, 0.42; 95% CI, 0.27, 0.67) and 21% further with ≥3 doses (OR, 0.21; 95% CI, 0.13, 0.35). Women with malaria at enrollment who received ≥2 doses vs 0-1 had 76% lower odds of any adverse birth outcome (OR, 0.24; 95% 0.09, 0.66), and Neisseria gonorrhoeae and/or Chlamydia trachomatis had 92% lower odds of any adverse birth outcome (OR, 0.08; 95% CI, 0.01, 0.64). Women with neither a malaria infection nor STIs/RTIs who received ≥2 doses had 73% fewer adverse birth outcomes (OR, 0.27; 95% CI, 0.11, 0.68).
IPTp-SP appears to protect against malaria, STIs/RTIs, and other unspecified causes of adverse birth outcome.
我们在赞比亚对接受磺胺多辛-乙胺嘧啶间歇性预防治疗(IPTp-SP)的孕妇进行了一项前瞻性队列研究。
我们计算了在7类疟疾感染以及性传播和生殖道感染(STIs/RTIs)中,IPTp-SP暴露(0 - 1剂,n = 126)与≥2剂(n = 590)以及≥2剂(n = 310)与≥3剂(n = 280)的不良出生结局的比值比(OR)。
我们发现不同IPTp-SP暴露组之间感染的基线患病率无显著差异。然而,与接受0 - 1剂的女性相比,接受2剂的女性出现任何不良出生结局的几率降低了45%(OR,0.55;95%置信区间[CI],0.36,0.86),接受≥3剂时进一步降低了13%(OR,0.43;95% CI,0.27,0.68)。与接受0 - 1剂相比,接受2剂或更多剂可使早产减少58%(OR,0.42;95% CI,0.27,0.67),接受≥3剂时进一步减少21%(OR,0.21;95% CI,0.13,0.35)。入组时感染疟疾且接受≥2剂与接受0 - 1剂的女性相比,出现任何不良出生结局的几率低76%(OR,