首页> 美国卫生研究院文献>The British Journal of Venereal Diseases >Safety and acceptability of vaginal disinfection with benzalkonium chloride in HIV infected pregnant women in west Africa: ANRS 049b phase II randomized double blinded placebo controlled trial. DITRAME Study Group
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Safety and acceptability of vaginal disinfection with benzalkonium chloride in HIV infected pregnant women in west Africa: ANRS 049b phase II randomized double blinded placebo controlled trial. DITRAME Study Group

机译:西非HIV感染孕妇接受苯扎氯铵阴道消毒的安全性和可接受性:ANRS 049b II期随机双盲安慰剂对照试验。 DITRAME研究组

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摘要

OBJECTIVES: To study the tolerance and acceptability in Africa of a perinatal intervention to prevent vertical HIV transmission using benzalkonium chloride disinfection. DESIGN: A randomized, double blinded phase II trial. SETTING: Prenatal care units in Abidjan (Cote d'Ivoire) and Bobo-Dioulasso (Burkina Faso). PATIENTS: Women accepting testing and counselling who were seropositive for HIV-1 and under 37 weeks of pregnancy were eligible. A total of 108 women (54 in each group) enrolled from November 1996 to April 1997, with their informed consent. INTERVENTION: Women self administered daily a vaginal suppository of 1% benzalkonium chloride or matched placebo from 36 weeks of pregnancy, and a single intrapartum dose. The neonate was bathed with 1% benzalkonium chloride solution or placebo within 30 minutes after birth. MAIN OUTCOME MEASURES: Adverse events were recorded weekly, with a questionnaire and speculum examination in women through delivery, and examination of the neonate through day 30. The incidence of genital signs and symptoms in the women and cutaneous or ophthalmological events in newborns were compared between groups on an intent to treat basis. RESULTS: The median duration of prepartum treatment was 21 days (range 0-87 days). Compliance was 87% for prepartum and 69% for intrapartum treatment, and 88% for the neonatal bath, without differences between the two groups. In women, the most frequent event was leucorrhoea; the incidence of adverse events did not differ between treatment groups. In children, the incidence of dermatitis and conjunctivitis did not differ between the benzalkonium chloride and placebo groups (p = 0.16 and p = 0.29, respectively). CONCLUSION: Vaginal disinfection with benzalkonium chloride is a feasible and well tolerated intervention in west Africa. Its efficacy in preventing vertical HIV transmission remains to be demonstrated.


机译:目的:研究使用苯扎氯铵消毒进行围产期干预以防止艾滋病毒垂直传播的非洲围产期干预措施的耐受性和可接受性。设计:一项随机,双盲的II期临床试验。地点:科特迪瓦阿比让和布基纳法索的波波-迪乌拉索的产前保健机构。患者:接受测试和咨询的血清HIV-1阳性且怀孕37周以下的妇女符合条件。 1996年11月至1997年4月,经知情同意,总共登记了108名妇女(每组54名)。干预措施:从怀孕36周起,妇女每天要自行服用1%的苯扎氯铵或配套安慰剂的阴道栓剂,并进行一次分娩。新生儿在出生后30分钟内用1%苯扎氯铵溶液或安慰剂沐浴。主要观察指标:每周记录不良事件,通过分娩对妇女进行问卷调查和镜检,并在第30天进行新生儿检查。比较了女性的生殖器体征和症状的发生率以及新生儿的皮肤或眼科事件。以治疗为目的的团体。结果:产前治疗的中位时间为21天(范围0-87天)。产前依从性为87%,产前治疗为69%,新生儿浴为88%,两组之间没有差异。在女性中,最常见的事件是白带。治疗组之间不良事件的发生率没有差异。在儿童中,苯扎氯铵组和安慰剂组的皮炎和结膜炎的发生率没有差异(分别为p = 0.16和p = 0.29)。结论:苯扎氯铵对阴道消毒是西非可行且耐受良好的干预措施。它在预防艾滋病毒垂直传播方面的功效仍有待证明。


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