Safety and acceptability of vaginal disinfection with benzalkonium chloride in HIV infected pregnant women in west Africa: ANRS 049b phase II randomised, double blinded placebo controlled trial

Citation
P. Msellati et al., Safety and acceptability of vaginal disinfection with benzalkonium chloride in HIV infected pregnant women in west Africa: ANRS 049b phase II randomised, double blinded placebo controlled trial, SEX TRANS I, 75(6), 1999, pp. 420-425
Citations number
22
Categorie Soggetti
Clinical Immunolgy & Infectious Disease","da verificare
Journal title
SEXUALLY TRANSMITTED INFECTIONS
ISSN journal
13684973 → ACNP
Volume
75
Issue
6
Year of publication
1999
Pages
420 - 425
Database
ISI
SICI code
1368-4973(199912)75:6<420:SAAOVD>2.0.ZU;2-R
Abstract
Objectives: To study the tolerance and acceptability in Africa of a perinat al intervention to prevent vertical HIV transmission using benzalkonium chl oride disinfection. Design: A randomised, 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 in formed consent. Intervention: Women self administered daily a vaginal suppository of 1% ben zalkonium chloride or matched placebo from 36 weeks of pregnancy, and a sin gle 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 questionn aire and speculum examination in women through delivery, and examination of the neonate through day ophthalmologi-30. The incidence of genital signs a nd symptoms in the women and cutaneous or o cal events in newborns were com pared 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 advers e events did not differ between treatment groups. In children, the incidenc e 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 a nd well tolerated intervention in west Ati ica. Its efficacy in preventing vertical HIV transmission remains to be demonstrated.