Ratanajamit Chaveewan, Vinther Skriver Mette, Jepsen Peter, Chongsuvivatwong Virasakdi, Olsen Jørn, Sørensen Henrik Toft
Department of Clinical Epidemiology, Institute of Epidemiology and Social Medicine, Aarhus University, Aarhus, Denmark.
Scand J Infect Dis. 2003;35(4):255-9. doi: 10.1080/00365540310000229.
This study aimed to examine the risk of adverse pregnancy outcomes in children born to mothers who redeemed a prescription for systemic or topical acyclovir during pregnancy. Data on prescriptions of acyclovir were obtained from the Danish North Jutland Prescription Database and data on pregnancy outcomes from the Danish Medical Birth Registry and the County Hospital Discharge Registry. The risk of malformations, low birth weight, preterm birth and stillbirth in users of acyclovir were compared with non-exposed women using a follow-up design, while the risk of spontaneous abortion was examined using a case-control design. 90 pregnant women had redeemed a prescription for systemic acyclovir, and 995 women for topical acyclovir, during 30 d before conception, or during their pregnancies from 1 January 1990 to 31 December 2001. The odds ratios (95% confidence intervals) of the exposed relative to the non-exposed for the systemic and topical acyclovir were: malformations, 0.69 (0.17-2.82) and 0.84 (0.51, 1.39); low birth weight, 2.03 (0.50-8.35) and 0.48 (0.21-1.07); preterm birth, 1.04 (0.38-2.85) and 0.95 (0.70-1.28); stillbirth (for topical acyclovir), 1.70 (0.80-3.60); and spontaneous abortion, 2.16 (0.60-7.80) and 1.29 (0.80-3.60). There is increasing evidence that the use of systemic acyclovir is not associated with an increased prevalence of malformations at birth and preterm delivery. The data for low birth weight and spontaneous abortion are still inconclusive, although the risk of spontaneous abortion is increased in women exposed to acyclovir during the first month of pregnancy. The use of topical acyclovir does not seem to be associated with any adverse pregnancy outcome, although data on stillbirth are inconclusive.
本研究旨在调查孕期使用全身性或局部性阿昔洛韦处方的母亲所生孩子出现不良妊娠结局的风险。阿昔洛韦处方数据来自丹麦北日德兰处方数据库,妊娠结局数据来自丹麦医疗出生登记处和郡医院出院登记处。采用随访设计,将阿昔洛韦使用者出现畸形、低出生体重、早产和死产的风险与未暴露女性进行比较,同时采用病例对照设计研究自然流产的风险。在1990年1月1日至2001年12月31日期间,90名孕妇在受孕前30天或孕期使用了全身性阿昔洛韦处方,995名孕妇使用了局部性阿昔洛韦处方。全身性和局部性阿昔洛韦暴露组相对于未暴露组的比值比(95%置信区间)分别为:畸形,0.69(0.17 - 2.82)和0.84(0.51,1.39);低出生体重,2.03(0.50 - 8.35)和0.48(0.21 - 1.07);早产,1.04(0.38 - 2.85)和0.95(0.70 - 1.28);死产(局部性阿昔洛韦),1.70(0.80 - 3.60);自然流产,2.16(0.60 - 7.80)和1.29(0.80 - 3.60)。越来越多的证据表明,使用全身性阿昔洛韦与出生时畸形患病率增加和早产无关。低出生体重和自然流产的数据仍无定论,尽管在怀孕第一个月接触阿昔洛韦的女性自然流产风险增加。使用局部性阿昔洛韦似乎与任何不良妊娠结局均无关联,尽管死产数据尚无定论。