孕期使用法莫替丁的影响:一项观察性队列研究。

IF 1.2 Q4 PHARMACOLOGY & PHARMACY
Ayako Nishimura, Ayako Furugen, Masaki Kobayashi, Yoh Takekuma, Naho Yakuwa, Mikako Goto, Masahiro Hayashi, Atsuko Murashima, Mitsuru Sugawara
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引用次数: 0

摘要

背景:法莫替丁是一种组胺2受体拮抗剂(H2Ras),被广泛用于治疗和预防孕期胃肠道症状。尽管有多项研究报告了妊娠期使用 H2Ras 的情况,但这些报告中关于法莫替丁的数据有限。因此,我们分析了妊娠结局数据,以评估孕期使用法莫替丁对胎儿的影响:妊娠结局数据用于1988年4月至2017年12月期间在日本两家提供孕期用药咨询的机构登记的女性。在主要终点方面,根据妊娠前三个月服用法莫替丁(n = 330)或被认为无致畸风险药物(对照组,n = 1 407)的孕妇的活产数据计算先天性畸形的发生率。考虑到次要终点,根据整个孕期服用法莫替丁(n = 347)和对照组(n = 1 476)的数据,计算了包括早产在内的产科结局发生率。先天性畸形发生率的粗略几率(cORs)采用单变量逻辑回归分析法计算,对照组作为参照。使用多变量逻辑回归分析计算调整后的几率比(aORs),并对其他各种因素进行调整:法莫替丁组和对照组的先天性畸形发生率分别为 3.9% 和 2.8%。法莫替丁组和对照组之间没有明显差异(cOR:1.40 [95% CI:0.68-2.71],aOR:1.06 [95% CI:0.51-2.16])。相反,法莫替丁组和对照组的早产率分别为 8.1%和 3.8%,差异显著(cOR:2.00 [95% CI:1.20-3.27])。然而,多变量分析排除了使用法莫替丁的混杂因素:这项观察性队列研究显示,妊娠头三个月期间接触法莫替丁与婴儿先天性畸形风险增加无关。虽然与对照组相比,法莫替丁使用者的早产率较高,但这可能是并发症等混杂因素造成的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of famotidine use during pregnancy: an observational cohort study.

Background: Famotidine, a histamine2-receptor antagonist (H2Ras), is widely used to treat and prevent gastrointestinal symptoms during pregnancy. Although several studies have reported the use of H2Ras during pregnancy, limited data on famotidine were included in these reports. Therefore, we analyzed pregnancy outcome data to evaluate the effects of famotidine use during pregnancy on the fetus.

Methods: Pregnancy outcome data were used for females enrolled in two Japanese facilities that provided counseling on drug use during pregnancy between April 1988 and December 2017. For the primary endpoint, the incidence of congenital malformations was calculated from the data of live birth to pregnant women who took famotidine (n = 330) or drugs considered to exert no teratogenic risk (control, n = 1,407) during the first trimester of pregnancy. Considering secondary endpoints, the incidence of obstetric outcomes, including preterm delivery, was calculated from data on the use of famotidine (n = 347) and controls (n = 1,476) during the entire pregnancy. The crude odds ratios (cORs) for the incidence of congenital malformations were calculated using univariate logistic regression analysis, with the control group used as the reference. Adjusted ORs (aORs) were calculated using multivariate logistic regression analysis adjusted for various other factors.

Results: The incidences of congenital malformations in the famotidine and control groups were 3.9% and 2.8%, respectively. There was no significant difference between the famotidine and control groups (cOR: 1.40 [95% CI:0.68-2.71], aOR: 1.06 [95% CI:0.51-2.16]). Conversely, the preterm delivery rates were 8.1% and 3.8% in the famotidine and control groups, respectively, indicating a significant difference (cOR: 2.00 [95% CI:1.20-3.27]). However, the multivariate analysis eliminated famotidine use as a confounding factor.

Conclusions: This observational cohort study revealed that exposure to famotidine during the first trimester of pregnancy was not associated with an increased risk of congenital malformations in infants. Although a higher rate of preterm delivery was detected in famotidine users when compared with controls, this could be attributed to confounding factors, such as complications.

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来源期刊
CiteScore
1.80
自引率
0.00%
发文量
29
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8 weeks
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