Ali Mohammad, Nelson Allyson, Luquero Francisco J, Azman Andrew S, Debes Amanda K, M'bang'ombe Maurice Mwesawina, Seyama Linly, Kachale Evans, Zuze Kingsley, Malichi Desire, Zulu Fatima, Msyamboza Kelias Phiri, Kabuluzi Storn, Sack David A
Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Lancet Infect Dis. 2017 May;17(5):538-544. doi: 10.1016/S1473-3099(16)30523-0. Epub 2017 Feb 2.
Pregnancy increases the risk of harmful effects from cholera for both mothers and their fetuses. A killed oral cholera vaccine, Shanchol (Shantha Biotechnics, Hydrabad, India), can protect against the disease for up to 5 years. However, cholera vaccination campaigns have often excluded pregnant women because of insufficient safety data for use during pregnancy. We did an observational cohort study to assess the safety of Shanchol during pregnancy.
This observational cohort study was done in two adjacent districts (Nsanje and Chikwawa) in Malawi. Individuals older than 1 year in Nsanje were offered oral cholera vaccine during a mass vaccination campaign between March 30 and April 30, 2015, but no vaccines were administered in Chikwawa. We enrolled women who were exposed to oral cholera vaccine during pregnancy in Nsanje district, and women who were pregnant in Chikwawa district (and thus not exposed to oral cholera vaccine) during the same period. The primary endpoint of our analysis was pregnancy loss (spontaneous miscarriage or stillbirth), and the secondary endpoints were neonatal deaths and malformations. We evaluated these endpoints using log-binomial regression, adjusting for the imbalanced baseline characteristics between the groups. This study is registered with ClinicalTrials.gov, number NCT02499172.
We recruited 900 women exposed to oral cholera vaccine and 899 women not exposed to the vaccine between June 16 and Oct 10, 2015, and analysed 835 in each group. 361 women exposed to the vaccine and 327 not exposed to the vaccine were recruited after their pregnancies had ended. The incidence of pregnancy loss was 27·54 (95% CI 18·41-41·23) per 1000 pregnancies among those exposed to the vaccine and 21·56 (13·65-34·04) per 1000 among those not exposed. The adjusted relative risk for pregnancy loss among those exposed to oral cholera vaccine was 1·24 (95% CI 0·64-2·43; p=0·52) compared with those not exposed to the vaccine. The neonatal mortality rate was 11·78 (95% CI 5·92-23·46) per 1000 livebirths for infants whose mothers were exposed to oral cholera vaccine versus 8·91 (4·02-19·77) per 1000 livebirths for infants whose mothers were not exposed to the vaccine (crude relative risk 1·32, 95% CI 0·46-3·84; p=0·60). Only three newborn babies had malformations, two in the vaccine exposure group and one in the no-exposure group, yielding a relative risk of 2·00 (95% CI 0·18-22·04; p=0·57), although this estimate is unreliable because of the small number of outcomes.
Our study provides evidence that fetal exposure to oral cholera vaccine confers no significantly increased risk of pregnancy loss, neonatal mortality, or malformation. These data, along with findings from two retrospective studies, support use of oral cholera vaccine in pregnant women in cholera-affected regions.
Bill & Melinda Gates Foundation.
妊娠会增加母亲及其胎儿因霍乱产生有害影响的风险。一种口服霍乱灭活疫苗Shanchol(印度海得拉巴的Shantha生物技术公司生产)可预防霍乱长达5年。然而,由于孕期使用的安全性数据不足,霍乱疫苗接种活动通常将孕妇排除在外。我们开展了一项观察性队列研究,以评估Shanchol在孕期的安全性。
这项观察性队列研究在马拉维相邻的两个地区(恩桑杰和奇夸瓦)进行。2015年3月30日至4月30日的大规模疫苗接种活动期间,为恩桑杰1岁以上的人群提供口服霍乱疫苗,但奇夸瓦未接种任何疫苗。我们纳入了在恩桑杰地区孕期接触口服霍乱疫苗的妇女,以及同期在奇夸瓦地区怀孕(因此未接触口服霍乱疫苗)的妇女。我们分析的主要终点是妊娠丢失(自然流产或死产),次要终点是新生儿死亡和畸形。我们使用对数二项回归评估这些终点,并对两组之间不均衡的基线特征进行了调整。本研究已在ClinicalTrials.gov注册,注册号为NCT02499172。
2015年6月16日至10月10日期间,我们招募了900名接触口服霍乱疫苗的妇女和899名未接触该疫苗的妇女,并对每组835名进行了分析。361名接触疫苗的妇女和327名未接触疫苗的妇女在妊娠结束后被纳入。接触疫苗组每1000例妊娠中妊娠丢失的发生率为27.54(95%CI 18.41 - 41.23),未接触疫苗组每1000例妊娠中妊娠丢失的发生率为21.56(13.65 - 34.04)。与未接触疫苗的妇女相比,接触口服霍乱疫苗的妇女妊娠丢失的校正相对风险为1.24(95%CI 0.64 - 2.43;p = 0.52)。母亲接触口服霍乱疫苗的婴儿每1000例活产中新生儿死亡率为11.78(95%CI 5.92 - 23.46),母亲未接触疫苗的婴儿每1000例活产中新生儿死亡率为8.91(4.02 - 19.77)(粗相对风险1.32,95%CI 0.46 - 3.84;p = 0.60)。只有3例新生儿有畸形,疫苗接触组2例,未接触组1例,相对风险为2.00(95%CI 0.18 - 22.04;p = 0.57),不过由于结局数量较少,该估计并不可靠。
我们的研究提供了证据,表明胎儿接触口服霍乱疫苗不会显著增加妊娠丢失、新生儿死亡或畸形的风险。这些数据以及两项回顾性研究结果支持在霍乱流行地区的孕妇中使用口服霍乱疫苗。
比尔及梅琳达·盖茨基金会。