Harrington K, Kurdi W, Aquilina J, England P, Campbell S
Homerton Hospital NHS Trust, London, UK.
Ultrasound Obstet Gynecol. 2000 Jan;15(1):13-8. doi: 10.1046/j.1469-0705.2000.00002.x.
To investigate the effect of low-dose, slow-release aspirin in reducing the incidence and/or severity of pregnancy complications in women identified as high risk of developing problems associated with uteroplacental insufficiency, namely pre-eclampsia or delivering a small-for-gestational age (SGA) baby.
A prospective, randomized management study. One thousand and twenty-two women of mixed parity underwent color flow/pulsed Doppler (CFPD) imaging of the uterine arteries at the time of the 17-23 week (mean 19.9) anomaly scan. Women who were screen positive were randomized to a control or treatment group. The treatment group was given 100-mg slow-release aspirin (Disprin CV) daily and followed up at regular intervals. Women in the routine group received routine antenatal care. Main outcome measures were pre-eclampsia and SGA < 3rd centile. Secondary outcome measures were: SGA < 10th centile, pre-eclampsia requiring delivery before 34 weeks, placental abruption, an Apgar score < 7 at 5 min, admission to neonatal intensive care unit or a pregnancy that resulted in a stillbirth or neonatal death. Odds ratios (OR) with 95% confidence intervals (CI) were calculated for severe and any complications.
Two hundred and sixteen women were screen positive according to the defined criteria. One hundred and three women were assigned to the treatment group and 113 to the control group. The difference in the incidence of pre-eclampsia and SGA < 3rd centile between the control and treatment groups did not reach statistical significance. There was a statistically significant reduction in any (OR 0.41 (CI 0.35-0.45), P < 0.01) and severe pregnancy complications (OR 0.43 (CI 0.21-0.84), P < 0.05) in the treatment group compared with the controls.
The administration of slow-release aspirin to women identified as high risk, using color Doppler imaging of the uterine arteries at 20 weeks' gestation, did not significantly alter the incidence of pre-eclampsia or delivery of a SGA baby. It did, however, improve the outcome by reducing the overall incidence of complications associated with uteroplacental insufficiency.
研究低剂量缓释阿司匹林对被确定为发生与子宫胎盘功能不全相关问题(即子痫前期或分娩小于胎龄儿(SGA))风险较高的女性妊娠并发症发生率和/或严重程度的影响。
一项前瞻性随机管理研究。1022名不同孕次的女性在妊娠17 - 23周(平均19.9周)进行异常扫描时接受了子宫动脉彩色血流/脉冲多普勒(CFPD)成像检查。筛查呈阳性的女性被随机分为对照组或治疗组。治疗组每天服用100毫克缓释阿司匹林(Disprin CV),并定期随访。常规组女性接受常规产前护理。主要结局指标为子痫前期和小于第3百分位数的SGA。次要结局指标为:小于第10百分位数的SGA、34周前因子痫前期需要分娩、胎盘早剥、5分钟时阿氏评分<7分、入住新生儿重症监护病房或导致死产或新生儿死亡的妊娠。计算严重并发症和任何并发症的比值比(OR)及95%置信区间(CI)。
根据既定标准,216名女性筛查呈阳性。103名女性被分配到治疗组,113名被分配到对照组。对照组和治疗组之间子痫前期和小于第3百分位数的SGA发生率差异无统计学意义。与对照组相比,治疗组任何妊娠并发症(OR 0.41(CI 0.35 - 0.45),P < 0.01)和严重妊娠并发症(OR 0.43(CI 0.21 - 0.84),P < 0.05)的发生率有统计学意义的降低。
在妊娠20周时,对经子宫动脉彩色多普勒成像确定为高危的女性给予缓释阿司匹林,并未显著改变子痫前期的发生率或小于胎龄儿的分娩率。然而,它确实通过降低与子宫胎盘功能不全相关的总体并发症发生率改善了结局。