Caritis S, Sibai B, Hauth J, Lindheimer M D, Klebanoff M, Thom E, VanDorsten P, Landon M, Paul R, Miodovnik M, Meis P, Thurnau G
Department of Obstetrics and Gynecology, University of Pittsburgh, PA 15213, USA.
N Engl J Med. 1998 Mar 12;338(11):701-5. doi: 10.1056/NEJM199803123381101.
Whether low-dose aspirin prevents preeclampsia is unclear. It is not recommended as prophylaxis in women at low risk for preeclampsia but may reduce the incidence of the disease in women at high risk.
We conducted a double-blind, randomized, placebo-controlled trial in four groups of pregnant women at high risk for preeclampsia, including 471 women with pregestational insulin-treated diabetes mellitus, 774 women with chronic hypertension, 688 women with multifetal gestations, and 606 women who had had preeclampsia during a previous pregnancy. The women were enrolled between gestational weeks 13 and 26 and received either 60 mg of aspirin or placebo daily.
Outcome data were obtained on all but 36 of the 2539 women who entered the study. The incidence of preeclampsia was similar in the 1254 women in the aspirin group and the 1249 women in the placebo group (aspirin, 18 percent; placebo, 20 percent; P=0.23). The incidences in the aspirin and placebo groups for each of the four high-risk categories were also similar: for women with pregestational diabetes mellitus, the incidence was 18 percent in the aspirin group and 22 percent in the placebo group (P=0.38); for women with chronic hypertension, 26 percent and 25 percent (P= 0.66); for those with multifetal gestations, 12 percent and 16 percent (P=0.10); and for those with preeclampsia during a previous pregnancy, 17 percent and 19 percent (P=0.47). In addition, the incidences of perinatal death, preterm birth, and infants small for gestational age were similar in the aspirin and placebo groups.
In our study, low-dose aspirin did not reduce the incidence of preeclampsia significantly or improve perinatal outcomes in pregnant women at high risk for preeclampsia.
低剂量阿司匹林能否预防子痫前期尚不清楚。不建议将其用于子痫前期低风险女性的预防,但可能会降低高风险女性患该病的发生率。
我们在四组子痫前期高风险孕妇中进行了一项双盲、随机、安慰剂对照试验,其中包括471例孕前接受胰岛素治疗的糖尿病女性、774例慢性高血压女性、688例多胎妊娠女性以及606例既往有子痫前期病史的女性。这些女性在孕13至26周期间入组,每天接受60毫克阿司匹林或安慰剂治疗。
在进入研究的2539名女性中,除36名外,其余所有人都获得了结局数据。阿司匹林组的1254名女性和安慰剂组的1249名女性子痫前期的发生率相似(阿司匹林组为18%,安慰剂组为20%;P = 0.23)。阿司匹林组和安慰剂组在四个高风险类别中的发生率也相似:对于孕前糖尿病女性,阿司匹林组的发生率为18%,安慰剂组为22%(P = 0.38);对于慢性高血压女性,分别为26%和25%(P = 0.66);对于多胎妊娠女性,分别为12%和16%(P = 0.10);对于既往有子痫前期病史的女性,分别为17%和19%(P = 0.47)。此外,阿司匹林组和安慰剂组的围产期死亡、早产以及小于胎龄儿的发生率相似。
在我们的研究中,低剂量阿司匹林并未显著降低子痫前期高风险孕妇子痫前期的发生率,也未改善围产期结局。