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作 者:张巍[1] 陈顺乐[1] 鲍春德[1] 顾越英[1] 张春燕[1]
机构地区:[1]上海交通大学医学院附属仁济医院风湿病科,200001
出 处:《上海医学》2008年第5期332-334,共3页Shanghai Medical Journal
摘 要:目的了解系统性红斑狼疮(SLE)肾炎患者妊娠的母婴风险。方法前瞻性观察我院1998—2006年47例SLE肾炎患者的妊娠结果,依据妊娠前SLE病情,将患者分为SLE缓解期妊娠(A组,37例)、非SLE缓解期妊娠(B组,6例)和妊娠期初发SLE(C组,4例),分别观察妊娠期及产后半年内母亲的SLE病情和胎儿结局。结果共45例患者分娩活婴(1例分娩双胎),2例患者因疾病活动而中止妊娠。无自然流产和死胎,无母婴死亡。A组中,妊娠期SLE肾炎活动7例,肾功能损害1例;中止妊娠1例,早产10例,足月产26例。B组中,妊娠期SLE肾炎活动5例,肾功能损害1例;中止妊娠1例,早产4例,足月产1例。C组中,妊娠期内无肾功能损害,早产2例,足月产2例。B组患者妊娠期SLE肾炎活动构成比显著低于A组(P<0.01)。结论SLE肾炎患者妊娠的关键在于妊娠时机的选择,疾病缓解期妊娠可有效降低母婴风险。Objective To evaluate the maternal fetal risks during pregnancy in patients with lupus nephritis. Methods A prospective observation was done on the outcomes of pregnancies in 47 patients with lupus nephritis between 1998--2006 in Renji Hospital. The patients were divided into 3 groups: controlled lupus (Group A, n=37), uncontrolled lupus (Group B, n=6) and lupus onset during pregnancy (Group C, n=4). The intra-partum and postpartum lupus disease activity and the fetal outcomes were observed in all group within half year after delivery. Results Totally 45 patients had live deliveries, including 1 with twin. Two patients received therapeutical abortion due to severe disease flare. There was no natural abortion and stillbirth, nor maternal-fetal deaths. Seven patients in Group A had intra-partum lupus nephritis flare (19 %); one had therapeutical abortion and 1 had transient renal damage; and 10 had preterm deliveries and 26 cases of full term deliveries. Five patients in Group B had intra-partum lupus nephritis flare (83%); 1 had therapeutical abortion and 1 had permanent renal damage; and 4 had preterm deliveries and 1 had full term delivery. No renal deterioration was found in Group C; 2 patients had pre-term delivery and 2 had therapeutical abortion. There was significant difference in intra-partum lupus nephritis flare between Group A and Group B(P〈0.01). Conclusion The key for a safe outcome of pregnancy in lupus nephritis patients is proper timing of conception. The control of lupus activity before pregnancy can effectively downregulate maternal-fetal risks. (Shanghai Med J, 2008,31 : 332-334)
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