妊娠合并慢性肾脏疾病的产科结局和预后因素评估

IF 1.5 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Hypertension in Pregnancy Pub Date : 2021-02-01 Epub Date: 2021-01-03 DOI:10.1080/10641955.2020.1869249
Riza Madazlı, Didem Kaymak, Verda Alpay, Aytac Mahmudova, Nurhan Seyahi
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引用次数: 0

摘要

目的:评价妊娠合并慢性肾脏疾病(CKD)的产科结局,并评估不良产科结局的预后因素。方法:回顾性分析101例CKD单胎妊娠。根据CKD分期探讨产科结局。综合产科不良结局定义为死产、新生儿死亡和分娩中至少一种。结果:CKD妊娠中子痫前期、胎儿生长受限、围产期死亡率和综合产科不良结局的发生率分别为40.5%、26.7%、14.8%和37.6%。与1期和蛋白尿相比,4-5期妊娠的综合产科不良结局明显高于其他期(p 3 g/24 h与综合产科不良结局相关(OR 43.2, p = 0.005和OR 6.08, p = 0.01)。结论:即使在早期CKD,产科不良结局的发生率也很高。CKD 4-5期和基线蛋白尿> 3g /24 h是不良预后因素。
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Evaluation of obstetric outcomes and prognostic factors in pregnancies with chronic kidney disease.

Objective: To evaluate the obstetric outcomes of pregnancies with chronic kidney disease (CKD) and to assess the prognostic factors on adverse obstetric outcomes. Methods: We retrospectively reviewed 101 singleton pregnancies with CKD. Obstetric outcomes were explored according to CKD stages. The composite adverse obstetric outcome was defined as at least one of stillbirth, neonatal death and delivery <34 weeks due to preeclampsia or fetal distress. Results: The incidences of preeclampsia, fetal growth restriction, perinatal mortality and composite adverse obstetric outcome were 40.5%, 26.7%, 14.8% and 37.6% respectively in pregnancies with CKD. Composite obstetric adverse outcome was significantly higher in pregnancies with CKD stage 4-5 than the other stages (p < 0.01). CKD stage 4-5 and baseline proteinuria >3 g/24 h were associated with composite obstetric adverse outcome (OR 43.2, p = 0.005 and OR 6.08, p = 0.01 respectively) comparing to stage 1 and proteinuria <0.5 g/24 h. Conclusion: Incidences of adverse obstetric outcomes are high even in early stages of CKD. CKD stage 4-5 and baseline proteinuria >3 g/24 h are poor prognostic factors.

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来源期刊
Hypertension in Pregnancy
Hypertension in Pregnancy 医学-妇产科学
CiteScore
3.40
自引率
0.00%
发文量
21
审稿时长
6 months
期刊介绍: Hypertension in Pregnancy is a refereed journal in the English language which publishes data pertaining to human and animal hypertension during gestation. Contributions concerning physiology of circulatory control, pathophysiology, methodology, therapy or any other material relevant to the relationship between elevated blood pressure and pregnancy are acceptable. Published material includes original articles, clinical trials, solicited and unsolicited reviews, editorials, letters, and other material deemed pertinent by the editors.
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