Pre-Pregnancy eGFR and the Risk of Adverse Maternal and Fetal Outcomes: A Population-Based Study.

IF 9.4 1区 医学 Q1 UROLOGY & NEPHROLOGY
Jessica Tangren, Lavanya Bathini, Nivethika Jeyakumar, Stephanie N Dixon, Joel Ray, Ron Wald, Ziv Harel, Ayub Akbari, Anna Mathew, Susan Huang, Amit X Garg, Michelle A Hladunewich
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引用次数: 0

Abstract

Significance statement: Pregnancies in women with CKD carry greater risk than pregnancies in the general population. The small number of women in prior studies has limited estimates of this risk, especially among those with advanced CKD. We report the results of a population-based cohort study in Ontario, Canada, that assessed more than 500,000 pregnancies, including 600 with a baseline eGFR < 60 ml/min per 1.73 m 2 . The investigation demonstrates increases in risk of different adverse maternal and fetal outcomes with lower eGFR and further risk elevation with baseline proteinuria.

Background: CKD is a risk factor for pregnancy complications, but estimates for adverse outcomes come largely from single-center studies with few women with moderate or advanced stage CKD.

Methods: To investigate the association between maternal baseline eGFR and risk of adverse pregnancy outcomes, we conducted a retrospective, population-based cohort study of women (not on dialysis or having had a kidney transplant) in Ontario, Canada, who delivered between 2007 and 2019. The study included 565,907 pregnancies among 462,053 women. Administrative health databases captured hospital births, outpatient laboratory testing, and pregnancy complications. We analyzed pregnancies with serum creatinine measured within 2 years of conception up to 30 days after conception and assessed the impact of urine protein where available.

Results: The risk of major maternal morbidity, preterm delivery, and low birthweight increased monotonically across declining eGFR categories, with risk increase most notable as eGFR dropped below 60 ml/min per 1.73 m 2 . A total of 56 (40%) of the 133 pregnancies with an eGFR <45 ml/min per 1.73 m 2 resulted in delivery under 37 weeks, compared with 10% of pregnancies when eGFR exceeded 90 ml/min per 1.73 m 2 . Greater proteinuria significantly increased risk within each eGFR category. Maternal and neonatal deaths were rare regardless of baseline eGFR (<0.3% of all pregnancies). Only 7% of women with an eGFR <45 ml/min per 1.73 m 2 received dialysis during or immediately after pregnancy.

Conclusions: We observed higher rates of adverse pregnancy outcomes in women with low eGFR with concurrent proteinuria. These results can help inform health care policy, preconception counseling, and pregnancy follow-up in women with CKD.

孕前 eGFR 与孕产妇和胎儿不良结局的风险:一项基于人群的研究
意义声明:与普通人群相比,患有慢性肾脏病的妇女怀孕的风险更大。以往研究中的女性人数较少,这限制了对这一风险的估计,尤其是晚期 CKD 患者。我们报告了在加拿大安大略省进行的一项基于人群的队列研究的结果,该研究评估了 50 多万名孕妇,其中包括 600 名基线 eGFR < 60 毫升/分钟/1.73 米 2 的孕妇。调查显示,随着 eGFR 的降低,孕产妇和胎儿出现不同不良后果的风险也会增加,而随着基线蛋白尿的增加,风险会进一步升高:背景:慢性肾脏病是妊娠并发症的一个风险因素,但对不良后果的估计主要来自单中心研究,其中只有少数妇女患有中度或晚期慢性肾脏病:为了研究孕产妇基线 eGFR 与不良妊娠结局风险之间的关系,我们对加拿大安大略省在 2007 年至 2019 年期间分娩的妇女(未接受透析或肾移植)进行了一项基于人群的回顾性队列研究。这项研究包括 462,053 名妇女中的 565,907 例妊娠。行政健康数据库记录了医院分娩、门诊实验室检测和妊娠并发症。我们对受孕 2 年内至受孕后 30 天内测量血清肌酐的孕妇进行了分析,并评估了尿蛋白(如有)的影响:主要孕产妇发病率、早产和低出生体重的风险随着 eGFR 值的下降而单调增加,当 eGFR 值下降到每 1.73 m 2 60 ml/min 以下时,风险增加最为显著。在 133 例 eGFR 下降的妊娠中,共有 56 例(40%)出现不良妊娠结局:我们观察到,低 eGFR 并发蛋白尿的妇女不良妊娠结局发生率较高。这些结果有助于为慢性肾脏病妇女的医疗保健政策、孕前咨询和孕期随访提供参考。
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来源期刊
Journal of The American Society of Nephrology
Journal of The American Society of Nephrology 医学-泌尿学与肾脏学
CiteScore
22.40
自引率
2.90%
发文量
492
审稿时长
3-8 weeks
期刊介绍: The Journal of the American Society of Nephrology (JASN) stands as the preeminent kidney journal globally, offering an exceptional synthesis of cutting-edge basic research, clinical epidemiology, meta-analysis, and relevant editorial content. Representing a comprehensive resource, JASN encompasses clinical research, editorials distilling key findings, perspectives, and timely reviews. Editorials are skillfully crafted to elucidate the essential insights of the parent article, while JASN actively encourages the submission of Letters to the Editor discussing recently published articles. The reviews featured in JASN are consistently erudite and comprehensive, providing thorough coverage of respective fields. Since its inception in July 1990, JASN has been a monthly publication. JASN publishes original research reports and editorial content across a spectrum of basic and clinical science relevant to the broad discipline of nephrology. Topics covered include renal cell biology, developmental biology of the kidney, genetics of kidney disease, cell and transport physiology, hemodynamics and vascular regulation, mechanisms of blood pressure regulation, renal immunology, kidney pathology, pathophysiology of kidney diseases, nephrolithiasis, clinical nephrology (including dialysis and transplantation), and hypertension. Furthermore, articles addressing healthcare policy and care delivery issues relevant to nephrology are warmly welcomed.
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