Subclinical and clinical chorioamnionitis, fetal vasculitis, and risk for preterm birth: A cohort study

被引:33
作者
Palmsten, Kristin [1 ,2 ]
Nelson, Katharine K. [3 ,4 ]
Laurent, Louise C. [4 ]
Park, Soojin [4 ,5 ]
Chambers, Christina D. [2 ,3 ,6 ]
Parast, Mana M. [4 ]
机构
[1] HealthPartners Inst, Mail Stop 23301A,POB 1524, Minneapolis, MN 55440 USA
[2] Univ Calif San Diego, Dept Pediat, 9500 Gilman Dr, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Pathol, 9500 Gilman Dr, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Sanford Consortium Regenerat Med, La Jolla, CA 92093 USA
[5] Univ Calif San Diego, Dept Obstet Gynecol & Reprod Sci, 9500 Gilman Dr, La Jolla, CA 92093 USA
[6] Univ Calif San Diego, Dept Family Med & Publ Hlth, 9500 Gilman Dr, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
Chorioamnionitis; Epidemiology; Preterm birth; Pregnancy; HISTOLOGIC CHORIOAMNIONITIS; INFLAMMATORY RESPONSE; PLACENTAL PATHOLOGY; HEART-RATE; OUTCOMES; DELIVERIES; INFECTION; INFANTS;
D O I
10.1016/j.placenta.2018.06.001
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective: To evaluate the association between subclinical and clinical chorioamnionitis and risk of preterm birth (PTB). Methods: Demographic and clinical characteristics were abstracted from medical records and placental examinations performed (N = 1371 pregnancies including spontaneous and medically-indicated PTBs). Pregnancies were classified as having clinical chorioamnionitis (with or without histologic chorioamnionitis), subclinical chorioamnionitis (histologic, but not clinical, chorioamnionitis), or no chorioamnionitis; pregnancies with histologic chorioamnionitis were further evaluated for fetal vasculitis. Relative risks for PTB, early and late PTB, and PTB +/- premature rupture of membranes (PROM) were adjusted for maternal characteristics. Results: Clinical (4.3%) and subclinical (24.5%) chorioamnionitis were not associated with PTB overall. In pregnancies without clinical or subclinical chorioamnionitis, the risk of PTB with PROM and early PTB was 2.2% and 8.6%, respectively. In comparison, clinical chorioamnionitis was associated with an increased risk of PTB with PROM (aRR: 3.42 (95% CI: 1.07, 10.98), whereas subclinical chorioamnionitis was associated with increased risk of PTB with PROM (aRR: 3.92 (95% CI: 2.15, 7.12)) and early PTB (aRR: 1.77 (95% CI: 1.18, 2.64)). Histologic chorioamnionitis with fetal vasculitis was associated with increased risk of PTB with PROM (aRR: 7.44 (95% CI: 3.68, 15.05)) and early PTB (aRR: 2.94 (95% CI: 1.78, 4.87)), whereas histologic chorioamnionitis without fetal vasculitis was associated with increased risk of PTB with PROM only (aRR: 2.64, 95% CI: 1.27, 5.50). Conclusions: Subclinical chorioamnionitis and histologic chorioamnionitis with fetal vasculitis were associated with early PTB and PTB with PROM but not with PTB overall, likely due to inclusion of indicated PTBs.
引用
收藏
页码:54 / 60
页数:7
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