Assessment of risk factors for cystic periventricular leukomalacia

被引:5
作者
Kurimoto, Tomonori [1 ]
Ibara, Satoshi [1 ]
Kamitomo, Masato [2 ]
Tokuhisa, Takuya [3 ]
Maeda, Takatsugu [2 ]
Maede, Yoshinobu [1 ]
Ishihara, Chie [1 ]
Naito, Yoshiki [1 ]
Hirakawa, Eiji [4 ]
Yamamoto, Tsuyoshi [1 ]
机构
[1] Kagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, Japan
[2] Kagoshima City Hosp, Dept Obstet & Gynecol, Perinatal Med Ctr, Kagoshima, Japan
[3] Imakiire Gen Hosp, Dept Neonatol, Perinatal Med Ctr, Kagoshima, Japan
[4] Nagasaki Harbor Med Ctr, Dept Neonatol, Perinatal Med Ctr, Nagasaki, Japan
关键词
cystic periventricular leukomalacia; late deceleration; late-onset circulatory dysfunction; loss of variability; risk factors; PRETERM INFANTS; CEREBRAL-PALSY; HEART-RATE; PATHOGENESIS; HYPOCAPNIA; FEATURES;
D O I
10.1111/jog.14473
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Aim Periventricular leukomalacia (PVL) is an important cause of cerebral palsy in premature infants, and cystic PVL is the most serious form of the disease. The risk factors for cystic PVL in singleton fetuses at a gestational age of The cystic PVL was associated with increased incidence of recurrent late deceleration (L/D) (43.4% vs. 15.9%,P= 0.004) and loss of variability (LOV) (10.0% vs. 0.0%,P= 0.03) in fetal heart rate monitoring and late-onset circulatory dysfunction (LCD) (33.3% vs. 11.1%,P= 0.02). Logistic regression analysis revealed that recurrent L/D (odds ratio [OR] = 3.57, 95% confidence interval [CI]: 1.29-10.15,P= 0.01) and LCD (OR = 3.41, 95% CI: 1.09-11.04,P= 0.03) were risk factors associated with cystic PVL. LOV was not included in the multivariate analysis as there were too few cases in both the cystic PVL and control groups. Conclusion Recurrent L/D, LOV and LCD are strongly associated with cystic PVL. In cases of fetal acidosis related to recurrent L/D or loss of variability, cystic PVL may occur.
引用
收藏
页码:2383 / 2389
页数:7
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