Assessment of risk factors for cystic periventricular leukomalacia
被引:5
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作者:
Kurimoto, Tomonori
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Kagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, JapanKagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, Japan
Kurimoto, Tomonori
[1
]
Ibara, Satoshi
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Kagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, JapanKagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, Japan
Ibara, Satoshi
[1
]
Kamitomo, Masato
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机构:
Kagoshima City Hosp, Dept Obstet & Gynecol, Perinatal Med Ctr, Kagoshima, JapanKagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, Japan
Kamitomo, Masato
[2
]
Tokuhisa, Takuya
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Imakiire Gen Hosp, Dept Neonatol, Perinatal Med Ctr, Kagoshima, JapanKagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, Japan
Tokuhisa, Takuya
[3
]
Maeda, Takatsugu
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Kagoshima City Hosp, Dept Obstet & Gynecol, Perinatal Med Ctr, Kagoshima, JapanKagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, Japan
Maeda, Takatsugu
[2
]
Maede, Yoshinobu
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Kagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, JapanKagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, Japan
Maede, Yoshinobu
[1
]
Ishihara, Chie
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Kagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, JapanKagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, Japan
Ishihara, Chie
[1
]
Naito, Yoshiki
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Kagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, JapanKagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, Japan
Naito, Yoshiki
[1
]
Hirakawa, Eiji
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Nagasaki Harbor Med Ctr, Dept Neonatol, Perinatal Med Ctr, Nagasaki, JapanKagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, Japan
Hirakawa, Eiji
[4
]
Yamamoto, Tsuyoshi
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Kagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, JapanKagoshima City Hosp, Dept Neonatol, Perinatal Med Ctr, 37-1 Uearata, Kagoshima 8908760, Japan
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
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.