ライフサイエンスコーパス: perinatal death

1 proven sepsis, necrotizing enterocolitis, or perinatal death).

2 aged >/=35 years may reduce overall rates of perinatal death.

3 nt should include discussion of the risks of perinatal death.

4 rm of ryanodine receptor; Ry1R) resulting in perinatal death.

5 on in rates of preterm birth, stillbirth, or perinatal death.

6 the risks of stillbirth, neonatal death, and perinatal death.

7 rm parturition, to prevent preterm birth and perinatal death.

8 The primary outcome was perinatal death.

9 gnancies, is a leading cause of maternal and perinatal death.

10 l intensive care/special care baby unit, and perinatal death.

11 architecture, causing severe proteinuria and perinatal death.

12 sive care, macrosomia, low Apgar scores, and perinatal death.

13 Whole-body deletion of Derlin-2 results in perinatal death.

14 interstitium, reduced airway branching, and perinatal death.

15 mphangiogenesis defects in mouse embryos and perinatal death.

16 th in the 7 days after birth, stillbirth, or perinatal death.

17 preterm birth, fetal-growth restriction, or perinatal death.

18 f routine induction of labour on the risk of perinatal death.

19 a 33% reduction in litter size and frequent perinatal death.

20 h caused congestive heart failure leading to perinatal death.

21 ice leads to cystic kidneys and embryonic or perinatal death.

22 r at 40 weeks would be required to prevent 1 perinatal death.

23 Prenatal induction resulted in perinatal death.

24 160 pregnancies and accounts for 50% of all perinatal deaths.

25 ed Scottish national databases of births and perinatal deaths.

26 There were no perinatal deaths.

27 associated with a lower risk of in-hospital perinatal death (0.08% versus 0.26%; adjusted risk ratio

28 I, 1.18-1.30; I2 = 80%; n = 18 studies); for perinatal death, 1.16 (95% CI, 1.00-1.35; I2 = 93.7%; n

29 more than 16,274 stillbirths, more than 4311 perinatal deaths, 11,294 neonatal deaths, and 4983 infan

30 5 singleton births, there were 13,027 (0.6%) perinatal deaths, 116,043 (5.6%) preterm live-births and

31 eated infertility also increased the risk of perinatal death (2.7 [1.5-4.7]); the risks associated wi

32 tio [OR] 3.3, 95% CI 1.2-9.0, I(2)=58%), and perinatal deaths (2.3, 1.2-4.1, I(2)=73%) compared with

33 was 7.0 per 1000 births, of which 3.6% were perinatal deaths, 20% prenatally diagnosed, and 5.6% TOP

34 e no significant differences in the rates of perinatal death (3.2% in the pessary group and 2.4% in t

35 reated infertility were at increased risk of perinatal death (3.3 [1.6-6.8]).

36 d in 2.0 per 1000 births, of which 8.1% were perinatal deaths, 40% were prenatally diagnosed, and 14%

37 (95% CI, 46-51), and 59 (95% CI, 55-63); for perinatal death, 66, 73 (95% CI, 67-81), and 86 (95% CI,

38 ir pregnancy ended with a livebirth (n=199), perinatal death (74), or a lost pregnancy (64).

39 ampsia is an important cause of maternal and perinatal death and complications.

40 or anxiety have higher risks of miscarriage, perinatal death and decisions to terminate a pregnancy i

41 y abruption result in increased frequency of perinatal death and decreased fetal size and gestational

42 ratory distress syndrome, a leading cause of perinatal death and morbidity in newborn infants.

43 ary outcome was a composite of stillbirth or perinatal death and neonatal complications, including hy

44 Whether supplementation reduces the risk of perinatal death and neonatal convulsions requires furthe

45 omposite outcome that included stillbirth or perinatal death and several neonatal complications, it d

46 Maternal deletion of Gtl2 resulted in perinatal death and skeletal muscle defects, indicating

47 n result in intrauterine growth retardation, perinatal death and spontaneous abortion.

48 There were 12 perinatal deaths and 5 neonatal convulsions in the contr

49 ulsions in the control group compared with 3 perinatal deaths and no neonatal convulsions in the DHA

50 studies (in which cases were stillbirths or perinatal deaths), and randomised controlled trials of m

51 estern Scotland with databases of maternity, perinatal death, and birth and death certifications to a

52 ffect with protection from preterm birth and perinatal death, and partial correction of reduced birth

53 , premature births, small full-term infants, perinatal deaths, and births of live healthy infants.

54 databases of maternity-hospital discharges, perinatal deaths, and death certifications.

55 riction and early delivery, the high risk of perinatal death associated with abruption persisted.

56 The risk of perinatal death associated with multiple births did not

57 f this analysis was to estimate the risks of perinatal death associated with treated and untreated in

58 The relative risks of perinatal death associated with treated and untreated in

59 The absolute risk of perinatal death associated with trial of labor following

60 There were no maternal or perinatal deaths associated with HELLP syndrome.

61 There were 18 perinatal deaths associated with uterine rupture among 1

62 vessel formation resulting in hemorrhage and perinatal death, but the mechanism of brain hemorrhage i

63 s a composite of adverse perinatal outcomes (perinatal death, chronic lung disease, neonatal sepsis,

64 Wnt1-expressing neural crest cells leads to perinatal death, cleft palate and other cranial bone def

65 Delivery-related perinatal death, defined as intrapartum stillbirth or ne

66 cterize the relationship between smoking and perinatal death, defined as the combination of stillbirt

67 enetic disruption of myomaker in mice causes perinatal death due to an absence of multi-nucleated mus

68 ant mice exhibit fragile stratum corneum and perinatal death due to dehydration.

69 to E18.5 reduced lung growth and resulted in perinatal death due to respiratory failure.

70 Wnt7b(lacZ-/-) mice exhibit perinatal death due to respiratory failure.

71 duced incidence of severe motor deficits and perinatal death following E22 hypoxia-ischemia.

72 n of proinflammatory cytokines, resulting in perinatal death from cachexia.

73 d1(tgCre) results in glomerular aneurysm and perinatal death from kidney failure.

74 d its homozygous deletion in mice results in perinatal death from respiratory failure due to the lack

75 evel rates of preterm birth, stillbirth, and perinatal death in Ontario between 2003 and 2012.

76 he effect of a trial of labor on the risk of perinatal death in otherwise uncomplicated term pregnanc

77 nd under-recording of induction of labour or perinatal death in the dataset.

78 ecropsy is done in less than 60% of cases of perinatal death in the UK, despite the value of the proc

79 r coagulation (both in the Foley group); ten perinatal deaths, including two stillbirths (both in the

80 The risks of stillbirth, neonatal death, and perinatal death increased with the amount smoked by the

81 The risk of cerebral palsy, like the risk of perinatal death, is lowest in babies who are of above av

82 ldbirth Checklist, on a composite outcome of perinatal death, maternal death, or maternal severe comp

83 l pregnancies and their outcome (live birth, perinatal death, miscarriage or termination) among women

84 ing policy would be lower than the number of perinatal deaths (n = 189) caused by lack of prenatal ca

85 spective of treatment, increased the risk of perinatal death (odds ratio 2.9 [95% CI 1.8-4.5]).

86 function has remained elusive because of the perinatal death of RIPK1 full knockout mice.

87 ational diabetes, fetal death or stillbirth, perinatal death, or admission to neonatal intensive care

88 g risk of a mother experiencing at least one perinatal death over the study was 9.0 per 1000 women.

89 women have a significantly increased risk of perinatal death, particularly associated with prematurit

90 ted with a reduction of 3.7 (95% CI 2.2-5.2) perinatal deaths per 1000 pregnancies and 2.3 (0.9-3.7)

91 omparison, the reductions were 4.1 (2.5-5.7) perinatal deaths per 1000 pregnancies and 2.4 (0.7-4.1)

92 se IIbeta (TopIIbeta) are known to exhibit a perinatal death phenotype.

93 how how the gestational age-specific risk of perinatal death (PND) can be decomposed as the product o

94 dorsal midline brain structure formation and perinatal death, presumably by interfering with expressi

95 In addition, the incidences of perinatal death, preterm birth, and infants small for ge

96 ries) and morbidities (acute and long-term), perinatal deaths, preterm birth, and intrauterine growth

97 Stillbirth and perinatal death rates were similarly not associated with

98 Using linkage of national pregnancy and perinatal death registries, the authors performed a retr

99 he population attributable risk fraction for perinatal death related to infertility was 6.2% (3.4-9.0

100 RR = 1.22, 95% CI: 1.14, 1.30 (n = 28)), and perinatal death (sRR = 1.33, 95% CI: 1.25, 1.41 (n = 46)

101 Qualitative reports have suggested that perinatal death takes a significant emotional toll on st

102 l birth was associated with a higher rate of perinatal death than was planned in-hospital birth (3.9

103 terval [CI], 0.81 to 1.22) or in the rate of perinatal death; there was a significant reduction in th

104 5 515), the overall rate of delivery-related perinatal death was 12.9 (95% confidence interval [CI],

105 A population-based case-control study of perinatal deaths was carried out in Leicestershire Healt

106 ations between active or passive smoking and perinatal death were included in the meta-analyses.

107 Of these, 567 perinatal deaths were associated with 542 women.

108 Mice deficient in MARCKS exhibited universal perinatal death with defects in neurulation, fusion of t

109 ion with preterm delivery; 55% of the excess perinatal deaths with abruption were due to early delive

110 ce were born small and weak and succumbed to perinatal death within 12 h because of neuromuscular res