ライフサイエンスコーパス: multiple birth

1 ivation, birthweight, maternal age, sex, and multiple birth.

2 dicator of higher embryo quality) on risk of multiple birth.

3 , maternal education, sex of the infant, and multiple births.

4 an intention-to-treat basis, accounting for multiple births.

5 erved elevated NTD risk was mediated through multiple births.

6 comes that are known to be more prevalent in multiple births.

7 with an aim toward reducing the incidence of multiple births.

8 iated with a substantial rise in the rate of multiple births.

9 s of twin births and triplet or higher-order multiple births.

10 ears), non-European American, or products of multiple births.

11 increase in the risk of low birth weight in multiple births.

12 other's age, method of delivery, parity, and multiple births.

13 Multiple births account for an increasing percentage of

14 rexia nervosa was independently predicted by multiple birth (adjusted hazard ratio = 1.33, 95% confid

15 We derived the rates of multiple births after natural conception from data on di

16 proposed as a strategy to reduce the risk of multiple birth and adverse pregnancy outcomes after in-v

17 tion, are associated with increased risks of multiple birth and concomitant sequelae and adverse outc

18 ficantly longer with birthweight 2.0-2.5 kg, multiple birth and increasing maternal age.

19 With the exception of monozygotic multiple birth and maternal hypertensive disorder, early

20 ogistic, or quantile regression adjusted for multiple birth and socioeconomic risk.

21 We identified an association between multiple births and early menopause, which connects even

22 Subgroup analyses for multiple births and preterm infants showed some differen

23 bryo transfer in the United States to reduce multiple births and related birth complications may be a

24 Women who had multiple births and their babies were excluded.

25 antenatal corticosteroids, whether single or multiple birth, and birth weight.

26 uded cesarean-section delivery, birthweight, multiple birth, and infant survival status.

27 Gestational age at birth, birth order, multiple birth, and parental age were not associated wit

28 Prenatal smoking exposure, being part of a multiple birth, and prematurity were not associated with

29 ncy diabetes mellitus, preterm preeclampsia, multiple birth, and termination of pregnancy.

30 Cesarean deliveries, multiple births, and births at less than 36 weeks' gesta

31 the youngest and oldest maternal age bands, multiple births, and deprivation (Index of Multiple Depr

32 t delivery, small for gestational age [SGA], multiple births, and male sex).

33 factors, in addition to GA at delivery, SGA, multiple births, and male sex.

34 s died, those with congenital abnormalities, multiple births, and mother and infant pairs who migrate

35 ity, household income, sex, gestational age, multiple births, and small for gestational age.

36 -binomial regression adjusted for race, sex, multiple birth, any maternal pregnancy risk factors (as

37 1.93), were primiparous (aOR = 2.03), had a multiple birth (aOR = 3.5), diabetes (aOR = 1.47), or ch

38 d their own estimate of the proportion of US multiple births attributable to non-ART ovulation stimul

39 ds that controlled for observed factors (eg, multiple birth, birth order, and parental sociodemograph

40 clinical and economic burden associated with multiple births can be prevented through single-embryo t

41 cle draws on official criminal histories for multiple birth cohorts spanning a 17-y difference in bir

42 lculations in consortia studies that include multiple birth cohorts.

43 crease in the age of asthma diagnosis across multiple birth cohorts.

44 lance data, they estimated proportions of US multiple births conceived naturally and by ART and assum

45 tion, history of CS, higher maternal age and multiple birth, consideration may be given to more conse

46 Almost 15% of inpatient costs for multiple births could have been avoided if ART twins and

47 as oral clefts, and individual patients with multiple birth defects (including clefts) have been show

48 rs in about 1 in 6000 live births and causes multiple birth defects in affected infants.

49 s are autosomal dominant disorders featuring multiple birth defects including ear, renal and branchia

50 ominant congenital disorder characterized by multiple birth defects including heart defects and myelo

51 Zika virus (ZIKV) is a flavivirus linked to multiple birth defects including microcephaly, known as

52 s an autosomal dominant disorder that causes multiple birth defects including renal, ear, anal and li

53 Hug mutants exhibit multiple birth defects typical of ciliopathies, includin

54 ion or activation of Shh signalling leads to multiple birth defects, including holoprosencephaly, neu

55 e it is associated with an increased risk of multiple birth defects, the effect of paternal MTX expos

56 ated SMO and increased Hh signaling, causing multiple birth defects.

57 The risk of perinatal death associated with multiple births did not explain this finding.

58 The unprecedented increase in multiple births during the past 3 decades is a major pub

59 account for statistical dependence owing to multiple births during the study period.

60 d by (in order of statistical significance): multiple birth; eclampsia/pre-eclampsia; maternal age 40

61 h (2.7 [1.5-4.7]); the risks associated with multiple births explained some, but not all, of this exc

62 fter adjusting for parental age at delivery, multiple births, fetal sex, obstetric comorbidities, and

63 al number of 9873 live births were reported (multiple births from 1 pregnancy were counted as 1 live

64 Based on these data, the risk of multiple births from IVF varies by maternal age and numb

65 at birth, postmenstrual age at scan, sex, or multiple birth in these populations.

66 tments has led to an increase in the rate of multiple births in the United States.

67 t adjusted for GA, small-for-GA status, sex, multiple birth, inborn status, antenatal steroid use, an

68 Compared with singletons, multiple-birth infants consume significantly more hospit

69 odevelopmental impairment or mortality among multiple-birth infants of mothers with diabetes (aRR = 1

70 A total of 6925 multiple-birth infants were studied; 5775 of 6925 (83.4%

71 ave low or very low birthweight or be from a multiple birth; infants with repeat specimens were less

72 maternal factors (age, parity, singleton vs multiple birth, insurance, and race) and neighborhood fa

73 with the polycystic ovary syndrome, although multiple birth is a complication.

74 While the above-mentioned increase in multiple births is well documented, the impact on the tw

75 Cesarean delivery, primiparity, multiple births, low birth weight, and prematurity were

76 We compared rates of livebirth, multiple births, low birthweight (<2.5 kg), preterm birt

77 g children with none/low maternal education, multiple births, low birthweight, short birth interval,

78 In Bangladesh, multiple birth measurements alone or in combination, par

79 eable to one or two ancestral proteins: "the multiple birth model" for the evolution of protein seque

80 nd higher S seroprevalences were observed in multiple births (odds ratio [OR], 0.84; 95% CI, 0.75-0.9

81 depression within 24 months before delivery, multiple births or stillbirth, or a diagnosis of breast

82 te 30.0/1,000) compared to 9,640 children of multiple births out of a total of 386,637 births in West

83 at diagnosis, birth weight, singleton versus multiple birth, parity, parental age, type of assisted c

84 the ART-NTD association was explained by the multiple-births pathway.

85 -reassuring fetal status, obstructed labour, multiple birth, placental weight >= 600 g, eclampsia/pre

86 a/abruptio placenta/ante-partum haemorrhage; multiple birth; pre-delivery LoS >= 3 days; placental we

87 conception and autism diagnosis mediated by multiple birth pregnancy and related birth complications

88 Multiple birth, preterm birth, and cesarean delivery joi

89 dds ratios and absolute risk differences for multiple birth, preterm birth, and low birthweight were

90 intensive use in 1981 and 1995 were having a multiple birth, primiparity, being married, and maternal

91 small for gestational age, mode of delivery, multiple birth, prolonged rupture of membranes, and cent

92 tion, small for GA status, mode of delivery, multiple birth, prolonged rupture of membranes, year of

93 6 eyes developing SROP, BW, gestational age, multiple births, race, per capita income in the mother's

94 cycles, ICSI use was associated with a lower multiple birth rate compared with conventional IVF (30.9

95 Among women aged 35 to 39 years, the multiple-birth rate was 29.4% if 3 embryos were transfer

96 Among women 40 to 44 years of age, the multiple-birth rate was less than 25% even if 5 embryos

97 through 2011 were used to determine national multiple birth rates, and data on in vitro fertilization

98 Live-birth and multiple-birth rates (percentage of live births that wer

99 ART use worldwide and persistently high ART multiple-birth rates in several countries highlight the

100 Multiple-birth rates increased as high as 45.7% for wome

101 Live-birth and multiple-birth rates may vary by patient age and embryo

102 Multiple-birth rates varied by age and the number of emb

103 With 2 embryos transferred, multiple-birth rates were 22.7%, 19.7%, 11.6%, and 10.8%

104 Embryo quality was not related to multiple birth risk but was associated with increased li

105 plied a fetal survival factor, and used this multiple-birth risk estimate and their own estimate of t

106 transferring more than two embryos increased multiple-birth risk, with no corresponding increase in t

107 Greater maternal age did not decrease multiple-birth risk.

108 fer multiple embryos, but this increases the multiple-birth risk.

109 = 1.54; 95% CI: 0.95, 2.49), and monozygotic multiple birth (RR = 1.94; 95% CI: 1.26, 2.99).

110 , comorbidities, parity, whether there was a multiple birth, socioeconomic deprivation, and the prese

111 h weight, gestational age, maternal age, and multiple birth status.

112 luding by gestational age, type of delivery, multiple birth, study year, and perinatal mortality.

113 re used to estimate the annual proportion of multiple births that were attributable to IVF and to non

114 Among multiple births, the prevalence of rectal and large inte

115 ertility by 1) increasing the probability of multiple births through the transfer of multiple embryos

116 nal age is associated with decreased risk of multiple birth; using donor eggs from younger women may

117 Being part of a multiple birth was strongly associated with early menopa

118 Women having a multiple birth were much more likely to have had intensi

119 Rates of multiple birth were related to number of embryos transfe

120 ment, preterm birth, perinatal asphyxia, and multiple births were associated with an increased risk o

121 Trends in multiple births were examined starting from 1998, the ye

122 eonate deaths, stillbirths, and higher order multiple births were excluded from analysis.

123 Multiple birth, which is associated with adverse fetal,

124 ncreased occurrence of both miscarriages and multiple births, which has resulted in a great deal of c

125 sociation is mediated through the pathway of multiple births, while the ART-NTD association was expla

126 Since 1981, the percentage of women with multiple births who received intensive prenatal care (de