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Observational study of cytomegalovirus from breast milk and necrotising enterocolitis

机译:从母乳和坏死性肠结肠炎的缩细胞病毒的观察研究

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To evaluate the relationship between cytomegalovirus (CMV) exposure from breast milk and risk of necrotising enterocolitis (NEC).Secondary analysis of a multicentre, observational cohort study. Maternal breast milk and infant serum or urine were serially evaluated by nucleic acid testing at scheduled intervals for CMV. Infants with evidence of congenital infection were excluded. Competing-risks Cox models, with adjustment for confounders, were used to evaluate the relationship between breast milk CMV exposure or postnatal CMV infection and NEC.Three neonatal intensive care units in Atlanta, Georgia.Infants with a birth weight≤1500 grams.Maximal CMV viral load in breast milk in the first 14 days after birth or postnatal CMV infection. Two different approaches were used to assess the timing of onset of CMV infection (midpoint or early).NEC, defined as Bell stage II or greater.Among 596 enrolled infants, 457 (77%) were born to CMV seropositive mothers and 33 developed postnatal CMV infection (cumulative incidence 7.3%, 95%?CI 5.0% to 10.1%). The incidence of NEC was 18% (6/33) among infants with CMV infection, compared with 7% (37/563) among infants without infection (adjusted cause-specific HR (CSHR): 2.81; 95%?CI 0.73 to 10.9 (midpoint); 6.02; 95%?CI 1.28 to 28.4 (early)). Exposure to higher breast milk CMV viral load was associated with a higher risk of NEC (adjusted CSHR per twofold increase 1.28; 95%?CI 1.06 to 1.54).CMV exposure from breast milk may be associated with the development of NEC in very low birth weight infants.
机译:评价患有母乳(CMV)暴露于母乳(CMV)暴露的关系,并进行病症内切肠炎(NEC)的风险。对多期一年,观察队列研究的认识性分析。母母乳和婴儿血清或尿液被CMV的预定间隔进行核酸测试。具有先天性感染证据的婴儿被排除在外。竞争风险的Cox模型,用于调整混淆,用于评估母乳CMV暴露或后期CMV感染和NEC.Three新生儿重症监护单位的关系,Georgia。出生体重≤1500克的那些.Aximal CMV在出生或产后CMV感染后的前14天在母乳中的病毒载荷。使用两种不同的方法来评估CMV感染(中点或早期)的时序。正在定义为贝尔阶段II或更大的巢级婴儿,457(77%)均出生于CMV血清阳性母亲和33次出版的后期CMV感染(累积发病率7.3%,95%?CI 5.0%至10.1%)。 NEC的发生率为CMV感染的婴儿18%(6/33),而没有感染的婴儿(37/563),而没有感染(调整原因特异性人力资源(CSHR):2.81; 95%?CI 0.73至10.9 (中点); 6.02; 95%?CI 1.28至28.4(早))。暴露于较高的母乳CMV病毒载荷与NEC的风险较高相关(每双重调整的CSHR增加1.28; 95%?CI 1.06至1.54)。母乳暴露可能与NEC的发育非常低的出生时重量婴儿。

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