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首页> 外文期刊>Pediatrics: Official Publication of the American Academy of Pediatrics >Very Low Birth Weight Preterm Infants With Surgical Short Bowel Syndrome: Incidence, Morbidity and Mortality, and Growth Outcomes at 18 to 22 Months
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Very Low Birth Weight Preterm Infants With Surgical Short Bowel Syndrome: Incidence, Morbidity and Mortality, and Growth Outcomes at 18 to 22 Months

机译:外科短肠综合征的极低出生体重早产儿:18至22个月的发病率,发病率和死亡率以及生长结局

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OBJECTIVES. The objective of this study was to determine the (1) incidence of short bowel syndrome in very low birth weight (1500 g) infants, (2) associated morbidity and mortality during initial hospitalization, and (3) impact on short-term growth and nutrition in extremely low birth weight (1000 g) infants.METHODS. Infants who were born from January 1, 2002, through June 30, 2005, and enrolled in the National Institute of Child Health and Human Development Neonatal Research Network were studied. Risk factors for developing short bowel syndrome as a result of partial bowel resection (surgical short bowel syndrome) and outcomes were evaluated for all neonates until hospital discharge, death, or 120 days. Extremely low birth weight survivors were further evaluated at 18 to 22 months' corrected age for feeding methods and growth.RESULTS. The incidence of surgical short bowel syndrome in this cohort of 12316 very low birth weight infants was 0.7%. Necrotizing enterocolitis was the most common diagnosis associated with surgical short bowel syndrome. More very low birth weight infants with short bowel syndrome (20%) died during initial hospitalization than those without necrotizing enterocolitis or short bowel syndrome (12%) but fewer than the infants with surgical necrotizing enterocolitis without short bowel syndrome (53%). Among 5657 extremely low birth weight infants, the incidence of surgical short bowel syndrome was 1.1%. At 18 to 22 months, extremely low birth weight infants with short bowel syndrome were more likely to still require tube feeding (33%) and to have been rehospitalized (79%). Moreover, these infants had growth delay with shorter lengths and smaller head circumferences than infants without necrotizing enterocolitis or short bowel syndrome.CONCLUSIONS. Short bowel syndrome is rare in neonates but has a high mortality rate. At 18 to 22 months' corrected age, extremely low birth weight infants with short bowel syndrome were more likely to have growth failure than infants without short bowel syndrome.
机译:目标这项研究的目的是确定(1)出生体重极低(<1500 g)的婴儿中短肠综合征的发生率,(2)初始住院期间的相关发病率和死亡率,以及(3)对短期生长的影响和极低出生体重(<1000 g)婴儿的营养。研究对象为2002年1月1日至2005年6月30日出生并加入美国国家儿童健康与人类发展研究所新生儿研究网络的婴儿。对所有新生儿评估因部分肠切除术(手术短肠综合征)而发展为短肠综合征的危险因素,直至出院,死亡或120天。在18至22个月的校正年龄下进一步评估了极低出生体重的幸存者的喂养方法和生长情况。该队列中的12316名极低出生体重婴儿的手术短肠综合征的发生率为0.7%。坏死性小肠结肠炎是与手术短肠综合征相关的最常见诊断。与没有坏死性小肠结肠炎或短肠综合征的婴儿相比,初诊期间死亡的极低出生体重的婴儿(20%)多于没有坏死性小肠结肠炎或小肠综合征的婴儿(12%),但比没有手术的坏死性小肠结肠炎婴儿(53%)少。在5657名极低出生体重的婴儿中,手术性短肠综合征的发生率为1.1%。在18到22个月时,患有短肠综合征的极低出生体重婴儿更可能需要管饲(33%)和再次住院(79%)。此外,这些婴儿比没有坏死小肠结肠炎或短肠综合症的婴儿具有更长的长度和更短的头围的生长延迟。结论。短肠综合征在新生儿中很少见,但死亡率很高。在矫正年龄为18至22个月时,患有短肠综合征的极低出生体重婴儿比没有短肠综合征的婴儿更有可能出现生长衰竭。

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