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首页> 外文期刊>Pediatrics: Official Publication of the American Academy of Pediatrics >Intestinal Transplantation for Short Gut Syndrome Attributable to Necrotizing Enterocolitis
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Intestinal Transplantation for Short Gut Syndrome Attributable to Necrotizing Enterocolitis

机译:肠道移植治疗坏死性小肠结肠炎所致的短肠综合征

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摘要

Background. Necrotizing enterocolitis (NEC) is a life-threatening condition of the neonatal age, which frequently requires surgical intervention. After extensive bowel resection, a small proportion of these patients may develop chronic short gut syndrome (SGS) and require chronic total parenteral nutrition (TPN) use. Intestinal transplantation has been performed in these patients as a life-saving option.This study reviews our experience with intestinal transplantation for SGS attributable to NEC emphasizing the mode of presentation, natural history, timing, and outcome.Methods. A retrospective chart review was performed for all pediatric patients who underwent small bowel transplantation for NEC at the University of Miami between August 1994 and March 1999.Results. Eleven transplants were performed for 10 patients with NEC (8 male and 2 female; median age: 1.75 years [range: 10 months to 10.1 years]). Procedures performed were isolated intestinal transplants ( n = 2), combined liver-intestinal transplants ( n = 6), and multivisceral transplants ( n = 3). All patients were born prematurely with median birth weight of 1.640 kg (range: 810 g to 2.730 kg). They developed NEC in the first few days of life and subsequently underwent an average of 5 surgeries per patient before transplant. Transplant was indicated for liver failure in 8 patients and recurrent central line sepsis in 2 others.At present, 6 patients are alive with an overall 1-year and 3-year actuarial survival of 60% and a median follow-up of 29 months (range: 9–46 months). Six children have been weaned off TPN after a median time of 71 days (range: 19–131) from transplantation. All survivors are at home with functional grafts.Conclusion. Intestinal transplantation provided a reasonable outcome in patients with NEC-associated SGS who had already developed life-threatening complications related to TPN. Intestinal transplantation replaced the diseased intestine and liver, enfranchised patients from TPN, and conferred improved quality of life. These patients should be actively considered for intestinal transplantation and referred to a transplant center as soon as possible.
机译:背景。坏死性小肠结肠炎(NEC)是威胁生命的新生儿年龄段,通常需要手术干预。广泛的肠切除术后,这些患者中的一小部分可能会发展为慢性短肠综合征(SGS),并需要长期使用全肠外营养(TPN)。在这些患者中进行肠移植是一种挽救生命的选择。本研究回顾了我们因NEC进行的SGS肠移植的经验,强调表现方式,自然史,时机和结局。 1994年8月至1999年3月在迈阿密大学对所有接受小肠移植NEC的儿科患者进行了回顾性图表审查。 10例NEC患者进行了11例移植(男8例,女2例;中位年龄:1.75岁[范围:10个月至10.1岁])。所执行的程序是单独的肠移植(n = 2),肝肠联合移植(n = 6)和多脏器移植(n = 3)。所有患者均早产,中位出生体重为1.640 kg(范围:810 g至2.730 kg)。他们在生命的最初几天发展出NEC,随后平均每位患者接受5例手术,然后再进行移植。移植指肝衰竭8例,中线败血症复发2例。目前有6例活着,总体1年和3年精算生存率为60%,中位随访29个月(范围:9-46个月)。移植后的中位时间为71天(范围:19-131),已经有6名儿童从TPN断奶。所有幸存者都在家中接受功能性移植。结论。对于已经发生威胁生命的与TPN相关的并发症的患者,肠移植为NEC相关SGS患者提供了合理的结果。肠移植取代了患病的肠和肝,使TPN的患者享有权利,并改善了生活质量。这些患者应积极考虑进行肠移植,并尽快转诊至移植中心。
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