Vennarecci G, Kato T, Misiakos E P, Neto A B, Verzaro R, Pinna A, Nery J, Khan F, Thompson J F, Tzakis A G
Department of Surgery, Division of Liver and Gastrointestinal Transplantation, University of Miami School of Medicine, Miami, Florida 33136, USA.
Pediatrics. 2000 Feb;105(2):E25. doi: 10.1542/peds.105.2.e25.
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.
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.
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.
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.
坏死性小肠结肠炎(NEC)是一种危及新生儿生命的疾病,常需手术干预。在广泛肠切除术后,一小部分此类患者可能会发展为慢性短肠综合征(SGS),需要长期使用全胃肠外营养(TPN)。肠道移植已作为一种挽救生命的选择应用于这些患者。本研究回顾了我们对因NEC导致SGS行肠道移植的经验,重点关注其临床表现形式、自然病程、手术时机及预后。
对1994年8月至1999年3月在迈阿密大学因NEC接受小肠移植的所有儿科患者进行回顾性病历审查。
为10例NEC患者实施了11例移植手术(8例男性,2例女性;中位年龄:1.75岁[范围:10个月至10.1岁])。实施的手术包括单纯肠道移植(n = 2)、肝肠联合移植(n = 6)和多脏器移植(n = 3)。所有患者均为早产儿,中位出生体重为1.640 kg(范围:810 g至2.730 kg)。他们在出生后的头几天发生NEC,随后在移植前平均每位患者接受了5次手术。8例患者因肝衰竭而进行移植,另外2例因反复发生中心静脉导管败血症而进行移植。目前,6例患者存活,总体1年和3年预期生存率分别为60%,中位随访时间为29个月(范围:9 - 46个月)。6名儿童在移植后中位时间71天(范围:19 - 131天)后停用了TPN。所有存活者在家中,移植肠功能良好。
对于已出现与TPN相关的危及生命并发症的NEC相关SGS患者,肠道移植提供了合理的预后。肠道移植替代了病变的肠和肝,使患者摆脱了TPN,提高了生活质量。应积极考虑对这些患者进行肠道移植,并尽快将其转诊至移植中心。