Literature DB >> 8078012

Isolated liver transplantation for liver failure in patients with short bowel syndrome.

J P Lawrence1, S P Dunn, D F Billmire, K Falkenstein, C D Vinocur, W H Weintraub.   

Abstract

The ultimate prognosis for patients with short bowel syndrome (SBS) has become progressively more favorable over the past decade. Advances in long-term total parenteral nutrition (TPN) have allowed this group of patients to meet nutritional needs while the process of intestinal adaptation occurs. Unfortunately, a subgroup of patients with SBS have hepatic failure (HF), most often secondary to TPN-induced cholestasis. Combined small bowel and liver transplantation (LT) offers a sound anatomic solution for cases of HF with SGS, but it remains experimental at this time. We propose that an isolated LT is a viable alternative mode of therapy for the patient with HF and SBS. The following characteristics were reviewed for five patients with SBS and HF who underwent LT: age at transplantation, weight, liver function, survival, intestinal length, volume of feeding before surgery, and current feeding tolerance and liver function. Four boys and one girl, aged 5.5 to 15 months (average, 11.9), had LT. The total bilirubin level at the time of transplantation was 14.4 to 37 mg/dL (average, 24.7). The patients weighed between 3.8 and 12 kg (average, 8.0), and feeding tolerance ranged from no enteric to complete enteric feeding (average, < 33% of calories by enteric feeding). Bowel loss was attributed to necrotizing enterocolitis in two cases, volvulus in two, and birth hypoxia in one. Bowel length ranged from 60 to 120 cm (average, 88.6). Four children (80%) survived LT, and the average follow-up period was 9.3 months. Three (75%) are home; one is on combined hyperalimentation and enteral feeding, and two are on full enteric feeding. One remains in a chronic care facility, on combined enteral and intravenous feeding. The average daily enteral feeding now comprises more than 70% of caloric requirements. The total bilirubin level is .6 to .8 mg/dL (average, .71). Isolated LT for HF in the patient with SBS effectively restores liver function, allowing time for further intestinal adaptation.

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Year:  1994        PMID: 8078012     DOI: 10.1016/0022-3468(94)90361-1

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  6 in total

Review 1.  Hepatobiliary abnormalities and parenteral nutrition.

Authors:  B S Tomar
Journal:  Indian J Pediatr       Date:  2000-09       Impact factor: 1.967

2.  Isolated liver transplantation in infants with end-stage liver disease associated with short bowel syndrome.

Authors:  Simon P Horslen; Debra L Sudan; Kishore R Iyer; Stuart S Kaufman; Angie K Iverson; Ira J Fox; Byers W Shaw; Alan N Langnas
Journal:  Ann Surg       Date:  2002-03       Impact factor: 12.969

3.  Effect of a valine-rich diet on a rat model of short bowel syndrome.

Authors:  Narito Takada; Keiko Ogita; Tomoaki Taguchi; Kouji Masumoto; Sachiyo Suita
Journal:  Pediatr Surg Int       Date:  2005-11       Impact factor: 1.827

Review 4.  The concept of gut rehabilitation and the future of visceral transplantation.

Authors:  Kareem Abu-Elmagd
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2015-01-20       Impact factor: 46.802

5.  Surgical approach to short-bowel syndrome. Experience in a population of 160 patients.

Authors:  J S Thompson; A N Langnas; L W Pinch; S Kaufman; E M Quigley; J A Vanderhoof
Journal:  Ann Surg       Date:  1995-10       Impact factor: 12.969

6.  Isolated liver transplantation for treatment of liver failure secondary to intestinal failure.

Authors:  Maria Immacolata Spagnuolo; Eliana Ruberto; Alfredo Guarino
Journal:  Ital J Pediatr       Date:  2009-09-15       Impact factor: 2.638

  6 in total

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