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DOI 10.1016/j.jpedsurg.2008.03.028

Медицинская библиотека · Journal of pediatric surgery · 2008

Intestinal transplantation for total intestinal aganglionosis: a series of 12 consecutive children.

Sauvat Frederique, Grimaldi Chiara, Lacaille Florence, Ruemmele Franck, Dupic Laurent, Bourdaud Nathalie, Fusaro Fabio, Colomb Virginie, Jan Dominique, Cezard Jean-Pierre, Aigrain Yves, Revillon Yann, Goulet Olivier

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Аннотация

BACKGROUND

Management of patients with total intestinal aganglionosis (TIA) is a medical challenge because of their dependency on parenteral nutrition (PN). Intestinal transplantation (ITx) represents the only alternative treatment for patients with irreversible intestinal failure for achieving intestinal autonomy.

METHODS

Among 66 patients who underwent ITx in our center, 12 had TIA. They received either isolated ITx (n = 4) or liver-ITx (LITx, n = 8) after 10 to 144 months of total PN. All grafts included the right colon.

RESULTS

After a median follow-up of 57 months, the survival rate was 62.5% in the LITx group and 100% in the ITx patients. The graft survival rate was 62.5% in the LITx group and 75% in the ITx group. All the surviving patients were fully weaned from total PN, after a median of 57 days. Pull through of the colon allograft was carried out in all patients. Fecal continence is normal in all but one of the surviving children.

CONCLUSION

These results suggest that ITx with colon grafting should be the preferred therapeutic option in TIA. Early referral to a transplantation center after diagnosis of TIA is critical to prevent PN-related cirrhosis and thereby to permit ITx, which is associated with a good survival rate.

Для цитирования: Sauvat Frederique, Grimaldi Chiara, Lacaille Florence, Ruemmele Franck, Dupic Laurent, Bourdaud Nathalie, Fusaro Fabio, Colomb Virginie, Jan Dominique, Cezard Jean-Pierre, Aigrain Yves, Revillon Yann, Goulet Olivier. Intestinal transplantation for total intestinal aganglionosis: a series of 12 consecutive children.. Journal of pediatric surgery. 2008. DOI: 10.1016/j.jpedsurg.2008.03.028.

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