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Combined liver and kidney transplantation and kidney after liver transplantation in children: Indication, postoperative outcome, and long‐term results
Author(s) -
Büscher Rainer,
Büscher Anja K.,
Cetiner Metin,
Treckmann Jürgen W.,
Paul Andreas,
Vester Udo,
Hoyer Peter F.
Publication year - 2015
Publication title -
pediatric transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.457
H-Index - 69
eISSN - 1399-3046
pISSN - 1397-3142
DOI - 10.1111/petr.12595
Subject(s) - medicine , transplantation , surgery , kidney transplantation , liver transplantation , dialysis , pediatrics
CLKT and sequential KALT are decided on a case‐by‐case basis in children for special indications such as ARPKD or PH 1. We report on 21 children who underwent CLKT or KALT at our hospital between 1998 and 2013. Eleven children were diagnosed with PH 1 and six with ARPKD . Other diagnosis were Joubert syndrome (n = 1), nephronophthisis (n = 1), CF (n = 1), and hepatocellular carcinoma (n = 1). Children (12 males, nine females) were aged 7.8 ± 6.2 yr (range, 10 months to 18 yr) at time of transplantation. Average wait time was 1.9 ± 0.9 yr (range, four months to 2.3 yr). Fifteen patients received dialysis prior to transplantation. In PH 1 patients, four children received CLKT , five received KALT , and two infants have received only an LTx, whereas all six patients with ARPKD received CLKT . In patients with other indications, CLKT was performed in three cases and KALT in one girl. Cumulative 10‐yr survival of all 21 patients was 78.4%. At the time of transfer into adult care, 13 patients retained stable liver and kidney function. Regardless the underlying diagnosis, CLKT and KALT can be performed in children with good surgical outcomes and long‐term survival.