{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,8]],"date-time":"2026-10-08T21:32:00Z","timestamp":1791495120162,"version":"4.3.4"},"reference-count":28,"publisher":"Wiley","issue":"8","license":[{"start":{"date-parts":[[2015,9,5]],"date-time":"2015-09-05T00:00:00Z","timestamp":1441411200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"Forschungsunterst\u00fctzungskreis Kindernephrologie e.V."}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatric Transplantation"],"published-print":{"date-parts":[[2015,12]]},"abstract":"Abstract<\/jats:title>CLKT<\/jats:styled-content> and sequential KALT<\/jats:styled-content> are decided on a case\u2010by\u2010case basis in children for special indications such as ARPKD<\/jats:styled-content> or PH<\/jats:styled-content>1. We report on 21 children who underwent CLKT<\/jats:styled-content> or KALT<\/jats:styled-content> at our hospital between 1998 and 2013. Eleven children were diagnosed with PH<\/jats:styled-content>1 and six with ARPKD<\/jats:styled-content>. Other diagnosis were Joubert syndrome (n\u00a0=\u00a01), nephronophthisis (n\u00a0=\u00a01), CF (n\u00a0=\u00a01), and hepatocellular carcinoma (n\u00a0=\u00a01). Children (12 males, nine females) were aged 7.8\u00a0\u00b1\u00a06.2\u00a0yr (range, 10\u00a0months to 18\u00a0yr) at time of transplantation. Average wait time was 1.9\u00a0\u00b1\u00a00.9\u00a0yr (range, four\u00a0months to 2.3\u00a0yr). Fifteen patients received dialysis prior to transplantation. In PH<\/jats:styled-content>1 patients, four children received CLKT<\/jats:styled-content>, five received KALT<\/jats:styled-content>, and two infants have received only an LTx, whereas all six patients with ARPKD<\/jats:styled-content> received CLKT<\/jats:styled-content>. In patients with other indications, CLKT<\/jats:styled-content> was performed in three cases and KALT<\/jats:styled-content> in one girl. Cumulative 10\u2010yr 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<\/jats:styled-content> and KALT<\/jats:styled-content> can be performed in children with good surgical outcomes and long\u2010term survival.<\/jats:p>","DOI":"10.1111\/petr.12595","type":"journal-article","created":{"date-parts":[[2015,9,5]],"date-time":"2015-09-05T09:40:12Z","timestamp":1441446012000},"page":"858-865","source":"Crossref","is-referenced-by-count":39,"title":["Combined liver and kidney transplantation and kidney after liver transplantation in children: Indication, postoperative outcome, and long\u2010term results"],"prefix":"10.1111","volume":"19","author":[{"given":"Rainer","family":"B\u00fcscher","sequence":"first","affiliation":[{"name":"Department of Pediatrics II University Hospital Essen Essen Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anja K.","family":"B\u00fcscher","sequence":"additional","affiliation":[{"name":"Department of Pediatrics II University Hospital Essen Essen 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