{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,17]],"date-time":"2026-09-17T04:53:56Z","timestamp":1789620836922,"version":"build-2803163510"},"reference-count":15,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2019,7,26]],"date-time":"2019-07-26T00:00:00Z","timestamp":1564099200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Br J Haematol"],"published-print":{"date-parts":[[2019,12]]},"abstract":"<jats:title>Summary<\/jats:title><jats:p>The prognosis of sickle cell disease (SCD) patients who need dialysis is poor, but experience with kidney transplantation is limited. This study assessed the characteristics of 36 SCD patients undergoing renal transplantation. Immediate post\u2010surgical complications occurred in 25% of cases. Cytomegalovirus and bacterial infections were frequently observed. Twelve patients died after a median follow\u2010up period of 17\u00b74\u00a0months. Overall patient survival was significantly lower in SCD than in the control group without significant difference for overall death\u2010censored graft survival. Our data suggest that renal transplantation should be systematically considered in SCD patients with end\u2010stage renal disease.<\/jats:p>","DOI":"10.1111\/bjh.16113","type":"journal-article","created":{"date-parts":[[2019,7,26]],"date-time":"2019-07-26T13:24:59Z","timestamp":1564147499000},"page":"676-680","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":19,"title":["Survival and specific outcome of sickle cell disease patients after renal transplantation"],"prefix":"10.1111","volume":"187","author":[{"given":"Christel","family":"G\u00e9rardin","sequence":"first","affiliation":[{"name":"AP\u2010HP (Assistance Publique\u2010H\u00f4pitaux de Paris), Department of Nephrology and Transplantation Rare French Disease Centre \u201cIdiopathic Nephrotic syndrome\u201d, Henri\u2010Mondor\/Albert\u2010Chenevier Hospital Cr\u00e9teil France"},{"name":"Inserm U955, Team 21, DHU VIC Paris\u2010Est University Cr\u00e9teil France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-6015-3979","authenticated-orcid":false,"given":"Anissa","family":"Moktefi","sequence":"additional","affiliation":[{"name":"Inserm U955, Team 21, DHU VIC Paris\u2010Est University Cr\u00e9teil France"},{"name":"AP\u2010HP, Department of Pathology Henri\u2010Mondor\/Albert\u2010Chenevier Hospital Cr\u00e9teil France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C\u00e9cile","family":"Couchoud","sequence":"additional","affiliation":[{"name":"REIN registry. 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