{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,7,30]],"date-time":"2025-07-30T12:43:31Z","timestamp":1753879411593,"version":"3.41.2"},"reference-count":19,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2022,11,17]],"date-time":"2022-11-17T00:00:00Z","timestamp":1668643200000},"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":["Pediatric Transplantation"],"published-print":{"date-parts":[[2023,3]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Pediatric heart transplant recipients are at risk for complications from prolonged exposure to immunosuppressive drugs, pharmacokinetic challenges in maintaining consistent immunosuppression, and medication non\u2010adherence. Basiliximab (BAS), an interleukin\u20102 receptor antagonist, is used for induction therapy across many pediatric heart transplant centers, but use as maintenance immunosuppression has not been well described.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>This was a retrospective, single pediatric center cohort study of heart transplant recipients who received BAS for maintenance immunosuppression (defined as &gt;2 monthly doses) from January 1, 2011, to December 31, 2021.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Ten patients met study criteria with a median age of 17.5 (5\u201322)\u00a0years and median 9.6 (1.2\u201318.9)\u00a0years since transplant at time of BAS initiation. The primary indications for BAS use were recurrent rejection (<jats:italic>n<\/jats:italic>\u00a0=\u00a04), fluctuating immunosuppression levels (<jats:italic>n<\/jats:italic>\u00a0=\u00a03), and renal dysfunction (<jats:italic>n<\/jats:italic>\u00a0=\u00a03). A median of 5.5 (3\u201332) monthly BAS doses were received. Three patients had a rejection event while on BAS. Calcineurin inhibitor exposure was reduced in 70% of patients. Three of the 10 patients were alive at last follow\u2010up. There was one documented infection during BAS use, and no hypersensitivity reactions.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>Monthly BAS infusions were well tolerated and allowed for reduced calcineurin inhibitor exposure in most patients. Mortality commonly occurred despite BAS use, potentially reflecting the acuity of this patient cohort. BAS can be considered for maintenance immunosuppression in pediatric patients with fluctuating immunosuppressive levels and\/or renal dysfunction. More studies are needed to determine long\u2010term outcomes and explore expanded use of BAS in the pediatric heart transplant population.<\/jats:p><\/jats:sec>","DOI":"10.1111\/petr.14438","type":"journal-article","created":{"date-parts":[[2022,11,18]],"date-time":"2022-11-18T05:23:40Z","timestamp":1668749020000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Basiliximab as maintenance immunosuppression in heart transplant recipients: A single pediatric center experience"],"prefix":"10.1111","volume":"27","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3449-5828","authenticated-orcid":false,"given":"Teaghan T.","family":"Chen","sequence":"first","affiliation":[{"name":"Children's Hospital Colorado  Aurora Colorado USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Megan M.","family":"Greene","sequence":"additional","affiliation":[{"name":"Children's Hospital Colorado  Aurora Colorado USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4117-2282","authenticated-orcid":false,"given":"Melanie D.","family":"Everitt","sequence":"additional","affiliation":[{"name":"Section of Cardiology, Department of Pediatrics University of Colorado School of Medicine  Aurora Colorado USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-6303-1264","authenticated-orcid":false,"given":"Kathleen E.","family":"Simpson","sequence":"additional","affiliation":[{"name":"Section of Cardiology, Department of Pediatrics University of Colorado School of Medicine  Aurora Colorado USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2022,11,17]]},"reference":[{"key":"e_1_2_9_2_1","doi-asserted-by":"publisher","DOI":"10.1161\/01.CIR.0000149745.83186.89"},{"key":"e_1_2_9_3_1","doi-asserted-by":"publisher","DOI":"10.1097\/00001573-200403000-00006"},{"key":"e_1_2_9_4_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.healun.2013.03.008"},{"key":"e_1_2_9_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.transproceed.2008.07.113"},{"volume-title":"Basiliximab. 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