{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,15]],"date-time":"2026-08-15T12:27:00Z","timestamp":1786796820931,"version":"build-2736575974"},"reference-count":46,"publisher":"SAGE Publications","license":[{"start":{"date-parts":[[2026,8,12]],"date-time":"2026-08-12T00:00:00Z","timestamp":1786492800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["The Cleft Palate Craniofacial Journal"],"abstract":"<jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To characterize the prevalence, spectrum, and healthcare burden of endocrine disorders across distinct orofacial cleft (OFC) phenotypes and to evaluate the impact of endocrine comorbidity on healthcare utilization and hospital outcomes.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Design<\/jats:title>\n                    <jats:p>Retrospective cross-sectional analysis of nationally representative inpatient data.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Setting<\/jats:title>\n                    <jats:p>United States hospitals included in the Kids\u2019 Inpatient Database (KID) for 2016, 2019, and 2022.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Participants<\/jats:title>\n                    <jats:p>Pediatric hospitalizations identified in the KID. Admissions involving isolated cleft were identified using ICD-10-CM codes and stratified by syndromic status.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Interventions<\/jats:title>\n                    <jats:p>None.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Main Outcome Measures<\/jats:title>\n                    <jats:p>The primary outcome was the presence of endocrine disorders (including hypothalamic, pituitary, thyroid, parathyroid, adrenal, metabolic, nutritional, and growth abnormalities). Secondary outcomes included length of stay (LOS), total hospital charges, and in-hospital mortality.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      A total of 41\u2005771 OFC hospitalizations were identified (5006: cleft Lip\u2014CL, 18\u2005109: cleft palate\u2014CP, and 18\u2005536: cleft lip and palate). Endocrine disorders were more common among children with OFCs than among noncleft controls (8.3% vs 6.0%,\n                      <jats:italic toggle=\"yes\">p<\/jats:italic>\n                      \u2009&lt;\u2009.001). Disease burden varied significantly across cleft phenotypes, with CP conferring the highest odds of any endocrine disorder (adjusted odds ratio: 2.68,\n                      <jats:italic toggle=\"yes\">p<\/jats:italic>\n                      \u2009&lt;\u2009.001). Hypothalamic\u2013pituitary disorders showed strong associations with all cleft phenotypes (all\n                      <jats:italic toggle=\"yes\">p<\/jats:italic>\n                      \u2009&lt;\u2009.001). Most associations persisted among patients without recognized syndromic diagnoses. Among children with OFCs, endocrine comorbidity was independently associated with a 131% increase in LOS, a 116% increase in total charges, and a 43% increase in in-hospital mortality (all\n                      <jats:italic toggle=\"yes\">p<\/jats:italic>\n                      \u2009\u2264\u2009.003).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>Despite substantial heterogeneity across cleft types, endocrine dysfunction may be a clinically significant but underrecognized comorbidity in children with OFCs and is associated with increased healthcare utilization, even among nonsyndromic patients.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1177\/10556656261477559","type":"journal-article","created":{"date-parts":[[2026,8,12]],"date-time":"2026-08-12T17:57:56Z","timestamp":1786557476000},"update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":0,"title":["Increased Endocrine Dysfunction in Children With Cleft Lip and Palate: A National Analysis of Pediatric Hospitalizations"],"prefix":"10.1177","author":[{"ORCID":"https:\/\/orcid.org\/0009-0002-8649-2079","authenticated-orcid":false,"given":"Kaan T.","family":"Oral","sequence":"first","affiliation":[{"name":"Icahn School of Medicine at Mount Sinai"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Martha M.","family":"MacDonald","sequence":"additional","affiliation":[{"name":"Icahn School of Medicine at Mount Sinai"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Katherine G.","family":"Stark","sequence":"additional","affiliation":[{"name":"Icahn School of Medicine at Mount Sinai"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Richard A.","family":"Hausman","sequence":"additional","affiliation":[{"name":"Icahn School of Medicine at Mount Sinai"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sheuli","family":"Chowdhury","sequence":"additional","affiliation":[{"name":"Icahn School of Medicine at Mount Sinai"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Peter W.","family":"Henderson","sequence":"additional","affiliation":[{"name":"Icahn School of Medicine at Mount Sinai"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Peter J.","family":"Taub","sequence":"additional","affiliation":[{"name":"Icahn School of Medicine at Mount Sinai"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2026,8,12]]},"reference":[{"key":"e_1_3_2_2_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.adnc.2004.12.006"},{"key":"e_1_3_2_3_2","doi-asserted-by":"publisher","DOI":"10.3390\/children9050757"},{"key":"e_1_3_2_4_2","doi-asserted-by":"publisher","DOI":"10.1097\/SCS.0b013e31822e5e4d"},{"key":"e_1_3_2_5_2","doi-asserted-by":"publisher","DOI":"10.1038\/nrg2933"},{"key":"e_1_3_2_6_2","doi-asserted-by":"publisher","DOI":"10.3390\/genes14081603"},{"key":"e_1_3_2_7_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(09)60695-4"},{"key":"e_1_3_2_8_2","doi-asserted-by":"publisher","DOI":"10.1067\/mpd.2002.121822"},{"key":"e_1_3_2_9_2","doi-asserted-by":"publisher","unstructured":"Akin MA Kurto\u011flu S Sarici D Akin L Hatipo\u011flu N Korkmaz L G\u00fcne\u015f T \u00d6zt\u00fcrk MA Ak\u00e7aku\u015f M . 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