{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,11]],"date-time":"2026-06-11T04:57:25Z","timestamp":1781153845658,"version":"3.54.1"},"reference-count":26,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2026,4,2]],"date-time":"2026-04-02T00:00:00Z","timestamp":1775088000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,4,2]],"date-time":"2026-04-02T00:00:00Z","timestamp":1775088000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["J Paediatrics Child Health"],"published-print":{"date-parts":[[2026,6]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Rationale<\/jats:title>\n                    <jats:p>Cystic fibrosis (CF) is characterised by chronic inflammation and malnutrition, significantly affecting disease progression and prognosis. The haemoglobin\u2010albumin\u2010lymphocyte\u2010platelet (HALP) score reflects inflammatory and nutritional status, and has prognostic associations in various chronic diseases; its role in paediatric CF is unclear.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>\n                      To evaluate the association between HALP measured during clinical stability and (i) baseline disease severity at the index assessment (FEV\n                      <jats:sub>1<\/jats:sub>\n                      , MSKS, and BMI z\u2010score), and (ii) subsequent 12\u2010month outcomes (hospitalisation\u2010requiring pulmonary exacerbations, PICU admission, and mortality) in children with CF.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Retrospective single\u2010centre cohort study of 152 children with CF aged 2\u201318\u2009years. HALP was calculated at clinical stability. Associations with index severity and 12\u2010month outcomes were analysed; logistic regression for low FEV\n                      <jats:sub>1<\/jats:sub>\n                      was restricted to participants with acceptable spirometry.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Lower HALP was associated with low FEV\n                      <jats:sub>1<\/jats:sub>\n                      (&lt;\u200970% predicted) at the index assessment (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u20090.001) and with a higher 12\u2010month burden of hospitalisation \u2010requiring pulmonary exacerbations (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u20090.001). PICU admission and mortality were infrequent and analysed exploratorily; HALP was lower in these groups (PICU\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u20090.001; mortality\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.004). In adjusted logistic regression among participants with spirometry (\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u2009101), HALP remained associated with low FEV\n                      <jats:sub>1<\/jats:sub>\n                      , although the effect size was modest and precision limited (adjusted OR 0.886, 95% CI 0.788\u20130.996;\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.043).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>HALP, reflecting nutritional and inflammatory status, may offer prognostic information in paediatric\u00a0CF.\u00a0Calculation from routine blood tests could make it a practical tool for identifying higher\u2010risk individuals and informing\u00a0clinical decision\u2010making. Further large\u2010scale studies are needed to validate its clinical utility in CF management.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/jpc.70382","type":"journal-article","created":{"date-parts":[[2026,4,3]],"date-time":"2026-04-03T04:15:30Z","timestamp":1775189730000},"page":"989-997","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Can the\n                    <scp>HALP<\/scp>\n                    Score Be Used as a Prognostic Marker in Paediatric Patients With Cystic Fibrosis?"],"prefix":"10.1111","volume":"62","author":[{"ORCID":"https:\/\/orcid.org\/0009-0004-7828-7504","authenticated-orcid":false,"given":"K\u00fcbra","family":"\u00d6zkaya","sequence":"first","affiliation":[{"name":"Department of Pediatric Pulmonology Ege University Faculty of Medicine  Izmir 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