{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,2]],"date-time":"2026-07-02T09:11:54Z","timestamp":1782983514383,"version":"3.54.5"},"reference-count":33,"publisher":"Elsevier BV","issue":"2","license":[{"start":{"date-parts":[[2018,3,1]],"date-time":"2018-03-01T00:00:00Z","timestamp":1519862400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2020,3,1]],"date-time":"2020-03-01T00:00:00Z","timestamp":1583020800000},"content-version":"vor","delay-in-days":731,"URL":"http:\/\/www.elsevier.com\/open-access\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.jp","clinicalkey.com","cysticfibrosisjournal.com","clinicalkey.es","clinicalkey.fr","clinicalkey.com.au","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of Cystic Fibrosis"],"published-print":{"date-parts":[[2018,3]]},"DOI":"10.1016\/j.jcf.2018.01.004","type":"journal-article","created":{"date-parts":[[2018,2,1]],"date-time":"2018-02-01T20:07:17Z","timestamp":1517515637000},"page":"264-270","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":11,"title":["The effect of enteral tube feeding in cystic fibrosis: A registry based study"],"prefix":"10.1016","volume":"17","author":[{"given":"Denis","family":"Libeert","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dimitri","family":"Declercq","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Simeon","family":"Wanyama","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Muriel","family":"Thomas","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sabine","family":"Van daele","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Frans","family":"De Baets","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Stephanie","family":"Van Biervliet","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"issue":"4","key":"10.1016\/j.jcf.2018.01.004_bb0005","doi-asserted-by":"crossref","first-page":"233","DOI":"10.1177\/0148607199023004233","article-title":"Effects of Pseudomonas colonization on body composition and resting energy expenditure in children with cystic fibrosis","volume":"23","author":"Vinton","year":"1999","journal-title":"JPEN J Parenter Enteral Nutr"},{"issue":"5","key":"10.1016\/j.jcf.2018.01.004_bb0010","doi-asserted-by":"crossref","first-page":"703","DOI":"10.1016\/j.jpeds.2007.10.021","article-title":"Longitudinal analysis of resting energy expenditure in patients with cystic fibrosis","volume":"152","author":"Magoffin","year":"2008","journal-title":"J Pediatr"},{"issue":"3","key":"10.1016\/j.jcf.2018.01.004_bb0015","doi-asserted-by":"crossref","first-page":"355","DOI":"10.1097\/MPG.0000000000000784","article-title":"Pancreatic enzyme replacement therapy and coefficient of fat absorption in children and adolescents with cystic fibrosis","volume":"61","author":"Woestenenk","year":"2015","journal-title":"J Pediatr Gastroenterol Nutr"},{"key":"10.1016\/j.jcf.2018.01.004_bb0020","article-title":"Enteral tube feeding for cystic fibrosis","volume":"4","author":"Morton","year":"2015","journal-title":"Cochrane Database Syst Rev"},{"issue":"7","key":"10.1016\/j.jcf.2018.01.004_bb0025","doi-asserted-by":"crossref","first-page":"881","DOI":"10.1007\/s00431-016-2719-5","article-title":"Beyond pancreatic insufficiency and liver disease in cystic fibrosis","volume":"175","author":"Demeyer","year":"2016","journal-title":"Eur J Pediatr"},{"issue":"6","key":"10.1016\/j.jcf.2018.01.004_bb0030","doi-asserted-by":"crossref","first-page":"583","DOI":"10.1016\/0895-4356(88)90063-7","article-title":"A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto","volume":"41","author":"Corey","year":"1988","journal-title":"J Clin Epidemiol"},{"issue":"6","key":"10.1016\/j.jcf.2018.01.004_bb0035","doi-asserted-by":"crossref","first-page":"505","DOI":"10.1097\/01.mcp.0000138995.08494.69","article-title":"Association of nutritional status and pulmonary function in children with cystic fibrosis","volume":"10","author":"Milla","year":"2004","journal-title":"Curr Opin Pulm Med"},{"issue":"5","key":"10.1016\/j.jcf.2018.01.004_bb0040","doi-asserted-by":"crossref","first-page":"832","DOI":"10.1016\/j.jada.2008.02.020","volume":"108","author":"Stallings","year":"2008","journal-title":"J Am Diet Assoc"},{"issue":"3 Pt 1","key":"10.1016\/j.jcf.2018.01.004_bb0045","doi-asserted-by":"crossref","first-page":"588","DOI":"10.1542\/peds.112.3.588","article-title":"Longitudinal changes in growth parameters are correlated with changes in pulmonary function in children with cystic fibrosis","volume":"112","author":"Peterson","year":"2003","journal-title":"Pediatrics"},{"issue":"10","key":"10.1016\/j.jcf.2018.01.004_bb0050","doi-asserted-by":"crossref","first-page":"746","DOI":"10.1136\/thorax.56.10.746","article-title":"Wasting as an independent predictor of mortality in patients with cystic fibrosis","volume":"56","author":"Sharma","year":"2001","journal-title":"Thorax"},{"issue":"3","key":"10.1016\/j.jcf.2018.01.004_bb0055","doi-asserted-by":"crossref","first-page":"382","DOI":"10.1016\/j.clnu.2012.08.017","article-title":"Stunting is an independent predictor of mortality in patients with cystic fibrosis","volume":"32","author":"Vieni","year":"2013","journal-title":"Clin Nutr"},{"key":"10.1016\/j.jcf.2018.01.004_bb0060","doi-asserted-by":"crossref","first-page":"33","DOI":"10.3389\/fped.2014.00033","article-title":"Body composition and pulmonary function in cystic fibrosis","volume":"2","author":"Sheikh","year":"2014","journal-title":"Front Pediatr"},{"issue":"Suppl. 1","key":"10.1016\/j.jcf.2018.01.004_bb0065","first-page":"31","article-title":"Nutritional outcomes in cystic fibrosis - are we doing enough?","volume":"16","author":"Connett","year":"2015","journal-title":"Paediatr Respir Rev"},{"issue":"3","key":"10.1016\/j.jcf.2018.01.004_bb0070","doi-asserted-by":"crossref","first-page":"557","DOI":"10.1016\/j.clnu.2016.03.004","article-title":"ESPEN-ESPGHAN-ECFS guidelines on nutrition care for infants, children, and adults with cystic fibrosis","volume":"35","author":"Turck","year":"2016","journal-title":"Clin Nutr"},{"issue":"2","key":"10.1016\/j.jcf.2018.01.004_bb0075","doi-asserted-by":"crossref","first-page":"244","DOI":"10.1016\/S0022-3476(94)70312-4","article-title":"Improvement of nutritional status and lung function after long-term nocturnal gastrostomy feedings in cystic fibrosis","volume":"124","author":"Steinkamp","year":"1994","journal-title":"J Pediatr"},{"issue":"1","key":"10.1016\/j.jcf.2018.01.004_bb0080","doi-asserted-by":"crossref","first-page":"53","DOI":"10.1097\/00005176-199807000-00009","article-title":"Pulmonary function correlates in the prediction of long-term weight gain in cystic fibrosis patients with gastrostomy tube feedings","volume":"27","author":"Walker","year":"1998","journal-title":"J Pediatr Gastroenterol Nutr"},{"issue":"1","key":"10.1016\/j.jcf.2018.01.004_bb0085","doi-asserted-by":"crossref","first-page":"87","DOI":"10.1136\/gut.44.1.87","article-title":"Percutaneous endoscopic gastrostomy feeding in patients with cystic fibrosis","volume":"44","author":"Williams","year":"1999","journal-title":"Gut"},{"issue":"2","key":"10.1016\/j.jcf.2018.01.004_bb0090","doi-asserted-by":"crossref","first-page":"191","DOI":"10.1016\/S0002-8223(99)00046-2","article-title":"Nutritional effects of long-term gastrostomy feedings in children with cystic fibrosis","volume":"99","author":"Rosenfeld","year":"1999","journal-title":"J Am Diet Assoc"},{"issue":"3","key":"10.1016\/j.jcf.2018.01.004_bb0095","first-page":"241","article-title":"Percutaneous endoscopic gastrostomy in cystic fibrosis: patient acceptance and effect of overnight tube feeding on nutritional status","volume":"67","author":"Van Biervliet","year":"2004","journal-title":"Acta Gastroenterol Belg"},{"issue":"4","key":"10.1016\/j.jcf.2018.01.004_bb0100","doi-asserted-by":"crossref","first-page":"324","DOI":"10.1002\/ppul.10321","article-title":"Factors affecting clinical outcome in gastrostomy-fed children with cystic fibrosis","volume":"37","author":"Oliver","year":"2004","journal-title":"Pediatr Pulmonol"},{"issue":"2","key":"10.1016\/j.jcf.2018.01.004_bb0105","doi-asserted-by":"crossref","first-page":"222","DOI":"10.1097\/01.mpg.0000189348.09925.02","article-title":"Long term nutritional rehabilitation by gastrostomy in Israeli patients with cystic fibrosis: clinical outcome in advanced pulmonary disease","volume":"42","author":"Efrati","year":"2006","journal-title":"J Pediatr Gastroenterol Nutr"},{"key":"10.1016\/j.jcf.2018.01.004_bb0110","doi-asserted-by":"crossref","first-page":"112","DOI":"10.2174\/1874306400903010112","article-title":"The long term efficacy of gastrostomy feeding in children with cystic fibrosis on anthropometric markers of nutritonal status and pulmonary function","volume":"3","author":"Truby","year":"2009","journal-title":"Open Respir Med J"},{"key":"10.1016\/j.jcf.2018.01.004_bb0115","doi-asserted-by":"crossref","first-page":"403","DOI":"10.1016\/j.jcf.2013.12.003","article-title":"The relative frequency of CFTR mutations classes in European patients with cystic fibrosis","author":"De Boeck","year":"2014","journal-title":"J Cyst Fibros"},{"key":"10.1016\/j.jcf.2018.01.004_bb0120","author":"Centers for Disease Control and Prevention"},{"issue":"1","key":"10.1016\/j.jcf.2018.01.004_bb0125","first-page":"13","article-title":"Body mass index variations: centiles from birth to 87\u202fyears","volume":"45","author":"Rolland-Cachera","year":"1991","journal-title":"Eur J Clin Nutr"},{"key":"10.1016\/j.jcf.2018.01.004_bb0130","doi-asserted-by":"crossref","first-page":"29","DOI":"10.1016\/S1569-1993(02)00141-8","article-title":"Evaluation of a new definition for chronic Pseudomonas aeruginosa infection in cystic fibrosis patients","volume":"2","author":"Lee","year":"2003","journal-title":"J Cyst Fibros"},{"key":"10.1016\/j.jcf.2018.01.004_bb0135","doi-asserted-by":"crossref","first-page":"751","DOI":"10.1093\/biomet\/73.3.751","article-title":"An improved Bonferroni procedure for multiple test of significance","volume":"73","author":"Simes","year":"1986","journal-title":"Biometrika"},{"key":"10.1016\/j.jcf.2018.01.004_bb0140","doi-asserted-by":"crossref","first-page":"724","DOI":"10.1016\/j.jcf.2016.08.004","article-title":"Enteral tube feeding for individuals with cystic fibrosis: cystic fibrosis foundation evidence-informed guidelines","volume":"15","author":"Schwarzenberg","year":"2016","journal-title":"J Cyst Fibros"},{"key":"10.1016\/j.jcf.2018.01.004_bb0145","author":"ISP\/WIV: BMR-RBM-BCFR"},{"issue":"6","key":"10.1016\/j.jcf.2018.01.004_bb0150","doi-asserted-by":"crossref","first-page":"616","DOI":"10.1016\/j.jcf.2013.05.003","article-title":"Enteral tube feeding in adults with cystic fibrosis; patient choice and impact on long term outcomes","volume":"12","author":"White","year":"2013","journal-title":"J Cyst Fibros"},{"issue":"3","key":"10.1016\/j.jcf.2018.01.004_bb0155","doi-asserted-by":"crossref","first-page":"334","DOI":"10.1097\/01.MPG.0000154656.64073.E1","article-title":"Attitudes toward percutaneous endoscopic gastrostomy placement in cystic fibrosis patients","volume":"40","author":"Gunnell","year":"2005","journal-title":"J Pediatr Gastroenterol Nutr"},{"issue":"8","key":"10.1016\/j.jcf.2018.01.004_bb0160","doi-asserted-by":"crossref","first-page":"743","DOI":"10.1002\/ppul.22507","article-title":"Nutritional outcomes following gastrostomy in children with cystic fibrosis","volume":"47","author":"Bradley","year":"2012","journal-title":"Pediatr Pulmonol"},{"issue":"3","key":"10.1016\/j.jcf.2018.01.004_bb0165","doi-asserted-by":"crossref","first-page":"179","DOI":"10.1016\/j.jcf.2008.12.002","article-title":"Nutritional decline in cystic fibrosis related diabetes: the effect of intensive nutritional intervention","volume":"8","author":"White","year":"2009","journal-title":"J Cyst Fibros"}],"container-title":["Journal of Cystic Fibrosis"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1569199318300079?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1569199318300079?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2020,3,1]],"date-time":"2020-03-01T02:46:09Z","timestamp":1583030769000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1569199318300079"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,3]]},"references-count":33,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2018,3]]}},"alternative-id":["S1569199318300079"],"URL":"https:\/\/doi.org\/10.1016\/j.jcf.2018.01.004","relation":{},"ISSN":["1569-1993"],"issn-type":[{"value":"1569-1993","type":"print"}],"subject":[],"published":{"date-parts":[[2018,3]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"The effect of enteral tube feeding in cystic fibrosis: A registry based study","name":"articletitle","label":"Article Title"},{"value":"Journal of Cystic Fibrosis","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jcf.2018.01.004","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2018 European Cystic Fibrosis Society. Published by Elsevier B.V.","name":"copyright","label":"Copyright"}]}}