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Cyproheptadine as an appetite stimulant in children with cystic fibrosis.
Grunert, Jodi; van der Haak, Natalie; La Vanda, Carol; Farrow, Nigel; Tai, Andrew.
Afiliação
  • Grunert J; Women's and Children's Hospital, Nutrition Department, 72 King William Road, North Adelaide, SA, Australia, 5006. Electronic address: jodi.grunert@sa.gov.au.
  • van der Haak N; Women's and Children's Hospital, Nutrition Department, 72 King William Road, North Adelaide, SA, Australia, 5006. Electronic address: Natalie.vanderhaak@sa.gov.au.
  • La Vanda C; SA Pharmacy, Women's and Children's Hospital, 72 King William Road, North Adelaide, SA, Australia, 5006. Electronic address: carol.lavanda@sa.gov.au.
  • Farrow N; Women's and Children's Hospital, Department of Respiratory and Sleep Medicine, 72 King William Road, North Adelaide, SA, Australia, 5006; University of Adelaide, Robinson Research Institute, Adelaide, Australia; University of Adelaide, Adelaide Medical School, Adelaide, Australia. Electronic address
  • Tai A; Women's and Children's Hospital, Department of Respiratory and Sleep Medicine, 72 King William Road, North Adelaide, SA, Australia, 5006; University of Adelaide, Robinson Research Institute, Adelaide, Australia. Electronic address: Andrew.tai@sa.gov.au.
Clin Nutr ESPEN ; 42: 407-409, 2021 04.
Article em En | MEDLINE | ID: mdl-33745614
BACKGROUND: Cystic fibrosis (CF) is a multi-organ genetically inherited disease that leads to progressive lung disease and nutrient malabsorption. The aim of this study was to assess the effectiveness of cyproheptadine (CH) (Periactin®) as an appetite stimulant on improving the nutrition status of paediatric patients with CF. METHODS: We conducted a retrospective study of 15 patients with a suboptimal nutrition status prescribed CH for ≥12 months from 2013 to 2018. Change in Body Mass Index (BMI) z-score and lung function before vs. after treatment with CH were measured as well as dose-response relationship. RESULTS: The mean change in BMI z-score over 12 months of treatment with CH was +0.91 compared to -0.52 in the previous 12 months (p∗∗∗ = 0.0002). There was also a trend towards an improvement in lung function over the 12 months of CH treatment compared to the 12 months prior (+2.79 vs -6.2% (p = 0.07)). No dose-response relationship was observed. CONCLUSION: These results suggest that CH is effective at improving the nutrition status of paediatric CF patients with suboptimal nutrition.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estimulantes do Apetite / Fibrose Cística Tipo de estudo: Observational_studies Limite: Child / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estimulantes do Apetite / Fibrose Cística Tipo de estudo: Observational_studies Limite: Child / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article