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Hypoglycaemia in cystic fibrosis in the absence of diabetes: A systematic review.
Armaghanian, N; Brand-Miller, J C; Markovic, T P; Steinbeck, K S.
Afiliación
  • Armaghanian N; Discipline of Paediatrics and Child Health, Sydney Medical School, University of Sydney, Australia; Academic Department of Adolescent Medicine, The Children's Hospital at Westmead, Australia. Electronic address: natasha.armaghanian@health.nsw.gov.au.
  • Brand-Miller JC; School of Molecular Bioscience, University of Sydney, Australia; Boden Institute of Obesity, Nutrition and Exercise, University of Sydney, Australia.
  • Markovic TP; Boden Institute of Obesity, Nutrition and Exercise, University of Sydney, Australia; Department of Endocrinology, Royal Prince Alfred Hospital, Sydney, Australia.
  • Steinbeck KS; Discipline of Paediatrics and Child Health, Sydney Medical School, University of Sydney, Australia; Academic Department of Adolescent Medicine, The Children's Hospital at Westmead, Australia; Department of Endocrinology, Royal Prince Alfred Hospital, Sydney, Australia.
J Cyst Fibros ; 15(3): 274-84, 2016 05.
Article en En | MEDLINE | ID: mdl-27025865
BACKGROUND: Hypoglycaemia in CF in the absence of diabetes or glucose lowering therapies is a phenomenon that is receiving growing attention in the literature. These episodes are sometimes symptomatic and likely have variable aetiologies. Our first aim was to conduct a systematic review of the literature to determine what is known about hypoglycaemia in CF. Our second aim was to assess evidence based guidelines for management strategies. METHODS: A comprehensive search of databases and guideline compiler entities was performed. Inclusion criteria were primary research articles and evidence based guidelines that referred to hypoglycaemia in CF in the absence of insulin treatment or other glucose lowering therapies. RESULTS: A total of 11 studies (four manuscripts and seven abstracts) and five evidence-based guidelines met the inclusion criteria. Prevalence rates of hypoglycaemia unrelated to diabetes varied between studies (7-69%). Hypoglycaemia was diagnosed during oral glucose tolerance testing or continuous glucose monitoring (CGM). Associations between hypoglycaemia and clinical parameters of BMI, lung function, liver disease and pancreatic insufficiency were measured in some studies. There was no unifying definition of hypoglycaemia in the absence of diabetes. Only two evidence based guidelines reported possible management strategies. CONCLUSION: The systematic review found limited data on this clinical problem and supports the need for high quality methodological studies that are able to describe the experience and the aetiology(ies) of hypoglycaemia in CF.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Fibrosis Quística / Hipoglucemia Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline / Prevalence_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: J Cyst Fibros Año: 2016 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Fibrosis Quística / Hipoglucemia Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline / Prevalence_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: J Cyst Fibros Año: 2016 Tipo del documento: Article