The screening and diagnosis of cystic fibrosis-related diabetes in the United Kingdom

被引:7
|
作者
Wickens-Mitchell, Kate L. [1 ]
Gilchrist, Francis J. [1 ,2 ]
McKenna, D. [3 ]
Raffeeq, P. [1 ]
Lenney, Warren [1 ,2 ]
机构
[1] Univ Hosp North Staffordshire, Acad Dept Child Hlth, Stoke On Trent ST4 6QG, Staffs, England
[2] Keele Univ, Guy Hilton Res Ctr, Inst Sci & Technol Med, Stoke On Trent 5T4 7QB, Staffs, England
[3] Univ S Manchester Hosp, Manchester Adult Cyst Fibrosis Ctr, Manchester M23 9LT, Lancs, England
关键词
Cystic fibrosis; Cystic fibrosis-related diabetes; GLUCOSE-TOLERANCE; CHILDREN; ADOLESCENTS; MORTALITY; MELLITUS;
D O I
10.1016/j.jcf.2014.01.008
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Introduction: The cystic fibrosis-related diabetes (CFRD) guidelines produced by the UK CF Trust differ from those used in Europe and the US. We conducted a study to establish current practice. Method: Paediatric and adult questionnaires were devised and emailed to the 48 specialist UK CF centres. Results: Completed questionnaires were returned by 39/48 (81%) centres. Only 3/21 (14%) paediatric centres begin annual screening at 12 years (as per UK guidelines), 11/21(52%) start to screen at 10 years (as per European and US guidelines) and 5/21 (24%) begin screening at a child's first annual review. The oral glucose tolerance test is used as a screening test in 33/39 (85%) of centres but only 3/33 (9%) use it in isolation. Home glucose monitoring is the most frequently used diagnostic test undertaken in 32/39 (82%) centres, and again this is rarely used in isolation. The decision to initiate insulin is often shared between specialist nurses and doctors. Conclusions: In the UK the majority of CF centres use the OGTT to screen and HUM to diagnose CFRD. The use of other tools varies with poor adherence to UK guidelines. These 2004 guidelines would benefit from being updated to reflect current best evidence. (C) 2014 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:589 / 592
页数:4
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