P291 Screening for Coeliac Disease in adults with cystic fibrosis in Wales
نویسندگان
چکیده
Emerging evidence suggests an increased prevalence of Coeliac Disease (CD) in People with Cystic Fibrosis (PwCF) when compared to the UK population. The objective was screen patients All Wales Adult Centre (AWACFC) for CD and compare results within adult general population, which is estimated be 1 100. serology tests (IgA anti-tissue Transglutaminase (tTG) antibodies) were added patient annual review blood testing from 2019 2021. An AWACFC Screening Management Flowchart created, based on , used interpret provide intervention guidance. 262 PwCF, 109 (42%) female, screened at review, one already known have CD. 215 (82%) had pancreatic insufficiency (PI). Of 261 without prior disease, two new identified. These reported symptoms gastrointestinal disturbance a skin rash (subsequently diagnosed as dermatitis herpetiformis), respectively. indicate our cohort 87, higher than three male symptom relief implementation gluten-free diet. screened, 16 low IgA therefore Anti-IgG tTG testing. support emerging that PwCF may Additionally, masked by PI, further supporting recommendation routine screening. Our experience shows ease feasibility adding this serological test
منابع مشابه
Cystic fibrosis and coeliac disease: coexistence
Goodchild, M. C., Nelson, R., and Anderson, C. M. (1973). Archives ofDisease in Childhood, 48, 684. Cystic fibrosis and coeliac disease: coexistence in two children. Two children, unrelated, in whom cystic fibrosis had been diagnosed at the ages of 14 weeks and 10 months, respectively, were found subsequently to suffer from coeliac disease as well. Both children are responding well to dietary g...
متن کاملAn infant with both cystic fibrosis and coeliac disease.
Coeliac disease (gluten enteropathy) and cystic fibrosis are both diagnosed fairly often in paediatric practice. The incidence of coeliac disease in London was estimated in 1959 as 1 in 3000 (Carter, Sheldon, and Walker, 1959), but this is almost certainly an underestimate, for the data were collected before the routine use of jejunal biopsy enabled the condition to be diagnosed more accurately...
متن کاملCystic fibrosis and coeliac disease: coexistence in two children.
Goodchild, M. C., Nelson, R., and Anderson, C. M. (1973). Archives ofDisease in Childhood, 48, 684. Cystic fibrosis and coeliac disease: coexistence in two children. Two children, unrelated, in whom cystic fibrosis had been diagnosed at the ages of 14 weeks and 10 months, respectively, were found subsequently to suffer from coeliac disease as well. Both children are responding well to dietary g...
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Background: Regional body composition was determined in adults with cystic fibrosis (CF). Our hypothesis was that dual energy x ray absorptiometry (DXA) scanning could assess the fat free mass, bone mineral content, and fat mass and determine the distribution of the changes. Method: Height squared indices were derived for fat mass (FMI), fat free mass (FFMI), and bone mineral content (BMCI) of ...
متن کاملScreening in cystic fibrosis
A few trials on prenatal CF carrier screening have been performed assessing what proportion of pregnant women are likely to be offered screening and what proportion are likely to accept the test if it is offered free by their own physician (Rowley PT, 1997; Loader S, 1996). A paucity of experience-database is available on CF carrier screening and to terminate CF affected pregnancies. Women foun...
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ژورنال
عنوان ژورنال: Journal of Cystic Fibrosis
سال: 2023
ISSN: ['1569-1993', '1873-5010']
DOI: https://doi.org/10.1016/s1569-1993(23)00662-8