Impact of COVID-19 on diagnosis and management of paediatric inflammatory bowel disease during lockdown: a UK nationwide study

被引:26
|
作者
Ashton, James John [1 ,2 ]
Kammermeier, Jochen [3 ]
Spray, Christine [4 ]
Russell, Richard K. [5 ]
Hansen, Richard [6 ]
Howarth, Lucy J. [7 ]
Torrente, Franco [8 ]
Deb, Protima [9 ]
Renji, Elizabeth [10 ]
Muhammed, Rafeeq [11 ]
Paul, Thankam [12 ]
Kiparissi, Fevronia [13 ]
Epstein, Jenny [14 ]
Lawson, Maureen [15 ]
Hope, Ben [16 ]
Zamvar, Veena [17 ]
Narula, Priya [18 ]
Kadir, Ahmed [19 ]
Devadason, David [20 ]
Bhavsar, Hemant [21 ]
Beattie, Robert Mark [1 ]
机构
[1] Southampton Childrens Hosp, Dept Paediat Gastroenterol, Southampton, Hants, England
[2] Univ Southampton, Human Genet & Genom Med, Southampton, Hants, England
[3] Evelina London Childrens Hosp, Dept Paediat Gastroenterol, London, England
[4] Bristol Royal Childrens Hosp, Dept Paediat Gastroenterol, Bristol, Avon, England
[5] Royal Hosp Sick Children, Dept Paediat Gastroenterol, Edinburgh, Midlothian, Scotland
[6] Royal Hosp Children Glasgow, Dept Paediat Gastroenterol, Glasgow, Lanark, Scotland
[7] Oxford Univ Hosp, Dept Paediat Gastroenterol, Oxford, England
[8] Addenbrookes Hosp, Dept Paediat Gastroenterol, Cambridge, England
[9] Royal London Hosp Barts Hlth NHS Trust, Dept Paediat Gastroenterol, London, England
[10] Alder Hey Childrens Hosp NHS Fdn Trust, Dept Paediat Gastroenterol, Liverpool, Merseyside, England
[11] Birmingham Childrens Hosp, Dept Paediat Gastroenterol, Birmingham, W Midlands, England
[12] St Georges Univ Hosp NHS Fdn Trust, Dept Paediat Gastroenterol, London, England
[13] Great Ormond St Hosp Sick Children, Dept Paediat Gastroenterol, London, England
[14] Chelsea & Westminster Hosp, Dept Paediat Gastroenterol, London, England
[15] Newcastle Upon Tyne Hosp NHS Fdn Trust, Dept Paediat Gastroenterol, Newcastle Upon Tyne, Tyne & Wear, England
[16] Kings Coll London, Dept Paediat Gastroenterol, London, England
[17] Leeds Childrens Hosp, Dept Paediat Gastroenterol, Leeds, W Yorkshire, England
[18] Sheffield Childrens NHS Fdn Trust, Dept Paediat Gastroenterol, Sheffield, S Yorkshire, England
[19] Manchester Childrens Hosp, Dept Paediat Gastroenterol, Manchester, Lancs, England
[20] Nottingham Univ Hosp NHS Trust, Dept Paediat Gastroenterol, Nottingham, England
[21] Univ Hosp Leicester NHS Trust, Dept Paediat Gastroenterol, Leicester, Leics, England
关键词
CROHNS-DISEASE; CHILDREN; IBD;
D O I
10.1136/archdischild-2020-319751
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background COVID-19 has impacted on healthcare provision. Anecdotally, investigations for children with inflammatory bowel disease (IBD) have been restricted, resulting in diagnosis with no histological confirmation and potential secondary morbidity. In this study, we detail practice across the UK to assess impact on services and document the impact of the pandemic. Methods For the month of April 2020, 20 tertiary paediatric IBD centres were invited to contribute data detailing: (1) diagnosis/management of suspected new patients with IBD; (2) facilities available; (3) ongoing management of IBD; and (4) direct impact of COVID-19 on patients with IBD. Results All centres contributed. Two centres retained routine endoscopy, with three unable to perform even urgent IBD endoscopy. 122 patients were diagnosed with IBD, and 53.3% (n=65) were presumed diagnoses and had not undergone endoscopy with histological confirmation. The most common induction was exclusive enteral nutrition (44.6%). No patients with a presumed rather than confirmed diagnosis were started on anti-tumour necrosis factor (TNF) therapy. Most IBD follow-up appointments were able to occur using phone/webcam or face to face. No biologics/immunomodulators were stopped. All centres were able to continue IBD surgery if required, with 14 procedures occurring across seven centres. Conclusions Diagnostic IBD practice has been hugely impacted by COVID-19, with >50% of new diagnoses not having endoscopy. To date, therapy and review of known paediatric patients with IBD has continued. Planning and resourcing for recovery is crucial to minimise continued secondary morbidity.
引用
收藏
页码:1186 / 1191
页数:6
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