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


Journal

Archives of disease in childhood
ISSN: 1468-2044
Titre abrégé: Arch Dis Child
Pays: England
ID NLM: 0372434

Informations de publication

Date de publication:
12 2020
Historique:
received: 22 05 2020
revised: 02 07 2020
accepted: 02 07 2020
pubmed: 1 8 2020
medline: 15 12 2020
entrez: 1 8 2020
Statut: ppublish

Résumé

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. 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. 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. 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.

Sections du résumé

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.

Identifiants

pubmed: 32732316
pii: archdischild-2020-319751
doi: 10.1136/archdischild-2020-319751
doi:

Substances chimiques

Tumor Necrosis Factor Inhibitors 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1186-1191

Informations de copyright

© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: RH has received consultancy or speaker’s fees and travel support from Nutricia and 4D pharma. All remaining authors declare no competing interests related to this manuscript.

Auteurs

James John Ashton (JJ)

Department of Paediatric Gastroenterology, Southampton Children's Hospital, Southampton, UK.
Human Genetics and Genomic Medicine, University of Southampton, Southampton, UK.

Jochen Kammermeier (J)

Department of Paediatric Gastroenterology, Evelina London Children's Hospital, London, UK.

Christine Spray (C)

Department of Paediatric Gastroenterology, Bristol Royal Childrens Hospital, Bristol, UK.

Richard K Russell (RK)

Department of Paediatric Gastroenterology, The Royal Hospital for Sick Children, Edinburgh, UK.

Richard Hansen (R)

Department of Paediatric Gastroenterology, Royal Hospital for Children Glasgow, Glasgow, UK.

Lucy J Howarth (LJ)

Department of Paediatric Gastroenterology, Oxford University Hospitals, Oxford, UK.

Franco Torrente (F)

Department of Paediatric Gastroenterology, Addenbrookes Hospital, Cambridge, UK.

Protima Deb (P)

Department of Paediatric Gastroenterology, The Royal London Hospital, Barts Health NHS Trust, London, UK.

Elizabeth Renji (E)

Department of Paediatric Gastroenterology, Alder Hey Children's Hospital NHS Foundation Trust, Liverpool, UK.

Rafeeq Muhammed (R)

Department of Paediatric Gastroenterology, Birmingham Children's Hospital, Birmingham, UK.

Thankam Paul (T)

Department of Paediatric Gastroenterology, St. Georges University Hospital NHS Foundation Trust, London, UK.

Fevronia Kiparissi (F)

Department of Paediatric Gastroenterology, Great Ormond Street Hospital, London, UK.

Jenny Epstein (J)

Department of Paediatric Gastroenterology, Chelsea and Westminster Hospital, London, UK.

Maureen Lawson (M)

Department of Paediatric Gastroenterology, The Newcastle Upon Tyne Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.

Ben Hope (B)

Department of Paediatric Gastroenterology, King's College London, London, UK.

Veena Zamvar (V)

Department of Paediatric Gastroenterology, Leeds Children's Hospital, Leeds, UK.

Priya Narula (P)

Department of Paediatric Gastroenterology, Sheffield Children's NHS Foundation Trust, Sheffield, UK.

Ahmed Kadir (A)

Department of Paediatric Gastroenterology, Manchester Children's Hospital, Manchester, UK.

David Devadason (D)

Department of Paediatric Gastroenterology, Nottingham University Hospitals NHS Trust, Nottingham, UK.

Hemant Bhavsar (H)

Department of Paediatric Gastroenterology, University Hospitals of Leicester NHS Trust, Leicester, UK.

Robert Mark Beattie (RM)

Department of Paediatric Gastroenterology, Southampton Children's Hospital, Southampton, UK mark.beattie@uhs.nhs.uk.

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Classifications MeSH