David Devadason

Dr. David Devadason

orcid

Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 November 2019 in The American Journal of Human Genetics
Verified
Journal Article
Closed access
HAHessa S. Alsaif
Hessa S. Alsaif
MAMohammad Al-Owain
Mohammad Al-Owain
MBMartin E. Barrios-Llerena
Martin E. Barrios-Llerena
GGGhada Gosadi
Ghada Gosadi
YBYousef Binamer
Yousef Binamer
FAFowzan S. Alkuraya
Fowzan S. Alkuraya

13 December 2019 in Diagnostics
Verified
Journal Article
Open access
PDF file
HSHayfa Sharif
Hayfa Sharif
DDDavid Devadason
David Devadason
NANichola Abrehart
Nichola Abrehart
RSRebecca Stevenson
Rebecca Stevenson
Luca MarcianiLuca Marciani
Luca Marciani
Background: functional gastrointestinal disorders (FGID) are common conditions in children and adults, often associated with abnormalities of whole gut transit. Currently, transit tests can be performed using several imaging methods, including tracking of radiopaque markers, gamma scintigraphy with the use of radioisotopes, magnetic tracking methods, tracking of movement of wireless motility capsules, and emerging magnetic resonance imaging (MRI) approaches. Objectives: to review recent literature on diagnostic imaging techniques used to investigate whole gut transit in FGIDs. Methods: a systematic review was carried out. The different techniques are described briefly, with particular emphasis on contemporary literature and new developments, particularly in the field of MRI. Conclusions: emerging MRI capsule marker methods are promising new tools to study whole gut transit in FGIDs.

1 November 2011 in Journal of Pediatric Gastroenterology and Nutrition
Verified
Journal Article
Closed access
DRDinesh Rawat
Dinesh Rawat
PGPeter M. Gillett
Peter M. Gillett
DDDavid Devadason
David Devadason
DWDavid C. Wilson
David C. Wilson
PMPatrick J. McKiernan
Patrick J. McKiernan

1 September 2020 in Gut
Verified
Journal Article
Open access
PDF file
RHRichard Hansen
Richard Hansen
SMSusanna Meade
Susanna Meade
RBR Mark Beattie
R Mark Beattie
MAMarcus Kh Auth
Marcus Kh Auth
NCNick Croft
Nick Croft
JKJochen Kammermeier
Jochen Kammermeier
Objective Paediatric acute severe colitis (ASC) management during the novel SARS-CoV-2/COVID-19 pandemic is challenging due to reliance on immunosuppression and the potential for surgery. We aimed to provide COVID-19-specific guidance using the European Crohn’s and Colitis Organisation/European Society for Paediatric Gastroenterology, Hepatology and Nutrition guidelines for comparison. Design We convened a RAND appropriateness panel comprising 14 paediatric gastroenterologists and paediatric experts in surgery, rheumatology, respiratory and infectious diseases. Panellists rated the appropriateness of interventions for ASC in the context of the COVID-19 pandemic. Results were discussed at a moderated meeting prior to a second survey. Results Panellists recommended patients with ASC have a SARS-CoV-2 swab and expedited biological screening on admission and should be isolated. A positive swab should trigger discussion with a COVID-19 specialist. Sigmoidoscopy was recommended prior to escalation to second-line therapy or colectomy. Methylprednisolone was considered appropriate first-line management in all, including those with symptomatic COVID-19. Thromboprophylaxis was also recommended in all. In patients requiring second-line therapy, infliximab was considered appropriate irrespective of SARS-CoV-2 status. Delaying colectomy due to SARS-CoV-2 infection was considered inappropriate. Corticosteroid tapering over 8–10 weeks was deemed appropriate for all. After successful corticosteroid rescue, thiopurine maintenance was rated appropriate in patients with negative SARS-CoV-2 swab and asymptomatic patients with positive swab but uncertain in symptomatic COVID-19. Conclusion Our COVID-19-specific adaptations to paediatric ASC guidelines using a RAND panel generally support existing recommendations, particularly the use of corticosteroids and escalation to infliximab, irrespective of SARS-CoV-2 status. Consideration of routine prophylactic anticoagulation was recommended.

3 November 2017 in Children
Verified
Journal Article
Open access
PDF file
ONOmar Nasher
Omar Nasher
DDDavid Devadason
David Devadason
RSRichard J. Stewart
Richard J. Stewart
The aim of this study was to review the aetiology, presentation and management of these patients with upper gastrointestinal bleeding (UGIB) at a tertiary children’s unit in the United Kingdom. This was a retrospective single-institution study on children (<16 years) who presented with acute UGIB over a period of 5 years using known International Classification of Diseases (ICD) codes. A total of 32 children (17 males, 15 females) were identified with a total median age at presentation of 5.5 years. The majority (24/32) of patients presented as an emergency. A total of 19/32 presented with isolated haematemesis, 8/32 with isolated melaena and 5/32 with a combination of melaena and haematemesis. On admission, the mean haemoglobin of patients who presented with isolated haematemesis was 11 g/dL, those with isolated melaena 9.3 g/dL and those with a combination 7.8 g/dL. Blood transfusion was required in 3/19 with haematemesis and 3/5 with haematemesis and melaena. A total of 19/32 underwent upper gastrointestinal endoscopy. Endoscopic findings were oesophageal varices (5/19) of which 4 required banding; bleeding gastric ulcer (1/19) requiring clips, haemospray and adrenaline; gastric vascular malformation (1/19) treated with Argon plasma coagulation therapy; duodenal ulcer (3/19) which required surgery in two cases; oesophagitis (5/19); and gastritis +/− duodenitis (3/19). A total of 13/32 patients did not undergo endoscopy and the presumed aetiology was a Mallory–Weiss tear (4/13); ingestion of foreign body (2/13); gastritis (3/13); viral illness (1/13); unknown (2/13). While UGIB is uncommon in children, the morbidity associated with it is very significant. Melaena, dropping haemoglobin, and requirement for a blood transfusion appear to be significant markers of an underlying cause of UGIB that requires therapeutic intervention. A multi-disciplinary team comprising gastroenterologists and surgeons is essential.

1 August 2019 in Journal of Pediatric Gastroenterology and Nutrition
Verified
Journal Article
Closed access
PNPriya Narula
Priya Narula
RBRaphael Broughton
Raphael Broughton
LHLucy Howarth
Lucy Howarth
APAnna Piggott
Anna Piggott
RBRonald Bremner
Ronald Bremner
DJDebbie Johnston
Debbie Johnston