Shria Kumar

Dr. Shria Kumar


Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

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

Representative Publications

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1 February 2020 in Gastroenterology
Verified
Journal Article
Closed access
PDF file
SKShria Kumar
Shria Kumar
DMDavid C. Metz
David C. Metz
SESusan Ellenberg
Susan Ellenberg
DKDavid Edward Kaplan
David Edward Kaplan
DGDavid S. Goldberg
David S. Goldberg

8 August 2016 in Frontline Gastroenterology
Verified
Journal Article
Open access
PDF file
SKShria Kumar
Shria Kumar
CRChristopher Ramos
Christopher Ramos
RGReuben J Garcia-Carrasquillo
Reuben J Garcia-Carrasquillo
PGPeter H Green
Peter H Green
BLBenjamin Lebwohl
Benjamin Lebwohl
Objectives To identify incidence and risk factors for new-onset gastrointestinal bleeding (GIB) in a medical intensive care unit (ICU), a topic for which there is a paucity of recent studies. Design Retrospective cohort study. Setting Medical ICUs at our tertiary-care hospital, from 2007 to 2013. Patients Patients who developed clinically significant GIB after entering the ICU. Interventions Univariable and multivariable analyses. Main outcome measures Incidence and risk factors for development of GIB. Results 4439 patients entered the medical ICU without a pre-existing GIB and 58 (1.3%) developed GIB while in the ICU. Risk factors included length of ICU stay (OR per additional day 1. 06; 95% CI 1.04 to 1.09) and elevated creatinine on ICU admission (OR 2.35; 95% CI 1.18 to 4.68, p=0.02). Elevated bilirubin on ICU admission (OR 2.08; 95% CI 0.97 to 4.47, p=0.06), and elevated aspartate transaminase (AST) on ICU admission (OR 2.20; 95% CI 0.96 to 5.03, p=0.06) trended towards increased risk of GIB that did not meet statistical significance. Age, gender, admission coagulation studies and mechanical ventilation were not predictive of GIB. Among those patients with new-onset GIB in the ICU, 47% died during that hospitalisation, as compared with those 30% of those without a GIB, p<0.01. Conclusions Onset of GIB is now an infrequent occurrence in the ICU setting; however those with elevated bilirubin, AST and creatinine upon admission, and with longer length of ICU stay appear at increased risk and may benefit from closer monitoring.

1 February 2021 in Clinical Gastroenterology and Hepatology
Verified
Journal Article
Closed access
SKShria Kumar
Shria Kumar
DMDavid C. Metz
David C. Metz
DKDavid Edward Kaplan
David Edward Kaplan
DGDavid S. Goldberg
David S. Goldberg

16 February 2022 in Cancers
Verified
Journal Article
Open access
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SKShria Kumar
Shria Kumar
NFNatalie Farha
Natalie Farha
CBCarol Burke
Carol Burke
BKBryson W Katona
Bryson W Katona
Lynch syndrome is a common hereditary cancer predisposition syndrome associated with increased digestive cancer risk including colorectal, gastric, and duodenal cancers. While colorectal cancer surveillance is widely accepted to be an important part of a comprehensive Lynch syndrome risk management plan, the use of upper gastrointestinal cancer surveillance in Lynch syndrome remains more controversial. Currently, upper gastrointestinal cancer surveillance guidelines for Lynch syndrome vary widely, and there is no consensus on who should undergo upper gastrointestinal cancer surveillance, how surveillance should be performed, the age at which to initiate surveillance, or how often individuals with Lynch syndrome should undergo upper gastrointestinal cancer surveillance. Fortunately, research groups around the world have been focusing on upper gastrointestinal cancer surveillance in Lynch syndrome, and recent evidence in this field has demonstrated that upper gastrointestinal cancer surveillance can be performed with identification of precancerous lesions as well as early-stage upper gastrointestinal cancers. In this manuscript, we review the upper gastrointestinal cancer risks in Lynch syndrome, differing guideline recommendations for surveillance, outcomes of upper gastrointestinal cancer surveillance, and controversies in the field, and we provide a framework based on our collective experience with which to incorporate upper gastrointestinal cancer surveillance into a risk management program for individuals with Lynch syndrome.

21 June 2021 in Pancreas
Verified
Journal Article
Closed access
SKShria Kumar
Shria Kumar
MSMonica Saumoy
Monica Saumoy
AOAaron Ba Oh
Aaron Ba Oh
YSYecheskel Schneider
Yecheskel Schneider
RBRandall E. Brand
Randall E. Brand
ARAnil K. Rustgi
Anil K. Rustgi
Objectives: Data from the International Cancer of the Pancreas Screening Consortium studies have demonstrated that screening for pancreatic ductal adenocarcinoma can be effective and that surveillance improves survival in high-risk individuals. Endoscopic ultrasound (EUS) and cross-sectional imaging are both used, although there is some suggestion that EUS is superior. Demonstration of the cost-effectiveness of screening is important to implement screening in high-risk groups. Methods: Results from centers with EUS-predominant screening were pooled to evaluate efficacy of index EUS in screening. A decision analysis model simulated the outcome of high-risk patients who undergo screening and evaluated the parameters that would make screening cost-effective at a US $100,000 per quality-adjusted life-year willingness to pay. Results: One-time index EUS has a sensitivity of 71.25% and specificity of 99.82% to detection to detect high-risk lesions. Screening with index EUS was cost-effective, particularly at lifetime pancreatic cancer probabilities of greater than 10.8%, or at lower probabilities if life expectancy after resection of a lesion that was at least 16 years, and if missed, lesion rates on index EUS are 5% or less. Conclusions: Pancreatic cancer screening can be cost-effective through index EUS, particularly for those individuals at high-lifetime risk of cancer.

4 March 2020 in Alimentary Pharmacology & Therapeutics
Verified
Journal Article
Closed access
PDF file
SKShria Kumar
Shria Kumar
DMDavid C. Metz
David C. Metz
GGGregory G. Ginsberg
Gregory G. Ginsberg
DKDavid E. Kaplan
David E. Kaplan
DGDavid S. Goldberg
David S. Goldberg