Po-Hung Chen

Dr. Po-Hung Chen

orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

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

Representative Publications

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28 September 2016 in Journal of Clinical and Translational Hepatology
Verified
Journal Article
Open access
NWNajeff Waseem
Najeff Waseem
PCPo-Hung Chen
Po-Hung Chen
Hypoxic Hepatitis: A Review and Clinical Update

26 February 2018 in Digestive Diseases and Sciences
Verified
Journal Article
Closed access
PDF file
BNBolin Niu
Bolin Niu
BKBrian Kim
Brian Kim
BLBerkeley N. Limketkai
Berkeley N. Limketkai
JSJing Sun
Jing Sun
ZLZhiping Li
Zhiping Li
PCPo-Hung Chen
Po-Hung Chen

24 December 2020 in Journal of Clinical Gastroenterology
Verified
Journal Article
Closed access
AMAbdul Mohammed
Abdul Mohammed
NPNeethi Paranji
Neethi Paranji
PCPo-Hung Chen
Po-Hung Chen
BNBolin Niu
Bolin Niu
The coronavirus disease 2019 (COVID-19) pandemic has brought challenges to clinicians caring for patients with chronic liver disease. In the past 6 months, COVID-19 has led to over 150,000 deaths in the United States and over 660,000 deaths around the world. Mounting evidence suggests that chronic liver diseases can have an adverse effect on the clinical outcomes of patients with COVID-19. We present a comprehensive review of the latest literature on preexisting liver diseases and its interrelationship with COVID-19 infection in cirrhosis, hepatocellular carcinoma, nonalcoholic fatty liver disease, autoimmune hepatitis, and viral hepatitis B. As social distancing and telemedicine gain new footing, we synthesize recommendations from 3 major hepatology societies [American Association for the Study of Liver Disease (AASLD), the European Association for the Study of Liver (EASL), and the Asian Pacific Association for the Study of Liver (APASL)] to present the best approaches for caring for patients with liver diseases as well as those requiring liver transplantation.

20 July 2022 in Inflammatory Bowel Diseases
Verified
Journal Article
Open access
PDF file
SHSusan Hutfless
Susan Hutfless
RJRyan A Jasper
Ryan A Jasper
ATAman Tilak
Aman Tilak
TGTamoghna Ghosh
Tamoghna Ghosh
SKSaurabh Kedia
Saurabh Kedia
SBSteven R Brant
Steven R Brant
Background: We sought to review Crohn’s disease (CD) case definitions that use diagnosis, procedure, and medication claims. Methods: We searched PubMed and Embase from inception through January 31, 2022, using terms related to CD, inflammatory bowel disease, administrative claims, or validity. Each article was scrutinized by 2 authors independently screening and abstracting data. Collected data included participant characteristics, case definition characteristics, and case definition validity. When diagnostic accuracy was provided for multiple case definitions, we extracted the case definition selected by the authors. All diagnostic accuracy characteristics were captured. Results: We identified 30 studies that evaluated a case definition using claims data to identify CD patients. The most common case definition included counts of diagnosis codes (57%) followed by a combination of diagnosis codes and medications (20%). All but 1 study validated the case definition with a medical chart review. In 2 studies, the patient’s primary care provider completed a survey to confirm disease status. The positive predictive value of the case definitions ranged from 18% (≥1 code at a single U.S. health plan) to 100% (≥1 code plus a relevant prescription at a U.S. hospital). More complex case definitions (eg, ≥1 code + prescription or ≥2 codes) had lower variability in positive predictive value (≥80%) and specificity (≥85%) than the ≥1 code requirement. Conclusions: Health services researchers should validate case definitions in their research cohorts. When such validation cannot be performed, we recommend using a more complex case definition. Studies without a validated CD case definition should use sensitivity analyses to confirm the robustness of their results.

30 October 2019 in Transplant Infectious Disease
Verified
Journal Article
Closed access
PDF file
Peng-sheng TingPeng-sheng Ting
Peng-sheng Ting
JHJames P. Hamilton
James P. Hamilton
AGAhmet Gurakar
Ahmet Gurakar
NUNathalie H. Urrunaga
Nathalie H. Urrunaga
MMMichelle Ma
Michelle Ma
PCPo-Hung Chen
Po-Hung Chen

15 September 2023 in Nutrients
Verified
Journal Article
Open access
PDF file
Tung-Sung TsengTung-Sung Tseng
Tung-Sung Tseng
WLWei-Ting Lin
Wei-Ting Lin
Peng-sheng TingPeng-sheng Ting
Peng-sheng Ting
CHChiung-Kuei Huang
Chiung-Kuei Huang
PCPo-Hung Chen
Po-Hung Chen
HLHui-Yi Lin
Hui-Yi Lin
Nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH) are fast becoming the most common chronic liver disease and are often preventable with healthy dietary habits and weight management. Sugar-sweetened beverage (SSB) consumption is associated with obesity and NAFLD. However, the impact of different types of SSBs, including artificially sweetened beverages (ASBs), is not clear after controlling for total sugar intake and total caloric intake. The aim of this study was to examine the association between the consumption of different SSBs and the risk of NAFLD and NASH in US adults. The representativeness of 3739 US adults aged ≥20 years old who had completed 24 h dietary recall interviews and measurements, including dietary, SSBs, smoking, physical activity, and liver stiffness measurements, were selected from the National Health and Nutrition Examination Survey 2017–2020 surveys. Chi-square tests, t-tests, and weighted logistic regression models were utilized for analyses. The prevalence of NASH was 20.5%, and that of NAFLD (defined without NASH) was 32.7% of US. adults. We observed a higher prevalence of NASH/NAFLD in men, Mexican-Americans, individuals with sugar intake from SSBs, light–moderate alcohol use, lower physical activity levels, higher energy intake, obesity, and medical comorbidities. Heavy sugar consumption through SSBs was significantly associated with NAFLD (aOR = 1.60, 95% CI = 1.05–2.45). In addition, the intake of ASBs only (compared to the non-SSB category) was significantly associated with NAFLD (aOR = 1.78, 95% CI = 1.04–3.05), after adjusting for demographic, risk behaviors, and body mass index. A higher sugar intake from SSBs and exclusive ASB intake are both associated with the risk of NAFLD.