Cited by 52

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Development and Validation of a Model Consisting of Comorbidity Burden to Calculate Risk of Death Within 6 Months for Patients With Suspected Drug-Induced Liver Injury

Ghabril, Marwan, Gu, Jiezhun, Yoder, Lindsay, Corbito, Laura, Ringel, Amit, Beyer, Christian D., Vuppalanchi, Raj, Barnhart, Huiman, Hayashi, Paul H., Chalasani, Naga·2019·Gastroenterology

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Crossref · 10.1053/j.gastro.2019.07.006

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  • DILI patients with pre-existing liver disease have an increased risk of 6-month mortality at 4.5% in validation cohort and 8.5% in discovery cohort in a DILIN study.

    “DILI patients with pre-existing liver disease have reported to demonstrate an increased risk of 6-month mortality at 4.5% in validation cohort and 8.5% in discovery cohort in a DILIN study [71].”
  • A validated model incorporating MELD score, serum albumin level, and Charlson comorbidity index may be useful in predicting the 6-month risk of death in patients with DILI.

    “Another validated model incorporating the Model for End-Stage Liver Disease score, the serum albumin level, and the Charlson comorbidity index as parameters may be useful in predicting the 6-month risk of death in patients with DILI [71].”
  • DILIN group established that significant comorbidities defined by Charlson ≥ 2, Model for End-Stage Liver Disease score and serum level of albumin at presentation were independently associated with 6-month mortality in both discovery (306 patients) and validation (247 patients) cohorts.

    “On the other hand, DILIN group established that significant comorbidities defined by Charlson ≥ 2, Model for End-Stage Liver Disease score and serum level of albumin at presentation were independently associated with 6-month mortality in both discovery (306 patients) and validation (247 patients) cohorts [33]”

    From DILI Differences and Similarities between the US and Europe (2026) · cites this paper as [33]

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Citations

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Research works printed but not linked: 19

  1. Chalasani, 2014, ACG Clinical Guideline: the diagnosis and management of idiosyncratic drug-induced liver injury, Am J Gastroenterol, 109, 950, 10.1038/ajg.2014.131 · DOI · Paper page
  2. Chalasani, 2015, Features and outcomes of 899 patients with drug-induced liver injury: the DILIN Prospective Study, Gastroenterology, 148, 1340, 10.1053/j.gastro.2015.03.006 · DOI · Paper page
  3. Hayashi, 2017, Death and liver transplantation within 2 years of onset of drug-induced liver injury, Hepatology, 66, 1275, 10.1002/hep.29283 · DOI · Paper page
  4. Natarajan, 2017, Role of non-hepatic medical comorbidity and functional limitations in predicting mortality in patients with HCV, Dig Dis Sci, 62, 76, 10.1007/s10620-016-4303-2 · DOI
  5. Ladha, 2015, The Deyo-Charlson and Elixhauser-van Walraven Comorbidity Indices as predictors of mortality in critically ill patients, BMJ Open, 5, 10.1136/bmjopen-2015-008990 · DOI
  6. Xu, 2017, Comparison of risk adjustment methods in patients with liver disease using electronic medical record data, BMC Gastroenterol, 17, 5, 10.1186/s12876-016-0559-4 · DOI
  7. Fontana, 2009, Drug-Induced Liver Injury Network (DILIN) prospective study: rationale, design and conduct, Drug Saf, 32, 55, 10.2165/00002018-200932010-00005 · DOI · Paper page
  8. Dakhoul, 2018, Heavy consumption of alcohol is not associated with worse outcomes in patients with idiosyncratic drug-induced liver injury compared to non-drinkers, Clin Gastroenterol Hepatol, 16, 722, 10.1016/j.cgh.2017.12.036 · DOI · Paper page
  9. Chalasani, 2017, Idiosyncratic drug induced liver injury in African-Americans is associated with greater morbidity and mortality compared to Caucasians, Am J Gastroenterol, 112, 1382, 10.1038/ajg.2017.215 · DOI · Paper page
  10. Fontana, 2015, Persistent liver biochemistry abnormalities are more common in older patients and those with cholestatic drug induced liver injury, Am J Gastroenterol, 110, 1450, 10.1038/ajg.2015.283 · DOI
  11. Fontana, 2014, Idiosyncratic drug-induced liver injury is associated with substantial morbidity and mortality within 6 months from onset, Gastroenterology, 147, 96, 10.1053/j.gastro.2014.03.045 · DOI
  12. Charlson, 1987, A new method of classifying prognostic comorbidity in longitudinal studies: development and validation, J Chronic Dis, 40, 373, 10.1016/0021-9681(87)90171-8 · DOI · Paper page
  13. Rattanasompattikul, 2012, Charlson Comorbidity score is a strong predictor of mortality in hemodialysis patients, Int Urol Nephrol, 44, 1813, 10.1007/s11255-011-0085-9 · DOI
  14. Formiga, 2018, High comorbidity, measured by the Charlson Comorbidity Index, associates with higher 1-year mortality risks in elderly patients experiencing a first acute heart failure hospitalization, Aging Clin Exp Res, 30, 927, 10.1007/s40520-017-0853-1 · DOI
  15. Fraccaro, 2016, Predicting mortality from change-over-time in the Charlson Comorbidity Index: a retrospective cohort study in a data-intensive UK health system, Medicine (Baltimore), 95, 10.1097/MD.0000000000004973 · DOI
  16. Chalasani, 2008, Causes, clinical features, and outcomes from a prospective study of drug-induced liver injury in the United States, Gastroenterology, 135, 1924, 10.1053/j.gastro.2008.09.011 · DOI
  17. Gottlieb, 2019, How to define acute liver failure patients with pre-existing liver disease without signs of cirrhosis, Dig Dis, 37, 147, 10.1159/000492869 · DOI
  18. Canbay, 2005, Overweight patients are more susceptible for acute liver failure, Hepatogastroenterology, 52, 1516
  19. Canbay, 2009, Acute liver failure in a metropolitan area in Germany: a retrospective study (2002–2008), Z Gastroenterol, 47, 807

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Metadata

Authors
Ghabril, M., Gu, J., Yoder, L., Corbito, L., Ringel, A., Beyer, C. D., Vuppalanchi, R., Barnhart, H., Hayashi, P. H., & Chalasani, N.
Venue
Gastroenterology
Publisher
Elsevier BV
Published
2019-11
Volume
157
Issue
5
Pages
1245-1252.e3
ISSN
0016-5085
Cited by
52
References
1
Language
en
Funders
  • National Institute of Diabetes and Digestive and Kidney Diseases
  • AbbVie
  • Eli Lilly and Company
  • Duke University (DK065201, DK065211)
  • Genentech
  • Indiana University (U01)
  • Siemens Foundation
  • University of North Carolina
  • Allergan Foundation
  • Gilead Sciences

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