The Indian Network of Drug-Induced Liver Injury: Etiology, Clinical Features, Outcome and Prognostic Markers in 1288 Patients.

AED, Anti-epileptic drugs ALF, Acute liver failure ALT, Alanine aminotransferase ART, Anti-retroviral drugs AST, Aspartate aminotransferase ATD, Anti- tuberculosis drugs Anti-tuberculosis drugs C.I, Confidence interval CAM, Complementary and alternative medicine Complimentary medicines DILI, Drug-induced liver injury DILIN, Drug induced liver injury network HE, Hepatic encephalopathy HIV, Human immunodeficiency virus INR, International normalised ratio Isoniazid Jaundice MELD, Model for end stage liver disease Mortality NSAID, Nonsteroidal anti-inflammatory drugs OR, Odds ratio Prognosis Pyrazinamide ROC, Receiver operating characteristic RUCAM, Roussel uclaf causality assessment method Rifampicin TB, Tuberculosis. TCM, Traditional chinese medicines. Traditional medicines ULN, Upper limit of normal USA, United states of america

Journal

Journal of clinical and experimental hepatology
ISSN: 0973-6883
Titre abrégé: J Clin Exp Hepatol
Pays: India
ID NLM: 101574137

Informations de publication

Date de publication:
Historique:
received: 21 06 2020
accepted: 09 11 2020
entrez: 17 5 2021
pubmed: 18 5 2021
medline: 18 5 2021
Statut: ppublish

Résumé

Etiology of and outcomes following idiosyncratic drug-induced liver injury (DILI) vary geographically. We conducted a prospective study of DILI in India, from 2013 to 2018 and summarize the causes, clinical features, outcomes and predictors of mortality. We enrolled patients with DILI using international DILI expert working group criteria and Roussel Uclaf causality assessment method. Follow-up was up to 3 months from onset of DILI or until death. Multivariate logistics regression was carried out to determine predictors of non-survival. Among 1288 patients with idiosyncratic DILI, 51.4% were male, 68% developed jaundice, 68% required hospitalization and 8.2% had co-existing HIV infection. Concomitant features of skin reaction, ascites, and encephalopathy (HE) were seen in 19.5%, 16.4%, and 10% respectively. 32.4% had severe disease. Mean MELD score at presentation was 18.8 ± 8.8. Overall mortality was 12.3%; 65% in those with HE, 17.6% in patients who fulfilled Hy's law, and 16.6% in those that developed jaundice. Combination anti-TB drugs (ATD) 46.4%, complementary and alternative medicines (CAM) 13.9%, anti-epileptic drugs (AED) 8.1%, non-ATD antimicrobials 6.5%, anti-metabolites 3.8%, anti-retroviral drugs (ART)3.5%, NSAID2.6%, hormones 2.5%, and statins 1.4% were the top 9 causes. Univariate analysis identified, ascites, HE, serum albumin, bilirubin, creatinine, INR, MELD score (p < 0.001), transaminases (p < 0.04), and anti-TB drugs (p = 0.02) as predictors of non-survival. Only serum creatinine (p = 0.017), INR (p < 0.001), HE (p < 0.001), and ascites (p = 0.008), were significantly associated with mortality on multivariate analysis. ROC yielded a C-statistic of 0.811 for MELD and 0.892 for combination of serum creatinine, INR, ascites and HE. More than 50 different agents were associated with DILI. Mortality varied by drug class: 15% with ATD, 13.6% with CAM, 15.5% with AED, 5.8% with antibiotics. In India, ATD, CAM, AED, anti-metabolites and ART account for the majority of cases of DILI. The 3-month mortality was approximately 12%. Hy's law, presence of jaundice or MELD were predictors of mortality.

Sections du résumé

BACKGROUND BACKGROUND
Etiology of and outcomes following idiosyncratic drug-induced liver injury (DILI) vary geographically. We conducted a prospective study of DILI in India, from 2013 to 2018 and summarize the causes, clinical features, outcomes and predictors of mortality.
METHODS METHODS
We enrolled patients with DILI using international DILI expert working group criteria and Roussel Uclaf causality assessment method. Follow-up was up to 3 months from onset of DILI or until death. Multivariate logistics regression was carried out to determine predictors of non-survival.
RESULTS RESULTS
Among 1288 patients with idiosyncratic DILI, 51.4% were male, 68% developed jaundice, 68% required hospitalization and 8.2% had co-existing HIV infection. Concomitant features of skin reaction, ascites, and encephalopathy (HE) were seen in 19.5%, 16.4%, and 10% respectively. 32.4% had severe disease. Mean MELD score at presentation was 18.8 ± 8.8. Overall mortality was 12.3%; 65% in those with HE, 17.6% in patients who fulfilled Hy's law, and 16.6% in those that developed jaundice. Combination anti-TB drugs (ATD) 46.4%, complementary and alternative medicines (CAM) 13.9%, anti-epileptic drugs (AED) 8.1%, non-ATD antimicrobials 6.5%, anti-metabolites 3.8%, anti-retroviral drugs (ART)3.5%, NSAID2.6%, hormones 2.5%, and statins 1.4% were the top 9 causes. Univariate analysis identified, ascites, HE, serum albumin, bilirubin, creatinine, INR, MELD score (p < 0.001), transaminases (p < 0.04), and anti-TB drugs (p = 0.02) as predictors of non-survival. Only serum creatinine (p = 0.017), INR (p < 0.001), HE (p < 0.001), and ascites (p = 0.008), were significantly associated with mortality on multivariate analysis. ROC yielded a C-statistic of 0.811 for MELD and 0.892 for combination of serum creatinine, INR, ascites and HE. More than 50 different agents were associated with DILI. Mortality varied by drug class: 15% with ATD, 13.6% with CAM, 15.5% with AED, 5.8% with antibiotics.
CONCLUSION CONCLUSIONS
In India, ATD, CAM, AED, anti-metabolites and ART account for the majority of cases of DILI. The 3-month mortality was approximately 12%. Hy's law, presence of jaundice or MELD were predictors of mortality.

Identifiants

pubmed: 33994711
doi: 10.1016/j.jceh.2020.11.002
pii: S0973-6883(20)30175-4
pmc: PMC8103312
doi:

Types de publication

Journal Article

Langues

eng

Pagination

288-298

Informations de copyright

© 2020 Indian National Association for Study of the Liver. Published by Elsevier B.V. All rights reserved.

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Auteurs

Harshad Devarbhavi (H)

Department of Gastroenterology, St. John's Medical College Hospital, Bangalore, India.

Tarun Joseph (T)

Department of Gastroenterology, St. John's Medical College Hospital, Bangalore, India.

Nanjegowda Sunil Kumar (N)

Department of Gastroenterology, Government Medical College, Kozhikode, India.

Chetan Rathi (C)

Department of Gastroenterology, LTM Medical College Hospital, Mumbai, India.

Varghese Thomas (V)

Department of Gastroenterology, Government Medical College, Kozhikode, India.

Shivaram Prasad Singh (S)

Department of Gastroenterology, S.C.B Medical College Hospital, Cuttack, India.

Prabha Sawant (P)

Department of Gastroenterology, LTM Medical College Hospital, Mumbai, India.

Ashish Goel (A)

Department of Gastroenterology, Christian Medical College, Vellore, India.

Chundamannil E Eapen (CE)

Department of Gastroenterology, Christian Medical College, Vellore, India.

Prakash Rai (P)

Department of General Medicine, Holy Spirit Hospital, Mumbai, India.

Anil Arora (A)

Department of Gastroenterology, Sir Ganga Ram Hospital, New Delhi, India.

Venkatakrishnan Leelakrishnan (V)

Department of Gastroenterology, P.S.G Institute of Medical Sciences, Coimbatore, India.

Gayathri Gopalakrishnan (G)

Department of Gastroenterology, Narayana Hrudayalaya Hospitals, Bangalore, India.

Vishnu Vardhan Reddy (V)

Department of Gastroenterology, St. John's Medical College Hospital, Bangalore, India.

Rajvir Singh (R)

Acute Care Surgery, HGH, Hamad Medical Corporation, Doha, Qatar.

Bhabadev Goswami (B)

Department of Gastroenterology, Dispur Hospitals, Guwahati, India.

Jayanthi Venkataraman (J)

Department of Hepatology, Gleneagles Global Health City, Chennai, India.

Girisha Balaraju (G)

Department of Gastroenterology, Kasturba Medical College Hospital, Manipal, India.

Mallikarjun Patil (M)

Department of Gastroenterology, St. John's Medical College Hospital, Bangalore, India.

Rakesh Patel (R)

Department of Gastroenterology, Suyash Endoscopy Centre, Thane, India.

Sunil Taneja (S)

Department of Hepatology, Post Graduate Institute of Medical Education & Research, Chandigarh, India.

Abraham Koshy (A)

Department of Gastroenterology, Lakeshore Hospital, Kochi, India.

Padaki Nagaraja Rao (P)

Department of Gastroenterology, Asian Institute of Gastroenterology, Hyderabad, India.

Shiv Kumar Sarin (S)

Department of Hepatology, Institute of Liver and Biliary Sciences, New Delhi, India.

Pravin Rathi (P)

Department of Gastroenterology, B.Y.L. Nair Hospital, Mumbai, India.

Radhakrishna Dhiman (R)

Department of Hepatology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.

Ajay K Duseja (AK)

Department of Hepatology, Post Graduate Institute of Medical Education & Research, Chandigarh, India.

Joy Vargese (J)

Department of Hepatology, Gleneagles Global Health City, Chennai, India.

Ajay Kumar Jain (A)

Department of Gastroenterology, Choithram Hospital and Research Centre, Indore, India.

Manav Wadhawan (M)

Department of Gastroenterology, BLK Super Speciality Hospital, New Delhi, India.

Piyush Ranjan (P)

Department of Gastroenterology, Sir Ganga Ram Hospital, New Delhi, India.

Dheeraj Karanth (D)

Department of Gastroenterology, Vikram Hospital, Bangalore, India.

Panchapakesan Ganesh (P)

Department of Gastroenterology, Sri Ramachandra Hospital, Chennai, India.

Sandeep Nijhawan (S)

Department of Gastroenterology, Sawai Man Singh Medical College, Jaipur, India.

Gopal Krishna Dhali (G)

School of Digestive and Liver Diseases, Institute of Post Graduate Medical Education & Research, Kolkata, India.

Channagiri K Adarsh (CK)

Department of Gastroenterology, BGS Gleneagles Global Hospitals, Bangalore, India.

Ajay Jhaveri (A)

Department of Gastroenterology, Jaslok Hospital and Research Center, Mumbai, India.

Aabha Nagral (A)

Department of Gastroenterology, Jaslok Hospital and Research Center, Mumbai, India.

Prasanna Rao (P)

Department of Gastroenterology, Apollo Hospitals, Bangalore, India.
Department of Gastroenterology and Hepatology, AIIMS, New Delhi, India.

Classifications MeSH