Importance of Hepatitis C Virus RNA Testing in Patients with Suspected Drug-Induced Liver Injury.


Journal

Digestive diseases and sciences
ISSN: 1573-2568
Titre abrégé: Dig Dis Sci
Pays: United States
ID NLM: 7902782

Informations de publication

Date de publication:
09 2019
Historique:
received: 14 12 2018
accepted: 12 03 2019
pubmed: 31 3 2019
medline: 24 3 2020
entrez: 31 3 2019
Statut: ppublish

Résumé

The aims were to review the diagnosis, testing and presentation of acute hepatitis C (HCV) in patients initially diagnosed to have drug-induced liver injury (DILI) enrolled in the US DILI Network. All patients with suspected DILI underwent testing for competing causes of liver injury and returned for 6-month follow-up. Causality was adjudicated by consensus expert opinion. Between 2004 and 2016, 1518 patients were enrolled and adjudicated and underwent 6 months of follow-up. Initial locally acquired anti-HCV results were available in 1457 (96%), but HCV RNA in only 795 (52%). Stored sera were available for repeat testing, so that results were available on all 1518 patients (1457 for anti-HCV and 1482 for HCV RNA). A total of 104 subjects (6.9%) had evidence of HCV infection-10 positive for HCV RNA alone, 16 for anti-HCV alone and 78 for both. All 104 HCV-positive cases were reviewed, and 23 cases were adjudicated as acute HCV. All presented with acute hepatocellular injury with median ALT 1448 U/L, alkaline phosphatase 232 U/L and total bilirubin 10.8 mg/dL. Twenty-two (96%) patients were jaundiced. While all 23 cases initially had been suspected of having DILI, 19 were adjudicated as acute HCV and not DILI at the 6-month follow-up; while 4 were still considered DILI. Twenty-three of 1518 (1.5%) cases of suspected DILI were due to acute HCV infection. We recommend that initial and follow-up HCV RNA testing should be performed to exclude HCV in patients with acute hepatocellular injury and suspected DILI.

Sections du résumé

BACKGROUND AND AIMS
The aims were to review the diagnosis, testing and presentation of acute hepatitis C (HCV) in patients initially diagnosed to have drug-induced liver injury (DILI) enrolled in the US DILI Network.
METHODS
All patients with suspected DILI underwent testing for competing causes of liver injury and returned for 6-month follow-up. Causality was adjudicated by consensus expert opinion.
RESULTS
Between 2004 and 2016, 1518 patients were enrolled and adjudicated and underwent 6 months of follow-up. Initial locally acquired anti-HCV results were available in 1457 (96%), but HCV RNA in only 795 (52%). Stored sera were available for repeat testing, so that results were available on all 1518 patients (1457 for anti-HCV and 1482 for HCV RNA). A total of 104 subjects (6.9%) had evidence of HCV infection-10 positive for HCV RNA alone, 16 for anti-HCV alone and 78 for both. All 104 HCV-positive cases were reviewed, and 23 cases were adjudicated as acute HCV. All presented with acute hepatocellular injury with median ALT 1448 U/L, alkaline phosphatase 232 U/L and total bilirubin 10.8 mg/dL. Twenty-two (96%) patients were jaundiced. While all 23 cases initially had been suspected of having DILI, 19 were adjudicated as acute HCV and not DILI at the 6-month follow-up; while 4 were still considered DILI.
CONCLUSIONS
Twenty-three of 1518 (1.5%) cases of suspected DILI were due to acute HCV infection. We recommend that initial and follow-up HCV RNA testing should be performed to exclude HCV in patients with acute hepatocellular injury and suspected DILI.

Identifiants

pubmed: 30927209
doi: 10.1007/s10620-019-05591-w
pii: 10.1007/s10620-019-05591-w
pmc: PMC6706305
mid: NIHMS1525764
doi:

Substances chimiques

Hepatitis C Antibodies 0
RNA, Viral 0
Alanine Transaminase EC 2.6.1.2
Alkaline Phosphatase EC 3.1.3.1
Bilirubin RFM9X3LJ49

Types de publication

Journal Article Multicenter Study Observational Study Research Support, N.I.H., Extramural Research Support, N.I.H., Intramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2645-2652

Subventions

Organisme : NIDDK NIH HHS
ID : U01 DK065211
Pays : United States
Organisme : NIDDK NIH HHS
ID : U24 DK065176
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK083027
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK083020
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001855
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK065184
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK065201
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK100928
Pays : United States

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Auteurs

Jawad Ahmad (J)

Division of Liver Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA. jawad.ahmad@mountsinai.org.

K Rajender Reddy (KR)

Division of Gastroenterology and Hepatology, University of Pennsylvania, Philadelphia, USA.

Hans L Tillmann (HL)

Division of Gastroenterology, Hepatology and Nutrition, East Carolina University, Greenville, USA.

Paul H Hayashi (PH)

Division of Gastroenterology and Hepatology, University of North Carolina School of Medicine, Chapel Hill, USA.

Naga Chalasani (N)

Division of Gastroenterology and Hepatology, Indiana University School of Medicine, Indianapolis, USA.

Robert J Fontana (RJ)

Division of Gastroenterology and Hepatology, University of Michigan Medical School, Ann Arbor, USA.

Victor J Navarro (VJ)

Einstein Medical Center, Philadelphia, USA.

Andrew Stolz (A)

Division of Gastrointestinal and Liver Diseases, Keck School of Medicine of University of Southern California, Los Angeles, USA.

Huiman Barnhart (H)

Duke Clinical Research Institute, Duke University, Durham, USA.

Gavin A Cloherty (GA)

Volwiler Society, Head Infectious Disease Research, Abbott Laboratories, Lake Bluff, USA.

Jay H Hoofnagle (JH)

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Bethesda, USA.

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