Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/33924
Title: Comorbidities and concomitant medications in patients with chronic hepatitis C virus infection receiving second-generation direct-acting antiviral regimens in Belgium : an observational study
Authors: Bourgeois, S.
Mulkay, J. P.
Cool, M.
Verhelst, X.
ROBAEYS, Geert 
Lasser, L.
Lefebvre, V
Colle, I
Van Steenkiste, C.
Decaestecker, J.
Coulon, S.
VENKEN, Koen 
Vanwolleghem, T.
Issue Date: 2021
Publisher: UNIV CATHOLIQUE LOUVAIN-UCL
Source: ACTA GASTRO-ENTEROLOGICA BELGICA, 84 (1) , p. 33 -41
Abstract: Objective : To describe comorbidities and concomitant medications in patients initiating treatment for hepatitis C virus (HCV) infection with direct-acting antiviral (DAA) regimens in Belgium. Methods : This was a noninterventional, observational, multi-center study of data from patient charts. Adult patients with HCV infection receiving second-generation DAA therapy were included. Comorbidities were assessed at the time of HCV treatment initiation. Concomitant medications were recorded at the time of diagnosis and at treatment initiation. Potential clinically relevant drug-drug interactions (DDIs) were assessed based on information available at www.hep-druginteractions.org. The primary objective was to describe concomitant medication use; secondary objectives were to describe modifications in concomitant therapies and comorbidities. Results : 405 patients were included. A total of 956 comorbidities were reported by 362 patients (median, 2; range, 0-15). The most common comorbidities were hypertension (27.2%); HIV coinfection (22.5%), and type 2 diabetes mellitus (14.3%). Overall, 1455 concomitant medications were being taken by 365 patients (90.1%; median, 3; range 0-16). The most common concomitant medications were psycholeptics (28.6%), antiviral agents (24.2%), and medications for acid-related disorders (21.0%) Overall, 74/365 (20.3%) patients receiving a concomitant medication required an adaptation to their concomitant medication. The medications that most frequently required change were drugs for acid-related disorders (n = 14) and antiviral drugs (n = 5); those that were most frequently stopped were lipid-modifying drugs (n = 25) and drugs for acid-related disorders (n = 13). Conclusion : Physicians are aware of the potential for DDIs with DAAs, but improved alignment between clinical practice and theoretical recommendations is required.
Notes: Bourgeois, S (corresponding author), ZNA Antwerp, Lindendreef 1, B-2020 Antwerp, Belgium.
stefan.bourgeois@zna.be
Other: Bourgeois, S (corresponding author), ZNA Antwerp, Lindendreef 1, B-2020 Antwerp, Belgium. stefan.bourgeois@zna.be
Keywords: hepatitis C;drug-drug interactions;direct-acting antivirals;Belgium;co-medication
Document URI: http://hdl.handle.net/1942/33924
ISSN: 1784-3227
e-ISSN: 1784-3227
ISI #: WOS:000624536600007
Category: A1
Type: Journal Contribution
Validations: ecoom 2022
Appears in Collections:Research publications

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