Rechallenge after anti-tuberculosis drug-induced liver injury in a high HIV prevalence cohort.

anti-tuberculosis drugs drug-induced liver injury positive rechallenge pyrazinamide treatment interruption tuberculosis

Journal

Southern African journal of HIV medicine
ISSN: 2078-6751
Titre abrégé: South Afr J HIV Med
Pays: South Africa
ID NLM: 100965417

Informations de publication

Date de publication:
2022
Historique:
received: 01 02 2022
accepted: 22 03 2022
entrez: 4 8 2022
pubmed: 5 8 2022
medline: 5 8 2022
Statut: epublish

Résumé

There are limited data on the outcomes of rechallenge with anti-tuberculosis therapy (ATT) following anti-tuberculosis drug-induced liver injury (AT-DILI) in a high HIV prevalence setting. To describe the outcomes of rechallenge with first-line ATT. Hospitalised participants with AT-DILI who were enrolled into a randomised controlled trial of N-acetylcysteine in Cape Town, South Africa, were followed up until completion of ATT rechallenge. We described rechallenge outcomes, and identified associations with recurrence of liver injury on rechallenge (positive rechallenge). Seventy-nine participants were rechallenged of whom 41 (52%) were female. Mean age was 37 years (standard deviation [s.d.] ±10). Sixty-eight (86%) were HIV-positive, of whom 34 (50%) were on antiretroviral therapy (ART) at time of AT-DILI presentation. Five participants had serious adverse reactions to an aminoglycoside included in the alternate ATT regimen given after first-line ATT interruption: acute kidney injury in three and hearing loss in two. The median time from first-line ATT interruption to start of first-line ATT rechallenge was 13 days (interquartile range [IQR]: 8-18 days). Antiretroviral therapy was interrupted for a median of 32 days (IQR: 17-58) among HIV-positive participants on ART before AT-DILI. Fourteen participants had positive rechallenge (18%). Positive rechallenge was associated with pyrazinamide rechallenge ( Rechallenge was successful in most of our cohort. Pyrazinamide rechallenge should be carefully considered.

Sections du résumé

Background UNASSIGNED
There are limited data on the outcomes of rechallenge with anti-tuberculosis therapy (ATT) following anti-tuberculosis drug-induced liver injury (AT-DILI) in a high HIV prevalence setting.
Objectives UNASSIGNED
To describe the outcomes of rechallenge with first-line ATT.
Method UNASSIGNED
Hospitalised participants with AT-DILI who were enrolled into a randomised controlled trial of N-acetylcysteine in Cape Town, South Africa, were followed up until completion of ATT rechallenge. We described rechallenge outcomes, and identified associations with recurrence of liver injury on rechallenge (positive rechallenge).
Results UNASSIGNED
Seventy-nine participants were rechallenged of whom 41 (52%) were female. Mean age was 37 years (standard deviation [s.d.] ±10). Sixty-eight (86%) were HIV-positive, of whom 34 (50%) were on antiretroviral therapy (ART) at time of AT-DILI presentation. Five participants had serious adverse reactions to an aminoglycoside included in the alternate ATT regimen given after first-line ATT interruption: acute kidney injury in three and hearing loss in two. The median time from first-line ATT interruption to start of first-line ATT rechallenge was 13 days (interquartile range [IQR]: 8-18 days). Antiretroviral therapy was interrupted for a median of 32 days (IQR: 17-58) among HIV-positive participants on ART before AT-DILI. Fourteen participants had positive rechallenge (18%). Positive rechallenge was associated with pyrazinamide rechallenge (
Conclusion UNASSIGNED
Rechallenge was successful in most of our cohort. Pyrazinamide rechallenge should be carefully considered.

Identifiants

pubmed: 35923608
doi: 10.4102/sajhivmed.v23i1.1376
pii: HIVMED-23-1376
pmc: PMC9257779
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1376

Informations de copyright

© 2022. The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no financial or personal relationships that may have inappropriately influenced them in writing this article.

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Auteurs

Muhammed Shiraz Moosa (MS)

Department of Medicine, New Somerset Hospital, Cape Town, South Africa.
Department of Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Gary Maartens (G)

Department of Medicine, Division of Clinical Pharmacology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Hannah Gunter (H)

Department of Medicine, Division of Clinical Pharmacology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Shaazia Allie (S)

Department of Medicine, Division of Clinical Pharmacology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Mohamed F Chughlay (MF)

Department of Medicine, Division of Clinical Pharmacology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Mashiko Setshedi (M)

Department of Medicine, Division of Gastroenterology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Sean Wasserman (S)

Department of Medicine, Division of Infectious Diseases, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

David F Stead (DF)

Department of Medicine, New Somerset Hospital, Cape Town, South Africa.
Department of Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Karen Cohen (K)

Department of Medicine, Division of Clinical Pharmacology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Classifications MeSH