Bictegravir/emtricitabine/tenofovir alafenamide combination in the management of kidney transplant patients with HIV receiving immunosuppressants.


Journal

Journal of chemotherapy (Florence, Italy)
ISSN: 1973-9478
Titre abrégé: J Chemother
Pays: England
ID NLM: 8907348

Informations de publication

Date de publication:
May 2022
Historique:
pubmed: 29 6 2021
medline: 23 4 2022
entrez: 28 6 2021
Statut: ppublish

Résumé

We report here a drug-drug interaction with tacrolimus in a HIV-positive patient with renal transplant, after switch from highly active antiretroviral therapy with boosted protease inhibitors to the combination bictegravir/emtricitabine/tenofovir alafenamide. Although the tacrolimus doses were adapted to take account of the pharmacokinetic interactions with protease inhibitors, a tacrolimus overdosage occurred in the patient nonetheless. Through this case report, we highlight the need to consider a sufficient timeframe of withdrawal of protease inhibitors, which induce a prolonged drug-drug interaction with tacrolimus. To conclude, we purport that the combination bictegravir/emtricitabine/tenofovir alafenamide could be an attractive alternative in the context of transplantation provided a discontinuation of boosted protease inhibitors for more than 48 hours before introducing tacrolimus.

Identifiants

pubmed: 34180378
doi: 10.1080/1120009X.2021.1940436
doi:

Substances chimiques

Amides 0
Anti-HIV Agents 0
Drug Combinations 0
Heterocyclic Compounds, 3-Ring 0
Heterocyclic Compounds, 4 or More Rings 0
Immunosuppressive Agents 0
Piperazines 0
Protease Inhibitors 0
Pyridones 0
bictegravir 8GB79LOJ07
Tenofovir 99YXE507IL
tenofovir alafenamide EL9943AG5J
Emtricitabine G70B4ETF4S
Adenine JAC85A2161
Alanine OF5P57N2ZX
Tacrolimus WM0HAQ4WNM

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

199-202

Auteurs

Jennifer Lagoutte-Renosi (J)

Service de Pharmacologie Clinique et Toxicologie, CHU Besançon, Besançon, France.
EA 3920, Université Bourgogne Franche-Comté, Besançon, France.

Mylène Flammang (M)

Service de Pharmacologie Clinique et Toxicologie, CHU Besançon, Besançon, France.

Didier Ducloux (D)

Service de Néphrologie, Dialyse et Transplantation Rénale, CHU Besançon, Besançon, France.
Université Bourgogne Franche-Comté, Besançon, France.

Jamal Bamoulid (J)

Service de Néphrologie, Dialyse et Transplantation Rénale, CHU Besançon, Besançon, France.
Université Bourgogne Franche-Comté, Besançon, France.

Pierre-Yves Royer (PY)

Hôpital Nord Franche-Comté, Montbéliard, France.

Quentin Lepiller (Q)

Service de Virologie, CHU Besançon, Besançon, France.
EA 3181, Université Bourgogne Franche-Comté, Besançon, France.

Anne-Laure Clairet (AL)

Université Bourgogne Franche-Comté, Besançon, France.
CHU Besançon, Besançon, France.

Siamak Davani (S)

Service de Pharmacologie Clinique et Toxicologie, CHU Besançon, Besançon, France.
EA 3920, Université Bourgogne Franche-Comté, Besançon, France.

Patrice Muret (P)

Service de Pharmacologie Clinique et Toxicologie, CHU Besançon, Besançon, France.
Université Bourgogne Franche-Comté, Besançon, France.

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Classifications MeSH