Onset of systemic arterial hypertension after initiation of elexacaftor/tezacaftor/ivacaftor in adults with cystic fibrosis: A case series.


Journal

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
ISSN: 1873-5010
Titre abrégé: J Cyst Fibros
Pays: Netherlands
ID NLM: 101128966

Informations de publication

Date de publication:
09 2022
Historique:
received: 17 12 2021
revised: 07 04 2022
accepted: 11 04 2022
pubmed: 23 4 2022
medline: 28 9 2022
entrez: 22 4 2022
Statut: ppublish

Résumé

Elexacaftor/tezacaftor/ivacaftor (ETI) is associated with major improvements in respiratory outcomes of individuals with cystic fibrosis (CF) and at least one Phe508del mutation. Although ETI was well tolerated in registration studies, the attention on adverse events not previously described is very high in the post-marketing phase. In this case series we report the onset of systemic arterial hypertension in 4 individuals with CF within the first weeks of starting therapy. All patients needed cardiac evaluation and started chronic anti-hypertensive therapy. Until more data is available, this report could foster the attention of CF physicians towards careful monitoring of cardiovascular parameters in patients starting ETI.

Identifiants

pubmed: 35450770
pii: S1569-1993(22)00099-6
doi: 10.1016/j.jcf.2022.04.010
pii:
doi:

Substances chimiques

Aminophenols 0
Antihypertensive Agents 0
Benzodioxoles 0
Chloride Channel Agonists 0
Drug Combinations 0
Indoles 0
Pyrazoles 0
Pyridines 0
Pyrrolidines 0
Quinolones 0
tezacaftor 0
Cystic Fibrosis Transmembrane Conductance Regulator 126880-72-6
ivacaftor 1Y740ILL1Z
elexacaftor RRN67GMB0V

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

885-887

Informations de copyright

Copyright © 2022. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors have no specific funding to report for this work.

Auteurs

Andrea Gramegna (A)

Department of Pathophysiology and Transplantation, University of Milan, Italy; Internal Medicine Department, Respiratory Unit and Cystic Fibrosis Adult Center. Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy. Electronic address: andrea.gramegna@unimi.it.

Claudia De Petro (C)

Department of Pathophysiology and Transplantation, University of Milan, Italy; Internal Medicine Department, Respiratory Unit and Cystic Fibrosis Adult Center. Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Gloria Leonardi (G)

Department of Pathophysiology and Transplantation, University of Milan, Italy; Internal Medicine Department, Respiratory Unit and Cystic Fibrosis Adult Center. Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Martina Contarini (M)

Internal Medicine Department, Respiratory Unit and Cystic Fibrosis Adult Center. Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Francesco Amati (F)

Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy; IRCCS Humanitas Research Hospital, Respiratory Unit, Rozzano, Italy.

Roberto Meazza (R)

Cardiology Unit, Internal Medicine Department, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Stefano Carugo (S)

Cardiology Unit, Internal Medicine Department, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Francesco Blasi (F)

Department of Pathophysiology and Transplantation, University of Milan, Italy; Internal Medicine Department, Respiratory Unit and Cystic Fibrosis Adult Center. Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

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