A case of complete atrioventricular block with extremely high blood concentration of azelnidipine

Abstract Background Azelnidipine, a dihydropyridine calcium channel blocker (CCB), has less adverse effects (e.g. hot flushes and reflex tachycardia) compared to other dihydropyridine CCBs. Azelnidipine has been reported to reduce heart rate as opposed to inducing tachycardia. No evidence of bradyca...

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Autores principales: Naohito Ide, Ayaka Mochizuki, Yoshiyuki Kagawa, Masaharu Ito
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Publicado: BMC 2021
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spelling oai:doaj.org-article:2f3bbe61056444408595b97b917db2e72021-12-05T12:03:12ZA case of complete atrioventricular block with extremely high blood concentration of azelnidipine10.1186/s40780-021-00230-x2055-0294https://doaj.org/article/2f3bbe61056444408595b97b917db2e72021-12-01T00:00:00Zhttps://doi.org/10.1186/s40780-021-00230-xhttps://doaj.org/toc/2055-0294Abstract Background Azelnidipine, a dihydropyridine calcium channel blocker (CCB), has less adverse effects (e.g. hot flushes and reflex tachycardia) compared to other dihydropyridine CCBs. Azelnidipine has been reported to reduce heart rate as opposed to inducing tachycardia. No evidence of bradycardia or complete atrioventricular block (CAVB) with azelnidipine treatment has been reported. Case presentation In the present study, a 92-year-old woman was diagnosed with CAVB while taking azelnidipine and simvastatin for an extended period of time, and referred to our medical center. It was thought that the CAVB may have been an adverse effect of azelnidipine treatment. Specifically, it was considered that in this patient, one of the causes might be the concomitant use of simvastatin inhibiting the metabolism of azelnidipine by cytochrome P450 enzyme 3A4. Consequently, it was suggested to the patient’s physician that the patient’s serum azelnidipine levels be measured and treatment with azelnidipine and simvastatin be discontinued. The patient’s serum concentration of azelnidipine at the time of her visit to our center was 63.4 ng/mL, higher than the normal acceptable level. There was no occurrence of CAVB for 4 weeks, to present, following discontinuation of azelnidipine and simvastatin treatment. Conclusions Azelnidipine has a different mechanism of action that other CCBs. In very rare cases, it may cause CAVB when combined with CYP3A4 inhibitors. If a patient taking azelnidipine is diagnosed with CAVB, physicians should suspect that the condition may be an adverse effect of azelnidipine and should consider discontinuing azelnidipine. And, in the elderly, it is necessary to avoid concomitant use of CYP3A4 inhibitors.Naohito IdeAyaka MochizukiYoshiyuki KagawaMasaharu ItoBMCarticleAzelnidipineAdverse eventsCalcium channel blockerComplete atrioventricular blockDrug interactionSimvastatinTherapeutics. PharmacologyRM1-950Pharmacy and materia medicaRS1-441ENJournal of Pharmaceutical Health Care and Sciences, Vol 7, Iss 1, Pp 1-6 (2021)
institution DOAJ
collection DOAJ
language EN
topic Azelnidipine
Adverse events
Calcium channel blocker
Complete atrioventricular block
Drug interaction
Simvastatin
Therapeutics. Pharmacology
RM1-950
Pharmacy and materia medica
RS1-441
spellingShingle Azelnidipine
Adverse events
Calcium channel blocker
Complete atrioventricular block
Drug interaction
Simvastatin
Therapeutics. Pharmacology
RM1-950
Pharmacy and materia medica
RS1-441
Naohito Ide
Ayaka Mochizuki
Yoshiyuki Kagawa
Masaharu Ito
A case of complete atrioventricular block with extremely high blood concentration of azelnidipine
description Abstract Background Azelnidipine, a dihydropyridine calcium channel blocker (CCB), has less adverse effects (e.g. hot flushes and reflex tachycardia) compared to other dihydropyridine CCBs. Azelnidipine has been reported to reduce heart rate as opposed to inducing tachycardia. No evidence of bradycardia or complete atrioventricular block (CAVB) with azelnidipine treatment has been reported. Case presentation In the present study, a 92-year-old woman was diagnosed with CAVB while taking azelnidipine and simvastatin for an extended period of time, and referred to our medical center. It was thought that the CAVB may have been an adverse effect of azelnidipine treatment. Specifically, it was considered that in this patient, one of the causes might be the concomitant use of simvastatin inhibiting the metabolism of azelnidipine by cytochrome P450 enzyme 3A4. Consequently, it was suggested to the patient’s physician that the patient’s serum azelnidipine levels be measured and treatment with azelnidipine and simvastatin be discontinued. The patient’s serum concentration of azelnidipine at the time of her visit to our center was 63.4 ng/mL, higher than the normal acceptable level. There was no occurrence of CAVB for 4 weeks, to present, following discontinuation of azelnidipine and simvastatin treatment. Conclusions Azelnidipine has a different mechanism of action that other CCBs. In very rare cases, it may cause CAVB when combined with CYP3A4 inhibitors. If a patient taking azelnidipine is diagnosed with CAVB, physicians should suspect that the condition may be an adverse effect of azelnidipine and should consider discontinuing azelnidipine. And, in the elderly, it is necessary to avoid concomitant use of CYP3A4 inhibitors.
format article
author Naohito Ide
Ayaka Mochizuki
Yoshiyuki Kagawa
Masaharu Ito
author_facet Naohito Ide
Ayaka Mochizuki
Yoshiyuki Kagawa
Masaharu Ito
author_sort Naohito Ide
title A case of complete atrioventricular block with extremely high blood concentration of azelnidipine
title_short A case of complete atrioventricular block with extremely high blood concentration of azelnidipine
title_full A case of complete atrioventricular block with extremely high blood concentration of azelnidipine
title_fullStr A case of complete atrioventricular block with extremely high blood concentration of azelnidipine
title_full_unstemmed A case of complete atrioventricular block with extremely high blood concentration of azelnidipine
title_sort case of complete atrioventricular block with extremely high blood concentration of azelnidipine
publisher BMC
publishDate 2021
url https://doaj.org/article/2f3bbe61056444408595b97b917db2e7
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