Should we still monitor QTc duration in frail older patients on low-dose haloperidol? A prospective observational cohort study.


Journal

Age and ageing
ISSN: 1468-2834
Titre abrégé: Age Ageing
Pays: England
ID NLM: 0375655

Informations de publication

Date de publication:
24 08 2020
Historique:
received: 02 04 2019
pubmed: 3 7 2020
medline: 29 7 2021
entrez: 3 7 2020
Statut: ppublish

Résumé

Haloperidol at high dosage is associated with QTc prolongation and polymorphic ventricular arrhythmia but the effects of low-dose haloperidol remain unknown. To evaluate the effects of low-dose haloperidol on QTc-duration in frail hospitalized elderly patients with delirium. A prospective observational study including hospitalized patients aged ≥70 years with Groningen Frailty Index-score > 3. We included 150 patients who received haloperidol and 150 age- and frailty-matched control patients. Serial ECG recordings were performed at hospital admission and during hospitalization. QT-interval was corrected according to Framingham (QTc). Patients were grouped according to baseline QTc in normal (nQTc), borderline (bQTc) or abnormal (aQTc). Primary outcome was change in QTc-duration between first and second ECG. Potentially dangerous QTc was defined as QTc >500 ms or an increase of >50 ms. Patients in the haloperidol group (48% male, mean age 85y, nQT n = 98, bQT n = 31, aQT n = 20) received an average dose of 1.5 mg haloperidol per 24 hours. QTc decreased in patients with borderline (mean - 15 ± 29 ms, P < 0.05) or abnormal (-19 ± 27 ms, P < 0.05) QTc at baseline, no patients developed dangerous QTc-duration. In the control group (41% male, mean age 84y, nQT n = 99 bQT n = 29, aQT n = 22) QTc decreased to a similar extent (bQT -7 ± 16 ms, aQTc -23 ± 20 ms). A trend to QTc shortening was seen, especially in patients with borderline or abnormal QTc at baseline, regardless of haloperidol use. These findings suggest that ECG monitoring of frail elderly patients who receive low-dose haloperidol, may not be necessary.

Sections du résumé

BACKGROUND
Haloperidol at high dosage is associated with QTc prolongation and polymorphic ventricular arrhythmia but the effects of low-dose haloperidol remain unknown.
OBJECTIVE
To evaluate the effects of low-dose haloperidol on QTc-duration in frail hospitalized elderly patients with delirium.
METHODS
A prospective observational study including hospitalized patients aged ≥70 years with Groningen Frailty Index-score > 3. We included 150 patients who received haloperidol and 150 age- and frailty-matched control patients. Serial ECG recordings were performed at hospital admission and during hospitalization. QT-interval was corrected according to Framingham (QTc). Patients were grouped according to baseline QTc in normal (nQTc), borderline (bQTc) or abnormal (aQTc). Primary outcome was change in QTc-duration between first and second ECG. Potentially dangerous QTc was defined as QTc >500 ms or an increase of >50 ms.
RESULTS
Patients in the haloperidol group (48% male, mean age 85y, nQT n = 98, bQT n = 31, aQT n = 20) received an average dose of 1.5 mg haloperidol per 24 hours. QTc decreased in patients with borderline (mean - 15 ± 29 ms, P < 0.05) or abnormal (-19 ± 27 ms, P < 0.05) QTc at baseline, no patients developed dangerous QTc-duration. In the control group (41% male, mean age 84y, nQT n = 99 bQT n = 29, aQT n = 22) QTc decreased to a similar extent (bQT -7 ± 16 ms, aQTc -23 ± 20 ms).
CONCLUSION
A trend to QTc shortening was seen, especially in patients with borderline or abnormal QTc at baseline, regardless of haloperidol use. These findings suggest that ECG monitoring of frail elderly patients who receive low-dose haloperidol, may not be necessary.

Identifiants

pubmed: 32614955
pii: 5837829
doi: 10.1093/ageing/afaa066
doi:

Substances chimiques

Antipsychotic Agents 0
Haloperidol J6292F8L3D

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

829-836

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the British Geriatrics Society. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Ellen Castro (E)

Geriatrics and Cardiology Department, Zuyderland Medical Centre, 6162 BG Sittard-Geleen, The Netherlands.

Frank Körver (F)

Geriatrics and Cardiology Department, Zuyderland Medical Centre, 6162 BG Sittard-Geleen, The Netherlands.

Audrey Merry (A)

Geriatrics and Cardiology Department, Zuyderland Medical Centre, 6162 BG Sittard-Geleen, The Netherlands.

Fieke van Moorsel (F)

Geriatrics and Cardiology Department, Zuyderland Medical Centre, 6162 BG Sittard-Geleen, The Netherlands.

Mark Hazebroek (M)

Cardiology Department, Maastricht University Medical Centre, Maastricht 6229 HX, The Netherlands.

Machiel Smid (M)

Geriatrics and Cardiology Department, Zuyderland Medical Centre, 6162 BG Sittard-Geleen, The Netherlands.

Sylvain Ploux (S)

IHU Liryc, Electrophysiology and Heart Modeling Institute, Foundation Bordeaux Université, F-33600 Pessac, Bordeaux, France.

Pierre Bordachar (P)

IHU Liryc, Electrophysiology and Heart Modeling Institute, Foundation Bordeaux Université, F-33600 Pessac, Bordeaux, France.

Frits Prinzen (F)

Cardiology Department, Maastricht University Medical Centre, Maastricht 6229 HX, The Netherlands.

Walther Sipers (W)

Geriatrics and Cardiology Department, Zuyderland Medical Centre, 6162 BG Sittard-Geleen, The Netherlands.

Marc Strik (M)

Cardiology Department, Maastricht University Medical Centre, Maastricht 6229 HX, The Netherlands.
IHU Liryc, Electrophysiology and Heart Modeling Institute, Foundation Bordeaux Université, F-33600 Pessac, Bordeaux, France.

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