Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Meta-Analysis
. 2022 Oct;45(10):1037-1048.
doi: 10.1007/s40264-022-01215-x. Epub 2022 Aug 10.

Use of Electrocardiogram Monitoring in Adult Patients Taking High-Risk QT Interval Prolonging Medicines in Clinical Practice: Systematic Review and Meta-analysis

Affiliations
Meta-Analysis

Use of Electrocardiogram Monitoring in Adult Patients Taking High-Risk QT Interval Prolonging Medicines in Clinical Practice: Systematic Review and Meta-analysis

Marijana Putnikovic et al. Drug Saf. 2022 Oct.

Abstract

Introduction: Electrocardiogram (ECG) monitoring is an important tool to detect and mitigate the risk of potentially fatal drug-induced QT prolongation and remains fundamental in supporting the quality use of high-risk QT interval prolonging medicines.

Objective: The aim of this systematic review was to determine the prevalence of baseline and/or follow-up ECG use in adult patients taking high-risk QT interval prolonging medicines in clinical practice.

Methods: CINAHL, Cochrane Library, Embase, PubMed, EThOS, OpenGrey and Proquest were searched for studies in adults that reported ECG use at baseline and/or at follow-up in relation to the initiation of a high-risk QT interval prolonging medicine in any clinical setting; either hospital or non-hospital. Two reviewers independently assessed the methodological quality of included studies. Proportional meta-analysis was conducted with all studies reporting baseline ECG use, before medicine initiation, and follow-up ECG use, within 30 days of medicine initiation.

Results: There was variability in baseline ECG use according to the practice setting. The prevalence of baseline ECG use for high-risk QT interval prolonging medicines was moderate to high in the hospital setting at 75.1% (95% CI 64.3-84.5); however, the prevalence of baseline ECG use was low in the non-hospital setting at 33.7% (95% CI 25.8-42.2). The prevalence of follow-up ECG use was low to moderate in the hospital setting at 39.2% (95% CI 28.2-50.8) and could not be determined for the non-hospital setting.

Conclusions: The use of ECG monitoring for high-risk QT interval prolonging medicines is strongly influenced by the clinical practice setting. Baseline ECG use occurs more in the hospital setting in comparison to the non-hospital setting. There is lower use of follow-up ECG in comparison to baseline ECG.

PubMed Disclaimer

Conflict of interest statement

Not applicable.

Figures

Fig. 1
Fig. 1
Flow diagram of search results and review process (PRISMA 2020) [13]
Fig. 2
Fig. 2
Proportional meta-analysis of baseline ECG use—hospital setting only and leave three out (studies with additional biases)
Fig. 3
Fig. 3
Proportional meta-analysis of baseline ECG use—non-hospital setting only
Fig. 4
Fig. 4
Proportional meta-analysis of follow-up ECG use—hospital setting only and leave two out (studies with additional biases)
Fig. 5
Fig. 5
Proportional meta-analysis of follow-up ECG use—hospital setting only and high-quality studies only; any clinical setting and high-quality studies only
Fig. 6
Fig. 6
Proportional meta-analysis of follow-up ECG use—any clinical setting and leave two out (studies with additional biases)

Comment in

  • Conundrum of Clinical QTc Monitoring.
    Malik M. Malik M. Drug Saf. 2022 Oct;45(10):1011-1014. doi: 10.1007/s40264-022-01229-5. Epub 2022 Aug 26. Drug Saf. 2022. PMID: 36018490 No abstract available.

Similar articles

Cited by

References

    1. Straus SM, et al. Non-cardiac QTc-prolonging drugs and the risk of sudden cardiac death. Eur Heart J. 2005;26(19):2007–2012. doi: 10.1093/eurheartj/ehi312. - DOI - PubMed
    1. Schwartz PJ, Woosley RL. Predicting the unpredictable: drug-induced QT prolongation and torsades de pointes. J Am Coll Cardiol. 2016;67(13):1639–1650. doi: 10.1016/j.jacc.2015.12.063. - DOI - PubMed
    1. QT interval and drug therapy. BMJ. 2016;353:i2732. - PubMed
    1. Jardin CG, Putney D, Michaud S. Assessment of drug-induced torsade de pointes risk for hospitalized high-risk patients receiving QT-prolonging agents. Ann Pharmacother. 2014;48(2):196–202. doi: 10.1177/1060028013512614. - DOI - PubMed
    1. Trinkley KE, et al. QT interval prolongation and the risk of torsades de pointes: essentials for clinicians. Curr Med Res Opin. 2013;29(12):1719–1726. doi: 10.1185/03007995.2013.840568. - DOI - PubMed

LinkOut - more resources