Literature DB >> 23529904

Agreement between ICU clinicians and electrophysiology cardiologists on the decision to initiate a QTc-interval prolonging medication in critically ill patients with potential risk factors for torsade de pointes: a comparative, case-based evaluation.

Justin M Fongemie1, Nada S Al-Qadheeb, N A Mark Estes, Russel J Roberts, Yutthapong Temtanakitpaisan, Robin Ruthazer, John W Devlin.   

Abstract

STUDY
OBJECTIVES: To measure concordance between different intensive care unit (ICU) clinicians and a consensus group of electrophysiology (EP) cardiologists for use of a common rate-corrected QT interval (QTc)-prolonging medication in cases containing different potential risk factor(s) for torsade de pointes (TdP).
DESIGN: Prospective case-based evaluation.
SETTING: Academic medical center with 320 beds.
SUBJECTS: Medical house staff (MDs) and ICU nurses (RNs) from one center and select critical care pharmacists (PHs). INTERVENTION: Completion of a survey containing 10 hypothetical ICU cases in which patients had agitated delirium for which a psychiatrist recommended intravenous haloperidol 5 mg every 6 hours. Each case contained different potential risk factor(s) for TdP in specific combinations. A group of five EP cardiologists agreed that haloperidol use was safe in five cases and not safe in five cases.
MEASUREMENTS AND MAIN RESULTS: For each case, participants were asked to document whether they would administer haloperidol, to provide a rationale for their decision, and to state their level of confidence in that decision. Most clinicians (92 of 115 [80%]) invited to participate completed the cases. Among the five cases where EP cardiologists agreed that haloperidol was not safe, 29% of respondents felt that haloperidol was safe. Conversely, in the five cases where EP cardiologists felt haloperidol was safe, 21% of respondents believed that it was not safe. Overall respondent-EP cardiologist agreement for haloperidol use across the 10 cases was moderate (κ = 0.51). MDs and PHs were in agreement with the EP cardiologists more than RNs (p=0.03). Interprofessional variability existed for the TdP risk factors each best identified. Clinician confidence correlated with EP cardiologist concordance for MDs (p=0.002) and PHs (p=0.0002), but not for RNs (p=0.69).
CONCLUSION: When evaluating use of a QTc interval-prolonging medication, ICU clinicians often fail to identify the TdP risk factors that EP cardiologists feel should prevent its use. Clinician-EP cardiologist concordance varies by the specific risk factor(s) for TdP and the ICU professional conducting the assessment.
© 2013 Pharmacotherapy Publications, Inc.

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Year:  2013        PMID: 23529904     DOI: 10.1002/phar.1242

Source DB:  PubMed          Journal:  Pharmacotherapy        ISSN: 0277-0008            Impact factor:   4.705


  5 in total

1.  Impact of clinical decision support preventing the use of QT-prolonging medications for patients at risk for torsade de pointes.

Authors:  Atsushi Sorita; J Martijn Bos; Bruce W Morlan; Robert F Tarrell; Michael J Ackerman; Pedro J Caraballo
Journal:  J Am Med Inform Assoc       Date:  2014-10-16       Impact factor: 4.497

2.  Risk management of QTc-prolongation in patients receiving haloperidol: an epidemiological study in a University hospital in Belgium.

Authors:  Eline Vandael; Bert Vandenberk; Joris Vandenberghe; Isabel Spriet; Rik Willems; Veerle Foulon
Journal:  Int J Clin Pharm       Date:  2016-01-09

Review 3.  A literature-based algorithm for the assessment, management, and monitoring of drug-induced QTc prolongation in the psychiatric population.

Authors:  M Zolezzi; L Cheung
Journal:  Neuropsychiatr Dis Treat       Date:  2018-12-24       Impact factor: 2.570

4.  Content Validation of an Algorithm for the Assessment, Management and Monitoring of Drug-Induced QTc Prolongation in the Psychiatric Population.

Authors:  Monica Zolezzi; Athar Elhakim; Waad M Elamin; Shorouk Homs; Doaa E Mahmoud; Iman A Qubaiah
Journal:  Neuropsychiatr Dis Treat       Date:  2021-11-19       Impact factor: 2.570

5.  Efficacy of halopeRIdol to decrease the burden of Delirium In adult Critically ill patiEnts (EuRIDICE): study protocol for a prospective randomised multi-centre double-blind placebo-controlled clinical trial in the Netherlands.

Authors:  Lisa Smit; Zoran Trogrlić; John W Devlin; Robert-Jan Osse; Huibert H Ponssen; Arjen J C Slooter; Nicole G M Hunfeld; Wim J R Rietdijk; Diederik Gommers; Mathieu van der Jagt
Journal:  BMJ Open       Date:  2020-09-23       Impact factor: 2.692

  5 in total

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