Kaden Shen, Kevin M Dube, Jeremy R DeGrado, Paul M Szumita, Kenneth E Lupi
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The major endpoint was a composite of the incidence of QTc prolongation (defined as QTc > 500 ms or QTc > 60 ms above baseline) following antipsychotic initiation. Univariable and multivariable analyses were performed to identify risk factors for QTc prolongation.</p><p><strong>Results: </strong>There was no statistical difference in the major composite endpoint between patients in the olanzapine and quetiapine groups (8/83 [9.6%] vs 19/129 [14.7%]; <i>P</i> = .28). The incidence of QTc > 500 ms (7/244 [2.9%] vs 20/427 [4.7%]; <i>P</i> = .25) and change from baseline >60 ms (5/244 [2.0%] vs 17/427 [4.0%]; <i>P</i> = .26) were not statistically different between the olanzapine and quetiapine groups, respectively. There were no occurrences of Torsades de Pointes or extrapyramidal symptoms in either group.</p><p><strong>Conclusion and relevance: </strong>The results of this study suggest olanzapine and quetiapine may have similar impact on QTc prolongation in critically ill patients. These findings could contribute to safer prescribing practices in the ICU.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Olanzapine Versus Quetiapine: Corrected QT Changes in Critically Ill Patients.\",\"authors\":\"Kaden Shen, Kevin M Dube, Jeremy R DeGrado, Paul M Szumita, Kenneth E Lupi\",\"doi\":\"10.1177/10600280241290254\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Olanzapine and quetiapine are frequently administered atypical antipsychotic medications and their effects on the corrected QT (QTc) in the critically ill population remain understudied.</p><p><strong>Objective: </strong>The objective of this study was to compare the impact of olanzapine and quetiapine on QTc changes in critically ill patients.</p><p><strong>Methods: </strong>This was a single-center, retrospective analysis. Adult patients admitted to the intensive care unit (ICU) from January 2023 through July 2023 were included if they received ≥2 doses of either olanzapine or quetiapine within a 48-hour period and had one QTc evaluated within 48 hours of antipsychotic initiation. The major endpoint was a composite of the incidence of QTc prolongation (defined as QTc > 500 ms or QTc > 60 ms above baseline) following antipsychotic initiation. Univariable and multivariable analyses were performed to identify risk factors for QTc prolongation.</p><p><strong>Results: </strong>There was no statistical difference in the major composite endpoint between patients in the olanzapine and quetiapine groups (8/83 [9.6%] vs 19/129 [14.7%]; <i>P</i> = .28). The incidence of QTc > 500 ms (7/244 [2.9%] vs 20/427 [4.7%]; <i>P</i> = .25) and change from baseline >60 ms (5/244 [2.0%] vs 17/427 [4.0%]; <i>P</i> = .26) were not statistically different between the olanzapine and quetiapine groups, respectively. There were no occurrences of Torsades de Pointes or extrapyramidal symptoms in either group.</p><p><strong>Conclusion and relevance: </strong>The results of this study suggest olanzapine and quetiapine may have similar impact on QTc prolongation in critically ill patients. 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引用次数: 0
摘要
背景:奥氮平和喹硫平是常用的非典型抗精神病药物,但它们对重症患者校正QT(QTc)的影响仍未得到充分研究:本研究旨在比较奥氮平和喹硫平对重症患者 QTc 变化的影响:这是一项单中心回顾性分析。从 2023 年 1 月到 2023 年 7 月入住重症监护室(ICU)的成人患者,如果在 48 小时内接受了≥2 次奥氮平或喹硫平治疗,并且在开始使用抗精神病药物的 48 小时内进行了一次 QTc 评估,则纳入研究对象。主要终点是开始使用抗精神病药物后QTc延长(定义为QTc > 500毫秒或QTc >基线以上60毫秒)发生率的综合结果。研究人员进行了单变量和多变量分析,以确定QTc延长的风险因素:奥氮平组和喹硫平组患者的主要复合终点无统计学差异(8/83 [9.6%] vs 19/129 [14.7%];P = .28)。奥氮平组与喹硫平组的 QTc > 500 ms 发生率(7/244 [2.9%] vs 20/427 [4.7%];P = .25)和基线变化 > 60 ms 发生率(5/244 [2.0%] vs 17/427 [4.0%];P = .26)分别没有统计学差异。两组患者均未出现心搏过速或锥体外系症状:本研究结果表明,奥氮平和喹硫平对重症患者 QTc 延长的影响相似。这些发现有助于在重症监护病房中采用更安全的处方。
Olanzapine Versus Quetiapine: Corrected QT Changes in Critically Ill Patients.
Background: Olanzapine and quetiapine are frequently administered atypical antipsychotic medications and their effects on the corrected QT (QTc) in the critically ill population remain understudied.
Objective: The objective of this study was to compare the impact of olanzapine and quetiapine on QTc changes in critically ill patients.
Methods: This was a single-center, retrospective analysis. Adult patients admitted to the intensive care unit (ICU) from January 2023 through July 2023 were included if they received ≥2 doses of either olanzapine or quetiapine within a 48-hour period and had one QTc evaluated within 48 hours of antipsychotic initiation. The major endpoint was a composite of the incidence of QTc prolongation (defined as QTc > 500 ms or QTc > 60 ms above baseline) following antipsychotic initiation. Univariable and multivariable analyses were performed to identify risk factors for QTc prolongation.
Results: There was no statistical difference in the major composite endpoint between patients in the olanzapine and quetiapine groups (8/83 [9.6%] vs 19/129 [14.7%]; P = .28). The incidence of QTc > 500 ms (7/244 [2.9%] vs 20/427 [4.7%]; P = .25) and change from baseline >60 ms (5/244 [2.0%] vs 17/427 [4.0%]; P = .26) were not statistically different between the olanzapine and quetiapine groups, respectively. There were no occurrences of Torsades de Pointes or extrapyramidal symptoms in either group.
Conclusion and relevance: The results of this study suggest olanzapine and quetiapine may have similar impact on QTc prolongation in critically ill patients. These findings could contribute to safer prescribing practices in the ICU.