Vandael Eline, Vandenberk Bert, Willems Rik, Reyntens Johan, Vandenberghe Joris, Foulon Veerle
From the *Department of Pharmaceutical and Pharmacological Sciences, University of Leuven, Leuven; †Scientific Institute of Public Health (WIV-ISP), Public Health and Surveillance, Brussels; ‡Department of Cardiovascular Sciences, University of Leuven; §Cardiology, University Hospitals Leuven, Leuven; ∥Sint-Jan Hospital, Eeklo; ¶Department of Neurosciences, University of Leuven; and #Psychiatry, University Hospitals Leuven, Leuven, Belgium.
J Clin Psychopharmacol. 2017 Oct;37(5):540-545. doi: 10.1097/JCP.0000000000000758.
PURPOSE/BACKGROUND: Drug-related QTc prolongation has been linked with Torsade de Pointes and sudden cardiac death. The objective of this study was to investigate the impact of starting an additional QTc-prolonging drug on the QTc interval of psychiatric inpatients.
An observational study was performed between May 2011 and December 2014 in 6 Belgian psychiatric hospitals. Inpatients who were already taking 1 QTc-prolonging drug or more could be included in the study when an additional QTc-prolonging drug was started. Electrocardiograms were performed at baseline and follow-up. Demographic, medical, medication, and laboratory data were collected. A risk score was used to estimate the risk of QTc prolongation based on patient-specific risk factors. A cutoff value of 8 points was set as high risk for QTc prolongation.
One hundred fifty-two patients (44.7% women; mean age, 44 [SD, 17] years) were included who received a prescription for an additional QTc-prolonging drug. There was a small but significant difference (P = 0.032) in mean QTc interval between baseline (409.1 [SD, 21.8] milliseconds) and follow-up (411.8 [SD, 21.7] milliseconds). Three patients developed a prolonged QTc interval in the follow-up electrocardiogram (QTc, ≥450 [men]/470 [women] milliseconds); 8 patients had a delta QTc of 30 milliseconds or longer. No cases of torsade de pointes or sudden cardiac death were identified. Fifty-eight patients (38.2%) had a risk score of 8 or higher; these patients had a significantly longer QTc interval at follow-up than did patients with a risk score of lower than 8 (P < 0.001).
IMPLICATIONS/CONCLUSIONS: Only a limited number of patients developed a prolonged QTc interval after the start of an additional QTc-prolonging drug. Nevertheless, it is still important to screen for high-risk patients at baseline. A risk score can help to select high-risk patients and to stimulate an appropriate and feasible risk management of QTc prolongation in psychiatry.
目的/背景:药物相关的QTc间期延长与尖端扭转型室速及心源性猝死有关。本研究的目的是调查加用一种可延长QTc间期的药物对精神科住院患者QTc间期的影响。
2011年5月至2014年12月期间,在比利时的6家精神病医院进行了一项观察性研究。已经服用一种或多种可延长QTc间期药物的住院患者,在加用另一种可延长QTc间期的药物时可纳入本研究。在基线和随访时进行心电图检查。收集人口统计学、医疗、用药及实验室数据。使用风险评分根据患者特定的危险因素估计QTc间期延长的风险。将8分的临界值设定为QTc间期延长的高风险。
共纳入152例患者(44.7%为女性;平均年龄44岁[标准差17岁]),这些患者接受了加用一种可延长QTc间期药物的处方。基线时(409.1毫秒[标准差21.8毫秒])与随访时(411.8毫秒[标准差21.7毫秒])的平均QTc间期存在微小但显著的差异(P = 0.032)。3例患者在随访心电图中出现QTc间期延长(男性QTc≥450毫秒/女性QTc≥470毫秒);8例患者的QTc变化值为30毫秒或更长。未发现尖端扭转型室速或心源性猝死病例。58例患者(38.2%)的风险评分为8分或更高;这些患者在随访时的QTc间期明显长于风险评分低于8分的患者(P < 0.001)。
意义/结论:加用另一种可延长QTc间期的药物后,仅有少数患者出现QTc间期延长。然而,在基线时筛查高风险患者仍然很重要。风险评分有助于选择高风险患者,并促进在精神病学中对QTc间期延长进行适当且可行的风险管理。