Ferraris Augusto, Szmulewicz Alejandro G, Vazquez Fernando J, Vollmer William M, Angriman Federico
From the *Pharmacology Department, School of Medicine, University of Buenos Aires; †Hospital de Emergencias Psiquiátricas Torcuato de Alvear; ‡Bipolar Disorder Program, Neuroscience Institute, Favaloro University; §Internal Medicine Department, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina; and ∥Kaiser Permanente Center for Health Research, Portland, OR.
J Clin Psychopharmacol. 2017 Aug;37(4):405-411. doi: 10.1097/JCP.0000000000000738.
Treatment with antipsychotic (AP) agents is associated with incident thromboembolic events. However, the underpinnings of this association remain unknown. We sought to evaluate the effect of AP agents-categorized by their metabolic/sedative and hyperprolactinemia adverse effect profile-on the risk of venous thromboembolic disease during long-term follow-up.
A retrospective cohort study of adult patients initiating AP treatment for the first time was conducted. Primary outcome was defined as the time to venous thromboembolism (VTE) (either deep venous thrombosis or acute pulmonary embolism). Antipsychotic agents were categorized by their risk (high vs low) of either drug-induced (a) sedation/metabolic adverse event or (b) hyperprolactinemia. We used a propensity score-adjusted Cox proportional hazards model to control for confounding.
One thousand eight patients (mean age, 72.4 y) were followed for a median of 36 months. Incident VTE occurred in 6.25% of patients, corresponding to an incidence rate of 184 cases per 10,000 person-years. We found no difference in the hazard of VTE during follow-up between high- and low-risk groups (hazard ratio, 1.23 [95% confidence interval, 0.74-2.04] for drug-induced sedation/metabolic adverse event risk categories, and hazard ratio 0.81 [95% confidence interval, 0.50-1.35] for high versus low hyperprolactinemia risk).
These results suggest that the risk of thromboembolic events in older adults who started AP treatment for the first time does not seem to be related to these drugs' risk of either sedation/metabolic adverse events or hyperprolactinemia. However, VTE remains a common problem in this subgroup of patients.
使用抗精神病药物(AP)治疗与血栓栓塞事件的发生有关。然而,这种关联的基础尚不清楚。我们试图评估根据其代谢/镇静和高催乳素血症不良反应特征分类的AP药物对长期随访期间静脉血栓栓塞性疾病风险的影响。
对首次开始AP治疗的成年患者进行了一项回顾性队列研究。主要结局定义为发生静脉血栓栓塞(VTE,包括深静脉血栓形成或急性肺栓塞)的时间。抗精神病药物根据其导致(a)镇静/代谢不良事件或(b)高催乳素血症的风险(高风险与低风险)进行分类。我们使用倾向评分调整的Cox比例风险模型来控制混杂因素。
1808名患者(平均年龄72.4岁)的中位随访时间为36个月。6.25%的患者发生了VTE事件,对应发病率为每10000人年184例。我们发现,在随访期间,高风险组和低风险组之间VTE风险没有差异(药物引起的镇静/代谢不良事件风险类别,风险比为1.23[95%置信区间,0.74 - 2.04];高催乳素血症风险高与低相比,风险比为0.81[95%置信区间,0.50 - 1.35])。
这些结果表明,首次开始AP治疗的老年人发生血栓栓塞事件的风险似乎与这些药物的镇静/代谢不良事件风险或高催乳素血症风险无关。然而,VTE在该亚组患者中仍然是一个常见问题。