无静脉血栓栓塞危险因素患者与低剂量奥氮平相关的急性肺栓塞

Case Reports in Vascular Medicine Pub Date : 2021-07-27 eCollection Date: 2021-01-01 DOI:10.1155/2021/5138509
Vu Hoang Vu, Nguyen Duong Khang, Mai Thanh Thao, Le Minh Khoi
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引用次数: 1

摘要

背景:奥氮平是第二代抗精神病药物,通常用于某些精神/情绪状况,如精神分裂症和双相情感障碍。这种药物被认为是静脉血栓形成的一个促发因素。先前报道的大多数病例与高剂量奥氮平治疗或有血栓栓塞高危因素的患者有关。案例演示。我们报告了一位长期服用低剂量奥氮平后发生肺栓塞的患者。患者66岁,女性,患有失眠症,服用奥氮平2.5 mg,帕罗西汀10 mg,两年。病人在家里突然晕厥,立即被送到医院。肺栓塞的诊断是在冠状动脉计算机断层扫描时偶然做出的。患者经常规治疗痊愈出院,病情稳定。出院两个月后的胸部电脑断层显示肺动脉树完全正常。结论:奥氮平相关性肺栓塞是一种罕见的疾病,如果主治医生不够警惕和了解情况,可能会漏诊。即使是低剂量的奥氮平,如果治疗时间延长,也可能与低典型危险因素患者的肺栓塞有关。在服用奥氮平的患者中,即使表现是非特异性的,也应寻求肺栓塞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Acute Pulmonary Embolism Associated with Low-Dose Olanzapine in a Patient without Risk Factors for Venous Thromboembolism.

Acute Pulmonary Embolism Associated with Low-Dose Olanzapine in a Patient without Risk Factors for Venous Thromboembolism.

Acute Pulmonary Embolism Associated with Low-Dose Olanzapine in a Patient without Risk Factors for Venous Thromboembolism.

Acute Pulmonary Embolism Associated with Low-Dose Olanzapine in a Patient without Risk Factors for Venous Thromboembolism.

Background: Olanzapine is a second-generation antipsychotic drug commonly prescribed for certain mental/mood conditions such as schizophrenia and bipolar disorders. This agent has been considered a precipitating factor for venous thromboembolism formation. Most of the cases previously reported were associated with high-dose olanzapine therapy or in patients with high-risk factors for the development of thromboembolism. Case Presentation. We report a patient who developed pulmonary embolism after a long course of low-dose olanzapine. A 66-year-old female patient suffering from insomnia had been prescribed olanzapine 2.5 mg and paroxetine 10 mg for two years. The patient suddenly developed a syncopal episode at home and was immediately brought to the hospital. The diagnosis of pulmonary embolism was made by chance during the computerized tomography of coronary arteries. The patient made a full recovery under conventional treatment and was discharged in stable condition. The thoracic computed tomography taken two months after discharge showed a completely normal pulmonary arterial tree.

Conclusion: Olanzapine-associated pulmonary embolism is a rare entity and might be missed if the physician in charge is not vigilant and well informed. Even low-dose olanzapine can be associated with pulmonary embolism in patients with low classic risk factors if the treatment is prolonged. Pulmonary embolism should be sought in patients taking olanzapine even though the presenting manifestations are nonspecific.

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