依鲁替尼诱发心房颤动并大咯血

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摘要

背景:肿瘤患者面临细胞毒性药物的多重不良反应,从组织损伤和中毒,可能从肌肉损伤,神经系统到心脏毒性。病例:这是一个79岁的女性病例,她到我们的急诊科就诊,主诉咯血一天,否认有任何相关的咳嗽、发烧、寒战、胸痛、哽咽、恶心、呕吐或腹痛。没有外伤史。病史包括高血压、子宫癌切除后情况。患者否认既往有类似发作,家族史。胸部x线显示双侧广泛浸润及心脏肿大。胸部CT排除肺栓塞,但显示广泛的多灶性肺炎与ARDS,淋巴增生性改变。在急诊科,患者开始出现鼻分泌物血性,需要鼻洗胃,发现深色血分泌物,然后开始大量咯血,迅速失代偿,需要气管内插管,缺氧呼吸衰竭。急诊支气管镜检查显示疑似肺泡出血(图1)。CBC显示活动性出血导致严重贫血,需要多次输血(表1)。患者被送入ICU。联系了患者的PCP以获得进一步的信息,报告了最近开始使用利伐沙班的心房颤动的新病史,伊鲁替尼的CLL和库姆斯溶血性贫血。住院过程因分布性休克和ARDS而复杂化。她使用了广谱抗生素,由于持续出血需要新鲜冷冻血浆。抗凝及依鲁替尼治疗后病情好转。患者最终拔管,需要物理治疗,然后出院。结论:该病例清楚地证明了适当的时间评估和病史的附带收集如何影响我们患者的结果。文献综述显示新发心房颤动和出血事件与依鲁替尼有关。考虑到利伐沙班有出血的风险,这两种药物联合使用可能导致大量肺泡出血,如果不及早发现,可能会致命。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ibrutinib induced atrial fibrillation complicated with massive hemoptysis
Background: The oncologic patient faces multiple adverse effects with cytotoxic medications, from tissue damage and intoxications that could be evident from muscle damage, neurologic to cardiac toxicity. Case: This is a case of a 79-year-old female who presented to our ED with the complaint of hemoptysis for one day, denied any associated cough, fever, chills, chest pain, SOB, nausea, vomiting, or abdominal pain. No history of trauma. Her medical history includes hypertension, uterine cancer status post-resection. The patient denied prior similar episodes, family history of similar complaints. Chest X-ray showed extensive bilateral infiltrates and cardiomegaly. CT chest ruled out pulmonary em-bolism but showed extensive multifocal pneumonia vs. ARDS, lymphoproliferative changes. While in the ED, the patient started having bloody nasal secretions noted, requiring nasogastric lavage revealing dark blood secretions, and then started having massive hemoptysis and rapidly decompensated requir-ing endotracheal intubation hypoxic respiratory failure. An emergent bronchoscopy was performed, which showed suspected alveolar hemorrhage (Figure 1). The CBC showed severe anemia requiring multiple transfusions due to active bleeding (Table 1). The patient was admitted to ICU. The patient’s PCP was contacted to obtain further information that reported a new history of atrial fi-brillation on rivaroxaban recently started, CLL on ibrutinib, and Coombs Hemolytic Anemia. The hospital course was complicated by distributive shock and ARDS. She was covered with broad-spectrum antibiotics and required fresh frozen plasma due to persistent bleeding. The patient improved after anticoagulation and ibrutinib were held. The patient was eventually extubated, required physical therapy for deconditioning, and then was discharged. Conclusion: This case represents clear evidence of how an appropriate assessment on time and the collateral gath-ering of medical history could impact the outcome of our patients. The literature review has shown new-onset atrial fibrillation and bleeding events related to ibrutinib. Given the risk for bleeding with rivaroxaban, their combination could present with massive alveolar hemorrhage that could become fa-tal if not recognized early.
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