Why the study?
Spontaneous hemothorax is an exceedingly rare bleeding event during rivaroxaban therapy for non-valvular atrial fibrillation.
Concomitant administration of rivaroxaban and fluconazole can lead to severe bleeding events such as spontaneous hemothorax, highlighting the need for vigilance regarding drug-drug interactions.
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Spontaneous hemothorax warrants consideration in dyspneic patients on rivaroxaban; this case leaves open a possible association pending further reports.
Introduction: Rivaroxaban, a novel oral anticoagulant, is widely used in patients with non-valvular atrial fibrillation. Bleeding events during rivaroxaban therapy most commonly include gastrointestinal bleeding and intracranial hemorrhage, while spontaneous hemothorax is exceedingly rare. We report a case of spontaneous hemothorax occurring during rivaroxaban administration. Methods: We report the case of a patient presenting primarily with dyspnea. The patient had been on long-term oral rivaroxaban for atrial fibrillation. Physical examination upon admission revealed diminished breath sounds in the left lung. Computed tomography imaging demonstrated a large left-sided pleural effusion with adjacent pulmonary atelectasis. Laboratory tests indicated significant coagulation abnormalities. After admission, the patient underwent therapeutic thoracentesis and chest tube placement, with bloody pleural fluid observed in the drainage. Due to the marked coagulation abnormalities on admission, the patient received fresh frozen plasma transfusion. Further history-taking revealed recent use of oral fluconazole. A review of the literature suggested that the spontaneous hemothorax might be associated with the concurrent use of rivaroxaban and fluconazole. Results: Following treatment, a follow-up computed tomography scan 3 months later showed no evidence of recurrent hemothorax. Discussion: Concomitant administration of rivaroxaban and fluconazole significantly increases the risk of bleeding events, necessitating clinician vigilance regarding potential drug-drug interactions when formulating therapeutic regimens.
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Li et al. (2025) studied this question.
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