Key result
Gemcitabine infusion induced severe chest pain and acute left bundle-branch block in a 59-year-old woman with preexisting coronary artery disease 30 minutes after administration.
Case Report (n=1)
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Gemcitabine infusion may induce acute coronary syndrome, particularly in patients with preexisting coronary artery disease, highlighting the need for intensive cardiac monitoring during administration.
OBJECTIVES: To report a case of metastatic leiomyosarcoma, in which a patient developed chest pain accompanied by acute left bundle-branch block (LBBB) after gemcitabine infusion. CLINICAL PRESENTATION AND INTERVENTION: A 59-year-old woman admitted with bilateral pulmonary nodules had classic risk factors for coronary heart disease and coronary stenosis as demonstrated by previous coronary angiography. She was treated with gemcitabine infusion, and 30 min later she experienced severe chest pain accompanied by acute LBBB confirmed by ECG. We suspected gemcitabine-induced coronary vasospasm exacerbated by the preexisting coronary artery disease as the cause of the acute coronary syndrome. The patient was subsequently treated with antianginal therapy and percutaneous coronary intervention. Her chest pain resolved and LBBB disappeared. She was discharged 2 days later without any further cardiac events. No additional cancer therapy was given and she died 5 months later, due to disease progression. CONCLUSION: This case showed that chemotherapeutic agents must be administered with intensive cardiac monitoring especially in patients with cardiac disease and well-known risk factors to prevent the development of cardiac complications, despite an agent not being known to be 'cardiotoxic'.
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Öztürk et al. (2008) conducted a case report in Metastatic leiomyosarcoma and acute coronary syndrome (n=1). Gemcitabine infusion was evaluated on Acute coronary syndrome (chest pain with acute LBBB). Gemcitabine infusion induced severe chest pain and acute left bundle-branch block in a 59-year-old woman with preexisting coronary artery disease 30 minutes after administration.
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