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Dual coronary emboli in peripartum cardiomyopathy
Lyndon C Box1, Viktor Hanak, Joaquin G Arciniegas
1Department of Internal Medicine, Carraway Methodist Medical Center, Birmingham, Alabama, USA. lcbox@yahoo.com
Insights
Peripartum cardiomyopathy can cause coronary artery emboli, leading to myocardial infarction. This case highlights successful treatment of multiple coronary emboli with eptifibatide, underscoring a rare complication of peripartum cardiomyopathy.
Area of Science:
- Cardiology
- Cardiovascular Medicine
- Reproductive Medicine
Background:
- Peripartum cardiomyopathy is a rare form of heart failure.
- Mural thrombus formation is a known complication of peripartum cardiomyopathy.
- Coronary artery embolism is a rare but serious complication of cardiac thrombus.
Observation:
- A 31-year-old woman with peripartum cardiomyopathy presented with acute myocardial infarction.
- Coronary angiography revealed two distinct emboli in the left anterior descending and left circumflex arteries.
- The patient had a known mural thrombus associated with her cardiomyopathy.
Findings:
- Local infusion of eptifibatide during angiography successfully resolved both coronary emboli.
- This case documents multiple coronary embolic events, unlike previous reports of single emboli.
- The findings reinforce the link between peripartum cardiomyopathy and embolic coronary occlusion.
Implications:
- This case expands the understanding of coronary embolism as a complication of peripartum cardiomyopathy.
- Prompt diagnosis and intervention, such as with eptifibatide, can be effective in managing acute coronary embolism.
- Further research is warranted to elucidate the mechanisms and optimal management strategies for coronary emboli in this patient population.
Abstract:
Coronary emboli are rare but devastating events. We present the case of a 31-year-old woman with peripartum cardiomyopathy and mural thrombus. She was admitted with an acute, non-ST elevation myocardial infarction. Two emboli were seen on the coronary angiogram: one in the left anterior descending coronary artery and a second in the left circumflex artery. Each embolus resolved after local infusion of eptifibatide at the time of angiography. There has been 1 report in the English-language medical literature of a similar coronary embolic event in the setting of peripartum cardiomyopathy; however, in that case, only 1 embolus was found. Our case further documents embolic coronary occlusion as a consequence of peripartum cardiomyopathy.
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