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Published on: May 28, 2019
Intracoronary administration of isosorbide dinitrate induced severely slow flow and transient ST-segment elevation
Kazuhito Yamashita1, Hiromi Tasaki
1Second Department of Internal Medicine, University of Occupational and Environmental Health, School of Medicine, Japan. wajinn@med.uoeh-u.ac.jp
Insights
Nitroglycerin is ineffective for angina in patients with syndrome X due to microvessel dysfunction. Isosorbide dinitrate caused coronary slow flow, suggesting impaired microvascular function in heart failure patients.
Area of Science:
- Cardiology
- Pharmacology
- Vascular Biology
Background:
- Nitroglycerin is a primary treatment for angina.
- Syndrome X and congestive heart failure can involve microvessel dysfunction.
- Microvascular impairment affects drug efficacy.
Observation:
- A patient with congestive heart failure experienced severe coronary slow flow and ST-segment elevation after intracoronary isosorbide dinitrate administration.
- Coronary angiograms were normal prior to the drug challenge.
- The patient reported mild chest pain during the event.
Findings:
- Intracoronary isosorbide dinitrate induced significant coronary slow flow in a patient with heart failure.
- This response suggests a delay in microvessel dilatation (less than 100 micrometers) due to dysfunction.
- Functional stenosis may occur in microvasculature with impaired function.
Implications:
- Microvascular dysfunction can lead to paradoxical reactions to nitrates.
- This finding highlights the importance of assessing microvascular function in heart failure.
- Current angina treatments may be ineffective in patients with underlying microvascular disease.
Abstract:
Nitroglycerin is one of the most widely used drugs in the treatment of angina. However, nitroglycerin fails to relieve angina in patients with syndrome X who have microvessel dysfunction. Microvessel function is impaired in several diseases. In this article, the authors report that despite normal coronary angiograms at control, intracoronary administration of isosorbide dinitrate induced severe coronary slow flow and transient ST-segment elevation with mild chest pain in a patient with congestive heart failure. The authors speculated that functional stenosis and a delay in the dilatation of microvessels less than 100 microm in diameter because of their dysfunction resulted in a severely slow flow after intracoronary administration of isosorbide dinitrate.
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