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Current strategies in the evaluation and management of cocaine-induced chest pain.

Authors :
Agrawal PR
Scarabelli TM
Saravolatz L
Kini A
Jalota A
Chen-Scarabelli C
Fuster V
Halperin JL
Source :
Cardiology in review [Cardiol Rev] 2015 Nov-Dec; Vol. 23 (6), pp. 303-11.
Publication Year :
2015

Abstract

With each successive year, the number of Emergency Department (ED) visits related to illicit drug abuse has progressively increased. Cocaine is the most common illegal drug to cause a visit to the ED. Cocaine use results in a variety of pathophysiological changes with regards to the cardiovascular system, such as constriction of coronary vessels, dysfunction of vascular endothelium, decreased aortic elasticity, hemodynamic disruptions, a hypercoagulable state, and direct toxicity to myocardial and vascular tissue. The clinical course of patients with cocaine-induced chest pain (CCP) is often challenging, and electrocardiographic findings can be potentially misleading in terms of diagnosing a myocardial infarction. In addition, there is no current satisfactory study regarding outcomes of use of various pharmacological drug therapies to manage CCP. At present, calcium-channel blockers and nitroglycerin are two pharmacological agents that are advocated as first-line drugs for CCP management, although the role of labetalol has been controversial and warrants further investigation. We performed an extensive search of available literature through a large number of scholarly articles previously published and listed on Index Medicus. In this review, we put forward a concise summary of the current approach to a patient presenting to the ED with CCP and management of the clinical scenario. The purpose of this review is to summarize the understanding of cocaine's cardiovascular pathophysiology and to examine the current approach for proper evaluation and management of CCP.

Details

Language :
English
ISSN :
1538-4683
Volume :
23
Issue :
6
Database :
MEDLINE
Journal :
Cardiology in review
Publication Type :
Academic Journal
Accession number :
25580707
Full Text :
https://doi.org/10.1097/CRD.0000000000000050