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2438: Dose-dependent nature of cocaine infusions on cardiovascular hemodynamics

OBJECTIVES/SPECIFIC AIMS: Cocaine use is a significant health problem in the United States and associated with increased risk of adverse cardiovascular outcomes. Our goal was to evaluate the effects of rapid cocaine infusions on cardiovascular hemodynamics among patients with cocaine abuse disorder....

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Autores principales: Carbone, Salvatore, Van Tassell, Benjamin, Abbate, Antonio, Canada, Justin, Buckley, Leo F., Johns, Sade, Kadariya, Dinesh, Moeller, F. Gerard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6799097/
http://dx.doi.org/10.1017/cts.2017.138
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author Carbone, Salvatore
Van Tassell, Benjamin
Abbate, Antonio
Canada, Justin
Buckley, Leo F.
Johns, Sade
Kadariya, Dinesh
Moeller, F. Gerard
author_facet Carbone, Salvatore
Van Tassell, Benjamin
Abbate, Antonio
Canada, Justin
Buckley, Leo F.
Johns, Sade
Kadariya, Dinesh
Moeller, F. Gerard
author_sort Carbone, Salvatore
collection PubMed
description OBJECTIVES/SPECIFIC AIMS: Cocaine use is a significant health problem in the United States and associated with increased risk of adverse cardiovascular outcomes. Our goal was to evaluate the effects of rapid cocaine infusions on cardiovascular hemodynamics among patients with cocaine abuse disorder. METHODS/STUDY POPULATION: Patients with a history of cocaine abuse but no overt cardiovascular disease received 4 consecutive intravenous infusions of cocaine (0, 10, 20, 40 mg) given in randomized, double-blinded order. The infusion procedure was repeated on 2 consecutive days (4 infusions each day). Following each dose, patients underwent continuous monitoring via fingertip plethysmography for 30 minutes, followed by an additional 30 minutes washout procedure. Patients were surveyed throughout this timeline to record symptoms of cocaine response. Finger tracings were then used to calculate arterial pressure curves and parameters of heart rate, blood pressure, cardiac output, stroke volume, and systemic vascular resistance according to device-specific algorithms. Mean values were calculated over the entire 30 minutes follow-up and peak values were defined as the maximum value sustained over any 60-second interval during the follow-up period. RESULTS/ANTICIPATED RESULTS: Seven patients were enrolled and received cocaine infusions of 2 consecutive days. Cocaine dose was positively associated with mean cardiac output (R=0.489, p<0.001), peak diastolic blood pressure (R=0.435, p=0.001), mean heart rate (R=0.401, p=0.003), peak systolic blood pressure (R=0.399, p=0.003), peak mean arterial pressure (R=0.362, p=0.008), mean systolic blood pressure (R=0.399, p=0.003), +dP/dt (R=0.346, p=0.012), and peak heart rate (R=0.334, p=0.015). Hemodynamic parameters were also predictive of patient-reported symptoms of cocaine response. DISCUSSION/SIGNIFICANCE OF IMPACT: These data confirm the known pharmacologic effect of cocaine to prevent reuptake of neurotransmitters and demonstrate the feasibility of conducting a noninvasive assessment of cardiovascular hemodynamics as a measure of responsiveness to cocaine infusions. This procedure also provides a benchmark to evaluate the potential impact of pharmacologic treatments on cocaine-induced hemodynamic changes and patient perceptions of cocaine response.
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spelling pubmed-67990972019-10-28 2438: Dose-dependent nature of cocaine infusions on cardiovascular hemodynamics Carbone, Salvatore Van Tassell, Benjamin Abbate, Antonio Canada, Justin Buckley, Leo F. Johns, Sade Kadariya, Dinesh Moeller, F. Gerard J Clin Transl Sci Clinical Trial OBJECTIVES/SPECIFIC AIMS: Cocaine use is a significant health problem in the United States and associated with increased risk of adverse cardiovascular outcomes. Our goal was to evaluate the effects of rapid cocaine infusions on cardiovascular hemodynamics among patients with cocaine abuse disorder. METHODS/STUDY POPULATION: Patients with a history of cocaine abuse but no overt cardiovascular disease received 4 consecutive intravenous infusions of cocaine (0, 10, 20, 40 mg) given in randomized, double-blinded order. The infusion procedure was repeated on 2 consecutive days (4 infusions each day). Following each dose, patients underwent continuous monitoring via fingertip plethysmography for 30 minutes, followed by an additional 30 minutes washout procedure. Patients were surveyed throughout this timeline to record symptoms of cocaine response. Finger tracings were then used to calculate arterial pressure curves and parameters of heart rate, blood pressure, cardiac output, stroke volume, and systemic vascular resistance according to device-specific algorithms. Mean values were calculated over the entire 30 minutes follow-up and peak values were defined as the maximum value sustained over any 60-second interval during the follow-up period. RESULTS/ANTICIPATED RESULTS: Seven patients were enrolled and received cocaine infusions of 2 consecutive days. Cocaine dose was positively associated with mean cardiac output (R=0.489, p<0.001), peak diastolic blood pressure (R=0.435, p=0.001), mean heart rate (R=0.401, p=0.003), peak systolic blood pressure (R=0.399, p=0.003), peak mean arterial pressure (R=0.362, p=0.008), mean systolic blood pressure (R=0.399, p=0.003), +dP/dt (R=0.346, p=0.012), and peak heart rate (R=0.334, p=0.015). Hemodynamic parameters were also predictive of patient-reported symptoms of cocaine response. DISCUSSION/SIGNIFICANCE OF IMPACT: These data confirm the known pharmacologic effect of cocaine to prevent reuptake of neurotransmitters and demonstrate the feasibility of conducting a noninvasive assessment of cardiovascular hemodynamics as a measure of responsiveness to cocaine infusions. This procedure also provides a benchmark to evaluate the potential impact of pharmacologic treatments on cocaine-induced hemodynamic changes and patient perceptions of cocaine response. Cambridge University Press 2018-05-10 /pmc/articles/PMC6799097/ http://dx.doi.org/10.1017/cts.2017.138 Text en © The Association for Clinical and Translational Science 2018 http://creativecommons.org/licenses/by/4.0/ This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Trial
Carbone, Salvatore
Van Tassell, Benjamin
Abbate, Antonio
Canada, Justin
Buckley, Leo F.
Johns, Sade
Kadariya, Dinesh
Moeller, F. Gerard
2438: Dose-dependent nature of cocaine infusions on cardiovascular hemodynamics
title 2438: Dose-dependent nature of cocaine infusions on cardiovascular hemodynamics
title_full 2438: Dose-dependent nature of cocaine infusions on cardiovascular hemodynamics
title_fullStr 2438: Dose-dependent nature of cocaine infusions on cardiovascular hemodynamics
title_full_unstemmed 2438: Dose-dependent nature of cocaine infusions on cardiovascular hemodynamics
title_short 2438: Dose-dependent nature of cocaine infusions on cardiovascular hemodynamics
title_sort 2438: dose-dependent nature of cocaine infusions on cardiovascular hemodynamics
topic Clinical Trial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6799097/
http://dx.doi.org/10.1017/cts.2017.138
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