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Transradial artery approach in STEMI patients reperfused early and late by either primary PCI or pharmaco-invasive approach()()

The purpose of the study was to investigate the safety and efficacy of transradial artery approach (TRA) in STEMI patients who reperfused early (≤3 h from symptoms onset) or late (>3 h from symptoms onset) by either PPCI or pharmaco-invasive strategy (PI), thrombolysis followed by CA. Therefore,...

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Autores principales: Sultan, El-Zahraa M., Rabea, Hoda M., abdelmeguid, Khaled R., Mahmoud, Hesham B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Egyptian Society of Cardiology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5883500/
https://www.ncbi.nlm.nih.gov/pubmed/29622990
http://dx.doi.org/10.1016/j.ehj.2017.04.001
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author Sultan, El-Zahraa M.
Rabea, Hoda M.
abdelmeguid, Khaled R.
Mahmoud, Hesham B.
author_facet Sultan, El-Zahraa M.
Rabea, Hoda M.
abdelmeguid, Khaled R.
Mahmoud, Hesham B.
author_sort Sultan, El-Zahraa M.
collection PubMed
description The purpose of the study was to investigate the safety and efficacy of transradial artery approach (TRA) in STEMI patients who reperfused early (≤3 h from symptoms onset) or late (>3 h from symptoms onset) by either PPCI or pharmaco-invasive strategy (PI), thrombolysis followed by CA. Therefore, a total 143 STEMI patients (who were presented within 12 h from symptoms onset or 12–24 h with an evidence of ongoing ischemia or suffered from an acute STEMI were randomized for either PI or PPCI. Eighty-two patients were assigned to PI arm while the rest assigned were to PPCI arm. Patients who were taken to a non-PCI capable hospital received streptokinase and were then transferred to our Hospital for CA. TRA was used in the catheterization laboratory for all patients. Each arm was divided according to reperfusion time into early and late subgroups. A primary endpoint was death, shock, congestive heart failure, or reinfarction up to 30 days. There was a non-significant difference regarding LVEF in both arms. Myocardium wall preservation was significant in the early PI arm (P = 0.023). TIMI flow had no discrepancy between both arms (P = 0.569). Mean procedural and fluoroscopic time were 35.1 ± 6.1 and 6.3 ± 0.9 min. There were no reported entry site complications. There was no difference in primary endpoint complications (P = 0.326) considering the different times of patients’ reperfusion (early; P = 0.696 vs. late; P = 0.424). In conclusion, it is safe and effective to use TRA in STEMI patients who reperfused by either early or late PPCI or PI. We recommend PI for STEMI patients with delay presentation if PPCI is not available.
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spelling pubmed-58835002018-04-05 Transradial artery approach in STEMI patients reperfused early and late by either primary PCI or pharmaco-invasive approach()() Sultan, El-Zahraa M. Rabea, Hoda M. abdelmeguid, Khaled R. Mahmoud, Hesham B. Egypt Heart J Acute Coronary Syndrome The purpose of the study was to investigate the safety and efficacy of transradial artery approach (TRA) in STEMI patients who reperfused early (≤3 h from symptoms onset) or late (>3 h from symptoms onset) by either PPCI or pharmaco-invasive strategy (PI), thrombolysis followed by CA. Therefore, a total 143 STEMI patients (who were presented within 12 h from symptoms onset or 12–24 h with an evidence of ongoing ischemia or suffered from an acute STEMI were randomized for either PI or PPCI. Eighty-two patients were assigned to PI arm while the rest assigned were to PPCI arm. Patients who were taken to a non-PCI capable hospital received streptokinase and were then transferred to our Hospital for CA. TRA was used in the catheterization laboratory for all patients. Each arm was divided according to reperfusion time into early and late subgroups. A primary endpoint was death, shock, congestive heart failure, or reinfarction up to 30 days. There was a non-significant difference regarding LVEF in both arms. Myocardium wall preservation was significant in the early PI arm (P = 0.023). TIMI flow had no discrepancy between both arms (P = 0.569). Mean procedural and fluoroscopic time were 35.1 ± 6.1 and 6.3 ± 0.9 min. There were no reported entry site complications. There was no difference in primary endpoint complications (P = 0.326) considering the different times of patients’ reperfusion (early; P = 0.696 vs. late; P = 0.424). In conclusion, it is safe and effective to use TRA in STEMI patients who reperfused by either early or late PPCI or PI. We recommend PI for STEMI patients with delay presentation if PPCI is not available. Egyptian Society of Cardiology 2018-03 2017-06-12 /pmc/articles/PMC5883500/ /pubmed/29622990 http://dx.doi.org/10.1016/j.ehj.2017.04.001 Text en © 2017 Egyptian Society of Cardiology. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Acute Coronary Syndrome
Sultan, El-Zahraa M.
Rabea, Hoda M.
abdelmeguid, Khaled R.
Mahmoud, Hesham B.
Transradial artery approach in STEMI patients reperfused early and late by either primary PCI or pharmaco-invasive approach()()
title Transradial artery approach in STEMI patients reperfused early and late by either primary PCI or pharmaco-invasive approach()()
title_full Transradial artery approach in STEMI patients reperfused early and late by either primary PCI or pharmaco-invasive approach()()
title_fullStr Transradial artery approach in STEMI patients reperfused early and late by either primary PCI or pharmaco-invasive approach()()
title_full_unstemmed Transradial artery approach in STEMI patients reperfused early and late by either primary PCI or pharmaco-invasive approach()()
title_short Transradial artery approach in STEMI patients reperfused early and late by either primary PCI or pharmaco-invasive approach()()
title_sort transradial artery approach in stemi patients reperfused early and late by either primary pci or pharmaco-invasive approach()()
topic Acute Coronary Syndrome
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5883500/
https://www.ncbi.nlm.nih.gov/pubmed/29622990
http://dx.doi.org/10.1016/j.ehj.2017.04.001
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