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Evaluation of fibrinolytic medical therapy for patients with acute myocardial infarction

BACKGROUND: Fibrinolytic therapy is the standard therapeutic method for patients with acute myocardial infarction (AMI). This study endeavored to assess the delay in arrival to the emergency department and door to needle time for thrombolytic therapy. METHODS: This study was conducted on 80 patients...

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Autores principales: Maleki, Ali, Shariari, Arman, Sadeghi, Masoumeh, Rashidi, Negin, Alyari, Farshid, Forughi, Saeid, Nabatchi, Behjat, Ghanavati, Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Isfahan Cardiovascular Research Center, Isfahan University of Medical Sciences 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448456/
https://www.ncbi.nlm.nih.gov/pubmed/23056101
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author Maleki, Ali
Shariari, Arman
Sadeghi, Masoumeh
Rashidi, Negin
Alyari, Farshid
Forughi, Saeid
Nabatchi, Behjat
Ghanavati, Reza
author_facet Maleki, Ali
Shariari, Arman
Sadeghi, Masoumeh
Rashidi, Negin
Alyari, Farshid
Forughi, Saeid
Nabatchi, Behjat
Ghanavati, Reza
author_sort Maleki, Ali
collection PubMed
description BACKGROUND: Fibrinolytic therapy is the standard therapeutic method for patients with acute myocardial infarction (AMI). This study endeavored to assess the delay in arrival to the emergency department and door to needle time for thrombolytic therapy. METHODS: This study was conducted on 80 patients with AMI whom referred to our clinic from January 2009 to January 2010. We measured time of arrival, needle time and door to needle time for all patients. Moreover, the relations of these times to some variables such as age, gender and the referred shift of emergency department personnel were calculated. RESULTS: A total of 80 patients, 62 (77.5%) male and 18 (22.5%) female were evaluated for thrombolytic therapy. The arrival time of overnight shifts was 14.59 ± 1.23 minutes shorter than other shifts. The median door to needle time was 46.56 minutes and the mean time of the onset of chest pain to arrival at the emergency department was 19.44 minutes. Seventy-two patients (90%) received fibrinolytic therapy within the first 30 minutes of arrival. The needle time was significantly longer in the night shift (P < 0.05) (between 8 to 14 minutes), while the time of receiving Streptokinase therapy in the other shifts was not meaningfully different. Finally there was a statistically significant difference between the referred shifts and needle time (P < 0.05). CONCLUSION: Despite our good results for door to needle time, to improve and attain the gold standard’s limits in administering fibrinolytic therapy, improvement of policies like training the personnel to shorten this time is recommend.
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spelling pubmed-34484562012-10-10 Evaluation of fibrinolytic medical therapy for patients with acute myocardial infarction Maleki, Ali Shariari, Arman Sadeghi, Masoumeh Rashidi, Negin Alyari, Farshid Forughi, Saeid Nabatchi, Behjat Ghanavati, Reza ARYA Atheroscler Original Article BACKGROUND: Fibrinolytic therapy is the standard therapeutic method for patients with acute myocardial infarction (AMI). This study endeavored to assess the delay in arrival to the emergency department and door to needle time for thrombolytic therapy. METHODS: This study was conducted on 80 patients with AMI whom referred to our clinic from January 2009 to January 2010. We measured time of arrival, needle time and door to needle time for all patients. Moreover, the relations of these times to some variables such as age, gender and the referred shift of emergency department personnel were calculated. RESULTS: A total of 80 patients, 62 (77.5%) male and 18 (22.5%) female were evaluated for thrombolytic therapy. The arrival time of overnight shifts was 14.59 ± 1.23 minutes shorter than other shifts. The median door to needle time was 46.56 minutes and the mean time of the onset of chest pain to arrival at the emergency department was 19.44 minutes. Seventy-two patients (90%) received fibrinolytic therapy within the first 30 minutes of arrival. The needle time was significantly longer in the night shift (P < 0.05) (between 8 to 14 minutes), while the time of receiving Streptokinase therapy in the other shifts was not meaningfully different. Finally there was a statistically significant difference between the referred shifts and needle time (P < 0.05). CONCLUSION: Despite our good results for door to needle time, to improve and attain the gold standard’s limits in administering fibrinolytic therapy, improvement of policies like training the personnel to shorten this time is recommend. Isfahan Cardiovascular Research Center, Isfahan University of Medical Sciences 2012 /pmc/articles/PMC3448456/ /pubmed/23056101 Text en © 2011 Isfahan Cardiovascular Research Center & Isfahan University of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Original Article
Maleki, Ali
Shariari, Arman
Sadeghi, Masoumeh
Rashidi, Negin
Alyari, Farshid
Forughi, Saeid
Nabatchi, Behjat
Ghanavati, Reza
Evaluation of fibrinolytic medical therapy for patients with acute myocardial infarction
title Evaluation of fibrinolytic medical therapy for patients with acute myocardial infarction
title_full Evaluation of fibrinolytic medical therapy for patients with acute myocardial infarction
title_fullStr Evaluation of fibrinolytic medical therapy for patients with acute myocardial infarction
title_full_unstemmed Evaluation of fibrinolytic medical therapy for patients with acute myocardial infarction
title_short Evaluation of fibrinolytic medical therapy for patients with acute myocardial infarction
title_sort evaluation of fibrinolytic medical therapy for patients with acute myocardial infarction
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448456/
https://www.ncbi.nlm.nih.gov/pubmed/23056101
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