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aVR ST‐segment changes and prognosis of ST‐segment elevation myocardial infarction
BACKGROUND: Clinical importance of aVR lead‐related changes in predicting the prognosis of acute myocardial infarction remains uncertain. The present study aimed to assess the value of ST‐segment changes in aVR lead and the outcome and sequels of the first episode of acute ST‐segment elevation myoca...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8485596/ https://www.ncbi.nlm.nih.gov/pubmed/34622021 http://dx.doi.org/10.1002/hsr2.387 |
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author | Sedighi, Sogol Fattahi, Mustafa Dehghani, Pooyan Aslani, Amir Mehdipour Namdar, Zahra Hassanzadeh, Mani |
author_facet | Sedighi, Sogol Fattahi, Mustafa Dehghani, Pooyan Aslani, Amir Mehdipour Namdar, Zahra Hassanzadeh, Mani |
author_sort | Sedighi, Sogol |
collection | PubMed |
description | BACKGROUND: Clinical importance of aVR lead‐related changes in predicting the prognosis of acute myocardial infarction remains uncertain. The present study aimed to assess the value of ST‐segment changes in aVR lead and the outcome and sequels of the first episode of acute ST‐segment elevation myocardial infarction. METHODS: This prospective cohort study was conducted on patients suffering first episode of ST‐segment elevation myocardial infarction and underwent percutaneous coronary intervention. Information was collected through hospital‐recorded files reading. The electrocardiogram (ECG) was taken from the patients upon entering the hospital and followed‐up for 30 days to assess cardiovascular complications. RESULTS: In patients with anterior STEMI, with the use of multivariate analysis, admission aVR ST elevation ≥1 mm was found to be a strong and independent predictor of major cardiovascular adverse events (MACE) within 30 days of discharging (P value for trend .002). In patients with inferior (± RV) ST‐segment elevation myocardial infarction (STEMI), with the use of multivariate analysis, admission aVR ST depression ≥1 mm was found to be a strong and independent predictor of MACE within 30 days of discharging (P value for trend .01). CONCLUSION: In patients with anterior STEMI, admission aVR STE ≥1 mm was found to be a strong and independent predictor of MACE within 30 days of discharging. On the other hand, in patients with inferior STEMI, aVR ST depression ≥1 mm was found to be a strong and independent predictor of MACE within 30 days of discharging. |
format | Online Article Text |
id | pubmed-8485596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84855962021-10-06 aVR ST‐segment changes and prognosis of ST‐segment elevation myocardial infarction Sedighi, Sogol Fattahi, Mustafa Dehghani, Pooyan Aslani, Amir Mehdipour Namdar, Zahra Hassanzadeh, Mani Health Sci Rep Research Articles BACKGROUND: Clinical importance of aVR lead‐related changes in predicting the prognosis of acute myocardial infarction remains uncertain. The present study aimed to assess the value of ST‐segment changes in aVR lead and the outcome and sequels of the first episode of acute ST‐segment elevation myocardial infarction. METHODS: This prospective cohort study was conducted on patients suffering first episode of ST‐segment elevation myocardial infarction and underwent percutaneous coronary intervention. Information was collected through hospital‐recorded files reading. The electrocardiogram (ECG) was taken from the patients upon entering the hospital and followed‐up for 30 days to assess cardiovascular complications. RESULTS: In patients with anterior STEMI, with the use of multivariate analysis, admission aVR ST elevation ≥1 mm was found to be a strong and independent predictor of major cardiovascular adverse events (MACE) within 30 days of discharging (P value for trend .002). In patients with inferior (± RV) ST‐segment elevation myocardial infarction (STEMI), with the use of multivariate analysis, admission aVR ST depression ≥1 mm was found to be a strong and independent predictor of MACE within 30 days of discharging (P value for trend .01). CONCLUSION: In patients with anterior STEMI, admission aVR STE ≥1 mm was found to be a strong and independent predictor of MACE within 30 days of discharging. On the other hand, in patients with inferior STEMI, aVR ST depression ≥1 mm was found to be a strong and independent predictor of MACE within 30 days of discharging. John Wiley and Sons Inc. 2021-10-01 /pmc/articles/PMC8485596/ /pubmed/34622021 http://dx.doi.org/10.1002/hsr2.387 Text en © 2021 The Authors. Health Science Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Sedighi, Sogol Fattahi, Mustafa Dehghani, Pooyan Aslani, Amir Mehdipour Namdar, Zahra Hassanzadeh, Mani aVR ST‐segment changes and prognosis of ST‐segment elevation myocardial infarction |
title | aVR ST‐segment changes and prognosis of ST‐segment elevation myocardial infarction |
title_full | aVR ST‐segment changes and prognosis of ST‐segment elevation myocardial infarction |
title_fullStr | aVR ST‐segment changes and prognosis of ST‐segment elevation myocardial infarction |
title_full_unstemmed | aVR ST‐segment changes and prognosis of ST‐segment elevation myocardial infarction |
title_short | aVR ST‐segment changes and prognosis of ST‐segment elevation myocardial infarction |
title_sort | avr st‐segment changes and prognosis of st‐segment elevation myocardial infarction |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8485596/ https://www.ncbi.nlm.nih.gov/pubmed/34622021 http://dx.doi.org/10.1002/hsr2.387 |
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