An international prospective cohort study evaluating major vascular complications among patients undergoing noncardiac surgery : the VISION Pilot Study
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/226227 |
Resumo: | Objectives: Among patients undergoing noncardiac surgery, our objectives were to: (1) determine the feasibility of undertaking a large international cohort study; (2) estimate the current incidence of major perioperative vascular events; (3) compare the observed event rates to the expected event rates according to the Revised Cardiac Risk Index (RCRI); and (4) provide an estimate of the proportion of myocardial infarctions without ischemic symptoms that may go undetected without perioperative troponin monitoring. Design: An international prospective cohort pilot study. Participants: Patients undergoing noncardiac surgery who were >45 years of age, receiving a general or regional anesthetic, and requiring hospital admission. Measurements: Patients had a Roche fourth-generation Elecsys troponin T measurement collected 6 to 12 hours postoperatively and on the first, second, and third days after surgery. Our primary outcome was major vascular events (a composite of vascular death [i.e., death from vascular causes], nonfatal myocardial infarction, nonfatal cardiac arrest, and nonfatal stroke) at 30 days after surgery. Our definition for perioperative myocardial infarction included: (1) an elevated troponin T measurement with at least one of the following defining features: ischemic symptoms, development of pathologic Q waves, ischemic electrocardiogram changes, coronary artery intervention, or cardiac imaging evidence of myocardial infarction; or (2) autopsy findings of acute or healing myocardial infarction. Results: We recruited 432 patients across 5 hospitals in Canada, China, Italy, Colombia, and Brazil. During the first 30 days after surgery, 6.3% (99% confidence interval 3.9–10.0) of the patients suffered a major vascular event (10 vascular deaths, 16 nonfatal myocardial infarctions, and 1 nonfatal stroke). The observed event rate was increased 6-fold compared with the event rate expected from the RCRI. Of the 18 patients who suffered a myocardial infarction, 12 (66.7%) had no ischemic symptoms to suggest myocardial infarction. Conclusions: This study suggests that major perioperative vascular events are common, that the RCRI underestimates risk, and that monitoring troponins after surgery can assist physicians to avoid missing myocardial infarction. These results underscore the need for a large international prospective cohort study. |
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Vision Pilot Study InvestigatorsDevereaux, Philip J.Chan, Matthew T.V.Walsh, MikeVillar, Juan CarlosPolanczyk, Carisi AnneSeligman, Beatriz Graeff SantosRohde, Luis Eduardo PaimSeligman, RenatoGuyatt, GordonAlonso-Coello, PabloSilva, Otávio Berwanger daHeels-Ansdell, DianeSimunovic, NicoleSchünemann, Holger J.Yusuf, Salim2021-08-27T04:18:07Z20111911-2092http://hdl.handle.net/10183/226227000907571Objectives: Among patients undergoing noncardiac surgery, our objectives were to: (1) determine the feasibility of undertaking a large international cohort study; (2) estimate the current incidence of major perioperative vascular events; (3) compare the observed event rates to the expected event rates according to the Revised Cardiac Risk Index (RCRI); and (4) provide an estimate of the proportion of myocardial infarctions without ischemic symptoms that may go undetected without perioperative troponin monitoring. Design: An international prospective cohort pilot study. Participants: Patients undergoing noncardiac surgery who were >45 years of age, receiving a general or regional anesthetic, and requiring hospital admission. Measurements: Patients had a Roche fourth-generation Elecsys troponin T measurement collected 6 to 12 hours postoperatively and on the first, second, and third days after surgery. Our primary outcome was major vascular events (a composite of vascular death [i.e., death from vascular causes], nonfatal myocardial infarction, nonfatal cardiac arrest, and nonfatal stroke) at 30 days after surgery. Our definition for perioperative myocardial infarction included: (1) an elevated troponin T measurement with at least one of the following defining features: ischemic symptoms, development of pathologic Q waves, ischemic electrocardiogram changes, coronary artery intervention, or cardiac imaging evidence of myocardial infarction; or (2) autopsy findings of acute or healing myocardial infarction. Results: We recruited 432 patients across 5 hospitals in Canada, China, Italy, Colombia, and Brazil. During the first 30 days after surgery, 6.3% (99% confidence interval 3.9–10.0) of the patients suffered a major vascular event (10 vascular deaths, 16 nonfatal myocardial infarctions, and 1 nonfatal stroke). The observed event rate was increased 6-fold compared with the event rate expected from the RCRI. Of the 18 patients who suffered a myocardial infarction, 12 (66.7%) had no ischemic symptoms to suggest myocardial infarction. Conclusions: This study suggests that major perioperative vascular events are common, that the RCRI underestimates risk, and that monitoring troponins after surgery can assist physicians to avoid missing myocardial infarction. These results underscore the need for a large international prospective cohort study.application/pdfengOpen Medicine. Otawa. Vol. 5, no. 4 (2011), p. e193-e200.Doenças vascularesEstudos de coortesCirurgiaAn international prospective cohort study evaluating major vascular complications among patients undergoing noncardiac surgery : the VISION Pilot StudyEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT000907571.pdf.txt000907571.pdf.txtExtracted Texttext/plain37071http://www.lume.ufrgs.br/bitstream/10183/226227/2/000907571.pdf.txt817f99e99e455c2ca9ea94a04f1bccafMD52ORIGINAL000907571.pdfTexto completo (inglês)application/pdf470041http://www.lume.ufrgs.br/bitstream/10183/226227/1/000907571.pdfaff86a44cba5ab0ac4d0e210457488c4MD5110183/2262272021-09-19 04:27:42.284635oai:www.lume.ufrgs.br:10183/226227Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-09-19T07:27:42Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
An international prospective cohort study evaluating major vascular complications among patients undergoing noncardiac surgery : the VISION Pilot Study |
title |
An international prospective cohort study evaluating major vascular complications among patients undergoing noncardiac surgery : the VISION Pilot Study |
spellingShingle |
An international prospective cohort study evaluating major vascular complications among patients undergoing noncardiac surgery : the VISION Pilot Study Vision Pilot Study Investigators Doenças vasculares Estudos de coortes Cirurgia |
title_short |
An international prospective cohort study evaluating major vascular complications among patients undergoing noncardiac surgery : the VISION Pilot Study |
title_full |
An international prospective cohort study evaluating major vascular complications among patients undergoing noncardiac surgery : the VISION Pilot Study |
title_fullStr |
An international prospective cohort study evaluating major vascular complications among patients undergoing noncardiac surgery : the VISION Pilot Study |
title_full_unstemmed |
An international prospective cohort study evaluating major vascular complications among patients undergoing noncardiac surgery : the VISION Pilot Study |
title_sort |
An international prospective cohort study evaluating major vascular complications among patients undergoing noncardiac surgery : the VISION Pilot Study |
author |
Vision Pilot Study Investigators |
author_facet |
Vision Pilot Study Investigators Devereaux, Philip J. Chan, Matthew T.V. Walsh, Mike Villar, Juan Carlos Polanczyk, Carisi Anne Seligman, Beatriz Graeff Santos Rohde, Luis Eduardo Paim Seligman, Renato Guyatt, Gordon Alonso-Coello, Pablo Silva, Otávio Berwanger da Heels-Ansdell, Diane Simunovic, Nicole Schünemann, Holger J. Yusuf, Salim |
author_role |
author |
author2 |
Devereaux, Philip J. Chan, Matthew T.V. Walsh, Mike Villar, Juan Carlos Polanczyk, Carisi Anne Seligman, Beatriz Graeff Santos Rohde, Luis Eduardo Paim Seligman, Renato Guyatt, Gordon Alonso-Coello, Pablo Silva, Otávio Berwanger da Heels-Ansdell, Diane Simunovic, Nicole Schünemann, Holger J. Yusuf, Salim |
author2_role |
author author author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Vision Pilot Study Investigators Devereaux, Philip J. Chan, Matthew T.V. Walsh, Mike Villar, Juan Carlos Polanczyk, Carisi Anne Seligman, Beatriz Graeff Santos Rohde, Luis Eduardo Paim Seligman, Renato Guyatt, Gordon Alonso-Coello, Pablo Silva, Otávio Berwanger da Heels-Ansdell, Diane Simunovic, Nicole Schünemann, Holger J. Yusuf, Salim |
dc.subject.por.fl_str_mv |
Doenças vasculares Estudos de coortes Cirurgia |
topic |
Doenças vasculares Estudos de coortes Cirurgia |
description |
Objectives: Among patients undergoing noncardiac surgery, our objectives were to: (1) determine the feasibility of undertaking a large international cohort study; (2) estimate the current incidence of major perioperative vascular events; (3) compare the observed event rates to the expected event rates according to the Revised Cardiac Risk Index (RCRI); and (4) provide an estimate of the proportion of myocardial infarctions without ischemic symptoms that may go undetected without perioperative troponin monitoring. Design: An international prospective cohort pilot study. Participants: Patients undergoing noncardiac surgery who were >45 years of age, receiving a general or regional anesthetic, and requiring hospital admission. Measurements: Patients had a Roche fourth-generation Elecsys troponin T measurement collected 6 to 12 hours postoperatively and on the first, second, and third days after surgery. Our primary outcome was major vascular events (a composite of vascular death [i.e., death from vascular causes], nonfatal myocardial infarction, nonfatal cardiac arrest, and nonfatal stroke) at 30 days after surgery. Our definition for perioperative myocardial infarction included: (1) an elevated troponin T measurement with at least one of the following defining features: ischemic symptoms, development of pathologic Q waves, ischemic electrocardiogram changes, coronary artery intervention, or cardiac imaging evidence of myocardial infarction; or (2) autopsy findings of acute or healing myocardial infarction. Results: We recruited 432 patients across 5 hospitals in Canada, China, Italy, Colombia, and Brazil. During the first 30 days after surgery, 6.3% (99% confidence interval 3.9–10.0) of the patients suffered a major vascular event (10 vascular deaths, 16 nonfatal myocardial infarctions, and 1 nonfatal stroke). The observed event rate was increased 6-fold compared with the event rate expected from the RCRI. Of the 18 patients who suffered a myocardial infarction, 12 (66.7%) had no ischemic symptoms to suggest myocardial infarction. Conclusions: This study suggests that major perioperative vascular events are common, that the RCRI underestimates risk, and that monitoring troponins after surgery can assist physicians to avoid missing myocardial infarction. These results underscore the need for a large international prospective cohort study. |
publishDate |
2011 |
dc.date.issued.fl_str_mv |
2011 |
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2021-08-27T04:18:07Z |
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1911-2092 |
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Open Medicine. Otawa. Vol. 5, no. 4 (2011), p. e193-e200. |
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