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The forgotten lead: does aVR ST-deviation add insight into the outcomes of ST-elevation myocardial infarction patients?

Publication ,  Journal Article
Alherbish, A; Westerhout, CM; Fu, Y; White, HD; Granger, CB; Wagner, G; Armstrong, PW
Published in: Am Heart J
August 2013

BACKGROUND: Lead aVR ST-segment deviation has been associated with increased mortality in ST-elevation myocardial infarction patients treated with fibrinolysis. However, its prognostic value in a contemporaneous population undergoing primary percutaneous coronary intervention is unknown. METHODS AND RESULTS: A core laboratory examined the 12-lead baseline electrocardiogram in 5,683 patients presenting within 6 hours of symptom onset in the APEX-AMI trial, and readers were blinded to study treatment and clinical outcomes. aVR ST-deviation was significantly associated with 90-day death when compared with patients with no aVR ST-deviation (aVR ST-depression [ST-D] 5%, aVR ST-elevation [ST-E] 10.2%, no ST-deviation [N] aVR 3.8%, P < .001). After multivariable adjustment, aVR ST-E was strongly associated with 90-day death in inferior myocardial infarction (MI) (adjusted hazard ratio [HR] 5.87, 95% CI 2.09-16.5), whereas aVR ST-D was associated with excess mortality in noninferior MI (1.53, 1.06-2.22; P [interaction] < .001). aVR ST-E was also significantly associated with the presence of left main coronary (N aVR 1.8%, aVR ST-E 7.7%, P ≤ .001) and multivessel coronary disease (N aVR 41.3%, aVR ST-E 53.3%, P ≤ .001). CONCLUSIONS: Lead aVR ST-deviation is common, occurring in one-third of all ST-elevation myocardial infarction patients and independently associated with increased 90-day death. Myocardial infarction location modulates the prognostic significance of aVR ST-deviation such that lead aVR ST-E in inferior MI and ST-D in noninferior MI represent 2 high-risk groups. There was also more frequent advanced coronary disease in patients with aVR ST-E.

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Published In

Am Heart J

DOI

EISSN

1097-6744

Publication Date

August 2013

Volume

166

Issue

2

Start / End Page

333 / 339

Location

United States

Related Subject Headings

  • Randomized Controlled Trials as Topic
  • Prognosis
  • Percutaneous Coronary Intervention
  • Myocardial Infarction
  • Middle Aged
  • Male
  • Kaplan-Meier Estimate
  • Humans
  • Female
  • Electrodes
 

Citation

APA
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ICMJE
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Alherbish, A., Westerhout, C. M., Fu, Y., White, H. D., Granger, C. B., Wagner, G., & Armstrong, P. W. (2013). The forgotten lead: does aVR ST-deviation add insight into the outcomes of ST-elevation myocardial infarction patients? Am Heart J, 166(2), 333–339. https://doi.org/10.1016/j.ahj.2013.05.018
Alherbish, Aws, Cynthia M. Westerhout, Yuling Fu, Harvey D. White, Christopher B. Granger, Galen Wagner, and Paul W. Armstrong. “The forgotten lead: does aVR ST-deviation add insight into the outcomes of ST-elevation myocardial infarction patients?Am Heart J 166, no. 2 (August 2013): 333–39. https://doi.org/10.1016/j.ahj.2013.05.018.
Alherbish A, Westerhout CM, Fu Y, White HD, Granger CB, Wagner G, et al. The forgotten lead: does aVR ST-deviation add insight into the outcomes of ST-elevation myocardial infarction patients? Am Heart J. 2013 Aug;166(2):333–9.
Alherbish, Aws, et al. “The forgotten lead: does aVR ST-deviation add insight into the outcomes of ST-elevation myocardial infarction patients?Am Heart J, vol. 166, no. 2, Aug. 2013, pp. 333–39. Pubmed, doi:10.1016/j.ahj.2013.05.018.
Alherbish A, Westerhout CM, Fu Y, White HD, Granger CB, Wagner G, Armstrong PW. The forgotten lead: does aVR ST-deviation add insight into the outcomes of ST-elevation myocardial infarction patients? Am Heart J. 2013 Aug;166(2):333–339.
Journal cover image

Published In

Am Heart J

DOI

EISSN

1097-6744

Publication Date

August 2013

Volume

166

Issue

2

Start / End Page

333 / 339

Location

United States

Related Subject Headings

  • Randomized Controlled Trials as Topic
  • Prognosis
  • Percutaneous Coronary Intervention
  • Myocardial Infarction
  • Middle Aged
  • Male
  • Kaplan-Meier Estimate
  • Humans
  • Female
  • Electrodes