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Stress-Delta B-Type Natriuretic Peptide Does Not Exclude ACS in the ED.

Publication ,  Journal Article
Susman, SJ; Bouffler, A; Gordee, A; Kuchibhatla, M; Leahy, JC; Griffin, SM; Christenson, RH; Newby, LK; Limkakeng, AT
Published in: J Appl Lab Med
September 1, 2022

BACKGROUND: There are many detectable changes in circulating biomarkers in the setting of myocardial ischemia. We hypothesize that there are associated changes in circulating B-type natriuretic peptide (BNP) level after stress-induced myocardial ischemia, which can be used for emergency department (ED) acute coronary syndrome (ACS) risk stratification. METHODS: In a prospective study, we enrolled 340 patients over the age of 30 receiving an exercise echocardiography stress test in an ED observational unit for suspected ACS. We collected blood samples at baseline and at 2 and 4 h post-stress test, measuring the relative and absolute changes (stress-delta) in plasma BNP concentrations. In addition, patients were contacted at 90 days and at 1 year posttest for a follow-up. We calculated the diagnostic test characteristics of stress-delta BNP for a composite outcome of ischemic imaging on stress echocardiogram, nonelective percutaneous coronary intervention, coronary artery bypass graft surgery, subsequent acute myocardial infarction, or cardiac death at 1 year via a logistic regression. We analyzed the 2-h BNP concentrations using an ANOVA model to adjust for the baseline BNP level. RESULTS: Baseline and 2-h post-stress BNP were both higher in the positive outcome group, but the stress-delta BNP was not. Stress-delta BNP had a sensitivity and specificity, respectively, of 53% and 76% at 2 h and 67% and 68% at 4 h. It was noted that patients with the composite outcome had a higher baseline BNP level. CONCLUSIONS: BNP stress-deltas are poor diagnostic means for ACS risk stratification, but resting BNP remains a promising prognostic tool for ED patients with suspected ACS.

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Published In

J Appl Lab Med

DOI

ISSN

2576-9456

Publication Date

September 1, 2022

Volume

7

Issue

5

Start / End Page

1098 / 1107

Location

England

Related Subject Headings

  • Prospective Studies
  • Natriuretic Peptide, Brain
  • Myocardial Ischemia
  • Myocardial Infarction
  • Humans
  • Emergency Service, Hospital
  • Coronary Artery Disease
  • Acute Coronary Syndrome
  • 3205 Medical biochemistry and metabolomics
  • 3202 Clinical sciences
 

Citation

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Susman, S. J., Bouffler, A., Gordee, A., Kuchibhatla, M., Leahy, J. C., Griffin, S. M., … Limkakeng, A. T. (2022). Stress-Delta B-Type Natriuretic Peptide Does Not Exclude ACS in the ED. J Appl Lab Med, 7(5), 1098–1107. https://doi.org/10.1093/jalm/jfac027
Susman, Stephen J., Andrew Bouffler, Alexander Gordee, Maragatha Kuchibhatla, J Clancy Leahy, S Michelle Griffin, Robert H. Christenson, L Kristin Newby, and Alexander T. Limkakeng. “Stress-Delta B-Type Natriuretic Peptide Does Not Exclude ACS in the ED.J Appl Lab Med 7, no. 5 (September 1, 2022): 1098–1107. https://doi.org/10.1093/jalm/jfac027.
Susman SJ, Bouffler A, Gordee A, Kuchibhatla M, Leahy JC, Griffin SM, et al. Stress-Delta B-Type Natriuretic Peptide Does Not Exclude ACS in the ED. J Appl Lab Med. 2022 Sep 1;7(5):1098–107.
Susman, Stephen J., et al. “Stress-Delta B-Type Natriuretic Peptide Does Not Exclude ACS in the ED.J Appl Lab Med, vol. 7, no. 5, Sept. 2022, pp. 1098–107. Pubmed, doi:10.1093/jalm/jfac027.
Susman SJ, Bouffler A, Gordee A, Kuchibhatla M, Leahy JC, Griffin SM, Christenson RH, Newby LK, Limkakeng AT. Stress-Delta B-Type Natriuretic Peptide Does Not Exclude ACS in the ED. J Appl Lab Med. 2022 Sep 1;7(5):1098–1107.

Published In

J Appl Lab Med

DOI

ISSN

2576-9456

Publication Date

September 1, 2022

Volume

7

Issue

5

Start / End Page

1098 / 1107

Location

England

Related Subject Headings

  • Prospective Studies
  • Natriuretic Peptide, Brain
  • Myocardial Ischemia
  • Myocardial Infarction
  • Humans
  • Emergency Service, Hospital
  • Coronary Artery Disease
  • Acute Coronary Syndrome
  • 3205 Medical biochemistry and metabolomics
  • 3202 Clinical sciences