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C-reactive Protein as a Predictor of Adverse outcome in Patients with Acute Coronary Syndrome
BACKGROUND AND OBJECTIVES: The acute-phase reactant C-reactive protein (CRP) has been shown to reflect systemic and vascular inflammation and to predict future cardiovascular events. The objective of this study was to evaluate the prognostic value of CRP in predicting cardiovascular outcome in patie...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3385197/ https://www.ncbi.nlm.nih.gov/pubmed/22754634 http://dx.doi.org/10.4103/1995-705X.96660 |
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author | Sheikh, A. S. Yahya, S. Sheikh, N. S. Sheikh, A. A |
author_facet | Sheikh, A. S. Yahya, S. Sheikh, N. S. Sheikh, A. A |
author_sort | Sheikh, A. S. |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: The acute-phase reactant C-reactive protein (CRP) has been shown to reflect systemic and vascular inflammation and to predict future cardiovascular events. The objective of this study was to evaluate the prognostic value of CRP in predicting cardiovascular outcome in patients presenting with acute coronary syndromes. PATIENTS AND METHODS: This prospective, single-centered study was carried out by the Department of Pathology in collaboration with the Department of Cardiology, Bolan Medical College Complex Quetta, Balochistan, Pakistan from January 2009 to December 2009. We studied 963 consecutive patients presenting with chest pain to Accident and Emergency Department. Patients were divided into four groups. Group-1 comprised patients with unstable angina; group-2 included patients with acute ST elevation myocardial infarction (STEMI); group-3 comprised patients with Non-ST elevation myocardial infarction (Non-STEMI) and group-4 was the control group. All four groups were followed-up for 90 days for occurrence of cardiovascular events. RESULTS: The CRP was elevated (>3 mg/L) among 27.6% patients in Group-1; 70.9% in group- 2; 77.9% in group-3 and 5.3% in the control group. Among cases with elevated CRP, 92.1% had a cardiac event compared to 34.3% among patients with CRP £3 mg/L (P < 0.0001). The mortality was significantly higher (P < 0.0001) in group-2 (8.9%) and group-3 (11.9%) as compared to group-1 (2.1%). There was no cardiac event or mortality in Group-4. CONCLUSIONS: Elevated CRP is a predictor of adverse outcome in patients with acute coronary syndromes and helps in identifying patients who may be at risk of cardiovascular complications. |
format | Online Article Text |
id | pubmed-3385197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-33851972012-07-02 C-reactive Protein as a Predictor of Adverse outcome in Patients with Acute Coronary Syndrome Sheikh, A. S. Yahya, S. Sheikh, N. S. Sheikh, A. A Heart Views Original Article BACKGROUND AND OBJECTIVES: The acute-phase reactant C-reactive protein (CRP) has been shown to reflect systemic and vascular inflammation and to predict future cardiovascular events. The objective of this study was to evaluate the prognostic value of CRP in predicting cardiovascular outcome in patients presenting with acute coronary syndromes. PATIENTS AND METHODS: This prospective, single-centered study was carried out by the Department of Pathology in collaboration with the Department of Cardiology, Bolan Medical College Complex Quetta, Balochistan, Pakistan from January 2009 to December 2009. We studied 963 consecutive patients presenting with chest pain to Accident and Emergency Department. Patients were divided into four groups. Group-1 comprised patients with unstable angina; group-2 included patients with acute ST elevation myocardial infarction (STEMI); group-3 comprised patients with Non-ST elevation myocardial infarction (Non-STEMI) and group-4 was the control group. All four groups were followed-up for 90 days for occurrence of cardiovascular events. RESULTS: The CRP was elevated (>3 mg/L) among 27.6% patients in Group-1; 70.9% in group- 2; 77.9% in group-3 and 5.3% in the control group. Among cases with elevated CRP, 92.1% had a cardiac event compared to 34.3% among patients with CRP £3 mg/L (P < 0.0001). The mortality was significantly higher (P < 0.0001) in group-2 (8.9%) and group-3 (11.9%) as compared to group-1 (2.1%). There was no cardiac event or mortality in Group-4. CONCLUSIONS: Elevated CRP is a predictor of adverse outcome in patients with acute coronary syndromes and helps in identifying patients who may be at risk of cardiovascular complications. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3385197/ /pubmed/22754634 http://dx.doi.org/10.4103/1995-705X.96660 Text en Copyright: © Heart Views http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Sheikh, A. S. Yahya, S. Sheikh, N. S. Sheikh, A. A C-reactive Protein as a Predictor of Adverse outcome in Patients with Acute Coronary Syndrome |
title | C-reactive Protein as a Predictor of Adverse outcome in Patients with Acute Coronary Syndrome |
title_full | C-reactive Protein as a Predictor of Adverse outcome in Patients with Acute Coronary Syndrome |
title_fullStr | C-reactive Protein as a Predictor of Adverse outcome in Patients with Acute Coronary Syndrome |
title_full_unstemmed | C-reactive Protein as a Predictor of Adverse outcome in Patients with Acute Coronary Syndrome |
title_short | C-reactive Protein as a Predictor of Adverse outcome in Patients with Acute Coronary Syndrome |
title_sort | c-reactive protein as a predictor of adverse outcome in patients with acute coronary syndrome |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3385197/ https://www.ncbi.nlm.nih.gov/pubmed/22754634 http://dx.doi.org/10.4103/1995-705X.96660 |
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