How Safe Is the Outpatient Management of Patients with Acute Chest Pain and Mildly Increased Cardiac Troponin Concentrations?

Author:

Meune Christophe12,Reichlin Tobias3,Irfan Affan1,Schaub Nora1,Twerenbold Raphael1,Meissner Julia1,Reiter Miriam1,Lüthi Adrian1,Haaf Philip1,Balmelli Cathrin1,Drexler Beatrice1,Winkler Katrin45,Hochholzer Willibald6,Osswald Stefan3,Mueller Christian13

Affiliation:

1. Department of Internal Medicine, University Hospital, Basel, Switzerland

2. Paris Descartes University, Cardiology department, Cochin Hospital, Assistance Publique–Hôpitaux de Paris, Paris, France

3. Department of Cardiology, University Hospital Basel, Basel, Switzerland

4. Servicio de Pneumologia, Hospital del Mar–Institut Municipal d'Investigació Mèdica (IMIM), Universitat Pompeu Fabra, Centro de Investigación en Red de Enfermedades Respiratorias, Instituto de Salud Carlos III, Barcelona, Spain

5. Servicio de Urgencias, Hospital del Mar–IMIM, Barcelona, Spain

6. Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA

Abstract

Abstract BACKGROUND The appropriate management of patients discharged from the emergency department (ED) with increased high-sensitivity cardiac troponin T (hs-cTnT) but normal or borderline-high conventional cardiac troponin concentrations is unknown. METHODS We investigated 643 consecutive ED patients with acute chest pain who had been discharged for outpatient management after acute myocardial infarction (AMI) had been ruled out by serial measurements of conventional cardiac troponin. hs-cTnT was measured blindly, and we calculated the rates of all-cause mortality (primary endpoint) and subsequent AMI (secondary endpoint) at 30, 90, and 360 days. RESULTS hs-cTnT concentrations were increased (>14 ng/L) in 114 patients (18%) but <30 ng/L in 95% of these patients. Of those 114 patients, 96 (84%) had an adjudicated noncoronary cause of chest pain. Thirty-day mortality (95% CI) was 0.9% (0.1%–6.1%), 90-day mortality was 2.7% (0.9%–8.1%), and 360-day mortality was 5.2% (2.2%–11.9%) in patients with increased hs-cTnT; respective rates (95% CI) of AMI were 0.0%, 1.9% (0.5%–7.2%), and 7.6% (3.7%–15.3%). Increased hs-cTnT was associated with increased mortality and AMI at 90 days (P = 0.006 and P = 0.081, respectively) and 360 days (P = 0.001 for both). CONCLUSIONS hs-cTnT is a strong prognosticator of intermediate and long-term mortality and AMI in low-risk patients discharged from the ED after AMI has been ruled out. The relatively low rate of 30-day events may suggest that patients without acute coronary syndrome and small increases in cardiac troponin are in need of further investigations and treatments, but not necessarily immediate hospitalization.

Funder

Freie Akademische Gesellschaft Basel

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Schweizerische Herzstiftung

Universität Basel

Department of Internal Medicine

University Hospital Basel

Roche

Brahms

Abbott

Nanosphere

Siemens

Publisher

Oxford University Press (OUP)

Subject

Biochemistry, medical,Clinical Biochemistry

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5. National Academy of Clinical Biochemistry Laboratory Medicine Practice Guidelines: clinical characteristics and utilization of biochemical markers in acute coronary syndromes;Morrow;Circulation,2007

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