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10.1136/heartjnl-2014-307288

http://scihub22266oqcxt.onion/10.1136/heartjnl-2014-307288
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suck abstract from ncbi


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pmid25691511
      Heart 2015 ; 101 (13 ): 1041-6
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  • A novel diagnostic protocol to identify patients suitable for discharge after a single high-sensitivity troponin #MMPMID25691511
  • Carlton EW ; Cullen L ; Than M ; Gamble J ; Khattab A ; Greaves K
  • Heart 2015[Jul]; 101 (13 ): 1041-6 PMID25691511 show ga
  • OBJECTIVE: To establish whether a novel accelerated diagnostic protocol (ADP) for suspected acute coronary syndrome (ACS) could successfully identify low-risk patients suitable for discharge after a single high-sensitivity troponin T (hs-cTnT) taken at presentation to the emergency department. We also compared the diagnostic accuracy of this ADP with strategies using initial undetectable hs-cTnT. METHODS: This prospective observational study evaluated the ability of the Triage Rule-out Using high-Sensitivity Troponin (TRUST) ADP to identify low-risk patients with suspected ACS. The ADP incorporated a single presentation hs-cTnT of <14?ng/L, a non-ischaemic ECG and a modified Goldman risk score. Diagnostic performance of the ADP was compared with the detection limit cut-offs of hs-cTnT (<5?ng/L and <3?ng/L). The primary end point was fatal/non-fatal acute myocardial infarction (AMI) within 30?days. RESULTS: 960 participants were recruited, mean age 58.0?years, 80 (8.3%) had an AMI. The TRUST ADP classified 382 (39.8%) as low-risk with a sensitivity for identifying AMI of 98.8% (95% CI 92.5% to 99.9%). hs-cTnT detection limits (<5?ng/L and <3?ng/L) had a sensitivity of 100% (94.3 to 100) and 100% (94.4 to 100), respectively. The TRUST ADP identified more patients suitable for early discharge at 39.8% vs 29.3% (<5?ng/L) and 7.9% (<3?ng/L) (p<0.001) with a lower false-positive rate for AMI detection; specificity 43.3% (95% CI 42.7% to 43.4%) vs 32.0% (95% CI 31.5% to 32.0%) and 8.6% (95% CI 8.1% to 8.6%), respectively. CONCLUSIONS: The TRUST ADP, which incorporates structured risk-assessment and a single presentation hs-cTnT blood draw, has potential to allow early discharge in 40% of patients with suspected ACS and has greater clinical utility than undetectable hs-cTnT strategies. TRIAL REGISTRATION NUMBER: ISRCTN No. 21109279.
  • |*Acute Coronary Syndrome/blood/diagnosis/physiopathology [MESH]
  • |Australia [MESH]
  • |Biomarkers/blood [MESH]
  • |Clinical Protocols/*standards [MESH]
  • |Diagnosis, Differential [MESH]
  • |Dimensional Measurement Accuracy [MESH]
  • |Female [MESH]
  • |Humans [MESH]
  • |Male [MESH]
  • |Middle Aged [MESH]
  • |Patient Discharge/*standards [MESH]
  • |Predictive Value of Tests [MESH]
  • |Prognosis [MESH]
  • |ROC Curve [MESH]
  • |Risk Assessment/methods [MESH]
  • |Severity of Illness Index [MESH]
  • |Time Factors [MESH]


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