Systematic review, meta-analysis and economic modelling of ...
Systematic review, meta-analysis and economic modelling of ...
Systematic review, meta-analysis and economic modelling of ...
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DOI: 10.3310/hta17010 Health Technology Assessment 2013 Vol. 17 No. 1Appendix 9 Final project descriptionProject titleCost-effectiveness <strong>of</strong> diagnostic strategies for suspected acute coronary syndrome (ACS).Planned investigationResearch objectives1. To estimate the diagnostic accuracy for myocardial infarction <strong>and</strong> prognostic accuracy for cardiacevents <strong>of</strong> biomarkers used to investigate suspected ACS.2. To estimate the cost-effectiveness <strong>of</strong> biomarker strategies for investigating suspected ACS.3. To estimate the diagnostic accuracy for coronary artery disease (CAD) <strong>and</strong> prognostic accuracy forcardiac events <strong>of</strong> multislice CT coronary angiography <strong>and</strong> exercise ECG in patients with suspected ACS.4. To estimate the cost-effectiveness <strong>of</strong> multislice CT coronary angiography <strong>and</strong> exercise ECG forinvestigating patients with troponin-negative suspected ACS.5. To identify the critical areas <strong>of</strong> uncertainty in the management <strong>of</strong> suspected ACS, where future primaryresearch would produce the most benefit.Existing researchACS typically occurs when a patient with CAD develops obstruction <strong>of</strong> their heart arteries. This can lead tomyocardial infarction (MI), heart failure, arrhythmia, cardiac arrest <strong>and</strong> death. ACS has 6-month mortality<strong>of</strong> up to 20% [2] <strong>and</strong> a fifth <strong>of</strong> patients are rehospitalised within 6 months <strong>of</strong> their initial admission [3].ACS usually presents as chest pain <strong>and</strong> must be differentiated from other common causes <strong>of</strong> chest pain,such as muscular pain, gastro-oesophageal pain <strong>and</strong> anxiety. Differentiation is difficult because clinicalassessment is unreliable <strong>and</strong> the ECG may be normal in the presence <strong>of</strong> ACS. Patients with suspected ACStherefore constitute a large <strong>and</strong> varied population, many <strong>of</strong> whom will not have ACS or CAD, but havenon-cardiac causes for their chest pain. Accurate identification <strong>of</strong> ACS <strong>and</strong> CAD are therefore required toguide subsequent intervention.Suspected ACS represents a substantial health-care problem <strong>and</strong> investigation represents a substantialchallenge. Chest pain is responsible for around 700,000 emergency department attendances in Engl<strong>and</strong><strong>and</strong> Wales [4], with the main reason for attendance being suspected ACS. Hospital Episodes Statistics forEngl<strong>and</strong> (2006–7) showed 158,342 emergency admissions with ischaemic heart disease, accounting foralmost 1 million bed-days. In addition, many <strong>of</strong> the 351,716 emergency admissions classified as ‘signs <strong>and</strong>symptoms involving the circulatory or respiratory system’ will have been due to suspicion <strong>of</strong> ACS.Investigation for suspected ACS has two main elements: (1) diagnosis <strong>of</strong> MI, <strong>and</strong> (2) diagnosis <strong>of</strong>underlying CAD. Diagnosis <strong>of</strong> unstable angina is another consideration but <strong>of</strong> decreasing importance forreasons outlined below.Diagnosis <strong>of</strong> MIThe term MI usually refers to NSTEMI in the context <strong>of</strong> investigating suspected ACS. Although ST-elevationMI is included in the definition <strong>of</strong> ACS it can usually be identified on the presenting ECG <strong>and</strong> thus doesnot form part <strong>of</strong> the typical diagnostic challenge <strong>of</strong> suspected ACS, although ECG interpretation <strong>and</strong>differentiation from other causes <strong>of</strong> ST elevation may present separate challenges.© Queen’s Printer <strong>and</strong> Controller <strong>of</strong> HMSO 2013. This work was produced by Goodacre et al. under the terms <strong>of</strong> a commissioning contract issued by the Secretary <strong>of</strong> Statefor Health. This issue may be freely reproduced for the purposes <strong>of</strong> private research <strong>and</strong> study <strong>and</strong> extracts (or indeed, the full report) may be included in pr<strong>of</strong>essional journalsprovided that suitable acknowledgement is made <strong>and</strong> the reproduction is not associated with any form <strong>of</strong> advertising. Applications for commercial reproduction should beaddressed to: NIHR Journals Library, National Institute for Health Research, Evaluation, Trials <strong>and</strong> Studies Coordinating Centre, Alpha House, University <strong>of</strong> Southampton SciencePark, Southampton SO16 7NS, UK.177