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DOI: 10.3310/hta17010 Health Technology Assessment 2013 Vol. 17 No. 1Representative spectrum?Acceptable reference st<strong>and</strong>ard?Acceptable delay between tests?Partial verification avoided?Differential verification avoided?Incorporation avoided?Reference st<strong>and</strong>ard results blinded?Index test results blinded?Body 2011 57 ++++++–+Cete 2010 58 ++++++??Charpentier 2010 59 ++++++++Di Serio 2005 63 ??+?++??Ecollan 2007 64 ++++++??Garcia-Valdecasas 2011 49 ++?+++++Haltern 2010 67 ++++++??Hjortshoj 2010 68 ++++++??Ilva 2009 50 ++++++??LeFevre 2007 72 ??++++++Li 2010 73 ++++++++Liao 2009 74 +??++?––Mad 2007 75 +??++?++McCann 2008 76 +++++?++Mion 2007 77 –+++?+??Naroo 2009 78 ++++++++Valle 2007 82 +?+++++?FIGURE 14 Quality assessment <strong>of</strong> diagnostic studies <strong>of</strong> H-FABP.test characteristics. Reporting <strong>of</strong> exclusion criteria was variable <strong>and</strong> some studies excluded patients withdiagnostic ECG changes. The prevalence <strong>of</strong> MI was generally high <strong>and</strong> varied from 18% to 73%. Themedian time from symptom onset to sampling varied from 2.2 to 7.8 hours. There was no consistencyin the diagnostic threshold used. It ranged from 51 to 150 µg/l <strong>and</strong> 5 out <strong>of</strong> 13 studies used differentthresholds for men <strong>and</strong> women, whereas 8 out <strong>of</strong> 13 studies used the same threshold. Several studies usedrelatively high thresholds for positivity for the reference st<strong>and</strong>ard troponin or did not report the timing <strong>of</strong>sampling or the assay used.Quality assessment <strong>of</strong> diagnostic studies <strong>of</strong> myoglobinFigure 21 shows the quality assessments for studies <strong>of</strong> myoglobin, whereas Figure 22 shows themethodological quality summary. The quality assessment <strong>of</strong> acceptability <strong>of</strong> the reference st<strong>and</strong>ard waslimited to whether or not the reference st<strong>and</strong>ard criteria were reported clearly <strong>and</strong> met the universal© 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.39

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