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DOI: 10.3310/hta17010 Health Technology Assessment 2013 Vol. 17 No. 1TABLE 16 Index <strong>and</strong> reference st<strong>and</strong>ard tests used in studies <strong>of</strong> other biomarkersStudyIndex test analyser(timing is at presentation unlessotherwise stated) Threshold Reference test assay <strong>and</strong> timingReference Tndiagnosticthreshold (µg/l)MI prevalencein sample (%)Apple 2009 55 CD40L, R&D Systems ELISA 1.08 ng/l Dade Behring Dimension or Stratus CS TnI at 8 hoursafter presentation0.1 5Apple 2009 55 MPO, Assay Designs ELISA 125 µg/l Dade Behring Dimension or Stratus CS TnI at 8 hoursafter presentation0.1 5Apple 2009 55 MMP9, Assay Designs ELISA 233 µg/l Dade Behring Dimension or Stratus CS TnI at 8 hoursafter presentation0.1 5Apple 2009 55 CRP, Dade Behring Dimension 1.0 <strong>and</strong> 3.0 mg/l Dade Behring Dimension or Stratus CS TnI at 8 hoursafter presentation0.1 5Apple 2009 55 NT-pro-BNP, Roche Elecsys 125 ng/l age < 75 years,450 ng/l age > 75 yearsDade Behring Dimension or Stratus CS TnI at 8 hoursafter presentation0.1 5Bassan 2005 56 Biosite immun<strong>of</strong>luorescence BNP assay 100 pg/ml Dade Behring TnI; within 9 hours post-admission; 1.0 11Body 2011 57 BNP Alere Fluorescence Immunoassay 73 ng/ml cTnT; Roche Elecsys; at least 12 hours after symptomonset0.01 18Body 2011 57 MPO Alere Fluorescence Immunoassay 510 pM cTnT; Roche Elecsys; at least 12 hours after symptomonset0.01 18Body 2011 46 PAPP-A, Demeditec Diagnostics ultrasensitiveELISA4.4 µg/l Roche fourth generation TnT at 12 hours 0.035 18Body 2011 46 CD40L, R&D Systems Quantikine kit 17.2 ng/l Roche fourth-generation TnT at 12 hours 0.035 18continued© 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.51

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