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Table 3 and Figure 6 summarise indirect comparison results.
                Overall, there was evidence that DSE (13 studies) had better test  cation and had reference thresholds ≥ 70% stenosis on coronary
                accuracy than MPS (9 studies) (P = 0.02). Using the results from  angiography were included in the analysis, there was no evidence
                the earlier analysis, DSE appeared to have a higher pooled sensi-  of a statistically significant difference between tests (P = 0.09).
                tivity (DSE: 0.79 (95% CI 0.67 to 0.88) versus MPS: 0.74 (95%  DSE (8 studies) appeared to have a higher pooled sensitivity: 0.78
                CI 0.54 to 0.87) and specificity DSE: 0.89 (95% CI 0.81 to 0.94)  (95% CI 0.59 to 0.89) than MPS 0.67 (95% CI 0.48 to 0.82) and
                versus MPS: 0.70 (95% CI 0.51 to 0.84). The variability in ac-  DSE specificity: 0.88 (95% CI 0.76 to 0.94) versus 0.77 (95% CI
                curacy was smaller for DSE than MPS, demonstrated by the dif-  0.61 to 0.88)] compared with MPS (7 studies), as well as a higher
                ference in size of the 95% confidence regions in HSROC space.  corresponding AUC.
                When we included only studies that used definitions of ≥ 70%
                stenosis on coronary angiography to diagnose severe CAD, DSE  Subgroup analyses
                (9 studies) had pooled sensitivity and specificity of 0.76 (95% CI
                                                                Sparse data, both in terms of numbers of studies and study par-
                0.60 to 0.87) and 0.88 (95% CI 0.78 to 0.94) respectively. MPS
                                                                ticipants, meant that we were unable to perform meaningful sub-
                (7 studies) had pooled sensitivity and specificity of 0.67 (95% CI
                                                                group analyses on the effect of DM or prevalence of angina and
                0.48 to 0.82) and 0.77 (95% CI 0.61 to 0.88) respectively. There
                                                                symptomatic ischaemic heart disease (IHD) on diagnostic test per-
                was no statistically significant difference between tests (P = 0.09)
                                                                formance. Only one study (Vandenberg 1996) included a patient
                (Figure 7). When we included only studies where partial verifi-
                                                                population who had no history of angina or IHD. Therefore, a
                cation bias was avoided, DSE (10 studies) had pooled sensitivity
                                                                sensitivity analysis of diagnostic accuracy in studies that enrolled
                and specificity of 0.80 (95% CI 0.64 to 0.90) and 0.89 (95% CI
                                                                only patients who had no symptoms of cardiac disease or history
                0.79 to 0.95) respectively. MPS (8 studies) had pooled sensitivity
                                                                of IHD could not be conducted.
                and specificity of 0.68 (95% CI 0.51 to 0.81) and 0.75 (95%
                CI 0.60 to 0.86) respectively. The difference in accuracy between
                MPS and DSE tests for these studies was statistically significant (P
                                                                Summary of results
                = 0.03) (Figure 8). When only studies that avoided partial verifi-
                Summary of results
                 Summary of results: Results of studies on cardiac testing in kidney transplant candidates

                 Review question: Comparison of non-invasive cardiac screening tests with coronary angiography for the detection of significant CAD
                 in potential kidney transplant recipients
                 Patient population: Kidney transplant candidates undergoing pre-transplant cardiac evaluation
                 Setting: Investigations performed in hospital or in an outpatient setting
                 Geographical location: Studies were conducted in USA (12 studies), Brazil (4 studies), India, (3 studies) the UK (3 studies), Australia
                 (1 study), Canada (1 study), and Spain (1 study)
                 Index test : Any non- or minimally invasive test used to assess risk of CAD
                 Reference standard: Coronary angiography
                 Included studies: DSE (13 studies; 745 participants), MPS (9 studies; 582 participants), EST (2 studies; 129 participants), EBCT
                 (1 study; 97 participants), DSF (1 study; 86 participants), exercise ventriculography (1 study; 35 participants), CIMT (1 study;
                 105 participants), resting wall motion abnormality on echocardiography (2 studies; 265 participants), left ventricular dysfunction
                 on echocardiography (1 study; 52 participants), mitral annular calcification on echocardiography (1 study; 125 participants), resting
                 ECG (3 studies; 263 participants)

                 Limitations

                 Only DSE and MPS were evaluated in detail, although these also had only a limited number of included comparisons with small
                 sample sizes. No studies were found investigating cardiopulmonary exercise testing, CT coronary angiography, magnetic resonance
                 angiography or cardiac magnetic resonance imaging. Fewer than five studies were found for each of EBCT, resting ECG, conventional
                 echocardiography, exercise ventriculography, DSF and CIMT. Sparse directly comparative data also resulted in low power to detect
                 important differences in accuracy between tests
                 Significant heterogeneity was present among studies investigating the same screening test. Although differences in study population

                Cardiac testing for coronary artery disease in potential kidney transplant recipients (Review)  21
                Copyright © 2011 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
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