Objectives: Identify the clinical and prognostic value of stress echocardiography (SE) appropriateness criteria for evaluation of valvular heart disease (VHD).
Background: Appropriateness criteria for patients undergoing SE have recently been published. There are no data which establish the clinical utility of these criteria for evaluation of VHD.
Methods: 100 consecutive patients undergoing SE for evaluation of VHD were identified. Patients were classified into appropriate, uncertain and inappropriate categories according to appropriateness criteria guidelines. A positive SE was defined according to VHD guidelines. The end-point was the composite of heart failure admission or death.
Results: Of the 100 patients undergoing SE 49%,36% and 15% of studies were classified as appropriate, uncertain and inappropriate, respectively. A positive test was identified in 32 (32%) patients. Of which a significantly greater proportion of positive tests occurred in patients classified as appropriate 19 (38.8%) or uncertain 13 (36.1%) compared to patients classified as inappropriate 0 (0%), p<0.0001. Over a median follow-up of 12.6 months, 24 events (16 deaths and 8 heart failure admissions) occurred. Of the 32 patients with a positive SE, events occurred in 18 (56.3%) patients compared to only 6 events (8.8%) in the 68 patients with a negative SE, p<0.0001. 12 month event free survival was significantly reduced in patients with appropriate or uncertain studies compared to patients with inappropriate studies (p=0.04, p=0.005 respectively). Of the important clinical and echocardiographic parameters, the only independent predictor of events was a positive SE (hazard ratio 15.5, p<0.0001).
Conclusion: Stress echocardiography for VHD has prognostic value when incorporated into clinical practice. The appropriateness criteria for evaluation of VHD provide the ability to differentiate between patients at high (appropriate group) and low risk (inappropriate group) of subsequent cardiac events. Patients with an uncertain indication for SE have reduced event free survival compared to patients classified as inappropriate. Re-classification of the uncertain group may improve their applicability to current clinical practice.