Patient characteristics
Sixty-five patients fulfilled the study protocol with complete RHC and echocardiography data sets. Of these, 28 (43%) patients were male. The mean age was 67.2 years (range 19–89 years). All of the patients were admitted to the cardiology department for diagnostic work-up of suspected PH. None of the patients had to be excluded due to poor image quality.
Invasive hemodynamic and echocardiographic measurements, classification of pulmonary hypertension
At RHC eleven (17%) patients had a mean pulmonary artery pressure (mPAPcath) of < 25 mmHg and were classified as non-PH. Fifty-four (83%) patients had an invasively measured mPAPcath of ≥ 25 mmHg and were classified as having PH. Eleven (17%) patients had mild pulmonary hypertension (mPAP 25–29 mmHg), and 43 (66%) patients had severe pulmonary hypertension (mPAP > 30 mmHg). Mean mPAWPcath was 13.6 ± 6.7 mmHg, mean sPAPcath was 61.0 ± 24.5 mmHg, and mean mPAPcath was 37.6 ± 14.9 mmHg. Left ventricular end-diastolic pressure was obtained in 53 patients (82%). Detailed echo characteristics are displayed in Table 1.
Table 1 Patient characteristics, echocardiographic and invasive data (n = 65)
Of the 54 patients with pulmonary hypertension, 15% had idiopathic pulmonary arterial hypertension, 43% had pulmonary hypertension due to left heart disease, 18% had pulmonary hypertension due to pulmonary disease, and 24% had chronic thromboembolic pulmonary hypertension (Table 1).
Echocardiographic TR velocity assessment
In 4 (6%) patients no TR signal could be measured. Considering all five windows sufficient TR signal was recorded in 61 (94%) patients. A TR signal was available in 30 (46%) patients in the parasternal long-axis view of the RV inflow, in 29 (45%) patients in the parasternal short axis view of the basal RV, in 61 (94%) in the RV modified apical four chamber view, in 50 (77%) patients in the apical long axis view of RV inflow, and in 17 (26%) patients in the subcostal four chamber view (Table 2). In concordance with clinical practice, we considered a missing signal as estimated normal pulmonary pressure.
Table 2 Sensitivity, Specificity, area under the curve (AUC) of multiple echocardiographic views
Compared with the other views peak TR velocity was highest in the parasternal long-axis view of the RV inflow in seven patients, in the parasternal short axis view of the basal RV in three patients, in the RV modified apical four chamber view in 20 patients, in the apical long axis view of RV inflow in 11 patients, and in the subcostal four chamber view in five patients. In 15 patients the same peak velocity was recorded from several angles. Compared to sole imaging from the RV modified apical four chamber view, additional imaging from atypical views resulted in higher overall peak TR velocity in 21 (32%) patients. The higher TR velocity did not change echocardiographic classification in 14 of the 21 patients. In four of the definite PH patients peak TR signal was below 2.9 m/s in the apical four chamber view but above 2.9 m/s in at least one other imaging window. In three of the PH patients peak TR signal was below 3.5 m/s in the apical four chamber view but above 3.5 m/s in at least one other imaging window. In none of the patients higher gradients from additional imaging windows resulted in an over-estimation of pulmonary hypertension. Since only higher but not lower velocities were accounted for in the additional views, there were no cases where a potential PH patient was downgraded via additional imaging.
Sufficient TR signal was available in 61 (94%) patients in the RV modified apical four chamber view. Sensitivity for correct classification of PH was 80%. Specificity was 91%. AUC was 0.85 (SD 0.06, 95% CI 0.75–0.95). Sufficient TR signal was available in 50 (77%) patients in the apical long axis view of RV inflow. Sensitivity for correct classification of PH was 66.7%. Specificity was 100%. AUC was 0.83 (SD 0.05, 95% CI 0.75–0.91). For sensitivity, specificity, and AUC of the remaining views see Table 2.
Considering all five imaging windows resulted in a sensitivity of 87%, and a specificity of 91% with an AUC of 0.89, which was significantly better as compared to sole imaging from the right ventricular modified apical four-chamber view (AUC 0.85, p = 0.0395). The multi-view approach resulted in a significantly better AUC compared to sole assessment of the parasternal long-axis view of the RV inflow (p < 0.01), the parasternal short axis view of the basal RV (p = 0.017), and the subcostal four chamber view (p < 0.01). TRvmax demonstrated good reproducibility with an interclass correlation coefficient for intra-observer variability of 0.99 (95% CI 0.976– 0.995) and for inter-observer variability of 0.969 (95% CI 0.0.931–0.985).
Bivariate correlation was calculated for maximal TR velocity of each of the imaging windows with invasively measured mean pulmonary artery pressure (mPAP). Correlation was statistically significant for each imaging window. The subcostal four chamber view showed the best correlation with r = 0.83 (p < 0.001). Both the RV modified apical four chamber view and the apical long axis view of RV inflow had the same correlation with r = 0.79 (p < 0.001). Correlation with the parasternal long axis view of the RV inflow was r = 0.51 (p < 0.001), correlation with the parasternal short axis view of the basal RV was r = 0.49 (p = 0.01). Overall peak TR velocity correlated with r = 0.78 (p < 0.001).
Correlation with invasively measured systolic pulmonary artery pressure (sPAPcath) was good as well. Correlation for overall peak TR velocity was r = 0.83 (p < 0.001), for values from the apical long axis view of RV inflow r = 0.82 (p < 0.001), for values from the subcostal four chamber view r = 0.81 (p < 0.001). Best correlation was achieved by the RV modified apical four chamber view (r = 0.85, p < 0.001). Measurements from the parasternal long axis view of the RV inflow correlated with r = 0.56 (p < 0.001), measurements from the parasternal short axis view of the basal RV with r = 0.62 (p < 0.001). For detailed correlations see Table 3.
Table 3 Correlation of peak TR signal with invasively measured mean PAP and PASP