Portopulmonary hypertension (POPH), a complication of chronic liver disease, may be a contraindication to liver transplantation (LT) because of the elevated risk of peritransplant and posttransplant morbidity and mortality. Because POPH is frequently asymptomatic, screening with echocardiography is recommended. The only reliable technique, however, for diagnosing POPH is right heart catheterization (RHC). The aims of this study were to evaluate the current estimated systolic pulmonary artery pressure (sPAP) cutoff value of 30 mm Hg and to determine a better cutoff value. One hundred fifty-two patients underwent pretransplant echocardiography between January 2005 and December 2010. These echocardiographic results were compared with pulmonary artery pressures measured during the pretransplant workup or at the beginning of the transplantation procedure (both by catheterization). With a cutoff value of 30 mm Hg, 74 of the 152 patients met the criteria for POPH on echocardiography, although the diagnosis was confirmed in only 7 patients during catheterization; this resulted in a specificity of 54%. It would have been more accurate to use a cutoff value of 38 mm Hg, which had a maximal specificity of 82% and, at the same time, guaranteed a sensitivity and negative predictive value of 100%. With the incorporation of the presence or absence of right ventricular dilatation, the specificity even increased to 93% for this new cutoff value. In conclusion, the prevalence of POPH was 4.6% among LT candidates in this study. We can recommend that LT candidates with an sPAP > 38 mm Hg should be referred for RHC. With the cutoff value increased from 30 to 38 mm Hg, the number of patients undergoing invasive RHC during their evaluation could be safely reduced. Liver Transpl 19:602-610, 2013. V C 2013 AASLD.Received November 11, 2012; accepted February 27, 2013.
See Editorial on Page 573Portopulmonary hypertension (POPH), the presence of pulmonary hypertension in association with portal hypertension, is a known complication of chronic liver disease.1-9 Prospective studies and case-control studies have documented that POPH occurs in approximately 5% to 6% of patients with advanced liver disease. 5 In patients with portal hypertension, the association with pulmonary hypertension is seen in 2% to 6%.10,11 The incidence of POPH in patients referred for liver transplantation (LT) is 4% to 6%.
12Abbreviations: CO, cardiac output; LT, liver transplantation; mPAP, mean pulmonary artery pressure; mRAP, mean right atrial pressure; NA, not applicable; ND, not determined; NS, not significant; PCWP, pulmonary capillary wedge pressure; POPH, portopulmonary hypertension; PVR, pulmonary vascular resistance; RHC, right heart catheterization; RVEDD, right ventricular end-diastolic diameter; sPAP, systolic pulmonary artery pressure; SVR, systemic vascular resistance; TPG, transpulmonary gradient.