Long-term outcome of patients with combined post- and pre-capillary pulmonary hypertension

Author:

Titz Anna12ORCID,Mayer Laura12,Appenzeller Paula1,Müller Julian12,Schneider Simon R12,Tamm Michael3,Darie Andrei M3,Guler Sabina A4,Aubert John-David5,Lador Frédéric6,Stricker Hans7,Fellrath Jean-Marc8,Pohle Susanne9,Lichtblau Mona12,Ulrich Silvia12ORCID

Affiliation:

1. Department of Pulmonology, University Hospital Zurich , Rämistrasse 100, Zurich 8091 , Switzerland

2. Department of Pulmonology, University of Zurich , Zurich , Switzerland

3. Clinic of Respiratory Medicine and Pulmonary Cell Research, University Hospital Basel , Basel , Switzerland

4. Department of Pulmonary Medicine and Department for BioMedical Research, Inselspital, Bern University Hospital, University of Bern , Bern , Switzerland

5. Department of Pulmonology, University Hospital Lausanne , Lausanne , Switzerland

6. Department of Pulmonology, University Hospital Geneva , Geneva , Switzerland

7. Department of Angiology, Ospedale La Carità , Locarno , Switzerland

8. Service of Pulmonology, Hospital Neuchâtelois , Neuchâtel , Switzerland

9. Lung Center, Cantonal Hospital St Gallen , St Gallen , Switzerland

Abstract

Abstract Aims Pulmonary hypertension (PH) is a complex clinical condition, and left heart disease is the leading cause. Little is known about the epidemiology and prognosis of combined post- and pre-capillary PH (CpcPH). Methods and results This retrospective analysis of the Swiss PH Registry included incident patients with CpcPH registered from January 2001 to June 2019 at 13 Swiss hospitals. Patient baseline characteristics [age, sex, mean pulmonary artery pressure (mPAP), pulmonary artery wedge pressure (PAWP), pulmonary vascular resistance (PVR), and risk factors, including World Health Organization (WHO)-functional class (FC), 6 min walk distance (6MWD), and N-terminal pro-brain natriuretic peptide (NT-proBNP), treatment, days of follow-up, and events (death or loss to follow-up) at last visit] were analysed by Kaplan–Meier and Cox regression analyses. Two hundred and thirty-one patients (59.3% women, age 65 ± 12 years, mPAP 48 ± 11 mmHg, PAWP 21 ± 5 mmHg, PVR 7.2 ± 4.8 WU) were included. Survival analyses showed a significantly longer survival for women [hazard ratio (HR) 0.58 (0.38–0.89); P = 0.01] and a higher mortality risk for mPAP > 46 mmHg [HR 1.58 (1.03–2.43); P = 0.04] but no association with age or PVR. Patients stratified to high risk according to four-strata risk assessment had an increased mortality risk compared with patients stratified to low-intermediate risk [HR 2.44 (1.23–4.84); P = 0.01]. A total of 46.8% of CpcPH patients received PH-targeted pharmacotherapy; however, PH-targeted medication was not associated with longer survival. Conclusion Among patients with CpcPH, women and patients with an mPAP ≤46 mmHg survived longer. Furthermore, risk stratification by using non-invasively assessed risk factors, such as WHO-FC, 6MWD, and NT-proBNP, as proposed for pulmonary arterial hypertension, stratified survival in CpcPH, and might be helpful in the management of these patients.

Publisher

Oxford University Press (OUP)

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