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Disease characteristics and clinical outcome over two decades from the Swiss pulmonary hypertension registry.
Appenzeller, Paula; Lichtblau, Mona; Berlier, Charlotte; Aubert, John-David; Azzola, Andrea; Fellrath, Jean-Marc; Geiser, Thomas; Lador, Frederic; Pohle, Susanne; Opitz, Isabelle; Schwerzmann, Markus; Stricker, Hans; Tamm, Michael; Saxer, Stéphanie; Ulrich, Silvia.
Afiliação
  • Appenzeller P; Clinic of Pulmonology, University Hospital Zurich Zurich Switzerland.
  • Lichtblau M; Clinic of Pulmonology, University Hospital Zurich Zurich Switzerland.
  • Berlier C; Clinic of Pulmonology, University Hospital Zurich Zurich Switzerland.
  • Aubert JD; Center of Pulmonology, CHUV Lausanne Switzerland.
  • Azzola A; Center of Pulmonology, Cantonal Hospital Lucerne Lucerne Switzerland.
  • Fellrath JM; Center of Pulmonology, Hôpital neuchâtelois Pourtalès Neuenburg Switzerland.
  • Geiser T; Interdisciplinary Center for Pulmonary Hypertension, Bern University Hospital and University of Bern Bern Switzerland.
  • Lador F; Pulmonary Hypertension Program, University Hospital of Geneva Geneva Switzerland.
  • Pohle S; Lung Center, Cantonal Hospital St. Gallen St. Gallen Switzerland.
  • Opitz I; Department of Thoracic Surgery University Hospital Zurich Zurich Switzerland.
  • Schwerzmann M; Interdisciplinary Center for Pulmonary Hypertension, Bern University Hospital and University of Bern Bern Switzerland.
  • Stricker H; Department of Angiology Ospedale La Carità Locarno Switzerland.
  • Tamm M; Center of Pulmonology, University Hospital Basel Basel Switzerland.
  • Saxer S; Clinic of Pulmonology, University Hospital Zurich Zurich Switzerland.
  • Ulrich S; Clinic of Pulmonology, University Hospital Zurich Zurich Switzerland.
Pulm Circ ; 12(1): e12001, 2022 Jan.
Article em En | MEDLINE | ID: mdl-35506112
ABSTRACT
Pulmonary hypertension (PH), especially pulmonary arterial and chronic thromboembolic pulmonary hypertension (PAH/CTEPH), are rare and progressive conditions. Despite recent advances in treatment and prognosis, PH is still associated with impaired quality of life and survival. Long-term PH-registry data provide information on the changing PH-epidemiology and may help to direct resources to patient's needs. This retrospective analysis of the Swiss Pulmonary Hypertension Registry includes patients newly diagnosed with PH (mainly PAH/CTEPH) registered from January 2001 to June 2019 at 13 Swiss hospitals. Patient characteristics (age, body mass index, gender, diagnosis), hemodynamics at baseline, treatment, days of follow-up, and events (death, transplantation, pulmonary endarterectomy, or loss to follow-up) at last visit were analyzed. Patients were stratified into four time periods according to their date of diagnosis. Survival was analyzed overall and separately for PAH/CTEPH and time periods. 1427 PH patients were included (thereof 560 PAH, 383 CTEPH). Over the years, age at baseline (mean ± SD) significantly increased from 59 ± 14 years in 2001-2005 to 66 ± 14 years in 2016-2019 (p < 0.001) while the gender distribution tended toward equality. Mean pulmonary artery pressure and pulmonary vascular resistance significantly decreased over time (from 46 ± 15 to 41 ± 11 mmHg, respectively, 9 ± 5 to 7 ± 4 WU, p < 0.001). Three-year survival substantially increased over consecutive periods from 69% to 91% (for PAH 63%-95%, for CTEPH 86%-93%) and was poorer in PAH than CTEPH independently of time period (p < 0.001). Most patients were treated with mono- or combination therapy and an increasing number of CTEPH underwent pulmonary endarterectomy (40% 2016-2019 vs. 15% 2001-2005). This long-term PH registry reveals that over two decades of observation, newly diagnosed patients are older, less predominantly female, have less impaired hemodynamics and a better survival.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article