Haemodynamic effects of riociguat in inoperable/recurrent chronic thromboembolic pulmonary hypertension
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't
PubMed
28011757
PubMed Central
PMC5529957
DOI
10.1136/heartjnl-2016-309621
PII: heartjnl-2016-309621
Knihovny.cz E-resources
- MeSH
- Antihypertensive Agents adverse effects therapeutic use MeSH
- Pulmonary Artery drug effects physiopathology MeSH
- Arterial Pressure drug effects MeSH
- Time Factors MeSH
- Vascular Resistance drug effects MeSH
- Chronic Disease MeSH
- Double-Blind Method MeSH
- Endarterectomy MeSH
- Middle Aged MeSH
- Humans MeSH
- Least-Squares Analysis MeSH
- Recovery of Function MeSH
- Pulmonary Embolism complications diagnosis MeSH
- Hypertension, Pulmonary diagnosis drug therapy etiology physiopathology MeSH
- Prospective Studies MeSH
- Pyrazoles adverse effects therapeutic use MeSH
- Pyrimidines adverse effects therapeutic use MeSH
- Recurrence MeSH
- Aged MeSH
- Walk Test MeSH
- Exercise Tolerance drug effects MeSH
- Treatment Outcome MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Randomized Controlled Trial MeSH
- Names of Substances
- Antihypertensive Agents MeSH
- Pyrazoles MeSH
- Pyrimidines MeSH
- riociguat MeSH Browser
OBJECTIVE: We compared the haemodynamic effects of riociguat in patients with inoperable chronic thromboembolic pulmonary hypertension (CTEPH) or persistent/recurrent CTEPH after pulmonary endarterectomy in the Chronic Thromboembolic Pulmonary Hypertension Soluble Guanylate Cyclase-Stimulator Trial 1 study. METHODS: Patients with inoperable or persistent/recurrent CTEPH (n=261; mean± SD age 59±14 years; 66% women) were randomised to riociguat (up to 2.5 mg three times daily) or placebo. Haemodynamic parameters were assessed at baseline and week 16. RESULTS: Riociguat decreased pulmonary vascular resistance (PVR) in inoperable (n=189; least-squares mean difference: -285 dyn s/cm5 (95% CI -357 to -213); p<0.0001) and persistent/recurrent (n=72; -131 dyn s/cm5 (95% CI -214 to -48); p=0.0025) patients. Cardiac index improved in inoperable patients by a least-squares mean difference of +0.6 L/min/m2 (95% CI 0.4 to 0.7; p<0.0001), while in persistent/recurrent patients the change was +0.2 L/min/m2 (95% CI -0.1 to 0.5; p=0.17). Mean pulmonary artery pressure decreased in inoperable and persistent/recurrent patients(-4.7 mm Hg (95% CI -6.9 to -2.6; p<0.0001 and -4.8 mm Hg (-8.2 to -1.5; p=0.0055), respectively). For all patients, changes in 6 min walk distance correlated with changes in PVR (r=-0.29 (95% CI -0.41 to -0.17); p<0.0001) and cardiac index (r=0.23 (95% CI 0.10 to 0.35); p=0.0004). CONCLUSIONS: Riociguat improved haemodynamics in patients with inoperable CTEPH or persistent/recurrent CTEPH. TRIAL REGISTRATION NUMBER: NCT00855465.
Center for Pulmonary Hypertension Thoraxclinic University Hospital Heidelberg Heidelberg Germany
Clinic for Respiratory Medicine Hannover Medical School Hannover Germany
Department of Medicine Imperial College London London UK
Division of Pulmonary Diseases Ludwig Maximilians University Munich Germany
German Center of Lung Research Giessen Germany
Global Clinical Development Bayer Pharma AG Wuppertal Germany
Kerckhoff Heart and Lung Center Bad Nauheim Germany
University of Giessen and Marburg Lung Center Giessen Germany
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NCT00855465