Effects of Exercise and Vasodilators on Cerebral Tissue Oxygenation in Pulmonary Hypertension

Background Arterial and thromboembolic pulmonary hypertension (PH) lead to arterial hypoxaemia. Objective To investigate whether cerebral tissue oxygenation (CTO) in patients with PH is reduced and whether this is associated with reduced exercise tolerance. Methods 16 patients with PH (mean pulmonar...

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Published in:Lung Vol. 193; no. 1; pp. 113 - 120
Main Authors: Müller-Mottet, Séverine, Hildenbrand, Florian F., Keusch, Stephan, Hasler, Elisabeth, Maggiorini, Marco, Speich, Rudolf, Bloch, Konrad E., Ulrich, Silvia
Format: Journal Article
Language:English
Published: Boston Springer US 01-02-2015
Springer
Springer Nature B.V
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Summary:Background Arterial and thromboembolic pulmonary hypertension (PH) lead to arterial hypoxaemia. Objective To investigate whether cerebral tissue oxygenation (CTO) in patients with PH is reduced and whether this is associated with reduced exercise tolerance. Methods 16 patients with PH (mean pulmonary arterial pressure ≥25 mmHg, 14 arterial, 2 chronic thromboembolic) and 15 controls underwent right heart catheterisation with monitoring of CTO at rest, during maximal bicycle exercise and during inhalation of oxygen and NO. The 6 min walk distance (6MWD) was measured. Results Median CTO in PH-patients at rest was 62 % (quartiles 53; 71), during exercise 60 % (53; 65); corresponding values in controls were 65 % (73; 73) (P = NS) and 68 % (66; 70) ( p  = .013 vs. PH). Inhalation of NO and oxygen improved CTO in PH. In multivariate regression analysis CTO at maximal exercise predicted the work load achieved when controlled for age, pulmonary vascular resistance and mixed venous oxygen saturation ( R 2  = .419, p  < .000); in addition, the 6MWD was predicted by CTO (adjusted R 2  = .511, p  < .000). Conclusion In PH-patients but not in controls CTO decreased during exercise. Since CTO was an independent predictor of the work load achieved and the 6MWD cerebral hypoxia may contribute to exercise limitation in PH. Clinicaltrials.gov: NCT01463514.
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ISSN:0341-2040
1432-1750
DOI:10.1007/s00408-014-9667-5