Literature DB >> 26277885

Severe pulmonary hypertension associated with COPD: hemodynamic improvement with specific therapy.

Anne Girard1, Stephane Jouneau, Céline Chabanne, Chahéra Khouatra, Morgane Lannes, Julie Traclet, Ségolène Turquier, P Delaval, J-F Cordier, Vincent Cottin.   

Abstract

BACKGROUND: There is no recommendation for treating pulmonary hypertension (PH) when associated with chronic obstructive pulmonary disease (COPD).
OBJECTIVE: To evaluate the effect of PH-specific therapy in patients with COPD.
METHODS: All successive patients with severe PH [mean pulmonary arterial pressure (mPAP) ≥35 mm Hg] and COPD, who received specific PH medication and who underwent right heart catheterization at baseline and after 3-12 months of treatment, were analyzed from a prospective database.
RESULTS: Twenty-six patients were included with a median follow-up of 14 months. Mean forced expiratory volume in 1 s was 57 ± 20% of predicted, and mean forced expiratory volume in 1 s/forced vital capacity was 47 ± 12%. Dyspnea was New York Health Association classification stage (NYHA) II in 15%, NYHA III in 81% and NYHA IV in 4%. First-line treatments were endothelin receptor antagonists in 11 patients, phosphodiesterase-5 inhibitors in 11 patients, calcium blocker in 1 patient, combination therapy in 3 patients including 2 with a prostanoid. After 6 ± 3 months, pulmonary vascular resistance decreased from 8.5 ± 3 to 6.6 ± 2 Wood units (p < 0.001), with significant improvement of cardiac index from 2.44 ± 0.43 to 2.68 ± 0.63 liters × min × m-2 (p = 0.015) and mPAP from 48 ± 9 to 42 ± 10 mm Hg (p = 0.008). There was no significant difference in dyspnea, 6-min walking distance, echocardiographic parameters or N-terminal pro-brain natriuretic peptide levels. There was no significant difference in arterial oxygen saturation after 3-12 months of treatment.
CONCLUSIONS: Specific PH medications may improve hemodynamic parameters in COPD patients with severe PH. Appropriate prospective randomized studies are needed to evaluate the potential long-term clinical benefit of treatment.
© 2015 S. Karger AG, Basel.

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Year:  2015        PMID: 26277885     DOI: 10.1159/000431380

Source DB:  PubMed          Journal:  Respiration        ISSN: 0025-7931            Impact factor:   3.580


  5 in total

1.  Mild parenchymal lung disease and/or low diffusion capacity impacts survival and treatment response in patients diagnosed with idiopathic pulmonary arterial hypertension.

Authors:  Robert A Lewis; A A Roger Thompson; Catherine G Billings; Athanasios Charalampopoulos; Charlie A Elliot; Neil Hamilton; Catherine Hill; Judith Hurdman; Smitha Rajaram; Ian Sabroe; Andy J Swift; David G Kiely; Robin Condliffe
Journal:  Eur Respir J       Date:  2020-06-04       Impact factor: 16.671

2.  Treatment of pulmonary hypertension associated with COPD: a systematic review.

Authors:  Ragdah Arif; Arjun Pandey; Ying Zhao; Kyle Arsenault-Mehta; Danya Khoujah; Sanjay Mehta
Journal:  ERJ Open Res       Date:  2022-02-21

Review 3.  Emerging phenotypes of pulmonary hypertension associated with COPD: a field guide.

Authors:  Agustín Roberto García; Lucilla Piccari
Journal:  Curr Opin Pulm Med       Date:  2022-07-16       Impact factor: 2.868

4.  Accuracy of CT Pulmonary Artery Diameter for Pulmonary Hypertension in End-Stage COPD.

Authors:  Firdaus A Mohamed Hoesein; Tim Besselink; Esther Pompe; Erik-Jan Oudijk; Ed A de Graaf; J M Kwakkel-van Erp; Pim A de Jong; Bart Luijk
Journal:  Lung       Date:  2016-07-16       Impact factor: 2.584

5.  Pre-Anesthesia Extracorporeal Membrane Oxygenation in Two Lung Transplant Recipients with Severe Pulmonary Hypertension.

Authors:  Liu Minqiang; Gao Hong; Chen Jingyu; Wang Yanjuan; Xu Bo; Wang Guilong; Wu Qiang; Hu Chunxiao
Journal:  Case Rep Med       Date:  2020-02-12
  5 in total

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