Literature DB >> 26492415

Pulmonary Arterial Hypertension-Specific Drug Therapy in COPD Patients with Severe Pulmonary Hypertension and Mild-to-Moderate Airflow Limitation.

George Calcaianu1, Matthieu Canuet, Armelle Schuller, Irina Enache, Ari Chaouat, Romain Kessler.   

Abstract

BACKGROUND: Patients with severe pulmonary hypertension (PH) associated with chronic obstructive pulmonary disease (COPD) present a poor outcome. Specific PH treatment could improve the clinical and hemodynamic status of these patients but may worsen arterial blood gases.
OBJECTIVES: Our study retrospectively included 28 patients with severe precapillary PH (mean pulmonary arterial pressure >35 mm Hg) associated with mild-to-moderate COPD [forced expiratory volume in 1 s (FEV1) >50% predicted]. All patients underwent specific pulmonary arterial hypertension (PAH) treatment as mono-, bi- or triple therapy.
METHODS: Our single-center study was conducted based on retrospective data of 537 right heart catheterizations (RHCs) performed on patients with COPD from January 2004 to June 2014. An echocardiography, comprehensive blood tests, pulmonary function tests, and a high-resolution computed tomography were performed before the RHCs. All patients underwent RHC with a Swan-Ganz catheter.
RESULTS: Compared to baseline, patients treated with specific PAH drugs showed a significant increase in cardiac index at long term (2.5 ± 0.7 liters/min/m2 at baseline vs. 3.2 ± 0.6 liters/min/m2 at 6/12 months; p = 0.003) as well as a decrease in pulmonary vascular resistance in the long term (8.4 ± 4.2 Wood units at baseline vs. 5 ± 1.7 Wood units at 6/12 months; p = 0.008). There was a slight decrease in arterial oxygen tension (PaO2) after 3 months of treatment (-2.4 ± 7.21 mm Hg; p = 0.066). During a median follow-up of 3 years, 12 patients (42.8%) died (including all causes of death).
CONCLUSIONS: This preliminary report suggests that the use of specific PH therapy in severe PH associated with mild-to-moderate COPD can improve pulmonary hemodynamic parameters, with worsening of PaO2, which had no clinical significance and did not lead to specific PAH therapy withdrawal in any patient.
© 2015 S. Karger AG, Basel.

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Year:  2015        PMID: 26492415     DOI: 10.1159/000441304

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


  10 in total

1.  Ginsenoside Rg1 attenuates hypoxia and hypercapnia-induced vasoconstriction in isolated rat pulmonary arterial rings by reducing the expression of p38.

Authors:  Mengxiao Zheng; Meiping Zhao; Lanlan Tang; Congcong Zhang; Longsheng Song; Wantie Wang
Journal:  J Thorac Dis       Date:  2016-07       Impact factor: 2.895

2.  Let-7a-transfected mesenchymal stem cells ameliorate monocrotaline-induced pulmonary hypertension by suppressing pulmonary artery smooth muscle cell growth through STAT3-BMPR2 signaling.

Authors:  Gesheng Cheng; Xingye Wang; Yongxin Li; Lu He
Journal:  Stem Cell Res Ther       Date:  2017-02-10       Impact factor: 6.832

3.  COPD as an endothelial disorder: endothelial injury linking lesions in the lungs and other organs? (2017 Grover Conference Series).

Authors:  Francesca Polverino; Bartolome R Celli; Caroline A Owen
Journal:  Pulm Circ       Date:  2018 Jan-Mar       Impact factor: 3.017

Review 4.  Updated Perspectives on Pulmonary Hypertension in COPD.

Authors:  Isabel Blanco; Olga Tura-Ceide; Victor Ivo Peinado; Joan Albert Barberà
Journal:  Int J Chron Obstruct Pulmon Dis       Date:  2020-06-09

5.  Pulmonary hypertension in chronic lung disease and hypoxia.

Authors:  Steven D Nathan; Joan A Barbera; Sean P Gaine; Sergio Harari; Fernando J Martinez; Horst Olschewski; Karen M Olsson; Andrew J Peacock; Joanna Pepke-Zaba; Steeve Provencher; Norbert Weissmann; Werner Seeger
Journal:  Eur Respir J       Date:  2019-01-24       Impact factor: 16.671

6.  Aquaporin-2 expression in the kidney and urine is elevated in rats with monocrotaline-induced pulmonary heart disease.

Authors:  Shao Ouyang; Wei Chen; Gaofeng Zeng; Changcheng Lei
Journal:  J Int Med Res       Date:  2020-01       Impact factor: 1.671

7.  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

8.  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 9.  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

Review 10.  Macrophage migration inhibitory factor (MIF) in the development and progression of pulmonary arterial hypertension.

Authors:  Mohamed Ahmed; Edmund Miller
Journal:  Glob Cardiol Sci Pract       Date:  2018-06-30
  10 in total

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