Literature DB >> 27602188

Can a Six-Minute Walk Distance Predict Right Ventricular Dysfunction in Patients with Diffuse Parenchymal Lung Disease and Pulmonary Hypertension?

Kamonpun Ussavarungsi1, Augustine S Lee2, Charles D Burger2.   

Abstract

OBJECTIVES: Pulmonary hypertension (PH) is commonly observed in patients with diffuse parenchymal lung disease (DPLD). The purpose of this study was to explore the influence of the 6-minute walk test (6MWT) as a simple, non-invasive tool to assess right ventricular (RV) function in patients with DPLD and to identify the need for an echocardiogram (ECHO) to screen for PH.
METHODS: We retrospectively reviewed 48 patients with PH secondary to DPLD, who were evaluated in the PH clinic at the Mayo Clinic in Jacksonville, Florida, from January 1999 to December 2014.
RESULTS: Fifty-two percent of patients had RV dysfunction. They had a significantly greater right heart pressure by ECHO and mean pulmonary arterial pressure (MPAP) from right heart catheterization (RHC) than those with normal RV function. A reduced 6-minute walk distance (6MWD) did not predict RV dysfunction (OR 0.995; 95% CI 0.980-1.001, p = 0.138). In addition, worsening restrictive physiology, heart rate at one-minute recovery and desaturation were not different between patients with and without RV dysfunction. However, there were inverse correlations between 6MWD and MPAP from RHC (r = -0.41, 
p = 0.010), 6MWD and RV systolic pressure (r = -0.51, p < 0.001), and 6MWD and MPAP measured by ECHO (r = -0.46, p =0.013). We also found no significant correlation between 6MWD and pulmonary function test parameters.
CONCLUSIONS: Our single-center cohort of patients with PH secondary to DPLD, PH was found to have an impact on 6MWD. In contrast to our expectations, 6MWD was not useful to predict RV dysfunction. Interestingly, a severe reduction in the 6MWD was related to PH and not to pulmonary function; therefore, it may be used to justify an ECHO to identify patients with a worse prognosis.

Entities:  

Keywords:  6-minute walk distance; Diffuse Parenchymal Lung Diseases; Echocardiogram.; Interstitial Lung Diseases; Pulmonary Hypertension

Year:  2016        PMID: 27602188      PMCID: PMC4996956          DOI: 10.5001/omj.2016.69

Source DB:  PubMed          Journal:  Oman Med J        ISSN: 1999-768X


  26 in total

1.  ATS statement: guidelines for the six-minute walk test.

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2.  Pulmonary hypertension in interstitial lung disease: prevalence, prognosis and 6 min walk test.

Authors:  Charlotte U Andersen; Søren Mellemkjær; Ole Hilberg; Jens Erik Nielsen-Kudsk; Ulf Simonsen; Elisabeth Bendstrup
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3.  Prevalence and outcomes of pulmonary arterial hypertension in advanced idiopathic pulmonary fibrosis.

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Authors:  Roland M du Bois; Carlo Albera; Williamson Z Bradford; Ulrich Costabel; Jonathan A Leff; Paul W Noble; Steven A Sahn; Dominique Valeyre; Derek Weycker; Talmadge E King
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Review 5.  Definitions and diagnosis of pulmonary hypertension.

Authors:  Marius M Hoeper; Harm Jan Bogaard; Robin Condliffe; Robert Frantz; Dinesh Khanna; Marcin Kurzyna; David Langleben; Alessandra Manes; Toru Satoh; Fernando Torres; Martin R Wilkins; David B Badesch
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Review 6.  Clinical course and prediction of survival in idiopathic pulmonary fibrosis.

Authors:  Brett Ley; Harold R Collard; Talmadge E King
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7.  Right ventricular function in patients with severe interstitial lung disease: a Tissue Doppler imaging study.

Authors:  J Nowak; D Jastrzebski; W Streb; P Rozentryt; J Wojarski; M Greif; J Kozielski; L Polonski; M Zembala; T Kukulski
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8.  Idiopathic pulmonary fibrosis and emphysema: decreased survival associated with severe pulmonary arterial hypertension.

Authors:  Mayra Mejía; Guillermo Carrillo; Jorge Rojas-Serrano; Andrea Estrada; Teresa Suárez; Delfino Alonso; Emilio Barrientos; Miguel Gaxiola; Carmen Navarro; Moisés Selman
Journal:  Chest       Date:  2009-02-18       Impact factor: 9.410

Review 9.  Pulmonary hypertension in interstitial lung disease.

Authors:  J Behr; J H Ryu
Journal:  Eur Respir J       Date:  2008-06       Impact factor: 16.671

10.  Pulmonary hypertension in patients with pulmonary fibrosis awaiting lung transplant.

Authors:  A F Shorr; J L Wainright; C S Cors; C J Lettieri; S D Nathan
Journal:  Eur Respir J       Date:  2007-07-11       Impact factor: 16.671

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