0
Pediatrics |

Exercise-Induced Pulmonary Arterial Hypertension in Pediatric and Young Adult Patients With Cystic Fibrosis FREE TO VIEW

Don Hayes, Jr.*, MD; Benjamin Kopp, MD; Heidi Mansour, PhD; Stephen Kirkby, MD; Andrew Yates, MD; Karen McCoy, MD; Curtis Daniels, MD
Author and Funding Information

The Ohio State University, Columbus, OH


Chest. 2012;142(4_MeetingAbstracts):773A. doi:10.1378/chest.1388349
Text Size: A A A
Published online

Abstract

SESSION TYPE: Pediatric Critical Care Posters

PRESENTED ON: Wednesday, October 24, 2012 at 01:30 PM - 02:30 PM

PURPOSE: Pulmonary arterial hypertension (PAH) has long been appreciated in cystic fibrosis (CF). Exercise-induced PAH is an evolving disorder that has not been well described in CF.

METHODS: A prospective cohort study was performed in CF patients with advanced lung disease undergoing evaluation for lung transplantation. The right heart catheterization (RHC) was performed with access via the right internal jugular vein with advancement of the catheter to the pulmonary artery wedge position under fluoroscopic guidance. There was continuous monitoring of the pulmonary artery pressure (PAP) while supine and during exercise on a stationary bicycle.

RESULTS: Five adult (mean age 26.8 ± 10.1 years) CF patients (3 males, 2 females) underwent RHC for evaluation for lung transplantation. The cohort had advanced lung disease with mean (± SD) FEV1 of 0.99 ± 0.17 (range 0.82-1.17) Liters and 26 ± 3 (range 23-30) % predicted. Each patient had no significant pathology or evidence of PAH on echocardiography. Using a paired t test, there was a significant elevation in the mean (± SD) PAP when comparing supine position to exercise, 24.80 ± 3.11 mmHg vs 45.20 ± 5.72 mmHg, P = 0.0003. There was no evidence of left heart failure with mean (± SD) pulmonary capillary wedge pressures of 8.6 ± 1.8 (range 6-11) mmHg.

CONCLUSIONS: An abnormal pulmonary vascular response to exercise in CF was identified in pediatric and young adult patients with advanced lung disease. The RHC was well tolerated and should possibly be considered sooner in CF patients with severe lung disease. Echocardiography was not helpful in estimating the PAP in this small cohort of CF patients.

CLINICAL IMPLICATIONS: Exercise-induced PAH should be considered as a contributing factor to clinical symptoms in pediatric and young adult patients with advanced lung disease due to CF despite normal echocardiography findings.

DISCLOSURE: The following authors have nothing to disclose: Don Hayes, Jr., Benjamin Kopp, Heidi Mansour, Stephen Kirkby, Andrew Yates, Karen McCoy, Curtis Daniels

No Product/Research Disclosure Information

The Ohio State University, Columbus, OH

Figures

Tables

References

NOTE:
Citing articles are presented as examples only. In non-demo SCM6 implementation, integration with CrossRef’s "Cited By" API will populate this tab (http://www.crossref.org/citedby.html).

Some tools below are only available to our subscribers or users with an online account.

Related Content

Customize your page view by dragging & repositioning the boxes below.

CHEST Journal Articles
CHEST Collections
PubMed Articles
  • CHEST Journal
    Print ISSN: 0012-3692
    Online ISSN: 1931-3543