Published ahead of print on July 6, 2006, doi:10.1164/rccm.200604-488OC
Am. J. Respir. Crit. Care Med., Volume 174, Number 7, October 2006, 803-809
A more recent version of this article appeared on October 1, 2006
Submitted on April 6, 2006
Accepted on June 30, 2006
Idiopathic Pulmonary Fibrosis: Prognostic Value of Changes in Physiology and Six Minute Hallwalk
Kevin R Flaherty1*, Adin-Cristian Andrei2, Susan Murray2, Chris Fraley1, Thomas V Colby3, William D Travis4, Vibha Lama1, Ella A Kazerooni5, Barry H Gross5, Galen B Toews1, and Fernando J Martinez1
1 Division of Pulmonary and Critical Care Medicine, University of Michigan Health System, Ann Arbor, MI, USA,
2 Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, MI, USA,
3 Department of Pathology, Mayo Clinic, Scottsdale, AZ, USA,
4 Department of Pathology, Memorial Sloan Kettering, New York, NY, USA,
5 Department of Radiology, University of Michigan Health System, Ann Arbor, MI, USA
* To whom correspondence should be addressed. E-mail: flaherty{at}umich.edu.
Rationale and hypothesis: Idiopathic pulmonary fibrosis is a fatal disease with a variable rate of progression. We hypothesized that changes in distance walked and quantity of desaturation during a six minute walk test would add prognostic information to changes in forced vital capacity or diffusing capacity for carbon monoxide.
Methods: One hundred and ninety-seven patients with idiopathic pulmonary fibrosis were evaluated. Desaturation during the six minute hallwalk was associated with increased mortality even if a threshold of 88% was not reached. Baseline walk distance predicted subsequent walk distance but was not a reliable predictor of subsequent mortality in multivariate survival models. The predictive ability of serial changes in physiology varied when patients were stratified by the presence/absence of desaturation 88% during a baseline six minute walk test. For patients with a baseline saturation 88% during a six minute walk test the strongest observed predictor of mortality was serial change in diffusing capacity for carbon monoxide. For patients with saturation > 88% during their baseline walk test serial decreases in forced vital capacity and increases in desaturation area, significantly predicted subsequent mortality while decreases in walk distance and in diffusing capacity for carbon monoxide displayed less consistent statistical evidence of increasing mortality in our patients.
Conclusion: These data highlight the importance of stratifying patients by degree of desaturation during a six minute walk test prior to attributing prognostic value to serial changes in other physiologic variables.
Key words: Idiopathic pulmonary fibrosis, six minute hall walk, prognosis, survival, pulmonary function
This article has been cited by other articles:

|
 |

|
 |
 
A U Wells, N Hirani, and on behalf of the British Thoracic Society Intersti
Interstitial lung disease guideline: the British Thoracic Society in collaboration with the Thoracic Society of Australia and New Zealand and the Irish Thoracic Society
Thorax,
September 1, 2008;
63(Suppl_V):
v1 - v58.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. M. Bourbonnais and L. Samavati
Clinical predictors of pulmonary hypertension in sarcoidosis
Eur. Respir. J.,
August 1, 2008;
32(2):
296 - 302.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. W. Voltz, J. W. Card, M. A. Carey, L. M. DeGraff, C. D. Ferguson, G. P. Flake, J. C. Bonner, K. S. Korach, and D. C. Zeldin
Male Sex Hormones Exacerbate Lung Function Impairment after Bleomycin-Induced Pulmonary Fibrosis
Am. J. Respir. Cell Mol. Biol.,
July 1, 2008;
39(1):
45 - 52.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. K. Han, S. Murray, C. D. Fell, K. R. Flaherty, G. B. Toews, J. Myers, T. V. Colby, W. D. Travis, E. A. Kazerooni, B. H. Gross, et al.
Sex differences in physiological progression of idiopathic pulmonary fibrosis
Eur. Respir. J.,
June 1, 2008;
31(6):
1183 - 1188.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Strange and J. R. Seibold
Scleroderma Lung Disease: "If You Don't Know Where You Are Going, Any Road Will Take You There"
Am. J. Respir. Crit. Care Med.,
June 1, 2008;
177(11):
1178 - 1179.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
T M Maher, M Gat, D Allen, A Devaraj, A U Wells, and D M Geddes
Reproducibility of dynamically represented acoustic lung images from healthy individuals
Thorax,
June 1, 2008;
63(6):
542 - 548.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A E Holland, C J Hill, M Conron, P Munro, and C F McDonald
Short term improvement in exercise capacity and symptoms following exercise training in interstitial lung disease
Thorax,
June 1, 2008;
63(6):
549 - 554.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. Giannakoulas, T. D. Karamitsos, G. Pitsiou, and H. I. Karvounis
Right ventricular dysfunction and functional limitation in idiopathic pulmonary fibrosis
Eur. Respir. J.,
January 1, 2008;
31(1):
219 - 220.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
T. E. King Jr., J. Behr, K. K. Brown, R. M. du Bois, L. Lancaster, J. A. de Andrade, G. Stahler, I. Leconte, S. Roux, and G. Raghu
BUILD-1: A Randomized Placebo-controlled Trial of Bosentan in Idiopathic Pulmonary Fibrosis
Am. J. Respir. Crit. Care Med.,
January 1, 2008;
177(1):
75 - 81.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. W. Kinder, K. K. Brown, M. I. Schwarz, J. H. Ix, A. Kervitsky, and T. E. King Jr
Baseline BAL Neutrophilia Predicts Early Mortality in Idiopathic Pulmonary Fibrosis
Chest,
January 1, 2008;
133(1):
226 - 232.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. K. Han, V. V. McLaughlin, G. J. Criner, and F. J. Martinez
Pulmonary Diseases and the Heart
Circulation,
December 18, 2007;
116(25):
2992 - 3005.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. W. Card, J. W. Voltz, M. A. Carey, J. A. Bradbury, L. M. DeGraff, F. B. Lih, J. C. Bonner, D. L. Morgan, G. P. Flake, and D. C. Zeldin
Cyclooxygenase-2 Deficiency Exacerbates Bleomycin-Induced Lung Dysfunction but Not Fibrosis
Am. J. Respir. Cell Mol. Biol.,
September 1, 2007;
37(3):
300 - 308.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
I. Noth and F. J. Martinez
Recent Advances in Idiopathic Pulmonary Fibrosis
Chest,
August 1, 2007;
132(2):
637 - 650.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. D. Nathan, P. W. Noble, and R. M. Tuder
Idiopathic Pulmonary Fibrosis and Pulmonary Hypertension: Connecting the Dots
Am. J. Respir. Crit. Care Med.,
May 1, 2007;
175(9):
875 - 880.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. U. Wells and C. M. Hogaboam
Update in Diffuse Parenchymal Lung Disease 2006
Am. J. Respir. Crit. Care Med.,
April 1, 2007;
175(7):
655 - 660.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. D. Fell and F. J. Martinez
The Impact of Pulmonary Arterial Hypertension on Idiopathic Pulmonary Fibrosis
Chest,
March 1, 2007;
131(3):
641 - 643.
[Full Text]
[PDF]
|
 |
|
Copyright © 2006 American Thoracic Society
|
|
|