Impact of Pulmonary Artery Pressure on Exercise Function in Severe COPD

被引:105
作者
Sims, Michael W. [1 ,2 ,3 ]
Margolis, David J. [2 ,3 ]
Localio, A. Russel [2 ,3 ]
Panettieri, Reynold A. [1 ]
Kawut, Steven M. [1 ,2 ,3 ]
Christie, Jason D. [1 ,2 ,3 ]
机构
[1] Univ Penn, Sch Med, Dept Biostat & Epidemiol, Pulm Allergy & Criti Care Div, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Biostat & Epidemiol, Dept Med,Airways Biol Initiat, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Dept Biostat & Epidemiol, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USA
关键词
RIGHT-VENTRICULAR-FUNCTION; OXYGEN-THERAPY; COR-PULMONALE; HYPERTENSION; DISEASE; DYSFUNCTION; IMPAIRMENT; SILDENAFIL; VALUES; SERIES;
D O I
10.1378/chest.08-2739
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: Although pulmonary hypertension commonly complicates COPD, the functional consequences of increased pulmonary artery pressures in patients with this condition remain poorly defined. Methods: We conducted a cross-sectional analysis of a cohort of 362 patients with severe COPD who were evaluated for lung transplantation. Patients with pulmonary hemodynamics measured by cardiac catheterization and available 6-min walk test results were included. The association of mean pulmonary artery pressure (mPAP) with pulmonary function, echocardiographic variables, and 6-min walk distance was assessed. Results: The prevalence of pulmonary hypertension (mPAP, > 25 mm Hg; pulmonary artery occlusion pressure [PAOP], < 16 mm Hg) was 23% (95% confidence interval, 19 to 27%). In bivariate analysis, higher mPAP was associated with lower FVC and FEV1, higher PCO2 and lower PO2 in arterial blood, and more right heart dysfunction. Multivariate analysis demonstrated that higher mPAP was associated with shorter distance walked in 6 min, even after adjustment for age, gender, race, height, weight, FEV1, and PAOP (-11 m for every 5 mm Hg rise in mPAP; 95% confidence interval, -21 to -0.7; p = 0.04). Conclusions: Higher pulmonary artery pressures are associated with reduced exercise function in patients with severe COPD, even after controlling for demographics, anthropomorphics, severity of airflow obstruction, and PAOP. Whether treatments aimed at lowering pulmonary artery pressures may improve clinical outcomes in COPD, however, remains unknown. (CHEST 2009; 136:412-419)
引用
收藏
页码:412 / 419
页数:8
相关论文
共 35 条
[2]  
[Anonymous], 2003, The Decline of the Steller Sea Lion in Alaskan Waters: Untangling Food Webs and Fishing Nets, P1
[3]   Echocardiographic assessment of pulmonary hypertension in patients with advanced lung disease [J].
Arcasoy, SM ;
Christie, JD ;
Ferrari, VA ;
Sutton, MS ;
Zisman, DA ;
Blumenthal, NP ;
Pochettino, A ;
Kotloff, RM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 167 (05) :735-740
[4]   Impaired flow-mediated dilation is associated with low pulmonary function and emphysema in ex-smokers - The emphysema and cancer action project (EMCAP) study [J].
Barr, R. Graham ;
Mesia-Vela, Sonia ;
Austin, John H. M. ;
Basner, Robert C. ;
Keller, Brad M. ;
Reeves, Anthony P. ;
Shimbo, Daichi ;
Stevenson, Lori .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2007, 176 (12) :1200-1207
[5]   Skeletal muscle dysfunction in patients with idiopathic pulmonary arterial hypertension [J].
Bauer, Ralf ;
Dehnert, Christoph ;
Schoene, Palma ;
Filusch, Arthur ;
Baertsch, Peter ;
Borst, Mathias M. ;
Katus, Hugo A. ;
Meyer, F. Joachim .
RESPIRATORY MEDICINE, 2007, 101 (11) :2366-2369
[6]   Pulmonary hypertension in COPD [J].
Chaouat, A. ;
Naeije, R. ;
Weitzenblum, E. .
EUROPEAN RESPIRATORY JOURNAL, 2008, 32 (05) :1371-1385
[7]  
CRAPO RO, 1982, B EUR PHYSIOPATH RES, V18, P419
[8]  
CRAPO RO, 1981, AM REV RESPIR DIS, V123, P185
[9]   IMPAIRMENT OF ENDOTHELIUM-DEPENDENT PULMONARY-ARTERY RELAXATION IN CHRONIC OBSTRUCTIVE LUNG-DISEASE [J].
DINHXUAN, AT ;
HIGENBOTTAM, TW ;
CLELLAND, CA ;
PEPKEZABA, J ;
CREMONA, G ;
BUTT, AY ;
LARGE, SR ;
WELLS, FC ;
WALLWORK, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (22) :1539-1547
[10]  
Falk Jeremy A, 2008, Proc Am Thorac Soc, V5, P543, DOI 10.1513/pats.200708-142ET