Quantifying change in pulmonary function as a prognostic marker in systemic sclerosis-related interstitial lung disease

被引:0
作者
Moore, O. A. [1 ,2 ]
Proudman, S. M. [3 ,4 ]
Goh, N. [5 ,6 ]
Corte, T. J. [7 ]
Rouse, H. [8 ]
Hennessy, O. [8 ]
Morrisroe, K. [1 ]
Thakkar, V. [1 ,9 ,10 ]
Sahhar, J. [11 ]
Roddy, J. [12 ]
Youssef, P. [13 ,14 ]
Gabbay, E. [15 ,16 ]
Nash, P. [17 ]
Zochling, J. [18 ]
Stevens, W. [1 ]
Nikpour, M. [1 ,19 ]
机构
[1] St Vincents Hosp Melbourne, Dept Rheumatol, Fitzroy, Vic 3065, Australia
[2] Derriford Hosp, Dept Rheumatol, Plymouth PL6 8DH, Devon, England
[3] Royal Adelaide Hosp, Rheumatol Unit, Adelaide, SA, Australia
[4] Univ Adelaide, Discipline Med, Adelaide, SA 5005, Australia
[5] Austin Hosp, Dept Resp Med, Melbourne, Vic 3084, Australia
[6] Alfred Hosp Melbourne, Dept Resp Med, Melbourne, Vic, Australia
[7] Royal Prince Alfred Hosp Sydney, Dept Resp Med, Sydney, NSW, Australia
[8] St Vincents Hosp Melbourne, Dept Radiol, Fitzroy, Vic 3065, Australia
[9] Liverpool Hosp Sydney, Dept Rheumatol, Sydney, NSW, Australia
[10] Univ Western Sydney, Sch Med, Penrith, NSW 1797, Australia
[11] Monash Med Ctr Melbourne, Dept Rheumatol, Melbourne, Vic, Australia
[12] Royal Perth Hosp, Dept Rheumatol, Perth, WA, Australia
[13] Royal Prince Alfred Hosp, Dept Rheumatol, Sydney, NSW, Australia
[14] Univ Sydney, Sydney, NSW 2006, Australia
[15] Royal Perth Hosp, Adv Lung Dis Unit, Perth, WA, Australia
[16] Notre Dame Univ, Fremantle, WA 6959, Australia
[17] Univ Queensland, Dept Med, Rheumatol Res Unit, Brisbane, Qld 4072, Australia
[18] Menzies Res Inst, Hobart, Tas, Australia
[19] Univ Melbourne, Dept Med, St Vincents Hosp Melbourne, Melbourne, Vic 3010, Australia
关键词
scleroderma; systemic sclerosis; interstitial lung disease; pulmonary function; prognosis; FORCED VITAL CAPACITY; SCLERODERMA LUNG; FIBROSIS; CLASSIFICATION; DECLINE; MANAGEMENT; STATEMENT; PREDICTOR; SURVIVAL; CRITERIA;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. Clinically meaningful change in systemic sclerosis (SSc) related interstitial lung (SSc-ILD) disease is unknown. The aim of this study was to quantify change in pulmonary function as a predictor of outcome in SSc-ILD. Methods. All patients had SSc-ILD defined by HRCT chest. All PFTs during follow-up, including FVC (L), DLCO (ml/min/mmHg) and KCO (DLCO/VA) volume ratio; DLCO/VA) (ml/min/mmHg/L) were retrieved. The rate of change over the first four years, and percentage change in the first year of follow-up were used in ROC curve analysis to determine the best cut-off points to predict adverse outcome (home oxygen, lung transplantation, or death). Results. Among 264 patients, there were 49 events (38 deaths, 10 supplemental oxygen, one lung transplant) over a mean (+/- SD) follow-up of 3.0 (+/- 1.7) years. The rates of decline over time and percentage change over one year in each of FVC, DLCO and KCO were predictive of adverse outcome. Stable PFTs over four years gave the optimal negative predictive values (NPVs) of 88-96%. The best sensitivity-specificity trade-off was a decline in FVC of 10% and in DLCO and KCO of 15% with NPVs of 92-93%. Conclusion. The course that SSc-ILD takes is evident within the first 1-4 years of follow up. Patients who have no decline in PFTs over 4 years have better outcomes. A decline within one year in DLCO or KCO of 15% or more is a poor prognostic factor, and identifies patients who should be monitored more closely and considered for therapy.
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页码:S111 / S116
页数:6
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