Connective tissue disease related fibrotic lung disease: high resolution computed tomographic and pulmonary function indices as prognostic determinants

被引:168
作者
Walsh, Simon L. F. [1 ]
Sverzellati, Nicola [2 ]
Devaraj, Anand [1 ]
Keir, Gregory J. [3 ]
Wells, Athol U. [3 ]
Hansell, David M. [1 ]
机构
[1] Royal Brompton Hosp, Dept Radiol, London SW3 6NP, England
[2] Univ Parma, Sect Radiol, Dept Surg Sci, I-43100 Parma, Italy
[3] Royal Brompton Hosp, Interstitial Lung Dis Unit, London SW3 6NP, England
关键词
USUAL INTERSTITIAL PNEUMONIA; REVISED CRITERIA; FIBROSIS; CLASSIFICATION; DIAGNOSIS; CT; POLYMYOSITIS; VARIABILITY;
D O I
10.1136/thoraxjnl-2013-203843
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Purpose: To determine high resolution computed tomography (HRCT) patterns and pulmonary function indices which are associated with increased mortality in patients with connective tissue disease related fibrotic lung disease (CTD-FLD). Methods: HRCTs from 168 patients with CTD-FLD were scored by 2 observers for a variety of HRCT patterns and traction bronchiectasis. A radiological diagnosis of usual interstitial pneumonia (UIP), fibrotic non-specific interstitial pneumonia (NSIP) or indeterminate was also assigned. Using Cox regression analysis, associations with mortality were identified. Honeycombing and traction bronchiectasis scores were converted to binary absence/presence scores and also tested. A subgroup analysis of patients with biopsy material (n=51) was performed by classifying patients according to radiological and histopathological diagnoses, as concordant UIP, discordant UIP and fibrotic NSIP. The prognostic separation of this classification was also evaluated. Results: Severity of traction bronchiectasis (HR 1.10, p=0.001, 95% CIs 1.04 to 1.17), increasing extent of honeycombing (HR 1.08, p=0.021, 95% CI 1.03 to 1.13) and reduction in DLco (HR 0.97, p=0.013, 95% CI 0.95 to 0.99) were independently associated with increased mortality. Interobserver agreement and prognostic strength were higher for binary traction bronchiectasis scores (weighted κ (κw)=0.69, HR 4.00, p=0.001, 95%CI 1.19 to 13.38), than binary honeycombing scores (κw=0.50, HR 2.87, p=0.022, 95% CI 1.53 to 5.43). The radiological-histopathological classification was strongly associated with increased mortality (HR 2.74, p<0.001, 95% CI 1.57 to 4.77) and patients with discordant UIP had a better prognosis than concordant UIP but worse prognosis than fibrotic NSIP. Conclusions: Severity of traction bronchiectasis, extent of honeycombing and DLco are strongly associated with mortality in CTD-FLD. Interobserver agreement for traction bronchiectasis is higher than for honeycombing. In CTD-FLD, radiological diagnosis has survival implications in biopsy proven UIP.
引用
收藏
页码:216 / 222
页数:7
相关论文
共 35 条
[1]  
Anon Alarcon-Segovia D., 1987, Mixed connective tissue disease and antinuclear antibodies, P33
[2]   LUNG-FUNCTION TESTING - SELECTION OF REFERENCE VALUES AND INTERPRETATIVE STRATEGIES [J].
不详 .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1991, 144 (05) :1202-1218
[3]   PRELIMINARY CRITERIA FOR THE CLASSIFICATION OF SYSTEMIC-SCLEROSIS (SCLERODERMA) [J].
不详 .
ARTHRITIS AND RHEUMATISM, 1980, 23 (05) :581-590
[4]   THE AMERICAN-RHEUMATISM-ASSOCIATION 1987 REVISED CRITERIA FOR THE CLASSIFICATION OF RHEUMATOID-ARTHRITIS [J].
ARNETT, FC ;
EDWORTHY, SM ;
BLOCH, DA ;
MCSHANE, DJ ;
FRIES, JF ;
COOPER, NS ;
HEALEY, LA ;
KAPLAN, SR ;
LIANG, MH ;
LUTHRA, HS ;
MEDSGER, TA ;
MITCHELL, DM ;
NEUSTADT, DH ;
PINALS, RS ;
SCHALLER, JG ;
SHARP, JT ;
WILDER, RL ;
HUNDER, GG .
ARTHRITIS AND RHEUMATISM, 1988, 31 (03) :315-324
[5]   POLYMYOSITIS AND DERMATOMYOSITIS .2. [J].
BOHAN, A ;
PETER, JB .
NEW ENGLAND JOURNAL OF MEDICINE, 1975, 292 (08) :403-407
[6]   STATISTICAL-METHODS FOR ASSESSING OBSERVER VARIABILITY IN CLINICAL MEASURES [J].
BRENNAN, P ;
SILMAN, A .
BMJ-BRITISH MEDICAL JOURNAL, 1992, 304 (6840) :1491-1494
[7]   Computed tomographic imaging in connective tissue diseases [J].
Devaraj, Anand ;
Wells, Athol U. ;
Hansell, David M. .
SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE, 2007, 28 (04) :389-397
[8]   Polymyositis-dermatomyositis-associated interstitial lung disease [J].
Douglas, WW ;
Tazelaar, HD ;
Hartman, TE ;
Hartman, RP ;
Decker, PA ;
Schroeder, DR ;
Ryu, JH .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 164 (07) :1182-1185
[9]   Fibrotic idiopathic interstitial pneumonias: HRCT findings that predict mortality [J].
Edey, Anthony J. ;
Devaraj, Anand A. ;
Barker, Robert P. ;
Nicholson, Andrew G. ;
Wells, Athol U. ;
Hansell, David M. .
EUROPEAN RADIOLOGY, 2011, 21 (08) :1586-1593
[10]  
European Respiratory Society, 2002, Am J Respir Crit Care Med, V165, P277, DOI [10.1164/ajrccm.165.2.ats01, DOI 10.1164/AJRCCM.165.2.ATS01]