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

被引:162
|
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
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