1 Division of Thoracic Radiology, University of Chicago, Chicago, Illinois.
2 Division of Pulmonary and Critical Care Medicine, Nanjing Drum Tower Hospital, Nanjing, Jiangsu, China.
Ann Am Thorac Soc. 2017 Oct;14(10):1533-1538. doi: 10.1513/AnnalsATS.201701-035OC.
Significant heterogeneity of computed tomography (CT) presentation exists within chronic hypersensitivity pneumonitis (HP). There are limited data aimed at delineating the prognostic value of specific CT features, distribution, and patterns in chronic HP.
To examine whether the presence of CT mosaic attenuation (MA) and air trapping (AT), and the distribution or patterns of fibrosis impact survival in subjects with chronic HP.
We retrospectively identified 110 consecutively enrolled, well-characterized, biopsy-proven adult subjects with chronic HP between 1982 and 2015 from the National Jewish Health interstitial lung disease research database. The first available CT scan of diagnostic quality from each subject was formally evaluated for specific CT findings associated with chronic HP and for overall CT pattern. A Cox proportional hazards model was used to identify independent predictors in time-to-death analysis, and bootstrap analysis was performed for internal model validation.
Fibrotic HP (65%; 72/110) was most often peripheral in the axial plane and lower lung preponderant. The distribution of lung disease in those without fibrosis was most often axially and zonally diffuse. There was no association between survival and CT distribution or CT pattern in the whole cohort or within the fibrotic subset of subjects. After multivariate adjustment, AT/MA was independently associated with survival in the whole cohort (HR = 0.26; 95% confidence interval = 0.07-0.97). Results were similar after restricting the analyses to fibrotic HP cases.
Among subjects with chronic HP, the presence of CT AT/MA may identify subjects with better prognosis.
慢性超敏性肺炎(HP)患者的计算机断层扫描(CT)表现存在明显异质性。目前针对 CT 特征、分布和模式的特定预后价值的相关数据有限。
研究慢性 HP 患者 CT 马赛克衰减(MA)和空气潴留(AT)的存在以及纤维化的分布或模式是否影响生存。
我们回顾性地从 1982 年至 2015 年全国犹太健康间质性肺病研究数据库中确定了 110 例连续入组、特征明确、经活检证实的成人慢性 HP 患者。对每位患者的首次可用的具有诊断质量的 CT 扫描进行正式评估,以确定与慢性 HP 相关的特定 CT 发现和整体 CT 模式。采用 Cox 比例风险模型进行时间到死亡分析中的独立预测因子识别,并进行 bootstrap 分析以进行内部模型验证。
纤维化性 HP(65%;72/110)在轴向平面上最常为外周性,下肺更常见。无纤维化患者的肺部疾病分布最常为轴向和区域性弥漫性。在整个队列或无纤维化亚组中,CT 分布或 CT 模式与生存均无相关性。多变量调整后,AT/MA 在整个队列中与生存独立相关(HR=0.26;95%置信区间=0.07-0.97)。在将分析限制在纤维化性 HP 病例后,结果相似。
在慢性 HP 患者中,CT AT/MA 的存在可能识别出预后较好的患者。