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比较支气管中心性肉芽肿病与肺移植后其他形式的慢性肺移植物功能障碍。

Comparison of bronchiolitis obliterans syndrome to other forms of chronic lung allograft dysfunction after lung transplantation.

机构信息

Department of Internal Medicine, Walter Reed Army Medical Center, Washington, DC 20307, USA.

出版信息

J Heart Lung Transplant. 2010 Oct;29(10):1159-64. doi: 10.1016/j.healun.2010.05.012. Epub 2010 Jun 26.

Abstract

BACKGROUND

The radiographic presence of allograft infiltrates is atypical of bronchiolitis obliterans (BO) and inconsistent with the definition of bronchiolitis obliterans requires that restrictive processes are ruled out. The natural history of these other forms of chronic allograft dysfunction has not been well characterized. We examined the prognostic significance of radiographic and spirometric restrictive processes in comparison to BOS among lung transplant recipients.

METHODS

We performed a retrospective review of lung transplant recipients with chronic lung allograft dysfunction (CLAD) as defined by spirometry. Subgroups based on the presence or absence of persistent radiographic abnormalities were labeled as non-specific (CLAD-NS) and CLAD due to BOS (CLAD-BOS), respectively. The CLAD-BOS group was further divided into obstructive (OBOS) and restrictive (RBOS) phenotypes based on spirometry. Groups were compared with respect to survival and decline in forced expiratory volume in 1 second (FEV(1)).

RESULTS

Among 241 lung transplant recipients, 96 (40%) were identified as having CLAD, of whom 62 (65%) had CLAD-BOS and 34 (35%) CLAD-NS. No difference between groups was identified with respect to post-CLAD survival or decline in FEV(1). CLAD-BOS subgroups included 35 (56%) patients with OBOS and 27 (44%) with RBOS. There was no difference in these subgroups with respect to survival or subsequent FEV(1) decline.

CONCLUSIONS

Patients with CLAD and persistent radiographic infiltrates have a similar prognosis to BOS patients but may still represent a clinically distinct phenotype. BOS patients frequently exhibited a restrictive pattern on spirometry, which also did not offer further prognostic information, but could still represent a unique disease phenotype.

摘要

背景

同种异体移植物浸润的放射学表现是非闭塞性细支气管炎(BO)的典型表现,与闭塞性细支气管炎的定义不一致,需要排除限制过程。这些其他形式的慢性同种异体移植物功能障碍的自然史尚未得到很好的描述。我们研究了放射学和肺量计限制性过程与肺移植受者 BO 相比的预后意义。

方法

我们对慢性肺同种异体功能障碍(CLAD)进行了回顾性审查,根据肺量计进行定义。基于持续存在放射异常的存在或不存在,将亚组分别标记为非特异性(CLAD-NS)和 BO 引起的 CLAD(CLAD-BOS)。根据肺量计,CLAD-BOS 组进一步分为阻塞性(OBOS)和限制性(RBOS)表型。比较各组的生存率和 1 秒用力呼气量(FEV1)下降情况。

结果

在 241 名肺移植受者中,有 96 名(40%)被确定为患有 CLAD,其中 62 名(65%)患有 CLAD-BOS,34 名(35%)患有 CLAD-NS。CLAD 后生存率或 FEV1 下降无组间差异。CLAD-BOS 亚组包括 35 名(56%)OBOS 患者和 27 名(44%)RBOS 患者。这些亚组在生存率或随后的 FEV1 下降方面没有差异。

结论

CLAD 伴持续放射学浸润的患者与 BO 患者的预后相似,但仍可能代表一种临床独特的表型。BO 患者的肺量计检查常表现为限制性模式,这也不能提供进一步的预后信息,但仍可能代表一种独特的疾病表型。

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