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合并性肺纤维化和肺气肿:临床特征、治疗及预后的回顾性分析

Combined pulmonary fibrosis and emphysema: a retrospective analysis of clinical characteristics, treatment and prognosis.

作者信息

Zhang Lijuan, Zhang Chunling, Dong Fushi, Song Qi, Chi Fangzhou, Liu Lu, Wang Yupeng, Che Chunli

机构信息

Department of Respiratory Medicine, First Affiliated Hospital of Harbin Medical University, 23 Youzheng Avenue, Nangang District, Harbin, Heilongjiang, China.

Department of Clinical Medicine, Harbin Medical University, Harbin, Heilongjiang, China.

出版信息

BMC Pulm Med. 2016 Nov 3;16(1):137. doi: 10.1186/s12890-016-0300-7.

Abstract

BACKGROUND

Combined pulmonary fibrosis and emphysema (CPFE) is increasingly acknowledged as a separate syndrome with distinct clinical, physiological and radiological characteristics. We sought to identify physiologic and radiographic indices that predict mortality in CPFE.

METHODS

Data on clinical characteristics, pulmonary function, high-resolution computed tomography (HRCT) and treatment were compared between patients with usual interstitial pneumonia (UIP) plus emphysema (CPFE group) and those with IPF alone (IPF group). Composite physiologic index (CPI) and HRCT scores at diagnosis and during follow-up were assessed.

RESULTS

CPFE group (N = 87) was characterized by the predominance of males and smokers, who were less likely to have viral infection prior to the diagnosis, and display basal crackles, finger clubbing and wheeze, as compared to that in the IPF group (N = 105). HRCT and CPI scores increased over time in both groups. Moreover, CPFE group had a poorer prognosis, lower 5-year survival rate (43.42 % vs. 65.56 %; P < 0.05), and higher mortality (39.47 % vs. 23.33 %; P < 0.05) as compared to that in the IPF group. All CPFE patients received oxygen therapy, antibiotics and oral N-acetylcysteine; > 50 % received bronchodilators, 40 % received corticosteroids and 14 % needed noninvasive mechanical ventilation. On survival analyses, pulmonary arterial hypertension (PAH) and ≥ 5-point increase in CPI score per year were predictors of mortality in the CPFE group (hazard ratio [HR]: 10.29, 95 % Confidence Interval [CI]: 2.69-39.42 and HR: 21.60, 95 % CI: 7.28-64.16, respectively).

CONCLUSION

Patients with CPFE were predominantly male and smokers and exhibited distinct clinical, physiological and radiographic characteristics. They had a poorer prognosis than IPF. PAH and ≥ 5-point increase in CPI score per year were predictors of mortality in these patients. Future studies are needed to identify the optimal treatment approach to CPFE.

摘要

背景

合并肺纤维化和肺气肿(CPFE)日益被公认为是一种具有独特临床、生理和放射学特征的独立综合征。我们试图确定预测CPFE患者死亡率的生理和影像学指标。

方法

比较了普通间质性肺炎(UIP)合并肺气肿患者(CPFE组)和单纯特发性肺纤维化(IPF)患者(IPF组)的临床特征、肺功能、高分辨率计算机断层扫描(HRCT)及治疗情况的数据。评估了诊断时及随访期间的综合生理指标(CPI)和HRCT评分。

结果

CPFE组(N = 87)以男性和吸烟者居多,与IPF组(N = 105)相比,诊断前病毒感染的可能性较小,且较少出现肺底部湿啰音、杵状指和喘息。两组的HRCT和CPI评分均随时间增加。此外,与IPF组相比,CPFE组预后较差,5年生存率较低(43.42%对65.56%;P < 0.05),死亡率较高(39.47%对23.33%;P < 0.05)。所有CPFE患者均接受了氧疗、抗生素和口服N - 乙酰半胱氨酸治疗;超过50%的患者接受了支气管扩张剂治疗,40%的患者接受了皮质类固醇治疗,14%的患者需要无创机械通气。生存分析显示,肺动脉高压(PAH)和每年CPI评分增加≥5分是CPFE组患者死亡率的预测因素(风险比[HR]分别为:10.29,95%置信区间[CI]:2.69 - 39.42;HR:21.60,95%CI:7.28 - 64.16)。

结论

CPFE患者以男性和吸烟者为主,具有独特的临床、生理和放射学特征。他们的预后比IPF患者差。PAH和每年CPI评分增加≥5分是这些患者死亡率的预测因素。未来需要开展研究以确定CPFE的最佳治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5c9/5093954/a8ccec63e6f1/12890_2016_300_Fig1_HTML.jpg

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