Radovic Milan, Ristic Lidija, Ciric Zorica, Dinic-Radovic Violeta, Stankovic Ivana, Pejcic Tatjana, Rancic Milan, Bogdanovic Dragan
Department of Internal Medicine, Faculty of Medicine, University of Nis, Nis, Republic of Serbia; Clinic for Lung Diseases, Clinical Centre of Nis, Nis, Republic of Serbia.
Clinic for Gastroenterology and Hepatology, Clinical Centre of Nis, Nis, Republic of Serbia.
Int J Chron Obstruct Pulmon Dis. 2016 Jun 16;11:1307-16. doi: 10.2147/COPD.S106875. eCollection 2016.
During the treatment phase of active pulmonary tuberculosis (PTB), respiratory function impairment is usually restrictive. This may become obstructive, as a PTB-associated airflow obstruction (AFO) or as a later manifestation of underlying COPD.
The aim of the study was to examine the potential causes and risks for AFO development in PTB by exploring the aspects of spirometry limitations and clinical implications for the underlying COPD detection, taking into account various confounding factors.
Prospective, nest case-control study on 40 new cases of PTB with initial restrictive respiratory function impairment, diagnosed and treated according to the directly observed treatment short course (DOTS) strategy.
From all observed patients, 37.5% of them developed AFO upon the completion of PTB treatment, with significantly increased average of forced vital capacity (%) (P<0.01). Their changes in forced expiratory volume in the first second (%) during the PTB treatment were strongly associated with the air pollution exposure in living (0.474%-20.971% for 95% confidence interval [CI]; P=0.041) and working environments (3.928%-20.379% for 95% CI; P=0.005), initial radiological extent of PTB lesions (0.018%-0.700% for 95% CI; P=0.047), leukocyte count (0.020%-1.328% for 95% CI; P=0.043), and C-reactive protein serum level (0.046%-0.205% for 95% CI; P=0.003) compared to the other patients. The multivariate logistic regression analysis model shows initial radiological extent of pulmonary tuberculosis lesions (OR 1.01-1.05 for 95% CI; P=0.02) and sputum conversion rate on culture (OR 1.02-1.68 for 95% CI; P=0.04) as the most significant predictors for the risk of AFO development.
AFO upon PTB treatment is a common manifestation of underlying COPD, which mostly occurs later, during the reparative processes in active PTB, even in the absence of major risk factors, such as cigarette smoking and biomass fuel dust exposure. Initial spirometry testing in patients with active PTB is not a sufficient and accurate approach in the detection of underlying COPD, which may lead to their further potential health deterioration.
在活动性肺结核(PTB)治疗阶段,呼吸功能损害通常为限制性。这可能会转变为阻塞性,表现为与PTB相关的气流阻塞(AFO)或潜在慢性阻塞性肺疾病(COPD)的后期表现。
本研究旨在通过探讨肺活量测定的局限性以及对潜在COPD检测的临床意义等方面,并考虑各种混杂因素,来研究PTB患者发生AFO的潜在原因和风险。
对40例初发限制性呼吸功能损害的PTB新病例进行前瞻性巢式病例对照研究,这些病例按照直接观察短程治疗(DOTS)策略进行诊断和治疗。
在所有观察的患者中,37.5%在PTB治疗结束时发生了AFO,其用力肺活量平均值(%)显著增加(P<0.01)。与其他患者相比,他们在PTB治疗期间第一秒用力呼气量(%)的变化与生活环境(95%置信区间[CI]为0.474%-20.971%;P=0.041)和工作环境(95%CI为3.928%-20.379%;P=0.005)中的空气污染暴露、PTB病变的初始放射学范围(95%CI为0.018%-0.700%;P=0.047)、白细胞计数(95%CI为0.020%-1.328%;P=0.043)以及血清C反应蛋白水平(95%CI为0.046%-0.205%;P=0.003)密切相关。多因素逻辑回归分析模型显示,肺结核病变的初始放射学范围(95%CI的比值比为1.01-1.05;P=0.02)和培养痰菌转阴率(95%CI的比值比为1.02-1.68;P=0.04)是AFO发生风险的最显著预测因素。
PTB治疗期间的AFO是潜在COPD的常见表现,大多在活动性PTB的修复过程后期出现,即使在没有吸烟和生物质燃料粉尘暴露等主要危险因素的情况下也是如此。对活动性PTB患者进行初始肺活量测定并不是检测潜在COPD的充分且准确的方法,这可能会导致其潜在健康状况进一步恶化。