|Year : 2018 | Volume
| Issue : 2 | Page : 128-133
Pulmonary functions' assessment in post-tuberculosis cases by spirometry: Obstructive pattern is predominant and needs cautious evaluation in all treated cases irrespective of symptoms
Shital Patil1, Rajesh Patil2, Anil Jadhav1
1 Department of Pulmonary Medicine, MIMSR Medical College, Latur, Maharashtra, India
2 Department of Internal Medicine, MIMSR Medical College, Latur, Maharashtra, India
|Date of Web Publication||13-Jun-2018|
Department of Pulmonary Medicine, MIMSR Medical College, Latur - 413 512, Maharashtra
Source of Support: None, Conflict of Interest: None
Background: Approximately 30%–40% patients suffer with lung function issues in spite of successful treatment outcome; and these problems are less documented routinely. Methods: Prospective multicentric study conducted during July 2013–June 2017, to find pulmonary function assessment in posttuberculosis (TB) cases irrespective of their symptoms, included 500 cases in symptomatic and asymptomatic group and subjected to inclusion and exclusion criteria. All cases were subjected to spirometry analysis. Statistical analysis was done using Chi-square test. Results: In spirometry assessment of symptomatic post-TB cases, obstructive pattern was predominant type documented in 42% cases. In spirometry assessment of asymptomatic post-TB cases, obstructive pattern is documented in 32%, mixed pattern in 14%, and normal spirometry is documented in 46% cases. In spirometry assessment in symptomatic and asymptomatic cases, obstructive pattern is documented in 210 cases and 160 cases, respectively (P < 0.00001). Abnormal lung function is documented in 70% and 54% in symptomatic and asymptomatic post-TB cases, respectively (P < 0.00001). Conclusions: Lung function impairment is known to occur after pulmonary TB irrespective of duration of treatment and outcome of disease. Obstructive lung disease is the predominant lung function impairment in symptomatic cases. Significant number of asymptomatic cases are also having obstructive pattern of lung function in spirometry analysis.
Keywords: Obstructive pattern, posttuberculosis, pulmonary functions, spirometry
|How to cite this article:|
Patil S, Patil R, Jadhav A. Pulmonary functions' assessment in post-tuberculosis cases by spirometry: Obstructive pattern is predominant and needs cautious evaluation in all treated cases irrespective of symptoms. Int J Mycobacteriol 2018;7:128-33
|How to cite this URL:|
Patil S, Patil R, Jadhav A. Pulmonary functions' assessment in post-tuberculosis cases by spirometry: Obstructive pattern is predominant and needs cautious evaluation in all treated cases irrespective of symptoms. Int J Mycobacteriol [serial online] 2018 [cited 2018 Jun 21];7:128-33. Available from: http://www.ijmyco.org/text.asp?2018/7/2/128/234330
| Introduction|| |
Tuberculosis (TB), the disease caused by Mycobacterium tuberculosis, remains a major public health problem globally. In 2014, >9.6 million people are estimated to have fallen ill with TB, while 1.5 million people died of the disease. Of the 6.3 million notified cases of TB that occurred in 2014, 81% had lung TB. Over the past two decades, treatment of TB has significantly improved and 61 million patients were successfully treated for TB globally since 1995. However, such successful treatment of TB based on either documentation of bacteriological clearance of M. tuberculosis bacilli from the involved site or completion of the prescribed drug dose does not assess structural and functional effects on the involved organ which is the hallmark of the pathology of TB.
Based on recent trends in treatment outcomes, about 86% of the new and relapse pulmonary TB (PTB) cases notified in 2014 were successfully treated. However, several studies have demonstrated the persistence of symptoms, reduced quality of life, abnormal radiological findings, and impaired pulmonary function tests (PFTs) in patients successfully treated for PTB.,,,
The presence of extensive residual lung lesions may be a predictor of permanent disability following tissue destruction, cor pulmonale, and susceptibility to opportunistic infections, leading to reduced quality of life. In addition, the extent of disease is one of the risk factors involved in TB mortality rates.
The histopathological findings resulting from TB include the formation of caseous granuloma, tissue liquefaction, and formation of pulmonary cavities. From these changes, residual lesions remain in many patients, resulting in pulmonary sequelae that are characterized by impairments in the bronchial and parenchymal structure. These structural changes include bronchovascular distortions, bronchiectasis, emphysema, and fibrosis.
PTB can involve the airways, leading to mucosal edema, hypertrophy, and hyperplasia of mucous glands, increased mucus secretion, and smooth muscle hypertrophy. This affects the caliber of the airways, increases its strength, and decreases airflow. Through the mechanism of cicatricial fibrosis, there is also a reduction of total lung capacity. Post-TB patients may have limited exercise tolerance and significant disability which may affect daily activities.
Studies of pulmonary function in individuals with PTB demonstrated variable patterns and severity of impairment.,,,,, Pulmonary function studies ,,,,, can show restrictive, obstructive, or mixed patterns and range from normal to severe impairment. These findings are currently incompletely characterized. The studies performed to date ,,,,, have been of highly selected populations, as follows: patients receiving only inpatient TB treatment; patients who have been referred for a symptom or preoperative evaluation; patients with an absence of other lung diseases; and persons sufficiently well to be currently employed in mining.,,,,, These patients do not completely represent the populations affected by TB. PFTs objectively quantify lung function and impairment and are used to evaluate persons with chronic lung disease.
In this study, we observed pulmonary functions by spirometry by categorizing patients as asymptomatic and symptomatic previously treated PTB cases.
| Methods|| |
A prospective multicentric observational study conducted in Venkatesh Chest hospital, and Pulmonary Medicine, MIMSR Medical College Latur during July 2013 to June 2017, to find out lung function assessment of previously treated PTB. We enrolled asymptomatic and symptomatic previously treated and declared cured as per national guidelines. A total of 500 asymptomatic and 500 symptomatic cases were enrolled in the study after IRB approval and written informed consent of the patient.
- PTB cases completed anti-TB treatment as per the standard guidelines for 6 months
- PTB cases completed treatment as per national guidelines and declared cured.
- Extrapulmonary TB cases
- Simultaneous involvement of lung and pleura
- Multidrug resistant TB cases
- Defaulted cases during treatment
- History of irregular treatment
- Cases with a history of smoking active or past to avoid spirometry analysis
- Cases with diabetes mellitus, hypertension, and ischemic heart disease
- Cases unable to cooperate during spirometry procedure or does not want to enroll in the study
- Cases who failed to fulfill acceptability and reproducibility criteria of spirometry were excluded from the study.
All study cases were undergone following assessment to rule out other comorbidities from pure respiratory system involvement
- Clinical assessment as vital parameters such as heart rate, respiratory rate, blood pressure, and documentation of respiratory adventitious sounds
- Laboratory parameters such as hemoglobin, renal functions, blood sugar level, kidney functions, and electrocardiography
- Spirometry performed.
Methodology of spirometry
Subsequently, spirometric evaluation was done by a portable spirometer, Spirolab II (manufactured by Medical International Research, Italy) and meets American Thoracic Society and European Respiratory Society standards (ATS and ERS), before and 15 min after administration of 400 microgram salbutamol using pressurized metered-dose inhaler with small-volume spacer device. All patients were instructed not to use any bronchodilator on the preceding night and on the day of procedure. Spirometric procedure was carried out as per ATS/ERS task force recommendation for standardization of lung function testing. Subjects who were found to have postbronchodilator forced expiratory volume in first second (FEV1)/forced vital capacity (FVC) <0.7 were taken up for final analysis as this value indicates the cutoff for diagnosis of obstructive airway disease according to GOLD guideline. Bronchodilator reversibility was defined as an improvement in FEV1 by at least 12% and 200 ml over prebronchodilator value. FEV1/FVC ≥ 0.7 was excluded as those patients had either a normal spirometry or a purely restrictive ventilatory abnormality. Furthermore, the individuals who failed to fulfill acceptability and reproducibility criteria of spirometry were excluded. FVC, FEV1, and FEV1/FVC ratio values for case patients were compared with gender-specific and race-specific adult predicted normative population values and the control group.
Interpretive algorithms were used in determining restrictive or obstructive patterns and spirometry results were analyzed and categorized in four groups as follows:,,,
- Normal - FEV1/FVC ratio of >70% and an FVC of >80% predicted
- Obstructive - airway obstruction was defined as an FEV1/FVC ratio of <70% and an FVC of >80% predicted
- Mixed-combined defects were FVC of <80% predicted and an FEV1/FVC ratio of <70%
- Restrictive-restrictive defects as an FEV1/FVC ratio of >70% with an FVC of <80% predicted.
The statistical analysis was done using Chi-squared test (three methods of Chi-squared test such as independence, goodness of fit, and proportion test). Significant values of Chi-squared were seen from probability table for different degrees of freedom required. P value was considered statistically significant if it was below 0.05 and highly significant in case if it was <0.001.
| Results|| |
In this study, a total of 500 cases were in symptomatic and asymptomatic group of post-TB cases. In both the groups, males were predominant with 64% and 56%, respectively. Mean age was 42 ± 11 years and 48 ± 9 years, respectively. Main symptoms in symptomatic group were shortness of breath in 79% cases, cough in 48% cases, and sputum production in 39% cases.
In spirometry assessment of symptomatic post-TB cases, obstructive pattern was predominant type documented in 42% cases [Table 1] and [Figure 1].
|Table 1: Spirometry assessment of symptomatic posttuberculosis cases (n=500)|
Click here to view
|Figure 1: Pie diagram showing spirometry assessment in symptomatic posttuberculosis cases|
Click here to view
In spirometry assessment of asymptomatic post-TB cases, obstructive pattern is documented in 32%, mixed pattern in 14%, and normal spirometry is documented in 46% cases [Table 2] and [Figure 2].
|Table 2: Spirometry assessment of asymptomatic posttuberculosis cases (n=500)|
Click here to view
|Figure 2: Pie diagram showing spirometry assessment in asymptomatic posttuberculosis cases|
Click here to view
In spirometry assessment in symptomatic and asymptomatic cases, obstructive pattern is documented in 210 cases and 160 cases, respectively (P< 0.00001) [Table 3].
|Table 3: Comparative spirometry analysis of symptomatic (n=500) and asymptomatic (n=500) cases in previously treated tuberculosis|
Click here to view
χ2 = 27.21, df = 4, P< 0.00001.
In spirometry assessment in symptomatic and asymptomatic cases, a significant difference is documented in normal and abnormal spirometry parameters in both groups (P< 0.00001)[Table 4].
|Table 4: Spirometry abnormality in symptomatic (n=500) and asymptomatic (n=500) cases in previously treated tuberculosis|
Click here to view
χ2 = 27.16, df = 1, P< 0.00001.
| Discussion|| |
Lung function pattern in symptomatic posttuberculosis cases
In this study, abnormal lung function is documented in 70% and 54% in symptomatic and asymptomatic post-TB cases, respectively (P< 0.00001). Pasipanodya et al. conducted a study in the United States showed that 59% of patients treated for TB subsequently had abnormal pulmonary function. In that study, more than half of the patients treated for PTB evolved to significantly impaired pulmonary function. These data suggest that impaired pulmonary function after PTB is a major cause of chronic lung disease. Agarwala et al. conducted a study in India and observed that 52.7% of treated PTB patients had an obstructive ventilatory defect. Manji et al. conducted a study in Tanzania and observed the prevalence of abnormal lung functions in 74% of cases.
In the present study, spirometry assessment of symptomatic post-TB cases, obstructive, restrictive, and mixed pattern was observed in 42%, 10%, and 18%, respectively. Manji et al. documented in their study, the prevalence of individual patterns of impairment was 42%, 13%, and 19% for obstructive, restrictive, and mixed patterns of lung disease, respectively. A study by Pasipanodya et al. observed that the prevalence of individual subtypes of impairment for obstructive, restrictive, and mixed was 15%, 31%, and 13%, respectively. Studies by Long et al., Willcox and Ferguson, Plit et al., and Lee and Chang  observed similar lung function abnormalities, and results are comparable to our study. Snider et al. found evenly distributed patterns of dysfunction among impaired patients, as follows: restrictive dysfunction, 24%; obstructive dysfunction, 23%; and mixed dysfunction, 19% cases. Verma et al. described similar findings in their study among 92 post-PTB individuals and they found restrictive pathology in 37 and mixed pattern in 21 patients as per spirometric criteria.
In the present study, spirometry assessment of symptomatic post-TB cases, mixed pattern was observed in 18% cases. Studies by Ramos et al., Di Naso et al., and Singla et al. observed predominantly mixed pattern of spirometric abnormality in the study population and such a high prevalence of mixed pattern can be explained by the extensive fibrosis coexisting with airflow obstruction.
Chushkin and Ots  observed that approximately half of all PTB patients treated at the local TB dispensary suffered from impaired pulmonary function, a prevalence much higher than that observed in the general population. Pulmonary impairment was identified in 102 (47.7%) of the patients, the pattern being obstructive in 74 (34.6%), restrictive in 18 (8.4%), and mixed in 8 (3.7%) cases.
Lung function pattern in asymptomatic posttuberculosis cases
In this study, abnormal lung function is documented in 70% and 54% in symptomatic and asymptomatic post-TB cases, respectively (P< 0.00001). Guilani et al. in their study documented that 62% of asymptomatic post-TB cases were having spirometry abnormality. In their study, they concluded that all cases of cured PTB are prone to develop pulmonary function impairment. Even asymptomatic cases may have defective lung function.
Anno and Tomashefski  in one of the early studies reported impairment of respiratory function in PTB patients. There was an increase in the residual volume (RV), RV/total lung capacity ratio, and a reduction in the maximal breathing capacity in a selected group of TB patients.
Obstructive is the most common abnormality documented in posttuberculosis cases?
In spirometry assessment in symptomatic and asymptomatic cases, obstructive pattern is documented in 210 cases and 160 cases, respectively (P< 0.00001). Overall prevalence of obstructive spirometry pattern in symptomatic and asymptomatic cases was 42% and 32%, respectively (P< 0.0001). The multicenter population-based PLATINO study  also evaluated the relationship between past history of TB and development of airflow obstruction in five Latin American countries. The overall prevalence of airflow obstruction was 30.7% among those with a history of TB.
Gaensler and Lindgren  in their study reported evidence of airflow obstruction in 61% TB patients. In a cross-sectional study performed in Chicago Municipal TB Sanatorium by Snider et al. reported airflow obstruction in 23% patients.
Indian studies by, Brashier et al. reported a 46% prevalence of airflow obstruction and the prevalence increased with the duration after treatment completion. In the Gothi et al. series, obliterative bronchiolitis was the cause of chronic airflow obstruction in 13% of patients and 78% of obliterative bronchiolitis was post-TB. Verma et al. reported a much lower prevalence of airflow obstruction. In fully treated PTB patients, obstructive spirometric pattern was seen in 15 (16.3%) patients and majority had irreversible airflow obstruction.
Baig et al. performed study in Pakistan and observed that 55.3% of treated PTB patients presenting with dyspnea and had an obstructive ventilatory defect. Study conducted by Patricio Jiménez et al. had also revealed that an obstructive pattern of pulmonary functional impairment following treated PTB was more common. In a larger study by Akkara et al., the authors found that, of 257 participants with cured PTB, 86.8% had spirometry readings consistent with obstructive airway disease, that is, FEV1:FVC <70%.
Di Naso et al. conducted a study in Brazilian population with severe obstructive pulmonary disease found that 15.7% of patients had PTB sequelae. Zhou et al. found a higher prevalence of obstructive disorders (68%) in previously treated TB cases.
Other important clinical intrusions observed in this study
Does past history of tuberculosis as independent risk factor for obstructive airway disease?
In the present study, spirometry assessment in symptomatic and asymptomatic cases, obstructive pattern, is documented in 210 cases and 160 cases, respectively (P< 0.00001).
Allwood et al. in a systematic review assessed the relation between PTB and the development of chronic airflow obstruction. A total of 19 studies including 1 case series, 3 case–control studies, 4 cohort studies, 8 single-center cross-sectional studies, and 3 multicenter cross-sectional studies were eligible for final analysis. The authors confirmed a positive association between a past history of TB and the presence of chronic airflow obstruction.
Lam et al. in a population-based study involving Guangzhou Biobank Cohort reported a past history of TB as an independent predictor of airflow obstruction with odds ratio of 1.37 after adjusting sex, age, and smoking exposure. Lee and Chang  in a cross-sectional population-based study based on data from Second Korea National Health and Nutrition Examination Survey 2001, analyzed the effects of the previous TB on the risk of obstructive lung disease development.
Plit et al. and Chung et al. documented that PTB patients usually develop maximum loss of lung function within 6 months of the diagnosis of TB and it stabilizes 18 months after completion of treatment.
The burden of obstructive lung disease (BOLD) study  had also shown past history of tuberculosis as a risk factor for developing airflow obstruction in later life with the adjusted odd ratio of 2.51. Two recent systemic reviews also confirmed this association.,,
Ehrlich et al. observed similar finding in their review of South African literature and showed a significant association between chronic airway obstruction and PTB. Inghammar et al. showed that impaired pulmonary function was associated with an increased risk of active TB. However, if decreased lung function is a risk factor for the development of TB, it is also possible that pulmonary impairment is a risk factor for its recurrence.
Indian studies by authors Verma et al., Rajasekaran et al., Krishna et al., and Salvi and Barness  observed that the obstructive airway disease is common in previously treated TB cases and documented within 1–10 years of follow-up.
Posttubercular pulmonary impairment emerges as a distinct entity in various patterns but mainly as airflow limitation and previous TB is considered as risk factor for COPD.,
Spirometry is less commonly used in routine evaluation of posttuberculosis cases!
In the present study, spirometry assessment in symptomatic and asymptomatic cases, abnormality was documented in 70% and 54%, respectively (P< 0.00001).
The presence of symptoms is not a sensitive and specific indicator of airway limitation, and the use of a symptom questionnaire appears to be an ineffective means of identifying pulmonary impairment.
However, evidence suggests that PFT is not used consistently. Even in developed countries, less than half of all patients newly diagnosed with chronic pulmonary diseases receive PFTs near the time of diagnosis.
In three large population studies, the authors Caballero et al., Lam et al., and Menezes et al. found a significant association between history of PTB and presence of airflow obstruction according to spirometry.
Using a mechanical peak expiratory flow meter or a pocket spirometer as a screening tool can reduce the number of diagnostic PFTs required. Although it has not been established that PFTs can predict recurrence, their use can probably help select a group of patients at higher risk of recurrence who require longer follow-up and prevention measures. This supports the idea that patients previously treated for PTB should undergo PFTs. However, PFTs has yet to be included in the guidelines for the treatment of TB.
| Conclusions|| |
Lung function impairment is known to occur after PTB irrespective of duration of treatment and outcome of disease. Routine use of spirometry is less utilized in these cases, and proportionate number of these cases were missed quality diagnosis and treatment, with simple spirometry technique.
Obstructive lung disease is the predominant lung function impairment in symptomatic post-TB cases. A significant number of asymptomatic post-TB cases are also having obstructive pattern of lung function in spirometry analysis. These cases are less evaluated and less efficiently treated in clinical setting. Prompt evaluation with the use of spirometry is must in all the cases of TB irrespective of symptoms.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Long R, Maycher B, Dhar A, Manfreda J, Hershfield E, Anthonisen N, et al.
Pulmonary tuberculosis treated with directly observed therapy: Serial changes in lung structure and function. Chest 1998;113:933-43.
Rajeswari R, Muniyandi M, Balasubramanian R, Naryanan PR. Perceptions of tuberculosis patients about their physical, menal and social wellbeing: A field report from South India. Soc Sci Med 2005;60:1845-53.
Banu Rekha VV, Ramachandran R, Kuppu Rao KV, Rahman F, Adhilakshmi AR, Kalaiselvi D, et al.
Assessment of long term status of sputum positive pulmonary TB patients successfully treated with short course chemotherapy. Indian J Tuberc 2009;56:132-40.
Lam KB, Jiang CQ, Jordan RE, Miller MR, Zhang WS, Cheng KK, et al.
Prior TB, smoking, and airflow obstruction: A cross-sectional analysis of the Guangzhou Biobank Cohort Study. Chest 2010;137:593-600.
Ross J, Ehlrich R, Hnizdo E. Excess lung function decline in gold miners following pulmonary tuberculosis. Thorax 2010;65:1010-5.
Pasipanodya JG, Miller TL, Vecino M, Munguia G, Garmon R, Bae S, et al.
Pulmonary impairment after tuberculosis. Chest 2007;131:1817-24.
Kim HY, Song KS, Goo JM, Lee JS, Lee KS, Lim TH. Thoracic sequalae and complications of tuberculosis. Radiographics 2001;21:839-58.
Fang X, Ma B, Yang X. Bronchial tuberculosis. Cytologic diagnosis of fiberoptic bronchoscopic brushings. Acta Cytol 1997;41:1463-7.
Zhou C, Nagayama N, Ohtsuka Y, Nagai H, Kawabe Y, Machida K, et al.
Long-term study of patients with sequelae of pulmonary tuberculosis after pneumonectomy – Obstructive impairment and its causes. Nihon Kyobu Shikkan Gakkai Zasshi 1995;33:416-21.
Rech V, Bervig D, Rodrigues LF. Effects of a physical exercise program in the effort tolerance by patients with pulmonary tuberculosis. Fisioter Pesqui 2005;12:35-40.
Gaensler EA, Lindgren I. Chronic bronchitis as an etiologic factor in obstructive emphysema; preliminary report. Am Rev Respir Dis 1959;80:185-93.
Snider GL, Doctor L, Demas TA, Shaw AR. Obstructive airway disease in patients with treated pulmonary tuberculosis. Am Rev Respir Dis 1971;103:625-40.
Willcox PA, Ferguson AD. Chronic obstructive airways disease following treated pulmonary tuberculosis. Respir Med 1989;83:195-8.
Weiner H. Changes in employment status associated with hospitalization for tuberculosis. I. Analysis of 163 consecutively admitted males. Am Rev Respir Dis 1963;87:17-22.
Hnizdo E, Singh T, Churchyard G. Chronic pulmonary function impairment caused by initial and recurrent pulmonary tuberculosis following treatment. Thorax 2000;55:32-8.
Crapo RO, Morris AH, Gardner RM. Reference spirometric values using techniques and equipment that meet ATS recommendations. Am Rev Respir Dis 1981;123:659-64.
Miller MR, Hankinson J, Brusasco V, Burgos F, Casaburi R, Coates A, et al.
Standardisation of spirometry. Eur Respir J 2005;26:319-38.
Evaluation of impairment/disability secondary to respiratory disorders. American Thoracic Society. Am Rev Respir Dis 1986;133:1205-9.
Enright PI, Hyatt RE. Office Spirometry: A Practical Guide to Selection and Use of Spirometers. Philadelphia, PA: Lea & Febiger; 1987.
Agarwala A, Maikap MK, Panchadhyayee P, Mandal P, Roy PP. Chronic airway obstruction in post tubercular fibrosis cases: A serious lung function changes. Int J Res Med Sci 2016;4:5294-6.
Manji M, Shayo G, Mamuya S, Mpembeni R, Jusabani A, Mugusi F, et al.
Lung functions among patients with pulmonary tuberculosis in Dar es Salaam – A cross-sectional study. BMC Pulm Med 2016;16:58.
Plit ML, Anderson R, Van Rensburg CE, Page-Shipp L, Blott JA, Fresen JL, et al.
Influence of antimicrobial chemotherapy on spirometric parameters and pro-inflammatory indices in severe pulmonary tuberculosis. Eur Respir J 1998;12:351-6.
Lee JH, Chang JH. Lung function in patients with chronic airflow obstruction due to tuberculous destroyed lung. Respir Med 2003;97:1237-42.
Verma SK, Narayan KV, Kumar S. A study on prevalence of obstructive airway disease among post pulmonary tuberculosis patients. Pulmonary 2009;11:4-7.
Ramos LM, Sulmonett N, Ferreira CS, Henriques JF, de Miranda SS. Functional profile of patients with tuberculosis sequelae in a university hospital. J Bras Pneumol 2006;32:43-7.
Di Naso FC, Pereira JS, Schuh SJ, Unis G. Functional evaluation in patients with pulmonary tuberculosis sequelae. Rev Port Pneumol 2011;17:216-21.
Singla N, Singla R, Fernandes S, Behera D. Post treatment sequelae of multi-drug resistant tuberculosis patients. Indian J Tuberc 2009;56:206-12.
Chushkin MI, Ots ON. Impaired pulmonary function after treatment for tuberculosis: The end of the disease? J Bras Pneumol 2017;43:38-43.
Guilani A, Bhalotra B, Parakh U, Jain N. Even asymptomatic patients may have serious lung impairment after successful TB treatment. Am J Respir Crit Care Med 2014;189:A3203.
Anno H, Tomashefski JF. Studies on the impairment of respiratory function in pulmonary tuberculosis. Am Rev Tuberc 1955;71:333-48.
Menezes AM, Hallal PC, Perez-Padilla R, Jardim JR, Muiño A, Lopez MV, et al.
Tuberculosis and airflow obstruction: Evidence from the PLATINO study in Latin America. Eur Respir J 2007;30:1180-5.
Brashier B, Gangavane S, Valsa S, Gaikwad SN, Ghorpade SV, Mandrekar S, et al
. Almost Half the Patients Treated for Pulmonary Tuberculosis (TB) Show Evidence of Obstructive Airways Disease (OAD). In: European Respiratory Society Annual Congress, Stockholm, Sweden; 15-19 September, 2007. [Abstr. E2585].
Gothi D, Shah DV, Joshi JM. Clinical profile of diseases causing chronic airflow limitation in a tertiary care centre in India. J Assoc Physicians India 2007;55:551-5.
Baig IM, Saeed W, Khalil KF. Post-tuberculous chronic obstructive pulmonary disease. J Coll Physicians Surg Pak 2010;20:542-4.
Patricio Jiménez P, Vivianne Torres G, Paula Lehmann F, Elisa Hernández C, Mauricio Alvarez M, Mónica Meneses M, et al
. Chronic airways obstruction in patients with tuberculosis sequel: A comparison with COPD. Rev Chil Enf Respir 2006;22:98-104.
Akkara SA, Shah AD, Adalja M, Akkara AG, Rathi A, Shah DN. Pulmonary tuberculosis: The day after. Int J Tuberc Lung Dis 2013;17:810-3.
Allwood BW, Myer L, Bateman ED. A systematic review of the association between pulmonary tuberculosis and the development of chronic airflow obstruction in adults. Respiration 2013;86:76-85.
Chung KP, Chen JY, Lee CH, Wu HD, Wang JY, Lee LN, et al.
Trends and predictors of changes in pulmonary function after treatment for pulmonary tuberculosis. Clinics (Sao Paulo) 2011;66:549-56.
Amaral AF, Coton S, Kato B, Tan WC, Studnicka M, Janson C, et al.
Tuberculosis associates with both airflow obstruction and low lung function: BOLD results. Eur Respir J 2015;46:1104-12.
Byrne AL, Marais BJ, Mitnick CD, Lecca L, Marks GB. Tuberculosis and chronic respiratory disease: A systematic review. Int J Infect Dis 2015;32:138-46.
Ehrlich RI, Adams S, Baatjies R, Jeebhay MF. Chronic airflow obstruction and respiratory symptoms following tuberculosis: A review of South African studies. Int J Tuberc Lung Dis 2011;15:886-91.
Inghammar M, Löfdahl CG, Winqvist N, Ljungberg B, Egesten A, Engström G, et al.
Impaired pulmonary function and the risk of tuberculosis: A population-based cohort study. Eur Respir J 2011;37:1285-7.
Rajasekaran S, Savithri S, Jeyaganesh D. Post-tuberculosis bronchial asthma. Indian J Tuberc 2001;48:139-42.
Krishna K, Bond S, Artvinli M, Reid KD, McHardy GJ, Crofton JW. Pulmonary function in treated tuberculosis; a long term follow-up. Am Rev Respir Dis 1977;115:402-4.
Salvi SS, Barness PJ. Chronic obstructive pulmonary disease in non-smokers. Lancet 2009;374:733-43.
Hassan IS, Al-Jandali HH. Obstructive airway disease in patients with significant post TB lung scarring. Saudi Med J 2005;26:1155-7.
Buffels J, Degryse J, Heyrman J, Decramer M; DIDASCO Study. Office spirometry significantly improves early detection of COPD in general practice: The DIDASCO study. Chest 2004;125:1394-9.
Lee TA, Bartle B, Weiss KB. Spirometry use in clinical practice following diagnosis of COPD. Chest 2006;129:1509-15.
Caballero A, Torres-Duque CA, Jaramillo C, Bolívar F, Sanabria F, Osorio P, et al.
Prevalence of COPD in five Colombian cities situated at low, medium, and high altitude (PREPOCOL study). Chest 2008;133:343-9.
Nelson SB, LaVange LM, Nie Y, Walsh JW, Enright PL, Martinez FJ, et al.
Questionnaires and pocket spirometers provide an alternative approach for COPD screening in the general population. Chest 2012;142:358-66.
Blumberg HM, Burman WJ, Chaisson RE, Daley CL, Etkind SC, Friedman LN, et al.
American Thoracic Society/Centers for Disease Control and Prevention/Infectious Diseases Society of America: Treatment of tuberculosis. Am J Respir Crit Care Med 2003;167:603-62.
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3], [Table 4]