Objective: The objective of this study is to determine the predominant spirometric pattern in patients with chronic airflow obstruction (CAO) due to pulmonary tuberculosis (PTB) sequelae (CAO-PTB) in family health center of La Florida, Talca.
Methods: Descriptive study of 17 patients (5 men, 12 women), with a mean age±SD of 72•8±8•4 years, with a CAO-PTB diagnostic, who underwent a basal and post bronchodilator spirometry. The measured variables were: basal and post bronchodilator FEV1/FVC, FEV1, FVC, FEF 25-75%, and change in FEV1 and FVC, measured in percentage and ml. The statistical analysis was made using the software SPSS, version 23.
Results: Of the 17 evaluated patients, 13 showed an obstructive spirometric pattern (76•5%), 3 a normal spirometric pattern (17•6%) and 1 a restrictive spirometric pattern (5•9%). Of the 13 patients with obstructive spirometric pattern, 7 presented a normal FVC (53•9%), and 6 a diminished FVC (46•1%). Regarding the changes post bronchodilator, 6 patients showed significant changes (35•3%), which were all obstructive, and 11 patients had no significant changes (64•7%), being 7 obstructive, 3 normal, and 1 restrictive.
Conclusion: The predominant spirometric pattern of the evaluated patients with CAO-PTB, in the family health center La Florida, Talca, was the obstructive with normal FVC, and no significant changes post bronchodilator were found.
Keywords: chronic airflow obstruction, pulmonary tuberculosis, spirometric pattern
The chronic airway obstruction (CAO) constitutes a group of obstructive diseases that have in common the narrowing of the airways, with a consequent airflow resistance and respiratory work increase. These diseases are: COPD, Irreversible Asthma, Bronchiectasis, Pneumoconiosis, Cystic Fibrosis, Obliterating Bronchiolitis, and the Pulmonary Tuberculosis (PTB) sequelae.1
Pulmonary Tuberculosis is characterized by the formation of granulomas and spots of caseous necrosis, which produce destructive effects in the Pulmonary parenchyma, affecting the apical lobes and generating sequelae after the bactereological cure of the disease.2 It has been described that nearly 70% of the ill people that cure and get pulmonary tuberculosis sequelae may develop, with the years, a CAO which may lead to a respiratory insufficiency and cor pulmonale.3,4 The ventilatory limitation that these patients develop has a restrictive component given the fibrous lesions and scars of the pulmonary parenchyma where the wound occurred, and an obstructive component due to the compensatory hyperinflation of the remaining healthy lung.5 In theory, this would correspond to an obstructive spirometric pattern with diminished FVC. This pattern is supported by the few studies about this topic, in which the authors agree that the predominant spirometric pattern in these patients would effectively be the obstructive one, and consider it similar to the COPD.6 This is why the objective of this research is to determine the predominant spirometric patter in the patients with chronic airflow obstruction (CAO) due to pulmonary tuberculosis (PTB) sequelae (CAO-PTB) in our family health center, and compare the results with the precedent studies, or to determine a different spirometric pattern to the one prescribed by the existent literature, so as to contribute to the general knowledge of this little studied group of patients.
The protocol of the study was approved by the health service scientific ethics committee of the Maule Region, and every involved subject signed a consent letter. Descriptive study of 17 patients (5 men, 12 women), with a mean age±SD of 72•8±8•4 years with a CAO-PTB diagnostic. Inclusion criteria were: patients over 50 years old with a medical diagnostic of CAO-PTB. Exclusion criteria were: patients with additional chronic respiratory diseases such as: COPD, Asthma, Interstitial lung diseases (ILD), including connective tissue diseases (CTD) compromising the lung and CAO produced by a cause different from tuberculosis. In addition, patients that presented contraindications regarding spirometry were excluded, such the ones suffering from: unstable cardiovascular status, recent myocardial infarction (within 1 month) or pulmonary embolism, uncontrolled hypertension or history of recent haemorrhagic cerebrovascular event, endocranean hypertension syndrome, recent pneumothorax (within 1 month), thoracic, abdominal or cerebral aneurysms, recent thoracic, abdominal or eye surgery, haemoptysis of unknown origin, thoracic pain of unknown origin and unlikely to be able to comply with instructions.7–9
All 17 selected patients were assessed in basal and post bronchodilator spirometry, following the standardized criteria of the European Respiratory Society (ERS).10,11 The spirometer used was the Vitalograph Model 6800, previously calibrated with a 3 litter calibrated syringe. Each patient got, at least, 3 acceptable and repeatable curves of forced expiration and the best values of FVC and FEV1 were selected.12,13 The dose and the bronchodilator used for the post test was 400µg of salbutamol through a valved spacer device. The measured variables were: basal and post bronchodilator FEV1/FVC, FEV1, FVC, FEF 25-75%, and change of FEV1 and FVC measured in percentage and ml. The statistical analysis was made using the SPSS software, version 23.
The characteristics of the selected patients, regarding their sex, age, time passed since the tuberculosis episode, body mass index (BMI), and the results of the basal and post bronchodilator pulmonary function, are summarized in Table 1 of the 17 evaluated patients, 13 showed an obstructive spirometric pattern (76•5%), 3 a normal spirometric pattern (17•6%) and 1 a restrictive spirometric pattern (5•9%). Of the 13 patients with obstructive spirometric pattern, 7 had normal FVC (53•9%), and 6 diminished FVC (46•1%) (Table 2). Regarding the changes post bronchodilator, 6 patients had significant changes (35•3%), which were all obstructive, and 11 patients had no significant changes (64•7%), being 7 obstructive, 3 normal, and 1 restrictive. A change was considered significant when the difference between the basal and post bronchodilator in FEV1 or FVC was higher than 12% and 200 ml. The difference post bronchodilator in FEV1 and FVC, in percentage and ml, can be seen in Table 3.
Basal values |
Post bronchodilator values |
|||||||||
---|---|---|---|---|---|---|---|---|---|---|
N |
Sex |
Age |
Years TB |
BMI |
FEV1* |
FVC * |
FEV1/FVC* |
FEV1 * |
FVC* |
FEV1/FVC* |
1 |
F |
61 |
42 |
26.2 |
93 |
104 |
73.9 |
96 |
100 |
78.7 |
2 |
F |
83 |
62 |
25.8 |
50 |
54 |
62.1 |
56 |
71 |
53 |
3 |
F |
69 |
47 |
32 |
53 |
63 |
67.6 |
58 |
61 |
75.9 |
4 |
F |
79 |
53 |
26.2 |
62 |
81 |
57.4 |
72 |
88 |
61 |
5 |
F |
63 |
15 |
25.3 |
56 |
81 |
56.9 |
60 |
85 |
58 |
6 |
M |
78 |
53 |
20.7 |
49 |
50 |
752 |
52 |
61 |
65.2 |
7 |
M |
82 |
68 |
22 |
123 |
155 |
60.3 |
130 |
157 |
63.4 |
8 |
F |
85 |
61 |
25.7 |
54 |
73 |
53.6 |
54 |
72 |
54.7 |
9 |
F |
68 |
46 |
26.7 |
42 |
62 |
54.8 |
50 |
75 |
54 |
10 |
F |
71 |
55 |
30.2 |
46 |
59 |
64.5 |
49 |
64 |
63.6 |
11 |
M |
83 |
50 |
22.9 |
76 |
114 |
51.2 |
79 |
109 |
55.8 |
12 |
M |
76 |
16 |
26.3 |
45 |
65 |
54.4 |
53 |
69 |
60 |
13 |
F |
70 |
34 |
16 |
39 |
54 |
60 |
50 |
65 |
64.1 |
14 |
M |
76 |
59 |
25.9 |
68 |
89 |
59.3 |
75 |
98 |
59.2 |
15 |
F |
68 |
30 |
32 |
103 |
96 |
87.2 |
114 |
101 |
90.9 |
16 |
F |
71 |
34 |
32.5 |
75 |
76 |
80 |
78 |
78 |
81.9 |
17 |
F |
55 |
18 |
32.1 |
61 |
79 |
63.5 |
88 |
88 |
61.3 |
Table 1 Results basal and post bronchodilator of the spirometric volumes
Years TB, years passed since the tuberculosis episode; BM I, body mass index; FEV1, forced expiratory volume in one second; FVC, forced vital capacity; FEV1/FVC, forced expiratory volume in one second/forced vital capacity ratio; *percentage of the predicted value
Spirometric pattern |
N =17 |
Obstructive with normal FVC |
7 |
Obstructive with low FVC |
6 |
Normal |
3 |
Restrictive |
1 |
Table 2 Results spirometric pattern
FVC, forced vital capacity
N |
Sex |
Age |
FEV1 chg (%) |
FEV1 chg (ml) |
FVC chg (%) |
FVC chg (ml) |
1 |
F |
61 |
3 |
50 |
-4 |
-90 |
2 |
F |
83 |
11 |
100 |
31 |
430 |
3 |
F |
69 |
10 |
100 |
-2 |
-30 |
4 |
F |
79 |
16 |
210 |
9 |
170 |
5 |
F |
63 |
7 |
80 |
5 |
100 |
6 |
M |
78 |
5 |
40 |
10 |
190 |
7 |
M |
82 |
6 |
150 |
1 |
30 |
8 |
F |
85 |
0 |
0 |
-2 |
-30 |
9 |
F |
68 |
19 |
150 |
21 |
300 |
10 |
F |
71 |
8 |
70 |
9 |
130 |
11 |
M |
83 |
4 |
70 |
-4 |
140 |
12 |
M |
76 |
18 |
210 |
7 |
150 |
13 |
F |
70 |
28 |
220 |
20 |
260 |
14 |
M |
76 |
10 |
170 |
10 |
290 |
15 |
F |
68 |
11 |
200 |
6 |
130 |
16 |
F |
71 |
4 |
60 |
2 |
30 |
17 |
F |
55 |
8 |
110 |
12 |
26 |
Table 3 Post bronchodilator changes of the FEV1 and FVC
FEV1 chg (%), change of the forced expiratory volume in one second in percentage; FEV1 chg (ml), change of the forced expiratory volume in one second in milliliters; FVC chg (%), change of the forced vital capacity in percentage; FVC chg (ml), change of the forced vital capacity in milliliters
Our results were compared to 3 of the few existent research in this topic, in which said results match with the previously published information. Lee et al.,14 South Korea, recruited 21 patients with CAO-PTB and compared them with patients COPD. All the patients had an obstructive spirometric pattern and diminished FVC.14 Jiménez et al.,6 Chile, recruited 25 patients with CAO-PTB, all of them with an obstructive spirometric pattern, specifically 20 with diminished FVC and 5 with normal FVC.6 Finally, Llanos-Tejada et al, in 2010, Peru, chose 104 patients with our diagnostic of interest. 83 were obstructive, 17 normal, and 14 restrictive. From the obstructive group, 59 out of 83 did not revert significantly post bronchodilator, and 24 did. The authors did not mention if the FVC is normal or diminished.15
Therefore, we concluded, as the majority of the studies on this topic did, that the predominant spirometric pattern in the patients with pulmonary tuberculosis sequelae (CAO-PTB patients) is the obstructive pattern with no significant changes post bronchodilator, and the tendency proposes that the obstruction is accompanied with a FVC diminish, although in our study only 6 patients had diminished FVC and 7 normal FVC, but we recognize that our sample was certainly small when compared with the ones of the aforementioned authors. Furthermore, this obstruction would not change significantly post bronchodilator, making it similar to the COPD.16,17 Notwithstanding, there is an important group of patients that did revert significantly post bronchodilator: 6 patients in our study, and an unspecified and undetermined number of patients in the cited studies. Nonetheless, evaluating the reversibility of the pulmonary function of these patients was not included in our study objectives. Considering the findings, we leave the door open for future research about why some patients with pulmonary tuberculosis sequelae would revert post bronchodilator. Maybe they had a bronchial asthma besides the CAO-PTB diagnostic. In fact, Ancic, in 1985, in Chile, assessed the bronchial hyperactivity in 19 patients with pulmonary tuberculosis sequelae through the bronchial incitement using histamine, where 9 resulted positive.18
In synthesis, we recognize the limits of our study, such as the small sample, and the minor quantity of studies made globally to compare ours with. Since pulmonary tuberculosis is not a considerable health problem in developed countries due to its low prevalence, these countries do not research it. Even so, we can conclude that, in theory, this group of patients has a restrictive component due to the fibrous apical lesion of the pathogen agent (Mycobacterium Tuberculosis), and an obstructive component given by the hyperinflation of the remaining healthy pulmonary parenchyma, and it is similar to the behavior in patients with COPD (6). This follows what Radovic et al.19 noted in 2016, in Serbia (Republic of Serbia), where it is mentioned that during the treatment phase of an active pulmonary tuberculosis, the pulmonary function is usually restrictive, which may become obstructive with the years, transforming in what we now know as CAO-PTB, or as a late manifestation of underlying COPD.19 We think that the restrictive component explains the decrease in the FCV, and the obstructive component the decrease in FEV1/FVC and FEV1. Nevertheless, we also know that we found some obstructive patients with normal FVC, which could be explained assuming the initial restrictive lesion produced by the tuberculosis was completely compensated with the hyperinflation of the remaining healthy pulmonary parenchyma, thus not being reflected in the spirometry years later, compensating in this way the loss of pulmonary volume.20 In any case, in order to clarify this disjunctive, including a Plethysmography in future studies would be convenient, in order to evaluate in an enhanced fashion the pulmonary volumes and objectify the degree of obstruction and restriction in these patients. Including de radiographic analysis of each subject would also be beneficial, for establishing a relation respecting the zone and extension of the pulmonary damage. We insist in suggesting future research on this topic, to even create a more specific guide to treat these patients, for there is no formal literature on the topic nowadays, and many of these patients are treated as COPD or asthmatics.
We deem important and convenient to treat the obstruction of these patients, which can be done through bronchodilators and pulmonary rehabilitation. We also can conclude that the degree of the ventilatory limitation has no relation with age nor amount of years passed after the PTB episode (6). This, because we found different degrees of spirometric limitation in either group of subjects: the ones who had the PTB many years ago and the ones who had it recently.
Finally, the importance of this research resides in the bibliographic contribution referring to the pulmonary function of patients with CAO-PTB, where we concluded and coincided with other researches, in that the predominant spirometric pattern of these patients would be the obstructive with no significant changes post bronchodilator, with some degree of controversy in the decrease or normality of the FVC, but similar to the pulmonary function in patients with COPD.
All authors were involved in the design of this study and the interpretation of study results, contributed to the manuscript from the outset, and read and approved the final draft. All authors vouch for the accuracy of the content included in the final manuscript.
None.
None.
The authors declare no conflict of interest.
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