Abstract
Both tuberculosis and COVID-19 being communicable and prevalent diseases in India, the co-existence can lead to worse outcomes, as seen in this study, where there was high mortality among active as well as treated TB patients with COVID-19 co-infection https://bit.ly/3jHcGbQ
To the Editor:
We read with interest the two articles by Tadolini et al. [1] and Stochino et al. [2], which described recent cohorts of either current or former tuberculosis (TB) patients with coronavirus disease 2019 (COVID-19) and studied their clinical course. India has the majority of global burden of TB, along with highest rising number of daily COVID-19 cases in the world [3, 4]. The information about COVID-19 and active/former TB co-infection reported so far is sparse, but it can be assumed that person with TB, when co-infected with COVID-19, may be at more risk of poor outcomes [1, 5]. The present study describes the first-ever cohort of current or treated TB patients co-infected with COVID-19 from a high TB burden country, recruited by a tertiary care hospital in India.
This was a retrospective observational study from 1 February 2020 to 14 June 2020, during which a total of 1073 consecutive COVID-19 patients were admitted. Out of these, 22 cases with a diagnosis of active/treated TB and COVID-19 co-infection were included in the study.
Among 22 patients with COVID-19 and TB co-infection, 13 (59.1%) patients had active TB (median age (interquartile range (IQR)) 36 (27–59.5) years) and nine (40.9%) patients had been treated for TB (median age (IQR) 44 (28–51) years) in the past. Among the active TB group, 11 (84.6%) were females and among the treated TB group, all patients were females. Out of the 13 active TB patients, 12 patients were already receiving anti-TB treatment (ATT) (median duration (IQR) 2 (1–3) months) at the time of admission, while one patient was newly diagnosed with pulmonary TB within a week of admission. The demographic, clinical, radiological and laboratory investigation details, and outcomes of each of the 22 patients, are described in table 1.
All patients, except one, were symptomatic at the time of presentation. All 12 patients with active TB, who were already receiving ATT at the time of admission, had become almost asymptomatic for TB symptoms. Among them, signs and symptoms attributed to COVID-19 included fever (100%), dry cough (53.8%) and dyspnoea (30.8%) (median (range) duration 2 (2–30) days). Nine treated TB patients were also almost asymptomatic for TB prior to the development of current COVID-19 infection. Among them fever (88.9%), dry cough (44.4%) and dyspnoea (33.3%), respectively were present (median (range) duration of 5 (2–30) days), which could be attributed to COVID-19 disease. Radiological examination, conducted at admission, revealed pulmonary parenchymal fibrosis in all patients in the treated TB group with three (33.3%) patients having accompanying residual cavitation as well. Among the 13 active TB patients, nine (69.2%) had pulmonary TB and four (30.8%) had extra-pulmonary TB. Among the nine active pulmonary TB patients, cavitation was present in three (33.3%), and six (66.7%) had parenchymal infiltrates/consolidation on chest radiography but no cavitation. Among four active extra-pulmonary TB patients, one had cerebral tuberculoma, two had pleural effusion, and one patient had only cervical lymphadenopathy. One active pulmonary TB patient had multidrug-resistant (MDR) TB (isoniazid and rifampicin resistant), receiving conventional MDR treatment regimen as per national guidelines. All treated TB cases had had pulmonary TB.
Lymphopenia was found in only one patient. In all, seven patients (31.8%) required critical care, 4/13 (30.7%) in the active TB group and 3/9 (33.3%) in the treated TB group. All but one patient who required critical care also required invasive mechanical ventilation. Among these, 3/13 (23.1%) patients were from the active TB group and 3/9 (33.3) patients were from the treated TB group. All these six patients died; this group also included one MDR-TB patient.
All six patients who died had hypoxaemia and a Glasgow Coma Scale (GCS) score of 3–4 on admission. Quick sepsis-related organ failure scores were 3 in four patients, and 2 and 1 in one patient each. Death in all deceased patients was attributed to COVID-19 co-infection, as all were otherwise responding clinically and radiologically to ATT in the active TB group or were clinically stable in the treated TB group. Comorbid diabetes mellitus was observed in 3/22 (13.6%) patients and two (66.7%) among them died. None of the patients had HIV. Of the 22 patients, 16 patients (72.7%) were discharged. During the study period, 14 days of admission was mandatory for COVID-19 patients as per national guidelines [6]. Among those discharged, the mean±sd duration of stay was 13.3±5.3 days.
In the present series, among 22 patients with TB and COVID-19 co-infection, the overall mortality rate was 27.3%. This mortality rate, though preliminary, is higher as compared to other studies by Tadolini et al. [1] (12.3%) and Motta et al. [7] (11.6%) in TB and COVID-19 co-infected patients. A review by Ong et al. [8] also found a higher mortality in TB with COVID-19. In India, a mortality rate of around 2.3% has been observed among COVID-19 patients, including patients with comorbid conditions such as diabetes, hypertension, malignancy and tuberculosis, etc. [4]. This higher mortality in TB and COVID-19 co-infection could be explained by damage to the lungs by fibrosis or cavitation in treated TB cases, or by active TB disease with superimposed insult of COVID-19 co-infection leading to further deterioration of already compromised lung function.
In the initial cohort of 40 COVID-19 patients who had been admitted to the authors' centre up to 31 March 2020, no patient had active or previously treated TB; however, over the subsequent 6 weeks, the incidence of active and treated TB went up to 1.21 and 0.83 per 100 hospital admissions for COVID-19, respectively [9].
The limitations of the study were that the role of pathological and biochemical factors, such as D-dimer, C reactive protein, IL-6 and ferritin, etc., and use of investigational drugs, such as tocilizumab, remdesivir, favipiravir and steroids, for patient management were not studied, as neither of these were a component of national treatment guidelines during the study period [6]. Also, because of the small sample size, analysis of various risk factors was not carried out.
In conclusion, patients with treated or active TB may be considered another vulnerable group for COVID-19 and may require special attention and appropriate preventive measures for development of COVID-19. Further, a high mortality, along with a greater need for critical care, was found in active as well as treated TB patients co-infected with COVID-19.
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Footnotes
Author contributions: All the 14 authors made substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work; or drafting the work or revising it critically for important intellectual content; and towards final approval of the version to be published; and agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
Declaration of patient consent: the authors certify that they have obtained written informed consent from the patients to publish their personal details and follow up. The patients understand that their name and initials will not be published but, anonymity cannot be guaranteed. Ethics committee approval was not required as it was a retrospective observational study.
Conflict of interest: N. Gupta has nothing to disclose.
Conflict of interest: P.Ish has nothing to disclose.
Conflict of interest: A. Gupta has nothing to disclose.
Conflict of interest: N. Malhotra has nothing to disclose.
Conflict of interest: J.A. Caminero has nothing to disclose.
Conflict of interest: R. Singla has nothing to disclose.
Conflict of interest: R. Kumar has nothing to disclose.
Conflict of interest: S.R. Yadav has nothing to disclose.
Conflict of interest: N. Dev has nothing to disclose.
Conflict of interest: S. Agrawal has nothing to disclose.
Conflict of interest: S. Kohli has nothing to disclose.
Conflict of interest: M.K. Sen has nothing to disclose.
Conflict of interest: S. Chakrabarti has nothing to disclose.
Conflict of interest: N.K. Gupta has nothing to disclose.
- Received September 6, 2020.
- Accepted October 13, 2020.
- Copyright ©ERS 2020
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