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EDITORIAL
Year : 2016  |  Volume : 33  |  Issue : 3  |  Page : 251-252  

Tuberculosis therapy in Mumbai: Critical importance of drug-susceptibility testing


McGill International TB Centre, McGill University, Montreal, Canada

Date of Web Publication21-Apr-2016

Correspondence Address:
Madhukar Pai
McGill International TB Centre, McGill University, Montreal
Canada
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0970-2113.180799

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How to cite this article:
Daftary A, Pai M. Tuberculosis therapy in Mumbai: Critical importance of drug-susceptibility testing. Lung India 2016;33:251-2

How to cite this URL:
Daftary A, Pai M. Tuberculosis therapy in Mumbai: Critical importance of drug-susceptibility testing. Lung India [serial online] 2016 [cited 2017 Jun 22];33:251-2. Available from: http://www.lungindia.com/text.asp?2016/33/3/251/180799

India is the ground zero for global tuberculosis (TB) epidemic, and Mumbai is the ground zero for India's epidemic of multidrug-resistant TB (MDR-TB) and extensively drug-resistant TB (XDR-TB). In this issue of Lung India, Udwadia et al. [1] present data that highlight major concerns with the use of standardized, empiric treatment regimens for MDR-TB in Mumbai. The alarming rates of MDR-TB, heterogeneous drug-resistance patterns and disproportionate number of cases that are found to be pre-XDR and XDR, mandate the early and comprehensive drug-susceptibility testing (DST) of all TB patients, to allow for individualized, DST-guided drug regimens.

The rationale to impose a standardized drug regimen for MDR-TB and harmonize medical practice is not unfounded. As in many other high-burden settings, upfront, universal DST is uncommon in India and hinders opportunities to devise optimal regimens for patients with MDR-TB. [2] Nearly half of all Indian TB patients are treated in the private sector [3] where the quality of care is highly variable, [4] and use of irrational drug regimens [5] urges stricter antibiotic stewardship, and makes a case for standardized protocols. However, there is an undeniable risk of amplifying drug resistance by promoting one regimen for all, without taking the local epidemiology into account.

In the cohort of 1539 MDR-TB cases identified by the TB laboratory at Hinduja Hospital in Mumbai (which included samples from both public and private patients), only 30% were truly MDR-TB; remaining cases represented pre-XDR, XDR, and resistance beyond XDR-TB. In other words, nearly two-thirds of this sample would have received a suboptimal drug regimen and have been at risk for developing secondary resistance, had they been empirically treated under the recommended standardized regimen for MDR-TB. [1] This is not unlike resistance profiles of cases reported by Dalal et al. and Dholakia and Shah, who have similarly suggested the need for individualized, DST-guided drug regimens in Mumbai. [6],[7] Other experts have argued that all TB patients in India deserve up-front DST, [8] and there are large-scale, programmatic data to support this. [9]

The importance of factoring in the local epidemiology of TB into empiric treatment regimens thus cannot be overemphasized. In India, a standardized empiric regimen for MDR-TB may perpetuate delays in DST and inadvertently feed into provider complacency in managing difficult cases. While patients' previous treatment histories have guided empiric drug regimens in other settings, this option would be futile in Mumbai, where primary drug resistance is common, and previously treated patients lack a complete medical history due to their high rate of switching between providers. [3],[10] The alternative recommendation suggested by Udwadia and colleagues [1] to use a tailored empiric drug regimen at their site based on data from their laboratory (and given their existing capacity to perform timely, comprehensive DST) is in line with the World Health Organization's most recent treatment guideline which emphasizes, "TB programs may need to adjust the (drug-resistant TB treatment) strategy to meet special circumstances and the local context." [11]

The argument against a one-size-fits-all approach to MDR-TB management is also congruent with recent trends to shift away from rigid, inflexible TB management in general toward more individualized, patient-centered approaches to care. [12],[13] Patient retention is a major challenge to MDR-TB treatment completion and cure, and the administration of suboptimal drug regimens may be considered an important determinant of nonadherence and loss to follow-up. [14],[15] A patient-centered approach to MDR-TB management begins with early diagnosis and DST, but equally incorporates stable access to the second-line drugs, treatment literacy, individualized education and counseling, and efforts to meet the medical, economic, and social needs of patients throughout their treatment course. [16] Alongside the push to tailor treatment regimens via DST, we cannot ignore the commensurate opportunity to refine current mechanisms of ensuring adherence and move beyond directly observed therapy-centered models of patient support.

The imposition of a standardized empiric drug regimen for MDR-TB, while feasible in lower burden settings with a more homogenous epidemic, may compound the existing challenges to MDR-TB management in settings with diverse patterns of TB drug resistance. It is time we shed universal dogmas when confronting strains of TB that are unpredictable, inconsistent, and increasingly untreatable. Given the profile of MDR-TB cases in Mumbai, DST-guided, individualized therapy is the safest option for patients and better aligned with the new End TB Strategy that calls for all countries to offer universal DST to all TB patients, at the time of diagnosis. [17] To meet the End TB Strategy goals, however, India must invest more in TB care and control, increase the budget of the Revised National TB Control Program, roll-out improved molecular diagnostics and daily drug regimens and scale-up successful models of private sector engagement. [18]

 
   References Top

1.
Udwadia ZF, Mullerpattan JB, Shah KD, Rodrigues CS. Possible impact of the standardized category IV reigmen on multidrug-resistant tuberculosis patients in Mumbai. Lung India 2016;33:253-6.  Back to cited text no. 1
  Medknow Journal  
2.
Brigden G, Nyang′wa BT, du Cros P, Varaine F, Hughes J, Rich M, et al. Principles for designing future regimens for multidrug-resistant tuberculosis. Bull World Health Organ 2014;92:68-74.  Back to cited text no. 2
    
3.
Kapoor SK, Raman AV, Sachdeva KS, Satyanarayana S. How did the TB patients reach DOTS services in Delhi? A study of patient treatment seeking behavior. PLoS One 2012;7:e42458.  Back to cited text no. 3
    
4.
Satyanarayana S, Subbaraman R, Shete P, Gore G, Das J, Cattamanchi A, et al. Quality of tuberculosis care in India: A systematic review. Int J Tuberc Lung Dis 2015;19:751-63.  Back to cited text no. 4
    
5.
Udwadia ZF, Pinto LM, Uplekar MW. Tuberculosis management by private practitioners in Mumbai, India: Has anything changed in two decades? PLoS One 2010;5:e12023.  Back to cited text no. 5
    
6.
Dalal A, Pawaskar A, Das M, Desai R, Prabhudesai P, Chhajed P, et al. Resistance patterns among multidrug-resistant tuberculosis patients in greater metropolitan Mumbai: Trends over time. PLoS One 2015;10:e0116798.  Back to cited text no. 6
    
7.
Dholakia YN, Shah DP. Clinical profile and treatment outcomes of drug-resistant tuberculosis before directly observed treatment strategy plus: Lessons for the program. Lung India 2013;30:316-20.  Back to cited text no. 7
[PUBMED]  Medknow Journal  
8.
Jain Y. India should screen all tuberculosis patients for drug resistant disease at diagnosis. BMJ 2015;350:h1235.  Back to cited text no. 8
    
9.
Sachdeva KS, Raizada N, Sreenivas A, Van′t Hoog AH, van den Hof S, Dewan PK, et al. Use of Xpert MTB/RIF in decentralized public health settings and its effect on pulmonary TB and DR-TB case finding in India. PLoS One 2015;10:e0126065.  Back to cited text no. 9
    
10.
Isaakidis P, Das M, Kumar AM, Peskett C, Khetarpal M, Bamne A, et al. Alarming levels of drug-resistant tuberculosis in HIV-infected patients in metropolitan Mumbai, India. PLoS One 2014;9:E110461.  Back to cited text no. 10
    
11.
World Health Organization. Companion Handbook to the WHO Guidelines for the Programmatic Management of Drug-Resistant Tuberculosis. Geneva: World Health Organization; 2014.  Back to cited text no. 11
    
12.
Udwadia ZF, Pinto LM. Review series: The politics of TB: The politics, economics and impact of directly observed treatment (DOT) in India. Chron Respir Dis 2007;4:101-6.  Back to cited text no. 12
    
13.
Metcalfe JZ, O′Donnell MR, Bangsberg DR. Moving beyond directly observed therapy for tuberculosis. PLoS Med 2015;12:E1001877.  Back to cited text no. 13
    
14.
Naidoo P, van Niekerk M, du Toit E, Beyers N, Leon N. Pathways to multidrug-resistant tuberculosis diagnosis and treatment initiation: A qualitative comparison of patients′ experiences in the era of rapid molecular diagnostic tests. BMC Health Serv Res 2015;15:488.  Back to cited text no. 14
    
15.
Shringarpure KS, Isaakidis P, Sagili KD, Baxi RK, Das M, Daftary A, et al. When treatment is more challenging than the disease: A qualitative study of MDR-TB patient retention. PLoS One 2016;11:e0150849.  Back to cited text no. 15
    
16.
O′Donnell MR, Daftary A, Frick M, Hirsch-Moverman Y, Amico KR, Senthilingam M, et al. Re-inventing adherence: Toward a patient-centered model of care for drug-resistant tuberculosis and HIV. Int J Tuberc Lung Dis 2016;20:430-4.  Back to cited text no. 16
    
17.
World Health Organization. The End TB Strategy. Geneva: World Health Organization; 2015.  Back to cited text no. 17
    
18.
Pai M, Daftary A, Satyanarayana S. TB control: Challenges and opportunities for India. Trans R Soc Trop Med Hyg 2016;110:158-60.  Back to cited text no. 18
    




 

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