Effectiveness of DOTS regime in terms of cure, failure, default and relapse in the treatment of TB patients

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International Journal of Advances in Medicine Jahnavi K et al. Int J Adv Med. 2018 Feb;5(1):170-174 http://www.ijmedicine.com pissn 2349-3925 eissn 2349-3933 Original Research Article DOI: http://dx.doi.org/10.18203/2349-3933.ijam20180079 Effectiveness of DOTS regime in terms of cure, failure, default and relapse in the treatment of TB patients Jahnavi K. 1, T. Sreenivasulu 2 * 1 Department of General Medicine, Malla Reddy Institute of Medical Sciences, Suraram, Hyderabad, Telangana, India 2 Department of General Medicine, Dr. Patnam Mahender Reddy Institute of Medical Sciences, Chevellam, Ranga Reddy Dist., Telangana, India Received: 01 December 2017 Accepted: 29 December 2017 *Correspondence: Dr. T. Sreenivasulu, E-mail: srinivasulujoins@gmail.com Copyright: the author(s), publisher and licensee Medip Academy. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. ABSTRACT Background: DOTS has given very good results in terms of cure and satisfaction among tuberculosis patients. But still some failure and relapse cases occur. Hence studies on effectiveness of DOTS are required. The objectives of research were to study the effectiveness of DOTS regime in terms of cure, failure, default and relapse in the treatment of TB patients Methods: A hospital based prospective follow up observational study was undertaken in the department of general medicine at a tertiary care medical college and hospital. The present study was conducted among the 60 eligible subjects as per the inclusion and exclusion criteria laid down for the present study. Results: 41 were pulmonary cases and 19 were extra pulmonary patients. intensive only 7 cases were sputum positive out of 37 which reduced to three at the end of extended intensive of treatment which further reduced to two at the end of two months of continuation. But by the end of completion of continuation, one case again became sputum positive i.e. failure case making a final tally to three. It was seen that there was significant weight gain over the period of time in both pulmonary and extra pulmonary cases. The cure rate was 78%. One patient died. Two defaulted and three were failure cases. Conclusions: The DOTS was found to be 78% effective in terms of cure rate. Still there is a huge gap of 22% found in the present scenario which needs to be addressed seriously and by all to prevent multi drug resistant tuberculosis. Keywords: Continuation, Effectiveness, Intensive INTRODUCTION RNTCP is successful in achieving its goals. That cure rate of 85% and case finding rate of 70%. But this is not enough. As more and more multi drug resistant tuberculosis cases are found and registered. There is no policy under RNTCP to follow the cases once it is declared cured as per RNTCP treatment guidelines. There are many reasons including compliance issues which lead to treatment failure and relapse of the cases of tuberculosis. There is a need to find out these reasons to prevent further disease transmission, for success of the program and control of the disease. 1 DOTS have given very good results in terms of cure and satisfaction among tuberculosis patients. But still some failure and relapse cases occur. Some patients land into multi drug resistance. Hence effectiveness of DOTS as 100% cure is doubtful. But ethical issues come while planning the randomized controlled trials for DOTS effectiveness studies. Patients in the control group are also tuberculosis patients and they cannot be denied the International Journal of Advances in Medicine January-February 2018 Vol 5 Issue 1 Page 170

right therapy as they are also exposed to the risk of developing the multi drug resistant tuberculosis and or complications associated with tuberculosis. So, it is important to adopt some other approach to study the effectiveness of DOTS therapy for the success of treatment of tuberculosis. Systematic review is one such way. 2 India carries the highest number of cases of tuberculosis compared to any country in the world. It shares almost 20% of the cases globally. The morbidity and mortality related to tuberculosis in India is also very high. 3 Inspite of achieving the good success rates under DOTS, incidence of tuberculosis continues on an increasing trend. It is not coming down. World Health Organization reported that the success rate of DOTS globally was 84% as per its 2004 report. But due to unexplored reasons or reasons unknown, tuberculosis continues to be the global public health problem. With arrival of HIV it has really been very difficult to control the tuberculosis. 4 As per DOTS program, two success outcomes are used. They are treatment completed and the second one is cured. If the sputum of the patient is negative for the tubercle bacilli at the end of the intensive of the treatment and also if the sputum of the patient is negative for the tubercle bacilli at the end of the six months or at the end of the treatment completed, then that patient is declared as cured. The bacilli are of two types. One is slow growers and one are of fast growers. Slow growing tubercle bacilli are the important reason for multi drug resistant tuberculosis. DOTS ensure to take care of these both the types of tubercle bacilli but in some cases, it may fail. 5 With this background present study was carried out to study the effectiveness of DOTS regime in terms of cure, failure, default and relapse in the treatment of TB patients. METHODS A hospital based prospective follow up observational study was undertaken in the department of general medicine at a tertiary care medical college and hospital. The present study was conducted among the 60 eligible subjects as per the inclusion and exclusion criteria laid down for the present study. The present study was conducted for a period of two years. Informed consent was obtained from every participating individual after explaining them the nature of the study. Almost all consented for the present study to participate as there was no intervention. It was only observation of the regular DOTS and the outcome. Inclusion criteria All registered cases of DOTS during the study period, All those who are ready to participate in the present study. Exclusion criteria All those who are not ready to participate in the present study, All those who are found to be seriously ill or having complications of tuberculosis. Once the patient came to the DOTS centre and was found to be having tuberculosis, either pulmonary tuberculosis or having extra pulmonary tuberculosis was asked for his consent to participate in the present study. Once the patient consented to participate in the present study, detailed history was taken in the proforma which was designed before the start of the study. Patient was classified as sputum positive or sputum negative in the present study. As per the DOTS protocol, sputum was again tested at the end of intensive. If it is negative, the patient was started with the continuation. If the sputum at the end of the intensive of two months was found to be positive, then the intensive was extended for one more month. this extended intensive, the sputum was again tested, and the result was recorded. The sputum was again tested at the end of two months of continuation and again at the end of completion of the continuation. All these results were carefully recorded in the proforma of the present study. Weight was recorded in the beginning of the treatment. Weight was recorded again at the end of intensive. this extended intensive, the weight was again tested, and the result was recorded. The weight was again recorded at the end of two months of continuation and again at the end of completion of the continuation. All these results were carefully recorded in the proforma of the present study. The outcome was recorded at the end of completion of the continuation. The outcome was classified as cured, failure, defaulted, relapses or died. Thus, all patients were followed till the treatment completion in the present study. All data was entered and analyzed using proportions. RESULTS Table 1 shows 37 out of 41 pulmonary cases were found to be positive by sputum AFB at presentation. Four cases were not sputum positive. 19 were extra pulmonary tuberculosis patients. Before the start of the treatment, 37 patients were sputum positive and four were sputum negative among the pulmonary cases. intensive of treatment, only 7 cases were sputum positive which reduced to three at the end of extended intensive of treatment which further reduced to two at the end of two International Journal of Advances in Medicine January-February 2018 Vol 5 Issue 1 Page 171

months of continuation. But by the end of completion of continuation, one case again became sputum positive i.e. failure case making a final tally to three as shown in Table 2. Table 1: Distribution of study subjects as per sputum positivity. Pre-treatment sputum AFB Pulmonary TB Extra-pulmonary TB Total Sputum negative 4 (9.8%) 19 (100%) 23 Sputum positive 37 (90.2%) 00 37 Total 41 19 60 Pulmonary cases Table 2: Sputum conversion during treatment among pulmonary cases. Pretreatment intensive extended intensive 2 months of continuation completion of continuation Sputum positive 37 (90.24%) 7 (18.91%) 3 (8.8%) 2 (5.4%) 3 (8.8%) Sputum negative 4 (9.86%) 30 (81.09%) 34 (91.2%) 35 (94.6%) 34 (91.2%) Table 3: Weight gain during treatment among pulmonary cases (n = 41). Weight Mean+SD Pre treatment 43.42+9.2 intensive 45.07+9.2 2 months of continuation 46.31+9.2 completion of continuation 47.42+9.1 Table 3 shows the w eight gain during treatment among pulmonary cases (n = 38). It was seen that there was significant weight gain over the period of time. The weight increased from 43.42+9.2 (pre treatment ) to 47.42+9.1. It increased to 45 kg at the end of the intensive and then it became 46 kg at the end of the 2 months of continuation. Table 4: Weight gain during treatment among extra pulmonary cases (n = 19). Weight Mean+SD Pre treatment 49.47+9.2 intensive 51.26+9.4 2 months of continuation 51.68+10.1 completion of continuation 52.94+11.1 P < 0.032 Table 4 shows weight gain during treatment among extra pulmonary cases (n = 19). In extra pulmonary cases also, the there was significant weight gain over the period of time. The weight increased from 49.47+9.2 (pre treatment ) to 52.94+11.1. It increased to 51 kg at the end of the intensive and then it became 52 kg at the end of the 2 months of continuation. Table 5: Outcome of DOTS therapy among pulmonary cases. Outcome Number Percentage Cured 32 78 Failure 3 7.3 Defaulted 2 4.9 Died 1 2.4 Total 38 100 X2 = 86.68, p = 0.000 Table 5 shows outcome of DOTS therapy among pulmonary cases. The cure rate was 78%. One patient died. Two defaulted and three were failure cases. DISCUSSION 41 were pulmonary cases and 19 were extra pulmonary patients. intensive only 7 cases were sputum positive out of 37 which reduced to three at the end of extended intensive of treatment which further reduced to two at the end of two months of continuation. But by the end of completion of continuation, one case again became sputum positive i.e. failure case making a final tally to three. It was seen that there was significant weight gain over the period of time in both pulmonary and extra pulmonary cases. The cure rate was 78%. One patient died. Two defaulted and three were failure cases. Verver S et al followed the patients for more than five years. The relapse rate was 18%. 5 Among them 14% were declared cured, 28% were defaulters. Thus, the authors concluded that defaulters were at more risk of relapse than the patients who took regular treatment. Dobler CC et al conducted a study in Australia. 6 They found that there were only three cases of repeated culture positive International Journal of Advances in Medicine January-February 2018 Vol 5 Issue 1 Page 172

cases. Two of these three patients had visited their country of origin which was having high incidence of tuberculosis. Third patient had reactivation of infection with same strain and was a case of secondary failure. This patient was found to have low compliance rate. du Plessis DG et al in their study used Multilesional strain genotyping. 7 They did this in HIV negative patients who had secondary tuberculosis. They observed that the secondary infection was caused by the same strain whether it is pulmonary tuberculosis or extra pulmonary tuberculosis. Shamputa IC et al from their study concluded that failure of the treatment and the relapse were mainly not caused by the re-infection by tubercle bacilli. 8 They carried out the matching of the DNA fingerprinting patterns before the start of the treatment and again at recurrence. In five cases it did not match. This indicated that there was reinfection. In remaining cases there was reactivation. Garcia de Viedma D et al observed that the strains involved in the primary and secondary infection of tuberculosis, were different in most of the cases. 9 The author studied the difference between the reactivation and reinfection groups. They found that it was statistically not significant. They thus concluded that in recurrent tuberculosis the reinfection has an important role. Kliiman K et al observed that the treatment success rate was 81.5%. 10 This is slightly more but comparable with the findings of the present study. The default rate in their study was 9.4% which is double than that observed in the present study. The author noted that the alcoholics were 3.2 times more likely to default than non-alcoholics. They also observed that unemployed were 3 times more likely to default than employed. They also found that those with multi drug resistant tuberculosis were 2 times more likely to default than those without multi drug resistant tuberculosis. They also noted that those from urban areas are 1.8 times multi drug resistant tuberculosis than those from rural areas. Blondal K et al observed that the treatment success rate was 61% which is lower than that observed in the present study. 11 But their study was among MDR and XDR tuberculosis patients. Our study was conducted among non MDR and non-xdr tuberculosis patients. In their study 22.3% of the patients defaulted which is very high compared to the findings of the present study. The authors concluded that the DOTS category IV regime was very effective and cured almost 75% of the patients. The risk factors for recurrence of MDR and XDR TB were previous treatment, and resistance development. Holtz TH et al found a sputum conversion rate of 77% which is similar to the findings of the present study. 12 The authors observed that 23% did not convert. The risk factors for delayed conversion or no conversion as studied by them were history of past treatment for MDR TB, increased culture colony count and on X ray presence of cavities on both the sides of the lung. CONCLUSION The DOTS was found to be 78% effective in terms of cure rate. Still there is a huge gap of 22% found in the present scenario which needs to be addressed seriously and by all to prevent multi drug resistant tuberculosis. Funding: No funding sources Conflict of interest: None declared Ethical approval: The study was approved by the institutional ethics committee REFERENCES 1. Revised National Tuberculosis Control Programme for India. TB India: RNTCP Status Report. Central TB Division, Directorate General of Health Services, Ministry of Health and Family Welfare; 2001. 2. Hill AR, Manikal VM, Riska PF. Effectiveness of directly observed therapy (DOT) for tuberculosis: a review of multinational experience reported in 1990-2000. Medicine (Baltimore). 2002;81(3):179-93. 3. Azhar GS. DOTS for TB relapse in India: A systematic review. Lung India. 2012;29(2):147-53. 4. WHO. Global tuberculosis control, surveillance, planning, financing Geneva: WHO,2007. Available at http://apps.who.int/iris/handle/10665/43629. 5. Verver S, Warren RM, Beyers N, Richardson M, van der Spuy GD, Borgdorff MW, et al. Rate of reinfection tuberculosis after successful treatment is higher than rate of new tuberculosis. Am J Respir Crit Care Med. 2005;171(12):1430-5. 6. Dobler CC, Marks GB, Simposon SE, Crawford AB. Recurrence of tuberculosis at a Sydney chest clinic between 1994 and 2006: reactivation or reinfection? Med J. 2008;188(3):153-5. 7. du Plessis DG, Warren R, Richardson M, Joubert JJ, van Helden PD. Demonstration of reinfection and reactivation in HIV-negative autopsied cases of secondary tuberculosis: multilesional genotyping of Mycobacterium tuberculosis utilizing IS 6110 and other repetitive element-based DNA fingerprinting. Tuberculosis (Edinb). 2001;81(3):211-20. 8. Shamputa IC, Van Deun A, Salim MA, Hossain MA, Fissette K, de Rijk P, et al. Endogenous reactivation and true treatment failure as causes of recurrent tuberculosis in a high incidence setting with a low HIV infection. Trop Med Int Heal. 2007;12(6):700-8. 9. Garcia de Viedma D, Marin M, Hernangomez S, Diaz M, Ruiz Serrano MJ, Alcala L, et al. Tuberculosis recurrences: reinfection plays a role in a population whose clinical/epidemiological characteristics do not favor reinfection. Arch Intern Med. 2002;162(16):1873-9. International Journal of Advances in Medicine January-February 2018 Vol 5 Issue 1 Page 173

10. Kliiman K, Altraja A. Predictors and mortality associated with treatment default in pulmonary tuberculosis. Int J Tuber Lung Dis. 2010;14(4):454-63. 11. Blondal K, Viiklepp P, Guomundsson LJ, Altraja A. Predictors of recurrence of multidrug-resistant and extensively drug-resistant tuberculosis. Int J Tuber Lung Dis. 2012;16(9):1228-33. 12. Holtz TH, Sternberg M, Kammerer S, Laserson KF, Riekstina V, Zarovska E, et al. Time to sputum culture conversion in multidrug-resistant tuberculosis: predictors and relationship to treatment outcome. Ann Intern Med. 2006;144(9):650-9. Cite this article as: Jahnavi K, T. Sreenivasulu. Effectiveness of DOTS regime in terms of cure, failure, default and relapse in the treatment of TB patients. Int J Adv Med 2018;5:170-4. International Journal of Advances in Medicine January-February 2018 Vol 5 Issue 1 Page 174