Tuberculosis, one of the oldest recorded human afflictions, is still one of the biggest killers among the infectious diseases, despite the worldwide use of a live attenuated vaccine and several antibiotics. This study was designed to assess the resistance rate distribution of MDR-TB among pulmonary tuberculosis patients attending Nnamdi Azikiewe University Teaching Hospital (NAUTH) Nnewi and St Patrick’s Hospital Mile 4 Abakaliki in the Southeast Nigeria. Patients with persistent cough for over two weeks were screened by Ziehl-Neelsen (ZN) technique for the presence of acid fast bacilli (AFB) in their sputum and a total of 103 patients with AFB positive sputum samples were recruited. The positive sputum samples were subjected to Xpert MTB/RIF assay (GeneXpert®, Cepheid USA) and culture on Lowestein Jensen medium for 42 days at 37°C. Drug susceptibility testing was done on the isolates using the nitrate reduction assay (NRA). Xpert MTB/RIF assay detected MTB in 83 (80.6%) samples out of which 45 (67.2%) were rifampicin resistant. Sixty-seven (80.7%) of the isolates were resistant to at least one of the first-line drugs. Primary resistance was 91% while 19.4%, 35.8%, 22.4% and 22.4% of the isolates were resistant to one, two, three and four drugs respectively. Isoniazid had the highest rate of resistance (57.8%) while Ethambutol had the least (34.9%) and 30 (44.8%) of the resistant isolates were MDR. Smoking (P=.002), gender (P=.002) and history of TB treatment (P=.012) were significantly associated with drug resistance. Educational status was significantly associated with MDR-TB (P=.020). NAUTH and St Patrick’s hospital had MDR-TB rates of 38.9% and 46.9% respectively. The findings of this study indicate high prevalence of MDR-TB among patients with pulmonary TB in the study sites and this portrays a menace to adequate TB control. Prompt diagnosis of TB, adequate patient compliance to therapy and increased awareness and mass education is recommended.
Published in | Chemical and Biomolecular Engineering (Volume 6, Issue 1) |
DOI | 10.11648/j.cbe.20210601.11 |
Page(s) | 1-10 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2021. Published by Science Publishing Group |
Resistance, MDR-TB, Tuberculosis, Patient
[1] | Raviglione MC, Narain JP, Kochi A. HIV-associated tuberculosis in developing countries: clinical features, diagnosis, and treatment. Bull WHO 1992; 70: 515-526. |
[2] | Raviglione MC, Snider DE Jr, Kochi A. 1995. Global epidemiology of tuberculosis; Morbidity and mortality of a worldwide epidemic. J Amer Med Ass 273: 220-226. |
[3] | World Health Organization 2009. Global Tuberculosis Control: Epidemiology, Strategy and Financing. WHO Report 2009 pg. 7. Report number WHO/HTM/TB/2009.411. Available at: http://www.who.int/tb/publications/global_report/2009/en/index.html. |
[4] | World Health Organization 2013. Global tuberculosis report 2013: http://www.who.int/tb/publications/global_report/en/ |
[5] | Leimane V, Leimans J. 2006. Tuberculosis control in Latvia: integrated DOTS and DOTS-Plus programmes. Eurosurveillance 11: 1-3. |
[6] | Telenti A, Imboden P, Marchesi F, Lowrie D, Cole S, Colston MJ, Matter L, Schopfer K, Bodmer T. 1993. Detection of rifampicin-resistance mutations in Mycobacterium tuberculosis. Lancet 341: 647-650. |
[7] | Traore H, Fissette K, Bastian I, Devleeschouwer M, Portaels F. 2000. Detection of rifampicin resistance in Mycobacterium tuberculosis isolates from diverse countries by a commercial line probe assay as an initial indicator of multidrug resistance. Inter J Tubecul and Lung Dis 4: 481-489. |
[8] | Sharma SK, Mohan A. 2006. Multidrug-resistant tuberculosis: A menace that threatens to destabilize tuberculosis control. Chest 130: 261-272. |
[9] | Zhang Y, Heym B, Allen B, Young D, Cole ST. 1992. The catalase-eroxidase gene and isoniazid resistance of Mycobacterium tuberculosis. Nature 358: 591-593. |
[10] | Piatek AS, Telenti A, Murray MR, El HH, Jacobs WJ, Kramer FR, Alland D. 2000. Genotypic analysis of Mycobacterium tuberculosis in two distinct populations using molecular beacons: implications for rapid susceptibility testing. Anti Agents and Chemo 44: 103-110. |
[11] | Nwadioha SI, Nwokedi EOP, Ezema GC, Eronini NC, Anikwe A, Audu F, Onwuezobe I. 2014 Drug resistant Mycobacterium tuberculosis in Benue, Nigeria. B Micro Res J 4: 988-995 |
[12] | Federal Republic of Nigeria Official Gazette. 2009. National Population Commission Abuja, Nigeria. |
[13] | Charan J, Biswas T. 2013. How to calculate sample size for different study designs in medical research. Ind J Psychol Med 35: 121-126. |
[14] | World Health Organization. 1999. Operational characteristics of commercially available assays to determine antibodies to HIV-1 and HIV-2 in human sera. (WHO/TB/99,1 Geneva) Report 11. |
[15] | Uzoewulu NG, Ibeh IN, Lawson L, Goyal M, Umenyonu N, Ofiaeli RO, Okonkwo R. 2014. Drug resistant Mycobacterium tuberculosis in tertiary hospital southeast, Nigeria. J Mel Micro and Diagn 3: 141-148. |
[16] | Manual on Technical SOPs for TB Labs. 2012. Nigeria Federal Ministry of Health, Department of Public Health Abuja. |
[17] | World Health Organization. Global tuberculosis report. Geneva: World Health. 2017. Google Scholar. |
[18] | Agarwal M, Gunai S, Durmaz R, Yang Z. 2010. Integration of Mycobacterium tuberculosis drug susceptibility testing and genotyping with epidemiological data analysis to gain insight into the epidemiology of drug resistant tuberculosis in Malaya, Turkey. J Clin Microbi 48: 3301-3305. |
[19] | Pai M, Behr MA, Dowdy D, Dheda K, Divangahi M, Boehme CC, Ginsberg A, Swaminathan S, Spigelman M, Getahum H, Menzies D, Ravigilone M. 2016. Molecular Basis of Tuberculosis Pathogenesis. Tuberculosis; 2: 1-23. |
[20] | Olusoji D, Osman E. 2011. Prevalence and risk factors associated with drug resistant TB in South West, Nigeria. Asian Paci J Trop Med 17: 148-151. |
[21] | Otu A, Umoh V, Habib A, Ameh S, Lawson L, Ansa V. 2013. Drug resistance among pulmonary tuberculosis patients in Calabar, Nigeria. Pulmonary Medicine; 2013: 76-84. |
[22] | Gaude GS, Hattiholli J, Kumar P. 2014. Risk factors and drug-resistance patterns among Pulmonary tuberculosis patients in Northern Karnataka region, India Nig Med J 55: 327-332. |
[23] | Shamaei M, Majid M, Ehsan C, Mehdi K, Mehdi E, Parisa F, Payam T, Majid V. A. 2009. First-line anti-tuberculosis drug resistance patterns and trends at the national TB referral center in Iran–eight years of surveillance. Elseveir 56: 236-241. |
[24] | Vashakldze L, Salakala A, Shubladze N, Cynamon M. 2009. Prevalence and risk factors for drug resistance among hospitalized pulmonary tuberculosis patients in Georgia. Inter J Tuber and Lung dis 13: 1148-1153. |
[25] | Lawson L, Habib AG, Okobi MI, Idiong D, Olajide I, Emenyonu N, Onuoha N, Cuevas LE, Ogiri SO. 2010. Pilot study on multidrug resistant tuberculosis in Nigeria. Ann Afr Med 9: 184-187. |
[26] | Eufrásio R. 2016. Pulmonary tuberculosis: Resistance pattern to first line anti-tuberculosis drugs in the Coimbra District, 2000-2011. Portuguese J Pulmono 116: 1-4. |
[27] | Lomtadze N, Aspindzelashvili R, Janjgava M, Mirtskhulava V, Wright A. 2009. Prevalence and risk factors for multidrug-resistant tuberculosis in the Republic of Georgia: a population based study. Inter J Tuber and Lung Dis 13: 68-73. |
[28] | Kaona FAD, Mary T, Seter S, Lenganji S. 2004. An assessment of factors contributing to treatment adherence and knowledge of TB transmission among patients on TB treatment. BMC Public Health 4: 68-76. |
[29] | Li W, Zhang Y, Xing J, Ma Z, Qu Y, Li X. 2015. Factors associated with primary transmission of multidrug-resistant tuberculosis compared with healthy controls in Henan Province, China. Infec Dis P 4: 1-7. |
[30] | Medea G, Matthew JM, Russell RK, Lagor K, Tsira C, Jonathan EG, Henry MB. 2015. Tobacco smoking and tuberculosis treatment outcomes: a prospective cohort study in Georgia. Bulletin of the World Health Organization 93: 390-399. |
[31] | McGrath M, GeyvanPiHius NC, Van Helden PD, Warren RM, Warner DF. 2013 Mutation rate and the emergence of drug resistance in Mycobacterium tuberculosis. J Anti Chemo 205: 1-11. |
[32] | Hamusse SD, Dejene T, Mohammed SH, Meaza D, Bernt L. 2016. Primary and secondary anti-tuberculosis drug resistance in Hitossa District of Arsi Zone, Oromia Regional State, Central Ethiopia. BMC Public Health 16: 593-563. |
[33] | Range N, Henrik F, Said M, Pascal M, John C, Andrew K, Apolinary M, Aase BA. 2012. Anti-tuberculosis drug resistance pattern among pulmonary tuberculosis patients with or without HIV infection in Mwanza, Tanzania. Tanzania J Health Res 14: 1-9. |
[34] | Lukoye D, Ssengooba W, Musisi K, Kasule GW, Cobelens FGJ, Joloba M, Gomez GB. 2015. Variation and risk factors of drug resistant tuberculosis in Sub-Saharan African: a systematic review and meta-analysis. BMC Public Health 15: 1-13. |
[35] | McBryde ES, Meehan IM, Doan TN, Ragonnet R, Marais JB Guernier V, Trauer JM. 2017. The risk of global epidemic replacement with drug resistant Mycobacterium tuberculosis strains. Inter J Infec Dise 2856: 1-7. |
[36] | Pourakbari B, Mamishi S, Mohammadzadeh M, Mahmoudi S. 2016. First-line Anti-Tubercular Drug Resistance of Mycobacterium tuberculosis in IRAN: A Systematic Review. Fron Micro 7: 1-11. |
[37] | Dasilva PEA, Palomino JC. 2011. Molecular Basis and mechanisms of drug resistance in Mycobacterium tuberculosis: classical and new drugs. J Ant Chemo 66: 1417-1430. |
[38] | Curry International Tuberculosis Center and California Department of Public Health, 2016: Drug Resistant Tuberculosis: A Survival Guide for Clinicians. Third Edition 31-56. |
APA Style
Chinenye Esther Okoro-Ani, Confort Nnenna Akujobi, Iniekong Philip Udoh, Stellamaris Ojiuzor Ibhawaegbele, Charles Ikechukwu Ezema, et al. (2021). Resistance Rate Distribution of MDR-TB Among Pulmonary Tuberculosis Patients Attending NAUTH and St Patrick’s Hospital Mile 4 Abakiliki in Southeast Nigeria. Chemical and Biomolecular Engineering, 6(1), 1-10. https://doi.org/10.11648/j.cbe.20210601.11
ACS Style
Chinenye Esther Okoro-Ani; Confort Nnenna Akujobi; Iniekong Philip Udoh; Stellamaris Ojiuzor Ibhawaegbele; Charles Ikechukwu Ezema, et al. Resistance Rate Distribution of MDR-TB Among Pulmonary Tuberculosis Patients Attending NAUTH and St Patrick’s Hospital Mile 4 Abakiliki in Southeast Nigeria. Chem. Biomol. Eng. 2021, 6(1), 1-10. doi: 10.11648/j.cbe.20210601.11
AMA Style
Chinenye Esther Okoro-Ani, Confort Nnenna Akujobi, Iniekong Philip Udoh, Stellamaris Ojiuzor Ibhawaegbele, Charles Ikechukwu Ezema, et al. Resistance Rate Distribution of MDR-TB Among Pulmonary Tuberculosis Patients Attending NAUTH and St Patrick’s Hospital Mile 4 Abakiliki in Southeast Nigeria. Chem Biomol Eng. 2021;6(1):1-10. doi: 10.11648/j.cbe.20210601.11
@article{10.11648/j.cbe.20210601.11, author = {Chinenye Esther Okoro-Ani and Confort Nnenna Akujobi and Iniekong Philip Udoh and Stellamaris Ojiuzor Ibhawaegbele and Charles Ikechukwu Ezema and Uchechukwu Anthonia Ezeugwu and Ogechukwu Calista Dozie-Nwakile and Aaron Chukwuemeka Okpe}, title = {Resistance Rate Distribution of MDR-TB Among Pulmonary Tuberculosis Patients Attending NAUTH and St Patrick’s Hospital Mile 4 Abakiliki in Southeast Nigeria}, journal = {Chemical and Biomolecular Engineering}, volume = {6}, number = {1}, pages = {1-10}, doi = {10.11648/j.cbe.20210601.11}, url = {https://doi.org/10.11648/j.cbe.20210601.11}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.cbe.20210601.11}, abstract = {Tuberculosis, one of the oldest recorded human afflictions, is still one of the biggest killers among the infectious diseases, despite the worldwide use of a live attenuated vaccine and several antibiotics. This study was designed to assess the resistance rate distribution of MDR-TB among pulmonary tuberculosis patients attending Nnamdi Azikiewe University Teaching Hospital (NAUTH) Nnewi and St Patrick’s Hospital Mile 4 Abakaliki in the Southeast Nigeria. Patients with persistent cough for over two weeks were screened by Ziehl-Neelsen (ZN) technique for the presence of acid fast bacilli (AFB) in their sputum and a total of 103 patients with AFB positive sputum samples were recruited. The positive sputum samples were subjected to Xpert MTB/RIF assay (GeneXpert®, Cepheid USA) and culture on Lowestein Jensen medium for 42 days at 37°C. Drug susceptibility testing was done on the isolates using the nitrate reduction assay (NRA). Xpert MTB/RIF assay detected MTB in 83 (80.6%) samples out of which 45 (67.2%) were rifampicin resistant. Sixty-seven (80.7%) of the isolates were resistant to at least one of the first-line drugs. Primary resistance was 91% while 19.4%, 35.8%, 22.4% and 22.4% of the isolates were resistant to one, two, three and four drugs respectively. Isoniazid had the highest rate of resistance (57.8%) while Ethambutol had the least (34.9%) and 30 (44.8%) of the resistant isolates were MDR. Smoking (P=.002), gender (P=.002) and history of TB treatment (P=.012) were significantly associated with drug resistance. Educational status was significantly associated with MDR-TB (P=.020). NAUTH and St Patrick’s hospital had MDR-TB rates of 38.9% and 46.9% respectively. The findings of this study indicate high prevalence of MDR-TB among patients with pulmonary TB in the study sites and this portrays a menace to adequate TB control. Prompt diagnosis of TB, adequate patient compliance to therapy and increased awareness and mass education is recommended.}, year = {2021} }
TY - JOUR T1 - Resistance Rate Distribution of MDR-TB Among Pulmonary Tuberculosis Patients Attending NAUTH and St Patrick’s Hospital Mile 4 Abakiliki in Southeast Nigeria AU - Chinenye Esther Okoro-Ani AU - Confort Nnenna Akujobi AU - Iniekong Philip Udoh AU - Stellamaris Ojiuzor Ibhawaegbele AU - Charles Ikechukwu Ezema AU - Uchechukwu Anthonia Ezeugwu AU - Ogechukwu Calista Dozie-Nwakile AU - Aaron Chukwuemeka Okpe Y1 - 2021/03/22 PY - 2021 N1 - https://doi.org/10.11648/j.cbe.20210601.11 DO - 10.11648/j.cbe.20210601.11 T2 - Chemical and Biomolecular Engineering JF - Chemical and Biomolecular Engineering JO - Chemical and Biomolecular Engineering SP - 1 EP - 10 PB - Science Publishing Group SN - 2578-8884 UR - https://doi.org/10.11648/j.cbe.20210601.11 AB - Tuberculosis, one of the oldest recorded human afflictions, is still one of the biggest killers among the infectious diseases, despite the worldwide use of a live attenuated vaccine and several antibiotics. This study was designed to assess the resistance rate distribution of MDR-TB among pulmonary tuberculosis patients attending Nnamdi Azikiewe University Teaching Hospital (NAUTH) Nnewi and St Patrick’s Hospital Mile 4 Abakaliki in the Southeast Nigeria. Patients with persistent cough for over two weeks were screened by Ziehl-Neelsen (ZN) technique for the presence of acid fast bacilli (AFB) in their sputum and a total of 103 patients with AFB positive sputum samples were recruited. The positive sputum samples were subjected to Xpert MTB/RIF assay (GeneXpert®, Cepheid USA) and culture on Lowestein Jensen medium for 42 days at 37°C. Drug susceptibility testing was done on the isolates using the nitrate reduction assay (NRA). Xpert MTB/RIF assay detected MTB in 83 (80.6%) samples out of which 45 (67.2%) were rifampicin resistant. Sixty-seven (80.7%) of the isolates were resistant to at least one of the first-line drugs. Primary resistance was 91% while 19.4%, 35.8%, 22.4% and 22.4% of the isolates were resistant to one, two, three and four drugs respectively. Isoniazid had the highest rate of resistance (57.8%) while Ethambutol had the least (34.9%) and 30 (44.8%) of the resistant isolates were MDR. Smoking (P=.002), gender (P=.002) and history of TB treatment (P=.012) were significantly associated with drug resistance. Educational status was significantly associated with MDR-TB (P=.020). NAUTH and St Patrick’s hospital had MDR-TB rates of 38.9% and 46.9% respectively. The findings of this study indicate high prevalence of MDR-TB among patients with pulmonary TB in the study sites and this portrays a menace to adequate TB control. Prompt diagnosis of TB, adequate patient compliance to therapy and increased awareness and mass education is recommended. VL - 6 IS - 1 ER -