Prevalence and Risk Factors of Adverse Drug Reactions Associated Multidrug Resistant Tuberculosis Treatments in Selected Treatment Centers in Addis Ababa Ethiopia

Abstract

Introduction: The key to successful elimination of tuberculosis (TB) is treatment of cases with optimum chemotherapy. Irrational anti-TB drug use over time has led to drug-resistant TB. The treatment of MDR-TB with second line drugs is long, complex and costly, and has a considerable rate of adverse effects. The level of ADR reporting is low in Ethiopia due to different factors. This Study conducted in a selected treated area in Addis Ababa, Ethiopia and helped the health care centers to understand the prevalence of ADR related MDR-TB and be aware of those adverse effects in order to detect them early and be prepared to take proper steps when they occur. Aim of the Study: To determine the prevalence and risk factor of adverse drug reactions associated treatments of Multidrug Resistant tuberculosis. Method: This was a cross sectional study, which was conducted between March 2012 and February 2013 at St. Peter TB specialized hospital and AHRI/ALERT. 73 MDR TB patients, who were on MDR TB treatments, enrolled to the study. Adverse Drug Reactions associated MDR TB treatments were assessed by patient history review and questionnaire. Chemistry laboratory was used to test renal function, thyroid function, liver enzyme and potassium level. Result: In 72 patients, at least two ADRs were found. The mean age of the study population (Mean ± SD) was 28 ± 8.8. In this study the most commonly found adverse drug reactions (ADRs) were: Anorexia 83.3%, Nausea and vomiting 82%, Gastritis 64%, Arteralgia 47%, Skin rash and itching 45%, Headache 29.2%, Depression 22.2% and Blurred vision 19.4%. Using binary logistic regression model older age (COR 8.71, 95% [CI] 1.06 - 71.9), alcoholism (COR 4.05, 95% [CI] 1.05 - 15.6), smoking (COR 0.24, 95% [CI] 0.06 - 0.87) and concomitant drug intake (COR 0.14, 95% [CI] 0.03 - 0.76) were independent predictors for ADRs. Conclusion: The prevalence of ADRs related MDR TB treatments is high. To minimize ADR occurrence, ADR predictors should be integrated into the clinical pathway. Monitoring of liver function, renal function, TSH and level of potassium during MDR TB treatment, helps to avoid complication caused by therapy and increase the adherence to the treatment.

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Bezu, H. , Seifu, D. , Yimer, G. and Mebrhatu, T. (2014) Prevalence and Risk Factors of Adverse Drug Reactions Associated Multidrug Resistant Tuberculosis Treatments in Selected Treatment Centers in Addis Ababa Ethiopia. Journal of Tuberculosis Research, 2, 144-154. doi: 10.4236/jtr.2014.23018.

Conflicts of Interest

The authors declare no conflicts of interest.

References

[1] Federal Ministry of Health (2009) Guideline for Program and Clinical Management of Drug Resistant Tuberculosis.
[2] Kocfa, C.D., Alejandro, R.M., Sonia Guillen, B., Eduardo, V.S., Andrea, S.M., Alexandra, N.G., Wilmer, S.C. and Antonio, B.O. (2011) Factors Associated with Anti-Tuberculosis Medication Adverse Effects: A Case-Control Study in Lima, Peru. PLoS One, 6, e27610. http://dx.doi.org/10.1371/journal.pone.0027610
[3] DOTS—Plus Guidelines (2010) Revised National Tuberculosis Control Programme. Central TB Division, Directorate General of Health Services, Ministry of Health & Family Welfare, Nirman Bhavan, New Delhi.
[4] Abate, G. (2002) Drug Resistant TB in Ethiopia: Problem Scenarios and Recommendation. Ethiopian Medical Journal, 40, 79-86.
[5] Ignacio, M. and Sandya, H. (2010) A Basis for the Clinical Management of Complicated MDR-TB Cases Summarise, Best Practice in the Often Lengthy and Complex Managemenet of Multidrug-Resistant Tuberculosis. Africa Health.
[6] Abiy, E., Getahun, G., Mengiste, M. and Assegid, M. (2011) Adverse Drug Reaction in Ethiopia, Analysis of Case Reports, 2002-2007. Ethiopian Journal of Health Development, 25, 168-173.
[7] Yimer, G., Aderaye, G., Amogne, W., Makonnen, E., Aklillu, E., Lindquist, L., et al. (2008) Anti-Tuberculosis Therapy Induced Hepatotoxicity among Ethiopian HIV Positive and Negative Patients. PLoS ONE, 3, e1809.
[8] PLoS ONE (2009) Study Reveals High Level of Adverse Drug Reactions in Hospitals. February 11, 2009.
[9] Saukkonen, J.J., Cohn, D.L., Jasmer, R.M., Schenker, S., Jereb, J.A., Nolan, C.M., Peloquin, C.A., Gordin, F.M., Nunes, D., Strader, D.B., Bernardo, J., Venkataramanan, R. and Sterling, T.R. (2006) Hepatotoxicity of Antituberculosis Therapy. American Journal of Respiratory and Critical Care Medicine, 174, 935-952. http://dx.doi.org/10.1164/rccm.200510-1666ST
[10] Tostmann, A., Boeree, M.J., Aarnoutse, R.E., de Lange, W.C., van der Ven, A.J. and Dekhuijzen, R. (2008) A Antituberculosis Drug-Induced Hepatotoxicity: Concise Up-to-Date Review. Journal of Gastroenterology and Hepatology, 23, 192-202.
[11] TB Policy, AFA (2011) Aids for Africa Health Care Professional Newsletter, June 2011-Issue 32. National Department of Health Guideline on the Management of Drug Resistant TB.
[12] World Health Organization (2008) Guidelines for the Programmatic Management of Drug-Resistant Tuberculosis. An Emergency Update. WHO/HTM/TB/2008.402, Geneva.
[13] TB Policy Guidelines (2004) DOTS-Plus for Standardized Management of Multidrug-Resistant Tuberculosis in South Africa Policy Guidelines.
[14] Joan, B.T. (2007) Risk Factors for Adverse Drug Reactions: The Merck Manual Home Health Hand Book.
[15] Knotek, M. (2013) Drug Induced Kidney Injury. Electronic Journal of IFFC, 20.
[16] Mahajan, S., Tandon, V.R. and Kuma, S. (2012) Women and Risk for Developing ADR’s. JK Science, 14, 1.
[17] Dominica, C., Cristian, D., Niculae, G., Radu, P. and Constantin, M. (2011) Individualized Treatment Regimens with Second Line Anti-TB Drugs (SLD) Compared to First Line Anti-TB Drug (FLD) Only in New Pulmonary TB Patients, Culture Confirmed with Full Sensibility at Drug Sensibility Test (DST). Thematic Poster Session, 4406.
[18] Serena, K. (2010) Management of Side Effects during MDR-TB Treatment Partners. In Health: Brigham and Women’s Hospital USAID TB CARE II.
[19] Shahina, Q., Iftekhar, A., Saifullah, B. and Nadeem R. (2011) Adverse Events in the Treatment of Multi Drug Resistant TB. Thematic Poster Session, 4402.
[20] Shin, S.S., Pasechnikov, A.D., Gelmanova, I.Y., Peremitin, G.G., Strelis, A.K., Mishustin, S., Barnashov, A., Karpeichik, Y., Andreev, Y.G., Golvbchikova, V.T., Tonkel, T.P., Yanova, G.V., Yedilbayev, A., Rich, M.L., Mukherjee, J.S., Furin, J.J., Atwood, S., Farmer, P.E. and Keshavjee, S. (2007) Adverse Drug Reaction among Patients Being Treated for Multi Drug Resistant TB Cohort in Tomsk, Russia. The International Journal of Tuberculosis and Lung Disease, 11, 1314-1320.
[21] Sin, C.I. (2011) Multi-Drug Resistant TB Drug Side Effect Management.
[22] Torun, T., Güngör, G., Ozmen, I., Bölükbasi, Y., Maden, E., Biçakçi, B., et al. (2005) Side Effects Associated with the Treatment of Multidrug-Resistant Tuberculosis. The International Journal of Tuberculosis and Lung Disease, 9, 1373- 1377.
[23] Bloss, E., Kuksa, L., Holtz, T.H., Riekstina, V., Skripconoka, V., Kammerer, S. and Leimane, V. (2010) Side Effects in Multi Drug Resistant TB Cohort in Lativa. The International Journal of Tuberculosis and Lung Disease, 14, 275-281.
[24] Duggal, P. and Sarkar, M. (2007) Audiologic Monitoring of Multi-Drug Resistant Tuberculosis Patients on Aminoglycoside Treatment with Long Term Follow-Up. BMC Ear, Nose and Throat Disorders, 7, 5.
[25] Sonya, S., Jennifer, F., Felix, A., Anne, H., Keith, J., Epifanio, S. and Michael, R. (2004) Hypokalemia among Patients Receiving Treatment for Multi Drug Resistant Tuberculosis. Chest, 125, 974-980.
[26] Evans, A. (2008) Multi-Drug Resistant Tuberculosis, a Challenge in the Management of Tuberculosis. African Journal of Health Sciences, 15, 6-13.
[27] Waseem, S., Arshad, N. and Jamal, A. (2009) Retrospective Audit of Patients Treated for MDR-TB in Retreatment Category. Journal of Ayub Medical College Abbottabad, 21, 94-98.
http://www.ayubmed.edu.pk/JAMC/PAST/21-2/Waseem.pdf
[28] Nathanson, E., Gupta, R., Huamani, P., Leimane, V., Pasechnikov, A.D., Tupasi, T.E., Vink, K., Jaramillo, E. and Espinal, M.A. (2004) Adverse Events in the Treatment of Multidrug-Resistant Tuberculosis: Results from the DOTS-Plus Initiative. International Journal of Tuberculosis and Lung Disease, 8, 1382-1384.
[29] Petros, I., Bhanumati, V., Homa, M., Helen, S.C., Joanna, L., Peter, S., Esdras, S., Samsuddin, K., Roma, P., Zarir, U., Giovanni, B.M., Giovanni, S. and Tony, R. (2012) Adverse Events among HIV/MDR-TB Co-Infected Patients Receiving Antiretroviral and Second Line Anti-TB Treatment in Mumbai, India. PLos ONE, 7, e40781.
[30] Owen, M.K. and Clenney, T.L. (2004) Management of Vaginitis. American Family Physician, 70, 2125-2132.
[31] Satti, H., Mafukidze, A., Jooste, P.L., McLaughlin, M.M., Farmer, P.E. and Seung, K.J. (2012) High Rate of Hypothyroidism among Treated for MDR TB in Lesotho. International Journal of Tuberculosis and Lung Disease, 16, 468-472. http://dx.doi.org/10.5588/ijtld.11.0615
[32] Marc, A.R. and Casillas, A.M. (2003) Adverse Drug Reaction: Types and Treatment Options. American Family Physician, 68, 1781-1791.
[33] National Health Service (NHS) Choices (2013) Alcoholic Unit. http://www.nsh.UK/livewell/Alcohol
[34] Abdullah, A.H. and Samir, A.A. (2002) Enemy within the Silent Epidemic of Substance Dependency in GCC Country. Sqc Journal for Scientific Research Medical Science, 4, 1-7.
[35] Redemarker, M. (2001) Female Patients Have Greater Risk for Developing Adverse Drug Reaction. American Journal of Clinical Dermatology, 2, 349-351.
[36] Zopf, Y., Rabe, C., Neubert, A., Hahn, E.G. and Dormann, H. (2008) Risk Factors Associated with Adverse Drug Reactions Following Hospital Admission: A Prospective Analysis of 907 Patients in Two German University Hospitals. European Journal of Clinical Pharmacology, 31, 789-798.

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