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. 2020 Nov 13;20:1705. doi: 10.1186/s12889-020-09827-7

Level of and associated factors for non-adherence to anti-tuberculosis treatment among tuberculosis patients in Gamo Gofa zone, southern Ethiopia: cross-sectional study

Dessalegn Ajema 1,, Tamiru Shibru 2, Temesgen Endalew 2, Selamawit Gebeyehu 1
PMCID: PMC7666453  PMID: 33187496

Abstract

Background

Non-adherence to anti-TB treatment is one of the crucial challenges in improving tuberculosis (TB) treatment outcomes and reducing healthcare costs. The poor adherence to anti-TB treatment among patients with TB is a major problem in Ethiopia. This study aimed to assess the level of and associated factors for non-adherence to anti-TB therapy among patients with tuberculosis in the Gamo Gofa Zone.

Methods

A cross-sectional study was conducted at Gamo Gofa Zone from July 20 – August 30, 2017. A multi-stage sampling technique was used. The study included 289 patients who were on anti-TB treatment. Data were collected by trained data collectors using a structured and pre-tested questionnaire through interviews. A multiple logistic regression model was fitted using SPSS 23 to identify factors associated with non-adherence to anti-TB treatment at a 5% significance level.

Results

We found that 16.5% of the participants were non-adherent for anti-TB treatment. Failure to disclose one’s TB status to his or her family (AOR = 31.7; 95% CI: 9.1–111.1), having no information on the expected adverse events (AOR = 31.1; 95% CI: 7.5–128.3), past anti-TB treatment history (AOR = 5.3; 95% CI: 1.5–18.8) and a smoking cigarette (AOR = 11.7; 95% CI: 3.2–43.03) were found to be associated with a higher odds of being non-adherent to anti-TB treatment.

Conclusions

The level of non-adherence to anti-TB treatment among TB patients was high. Health care providers should counsel TB patients on the expected adverse events and measures to be taken when patients face the expected adverse events. They should also counsel their patients to disclose their TB status to his or her family and for ceasing cigarette smoking.

Supplementary Information

The online version contains supplementary material available at 10.1186/s12889-020-09827-7.

Keywords: TB, Non-adherence, Gamo Gofa, Ethiopia

Background

Tuberculosis (TB) is an infectious disease caused by the bacillus Mycobacterium tuberculosis. It typically affects the lungs (pulmonary TB), but can also affect other sites (extrapulmonary TB) [1]. Most people who had TB disease can be cured with early diagnosis and correct treatment. Despite this, it has been continued as a leading cause of death from a single infectious agent ranking on top of HIV/AIDS for the past five years [2].

In 2018, TB caused an estimated 1.2 million deaths (range, 1.1–1.3 million) among HIV-negative people and 10.0 million people developed the disease. The biggest burden (83%) of TB deaths among HIV-negative people shouldered by the African and South-East Asia Region. Ethiopia is in the list of 30 high burden countries (HBCs), with an estimated total incidence of TB 165 per 100,000 population [3].

Based on the evidence that TB is a global public health challenge, WHO launched different strategies like the Directly Observed Treatment, Short-course (DOTS), STOP TB Strategy and End TB strategy for TB control [15]. Almost all countries, including Ethiopia, have adopted this strategy and have been implementing for years. Similarly, in recent years, they committed and have targeted to end the epidemics of AIDS, TB, and other communicable diseases by 2030 [2].

Even though many national and international efforts have been implemented against TB prevention and control, currently, the world as a whole, are not on track to reach the 2020 milestones of the End TB Strategy [3]. Besides this, drug-resistant TB threatens global TB care and prevention and remains a major public health concern in many countries [2]. The year 2019 WHO report shows in 2018, there were about half a million new cases of rifampicin-resistant TB (of which 78% had multidrug-resistant TB (MDR-)TB, and many cases are developing Extensively Drug resistance (XDR) TB among retreatment cases throughout the world [3].

Drug-resistant (DR-) TB emerges at least in part due to inappropriate treatment or suboptimal adherence to the treatment regimen [6]. Thus poor adherence to a prescribed treatment increases the risks of morbidity, mortality, and drug resistance [7]. As a result, patients with TB are expected to have non-adherence levels of less than 10% to facilitate cure [8, 9].

Non-adherence rates to long-term medication including TB and HIV/AIDS patients in developing countries seem to be higher and remain a challenge [7, 10]. In sub-Saharan Africa, there is a high rate of losses to follow-up of TB patients that range from 11.3 to 29.6% [11]. Mapping of TB treatment outcomes in Ethiopia stated that 0.7% of the patients had treatment failure, and 5.5% were lost to follow-up. The overall prevalence of poor TB treatment outcomes was 9.0%, which is most probably due to treatment non-adherence and loss to follow up [12]. A systematic review done to estimate the pooled prevalence of non-adherence to anti TB treatment in Ethiopia showed Southern Nations and Nationalities of Ethiopia had the highest (23.61%) pooled prevalence estimate of non-adherence to anti TB treatment [13].

To improve TB treatment outcomes, it requires a better understanding of factors that influence TB treatment non-adherence. Studies conducted in different parts of Ethiopia revealed several factors associated with anti-TB treatment non-adherence, including factors related to the health system, patient and socio-economic characteristics, [1416]. As TB treatment non-adherence is an “unavoidable by-product of collisions between the clinical world and the other competing worlds of work, play, friendships and family life” the factors affecting it can be changed over time [7]. The present study was therefore conducted to assess the level and factors associated with non-adherence to anti-TB treatment among TB patients in Gamo Gofa Zone, Ethiopia.

Methods

Study setting

The study was conducted in the Gamo Gofa Zone of Southern Nations, Nationalities and Peoples` Regional State (SNNPR), Ethiopia. It is found at 50 57–60 71′ N 360 37′- 37098′ E and altitude of 680 to 4207 masl. The general elevation of the Gamo Gofa zone ranges from 680 to 4207 m above sea level. Gamo Gofa has a population of about 2,040,972. DOTS services have been provided for years in the area. Seventeen health facilities within this zone register and treat all diagnosed TB patients under the DOTS. In this facility’s diagnosis, treatment, and prevention services have been given. Health extension workers play an important role in the identification of presumptive cases at the community level. Once a presumptive case is identified they immediately refer to a health facility providing DOTS service for diagnosis and treatment. In line with the national TB and leprosy control program guidelines [17], once diagnosis is made, patients are provided with anti-TB medication and care free of charge. According to the zonal report, TB morbidity is decreased from 41% in 2017 to 37% in 2019, while the mortality also decreased from 2.4% in 2017 to 2.3% in 2019. Moreover, there were 3.2% treatment failure cases in 2017 and 1.2% cases in 2019. The report also stated that the drug-resistant (DR) TB rate was 3.4% in 2017 increased to 4.2% in 2019 among new cases and 12.5% in 2017 increased to 15.2% in 2019 among previously treated cases. The study was conducted from July 20, 2017 – August 30, 2017.

Study design and population

A health facility-based cross-sectional study was conducted. All patients aged over 15 years, who had started anti- TB treatment and on treatment follow-up in selected health facilities were eligible.

Sample size and sampling procedures

To reach the participants, a Multi-stage sampling method was used. From 17 woreda health offices and one general hospital, by using a simple random sampling method four of the registry centers were selected. Proportionate allocation to size was made. Finally, the study participants were selected by simple random sampling from the sampling frame (patients’ register). The sample size was calculated using a single population proportion formula; considering 13.6% level of non-adherence [15] with a 5% margin of error and 95% confidence, it was 183. The design effect was taken into consideration and the sample size was multiplied by 1.5, giving 275. By adding a 5% none response rate the final sample size was 289.

Data collection tool

Data were collected using an interviewer-administered questionnaire. The questionnaire was developed based on the comparable studies [6, 1416, 1820] and included demographics (age and sex), economic status (monthly income), social (residence, level of education, employment, religious status, ethnicity, and marital status), medical history(number of doses taken in the month before the study interview, history of previous anti-TB treatment and history of opportunistic infection), TB knowledge (etiology, mode of transmission, symptoms, treatment duration and effectiveness, and expected adverse events), health provider (counseling about the expected adverse effect), and health system (time to reach a health facility, waiting time and mode of transportation) and patients behaivor (smoking, alcohol drinking, khat chewing and disclosing one’s TB status),(See additional file questionnaire for the study). It was initially prepared in English and then translated into Amharic and back-translated to English to ensure its consistency. The questionnaire was pretested before the actual data collection. Data was collected through a face-to-face exit interview. It was collected after verbal informed consent was obtained. Interviewers were specifically trained for this study.

Operational definitions

Non-adherence for TB treatment: If the patient had taken less than 90% of the dose prescribed within a month he/she was regarded as non-adherent [5, 10].

Data analysis

Data were coded and entered into Epi Data version 3.1 [21] and exported to SPSS version 23 [22] for analysis. The participant’s characteristics were summarized using frequencies and percentages for categorical variables. Furthermore, patients who had the correct answer to three questions was taken as having good knowledge while the incorrect answer to three or more question was taken as having poor knowledge. Bivariate logistic regression analysis was conducted to assess the association between each categorical variable and the non-adherence to anti-TB treatment. The variables with p-value ≤0.25 were included in the multivariable logistic regression model. The multiple logistic regression model was fitted using a backward stepwise selection method to identify variables independently associated with the outcome variable of interest at a 5% significance level. The final model was assessed using the Hosmer and Lemeshow goodness of fit test. The adjusted odds ratios (aORs) and the corresponding 95% confidence intervals (CIs) of the variables in the final model were reported.

Ethical consideration

Ethical clearance was obtained from Arba Minch University research and community service core process ethical review board, and permission was secured from the Gamo Gofa zone health Department. Participants were informed about the objectives, risks, and benefits of the study. Verbal consent was obtained for those study participants who were18 years and above. Verbal Assent was obtained for participants less than 18 years from themselves and if families were available parental permission was asked; if parents were not available permission was taken from the health facility or health service provider. Participant’s involvement in the study was voluntary and those who wish to quit their participation at any stage were informed to do so without any restriction.

Results

A total of 249 participants were included in this study with a response rate of 86.2%. One hundred fifty-five (62.2%) of study participants were rural residents and 148 (59.4%) were males. One hundred twenty-three (50.4%) of them did not attend any formal education and 77 (30.9%) of the respondents were farmers. One hundred forty-eight (59.4%) were protestants and 194 (77.9%) participants were Gamo in Ethnicity (Table 1). One hundred eighty-nine (75.9%) of the participants walk to the health facility. For one hundred twenty-five (50.2%) participants, it took them more than 30 min to reach a health facility.

Table 1.

Socio-demographic and economic characteristics of participants who started anti-tuberculosis treatment and are on follow up in health institutions of Gamo Gofa Zone, 2017 (n = 249)

Variable Number Percent (%)
Residence Urban 94 37.8
Rural 155 62.2
sex of respondent Male 148 59.4
Female 101 40.6
Age of respondent (years) 15–24 80 32.1
25–34 72 28.9
35–44 44 17.7
≥45 53 24.3
Marital status Married 149 59.8
Single 82 32.9
Divorced/Widowed 18 7.2
Level of education Unable to read and write 87 34.9
Read & write 36 14.5
grade1–8 57 22.9
grade 9–12 43 17.3
College and above 26 10.4
Religion Orthodox 84 33.7
protestant 148 59.4
Muslim 17 6.8
Ethnicity Gamo 194 77.9
Gofa 16 6.4
other 39 15.6
occupation Housewife 42 16.9
Daily laborer 46 18.5
Government employee 19 7.6
farmer 77 30.9
Private employee 20 8.0
Other (specify) 45 18.1
Income (in birr) <  500 91 36.8
≥500 158 63.5

The overall level of non-adherence to anti-TB treatment over one month and the last four days before the survey were 16.5 and 10%, respectively. One hundred sixty-six (66.7%) participants had good knowledge about TB. From all participants, 185 (74.3%) of them had a family member or friend who reminds the patient to take treatment, and 37(13.4%) smoke cigarettes; the adverse event was experienced by 102(41.0%) participants. From different adverse events, urine discoloration was experienced by 56(54.9%) of them. Symptoms of TB were reported by 36(14.5%) of the participants at the time of the interview. One hundred eighty-two (73.1%) of them acquired Pulmonary TB confirmed with sputum and 36(14.5%) of them had pulmonary TB without sputum. Extra-pulmonary TB (EPTB) was found among 31 (12.4%) of the participants. From all participants, 198 (79.5%) had no history of previous anti-TB treatment. Nearly all of them 248(99.6%) had screened for HIV and 14(5.6%) of them were positive for HIV. Those participants who were positive for HIV had started Anti-Retroviral Treatment (ART) and had no other Opportunistic Infections (OIs) (Table 2).

Table 2.

Determinants of anti-TB treatment non-adherence among participants who started anti-tuberculosis treatment and are on follow up in health institutions of Gamo Gofa Zone, 2017

Variable number percent
Family member or friend who reminds the patient to take treatment yes 185 74.3
no 64 25.7
Knowledge about TB good 166 66.7
poor 83 33.3
TB status disclosure to the family disclose 211 84.7
not disclose 38 15.3
Felt discriminated by family/Community Discriminated 23 9.2
Non discriminated 226 90.8
Support for medication health professional 26 10.4
family member 185 74.3
No treatment supporter 38 15.3
Chewing khat yes 27 10.8
no 222 89.2
Addicted to alcohol yes 43 17.3
no 206 82.7
Smoking yes 34 13.7
no 215 86.3

Income, marital status, time to reach a health facility, waiting time to get served, information on the expected adverse event, missing drug in the last four day, alert for medication, knowledge about the disease, disclose one’s TB status, discrimination from family and society, use of alcohol, Khat, smoking cigarette, having adverse event t and past anti-TB treatment history had a p-value of less than 0.25 in the bivariate analysis. Thus, these variables were considered for the multivariable logistic regression analysis. In the multivariable analysis, information on the expected adverse event, having past anti-TB treatment history, disclose one’s TB status to family, and smoking cigarettes had a statistically significant association with the level of non-adherence to anti-TB treatment (Table 3).

Table 3.

The result of Bivariate and multivariable logistic regression for non-adherence among participants on anti-tuberculosis treatment and on follow up in health institutions of Gamo Gofa Zone,2017

Variable non-adherence COR(95%CI) AOR(95%CI)
Yes n (%) No n (%)
Sex
Male 24 (16.2) 124 (83.8) 1
Female 17 (16.8 84 (83.2) 1.05 (0.53–2.06)
Age
15–24 13 (16.3) 67 (83.8) 1
25–34 14 (19.4) 58 (80.6) 1.24 (0.54–2.86)
35–44 9 (20.5) 35 (79.5) 1.33 (0.52–3.4)
  ≥ 45 5 (9.4) 48 (90.6) 0.54 (0.179–1.61)
Income
  < 500 21 (23.1) 70 (76.9) 2.07 (1.05–4.072)a 1
  ≥ 500 20 (12.6) 138 (87.3) 1 1.7 (0.4–7.6)
Marital status
married 14 (9.3) 135 (90.6) 1 1
single 20 (24.4) 62 (75.6) 3.11 (1.47–6.56)a 5.1 (0.98–26.4)
divorced 7 (38.9) 11 (61.1) 6.14 (2.05–18.35)a 23.8 (2.4–231.1)
Mode of transportation
waking 27 (14.3) 162 (85.7) 0.55 (0.27–1.13)
public 14 (23.3) 46 (76.7) 1
Time to reach a health facility
  ≤ 30 min 12 (9.6) 112 (90.3) 1 1
  > 30 min 29 (23.2) 96 (76.8) 2.82 (1.36–5.83)a 1.4 (0.3–2.7)
Waiting time
  ≤ 30 min 20 (9.4) 192 (90.6) 1 1
  > 30 min 21 (56.7) 16 (43.2) 12.6 (5.68–27.66)a 5.2 (0.8–30.4)
Have you consulted
Yes 40 (16.5) 203 (83.5) 1
No 1 5 1.01 (0.12–8.92)
Information on the expected adverse event
Yes 21 (9.4) 202 (90.6) 1 1
No 20 (76.9) 6 (23.1) 32.06 (11.6–88.7)a 31.1 (7.5–128.3)b
Knowledge
Good 13 (7.8) 153 (92.2) 1 1
Poor 28 (33.7) 55 (66.3) 5.99 (2.89–12.38)a 5.5 (0.94–30.7)
use traditional medicine
yes 11 (23.9) 35 (76) 1.81 (0.83–3.95)
No 30 (14.8) 173 (85.2) 1
Alert
Yes 16 (8.6) 169 (91.4) 1 1
No 25 (39.1) 39 (60.9) 6.77 (3.3–13.87)a 2.6 (0.43–15.1)
Disclosing one’s TB status
Yes 15 (7.1) 196 (92.8) 1 1
No 26 (40) 39 (60) 28.3 (11.95–67.05)a 31.7(9.1–111.1)
Discriminated
Yes 9 (39.1) 14 (60.8) 3.89 (1.56–9.75)a 5.9 (0.7–48.6)
No 32 (14.2) 194 (85.8) 1 1
Addicted to alcohol
Yes 16 (37.2) 27 (62.8) 4.29 (2.03–9.05)a 0.6 (0.1–3.95)
No 25 (12.1) 181 (87.8) 1 1
Addicted to khat
Yes 18 (66.7) 9 (3.3) 17.3 (6.97–42.95)a 2.03 (0.02–18.05)
No 23 (10.4) 199 (89.6) 1 1
Smoke cigarette
Yes 24 (70.6) 10 (29.4) 27.9 (11.5–67.9)a 11.7 (3.2–43.03)b
No 17 (7.9) 198 (92.1) 1 1
Adverse event
Yes 23 (22.5) 79 (77.5) 2.08 (1.06–4.108)a 1.3 (0.3–6.4)
No 18 (12.2) 129 (87.7) 1 1
Previous TB treatment
Yes 16 (31.4) 35 (68.6) 3.16 (1.53–4.6.53)a 5.3(1.5–18.8)b
No 25 (12.6) 173 (87.4) 1 1
Having a symptom of TB
Yes 10 (27.9) 26 (72.2) 2.3 (0.99–5.14)
No 31 (14.6) 182 (85.4) 1

a P-value≤0.25; b P-value< 0.05

The odds of TB treatment non-adherence among the study participants who didn’t disclose their TB status to their families was higher compared to those who did disclose their TB status told (aOR = 31.7; 95% CI: 9.1–111.1). The study participants who had no information on the expected adverse events had higher odds of the TB treatment non-adherence compared to those who had information (aOR = 31.1;95% CI:7.5–128.3). Furthermore, the non-adherence to TB treatment was higher among those with TB treatment in the past (aOR = 5.3; 95% CI: 1.5–18.8) and those who smoke a cigarette (aOR = 11.7; 95% CI: 3.2–43.03).

Discussion

In the present study, 16.5% were non-adherent to anti-TB therapy in the last month before the interview. This finding was higher than the levels of non-adherence reported from another study in Northwest Ethiopia (10%) [15]. This variation might be from differences in participants. Such that, in this study, we included both new TB cases and patients who had past treatment but the study in Northwest Ethiopia included only new TB cases. So, patients who had past treatment might be reluctant or unwilling to try it again because of the previous experience which could be treatment failure. The level of non-adherence among new TB cases in this study was 10% which is similar to the report from the study in Northwest, Ethiopia [15].

However, the present non-adherence level over one month was lower than the previous reports from Southern Ethiopia (24.7%), Mekelle (55.8%), and Uganda (25%) [14, 16, 18]. This is probably due to variation in the participant characteristics and duration in which adherence was measured. For example, in this study, we included both HIV-positive and HIV-negative patients but the study in Mekelle, Uganda, included only TB/HIV co-infected patients in which HIV co-infected patients are more likely to be non-adherent because they have to get HIV care in addition to the TB care [8]. Besides, this variation may be attributable to the duration in which the adherence was calculated. In the case of the Ugandan study, adherence was estimated over the last five days.

Disclosing one’s TB status for the family is important to get family support and reminder which helps to adhere. In this study, 15.3% of the participants did not get family support. This is supported by a study done in Mekelle which stated a lack of caregivers and people who remind the TB patients to take their medications were associated with non-adherence [14]. A systematic review stated Social support, support from family were identified as extremely important for TB treatment adherence [20]. Patients usually did not disclose their status because of fear of discrimination [23]. So, disclosing one’s status is important to get different support which can help to adhere to treatment.

In this study, one of the reasons for non-adherence to anti-TB treatment was past anti-TB treatment history. This is in line with studies done in Northeast Ethiopia, Northern Ethiopia, and Gambella Regional State, Ethiopia stated Patients with previously treated cases have a high level of treatment failure, and patients who had lost to follow-up history could be reluctant and tend to interrupt their treatment again and be non-adherent [2426].

Having no information about the expected adverse event was also another reason for non-adherence to anti-TB treatment. This is supported by a qualitative study done in India which patients who had inadequate information on the management of the expected adverse event or problems to be non-adherent [23]. This could be when participants had counseled and had information on the expected adverse event they expect the adverse event and know the measures to take when they experienced these effects which help to adhere.

The other reason for anti-TB nonadherence among TB patients was smoking cigarettes. This finding is supported by a study done in Nigeria which stated that cigarette smokers had poorer TB treatment than a non-smoker [27]. This might be due to Cigarette smoke is known to damage the lungs and suppresses the individual adaptive immune responses affecting patients’ response to TB treatment which could lead to non-adherence [7, 28]. In contrast, a study done in southern Ethiopia mentioned smoking has no association with non-adherence.

In this study, some factors which were associated in different studies were not found to be significant determinants of non-adherence. For example, distance from a health facility, transportation cost, relationship with a health worker, and proper counseling [15, 16, 25].

One limitation of this study was the level of non-adherence to anti-TB treatment was self-reported. One of the main limitations of self-reporting adherence measurement is lack of reliability. This can be explained by patient recall bias and other information biases, social desirability, or the interviewer’s skills and construction of the questions. A close relationship between the patient and the healthcare professional could also result in an underestimation of non-adherence rates. So, it has been strongly recommended to use them as a complement of another method like the direct methods, for example, measurement of drug or metabolites and ingestible sensors which are more accurate [29]. Another limitation was a cross-sectional study was conducted, it might suffer from temporal relationship establishment with some variables and might not provide much stronger evidence of causality.

Conclusions

The level of Non-adherence among TB patients was high. Information on the expected adverse event, having past anti-TB treatment history, disclose TB status to family, and smoking cigarettes were factors independently associated with non-adherence to anti-TB treatment.

Health care providers should counsel TB patients about anti-TB treatment adverse events and measures to be taken when patients face adverse events. They should also counsel their patients to disclose their TB status to family and the effect of smoking on the treatment outcome.

Additional file

Additional file 1 (26.4KB, docx)

Questionnaire for the study.

Acknowledgments

Our sincere acknowledgment extends to the study participants and Gamo Gofa Zone Health Department for the baseline information. We thank data collectors and supervisors for their contribution to the success of the study.

Abbreviations

AMGH

Arba Minch General Hospital

AMU

Arba Minch University

HIV/AIDS

Human Immune Deficiency Virus/ Acquired Immune Deficiency Syndrome

MDR

Multi-Drug Resistant

PTB-SM + ve

Smear Positive Pulmonary Tuberculosis

PTB-SM –ve

Smear Negative Pulmonary Tuberculosis

RVI

Retroviral Infection

ART

Antiretroviral therapy

OIs

Opportunistic Infections

Authors’ contributions

TS and DA have made substantial intellectual contributions to the conception, design, and acquisition of data, analysis, and interpretation of data to this study. TS, TE, DA, and SG have made substantial contributions to the analysis and interpretation of data and participated in the critical review and editing of all the manuscript drafts for scientific merit and depth. All authors read and approved the final manuscript and agreed 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.

Funding

Arbaminch University supports this research financially. The university has no role in the design of the study, collection, analysis, and interpretation of the data and in writing the manuscript.

Availability of data and materials

The data used to support the findings of this study are not publicly available due to restrictions on the publication of human subjects’ data but these data can be available from the corresponding author upon reasonable request.

Ethics approval and consent to participate

Ethical clearance was obtained from the institutional review board of college of medicine and health sciences, Arba Minch University with IRB ref. no. CMHS/907/07. A permission letter was written for the Gamo Gofa zone health department and the informed verbal consent was obtained for those study participants who were 18 years and above. Verbal Assent was obtained for participants less than 18 years from themselves and if families were available parental permission was asked; if parents were not available permission was taken from the health facility or health service provider and this was approved by the ethics committee. The assurance of confidentiality was performed by omitting the name of the study participants from the questionnaire, by telling the safety of the place where the questionnaire was stored after data collection and also the analysis was not for individual it is for groups.

Consent for publication

Not applicable.

Competing interests

The authors declare that there is no conflict of interest regarding the publication of this paper.

Footnotes

Publisher’s Note

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Contributor Information

Dessalegn Ajema, Email: dessu.aj@gmail.com.

Tamiru Shibru, Email: drtamshib1@gmail.com.

Temesgen Endalew, Email: dolceru.enda@gmail.com.

Selamawit Gebeyehu, Email: emugebe.sg@gmail.com.

References

  • 1.World Health Organization. Global Tuberculosis Report. 2018. 1–162 p. Available from http://www.who.int/tb.
  • 2.World Health Organization. Global tuberculosis report [internet]. Geneva: WHO press; 2017. 147 p. Available from http://www.who.int/tb.
  • 3.World Health Organization. Global Tuberculosis report 2019. 2019. 1–283 p. Available from http://www.who.int/tb.
  • 4.World Health Organization. Global Tuberculosis Control [Internet]. 2010. Available from: http://www.who.int/tb.
  • 5.WHO. WHO treatment guidelines for drug-resistant tuberculosis 2016. 2016 Available from http://www.who.int/tb.
  • 6.Cadosch D, Abel P, Kouyos R, Bonhoeffer S. The role of adherence and retreatment in De novo emergence of MDR-TB. PLoS Comput Biol. 2016;12(3):1–19. doi: 10.1371/journal.pcbi.1004749. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.World Health Organization. Adherence to long-term therapies. Vol. 30, Am J Hosp Palliat Med. 2013. 334–338 p.
  • 8.World Health Organization TB/HIV: A clinical manual. Trans R Soc Trop Med Hyg. 2004;91(6):731–732. [Google Scholar]
  • 9.Tola HH, Holakouie-Naieni K, Tesfaye E, Mansournia MA, Yaseri M. Prevalence of tuberculosis treatment non-adherence in Ethiopia: a systematic review and meta-analysis. Int J Tuberc Lung Dis. 2019;23(6):741–749. doi: 10.5588/ijtld.18.0672. [DOI] [PubMed] [Google Scholar]
  • 10.Méda ZC, Lin YT, Sombié I, Maré D, Morisky DE, Chen YMA. Medication-adherence predictors among patients with tuberculosis or human immunodeficiency virus infection in Burkina Faso. J Microbiol Immunol Infect. 2014;47(3):222–232. doi: 10.1016/j.jmii.2013.05.001. [DOI] [PubMed] [Google Scholar]
  • 11.Castelnuovo B. A review of compliance with anti-tuberculosis treatment and risk factors for defaulting treatment in sub Saharan Africa. Res Heal Sci 2010;10(April):320–324. Available from: https://www.researchgate.net/publication/50420790. [PMC free article] [PubMed]
  • 12.Alene KA, Viney K, Gray DJ, Mcbryde ES, Wagnew M, Clements ACA. Mapping tuberculosis treatment outcomes in Ethiopia. BMC Infect Dis. 2019;19(474):1–11. doi: 10.1186/s12879-019-4099-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Zegeye A, Dessie G, Wagnew F, Gebrie A, Islam SMS, Tesfaye B, et al. Prevalence and determinants of anti-tuberculosis treatment non-adherence in Ethiopia: a systematic review and meta-analysis. PLoS One. 2019;14(1):1–15. Available from: 10.1371/journal.pone.0210422. [DOI] [PMC free article] [PubMed]
  • 14.Eticha T, Kassa E. Non-adherence to anti-TB drugs and its predictors among TB/HIV co-infected patients in Mekelle, Ethiopia. J Bioanal Biomed. 2014;6(6):61–64. [Google Scholar]
  • 15.Adane AA, Alene KA, Koye DN, Zeleke BM. Non-Adherence to Anti-Tuberculosis Treatment and Determinant Factors among Patients with Tuberculosis in Northwest Ethiopia. PLoS One. 2013;8(11). [DOI] [PMC free article] [PubMed]
  • 16.Gube AA, Debalkie M, Seid K, Bisete K, Mengesha A, Zeynu A, et al. Assessment of anti-TB drug nonadherence and associated factors among TB patients attending TB clinics in Arba Minch governmental health institutions, southern Ethiopia. Hindawi Tuberc Res Treat. 2018;2018:7. Available from: 10.1155/2018/3705812%0AResearch. [DOI] [PMC free article] [PubMed]
  • 17.Federal MinistryHealth Ethiopia. Tuberculosis, Leprosy, and TB/HIV Prevention and Control Programme. Vol. Fourth Edi, Manual Fourth Edition. 2008.
  • 18.Amuha MG, Kutyabami P, Kitutu FE, Odoi-adome R, Kalyango JN. Non-adherence to anti-TB drugs among TB / HIV co-infected patients in Mbarara Hospital Uganda : Prevalence and associated factors. Afr Health Sci. 2009;9(Special Issue1):8–15. [PMC free article] [PubMed]
  • 19.Zhou C, Chu J, Liu J, Tobe RG, Gen H, Wang X, et al. Adherence to Tuberculosis Treatment among Migrant Pulmonary Tuberculosis Patients in Shandong , China : A Quantitative Survey Study. PLoS One. 2012;7(12):1–6. doi: 10.1371/journal.pone.0052334. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Tola HH, Tol A, Shojaeizadeh D. Tuberculosis treatment non-adherence and lost to follow up among TB patients with or without HIV in developing countries : a systematic review. Iran J Public Heal. 2015;44(1):1–11. [PMC free article] [PubMed] [Google Scholar]
  • 21.Lauritsen JM, Bruus M. EpiData Help File v3.1. EpiData Assoc Odense Denmark [Internet]. 2004; Available from: www.epidata.dk.
  • 22.Mallery DG and Mallery P. IBM SPSS Statistics 23 [Internet]. 2016. Available from: https://www.ibm.com/support/pages/how-cite-ibm-spss-statistics-or-earlier-versions-spss.
  • 23.Deshmukh RD, Dhande DJ, Sachdeva KS. Patient and provider reported reasons for lost to follow up in MDRTB treatment : a qualitative study from a drug-resistant TB Centre in India. PLoS One. 2015;10(8):1–11. doi: 10.1371/journal.pone.0135802. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Malede A, Shibabaw A, Hailemeskel E, Atnafe SA. Treatment Outcome of Tuberculosis Patients and Associated Risk Factors at Dessie and Woldiya Town Health Institutions, Northeast Ethiopia : J Bacteriol Parasitol. 2017;(August).
  • 25.Berhe G, Enquselassie F, Aseffa A. Treatment outcome of smear-positive pulmonary tuberculosis patients in Tigray region. Northern Ethiopia: BMC Public Health; 2012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Ejeta E, Beyene G, Balay G, Bonsa Z, Abebe G. Factors associated with unsuccessful treatment outcome in tuberculosis patients among refugees and their surrounding communities in Gambella regional state. PLoS One. 2018;13(10):1–15. doi: 10.1371/journal.pone.0205468. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Ibrahim LM, Hadejia IS, Nguku P, Lakda GM, Ogiri S. Factors Associated with Outcomes of Treatment among Pulmonary Tuberculosis Patients in Plateau State, Nigeria, 2011. J US-China Med Sci 12. 2015;12:172–179. [DOI] [PMC free article] [PubMed]
  • 28.Leung CC, Yew WW, Chan CK, Chang KC, Law WS, Lee SN, et al. Smoking adversely affects treatment response, outcome, and relapse in tuberculosis. Eur Respir J. 2015;45(3):738–745. doi: 10.1183/09031936.00114214. [DOI] [PubMed] [Google Scholar]
  • 29.Valencia S, León M, Losada I, Sequera VG, Fernández Quevedo M, García-Basteiro AL. How do we measure adherence to anti-tuberculosis treatment? Expert Rev Anti Infect Ther. 2017;15(2):157–165. doi: 10.1080/14787210.2017.1264270. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Additional file 1 (26.4KB, docx)

Questionnaire for the study.

Data Availability Statement

The data used to support the findings of this study are not publicly available due to restrictions on the publication of human subjects’ data but these data can be available from the corresponding author upon reasonable request.


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