Background
Tuberculosis is a major public health problem in Ethiopia, with an estimated incidence of 379 per 100 000 and a prevalence of 643 per 100 000 [
1]. According to hospital statistics data, TB is the leading cause of morbidity, the third cause of hospital admission and the second cause of death in Ethiopia [
2]. There is a high rate of HIV among patients with TB in Ethiopia. The WHO Global Report 2008 estimated that 40% of patients treated for TB are HIV positive [
2].
Effective treatment exists for both TB and HIV. Evidence shows that ART treatment can have a significant impact on the HIV and TB related morbidity and mortality in co-infected patients; but concomitant treatment is complicated by factors such as overlapping drug toxicities, drug-drug interactions and possible paradoxical reactions [
3‐
7]. Concomitant treatment also leads to a higher pill burden. There is an association between poor adherence and the pill burden associated with a regimen, the regimen's complexity, and the extent to which the regimen impacts on the patient's daily life [
8‐
11]. Co-infected patients on concomitant treatment may thus be at risk for decreased adherence to either or both treatments. Low adherence to TB treatment can lead to an increased risk of drug resistance, relapse, death, and may prolong infectiousness [
12].
Adherence is defined by WHO as "the extent to which a person's behavior- taking medication, following a diet, and or executing lifestyle changes, corresponds with agreed recommendations from a health care provider" [
13]. Adherence it is a concept that allows for a comprehensive assessment of factors related to medication intake such as characteristics of the regimen; attitudes of the providers; socio-economic, cultural and environmental factors [
14,
15].
Studies of patients' adherence to TB treatment in Ethiopia have identified socio-economic and structural barriers to adherence, including lack of money to pay for transportation, high distance from clinics, the difficulties associated with daily treatment and rigid routines at health facilities [
12,
16‐
23]. Inadequate knowledge about the illness was also found to adversely impact adherence. The studies also showed that family support, involvement in TB clubs, and adequate knowledge about the disease were facilitators of TB treatment adherence [
12,
16‐
23].
To our knowledge, no study has explored the experiences of TB/HIV co-infected patients receiving concomitant treatment in Ethiopia. How concomitant treatment affects TB treatment adherence has similarly not been explored. A review of qualitative studies of factors considered as important by patients, caregivers and health care providers for TB medication adherence indicated a lack of evidence on the experiences of patients living with HIV/AIDS and taking treatment for TB or for both illnesses [
11]. There is a need for more knowledge about factors influencing treatment adherence in co-infected patients on concomitant treatment. We thus conducted a study to explore patients' and health care professionals' views about barriers and facilitators to TB treatment adherence in co-infected patients who received concomitant treatment for TB and HIV.
Methods
Setting
The study was conducted in Addis-Ababa, the capital city of Ethiopia, in the period July 2008 to October 2008. The health service coverage in Addis-Ababa, with regards to geographical accessibility, is 100% [
24]. Out-patient TB treatment is mainly provided by governmental health centers. These health centers are administered by the Addis Ababa Health Bureau and provide medical services for the populations within their catchments areas. TB clinics have been operating for many years in local health centers, and ART clinics were established in 2006, as part of the expansion of HAART provision program initially started in hospitals [
25]. The health centers offer free ART service and care for patients with HIV infection. In addition to diagnosis and treatment of patients with TB, the TB clinics also offer the Provider Induced Counseling and Treatment (PICT) service through which all patients coming to the TB clinics are offered screening for HIV. Both TB and ART treatments are offered free of charge in these health centers. The different health centers in general do not have significant differences in terms of services they provide and in terms of health personnel and equipments available.
Participants
We collected data using in-depth interviews and focus group discussions. We conducted individual interviews with 15 patients (7 men, 8 women) who had been on concomitant treatment for TB and HIV, and we interviewed nine health professionals (6 clinical nurses, 2 health officers and 1 doctor) who were involved in the treatment of these patients. We conducted a preliminary analysis of our in-depth interviews, identifying major themes emerging from our data. We subsequently conducted two focus group discussions with a total of 14 patients (7 men, 7 women), in order to further explore and validate our preliminary findings from the in-depth interviews. Participants were recruited from three out of 21 health centres: Bole Health Center, Arada Health Center and Woreda 7 Health Center.
We used a maximum variation sampling strategy when recruiting participants, to ensure diversity in views and experiences. We thus included participants with diversity with regards to age, gender, education, and occupation. In addition, we included patients for whom ART was started at different stages during TB treatment (before anti-TB initiation, in intensive phase, in continuation phase). We ensured diversity of treatment experiences by interviewing an equal number of patients who had defaulted treatment and with successful treatment; we also included three patients who were on retreatment.
Patients with pre-specified characteristics were invited to participate in the study through an invitation letter provided by health personnel. Patients who had defaulted treatment were contacted by health personnel on our behalf while being traced after treatment discontinuation at the TB clinics and two were contacted through personnel at the ART clinic. Only one patient declined to participate in the study. Health personnel were directly invited by the first author (MK) to participate in the study. We interviewed patients who had either completed or discontinued treatment in the past six months before data collection.
Data collection
Audio-recorded individual interviews and focus group discussions were conducted by MK in Amharic. Individual interviews took place in private rooms, and a semi-structured format with open-ended questions was used. The questions covered participants' perceptions about TB, HIV and co-infection; experiences of concomitant medication intake; factors positively and adversely influencing TB medication intake while on concomitant ART treatment; and experiences at both TB and HIV clinics. Similar topics were covered in the focus group discussions, and issues that arose in the interviews were brought up for further discussion. We used this triangulation of data sources in order to increase the validity of findings in our study.
We developed a semi-structured interview guide for patients that was inspired by a theoretical framework for health related behaviors, in which the following six major categories are essential: accessibility of health care; evaluation of health care; perception of symptoms and threat of disease; social network characteristics; knowledge about disease; demographic characteristics [
26]. The interview guide was also inspired by further review of literature on adherence which indicates the importance of other factors such as regimen related factors and health service related factors [
8‐
11,
27].
We developed an interview guide for health workers, and we explored their experiences with adherence to treatment in co-infected patients on concomitant treatment, with a focus on barriers and facilitators to adherence. Other questions such as what they do to try and assist patients with adherence, what they would recommend would assist patients with their medication intake were also included.
Data analysis
Audio-recorded data from interviews of patients was transcribed verbatim and translated into English. A preliminary analysis of interviews was done, and used for validation of results and further exploration using focus group interviews. Data from health worker interviews and focus group discussions which were also audio-recorded were also transcribed verbatim and translated into English.
The final analysis involved identification and coding of material about participants' perceptions about TB and HIV, perceived barriers and facilitators of TB treatment adherence using Giorgi's phenomenological method, as modified by Malterud [
28]. MK read the material to get an overview and subsequently identified units of meaning that represent different aspects of participants' perceived barriers and facilitators to adherence. MK and the third author (JCF) agreed on a list of codes and then MK coded the material. All authors participated in condensing and summarizing the content of each code in order to make generalized descriptions concerning barriers and facilitators to TB treatment.
Ethics
Informed consent was obtained from all participants prior to data collection. Anonymity and confidentiality were ensured. The study has been approved by the Regional Committees for Medical and Health Research Ethics (REK) in Norway and was granted ethical clearance by Addis Ababa Health Bureau in Ethiopia.
Results
We found that interplay of factors is involved in the decision making about medication intake. Factors that influenced adherence to TB treatment positively were beliefs in the curability of TB, and in the severity of TB in the presence of HIV infection, support from families and health professionals. Barriers to treatment adherence were experiencing side effects, pill burden, economic constraints, stigma with lack of disclosure, and lack of adequate communication with health professionals. Table
1 presents a summary of study findings and their relationship to categories from our theoretical framework.
Table 1
Relationship between study findings and categories from theoretical framework
Accessibility of health care | Challenges of DOT |
Evaluation of health care | Interaction with health personnel |
Perception of symptoms and threat of disease | Beliefs about TB, TB treatment and co-infection |
Social network characteristics | Social support, Stigma |
Knowledge about disease | Beliefs about TB and co-infection |
Demographic characteristics (social status, income and education) | Lack of food (poverty related) |
Regimen factors | Pill burden, Side effects |
Health care related factors | Interaction with health personnel, Challenges of DOT |
Beliefs about TB, TB treatment and co-infection
A majority of patients explained that TB could be cured, despite the presence of a concomitant HIV infection; but many also thought that it was more difficult to be cured when one had HIV. "Weakening" of the body by HIV was mentioned by one group of participants who explained that the two diseases "support each other" to weaken the body.
"If you have HIV, TB can be strong, because they can collide. If you do not have HIV, TB will disappear soon. Like any person who has TB, you take your drug, and it disappears, but if you have HIV, it will not disappear fast." (20 year-old female participant)
This in turn was mentioned by patients as being a reason to take TB medications properly when one was infected with HIV. A woman explained:
"You have to take what the doctors give you, you can not stop that. You can only live if you take the drugs. Two diseases, it will kill you at once, your body can not support that. We are different from those who have TB only." (50 year-old female participant)
Health professionals underlined the presence of this belief among patients, and said that many patients co-infected with TB and HIV are motivated to take their TB treatment properly because of the fear of getting severe TB symptoms because of the HIV.
There were divergent views among patients about which disease they thought was the most severe when comparing TB and HIV. One group mentioned HIV as being the most serious illness that they feared more, while another group thought that TB was more dangerous. Patients' views about severity affected the decision about which drugs to discontinue for those patients who decided to take one of the drugs and stop the other. A 36 years old male defaulter explained the reason why he decided to discontinue his anti-TB drugs and continue with the ART after experiencing side effects aggravated by lack of food:
"I have to take at least one of the drugs. I wanted to survive. I said, I will take the HIV drugs only. Interviewer: Why the HIV drugs and not the TB drugs? The HIV, it will kill you, it will kill you fast. Samba (TB) will not kill me if I take these drugs (ARV drugs) properly." (36 year-old male participant)
A factor that most health professionals believed helped patients to gain hope was the improvement they observed in other patients who had previously been critically ill. According to health professionals, that helped patients believe in the efficacy of treatment and hence gave them hope for themselves. A medical doctor stated:
"I think many patients are encouraged to come because they see critically ill patients with co-infection who have improved. That gives them a lot of hope." (medical doctor)
Pill burden and side effects
Patients mentioned pill burden as being one of the major challenges of concomitant treatment, and they used expressions such as "becoming a drug bag", and "becoming a pharmacy". In addition to anti-TB drugs and ARV drugs, patients were also taking co-trimoxazole for PCP prophylaxis; and some in addition had to take drugs for other illnesses. From the perspective of some patients, a high number of pills was associated with potential damage to the body and a higher risk of not tolerating the drugs.
"Swallowing so many drugs, it was very difficult. I was scared that it would harm my body. Drugs can harm you if they are too many." (36-year-old male participant)
This belief was reinforced by some health professionals, as noted by a medical doctor:
"When they think about pill burden, they say, can I tolerate this, won't this kill me? Taking many pills is perceived as lethal by some. Patients worry a lot about whether their body will be able to handle so many pills every day." (medical doctor)
Forgetfulness and mix up of drugs as a result of high pill burden were also reported by some patients.
Side effects were experienced by more than half of the participants, mainly at the beginning of anti-TB treatment or upon initiation of concomitant treatment. Among side effects patients mentioned were generalized body weakness, burning of the stomach, "turning of the head", headache, bad dreams, rash and vomiting. A 57 year-old male participant who discontinued both his anti-TB and ART treatment after experiencing severe side effects explains:
"I continued the drugs but the nightmares and the hunger became too much. And then, I don't really even know how, my mind was also disturbed, so I took the drugs for some time, and stopped all drugs. You know the nightmare! And since I had no one beside me, and since the medications were disturbing me at night, and since it was pushing me to run away, I got scared and stopped the drugs." (57 year-old male participant)
Lack of food
The majority of patients believed that lack of food or intake of inadequate food was associated with more severe side effects and a difficulty to tolerate the drugs. The amount and quality of food needed and the degree of possible side effects were also believed by some patients to be proportional to the drugs taken. Lack of food was mentioned as a factor adversely affecting their treatment by those patients who had insufficient income. Patients mentioned drugs could be harmful on an empty stomach, and that it was better not to take drugs if one had not eaten. Health professionals recognized the problem of food as being common, especially with the gain in appetite related to improvement. A clinical nurse explained:
"That (food) is a very serious problem for many of our patients. They almost want to kill us wanting help. They come here asking for help from NGOs. They say that especially TB drugs increase appetite. They feel hungry after they start feeling well a bit, and food becomes a problem." (nurse)
Interaction with health personnel
The majority of patients in the study were happy about the way health professionals received and treated them at the health centers. Some said they were encouraged to come for treatment because health professionals were receiving them with a "good face", and were encouraging them to finish their treatment. A patient explained the support she received from health professionals:
"They [health professionals] were very good to me. They are like friends, did you not see? Since my head was not good, they were giving me the drugs in a certain way, in a bag, so that I know which drug to take when, they translated it in Amharic for me. They gave me a watch, they helped me a lot. They were like relatives. I have no words to thank them. I am standing today because of them. They told me what drugs to take at what time." (20 years old female patient)
When being asked about whether they received information about TB, or about the drugs and potential side effects, patients often replied that they did not get information. A patient said:
"Someone might be kind, that is not because they always give me drugs, they should also ask me what did it cause on you, is it good, did it cause any harm, what can we do for you? They have to say this. I come, they see my card, I get my drugs, and I go. That's all. Someone might be good naturally, but when I see from profession, it is less than I expected." (male focus group participant)
Few patients had asked health professionals at the TB clinics the information they needed. Those who asked questions tended to be more educated in general. For most of the other patients, the information that they had about TB and its treatment came from the community, from other patients at the health centers and mainly from the media. But many patients said that they were given information regarding ART and its side effects at the ART clinics. Health professionals said that adherence counseling is critical for patients, and that patients should be evaluated for their drug intake every time they come for a visit. Some nevertheless said that it had been difficult to do so, mainly because of time constraints. A clinical nurse said:
"What we do is not enough. The counseling should be done every time they come for treatment. Sometimes, we just give them their drug and send them home. You do not even know if they are taking the drugs the right way." (clinical nurse)
The challenges of DOT
The majority of patients said that DOT with daily supervision of treatment for the first two months is a very difficult task to accomplish. The initial phase of treatment during which daily supervision is made was the phase when many patients were ill and weak, and for such patients, it meant that they often had to come to the clinic accompanied by their families. This meant that families were also bearing the burden of treatment. In addition to physical weakness, transport costs were also a problem for many patients who had financial difficulties:
"I had to come every day for injections. I tell you the truth, there was a time when I had to sell my jewellery: my rings, my necklace, everything. I had to run here without even eating breakfast." (35 year-old female patient)
DOT was particularly problematic for those patients who had irregular jobs and who had to go looking for a job on a daily basis. A 36 year-old daily laborer explained his situation:
"I have to go in the morning. We stand at the roundabout and wait for someone to give us a job. If I don't go, someone else will take it. It will not stand and wait for me." (36 year old male patient)
All health professionals agreed that DOT with daily supervision is a difficult task for most of their patients, and in particular co-infected patients who needed to attend the clinics for ART as well. Most believed that DOT is too rigid, and some stated that something needs to be done to modify the daily schedule into a better schedule for patients. A medical doctor explains:
"Asking a person to come every day is a punishment. We should change something; find a certain schedule, for example weekly for the first month." (medical doctor)
Timing of ART
Participants in this study had started ART at different phases during TB treatment. Some were initiated on ART in the intensive phase of TB treatment, some in the continuation phase, and a few were already on ART when they were started on treatment for TB. Patients who had been told by health professionals that ART would be delayed until the end of the intensive phase of TB treatment were positive about this, since they had fears and doubts about starting concomitant treatment immediately. One group believed that their body would "adapt" to the TB drugs with time, and it will make it easier for them to tolerate the ART, hence allowing them to follow both treatments properly. Three of the patients who had defaulted treatment in this study said that initiation of ART in the intensive phase of their TB treatment had been too difficult, and that they were unable to tolerate treatment. They said that delaying the ART would have been better in their cases. A 36 years old male defaulter who had discontinued both anti-TB and ART drugs explained:
"It is better to take one drug and then the other drug. Your stomach can tolerate it. Your body can tolerate it. Together, it is too much. That is why I stopped my drugs." (36 year-old male participant)
Stigma
Many patients believed that they were predisposed to stigma because of TB. For many of these patients, that was mainly due to the fact that people associated TB with HIV. Many had seen other HIV patients suffering from stigma and discrimination in their communities, and feared that the same might happen to them. Some shared their experiences, such as being pointed at in their neighborhoods, neighbors gossiping about their illness behind their backs and exclusion from social events. Some patients said the stigma was directly related to the TB because they were believed to be infectious. These actual experiences and anticipations of stigma resulted in many patients hiding their diagnosis of TB or only disclosing it to selected people, mostly close families. A male focus group participant said:
"Before, I knew a lot of people with TB who did not have HIV. But now, if you say you have TB, people will take it to HIV. Me, even when I take these TB drugs, I don't tell to anyone." (male focus group participant)
Fear of stigma not only lead to such patients not disclosing their illnesses but also made seeking TB treatment in their catchments areas difficult as mentioned earlier, for fear of being identified by neighbors:
"I don't want neighbors to see me here [at the TB clinic]. One day, I saw this girl from my neighborhood here; I was sitting outside and waiting. I wished the earth would open and swallow me. I know she would spread the gossip. I tried to hide behind the man sitting next to me. I don't think she saw me." (36 years old male patient)
This fear was confirmed by many health professionals who explained that they have faced difficulties with patients who do not want to receive treatment in the health centers located in their vicinity, for fear of being identified by neighbors.
Social support
Social support was found to be crucial for patients' treatment. Some patients had been seriously ill when treatment was initiated and needed someone to accompany them for treatment. In addition, families provided food and transportation money since some patients had no income and others had to stop working for some time. Families were also a source of encouragement and comfort for those patients who had lost hope.
"My family members supported me a lot. They encouraged me. After the TB, when they found the HIV, I wanted to die. I did not want to live. But my families, especially my brothers and sisters, they said: you are not the only one. Look, many people have this. It is because of them that I am alive today." (female focus group participant)
Some health professionals also noted that patients who had family support and come to the clinics accompanied are usually those who successfully complete their treatment.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
MK designed the study in collaboration with GAB and JCF. MK collected the data. MK coded the data and all authors contributed in the subsequent analysis. All authors have critically revised the manuscript.