Skip to main content
Erschienen in: BMC Public Health 1/2015

Open Access 01.12.2015 | Research article

Tuberculosis retreatment ‘others’ in comparison with classical retreatment cases; a retrospective cohort review

verfasst von: Mary G. Nabukenya-Mudiope, Herman Joseph Kawuma, Miranda Brouwer, Peter Mudiope, Anna Vassall

Erschienen in: BMC Public Health | Ausgabe 1/2015

Abstract

Background

Many of the countries in sub-Saharan Africa are still largely dependent on microscopy as the mainstay for diagnosis of tuberculosis (TB) including patients with previous history of TB treatment. The available guidance in management of TB retreatment cases is focused on bacteriologically confirmed TB retreatment cases leaving out those classified as retreatment ‘others’. Retreatment ‘others’ refer to all TB cases who were previously treated but with unknown outcome of that previous treatment or who have returned to treatment with bacteriologically negative pulmonary or extra-pulmonary TB. This study was conducted in 11 regional referral hospitals (RRHs) serving high burden TB districts in Uganda to determine the profile and treatment success of TB retreatment ‘others’ in comparison with the classical retreatment cases.

Methods

A retrospective cohort review of routinely collected National TB and Leprosy Program (NTLP) facility data from 1 January to 31 December 2010. This study uses the term classical retreatment cases to refer to a combined group of bacteriologically confirmed relapse, return after failure and return after loss to follow-up cases as a distinct group from retreatment ‘others’. Distribution of categorical characteristics were compared using Chi-squared test for difference between proportions. The log likelihood ratio test was used to assess the independent contribution of type of retreatment, human immunodeficiency virus (HIV) status, age group and sex to the models.

Results

Of the 6244 TB cases registered at the study sites, 733 (11.7 %) were retreatment cases. Retreatment ‘others’ constituted 45.5 % of retreatment cases. Co-infection with HIV was higher among retreatment ‘others’ (70.9 %) than classical retreatment cases (53.5 %). Treatment was successful in 410 (56.2 %) retreatment cases. Retreatment ‘others’ were associated with reduced odds of success (AOR = 0.44, 95 % CI 0.22,0.88) compared to classical cases. Lost to follow up was the commonest adverse outcome (38 % of adverse outcomes) in all retreatment cases. Type of retreatment case, HIV status, and age were independently associated with treatment success.

Conclusion

TB retreatment ‘others’ constitute a significant proportion of retreatment cases, with higher HIV prevalence and worse treatment success. There is need to review the diagnosis and management of retreatment ‘others’.
Hinweise
Herman Joseph Kawuma Peter Mudiope and Anna Vassall contributed equally to this work.

Competing interests

The authors declare no conflict of interest.

Authors contributions

Substantial contributions to conception and design, acquisition of data or analysis and interpretation of data (MGN, HJK, PM, AV). Manuscript writing and revising for intellectual content and approval for journal submission (MGN, HJK, MB, PM, AV). All authors read and approved the final manuscript.
Abkürzungen
AFB
Acid fast bacilli
AOR
Adjusted odds ratio
ART
Antiretroviral therapy
CI
Confidence interval
CPT
Cotrimoxazole preventive therapy
DST
Drug susceptibility testing
DTLS
District TB and Leprosy supervisor
E
Ethambutol
H
Isoniazid
HIV
Human immunodeficiency virus
LFTU
Lost to follow up
LSHTM
London School Of Hygiene and Tropical Medicine
MTB/RIF
Mycobacterium tuberculosis and rifampicin-resistance mutations
NTLP
National Tuberculosis and Leprosy Programme
OR
Odds ratio
R
Rifampicin
RRHs
Regional referral hospitals
S
Streptomycin
TB
Tuberculosis
WHO
World Health Organization
Z
Pyrazinamide
ZN
Ziehl Neelsen

Background

The World Health Organization (WHO) treatment guidelines recommend that all previously-treated TB patients should be managed according the TB retreatment category, while their sputum is cultured and tested for drug susceptibility (DST) [1]. However, few countries have the required laboratory capacity to improve access to DST services to all TB retreatment patients. Therefore, many countries remain unclear on the best management of TB retreatment cases. Of particular concern is the category of TB patients classified as retreatment ‘others’. These refer to all TB cases, previously treated but with unknown outcome of that previous treatment or who return for treatment with bacteriologically negative pulmonary or extra-pulmonary TB. This study uses the term classical retreatment cases to refer to all bacteriologically confirmed relapse, return after failure and return after lost to follow-up (LTFU) cases as a distinct group from retreatment ‘others’.
Uganda has limited capacity to conduct culture and DST investigations in TB retreatment patients. A study conducted in three regional referral hospitals (RRHs) in Uganda showed that only 13 % of 114 registered relapse smear-positive or treatment after failure cases had their sputum samples sent to National TB Reference Laboratory for culture and DST [2]. Since 2002, Uganda has notified an increasing number of TB retreatment cases from 1500 to about 4000 cases per year [3]. Of the 47,650 total TB cases Uganda notified to the WHO in 2013, 4028 (8.5 %) were TB retreatment cases [4]. TB retreatment ‘others’ constituted a third of the total retreatment cases notified in 2012 [3].
An important step in understanding how to manage retreatment ‘others’ is to better understand their outcomes. Previous studies in other settings have observed different treatment outcomes, HIV status and management approaches between classical TB retreatment cases and retreatment ‘others’ [57]. A study in India found that retreatment ‘others’ significantly had better treatment outcomes than classical retreatment cases [7]. Another study in Zimbabwe found that retreatment ‘others’ constituted 40 % of recurrent TB with no difference in treatment outcomes by HIV status [6]. 65 % of retreatment cases in Malawi were retreatment ‘others’ with over half of them treated with standard TB regimen for new cases [5]. This study seeks to add this emerging evidence base on how this group of patients differs by setting, to answer the following research question: what is the profile and treatment success of TB retreatment ‘others’ compared to the classical retreatment cases in Uganda?

Methods

A retrospective hospital-based review of routinely collected TB data on TB retreatment patients started on TB treatment from 1st January to 31st December 2010. The data were extracted between May and June 2012.

Study setting

This study was conducted in 11 RRHs of Uganda serving mostly districts with high TB burden. In 2009, it was observed that districts with RRHs notified an average of 114 retreatment cases each compared to an average of 32 retreatment cases notified by districts without RRHs (unpublished NTLP reports). The study thus systematically selected 11 high burden RRHs based on the burden of TB. The study sites were: Arua, Fort-Portal, Gulu, Hoima, Jinja, Kabale, Lira, Masaka, Mbarara, Mbale and Soroti RRHs.

Case definitions and treatment of retreatment TB patients

In Uganda, a TB retreatment case is defined as a person previously treated with anti-TB drugs for a month or more and is being treated again, in line with WHO definitions [1, 8]. The retreatment category is further classified either as ‘relapse’, ‘treatment after failure’, ‘return after LTFU’ or ‘others’. Relapses are patients who become bacteriologically positive after having been treated for TB and declared cured or treatment completed. Treatment after failure are patients who, while on first line anti-TB treatment are bacteriologically positive at 5 months or later during the course of treatment. Return after LTFU patients are those who return to treatment and are bacteriologically positive after having interrupted treatment for more than 2 months. Retreatment ‘others’ refer to all TB cases that do not fit the above definitions such as patients with history of TB treatment for a month or more but with no bacteriological confirmation of TB for the current episode.
In line with WHO definitions, Ugandan NTLP classifies treatment outcomes as; cured, treatment completed, treatment failure, died, LTFU and transferred-out. Treatment success refers to a combination of cured and treatment completed. In this study, adverse outcome refers to a combination of LTFU, died, treatment failure and transferred-out.
The retreatment regimen in Uganda consists of two (2) months streptomycin (S), rifampicin (R), isoniazid (H), pyrazinamide (Z), and ethambutol (E). This is followed by one (1) month RHZE and five (5) months RHE. The retreatment regimen(2SRHZE/1RHZE/5RHE) is recommended for all bacteriologically positive TB retreatment cases [1, 8]. Both NTLP and WHO guidelines are silent on the management of TB retreatment ‘others’ in settings with limited TB DST capacity. In Uganda, it is at the discretion of the clinician to decide the TB treatment regimen to use in the management of retreatment ‘others’. At the time of the study, routine culture and DST for retreatment cases had been rolled out to the study sites with varying levels of implementation [2].

Study variables, source of information and data collection

Records of routinely collected variables within the hospitals’ unit TB registers that were analyzed included: patient demographic (age and sex); clinical (disease classification, pre-treatment smear status and HIV status); treatment-related (type of retreatment and treatment regimen) characteristics and treatment outcomes. In Uganda, each TB patient is registered in the unit TB register by the health facility staff at the start of treatment and individual patient records updated at every visit during the course of treatment. The district TB and Leprosy supervisor (DTLS) enters TB patients registered on treatment from all TB diagnostic and treatment health facilities within that particular district into the district TB register. Information on patients that transferred to other facilities within the same district is captured by the DTLS and conveyed back to the registering facility. More information on patients transfers between districts in the same zone is exchanged during quarterly zonal performance reviews attended by DTLSs before compiling quarterly district TB and Leprosy reports on notification and treatment outcomes. At the time of the study, the reporting unit at the NTLP central unit was the district. Using an anonymous standardized data collection tool, study variables were extracted from the hospital’ TB unit registers by one trained research assistant and all entries were verified by the first author. The respective district TB registers were used to ascertain definitive patient treatment outcomes that were missing in the unit registers.

Data entry and analysis

Data was entered into EpiData version 3.1 (The EpiData Association, Odense, Denmark)and analyzed in STATA version 11.2 (Stata Corp, College Station, TX, USA).
HIV status was categorized into positive, negative and unknown. Age was categorized using cut offs that made meaningful differences between the categories. Descriptive analysis of patient characteristics was computed. Distribution of patient characteristics by type of retreatment cases (classical vs. retreatment ‘others’) was computed. The differences in distribution of categorical characteristics were compared using Chi-square test for difference between proportions at a significance level of P-value equal to 0.05.
Treatment outcome was analyzed as a binary variable of success versus all other outcomes. Odds ratio was the measure of association. Logistic regression was used to identify patient characteristics that were independently associated with treatment success. Characteristics that had P-value equal or less than 0.05 at bivariate level were assessed further in a multivariate model. In the multivariate analysis, characteristics that were not significant at p-value equal or less than 0.05 were dropped. The multivariable model was determined using forward regression with a two-sided P-value equal or less than 0.05. Sex was included as a priori in the final model. The log likelihood ratio test was used to assess the independent contribution of explanatory variables to the models.

Ethical approval

As this study was a review of routinely collected NTLP data at RRHs, approval was obtained from Ministry of Health and Joint Clinical Research Centre Institutional Review Board as the local ethical body. The protocol was also approved by London School of Hygiene Tropical Medicine ethics review committee.

Results

Of the 6244 TB cases registered at the 11 RRHs, 733 (11.7 %) were retreatment cases (Fig. 1). Three retreatment cases were excluded from subsequent analyzes due to contradictory records. Table 1 shows that majority of retreatment cases were males (71.6 %) and in age group 15–44 years (70 %). Overall, 690 (94.5 %) retreatment cases had a documented HIV test result.
Table 1
Frequency of retreatment TB patients’ characteristics and their distribution by type of retreatment cases registered at the eleven RRHs, 2010 (n = 730 cases)
Characteristic
All retreatment cases
Type of retreatment cases
P-value*
 
Classical TB retreatment cases;
TB retreatment ‘others’;
n (%)
n = 398 (%)
n = 332 (%)
 
Sex
    
 Male
523 (71.6)
308 (77.4)
215 (64.8)
<0.001
 Female
207 (28.4)
90 (22.6)
117 (35.2)
 
Age (years)a
    
 <15
39 (5.4)
3 (0.8)
36 (10.8)
<0.001
 15-44
509 (69.8)
293 (73.8)
216 (65.1)
 
 >44
181 (24.8)
101 (25.4)
80 (24.1)
 
Anatomical site
    
 Pulmonary
689 (94.4)
398 (100.0)
291 (87.7)
<0.001
 Extrapulmonary
41 (5.6)
0 (0.0)
41 (12.3)
 
Disease classification
    
 Sputum smear-positive
400 (54.8)
398 (100.0)
2 (0.6)
<0.001
 Sputum smear-negative
267 (36.6)
0 (0.0)
267 (80.4)
 
 No smear done
22 (3.0)
0 (0.0)
22 (6.6)
 
 Extrapulmonary
41 (5.6)
0 (0.0)
41 (12.4)
 
HIV status
    
 Negative
266 (36.4)
174 (43.7)
92 (27.7)
<0.001
 Positive
424 (58.1)
200 (50.3)
224 (67.5)
 
 Unknown
40 (5.5)
24 (6.0)
16 (4.8)
 
Retreatment sub-category
    
 Sputum smear-positive relapse
196 (26.9)
196 (49.3)
0 (0.0)
<0.001
 Sputum smear-positive failure
44 (6.0)
44 (11.1)
0 (0.0)
 
 Sputum smear-positive return after LTFU
158 (21.6)
158 (39.7)
0 (0.0)
 
 Retreatment ‘others’
332 (45.5)
0 (0.0)
332 (100.0)
 
Treatment regimen
    
 Retreatment: 2SRHZE/1RHZE/5RHE
582 (79.7)
378 (95.0)
204 (61.5)
<0.001
 New: 2RHZE/6EH or 2RHZ/4RH
116 (15.9)
19 (4.8)
97 (29.2)
 
 Other regimenb
32 (4.4)
1 (0.2)
31 (9.3)
 
*P-values are from Pearson’s chi-squared test or Fisher’s exact test for the difference in the distribution of the categorical characteristics across the types of retreatment cases
a1 patient had missing data
bOther regimen included: 3RHZE/5RHE = 13; 2SRHZ/4-12RH = 14; 2SRHZE/6EH = 2; 3SRH/6RH = 1; unknown = 2
Retreatment ‘others’ constituted 45.5 % of retreatment cases. Like the classical retreatment cases, retreatment ‘others’ were mostly males (65 %), and in the age group 15–44 years (65 %). Significantly, lesser (62 %) of retreatment ‘others’ were treated with the standard retreatment regimen (2SRHZE/1RHZE/5RHE) compared to 95 % of classical retreatment cases. About a third of the retreatment ‘others’ were treated with the standard regimen for new TB patients.
Table 2 shows that HIV prevalence was higher among retreatment ‘others’ (70.9 %) than classical retreatment cases (53.5 %). HIV co-infection was 61.5 % among 690 retreatment patients that had a documented HIV test result. Females had a higher HIV prevalence (70.7 %) than males (57.8 %). Of the 424 patients with an HIV-positive test result, 385 (91 %) and 221 (52 %) were provided with Cotrimoxazole preventive therapy (CPT) and antiretroviral therapy (ART) respectively.
Table 2
Prevalence of HIV by patient characteristics, retreatment type among retreatment TB patients with known HIV test results at eleven RRHs, Uganda (n = 690)
Characteristic
Total
Classical retreatment cases
‘Others’ retreatment cases
P-value*
 
HIV Positive
 
HIV Positive
 
HIV Positive
n (%)
n (%)
n (%)
Overall
690
424b (61.4)
374
200 (53.5)
316
224 (70.9)
<0.001**
Sex
       
 Male
492
284 (57.8)
289
145 (50.2)
203
139 (68.5)
0.022
 Female
198
140 (70.7)
85
55 (64.7)
113
85 (75.2)
 
Age group, yearsa
       
 <15
35
24 (68.6)
3
2 (66.7)
32
22 (68.8)
<0.001
 15-44
488
316 (64.8)
277
157 (56.7)
211
159 (75.4)
 
 >44
166
83 (50.0)
94
40 (42.6)
73
43 (58.9)
 
Anatomical site
       
 Pulmonary
650
391 (60.2)
374
200 (53.5)
276
191 (69.2)
<0.001
 Extrapulmonary
40
33 (82.5)
0
0 (0.0)
40
33 (82.5)
 
Treatment regimen
       
 Retreatment: 2SRHZE/1RHZE/5RHE
553
329 (59.5)
357
192 (53.8)
196
137 (69.9)
<0.001
 New:2RHZE/6EH or 2RHZ/4RH
106
73 (68.9)
16
8 (50.0)
90
65 (72.2)
 
 Other regimen
31
22 (71.0)
1
0 (0.0)
30
22 (73.3)
 
*P-values are from either Pearson’s chi-squared test of Fischer’s exact tests for the difference between given characteristics and the type of retreatment among only HIV positive patients
**P-value from Z-test for two proportions
a1 patient had missing data on this variable
bCotrimoxazole preventive therapy and antiretroviral treatment were documented among 385 (91 %) and 221 (52 %) of all HIV positive TB retreatment patients respectively
Table 3 shows that treatment was successful in 410 (56.2 %) of the 730 retreatment cases. Adverse outcomes were; 16.4 % LTFU, 9.9 % died, 2.6 % failed on treatment while 5.1 % transferred-out and 9.9 % were not-evaluated. Table 4 shows that retreatment ‘others’ were associated with reduced odds of treatment success [odds ratio (OR) =0.65, 95 % CI 0.48, 0.87] compared to the classical retreatment cases. Anatomical site and treatment regimen were not associated with treatment success. Using multivariable analysis, odds of treatment success remained lower among retreatment ‘others’ compared to the classical retreatment cases after adjusting for age group, HIV status and sex (Adjusted OR (AOR)) = 0.60, 95% CI 0.44, 0.82). Unknown HIV status was significantly associated with lower odds of treatment success compared to known HIV status (AOR = 0.44, 95% CI 0.22, 0.88). Together with type of retreatment case, age group (less than 15 years) became significantly associated with treatment success (AOR = 2.32, 95% CI 1.12, 4.81).
Table 3
Outcomes of retreatment cases by WHO retreatment category
Type of retreatment
Treatment outcome
Adverse outcomes
Successful
Adverse
Failure
Died
LTFU
Transfer-out
Not -evaluated
n (%)
n (%)
n (%)
n (%)
n (%)
n (%)
n (%)
Smear-positive relapse: n = 196
134 (68.4)
62 (31.6)
9 (4.6)
9 (4.6)
23 (11.7)
7 (3.6)
14 (7.0)
Smear-positive return after failure: n = 44
30 (68.2)
14 (31.8)
4 (9.1)
3 (6.9)
5 (11.4)
0 (0.0)
2 (4.5)
Smear-positive return after LTFU: n = 158
79 (50)
79 (50.0)
3 (1.9)
19 (12)
26 (16.4)
12 (7.6)
19 (12.0)
Retreatment ‘others’: n = 332
167 (50.3)
165 (49.7)
3 (0.9)
41 (12.3)
66 (19.9)
18 (5.4)
37 (11.0)
Total; n = 730
410 (56.2)
320 (43.8)
19 (2.6)
72 (9.9)
120 (16.4)
37 (5)
72 (9.9)
P < 0.001 for the difference between the type of retreatment and treatment outcome using Pearson’s chi-squared test
Table 4
Patient characteristics associated with binary treatment success among TB retreatment cases registered in eleven RRHs of Uganda (n = 730)
Characteristics
Total
Treatment Success n (%)
Unadjusted OR (95 % CI)
P-value*
Adjustedb OR (95 % CI)
P-value*
Overall
730
410 (56.2)
    
Type of retreatment case
      
Classical retreatment cases
398
243 (61.1)
1.00
 
1.00
 
 Retreatment ‘others’
332
167 (50.3)
0.65 (0.48, 0.87)
0.004**
0.60 (0.44, 0.82)
0.001**
HIV status
      
 Positive
424
236 (55.7)
1.00
 
1.00
 
 Negative
266
159 (59.8)
1.18 (0.87, 1.62)
0.288
1.13 (0.82, 1.56)
0.452
 Unknown
40
15 (37.5)
0.48 (0.24, 0.93)
0.030**
0.44 (0.22, 0.88)
0.020**
Age groupa
      
 15-44
509
292 (57.4)
1.00
 
1.00
 
 <15
39
27 (69.2)
1.67 (0.83, 3.37)
0.143
2.32 (1.12, 4.81)
0.024**
 ≥45
181
90 (49.7)
0.73 (0.52, 1.03)
0.073
0.75 (0.53, 1.06)
0.102
Sex
      
 Male
523
296 (56.6)
1.00
 
1.00
 
 Female
207
114 (55.1)
0.94 (0.68, 1.30)
0.708
0.97 (0.69, 1.35)
0.844
Anatomical site
      
 Pulmonary
689
388 (56.3)
1.00
   
 Extrapulmonary
41
22 (53.7)
0.90 (0.48, 1.69)
0.739
  
Treatment regimen
      
 Retreatment: 2SRHZE/1RHZE/5RHE
582
322 (55.3)
1.00
   
 New: 2RHZE/6EH or 2RHZ/4RH
116
66 (56.9)
1.07 (0.71, 1.59)
0.756
  
 Other regimen
32
22 (68.8)
1.78 (0.83, 3.82)
0.137
  
*Wald P-value
**Significant at P = 0.05
a1 patient had missing data
bAdjusted for HIV status, age, and sex

Discussion

Retreatment ‘others’ constitute almost half of the retreatment cases in the RRHs of Uganda. Compared to the classical retreatment cases, more cases of retreatment ‘others’ were HIV positive. And more than a third of retreatment ‘others’ were not managed with the standard retreatment regimen. Fewer (half) retreatment ‘others’ succeeded on treatment (50.3 %) compared to six in ten of the classical retreatment cases (61.1 %). Lost to follow up was the commonest adverse outcome for both retreatment groups.
Nearly half of the retreatment cases in this study were retreatment ‘others’ compared to one in three cases notified nationally [3]. Probably, RRHs receive mostly very sick patients whose sputum is likely to test negative on Ziehl Neelsen (ZN) smear test due to their inability to mount an immune response and/ or produce sufficient sputum for microscopy. In addition, the TB diagnosis in RRHs is likely to be made by relatively highly qualified clinicians with capacity and/or bias to rely on their clinical acumen to diagnose TB even in the absence of a positive AFB sputum result. The presence of high TB-HIV co-infection rates in our study may account for the observed high proportion of retreatment ‘others’ [9]. The proportion of retreatment ‘others’ in this study is comparable to those from Zimbabwe and India [6, 7], but less than the proportion observed from a study conducted in a large registration centre of Malawi [5].
Overall, treatment success was low at 50 % in retreatment ‘others’ and 61 % in classical retreatment cases, compared to 71 % treatment success notified to WHO [3]. This study considered patients in referral hospitals who may be different from other TB patients from lower levels of care on a number of factors. Due to the referral cascade, patients with atypical forms of TB or drug-resistant TB are likely to be managed at RRHs and hence likely to exhibit poor treatment outcomes. However, the observed factors like the weakness in recording and reporting system, inability to track these patients (15 % of participants didn’t have definitive outcomes) and the low uptake of ART (52 %) among HIV co-infected patients may also explain the low treatment success. The 52 % ART uptake observed in the study population was higher than the national average of 24 % [10]. The difference between treatment success in this study and that reported to WHO may be because we evaluated all retreatment cases registered and not only classical retreatment cases that are routinely evaluated. Nonetheless, the results support previous findings from a smaller study conducted in three RRHs in Uganda [2].
The outcomes for retreatment ‘others’ in this study were worse than those of retreatment ‘others’ reported in India as compared to the classical retreatment cases [7]. This difference across settings may be influenced by factors such as difference in treatment regimens’ [5], drug resistance [11], co-morbidity [12], delay in diagnosis or even misdiagnosis [5, 13], adherence levels or having another pulmonary or extra-pulmonary disease for which they are not adequately treated.
Similar to the results reported in previous studies [5, 6], this study found that a higher proportions of retreatment ‘others’ were co-infected with HIV compared to the classical retreatment cases. Just like in other studies, we found that patients’ knowledge of their HIV status is beneficial [9, 14, 15]. 90 % of study participants that were found to be HIV-positive were started on CPT and half of them started on ART as well. The high uptake of HIV testing coupled with good initiation of CPT in this study could have resulted in observing no difference in treatment success between HIV-positive and negative patients. Age group and unknown HIV status were only significant independent predictors, but did not modify the effect of type of TB retreatment case on treatment outcome.
The findings of this study should be viewed with the following limitations. Firstly, this was a retrospective study utilizing hospital TB registers which could be prone to inaccuracies resulting from poor recording and completeness in the patient data and compromise the validity of the finding. However, this study found that 94.5 % of smear-positive retreatment cases had smear result correctly recorded. In addition, completeness of treatment outcomes was improved by use of the district TB registers whereby 28 % (176/621) of definitive outcomes among study participants were obtained.
We could not establish treatment outcomes in 15 % of the study participants even after reviewing district TB registers. There were no differences in patient characteristics between those who had complete information on the outcomes and those who had missing outcomes. However, the high proportion of missing treatment outcome could have introduced bias in determining treatment success or underreported deaths or LTFU among the study participants.
This study highlights the importance of ensuring appropriate management for retreatment ‘others’ given the relatively poor outcomes. A first key step is to ensure that this high number of retreatment ‘others’ is not a result of misdiagnosing drug-resistant TB or a false positive diagnosis of TB. More accurate TB diagnostic tools like the GeneXpert MTB/RIF that are currently available in all the study sites may have a role in providing access to a confirmation of TB in this special group.
Secondly, the continued notification of high proportions of retreatment ‘others’ to national authorities and Global TB Program calls for clear guidance on the management of retreatment ‘others’ including further definition of treatment regimen(s) in high HIV prevalence settings and limited TB diagnostic capacity. A future prospective study involving culture and drug-susceptibility testing could be conducted in programmatic settings to further understand the appropriate treatment regimens in such patients.
Thirdly, the observed high LTFU in the retreatment patients especially the retreatment ‘others’ calls for focused and innovative interventions to ensure treatment adherence in this group of patients. Social incentives and community outreach may have a role to play in reducing the loss to follow-up of these groups.
Fourthly, high HIV prevalence among retreatment cases especially the TB retreatment ‘others’ calls for better strategies of improving provision of the full range of TB/HIV collaborative services to reduce the burden of HIV in this group of patients.
Finally, further research is recommended at different levels of the TB treatment program to further clarify the importance of patient, health worker and system related factors on treatment success among retreatment cases to complement the findings of this study; and design the most appropriate response to ensure favorable outcomes from this underserved and evaluated group of TB patients.

Acknowledgements

This paper was extracted from results of a Master of Science in Public Health Project at University of London International Programmes and therefore thank the PH Project staff at London School of Hygiene and Tropical Medicine (LSHTM) who provided enormous support for the successful completion of this project.
The authors thank the Ugandan Ministry of Health, National Tuberculosis and Leprosy Programme and Directors of Arua, FortPortal, Gulu, Hoima, Jinja, Kabale, Lira, Masaka, Mbale, Mbarara and Soroti regional referral hospitals who granted permission to conduct this study.
The authors also thank the Zonal TB/Leprosy Supervisors (ZTLS), District TB/Leprosy Supervisors (DTLS) and the TB clinic staff who availed the source documents. The authors thank C Mpambaara who entered the data.
Funding for the study was provided through the German Leprosy and TB Relief Association (GLRA) Uganda Medical Advisors’ grant 2012.
Open AccessThis article is 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, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.

Competing interests

The authors declare no conflict of interest.

Authors contributions

Substantial contributions to conception and design, acquisition of data or analysis and interpretation of data (MGN, HJK, PM, AV). Manuscript writing and revising for intellectual content and approval for journal submission (MGN, HJK, MB, PM, AV). All authors read and approved the final manuscript.
Literatur
2.
Zurück zum Zitat Nakanwagi-Mukwaya A, Reid AJ, Fujiwara PI, Mugabe F, Kosgei RJ, Tayler-Smith K, et al. Characteristics and treatment outcomes of tuberculosis retreatment cases in three regional hospitals, Uganda. Public Health Action. 2013;3:149–55.CrossRefPubMedPubMedCentral Nakanwagi-Mukwaya A, Reid AJ, Fujiwara PI, Mugabe F, Kosgei RJ, Tayler-Smith K, et al. Characteristics and treatment outcomes of tuberculosis retreatment cases in three regional hospitals, Uganda. Public Health Action. 2013;3:149–55.CrossRefPubMedPubMedCentral
3.
Zurück zum Zitat World Health Organisation. G: Global Tuberculosis Report 2013.pdf. annual report. Geneva: World Health Organization; 2013. p. 133 [Communicable Diseases and Their Control]. World Health Organisation. G: Global Tuberculosis Report 2013.pdf. annual report. Geneva: World Health Organization; 2013. p. 133 [Communicable Diseases and Their Control].
5.
Zurück zum Zitat Tweya H, Kanyerere H, Ben-Smith A, Kwanjana J, Jahn A, Feldacker C, et al. Re-Treatment Tuberculosis Cases Categorised as “Other”: Are They Properly Managed? PLoS ONE. 2011;6, e28034.CrossRefPubMedPubMedCentral Tweya H, Kanyerere H, Ben-Smith A, Kwanjana J, Jahn A, Feldacker C, et al. Re-Treatment Tuberculosis Cases Categorised as “Other”: Are They Properly Managed? PLoS ONE. 2011;6, e28034.CrossRefPubMedPubMedCentral
6.
Zurück zum Zitat Takarinda KC, Harries AD, Srinath S, Mutasa-Apollo T, Sandy C, Mugurungi O. Treatment outcomes of adult patients with recurrent tuberculosis in relation to HIV status in Zimbabwe: a retrospective record review. BMC Public Health. 2012;12:124.CrossRefPubMedPubMedCentral Takarinda KC, Harries AD, Srinath S, Mutasa-Apollo T, Sandy C, Mugurungi O. Treatment outcomes of adult patients with recurrent tuberculosis in relation to HIV status in Zimbabwe: a retrospective record review. BMC Public Health. 2012;12:124.CrossRefPubMedPubMedCentral
7.
Zurück zum Zitat Srinath S, Sharath B, Santosha K, Chadha SS, Roopa S, Wares F, et al. Tuberculosis retreatment others: profile and treatment outcomes in the state of Andhra Pradesh, India. Int J Tuberc Lung Dis. 2011;15:105–9.PubMed Srinath S, Sharath B, Santosha K, Chadha SS, Roopa S, Wares F, et al. Tuberculosis retreatment others: profile and treatment outcomes in the state of Andhra Pradesh, India. Int J Tuberc Lung Dis. 2011;15:105–9.PubMed
9.
Zurück zum Zitat Maher D, Harries A, Getahun H. Tuberculosis and HIV interaction in sub-Saharan Africa: impact on patients and programmes; implications for policies. Trop Med Int Health. 2005;10:734–42.CrossRefPubMed Maher D, Harries A, Getahun H. Tuberculosis and HIV interaction in sub-Saharan Africa: impact on patients and programmes; implications for policies. Trop Med Int Health. 2005;10:734–42.CrossRefPubMed
10.
Zurück zum Zitat World Health Organization. Global Tuberculosis Control, WHO report 2011. 2011. World Health Organization. Global Tuberculosis Control, WHO report 2011. 2011.
11.
Zurück zum Zitat Temple B, Ayakaka I, Ogwang S, Nabanjja H, Kayes S, Nakubulwa S, et al. Rate and Amplification of Drug Resistance among Previously-Treated Patients with Tuberculosis in Kampala, Uganda. Clin Infect Dis. 2008;47:1126–34.CrossRefPubMedPubMedCentral Temple B, Ayakaka I, Ogwang S, Nabanjja H, Kayes S, Nakubulwa S, et al. Rate and Amplification of Drug Resistance among Previously-Treated Patients with Tuberculosis in Kampala, Uganda. Clin Infect Dis. 2008;47:1126–34.CrossRefPubMedPubMedCentral
12.
Zurück zum Zitat Lawn SD, Churchyard G. Epidemiology of HIV-associated tuberculosis: Curr Opin HIV. AIDS. 2009;4:325–33. Lawn SD, Churchyard G. Epidemiology of HIV-associated tuberculosis: Curr Opin HIV. AIDS. 2009;4:325–33.
13.
Zurück zum Zitat Harries AD, Nyirenda TE, Kemp JR, Squire BS, Godfrey-Faussett P, Salaniponi FML. Management and outcome of tuberculosis patients who fail treatment under routine programme conditions in Malawi. Int J Tuberc Lung Dis. 2003;7:1040–4.PubMed Harries AD, Nyirenda TE, Kemp JR, Squire BS, Godfrey-Faussett P, Salaniponi FML. Management and outcome of tuberculosis patients who fail treatment under routine programme conditions in Malawi. Int J Tuberc Lung Dis. 2003;7:1040–4.PubMed
14.
Zurück zum Zitat Golub JE, Durovni B, King BS, Cavalacante SC, Pacheco AG, Moulton LH, et al. Recurrent tuberculosis in HIV-infected patients in Rio de Janeiro, Brazil. AIDS. 2008;22:2527–33.CrossRefPubMedPubMedCentral Golub JE, Durovni B, King BS, Cavalacante SC, Pacheco AG, Moulton LH, et al. Recurrent tuberculosis in HIV-infected patients in Rio de Janeiro, Brazil. AIDS. 2008;22:2527–33.CrossRefPubMedPubMedCentral
15.
Zurück zum Zitat Harries AD, Zachariah R, Corbett EL, Lawn SD, Santos-Filho ET, Chimzizi R, et al. The HIV-associated tuberculosis epidemic—when will we act? Lancet. 2010;375:1906–19.CrossRefPubMed Harries AD, Zachariah R, Corbett EL, Lawn SD, Santos-Filho ET, Chimzizi R, et al. The HIV-associated tuberculosis epidemic—when will we act? Lancet. 2010;375:1906–19.CrossRefPubMed
Metadaten
Titel
Tuberculosis retreatment ‘others’ in comparison with classical retreatment cases; a retrospective cohort review
verfasst von
Mary G. Nabukenya-Mudiope
Herman Joseph Kawuma
Miranda Brouwer
Peter Mudiope
Anna Vassall
Publikationsdatum
01.12.2015
Verlag
BioMed Central
Erschienen in
BMC Public Health / Ausgabe 1/2015
Elektronische ISSN: 1471-2458
DOI
https://doi.org/10.1186/s12889-015-2195-2

Weitere Artikel der Ausgabe 1/2015

BMC Public Health 1/2015 Zur Ausgabe