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Epidemiology and Infection logoLink to Epidemiology and Infection
. 2017 Apr 11;145(9):1805–1814. doi: 10.1017/S0950268817000656

Risk factors for the treatment outcome of retreated pulmonary tuberculosis patients in China: an optimized prediction model

X-M WANG 1,, S-H YIN 1,, J DU 2,, M-L DU 1,*, P-Y WANG 3, J WU 4, C M HORBINSKI 5, M-J WU 5, H-Q ZHENG 1, X-Q XU 1, W SHU 2, Y-J ZHANG 6
PMCID: PMC9203337  PMID: 28397611

SUMMARY

Retreatment of tuberculosis (TB) often fails in China, yet the risk factors associated with the failure remain unclear. To identify risk factors for the treatment failure of retreated pulmonary tuberculosis (PTB) patients, we analyzed the data of 395 retreated PTB patients who received retreatment between July 2009 and July 2011 in China. PTB patients were categorized into ‘success’ and ‘failure’ groups by their treatment outcome. Univariable and multivariable logistic regression were used to evaluate the association between treatment outcome and socio-demographic as well as clinical factors. We also created an optimized risk score model to evaluate the predictive values of these risk factors on treatment failure. Of 395 patients, 99 (25·1%) were diagnosed as retreatment failure. Our results showed that risk factors associated with treatment failure included drug resistance, low education level, low body mass index (<18·5), long duration of previous treatment (>6 months), standard treatment regimen, retreatment type, positive culture result after 2 months of treatment, and the place where the first medicine was taken. An Optimized Framingham risk model was then used to calculate the risk scores of these factors. Place where first medicine was taken (temporary living places) received a score of 6, which was highest among all the factors. The predicted probability of treatment failure increases as risk score increases. Ten out of 359 patients had a risk score >9, which corresponded to an estimated probability of treatment failure >70%. In conclusion, we have identified multiple clinical and socio-demographic factors that are associated with treatment failure of retreated PTB patients. We also created an optimized risk score model that was effective in predicting the retreatment failure. These results provide novel insights for the prognosis and improvement of treatment for retreated PTB patients.

Key words: Pulmonary tuberculosis, retreatment, risk factors, risk score

INTRODUCTION

Tuberculosis (TB) remains a critical health issue worldwide, particularly in developing countries. According to the World Health Organization (WHO) [1], 6·31 million TB cases were reported in 2014, including 6·05 million new cases and 260 000 retreated patients. Moreover, TB is also one of the top 10 causes of death in the world, with 1·5 million deaths from the disease in 2014. Despite great efforts in prevention and treatment, China still has the third largest population of TB patients in the world. In 2014, 94 000 new TB cases and 40 000–50 000 retreated TB cases were reported in China [1]. Meanwhile, there are several new challenges in the battle against TB, including the spread of multi-drug-resistant tuberculosis (MDR-TB) and co-infection of HIV and TB. WHO is making great efforts to control TB, as exemplified by the MDGs (Millennium Development Goals), Stop TB Strategy, SDGs (Sustainable Development Goals), and the End TB Strategy [24]. The most recent five TB epidemiological surveys in China showed that, among total TB cases, the frequency of retreated cases were 45·6%, 48·5%, 38·9%, 26·1%, and 11·8%, respectively [5]. Although the frequency of retreated TB cases is decreasing, there are still a big number of retreated TB cases. TB patients with retreatment failure are usually considered as MDR-TB, and thus receive complicated and expensive treatment [6].Many factors have been reported to be associated with the treatment failure of retreated TB patients, including biological factors, susceptibility test and socio-economic factors, such as bacillus Calmette-Guérin (BCG) vaccination, drug susceptibility test, occupation, education level, and compliance [711]. However, their exact roles and values in predicting the treatment failure remain unclear. As pulmonary tuberculosis (PTB) patients account for about 95% of the TB cases, in this study, we aimed to identify the risk factors for treatment failure in retreated PTB patients, using an optimized model to assess their values in predicting treatment failure.

METHODS

Study participants and definition of index

Study participants

Participants of this study included PTB patients who received retreatment between July 2009 and July 2011 from one of the 24 hospitals or TB prevention and control institution in Beijing, Harbin, Inner Mongolia, Guangdong, Zhejiang, and other provinces in China.

Inclusion criteria
  1. Retreated TB patients with clear treatment outcome in prior treatment,

  2. Sputum smear positive,

  3. No serious complication,

  4. Voluntarily participated in the study and signed the informed consent form.

Exclusion criteria
  1. Nontuberculous mycobacteria (NTM) lung disease,

  2. Negative in smear test,

  3. MDR-TB or extensively drug-resistant tuberculosis (XDR-TB) as suggested by drug susceptibility test,

  4. Allergic to any kind of anti-TB drugs.

Definition of index

Retreatment type

According to National TB control program implementation guide in China (version 2009), retreated patients was categorized into three types:

  1. Relapse: A PTB patient was declared cured or treatment completed by a physician at the end of their most recent course of treatment, but is now found to be sputum smear positive;

  2. Initial treatment failure: A PTB patient is found to be sputum smear positive at month 5 or later during treatment;

  3. Others: when a PTB patient cannot be defined as ‘relapse’ or ‘initial treatment failure’, including the one who returns, immigrates, or irregularly and irrationally uses anti-TB drugs over 1 month.

Treatment outcome

The treatment outcome was categorized according to National TB control program implementation guide in China (version 2008). These categories include:

  1. Cure: A smear-positive PTB patient who completes prescribed medication and has two consecutive negative smear results in the last month of the treatment;

  2. Treatment completion: A smear-positive PTB patient who completes prescribed medication with negative smear result at the most recent check-up, but no result available at the end of treatment;

  3. Treatment success: A PTB patient who completes the treatment and is cured;

  4. Treatment failure: A PTB patient whose sputum smear is positive at month 5 or later during treatment, or a smear-negative PTB patient who becomes smear positive during treatment;

  5. Death: includes TB-specific death and non-TB-specific death.
    • TB-specific death: A PTB patient who dies from disease progression or complications, including hemoptysis, pneumothorax, pulmonary heart disease, systemic failure, extra-PTB etc.
    • Non-TB-specific death: A PTB patient who dies from other causes rather than TB;
  6. Lost to follow-up: A PTB patient who did not start treatment or whose treatment was interrupted for two consecutive months or more.

Treatment regimen
  1. Standard retreatment regimen: defined as WHO recommended standard regimen for retreatment of PTB (2HREZS/6HRE and 3HRZE/6HRE);

  2. Optimal regimen: includes high-dose regimen (2HL2ZS/2HL2EZS/4HL2E), long-treatment-duration regimen (2HL2EZS/2HL2EZS3/8HL2E) and individual regimen.

High-dose regimen: when the duration of intensive treatment is prolonged to 4 months. The dose will be given to a patient according to his/her weight, at H(0·3)/d for weight <50 kg, and H (0·4–0·5)/d, L2 (0·6) 2 times/week for weight ⩾50 kg. Regular dose will be used for ethambutol and pyrazinamide, and the course of treatment will last 8 months.

Long-treatment-duration regimen: when the duration of intensive treatment is prolonged to 4 months. The dose will be given at H (0·3)/d, L2 (0·45–0·6) 2 times/week. Regular dose will be used for ethambutol and pyrazinamide, and the course of treatment will last 12 months;

Individual regimen: Drug replacement based on standard retreatment regimen according to drug resistance result of each patient.

Ethics statement

Ethical approval was obtained from Inner Mongolia Medical University and IRB of the Beijing Tuberculosis and Thoracic Tumor Institution, Capital Medical University affiliated Beijing Chest Hospital, and the other collaboration institutions. All patients had signed informed consent prior to enrollment into the study.

Statistical analysis

All statistical analyses were performed using SPSS 19·0; significance tests were two-sided with P ⩽ 0·05 considered statistically significant. Univariable logistic regression was used to compare socio-demographic characteristics, health-related behavior, previous treatment information, clinical features of diagnosis between treatment success and failure groups in retreated PTB patients, with treatment outcome as the independent variable (treatment success was assigned as 0, treatment failure as 1). Dummy variables and variable assignment could be seen in Table 1. The variables with P-values ⩽0·10 in the univariable analysis were then included in the multivariable logistic regression model and further filtered at P-value ⩽0·05. The selected variables in the final multivariable prediction model were considered as the risk factors for treatment failure. Odds ratio (OR) and the 95% confidence interval (CI) for each variable were calculated. Receiver operating characteristic (ROC) curve was then used to assess the predicted ability of the final multivariable model, determine the cut-off value of predicted probability, obtain the area under curve (AUC), and calculate sensitivity and specificity for predicted probability of retreatment failure. The diagnostic accuracy of the multivariable model was considered as non-significant when AUC < 0·5, poor when AUC between 0·5 and 0·7, good when AUC between 0·7 and 0·9, and high when AUC > 0·9. The larger the AUC, the better the predicted ability. Optimized Framingham risk model was then used to calculate risk scores based on the selected risk factors and the corresponding coefficients from the multivariable prediction model [12] (Method 1, Table S1). Risk scores were then categorized into three groups according to estimated probability of treatment failure: low (<19%), moderate (19% to 70%), and high (>70%).

Table 1.

Variable assignment

Variable Variable assignment
BMI (kg/m2) 0 = BMI ⩾ 18·5,1 = BMI  < 18·5
Level of education 0 = Low (illiteracy, elementary school, or middle school), 1 = high (college, university, or above)
Institution where the first diagnosis was made 0 = TB prevention and control institution, specialized hospital, 1 = general hospital, 2 = private hospital or others
Place where first medicine was taken 0 = Home, 1 = medical institutions (TB prevention and control institution, TB specialized hospital, or general hospital), 2 = temporary living places (short-term living place, hotel or the places where homeless people stay)
Number of treatment 0 = 1, 1 = 2 or more
History of BCG vaccination 0 = No, 1 = yes
Previous treatment duration 0 = ⩽6 months,1 = >6 months
Type of retreatment 0 = Relapse, 1 = initial treatment failure, 2 = others (patients with returning, immigration, or irregular and irrational use of anti-TB drugs over 1 month)
Treatment regimen 0 = Standard retreatment regimen, 1 = optimal regimen
Medication supervision 0 = No, 1 = yes
Culture result after 2 months of treatment 0 = Negative, 1 = positive
Drug resistance 0 = No, 1 = yes

RESULTS

Baseline characteristics of retreated PTB patients

Among 395 retreated smear-positive PTB patients, 99 (25·1%) of them were in the treatment failure group and 296 (74·9%) were treatment success group. The median age of all the patients was 43 (Q1–Q3: 31·75–53·00 years, minimum–maximum: 12–79 years). The majority of patients were male, Han, low educated, married, and local residence, which accounted for 75·9%, 94·7%, 88·4%, 76·2%, and 69·6%, respectively. The 63·5% of them were relapsed PTB. Patients in the failure group were younger than those in success group. Patients with drug resistance had a higher treatment failure rate than those sensitive with drug. The univariable logistic regression identified 15 variables statistically associated with higher treatment failure rate. Those variables included low body mass index (BMI < 18·5), low education level, first diagnosed at private hospital, living alone, no history of BCG vaccination, long duration of previous treatment (>6 months), other retreatment type rather than relapse or initial treatment failure, receiving more than two episodes of treatment, high symptom scores before treatment (⩾5), having medical supervision this time, receiving standard treatment regimen, having positive culture result after 2 months of treatment. Patients who took first medicine at home had the lowest treatment failure rate, compared with those at medical institutions (TB prevention and control institution, TB specialized hospital, or general hospital), or temporary living places, other retreatment type rather than relapse or initial treatment failure (defined as patients who return, immigrate, or irregularly and irrationally use of anti-TB drugs over 1 month), (Tables 2 and 3 could be seen in the final document).

Table 2.

Baseline characteristics in retreatment PTB patients with different treatment outcomes

Characteristics Study population Treatment failure (n = 99) Treatment success (n = 296)
(n = 395)
Age (years) 43 (31·75–53·00) 41 (31·00–52·00) 46 (37·00–54·00)
Gender
Male 300 (75·9) 76 (25·3) 224 (74·7)
Female 95 (24·1) 23 (24·2) 72 (75·8))
Drug susceptibility
Drug resistance 185 (48·8) 58 (31·4) 127 (68·6)
Drug sensitivity 194 (51·2) 35 (18·0) 159 (82·0)
BMI (kg/m2)
<18·5 105 (26·9) 34 (32·4) 71 (67·6)
⩾18·5 286 (73·1) 64 (22·4) 222 (77·6)
Household register
Local residence 275 (69·6) 66 (24·0) 209 (76·0)
Non-local residence 120 (30·4) 33 (27·5) 87 (72·5)
Ethnicity
Han 374 (94·7) 94 (25·1) 280 (74·9)
Minorities 21 (5·3) 5 (23·8) 16 (76·2)
Level of education
Low 349 (88·4) 96 (27·5) 253 (72·5)
High 46 (11·6) 3 (6·5) 43 (93·5)
Marital status
Single 77 (19·5) 16 (20·8) 61 (79·2)
Married 301 (76·2) 79 (26·2) 222 (73·8)
Others 17 (4·3) 4 (23·5) 13 (76·5)
Smoking status
No smoking 168 (42·9) 37 (22·0) 131 (78·0)
Former smoking 167 (42·6) 44 (26·3) 123 (73·7)
Current smoking 57 (14·5) 17 (29·8) 40 (70·2)
Alcohol use
No drinking 216 (55·2) 48 (22·2) 168 (77·8)
Former drinking 154 (39·4) 41 (26·6) 113 (73·4)
Current drinking 21 (5·4) 9 (42·9) 12 (57·1)
History of BCG vaccination
Yes 196 (49·7) 40 (20·4) 156 (79·6)
No 198 (50·3) 59 (29·8) 139 (70·2)
Previous treatment duration
⩽6 months 232 (59·2) 51 (22·0) 181 (78·0)
>6 months 160 (40·8) 48 (30·0) 112 (70·0)
Number of treatment
1 349 (88·4) 82 (23·5) 267 (76·5)
⩾2 46 (11·6) 17 (37·0) 29 (63·0)
Retreatment type
Relapse 251 (63·5) 58 (23·1) 193 (76·9)
Initial treatment failure 67 (17·0) 13 (19·4) 54 (80·6)
Others 77 (19·5) 28 (36·4) 49 (63·6)
Complications
Yes 93 (24·0) 26 (28·0) 67 (72·0)
No 294 (76·0) 72 (24·5) 222 (75·5)
Adverse reaction this time
Yes 95 (24·1) 29 (30·5) 66 (69·5)
No 300 (75·9) 70 (23·3) 230 (76·7)
Treatment regimen
Standard regimen 110 (27·8) 42 (38·2) 68 (61·8)
Optimal regimen 285 (72·2) 57 (20·0) 228 (80·0)
Culture result after 2 months of treatment
Negative 302 (79·7) 56 (18·5) 246 (81·5)
Positive 77 (20·3) 32 (41·6) 45 (58·4)

Table 3.

Univariable and multivariable analysis of clinical predictors for retreatment PTB patients with treatment failure

Characteristics Univariable analysis (OR 95% CI) P Multivariable analysis (OR 95% CI) P
Age (years) 1·023 (1·005–1·041) 0·013*
Gender (female) 1·062 (0·621–1·817) 0·826
Drug susceptibility (no) 2·075 (1·284–3·353) 0·003* 2·060 (1·165–3·643) 0·013*
BMI (⩾18·5 kg/m2) 1·661 1·013–2·723) 0·044* 2·150 (1·138–4·061) 0·018*
Household register (local residence) 1·201 (0·738–1·955) 0·461
Ethnicity (Han) 0·931 (0·332–2·610) 0·892
Level of education (high) 5·439 (1·648–17·945) 0·005* 3·732 (1·043–13·356) 0·043*
Marital status (single)
Married 1·357 (0·739–2·491) 0·325
Others 1·173 (0·337–4·089) 0·802
Marital status (no smoking)
Former smoking 1·267 (0·767–2·092) 0·356
Current smoking 1·505 (0·766–2·954) 0·235
Alcohol use (no drinking)
Former drinking 1·270 (0·786–2·053) 0·329
Current drinking 2·625 (1·044–6·599) 0·040
Paid by themselves (yes) 0·860 (0·531–1·391) 0·538
Institution where the first diagnosis was made (TB-specialized hospital)
General hospital 0·814 (0·469–1·414) 0·466
Private hospital 4·479 (1·229–16·321) 0·023
Living alone (no) 2·307 (0·899–5·919) 0·082
History of BCG vaccination (yes) 1·655 (1·043–2·627) 0·032*
Previous treatment duration (⩽6 months) 1·521 (0·961–2·407) 0·073 1·984 (1·109–3·551) 0·021*
Number of treatment (1) 1·909 (0·999–3·648) 0·050*
History of allergies (no)
Yes 0·589 (0·167–2·081) 0·411
Unknown 1·263 (0·320–4·983) 0·739
Previous adverse reaction (no) 1·166 (0·623–2·182) 0·631
Initial diagnosed type (invasive)
Fibrocavitary 1·147 (0·589–2·235) 0·686
Others 0·562 (0·187–1·686) 0·304
Regularly taking medicine at first diagnosis (yes) 1·210 (0·740–1·981) 0·447
Medication supervision at first diagnosis(yes) 1·279 (0·779–2·100) 0·330
Place where first medicine was taken (home)
Medical institutions 1·615 (0·912–2·859) 0·100 2·011 (0·950–4·257) 0·068
Temporary living places 5·176 (1·421–18·849) 0·013 9·329 (1·716–50·722) 0·010*
Retreatment type (relapse)
Initial treatment failure 0·801 (0·409–1·570) 0·518 0·695 (0·305–1·584) 0·387
Others 1·901 (1·098–3·293) 0·022 2·081 (1·057–4·096) 0·034*
Symptom scores before treatment (<5) 1·634 (1·031–2·589) 0·037*
Fibrocavitary 1·478 (0·911–2·398) 0·113
Others 0·719 (0·200–2·587) 0·614
Complications (no) 1·197 (0·708–2·023) 0·503
Adverse reaction this time (no) 1·444 (0·865–2·409) 0·160
Hospitalization (no) 0·854 (0·538–1·356) 0·503
DOT distance (<1 km)
1~5 km 0·643 (0·257–1·612) 0·347
6~10 km 1·117 (0·421–2·964) 0·823
>10 km 0·826 (0·357–1·909) 0·654
Medical supervision this time (yes) 3·143 (1·147–8·612) 0·026*
Treatment regimen (optimal regimen) 2·471 (1·526–4·000) <0·001* 3·329 (1·778–6·234) <0·001*
Culture result after 2 months of treatment month (negative) 3·124 (1·824–5·351) <0·001* 3·498 (1·811–6·754) <0·001*

Note: *P < 0·05.

Variables in brackets represent control groups.

Risk factors associated with treatment failure among retreated PTB patients

A multivariable logistic regression model was conducted, including the 15 variables significantly associated with treatment outcome in the univariable logistic regression. The results indicated that patients were at a higher risk of treatment failure when they were having drug resistance, receiving standard retreatment regimen or positive culture result after 2 months. Moreover, patients were more likely to experience treatment failure if they had low education level, low BMI (<18·5), or long duration of previous treatment duration (>6 months). Patients who took first medicine at home had a lower risk of failure, compared with those at temporary living places other than home or medical institutions. Moreover, retreatment type was also a risk factor for treatment failure (Table 3). The sensitivity, specificity, and positive predictive value of the multivariable prediction model were 75·0%, 65·0%, and 38·4%, respectively (Table 4). The predictive ability (as assessed by AUC) of the multivariable prediction model was 0·774 (95% CI 0·715–0·883) (Fig. 1).

Table 4.

Performance characteristics for diagnosing retreatment failure using multivariable prediction model

Value TPR TNR PPV NPV
Predicted probability 75·0% 65·0% 38·4% 90·4%

TPR, true-positive rate (sensitivity); TNR, true-negative rate (specificity); PPV, positive predictive value; NPV, negative predictive value.

Fig. 1.

Fig. 1.

ROC curves of final multivariable prediction model for retreated PTB patients with treatment failure.

Risk score for predicting treatment failure in retreated PTB patients with complete data

In total, 359 patients (91%) had complete data for all selected predictors from the multivariable prediction model. There were no significant differences between all the patients and those with complete data in all the selected predictors (P > 0·05) (Table S2). Thus, those predictors were used to calculate the risk scores in the patients with complete data. The predicted probability of treatment failure increased with increasing risk score (Fig. 2). The risk score of each risk factor was also calculated. Patients whose first medicines were taken at the temporary living places other than home or medical institutions had the highest score of 6 (Table 5). Ten out of 359 patients had a risk score >9, which corresponded to a probability of treatment failure higher than 70% (Table S3).

Fig. 2.

Fig. 2.

Risk of retreated PTB patients with treatment failure corresponding to treatment failure risk score.

Table 5.

Risk factors and the corresponding risk score assigned by multivariable logistic regression to predict retreatment failure

Category Risk score
Level of education
Low 0
High 2
BMI (kg/m2)
⩾18·5 0
<18·5 1
Retreatment type
Relapse 0
Initial treatment failure 1
Others 2
Treatment regimen
Standard regimen 0
Optimal regimen 2
Drug susceptibility
Drug resistance 0
Drug sensitivity 1
Place where first medicine was taken
Home 0
Medical institutions 1
Temporary living places 6
Previous treatment duration
⩽6 months 0
>6 months 1
Culture result after 2 months of treatment
Negative 0
Positive 2

DISCUSSION

In China, the emergence of large number of retreated cases may be due to irrational drug use, mismanagement, irregular treatment, and many other reasons [1315].Retreated TB patients usually have severe adverse reactions and tend to have mood disorders such as depression. The failure of retreatment not only affects treatment compliance and confidence, but also influences the burden on families and caregivers. Therefore, in order to enhance the prevention and improvement of retreatment regimens, it is of great importance to identify risk factors and assess their predictive value. Here, we analyzed the data from a larger survey in China to identify predictors of treatment failure for retreated PTB patients. We used an optimized risk score model to assess the value of these factors in predicting treatment failure. Our findings add novel insights for the prognosis and treatment of retreated PTB patients in China and throughout the world.

The Optimized Framingham Heart Profile (FHP) is widely used in various fields [16], including stroke, coronary heart disease, metabolic syndrome, hypertension, TB, and other diseases [1722]. In addition, optimized FHP was also used to predict the risk of bacteremia for TB patients with HIV, which showed that predicted probability of bacteremia for TB patients with HIV increased with increasing risk score. Our results indicated that, with certain adjustments, the model could be effective in evaluating risk factors for PTB patients in China.

In this study, we found that place where first medicine was taken was an independent risk factor for the treatment failure of retreated PTB patients. Compared with patients who took medicine at home, risk score of patients who took medicine at temporary living places was much higher (6 points), which corresponded to the highest risk of treatment failure (OR 9·3293, 95% CI 1. 716–50·722). These patients may be part of migrating populations who cannot take medicine at home, and lack the supervision of TB prevention and control institutions or community stations. In addition, our study found that patients with previous treatment duration >6 months had higher risk of treatment failure (OR 1·984, 95% CI 1·109–3·551). Inappropriate treatment regimen, poor compliance and migrating may prolong treatment period. Previous study [23] had shown that prolonged initial treatment duration was a risk factor for drug resistance (OR 2·18), which could result in retreatment failure. Therefore, for these patients who take first medicine at temporary living places or have previous treatment duration >6 months, we should take proper interventions during their retreatment to decrease the failure rate.

The standard WHO recommended retreatment regimen (category II) for PTB is an economic and efficient regimen [2426]. However, in past two decades, the collaborative researches were conducted in many countries have provided a lot of evidence that patients ultimately failed with standard retreatment regimen [2732]. Our study showed that the risk score of standard retreatment regimen was 2 points, which indicated a relatively high risk for retreatment failure (OR 3·329, 95% CI 1·778–6·234). This was probably because the standard retreatment regimen, comprising four kinds of first-line drug combination regimen in initial treatment plus streptomycin, was mainly proposed based on the experiences of expert. Therefore, the Standard Retreatment Regimen recommended by WHO may not be appropriate for every PTB patient. More effective treatment regimen should be developed according to the characteristics and the condition of retreated PTB patients.

Our study showed that the risk score of drug resistance was 1 point, which corresponded to a higher risk of retreatment failure than drug-sensitive TB (OR 2·060, 95% CI 1·165–3·643). Consistent with these findings, a study from South Korea indicated that success rate for new patients with drug resistance (68·8%) was much higher than that of retreated TB patients (40·7%) [33]. Another study in China showed that the chance of treatment failure for MDR-TB was 4·7 times more than that in drug-sensitive patients [34].

Culture result after 2 months of treatment can be used as a comprehensive treatment effect indicator for patients after intensive treatment. Our study showed that positive culture after 2 months of treatment was an independent risk factor for treatment failure in retreated PTB patients, with a risk score of 2 points. Patients with positive culture were 2·498 times more likely to fail during treatment than those with negative results, which was consistent with the study of Zhou and co-workers [35]. Besides, our study found that the risk score of treatment failure in PTB patients with other type of retreatment was higher than patients who relapsed, with an OR of 2·081 (95% CI 1·057–4·096). This might be associated with definite microbiological diagnosis in patients with relapsed PTB, while the others who return, immigrate, or irregularly and irrationally use of anti-TB drugs over 1 month were more likely to be combined with other disease, such as HIV, lung, or heart disease, which could lead to immune function impairment and increase the risk of poor treatment outcome.

Our study also found that the risk score of low education level and low BMI (<18·5) were 2 and 1, respectively. The reason may be that lack of education and low BMI were associated with poor socio-economic factors. Patients who had less awareness of health issues and self-care might delay in the diagnosis and treatment. Also patients with low education level will be more likely to misuse drug and discontinue drug use during treatment.

We acknowledged that this study had some limitations. First, our model may need to validate with a second cohort to strengthen our conclusions. Second, the study was performed with the data from China, thus the application of the model in other countries may require further examination. However, our study provides a good starting point for international studies on this topic, and our further study is also in progress.

CONCLUSIONS

In summary, predictors of treatment failure for retreated PTB patients included drug susceptibility, BMI, level of education, previous treatment duration, location where first medicine was taken, retreatment type, treatment regimen, and culture result after two months of treatment. The Optimized Framingham risk model built with those risk factors was proven to be effective in predicting the treatment failure, which could improve early diagnosis of treatment failure in retreated PTB patients using risk scores, especially when using standard treatment regimen. Our findings add novel insights for the prognosis and treatment of retreated PTB patients in China.

ACKNOWLEDGEMENTS

This study was supported by One million projects of Science and Technology of Inner Mongolia Medical University (YKD2013KJBW006), Intelligent health monitoring and modern medical information system development based on technology of Internet of Things and National Science and Technology Major Projects (2008ZX10003-015-2).

Supplementary material

For supplementary material accompanying this paper visit https://doi.org/10.1017/S0950268817000656.

S0950268817000656sup.zip (35.7KB, zip)

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DECLARATION OF INTERESTS

None.

REFERENCES

  • 1.WHO. Global Tuberculosis Report 2015. Geneva: World Health Organization, 2015. [Google Scholar]
  • 2.Jaramillo M. The Stop TB Strategy: building on and enhancing DOTS to meet the TB-related Millennium Development Goals. Geneva, Switzerland: World Health Organization [WHO], 2006. [Google Scholar]
  • 3.MCR. The Global Plan to Stop TB, 2006–2015. International Journal of Tuberculosis & Lung Disease the Official Journal of the International Union against Tuberculosis & Lung Disease 2006; 10(2): 238–239. [PubMed] [Google Scholar]
  • 4.WHO. Global tuberculosis control 2015. Global Tuberculosis Control 2015.
  • 5.Lixia W, et al. Survey of the Fifth National epidemiological sampling of tuberculosis in 2010. Chinese Journal of Tuberculosis Prevention 2012; 34(08): 485–508. [Google Scholar]
  • 6.World Health Organization. Stop TB Department Guidelines for the Programmatic Management of Drug-Resistant Tuberculosis. Geneva: World Health Organization, 2006. [Google Scholar]
  • 7.Qianghong D, et al. Treatment outcomes and risk factors for retreated smear positive pulmonary tuberculosis in Wuhan City. Chinese Journal of Tuberculosis Prevention 2013; 35(10): 788–792. [Google Scholar]
  • 8.Yingjie Y. Risk factors for the efficacy of retreated smear positive tuberculosis patients and nursing intervention. Jilin Medicine 2010; 31(34): 6350–6351. [Google Scholar]
  • 9.Vicentin G. Evoluçäo da mortalidade por tuberculose no município do Rio de Janeiro, 1979–1995. São Paulo, Brazil: Universidade de São Paulo, 2000. [Google Scholar]
  • 10.Volmink J, Garner P. Systematic review of randomised controlled trials of strategies to promote adherence to tuberculosis treatment. BMJ (Clinical Research edn) 1997; 315(7120): 1403–1406. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Yaqin L, Yuan M, Wei C. Risk factors for compliance of retreated tuberculosis patients. Nursing Research 2011; 25(29): 2649–2651. [Google Scholar]
  • 12.Sullivan LM, Massaro JM, D'Agostino RB. Sr Presentation of multivariate data for clinical use: the Framingham Study risk score functions. Statistics in Medicine 2004; 23(10): 1631–1660. [DOI] [PubMed] [Google Scholar]
  • 13.Shiming C, et al. Investigation and analysis on social factors of retreated smear positive pulmonary tuberculosis patients in Hunan Province. Practical Preventive Medicine 2003; 10(02): 132–134. [Google Scholar]
  • 14.Kherosheva T, et al. Encouraging outcomes in the first year of a TB control demonstration program: Orel Oblast, Russia. The International Journal of Tuberculosis and Lung Disease: the Official Journal of the International Union against Tuberculosis and Lung Disease 2003; 7(11): 1045–1051. [PubMed] [Google Scholar]
  • 15.Talay F, Kumbetli S, Altin S. Factors associated with treatment success for tuberculosis patients: a single center's experience in Turkey. Japanese Journal of Infectious Diseases 2008; 61(1): 25–30. [PubMed] [Google Scholar]
  • 16.D'Agostino RB, et al. Stroke risk profile: adjustment for antihypertensive medication. The Framingham Study. Stroke; a Journal of Cerebral Circulation 1994; 25(1): 40–43. [DOI] [PubMed] [Google Scholar]
  • 17.Yousefzadeh G, et al. Applying the Framingham risk score for prediction of metabolic syndrome: the Kerman Coronary Artery Disease Risk Study, Iran. ARYA Atherosclerosis 2015; 11(3): 179–185. [PMC free article] [PubMed] [Google Scholar]
  • 18.Goldstein LB BC, Adams RJ, Appel LJ, Braun LT, Chaturvedi S, Creager MA, Culebras A, Eckel RH, Hart RG, Hinchey JA, Howard VJ, Jauch EC, Levine SR, Meschia JF, Moore WS, Nixon JV, Pearson TA; American Heart Association Stroke Council; Council on Cardiovascular Nursing; Council on Epidemiology and Prevention; Council for High Blood Pressure Research; Council on Peripheral Vascular Disease and Interdisciplinary Council on Quality of Care and Outcomes Research. Guidelines for the primary prevention of stroke: a guideline for healthcare professionals from the American Heart Association/American Stroke Association. Stroke 2011; 42(2): 517–584. [DOI] [PubMed] [Google Scholar]
  • 19.Wang H, et al. Longitudinal association of dairy consumption with the changes in blood pressure and the risk of incident hypertension: the Framingham Heart Study. The British journal of nutrition 2015; 114(11): 1887–1899. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Jacob ST, Pavlinac PB, Nakiyingi L, Banura P, Baeten JM, Morgan K, et al. Mycobacterium tuberculosis Bacteremia in a Cohort of HIV-infected patients hospitalized with severe sepsis in Uganda–high frequency, low clinical sand derivation of a Clinical Prediction Score. PLoS ONE 2013; 8(8): e70305. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Joshi PH, et al. Remnant lipoprotein cholesterol and incident coronary heart disease: the Jackson Heart and Framingham Offspring Cohort Studies. Journal of the American Heart Association 2016; 5(5). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Parikh NI, et al. A risk score for predicting near-term incidence of hypertension: the Framingham Heart Study. Annals of Internal Medicine 2008; 148(2): 102–110. [DOI] [PubMed] [Google Scholar]
  • 23.Chen S, et al. Risk factors for multidrug resistance among previously treated patients with tuberculosis in eastern China: a case–control study. International Journal of Infectious Diseases: IJID: Official Publication of the International Society for Infectious Diseases 2013; 17(12): e1116–1120. [DOI] [PubMed] [Google Scholar]
  • 24.Lenjisa J. Assessment of tuberculosis retreatment case rate and its treatment outcomes at Adama Hospital Medical College, East Showa, Ethiopia. Journal of Steroids & Hormonal Science 2015; 06(1). [Google Scholar]
  • 25.Jones-Lopez EC, et al. Effectiveness of the standard WHO recommended retreatment regimen (category II) for tuberculosis in Kampala, Uganda: a prospective cohort study. PLoS Medicine 2011; 8(3): e1000427. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Mpagama SG, et al. The influence of mining and human immunodeficiency virus infection among patients admitted for retreatment of tuberculosis in Northern Tanzania. The American Journal of Tropical Medicine and Hygiene 2015; 93(2): 212–215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Kritski AL, et al. Retreatment tuberculosis cases. Factors associated with drug resistance and adverse outcomes. Chest 1997; 111(5): 1162–1167. [DOI] [PubMed] [Google Scholar]
  • 28.Espinal MA, et al. Standard short-course chemotherapy for drug-resistant tuberculosis: treatment outcomes in 6 countries. Jama 2000; 283(19): 2537–2545. [DOI] [PubMed] [Google Scholar]
  • 29.He GX, et al. Follow-up of patients with multidrug resistant tuberculosis four years after standardized first-line drug treatment. PLoS ONE 2010; 5(5): e10799. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Green E, et al. Drug-susceptibility patterns of Mycobacterium tuberculosis in Mpumalanga province, South Africa: possible guiding design of retreatment regimen. Journal of Health, Population, and Nutrition 2010; 28(1): 7–13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Mak A, et al. Influence of multidrug resistance on tuberculosis treatment outcomes with standardized regimens. American Journal of Respiratory and Critical care Medicine 2008; 178(3): 306–312. [DOI] [PubMed] [Google Scholar]
  • 32.Faustini A, Hall AJ, Perucci CA. Risk factors for multidrug resistant tuberculosis in Europe: a systematic review. Thorax 2006; 61(2): 158–163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Choi H, et al. Predictors of pulmonary tuberculosis treatment outcomes in South Korea: a prospective cohort study, 2005–2012. BMC Infectious Diseases 2014; 14(1): 360. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Jian D, et al. Reasons for failure of Standardized short term chemotherapy regimen for initial or retreated pulmonary tuberculosis patients. Chinese Journal of Parasitic Disease 2012; 7(07): 523–526. [Google Scholar]
  • 35.Yang Z, et al. Risk factors for sputum culture result at the end of 2nd month of treatment in MDR-TB patients. Chinese Journal of Tuberculosis Prevention 2015; 37(1): 74–79. [Google Scholar]

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