Literature DB >> 35831812

Factors contributing to the high prevalence of multidrug-resistance/Rifampicin-resistance in patients with tuberculosis: an epidemiological cross sectional and qualitative study from Khabarovsk krai region of Russia.

Ilia Bykov1,2, Olga Dyachenko3, Pavel Ratmanov2, Huan Liu1, Libo Liang1, Qunhong Wu4.   

Abstract

BACKGROUND: Growing prevalence of multidrug-resistant/Rifampicin-resistant tuberculosis (MDR/RR-TB; resistance to Isoniazid and Rifampicin/Isolated resistance to Rifampicin) is putting in jeopardy the WHO End TB strategy. This study aimed to identify factors contributing to the high prevalence of MDR/RR-TB in Khabarovsk krai region of Russia.
METHODS: A cross-sectional retrospective study was conducted, analyzing clinical, demographic, and drug susceptibility testing data on 1440 patients. As a source of raw data, the national electronic TB surveillance system was used. Anonymous data was collected on every patient diagnosed with TB in all healthcare facilities of the region from January 2018 to December 2019. Only patients with proven excretion of m. tuberculosis were included in the study. Factors associated with MDR/RR-TB were identified through logistic regression analysis, in conjunction with in-depth interviews with eight patients, five healthcare managers and five doctors.
FINDINGS: 2661 patients were identified with TB, 1440 were incorporated in the study based on inclusion criteria. Of these, 618 (42.9%) were identified with MDR/RR-TB. Patients with a history of imprisonment were 16.53 times (95% CI 5.37 to 50.88,) more likely to have MDR/RR-TB, whereas re-treatment patients were 2.82 times (95% CI 2.16 to 3.66) more likely to have MDR/RR-TB. Other influencing factors included presence of disability (AOR is 2.32, 95% CI 1.38 to 3.89), cavitary disease (AOR is 1.76, 95% CI 1.37 to 2.25), and retirement status (AOR 0.65, 95% CI 0.43 to 0.98, p = 0.042). Poor patient knowledge and understanding of the disease, progressive weariness of prolonged TB treatment, and inability hospitalize infectious patients without their consent were perceived by the interviewees as major influencing factors.
CONCLUSIONS: Incarceration and treatment history, regardless of outcome, were identified as major factors influencing MDR/RR-TB prevalence. It is essential for the TB care system to eliminate legal loopholes, which deprive doctors of means to enforce quarantine procedures and epidemiological surveillance on infected patients, former and current inmates. Increasing people's awareness of TB, early detection and appropriate treatment of patients with TB are needed for successfully combating MDR/RR-TB.
© 2022. The Author(s).

Entities:  

Keywords:  Disability; Multidrug-resistant/Rifampicin-resistant tuberculosis; Penitentiary facilities; Risk factors; Tuberculosis

Mesh:

Substances:

Year:  2022        PMID: 35831812      PMCID: PMC9281178          DOI: 10.1186/s12879-022-07598-7

Source DB:  PubMed          Journal:  BMC Infect Dis        ISSN: 1471-2334            Impact factor:   3.667


Introduction

The continuous increase of multidrug-resistant/Rifampicin-resistant tuberculosis (MDR/RR-TB; resistance to Isoniazid and Rifampicin/Isolated resistance to Rifampicin) throughout the globe is a major public health issue. In 2020, the WHO reported that the global treatment success rate for MDR/RR-TB was only 59%. Treatment of MDR/RR-TB is more toxic to the patient, less effective, and it carries a much higher economic burden on the patients and the healthcare system, jeopardizing TB control efforts in developed and developing countries alike [1-4]. Russia carries one of the greatest burdens of MDR/RR-TB in the world. In 2018, MDR/RR-TB accounted for 35% of all new TB cases and 71% of all previously treated TB cases, with an MDR/RR-TB incidence of 27 per 100,000 and second highest in the world MDR/RR-TB prevalence rate [5, 6]. Such situation develops despite what seems to be a well-designed TB care system, in which all aspects of TB care in Russia are free of charge to the public. The entire system was designed to provide universal, quality, and specialized care that is centralized in TB-designated facilities (TBDF), as depicted in Fig. 1. All healthcare facilities and schools are participating in detection of asymptomatic TB by performing a mandatory annual chest x-ray in adults and Tuberculin Skin Testing (TST) in children. If TB is suspected, the healthcare facility is legally obliged to transfer such a patient to the TBDF, so the final diagnosis of suspected TB patients and provision of TB treatment are reserved only for TBDF [7]. The only exception to this system are penitentiary facilities, which screen, diagnose and treat inmates themselves. Such independence has been already proposed by researchers as a main reason for the high incidence of TB in Russian prisons, but little has been done to improve this situation [8].
Fig. 1

Organization of TB care in Russia. PHF primary healthcare facility, HF healthcare facility, TBDF TB designated facility, DOT directly observed treatment, PCR polymerase chain reaction, TST tuberculin skin test, DST drug susceptibility testing, DST Diaskin skin test, CT computed tomography, MTB mycobacterium tuberculosis

Organization of TB care in Russia. PHF primary healthcare facility, HF healthcare facility, TBDF TB designated facility, DOT directly observed treatment, PCR polymerase chain reaction, TST tuberculin skin test, DST drug susceptibility testing, DST Diaskin skin test, CT computed tomography, MTB mycobacterium tuberculosis High MDR/RR-TB incidence encourages the government of the Russian Federation and the Russian society of Phthisiatricians1 have developed specific policies and guidelines to address the issues [9]. Joint TB control programs with international partners have been initiated, research funds have been extended, a centralized national electronic database of TB patients created, and new diagnostic techniques and policies implemented. However, the progress has been far from satisfactory, as despite the decrease in total TB incidence, the prevalence of MDR/RR-TB is continuing to rise [5-8]. It is crucial to identify the underlying reasons for such high MDR/RR-TB prevalence so that more feasible and cost-effective approaches can be developed to control this trend. International reviews, and some country-level studies, have identified that risk factors for MDR/RR-TB vary depending on country, region, or locality. Among the most prevalent are poor adherence to TB treatment on the part of patients, poor monitoring and management of TB treatment adverse events, poverty, overcrowding, HIV co-infection, diabetes, alcoholism, smoking, cavitary disease and young age [10-18]. This study was undertaken in Khabarovsk Krai, in the Far East of Russia, where the proportion of MDR-TB among newly diagnosed cases (38%) was estimated to be the third highest in the country, significantly higher than the national average of 29.3% in 2018 [19]. Unfortunately, there is a notable gap in research into MDR/RR-TB rates between high and low prevalence regions of Russia. Despite some studies carried out in low-prevalence regions, factors influencing MDR/RR-TB in high- prevalence regions have rarely been investigated [20-22].

Methods

Data collection

Khabarovsk Krai is a region in the Far East of the Russian Federation, and it considered one of its high-prevalence TB regions. The TB incidence there is 87.7 per 100,000 in 2019 (almost twice the national average) with a population of only 1.2 million. These figures relegate region to ninth place by total TB incidence out of all 85 regions of Russia [19]. The mixed epidemiological, cross-sectional, retrospective and a qualitative study was conducted in the central “Tuberculosis Hospital” of Khabarovsk Krai. This institution collects and processes information about all patients with tuberculosis in region and functions as a reference laboratory at the regional level. The Federal Register of TB patients (FRTP) was used as a source of data, which is a subsystem of the digital Unified State Healthcare Information System (USHIS). FRTP stores data of TB patients in form of electronic medical records, which were accessed by the investigator in April 2021. Anonymous demographic and clinical characteristics of every patient that was diagnosed with TB from January 2018 to December 2019 was collected and summarized into single data set for further analysis. The surveillance covered all healthcare institutions in the region and strictly followed the guidelines developed by the WHO and the International Union against Tuberculosis and Lung Disease [23, 24].

Diagnostic methods

In all patients with suspected TB in the region, an acid-fast bacilli sputum smear, culture (with both liquid and solid media), real-time PCR, and Drug Susceptibility Testing (DST) are routinely implemented as initial diagnostic tests. Various DST techniques were employed to detect MDR/RR-TB in patients. A liquid and solid media sputum culture tested MTB resistance to the following agents: Isoniazid, Rifampicin, Ethambutol, Streptomycin, Linezolid, Capreomycin, Amikacin, Ofloxacin, Levofloxacin, Kanamycin, Ethionamide, Para-aminosalicylic acid and Cycloserine. DST in direct PCR was performed with Allele-specific polymerase chain reaction aimed to identify rpoB, katG, inhA, embB and gyrA genes mutations associated with resistance to Isoniazid, Rifampicin, Ethambutol and fluoroquinolones [25]. All DST strictly followed the procedures and methods set out by WHO and the International Union against Tuberculosis and Lung Disease [24]. A new patient was defined as a patient with TB who had never been treated for TB previously, or who had received anti-TB drugs treatment for less than 1 month. A re-treatment patient was defined as a patient who had received anti-TB drug treatment for more than 1 month [10].

Inclusion/Exclusion criteria

A patient whose sample tests positive for mycobacterium tuberculosis (MTB) in at least one of the four initial diagnostic tests was defined as having active pulmonary TB. Patients whose samples are negative for the MTB in all four initial diagnostic tests were defined as having non-active pulmonary TB. Such patients were excluded from the study. Patients with mono-resistance (resistance to one first-line anti-TB drug only), poly-resistance (resistance to more than one first-line anti-TB drug, other than both isoniazid and rifampicin) and extensive drug resistance (resistance to any fluoroquinolone, and at least one second-line injectable TB medication, in addition to multidrug resistance) were excluded from the study. Patients whose electronic medical records contained incomplete set of data were also excluded from the study.

In-depth interviews

The interviewees were purposely selected based on their roles and experience in TB control. A total of 8 re-treatment and newly diagnosed patients completed the interviews, including one with a history of incarceration. 10 healthcare workers involved with their treatment completed interviews, including 5 physicians and 5 health administrative officials. Patients with TB were asked to answer when, where, and why they had received TB services, how they were treated and what problems they faced. The administrative officials were asked to answer questions about the arrangement of treatment regimens and compliance of providers and patients. The physicians were asked to answer questions about their experiences and problems in treating TB patients. The interviews were digitally recorded, transcribed, and thematically coded. The final sample size was determined by a saturation of information when no new categories emerged.

Quantitative data analysis

Quantitative variables of demographic and clinical characteristics of the patients with MDR/RR-TB were compared with those without MDR/RR-TB. Three regression models were constructed for all cases combined—only new cases and only re-treatment cases, respectively. Tested in the regression analysis were the following independent variables: gender, age, social status, place of residence, living conditions, substances abuse, a history of imprisonment, partial or total permanent inability to work (further—disability), HIV status, a history of treatment with Rifampicin and Isoniazid, TB localization, cavitary disease, and circumstances of TB discovery. For the re-treatment patients, additional variables of previous therapy outcome and length of previous treatment with Rifampicin and Isoniazid were added. Three separate binary logistic regression models were created. Chi square tests were used for testing the statistical significance of the models as a whole. Fitness of the models to the data were tested with the Hosmer & Lemeshow test. Regression coefficient, Odds ratio with 95% confidence interval (95% CI) for each variable category was calculated and Wald statistics method used to determine their statistical significance [26]. An analysis was performed using SPSS software V24.0.01.

Qualitative data analysis

The interview data was analyzed thematically, with the coding framework developed inductively from the data. The initial coding used open coding and theoretical coding. The initial codes were then refined to produce a smaller set of themes. The coding framework was subject to continuing revision with each iteration during analysis. Main objectives of the analysis were to receive clinical explanation for the results of quantitative data analysis, identify non-apparent factors influencing MDR/RR-TB incidence, determine features of the TB care system organization and limitations of the study. An analysis was performed using Nvivo software V11.0.

Results

Characteristics of the study population

During the study period, in all healthcare institutions of the region, 2661 patients were diagnosed with TB, of which 1544 patients had an active pulmonary tuberculosis, and 101 patients were excluded from the study due to resistance types other then MDR/RR-TB, three patients were excluded due to an incomplete set of variables leaving 1440 patients for further analysis (Fig. 2).
Fig. 2

Flow chart of patients enrollment. PCR polymerase chain reaction, DST drug susceptibility testing, MDR/RR-TB multidrug-resistant/Rifampicin-resistant tuberculosis

Flow chart of patients enrollment. PCR polymerase chain reaction, DST drug susceptibility testing, MDR/RR-TB multidrug-resistant/Rifampicin-resistant tuberculosis Participants had a median age of 41 years, and 73.5% of them were male. MDR/RR was detected in 618 participants (42.9%, 95% CI 40.3% to 45.5%). The proportion of participants residing in cities was 69.4%, and 989 of them (68.7%) had no record of employment. By residence type, 61.5% were living in separate apartments and 151 (10.5%) were homeless at the time of TB diagnosis. There were 2.01 times more homeless among re-treatment cases than in newly diagnosed cases (16,5% vs 8.2%). Alcoholism was reported in 3.5% of all cases and in 62.5% of TB was discovered actively with an annual chest x-ray in primary healthcare facilities (PHF). More than half of all cases (55.1%) showed signs of cavitary disease. Disabilities were reported in 6% of the entire sample, while 8.3% were tested positive for HIV. 78 patients (5.4%) were in detention or had an official history of incarceration at the time of diagnosis. Overall, incarcerated patients had a much higher prevalence MDR/RR (93.6%, 95% CI 85.6% to 97.8%) compared to the population without a history of imprisonment (40.0%, 95% CI 37.4% to 42.7%) (p < 0.001). Out of the 1440 patients, 394 were re-treatment patients, totaling 27.4% of the overall sample. The re-treatment patients had greater prevalence of MDR/RR (64.6%, 95% CI 59.8% to 69.4%) than the new patients (34.8%, 95% CI 31.8% to 37.7%) (p < 0.001) (Table 1).
Table 1

Demographical and clinical characteristics of the recruited patients:

VariableEntire sample N and % (n = 1440)New cases N and % (n = 1046)Retreatment cases N and % (n = 394)MDR/RR/Non-MDR/RR-TB (p value)
MDR/RR
 MDR/RR618 (42.9)363 (34.7)255 (64.7)(in applicable)
 No MDR/RR822 (57.1)683 (65.3)139 (35.3)
Gender
 Male1058 (73.5)755 (72.2)303 (76.9)0.856
 Female382 (26.5)291 (27.8)91 (23.1)
Age, median years (range)
 < 41 years715 (43.7)524 (50.1)191 (48.5) < 0.001
  ≥41 years725 (50.3)522 (49.9)203 (51.5)
Place of residence
 Country side440 (30.6)311 (29.7)129 (32.7)0.149
 City1000 (69.4)735 (70.3)265 (67.3)
Social status
 Not working989 (68.7)675 (64.5)314 (79.7)(inapplicable)
 Working244 (16.9)203 (19.4)41 (10.4)
 Retired173 (12.0)136 (13.0)37 (9.4)
 Student28 (1.9)26 (2.5)2 (0.5)
 Not organized child4 (0.3)4 (0.4)0
 In military service2 (0.1)2 (0.2)0
Living conditions:
 Homeless151 (10.5)86 (8.2)65 (16.5)(inapplicable)
 Bed in designated facility44 (3.1)12 (1.1)32 (8.1)
 Room in Dormitory13 (0.9)9 (0.9)4 (1.0)
 Room in separate apartment11 (0.8)10 (1.0)1 (0.3)
 Separate house335 (23.3)241 (23.0)94 (23.9)
Substances abuse
 No official records1385 (96.2)1006 (97.8)379 (96.2)(inapplicable)
 Alcoholism51 (3.5)37 (3.5)14 (3.6)
 Drug abuse4 (0.3)3 (0.3)1 (0.3)
Circumstance of TB discovery
 Visit with symptoms to healthcare facility540 (37.5)422 (40.3)118 (29.9)0.005
 Discovered actively by healthcare facility900 (62.5)624 (59.7)276 (70.1)
 Imprisonment history
 No official history of detention1362 (94.6)1023 (97.8)339 (86.0) < 0.001
 Being in detention or history of detention78 (5.4)23 (2.2)55 (14.0)
Cavitary disease
 No cavities646 (44.9)483 (46.2)163 (41.4) < 0.001
 Presence of cavities794 (55.1)563 (53.8)231 (58.6)
Disabilities
 No disability1354 (94.0)1001 (95.7)353 (89.6) < 0.001
 Presence of disability86 (6.0)45 (4.3)41 (10.4)
TB localization:
 Pulmonary TB1401 (97.3)1011 (96.7)390 (99.0)(inapplicable)
 TB of lungs’ lymph system, pleural29 (2.0)26 (2.5)3 (0.8)
 Non thoracic TB10 (0.7)9 (0.9)1 (0.2)
HIV status
 Negative1321 (91.7)967 (92.4)354 (89.8) < 0.001
 Positive119 (8.3)79 (7.6)40 (10.2)

HIV human immunodeficiency virus, TB tuberculosis, MDR/RR multidrug resistance/Rifampin resistance

Demographical and clinical characteristics of the recruited patients: HIV human immunodeficiency virus, TB tuberculosis, MDR/RR multidrug resistance/Rifampin resistance

Factors associated with MDR/RR-TB

Data of 1440 patients undergone logistic regression analysis. The strongest associative factors for MDR/RR-TB were a history of imprisonment and history of previous treatment. In these cases, the risk of having MDR/RR-TB was 16.53 (95% CI 5.37 to 50.88, p < 0.001) and 2.82 times higher (95% CI 2.16 to 3.66, p < 0.001) respectively. Other influencing factors included presence of disability (AOR is 2.32, 95% CI 1.38 to 3.89, p = 0.001), cavitary disease (AOR is 1.76, 95% CI 1.37 to 2.25, p < 0.001), positive HIV status (AOR 1.55, 95% CI 1.01 to 2.39, p = 0.046), age (AOR for being older than 41 years is 1.36, 95% CI 1.06 to 1.76, p = 0.013), place of residence (AOR for residing in the city is 1.44, 95% CI 1.09 to 1.89, p = 0.01). The only variable that showed protective effect against MDR/RR-TB was retirement status (AOR 0.65, 95% CI 0.43 to 0.98, p = 0.042) (Table 2).
Table 2

Analysis for estimation of prevalence of MDR/RR-TB in the entire sample (n = 1440)

VariablePrevalence of MDR/RR-TB (%)AOR (95% CI)P value
Gender
 Female43.11.21 (0.93 to 1.57)0.156
 Male41.41 (reference)
Age, median years (range)
 ≥41 years481.36 (1.06 to 1.76)0.013
  < 41 years37.91 (reference)
Place of residence
 City44.21.43 (1.09 to 1.89)0.010
 Countryside40.01 (reference)
Social status (whole variable)(–)
 Working39.30.75 (0.09 to 6.53)0.432
 Retired29.30.65 (0.43 to 0.98)0.792
 Student35.70.94 (0.41 to 2.15)0.042
 Not organized child501.08 (0.79 to 1.47)0.879
 In military service1000.639
 Not working46.31 (reference)0.999
Living conditions (whole variable)0.125
 Bed in designated facility51.30.98 (0.29 to 3.37)0.608
 Room in dormitory86.4(–)0.656
 Room in separate apartment46.20.84 (0.45 to 1.56)0.569
 Separate house9.12.35 (0.23 to 24.25)0.475
 Separate apartment43.91 (reference)-
Substances abuse (whole variable)(–)0.656
 Alcoholism39.20.84 (0.45 to 1.56)0.569
 Drug abuse752.35 (0.23 to 24.25)0.475
 No official records431 (reference)-
Circumstance of TB discovery
 Discovered actively by healthcare facility45.81.24 (0.97 to 1.60)0.088
 Visit with symptoms to healthcare facility38.11(reference)
Imprisonment history
 Being in detention or history of detention93.616.53 (5.37 to 50.88) < 0.001
 No official history of detention40.01 (reference)
Cavitary disease
 Presence of cavities47.41.76 (1.37 to 2.25) < 0.001
 No cavities37.51 (reference)
Disabilities
 Presence of disability67.42.32 (1.38 to 3.89)0.001
 No disability41.41 (reference)
TB localization(–)0.859
 Pulmonary TB43.41.27 (0.55 to 2.94)0.581
 Non thoracic TB0
 TB of lungs’ lymph system, pleural34.51 (reference)0.999
HIV status
 Positive53.81.55 (1.01 to 2.39)0.046
 Negative41.91 (reference)
Treatment history with I and R
 Retreatment64.62.82 (2.16 to 3.66) < 0.001
 No history34.81 (reference)

HIV human immunodeficiency virus, TB tuberculosis, MDR/RR multidrug resistance/Rifampin resistance, AOR adjusted odds ratio

Analysis for estimation of prevalence of MDR/RR-TB in the entire sample (n = 1440) HIV human immunodeficiency virus, TB tuberculosis, MDR/RR multidrug resistance/Rifampin resistance, AOR adjusted odds ratio The multilevel model for the newly diagnosed patients was composed of 1047 cases. Of these, 364 had MDR/RR-TB (34.7%). History of imprisonment was the strongest associative factor, with 11.9 times higher risk of MDR/RR-TB (95% CI 2.94 to 43.78, p < 0.001). Among remaining factors, three showed association with presence of MDR/RR-TB. Cases with underlying cavitary disease were 1.96 times more likely to have MDR/RR-TB (95% CI 1.46 to 2.63, p < 0.001). Patients living in cities were 1.841 times more likely to have MDR/RR-TB (95% CI 1.25 to 2.44, p = 0.001). Positive HIV status was associated with 1.67 times increase in MDR/RR-TB risk (95% CI 1.01 to 2.77, p = 0.047) (Table 3).
Table 3

Analysis for estimation of prevalence of MDR-TB in the new cases (n = 1046) and retreatment cases (n = 394)

VariableNew cases (n = 1046)Retreatment cases (n = 394)
Prevalence of MDR-TB (%)AOR (95% CI)p valuePrevalence of MDR-TB (%)AOR (95% CI)p value
Gender
 Female36.41.25 (0.92 to 1.69)0.15765.61.24 (0.71 to 2.18)0.441
 Male34.11 (reference)-61.51 (reference)
Age, median years (range)
 ≥41 years39.51.34 (0.99 to 1.81)0.01358.10.65 (0.38 to 1.09)0.108
  < 41 years30.01 (reference)71.61 (reference)
Place of residence
 City37.21.841 (1.32 to 2.57)0.01066.71.27 (0.72 to 2.26)0.408
 Countryside28.91 (reference)-63.61 (reference)
Social status (whole variable)(–)0.604(–)0.008
 Working30.50,83 (0.58 to 1.19)0.63982.94,32 (0.58 to 1.19)0.002
 Retired24.80.66 (0.41 to 1.07)0.04245.90.66 (0.29 to 1.49)0.042
 Student30.80.75 (0.31 to 1.86)0.879100.00.999
 Not organized child50.00.81 (0.09 to 6.81)0.7920.00.999
 In military service100.00.9990.00.999
 Not working37.91 (reference)64.21 (reference)
Living conditions (whole variable)(–)0.534(–)0.526
 Bed in designated facility66.70.73 (0.12 to 4.37)0.60893.80.43 (0.05 to 3.68)0.439
 Room in dormitory22.20.64 (0.12 to 3.43)0.978100.00.999
 Room in separate apartment0.00.999100.00.999
 Separate house37.31.379 (0.79 to 2.40)0.59560.60.78 (0.35 to 1.77)0.560
 Separate apartment33.70.98 (0.60 to 1.61)0.2859.10.52 (0.26 to 1.05)0.070
 Homeless37.21 (reference)70.31 (reference)
Substances abuse (whole variable)(–)0.991(–)0.539
 Alcoholism32.40.97 (0.47 to 1.99)0.93557.10.48 (0.13 to 1.73)0.266
 Drug abuse66.71.15 (0.09 to 14.14)0.914100.00.999
 No official records34.81 (reference)64.81 (reference)
Circumstance of TB discovery
 Discovered actively by healthcare facility35.31.18 (0.88 to 1.57)0.27869.61.79 (1.06 to 3.05)0.030
 Visit with symptoms to healthcare facility34.0(reference)53.01 (reference)
Imprisonment history
 Being in detention or history of detention82.611.9 (3.08 to 45.93) < 0.00198.238.55 (3.65 to 407.42)0.002
 No official history of detention33.71 (reference)59.21 (reference)
Cavitary disease
 Presence of cavities40.11.95 (1.45 to 2.62) < 0.00165.21.46 (0.87 to 2.44)0.151
 No cavities28.61 (reference)63.81 (reference)
Disabilities0.008
 Presence of disability48.91.66 (0.87 to 3.15)0.11987.84.44 (1.47 to 13.38)
 No disability34.11 (reference)61.91 (reference)
TB localization:(–)0.494(–)0.999
 TB of lungs’ lymph system, pleural38.51.69 (0.71 to 4.04)0.2350.0
 Non thoracic TB0.00.9990.0
 Pulmonary TB35.01 (reference)65.31 (reference)
HIV status
 Positive46.81.67 (1.01 to 2.77)0.04767.51.48 (0.62 to 3.53)0.378
 Negative33.81 (reference)64.31 (reference)
Previous therapy
 More than 180 days61.40.92 (0.56 to 1.51)0.732
 Less than 180 days69.71 (reference)
Previous therapy outcome (whole variable)0.061
 Not effective course-79.3(–)0.621
 Other0.01.379 (0.79 to 2.40)0.999
 Transferred100.00.999
 Interrupted course52.50.089
 Effective course61.40.98 (0.60 to 1.61)

HIV human immunodeficiency virus, TB tuberculosis, MDR/RR multidrug resistance/Rifampin resistance, AOR adjusted odds ratio

Analysis for estimation of prevalence of MDR-TB in the new cases (n = 1046) and retreatment cases (n = 394) HIV human immunodeficiency virus, TB tuberculosis, MDR/RR multidrug resistance/Rifampin resistance, AOR adjusted odds ratio 393 re-treatment patients were analyzed in the separate multilevel model. Four variables proved to be significant, with a history of incarceration remaining the strongest associative factor. Such patients were 38.5 times more likely to have MDR/RR-TB (95% CI 3.64 to 407.42, p = 0.002). The presence of disability led to a 4.43 times greater likelihood of contracting MDR/RR-TB (95% CI 1.47 to 13.38, p = 0.008). A final two significant variables were official records of employment (AOR 4.32, 95% CI 1.74 to 10.71, p = 0.002) and being discovered actively by PHF (AOR 1.79, 95% CI 1.05 to 3.05, p = 0.03) (Table 3).

Interpretation of interviews

Healthcare providers confirmed that former inmates are the most problematic group of TB patients. TB care in penitentiary facilities is provided on site, by the often undertrained medical stuff with insufficient funding and equipment. This medical service is not controlled by the authorities of general TB care system and operates without supervision. Lack of centralized control in tandem with poor nutrition and living conditions, overcrowding, treatment regimen neglect by prisons’ medical staff and inmates, make prisons the clearest breeding ground for drug resistance. After being released, prisoners mostly disappear from epidemiological surveillance and, even if they show up for further treatment, they often fail to adhere to the regimen and follow-up procedures and there are no legal tools for healthcare providers to enforce surveillance on them. Among interviewees, there was a consensus that the main obstacle toward achieving full patient’s compliance is the length of therapy. Patients become progressively tired as the treatment advances, especially those with drug resistance, whose regimens typically last for 24 months or more. In these cases, all patients with MDR/RR-TB receive treatment in inpatient conditions for at least twelve months in TBDF. After that period, the patient can be transferred to an outpatient treatment regimen. This option is reserved for patients who have proven themselves trustworthy, showing full compliance during inpatient treatment, and not actively secreting TB mycobacterium so as not to be an ongoing source of infection to others. Patients who do not meet those criteria continue their treatment in inpatient conditions until the end of the course. Such prolonged treatment, combined with insufficient awareness about consequences of intermittent treatment, leads patients to forgo treatment, usually as soon as symptoms disappear. Outpatients phase of regimens provide many opportunities for the patients to drop out due to various reasons. Local TBDF in collaboration with the Russian Red Cross NGO are trying to address this issue by more thoroughly educating patients about TB treatment, giving out free monthly food packages and reimbursement of travel expenses to fully compliant patients. According to physicians, this has been especially effective in encouraging economically disadvantaged patients to continue their treatment. Neither patients nor healthcare providers reported adverse effects to be a significant issue in achieving full treatment adherence. During an inpatient stay, patients are closely monitored for occurrence of adverse effects, where they are also given medication for side effects prevention. Physicians stated that they are equipped with all the necessary medications for the effective management of adverse effects. Monitoring the occurrence of the adverse events among outpatients is carried out through mandatory monthly examination. The only issue here, that during ambulatory phase of the treatment, patients pay out-of-pocket for drugs to combat minor side effects, but in event of adverse effects occurrence during this phase physicians try to hospitalize such patients in TBDF so they could receive free medication and avoid financial burden. Same couldn’t be said about medical service in penitentiary facilities, according to patients, monitoring procedures are next to non-existing and medications for combating adverse events are scarce there. So, it is common for the inmates to discontinue medications as soon as adverse event occurs. Both physicians and healthcare managers reported that TBDF of the region are sufficiently supplied with quality anti-TB medication and all the necessary diagnostic equipment. Healthcare providers stated that both outcome and history of previous treatment contributed to the resistance development contrary to our results that mere fact of previous treatment history is increasing risk of resistance presence regardless of its outcome. Same goes for social status and living conditions, which, according to our statistical data, do not influence resistance development, but from a clinical standpoint, socially disadvantaged patients (particularly homeless ones) display a greater tendency to acquire MDR/RR TB. Another substantial problem that was not supported by data but reported by interviewees, is a greater frequency of alcohol and substances abuse. MDR/RR–TB prevalence in those groups is significantly higher than average. Physicians did not report any association between presence of disability and risk of MDR/RR-TB development but they stated that some patients purposely do not comply with treatment to worsen their condition and acquire disability status for receiving social security benefits.

Discussion

Besides the TB mycobacterium’s major biological features leading to the prevalence of MDR/RR-TB, such as mutation potential [27], strains [28] and draft genome sequences [29], TB related service patterns, demographics and clinical factors also have a significant impact on the development of MDR/RR-TB. Based on the statistical analysis of 1440 TB patients, we identified several factors influencing incidence of MDR/RR-TB in the Khabarovsk region of Russia. Among them are incarceration and previous anti TB treatment history, cavitary disease, HIV co-infection, age, place of residence, retirement status, presence of disability, circumstance of TB discovery and social status. We also concluded that newly diagnosed patients and retreatment patients tend to have different risk factors for contracting and developing MDR/RR-TB. Qualitative survey showed that organization of the TB care system, features of TB treatment process, healthcare and social security legislation play important role in TB epidemiology and may influence incidence of MDR/RR-TB both directly and indirectly. Findings of quantitative data analysis were partially supported by interviews with patients, health managers, and physicians. Incarceration history was identified as the strongest risk factor associated with MDR/RR-TB in all studied groups. In this data, a high prevalence of TB and its drug resistant forms can be seen in prisons all around the world, developed and developing countries alike [30-32]. In 2021, according to Birkbeck University of London, Russia occupied 5th place in the world in terms of total prison population [33]. Based on literature reports and the interpretation of interviews, we can conclude that persistent unhygienic incarceration conditions and low quality of medical care in penitentiary facilities cause high prevalence of MDR/RR among TB infected inmates [7]. This creates a substantial pool of hosts, carrying drug resistant TB in the general population. Contrary to all other healthcare facilities in Russia, penitentiary institutions’ medical service operates independently from the general TB care system (Fig. 1). Such demarcation deprives inmates of proper care and follow up, which they can receive in TBDF. Either a considerable reduction in the total prison population and/or inclusion of penitentiary facilities in the TB care system may address the problem. This predicament of prisons is explained by a contradiction of Russian laws in the field of healthcare. No medical procedures can be instituted without a patient's consent, including hospitalization, so some patients simply leave TBDF at will. To ensure epidemiological surveillance, healthcare providers have to file a claim for forced hospitalization to the court, but there are no legal mechanisms to execute positive court decisions without a patient's written consent. Thereby, infectious TB patients can leave TBDF even with a court decision of forced hospitalization. In 2011 it was that 3500 out of 6000 lawsuits were satisfied in favor of forced hospitalization, and it took an average of 3 months to obtain a court decision and up to 30% of patients left TBDF after forced hospitalization [34]. To ensure proper TB surveillance, measures should be taken to eliminate such a loophole in the legal framework. For reducing the pool of former inmates with MDR/RR-TB, better treatment conditions and epidemiological surveillance in penitentiary facilities must be established. Such intervention of providing TB care for inmates in civil clinics has been implemented in the Tomsk oblast region of Russia from 2000 to 2002 [7], which consisted of two phases of DOTS-plus individualized MDR-TB treatment regimens. In first “intensive” inpatient phase, patients received a high calories and protein rich diet, a separate and better accommodation, and were closely monitored for occurrence of treatment’s side effects. In the second “continuation” ambulatory phase, a community-based approach was used to provide directly observed therapy in outpatient clinics. For avoiding treatment discontinuation, adverse effects were managed aggressively, alongside with provision of monthly food packages to fully compliant patients and reimbursement of travel expenses. The results showed significant increase in compliance, reduction in adverse effects, decrease in mortality rate, and increased treatment efficiency among incarcerated patients. Listed interventions, contrary to penitentiary facilities, are common practice in civil TB designated clinics therefore success of this study supports the necessity of centralized TB care for all TB patients [8]. As it was reported by numerous studies, poor adherence to drug susceptible TB treatment and poor screening for MDR/RR-TB are the major threats to MDR/RR-TB spread. According to the WHO, in 2020 DST underwent 92% and 94% of all newly diagnosed and retreatment TB cases respectively [4]. Such large-scale testing combined with routine usage of direct PCR DST and culture-based DST methods in all TB suspected patients provide a reliable and effective system of monitoring and detection of MDR/RR-TB. This conclusion is supported by the results of healthcare providers’ interviews. A much larger concern is the problem of the poor adherence to the TB treatment. Implementation of DOT and DOTS plus were beneficial but didn’t fully address this problem in Russia [7, 34]. As was reported, the length of therapy seems to be a major factor affecting a patient’s drop-out rate. Because of Russian legislation, it is challenging to keep patients in hospitals against their will but attempts to overcome this obstacle are present. For example, a special mobile medical team may visit some infected patients daily in their homes to deliver DOT. Those patients are typically not from economically disadvantaged groups, and their living conditions are much better than those of inpatient TB designated facilities, so their compliance is much higher when they stay in conditions that can be compared to home confinement but not in inpatient facility. Another instance is that pediatric TBDF provides compulsory school education to children, so they don’t disrupt their studies during a hospital stay. A study from Belarus performed in 2009 identified positive association between disability and MDR/RR-TB prevalence [35]. Concerning another type of social security policies, influence of retirement social status on the risk of MDR/RR-TB development is uncertain as both positive and negative relationships were reported in the literature [13, 36]. A study conducted in Ethiopia revealed a tenfold increase in risk of MDR-TB for the military pensioners, explaining it as pensioners receive much fewer social benefits compared to the active military servicemen [13]. At the same time, researchers from Belarus describe a protective effect similar to results received in our study with a reported AOR of 0.6 [36]. Such consistency in results may be due to that Russia and Belarus, both being part former Soviet Union members, have similar social security policies regarding retirement benefits and benefits for people with permanent inability to work. There is a need for further investigation of that phenomenon in countries with and without such policies. Such studies may support disability status as a risk factor or reveal its connection to social security policies. It should be mentioned as limitation, that we had no data on whether disability was TB-related or determined by another disease, thus the full statistical meaning of this variable remains uncertain. Our results concerning association between MDR/RR-TB with younger age, cavitary disease, and positive HIV status correspond with previous studies [28, 37, 38]. Regarding place of residency, city dwellers have better access to healthcare in general and have a far greater capacity to complete annual chest X-rays. Therefore, cities tend to see greater number of people diagnosed with TB than in rural areas. Likewise, the increased population density in cities provides more chances to contract MDR/RR–TB. This can explain an emerging trend observed by physicians—the increase in the prevalence of MDR / RR-TB among newly diagnosed patients. Our study has several limitations. We failed to explain the significance of official employment status as a risk factor among re-treatment patients and insignificance of social status and living conditions, as these results contradict with previous studies [12, 38–40]. Also, our data indicates that outcome of previous treatment does not influence risk of MDR/RR-TB development which contradicts with previous studies and healthcare providers’ interviews [38]. During patients selection process, gyrB mutation of m.tuberculosis in DST was not tested due to usage of premanufactured reagent in allele-specific PCR [25], but because of simultaneous use of cultural DST methods we are confident that no patient with fluoroquinolones resistance was enrolled in the study. It should be stated that data on narcotics and alcohol use disorders was based on official records of seeking medical attention for such conditions. Because significantly few patients in Russia seek medical attention for addiction-related problems [41] based on this and interviewee reports of high prevalence of these conditions in TB patients and corresponding literature [19], we acknowledge that our data may not fully represent the overall prevalence of substance abuse in the studied population. It is worth mentioning that, even so according to the healthcare professionals’ interviews, TBDF is sufficiently supplied with medications of proper quality, our quantitative data didn’t contain information about supply and quality of anti-TB drugs. Another piece of valuable information that has not been represented in the quantitative data set was the occurrence of adverse effects. But based on the in-depth interview results, we can conclude that adverse events don’t affect compliance of patients receiving TB care in TBDF. Contrary to the penitentiary institutions where treatment drop-out due to adverse events occurrence is a major problem [31].

Conclusion

Incarceration and treatment history, regardless of outcome, seems to be a major factor influencing MDR/RR-TB prevalence in Russia. It is essential for the TB care system to eliminate legal loopholes, which deprive doctors of means to enforce quarantine procedures and epidemiological surveillance on infected patients, former and current inmates, who seem to be the main source of MDR/RR-TB hosts in the general population. The last can be addressed by treating inmates in the facilities of the general TB care system. In the end, we want to say that further attempts to better patients’ education and public awareness about TB, with continuing coordinated and centralized care for patients with TB, in tandem with greater compliance by patients with TB treatment guidelines, are the keys to success in the battle against MDR/RR-TB globally.
  27 in total

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Authors:  H Ohno; H Koga; S Kohno
Journal:  Kekkaku       Date:  1998-11

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3.  Risk factors for poor engagement in drug-resistant TB care in South Africa: a systematic review.

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4.  Evaluation of risk factors associated with the development of MDR- and XDR-TB in a tertiary care hospital: a retrospective cohort study.

Authors:  Amna Saifullah; Tauqeer Hussain Mallhi; Yusra Habib Khan; Muhammad Shahid Iqbal; Nasser Hadal Alotaibi; Abdulaziz Ibrahim Alzarea; Maria Rasheed
Journal:  PeerJ       Date:  2021-03-18       Impact factor: 2.984

Review 5.  Global burden of HIV, viral hepatitis, and tuberculosis in prisoners and detainees.

Authors:  Kate Dolan; Andrea L Wirtz; Babak Moazen; Martial Ndeffo-Mbah; Alison Galvani; Stuart A Kinner; Ryan Courtney; Martin McKee; Joseph J Amon; Lisa Maher; Margaret Hellard; Chris Beyrer; Fredrick L Altice
Journal:  Lancet       Date:  2016-07-14       Impact factor: 79.321

6.  Risk factors of multidrug-resistant tuberculosis: A global systematic review and meta-analysis.

Authors:  Ivan Surya Pradipta; Lina Davies Forsman; Judith Bruchfeld; Eelko Hak; Jan-Willem Alffenaar
Journal:  J Infect       Date:  2018-10-16       Impact factor: 6.072

7.  High time to use rapid tests to detect multidrug resistance in sputum smear-negative tuberculosis in Belarus.

Authors:  V Rusovich; A M V Kumar; A Skrahina; H Hurevich; A Astrauko; P de Colombani; K Tayler-Smith; M Dara; R Zachariah
Journal:  Public Health Action       Date:  2014-12-21

8.  Whole-genome sequencing for prediction of Mycobacterium tuberculosis drug susceptibility and resistance: a retrospective cohort study.

Authors:  Timothy M Walker; Thomas A Kohl; Shaheed V Omar; Jessica Hedge; Carlos Del Ojo Elias; Phelim Bradley; Zamin Iqbal; Silke Feuerriegel; Katherine E Niehaus; Daniel J Wilson; David A Clifton; Georgia Kapatai; Camilla L C Ip; Rory Bowden; Francis A Drobniewski; Caroline Allix-Béguec; Cyril Gaudin; Julian Parkhill; Roland Diel; Philip Supply; Derrick W Crook; E Grace Smith; A Sarah Walker; Nazir Ismail; Stefan Niemann; Tim E A Peto
Journal:  Lancet Infect Dis       Date:  2015-06-23       Impact factor: 25.071

9.  Factors associated with multidrug-resistant tuberculosis (MDR-TB) in Bhutan: A nationwide case-control study.

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Journal:  BMC Public Health       Date:  2021-06-24       Impact factor: 3.295

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