Next Article in Journal
Social Network Analysis of COVID-19 Sentiments: 10 Metropolitan Cities in Italy
Previous Article in Journal
Tribal Tobacco Use Project II: Planning, Implementation, and Dissemination Using Culturally Relevant Data Collection among American Indian Communities
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Tuberculosis among People Living on the Street and Using Alcohol, Tobacco, and Illegal Drugs: Analysis of Territories in Extreme Vulnerability and Trends in Southern Brazil

by
Alessandro Rolim Scholze
1,*,
Josilene Dália Alves
2,
Thaís Zamboni Berra
1,
Antônio Carlos Vieira Ramos
1,
Flávia Meneguetti Pieri
3,
Sandra Cristina Pillon
4,
Júlia Trevisan Martins
3,
Maria José Quina Galdino
5,
Emiliana Cristina Melo
5,
Felipe Mendes Delpino
1,
Ariela Fehr Tártaro
1,
Inês Fronteira
6 and
Ricardo Alexandre Arcêncio
1
1
Department of Maternal-Infant and Public Health Nursing, Ribeirão Preto College of Nursing, University of São Paulo, Ribeirão Preto 14040-902, Brazil
2
Institute of Biological Sciences and Health, Federal University of Mato Grosso, Barra do Garças 78605-091, Brazil
3
Department of Nursing, State University of Londrina, Londrina 86057-970, Brazil
4
Department of Psychiatric Nursing and Human Sciences, Ribeirão Preto College of Nursing, University of São Paulo, Ribeirão Preto 14040-902, Brazil
5
Department of Nursing, State University of Northern Paraná, Bandeirantes 86360-000, Brazil
6
Global Health and Tropical Medicine, Instituto de Higiene e Medicina Tropical, University Nova de Lisboa, 1349-008 Lisboa, Portugal
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2022, 19(13), 7721; https://doi.org/10.3390/ijerph19137721
Submission received: 26 March 2022 / Revised: 15 June 2022 / Accepted: 21 June 2022 / Published: 23 June 2022
(This article belongs to the Topic Impact of Globalization on Healthcare)

Abstract

:
(1) Background: Tuberculosis presents an epidemiological trend toward inequality, especially among people in social exclusion and situations of vulnerability. This study aimed to analyze territories with a concentration of people diagnosed with tuberculosis in a street situation and who partake in chronic use of alcohol, tobacco, and illicit drugs. We also analyzed trends in this health condition in southern Brazil. (2) Methods: Ecological study, developed in the 399 municipalities of Paraná, southern Brazil, with all tuberculosis cases in the homeless population registered in the Information System of Notifiable Diseases between 2014 and 2018. For data analysis, we used descriptive statistics, the Prais–Winsten autoregression method for the time series, and the Getis-Ord Gi technique* for spatial analysis. (3) Results: in total, 560 cases were reported. We found a predominance of alcohol, smoking, and illicit drug users, with an increasing trend in the state and clusters of spatial risk in the East health macro-region. (4) Conclusions: We observed territories with critical levels of highly vulnerable people who use psychoactive substances and are in a street situation. The results highlight the importance of incorporating public policies of social protection for these individuals and resolutive health services that receive these cases and assist in eradicating TB.

1. Introduction

Tuberculosis (TB) is an infectious disease caused by Mycobacterium tuberculosis. Considered a serious public health problem, it is among the ten most common causes of preventable death in the world [1,2,3]. Historically, TB presents an epidemiological trend toward inequality, especially among people in social exclusion and situations of vulnerability [4]. Thus, the homeless population, the population deprived of liberty (PPL), people infected with human immunodeficiency virus (HIV), and users or addicts of psychoactive substances, alcohol, tobacco, and other drugs [5,6] are considered at high risk of contributing to the spread of this disease.
In this sense, the homeless population is defined as a heterogeneous population that has extreme poverty, interrupted or weakened family ties, and the absence of regular conventional housing in common. This population uses public spaces and degraded areas as a living and subsistence space, temporarily or permanently, as well as reception units for temporary accommodation or as temporary housing [7].
Being homeless is an aggravating factor for the spread of TB in social exclusion groups since TB infection is transmitted via the respiratory route by inhaling the sputum droplets expelled by an infected person [6]. Given the social situation of homeless people, there may be a considerable spread of the disease among them since they tend to congregate in groups. Especially among the homeless population, TB has a high prevalence due to close contact within a large contingent of homeless people and frequent movement between different shelters and territories [8].
In addition, most infected people do not present signs and symptoms of the disease and are classified as carriers of latent infection by TB. The absence of signs and symptoms prevents the search for treatment and intensifies the spread of the disease. It is estimated that approximately 2 to 3 billion people in the world are infected with TB, and of these, about 5% to 15% will evolve to active TB during their lifetime [9,10]. Studies point out that TB among the homeless population is the third-largest cause of illness and has a 10 to 85 times higher rate of developing into latent or active TB infection when compared with the general population [11]. In the United States, about 5% of TB cases have been homeless at some point in the 12 months prior to diagnosis [12].
Among individuals diagnosed with TB in the United States, the incidence rate is 36 to 47 cases per 100 inhabitants, compared to the incidence in the general population of 2.8 cases per 100 inhabitants [13]. In Germany, TB in the homeless has 30 cases per 100 inhabitants, compared to the general population of 18 cases per 100 inhabitants [8]. In western Europe, the prevalence of TB among homeless people ranges from 1% to 2% for active TB infection and up to 45% for latent infection [14].
TB among the homeless population is a challenge since even those countries with low endemicity show a high TB incidence among homeless people. This factor contributes to the maintenance of the TB burden in these countries, thus making it difficult to achieve the goals established by the End TB strategy.
This evidence indicates that vulnerable populations have become a major challenge for countries to develop strategies and achieve their TB elimination goals globally. In social epidemiology, there are several resources available that demonstrate the strength of the social determinants of territories in the TB progression chain, with a large number of studies using spatial analysis in the general population. However, this is not the reality for the homeless population since an address is an aspect required for geoprocessing/georeferencing; as such, many studies using these approaches exclude this population.
Another gap is that vulnerability is multifaceted. Within the same context, many vulnerabilities end up countering each other, causing cases to become overly complex, requiring equally complex approaches toward alleviating suffering and bringing solutions to the problem. Given the presented problems, the present study is of great importance. It brings together the question of territories and the homeless population with TB and the relationship with alcohol, tobacco, and illicit drugs; as a result, disease control is far from being achieved in some regions and territories. Therefore, this study aimed to analyze territories where there is a concentration of people diagnosed with tuberculosis, in a street situation, and who partake in chronic use of alcohol, tobacco, and illicit drugs. We also analyzed trends in this health condition in southern Brazil.

2. Materials and Methods

2.1. Study Design

Ecological study [15].

2.2. Study Location and Population

This study was carried out in the 399 municipalities of Paraná, located in the southern region of Brazil at the geographic coordinates 24°59′ S latitude and 53°56′ W longitude; the estimated population is 11.34 million inhabitants. It is the fifteenth state of Brazil with the largest national territory and the fifth-highest population [5].
In 2020, Paraná had 2,190 TB cases, obtaining an incidence of 19 cases per 100,000 inhabitants; there were 157 deaths, with an incidence of 1.4 per 100,000 inhabitants. About 6.2% of patients abandon treatment [3].
According to the Inter-sector Committee for Monitoring and Monitoring the Population Policy in Street Situation (CIAMP Street/PR), which aims to enable and assist in the implementation and monitoring of public policies aimed at the population in a street situation, it is estimated that, in 2021, the state had about 8,659 people registered at CIAMP street/PR. It is noteworthy that this may be an under notification, indicating that the number should be higher, mainly due to the current situation in the country, as well as the high turnover of homeless people. Between 2015 and 2020, the state showed a 65% increase in TB cases in the homeless population, and in 2020, a 6.8% increase in the percentage of cases [16].
To develop the spatial distribution, we subdivided the 399 municipalities that make up the state of Paraná into four health macro-regions (East, North, Northwest, and West) and used these as a unit of geographical analysis. Figure 1 illustrates the location of the state and its health macro-regions.

2.3. Inclusion Criteria

We considered all cases of TB in the homeless population obtained in the Information System of Notifiable Diseases (SINAN) from 2014 to 2018. These data were made available by the Health Department of the State of Paraná in an electronic spreadsheet in Excel.
The adopted inclusion criteria were people diagnosed with TB, included in the notification form as a person living on the street, alcohol, tobacco, or illicit drug user, and aged 18 years or older. To identify risk areas and time series, the population was subdivided into general TB, TB alcoholism, TB smoking, and TB users of illicit drugs. It is emphasized that an individual may belong simultaneously to one or more study groups.

2.4. Analysis Plan

First, the descriptive statistics of the data were performed utilizing absolute and relative frequency, which used the following variables: alcoholism, smoking, and illicit drugs, sex, age group, race/color and education, TB/HIV coinfection, diabetes mellitus, mental disorder, and data related to the clinical profile of TB, such as type of entry, form, radiography, sputum smear, histopathology, molecular test, and case closure. It should be noted that the terminologies described in the Sinan notification form were kept in full; it should be noted that this form is a structured document recommended by the Ministry of Health and applies throughout the national territory of Brazil.
The IBM SPSS software version 25 was used to analyze the data.

2.5. Time Series

Time series are characterized as observations taken sequentially over time [17]. It is worth noting that the temporal trend refers to the direction in which the time series develops according to a determined time interval, which may follow a growth, decrease, or stationary pattern [18,19]. The month and year of notification of TB cases were used to perform the analysis.
The Prais–Winsten autoregression method [18] was performed in STATA software, version 14, to classify the event’s temporal trend as increasing, decreasing, or stationary in the study period. When the temporal trend was classified as increasing or decreasing, the percentage of monthly variation (MPC—monthly percent change) and their respective 95% confidence intervals (95 CI) were calculated [17].
Next, we used the robust time series decomposition method called seasonal trend by Loess (STL by Loess) [16]. This decomposition method is based on a locally weighted regression (Loess). It is the method used to estimate nonlinear relations, managing to separate the components that make up a time series: trend, seasonality, and noise [19,20]. For the analysis, RStudio software and the forecast package were used.
In contrast to the Prais–Winsten method, where the time trend assessment is global and a constant is generated by classifying the whole period under study, the STL method allows for the evaluation of the time trend over the whole period under analysis, notes variations over time, checks if the trend has always been increasing/decreasing/stationary, or if there have been periods of variations with peaks and/or decreases.

2.6. Spatial Analysis

The techniques called Getis-Ord General G and Getis-Ord Gi* were used to identify whether clusters were formed, using the number of cases per municipality. The Getis-Ord General G technique is based on the Moran Global Index, and, as in inferential statistics, the results are based on the null hypothesis that there is no spatial grouping. If p is significant, the null hypothesis can be rejected, and the z-score value becomes important, where its values of ±3 represent a 99% confidence level [21,22]. If the z-score value is positive, the observed G-Index is higher than expected, indicating high event indices grouped in the area under study. A negative z-score value of the G-index is considered lower than the expected index, indicating that low values are grouped in the study area [23].
The Getis-Ord Gi* technique indicates a local association, considering the values for each census tract from a neighborhood matrix. In this analysis, a z-score was generated for statistically significant municipalities, and the higher the z-score, the more intense the grouping of high values is (hotspot). The logic is the same for the z-negative score, i.e., the lower the z-score, the more intense the grouping of low values (cold spot) [23].
In addition to the z-score, the p-value and significance level (Gi-Bin) are also provided, which identify statistically significant hot and cold spots. The values may vary between +/− 3 and reflect statistical significance with a confidence level of 99%, +/− 2 with a confidence level of 95%, and +/− 1 with a confidence level of 90%, with a zero-value corresponding to non-statistically significant areas [23].

2.7. Ethical Aspects

The study was approved by the Research Ethics Committee of the Escola de Enfermagem de Ribeirão Preto da Universidade de São Paulo, under CAAE (Process number: 24963319.1.0000.5393).

3. Results

Between 2014 and 2018, 560 cases of TB were reported among the homeless population. The analysis showed that the consumption of psychoactive substances was prevalent in homeless users (n = 420; 36.30%), as were smokers (n = 382; 33.02%), and users of other drugs (n = 355; 30.68%).
Table 1 shows the characterization of TB cases in the homeless population subdivided by type of psychoactive substance. The total sample showed a higher predominance of TB in males, in the age group above 40 years of white race/color, with education from the fifth to eighth grade of elementary school, and living in the urban perimeter. The sociodemographic characteristics of the homeless population of users of alcohol, tobacco, and illicit drugs are similar to that of the general homeless population. Some peculiarities were noted, such as one-third of alcohol and tobacco users had a poor education (first to fourth grade), 43.1% (n = 153) of other drug users were younger (30 to 39 years of age) when compared to alcohol users (50.2%; n = 211) and tobacco (47.1%; n = 180) users, who were in the age group of 40 years or older. Notably, 73.7% (n = 412) of the general street population who had TB did not receive government benefits. Regarding the presence of chronic diseases, it was observed that TB-AIDS coinfection was the most prevalent among all variables studied, followed by the categories “other diseases” and mental illness.
Regarding the clinical profile of TB cases in the homeless population (Table 2), in the general street population, there was a prevalence of new cases, pulmonary TB, with suspect chest radiography, positive sputum culture, histopathology not performed, HIV negative test, molecular tests not performed, sensitivity tests not reported, and curative TB treatment. When analyzing the clinical profile of cases associated with the type of drug, it was found that the same specificities of the total population occurred, noting that, regarding the closure situation, abandonment and death due to TB and other causes were more present among patients who used alcohol, tobacco, and other drugs.
The temporal trend of TB cases in the homeless population (Table 3) presented an increasing scenario for all categories analyzed. For the population using alcohol, the growth was 29.71% per month (95% CI 18.03–42.56), tobacco 27.93% per month (95% CI 16.68–39.95), other drugs 30.31% per month (95% CI 18.57–43.21), and general drugs 38.35% (95% CI 23.31–55.23).
Figure 2 shows the time series decomposition technique. We found an increase in the temporal trend of TB cases in the homeless population for alcohol, tobacco, and other drugs and in the general street population. We identified slight fluctuations of the temporal trend concerning the number of cases over the months, thus corroborating the findings presented in Table 1 referring to the Prais–Winsten analysis.
For the results of the global spatial association (G), we observed that the values of the z-score and the pseudo-significance test confirmed the non-randomness of TB cases in the population using alcohol (z-score of 3.00 and p <0.00), tobacco (z-score 3.12 and p < 0.00), illicit drugs (z-score 2.79 and p < 0.00), and general drugs (total) (z-score 3.78 and p < 0.00). Figure 3 shows the local spatial association (Gi*) of TB cases, which shows hotspots in the Eastern macro-region in the metropolitan region of Curitiba for users of alcohol, tobacco, and illicit drugs and in the general street population.

4. Discussion

We analyzed territories with a concentration of people diagnosed with tuberculosis, in a homeless situation, and who partake in the chronic use of alcohol, tobacco, and illicit drugs; we also assessed the trends of this health condition in southern Brazil. We observed that, in the south of Brazil, despite being considered one of the most developed regions of the country, there were still clusters or areas of the population with extreme vulnerability, people diagnosed with TB, using psychoactive substances, and still on the street. There was also a growing increase in this situation in the East health macro-region (metropolitan region of Curitiba, the state capital).
International and national studies indicate that the homeless population has a high prevalence of TB associated with the use of alcohol, tobacco, and illicit drugs, which are risk factors that favor the development of new cases and the maintenance of the TB transmission cycle [4,8,24]. Thus, the homeless population has a 48 to 67 times greater chance of developing TB when compared to the general population [25].
A study conducted in the United States between 2006 and 2010 found that the annual incidence of TB among the homeless population ranged from 36 to 47 cases per 100,000 inhabitants [26]. In Germany, the incidence of TB is 30 cases per 100,00 inhabitants [8], whereas, in Brazil, there are no specific data that address this population.
It is worth noting that Brazil does not have official data on the size of the homeless population, considering that the demographic census does not include homeless residents in the investigation. Since these data are collected in fixed residences, it is impossible to correctly quantify these individuals, which makes them invisible [27].
The high prevalence of TB in this population is related to precarious urbanization, sanitary conditions (close contact with a contingent of people and movement between different shelters), social exclusion, and extreme poverty [28]. These individuals experience a highly vulnerable environment on a daily basis, which leads to health problems and infections, including TB [8]. This population also has high rates of avoidable death from all causes compared to the general population, which exemplifies the influence of inequalities and social determinants of health in the illness process of these individuals [29].
In addition, this population has specificities that favor the development of health problems, such as poor education, which consequently generates ignorance regarding primary health care and the health-disease process. Moreover, many have difficulties in accessing health services, experience stigma, prejudice, conflicting or nonexistent family ties, and the lack of a life project, among other factors [4,28].
The homeless population presents a deficit in self-care concerning hygiene and eating habits, which contributes to a precarious lifestyle and a high prevalence of complications due to chronic diseases, infectious conditions, and injuries related to violence [30]. Therefore, strategic actions should be implemented for the coverage and supply of health services, social assistance, and effective housing to these individuals so that basic human needs are guaranteed.
When evaluating the spatial determinants and the conformation of the clusters when applying the Getis-Ord Gi* technique, clusters of hotspots were identified in the East health macro-region. It is estimated that, in Brazil, there is a population of approximately 100,000 homeless and that 75% of this population lives in municipalities with more than 100,000 inhabitants [27].
Access to housing is understood as an important determinant of health, and homelessness is directly related to an increase in morbidity and mortality compared to the sheltered population. Mortality among the homeless population is 3 to 11 times higher [31].
In addition, it can be highlighted that mobility among homeless people, loss of follow-up, lack of attendance to follow-up appointments, unstable housing, incarceration, fear of invasive investigations and the side effects of TB treatment, transportation and location of health services, lack of flexible hours of care, and problems with remembering commitments and the correct use of medicines are some barriers that hinder a favorable outcome of TB treatment among the homeless population and users/addicts of psychoactive substances [32].
It is necessary to recognize the magnitude of the public health problem present in large cities among the street population and to implement public policies aimed at this heterogeneous group that is in extreme social vulnerability [33,34]. Thus, implementing policies in terms of social support and reintegration of the street population into society is extremely important, as are programs aimed at income distribution, such as the Bolsa Família Program. The Bolsa Família Program aims to provide income to families in poverty and extreme poverty. The aid seeks to overcome the situation of vulnerability and poverty, thus ensuring the right to food and access to education and health [35]. The implementation of the Bolsa Família Program provided an increase in the rate of adherence and cure of patients with TB, highlighting the need to implement policies aimed at social support [36].
Another behavior analyzed in this study was that TB is growing among alcohol, tobacco, and illicit drug users. This result is extremely important since the higher the consumption of psychoactive substances by the homeless population, the worse the prognosis of these individuals; other problems include maintenance, increased incidence, and the recurrence of new cases of TB and drug-resistant TB TB-DR. In addition, homeless people who use psychoactive substances move through spaces/territories with a high number of individuals, a characteristic that contributes to a greater spread of the disease.
Therefore, the use of psychoactive substances is considered an aggravating and complicating factor for the containment and eradication of TB in the world. It is noteworthy that the Sustainable Development Goals of the World Health Organization reinforce the importance of implementing prevention and treatment of disorders related to the use of alcohol and other drugs among vulnerable populations [37].
In this sense, investing in public policies, health services targeted at vulnerable populations, and skilled professionals can be an effective tool for early diagnosis, correct treatment, a decrease in the incidence of TB, guaranteed access to health services and social support, and a direction for the social reintegration of individuals who are on the street.
Moreover, the use of psychoactive substances among vulnerable populations promotes community transmission and TB contamination since these individuals live in an environment of extreme sanitary prevarication and share objects and materials such as pipes and needles to make use of psychoactive substances. This characteristic contributes to the spread and dissemination of latent and active TB in these territories [38].
It was also observed that the worst outcomes in treatment and death were present in vulnerable populations that used or were dependent on any substance. Therefore, the vulnerable population has a high TB infectivity rate and thus makes it a strategic population for actions aimed at eradicating TB in the world. Developing public policies aimed at vulnerable populations is a way to contain the spread of the disease in these territories [33,39] and thus achieve the goals established through the End TB strategy.
In order to reduce the infection rate and decrease the number of new cases of TB or relapses, countries need to develop specific strategies aimed at vulnerable populations, such as users of alcohol, tobacco, and other drugs, whereas by implementing health actions directed at these individuals, it is possible to ensure early detection and diagnosis of TB and, consequently, effective treatment [39]. It should be emphasized that countries need to act and invest in research to highlight the territories with the greatest risk of illness and thus identify why people get sick in different territorial regions [40].
Ensuring health services that are responsive and targeted to vulnerable populations is of utmost importance, as is ensuring reception and, consequently, providing the correct sequence during treatment. However, what is observed in health services is a barrier to access and health care for vulnerable populations, which makes these people invisible to the public health system and contributes to the maintenance of TB and other health problems [41].
Strategies that can enhance and provide more comprehensive health care to these populations are the incorporation of health services within vulnerable territories and the implementation of street offices and health care within prisons. The purpose of street offices is to expand the access of the homeless population to health services and to provide comprehensive health care to individuals who are in vulnerable conditions or with fragile family ties [41,42].
The street office has a work dynamic that allows for the active search for people living on the street in several places in the city, valuing welcoming and the creation of links in order to supply the needs of these individuals, without judgment or social standards, and guaranteeing them the right to health advocated in the constitution [43].
It is also relevant to consider the implementation in the country of networks that seek better social protection for vulnerable populations, considering that, when investing in measures that aid equity in health and poverty reduction, a reversal will occur in the context of morbidity and mortality of TB. This strategy is emphasized and recommended by the World Health Organization.
Another measure to be adopted is the incorporation of health policies aimed at reducing the consumption of psychoactive substances in vulnerable territories and throughout society. One aim is the development of prevention and promotion actions related to early consumption among children and adolescents, promoting actions in vulnerable populations, and, in general, a conscious consumption of the substance; by incorporating measures aimed at conscious consumption, this factor reduces exposure to risk, as well as health problems [16].
When analyzing the strategies used to control TB in other countries, it was found that, in the United States, actions such as monetary incentives and education programs are implemented to improve adherence to treatment since these measures help in adherence to treatment and contribute to a better level of treatment completion and thus interruption of the TB transmission cycle [44].
Another feature that helps to reduce the risk of infection and improves the chance of successful treatment is the implementation of programs focused on the health education of the homeless population. In other words, the development of early interventions aimed at preventing TB infection, promoting early diagnosis, and reducing treatment abandonment, drug-resistant TB, and death.
Finally, this study provides significant contributions and joins the global effort to control TB since it was possible to incorporate statistical methods that identified areas of spatial risk for TB among users dependent on alcohol, tobacco, and illicit drugs.

5. Conclusions

This study advances scientific knowledge since few studies have addressed the geoepidemiology of TB between the homeless population and the relation of chronic use of alcohol, tobacco, and illicit drugs. In this sense, it was possible to highlight territories at risk for the development of TB in the homeless population and their relationship with the territories that have a large number of people.
It is necessary to incorporate public policies of social protection for these individuals and resolutive, welcoming health services that will assist in eradicating TB.

Author Contributions

Conceptualization, A.R.S., J.D.A. and R.A.A.; methodology, A.R.S., J.D.A., T.Z.B., F.M.P. and R.A.A.; software, A.R.S. and A.C.V.R.; formal analysis, A.R.S., J.D.A., T.Z.B., A.C.V.R., I.F. and R.A.A.; investigation, A.R.S.; data curation, A.R.S., J.D.A., T.Z.B., A.C.V.R. and R.A.A.; writing—original draft preparation, A.R.S.; writing—review and editing, A.R.S., F.M.P., S.C.P., J.T.M., M.J.Q.G., E.C.M., F.M.D., F.M.P., A.F.T., I.F. and R.A.A.; supervision, R.A.A.; project administration, A.R.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was approved by the Research Ethics Committee of the Escola de Enfermagem de Ribeirão Preto da Universidade de São Paulo, under CAAE (Process number: 24963319.1.0000.5393).

Informed Consent Statement

Consent was waived for all subjects involved in the study.

Data Availability Statement

The data presented in this study are available on request from the corresponding author on reasonable request.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Adjobimey, M.; Ade, S.; Wachinou, P.; Esse, M.; Yaha, L.; Bekou, W.; Campbell, J.R.; Toundoh, N.; Adjibode, O.; Attikpa, G.; et al. Prevalence, acceptability, and cost of routine screening for pulmonary tuberculosis among pregnant women in Cotonou, Benin. PLoS ONE 2022, 17, e0264206. [Google Scholar] [CrossRef]
  2. Word Health Organization. Global Tuberculosis Report 2020; WHO: Geneva, Switzerland; p. 208. Available online: https://apps.who.int/iris/bitstream/handle/10665/336069/9789240013131-eng.pdf (accessed on 14 December 2021).
  3. Ministry of Health. Health Surveillance Secretariat. In Epidemiological Bulletin, Brasília. Special Issue. March 2021. Available online: https://www.gov.br/saude/pt-br/media/pdf/2021/marco/24/boletim-tuberculose-2021_24.03 (accessed on 14 December 2021).
  4. Dos Santos, A.C.E.D.; Brunfentrinker, C.; Pena, L.D.S.; Saraiva, S.D.S.; Boing, A.F. Analysis and comparison of tuberculosis treatment outcomes in the homeless population and in the general population of Brazil. J. Bras. Pneumol. 2021, 47, e20200178. [Google Scholar] [CrossRef]
  5. Pedro, A.S.; Gibson, G.; Santos, J.P.C.; Toledo, L.M.; Sabroza, P.C.; Oliveira, R.M. Tuberculosis as a marker of inequities in the context of socio-spatial transformation. J. Public Health 2017, 51. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Eddabra, R.; Neffa, M. Epidemiological profile among pulmonary and extrapulmonary tuberculosis patients in Laayoune, Morocco. Pan Afr. Med J. 2020, 37, 56. [Google Scholar] [CrossRef]
  7. Presidency of the Republic. Establishes the National Policy for the Homeless Population and Its Intersectoral Follow-Up and Monitoring Committee and Other Measures; Decree No. 7053, of 23 December 2009; Official Federal Gazette: Brasilia, Brazil, 2009. Available online: http://www.planalto.gov.br/ccivil_03/_ato2007-2010/2009/decreto/d7053.htm (accessed on 14 December 2021).
  8. Von Streit, F.; Bartels, C.; Kuczius, T.; Cassier, C.; Gardemann, J.; Schaumburg, F. Prevalence of latent tuberculosis in homeless persons: A single-centre cross-sectional study, Germany. PLoS ONE 2019, 14, e0214556. [Google Scholar] [CrossRef]
  9. Anton, C.; Machado, F.D.; Ramirez, J.M.A.; Bernardi, R.M.; Palominos, P.E.; Brenol, C.V.; Mello, F.C.D.Q.; Silva, D.R. Latent tuberculosis infection in patients with rheumatic diseases. J. Bras. Pneumol. 2019, 45, e20190023. [Google Scholar] [CrossRef]
  10. Sterling, T.R.; Njie, G.; Zenner, D.; Cohn, D.L.; Reves, R.; Ahmed, A.; Menzies, D.; Horsburgh, C.R.; Crane, C.M.; Burgos, M.; et al. Guidelines for the Treatment of Latent Tuberculosis Infection: Recommendations from the National Tuberculosis Controllers Association and CDC, 2020. MMWR. Recomm. Rep. 2020, 69, 1–11. [Google Scholar] [CrossRef]
  11. Chekesa, B.; Gumi, B.; Chanyalew, M.; Zewude, A.; Ameni, G. Prevalence of latent tuberculosis infection and associated risk factors in prison in East Wollega Zone of western Ethiopia. PLoS ONE 2020, 15, e0233314. [Google Scholar] [CrossRef]
  12. Schmit, K.M.; Wansaula, Z.; Pratt, R.; Price, S.F.; Langer, A.J. Tuberculosis—United States, 2016. MMWR. Morb. Mortal. Wkly. Rep. 2017, 11, 289–294. [Google Scholar] [CrossRef] [Green Version]
  13. Nwana, N.; Marks, S.M.; Lan, E.; Chang, A.H.; Holcombe, M.; Morris, S.B. Treatment of latent Mycobacterium tuberculosis infection with 12 once weekly directly-observed doses of isoniazid and rifapentine among persons experiencing homelessness. PLoS ONE 2019, 3, e0213524. [Google Scholar] [CrossRef] [Green Version]
  14. Janssens, J.-P.; Wuillemin, T.; Adler, D.; Jackson, Y. Screening for tuberculosis in an urban shelter for homeless in Switzerland: A prospective study. BMC Infect. Dis. 2017, 17, 347. [Google Scholar] [CrossRef] [Green Version]
  15. Morgenstern, H. Ecologic Studies. In Modern Epidemiology, 3rd ed.; Rothman, K.J., Greenland, S., Lash, T.L., Eds.; Lippincott Williams & Wilkins: Philadelphia, PA, USA, 2008; pp. 512–531. [Google Scholar]
  16. Secretary of Justice, Family and Labor. Intersectoral Committee for Follow-Up and Monitoring of Homeless Population Policy. In Period from July 2021 to December 2021. Available online: https://www.justica.pr.gov.br/Pagina/CIAMP-Rua#:~:text=Atualmente%2C%20o%20Cadastro%20%C3%9Anico%20do,em%20situa%C3%A7%C3%A3o%20de%20rua%20cadastradas (accessed on 6 January 2022).
  17. Antunes, J.L.F.; Cardoso, M.R.A. Using time series analysis in epidemiological studies. Epidemiol. Serv. Saude 2015, 24, 565–576. [Google Scholar] [CrossRef]
  18. Prais, S.J.; Winsten, C.B. Trend estimators and serial correlation. In Trend Estimates and Serial Correlation; Cowles Commission Discussion Paper, Stat. No. 383; University of Chicago: Chicago, IL, USA, 1954. [Google Scholar]
  19. Cleveland, R.B.; Cleveland, W.S.; McRae, J.E.; Terpenning, I. STL: A seasonal-trend decomposition procedure based on Loess. J. Off. Stat. 1990, 6, 3–73. [Google Scholar]
  20. Brockwell, P.J.; Davis, R.A. Introduction to Time Series and Forecasting, 2nd ed.; Springer-Verlag: New York, NY, USA, 2002. [Google Scholar]
  21. Caliari, J.S.; Figueiredo, R.M. Tuberculosis: Patient profile, service flowchart, and nurses opinions. Acta Paul. Enferm. 2012, 25, 43–47. [Google Scholar] [CrossRef] [Green Version]
  22. Furlan, M.C.R.; Oliveira, S.P.; Marcon, S.S. Factors associated with nonadherence of tuberculosis treatment in the state of Paraná. Acta Paul. Enferm. 2012, 25, 108–114. [Google Scholar]
  23. Getis, A.; Ord, J.K. The analysis of spatial association by use of distance statistics. Geogr. Anal. 1992, 24, 189–206. [Google Scholar]
  24. Aldridge, R.W.; Hayward, A.C.; Hemming, S.; Yates, S.K.; Ferenando, G.; Possas, L.; Garber, E.; Watson, J.M.; Geretti, A.M.; McHugh, T.D.; et al. High prevalence of latent tuberculosis and bloodborne virus infection in a homeless population. Thorax 2018, 73, 557–564. [Google Scholar] [CrossRef] [Green Version]
  25. Alecrim, T.F.; Mitano, F.; Reis, A.A.; Roos, C.M.; Palha, P.F.; Protti-Zanatta, S.T. Experience of health professionals in care of the homeless population with tuberculosis. Rev. Esc. Enferm. USP 2016, 50, 808–815. [Google Scholar] [CrossRef] [Green Version]
  26. Agarwal, S.; Nguyen, D.T.; Graviss, E.A. Homelessness and Mortality Among Persons With Tuberculosis in Texas, 2010–2017. Public Health Rep. 2019, 134, 643–650. [Google Scholar] [CrossRef]
  27. Hungaro, A.A.; Gavioli, A.; Christóphoro, R.; Marangoni, S.R.; Altrão, R.F.; Rodrigues, A.L.; De Oliveira, M.L.F. Homeless population: Characterization and contextualization by census research. Rev. Bras. Enferm. 2020, 73, e20190236. [Google Scholar] [CrossRef]
  28. Hino, P.; Yamamoto, T.T.; Bastos, S.H.; Beraldo, A.A.; Figueiredo, T.M.R.M.; Bertolozzi, M.R. Tuberculosis in the street population: A systematic review. Rev. Esc. Enferm. USP 2021, 55, e03688. [Google Scholar] [CrossRef]
  29. Hashmi, S.S.; Saad, A.; Leps, C.; Gillies-Podgorecki, J.; Feeney, B.; Hardy, C.; Falzone, N.; Archibald, D.; Hoang, T.; Bond, A.; et al. A student-led curriculum framework for homeless and vulnerably housed populations. BMC Med. Educ. 2020, 20, 232. [Google Scholar] [CrossRef]
  30. Wiens, J.D.; Dugger, K.M.; Higley, J.M.; Lesmeister, D.B.; Franklin, A.B.; Hamm, K.A.; White, G.C.; Dilione, K.E.; Simon, D.C.; Bown, R.R.; et al. Invader removal triggers competitive release in a threatened avian predator. Proc. Natl. Acad. Sci. USA 2021, 118, e2102859118. [Google Scholar] [CrossRef]
  31. Baxter, N.T.; Schmidt, A.W.; Venkataraman, A.; Kim, K.S.; Waldron, C.; Schmidt, T.M. Dynamics of Human Gut Microbiota and Short-Chain Fatty Acids in Response to Dietary Interventions with Three Fermentable Fibers. mBio 2019, 10, e02566-18. [Google Scholar] [CrossRef] [Green Version]
  32. Johnson, L.; Lewer, D.; Aldridge, R.W.; Hayward, A.C.; Story, A. Protocol for a systematic review of treatment adherence for HIV, hepatitis C and tuberculosis among homeless populations. Syst. Rev. 2020, 9, 211. [Google Scholar] [CrossRef] [PubMed]
  33. Omerov, P.; Craftman, Å.G.; Mattsson, E.; Klarare, A. Homeless persons’ experiences of health- and social care: A systematic integrative review. Health Soc. Care Community 2020, 28, 1–11. [Google Scholar] [CrossRef] [Green Version]
  34. Andrade, R.; Costa, A.A.S.; Sousa, E.T.; Rocon, P.C. Access to health services by the homeless population: An integrative review. Health Debate 2022, 46, 227–239. [Google Scholar] [CrossRef]
  35. Baroni, L.; Alves, R.F.S.; Boccolini, C.S.; Salles, R.; Gritz, R.; Paixão, B.; Boccolini, P.D.M.M. Database on the coverage of the “Bolsa-Família” conditioning cash-transfer program: Brazil, 2005 to 2021. BMC Res. Notes 2021, 14, 435. [Google Scholar] [CrossRef]
  36. Torrens, A.W.; Rasella, D.; Boccia, D.; Maciel, E.L.N.; Nery, J.S.; Olson, Z.D.; Barreira, D.C.N.; Sanchez, M.N. Effectiveness of a conditional cash transfer programme on TB cure rate: A retrospective cohort study in Brazil. Trans. R. Soc. Trop. Med. Hyg. 2016, 110, 199–206. [Google Scholar] [CrossRef]
  37. Silva, D.R.; Muñoz-Torrico, M.; Duarte, R.; Galvão, T.; Bonini, E.H.; Arbex, F.F.; Arbex, M.A.; Augusto, V.M.; Rabahi, M.F.; Mello, F.C.D.Q. Risk factors for tuberculosis: Diabetes, smoking, alcohol use, and the use of other drugs. J. Bras. Pneumol. 2018, 44, 145–152. [Google Scholar] [CrossRef] [Green Version]
  38. Cruz, V.D.; Harter, J.; Oliveira, M.M.; Gonzales, R.I.C.; Alves, P.F. Consumo de crack y la tisis: Una revisión integrativa. Rev. Eletrônica Saúde Ment. Álcool Drog. 2013, 9, 48–55. [Google Scholar] [CrossRef] [Green Version]
  39. Heuvelings, C.C.; Greve, P.F.; De Vries, S.G.; Visser, B.J.; Bélard, S.; Janssen, S.; Cremers, A.L.; Spijker, R.; Shaw, E.; Hill, R.; et al. Effectiveness of service models and organisational structures supporting tuberculosis identification and management in hard-to-reach populations in countries of low and medium tuberculosis incidence: A systematic review. BMJ Open 2018, 8, e019642. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  40. Breilh, J. Critical Epidemiology: Emancipatory Science and Interculturality; FIOCRUZ: Rio de Janeiro, Brazil, 2006. [Google Scholar]
  41. Viegas, S.M.F.; Nitschke, R.G.; Bernardo, L.A.; Tholl, A.D.; Borrego, M.A.R.; Soto, P.J.L. The routine of the street outreach office team: Weaving networks for health promotion. Esc. Anna Nery Rev. Enferm. 2021, 25, e20200222. [Google Scholar] [CrossRef]
  42. Marques, L.S.; Costa, J.H.M.; Gomes, M.M.; Silva, M.M. Knowledge, territories, and drug use: Street ways of life and reinventing care. Cien. Saude Colet. 2022, 27, 123–132. [Google Scholar] [CrossRef]
  43. Timóteo, A.V.G.; Silva, J.V.S.; Gomes, L.K.G.; Alves, A.S.S.; Barbosa, V.M.S.; Brendão, T.M. Characterization of the work and actions developed by the consultant’s teams in the street of Maceió—AL. Enferm. Foco 2020, 11, 126–130. [Google Scholar]
  44. Lutge, E.E.; Wiysonge, C.S.; Knight, S.E.; Sinclair, D.; Volmink, J. Incentives and enablers to improve adherence in tuberculosis. Cochrane Database Syst. Rev. 2015, 9, CD007952. [Google Scholar] [CrossRef] [Green Version]
Figure 1. Geographical location of health macro-regions according to municipalities in the state of Paraná.
Figure 1. Geographical location of health macro-regions according to municipalities in the state of Paraná.
Ijerph 19 07721 g001
Figure 2. Time series of the homeless population diagnosed with tuberculosis in the state of Paraná, Brazil (2014–2018). (A) Alcohol; (B) Tobacco; (C) Illicit drugs; (D) General street population.
Figure 2. Time series of the homeless population diagnosed with tuberculosis in the state of Paraná, Brazil (2014–2018). (A) Alcohol; (B) Tobacco; (C) Illicit drugs; (D) General street population.
Ijerph 19 07721 g002
Figure 3. High clusters and low clusters of tuberculosis cases in the homeless population in the state of Paraná, Brazil (2014–2018).
Figure 3. High clusters and low clusters of tuberculosis cases in the homeless population in the state of Paraná, Brazil (2014–2018).
Ijerph 19 07721 g003
Table 1. Sociodemographic characterization of tuberculosis cases in the homeless population of the state of Paraná, Brazil (2014–2018).
Table 1. Sociodemographic characterization of tuberculosis cases in the homeless population of the state of Paraná, Brazil (2014–2018).
VariablesStreet Population Using AlcoholStreet Population Using TobaccoStreet Population Using Illicit DrugsGeneral Street Population
n%n%n%n%
Gender
Male36282.331883.228179.247284.4
Female5813.26416.87420.88715.6
Age group
18 to 29 years6114.56517.07721.79717.4
30 to 39 years14835.213735.915343.119735.2
40 or more21150.218047.112535.226547.4
Race
White21751.719751.618050.729252.2
Black5112.14712.33911.06110.9
Yellow20.510.341.140.7
Brown14334.012532.712234.418332.7
Indigenous10.210.310.320.4
Schooling
Illiterate112.6112.9113.1173.0
First to fourth grade12630.011129.18423.714926.7
Fifth to eighth grade11226.710327.010830.415728.1
> Eight years of study399.34110.7359.9559.8
Housing perimeter
Urban36787.433487.432391.048586.8
Rural163.8164.2102.8254.5
Periurban10.2----20.4
Government benefit
Yes225.2246.3246.8397.0
No31274.328875.426674.941273.7
Alcoholism
Yes420100.031883.228480.042075.1
No--5614.76016.911821.1
Smoking
Yes31875.7382100.027477.238268.3
No8219.5--6518.314025.0
Other drugs
Yes28467.627471.7355100.035563.5
No11026.29424.6--16329.2
HIV/AIDS
Yes11026.210627.711733.015327.4
No29169.325867.522463.137867.6
Diabetes mellitus
Yes153.6143.7113.1193.4
No38992.635492.733193.251191.4
Mental illness
Yes286.7287.3267.3366.4
No37188.333888.531087.348787.1
Other diseases
Yes5011.94612.04111.56411.4
No28768.326368.824569.038969.6
Table 2. Clinical profile of tuberculosis cases in the homeless population of the state of Paraná, Brazil (2014–2018).
Table 2. Clinical profile of tuberculosis cases in the homeless population of the state of Paraná, Brazil (2014–2018).
VariablesStreet Population Using AlcoholStreet Population Using TobaccoStreet Population Using Illicit DrugsGeneral Street Population
n%n%n%n%
Type of entry
New case25661.023260.721761.135162.8
Recurrence378.8338.6318.7468.2
Reentry after loss to follow-up8019.07319.17220.310218.2
Do not know20.5--20.630.5
Transfer419.84110.7318.7519.1
Clinical form
Pulmonary37890.034389.831388.250490.2
Extrapulmonary204.8174.5195.4244.3
Pulmonary + extrapulmonary225.2225.8236.5315.5
Chest radiography
Suspect35684.832986.129282.346683.4
Normal71.751.372.091.6
Other pathology10.210.310.310.2
Not performed5212.44311.35214.67814.0
Sputum smear microscopy
Positive26563.124764.722262.535964.2
Negative6315.06216.25214.68515.2
Not performed8821.07118.67822.011019.7
Sputum culture
Positive16840.015340.114540.822139.5
Negative8019.08221.57721.710619.0
In progress153.6143.7113.1183.2
Not performed15737.413334.812234.421438.3
Histopathology
Baar positive4611.04511.84111.56712.0
Suggestive of TB122.9102.692.5142.5
Non-suggestive of TB20.530.841.140.7
In progress122.992.461.7132.3
Not performed34381.731181.429182.045481.2
HIV test
Positive11326.910728.012033.815627.9
Negative27064.324764.720858.635263.0
Not performed368.6277.1277.6508.9
Final status
Cure15236.214939.011432.120035.8
Primary abandonment133.1102.6102.8142.5
Abandonment9121.78522.38523.913724.5
Death by TB317.4266.8236.5397.0
Death from other causes4410.5369.43911.0529.3
Transference6816.26416.86718.99116.3
TB-DR122.9102.682.3132.3
Molecular testing
Detectable at rifampin11226.710728.010830.415828.3
Detectable rifampin resistant92.161.682.3112.0
Undetectable133.1133.4113.1142.5
Inconclusive61.451.341.161.1
Not performed26262.423561.521360.034461.5
Not reported184.3164.2113.1264.7
Sensitivity test
Resistant to isoniazid only61.461.630.871.3
Resistance to rifampin only20.510.320.630.5
Resistant to isoniazid and rifampin41.041.020.650.9
Resistant to other first line drugs 30.741.041.140.7
Sensitive7417.66617.36217.59817.5
In progress61.471.841.181.4
Not performed6114.55113.44512.77713.8
Not reported26462.924363.623365.635763.9
Table 3. Temporal trend of tuberculosis incidence in the street population according to the consumption of psychoactive substances, Paraná, Brazil (2014–2018).
Table 3. Temporal trend of tuberculosis incidence in the street population according to the consumption of psychoactive substances, Paraná, Brazil (2014–2018).
VariableCoefficient (CI * 95%)Temporal TrendMPC ** (CI95%)
Street population using alcohol2.47 (1.50–3.54)Crescent29.71 (18.03–42.56)
Street population using tobacco3.32 (1.39–3.32)Crescent27.93 (16.68–39.95)
Street population of illicit drugs2.52 (1.54–3.60)Crescent30.31 (18.57–43.21)
General street population3.19 (1.94–4.60)Crescent38.35 (23.31–55.23)
* Confidence interval ** Monthly percent change.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Scholze, A.R.; Alves, J.D.; Berra, T.Z.; Ramos, A.C.V.; Pieri, F.M.; Pillon, S.C.; Martins, J.T.; Galdino, M.J.Q.; Melo, E.C.; Delpino, F.M.; et al. Tuberculosis among People Living on the Street and Using Alcohol, Tobacco, and Illegal Drugs: Analysis of Territories in Extreme Vulnerability and Trends in Southern Brazil. Int. J. Environ. Res. Public Health 2022, 19, 7721. https://doi.org/10.3390/ijerph19137721

AMA Style

Scholze AR, Alves JD, Berra TZ, Ramos ACV, Pieri FM, Pillon SC, Martins JT, Galdino MJQ, Melo EC, Delpino FM, et al. Tuberculosis among People Living on the Street and Using Alcohol, Tobacco, and Illegal Drugs: Analysis of Territories in Extreme Vulnerability and Trends in Southern Brazil. International Journal of Environmental Research and Public Health. 2022; 19(13):7721. https://doi.org/10.3390/ijerph19137721

Chicago/Turabian Style

Scholze, Alessandro Rolim, Josilene Dália Alves, Thaís Zamboni Berra, Antônio Carlos Vieira Ramos, Flávia Meneguetti Pieri, Sandra Cristina Pillon, Júlia Trevisan Martins, Maria José Quina Galdino, Emiliana Cristina Melo, Felipe Mendes Delpino, and et al. 2022. "Tuberculosis among People Living on the Street and Using Alcohol, Tobacco, and Illegal Drugs: Analysis of Territories in Extreme Vulnerability and Trends in Southern Brazil" International Journal of Environmental Research and Public Health 19, no. 13: 7721. https://doi.org/10.3390/ijerph19137721

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop