Skip to main content
PLOS Neglected Tropical Diseases logoLink to PLOS Neglected Tropical Diseases
. 2020 Jun 29;14(6):e0008399. doi: 10.1371/journal.pntd.0008399

Impact of the social context on the prognosis of Chagas disease patients: Multilevel analysis of a Brazilian cohort

Ariela Mota Ferreira 1,*, Éster Cerdeira Sabino 2, Lea Campos de Oliveira 2, Cláudia Di Lorenzo Oliveira 3, Clareci Silva Cardoso 3, Antônio Luiz Pinho Ribeiro 4, Renata Fiúza Damasceno 1, Maria do Carmo Pereira Nunes 4, Desirée Sant’ Ana Haikal 1
Editor: Walderez O Dutra5
PMCID: PMC7351237  PMID: 32598390

Abstract

The present study aims to investigate how the social context contributes to the prognosis of Chagas disease (CD). This is a multilevel study that considered individual and contextual data. Individual data came from a Brazilian cohort study that followed 1,637 patients who lived in 21 municipalities to which CD is endemic, over two years. Contextual data were collected from official Brazilian government databases. The dependent variable was the occurrence of cardiovascular events in CD during the two-year follow-up, defined from the grouping of three possible combined events: death, development of atrial fibrillation, or pacemaker implantation. Analysis was performed using multilevel binary logistic regression. Among the individuals evaluated, 205 (12.5%) manifested cardiovascular events in CD during two years of follow-up. Individuals living in municipalities with a larger rural population had protection for these events (OR = 0.5; 95% CI = 0.4–0.7), while those residing in municipalities with fewer physicians per thousand inhabitants (OR = 1.6; 95% CI = 1.2–2.5) and those living in municipalities with lower Primary Health Care (PHC) coverage (OR = 1.4; 95% CI = 1.1–2.1) had higher chances of experiencing cardiovascular events. Among the individual variables, the probability of experiencing cardiovascular events was higher for individuals aged over 60 years (OR = 1.4; 95% CI = 1.01–2.2), with no stable relationship (OR = 1.4; 95% CI = 0.98–2.1), without previous treatment with Benznidazole (OR = 1.5; 95% CI = 0.98–2.9), with functional class limitation (OR = 2.0; 95% CI = 1.4–2.9), with a QRS complex duration longer than 120 ms (OR = 1.5; 95% CI = 1.1–2.3), and in individuals with high NT-proBNP levels (OR = 6.4; 95% CI = 4.3–9.6). CONCLUSION: The present study showed that the occurrence of cardiovascular events in individuals with CD is determined by individual conditions that express the severity of cardiovascular involvement. However, these individual characteristics are not isolated protagonists of this outcome, and the context in which individuals live, are also determining factors for a worse clinical prognosis.

Author summary

Chagas disease (CD) is a serious public health problem in Latin America and has a strong social impact worldwide. Up to 30% of the infected people may have cardiac alterations, which are associated with a worse prognosis and with high mortality rates. The occurrence of CD is associated with contexts of social vulnerability. However, no studies have been identified that assessed whether unfavorable social contexts are related to the prognosis and evolution of CD, which is the purpose of our study. We evaluated 1,637 patients with CD who lived in 21 municipalities located in regions to which CD is endemic in Brazil, over a two-year period. Of these people, 12.5% ​​evolved into a worse prognosis. Our study revealed that socio-demographic and clinical characteristics of individuals were not isolated protagonists of the evolution of CD. The context in which individuals lived was also a determining factor of a worse prognosis, including living in municipalities with a smaller rural population, fewer physicians, and a smaller Primary Health Care (PHC) coverage. Thus, we observed that characteristics related to the health care available in the municipalities influenced the evolution of CD. This knowledge has the potential to support health care planning that is more appropriate for the evolution of patients with CD, especially considering poor and remote regions.

Introduction

Chagas disease (CD) is a serious public health problem in Latin America and one of the main Brazilian medical and social problems. CD represents one of the top four causes of deaths from neglected infectious and parasitic diseases in the world and it is included in the group of infectious diseases classified as neglected [1, 2]. The World Health Organization (WHO) estimates a high concentration of CD patients in Latin America, to which the disease is endemic. In Brazil it is estimated that more than 1,100,000 people are affected by CD [1], which remains a major cause of morbidity, mortality, and disability in several Latin American countries. CD was the leading cause of disability-adjusted lost years of life (DALY) among all neglected tropical diseases, and in this group as well as in general, the Brazilian state of Minas Gerais is cited as having one of the highest age-standardized DALY rates [3].

Most patients with CD remain in the “undetermined chronic form”, defined as a persistent asymptomatic infection without cardiac or gastrointestinal tract alterations [4]. However, up to 30% of chronically infected people may develop cardiac alterations, which is the most serious complication of CD [5]. Chagasic cardiomyopathy is associated with a worse prognosis, with higher mortality rates compared to other causes of heart failure [4, 68].

The prognosis of CD is still strongly impacted by it being neglected, with important problems related to late diagnosis and lack of opportunity for treatment, such as deaths that result from the lack of timely intervention, especially for the cardiac form of the disease [9]. Previous studies estimated that more than 80% of people with CD worldwide will not have access to diagnosis and continued treatment, which support the high morbidity and mortality rates and the social cost of the disease [4, 10].

Despite the knowledge about contextual influence and social determination in the occurrence of some diseases, little has been investigated about the influence of contexts on their evolution and prognosis, which demands more studies to be developed to understand this issue [10]. The occurrence of CD it is admittedly related to contexts of social vulnerability that have been neglected to varying degrees and perspectives [11]. Addressing this problem requires urgent responses, with emphasis on specific actions by the healthcare network [12] adjusted to the characteristics of each reality [13].

In Brazil the great territorial extent and diversity, with specificities in the ecological, demographic, social, and economic dynamics of the regions, imply multiple and complex clinical, epidemiological, and operational scenarios [14]. These need to be considered in studies related to CD, although no previous studies on the social context related to the prognosis of CD have been identified.

The present study has the objective to investigate the contribution of the social context to the occurrence of cardiovascular events in CD using multilevel modeling, considering a two-year follow-up cohort with more than 1,600 patients with CD who lived in regions of Brazil to which the disease is endemic.

Methods

Ethical approval

Ethical approval was obtained from the relevant ethics committee: National Commission of Ethics in Research (CONEP: 179,685/2012). All subjects agreed to participate and signed the informed consent form prior to the beginning of the study.

Study design

This is a multilevel study on CD that considered individual and contextual data. The individual data came from a prospective two-year follow-up cohort study entitled SaMi-Trop (Research on Biomarkers of Neglected Tropical Diseases in São Paulo/Minas Gerais). This study, conducted in Brazil from 2013 to 2019, covers 21 municipalities, and has been conducted in a multicenter manner, with the participation of four Brazilian public universities. The contextual data used were extracted from an official database of the Brazilian government, and collected at the municipal level.

Individual data

The SaMi-Trop methodology has been presented in detail in previous publications [14, 15]. The main points of the methodology of this cohort are described in the following paragraphs.

The study was carried out in 21 municipalities selected for showing a high prevalence of CD. These municipalities belong to two regions to which CD is endemic in the state of Minas Gerais, Brazil: the northern region of the state and the Jequitinhonha Valley region.

Patients older than 18 years were recruited to participate in the study based on their CD self-report, during the execution of electrocardiogram (ECG) exams in 2012 by a Telehealth program, which provides distance support to municipal public health services by providing ECG reports and clinical discussions with university specialists [16].

To date, patients followed in this cohort have undergone two assessments, baseline and follow-up. Baseline consisted of 2,161 individuals. At follow-up, performed two years after baseline, 1,709 individuals were evaluated but 145 of the baseline participants had died, totaling 1,854 individuals eligible to be included in the sample (death is one of the events of interest in the present study). However, 217 individuals were excluded from analysis (161 because they did not have positive serology for the anti-T. cruzi antibody and 56 because they did not respond to the dependent variable adopted). Consequently, 1,637 individuals were included in the sample (Fig 1).

Fig 1. Flowchart showing the number of eligible, lost, and excluded CD patients in the study.

Fig 1

Baseline data collection occurred between 2013 and 2014, with interviews with the patients, peripheral blood collection, and ECG exams. Follow-up data collection occurred between 2015 and 2016, for which all baseline activities were repeated and the echocardiogram exam was added. The baseline interview included socio-demographic, lifestyle, physical activity, quality of life, and clinical information, in addition to the therapeutic history of CD. In the follow-up interview, data regarding the use of health services, health literacy, and hospitalization were added.

Contextual data

Contextual data collection was carried out considering the 21 municipalities included in SaMi-Trop. For the social, economic, demographic, epidemiological, and health services characterization of these 21 municipalities, 13 contextual variables were collected from publicly accessible institutional platforms and information systems of the Brazilian government. Table 1 shows these variables, the year adopted as reference for collection (most recent data available), their source, their concept, and the way the data were categorized to carry out the analyses.

Table 1. Contextual variables collected in publicly accessible institutional platforms and information systems, according to the year, source, concept, and cutoff point adopted in the study.

Contextual variables Collection Year Source Concept Adopted cutoff
1. Total population 2010 Atlas of Human Development in Brazil Population consisting of people living in the municipality 75th percentile = 31,003
2. Percentage of the rural population 2010 Atlas of Human Development in Brazil Proportion of the rural population, which covers the whole area outside urban limits 25th percentile = 33.11%
3. Municipal human development index (MHDI) 2010 Atlas of Human Development in Brazil Geometric average of the dimensions indices: Income, Education, and Longevity, with equal weights Dichotomized into low vs. high and medium, according to the international standard
4. Gini index 2010 Atlas of Human Development in Brazil Measures the degree of inequality in the distribution of individuals according to the per capita household income. Its value ranges from 0 (when there is no inequality) to 1 (when inequality is maximum) 25th percentile = 0.46
5. % of the population living in extreme poverty 2010 Department of Primary Care–Ministry of Health Proportion of individuals with a per capita household income equal to or lower than R$ 70.00 per month (U$ 39.54, considering the US dollar exchange rate for January 2010) 25th percentile = 10.88%
6. Social vulnerability index–SVI 2010 Social Vulnerability Atlas Signals the access, absence, or insufficiency of some civil rights. The three subindices of which it consists are: Urban Infrastructure, Human Capital, and Income/Work 25th percentile = 0.32
7. Unified health system performance index (IDSUS) 2010 Unified health system performance index Evaluates the performance of the Unified Health System (SUS) regarding: universality of access, comprehensiveness, equality, resolvability and equity of care, decentralization with single command by management sphere, tripartite responsibility, regionalization, and hierarchization of the health services network Categorized according to the Brazilian standard and dichotomized into 0.500–0.599 vs. 0.600–0.699 and 0.700–0.799
8. Total health expenditure per inhabitant 2016 Public Health Budgets Information System—SIOPS Measures the total public health expenditure per inhabitant 75th percentile = R$ 610.72 (U$ 150.79), considering the dollar exchange rate in Jan 2016
9. Number of doctors per thousand inhabitants 2017 National Register of Health Establishment—CNES Number of doctors present in the municipality per thousand inhabitants 75th percentile = 0.79
10. Presence of cardiologists 2017 National Register of Health Establishment—CNES Number of cardiologists present in the municipality hired by the SUS. 75th percentile = 1 (present vs. absent)
11. Number of existing electrocardiographs in SUS facilities per thousand inhabitants 2017 National Register of Health Establishment—CNES Number of electrocardiographs present in the municipality to be used by the SUS per thousand inhabitants 75th percentile = 0.21
12. Percentage of the population with health insurance 2017 Department of Primary Care—Ministry of Health Proportion of the population with health insurance 75th percentile = 3.03%
13. Family Health Strategy (FHS) coverage 2017 Department of Primary Care—Ministry of Health Percentage of the population coverage by Family Health Strategy teams. 75th percentile = 100%

*SUS = public health model currently in force in Brazil

Sources: Atlas of Human Development http://www.atlasbrasil.org.br/2013/en/o_atlas/idhm/

Department of Primary Care—Ministry of Health: http://dab.saude.gov.br/portaldab/. Technical Note for October 2017.

Atlas of Social Vulnerability: http://ivs.ipea.gov.br/index.php/en/

Unified Health System Performance Index: http://idsus.saude.gov.br/

CNES—National Register of Health Establishment: http://cnes.datasus.gov.br/

Theoretical model/variables

The organization of variables in the present study followed Andersen & Davidson's [17] conceptual theoretical model, which considers “evaluated health” as an outcome of interest. Following this model, the occurrence of cardiovascular events was adopted as outcome (dependent variable), dichotomized into two categories (absent or present) (Fig 2), considering the two years of follow-up. This variable was constructed from the grouping of three possible events that may have occurred between baseline and follow-up: death (all-cause mortality), obtained from loss of follow-up for this reason and identified by death certificates from the Health Department of Minas Gerais; development of atrial fibrillation (AF) (absent at baseline and present at follow-up) obtained by ECG analysis and defined as sinus rhythm at baseline and AF (presence of irregular trace) on ECG at the follow-up visit; and pacemaker implantation (absent at baseline and present at follow-up) obtained by participants’ self-report and confirmed by follow-up ECG through the presence of the image of the pacemaker spike and by ventricular depolarization. The development of the dependent variable including markers that express disease progression aimed to capture changes in the health status of individuals with CD, characterized by over a two-year period. The development of atrial fibrillation and the appearance of atrioventricular blocks, especially total atrioventricular block that requires pacemaker implantation, express progression of heart disease and increased risk of death [18]. To be classified in the category “absent”, participants could not have shown new cardiovascular events during the follow-up period.

Fig 2. The adopted behavioral theoretical model.

Fig 2

The independent variables were grouped according to the theoretical model [17] (Fig 2) which has three levels, the first being contextual (first level) and the other two, consisting of individual variables, being individual characteristics (second level) and health-related behavior (third level). Information from the last two levels was extracted from baseline (Fig 2).

In the first level, contextual characteristics related to the municipalities were included considering the variables shown in Table 1, subgrouped into: 1) Predisposing characteristics and 2) Capacitating factors. The variables Municipal Human Development Index (MHDI) and Unified Health System Performance Index (IDSUS) were collected, categorized according to the Brazilian standard, and subsequently dichotomized. The other contextual variables were collected numerically and later dichotomized by adopting the 25th or 75th percentiles as the cutoff point, depending on whether the variable represented a negative measure (low values indicating a better situation) or a positive measure (high values indicating a better situation). The objective was to separate the 25% of the better-off municipalities vs. 75% of the worst-off municipalities, given that in general, the municipalities included had similar profiles and most of them had unfavorable social conditions (Table 1).

The second level (individual characteristics) considered three subgroups. The first subgroup was predisposing characteristics: gender (male, female); age (up to 60 years, 60 years or older); self-declared skin color (white, non-white); marital status (stable relationship, no stable relationship); and literacy (yes, no). Age was calculated using the informed date of birth and later dichotomized for the purpose of differentiating adults and the elderly, according to the criteria adopted by WHO for developing countries [19]. The second was capacitating factors: income (above one minimum wage, up to one minimum wage), dichotomized considering the value of the minimum wage in force in the country (R$ 724.00—U$ 304.20) at the time of data collection. The third subgroup was perceived/evaluated needs: self-reported diabetes diagnosis (no, yes); self-reported hypertension diagnosis (no, yes); self-reported CD diagnostic time (up to ten years, over ten years); use of benznidazole (BZN) sometime in life (yes, no); and functional class (no limitations—class I, with limitations—class II, III, and IV) [20]. The QRS complex duration (up to 119 ms, longer than or equal to 120 ms) [21] and NT-proBNP categorized by age [22] (normal, abnormal) were obtained from ECG examination and blood samples, respectively. The assessment of self-rated health was based on the question: “How would you rate your health today?” and a Likert scale was adopted with the response options and then dichotomized as positive (good, very good, and medium) vs. negative (bad and very bad).

The third level (health behavior) considered only one subgroup related to personal health practices: physical activity practice (yes, no); alcohol consumption (infrequent use of alcohol, frequent use of alcohol); and smoking (never smoked or former smoker, smoker). Data about the practice of physical activity were not changed after collection. Alcohol consumption was measured by asking the question “how many times have you consumed alcoholic beverages in the past thirty days?” with the answer options being: have not consumed, consumed less than once per week, consumed one to two times per week, consumed three to five times per week, and consumed every day. The answers to this question were dichotomized and grouped into two categories: infrequent use (have not consumed/consumed less than once a week/consumed one to two times a week) vs. frequent use (consumed three to five times a week/consumed every day). Smoking was evaluated by asking the question: “Which of the following phrases best defines your smoking habits?” with the answer options being: “I have never smoked”, “I have smoked but no longer smoke”, and “I am currently a smoker”. Smokers were considered as those who had the habit of smoking at the time of data collection, and former smokers and those who had never smoked were included in the non-smokers category.

Statistical analyses

Analysis was carried out to assess differential loss that is, comparing the characteristics of study participants with the characteristics of individuals who were lost and/or excluded. The objective of this step was to verify whether the individuals who continued to be analyzed showed comparability to those lost/excluded. The compared characteristics were gender, self-declared skin color, literacy, age, and income. To perform this type of analysis, descriptive data were obtained and bivariate analyses (chi-square tests) were conducted.

Descriptive analysis of all individual variables involved was subsequently performed. Absolute (n) and relative (%) frequencies were estimated. The outcome was explored, and its frequency was estimated for each municipality included in the present study. Bivariate analysis was subsequently carried out using Pearson's chi-square test. Variables with p value ≤ 0.20 were selected for the multivariate model. Before beginning the multiple analysis, absence of multicollinearity between the independent variables (correlation lower than 0.7) was confirmed. In multivariate analysis, multilevel binary logistic regression was adopted so the variables were introduced in the model by grouping levels, according to the adopted theoretical model. The effects of individual and contextual characteristics on the outcome were analyzed using multilevel models. The multilevel analysis used the fixed effects model (intercept model). Odds ratios (OR) with 95% CI were calculated to assess associations between the outcome and the individual and contextual variables. The model was adjusted upon the introduction of each level, in a hierarchical manner, keeping only variables with statistical significance. Deviance was the indicator used to assess the adjustment quality, making it possible to compare likelihood functions, and is represented by the “-2 loglikelihood”. Analyses were run using Predictive Analytics Software (PASW/SPSS) version 18.0 for Windows and STATA version 14.0 (StatCorp, College Station, Texas, USA) statistical software.

Results

Among the 1,637 patients with CD evaluated in the SaMi-Trop cohort, 205 (12.5%) showed new cardiovascular events between baseline and follow-up, of whom 134 (8.2%) died; 28 (1.7%) developed AF, and 43 (2.6%) required pacemaker implantation. The variation in the occurrence of these events according to each municipality investigated can be seen in Fig 3.

Fig 3. Occurrence of cardiovascular events over two years in Chagas Disease (CD) patients and their distribution by municipality (n = 21).

Fig 3

Minas Gerais, Brazil. Created with QGIS.

Differential loss analysis showed that, except for the variable age, the other tested variables did not differ significantly in the group of lost individuals when compared with data of those who remained in the study (p > 0.05). However, among the lost individuals there was a significantly higher proportion of older people (55% vs. 45%). The mean age in the group of people who remained in the sample was 58.6 (± 12.6) years, while in the group of lost individuals it was 61 (± 13.6) years (p < 0.05). Additionally, in the group of lost individuals with negative and inconclusive serology (n = 161), it was identified 10 (6%) individuals that manifested cardiac events (8 deaths, 1 developed AF, and 1 implanted a pacemaker).

The distribution of participants according to individual characteristics and health behaviors can be seen in Table 2. There was a predominance of individuals under 60 years (53.5%), women (66.6%), non-white self-reported skin color (78.6%), and people with a monthly income of up to one minimum wage (51.8%). The mean age of the individuals was 59.81 (±12.3) years and 65.33 (±13.0) years, among those who did not have, and had cardiovascular events, respectively.

Table 2. Descriptive and bivariate analysis of individual socio-demographic, lifestyle, and health condition-related characteristics and their association with the occurrence of cardiovascular events over two years in Chagas Disease (CD) patients. Minas Gerais, Brazil (n = 1,637).

Characteristics Descriptive analysis Bivariate analysis p-valueπ
Cardiovascular events

n (%)
Absent
n (%)
Present
n (%)
Individual
Gender
    Male 547 (33.4%) 459/1432 (32%) 88/ 205 (42.9%) 0.002¥
Age
    Up to 60 years 876 (53.5%) 805/1432 (56.2%) 71/205 (34.6%) <0.001¥
Self-reported skin color*
    White 349 (21.4%) 296/1426 (20.7%) 53/202 (26.2%) 0.076¥
Marital Status*
    Stable relationship 1048 (64.3%) 936/1428 (65.5%) 112/203 (55.1%) 0.004¥
Literate*
    Yes 899 (55.2%) 816/1427 (57.1%) 83/203 (40.8%) <0.001¥
Income*
    Above one minimum wage 786 (48.2%) 684/1428 (47.8%) 102/203 50.2%) 0.531
Diabetes mellitus
    No 1481 (90.5%) 1294/1432 (30.3%) 187/205 (91.2%) 0.696
Arterial hypertension*
    No 582 (35.6%) 528/1432 (36,8%) 54/205 (26.3%) 0.003¥
CD diagnosis time*
    Up to ten years 278 (21.9%) 248/1112 (22.3%) 30/157 (19.1%) 0.365
BZN use*
    Yes 410 (27.1%) 384/1337 (28.7%) 26/176 (14.7%) <0.001¥
Functional class*
    No limitations 904 (55.7%) 832/1420 (58.6%) 72/203 (35.4%) <0.001¥
QRS complex duration*
    Up to 119 ms 927 (58.2%) 845/1396 (60.5%) 82/198 (41.4%) <0.001¥
NT-proBNP*
    Normal 1435 (88%) 1313/1425 (92.1%) 122/205 (59.5%) <0.001¥
Health self-perception*
    Positive 1408 (86.8%) 1236/1419 (87.1%) 172/203 (84.7%) 0.350
Health Behavior
Practice of physical activity*
    Yes 374 (23%) 340/1421 (23.9%) 34/205 (16.5%) 0.020¥
Alcohol consumption*
    Does not consume alcohol frequently 1594 (97.9%) 1394/1426 (97.7%) 200/202 (99%) 0.243
Smoking*
    Never smoked or former smoker 1513 (92.8%) 1328/1428 (92.9%) 185/202 (91.5%) 0.466

* Variation of n = 1,637 because of missing information.

π Pearson’s chi-squared test

¥ p ≤ 0.20

In bivariate analysis, the individual variables selected to make up the initial multiple model (p ≤ 0.20) were: gender, age, self-reported skin color, marital status, literacy, hypertension, BZN use, functional class, QRS complex duration, NT–proBNP, and physical activity practice (Table 2).

The adjusted multiple model revealed that three contextual variables influenced the outcome. Among the contextual characteristics, there was protection for cardiovascular events among those who lived in municipalities with the largest rural population; and higher chances of cardiovascular events among those who lived in municipalities with fewer physicians per thousand inhabitants and those who lived in municipalities with lower Family Health Strategy (FHS) coverage. In the second level of the individual characteristics there was a higher probability of cardiovascular events among the people who were over 60 years old, did not have a stable relationship, had not used BZN, belonged to a worse functional class, had a QRS complex duration higher than 120 ms, and showed an abnormal age-adjusted NT-proBNP level. No third level variables remained in the model after adjustment (Table 3).

Table 3. Final hierarchical multilevel logistic regression model for the factors associated with the occurrence of cardiovascular events over two years in patients with Chagas disease. Minas Gerais, Brazil (n = 1,637).

MODELS VARIABLES OR (CI95%) p value
Empty model Deviance (-2log Log likelihood) = 123.406
Level 1
Contextual characteristics
Rural population
Smaller rural population 1
Larger rural population 0.509 (0.359–0.721) <0.001
Number of physicians per thousand inhabitants
Higher number of physicians 1
Lower number of physicians 1.698 (1.157–2.490) 0.007
FHS coverage
Higher FHS coverage 1
Lower FHS coverage 1.468 (1.037–2.079) 0.030
Deviance (-2log Log likelihood) = 121.810
Level 2
Contextual characteristics Individual characteristics
Age
Up to 60 years 1
60 years or over 1.474 (1.010–2.151) 0.044
Marital status
Stable relationship 1
Not in a stable relationship 1.420 (0.987–2.043) 0.058
Use of benznidazole
Yes 1
No 1.599 (0.985–2.956) 0.057
Functional class
No limitations 1
With limitations 2.007 (1.402–2.873) <0.001
QRS complex duration
<120 ms 1
>120 ms 1.583(1.095–2.289) 0.014
Age-adjusted NT-proBNP level
Normal 1
Abormal 6.424 (4.297–9.603) <0.001
Deviance (-2log Log likelihood) = 87.861

Discussion

The present study showed that more than 12% of the patients with CD had cardiovascular events over the two-year follow-up. This outcome was associated with the contextual variables: rural population, number of physicians per thousand inhabitants, and FHS coverage; and the individual variables: age, functional class, QRS complex duration and NT-proBNP level. The BZN use and marital status variables showed a borderline association with the outcome and were also maintained in the final model. The high incidence of individuals showing progression of the disease over two years (12%) corroborates the literature regarding the severity of the cardiac form of CD [4, 23]. One may also suspect the difficulty of accessing a quality clinical evaluation in these remote regions.

The methodological approach of the present study goes beyond the individual level of understanding of the health-disease process and reaches the population level, making it possible to grasp the essence of the collective and social character of epidemiology [24]. Previous studies that have adopted a multilevel methodology related to the prognosis of patients with CD have not been identified, making comparisons of this nature impossible.

Regarding the comparative analyses of the groups of patients kept and lost in the present study, it is known that the latter during the follow-up period may differ from those who remain. Individuals who are lost often are those showing the highest proportion of worst socio-demographic indicators, which may represent risk factors relevant to the study [25]. To address this issue, an analysis was carried out to test the presence of this type of bias in the sample. It was observed that there were no significant differences for most of the socio-demographic variables considered in the comparison of the groups, suggesting that they were relatively homogeneous.

The dependent variable was innovatively developed by combining three important events that mark the progression of heart disease: death, development of AF, and pacemaker implantation. Death, the most serious event, is one of the most commonly used health status indicators, especially in studies on health and social inequality [26]. In areas to which CD is endemic, the illness is a leading cause of death from cardiovascular disease [27]. A meta-analysis identified that CD is statistically associated with high mortality rates, regardless of the clinical condition, with a relative risk of 1.74 (95% CI 1.49–2.03) and attributable risk of 42.5% considering the exposed group [28]. AF is associated with an unfavorable prognosis [29, 30]. Previous studies, including a meta-analysis, showed that AF has an independent prognostic value for death, with an OR ranging from 1.14 to 2.8 [30,31]. Pacemaker implantation also represents an important event resulting from chronic Chagas heart disease, which is the most important cardiac consequence of CD [4, 30]. The prevalence of pacemakers among patients with CD has been reported by few studies, ranging from 6.2 to 14.3% [14, 32]. Patients with CD are 13 times more likely to have a pacemaker implanted when compared to people in the general population [4]. In the present study, an incidence of 2.6% of pacemaker implantation was identified in patients with CD over the two-year follow-up. Previous studies showing the incidence of pacemaker implantation in patients with CD were not found.

In the present study, individuals living in municipalities with a larger rural population showed protection against cardiovascular events. The hypothesis proposed by the authors is that this can be explained by the expansion of the Primary Health Care (PHC) coverage through the FHS, especially in smaller and rural municipalities [33]. The FHS represents the “gateway” to the Unified Health System (Sistema Único de Saúde—SUS, the public health model currently available in Brazil [34]. With the expansion mentioned, residents and health workers in more rural areas are more likely to know each other, have a stronger bond, and undertake follow up more closely, facilitating access to information and the scheduling of appointments and tests. In addition, the Brazilian policy of permanent education of SUS workers [35] has aimed to offer training to SUS professionals according to their demands, which originate in the realities that they experience in their practice in health services.

Individuals living in municipalities with fewer physicians per thousand inhabitants had a higher probability of experiencing cardiovascular events. This indicator in isolation may have little significance. Therefore, the WHO does not establish the numerical ratio of physicians per thousand inhabitants considered adequate, as this number depends on regional, socioeconomic, cultural, and epidemiological factors, and consequently it is not possible to establish a generalized "ideal rate" for all countries [36]. Despite these limitations, this indicator is the most used because of the absence of others that encompass the complexity of current care models.

Brazil still has one of the lowest rates of physicians per thousand inhabitants, and in January 2018 this number was 2.18 physicians per thousand inhabitants. There are significant inequalities in the distribution of physicians throughout the Brazilian territory, with the state capitals accounting for 23.8% of the population and 55% of the physicians. The ratio calculated for the set of capitals is 5.07 physicians per thousand inhabitants. In municipalities located in the interior of states, this ratio decreases to 1.28 [37]. The municipalities examined in the present study had an average of 0.68 (± 0.4) physicians per thousand inhabitants, which is almost three times lower than the Brazilian average and half the average calculated for municipalities in the interior of the states, which shows that the analyzed area is economically disadvantaged and has an insufficient healthcare structure, even when Brazilian data is used as a reference. The group of municipalities considered as having the highest number of physicians had an average of 1.21 (± 0.4) physicians per thousand inhabitants, and the group with the lowest number of physicians had an average of 0.51 (± 0.1). Consequently, it must be emphasized that this difference in the number of physicians in the municipalities was important in the occurrence of cardiovascular events. This finding stresses the importance of this marker and provides resources to hypothesize that there will be no improvement in the prognosis of CD if there are no public investments in maintaining more medical professionals in these municipalities, whose health sector can be considered, in general, neglected. No previous studies that considered the number of physicians per thousand inhabitants with outcomes measured at the individual level were identified.

Similarly, individuals living in municipalities with a lower FHS coverage had higher chances of experiencing cardiovascular events. The result obtained in the present study agrees with the literature that points PHC, represented by the FHS, as being associated with better health outcomes [38]. Studies show that PHC-oriented countries have better health indicators, such as lower early mortality caused by preventable causes and longer life expectancy. These countries also encourage population empowerment and provide support to reduce vulnerabilities [39, 40, 41]. Thus, this finding shows the importance of PHC in facing Brazilian health realities, which are extremely heterogeneous and with historical social inequalities, even in the face of commonly neglected health conditions.

There is evidence that social inequalities are strong determinants of a population’s health [42]. Individuals literally incorporate the world where they live, producing health, illness, disability, and death standards [24]. According to the WHO, most health illnesses and inequities occur as a consequence of the so-called “social determinants of health,” a term that brings together social, economic, political, cultural, and environmental health issues. The social determinants most commonly associated with the occurrence of diseases are those that generate social stratification and are entitled structural determinants [42]. However, among the several contextual variables tested in the present study, the three that showed association with the outcome of cardiovascular events incite issues that relate more to care than to structural determinants. Structural contextual factors are risk factors for the occurrence of diseases [42], but care contextual factors were more significant in assessing the disease prognosis. This finding is fundamental for a better understanding that care plays a leading role compared to structural issues once the disease is present and taking into account its progression. Proper management of these care determinants must complement individual-level interventions for healthcare professionals to achieve greater effectiveness in CD-targeted actions. It should be noted that the present study did not assess any factor related to access or the quality of care provided.

The individual demographic variables associated with cardiovascular events were marital status and age, corroborating previous studies [43, 44, 45, 46]. Although in our study marital status showed a borderline association with the outcome (p = 0.058), the maintenance of this variable improved the fit of the final model. Furthermore, marital status has been found to play a significant role in adult mortality in previous studies, with married individuals tending to have longer life expectancy when compared to divorced/separated people, widow(er)s, or people who never married [43, 44]. Older individuals were also more likely to have cardiovascular events. Age is widely recognized as an independent factor associated with worse cardiac health and death [4, 29, 30, 45, 46].

The individual clinical variables that remained in the final model are well established and known to be related to the prognosis of the disease [22, 47, 48, 49, 50]. It has been found that more advanced functional class is associated with death caused by increased myocardial dysfunction [47]. Not using BZN also increased the probability of experiencing cardiovascular events, but the p value observed in this association was borderline (p = 0.057) and this result needs to be analyzed with caution. Previous use of this drug is still considered reduced among patients with CD in Brazilian endemic regions (27%) [15]. Previous studies have found that BZN use has been associated with a significant reduction in parasitemia [32], lower prevalence of severe cardiomyopathy markers, and lower mortality [48]. The age-adjusted abnormal NT-proBNP level was the factor most strongly associated with the occurrence of cardiovascular events in the present study. NT-proBNP levels are accurate discriminators of the diagnosis of heart failure, powerful predictors of death, and aid in patient risk stratification [50]. Prolonged QRS complex duration was also associated with the outcome, corroborating a study that identified its prolonged duration as an independent predictor of death in CD [49].

The longitudinal evaluation of a large sample of CD patients who lived in endemic areas and small municipalities, far from the large urban centers commonly depicted in studies in the literature, stands out as one of the strengths of the present study. This allows to extend the results to similar locations, given that the populations with CD usually have a similar epidemiological profile [51]. The creation of a dependent variable considering three cardiovascular events simultaneously is innovative and increases the understanding of factors that may influence the prognosis of CD, unlike other studies that adopt only one event of interest. Results were reliably measured, reflecting the patients' clinical condition as well as their parasitological status.

Study limitations

An important cardiovascular event assessed in this study was death. Although we acknowledge that the use of all cause mortality is a limitation, in general deaths associated with CD are due to cardiovascular causes, mainly sudden death or progressive heart failure. In the present study, only 4 non-cardiovascular deaths occurred (one accidental death, two due to cancer and one non-specified death). However, as we were unable to assess the cause of death of each patient, all cause mortality was defined as the outcome.

In the present study the patients were dichotomized according to NYHA functional class into good exercise capacity (Class I) versus others, which may include patients who have different exercise tolerance in the same classification. However, functional class is a subjective estimate of a patient’s functional ability based on symptoms that do not always correlate with the objective measures of functional capacity.

Some collected information originated in self-reporting, which may result in measurement bias. However, high accuracy of self-reported data for chronic conditions has already been verified [52]. Additionally, investigating the effect of context on an individual outcome related to the occurrence of cardiovascular events in CD is important, useful, and necessary, because it reveals a reality that is often neglected in many spheres, paving the way for targeted actions and future investigations.

The occurrence of cardiovascular events in CD over two years can be considered high (12.5%) and related to the limitations of the organization/provision of the Brazilian public health service and the organization of the urban/rural space of populations with CD, in addition to socio-demographic and clinical issues already established in the literature. The findings showed that individual conditions are not isolated protagonists in the occurrence of cardiovascular events and that the context in which individuals live also determines this prognosis. The absence of public policies that take into account the context in the health condition of patients with CD can contribute significantly to the high morbidity and mortality in CD. Appropriate investments to expand health care for people with CD in remote and neglected areas need to be made.

Supporting information

S1 Checklist. STROBE checklist.

(DOCX)

S1 Table. Database.

(XLS)

Acknowledgments

We would like to thank all of the SaMi-Trop patients and the health teams in each municipality for their valuable contributions to this study.

Data Availability

All relevant data are within the manuscript and its Supporting Information files.

Funding Statement

The study is supported by the National Institute of Health: P50 AI098461-02 and U19AI098461-06. ECS is the author who receives funding. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References

  • 1.WHO- World Health Organization. Chagas disease in Latin America: an epidemiological update based on 2010 estimates. 6 FEBRUARY 2015, 90th YEAR / 6 FÉVRIER 2015, 90e ANNÉE No. 6, 2015, 90, 33–44 [PubMed] [Google Scholar]
  • 2.Brasil. Ministério da Saúde. https://www.saude.gov.br/saude-de-a-z/doenca-de-chagas/situacao-epidemiologica. Acesso em 18/04/2020.
  • 3.Martins-Melo FR, Carneiro M, Ribeiro ALP, Bezerra JMT, Werneck GL. Burden of Chagas disease in Brazil, 1990–2016: findings from the Global Burden of Disease Study 2016. Int J Parasitol. 2019. March;49(3–4):301–310. 10.1016/j.ijpara.2018.11.008 [DOI] [PubMed] [Google Scholar]
  • 4.Nunes MCP, Beaton A, Acquatella H, Bern C, Bolger AF, Echeverría LE, et al. American Heart Association Rheumatic Fever, Endocarditis and Kawasaki Disease Committee of the Council on Cardiovascular Disease in the Young; Council on Cardiovascular and Stroke Nursing; and Stroke Council. Chagas Cardiomyopathy: An Update of Current Clinical Knowledge and Management: A Scientific Statement From the American Heart Association. Circulation. 2018. September 18;138(12):e169–e209 10.1161/CIR.0000000000000599 [DOI] [PubMed] [Google Scholar]
  • 5.Sabino EC, Ribeiro AL, Salemi VM, Di Lorenzo Oliveira C, Antunes AP, Menezes MM, et al. Ten-year incidence of Chagas cardiomyopathy among asymptomatic Trypanosoma cruzi-seropositive former blood donors. Circulation. 2013;127(10):1105–15. Epub 2013/02/09. 10.1161/CIRCULATIONAHA.112.123612 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Freitas HF, Chizzola PR, Paes AT, Lima AC, Mansur AJ. Risk stratification in a Brazilian hospital-based cohort of 1220 outpatients with heart failure: role of Chagas' heart disease. International journal of cardiology 2005; 102(2): 239–47. 10.1016/j.ijcard.2004.05.025 [DOI] [PubMed] [Google Scholar]
  • 7.Braga JC, Reis F, Aras R Jr, Dantas N, Bitencourt A, Neves FS, et al. Is Chagas cardiomyopathy an independent risk factor for patients with heart failure? International journal of cardiology 2008; 126(2): 276–8. 10.1016/j.ijcard.2007.01.097 [DOI] [PubMed] [Google Scholar]
  • 8.Pereira Nunes M do C, Barbosa MM, Ribeiro AL, Amorim Fenelon LM, Rocha MO. Predictors of mortality in patients with dilated cardiomyopathy: relevance of chagas disease as an etiological factor. Rev Esp Cardiol 2010; 63(7): 788–97 10.1016/s1885-5857(10)70163-8 [DOI] [PubMed] [Google Scholar]
  • 9.Dias JCP, Ramos AN Jr., Gontijo ED, Luquetti A, Shikanai-Yasuda MA, Coura JR et al. II Consenso Brasileiro em Doença de Chagas, 2015. Epidemiol. Serv. Saúde. 2016. June; 25 (spe): 7–86. 10.5123/S1679-49742016000500002 [DOI] [PubMed] [Google Scholar]
  • 10.Borde E, Akerman M, Pellegrini FA. Mapping of capacities for research on health and its social determinants in Brazil. Cad. Saúde Pública. 2014. October; 30 (10): 2081–2091 10.1590/0102-311x00162513 [DOI] [PubMed] [Google Scholar]
  • 11.Victora CG, Wagstaff A, Schellenberg JA, Gwatkin D, Claeson M, Habicht JP. Applying an equity lens to child health and mortality: more of the same is not enough. Lancet. 2003. July;362(9379):233–41. 10.1016/S0140-6736(03)13917-7 [DOI] [PubMed] [Google Scholar]
  • 12.Mendes EV. O cuidado das condições crônicas na atenção primária à saúde: o imperativo da consolidação da estratégia da saúde da família. Brasília: Organização Pan-Americana da Saúde; 2012. [Google Scholar]
  • 13.Dias JCP, Ramos AN Jr., Gontijo ED, Luquetti A, Shikanai-Yasuda MA, Coura JR et al. II Consenso Brasileiro em Doença de Chagas, 2015. Epidemiol. Serv. Saúde. 2016. June; 25 (spe): 7–86. 10.5123/S1679-49742016000500002 [DOI] [PubMed] [Google Scholar]
  • 14.Cardoso CS, Sabino EC, Oliveira CDL, Oliveira LC, Ferreira AM, Cunha-Neto E, et al. Longitudinal study of patients with chronic Chagas cardiomyopathy in Brazil (SaMi-Trop project): a cohort profile. BMJ Open. 2016; 6: e011181 10.1136/bmjopen-2016-011181 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Ferreira AM, Sabino EC, De Oliveira LC, Oliveira CDL, Cardoso CS, Ribeiro ALP, et al. Benznidazole use among patients with chronic Chagas' cardiomyopathy in an endemic region of Brazil. PLoS ONE, 2016; 11 (11). e0165950 10.1371/journal.pone.0165950 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Alkmim MB, Minelli Figueira R, Soriano Marcolino M, Silva Cardoso C, Pena de Abreu M, Rodrigues Cunha L, et al. Improving patient access to specialized health care: the Telehealth Network of Minas Gerais, Brazil. Bull World Health Organ. 2012; 90: 373±378. 10.2471/BLT.11.099408 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Andersen RM, Davidson PL. (2014). Improving access to care in America: Individual and contextual indicators Changing the US Health Care System: Key Issues in Health Services Policy and Management. In Andersen R. M., Rice T. H., & Kominski G. F. (Eds.), Changing the U.S. health care system: Key issues in health services policy and management; 2007. pp. 3–31. [Google Scholar]
  • 18.Ribeiro AL, Nunes MP, Teixeira MM, Rocha MO. Diagnosis and management of Chagas disease and cardiomyopathy. Nat Rev Cardiol. 2012; 9, 576–589. 10.1038/nrcardio.2012.109 [DOI] [PubMed] [Google Scholar]
  • 19.WHO- World Health Organization. Active Ageing- A Policy Framework. A contribution of the World Health Organization to the Second United Nations World Assembly on Ageing; Madri, April 2002, p. 4 [Google Scholar]
  • 20.New York Heart Association Chacko KA. AHA Medical/Scientific Statement: 1994 revisions to classification of functional capacity and objective assessment of patients with diseases of the heart. Circulation 1995; 92(7):2003–5. [PubMed] [Google Scholar]
  • 21.Pastore CA, Nelson S, Pereira-Filho HG. III Diretrizes SBC para Análise e Emissão de Laudos Eletrocardiográficos—Resumo Executivo. Arq. Bras. Cardiol. 2016. November 107 (5): 392–402. 10.5935/abc.20160173 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Maisel A, Mueller C, Adams K Jr., Anker SD, Aspromonte N, Cleland JG, et al. State of the art: using natriuretic peptide levels in clinical practice. Eur J Heart Fail. 2008. September;10(9):824–39. 10.1016/j.ejheart.2008.07.014 [DOI] [PubMed] [Google Scholar]
  • 23.Nadruz W, Gioli-Pereira L, Bernardez-Pereira S, Marcondes-Braga FG, Fernandes-Silva MM, Silvestre OM, et al. Temporal trends in the contribution of Chagas cardiomyopathy to mortality among patients with heart failure. Heart 2018;104:1522–1528. 10.1136/heartjnl-2017-312869 [DOI] [PubMed] [Google Scholar]
  • 24.Rita Barradas Barata. Epidemiologia social. Rev. bras. epidemiol. 2005. March; 8 (1): 7–17. [Google Scholar]
  • 25.Barreto SM, Ladeira RM, Bastos MSCBO, Diniz MFHS, Jesus EA, Kelles SMB et al. Estratégias de identificação, investigação e classificação de desfechos incidentes no ELSA-Brasil. Rev. Saúde Pública. 2013; 47 (Suppl 2): 79–86. [DOI] [PubMed] [Google Scholar]
  • 26.Kennedy B, Kawachi I, Prothrow-Stith D. Income distribution and mortality: cross sectional ecological study of the Robin Hood index in the United States. BMJ 1996;312:1004–7. 2. 10.1136/bmj.312.7037.1004 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Capuani L, Bierrenbach AL, Alencar AP, Mendrone A Jr, Ferreira JE, Custer B, et al. Mortality among blood donors seropositive and seronegative for chagas disease (1996–2000) in são paulo, brazil: A death certificate linkage study. PLoS neglected tropical diseases. 2017;11:e0005542 10.1371/journal.pntd.0005542 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Cucunubá ZM, Okuwoga O, Basáñez M-G, Nouvellet P. Increased mortality attributed to chagas disease: A systematic review and meta-analysis. Parasites & vectors. 2016; 9:42. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Camm AJ, Lip GY, De Caterina R, Savelieva I, Atar D, Hohnloser SH, et al. ; ESC Committee for Practice Guidelines (CPG). 2012 focused update of the ESC Guidelines for the management of atrial fibrillation: an update of the 2010 ESC Guidelines for the management of atrial fibrillation. Developed with the special contribution of the European Heart Rhythm Association. Eur Heart J. 2012;33(21):2719–47. Erratum in: Eur Heart J. 2013;34(10):790; Eur Heart J. 2013;34(36):2850–1. [DOI] [PubMed] [Google Scholar]
  • 30.Ribeiro AL, Marcolino MS, Prineas RJ, Lima-Costa MF. Electrocardiographic abnormalities in elderly Chagas disease patients: 10-year follow-up of the Bambui Cohort Study of Aging. J Am Heart Assoc. 2014. February 7;3(1):e000632 10.1161/JAHA.113.000632 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Mamas MA, Caldwell JC, Chacko S, Garrat CJ, Fath-Ordoubadi F, Neyses L. A meta-analysis of the prognostic significance of atrial fibrillartion in chronic heart failure. Eur J Heart Fail. 2009;11:676–83. 10.1093/eurjhf/hfp085 [DOI] [PubMed] [Google Scholar]
  • 32.Morillo CA, Marin-Neto JA, Avezum A, Sosa-Estani S, Rassi A Jr, Rosas F, et al. BENEFIT Investigators. Randomized Trial of Benznidazole for Chronic Chagas' Cardiomyopathy. N Engl J Med. 2015;373(14):1295–306. 51. 10.1056/NEJMoa1507574 [DOI] [PubMed] [Google Scholar]
  • 33.Malta DC, Santos MAS, Stopa SR, Vieira JEB, Melo EA, Reis AAC. A Cobertura da Estratégia de Saúde da Família (ESF) no Brasil, segundo a Pesquisa Nacional de Saúde, 2013. Ciênc. saúde coletiva. 2016. February; 21 (2): 327–338. [Google Scholar]
  • 34.Brasil. Ministério da Saúde. Secretaria de Assistência à Saúde. Coordenação de Saúde da Comunidade Saúde da Família: uma estratégia para a reorientação do modelo assistencial. Brasília: Ministério da Saúde, 1997. 36p. [Google Scholar]
  • 35.BRASIL. Ministério da Saúde. Portaria nº 1.996, de 20 de agosto de 2007.BRASIL: Ministério da Saúde; Portaria nº 1.996, de 20 de agosto de 2007. Brasilia, v. 144, n. 162, 20 Ago 2007. Seção 1, p.34–38 [Google Scholar]
  • 36.OMS—Organização Mundial Da Saúde. Departamento de Recursos Humanos para a Saúde. Spotlight: estatísticas da força de trabalho em saúde. Edição nº 8; Outubro de 2009. [Google Scholar]
  • 37.Scheffer M. Demografia Médica no Brasil 2018. São Paulo, SP: FMUSP, CFM, Cremesp; 2018. [Google Scholar]
  • 38.Shi L. The relation between primary care and life chances. J Health Care Poor Underserved. 1992;3:321–35 10.1353/hpu.2010.0460 [DOI] [PubMed] [Google Scholar]
  • 39.Ayres JRCM, França Junior I, Calazans GJ. O Conceito de Vulnerabilidade e as práticas de saúde: novas perspectivas e desafio In: Ayres JRCM, França Junior I, Calazans GJ. Promoção de saúde. Rio de Janeiro: Ed. Fiocruz; 2009. [Google Scholar]
  • 40.Starfield B. New Paradigms for Quality in Primary Care. Br J Gen Pract. 2001; 51(465):303–309 [PMC free article] [PubMed] [Google Scholar]
  • 41.Shi L, Macinko J, Starfield B, Xu J, Regan J, Politzer R, Wulu J. Primary Care, Infant Mortality, and Low Birth Weight in the States of the USA. J Epidemiol Community Health 2004; 58(5):374–380. 10.1136/jech.2003.013078 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.OMS—Organização Mundial Da Saúde. Diminuindo as diferenças: a prática das políticas sobre determinantes sociais da saúde. [Documento de Discussão]. Rio de Janeiro, Conferência Mundial sobre Determinantes Sociais da Saúde, 19–21 Outubro; 2011. 47p.
  • 43.Murphy M, Grundy E, Kalogirou S. The increase in marital status differences in mortality up to the oldest age in seven European countries, 1990–99. Popul Stud 2007; 61:287–98. [DOI] [PubMed] [Google Scholar]
  • 44.Johnson NJ, Backlund E, Sorlie PD, Loveless CA. Marital status and mortality: the national longitudinal mortality study. Ann Epidemiol 2000; 10: 224–38 10.1016/s1047-2797(99)00052-6 [DOI] [PubMed] [Google Scholar]
  • 45.Lorga FA, Lorga AM, Lopes ANG,Ângelo AVP, Costa AB, Péres AK et al. Diretriz de fibrilação atrial. Arq. Bras. Cardiol. 2003. November; 81 (Suppl 6): 2–24. [PubMed] [Google Scholar]
  • 46.Benjamin EJ, Virani SS, Callaway CW, Chamberlain AM, Chang AR, Cheng S,, et al. Heart Disease and Stroke Statistics—2018 Update: A Report From the American Heart Association. Circulation. 2018;137:e67–e492 10.1161/CIR.0000000000000558 [DOI] [PubMed] [Google Scholar]
  • 47.Rassi S, Barretto ACP, Porto CC, Pereira CR, Calaça BW, Rassi DC. Sobrevida e fatores prognósticos na insuficiência cardíaca sistólica com início recente dos sintomas. Arq. Bras. Cardiol. 2005. April; 84 (4): 309–313. 10.1590/s0066-782x2005000400007 [DOI] [PubMed] [Google Scholar]
  • 48.Cardoso CS, Ribeiro ALP, Oliveira CDL, Oliveira L, Ferreira AM, Bierrenbach AL, et al. Beneficial effects of benznidazole in Chagas disease: NIH SaMi-Trop cohort study. PLoS Negl Trop Dis. 2018; 12(11): e0006814 10.1371/journal.pntd.0006814 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Ribeiro AL, Cavalvanti PS, Lombardi F, Nunes MC, Barros MV, Rocha MOC. Prognostic Value of Signal-averaged Electrocardiogram in Chagas Disease. J Cardiovasc Electrophysiol. 2008;19:502–9. 10.1111/j.1540-8167.2007.01088.x [DOI] [PubMed] [Google Scholar]
  • 50.Lima-Costa MF, Cesar CC, Peixoto SV, Ribeiro AL. Plasma B-type natriuretic peptide as a predictor of mortality in community-dwelling older adults with Chagas disease: 10-year follow-up of the Bambui Cohort Study of Aging. Am J Epidemiol. 2010. July 15;172(2):190–6. 10.1093/aje/kwq106 [DOI] [PubMed] [Google Scholar]
  • 51.Nunes MC, Dones W, Morillo CA, Encina JJ, Ribeiro AL. ChD: an overview of clinical and epidemiological aspects. Journal of the American College of Cardiology. 2013;62(9):767–76. 10.1016/j.jacc.2013.05.046 [DOI] [PubMed] [Google Scholar]
  • 52.Francisco PMSB, Barros MBA, Segri NJ, Alves MCGP, Cesar CLG, Malta DC. Comparação de estimativas para o auto-relato de condições crônicas entre inquérito domiciliar e telefônico—Campinas (SP), Brasil. Rev. bras. epidemiol. 2011. September; 14 (Suppl 1): 5–15.22002138 [Google Scholar]
PLoS Negl Trop Dis. doi: 10.1371/journal.pntd.0008399.r001

Decision Letter 0

Walderez O Dutra

3 Feb 2020

Dear Ferreira,

Thank you very much for submitting your manuscript "Impact of the social context on the prognosis of Chagas disease patients: multilevel analysis of a Brazilian cohort" for consideration at PLOS Neglected Tropical Diseases. As with all papers reviewed by the journal, your manuscript was reviewed by members of the editorial board and by several independent reviewers. In light of the reviews (below this email), we would like to invite the resubmission of a significantly-revised version that takes into account the reviewers' comments.

We cannot make any decision about publication until we have seen the revised manuscript and your response to the reviewers' comments. Your revised manuscript is also likely to be sent to reviewers for further evaluation.

When you are ready to resubmit, please upload the following:

[1] A letter containing a detailed list of your responses to the review comments and a description of the changes you have made in the manuscript. Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.

[2] Two versions of the revised manuscript: one with either highlights or tracked changes denoting where the text has been changed; the other a clean version (uploaded as the manuscript file).

Important additional instructions are given below your reviewer comments.

Please prepare and submit your revised manuscript within 60 days. If you anticipate any delay, please let us know the expected resubmission date by replying to this email. Please note that revised manuscripts received after the 60-day due date may require evaluation and peer review similar to newly submitted manuscripts.

Thank you again for your submission. We hope that our editorial process has been constructive so far, and we welcome your feedback at any time. Please don't hesitate to contact us if you have any questions or comments.

Sincerely,

Walderez O. Dutra, PhD.

Deputy Editor

PLOS Neglected Tropical Diseases

Alvaro Acosta-Serrano

Deputy Editor

PLOS Neglected Tropical Diseases

***********************

Reviewer's Responses to Questions

Key Review Criteria Required for Acceptance?

As you describe the new analyses required for acceptance, please consider the following:

Methods

-Are the objectives of the study clearly articulated with a clear testable hypothesis stated?

-Is the study design appropriate to address the stated objectives?

-Is the population clearly described and appropriate for the hypothesis being tested?

-Is the sample size sufficient to ensure adequate power to address the hypothesis being tested?

-Were correct statistical analysis used to support conclusions?

-Are there concerns about ethical or regulatory requirements being met?

Reviewer #1: Generally it is appropriated, Minor corrections are suggested

Reviewer #2: Introduction section

- Lines 75 and 76. Authors speaks about social problem and social impact, based on data of reference 1. Please, explain what social impact means, because it is not explained into this reference, or alternatively, provide a reference to address it.

- Line 100. Authors said that CD is classically associated with poverty in rural areas (ref 11). I don’t agree with this statement given that in periurban areas of endemic countries, CD transmission (and prevalence) is even higher that in rural areas, due to internal migrant movements. I suggest authors to reformulate the statement

Methods section

- Study design. Why were negatives excluded from the analysis? How do you ensure that also negatives patients did not suffer from the same cardiological affections?

I suggest authors to provide information about this group, if they have. If not, I consider this lack of information a study major limitation.

- Line 179: Theoretical model and variables. I think that this section should be better organized and included in Study design section

- In this same section (Theoretical model and variables), and even if authors include this information after, I suggest to provide information why (based on which data) AF and QRS complex duration were selected among arrhythmia types and EKG values.

- Line 199: If I understood well, health related behavior variables were asked only at the beginning. From my point of view, it is possible that these value change during the follow-up period. Please provide information of this timepoint evaluation, and if you don’t have it, provide a rational why it was not considered to be included.

- Line 206: why authors selected range 25-75 to dichotomize variables? Based on what? Please, provide more information on this decision.

--------------------

Results

-Does the analysis presented match the analysis plan?

-Are the results clearly and completely presented?

-Are the figures (Tables, Images) of sufficient quality for clarity?

Reviewer #1: Table 2 should be improved

Figures provided in portuguese and in a very poor quality

Reviewer #2: In case of the results, the analysis presented matched with the analysis plan. Results were mainly clearly presented.

Table 2.

- Regarding self-reporting skin color, and given the high variety and variability of the variable. As a curiosity, why authors decide white/ non-white variables?

- Functional class: At /with limitations/ variable, did authors considered degree limitation? I think that information is scarce as dichotomized in this case. Please provide an explanation why the variable was established this way.

Figure 1 should be translated into English

--------------------

Conclusions

-Are the conclusions supported by the data presented?

-Are the limitations of analysis clearly described?

-Do the authors discuss how these data can be helpful to advance our understanding of the topic under study?

-Is public health relevance addressed?

Reviewer #1: ok

Reviewer #2: - Line 324. 12% of the patients with CD had Cvascular events. Among them, how many were treated? Please, provide information of the analysis of patients by treatment condition

- Lines 376-380. I think that this assumption is not based on the manuscript results presented. To provide information of this assumption was not the objective of the research, so there is no data to support this hypothesis. I suggest authors to reformulate or eliminate it.

- Same comment to 436-438 lines.

- Line 453-454: there were people with altered NTproBNP without cardiovascular events? It seems clear that, as ventricular disfunction marker, proBNP is proven to be higher in older people. Please highlight if new information on this concern regarding this study results

--------------------

Editorial and Data Presentation Modifications?

Use this section for editorial suggestions as well as relatively minor modifications of existing data that would enhance clarity. If the only modifications needed are minor and/or editorial, you may wish to recommend “Minor Revision” or “Accept”.

Reviewer #1: see attached document

Reviewer #2: (No Response)

--------------------

Summary and General Comments

Use this section to provide overall comments, discuss strengths/weaknesses of the study, novelty, significance, general execution and scholarship. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. If requesting major revision, please articulate the new experiments that are needed.

Reviewer #1: see attached document

Reviewer #2: First of all, I would like congratulate researches for the comprehensive view that a disease like Chagas, and that is reflected in the research results and the manuscript.

Nevertheless, and spite of the necessary and positive approach, I would have needed a little more information to arrive to authors’ conclusions.

--------------------

PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: No

Figure Files:

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email us at figures@plos.org.

Data Requirements:

Please note that, as a condition of publication, PLOS' data policy requires that you make available all data used to draw the conclusions outlined in your manuscript. Data must be deposited in an appropriate repository, included within the body of the manuscript, or uploaded as supporting information. This includes all numerical values that were used to generate graphs, histograms etc.. For an example see here: http://www.plosbiology.org/article/info%3Adoi%2F10.1371%2Fjournal.pbio.1001908#s5.

Reproducibility:

To enhance the reproducibility of your results, PLOS recommends that you deposit laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. For instructions see https://journals.plos.org/plosntds/s/submission-guidelines#loc-methods

Attachment

Submitted filename: mpact of the social context on the prognosis of Chagas disease patients REVIEW.docx

PLoS Negl Trop Dis. doi: 10.1371/journal.pntd.0008399.r003

Decision Letter 1

Walderez O Dutra

3 Apr 2020

Dear Ferreira,

Thank you very much for submitting your manuscript "Impact of the social context on the prognosis of Chagas disease patients: multilevel analysis of a Brazilian cohort" for consideration at PLOS Neglected Tropical Diseases. As with all papers reviewed by the journal, your manuscript was reviewed by members of the editorial board and by several independent reviewers. In light of the reviews (below this email), we would like to invite the resubmission of a significantly-revised version that takes into account the reviewers' comments.

Given the comments by one of the reviewers were not addressed, please consider if you would like to address the comments and resubmit. We will not consider a resubmission without proper response to the points raised.

We cannot make any decision about publication until we have seen the revised manuscript and your response to the reviewers' comments. Your revised manuscript is also likely to be sent to reviewers for further evaluation.

When you are ready to resubmit, please upload the following:

[1] A letter containing a detailed list of your responses to the review comments and a description of the changes you have made in the manuscript. Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.

[2] Two versions of the revised manuscript: one with either highlights or tracked changes denoting where the text has been changed; the other a clean version (uploaded as the manuscript file).

Important additional instructions are given below your reviewer comments.

Please prepare and submit your revised manuscript within 60 days. If you anticipate any delay, please let us know the expected resubmission date by replying to this email. Please note that revised manuscripts received after the 60-day due date may require evaluation and peer review similar to newly submitted manuscripts.

Thank you again for your submission. We hope that our editorial process has been constructive so far, and we welcome your feedback at any time. Please don't hesitate to contact us if you have any questions or comments.

Sincerely,

Walderez O. Dutra, PhD.

Deputy Editor

PLOS Neglected Tropical Diseases

Alvaro Acosta-Serrano

Deputy Editor

PLOS Neglected Tropical Diseases

***********************

Reviewer's Responses to Questions

Key Review Criteria Required for Acceptance?

As you describe the new analyses required for acceptance, please consider the following:

Methods

-Are the objectives of the study clearly articulated with a clear testable hypothesis stated?

-Is the study design appropriate to address the stated objectives?

-Is the population clearly described and appropriate for the hypothesis being tested?

-Is the sample size sufficient to ensure adequate power to address the hypothesis being tested?

-Were correct statistical analysis used to support conclusions?

-Are there concerns about ethical or regulatory requirements being met?

Reviewer #1: Authors have adressed all comments properly

Reviewer #2: Same comments than in R1: there were no answered by authors (nor in the text, neither in the letter of response)

--------------------

Results

-Does the analysis presented match the analysis plan?

-Are the results clearly and completely presented?

-Are the figures (Tables, Images) of sufficient quality for clarity?

Reviewer #1: Authors have adressed all comments properly

Reviewer #2: Same comments than in R1: there were no answered by authors (nor in the text, neither in the letter of response)

--------------------

Conclusions

-Are the conclusions supported by the data presented?

-Are the limitations of analysis clearly described?

-Do the authors discuss how these data can be helpful to advance our understanding of the topic under study?

-Is public health relevance addressed?

Reviewer #1: Authors have adressed all comments properly

Reviewer #2: Same comments than in R1: there were no answered by authors (nor in the text, neither in the letter of response)

--------------------

Editorial and Data Presentation Modifications?

Use this section for editorial suggestions as well as relatively minor modifications of existing data that would enhance clarity. If the only modifications needed are minor and/or editorial, you may wish to recommend “Minor Revision” or “Accept”.

Reviewer #1: Accept

Reviewer #2: No comments

--------------------

Summary and General Comments

Use this section to provide overall comments, discuss strengths/weaknesses of the study, novelty, significance, general execution and scholarship. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. If requesting major revision, please articulate the new experiments that are needed.

Reviewer #1: Obrigado por ter considerado minhas sugestões.

Reviewer #2: No comments

--------------------

PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: No

Figure Files:

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email us at figures@plos.org.

Data Requirements:

Please note that, as a condition of publication, PLOS' data policy requires that you make available all data used to draw the conclusions outlined in your manuscript. Data must be deposited in an appropriate repository, included within the body of the manuscript, or uploaded as supporting information. This includes all numerical values that were used to generate graphs, histograms etc.. For an example see here: http://www.plosbiology.org/article/info%3Adoi%2F10.1371%2Fjournal.pbio.1001908#s5.

Reproducibility:

To enhance the reproducibility of your results, PLOS recommends that you deposit laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. For instructions see https://journals.plos.org/plosntds/s/submission-guidelines#loc-methods

PLoS Negl Trop Dis. doi: 10.1371/journal.pntd.0008399.r005

Decision Letter 2

Walderez O Dutra

19 May 2020

Dear Ferreira,

We are pleased to inform you that your manuscript 'Impact of the social context on the prognosis of Chagas disease patients: multilevel analysis of a Brazilian cohort' has been provisionally accepted for publication in PLOS Neglected Tropical Diseases.

Before your manuscript can be formally accepted you will need to complete some formatting changes, which you will receive in a follow up email. A member of our team will be in touch with a set of requests.

Please note that your manuscript will not be scheduled for publication until you have made the required changes, so a swift response is appreciated.

IMPORTANT: The editorial review process is now complete. PLOS will only permit corrections to spelling, formatting or significant scientific errors from this point onwards. Requests for major changes, or any which affect the scientific understanding of your work, will cause delays to the publication date of your manuscript.

Should you, your institution's press office or the journal office choose to press release your paper, you will automatically be opted out of early publication. We ask that you notify us now if you or your institution is planning to press release the article. All press must be co-ordinated with PLOS.

Thank you again for supporting Open Access publishing; we are looking forward to publishing your work in PLOS Neglected Tropical Diseases.

Best regards,

Walderez O. Dutra, PhD.

Deputy Editor

PLOS Neglected Tropical Diseases

Alvaro Acosta-Serrano

Deputy Editor

PLOS Neglected Tropical Diseases

***********************************************************

Reviewer's Responses to Questions

Key Review Criteria Required for Acceptance?

As you describe the new analyses required for acceptance, please consider the following:

Methods

-Are the objectives of the study clearly articulated with a clear testable hypothesis stated?

-Is the study design appropriate to address the stated objectives?

-Is the population clearly described and appropriate for the hypothesis being tested?

-Is the sample size sufficient to ensure adequate power to address the hypothesis being tested?

-Were correct statistical analysis used to support conclusions?

-Are there concerns about ethical or regulatory requirements being met?

Reviewer #2: Authors answered the most of the queries raised at the first review, and at this moment methods section is pretty clear and complete.

**********

Results

-Does the analysis presented match the analysis plan?

-Are the results clearly and completely presented?

-Are the figures (Tables, Images) of sufficient quality for clarity?

Reviewer #2: Authors answered the most of the queries raised at the first review: results are clear and well structured.

**********

Conclusions

-Are the conclusions supported by the data presented?

-Are the limitations of analysis clearly described?

-Do the authors discuss how these data can be helpful to advance our understanding of the topic under study?

-Is public health relevance addressed?

Reviewer #2: The conclusions are supported by the data presented, and limitations of the study clearly established.

**********

Editorial and Data Presentation Modifications?

Use this section for editorial suggestions as well as relatively minor modifications of existing data that would enhance clarity. If the only modifications needed are minor and/or editorial, you may wish to recommend “Minor Revision” or “Accept”.

Reviewer #2: NA

**********

Summary and General Comments

Use this section to provide overall comments, discuss strengths/weaknesses of the study, novelty, significance, general execution and scholarship. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. If requesting major revision, please articulate the new experiments that are needed.

Reviewer #2: I think that the content of the manuscript contains valuable data and information, and add knowledge for better address Chagas Disease with a interdisciplinar view.

**********

PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #2: No

PLoS Negl Trop Dis. doi: 10.1371/journal.pntd.0008399.r006

Acceptance letter

Walderez O Dutra

22 Jun 2020

Dear Ferreira,

We are delighted to inform you that your manuscript, "Impact of the social context on the prognosis of Chagas disease patients: multilevel analysis of a Brazilian cohort," has been formally accepted for publication in PLOS Neglected Tropical Diseases.

We have now passed your article onto the PLOS Production Department who will complete the rest of the publication process. All authors will receive a confirmation email upon publication.

The corresponding author will soon be receiving a typeset proof for review, to ensure errors have not been introduced during production. Please review the PDF proof of your manuscript carefully, as this is the last chance to correct any scientific or type-setting errors. Please note that major changes, or those which affect the scientific understanding of the work, will likely cause delays to the publication date of your manuscript. Note: Proofs for Front Matter articles (Editorial, Viewpoint, Symposium, Review, etc...) are generated on a different schedule and may not be made available as quickly.

Soon after your final files are uploaded, the early version of your manuscript will be published online unless you opted out of this process. The date of the early version will be your article's publication date. The final article will be published to the same URL, and all versions of the paper will be accessible to readers.

Thank you again for supporting open-access publishing; we are looking forward to publishing your work in PLOS Neglected Tropical Diseases.

Best regards,

Shaden Kamhawi

co-Editor-in-Chief

PLOS Neglected Tropical Diseases

Paul Brindley

co-Editor-in-Chief

PLOS Neglected Tropical Diseases

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Checklist. STROBE checklist.

    (DOCX)

    S1 Table. Database.

    (XLS)

    Attachment

    Submitted filename: mpact of the social context on the prognosis of Chagas disease patients REVIEW.docx

    Attachment

    Submitted filename: letter_to_the_reviewer_.docx

    Attachment

    Submitted filename: letter_to_the_reviewer_2 (2).docx

    Data Availability Statement

    All relevant data are within the manuscript and its Supporting Information files.


    Articles from PLoS Neglected Tropical Diseases are provided here courtesy of PLOS

    RESOURCES