INTRODUCTION
In recent decades, dengue fever has gained prominence as one of the most important arboviral diseases in Brazil and worldwide because of the increasing number of people living in endemic areas as well as increases in severe clinical manifestations and lethality rates1.
Brazil accounts for more than 70% of notified cases in the Americas, and the City of Rio de Janeiro has become one of the most endemic cities in Brazil with a long history of dengue virus circulation2–5.
Successive epidemics have been reported in Rio de Janeiro, beginning in 1986 with the introduction of dengue virus serotype-1 (DENV-1)6. After an interval of four years, the city experienced an epidemic of dengue virus serotype-2 (DENV-2) from 1990-1991. During this epidemic, only a few cases of hemorrhagic fever were reported7. From 2001-2002, the largest epidemic to date, in terms of total cases, attributed to dengue virus serotype-3 (DENV-3) occurred in the city. This epidemic resulted in more than 288,000 notified cases with 1,831 cases of hemorrhagic fever and 91 deaths8,9. Subsequently, the City of Rio de Janeiro was affected in 2008 by the largest dengue epidemic ever reported in terms of mortality. The 2008 epidemic was associated with a variant strain of the DENV-2 serotype, which was characterized by a greater proportion of severe cases in children compared with previous epidemics2,5,10,11.
No consensus is currently available on the determinants of a poor clinical prognosis in dengue patients; however, the excessive number of severe cases in Rio de Janeiro in 2008 may be explained by a combination of factors that range from proximal determinants, such as the genetic variant of the DENV-2 serotype, the immune status of the population, the supply and quality of health services, and the socioeconomic context from which the severe cases emerged2,4,5,11.
Therefore, this ecological study aimed to analyze the association between the occurrence of severe cases of dengue in the 2008 epidemic and socioeconomic indicators, as well as indicators of health service availability and previous circulation of the DENV-3 serotype.
METHODS
Study area
The study area was Rio de Janeiro, the capital of the State of Rio de Janeiro in the southeast region of Brazil. According to 2010 census data, the city has a population of 6,323,037 inhabitants within an area of 1,182km2 that is divided into 160 districts. These districts were the units of analysis in this ecological study.
Data sources
This study analyzed confirmed cases of severe dengue fever [dengue hemorrhagic fever (DHF); dengue shock syndrome (DSS); and dengue with complications (DCC)] that occurred in Rio de Janeiro in 2008. Data were collected from the National System for Notifiable Diseases [Sistema Nacional de Agravos de Notificação (SINAN)]. Duplicate records and inconsistencies were removed from the database, and the cases were categorized according to the district of residence.
In Brazil, the Ministry of Health has adopted the definitions for suspected and confirmed cases of dengue fever and hemorrhagic dengue fever that were proposed by the World Health Organization (WHO). However, because of difficulties in classifying severe cases of disease, an intermediate classification called dengue with complications [dengue com complicações (DCC)] was adopted in Brazil12. Dengue with complications is assigned to cases with clinical outcomes that do not completely meet the traditional WHO classification criteria for dengue hemorrhagic fever. Additionally, DCC may indicate cases in which the dengue fever rating is unsatisfactory given the severity of the clinical and laboratory manifestations. Therefore, DCC includes cases with at least one of the following clinical and laboratory changes: cardio-respiratory dysfunction, liver failure, massive gastrointestinal bleeding, neurological abnormalities, a leukocyte count equal to or less than 1,000 cells/ml, a platelet count less than 20,000/ml, pleural effusion, pericardial effusion or ascites. In addition, fatal dengue cases that do not meet the criteria for hemorrhagic fever may be classified as DCC12.
The data on health facilities were extracted from the National Register of Health Establishments [Cadastro Nacional de Estabelecimentos de Saúde (CNES)]. We selected only public health units and classified them according to type and location. The data used to construct the socioeconomic indicators were obtained from the 2010 census from the Brazilian Institute of Geography and Statistics [Instituto Brasileiro de Geografia e Estatística (IBGE)]. The district populations for 2001 and 2008 (inter-census) were estimated based on the geometric growth model.
Data analysis
Using the available data from the 2010 census, we constructed 15 possible indicators related to the disease. The following indicators were calculated per district: the number of severe dengue cases in the 2001 epidemic (considered to be a proxy for the prior circulation of the DENV-3 serotype); the percentage of residents who declared their skin color or race as black; the proportion of permanent private domiciles that store rain water in cisterns; the proportion of permanent private domiciles that discharge domestic waste on empty lots or on the street; the ratio of the population within a given district to the district area in km2; the proportion of permanent private domiciles in substandard settlements; the proportion of residents who live in substandard settlements; the proportion of permanent domiciles in substandard settlements in which domestic waste is collected by open skip (waste is accumulated in a large dumpster without a lid, which is shared with the whole neighborhood and collected at time intervals that are usually longer than those of standard domestic waste collection service); the proportion of permanent private domiciles with no connection to the sewage system and no septic tank; the proportion of permanent private domiciles in which the head of the family has an income less than the Brazilian monthly minimum wage (approximately US$290); the proportion of residents in permanent private domiciles with no exclusive bathroom available and no toilet; the proportion of permanent private domiciles in which domestic waste is collected by open skip; the proportion of permanent private domiciles in which the water supply is from a well or spring on the property; the number of primary health facilities; and the number of Family Health Strategy (FHS) clinics.
The Family Health Strategy program was designed to reorient the Brazilian health care model by implementing multidisciplinary teams in primary care units. These teams are responsible for monitoring families who reside in a particular geographical area, and they usually work in the community on initiatives for health promotion and prevention, including the rehabilitation of diseases and health disorders. The aim of the FHS is to achieve health assistance that is equitable and comprehensive13,14,15.
Subsequently, the indicators were separated into groups according to subject (sanitation, income, health services and education) and a collinearity diagnostic was performed using the variance inflation factor (VIF) test (with a tolerance value greater than 10) to select variables for the model. The explanatory variables were tested separately in univariate models, and the variables with statistical significance were analyzed in multivariate models using forward selection logistic regression. The likelihood ratio test was used to assess the best-fit model. Only the results of the negative binomial model with the best fit are presented. Moran’s index was used to measure the spatial autocorrelation of the residuals from the model. The analyses were performed using the R software environment (R Development Core Team 2011; R Foundation for Statistical Computing, Vienna, Austria).
The distribution of the means and standard deviations of the explanatory variables was calculated for the overall set of districts; the values were subsequently standardized using the Z-scale [(X-mean)/standard deviation]. Using this method, the magnitude of the change in the incidence rate ratio for severe dengue cases was compared for each predictive variable13,16.
The data were incorporated into a negative binomial regression model, which is commonly used for counting data and when the variance exceeds the mean17. Because the dependent variable (severe dengue cases) was influenced by the incidence rate of dengue fever, the analysis was adjusted for the number of dengue fever cases in 2008.
The dependent variable Yi for each district (i= 1, 2, 3…, 156) has an expected value of µi and a dispersion parameter θ, which was used to capture the extra-variation in the data17. The overdispersion of error terms was tested using the poisgof function in the epicalc package, which was included in the R software program 2.11.1 (p-value= 0.0082). The model was expressed as log (µ)= βχ + ε, where χi is the standardized independent variable (with its associated regression coefficient, βi) and ε represents the error term17. The natural logarithm of the district population was included as the offset variable. The exponential of each βi regression coefficient provides the incidence rate ratio for each 1-standard-deviation change in the corresponding independent variable.
RESULTS
In 2008, a total of 59,395 cases of dengue were reported in Rio de Janeiro, of which 12,620 cases were classified as DF, 5,082 as DCC, 621 as DHF, and 18 as DSS. A final classification was not available for 41,054 cases; therefore, approximately 31% of the total cases were classified. The age group that was most affected by all clinical forms of the disease were children and adolescents 6-15 years of age. Higher incidence rates were found in this age group compared with other age groups (Table 1).
Age group (years) | Dengue fever | Severe dengue | NM+ | Total | ||
---|---|---|---|---|---|---|
cases | incidence* | cases | incidence* | |||
≤ 5 | 1,016 | 204.1 | 410 | 82.4 | 3,668 | 5,094 |
6-15 | 3,269 | 364.1 | 2,632 | 293.1 | 11,017 | 16,918 |
16-20 | 1,099 | 308.8 | 365 | 102.6 | 3,810 | 5,274 |
21-35 | 2,956 | 194.8 | 784 | 51.7 | 10,667 | 14,407 |
36-50 | 2,335 | 180.6 | 766 | 59.2 | 7,101 | 10,202 |
51-60 | 1,141 | 159.9 | 377 | 52.8 | 2,888 | 4,406 |
> 60 | 804 | 90.8 | 387 | 43.7 | 1,903 | 3,094 |
Total | 12,620 | 204.8 | 5,721 | 92.9 | 41,054 | 59,395 |
+ Number of missings: cases with missing classification. *Incidence per 100,000 inhabitants; +the number of case records in which the final classification was ignored or not completed; the cases classified as dengue hemorrhagic fever, dengue shock syndrome, and dengue with complications were considered to be severe infections.
Furthermore, according to the data provided by Sistema Nacional de Agravos de Notificação (SINAN), a total of 5,463 patients with dengue were hospitalized in Rio de Janeiro in 2008, representing 9% of the 59,395 dengue cases reported in the city. The highest proportion of death was found in patients who were 6-15 years and those older than 60 years.
In the univariate analysis, two variables were significantly associated with the occurrence of severe dengue cases in the 2008 epidemic: the number of dengue fever cases per district in the epidemic year of 2001and the percentage of residents who declared their skin color or race as black. The number of FHS clinicsand the proportion of permanent domiciles in substandard settlements in which domestic waste was collected by open skip were inversely associated with the incidence of severe dengue, and these associations were significant. However, when these variables were combined in a multivariate model, theproportion of permanent domiciles in substandard settlements in which domestic waste was collected by open skip lost statistical significance as an explanatory factor and was therefore eliminated from the final model. Additionally, a direct association was observed between the number of dengue fever cases and the incidence of severe cases in 2008 (Table 2).
Indicator | Univariate analysis | Multivariate analysis | ||
---|---|---|---|---|
IRR | 95% CI | IRR | 95% CI | |
Previous circulation of DENV-3 serotype (number of dengue cases in the 2001 epidemic)* | 1.23 | [1.04-1.46] | 1.21 | [1.05-1.40] |
Family Health Strategy clinics* | 0.89 | [0.58-0.92] | 0.81 | [0.70-0.93] |
Self-declaration of race or skin color as black* | 1.30 | [1.12-1.51] | 1.34 | [1.16-1.54] |
Number of dengue fever cases in 2008 | 1.28 | [1.11-1.48] | 1.21 | [1.05-1.39] |
Water supply | 1.15 | [0.99-1.33] | ||
Population density | 1.04 | [0.89-1.20] | ||
Population living in favelas | 1.10 | [0.95-1.28] | ||
Primary health care clinics | 0.99 | [0.86-1.15] | ||
Low income | 1.07 | [0.87-1.31] | ||
Domestic waste collection service | 1.02 | [0.88-1.19] | ||
Domestic waste collection service in substandard settlements* | 0.84 | [0.73-0.98] |
IRR: incidence rate ratio; 95% CI: 95% confidence interval; DENV-3: dengue virus serotype-3.
*Variables with statistical significance in the univariate analysis; IRR reflects the variation in the incidence rate per each 1-standard-deviation increment in the mean of the predictive variable. The indicator domestic waste collection service in substandard settlements lost statistical significance as an explanatory variable in the multivariate analysis and was therefore eliminated from the final model.
The districts with more cases of dengue during the 2001 epidemic (an epidemic attributed to the DENV-3 serotype) presented higher incidence rates of severe dengue during the 2008 epidemic, both in the univariate and multivariate models. Similarly, the districts with a higher percentage of residents who declared their skin color or race as black were more likely to have higher incidence rates of severe dengue in 2008 in both the univariate and multivariate models. In contrast, the districts with more FHS clinics were more likely to have lower incidence rates of severe dengue in the 2008 epidemic. All of the multivariate analyses were adjusted for the number of dengue fever cases in 2008 (Table 2). The incidence rates of dengue fever and severe dengue in 2008 for each district in Rio de Janeiro are shown in Figure 1 and Figure 2.
For each increment of one standard deviation in the mean number of dengue cases in 2001 (approximately from 166 to 263), the incidence rate of severe dengue in 2008 increases 1.21 times (assuming the other variables remained constant). Similarly, for each increment of one standard deviation in the mean percentage of residents who declared their skin color or race as black (approximately from 11.5% to 16%), the incidence rate of severe dengue in 2008 increases 1.34 times. For each increment of one standard deviation in the mean number of FHS clinics (from 0.2 to 0.6), the incidence rate of severe dengue in 2008 was 0.2 times lower (Table 2 and Table 3).
Variables/indicators per district | Mean | Standard deviation | Range [min-max] |
---|---|---|---|
Population per district in 2008 | 38,807.9 | 54,491.6 | [160-321,949] |
Number of severe dengue cases in 2008 | 36.6 | 42.7 | [0-241] |
Number of dengue fever cases in 2008 | 80.6 | 154.0 | [0-1,575] |
Water supply servicea | 0.02 | 0.05 | [0-0.47] |
Number of Family Health Strategy clinics | 0.21 | 0.59 | [0.0-4.0] |
Previous circulation of the DENV-3 serotypeb | 65.7 | 197.23 | [1.0-898.0] |
Population densityc | 14,878.6 | 12,402.7 | [17.4-96,515.8] |
Population living in favelasd | 16.07 | 15.76 | [0.0-71.7] |
Number of primary health care clinics | 0.47 | 0.90 | [0.0-6.0] |
Low-income populatione | 0.11 | 0.42 | [0.0-4.2] |
Self-declared black populationf | 11.15 | 4.68 | [1.5-27.7] |
Domestic waste collection serviceg | 0.54 | 1.32 | [0.0-10.6] |
Domestic waste collection service in substandard settlementsh | 34.69 | 31.82 | [0.0-98.7] |
DENV-3: dengue virus serotype-3.
aProportion of permanent private domiciles that store rain water in cisterns.
bNumber of cases in the 2001 dengue epidemic.
cRatio of the district population to its area in km2.
dProportion of residents living in substandard settlements.
eProportion of residents in permanent private domiciles with no exclusive bathroom access and no toilet.
fPercentage of residents who declared their skin color or race as black.
gThe proportion of permanent private domiciles that discharge domestic waste on empty lots or on the street.
hProportion of permanent domiciles in substandard settlements in which domestic waste is collected by open skip.
Regarding the number of dengue cases in 2001 (considered to be a proxy for the prior circulation of the DENV-3 serotype), the districts presented an average of 65.7 cases with a range of 1-898 cases and a standard deviation of 197.2 cases (Table 3). Overall, the distribution pattern of dengue cases in 2001 suggests that cases were concentrated in the center, western and northern districts of the city.
The quartile with the highest percentage of self-declared black residents ranged from 14.7%-27.7% and comprised 38 districts. Notably, the overall mean percentage of self-declared black residents per district was 11.1% with a range of 1.5%-27.7% and a standard deviation of 1.3 (Table 3). The distribution pattern of self-declared black residents suggests that higher percentages of these individuals were located in the western and northern districts of the city.
The spatial distribution of the FHS clinics revealed only one district with four FHS clinics and one district with three clinics. Furthermore, six districts had two FHS clinics each, whereas 13 had only one clinic each. Therefore, of the 156 districts that were examined, 135 did not have FHS clinics. Both the location and quantity of FHS units are determined according to the population size, political-administrative factors and the local demand for health services.
Moran’s coefficient for the residuals from the final multivariate model was not statistically significant (p-value= 0.183), indicating a lack of spatial correlation.
DISCUSSION
The higher incidence rates of severe dengue in 2008 in the districts with a higher incidence of dengue fever during the 2001 epidemic (attributed to DENV-3) suggests that more individuals were susceptible to secondary infection in these areas which may partially explain the substantial increase in severe cases, particularly in the 8- to 17-year-old age group. In 2008, 8- to 17-year-olds represented a large contingent of individuals who had been exposed to the DENV-3 serotype in the 2001 epidemic; however, these individuals were also susceptible to DENV-2 because they were born after the emergence of this serotype in 1990-19913,5.
Although several studies have demonstrated the occurrence of severe and fatal cases in primary dengue infection, sequential infection by multiple serotypes has been suggested as one of the main risk factors for the severe clinical evolution8,18. According to Barraquer et al.19, the accumulation of homotypic and heterotypic immunity against dengue virus serotypes in the Brazilian population since 1986 when dengue reemerged in Brazil created the conditions responsible for the changes that are now being observed in the clinical and epidemiological profiles of the disease. To the extent of a hyper-endemic scenario, adult individuals are acquiring new infections and accumulating heterotypic immunity to various serotypes.
However, when only severe cases of dengue (DHF and DSS), classified according to the WHO criteria, were used as the dependent variable in the regression analysis of this study, the explanatory variable confirmed dengue fever cases in 2001 lost statistical significance in the final multivariate model.
At the individual level, several genetics studies on the relationship between dengue severity and ethnicity/ancestry have demonstrated that afro-descendant individuals are less susceptible to the severe forms of the disease20,21. In contrast, at the ecological level, our findings indicate a higher risk of severe dengue in districts with a higher percentage of self-declared black residents.
This finding may be related to the historical socioeconomic vulnerability of this group, which in turn reflects the morbidity and mortality patterns of many health problems, including dengue and its severe forms22,23. These social inequalities may lead to several disadvantages, ranging from a lack of health promotion to a reduced capability to successfully treat severe and potentially fatal cases, resulting from limited access to early diagnosis and timely clinical management23,24.
Most of the districts with a higher percentage of self-declared black residents have large areas of substandard settlements and favelas, which are generally associated with poor living conditions.
The national health system in Brazil is guided by the underlying principle of universal and egalitarian access to health care among socially disparate individuals; however, health inequities persist due to differences in living conditions and the availability and accessibility of health services22,25. Several authors have argued that income constitutes an enabling resource, whose availability positively influences health service access, i.e., the ability to use health services when necessary23,25,26.
Moreover, the characteristics of healthcare supply, such as availability and geographical location (proximity of health resources and services), can facilitate or hinder health service utilization25. The results of this study demonstrate a protective effect against various forms of severe dengue in the districts with FHS clinics.
The introduction of the FHS was aimed at reorienting and strengthening the healthcare model in Brazil; therefore, the districts that have FHS clinics should have their health needs better met. Accordingly, ease of access to health care for individuals at the family level, in addition to preventive actions and health promotion, might have attenuated the vulnerability to dengue and its severe forms15.
Roriz-Cruz et al.14 emphasized the importance of structuring primary health care, especially the FHS, to achieve control of dengue in a comparison of Rio de Janeiro with its neighbor City, Niterói. They argue that although the cities are close and have similar profiles in terms of population density, climate and levels of sanitation, the incidence of dengue and related vector infestation rates are considerably lower in Niterói than in Rio de Janeiro. They attribute this difference to the high level of coverage by primary health care and the FHS, as the coverage in Niterói has increased from less than 1% to 77.4% over 20 years compared with 7.2% coverage in Rio de Janeiro. Accordingly, the actions of community health workers at FHS clinics are directed at eliminating the foci of vectors and educating the community, which are critical factors to understanding the differences between the two cities in terms of the epidemiological profile of dengue14.
Most FHS clinics are not directly integrated with the dengue vector control program (Aedes aegypti); however, the actions of FHS are essential to health promotion and disease prevention, which includes reducing the risk of exposure to and transmission of dengue. Moreover, FHS teams are trained in early disease recognition, ensuring the referral of these patients to other care levels within the health system when necessary15,16.
This study had several limitations, such as the low rate of final classifications in the case records. The overloading of health care facilities, particularly during the dengue epidemic, may have contributed to information loss with respect to the classification of dengue cases. Therefore, even though severe cases tend to be recorded more carefully than are classic dengue cases, this issue should be considered while interpreting the results.
In conclusion, our results indicate the need for further studies to address the routine practices of the FHS with regard to dengue fever and its severe forms, including studies on the development of policies and procedures aimed at effective disease prevention from the perspective of primary health care at the local level.