- Research article
- Open Access
30 years of fatal dengue cases in Brazil: a review
BMC Public Health volume 19, Article number: 329 (2019)
Over the last 30 years, extensive dengue epidemics have occurred in Brazil, characterized by emergences and re-emergences of different serotypes, a change in the epidemiological profile and an increase in the number of severe and fatal cases. Here, we present a review on the dengue fatal cases that occurred in Brazil in 30 years (1986–2015).
We performed an ecological study by using secondary data on dengue fatal cases obtained in the National System of Reported Diseases (Sistema de Informação de Agravos de Notificação -SINAN) and in the Mortality Information System (SIM), both maintained by the Brazilian Ministry of Health. Cases were analyzed by region, demographic variables, clinical classification and complications based on the data available.
In 30 years (1986–2015), the Southeast region reported 43% (n = 2225) of all dengue deaths in the country. The Midwest region was responsible for 18% of the fatal cases. After 2000, deaths occurred in almost all states, with the exception of Santa Catarina and Rio Grande do Sul, South region. From 2006 to 2010, the number of deaths increased, with higher rates of mortality, especially in Goiás and Mato Grosso. From 2011 to 2015, Goiás became the state with the highest mortality rate in the country, and Rio Grande do Sul reported its first dengue deaths. In 30 years, a total of 2682 dengue deaths occurred in males and 2455 in females, and an equal distribution between the sexes was observed. From 1986 to 2006, dengue deaths occurred predominantly in individuals over 15 years old, but this scenario changed in 2007–2008. After 2009, fatal cases on individuals above 15 years old became more frequent, with peaks in the years of 2010, 2013 and 2015.
The Brazil is experiencing a hyperendemic scenario, which has resulted in the co-circulation of the four DENV serotypes and with the increasing occurrence of severe and fatal cases. The disease surveillance and studies characterizing what has been reported overtime, are still important tools to better understand the factors involved in the disease outcome.
Dengue viruses (DENV) are arboviruses belonging to the Flaviviridae family and the genus Flavivirus, and are represented by four antigenically distinct serotypes (DENV-1 to 4) causing a mild self-limiting illness or more severe forms of the disease and death . According to WHO , currently dengue cases can be classified as dengue without warning signs, dengue with warning signs and severe dengue. A severe dengue case is characterized by severe bleeding, severe organ involvement and severe plasma leakage. The viruses are responsible for high rates of disease and mortality . Dengue is a mosquito-borne viral disease endemic in several tropical and sub-tropical countries worldwide and, in recent decades the disease has grown drastically throughout the world . Globally, it is estimated an average of 9 thousand dengue deaths per year from 1990 to 2013 have occurred . In the Americas, dengue has an endemo-epidemic pattern with outbreaks occurring every 3 to 5 years .
From 1995 to 2015, more than 18 million cases of dengue were reported throughout the American continent and, about 14 million cases were reported only in South American countries. Brazil contributed 55% of the cases reported in the Americas over this period. A total of 8788 fatal cases were confirmed in the Americas, and Brazil accounted for 48% of those cases . Despite that, dengue cases are still underreported and many cases are incorrectly classified, with one notification for every twenty cases of dengue fever (95%) [7, 8].
Over the last 30 years, extensive dengue epidemics have occurred in Brazil, characterized by the emergence and re-emergence of different serotypes, a change in the epidemiological profile and an increase in the number of severe and fatal cases. Here, our goal is to present a review on the fatal dengue cases that occurred in Brazil over 30 years (1986–2015) based on the Brazilian Dengue Surveillance Systems, as understanding the patterns of case fatalities, may be critical for dengue case management in the country.
We performed an ecological study by using secondary data from the dengue epidemics available in Brazil. Official data on dengue fatal cases occurred from 1986 to 2013, from TabNet (DATASUS) from the National System of Reported Diseases (Sistema de Informação de Agravos de Notificação -SINAN) and from the Mortality Information System (SIM), both maintained by the Brazilian Ministry of Health (MoH), were obtained. Cases occurring in 2014 and 2015 were obtained from epidemiological reports available at http://portalms.saude.gov.br/boletins-epidemiologicos.
Dengue severity was considered according to the final classification of the Brazilian MoH and to the epidemiological reports available, as follows: Dengue with complications (DCC), Dengue Hemorrhagic Fever (DHF), Dengue Shock Syndrome (DSS) and Severe Dengue (SD). In this study, the 1997 World Health Organization (WHO) dengue case classification (DHF and DSS) was used from 1986 to 2000. From 2000 to 2013, the Brazilian MoH DCC classification was used to define severe dengue cases that did not meet the WHO criteria for DHF/DSS and, from 2014 and on, the 2009 WHO dengue case classification, Dengue with warning signs (DwWS) and SD were employed [1,2,3,4,5,6, 9]. Here, we considered dengue deaths to be reported in the SINAN database filled out as “death due to dengue,” or from the SIM database where cause of death was with the code “A90” or “A91,” according to the 10th International Classification of Diseases (ICD-10).
The case fatality rate of each classification was calculated using number of deaths from DHF/DSS, DCC, DwWS or SD per number of confirmed cases from each classification × 100. The overall fatality rate was calculated by the sum of each classification per number of dengue confirmed cases × 100. The mortality rate was calculated using the number of deaths per dengue per total number of the locality’s population, per year × 100,000 inhabitants. The population data of each year and by region were obtained from Instituto Brasileiro de Geografia e Estatística (IBGE) available at https://www.ibge.gov.br. Cases were analyzed by region, demographic variables and clinical classification based on the data available on the reporting and investigation forms using a database in Excel Software. The maps were made using the TerraView 4.2.2 (INPE, SP, Brazil) software.
Odds ratio (OR) of dengue fatal cases occurred in Brazil from 1987 to 2015 was calculated with a 95% confidence interval (CI) and p-values for each year, with 1986 as the reference year. The analysis was performed by GraphPad Prism software version 6. We used 1986 as the reference year as it was the first year of dengue introduction in Brazil and the first year of data availability on the Brazilian MoH database. All data are available from the Brazilian MoH and do not need permission for access.
Overview on dengue epidemics in Brazil
The first reports of a disease with signs and symptoms compatible with dengue fever in Brazil, date back to 1846 . Late 1981 and early 1982, a first dengue outbreak, caused by DENV-1 and DENV-4 was characterized in Brazil, which was restricted to the city of Boa Vista, Roraima (RR) in the north region . In1986, after 4 years without dengue cases confirmation, an epidemic occurred due to the DENV-1 introduction in the state of Rio de Janeiro (RJ), which spread to other states . Five fatal cases were confirmed in 1986. DENV-2 was detected, for the first time in RJ, in 1990 , when the first DHF/SCD cases occurred (n = 8). In the following years, DENV-1 and DENV-2 co-circulated and caused epidemics throughout the country  . Through 1999, a total of 75 fatal cases were reported (1991–1999), Fig. 1.
In December 2000, a newly introduced serotype, DENV-3, was initially detected in RJ  and quickly spread to other states of the country. The 2002 epidemic, caused mainly by DENV-3, was the largest and most severe epidemic experienced in the country so far, with increased hospitalizations and 150 deaths confirmed. It was suggested that, the introduction of a new serotype of Asian origin (Genotype III), would have been an explanation for the severity of the epidemic . Despite the prevalence of Genotype III in Brazil, the co-circulation of Genotypes III and V was detected in Rondônia . In 2002, the number of DHF deaths exceeded malaria deaths for the first time in the country .
Seventeen years after its introduction, DENV-2 reemerged in 2007 causing a major epidemic in 2008, with a higher proportion of DHF, more than double the number of cases reported in previous years . A total of 561 deaths, mainly caused by this serotype, were reported only in that year (Fig. 1A). Oliveira et al.  observed that the DENV-2 emerged in the 2008 epidemic was genetically different from the strain introduced in 1990, and despite belonging to the same genotype, those viruses were considered a new lineage (Lineage II). Studies by Faria et al.  concluded that there were no nucleotide changes between the two strains that led to an increase in the severity of Lineage II viruses. On the other hand, Nunes et al.  demonstrated that the viremia of the DENV- 2 Lineage I cases was lower than that observed by Lineage II cases. Furthermore, severe cases caused by Lineage II, had 1000 times more circulating virus than those from Lineage I. The factors that led to the severity of this particular epidemic are still unclear. However, one cannot exclude the difficulties experienced in public health systems in controlling the epidemic, and the situation caused panic and insecurity throughout the Brazilian society [22, 23].
In 2009, DENV-1 reemerged with the possibility of a new epidemic, considering the low circulation of this serotype since the beginning of the decade. The 2010 epidemic presented a pattern quite different from the 2002 and 2008 epidemics, with the highest number of deaths (n = 656), reported. The DENV-1 isolated in Brazil between 2009 and 2010, belonged to Genotype V (American /African) and grouped in a clade (Lineage II) distinct from that of the previous isolates (Lineage I). Moreover, strains isolated in 2011 grouped in another distinct clade (Lineage III) . The introduction of new strains resulted in the substitution of the circulating lineage and the increase in the genetic diversity of DENV-1, probably as a result of local evolution, or introduction of exogenous viruses during the same period or at different times .
In 2010, the risk of DENV-4 reintroduction into the country was imminent, as this serotype circulated in neighboring countries such as Venezuela and Colombia . However, only in July of 2010, the first DENV-4 cases were identified in RR and Amazonas (AM), about 30 years after its first detection in the country. Less than 20 cases of DENV-4 were confirmed during the second half of 2010, and the first cases resulting from the spread of the virus, were detected only in January 2011, isolated in Amazonas and Pará. In March of 2011, the first DENV-4 cases were reported in RJ, introduced by the municipality of Niteroi [27, 28].
An increase in deaths was evidenced, especially in 2015, with an explosive epidemic of 1,649,008 dengue cases reported and 986 fatal cases confirmed. In 30 years a total of 11,084,755 suspected dengue cases were reported, with the confirmation of 5399 deaths nationwide (Fig. 1). The years that had the greatest chances of death were 2007–2009 (CI 95% 2.23–19.8), mainly due to the DENV-2 epidemic. The years of 2014–2015 had OR of 3.08–17.97 and, despite the co-circulation of the four serotypes, DENV-4 was predominant. In 2010–2011 OR were (CI 95% 2.492–14.48), when DENV-1 reemerged and DENV-4 was introduced (Table 1).
Fatal dengue and regions
In 30 years, the Southeast region reported 43% (n = 2225) of all dengue deaths in the country. São Paulo (SP) confirmed 945 fatal cases, RJ, 738, Minas Gerais (MS) and Espírito Santo (ES) registered 430 and 196 deaths, respectively. In the Northeast, the states with the highest number of fatal cases were Ceará (CE) with 506, Pernambuco (PE) with 277, Bahia (BA) with 228 and Maranhão (MA) with 166. The Midwest region was responsible for 18% of the fatal cases, where the state of Goiás (GO) reported 600 deaths, Mato Grosso (MT), 187, Mato Grosso do Sul (MS), 128 and Distrito Federal (DF), 66. In the North region, only 7% of the deaths were confirmed. Pará (PA) was the state that reported the highest number of dengue deaths (n = 141) in the period. The South region, historically less affected by dengue cases, reported consequently the lowest number of dengue fatal cases (2%). Only Paraná (PR) (n = 108) and Rio Grande do Sul (RS) (n = 4) reported dengue deaths.
During 30 years of epidemics, we have observed that RJ historically contributed to the introduction and dissemination of DENV-1, 2 and 3, and since then, has constantly reported dengue fatal cases (Fig. 2). After 2000, deaths occurred in almost all states, with the exception of Santa Catarina (SC) and RS. From 2006 to 2010, possibly due to the introduction of DENV-3 and DENV-4, and re-emergence of DENV-1 and DENV-2, the number of deaths increased, with higher mortality rates in the states of RJ, Sergipe (SE), MS, Rondônia (RO) and RR. Rates were even higher in GO, but the state of MT had the highest mortality rate in this period. From 2011 to 2015, GO became the state with the highest mortality rate in the country, and RS reported the first dengue fatal outcomes.
The analysis of the mortality rates by municipality showed an increase of dengue fatal cases and distribution by the Brazilian territory over the years. In 2008, the North, Northeast and Southeast regions had higher mortality rates. In 2009, dengue deaths were distributed in the North and Midwest regions. From 2010 to 2012, dengue deaths occurred throughout the Brazilian regions (Fig. 2).
According to the WHO  dengue case criteria, infections were classified as dengue fever (DF), DHF and DSS. However, in 2000, the Brazilian MoH proposed the DCC classification, to define severe dengue cases that did not meet the WHO criteria for DHF/DSS. From January 2014 and on, Brazil adopted the new WHO 2009 classification. Therefore, in this analysis, DHF/DSS, DCC, DwWS and SD denominations were used, considering the epidemic year analyzed. The timeline and the characteristics of each classification are available in Table 2.
DHF cases fatality rates were high in 1994, 1997, 1998, 2006, 2012, and 2013. By DCC, deaths were more frequently reported in 2003, 2006, 2007, with increasing numbers from 2008 to 2013 and the latter, being the highest peak of DCC mortality. Considering the new classification, 3% of DwWS patients died in 2014. In 2014 and 2015, 8 and 7% of SD cases died, respectively (Fig. 3A).
The five-year case fatality rate of each state is shown in Fig. 4. From 1986 to 1990 the DHF fatality rate was up to 10% in RJ and Alagoas (AL). From 1991 to 1995, only RJ reported a DHF fatality rate up to 10%. That rate was five times higher (up to 50%) in CE, from 1996 to 2001. On the following years (2001 to 2005), fatality rates were up to 50% in MS, followed by GO (up to 40%), PB (up to 20%), and RJ, ES and PE with up to 10% of DHF cases evolving to death. From 2006 to 2010, this scenario changed and case fatality rate increased in almost all states, being higher in DF (up to 50%), PR (up to 40%), PA and RR (up to 30%) and TO (up to 20%). From 2011 to 2013, the states of PR, SP, MG, TO, PI, AP had up to 20% DHF fatality rate, however those were higher in CE with 21–30% and DF with 31–40% (Fig. 4A). In the years of 1999–2003, 11 to 20% of the cases with DCC died in RR, and in MT, MS, PR, SP, RJ, BA, SE, AL, CE, MA and AP, up to 10% (Fig. 4B).
From 2004 to 2008, increased numbers of fatal cases by DCC were also reported in other Brazilian states, and AC, MS, PR reported up to 20%, RJ up to 30% and DF up to 40% of fatality rates, Fig. 3B. In 2009 and 2013 the number of deaths was lower, and the states of MA, CE, MS, MG, RJ, ES and PR had up to 20% of case fatality rate. Only the state of SC did not report fatal cases by DCC (Fig. 4B).
Considering the new WHO  criteria, case fatality rate by DwWS in PA, AC, RO, MT, MS, PR, SP, MG, RJ, ES, BA, CE RN and PE was around 5%, however in PB and AM, it reached 15% in 2014–2015 (Fig. 4C). In the same period, deaths from SD occurred in all states, except in SC, with high case fatality rates in the states of AC and RS (100%), AM, PB and DF with 81 to 99%, MG, SP, MS, MT, MA, PE, PB, CE, PA, RO with 51 to 80%, RJ, ES, BA, GO, TO, RR, SE, AL with 21 to 51% and in PR, PE and AP, with up to 20%, Fig. 4D.
Demographic variables associated to dengue fatal cases: sex and age
In the 30 years period (1986–2015), a total of 2682 dengue deaths occurred on males and 2455 on females and, during the years, an equal distribution between the sexes, was observed.
From 1986 to 2006, dengue deaths occurred more often in individuals over 15 years old, Fig. 4B. This changed in 2007–2008, with the DENV-2 re-emergence, as more than 53% of the dengue deaths cases occurred in children 15 years old and under. In 2008 alone, 190 fatal cases on children from that age group were reported (Fig. 3C). After 2009, there was a decrease in fatal cases in children 15 years old and under, while fatal cases on individuals above 15 years old became more frequent, with peaks in the years 2010, 2013 and 2015.
The consecutive introduction of distinct DENV serotypes overtime, resulted in a hyperendemic scenario, with the co-circulation of all serotypes and, an increase in deaths, was evidenced, especially in 2015. However, the years that had the greatest chances of death were between 2007 and 2009, mainly due to the DENV-2 epidemic.
As Brazil is the second largest and most populated country in the Americas, it is important to understand the contribution of the distinct regions in the occurrence of dengue deaths. Historically, the regions in the country with highest dengue incidences and fatal cases have been the Southeast, followed by the Northeast region. During 30 years of epidemics, RJ, in the Southeast region, has historically contributed to the introduction and dissemination of three of the four DENV serotypes (DENV-1 to 3), and since then, has constantly reported dengue fatal cases.
One well-characterized study by Paixão  analyzed the trends and factors associated with dengue mortality and fatality in Brazil from 2001 to 2011, and reported the results on the analysis of 3156 deaths. It was shown that the Southeast and Northeast regions accounted for more than 70% of fatal cases. Moreover, mortality rates increased during the period and that the factors associated with mortality were inequality, high income per capita and higher populations inhabiting urban areas .
According to the WHO  dengue case criteria, infections were classified as dengue fever (DF), DHF and DSS. However, due to difficulties in using this classification , mostly due to changes in the disease epidemiology, a new classification was needed. In 2000, the Brazilian MoH proposed the DCC classification, to define severe dengue cases that did not meet the WHO criteria for DHF/DSS [31, 32]. DCC was characterized when the dengue patient presented at least one of the following: neurological abnormalities, liver failure, cardiorespiratory dysfunction, gastrointestinal bleeding, low platelet count (leukocyte count ≤1000 cells/ml), pleural and pericardial effusion and ascites or death. It was a mandatory classification after 2007 .
Based on the results of a multicenter study (Dengue Control, DENCO) to assess the limitations of the 1997 WHO classification, experts from dengue endemic regions agreed on a binary classification represented by two clear entities, severe dengue and dengue and, the term “non-severe dengue” should be avoided, as any dengue case can become severe. Moreover, it was shown that patients exhibiting warning signs are at increased risk of severe disease progression and deserve careful observation . This new classification proposed in 2009, characterized dengue infections in dengue without signs (DWoWS), DwWS and SD [1, 9, 35]. From January 2014 and on, Brazil adopted this new proposed classification. Therefore, in this analysis, DHF/DSS, DCC, DwWS and SD denominations were used, considering the epidemic year analyzed.
A higher sensitivity to detect increased disease severity has been shown by the new WHO 2009 dengue classification [36,37,38,39]. Its specificity, however, is much lower (73.0%) compared to the 1997 classification (93.4%). The higher sensitivity allows better patients’ management, reducing mortality [40, 41], on the other hand, may also result in the misclassification of some severe cases . In fact, the lower specificity of this new classification is attributed, partly, to the lack of clear criteria for the definition of the warning signs .
DHF cases fatality rates were high in 1994, 1997, 1998, 2006, 2012, and 2013. By DCC, deaths were more frequently reported in 2003, 2006, 2007, with increasing numbers from 2008 to 2013. In 2014, 3% of DwWS patients died, while in 2014 and 2015, 8 and 7% of SD cases died, respectively. From 1986 to 1990 the DHF fatality rate was up to 10% in RJ and AL, but was five times higher in CE, from 1996 to 2001, however, from 2006 to 2010, case fatality rates increased in almost all states.
Sex has also been considered by some authors, as risk factor for the disease severity. Studies in Asia and the Americas, show that women are more likely to have the disease and are at greater risk of developing more severe forms than men [44,45,46,47]. In the 30 years period, an equal distribution of dengue fatal cases was observed between the sexes. Previous studies on dengue incidence have sometimes found equal attack rates between the sexes [48,49,50,51], and sometimes found uneven distribution of cases, with no clear tendency for males or females to be more affected [45, 52,53,54,55].
From 1986 to 2006, dengue deaths occurred more often in individuals over 15 years old. This changed in 2007–2008, with the DENV-2 re-emergence, as more than 53% of the dengue deaths cases occurred in children 15 years old and under . Likewise, the study by Paixão et al.  analyzing dengue mortality from 2001 to 2011 in Brazil, showed the highest DHF case fatality rates on individuals over 15 years old and especially on those 80 years old and over. However, children under 1 year old experienced increased fatality rates.
After 2009, there was a decrease in fatal cases in children 15 years old and under, while fatal cases on individuals above 15 years old became more frequent, especially in the years of 2010, 2013 and 2015. The increased risk of death in the older age group may be associated with the difficulty in managing the disease in a population with a high frequency of comorbidities . Cases coincident with sickle cell anemia, autoimmune diseases, asthma, hypertension, uremia and diabetes mellitus have been described in more severe outcomes of dengue [56,57,58,59,60].
Currently, Brazil is experiencing a hyperendemic scenario, with the co-circulation of the four DENV serotypes and occurrence of severe and fatal cases and, more recently, the co-circulation with other arboviruses such as Zika, Yellow Fever and Chikungunya, Therefore, the possibility of misdiagnosis and even co-infections in a same individual and the its impact in the disease outcome, can not be neglected and need further investigation.
One point to be addressed here and pointed out in a previous study, is the challenge in determining whether a death occurs due to DENV infection or in a patient with DENV infection, meaning the disease is the cause of death or is the underlying cause of it . Either way, the disease surveillance and studies characterizing what has been reported overtime, are still important tools to better understand the factors involved on the disease outcome.
It is a fact that, there are many dengue-related deaths underestimated in many health services, even after 30 years of dengue surveillance in Brazil and it has been shown that the structuring and organization of surveillance, autopsy and laboratory teams, may significantly improve this scenario [61,62,63].
Despite that, the use of secondary data as those analyzed here, imposes some limitations to the study and those include the lack of some clinical and/or demographic information, description of disease course during hospitalization and until death, delay in diagnosis and low adherence to notification by health professionals. Dengue cases are under-reported in Brazil and improvements are needed in the proper filing of report forms [7, 64,65,66].
Dengue with complications
Dengue Hemorrhagic Feverx
Dengue Shock Syndrome
Dengue with warning signs
Instituto Brasileiro de Geografia e Estatística
10th International Classification of Diseases
Brazilian Ministry of Health
Mato Grosso do Sul
Rio de Janeiro
Rio Grande do Norte
Rio Grande do Sul
Mortality Information System
Sistema de Informação de Agravos de Notificação
World Health Organization
WHO (World Health Organization). Dengue Guidelines for Diagnosis, Treatment, Prevention and Control. Geneva; 2009.
Mukhopadhyay S, Kuhn RJ, Rossmann MG. A structural perspective of the flavivirus life cycle. Nat Rev Microbiol. 2005;3:13–22.
WHO (World Health Organization). Dengue and severe dengue: Fact Sheet No 117. 2016.
Stanaway JD, Shepard DS, Undurraga EA, Halasa YA, Coffeng LE, Brady OJ, et al. The global burden of dengue: an analysis from the global burden of disease study 2013. Lancet Infect Dis. 2016;16:712–23.
Brathwaite Dick O, San Martín JL, Montoya RH, del Diego J, Zambrano B, Dayan GH. The history of dengue outbreaks in the Americas. Am J Trop Med Hyg. 2012;87:584–93.
PAHO PAHO. Reported cases of dengue fever in th Americas, by country or territory 1995–2017 (until October 2017). 2017.
Silva MMO, Rodrigues MS, Paploski IAD, Kikuti M, Kasper AM, Cruz JS, et al. Accuracy of dengue reporting by National Surveillance System. Brazil. Emerging Infect Dis. 2016;22:336–9.
Melo MA, De S, LLM DS, Melo AL, De S, Castro AM. Subnotificação no Sinan e fatores gerenciais e operacionais associados: revisão sistemática da literatura. RAU/UEG – Revista de Administração da UEG. 2018;9:25–43.
WHO (World Health Organization). Dengue haemorrhagic fever Diagnosis, treatment, prevention and control. SECOND EDITION. 1997.
Mariano F. A dengue: Considerações a respeito de sua incursão no Rio Grande do Sul em 1916. Arch Bras Med. 1917;8:272–7.
Osanai CH, Travassos da Rosa AP, Tang AT, do Amaral RS, Passos AD, Tauil PL. Dengue outbreak in Boa Vista, Roraima. Preliminary report. Rev Inst Med Trop Sao Paulo. 1983;25:53–4.
Schatzmayr HG, Nogueira RM, Travassos da Rosa AP. An outbreak of dengue virus at Rio de Janeiro--1986. Mem Inst Oswaldo Cruz. 1986;81:245–6.
Nogueira RM, Miagostovich MP, Lampe E, Schatzmayr HG. Isolation of dengue virus type 2 in Rio de Janeiro. Mem Inst Oswaldo Cruz. 1990;85:253.
Siqueira JB, Martelli CMT, Coelho GE, Simplicio AC, Da R, Hatch DL. Dengue and dengue hemorrhagic fever, Brazil, 1981-2002. Emerging Infect Dis. 2005;11:48–53.
Nogueira RMR, Filippis AMB, Coelho JMO, Sequeira PC, Schatzmayr HG, Paiva FG, et al. Dengue virus infection of the central nervous system (CNS): a case report from Brazil. Southeast Asian J Trop Med Public Health. 2002;33:68–71.
de Araújo JMG, Schatzmayr HG, de Filippis AMB, Dos Santos FB, Cardoso MA, Britto C, et al. A retrospective survey of dengue virus infection in fatal cases from an epidemic in Brazil. J Virol Methods. 2009;155:34–8.
Nogueira MB, Stella V, Bordignon J, Batista WC, de Borba L, da Silva LHP, et al. Evidence for the co-circulation of dengue virus type 3 genotypes III and V in the northern region of Brazil during the 2002-2004 epidemics. Mem Inst Oswaldo Cruz. 2008;103:483–8.
Teixeira MG, Costa MCN, Coelho G, Barreto ML. Recent shift in age pattern of dengue hemorrhagic fever. Brazil Emerging Infect Dis. 2008;14:1663.
Oliveira MF, Galvao Araujo JM, Ferreira OC, Ferreira DF, Lima DB, Santos FB, et al. Two lineages of dengue virus type 2. Brazil. Emerging Infect Dis. 2010;16:576–8.
Faria NR, Da C, RMR N, AMB DF, JBS S, Nogueira F, De B, Da Rocha Queiroz Lima M, et al. Twenty years of DENV-2 activity in Brazil: molecular characterization and phylogeny of strains isolated from 1990 to 2010. PLoS Negl Trop Dis. 2013;7:–e2095.
Nunes PCG, Sampaio SAF, da Costa NR, de Mendonça MCL, Lima M, Da RQ, SEM A, et al. Dengue severity associated with age and a new lineage of dengue virus-type 2 during an outbreak in Rio De Janeiro, Brazil. J Med Virol. 2016;88:1130–6.
Barreto ML, Teixeira MG. Dengue fever: a call for local, national, and international action. Lancet. 2008;372:205.
Teixeira MG, Costa M. da CN, Barreto F, Barreto ML. Dengue: twenty-five years since reemergence in Brazil. Cad Saude Publica. 2009;25(Suppl 1):S7–18.
dos Santos FB, Nogueira FB, Castro MG, Nunes PC, de Filippis AMB, Faria NR, et al. First report of multiple lineages of dengue viruses type 1 in Rio de Janeiro. Brazil Virol J. 2011;8:387.
Drumond BP, Mondini A, Schmidt DJ, Bosch I, Nogueira ML. Population dynamics of DENV-1 genotype V in Brazil is characterized by co-circulation and strain/lineage replacement. Arch Virol. 2012;157:2061–73.
Guzmán MG, Kourí G. Dengue: an update. Lancet Infect Dis. 2002;2:33–42.
Nogueira RMR, Eppinghaus ALF. Dengue virus type 4 arrives in the state of Rio de Janeiro: a challenge for epidemiological surveillance and control. Mem Inst Oswaldo Cruz. 2011;106:255–6.
Temporão JG, Penna GO, Carmo EH, Coelho GE. Azevedo R do SS, Nunes MRT, et al. dengue virus serotype 4, Roraima state, Brazil. Emerg Infect Dis. 2011;17:938–40.
Paixão ES. Costa M da CN, Rodrigues LC, Rasella D, Cardim LL, Brasileiro AC, et al. Trends and factors associated with dengue mortality and fatality in Brazil Revista da Sociedade Brasileira de Medicina Tropical. 2015;48:399–405.
Bandyopadhyay S, Lum LCS, Kroeger A. Classifying dengue: a review of the difficulties in using the WHO case classification for dengue haemorrhagic fever. Tropical Med Int Health. 2006;11:1238–55.
MS (Ministério da Saúde). Diretrizes nacionais para prevenção e controle de epidemias de dengue. 2009.
MS (Ministério da Saúde). Saúde Brasil 2010: uma análise da situação de saúde e de evidências selecionadas de impacto de ações de vigilância em saúde/Ministério da Saúde, Secretaria de Vigilância em Saúde. Brasília; 2011.
MS (Ministério da Saúde). Guia de Vigilância Epidemiológica. Brasília; 2005.
Horstick O, Farrar J, Lum L, Martinez E, San Martin JL, Ehrenberg J, et al. Reviewing the development, evidence base, and application of the revised dengue case classification. Pathog Glob Health. 2012;106:94–101.
Barniol J, Gaczkowski R, Barbato EV, da Cunha RV, Salgado D, Martínez E, et al. Usefulness and applicability of the revised dengue case classification by disease: multi-Centre study in 18 countries. BMC Infect Dis. 2011;11:106.
Horstick O, Jaenisch T, Martinez E, Kroeger A, See LLC, Farrar J, et al. Comparing the usefulness of the 1997 and 2009 WHO dengue case classification: a systematic literature review. Am J Trop Med Hyg. 2014;91:621–34.
Cavalcanti LP, De G, LAM M, Lustosa GP, Fortes MC, DAM M, AAB L, et al. Evaluation of the WHO classification of dengue disease severity during an epidemic in 2011 in the state of Ceará. Brazil Mem Inst Oswaldo Cruz. 2014;109:93–8.
Khursheed M, Khan UR, Ejaz K, Fayyaz J, Qamar I, Razzak JA. A comparison of WHO guidelines issued in 1997 and 2009 for dengue fever - single Centre experience. J Pak Med Assoc. 2013;63:670–4.
Vieira Machado AA, Estevan AO, Sales A, Brabes KC, Da S, Croda J, Negrão FJ. Direct costs of dengue hospitalization in Brazil: public and private health care systems and use of WHO guidelines. PLoS Negl Trop Dis. 2014;8:e3104.
Alexander N, Balmaseda A, Coelho ICB, Dimaano E, Hien TT, Hung NT, et al. Multicentre prospective study on dengue classification in four south-east Asian and three Latin American countries. Tropical Med Int Health. 2011;16:936–48.
Basuki PS, Null B, Puspitasari D, Husada D, Darmowandowo W, Null I, et al. Application of revised dengue classification criteria as a severity marker of dengue viral infection in Indonesia Southeast Asian. J Trop Med Public Health. 2010;41:1088–94.
Macedo GA, Gonin MLC, Pone SM, Cruz OG, Nobre FF, Brasil P. Sensitivity and specificity of the World Health Organization dengue classification schemes for severe dengue assessment in children in Rio de Janeiro. PLoS One. 2014;9:e96314.
Morra ME, Altibi AMA, Iqtadar S, Minh LHN, Elawady SS, Hallab A, et al. Definitions for warning signs and signs of severe dengue according to the WHO 2009 classification: Systematic review of literature. Rev Med Virol. 2018;:e1979.
Halstead SB, Nimmannitya S, Cohen SN. Observations related to pathogenesis of dengue hemorrhagic fever. IV. Relation of disease severity to antibody response and virus recovered. Yale J Biol Med. 1970;42:311–28.
Anders KL, Nguyet NM, Chau NVV, Hung NT, Thuy TT, Lien LB, et al. Epidemiological factors associated with dengue shock syndrome and mortality in hospitalized dengue patients in Ho Chi Minh City. Vietnam Am J Trop Med Hyg. 2011;84:127–34.
García G, González N, Pérez AB, Sierra B, Aguirre E, Rizo D, et al. Long-term persistence of clinical symptoms in dengue-infected persons and its association with immunological disorders. Int J Infect Dis. 2011;15:e38–43.
Dettogni RS, Tristão-Sá R, dos Santos M, da Silva FF, Louro ID. Single nucleotide polymorphisms in immune system genes and their association with clinical symptoms persistence in dengue-infected persons. Hum Immunol. 2015;76:717–23.
Vasconcelos PF, Lima JW, da Rosa AP, Timbó MJ, da Rosa ES, Lima HR, et al. Dengue epidemic in Fortaleza, Ceará: randomized seroepidemiologic survey. Rev Saude Publica. 1998;32:447–54.
De Figueiredo RMP, Thatcher BD, de Lima ML, Almeida TC, Alecrim WD, Guerra MV de F. Exanthematous diseases and the first epidemic of dengue to occur in Manaus, Amazonas state, Brazil, during 1998-1999. Rev Soc Bras Med Trop. 2004;37:476–9.
Wang W-K, Chao D-Y, Kao C-L, Wu H-C, Liu Y-C, Li C-M, et al. High levels of plasma dengue viral load during defervescence in patients with dengue hemorrhagic fever: implications for pathogenesis. Virology. 2003;305:330–8.
Thomas L, Verlaeten O, Cabié A, Kaidomar S, Moravie V, Martial J, et al. Influence of the dengue serotype, previous dengue infection, and plasma viral load on clinical presentation and outcome during a dengue-2 and dengue-4 co-epidemic. Am J Trop Med Hyg. 2008;78:990–8.
Moraes GH, de Fátima DE, Duarte EC. Determinants of mortality from severe dengue in Brazil: a population-based case-control study. Am J Trop Med Hyg. 2013;88:670–6.
Leo Y-S, Thein TL, Fisher DA, Low JG, Oh HM, Narayanan RL, et al. Confirmed adult dengue deaths in Singapore: 5-year multi-center retrospective study. BMC Infect Dis. 2011;11:123.
Araújo FMC, Araújo MS, Nogueira RMR, Brilhante RSN, Oliveira DN, Rocha MFG, et al. Central nervous system involvement in dengue: a study in fatal cases from a dengue endemic area. Neurology. 2012;78:736–42.
Pinto RC, de Castro DB, de Albuquerque BC, de Sampaio V. S, Passos RAD, Costa CF da, et al. mortality predictors in patients with severe dengue in the state of Amazonas, Brazil. PLoS One. 2016;11:e0161884.
Amâncio FF, Pereira MA, Iani FC, De M, D’anunciação L, JLC DA, JAS S, et al. Fatal outcome of infection by dengue 4 in a patient with thrombocytopenic purpura as a comorbid condition in Brazil. Rev Inst Med Trop Sao Paulo. 2014;56:267–70.
Bravo JR, Guzmán MG, Kouri GP. Why dengue haemorrhagic fever in Cuba? 1. Individual risk factors for dengue haemorrhagic fever/dengue shock syndrome (DHF/DSS). Trans R Soc Trop Med Hyg. 1987;81:816–20.
Cunha RV, Schatzmayr HG, Miagostovich MP, Barbosa AM, Paiva FG, Miranda RM, et al. Dengue epidemic in the state of Rio Grande do Norte, Brazil, in 1997. Trans R Soc Trop Med Hyg. 1999;93:247–9.
Figueiredo MAA, Rodrigues LC, Barreto ML, Lima JWO, Costa MCN, Morato V, et al. Allergies and diabetes as risk factors for dengue hemorrhagic fever: results of a case control study. PLoS Negl Trop Dis. 2010;4:e699.
Lee M-S, Hwang K-P, Chen T-C, Lu P-L, Chen T-P. Clinical characteristics of dengue and dengue hemorrhagic fever in a medical center of southern Taiwan during the 2002 epidemic. J Microbiol Immunol Infect. 2006;39:121–9.
Cavalcanti LP, De G, ARR F, Brasil P, da Cunha RV. Surveillance of deaths caused by arboviruses in Brazil: from dengue to chikungunya. Mem Inst Oswaldo Cruz. 2017;112:583–5.
Braga DN de M. Aspectos Laboratoriais e Anatomopatológicos no Diagnóstico da Dengue no Ceará em 2011 e 2012: Papel do Serviço de Verificação de Óbitos de Fortaleza: Universidade Federal do Ceará; 2014.
Cavalcanti LP, De G, Braga DN, De M, LMA DS, Aguiar MG, Castiglioni M, Silva-Junior JU, et al. Postmortem diagnosis of dengue as an epidemiological surveillance tool. Am J Trop Med Hyg. 2016;94:187–92.
Nunes PCG, de Filippis AMB, Lima MQ, Da R, Faria NR, Da C, De Bruycker-Nogueira F, Santos JB, et al. 30 years of dengue fatal cases in Brazil: a laboratorial-based investigation of 1047 cases. BMC Infect Dis. 2018;18:346.
Martínez-Vega RA, Díaz-Quijano FA, Villar-Centeno LA. Low concordance between early clinical suspicion of dengue and its serological confirmation. Rev Med Chil. 2006;134:1153–60.
Diaz-Quijano FA. Dengue severity: a key determinant of underreporting. Tropical Med Int Health. 2015;20:1403.
Ethical approval and consent to participate
This is an anonymous secondary data-based study from National available databases and it is part of a goal from an ongoing Project approved by the Oswaldo Cruz Institute Ethical Committee (CAAE 57221416.0.1001.5248). Consent to participate not applicable.
To Conselho Nacional de Desenvolvimento Científico e Tecnológico/CNPq [grant number 302462/2018-0] and Priscila’s Nunes fellowship. The funder had no role on the study design, data collection and analysis, data interpretation and in the decision to publish.
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The data that support the findings of this study are available from the Ministry of Health, this data is publically available from http://sinan.saude.gov.br/sinan/login/login.jsf and http://sim.saude.gov.br/default.asp, therefore, no permissions were required.
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Nunes, P.C.G., Daumas, R.P., Sánchez-Arcila, J.C. et al. 30 years of fatal dengue cases in Brazil: a review. BMC Public Health 19, 329 (2019). https://doi.org/10.1186/s12889-019-6641-4
- Dengue mortality
- 30 years