Find information on thousands of medical conditions and prescription drugs.

Dengue fever

Dengue and dengue hemorrhagic fever (DHF) are acute febrile diseases, found in the tropics, with a geographical spread similar to malaria. Caused by one of four closely related virus serotypes of the genus Flavivirus, family Flaviviridae, each serotype is sufficiently different that there is no cross-protection and epidemics caused by multiple serotypes (hyperendemicity) can occur. Dengue is transmitted to humans by the mosquito Aedes aegypti (rarely Aedes albopictus). more...

Home
Diseases
A
B
C
D
Dandy-Walker syndrome
Darier's disease
Dementophobia
Demyelinating disease
Dendrophobia
Dengue fever
Dental fluorosis
Dentinogenesis imperfecta
Dentophobia
Depersonalization disorder
Dermatitis herpetiformis
Dermatofibroma
Dermatographic urticaria
Dermatomyositis
Dermatophytosis
Desmoplastic small round...
Dextrocardia
Diabetes insipidus
Diabetes mellitus
Diabetes, insulin dependent
Diabetic angiopathy
Diabetic nephropathy
Diabetic neuropathy
Diamond Blackfan disease
Diastrophic dysplasia
Dibasic aminoaciduria 2
Diethylstilbestrol...
DiGeorge syndrome
Dilated cardiomyopathy
Diphallia
Diphtheria
Dipsophobia
Dissociative amnesia
Dissociative fugue
Dissociative identity...
Distemper
Diverticulitis
Diverticulosis
Dk phocomelia syndrome
Doraphobia
Double outlet right...
Downs Syndrome
Dracunculiasis
Duane syndrome
Dubin-Johnson syndrome
Dubowitz syndrome
Duchenne muscular dystrophy
Dupuytren's contracture
Dwarfism
Dysbarism
Dysgerminoma
Dyskeratosis congenita
Dyskinesia
Dysmorphophobia
Dysplasia
Dysplastic nevus syndrome
Dysthymia
Dystonia
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
Medicines

Signs and symptoms

The disease is manifested by a sudden onset of fever, with severe headache, joint and muscular pains (myalgias and arthralgias — severe pain gives it the name break-bone fever) and rashes; the dengue rash is characteristically bright red petechia and usually appears first on the lower limbs and the chest - in some patients, it spreads to cover most of the body. There may also be gastritis with some combination of associated abdominal pain, nausea, vomiting or diarrhoea.

Some cases develop much milder symptoms, which can, when no rash is present, be misdiagnosed as a flu or other viral infection. Thus, travelers from tropical areas may inadvertently pass on dengue in their home countries, having not being properly diagnosed at the height of their illness. Patients with dengue can only pass on the infection through mosquitoes or blood products while they are still febrile.

The classic dengue fever lasts about six to seven days, with a smaller peak of fever at the trailing end of the fever (the so-called "biphasic pattern"). Clinically, the platelet count will drop until the patient's temperature is normal.

Cases of DHF also shows higher fever, haemorrhagic phenomena, thrombocytopenia and haemoconcentration. A small proportion of cases leads to dengue shock syndrome (DSS) which has a high mortality rate.

Diagnosis

The diagnosis of dengue is usually made clinically. The classic picture is high fever with no localising source of infection, a petechial rash with thrombocytopenia and relative leukopenia.

Serology and PCR (polymerase chain reaction) studies are available to confirm the diagnosis of dengue if clinically indicated.

Treatment

The mainstay of treatment is supportive therapy. The patient is encouraged to keep up oral intake, especially of oral fluids. If the patient is unable to maintain oral intake, supplementation with intravenous fluids may be necessary to prevent dehydration and significant hemoconcentration. A platelet transfusion is indicated if the platelet level drops significantly.

Epidemiology

The first epidemics occurred almost simultaneously, in Asia, Africa, and North America in the 1780s. The disease was identified and named in 1779. A global pandemic began in Southeast Asia in the 1950s and by 1975 DHF had become a leading cause of death among children in many countries in that region. Epidemic dengue has become more common since the 1980s - by the late 1990s, dengue was the most important mosquito-borne viral disease affecting humans after malaria, there being around 40 million cases of dengue fever and several hundred thousand cases of dengue hemorrhagic fever each year. In February 2002 there was a serious outbreak in Rio De Janeiro, affecting around one million people but only killing sixteen.

Read more at Wikipedia.org


[List your site here Free!]


Dengue and dengue hemorrhagic fever, Brazil, 1981-2002
From Emerging Infectious Diseases, 1/1/05 by Joao Bosco Siqueira, Jr.

In the last 5 years, Brazil has accounted for [approximately equal to] 70% of reported dengue fever cases in the Americas. We analyzed trends of dengue and dengue hemorrhagic fever (DHF) from the early 1980s to 2002 by using surveillance data from the Brazilian Ministry of Health. Two distinct epidemiologic patterns for dengue were observed: localized epidemics (1986-1993), and endemic and epidemic virus circulation countrywide (1994-2002). Currently, serotypes 1, 2, and 3 cocirculate in 22 of 27 states. Dengue and DHF affected mainly adults; however, an increase in occurrence of DHF among children has been recently detected in northern Brazil, which suggests a shift in the occurrence of severe disease to younger age groups. In 2002, hospitalizations increased, which points out the change in disease severity compared to that seen in the 1990s. We describe the epidemiology of dengue in Brazil, characterizing the changing patterns of it and DHF during the last 20 years.

**********

Brazil accounted for nearly 70% of the 3,141,850 reported cases of dengue fever in the American regions in the last 5 years (1). Dengue fever and a severe manifestation of the illness known as dengue hemorrhagic fever/dengue shock syndrome (DHF/DSS) are increasingly important health, environmental, and economic concerns in the Americas (2,3). Dengue/DHF is a febrile illness caused by a flavivirus with four known serotypes (dengue virus [DENV] 1, 2, 3, 4), and infection is mainly transmitted by the mosquito Aedes aegypti (4). Currently, no vaccine is available for dengue fever, and disease control and prevention have mainly focused on vector control activities and surveillance that incorporates community participation (5,6). Despite vector control programs and heightened public awareness, outbreaks have occurred in several highly urbanized areas in Central and South America (7-9).

The reemergence of dengue in Latin America occurred during the 1960s with epidemics in the Caribbean and Venezuela and in the 1970s in Colombia (3). Brazil remained free of A. aegypti until 1976 as a result of the successful eradication program to prevent urban yellow fever coordinated by the Pan American Health Organization (PAHO) in previous decades (10,11). The subsequent reinfestation of A. aegypti into urban areas of Brazil and the introduction of DENV in 1986 led to resurgence of dengue fever outbreaks and an increased risk for urbanization of yellow fever in the country (12).

The Brazilian system for dengue/DHF reporting relies on passive surveillance, with laboratory diagnosis for case ascertainment and identification of circulating serotypes. A parallel system for entomologic surveillance exists to monitor virus and vector dispersion. Analyses of data reported to the state and national level are used to evaluate the impact of disease, time trends, and geographic distribution, with the objective of supporting and improving public health interventions (13). In a previous report, we analyzed the dengue situation, focusing on the main policies regarding prevention and control strategies adopted in Brazil (8). Here, on the basis of national surveillance data, we analyze the trends of dengue/DHF from the early 1980s to 2002 and contrast the changes in the epidemiologic pattern of disease for regions in Brazil.

Methods

Brazil is the largest and most populated country in Latin America, covering >8 million [km.sup.2] with an estimated 2002 population of 174,632,932 inhabitants. High population density areas and cities (up to 12,901 inhabitants/[km.sup.2]) are located mainly on the Atlantic Coast. Most of Brazil has a tropical climate; in the southern region, the climate is subtropical. The rainy season is observed in the first several months of the year, and the average temperature is >20 [degrees]C (14).

Sources of Data

Dengue/DHF is a reportable disease in Brazil, and the ministry of health has implemented a surveillance system since the first epidemic in the early 1980s. We reviewed available data compiled from 1986 to 2003 by the official surveillance system. We also used the available computerized data from the Hospitalization Information System of the Unified Health System (SIH-SUS), which covers [approximately equal to] 70%-80% of overall hospitalizations in the country (15,16). This system permits recovery of information on hospital admissions according to the International Disease Classification system (ICD versions 9 and 10). For this analysis, we selected hospitalizations due to dengue fever and DHF stratified by state from 1990 to 2003.

Case Definition and Surveillance Forms

During the study period, case definitions used for suspected, probable, and confirmed dengue/DHF adhered to PAHO guidelines (17). Information on persons with suspected dengue/DHF is routinely reported by using standardized forms completed by clinicians or health staff and subsequently sent to local health surveillance officials for data checking. This dengue/DHF case investigation form includes information on basic demographic data, dates of symptom onset and sample collection, case classification (dengue fever, DHF, DSS, or discarded case), and outcome. Individual data are locally entered into the electronic information system and subsequently transmitted to state and national levels.

Laboratory Confirmation and Entomologic Surveillance

Laboratory confirmation was based on the following: 1) serologic tests (immunoglobulin M antibody-capture enzyme-linked immunosorbent assay) performed on serum samples collected [greater than or equal to] 6 days after the onset of symptoms (18); or 2) virus isolation in C6/36 mosquito cell culture from blood samples collected <6 days after symptom onset (19). Immunohistochemical studies with formalin-fixed tissues were performed on samples from selected patients who died (20).

Initially, 3 public health laboratories were responsible for DENV laboratory confirmation: Evandro Chagas Institute (located in Belem, Para State), which is the Ministry of Health reference laboratory; Oswaldo Cruz Foundation (Rio de Janeiro); and Adolfo Lutz Institute (Sao Paulo). During the 1990s, the Public Health Laboratory Network was set up for the dengue-endemic states to respond to increasing requests for laboratory confirmation. By 2001, a total of 27 public laboratories at state level were in charge of serologic tests and quality control. Information on circulating serotypes was obtained from viral isolation by the 3 national reference laboratories during the 1980s and subsequently from 13 public health laboratories at the state level. Laboratory results are routinely linked to individual data. Classification of DHF required laboratory confirmation throughout the study period. Approximately 30% of dengue fever cases are also laboratory-confirmed. During epidemics, dengue cases were mostly classified by clinical and epidemiologic criteria because of limits in laboratory capacity.

The number of municipalities documented with A. aegypti infestations and information on vector dispersion were abstracted from data compiled by the national vector information system for yellow fever and dengue.

Data Analysis

A descriptive analysis of dengue incidence was performed by region (using residence of reported cases) from 1986 to 2002. Incidence and hospitalization rates by age group were calculated by using census population data as denominators. The ratio of incident versus hospitalized cases was also calculated. Exploratory data analysis of the age group of reported patients focused on data from 1998 to 2002, since standardized data in electronic format for these variables were available for this period.

Results

The epidemiologic pattern of dengue fever in Brazil during the last 20 years can be divided into 2 distinct periods: 1) epidemic waves in localized areas (1986-1993) and 2) epidemic and endemic virus circulation countrywide (1994-2002) (Figure 1 and Table 1). The main dengue-related events occurring in these 2 periods are summarized in Table 1. In 1981, the first laboratory-confirmed cases of dengue (DENV 1 and DENV4) occurred in an isolated area in the northwest Amazon region (Roraima State). After a 5-year interval without confirmed dengue fever, an epidemic due to DENV1 occurred in Rio de Janeiro State and was followed by several epidemics in highly populated cities in the southeast and northeast regions of Brazil. The number of dengue fever cases peaked at [approximately equal to] 100,000 in 1987 and 1991, probably because different serotypes (DENV1 and DENV2, respectively; Figure 2) were introduced. From 1986 to 1993, a total of 76.6% of the 294,419 reported dengue cases occurred in the rainy season from December to May, showing a marked seasonal pattern (Figure 1B). A cyclical pattern of 2-year intervals between large outbreaks was observed, which suggested low viral activity in the dry season (June to November).

[FIGURES 1-2 OMITTED]

In the second period (1994-2002), a total of 2,826,948 dengue cases were reported, indicating an upward trend in the incidence from 37 to 454 per 100,000 inhabitants. Although large outbreaks were observed in the rainy season, 482,163 cases were reported in the nonrainy season, which demonstrated increased dengue virus activity during the entire year. The bulk of incident cases were generated from metropolitan areas, although several outbreaks occurred in smaller urban settings in 25 out of 27 states. Two unprecedented epidemics occurred in 1998 and 2002, with 528,388 and 794,219 dengue fever cases reported, respectively. During this second period, vector surveillance to monitor A. aegypti infestation was extended to most of the country, covering 69.7% (n = 3,878) of the municipalities in 1996 and 89.6% (n = 4,985) in 2002. According to this vector information system, the number of infested municipalities ranged from 1,726 (44.5%) in 1996 to 2,905 (58.3%) in 2002. To date, Santa Catarina and Rio Grande do Sul States, located in southernmost Brazil, remain free of autochthonous dengue transmission; they report only imported cases.

The overall age distribution among reported cases during the last 5 years is presented in Figure 3. Approximately 50% of all reported dengue cases occurred in adults 2040 years of age. During this period, dengue incidence was consistently higher in adults, reaching up to 432.7/100,000 population in the 30- to 49-year-old age group in 2002 (Table 2). The male:female ratio was constant at [approximately equal to] 1.1:1 during this 5-year period. Sex and age group distribution were very similar when the data for the 5 regions of the country were stratified (data not shown).

[FIGURE 3 OMITTED]

The first DHF cases were confirmed in 1990, after DENV2 was introduced into Brazil. During the decade that followed, 893 confirmed DHF cases with 44 deaths (rate of 4.9%) occurred; 75% of these deaths occurred in Rio de Janeiro State. During 2001-2002, a striking increase in the number of DHF cases was detected, with incidence rates of 2.9/100,000 population (n = 682) in 2001 and 12.9/ 100,000 population (n = 2,714) in 2002 (Figure 2). DHF cases increased 45-fold from 2000 to 2002, compared to a 3.3-fold increase in dengue fever cases during the same period. In the epidemic year of 2002, the overall ratio of dengue fever to DHF cases was 292.6; in Rio de Janeiro State, the most affected area, this ratio was 134.8. From 1998 to 2002, the case-fatality rate was 5.4% (195/3,632). During this period, the sex distribution of DHF was similar, and cases occurred mainly in adults (median age 33 years) (Figure 3A). Recently, a different pattern in the age distribution of DHF was observed in Amazonas State, where unlike the national level, a higher proportion of DHF cases occurred among children. In Amazonas State, 30.9% (17/55) and 28.8% (15/52) of DHF cases occurred among children <15 years of age in 2001 and 2003, respectively (Figure 3B).

Countrywide, an upward trend in hospitalized dengue cases has been apparent since 1994, peaking with >54,000 hospitalizations in 2002 (Figures 2 and 4). Hospitalization rates were consistently higher among adults from 1998 to 2002. Comparing the 2 largest epidemic years (1998 and 2002), hospitalization rates in all age groups increased [approximately equal to] 8-fold (Table 2). The ratio of reported to hospitalized cases decreased from 29.4 in 1998 to 10.6 in 2002, which represents 1 hospitalization for every 10 reported dengue cases. Despite this increased proportion of hospitalized cases, >90% of the total reported cases were considered mild or moderate cases by the health system.

[FIGURE 4 OMITTED]

In Brazil, the chronology of the appearance of DENV serotypes occurred in the following sequence: DENV1 in 1986, DENV2 in 1990, and DENV3 in 2000 (Figure 2). The simultaneous circulation of these 3 serotypes was first detected in multiple states during the last 2 years. Molecular epidemiology of DENV in Brazil has identified the Caribbean, Jamaican, and Sri Lankan genotypes for the DENV1, DENV2, and DENV3 viruses, respectively (21).

Discussion

Analysis of 20 years of dengue/DHF surveillance data showed 2 distinct periods: an initial phase from 1986 to 1993, characterized by localized, sporadic epidemic waves in urban centers, and a nationwide endemic and epidemic pattern from 1994 to 2002. In this latter period, several epidemics of dengue progressed towards hyperendemicity in multiple urban centers. Since 1999, dramatic increases in both the incidence and hospitalizations due to dengue fever and DHF have occurred, indicating a likely increase in disease severity in recent years. Changes in surveillance coverage might explain part of this increase, but this explanation seems unlikely since no major changes were made in surveillance definitions. The current intense virus transmission pattern can be explained by the number of municipalities infested with A. aegypti mosquitoes, the mobility of the population, and the introduction and cocirculation of 3 different virus serotypes (DENV1, 2, and 3).

The epidemiology of dengue in Brazil presents some unusual features, characterized by dengue/DHF affecting mainly adults, with a predominance of milder infection in persons treated at outpatient clinics. In contrast, severe forms of the disease among children requiring hospitalization have been described in DHF epidemics in South and Central American countries (3,22,23). This endemic pattern has also been reported from Southeast Asia in recent decades (24,25). Cuban children with secondary infection by DENV2 showed a higher frequency of DHF and DHF-related deaths during the epidemic of 1981, which had been preceded by a DENV1 outbreak 4 years earlier (26). Apparently, similar events in Brazil, which also experienced the sequential introduction of DENV 1 (during 1986) followed by DENV2 4 years later, led to a different outcome: most reported dengue/DHF occurred in adults. These findings may be explained by the distinct DENV2 strains circulating in Cuba (New Guinea) and Brazil (Jamaica) (21,27,28). Another possibility is the underdiagnosis of DHE in children in Brazil, although it seems unlikely that severe clinical manifestations would not likely be misdiagnosed or fail to draw the attention of public health authorities.

During the 20-year period examined, dengue/DHF in Brazil most commonly affected the adult population, even with the observed increase of dengue/DHF cases. Despite these findings, current data underscore a different pattern in the Amazon region, where an increased proportion of severe cases occurs among children. This finding represents a warning to pediatric practitioners and health officials. In the future, if the current intense DENV circulation persists, Brazil could resemble Southeast Asia, with DHF occurring mainly in younger age groups.

In 2002, the absolute number of deaths due to DHF (N = 150) exceeded malaria deaths for the first time in Brazil, demonstrating that malaria is not the only major endemic vector-borne disease in this tropical region. During that year, the largest epidemic yet recorded, including 250,000 dengue cases in the metropolitan area of Rio de Janeiro, caused major public health and political concern (7,8). Hemorrhagic fever and dengue-related deaths also clustered in this city. These findings probably reflect the recent introduction and predominance of DENV3, which suggests a possible role of this serotype in disease severity and the potential for additional DHF epidemics in the future (29). Another possible explanation for the increase in DHF is the association between secondary infection with disease severity (10); however, routine surveillance data only indicate patients' immune status. In addition, some highly urbanized areas have substantial proportions of the population living in crowded, impoverished areas with poor sanitation (30). These complex urban settings are present in many regions in Brazil, resulting in a major challenge for vector control activities (8).

Several seroepidemiologic studies in Brazil have shown that up to 70% of urban populations had previous dengue infection, outnumbering reported cases. These results suggest that seroprevalence increases with age and that subclinical outcomes are a common feature of DENV exposure (31,32). Access to health services is considered nearly universal in Brazil, particularly in urban settings; therefore, dengue/DHF reports should be representative of the disease in the population. Incidence and hospitalization rates by age group showed similar patterns when surveillance system and hospitalization database were analyzed. The consistent patterns of age and sex distribution for all regions during epidemic and nonepidemic periods also suggest reliability of these surveillance data.

The high case-fatality rate for DHF observed in the last 5 years may be due to difficulties in classifying case severity according to the standard World Health Organization/ PAHO dengue case definition (33). The Brazilian Ministry of Health has been strongly committed to improving surveillance and patient care in a major effort to reduce dengue-related deaths (34). The aim of this policy is to rapidly identify patients at risk of developing DHF and to initiate prompt, adequate treatment (e.g., intravenous fluid infusion) to prevent DSS. As result of this early and effective replacement of plasma loss, hemoconcentration (one of the classification criteria for DHF) has become a less frequently observed event during the course of the disease, and therefore, a proportion of these cases may not fulfill DHF criteria. Different applications or interpretations of this case definition by countries may limit the ability to make valid comparisons, particularly in Latin America compared to Southeast Asia (23,33).

The current epidemiologic trend underscores the importance of dengue/DHF and the need for long-term improvements in disease control and surveillance in Brazil. We have described the changing patterns and epidemiologic profile of dengue/DHF during the last 20 years in one of the most severely affected countries in the Americas, highlighting the recent increase in disease severity.

Acknowledgments

We thank Jarbas Barbosa da Silva, Jr. and Fabiano Geraldo Pimenta, Jr. for sharing their vast knowledge and the National Dengue Control Program staff for their support.

J.B. Siqueira, Jr. received a postgraduate scholarship from CNPq and Martelli CMT Research grant CNPq ID 300443/97-8.

References

(1.) Pan American Health Organization. Surveillance-featured surveillance items. [cited 2003 Nov 23]. Available from http://www. paho.org/english/ad/dpc/cd/dengue.htm

(2.) Gubler DJ, Clark GG. Dengue/dengue hemorrhagic fever: the emergence of a global health problem. Emerg Infect Dis. 1995;1:55-7.

(3.) Pinheiro FP, Corber SJ. Global situation of dengue and dengue haemorrhagic fever, and its emergence in the Americas. World Health Stat Q. 1997;50:161-9.

(4.) Gubler DJ. Dengue and dengue hemorrhagic fever. Clin Microbiol Rev. 1998;11:480-96.

(5.) Pan American Health Organization. Directing Council Resolution CD43.R4. Washington: Pan American Health Organization. [cited 2003 Jun 2]. Available from http://Paho.org/English/GOV/CD/ cd43_12-e.pdf

(6.) Halstead SB, Deen J. The future of dengue vaccines. Lancet. 2002;360:1243-5.

(7.) Halstead SB. Dengue. Curt Opin Infect Dis. 2002;15:471-6.

(8.) Barbosa da Silva J Jr, Siqueira JB Jr, Coelho GE, Vilarinhos PT, Pimenta FG Jr. Dengue in Brazil: current situation and prevention and control activities. Epidemiol Bull. 2002;23(1):3-6.

(9.) Guzman MG, Kouri G. Dengue and dengue hemorrhagic fever in the Americas: lessons and challenges. J Clin Virol. 2003;27:1-13.

(10.) Rigau-Perez JG, Clark GG, Gubler DJ, Reiter P, Sanders EJ, Vorndam AV. Dengue and dengue haemorrhagic fever. Lancet. 1998; 352:971-7.

(11.) Tauil PL. Urbanization and dengue ecology [article in Portuguese]. Cad Saude Publica. 2001;17(Suppl):99-102.

(12.) Massad E, Coutinho FA, Burattini MN, Lopez LF. The risk of yellow fever in a dengue-infested area. Trans R Soc Trop Med Hyg. 2001;95:370-4.

(13.) Gubler DJ. Surveillance for dengue and dengue hemorrhagic fever. Bull Pan Am Health Organ. 1989;23:397-404.

(14.) Instituto Brasileiro de Geografia e Estatistica--IBGE. Censo demografico 2000. [cited 2003 Sep 1]. Available from http://www.ibge.gov.br

(15.) Ministerio da Saude--DATASUS. Morbidade Hospitalar do SUS--por local de internacao--Brasil. Brasilia, 2004 [Cited 2004 May 8]. Available from http://tabnet.datasus.gov.br/cgi/sih/mimap.htm

(16.) Pinheiro RS, Travassos C, Gamerman D, Carvalho MS. Urban hospital markets: a methodological approach [article in Portuguese]. Cad Saude Publica. 2001;17:1111-21.

(17.) Organizacion Panamericana de la Salud. Dengue y dengue hemorragico en las Americas: guias para su prevencion y control. Publicacion Cientifica no. 548. Washington: The Organization; 1995.

(18.) Burke DS, Nisalak A, Ussery MA. Antibody capture immunoassay detection of Japanese encephalitis virus immunoglobulin M and G antibodies in cerebrospinal fluid. J Clin Microbiol. 1982; 16:1034-42.

(19.) Gubler DJ, Kuno G, Sather GE, Velez M, Oliver A. Mosquito cell cultures and specific monoclonal antibodies in surveillance for dengue viruses. Am J Trop Med Hyg. 1984;33:158-65.

(20.) Hall WC, Crowell TP, Watts DM, Barros VL, Kruger H, Pinheiro F, et al. Demonstration of yellow fever and dengue antigens in formalin-fixed paraffin-embedded human liver by immunohistochemical analysis. Am J Trop Med Hyg. 1991;45:408-17.

(21.) Nogueira RM, Miagostovich MP, de Filippis AM, Pereira MA, Schatzmayr HG. Dengue virus type 3 in Rio de Janeiro, Brazil. Mem Inst Oswaldo Cruz. 2001 ;96:925-6.

(22.) Pan American Health Organization. Dengue in Central America: the epidemics of 2000. Epidemiol Bull. 2000;21(4):4-8.

(23.) Harris E, Videa E, Perez L, Sandoval E, Tellez Y, Perez ML, et al. Clinical, epidemiologic, and virologic features of dengue in the 1998 epidemic in Nicaragua. Am J Trop Med Hyg. 2000;63:5-11.

(24.) Barbazan P, Yoksan S, Gonzalez JP. Dengue hemorrhagic fever epidemiology in Thailand: description and forecasting of epidemics. Microbes Infect. 2002;4:699-705.

(25.) World Health Organization. Dengue haemorrhagic fever: diagnosis, treatment and control. Geneva: The Organization; 1987.

(26.) Guzman MG, Kouri G, Valdes L, Bravo J, Vazquez S, Halstead SB. Enhanced severity of secondary dengue-2 infections: death rates in 1981 and 1997 Cuban outbreaks. Rev Panam Salud Publica. 2002;11(4):223-7.

(27.) Sariol CA, Pelegrino JL, Martinez A, Arteaga E, Kouri G, Guzman MG. Detection and genetic relationship of dengue virus sequences in seventeen-year-old paraffin-embedded samples from Cuba. Am J Trop Med Hyg. 1999;61:994-1000.

(28.) Guzman MG, Deubel V, Pelegrino JL, Rosario D, Marrero M, Sariol C, et al. Partial nucleotide and amino acid sequences of the envelope and the envelope/nonstructural protein-1 gene junction of four dengue-2 vires strains isolated during the 1981 Cuban epidemic. Am J Trop Med Hyg. 1995;52:241-6.

(29.) Messer WB, Gubler DJ, Harris E, Sivananthan K, de Silva AM. Emergence and global spread of a dengue serotype 3, subtype III virus. Emerg Infect Dis. 2003;9:800-9.

(30.) World Bank. World development report 1995. Workers in an integrating world. Washington: World Bank; 1995.

(31.) Figueiredo LT, Cavalcante SM, Simoes MC. Dengue serologic survey of schoolchildren in Rio de Janeiro, Brazil, in 1986 and 1987. Bull Pan Am Health Organ. 1990;24:217-25.

(32.) Teixeira MG, Barreto ML, Costa MC, Ferreira LD, Vasconcelos PF, Cairncross S. Dynamics of dengue virus circulation: a silent epidemic in a complex urban area. Trop Med Int Health. 2002;7:757-62.

(33.) Rigau-Perez JG, Bonilla GL. An evaluation of modified case definitions for the detection of dengue hemorrhagic fever. Puerto Rico Association of Epidemiologists. PR Health Sci J. 1999;18:347-52.

(34.) Fundacao Nacional de Saude. Programa Nacional de Controle da Dengue. Brasilia, Brasil: Ministerio da Saude; 2002.

Joao Bosco Siqueira, Jr., * ([dagger]) Celina Maria Turchi Martelli, ([dagger]) Giovanini Evelim Coelho, * Ana Cristina da Rocha Simplicio, * and Douglas L. Hatch* ([double dagger])

* Ministry of Health, Brasilia, Brazil; ([dagger]) Federal University of Goias, Goiania, Brazil; and ([double dagger]) Centers for Disease Control and Prevention, Atlanta, Georgia, USA

Address for correspondence: Joao Bosco Siqueira Junior, Secretaria de Vigilancia em Saude, SAS--Quadra 4--Bloco "N"--7 andar Sala 715, 70 070 -040 Brasilia--DF Brazil; fax: 5561-2264488; email: joao.siqueira@funasa.gov.br

Dr. Siqueira is a staff member of the national dengue branch at Health Surveillance Secretariat, Ministry of Health, Brazil, and a researcher at the Tropical Pathology and Public Health Institute, Federal University of Goias. His main research interests are epidemiology, control of infectious diseases, and outbreak investigations.

COPYRIGHT 2005 U.S. National Center for Infectious Diseases
COPYRIGHT 2005 Gale Group

Return to Dengue fever
Home Contact Resources Exchange Links ebay