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Brote urbano de enfermedad aguda de Chagas en la region amazonica de Brasil: seguimiento de cuatro anos despues del tratamiento con benznidazol.

Urban outbreak of acute Chagas disease in Amazon region of Brazil: four-year follow-up after treatment with benznidazole

Despite efforts to eliminate American trypanosomiasis (Chagas disease) through vector control, the disease continues to be a public health problem in Latin America. The infection is caused by Try-panosoma cruzi, a parasite transmitted primarily by triatomine vectors found in Mexico and Central and South America. Chagas disease is a complex zoonosis, and the life cycle of the parasite involves a variety of mammal hosts. T. cruzi infection in humans manifests with acute symptomatic or asymptomatic phases and progressive chronic forms with myocardial, esophageal, and intestinal involvement.

An estimated 15 million people in Latin America are infected with T. cruzi, but acute cases are detected in only 1%- 2% of those infected (1). Some authors point out that there has been an increase in the number of acute cases recorded in some Latin American countries, leading to predictions that the situation regarding Chagas at the beginning of the 21st century will be similar to that in the early years of the 20th century (2, 3).

Prior to 1996, acute Chagas disease was rarely reported in the Amazon region of Brazil, despite evidence of the complete enzootic cycle of T. cruzi in the region. Outbreaks have since been reported in the region, characterized as short outbreaks involving 2 to 16 acute cases per episode (4). Only five chronic cases are considered autochthonous to the Amazon region. Two of the five patients were symptom-free, two had dilated cardiomyopathy, and one had the digestive form of Chagas disease (5-7).

Acute Chagas disease in the Amazon region of Brazil was first documented by Shaw et al. in 1969 in a low-income area of Belem, Para state (8). The outbreak involved four family members who fell ill simultaneously in 1968. The absence of triatomine vectors in the family dwelling suggested oral transmission of T. cruzi for the first time in Brazil's Amazon region (8).

Belem is located between Guajara Bay and the Guama River and has an urban area of 516 [km.sup.2] with some 1.3 million inhabitants. Preserved forest areas, such as Utinga National Park are on the outskirts of the city. Between 1967 and 1977, single adult insects infected with T. cruzi, particularly Panstrongylus geniculatus and Rhodnius pictipes, were found in households of poor, low-lying suburbs of Belem (9, 10). Mammals trapped in forest areas bordering the Pedreira district of Belem, where the 1968 outbreak occurred, had a high prevalence of T. cruzi-like trypanosomes (9, 10).

Outbreaks in the Amazon region are a target of epidemiological surveillance programs by the Brazilian Ministry of Health because of suspected oral transmission of the parasite. It is problematic to distinguish clinical features of acute Chagas disease in patients infected by vectors and those infected by the oral route. In part this is due to difficulties in obtaining data on acute cases from endemic areas where transmission typically occurs through vectors. Outbreaks involving oral transmission show prolonged febrile illness, a broad spectrum of symptoms, high mortality rates between outbreaks, and no inoculation sites on the body (11, 12).

When the acute phase of T. cruzi infection is not detected and treated, it can persist in the indeterminate phase for the life of a patient. Treatment of the acute infection with tripanocidal drugs (benznidazole) has moderate efficacy (60%) in eradicating parasites, mainly in patients with a prolonged subacute phase (11, 12). Trials with patients suffering from chronic or indeterminate phase Chagas disease do not indicate a treatment benefit (13, 14). Andrade et al. presented encouraging findings regarding the efficacy of benznidazole in a randomized controlled trial of children with early chronic T. cruzi infection. Their data showed negative seroconversion at the end of a three-year follow-up study in 55.8% of the children treated with benznidazole, when compared with the placebo group (15). Results from a study in the same cohort of children using the polymerase chain reaction (PCR) method support the notion that negative serology post-treatment corresponds to cure (16).

Better evidence about the clinical profile and treatment outcome of acute phase Chagas disease patients is needed.

We describe an outbreak of acute trypanosomiasis that occurred in September 2000, in the city of Belem. Eleven members of four neighboring families were affected simultaneously, likely as a result of ingesting contaminated food. We describe clinical and laboratory findings during the outbreak and in a four-year follow-up study. The treatment outcome and relevance of serial parasitological examinations of patients with acute Chagas disease are discussed.

MATERIALS AND METHODS

Eleven patients from four families were enrolled in the study. The first two patients, a 17-year-old female and her 58-year-old mother, visited the Evandro Chagas Institute in Belem following diagnosis with supposed typhoid fever and treatment with chloramphenicol. Both mother and daughter showed negative results for typhoid fever. Based on clinical evidence of prolonged fever and information about febrile illness in a relative and in neighbors, acute Chagas disease was suspected.

These two patients and nine of their relatives or neighbors with the same history of extensive febrile illness were subsequently diagnosed with trypanosomiasis by parasitological and serologic tests. As far as could be ascertained, all 11 of these individuals were born in the city of Belem and had always lived in the district of Pedreira.

Forty contacts (relatives and neighbors) of the infected individuals were questioned about febrile illness and underwent blood sample collection, regardless of whether symptoms were present. Blood samples were examined using immunofluorescence assay (IFA) for immunoglobulin M (IgM) and immunoglobulin G (IgG), and indirect hemagglutination assay (IHA).

The houses of all patients and their contacts were rigorously searched for triatomine bugs, but none were found.

Case definition

The case definition for acute Chagas disease is a positive T. cruzi parasitological test (Strout method or thick smear) or a positive serologic test for immunoglobulin M (IgM) anti-T. cruzi antibodies by IFA. When a case is detected, contacts (relatives or neighbors) are immediately screened for infection with blood and parasitological exams, whether or not they are symptomatic (17). Infection cure is defined when three sequential serologic tests, using two different methods, give negative results (17).

A suspicious case is defined as a contact of a diagnosed case who presents febrile illness [+ or -] 15 days from the time the first diagnosed patient became ill.

Clinical and laboratory evaluation

During the initial evaluation (acute phase), all patients were submitted to clinical and physical examination and blood sampling. Seven series of blood samples were collected: one before onset of treatment (initial), one during treatment (30 days after the onset of treatment), and five following the conclusion of treatment (at 60 days and at 12, 24, 36, and 48 months post-treatment).

The samples collected before treatment were processed using IFA and quantitative buffy coat (QBC) (18).

We added two indirect parasitological methods--artificial xenodiagnosis and blood culture for T. cruzi--to the follow-up series of examinations. For serum blood culture, a 3 mL sample of heparinized blood was overlaid on a Hoff agar slant. The overlay was examined by phase contrast microscopy at 400x magnification every 2 weeks; cultures were discarded as negative after 10 weeks. Xenodiagnosis was performed using 40 fifth-stage nymphs of Triatoma infestans, Triatoma maculata, Triatoma tibiamaculata, Triatoma dimidiata, Panstrongylus megistus, and Dipetalogaster maximus. Rectal contents of individual insects were examined for trypanosomes at 400x magnification one and two months after feeding. Leukocyte counts and hemoglobin concentration studies were made before and after treatment.

Standard 12-lead electrocardiograms (ECG) with the patient at rest and echocardiograms were performed during the first week of treatment and in the third month and fourth year of post-treatment follow-up.

Treatment procedures

The 11 confirmed cases in the study were treated with benznidazole at doses of 5 to 7 mg/Kg daily for 60 to 90 days (17). Ten patients received daily treatment for 60 days and, because of treatment failure, one patient received treatment for 90 days.

The ethics committee of the Evandro Chagas Institute approved the study, and all subjects gave informed consent for their participation in this investigation.

RESULTS

All 11 patients included in this study presented febrile illness and asthenia beginning 7 or 9 September 2000, lasting between 23 and 43 days. Other reported symptoms and signs were dyspnea, chills, abdominal pain, vomiting, paleness, myalgia, arthralgia, leg swelling, face swelling, cutaneous rash, coughing, and variable degrees of myositis, mainly in the females (Figure 1). Three patients had palpitations, tachycardia, and chest pain. Six patients developed myocarditis and five presented with myopericarditis during the acute phase. Two had serious cardiac manifestations during the acute phase of the disease and required hospitalization. Neither Romana sign nor other indication of insect inoculation was found on physical examination of the patients.

[FIGURE 1 OMITTED]

Parasitological tests made immediately after the completion of 30 days of treatment were negative in nine patients. Xenodiagnosis was positive for one 31-year-old female at the 30th day of treatment and positive for another 58-year-old female on the 60th day of treatment, indicating treatment failure (Table 1).

Follow-up serologic tests in all patients detected IgM antibodies for a short period and persistent IgG anti-T. cruzi antibodies four years after acute infection. No patients had negative serologic tests until September 2004, four years after treatment (Figure 2).

During the acute phase, five patients presented with anemia (hemoglobin 8.9- 10.2 g/dL). Leukocyte counts increased in two patients who presented with acute pulmonary infections simultaneously with acute Chagas disease. Four patients had lymphocytosis (1 702-8 979 lymphocytes/ [mm.sup.3]) during the acute illness, with improvement after two months. Three patients presented with leukopenia (3 200-4 700 leukocytes/[mm.sup.3]).

ECG and echocardiogram results during the acute illness and at four years post-treatment are shown in Table 2. Five patients had no ECG changes through the follow-up period. One patient had low QRS voltage due to pericardial effusion. Four patients presented non-specific ventricular repolarization with or without associated conduction disturbances. Of these four, the ECGs of two patients normalized, one 17-year-old female remained with atrioventricular (AV) dissociation and intermittent left bundle-branch block, and one 15-year-old female developed right bundle-branch block plus fascicular left bundle-branch block.

[FIGURE 2 OMITTED]

Three patients presented pericardial effusion that resolved shortly after onset of treatment. One 28-year-old male had a moderate amount of fluid in the pericardium and significant myositis in both lower limbs. Echocardiography of a 70-year-old female with prior history of arterial hypertension showed abnormalities before and after treatment that were consistent with diastolic dysfunction and signs of hypertrophy due to her previous condition. None of the patients presented decreased ejection fraction either during acute illness or later (see Table 2).

All 40 contacts (relatives and neighbors) examined were asymptomatic and had negative serologic tests.

DISCUSSION

The signs and symptoms described in the Chagas outbreak reviewed in this study reveal a prolonged, febrile syndrome illness and positive parasitological and serologic tests. All patients showed persistent titers of IgG anti-T. cruzi antibodies four years after acute infection, but with an important decrease over time. While these lowered titers suggest a high possibility of cure, the outcomes for the patients remain uncertain.

Despite the low sensitivity of parasitological tests in cure assessment, we performed these tests during, before, and after treatment. Xenodiagnosis showed that two patients had persistent parasitemia at days 30 and 60 of treatment. Both continued medication for an additional 30 days. There was no difference in response to treatment between the patient receiving benznidazole for 90 days and the patient receiving it for 60 days. Four years after treatment, both of these patients showed low IgG antibody titers (1/40) and negative parasitological tests. We cannot be certain that these two patients followed the prescribed dosing schedules during the first 60 days of treatment.

Our findings show the potential benefits of benznidazole for clinical improvement of acute cases. However, the failure of benznidazole to clear parasitemia (as shown by xenodiagnosis and blood culture) in two patients by days 30 and 60 of treatment, suggests the need for new treatment schedules with longer duration. In addition, we do not know the significance of low IgG titers during the follow-up series of tests, but we hypothesize that it represents immunological memory rather than parasite persistence. More extensive follow-up or other effective tests are necessary to evaluate cure.

The rates of ECG abnormalities and cardiac disease during the acute phase reported in this study are similar to those reported in endemic areas (19, 20). Abnormalities compatible with acute Chagas disease showed rapid clinical improvement following treatment. One patient showed minimal echocardiography alterations consistent with acute myocarditis that disappeared after treatment. Similar results were encountered in a study of 37 patients with acute Chagas disease in an endemic area. These patients had temporary alterations of the cardiac autonomic conduction system (19, 3).

Early lesions of the cardiac conduction system have been documented in patients from a Chagas endemic area in Brazil. Pazin-Filho et al. showed that mild segmental left ventricular wall motion abnormalities in echocardiograms of patients with chronic disease could indicate future worsening of systolic function (21). In our post-treatment follow-up, chronic Chagas disease is indicated in three patients on the basis of these ECG findings: left anterior fascicular block, atrioventricular dissociation and intermittent left bundle-branch block, and right bundle-branch block and left posterior fascicular block, despite there being no clinical manifestation of these conditions. We do not know if the persistent ECG abnormalities indicate chronic phase of Chagas disease despite all patients having undergone treatment during the acute phase, or if these abnormalities represent sequelae of acute myocardial attack in patients who are free of the parasite. Patients with abnormal ECGs four years after treatment suggest that these early lesions are common and can go undetected, as we observed in the follow-up of patients. Long-term observation is needed to determine whether overt clinical disease will appear or if these abnormalities persist as mild sequelae of the acute phases.

Pericardial effusion resulting in death has been documented in patients with acute Chagas disease in outbreaks in the municipalities of Abaetetuba and Cameta, both in Para state in Brazil's Amazon region. In the Cameta outbreak, two deaths due to acute myopericarditis occurred (22, 23). In our study, three patients presented mild pericardial effusion without relationship either to ECG conduction disturbances or low ejection fraction in echocardiogram. This suggests that the presence of pericardial effusion may be part of a generalized process of inflammation with important repercussions for the pericardium rather than the myocardium. While myocarditis is more consistent with acute Chagas disease, pericarditis is described as a consequence of direct parasite lesions in acute cases from endemic areas, and should not be disregarded in cases in the Amazon region.

[FIGURE 3 OMITTED]

Epidemiologic investigation found no signs of triatomine vectors in the households of the patients and their contacts in our study. Onset of symptoms occurred within two to four days for all 11 of the affected individuals, suggesting oral transmission due to indirect contact with triatomine bugs. The presence of triatomines infected with T. cruzi in Pedreira district has been documented, as well as a 17.4% T. cruzi infection rate in wild mammals on the outskirts and in forests bordering Belem, mainly in the National Park of Utinga located near the Pedreira district (see the map in Figure 3) (9). This could be evidence of indirect and accidental human contact with this vector in this well-defined area of Belem, where acute cases of Chagas disease have occurred. The four families included in this study did not participate in gatherings where they would have shared food. It is improbable that infected triatomine bugs could infect three or more people concurrently, and that symptoms would present nearly simultaneously. We suggest that transmission of T. cruzi in this group of patients occurred orally, possibly involving an unprocessed beverage frequently consumed by this population. When prepared in unclean conditions this drink could be contaminated, as documented in a similar outbreak in Amapa state (24).

Brazilian researchers suggest that the increased risk for endemic Chagas disease in the Amazon is related to deforestation, population settlements, shifting cultivation, human colonization of the vector's natural ecotopes, and human migration to the Amazon region from endemic areas. Chagas disease in humans has been described in limited geographic areas in the Amazon region, especially northeastern Para state and southeastern Amapa state, related to sylvatic and port areas or areas that have experienced rapid urbanization and increased population density in the last 10 years (4, 25-29). In northeastern Para state, an extensive highway project may have caused an important ecological imbalance that has contributed to disturbing triatomine ecotopes.

There are many unanswered questions regarding contact between sylvatic vectors and human hosts of Trypanosomas in the Brazilian Amazon. We know that acute infection is benign in the majority of cases of Chagas, but poor clinical outcomes are possible when delayed diagnosis and delayed host response occurs. Serious pericarditis may be lethal to patients in the acute phase of the disease.

Clinical outcomes of patients during this brief follow-up of an urban Trypanosomiasis outbreak suggest that chronic Chagas disease in the Amazon region may be underestimated, although all patients in this study were symptomatic during the acute phase, unlike those affected in endemic areas. The authors underscore the need for a strong surveillance system for Chagas disease in the Amazon region of Brazil.

Acknowledgments. We are grateful to Jose Elson Abud, Francisco Gomes, Aguinaldo Ferreira, and Gilberto Cesar Rodrigues for technical support in carrying out this study. We acknowledge Ralph Lainson who gave us permission to adapt the published version of the map of Belem, and Nelson Veiga and his colleagues for adapting the map. We are indebted to Sheila Maria Almeida Ferreira Gomes for comments on the text. Financial support was provided by the Evandro Chagas Institute, UNESCO, and the Luiz Decourt Foundation (Belem).

Manuscript received on 1 January 2008. Revised version accepted for publication on 2 April 2008.

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(2.) Medrano-Mercado N, Luz M, Torrico F, Tapia G, Van Leuven F, Araujo-Jorge TC. Acutephase proteins and serological profiles of chagasic children from an endemic area in Bolivia. Am J Trop Med and Hyg. 1996;54(2): 154-61.

(3.) Parada H, Carrasco HA, Anez N, Fuenmayor C, Inglessis I. Cardiac involvement is a constant finding in acute Chagas' disease: a clinical, parasitological and histopathological study. Int J Cardiol. 1997; 60(1):49-54.

(4.) Valente SA, Valente VC, Fraiha H. Considerations on the epidemiology and transmission of Chagas disease in the Brazilian Amazon. Mem Inst Oswaldo Cruz. 1999;94(Suppl 1): 395-8.

(5.) Valente VC, Crescente JA, Valente SAS, Araujo JEA. Doenca de Chagas em fase indeterminada detectada em 2 doadores de sangue no Estado do Para. Summary presented at the XXVIII Congresso da Sociedade Brasileira de Medicina Tropical; Belem, March 1992. Pp. 37-8.

(6.) Valente VC, Pinto AYN, Valente SAS, Ostermayer AL. Consideracoes sobre um possivel caso de megacolon por doenca de Chagas autoctone no Estado do Para. Rev Soc Bras Med Trop. 1995;28(Suppl III):99-100.

(7.) Albajar PV, Laredo SV, Terrazas MB, Coura JR. Miocardiopatia dilatada em pacientes com infeccao chagasica cronica. Relato de dois casos fatais autoctones no Rio Negro, estado do Amazonas. Rev Soc Bras Med Trop. 2003; 36(3):401-7.

(8.) Shaw JJ, Lainson R, Fraiha H. Consideracoes sobre a epidemiologia dos primeiros casos autoctones de doenca de Chagas registrados em Belem, Para, Brasil. Rev Saude Publica. 1969;3(2):153-7.

(9.) Lainson R, Shaw JJ, Fraiha H, Miles MA, Draper CC. Chagas disease in the Amazon Basin 1. Trypanosoma cruzi infections in sylvatic mammals, triatomine bugs and man in the State of Para, north Brazil. Trans R Soc Trop Med Hyg. 1979;73(2):193-204.

(10.) Miles MA, Souza AA, Povoa M. Chagas disease in the Amazon basin III. Ecotopes of ten triatomine bug species (Hemiptera: Reduviidae) from the vicinity of Belem, Para State, Brazil. J Med Entomol. 1981;18(4):266-78.

(11.) Brazil, Ministry of Health, Department of Health Surveillance [Secretaria de Vigilancia em Saude]. Doenca de Chagas aguda relacionada a ingestao de caldo de cana em Santa Catarina. Brasilia, 2005 [Internet site]. Available from: http://www.anvisa.gov.br/ DIVULGA/NOTICIAS/2005/240305_nota. pdf. Accessed 17 July 2008.

(12.) Valente SA, Valente VC, Pinto AYN. Epidemiologia e transmissao oral da doenca de Chagas na Amazonia brasileira. In: Organizacion Panamericana de la Salud/Organizacion Mundial de la Salud. Unidad Regional de Prevencion y Control de Enfermedades Transmisibles, Grupo Tecnico Especializado en Inocuidad de Alimentos. Informe de la consulta tecnica en Epidemiologia, Prevencion y Manejo de la Transmision de la Enfermedad de Chagas como Enfermedad Transmitida por Alimentos (ETA), Rio de Janeiro, May 2006. Pp. 21-6.

(13.) Ferreira HO. Tratamento da forma indeterminada da doenca de Chagas com nifurtimox e benzonidazol. Rev Soc Bras Med Trop. 1990; 23(4):209-11.

(14.) Villar JC, Villar LA, Marin-Neto JA, Ebrahim S, Yusuf S. Trypanocidal drugs for chronic asymptomatic Trypanosoma cruzi infection. Cochrane Database Syst Rev. 2002;(1): CD003463.

(15.) Andrade AL, Martelli CM, Oliveira RM, Silva SA, Aires AI, Soussumi LMT, et al. Short report: benznidazole efficacy among Trypanosoma cruzi-infected adolescents after a sixyear follow-up. Am J Trop Med Hyg. 2004; 71(5):594-7.

(16.) Galvao LM, Chiari E, Macedo AM, Luquetti AO, Silva SA, Andrade AL. PCR assay for monitoring Trypanosoma cruzi parasitemia in childhood after specific chemoterapy. J Clin Microbiol. 2003;41(11):5066-70.

(17.) Brazil, Ministry of Health, Department of Health Surveillance [Secretaria de Vigilancia em Saude]. Consenso brasileiro em doenca de Chagas. Rev Soc Bras Med Trop. 2005;38 (Suppl. III):30.

(18.) Levine RA, Wardlaw SC, Patton CL. Detection of haemotoparasites using quantitative buffy coat analysis tubes. Parasitol Today. 1989;5(4):132-4.

(19.) Rassi A, Ferreira HO. Tentativa de tratamento especifico da fase aguda de doenca de chagas com nitrofuranos em esquemas de duracao prolongada. Rev Soc Bras Med Trop. 1971; 5(5):235-62.

(20.) Cancado JR. Tratamento etiologico da Doenca de Chagas pelo benzonidazol. In: Brener Z, Andrade Z, Barra-Neto M, eds. Trypanosoma cruzi e doenca de Chagas. 2nd edition. Rio de Janeiro: Guanabara Koogan; 2000. Pp. 389-405.

(21.) Pazin-Filho A, Romano MMD, Almeida-Filho JA, Marin-Neto OC, Furuta MS, Viviani LF, et al. Minor segmental wall motion abnormalities detected in patients with Chagas[acute accent] disease have adverse prognostic implications. Braz J Med Biol Res. 2006;39(4);483-7.

(22.) Pinto AYN, Harada GS, Valente VC, Abud JEA, Gomes FS, Souza GCR, et al. Acometimento cardiaco em pacientes com doenca de Chagas aguda em microepidemia familiar, em Abaetetuba, na Amazonia brasileira. Rev Soc Bras Med Trop. 2001;34(5):413-9.

(23.) Pinto AY, Valente SA, Valente VC. Emerging acute Chagas disease in Amazonian Brazil: case reports with serious cardiac involvement. Braz J Infect Dis. 2004;8(6):454-60.

(24.) Valente SAS, Valente VC, Cesar MJB, Santos MP. Registro de 15 casos autoctones de doenca de Chagas no Estado do Amapa com evidencias de transmissao oral. Summary presented to the XXXIII Congresso da Sociedade Brasileira de Medicina Tropical, 4-7 March 1997; Belo Horizonte.

(25.) Valente VC, Valente SA, Noireau F, Carrasco HJ, Miles MA. Chagas' disease in the Amazon Basin: association of Panstrongylus geniculatus (Hemiptera: Reduviidae) with domestic pigs. J Med Entomol. 1998;35(2):99-103.

(26.) Coura JR, Junqueira AC, Fernandes O, Valente SA, Miles MA. Emerging Chagas disease in Amazonian Brazil. Trends Parasitol. 2002; 18(4):171-6.

(27.) Ferraroni JJ, Melo JA, Camargo ME. Molestia de Chagas na Amazonia: ocorrencia de seis casos suspeitos, autoctones, sorologicamente positivos. Acta Amazonica. 1977;7(3):438-40.

(28.) Rodrigues CI, Souza AA, Terceros R, Valente SA. Doenca de Chagas na Amazonia: registro de oito casos autoctones em Macapa. Rev Soc Bras Med Trop. 1988;21(4):193-7.

(29.) Teixeira AR, Monteiro PS, Rebelo JM, Arganaraz ER, Vieira D, Lauria Pires L, et al. Emerging Chagas disease: trophic network and cycle of transmission of Trypanosoma cruzi from palm trees in the Amazon. Emerg Infect Dis. 2001;7(1):100-12.

Ana Yece das Neves Pinto, [1] Alberto Gomes Ferreira Jr., [2] Vera da Costa Valente, [1] Geraldo Saburo Harada, [3] and Sebastiao Aldo da Silva Valente [1]

[1] Chagas Disease Laboratory, Evandro Chagas Institute, Department of Health Surveillance, Ministry of Health, Belem, Brazil. Send correspondence to: Ana Yece das Neves Pinto, Secao de Parasitologia, Instituto Evandro Chagas, Secretaria de Vigilancia em Saude, BR 316 Km7, Levilandia, Postal code 67030070, Ananindeua, PA, Brazil. Tel: 91 3214 2150/3214 2043/3214 2151; e-mail: ayece@iec.pa. gov.br.

[2] Luiz Decourt Foundation, Belem, Brazil.

[3] Instituto do Coracao de Belem, Belem, Para, Brazil.
TABLE 1. Parasitological results in follow-up of treatment of 11
patients presenting acute Chagas disease, Belem, Brazil;
2000-2004

                           Test results for patients

                  Quantitative buffy coat         Blood culture

                   Positive     Negative     Positive     Negative
Days following
treatment          No.    %     No.    %     No.    %     No.    %

First day           8   72.3     3   27.3     8   72.3     3   27.3
30 days             0           11    100     0           11    100
60 days             0           11    100     0           11    100
1 year              0           11    100     0           11    100
3 years             0           11    100     0           11    100

                 Test results for patients

                     Xenodiagnosis

                  Positive     Negative

Days following
treatment          No.    %     No.    %

First day          11    100     0
30 days             2     18     9     82
60 days             1      9    10     91
1 year              0           11    100
3 years             0           11    100

TABLE 2. Results of electrocardiograms and echocardiograms during
acute phase and four years post-treatment in 11 Chagas disease
patients in  Belem, Brazil, 2000-2004

                                             Acute phase
             Age                          electrocardiogram
Case No.   (years)   Gender                    results

1            24        M      Low QRS voltage

2            28        F      Normal

3            31        F      Left axis deviation

4            70        F      Non-specific repolarization changes

5            28        M      First-degree atrioventricular block;
                              non-specific repolarization changes

6            17        F      Non-specific repolarization changes;
                              atrioventricular dissociation; left axis
                              deviation

7            22        M      Normal

8            19        M      Normal

9            15        F      Non-specific repolarization changes

10           24        F      Normal

11           58        F      Normal

                        Post-treatment
                       electrocardiogram
                            results
Case No.                 (fourth year)

1          Normal

2          Normal

3          Left axis deviation, left anterior
           fascicular block

4          Normal

5          Normal

6          Atrioventricular dissociation;
           intermittent left bundle-branch
           block

7          Normal

8          Normal

9          Right bundle-branch block,
           left posterior fascicular block

10         Normal

11         Normal

                          Acute phase
                        echocardiogram
Case No.                    results

1          Mild pericardial efusion; EF = 64%

2          ...

3          Normal; EF = 69%

4          Left ventricular hypertrophy;
           diastolic dysfunction; pericardial
           effusion; EF = 66%

5          Moderate pericardial effusion;
           EF = 63%

6          Mild pericardial effusion; left
           ventricular dilatation with diffuse
           hypokinesis; moderate mitral
           regurgitation; EF= 56%

7          Normal; EF= 66%

8          ...

9          Normal; EF= 74%

10         Mild pericardial effusion; EF= 70%

11         Left ventricular hypertrophy;
           EF = 68%

                        Post-treatment
                        echocardiogram
                            results
Case No.                 (fourth year)

1          Normal

2          Normal

3          Normal

4          Diastolic
           dysfunction;
           left ventricular
           hypertrophy

5          Normal

6          Normal

7          Normal

8          Normal

9          Normal

10         Normal

11         Normal

QRS = QRS complex; EF = Ejection fraction; ... = echocardiogram
not carried out.
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Title Annotation:Informe especial
Author:das Neves Pinto, Ana Yece; Gomes Ferreira, Alberto, Jr.; da Costa Valente, Vera; Saburo Harada, Gera
Publication:Revista Panamericana de Salud Publica
Date:Jan 1, 2009
Words:4576
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