SciELO - Scientific Electronic Library Online

 
vol.37 issue3Occurrence of Aedes albopictus in the state of Pará, Brazil author indexsubject indexarticles search
Home Page  

Services on Demand

Article

  • pdf in English
  • Article in xml format
  • Article references
  • How to cite this article
  • Curriculum ScienTI
  • Automatic translation
  • Send this article by e-mail

Indicators

Related links

Share


Revista de Saúde Pública

Print version ISSN 0034-8910

Rev. Saúde Pública vol.37 n.3 São Paulo Jun. 2003

http://dx.doi.org/10.1590/S0034-89102003000300021 

COMUNICAÇÕES BREVES BRIEF COMMUNICATIONS

 

Performance of an immunochromatography test for vivax malaria in the Amazon region, Brazil

 

Desempenho de um teste de imunocromatografia para malária por P. vivax na Amazônia

 

 

Alberto Ferreira Figueiredo FilhoI,III; Maria Cristina FigueredoI; José Maria NascimentoI; Vanja Suely Pachiano CalvosaI; Marinete Marins PóvoaI; Ricardo Luiz Dantas MachadoI,II

IServiço de Parasitologia do Instituto Evandro Chagas. Belém, PA, Brazil
IIDepartamento de Doenças Dermatológicas, Infecciosas e Parasitárias da Faculdade de Medicina de São José do Rio Preto. São Jose do Rio Preto, SP, Brazil
IIIAluno bolsista da Faculdade de Medicina da Universidade Federal do Pará

Correspondence

 

 


ABSTRACT

The study was carried out to evaluate the diagnostic performance of the ICT malaria Pf/PvTM test for vivax malaria diagnosis in Belém, Amazon region, Brazil. The results of blood malaria parasites examination using an immunochromatography test were compared with thick blood film (TBF) examination. It was also evaluated the performance of this test storaged at three different temperatures (25°C, 30°C, and 37°C) for 24 hours before use. Overall sensitivity of ICT Pf/PvTM was 61.8% with a specificity of 100%, positive and negative predictive value of 100% and 71.8%, respectively and accuracy of 80.6%. The test sensitivity was independent of the parasite density. This test needs to be further reviewed in order to have better performance for P. vivax malaria diagnosis.

Keywords: Malaria, vivax, diagnosis. Plasmodium vivax. Cromatography.


RESUMO

Avaliação do teste ICT malaria Pf/PvTM para o diagnóstico da malária por P. vivax em Belém, Estado do Pará. Foram comparados os resultados do teste imunocromatográfico com a gota espessa (GE) e avaliados o comportamento desse teste, estocado a três temperaturas distintas (250C/ 300C/ 370C), 24 horas antes de seu uso. A sensibilidade do ICT malaria Pf/PvTM foi de 61,8% com especificidade de 100%, valores preditivo positivo e negativo de 100% e 71,8%, respectivamente, e acurácia de 80,67%. A sensibilidade desse teste foi independente da densidade parasitária. Este teste necessita de reavaliação para melhorar o seu comportamento no diagnóstico da malária por P. vivax.

Descritores: Malária vivax, diagnóstico. Plasmodium vivax. Cromatografia.


 

 

Malaria is one of the most prevalent infectious diseases in tropical areas world-wide and is one of the main causes of human morbidity in the Amazon region, north of Brazil. In this area, Plasmodium vivax is the most common human malaria parasite, causing more than 80.2% of all cases reported in 2000.

The rapid and accurate diagnosis of malaria is essential for reducing its morbidity and mortality as well as for its control. The diagnosis of malaria has been traditionally based on microscopic examination of thick and thin blood films. Although simple and cheap, this procedure is however labor-intensive, time consuming and dependent upon training and expert knowledge of morphologic differentiation of plasmodial species.3 Alternative immunochromatography tests have been developed, particularly for Plasmodium falciparum that showed to be effective, quick and easy to use.1 P. vivax malaria blood samples from Turkey were analyzed by ICT-Malaria PvTM test (it detects P. vivax histidine-rich protein (HRP)-2 antigen) and showed 85.7% sensitivity, 100% specificity, and positive and negative predictive values of 100% and 87.1%, respectively.2 It has been suggested that this test is simple, rapid and reliable, allowing diagnosis where traditionally diagnostic tests are not available (rural and remote areas). Recently, it came out the ICT Malaria Pf/PvTM (ICT-Malaria Pf/Pv, AMRAD, Australia), a commercial in-vitro immunochromatography test for the detection and speciation of both P. falciparum and P. vivax malaria parasites. The aim of this study is to evaluate the diagnostic performance of the ICT Pf/PvTM test for diagnosis of vivax malaria in Belém, Amazon region, Brazil.

Subjects seen at the Evandro Chagas Institute, Belém, from January to March 2000 with symptoms and signs suggestive of malaria and later had a positive slide test for P. vivax malaria were randomly tested using ICT Pf/PvTM. Informed consent was obtained and symptoms details were registered. There were 20 asymptomatic individuals in the negative control groups, and the same number of P. falciparum infected individuals with positive thick blood film (TBF) was selected. P. vivax malaria patients had been treated with chloroquine 25 mg/kg of body weight divided in three days (10 mg/kg in day 1 and 7.5 mg/kg in days 2 and 3) plus primaquine 0.25 mg/kg of body weight for 14 days starting five days after the vivax malaria diagnosis.

The results of blood obtained through finger-prick and immediate evaluation using ICT Malaria Pf/PvTM test (as by the manufacturer's instructions) on day 0 and days 1, 2, 3 and 4 after treatment start were compared with standard microscopy examination of malaria parasites in TBF. Fifteen samples were also evaluated using ICT Malaria Pf/PvTM test storaged at three different temperatures (25°C, 30°C and 37°C) for 24 hours before use. TBF were examined by independent experienced microscopists who were unaware of the results, following the World Health Organization5 recommended procedures.

In order to compare the performance of ICT Pf/PvTM test, 30 vivax malaria patients before (day 0) and after chloroquine treatment (day 1 to 4) were included in the study. On day 0, 30 samples of P. vivax patients showed parasite density between 200 and 7,750 infected red blood cells/mm3, while on day 1 the parasitemia had ranged from 10 to 1,020 infected red blood cells/mm3. Three samples were negative. On day 2 15 samples had parasite density between 10 and 300 infected red blood cells/mm3, and 15 samples were negative. The parasitemia in day 3 was detected only in four samples and ranged from 10 to 40 infected red blood cells/mm3. In day 4 all 30 samples were negative. The ICT Pf/PvTM test detected P. vivax in 28 samples in day 0, while in day 1 it was detected in sixteen and in day 2 only in four samples. None P. vivax sample was detected using ICT Pf/PvTM test in day 3. Both TBF and ICT Pf/PvTM test were negative in day 4. The ICT Pf/PvTM was negative in all 20 samples (control group) with no parasites in the microscopy examination. The ICT Pf/PvTM test detected all 20 P. falciparum samples that were seen in the microscopy examination.

A total of 150 paired samples were analyzed. The test performance was assessed in terms of its sensitivity and specificity. Overall sensitivity of ICT Pf/PvTM for vivax malaria diagnosis was 61.8%, specificity of 100%, positive and negative predictive values of 100% and 71.8%, respectively and accuracy of 80.7% (Table). The results of ICT Pf/PvTM were variable for the three different temperatures tested. It was observed that the color of positive results (pink line) losses its intensity with increasing temperatures.

 

 

The great area of land and water, and the uncontrolled occupation of the Brazilian Amazon region, associated with the lack of personnel to carry out rapid diagnosis, all contribute to the elevated number of malaria cases in this region.

The Quantitative Buffy CoatÒ and serological tests are useful but have limitations for the diagnosis of malaria infections and alternative methods are needed to overcome these problems. Molecular techniques are sensitive, accurate and specific4 but expensive and require expert knowledge. Complementary and alternative diagnosis methods not dependent on microscopy are commercially available.

Although the ICT Pf/PvTM test is known for its ease of use even for personnel not familiar with the test format, it has showed variable results in P. vivax detection and low sensitivity in the present study. The study results suggest that differences in the sensitivity of ICT Pf/PvTM test for vivax malaria infections were independent of P. vivax density in blood samples. Storage temperature is a crucial factor for the efficiency of the ICT Pf/PvTM test, especially in the north of Brazil where temperatures can reach more than 30°C (maximum storage temperature recommended by the kit).

Although the cost of ICT Pf/PvTM (US$ 1.50) is higher than microscopy technique (US$ 0.70), this method is simple and rapid, allowing diagnosis where specialized laboratory and personnel are not available. This test can play a useful role in assessing P. vivax malaria diagnosis in developing countries, but it needs to be further reviewed for a better performance. The TBF is still the best indicator of P. vivax malaria in infected patients.

The study protocol was reviewed and approved by the Research Board of the Evandro Chagas Institute.

 

ACKNOWLEDMENTS

To all patients enrolled in this study and staff of the Malaria Laboratory at the Evandro Chagas Institute for their technical assistance.

 

REFERENCES

1. Abul Faiz MA, Rashid R, Palit R, Rahman MR, Bin Yunus E, Hussain A et al. ParaSightTM- F test results in cerebral malaria patients before and after treatment in Chittagong Medical College Hospital, Bangladesh. Trans R Soc Trop Med Hyg 2000;94:56-7.        [ Links ]

2. Araz E, Tanyhksel M, Ardic N, Tabuk C. Performance of a commercial immunochromatografic test for the diagnosis of vivax malaria in Turkey. Trans R Soc Trop Med Hyg 2000;94:55-6.        [ Links ]

3. Chiodini PL. Non-microscopic methods for diagnosis of malaria. Lancet 1998;351:80-1.        [ Links ]

4. Machado RLD, Garret DO, Adagu IS, Warhurst DC, Póvoa MM. Simplified diagnosis of malaria infection: GFM/PCR/ELISA a simplified nucleic acid amplification technique by PCR/ELISA. Rev Inst Med Trop S Paulo 1998;40:333-4.        [ Links ]

5. World Health Organization. Basic malaria microscop. Geneva; 1991. Part I p.17-68.        [ Links ]

 

 

Correspondence to
Ricardo Luiz Dantas Machado
Departamento de Doenças Dermatológicas, Infecciosas e Parasitárias
Av. Brigadeiro Faria Lima, 5416
15090-000 São José do Rio Preto, SP, Brazil
E-mail: ricardomachado@famerp.br

Received on 9/9/2002
Reviewed on 15/2/2003
Approved on 12/3/2003