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Jornal de Pediatria

Print version ISSN 0021-7557

J. Pediatr. (Rio J.) vol.83 no.5 Porto Alegre Sept./Oct. 2007

http://dx.doi.org/10.1590/S0021-75572007000600012 

ORIGINAL ARTICLE

 

Early diagnosis of streptococcal pharyngotonsillitis: assessment by latex particle agglutination test

 

 

Maria Jussara F. FontesI; Flávia B. BottrelII; Maria Teresa M. FonsecaIII; Laura B. LasmarIII; Rosângela DiamanteIV; Paulo Augusto M. CamargosV

IDoutora. Professora adjunta, Disciplina de Pneumologia, Departamento de Pediatria, Faculdade de Medicina, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG, Brazil
IIEspecialista em Pediatria, Sociedade Brasileira de Pediatria. Pós-graduanda, Curso de Especialização em Pneumologia Pediátrica, UFMG, Belo Horizonte, MG, Brazil
IIIDoutora. Professora adjunta, Disciplina de Pneumologia, Departamento de Pediatria, Faculdade de Medicina, UFMG, Belo Horizonte, MG, Brazil.
IVProfessora assistente, Departamento de Pediatria, Faculdade de Medicina, UFMG, Belo Horizonte, MG, Brazil
VDoutor. Professor titular, Departamento de Pediatria, Faculdade de Medicina, UFMG, Belo Horizonte, MG, Brazil. Chefe, Unidade de Pneumologia Pediátrica, Hospital das Clínicas, UFMG, Belo Horizonte, MG, Brazil

Correspondence

 

 


ABSTRACT

Objectives: Acute pharyngitis is one of the most common diseases in pediatric practice, and the most common bacterial etiology is group A beta-hemolytic streptococcus (GABHS). Correct diagnosis and treatment are primarily of importance to the prevention of non-suppurative sequelae. Rapid tests for detecting the antigen of group A streptococcus are a useful tool for the diagnosis of streptococcal pharyngotonsillitis, due to the speed of results, accuracy and low cost; however, in our country they are little used and have been little studied. The objective of this study was to evaluate the accuracy of a GABHS rapid antigen detection test kit, in comparison with oropharynx swab culture.
METHODS: Children aged 1 to 18 years with clinical diagnoses of acute pharyngitis were chosen at public emergency and private clinical services in Belo Horizonte, Minas Gerais, Brazil, with children being excluded if they had taken antibiotics within 30 days of their consultation. The final sample consisted of 229 patients, each of whom had two oropharynx swabs taken, one for rapid GABHS testing and the other to be sent for culture.
RESULTS: We observed sensitivity of 90.7%, specificity of 89.1%, a positive predictive value of 72.1%, a negative predictive value of 96.9% and a positive likelihood ratio of 9.0 for the rapid test used here, compared with culture.
CONCLUSIONS: The rapid test studied exhibited a good correlation with culture and is, therefore, of great use in clinical practice for detection of GABHS.

Keywords: Pharyngitis, tonsilitis, Streptococcus pyogenes, diagnosis, latex fixation test.


 

 

Introduction

Acute pharyngitis (AP) is one of the most common diseases in pediatric practice.1 Although the majority of APs is of viral origin, group A b-hemolytic streptococcus (GABHS) is the most common bacterial etiology (15-30% of AP).1-3 Therefore, early diagnosis of this infection, followed by appropriate antimicrobial treatment, is extremely relevant to the prevention of rheumatic fever (RF) and suppurative complications (peritonsillar abscess, cervical lymphadenitis and mastoiditis), to the improvement of signs and symptoms, to reducing of GABHS transmission and in order to minimize the adverse effects of inappropriate antibiotics use,1,4,5 including the emergence of resistance to antibiotics.2

In developing countries, RF is one of the principal causes of acquired heart disease among school-aged and adolescent children and young adults.6,7 In Brazil, according to a World Health Organization epidemiological model, there is an estimated annual frequency of 6 million streptococcal AP, 0.3% of which, under non-epidemic conditions, result in episodes of acute RF, which equates to an incidence of 15,000 to 18,000 new cases annually. Around one third, i.e. 6000, of these cases progress to chronic rheumatic heart disease. The majority of mitral valve interventions carried out in our country are the result of rheumatic heart disease.8 In Belo Horizonte, Minas Gerais, Brazil, a study carried out at a school belonging to the public education system demonstrated a prevalence of rheumatic disease of 3.6 in every 1,000 students aged 10-20 years.9

A large proportion of the signs and symptoms of pharyngitis due to GABHS are the same as those of non-streptococcal pharyngitis, which makes it difficult to make etiologic diagnosis on the basis of clinical signs and symptoms alone.1,4 Many attempts have been made to develop reliable clinical criteria by means of scores and flow diagrams,1,3,10-13 but, unfortunately, few have managed to achieve a level of accuracy comparable to that of confirmatory laboratory tests.12

The current recommendations of the American Academy of Pediatrics (AAP), the Centers for Disease Control and Prevention (CDC), the American Heart Association (AHA) and the Infectious Diseases Society of America (IDSA) are that, when there is a clinical suspicion of AP due to GABHS, diagnosis should be confirmed by laboratory tests employing either cultures of peritonsillar exsudate swabs or rapid antigen detection tests (RADT) of the same swabs.

The high specificity (> 95%) of RADT, observed by several authors, means that treatment can be initiated if the result is positive. However, a negative result from a test the sensitivity of which varies between 80 and 90% does not exclude a diagnosis of AP due to GABHS and should be confirmed by culture, which, if positive, demands immediate treatment.1,2,14,15 According to the AAP and the IDSA, this last recommendation can be ignored if the specific RADT being used has a sensitivity that is proven to be comparable to culture.

Culture of pharyngotonsillar secretions is the conventional method and the gold standard for diagnosis of AP due to GABHS, but it has practical limitations. The wait for results (18-48 hours) causes a delay in treatment or use of antibiotics too early, causes anxiety among patients and family members and prolongs symptomatology and the period during which streptococcus dissemination occurs in cases of AP due to GABHS.

Rapid antigen detection tests have been widely studied and validated at many different centers for the diagnosis of streptococcal AP.1,14,16-18 These tests offer results in up to 30 minutes and exhibit good concordance with culture results, making them a reliable resource that is easily accessed, is cheaper than culture and is a great aid in the correct diagnosis of AP and to judicious use of antimicrobials.

Both the AAP and the IDSA recommend that each center that employs RADT for diagnosis of AP should validate them and compared their sensitivity and specificity with results from culture.1,14

Brazilian data on RADT remain scarce.19-21 This study aims to evaluate the sensitivity, specificity, positive predictive value, negative predictive value and positive likelihood ratio (LR) of an RADT compared with culture in a sample of patients in the pediatric age group seen at primary care services.

 

Methods

This is a cross-sectional study, undertaken in Belo Horizonte, Minas Gerais, Brazil, during the period from January 1997 to January 2001. Pediatric patients aged 1 to 18 years were selected at public emergency and private clinical services, with a clinical presentation of acute pharyngitis. Use of benzathine penicillin within the previous 30 days and/or other antimicrobial drugs within the previous 15 days were exclusion criteria. The present study was approved by the Ethics Committee at the Universidade Federal de Minas Gerais.

After consent had been obtained, each child was interviewed, in the presence of a parent, by a first examiner who filled out a specific protocol and took two swabs simultaneously from the tonsils and posterior pharyngeal region. A second examiner (double-blind test), performed latex particle agglutination testing (Patho Dx®, DPC, Los Angeles, United States) on one of the swabs, according to the manufacturer's instructions. The second swab was used to seed an agar and 5% lamb's blood plate within 20 minutes, which was then incubated for 18 to 24 hours in microaerophilic conditions at 37ºC. The plate was subsequently interpreted based on colony morphology and hemolysis pattern by a microbiologist who was unaware of the result of the latex test. Suspect colonies were confirmed as beta-haemolytic streptococcus by means of latex agglutination testing (Pastorex®, Sanofi Pasteur, France).

The patients included had presented with signs of pharyngotonsillitis, among others, complaining of sore throat and/or hyperemic tonsils or oropharynx, observed during the clinical examination performed at the time of enrollment on the study.

Streptococcal AP due to GABHS (case): patients with clinical diagnosis of AP and a culture positive for GABHS.

Negative (control): patients with clinical diagnosis of AP and a culture negative for GABHS.

The sample size was calculated, using Epi-Info version 6.0, at 126 patients in order to achieve a sensitivity of 91%, and at 138 patients in order to achieve a specificity of 90%, taking the culture as gold standard and with an alpha error of 5%, with amplitude of variation of 15% of the 95% confidence interval.

Frequency distributions were employed to assess the population's characteristics in terms of sex, age, number of inhabitants in family home and parents' education.

The sensitivity, specificity, positive predictive value, negative predictive value and accuracy, with their respective 95% confidence intervals, and the positive LR of the RADT were all calculated in relation to culture.

The protocol, database and statistical analysis were all produced electronically using Epi-Info, versions 6.0 and 2002.

 

Results

Initially, 238 patients were included; eight of these were excluded due to doubtful latex results and/or contaminated culture. The sample analyzed comprised 229 children.

The characteristics of the study population are given in Table 1.

There was a predominance of females (56.8%) and of patients aged from 4 to 10 years (74.9%). We observed that parents had a low educational level, with a predominance of those who had had 0 to 8 years' schooling (63.5%).

The most common clinical findings were fever (88%), swollen tonsils (73.8%), pain when swallowing (73.4%) and prostration (73.4%). The frequency distribution of clinical signs and symptoms across the study group can be observed in Table 2.

The data in Table 3 demonstrate that the age group with most positive latex results was the over-fives (n = 64; 30.1%). There was no difference in the proportion of positive cultures between patients younger than 5 years (n = 4; 23.5%) and those older than 5 years (n = 50, 23.6%).

 

 

Table 4 illustrates the comparison of the RADT results with those of the oropharynx swab culture.

 

 

The figures observed for the test were: sensitivity (S) of 90.7% (95%CI 85.1-96.4); specificity (SP) of 89.1% (95%CI 83.0-95.2); positive predictive value (PPV) of 72.1% (95%CI 63.3-80.9); negative predictive value (NPV) of 96.9% (95%CI 93.5-100.3) and a positive LR of 9. All calculations were performed to a confidence interval of 95%.

 

Discussion

The sensitivity of RADT for detecting GABHS (90.7%) found in this study is comparable with the results of previous publications (80-90%).1,3,10,19,20,22,23 Possible explanations for the presence of the false negatives observed in this study include the culture incubation time, which was 24 hours (increasing the incubation period to 48 hours increases positivity and, therefore, the sensitivity of the test1,22), and the possibility of low numbers of colonies with this test, which was not assessed in our analysis.

The observed specificity of 89.1% was lower than the average in the literature, where figures are above 95%. We could speculate that there might be a high prevalence of healthy carriers of GABHS, the prevalence of whom is unknown in our country, since the test does not allow differentiation between colonized and infected patients, and that this increased the number of false positives. Another possible explanation is that different test kits were used in different studies.

Hjortdahl et al. used the same RADT kit used here and observed a specificity of 91%, but they attributed the divergence from other study results not to the kit itself, but to the low level of precision of results caused by the introduction of a new laboratory diagnostic test; the subjectivity of RADT readings (a reaction that is weakly positive may be interpreted as positive); problems inherent to the "gold standard" employed, since oropharynx swab cultures can produce around 10% false-negatives; and to the occurrence of other streptococci with hemolysis patterns and antigens A, C, F or G.24,25

Berezin et al. observed sensitivity and specificity of 78 and 90%, respectively,19 whereas Santos et al. found 96.7 and 94.4%.20 In this last study, the elevated specificity was the result of the exclusion of patients with signs and symptoms of viral infection, which was not performed in our study. The present analysis included patients (with nonspecific complaints) with uncertain clinical status of GABHS infection with the intention of assessing a sample that was representative of the reality faced by the majority of professionals working at emergency services and in primary care. Earlier studies have shown that prior selection of patients to be investigated with RADT with presentation strongly suggestive of AP of streptococcal etiology (sudden onset of fever, sore throat, without conjunctivitis, coryza, coughing, hoarseness or diarrhea) increases the pre-test prevalence and, consequently, the sensitivity and specificity of the test.23,26,27

In a study carried out by Araújo Filho et al. with the adult population (18 to 69 years), the values observed for the sensitivity and specificity of the latex test were 93.9 and 68.7%, respectively. In that case, the specificity was lower than found in this article.

The LR is a statistical analysis that assesses the quality of a diagnostic test and helps with the selection of an appropriate diagnostic test.28 It offers advantages over determination of sensitivity and specificity because it alters less in response to the prevalence of a given disease. In a review of the literature, just one study was identified which had calculated the LR of an RADT, coming up with a value of 17.20 Our study found a positive LR of 9, which means that it is nine times more likely to observe a positive latex result in a patient who has a positive culture than in a patient with a negative culture.

The figures for sensitivity, specificity, NPV, PPV and positive LR observed here for the RADT used allow us to consider it a clinically useful method. In cases where the RADT result is negative, the current recommendations of the AAP, CDC, AHA and IDSA should be followed and an oropharynx swab culture be taken with the objective of maximizing conclusive etiologic diagnoses.

 

Acknowledgements

We are grateful to Dr. Zilda Maria Alves Meira for her help with data collection and to FAPEMIG - Fundação de Amparo à Pesquisa do Estado de Minas Gerais for partially funding the study, grant number CDS 873/90 (awarded to PAMC).

 

References

1. Bisno AL, Gerber MA, Gwaltney JM, Kaplan EL, Schwartz RH; Infectious Diseases Society of America. Practice guidelines for the diagnosis and management of group A streptococcal pharyngitis. Clin Infect Dis. 2002;35:113-25.        [ Links ]

2. Schwartz B, Marcy M, Phillips WR, Gerber MA, Dowell SF. Pharyngitis: principles of judicious use of antimicrobial agents. Pediatrics. 1998;101:171-4.        [ Links ]

3. Putto A. Febrile exudative tonsillitis: viral or streptococcal? Pediatrics. 1987;80:6-12.        [ Links ]

4. Dajani A, Taubert K, Ferrieri P, Peter G, Shulman S. Treatment of acute streptococcal pharyngitis and prevention of rheumatic fever: a statement for health professionals. Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease of the Council on Cardiovascular Disease in the Young, the American Heart Association. Pediatrics. 1995;96:758-64.        [ Links ]

5. Park SY, Gerber MA, Tanz RR, Hickner JM, Galliher JM, Chuang I, et al. Clinicians' management of children and adolescents with acute pharyngitis. Pediatrics. 2006;117:1871-8.         [ Links ]

6. Mattos C, Braga SL, Esteves CA, Branco JM, Gomes NL, Maldonado M, et al. Valvotomia mitral percutânea em pacientes com idade menor ou igual a 18 anos. Resultados imediatos e tardios. Arq Bras Cardiol. 1999;73:373-7.        [ Links ]

7. Bitar FF, Hayek P, Obeid M, Gharzeddine W, Mikati M, Dbaibo GS. Rheumatic fever in children: a 15-year experience in a developing country. Pediatr Cardiol. 2000;21:119-22.        [ Links ]

8. Provenzano Júnior SC, Sá MP, Bastos ES, Azevedo JA, Murad H, Gomes EL, et al. Plastia valvar mitral na doença cardíaca reumática e degeneração mixomatosa: estudo comparativo. Rev Bras Cir Cardiovasc. 2002;17:24-34.        [ Links ]

9. Mota CC, Meira ZM. Febre Reumática. In: Leão E, Correa EJ, Mota JA, Viana MB. Pediatria Ambulatorial. 4ª ed. Belo Horizonte: Coopmed; 2005. p. 733-9.        [ Links ]

10. McIsaac WJ, Kellner JD, Aufricht P, Vanjaka A, Low DE. Empirical validation of guidelines for the management of pharyngitis in children and adults. JAMA. 2004;291:1587-95.         [ Links ]

11. Breese BB. A simple scorecard for the tentative diagnosis of streptococcal pharyngitis. Am J Dis Child. 1977;131:514-7.        [ Links ]

12. Kaplan EL. Clinical guidelines for group A streptococcal throat infectious. Lancet. 1997;350:899-900.         [ Links ]

13. Hoffmann S. An algorithm for a selective use of throat swabs in the diagnosis of group A estreptococcal pharyngo-tonsillitis in general practice. Scand J Prim Health Care. 1992;10:295-300.        [ Links ]

14. American Academy of Pediatrics. Group A streptococcal infections. In: Pickering LK, editor. Red Book 2003: report of the Committee on Infectious Diseases. 26th ed. Elk Grove Village, IL: American Academy of Pediatrics; 2003. p. 573-84.        [ Links ]

15. Kobringer ME, Bresolin AM, Novaes HM. Afecções das vias aéreas superiores. In: Sucupira AC, Bresolin AM, Marcondes E, Souto MI, Dias MG, Zucolotto SM. Pediatria em Consultório. 3ª ed. São Paulo: Savier; 1996. p. 632.        [ Links ]

16. Miceika BG, Vitous AS, Thompson KD. Detection of group A streptococcal antigen directly from throat swabs with a ten-minute latex agglutination test. J Clin Microbiol. 1985;21:467-9.         [ Links ]

17. Fujikawa S, Ohkuni M. A new latex agglutination test for rapid diagnosis of group A strptococci. Jpn Circ J. 1986;50:25-31.        [ Links ]

18. Gupta R, Rattan A, Prakash K, Talwar GP, Gupta SK. Imunodiagnosis of group-A streptococci by latex agglutination assays with monoclonal or monospecific polyvalent antibodies. Indian J Med Res. 1993;97:25-31.        [ Links ]

19. Berezin EN, Jasinowodolinski D, Massarato LC, Gazzeta RE, Designe R, Raphaelian T, et al. Faringite estreptocócica: diagnóstico clínico e laboratorial. Rev Paul Pediatr. 1996;14:177-9.        [ Links ]

20. dos Santos AG, Berezin EN. Comparação entre métodos clínicos e laboratoriais no diagnóstico das faringotonsilites estreptocócicas. J Pediatr (Rio J). 2005;81:23-8.        [ Links ]

21. Araújo Filho BC, Imamura R, Sennes LU, Sakae FA. Papel do teste de detecção rápida do antígeno do estreptococcus beta-hemolítico do grupo A em pacientes com faringoamigdalites. Rev Bras Otorrinolaringol. 2006;72:12-6.        [ Links ]

22. Armengol CE, Schlager TA, Hendley JO. Sensitivity of a rapid antigen detection test for group A strepococci in a private pediatric office setting: answering the Red Book's request for validation. Pediatrics. 2004;113:924-6.         [ Links ]

23. Gieseker KE, Roe MH, MacKenzie T, Todd JK. Evaluating the American Academy of pediatrics diagnostic standard for Streptococcus pyogenes pharyngitis: backup culture versus repeat rapid antigen testing. Pediatrics. 2003;11:666-70.         [ Links ]

24. Hjortdahl P, Laerum E, Gaustad P. How reliable and useful is the latex agglutination test in diagnosing streptococcal throat infection in general practice? Scand J Prim Health Care. 1987;5:151-4.        [ Links ]

25. Schroeder S, Procop GW. False-positive strep A antigen test. Pediatr Infec Dis J. 2000;19:1114-5.        [ Links ]

26. Hall MC, Kieke B, Gonzales R, Belongia EA. Spectrum bias of a rapid antigen detection test for group a beta-hemolitic streptococcal pharyngitis in a pediatric population. Pediatrics. 2004;114:182-6.         [ Links ]

27. Edmonson MB, Farwell KR. Relationship between the clinical likelihood of group A streptococcal pharyngitis and the sensitivity of a rapid antigen-detection test in a pediatric practice. Pediatrics. 2005;115:280-5.         [ Links ]

28. Jaeschke R, Guyatt GH, Sackett DL. User's guide to the medical literature. III. How to use an article about a diagnosis test: What are the results and will they help me in caring for my patients? The Evidence-Based Medicine Working Group. JAMA. 1994;271:703-7.         [ Links ]

 

 

Correspondence:
Paulo A. M. Camargos
Departamento de Pediatria da Faculdade de Medicina da UFMG
Avenida Alfredo Balena, 190/4061
CEP 30130-100 - Belo Horizonte, MG - Brazil
Tel.: +55 (31) 3248.9773
Fax: +55 (31) 3248.9664
Email: pcamargs@medicina.ufmg.br, pauloamcamargos@gmail.com

Manuscript received Apr 20 2007, accepted for publication July 25 2007.

 

 

Partially supported by Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG), grant no. CDS 873/90.