See related research article on page 23 and at www.cmaj.ca/lookup/doi/10.1503/cmaj.140772; see also case on page 50 and at www.cmaj.ca/lookup/doi/10.1503/cmaj.140155
Pharyngitis is common and a frequent presentation to family physicians and pediatricians.1 Most of these infections are caused by viruses, but about 20%–40% of cases in children are due to group A streptococcal infection.2,3 Differentiating between streptococcal and viral causes has proven difficult, because individual signs and symptoms are not sufficiently discerning.4 Thus, some expert guidelines recommend microbiologic testing.5 However, given the rarity of complications such as rheumatic fever in high-resource countries, the delay in obtaining throat culture results, an the large number of negative tests, physicians have frequently used a selective strategy of testing in some cases and starting antibiotic therapy before test results are received in others.1
Clinical prediction rules have been developed to help clinicians predict the likelihood of streptococcal infection more accurately, and to guide selective treatment decisions. Although several such rules have been developed,6 is has been suggested that none has the necessary sensitivity or specificity to eliminate the need for children to undergo microbiologic testing. Cohen and colleagues7 have reviewed the available clinical prediction rules for diagnosing and managing streptococcal pharyngitis in children and directly compared their diagnostic accuracy. They found that each clinical prediction rule required some degree of adaptation to incorporate rapid antigen detection testing. They then applied the adapted rules to patients in a validation cohort to classify each patient as being at low (no further testing or antibiotic therapy), intermediate (rapid antigen detection testing for all, antibiotics for those with positive test results) and high risk (empiric treatment) of streptococcal infection. With this strategy, they were unable to identify patients at low or high risk in whom microbiologic testing could be avoided.
Microbiologic testing for group A streptococcus includes culture-based approaches and rapid antigen detection tests. Throat culture is considered the gold standard and has a high sensitivity, but it may be associated with higher cost and delayed treatment. Rapid antigen detection tests are highly specific (95%) and can aid in making immediate clinical decisions, but they are limited by low sensitivity (70%–90%),8 which varies with disease spectrum, size of the bacterial inoculum and the person performing the test. A limitation of both test modalities is the inability to distinguish between colonization or carriage (occurring in 5%–20% of children age 3–15 yr) and infection.
Cohen and colleagues’ study is the first to use a validation cohort to evaluate the utility of various clinical prediction rules specifically in children. However, there are two caveats to keep in mind when interpreting the results. First, the children in the validation cohort were recruited by a relatively select group of academic French pediatricians in urban areas. The severity of illness in the validation cohort may have been toward the sicker end of the spectrum. The prevalence of positive test results in the low- and high-risk strata were similar using the various clinical prediction rules. Second, the study did not attempt to discern age-related differences in the utility of the clinical prediction rules. Achieving results for older children similar to those seen in adults is plausible.9 Despite these limitations, however, this paper highlights the need for further guidance in diagnosing and treating pharyngitis in children.
Owing to a substantial decline in the incidence of suppurative and nonsuppurative complications of group A streptococcal infection in high-resource settings, the importance of universally treating pharyngitis has been questioned.10 However, a Cochrane review has shown that antibiotic treatment of sore throat reduces the risk of otitis media and peritonsillar abscess, the duration of symptoms and the rate of acute rheumatic fever.11,12 In the United Kingdom, a reduction in prescribing antibiotics may have been a contributing factor for increased admissions for peritonsillar and retropharyngeal abscesses.13 Currently, many European guidelines recommend antibiotic treatment only for high-risk patients, whereas North American guidelines focus on treatment for all patients with group A streptococcal pharyngitis.10
So, which patients with sore throat should receive treatment? Given that most sore throats are caused by viruses, giving treatment to all patients would result in unnecessary antibiotic use in an era of increasing antimicrobial resistance.3 Having all patients undergo testing will reduce antibiotic exposure, but may be less desirable to physicians who have to follow-up with patients after their appointments to provide results or call in prescriptions. This strategy also involves higher cost and may lead to increased symptom duration.
Cohen and colleagues argue against a selective strategy for testing and treating owing to insufficient diagnostic accuracy of the clinical prediction rules. However, they make no comment on the cost-effectiveness of a universal testing strategy. Furthermore, for any strategy to be effective, it must be simple and have buy-in from frontline physicians. Data from the United States suggest that only half of physicians perform throat swabs, and half write a prescription before the results of the test are available.1 Similarly, a recent paper from Israel showed that only 54% of physicians adhered to guidelines recommending testing in all children.14 Cohen and colleagues do not address this question.
Currently, no Canadian consensus guideline on the approach to sore throat in children exists. We need to define a strategy that is safe, cost-effective and useful in both urban and rural settings. Canadian health organizations for family physicians, pediatricians and other relevant stakeholders should work together to define such a strategy. Whatever strategy they recommend should be accompanied by ongoing surveillance for group A streptococcal pharyngitis and its complications, antibiotic use and resistance rates. Further research is needed to determine whether clinical prediction rules could be useful, perhaps by focusing on specific age strata.
Key PointsCurrent clinical prediction rules are insufficiently sensitive and specific to guide management of acute pharyngitis in children.
Increasing antibiotic resistance and the rarity of complications associated with group A streptococcal pharyngitis in high-resource countries suggest that a new approach is needed in the approach to acute pharyngitis.
The time has come for a Canadian strategy that will take into account safety, cost, antimicrobial resistance and physician practices.
Footnotes
Competing interests: Warren McIsaac developed one of the clinical decision rules that was evaluated in the article by Cohen and colleagues. No other competing interests were declared.
This article was solicited and has not been peer reviewed.
Contributors: Each of the authors conceived the idea for the manuscript. Michelle Science drafted the manuscript, which was revised by Ari Bitnun and Warren McIsaac for important intellectual content. All of the authors approved the final version submitted for publication.