Streptococcal Pharyngitis: Rapid Evidence Review

Jennifer L. Hamilton, MD, PhD
Leon McCrea, II, MD, MPH

American Family Physician. 2024;109(4):343-349.

Author disclosure: No relevant financial relationships.

Group A beta-hemolytic streptococcal pharyngitis is a common infection responsible for more than 6 million office visits in the United States annually. Only 10% of adults seeking care for a sore throat have group A beta-hemolytic streptococcal pharyngitis; however, 60% or more are prescribed antibiotics. Guidelines recommend using clinical decision rules to assess the risk of group A beta-hemolytic streptococcal infection, followed by rapid antigen testing if a diagnosis is unclear, before prescribing antibiotics. Fever, tonsillar exudate, cervical lymphadenitis, and patient ages of 3 to 15 years increase clinical suspicion. A cough is more suggestive of a viral etiology. The limited history used in these decision rules is amenable to virtual visits. After a negative rapid antigen test result, a throat culture is recommended in children and adolescents. Penicillin and amoxicillin are first-line antibiotics, with a recommended course of 10 days; first-generation cephalosporins are recommended for patients with nonanaphylactic allergies to penicillin. There is significant resistance to azithromycin and clarithromycin in some parts of the United States. Steroids are not recommended for symptomatic treatment. Patients with worsening symptoms after appropriate antibiotic initiation or with symptoms lasting 5 days after the start of treatment should be reevaluated. Tonsillectomy is rarely recommended as a preventive measure: seven episodes of streptococcal pharyngitis in 1 year, five episodes in each of the past 2 years, or three episodes in each of the past 3 years are commonly used thresholds for considering surgery.

More than 24 million episodes of pharyngitis are diagnosed annually in the United States, with more than 6 million office visits attributable to group A beta-hemolytic streptococcal infection.1 This article provides a summary of the best available patient-oriented evidence about streptococcal pharyngitis and guideline recommendations using clinical decision rules to assess the risk of group A beta-hemolytic streptococcal infection, followed by rapid antigen testing if a diagnosis is unclear.

WHAT'S NEW ON THIS TOPIC

Streptococcal Pharyngitis
A 2021 study of patients who had telemedicine and face-to-face visits on the same day noted that patients assessed as having low-risk McIsaac scores in the telemedicine visit also had low-risk scores in face-to-face visits.
In a cohort study, the use of broad-spectrum antibiotics for children with group A beta-hemolytic streptococcal pharyngitis was not associated with a reduction in the rate of treatment failure compared with narrow-spectrum antibiotics.
Acute rheumatic fever is increasingly rare. It has an estimated incidence of 0.5 episodes per 100,000 people in the continental United States, with higher rates in the Pacific Islands. Rheumatic heart disease develops in 50% to 70% of people with rheumatic fever.

SORT: KEY RECOMMENDATIONS FOR PRACTICE

GABHS = group A beta-hemolytic streptococcal.

A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For information about the SORT evidence rating system, go to https://www.aafp.org/afpsort.

JENNIFER L. HAMILTON, MD, PhD, FAAFP, is the associate dean for medical education – simulation, the family medicine pathway director, and a professor in the Department of Family, Community, and Preventive Medicine at Drexel University College of Medicine, Philadelphia, Pa.

LEON MCCREA II, MD, MPH, FAAFP, is the Deborah J. Tuttle, MD, and John P. Piper, MD, vice dean for educational affairs and an associate professor in the Department of Family, Community, and Preventive Medicine at Drexel University College of Medicine.

Address correspondence to Jennifer L. Hamilton, MD, PhD, FAAFP, Drexel University College of Medicine, 60 N. 36th Street, HSB Room 7E09, Philadelphia, PA 19104 (jlh88@drexel.edu). Reprints are not available from the authors.

Author disclosure: No relevant financial relationships.

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