eMedicine Specialties > Infectious Diseases > HEENT Infections

Pharyngitis, Bacterial: Treatment & Medication

Author: Eric S Halsey, MD, Chief, Department of Infectious Diseases, Wright-Patterson Air Force Base; Assistant Professor of Medicine, Uniformed Services University of the Health Sciences; Assistant Professor of Medicine, Wright State University
Contributor Information and Disclosures

Updated: May 19, 2009

Treatment

Medical Care

Overzealous prescription of antibiotics for pharyngitis has been estimated to cost health payers $1.2 billion annually.27 Therefore, treatment of GABHS pharyngitis should be initiated only after confirmation with a RADT or throat culture.13 Alternatively, treatment in high-risk patients may be started before throat culture results are available, but antibiotics should be stopped if the culture returns negative results. Even though most cases of GABHS pharyngitis resolve after 3-4 days without treatment, antibiotics decrease the likelihood of local suppurative complications and acute rheumatic fever. Oral antibiotics should be administered for 10 days, although many recent studies show similar efficacy with shorter courses.28 Antibiotic therapy does not decrease the likelihood of poststreptococcal glomerulonephritis.

Oral penicillin V remains the preferred antibiotic to treat GABHS pharyngitis.13 In vitro, no isolate of GABHS has ever been resistant to penicillin. Other reasons favoring oral penicillin include its narrow spectrum, low cost, infrequent adverse effects, and proven track record. Nevertheless, GABHS is sensitive to many other antibiotics, thereby allowing flexibility based on numerous factors.

The following circumstances dictate that a choice other than penicillin V should be used:

  • Compliance: Oral penicillin requires multiple daily doses and a 10-day course. In patients unlikely to adhere to this regimen, one dose of intramuscular benzathine penicillin provides a depot that releases medication over the course. Azithromycin, cefdinir, and cefpodoxime may all be given in 5-day courses, although none of these medications is yet considered a first-line agent.13,29 Recent reports have supported the use of once-daily amoxicillin and verified its noninferiority to twice-daily penicillin30 or twice-daily amoxicillin.31
  • Palatability: Some young children find oral penicillin unpalatable. Taste tests and many doctors’ experiences have shown amoxicillin to be much better tolerated.32 Amoxicillin’s similar spectrum and low cost make it a reasonable substitute.
  • Allergy: In patients with an immunoglobulin E (IgE)–mediated penicillin allergy, antibiotics that contain a beta-lactam ring (cephalosporins, amoxicillin) should be used with extreme caution. Although cross-reactivity between penicillin and cephalosporins is probably less than 10%, the risk of anaphylaxis justifies the consideration of other viable agents.33 Macrolides such as azithromycin and erythromycin may be used, although resistance has been reported in the United States34 and internationally.35
  • Recurrence: Test of cure is not indicated when pharyngitis symptoms have resolved following treatment. In patients with recurrent symptoms, retreatment with an initial first-line agent (oral penicillin, benzathine penicillin, erythromycin, or a first-generation cephalosporin) is reasonable. Worth noting is the difficulty in differentiating between viral pharyngitis with GABHS carriage and actual GABHS pharyngitis. This becomes even more of an issue in patients with multiple recurrences. Between 5% and 15% of children are asymptomatic carriers during seasons when GABHS pharyngitis is most prevalent.36 A positive test result during a time of wellness may indicate GABHS carriage. When multiple recurrences are believed to be due to GABHS infection, clindamycin or amoxicillin/clavulanic acid is indicated.13 Benzathine penicillin with or without rifampin may be given when noncompliance is suspected to have been responsible for previous failures.

Surgical Care

In rare cases, pharyngitis spreads to adjacent structures and forms abscesses. In these cases, a drainage procedure performed by an interventional radiologist or otolaryngologist should be considered.

Consultations

  • An otolaryngologist should be consulted for local suppurative complications such as peritonsillar abscess and mastoiditis. Tonsillectomy may be considered in recurrent GABHS infection.37
  • An infectious diseases expert may be consulted for patients with immunocompromising conditions or when an agent other than GABHS (eg, HIV) is suspected or confirmed.

Diet

Allow a regular diet as tolerated in patients with bacterial pharyngitis. Warm liquids may provide symptomatic relief.

Activity

Encourage rest during the acute illness.

Medication

The goals of pharmacotherapy are to eradicate the infection, to reduce morbidity, and to prevent complications.

Antibiotics

Oral penicillin is currently the drug of choice for GABHS pharyngitis.13 Amoxicillin remains a reliable alternative and offers advantages in terms of easier dosing and increased palatability.

Tetracyclines and trimethoprim/sulfamethoxazole should not be used to treat GABHS pharyngitis owing to higher rates of resistance.


Penicillin G benzathine (Bicillin L-A, Permapen)

Interferes with synthesis of cell wall by binding to penicillin-binding proteins. Penicillin is the drug of choice to treat GABHS pharyngitis, as recommended by expert committees of the American Heart Association, American Academy of Pediatrics, and the Infectious Disease Society of America, because of proven efficacy, safety, narrow spectrum, and low cost. Preferred for patients unlikely to complete a full 10-d PO course. S pyogenes remains universally sensitive to penicillin.

Adult

1.2 million U IM once

Pediatric

<27 kg: 600,000 U IM once
>27 kg: Administer as in adults

Probenecid can increase penicillin effectiveness by decreasing clearance

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Caution in impaired renal function


Penicillin VK (Beepen VK)

Treatment of choice for GAS pharyngitis, as recommended by expert committees of the American Heart Association, American Academy of Pediatrics, and the Infectious Disease Society of America, because of its proven efficacy, safety, narrow spectrum, and low cost. Inhibits biosynthesis of cell wall by binding to penicillin-binding proteins. Bactericidal against sensitive organisms when adequate concentrations are reached and most effective during stage of active multiplication. Inadequate concentrations may be ineffective. GABHS remains uniformly susceptible in vitro.

Adult

250 mg PO tid/qid or 500 mg PO bid for 10 d

Pediatric

Children: 250 mg PO bid/tid for 10 d
Adolescents: 250 mg PO tid/qid for 10 d or 500 mg PO bid for 10 d

Probenecid may increase effectiveness by decreasing clearance

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in renal impairment


Amoxicillin (Amoxil, Biomox, Trimox)

Interferes with synthesis of cell wall mucopeptides by binding to penicillin-binding proteins. Often used in place of oral penicillin VK in young children. Efficacy equal to penicillin, and often chosen because of the unpalatability of the penicillin susp.

Adult

500 mg PO bid for 10 d; recent studies have shown that once-daily dosing has equal efficacy; forthcoming guidelines may include this as an option

Pediatric

<40kg, 375mg PO bid for 10 d
>40kg, 500mg PO bid for 10 d; recent studies have shown that once daily dosing has equal efficacy; forthcoming guidelines may include this as an option

Reduces efficacy of oral contraceptives

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in renal impairment; may enhance risk of candidiasis; patients with infectious mononucleosis may develop a rash if given this antibiotic


Azithromycin (Zithromax)

Inhibits RNA-dependent protein synthesis at the 50s ribosome. Can be given as a single daily dose, is better tolerated than erythromycin in patients who are allergic to penicillin, and is effective in a 5-d course. However, much more expensive and should be avoided as first-line therapy in patients with streptococcal pharyngitis. Sporadic resistance has been reported.

Adult

Day 1: 500 mg PO
Days 2-5: 250 mg PO qd

Pediatric

<6 months: Not established
>6 months
Day 1: 10 mg/kg PO once; not to exceed 500 mg/d
Days 2-5: 5 mg/kg PO qd; not to exceed 250 mg/d

May increase toxicity of theophylline, warfarin, and digoxin; effects are reduced with coadministration of aluminum and/or magnesium antacids; nephrotoxicity and neurotoxicity may occur when coadministered with cyclosporine

Documented hypersensitivity; hepatic impairment; do not administer with pimozide

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Bacterial or fungal overgrowth may result with prolonged antibiotic use; may increase hepatic enzymes and cholestatic jaundice; caution in patients with impaired hepatic function, prolonged QT intervals, or pneumonia; caution in patients who are hospitalized, elderly, or debilitated


Erythromycin (E.E.S., E-Mycin, Ery-Tab, Erythrocin)

Inhibits RNA-dependent protein synthesis at the 50s ribosome. An option in those with severe allergic reactions to beta-lactam antibiotics. Sporadic resistance has been reported.

Adult

333 mg PO tid for 10 d or 500 mg PO qid for 10 d

Pediatric

20-40 mg/kg/d PO in 2-4 divided doses for 10 d

Coadministration may increase toxicity of theophylline, digoxin, carbamazepine, and cyclosporine; may potentiate anticoagulant effects of warfarin; coadministration with lovastatin and simvastatin increases risk of rhabdomyolysis

Documented hypersensitivity; hepatic impairment

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Liver disease; estolate formulation may cause cholestatic jaundice; adverse GI effects are common; discontinue use if nausea, vomiting, malaise, abdominal colic, or fever occur


Clindamycin (Cleocin)

Belongs to the lincosamide class of antibiotics. Binds to the 50s ribosome and prevents bacterial protein synthesis. Is an option for symptomatic patients with multiple, recurrent episodes of pharyngitis proven by culture or rapid antigen testing.

Adult

600 mg/d PO divided bid/qid for 10 d

Pediatric

20-30 mg/kg/d PO tid for 10 d

Increases duration of neuromuscular blockade induced by tubocurarine and pancuronium; erythromycin may antagonize effects

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in severe hepatic dysfunction; no adjustment necessary in renal insufficiency; associated with severe and possibly fatal colitis by allowing overgrowth of Clostridium difficile


Cephalexin (Keflex)

First-generation cephalosporin that arrests bacterial growth by inhibiting bacterial cell wall synthesis. Bactericidal activity against rapidly growing organisms. Oral cephalosporins are highly effective for streptococcal pharyngitis, and several studies have found them to have slightly higher eradication rates than those of penicillin. Second-line agents in the treatment of patients with GABHS pharyngitis.

Adult

500 mg PO bid for 10 d

Pediatric

25-50 mg/kg/d PO divided bid for 10 d

May increase level of metformin

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in renal impairment

More on Pharyngitis, Bacterial

Overview: Pharyngitis, Bacterial
Differential Diagnoses & Workup: Pharyngitis, Bacterial
Treatment & Medication: Pharyngitis, Bacterial
Follow-up: Pharyngitis, Bacterial
Multimedia: Pharyngitis, Bacterial
References

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Further Reading

Keywords

bacterial pharyngitis, tonsillopharyngitis, acute tonsillitis, sore throat, group A Streptococcus, GAS, streptococcal pharyngitis, Streptococcus pyogenes, S pyogenes, acute pharyngitis, upper respiratory tract infections, streptococcal fever, rheumatic fever, rheumatic heart disease, acute rheumatic fever, scarlet fever, acute glomerulonephritis, poststreptococcal glomerulonephritis, Yersinia enterocolitica, Y enterocolitica, Neisseria gonorrhoeae, N gonorrhoeae, Mycoplasma pneumoniae, M pneumoniae, Corynebacterium diphtheriae, C diphtheriae, Chlamydia pneumoniae, C pneumoniae, Arcanobacterium haemolyticum, A haemolyticum, Corynebacterium diphtheriae, respiratory diphtheria, non-group A Streptococcus, non-GAS infection, GABHS

Contributor Information and Disclosures

Author

Eric S Halsey, MD, Chief, Department of Infectious Diseases, Wright-Patterson Air Force Base; Assistant Professor of Medicine, Uniformed Services University of the Health Sciences; Assistant Professor of Medicine, Wright State University
Eric S Halsey, MD is a member of the following medical societies: American College of Physicians, Armed Forces Infectious Diseases Society, HIV Medicine Association of America, and Infectious Diseases Society of America
Disclosure: Nothing to disclose.

Medical Editor

Kenneth C Earhart, MD, Deputy Head, Disease Surveillance Program, United States Naval Medical Research Unit #3
Kenneth C Earhart, MD is a member of the following medical societies: American College of Physicians, American Society of Tropical Medicine and Hygiene, Infectious Diseases Society of America, and Undersea and Hyperbaric Medical Society
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

Managing Editor

Gordon L Woods, MD, Consulting Staff, Department of Internal Medicine, University Medical Center
Gordon L Woods, MD is a member of the following medical societies: Society of General Internal Medicine
Disclosure: Nothing to disclose.

CME Editor

Eleftherios Mylonakis, MD, Clinical and Research Fellow, Department of Internal Medicine, Division of Infectious Diseases, Massachusetts General Hospital
Eleftherios Mylonakis, MD is a member of the following medical societies: American Association for the Advancement of Science, American College of Physicians, American Society for Microbiology, and Infectious Diseases Society of America
Disclosure: Nothing to disclose.

Chief Editor

Burke A Cunha, MD, Professor of Medicine, State University of New York School of Medicine at Stony Brook; Chief, Infectious Disease Division, Winthrop-University Hospital
Burke A Cunha, MD is a member of the following medical societies: American College of Chest Physicians, American College of Physicians, and Infectious Diseases Society of America
Disclosure: Nothing to disclose.

 
 
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