eMedicine Specialties > Emergency Medicine > Ear, Nose, & Throat

Otitis Media: Treatment & Medication

Author: Brenda Liz Natal, MD, Clinical Assistant Instructor and Staff Physician, Department of Emergency Medicine, Kings County Hospital and State University of New York Downstate, Brooklyn
Coauthor(s): Jennifer H Chao, MD, FAAP, Clinical Assistant Professor of Pediatric Emergency Medicine, University Hospital of Brooklyn; Attending Physician, Pediatric Emergency Department, Kings County Hospital, Brooklyn
Contributor Information and Disclosures

Updated: Nov 2, 2009

Treatment

Emergency Department Care

According to American Academy of Pediatrics (AAP) and American Academy of Family Physicians (AAFP) guidelines for the treatment of acute otitis media, an observation period may be recommended depending on the patient's age, the diagnostic certainty, and the severity of illness.6

  • Diagnostic certainty is based on all 3 of the following criteria: acute onset, middle ear effusion (MEE), and middle ear inflammation.
  • Severe illness is defined as moderate-to-severe otalgia or temperature greater than 39°C, whereas nonsevere illness is defined as mild otalgia and temperature less than 39°C.

Diagnosis: The definition of acute otitis media (AOM) is relatively uniform; however, the diagnosis is not always as clear. It is this uncertainty in diagnosis which may lead to overdiagnosis and unnecessary antibiotic use or to underdiagnosis and an increase in complications.

  • Overdiagnosis of acute otitis media is frequently a result of all of the following:
    • Difficulty in differentiating AOM from otitis media with effusion (OME)
    • Difficulty in confirming middle ear effusion
    • Poor compliance with guidelines for diagnosis (Diagnosis of AOM meets all 3 of the criteria: rapid onset, presence of MEE, and signs and symptoms of middle ear inflammation.)
  • Several studies have demonstrated the difficulty and inconsistency with which practitioners diagnose acute otitis media.7,8 In a study of inter-rater agreement of AOM in children, Blomgren et al noted a substantial discrepancy concerning practitioner impressions of the tympanic membrane. The clinicians agreed only on 64% of the diagnoses of AOM. The use of a pneumatic otoscopy and tympanometry reduces the number of acute otitis media diagnoses by greater than 30%, suggesting that acute otitis media is misdiagnosed often.9

Treatment recommendations are as follows:

  • Infants younger than 6 months should receive antibiotics.
  • Children aged 6 months to 2 years should receive antibiotics if the diagnosis is certain. If the diagnosis is uncertain, an observation period can be considered if the illness is nonsevere, and antibiotic therapy can be considered for severe illness.
  • Children aged 2 years and older should receive antibiotics if the diagnosis is certain and if the illness is severe. An observation period is an option when the diagnosis is uncertain or when it is certain and nonsevere.
    • The observation option is a 48- to 72-hour period of symptomatic treatment with analgesics and without antibiotics.
    • For an observation option to be considered, the parent or caregiver must be able to communicate with the clinician and have access to follow-up care whenever problems ensue or symptoms worsen.
    • Pain management is an important part of treating AOM. Appropriate analgesics should be offered.
    • If prescribed antibiotics, children younger than 2 years old and those aged 2-5 years with severe disease should receive 10-days of therapy. For those who are 6 years old and older with mild to moderate disease, 5-7 days is appropriate.
    • Studies in the ED setting have shown that the observation option is both feasible and well accepted.10,11
  • Recent studies have also shown that, despite adequate access to clinical guidelines, the prescribing rates for antibiotics in AOM in some emergency departments remain high.12

Criteria for Initial Antibacterial Agent Treatment or Observation in Children With Acute Otitis Media2

Open table in new window

Table
AgeCertain DiagnosisUncertain Diagnosis
<6 moAntibacterial therapyAntibacterial therapy
6 mo–2 yAntibacterial therapyAntibacterial therapy if severe illness; observation option* if nonsevere illness
>2 yAntibacterial therapy if severe illness; observation option* if nonsevere illnessObservation option*
AgeCertain DiagnosisUncertain Diagnosis
<6 moAntibacterial therapyAntibacterial therapy
6 mo–2 yAntibacterial therapyAntibacterial therapy if severe illness; observation option* if nonsevere illness
>2 yAntibacterial therapy if severe illness; observation option* if nonsevere illnessObservation option*
*Observation is an appropriate option only when follow-up can be ensured and antibacterial agents started if symptoms persist or worsen. Nonsevere illness is mild otalgia and fever less than 39°C in the past 24 hours. Severe illness is moderate-to-severe otalgia or fever greater than or equal to 39°C. A certain diagnosis of acute otitis media meets all 3 criteria: (1) rapid onset, (2) signs of middle ear effusion (MEE), and (3) signs and symptoms of middle-ear inflammation.2

Consultations

  • In general, patients with acute otitis media seen in the ED should be referred to a primary care provider for follow-up care.
  • Patients discharged with or without antibiotic therapy should be reexamined 4-6 weeks after their initial presentation for evidence of middle ear aeration.
  • Patients whose symptoms (eg, pain, fever) do not resolve within 48-72 hours of treatment should be reevaluated.  
  • Patients with persistent symptoms or recurrent acute otitis media (AOM) should be referred to an otorhinolaryngologist for evaluation and possible tympanocentesis.

Medication

  • Studies have shown that antibiotics provide little benefit beyond placebo in mild cases of acute otitis media (AOM).
  • Infants with frequent recurrences may be considered for daily antibiotic prophylaxis with sulfamethoxazole or amoxicillin for a period of several months. However, the decrease in frequency of recurrent episodes is small to none.13,14
  • The potential consequences of excessive antibiotic use are also well known, and newer recommendations are that antibiotic prophylaxis for AOM should be avoided whenever possible.
  • The management of AOM should always include assessment of pain and fever. Antipyretics and analgesics may be necessary and should be prescribed liberally. Steroids, decongestants, and antihistamines are not effective in the treatment of AOM, and they may cause complications.
  • Several complimentary and/or alternative medicine (CAM) therapies, such as homeopathy, acupuncture, herbal remedies, chiropractic treatments, and nutritional supplements, have been used by parents/caregivers for the treatment of AOM. The preferred therapy is largely dependent on cultural background and/or practices. Data supporting complimentary and alternative therapies are limited and controversial. Currently, there are no recommendations for the use of CAM for the treatment of AOM.2
  • If antibiotic therapy is chosen, the AAP and FAAP recommend that amoxicillin 80-90 mg/kg/d is the antibiotic of choice. The length of treatment is 10 days for younger children and patients with severe illness, otherwise, a 5- to 7-day course is appropriate.
  • Routine use of the conjugated heptavalent pneumococcal vaccine (PCV 7) in children younger than 2 years may have changed the microbiology of AOM in vaccinees, by increasing the proportion of gram-negative bacteria as a cause; in which case, an antibiotic with beta-lactamase activity may be preferable. Currently though, the recommendations for antibiotics remain unchanged.15
  • If additional beta-lactamase-positive H influenzae and/or Moraxella catarrhalis coverage is desired, high-dose amoxicillin and clavulanate potassium is recommended.
  • If the patient is allergic to amoxicillin, alternatives are cefdinir, cefpodoxime, or cefuroxime if the allergic reaction is not a type 1 hypersensitivity. Patients with type 1 hypersensitivity should be given azithromycin or clarithromycin. Other alternatives are clindamycin and ceftriaxone given intravenously or intramuscularly. Ceftriaxone 50 mg/kg/d is recommended for children who are unable to take oral antibiotics and for patients with compliance problems.
  • In patients whose condition fails to improve after initial antibiotic therapy, a 3-day course of ceftriaxone offers outcomes better than those of a 1-day course.
  • When prescribing antibiotics to the pediatric population, one also has to consider the probability of noncompliance to therapy. In this age group, the palatability of a drug may influence adherence to treatment. If prescribing cephalosporins, consider the use of cefdinir (Omnicef) as it has a more accepted taste when compared with the other recommended cephalosporins (eg, cefuroxime).16
  • Topical quinolones are the preferred agents for the treatment of AOM in children with tympanostomy tubes (AOMT) and/or perforations. The treatment options for AOMT, as discussed in a clinical review by Schmelzle et al include systemic or topical antibiotics. Topical treatment with fluoroquinolones is superior than systemic antibiotics and results in less antibiotic resistance and fewer adverse effects (ototoxicity) than other treatments.17
  • Topical aminoglycosides should be avoided and not used to treat the draining ear because of potential ototoxicity.17
  • Addition of dexamethasone to a topical antibiotic may decrease the length of time necessary for middle ear drainage when compared with a topical antibiotic alone. The evidence for superior outcomes with the addition of steroids is lacking strength, and the addition of the steroids to the management exacerbates overall treatment costs; and this may lead to nonadherence to treatment.17

Antibiotics

Empiric antimicrobial therapy must be comprehensive and should cover all likely pathogens in the context of the clinical setting.


Cefdinir (Omnicef)

Used to treat acute bacterial otitis media. Classified as a third-generation cephalosporin and inhibits mucopeptide synthesis in the bacterial cell wall. Typically bactericidal, depending on organism susceptibility, dose, and serum or tissue concentrations.

Adult

300 mg PO q12h for 5-10 d
Alternative: 600 mg PO qd for 10 d

Pediatric

<6 months: Not established
6 months to 13 years: 7 mg/kg PO q12h or 14 mg/kg PO qd; not to exceed 600 mg/d
>13 years: Administer as in adults

May increase hypoprothrombinemic effects of anticoagulants; coadministration with potent diuretics and aminoglycosides (eg, loop diuretics) may increase nephrotoxicity

Pregnancy

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

Precautions

Reduce dosage by 1/2 if creatinine clearance is 10-30 mL/min, and by 3/4 if <10 mL/min; bacterial or fungal overgrowth of nonsusceptible organisms may occur with prolonged or repeated therapy


Ofloxacin (Floxin)

Inhibits bacterial growth by inhibiting DNA gyrase.

Adult

5-10 gtt in affected ear bid

Pediatric

Administer as in adults

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Failure to respond after treating for 2-3 d may indicate presence of resistant organism or another causative agent


Amoxicillin (Amoxil, Biomox)

Interferes with synthesis of cell wall mucopeptides during active multiplication, resulting in bactericidal activity against susceptible bacteria. Inexpensive and effective, even in populations with certain highly resistant bacteria.

Adult

250-500 mg PO q8h

Pediatric

80-90 mg/kg/d PO divided q8h for 10 d in younger children and in patients with severe disease

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; use in Ebstein-Barr viral mononucleosis increases risk of severe rash


Amoxicillin and clavulanate potassium (Augmentin)

Drug combination treats bacteria resistant to beta-lactam antibiotics. For children >3 mo, base dosing protocol on amoxicillin content. Because of different amoxicillin and clavulanate ratios in 250-mg tab (250/125) vs 250-mg chewable tab (250/62.5), do not use 250-mg tab until child weighs >40 kg.

Adult

500-875 mg PO q12h PO or 250-500 mg PO q8h

Pediatric

90 mg/kg (amoxicillin) with 6.4 mg/kg (clavulanate) divided PO q12h

Coadministration with warfarin or heparin increases risk of bleeding

Pregnancy

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

Precautions

Give for minimum of 10 d to eliminate organism and prevent sequelae (eg, endocarditis, rheumatic fever); after treatment, perform cultures to confirm eradication of streptococci

Analgesics

Relief of pain is one of the prime functions of effective treatment. Oral analgesics or topical medications may be required for relief of pain. Appropriate doses of acetaminophen or ibuprofen are available in tablet or liquid form. Codeine may be used as an ancillary agent; however, it may provoke emesis or constipation.


Benzocaine (Americaine, Cylex)

Inhibits neuronal membrane depolarization, blocking nerve impulses. Drops may be used as local anesthetic, with some benefit.

Adult

2-3 gtt q4-6h prn

Pediatric

Administer as in adults

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Not intended for use when infection present


Acetaminophen (Tylenol, Tempra, Panadol)

Used worldwide for antipyretic effects and mild analgesic effects. DOC for pain in patients with documented hypersensitivity to aspirin or NSAIDs, with upper GI disease, or with oral anticoagulation. May be used with ibuprofen for additive effects.

Adult

650 mg PO q4-6h; not to exceed 4 g/d

Pediatric

15-20 mg/kg/dose q4-6h; not to exceed 2.6 g/d

Rifampin can reduce analgesic effects; coadministration with barbiturates, carbamazepine, hydantoins, and isoniazid may increase hepatotoxicity

Documented hypersensitivity; G-6-PD deficiency

Pregnancy

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

Precautions

Hepatotoxicity possible in chronic alcoholism at various doses; severe or recurrent pain or high or continued fever may indicate serious illness; acetaminophen contained in many OTC products, and combined use of acetaminophen products may result in cumulative doses exceeding recommended maximum


Ibuprofen (Motrin, Ibuprin, Advil)

DOC for mild to moderate pain. Inhibits inflammatory reactions and pain by decreasing prostaglandin synthesis. Approved for use in children. Available as inexpensive liquid form, allowing for effective dosing in infants.

Adult

400-800 mg PO q6-8h for pain or fever; not to exceed 3.2 g/d

Pediatric

10 mg/kg PO (100 mg/5 mL) q6h for pain or fever

Coadministration with aspirin increases risk of inducing serious NSAID-related adverse effects; probenecid may increase concentrations and, possibly, toxicity of NSAIDs; may decrease effect of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; closely monitor PT (instruct patients to watch for signs of bleeding); may increase risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently

Documented hypersensitivity; peptic ulcer disease; recent GI bleeding or perforation; renal insufficiency; high risk of bleeding

Pregnancy

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

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

At therapeutic doses, can cause renal failure and/or gastric upset (more common in elderly persons but also described in children); caution in congestive heart failure, hypertension, and decreased renal and hepatic function; caution in anticoagulation abnormalities or during anticoagulant therapy

More on Otitis Media

Overview: Otitis Media
Differential Diagnoses & Workup: Otitis Media
Treatment & Medication: Otitis Media
Follow-up: Otitis Media
Multimedia: Otitis Media
References

References

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Further Reading

Keywords

OM, otitis media, ear infection, otitis media symptoms, otitis media causes, otitis media treatment, middle ear inflammation, acute otitis media, AOM, middle ear infection, middle ear effusion, MEE, otitis media with effusion, OME, bulging tympanic membrane, upper respiratory infection, viral infection

Contributor Information and Disclosures

Author

Brenda Liz Natal, MD, Clinical Assistant Instructor and Staff Physician, Department of Emergency Medicine, Kings County Hospital and State University of New York Downstate, Brooklyn
Brenda Liz Natal, MD is a member of the following medical societies: American College of Emergency Physicians and American Medical Association
Disclosure: Nothing to disclose.

Coauthor(s)

Jennifer H Chao, MD, FAAP, Clinical Assistant Professor of Pediatric Emergency Medicine, University Hospital of Brooklyn; Attending Physician, Pediatric Emergency Department, Kings County Hospital, Brooklyn
Jennifer H Chao, MD, FAAP is a member of the following medical societies: American Academy of Pediatrics
Disclosure: Nothing to disclose.

Medical Editor

Jerry Balentine, DO, Professor of Emergency Medicine, New York College of Osteopathic Medicine; Executive Vice President, Chief Medical Officer, Attending Physician in Department of Emergency Medicine, St. Barnabas Hospital
Jerry Balentine, DO is a member of the following medical societies: American College of Emergency Physicians, American College of Osteopathic Emergency Physicians, American College of Physician Executives, American Osteopathic Association, and New York Academy of Medicine
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

Mark W Fourre, MD, Program Director, Department of Emergency Medicine, Maine Medical Center; Associate Clinical Professor, Department of Surgery, University of Vermont School of Medicine
Disclosure: Nothing to disclose.

CME Editor

John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center
John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Chief Editor

Pamela L Dyne, MD, Professor of Clinical Medicine/Emergency Medicine, David Geffen School of Medicine at UCLA; Attending Physician, Department of Emergency Medicine, Olive View-UCLA Medical Center
Pamela L Dyne, MD is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

 
 
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