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Brief Summary

GUIDELINE TITLE

Diagnosis and management of acute otitis media.

BIBLIOGRAPHIC SOURCE(S)

GUIDELINE STATUS

This is the current release of the guideline.

American Academy of Pediatrics (AAP) Policies are reviewed every 3 years by the authoring body, at which time a recommendation is made that the policy be retired, revised, or reaffirmed without change. Until the Board of Directors approves a revision or reaffirmation, or retires a statement, the current policy remains in effect.

** REGULATORY ALERT **

FDA WARNING/REGULATORY ALERT

Note from the National Guideline Clearinghouse: This guideline references a drug(s) for which important revised regulatory information has been released.

  • September 11, 2007, Rocephin (ceftriaxone sodium): Roche informed healthcare professionals about revisions made to the prescribing information for Rocephin to clarify the potential risk associated with concomitant use of Rocephin with calcium or calcium-containing solutions or products.

BRIEF SUMMARY CONTENT

 ** REGULATORY ALERT **
 RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

A definition of the recommendations rating scheme is provided at the end of the "Major Recommendations" field.

Recommendation 1: To diagnose acute otitis media (AOM), the clinician should confirm a history of acute onset, identify signs of middle-ear effusion, and evaluate for the presence of signs and symptoms of middle-ear inflammation. (Recommendation) (See Table 2 in the original guideline document.)

Recommendation 2: The management of AOM should include an assessment of pain. If pain is present, the clinician should recommend treatment to reduce pain. (Strong Recommendation)

Recommendation 3A: Observation without use of antibacterial agents in a child with uncomplicated AOM is an option for selected children based on diagnostic certainty, age, illness severity, and assurance of follow-up. (Option)

Recommendation 3B: If a decision is made to treat with an antibacterial agent, the clinician should prescribe amoxicillin for most children. (Recommendation) When amoxicillin is used, the dose should be 80 to 90 mg/kg/day. (Option)

Recommendation 4: If the patient fails to respond to the initial management option within 48 to 72 hours, the clinician must reassess the patient to confirm AOM and exclude other causes of illness. If AOM is confirmed in the patient initially managed with observation, the clinician should begin antibacterial therapy. If the patient was initially managed with an antibacterial agent(s), the clinician should change the antibacterial agent(s). (Recommendation)

Recommendation 5: Clinicians should encourage the prevention of AOM through reduction of risk factors. (Recommendation)

Recommendation 6: There is insufficient evidence to make a recommendation regarding the use of complementary and alternative medicine (CAM) for AOM. (No Recommendation)

Definitions:

Strong Recommendation

A strong recommendation in favor of a particular action is made when the anticipated benefits of the recommended intervention clearly exceed the harms (as a strong recommendation against an action is made when the anticipated harms clearly exceed the benefits) and the quality of the supporting evidence is excellent. In some clearly identified circumstances, strong recommendations may be made when high-quality evidence is impossible to obtain and the anticipated benefits strongly outweigh the harms. Clinicians should follow a strong recommendation unless a clear and compelling rationale for an alternative approach is present.

Recommendation

A recommendation in favor of a particular action is made when the anticipated benefits exceed the harms, but the quality of evidence is not as strong. Again, in some clearly identified circumstances, recommendations may be made when high-quality evidence is impossible to obtain but the anticipated benefits outweigh the harms. Clinicians would be prudent to follow a recommendation, but should remain alert to new information and sensitive to patient preferences.

Option

Options define courses that may be taken when either the quality of evidence is suspect or carefully performed studies have shown little clear advantage to one approach over another. Clinicians should consider the option in their decision making, and patient preference may have a substantial role.

No Recommendation

No recommendation indicates that there is a lack of pertinent published evidence and that the anticipated balance of benefits and harms is presently unclear. Clinicians should be alert to new published evidence that clarifies the balance of benefit versus harm.

CLINICAL ALGORITHM(S)

A clinical algorithm is provided in the original guideline document for the management of acute otitis media.

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

Recommendation 1: Based on observational studies and a preponderance of benefit over risk

Recommendation 2: Based on randomized, clinical trials with limitations and a preponderance of benefit over risk

Recommendation 3A: Based on randomized controlled trials with limitations and a relative balance of benefit and risk

Recommendation 3B:

  • Amoxicillin use: Based on randomized controlled trials with limitations and a preponderance of benefit over risk
  • Dosage: Based on extrapolation from microbiologic studies and expert opinion, with a preponderance of benefit over risk

Recommendation 4: Based on observational studies and a preponderance of benefit over risk

Recommendation 5: Based on strong observational studies and a preponderance of benefits over risks

Recommendation 6: Based on limited and controversial data

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

ADAPTATION

Not applicable: The guideline was not adapted from another source.

DATE RELEASED

2004

GUIDELINE DEVELOPER(S)

American Academy of Family Physicians - Medical Specialty Society
American Academy of Pediatrics - Medical Specialty Society

SOURCE(S) OF FUNDING

American Academy of Pediatrics

GUIDELINE COMMITTEE

Subcommittee on Management of Acute Otitis Media

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Committee Members: Allan S. Lieberthal, MD, Co-chairperson, AAP; Theodore G. Ganiats, MD, Co-chairperson, AAFP; Edward O. Cox, MD, AAP; Larry Culpepper, MD, MPH, AAFP; Martin Mahoney, MD, PhD, AAFP; Donald Miller, MD, MPH, AAP; Desmond K. Runyan, MD, DrPH, AAP; Nina Lisbeth Shapiro, MD, AAP; Ellen Wald, MD, AAP

Liaisons: Richard Besser, MD, Centers for Disease Control and Prevention; Ellen Friedman, MD, American Academy of Otolaryngology-Head and Neck Surgery; Norman Wendell Todd, MD, American Academy of Otolaryngology-Head and Neck Surgery

Consultants: S. Michael Marcy, MD; Richard M. Rosenfeld, MD, MPH; Richard Shiffman, MD

Staff: Maureen Hannley, PhD, AAO-HNS; Carla Herrerias, MPH, AAP; Bellinda Schoof, MHA, CPHQ, AAFP

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

Not stated

GUIDELINE STATUS

This is the current release of the guideline.

American Academy of Pediatrics (AAP) Policies are reviewed every 3 years by the authoring body, at which time a recommendation is made that the policy be retired, revised, or reaffirmed without change. Until the Board of Directors approves a revision or reaffirmation, or retires a statement, the current policy remains in effect.

GUIDELINE AVAILABILITY

Electronic copies: Available from the American Academy of Pediatrics (AAP) Policy Web site.

Print copies: Available from American Academy of Pediatrics, 141 Northwest Point Blvd., P.O. Box 927, Elk Grove Village, IL 60009-0927.

AVAILABILITY OF COMPANION DOCUMENTS

PATIENT RESOURCES

None available

NGC STATUS

This summary was completed by ECRI on June 8, 2004. The information was verified by the guideline developer on July 6, 2004. This summary was updated on May 3, 2005 following the withdrawal of Bextra (valdecoxib) from the market and the release of heightened warnings for Celebrex (celecoxib) and other nonselective nonsteroidal anti-inflammatory drugs (NSAIDs). This summary was updated by ECRI on June 16, 2005, following the U.S. Food and Drug Administration advisory on COX-2 selective and non-selective non-steroidal anti-inflammatory drugs (NSAIDs). This summary was updated by ECRI Institute on October 3, 2007 following the U.S. Food and Drug Administration (FDA) advisory on Rocephin (ceftriaxone sodium).

COPYRIGHT STATEMENT

This NGC summary is based on the original guideline, which is subject to the guideline developer's copyright restrictions. Please contact the Permissions Editor, American Academy of Pediatrics (AAP), 141 Northwest Point Blvd, Elk Grove Village, IL 60007.

DISCLAIMER

NGC DISCLAIMER

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