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Brief Summary

GUIDELINE TITLE

Practice guidelines for outpatient parenteral antimicrobial therapy.

BIBLIOGRAPHIC SOURCE(S)

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: Practice guidelines for community-based parental anti-infective therapy. Clin Infect Dis 1997 Oct;25(4):787-801.

** REGULATORY ALERT **

FDA WARNING/REGULATORY ALERT

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

BRIEF SUMMARY CONTENT

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

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Executive Summary

These guidelines were formulated to assist physicians and other health care professionals with various aspects of the administration of outpatient parenteral antimicrobial therapy (OPAT). Although there are many reassuring retrospective studies on the efficacy and safety of OPAT, few prospective studies have been conducted to compare the risks and outcomes for patients who receive treatment as outpatients rather than as inpatients. Because truly evidence-based studies are lacking, the present guidelines are formulated from the collective experience of the committee members and advisors from related organizations.

Important aspects of OPAT are described in the text and tables in the original guideline document and include the following:

  1. The literature supports the effectiveness of OPAT for a wide variety of infections (see below).
  2. A thorough assessment of the patient’s general medical condition, the infectious process, and the home situation is necessary before starting therapy (see Table 2 of the original guideline document)
  3. Prescribing physicians should be aware of a number of aspects of OPAT which distinguish it from other forms of therapy. These include the required teamwork, communication, monitoring, and outcome measurements (see Tables 3 and 4 of the original guideline document).
  4. The physician has a unique role on the OPAT team, which may also include nursing, pharmacy, and social services. These responsibilities include establishing a diagnosis, prescribing treatment, determining the appropriate site of care, monitoring during therapy, and assuring the overall quality of care.
  5. Antimicrobial selection for OPAT is different from that for therapy in the hospital. Once-daily drug administration has many advantages. Potential for adverse effects and the stability of an antimicrobial once it is mixed must be considered (see Tables 5–7 of the original guideline document).
  6. The importance of administering the first dose of an antibiotic in a supervised setting is emphasized.
  7. Regular clinical and laboratory monitoring of patients receiving OPAT is essential and varies with the antimicrobial chosen (see Table 8 of the original guideline document).
  8. Outcomes measures should be an integral part of any OPAT program, to assure the effectiveness and quality of care (see Table 9 of the original guideline document).
  9. Children receiving OPAT must be considered differently because of their special needs. (See the section "Considerations for Pediatric Patients" in the original guideline document)

Table 1. Infections Treated with Outpatient Parenteral Antimicrobial Therapy (OPAT) and the Antibiotics Used in 4 Studies or Sites

OPAT Network (1996–2002)a Cleveland Clinic (1986–2000)b Minneapolis area (1978–1990)c Children’s Hospital San Diego (2000)d
Type of infection, ranked by frequency (% of OPAT courses)

Skin and soft tissue (23)

Osteomyelitis (15)

Septic arthritis/bursitis (5)

Bacteremia (5)

Wound (4)

Pneumonia (4)

Pyelonephritis (3)

Musculoskeletal

Infected devices

Bacteremia

Intra-abdominal

Skin and soft tissue

...

...

Cellulitis (15)

Osteomyelitis (13)

Late-stage Lyme disease (10)

Pyelonephritis and UTI (9)

Septic arthritis (7)

Other (46)

...

Bacteremia (16)

Pyelonephritis (13)

Meningitis (13)

Intra-abdominal (8)

Cellulitis (7)

Osteomyelitis (7)

Wound (7)

Antimicrobial, ranked by frequency of use (% of OPAT courses)

Ceftriaxone (33)

Vancomycin (20)

Cefazolin (6)

Oxacillin/nafcillin (5)

Aminoglycosides (5)

Clindamycin (3)

Ceftazidime (3)

Vancomycin (31)

Penicillins (20)

Antivirals (12)

Cephalosporins (9)

Aminoglycosides (5)

Other beta-lactams (4)

...

...

...

...

...

...

Ceftriaxone (42)

Meropenem (11)

Cefazolin (11)

Cefepime (6)

Ceftazidime (6)

Vancomycin (6)

Abbreviation: UTI, urinary tract infection

a Data from OPAT Outcomes Registry (available at http://www.opat.com).

b Data from Susan Rehm, personal communication. Percentage of infections not recorded.

c Data from Williams DN. Home intravenous antibiotic therapy (HIVAT): Indications, patients and antimicrobial agents. Int J Antimicrobial Agents. 1995; 5:3–8.

d Data from John Bradley, personal communication.

CLINICAL ALGORITHM(S)

None provided

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The guidelines were formulated on the basis of the collective clinical experience of the Guideline Committee. Wherever possible, the strength of the recommendation and quality of evidence available to support the recommendation were assessed with use of previously published criteria.

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

ADAPTATION

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

DATE RELEASED

1997 (revised 2004 Jun 15)

GUIDELINE DEVELOPER(S)

Infectious Diseases Society of America - Medical Specialty Society

SOURCE(S) OF FUNDING

Infectious Diseases Society of America (IDSA)

GUIDELINE COMMITTEE

IDSA Practice Guidelines Committee

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Names of Committee Members: Alan D. Tice, John A. Burns School of Medicine, University of Hawaii, Honolulu; Susan J. Rehm, Department of Infectious Diseases, Cleveland Clinic Foundation, Cleveland, Ohio; Joseph R. Dalovisio, Ochsner Clinic, Department of Infectious Diseases, New Orleans, Louisiana; John S. Bradley, Division of Infectious Diseases, Children’s Hospital of San Diego, San Diego, California; Lawrence P. Martinelli, Consultants in Infectious Diseases, Lubbock, Texas; Donald R. Graham, Springfield Clinic, Springfield, Illinois; R. Brooks Gainer, Morgantown Internal Medicine Group, Morgantown, West Virginia; Mark J. Kunkel, Pfizer, Inc.; Robert W. Yancey, Florida Infection Physicians, Gainesville; David N. Williams, Hennepin County Medical Center, Minneapolis, Minnesota

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

John S. Bradley has received research funding from Roche, AstraZeneca, Bristol-Myers Squibb, Johnson and Johnson, and Pfizer; he has consulted for AstraZeneca, Bristol-Myers Squibb, Johnson and Johnson, and Bayer. R. Brooks Gainer belongs to the speakers’ bureaus of Roche, Merck, Pfizer, Glaxo-SmithKline, and Wyeth-Ayerst. Mark J. Kunkel is employed by Pfizer.

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: Practice guidelines for community-based parental anti-infective therapy. Clin Infect Dis 1997 Oct;25(4):787-801.

GUIDELINE AVAILABILITY

Electronic copies: Available from the Infectious Diseases Society (IDSA) Web site.

Print copies: Available from Infectious Diseases Society of America, 1300 Wilson Boulevard, Suite 300, Arlington, VA 22209.

AVAILABILITY OF COMPANION DOCUMENTS

PATIENT RESOURCES

None available

NGC STATUS

This summary was completed by ECRI on January 15, 1999. The information was verified by the guideline developer as of March 22, 1999. This summary was updated by ECRI on August 11, 2004. 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). This summary was updated by ECRI Institute on July 28, 2008 following the U.S. Food and Drug Administration advisory on fluoroquinolone antimicrobial drugs.

COPYRIGHT STATEMENT

This NGC summary is based on the original guideline, which is subject to the guideline developer's copyright restrictions.

DISCLAIMER

NGC DISCLAIMER

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