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Brief Summary

GUIDELINE TITLE

Clinical policy: evidence-based approach to pharmacologic agents used in pediatric sedation and analgesia in the emergency department.

BIBLIOGRAPHIC SOURCE(S)

GUIDELINE STATUS

This is the current release of the guideline.

BRIEF SUMMARY CONTENT

 
RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Definitions for the strength of evidence (Class I-III) and strength of recommendations (Level A-C) are repeated at the end of the "Major Recommendations" field.

Etomidate

Is etomidate effective for providing procedural sedation in children in the emergency department (ED)?

  • Level A recommendations. None specified.
  • Level B recommendations. None specified.
  • Level C recommendations. Etomidate is an effective agent for procedural sedation in the pediatric patient population within the ED.

Is etomidate safe for providing procedural sedation in children in the ED?

  • Level A recommendations. None specified.
  • Level B recommendations. None specified.
  • Level C recommendations. Etomidate is a safe agent for procedural sedation in the pediatric patient population within the ED.

Fentanyl/Midazolam

Are fentanyl and midazolam effective for providing procedural sedation in children in the ED?

  • Level A recommendations. None specified.
  • Level B recommendations. Intravenous use of fentanyl and midazolam is effective for pediatric sedation during painful procedures in the ED.
  • Level C recommendations. None specified.

Is the use of fentanyl and midazolam safe for providing procedural sedation for painful procedures in children in the ED?

  • Level A recommendations. None specified.
  • Level B recommendations. The combination of fentanyl and midazolam appears to result in a greater risk of respiratory depression; therefore, the clinician should take particular care to monitor the patient for signs of respiratory depression and should have appropriate training and support to treat apnea.
  • Level C recommendations. None specified.

Ketamine

Is ketamine effective for providing procedural sedation in children in the ED?

  • Level A recommendations. Ketamine is effective either as a sole agent or in combination with a benzodiazepine for brief painful procedures in children.
  • Level B recommendations. None specified.
  • Level C recommendations. None specified.

Is ketamine safe for providing procedural sedation in children in the ED?

  • Level A recommendations. Ketamine can be safely used for procedural sedation in children in the ED, but may require head positioning, supplemental oxygen, occasional bag-valve-mask ventilatory support, and measures to address laryngospasm.
  • Level B recommendations. None specified.
  • Level C recommendations. None specified.

Does the addition of midazolam as an adjunct to ketamine for procedural sedation for children in the ED reduce recovery agitation or vomiting?

  • Level A recommendations. The addition of midazolam as an adjunct to ketamine for procedural sedation for children in the ED does not decrease the incidence of emergent reactions.
  • Level B recommendations. The addition of midazolam as an adjunct to ketamine for procedural sedation for children decreases the incidence of emesis.
  • Level C recommendations. None specified.

Methohexital

Is methohexital effective for providing procedural sedation in children in the ED?

  • Level A recommendations. None specified.
  • Level B recommendations. Methohexital administered by either the intravenous, intramuscular, or rectal routes can provide effective sedation for children undergoing painless diagnostic studies.
  • Level C recommendations. None specified.

Is methohexital safe for providing procedural sedation in children in the ED?

  • Level A recommendations. None specified.
  • Level B recommendations. Methohexital can be safely used for procedural sedation but may require head positioning, supplemental oxygen, and occasional bag-valve-mask ventilatory support.
  • Level C recommendations. None specified.

Pentobarbital

Is pentobarbital effective for providing procedural sedation in children in the ED?

  • Level A recommendations. None specified.
  • Level B recommendations. Pentobarbital alone is effective in producing cooperation for painless diagnostic procedures. Best sedation results are seen in children younger than 8 years.
  • Level C recommendations. None specified.

Is pentobarbital safe for providing procedural sedation in children in the ED?

  • Level A recommendations. None specified.
  • Level B recommendations. Pentobarbital can be safely used for procedural sedation but may require head positioning, supplemental oxygen, and occasional bag-valve-mask ventilatory support.
  • Level C recommendations. None specified.

Propofol

Is propofol effective for providing procedural sedation in children in the ED?

  • Level A recommendations. None specified.
  • Level B recommendations. Propofol combined with opiate agents is effective in producing cooperation for painful therapeutic or diagnostic studies.
  • Level C recommendations. Propofol alone, without the concomitant use of opiate agents, is likely to be effective in producing sedation for painless diagnostic studies in ED patients.

Is propofol safe for providing procedural sedation in children in the ED?

  • Level A recommendations. None specified.
  • Level B recommendations. Propofol combined with opiate agents can be safely used for procedural sedation but may require head positioning, supplemental oxygen, and occasional bag-valve-mask ventilatory support.
  • Level C recommendations. Propofol alone, without the concomitant use of opiate agents, can be safely used for procedural sedation but may require head positioning, supplemental oxygen, and occasional bag-valve-mask ventilatory support.

Definitions:

Strength of Evidence

Strength of evidence Class I - Interventional studies including clinical trials, observational studies including prospective cohort studies, aggregate studies including meta-analyses of randomized clinical trials only

Strength of evidence Class II - Observational studies including retrospective cohort studies, case-controlled studies, aggregate studies including other meta-analyses

Strength of evidence Class III - Descriptive cross-sectional studies, observational reports including case series and case reports, consensus studies including published panel consensus by acknowledged groups of experts

Strength of Recommendation

Level A recommendations - Generally accepted principles for patient management that reflect a high degree of clinical certainty (i.e., based on strength of evidence Class I or overwhelming evidence from strength of evidence Class II studies that directly address all the issues)

Level B recommendations - Recommendations for patient management that may identify a particular strategy or range of management strategies that reflect moderate clinical certainty (i.e., based on strength of evidence Class II studies that directly address the issue, decision analysis that directly addresses the issue, or strong consensus of strength of evidence Class III studies)

Level C recommendations - Other strategies for patient management based on preliminary, inconclusive, or conflicting evidence, or in the absence of any published literature, based on panel consensus

There are certain circumstances in which the recommendations stemming from a body of evidence should not be rated as highly as the individual studies on which they are based. Factors such as heterogeneity of results, uncertainty about effect magnitude and consequences, strength of prior beliefs, and publication bias, among others, might lead to such a downgrading of recommendations.

CLINICAL ALGORITHM(S)

None provided

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of evidence supporting the recommendations is identified and graded in the "Major Recommendations" field.

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

ADAPTATION

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

DATE RELEASED

2004 Oct

GUIDELINE DEVELOPER(S)

American College of Emergency Physicians - Medical Specialty Society

SOURCE(S) OF FUNDING

This clinical policy was developed by a multidisciplinary panel and supported in part by grant 02-MCHB-48A from the Department of Health and Human Services (DHHS), Health Resources and Services Administration, Maternal and Child Health Bureau, Emergency Medical Services for Children Program in cooperation with the US Department of Transportation (DOT), National Highway Traffic Safety Administration. The contents are the sole responsibility of the authors and do not necessarily represent the official views of DHHS or DOT.

GUIDELINE COMMITTEE

EMSC Grant Panel (Writing Committee) on Pharmacologic Agents Used in Pediatric Sedation and Analgesia in the Emergency Department

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

EMSC Grant Panel (Writing Committee) on Pharmacologic Agents Used in Pediatric Sedation and Analgesia in the Emergency Department Members: Sharon E.Mace, MD (Chair) (ACEP); Isabel A. Barata, MD (ACEP); Joseph P. Cravero, MD (American Society of Anesthesiologists); William C. Dalsey, MD (ACEP); Steven A. Godwin, MD (ACEP); Robert M. Kennedy, MD (American Academy of Pediatrics); Kelly C. Malley, CPNP, RN (Emergency Nurses Association); R. Lawrence Moss, MD (American Pediatric Surgical Association); Alfred D. Sacchetti, MD (ACEP); Craig R. Warden, MD, MPH (ACEP); Robert L. Wears, MD, MS, Methodologist (ACEP).

Other Panel Members:

ACEP Board Liaison: John A. Brennan, MD

Clinical Policies Manager, ACEP: Rhonda R. Whitson, RHIA

EMSC, Public Policy and Partnerships Specialist: Heather Crown, MRC

EMSC Program Director: Dan Kavanaugh, MSW

EMSC, Public Policy and Partnerships Director: Susan Eads Role, JD, MSLS

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

Not stated

ENDORSER(S)

American Academy of Pediatrics - Medical Specialty Society
American Pediatric Surgical Association - Medical Specialty Society
Emergency Nurses Association - Medical Specialty Society

GUIDELINE STATUS

This is the current release of the guideline.

GUIDELINE AVAILABILITY

AVAILABILITY OF COMPANION DOCUMENTS

None available

PATIENT RESOURCES

None available

NGC STATUS

This NGC summary was completed by ECRI on November 24, 2004. The information was verified by the guideline developer on January 14, 2005.

COPYRIGHT STATEMENT

DISCLAIMER

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