National Survey to Describe the Current Patterns of Procedural Sedation Practices Among Pediatric Emergency Medicine Practitioners in the United States
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Published on: July 30, 2009
Deepak Choudhary1, Reshvinder Dhillon2, Kunal Chadha2
1From the Department of Pediatric Emergency Medicine, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, AR.
Insights
Pediatric procedural sedation (PPS) practices vary widely across the US, with many practitioners not adhering to national guidelines. This survey highlights significant differences in personnel, monitoring, and medication choices for pediatric sedation.
Area of Science:
- Emergency Medicine
- Pediatric Sedation
- Clinical Practice Guidelines
Background:
- Pediatric procedural sedation (PPS) is crucial for ensuring safety and cooperation during medical procedures in children.
- Variations in PPS practices may impact patient outcomes and adherence to established guidelines.
Purpose of the Study:
- To describe current pediatric procedural sedation practices nationwide.
- To identify variations in PPS and assess adherence to national guidelines.
Main Methods:
- A nationwide survey was conducted using a secure web-based platform.
- Data collected included practitioner demographics, sedation approach, monitoring, equipment, and medication preferences for common scenarios.
Main Results:
- 211 surveys were completed from 34 states, primarily from pediatric emergency medicine attendings in teaching hospitals.
- Significant variability was observed in training methods, BMI cutoffs, post-sedation observation times, and the availability of bedside reversal agents and defibrillators.
- Common medication preferences included ketamine for fracture reduction and local anesthesia with intranasal midazolam for laceration repair.
Conclusions:
- Current pediatric procedural sedation practices exhibit considerable variability across the United States.
- There is a notable lack of adherence to national guidelines in several aspects of PPS.
Objective:
Pediatric procedural sedation (PPS) is used to maintain children's safety, comfort, and cooperation during emergency department procedures. Our objective was to gather data describing PPS practice across the United States to highlight the variations in practice and adherence to National Guidelines.
Methods:
We performed a nationwide survey of PPS practitioners using a secure web-based software program. A link to the survey was sent to all subscribers of a pediatric emergency medicine listserv. We collected participant demographics, their PPS approach for personnel, monitoring, equipment, postsedation observation, and side effects, as well as providers' medication preferences for 3 common PPS scenarios.
Results:
We received 211 completed surveys from 34 States. There were 20.6% respondents that were based in New York, 83.4% were pediatric emergency medicine attendings, and 91.7% were based in the United States teaching hospitals. Our participants learned PPS by various methods, most commonly: observation of at least 10 PPS (29.9%); self-study (24.8%); and classroom lectures (24.5%). Seventy-seven percent of our participants reported no body mass index cutoff to do PPS. There were 31.5% of our participants that observe children after PPS up to 1 hour, 30.1% up to 2 hours. There were 67.7% of the PPS providers that were a separate person from the practitioner doing the procedure, and 98.2% required a separate trained nurse to be present for monitoring. There were 92.6% of PPS providers that measure end-tidal carbon dioxide (ETCO2) during the sedation. Most PPS providers reported having no reversal agents (71.4%) and no defibrillator (65.9%) at bedside. For the abscess drainage scenario, 22% of participants preferred local anesthetic alone, and 22.5% preferred utilizing local anesthetic in combination with intravenous ketamine. For a forearm fracture reduction scenario, 62.8% of participants would choose intravenous ketamine alone. For the laceration repair scenario, the most favored drug combination was local anesthesia + intranasal midazolam by 39.8% of participants.
Conclusions:
Our study demonstrates a wide variability in several aspects of PPS and low adherence to national PPS guidelines.
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