Pediatrics/editorial
Procedural Sedation Goes Utstein: The Quebec Guidelines

https://doi.org/10.1016/j.annemergmed.2008.10.029Get rights and content

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Cited by (24)

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    The clinical characteristics of patients who had SAEs are presented in Table II (available at www.jpeds.com). None of the patients experienced complete airway obstruction,15 clinically apparent pulmonary aspiration, permanent neurologic injury, or death. Table III summarizes the associations between sedation-related adverse events and the patient-level variables.

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    One major obstacle to large-scale audit is the lack of consensus over what to report and also how events should be defined and classified. This inconsistency means that data collected from individual studies are difficult to aggregate and compare, limiting efforts to produce evidence-based recommendations (Green & Yealy 2009). As a consequence, the development of uniform definitions and reporting templates has been recommended in human medicine (Cummins et al. 1991; Bhatt et al. 2009; Mason et.

  • Emergency nurses practices in assessing and administering continuous intravenous sedation for critically ill adult patients: A retrospective record review'

    2015, International Emergency Nursing
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    Textual data from medical and nursing clinical documentation and medication charts were transcribed verbatim into NVivo (version 10) software (QRS International Pty Ltd, 2012). Initial tool development was informed by studies exploring procedural sedation and intubation practices in the ED (Green and Yealy, 2009; Innes et al., 1999). In addition, all relevant national and international guidance were reviewed to further inform the creation of the final audit tool (Fig. 1).

  • Propofol for adult procedural sedation in a UK emergency department: Safety profile in 1008 cases

    2013, British Journal of Anaesthesia
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    For example, hypoxia is defined as oxygen saturations <93%,11 <90% for >10 s12 and by a selection of interventional criteria13 in just three recent emergency medicine publications. Standardization in reporting adverse events has been recommended,14 15 latterly by the World SIVA International Sedation Task Force. In this study, we report a safety analysis of our use of propofol, using the consensus-based World SIVA adverse sedation event reporting tool (Supplementary Appendix 1).

  • Outcomes of Procedural Sedation: What Are the Benchmarks?

    2021, Pediatric Sedation Outside of the Operating Room: A Multispecialty International Collaboration
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Supervising editor: Michael L. Callaham, MD

Dr. Callaham was the supervising editor on this article. Dr. Green and Dr. Yealy did not participate in the editorial review or decision to publish this article.

Funding and support: By Annals policy, all authors are required to disclose any and all commercial, financial, and other relationships in any way related to the subject of this article that might create any potential conflict of interest. The authors have stated that no such relationships exist. See the Manuscript Submission Agreement in this issue for examples of specific conflicts covered by this statement.

Reprints not available from the authors.

Publication date: Available online December 20, 2008.

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