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RSICZ: Rapid Sequence Induction Czech Republic: Survey

Sponsor
Brno University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT02985970
Collaborator
(none)
164
Enrollment
4
Duration (Months)

Study Details

Study Description

Brief Summary

Rapid sequence induction (RSI) is a common part of routine anesthesiology practice.However several steps of RSI are not based on evidence based data (EBM) and are considered controversial. In an electronic evaluation form that will be send to Czech society of anesthesiology, resuscitation and intensive care (ČSARIM) members, the investigators bring 4 clinical scenarios in which RSI should be used. In the questionnaire the participants have to choose RSI or no and they have to describe all the next steps on anesthesia induction process in each single clinical scenario.

Condition or Disease Intervention/Treatment Phase
  • Other: questionnaire

Detailed Description

Rapid sequence induction (RSI) is a common part of routine anesthesiology practice.However several steps of RSI are not based on evidence based data (EBM) and are considered controversial. In an electronic evaluation form that will be send to Czech society of anesthesiology, resuscitation and intensive care (ČSARIM) members, the investigators bring 4 clinical scenarios in which RSI should be used. In the questionnaire the participants have to choose RSI or no and they have to describe all the next steps on anesthesia induction process in each single clinical scenario.

  • 1st. scenario - adult patient with acute abdomen in the OR to be anesthetized

  • 2nd. scenario - 4 years old child with acute abdomen in the OR scheduled for an acute surgery

  • 3rd. scenario - pregnant women scheduled for an elective caesarean section in the OR

  • 4th. scenario - geriatric patient with hiatal hernia scheduled for an elective laparoscopic cholecystectomy.

In each scenario the several steps of the RSI sequence has to be answered:

Is RSI indicated? Y N

Peripheral vein line before induction? Y N

Nasogastric tube before/after induction or without?

Patients position: neutral, head-up, head-down?

Preoxygenation - 3/5minutes, breaths, (CPAP)/Positive end-expiratory pressure (PEEP)?

Sellick manoeuver? Y N

Drugs for induction (order with the number in the row) - propofol, etomidate, ketamine, thiopental, midazolam, suxamethonium, rocuronium, cisatracurium, atracurium, vecuronium

Manual hand-bag ventilation after induction: with limited pressure/contraindicated

Airway: tracheal tube with the cuff/without cuff/laryngeal mask

Comments

Study Design

Study Type:
Observational
Actual Enrollment :
164 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Rapid Sequence Induction in Czech Republic: Survey
Study Start Date :
Dec 1, 2016
Actual Primary Completion Date :
Feb 1, 2017
Actual Study Completion Date :
Apr 1, 2017

Arms and Interventions

Arm Intervention/Treatment
ČSARIM - questionnaire

Members of Czech society of anesthesiology, resuscitation and intensive care will obtain the questionnaire

Other: questionnaire
The questionnaire will be send to all members of ČSARIM with the selected 4 controversial clinical scenarios in which the RSI should be used
Other Names:
  • survey

    		•

    Outcome Measures

    Primary Outcome Measures

    1. RSI practice in Czech Republic - questionnaire [one month]

      Evaluation of the clinical practice of the RSI in Czech Republic

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    4 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    Exclusion Criteria:

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Brno University Hospital

    Investigators

    • Study Chair: Petr Štourač, doc.MD.Ph.D, University Hospital Brno

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Petr Štourač, MD, Doc.MD.Ph.D, Brno University Hospital
    ClinicalTrials.gov Identifier:
    NCT02985970
    Other Study ID Numbers:
    • RSI 2016CZ
    First Posted:
    Dec 7, 2016
    Last Update Posted:
    Apr 24, 2017
    Last Verified:
    Apr 1, 2017
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Keywords provided by Petr Štourač, MD, Doc.MD.Ph.D, Brno University Hospital
    crush induction, RSI

    Study Results

    No Results Posted as of Apr 24, 2017