Implementation of a second generation laryngeal mask in a large hospital
- Conditions
- Degree of application of pro-seal laryngeal masks in defined surgical interventions
- Registration Number
- DRKS00029771
- Lead Sponsor
- Schwarzwald-Baar Klinikum Villingen-Schwenningen GmbH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 3578
Inclusion Criteria
We don't select patient groups. Complete documentation according to the outcome.
Exclusion Criteria
Incomplete data
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The aim of this study is to evaluate the degree of application of the pro-seal laryngeal masks in relation to further indications (ratio of an endotracheal tube or a laryngeal mask per intervention and reference interval). The data collection will be retrospective from narcotic protocols from our own clinical system Orbis. The generally anesthesiologic handling will be the same and is not part of this study. We don't want to show a benefit for one of those methods, as this occurred already at another placement.
- Secondary Outcome Measures
Name Time Method We hypothesize that there will be according to the handling of pro-seal laryngeal masks differences between surgical interventions (laparoscopic surgeries versus laparotomies), the age of the patients and the shift plan (regular work versus on-call duty). Beside the data collection we will make a questionnaire, which should evaluate possible retentions and their reasons against further indications of laryngeal masks of second generation.