About this trial
The aim of this study was to determine the independent association of frailty with cardiopulmonary resuscitation and predictive factors in patients triggering code blue response
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
pediatric patients
Disqualifiers
pregnant patients
Trial population
Adult patients with hospitalization and those who are not inpatients (in the outpatient clinic system) requiring Code Blue will be included in the study.
Trial design
Cohort
Prospective
Treatments tested in this trial
Edmonton frailty scale calculation
Other interventionThe frailty status of the patients will be assessed using the Edmonton frailty scale. According to the Edmonton frailty scale; * (0-5): not frail * (6-7): sensitive * (8-9): slightly fragile * (10-11): moderately fragile, * (12-17): extremely fragile
Treatment groups
Trial outcomes
Primary outcomes
code blue reason
comorbid disease and dog usage
duration of CPR time
between the time of giving the blue code and the end of CPR
Secondary outcomes
the airway equipment used
intubation, supraglottic airway devices, tracheostomy, cricothyroidectomy, fiberbronchoscopy
mortality and morbidity
presence and duration of intensive care unit stay
Sponsors and contacts
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