major project
Conditions
Interventions
Intervention Group (Task 3):Synchronized bag-mask ventilation at 10 breaths per minute will be administered, and the oropharyngeal airway will be used to maintain the airway open throughout the proced
Control Group (Task 3):Two bag-mask ventilation sessions will be administered after every 30 compressions, and the oropharyngeal airway will be used to maintain the airway open throughout the procedur
High quality ventilation group and Low quality ventilation control group (Task 2):Task 2 is a prospective observational cohort study. The patients will be treated according to the current routine card
Patients in task 1:Task 1 is a real world study, in which patients will be treated according to the current routine cardiopulmonary resuscitation without grouping.
Sponsors
China-Japan Friendship Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 120 Years
Inclusion criteria
Inclusion criteria: The inclusion criteria for task 1, task 2 and task 3 are consistent: 1.18 years of age or above; 2. Patients with cardiac arrest of cardiac origin or suspected cardiac origin.
Exclusion criteria
Exclusion criteria: The exclusion criteria for task 1, task 2, and task 3 are consistent: 1.Patients with asphyxia, bleeding, trauma, tracheotomy; 2.Pregnant woman.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Prehospital return of spontaneous circulation; | — |
Secondary
| Measure | Time frame |
|---|---|
| Survival rate at discharge;Neurological outcome at discharge;30-Day Survival rate;Quality of ventilation;Quality of compression; | — |
Countries
China
Contacts
Public ContactZhang Guoqiang
Department of Emergency, China-Japan Friendship Hospital, Beijing 100029, China.
Outcome results
None listed