Investigating and comparing the effectiveness of manual and mechanical ventilation on blood gases in patients under mechanical ventilatio
Not Applicable
Recruiting
- Conditions
- cardiopulmonary arrest in patients with neuropathy diseases.Cardiac arrest, cause unspecifiedI46.9
- Registration Number
- IRCT20240106060630N1
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 66
Inclusion Criteria
Age > 18
Definitive cardiopulmonary arrest diagnosis (no response, no carotid pulse, no breath)
Patients with neuropathy diseases
Patients with cv-line
Exclusion Criteria
Traumatic cardiac arrest
Irreversible death
Suspected COVID-19
Suspected pneumothorax
Pregnant
ROSC was achieved before intervention
The patient's withdrawal from the research plan at the doctor's discretion
Patients admitted to the hospital under cardiopulmonary resuscitation.
Patients from whom initial arterial blood gas samples cannot be taken 2 minutes immediately after starting CPR.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method End-tidal carbon dioxide. Timepoint: During cardiopulmonary resuscitation every 2 minutes. Method of measurement: A Sidestream portable capnography device from Comdek company, model MD-660P, made in Taiwan and manufactured in 2005.;Arterial oxygen saturation. Timepoint: During cardiopulmonary resuscitation every 2 minutes. Method of measurement: A SP-20 handheld pulse oximeter made in Germany in 2019.;Arterial blood gases. Timepoint: 2 minutes immediately after starting CPR and 1 minute after achieving ROSC. Method of measurement: ABG device made in America model GEM 2000.
- Secondary Outcome Measures
Name Time Method Perfusion index. Timepoint: Every two minutes during CPR. Method of measurement: With pulseoximeter.