Monitoring of Non-invasive Ventilation
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Hypoventilation
- Sponsor
- Oslo University Hospital
- Enrollment
- 67
- Locations
- 1
- Primary Endpoint
- Frequency of transcutaneous co2 revealing sleep hypoventilation, when nocturnal pulseoximeter is normal
- Status
- Completed
- Last Updated
- 11 years ago
Overview
Brief Summary
The purpose of this study is to determine whether clinical examination, report from ventilator software, nocturnal Sp02 and daytime arterial blood gas are sufficient as screening tools to reveal clinical relevant problems with patients receiving long term treatment with non invasive ventilation.
Detailed Description
Patient with chronic hypoventilation with stable on long term treatment (LTMV) with non-invasive ventilation for at least 3 month taking part of our LTMV program will be included. In addition to clinical examination,report from ventilator software, nocturnal Sp02 and daytime arterial blood gas all patients will be investigated with sleep polygraphy and transcutaneous Co2.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •Under 18 years old
- •Lack of cooperation
- •Acute exacerbation last 3 month leading to hospital admission.
- •Change of treatment last 3 month
Outcomes
Primary Outcomes
Frequency of transcutaneous co2 revealing sleep hypoventilation, when nocturnal pulseoximeter is normal
Time Frame: single night study
Secondary Outcomes
- Frequency of patient-ventilator asynchrony during non invasive ventilation ?(Single night study)