Critical Illness
Conditions
Brief summary
Partial blood oxygen and carbon dioxide pressures obtained in critical ill neonates by transcutaneous sensors will be compared to respective values obtained by medically indicated arterial and capillary blood gas analyses. The influence of blood withdrawal method, sensor operational temperature and application time, presence of cyanotic heart malformations and/or intra or extra cardiac right to left shunt, vasoactive drugs, elevated non-conjugated bilirubin, and skin and soft tissue oedema, skin colour and perfusion conditions will be elucidated as well as sensor's safety. Study duration will be 48 hours with sensors applied and additional 4 hours of further surveillance for thermal injury.
Interventions
DEVICESentec (SenTec) Digital Monitoring System with OxiVenT Sensor
The sensor will be attached to four anatomical positions (thoracic left and right; abdominal left and right), starting with the left thoracic position followed by 4-hourly clockwise position rotation. In case of severe oedema, the ear lobes will be used as anatomical measurement sites and changes to the contralateral ear lobe are made every 4 hours.
Sponsors
Vera Bernet, MD
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
No minimum to 10 Weeks
Healthy volunteers
No
Inclusion criteria
* Late premature or term birth newborn infants (34 0/7 until 43 6/7 weeks gestational age (GA)). * Age between first day of life and 43 6/7 weeks postmenstrual age. * Ability of care taker to understand verbal and written instructions and informed consent in German.
Exclusion criteria
* Care taker unable or unwilling to give written informed consent in German. * Care taker not understanding German and without a family member able to translate. * Written informed consent cannot be obtained for any other reason.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Bias and precision of the transcutaneous oxygen and carbon dioxide measurements | 52 hours | Agreement of transcutaneous measurements with capillary and arterial blood gas values at two operational sensor temperatures (42 and 43°C). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Bias and precision of oxygen and carbon dioxide transcutaneous measurements under the influence of vasoactive drugs (Adrenalin, Noradrenalin, Dopamine, Dobutamine, Vasopressin, Milrinone) | 52 hours | — |
| Bias and precision of oxygen and carbon dioxide transcutaneous measurements under the influence of elevated indirect bilirubin | 52 hours | — |
| Bias and precision of the oxygen and carbon dioxide transcutaneous measurements over time at one anatomical site with determination of technical drift and physiological drift | 52 hours | — |
| Agreement of partial transcutaneous oxygen and carbon dioxide pressures with arterial and capillary values in children with echocardiographically determined congenital cyanotic heart disease and/or intra or extra cardiac right to left shunt | 52 hours | — |
| Bias and precision of transcutaneous partial oxygen and carbon dioxide pressure measurements with changing peripheral perfusion | 52 hours | — |
| Bias and precision of transcutaneous partial oxygen and carbon dioxide pressure measurements with different skin colour types | 52 hours | — |
| Safety of OxiVenT sensor: Appearance of signs of thermal injury (redness, blisters, necrosis) under application of transcutaneous sensor temperatures of 42 and 43°C | 52 hours | While operated at sensor temperatures of 42 and 43°C, the skin will be closely observed for any kind of thermic tissue damage |
| Bias and precision of transcutaneous partial oxygen and carbon dioxide pressure measurements in patients with skin and soft tissue oedema | 52 hours | — |
Countries
Switzerland
Outcome results
None listed