Measurement of Serum Potassium Rate During Accidental Hypothermia.
- Conditions
- HyperkalemiaAccidental HypothermiaCardiac Arrest
- Interventions
- Diagnostic Test: blood draw from three different vessels
- Registration Number
- NCT03096561
- Lead Sponsor
- University Hospital, Grenoble
- Brief Summary
Serum Potassium Rate (PR) is a key indicator for medical management of patients with accidental hypothermia particularly for hypothermia related cardiac arrest (CA).
Experts recommend a cut-off value for PR of 12 mmol/l for all hypothermic victims and 8 mmol/l for avalanche casualties. Any patient presenting a PR lower than the cut-off value should be considered for Extracorporeal Rewarming. This therapeutic strategy is vital for patient survival.
However, there is no consensus about what type of vessels should be punctured in order to obtain an accurate potassium rate and what type of measurement technics should be used to measure this potassium rate.
The investigators hypothesize that potassium rate in these patients will differ by 1 mmol/l in blood samples collected from a peripheral vein in contrast to a central vein.
The investigators study is a prospective observational, multicentre study.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 12
- Hypothermia related cardiac arrest
- Age > 18 years
- Core temperature < 30° C measured in oesophagus at hospital admission
- Age < 18 years
- Known condition of pregnancy or breastfeeding women
- Evidence of trauma-related cardiac arrest
- Cardiac arrest in which reanimation is not justified (frozen body, final stadium of an incurable disease, advance health care directive)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Hypothermia related cardiac arrest blood draw from three different vessels blood draw from three different vessels punctured in the emergency room (central vein, peripheral vein, artery) and comparison of potassium rate and other biological values between the different sites of blood draw and two different measuring techniques (laboratory vs. blood gas analyser)
- Primary Outcome Measures
Name Time Method Comparison of potassium rate in central venous blood and blood from a peripheral vein (measured in mmol/l) 24 hours Comparison of PR in central venous blood and blood from a peripheral vein (measured in mmol/l)
- Secondary Outcome Measures
Name Time Method Comparison of potassium rate in venous and arterial blood (measured in mmol/l) 24 hours Comparison of potassium rate in venous and arterial blood (measured in mmol/l)
Comparison of potassium rate from laboratory analysis and at bedside via blood gas analyser (measured in mmol/l) 24 hours Comparison of potassium rate from laboratory analysis and at bedside via blood gas analyser (measured in mmol/l)
Comparison of the time difference between laboratory analysis and blood gas analyzer at bed side (measured in minutes) 24 hours Comparison of the time difference between laboratory analysis and blood gas analyzer at bed side (measured in minutes)
Survival and neurological outcome as measured by the Cerebral Performance Category Scale 3 months Survival and neurological outcome as measured by the Cerebral Performance Category Scale
Study of biological parameters to calculate the Strong Ion Gap (measured in mEq/l) according to the Stewart Approach 24 hours 1. For each sample, the apparent strong ion difference (SIDa) will be calculated as SIDa =(Na+ +K+ +Ca2+ +Mg2+)-(Cl- +Lac-)
2. The amount of weak plasma acid (A-) will be calculated as:
A- = \[Alb\] × (0.123 × pH - 0.631) + \[PO4\] × (0.309 × pH - 0.469)
3. The effective strong ion difference (SIDe) will be calculated as:
SIDe = 1000 × 2.46 × 10-11 × PaCO2/(10-pH) + \[A-\]
To quantify unmeasured charges, the SIG will be calculated as:
SIG = SIDa - SIDe
Trial Locations
- Locations (2)
Hospital of Valais
🇨🇭Sion, Valais, Switzerland
University Hospital Vaudois
🇨🇭Lausanne, Valais, Switzerland