To assess the comparability of routine blood analysis from intraosseous cannulation and peripheral venous blood in the emergency setting.
ID
Source
Brief title
Condition
- Other condition
Synonym
Health condition
hemodynamisch instabiele patiënten op de SEH
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The main study parameter is the comparability of laboratory values (i.e.
sodium, potassium, magnesium, calcium, glucose, lactate, albumin, creatinine,
urea, alkalin phosphatase, γ-GT, LD, ALAT, ASAT, CK, TnT, CBC, PT and APTT) )in
blood samples obtained by intraosseal cannulation and peripheral venous access.
Secondary outcome
Is the preanalytical quality of the bone marrow material sufficient for
laboratory analysis. Quality will be assessed by using parameters such as
hemolysss, lipaemia and the presence of bone fragments. The endpoint is the
number of rejecte samples .
Number and type of the complications that are related to the use of the
intraosseous canulle in comparison to complications when using an intraveneous
catheter.
Background summary
In the emergency setting the use of intraosseous cannulation and infusion is
becoming more widely used. In need of fast access it is a save method for
gaining access to the vascular system to infuse drugs and fluids when access
through the peripheral venous route is difficult or impossible. It is under
debate whether blood taken from intraosseous cannulation can be used for blood
analysis. It would be an enormous advantage to the patient in the acute setting
if blood obtained from intraosseous cannulation could also be used for
laboratory assays. Important laboratory results will be faster known and
consequently treatment will be started in an earlier stage. However, there is
currently no evidence that reliable and comparable to peripheral venous levels
can be obtained in blood samples taken from intraosseous cannulation in the
acute setting.
Study objective
To assess the comparability of routine blood analysis from intraosseous
cannulation and peripheral venous blood in the emergency setting.
Study design
Non-therapeutic, prospective, descriptive study
Study burden and risks
The only deviation from the standard procedure is the earlier use of
intraosseous cannulation. An intraosseous cannulation is regularly being used
in critically ill patients for the infusion of fluids. The usage is even being
recommended by European and American guidelines. Our research population is
only one step away in receiving an intraosseous cannula using the standard
protocols. The potential risk for patients in this study will be the use of
the intraosseous cannula, which is generally regarded as a safe method.
Complications that may occur include the release of bone and/or fat fragments
in the circulation, fracture at the entrance site, local infections of the bone
or skin, subcutaneous spill of infusion fluids and the compartment syndrome.
Research has shown that these complications are rare. Reported incidence varies
from 0.9% to 4.8%. Risk of complications are even less as has been described
for (deep) venous catheters in which complications such as infection, arterial
puncture, pneumothorax and thrombosis. In addition, insertion of such a
catheter is more time consuming than that of an intraosseous canulla (2,3min
vs. 9.9min). Moreover, change of success is much larger by using an
intraosseous canulla.
Not inserting an intraosseous canulla could be a greater risk to the patient in
case of an emergency, as fluids and/or medication cannot be administered on
time, which could be potentially fatal. This justifies the minimal risk of
using an intraoseous canulla. In some instances the infusion of fluids through
an intraoseous canulla can be painful, which can easily be treated by using
lidocain before infusion. However, most patients will be unconscious.
Patients in the study protocol will only endure minimal discomfort and risks
for complications are minimal.
postbus 4446
6401CX Heerlen
NL
postbus 4446
6401CX Heerlen
NL
Listed location countries
Age
Inclusion criteria
- Age: 18-80 years
- Hemodynamic unstable patients in need of two vascular access routes.For example.:
o Trauma
o Shock
o Cardiac arrest / resuscitation
o Burnwounds.
o Etc.
Exclusion criteria
- Age: < 18 years or > 80 year
- Hemodynamic stable patients
- Fracture of the proximale tibia
- (Skin)infection of the proximale tibia
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL33727.096.10 |