Radial Artery Cannulation Clinical Trial
Official title:
Dynamic Need Tip Positioning With Ultrasound Versus Palpation Technique for Radial Artery Cannulation: A Prospective Randomized Controlled Trial
Invasive blood pressure monitoring is achieved by cannulating an artery and transducing the
pressure. During arterial cannulation the artery can be located by palpation, but use of
ultrasound has increased the success rate of cannulation. A new ultrasound technique for
vascular cannulation (dynamic needle tip positioning) has been described. Investigators aim
to compare this technique to the palpation technique for arterial cannulation. Investigators
hypothesize that the use of this novel ultrasound technique will result in a higher first
attempt success rate and overall success compared to palpation.
Investigators plan to enroll 310 patients in this study. The participants in the study will
have been deemed by the attending anesthesiologist to require a radial arterial line for the
operation and thus the research protocol will not involve a deviation from the standard of
care.
Participants will be brought to the main operating rooms. The patient will not be required
to do anything different than if they were not enrolled in the study. The anesthesiologist
will be asked to confirm that the patient still requires an arterial line. The patient will
be randomized either to palpation or ultrasound group. Patients would be placed in supine
position on the operating room table and all regular monitors (electrocardiogram, pulse
oximeter, non-invasive blood pressure) applied. After preoxygenation, the patient would be
induced and the airway secured. For those requiring an arterial catheter before induction of
general anesthesia, subcutaneous lidocaine will be used to anesthetize the planned puncture
site.
The arms would be abducted and the decision on which side to place the arterial line will be
determined by the operator after palpation or scanning the wrists with ultrasound. An
ultrasound image of the radial artery to be cannulated will be obtained. A wrist roll would
then be placed under the wrist and the hand secured with tape. The wrist would then be
prepped with chlorhexidine and sterile towels placed around the prepped site. Timing would
begin once the ultrasound or the operator fingers touch the prepped wrist. For those
randomized to ultrasound, a Sonosite linear ultrasound probe would then be used to locate
the radial artery. After satisfactory position is obtained, a 20 ga angiocath 45mm long
would be used to puncture the artery and then would be advanced until the tip appears on the
ultrasound view. When this happens the ultrasound is advanced about 2mm proximal along the
artery. The needle is advanced until the tip is again visualized. This is repeated until the
needle tip is in the lumen of the radial artery. At this point the needle is sequentially
advanced in the lumen of the artery in small steps under ultrasound vision and then the
cannula is advanced over the needle. The needle core is then retracted and the transducer is
connected to the cannula. If the first attempt is unsuccessful, then more attempts may be
made until 5 minutes elapse. Success is defined as arterial cannulation as shown by an
arterial waveform that is obtained within 5 minutes of touching the prepped skin with an
ultrasound probe or the operator fingers. After that the operator may use the arterial
cannulation method of choice or decide to change to the other wrist.
For the palpation method, the radial artery would be palpated and then a 20 ga angiocath
used to puncture the artery. After a return of blood in the catheter an attempt will be made
to advance the catheter over the needle core. If this is not successful, the operator can
make multiple attempts until 5 minutes elapse. After this time, the operator can use any
desired method to cannulate the artery and may also decide to use the other wrist.
Investigators will record the successful first pass cannulation, and time to cannulate the
vessel. Other measures will be number of attempts, number of catheters, radial artery depth,
radial artery diameter, blood pressure, heart rate, and failure rate. Other data that will
be recorded will include patient age, gender, weight, height , body mass index, and history
of peripheral vascular disease, and diabetes.
Patients will not require any followup for the study.
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