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The procedure for inserting an arterial line and withdrawing blood using a pressure system and an open system. It includes steps for preparing the pressure system, attaching the open end of the cable to the transducer, securing the transducer, assessing the limb distal to the insertion site, and collecting blood specimens. The document also includes safety precautions and considerations for different arterial sites.
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NURSING PROCEDURE TITLE: ARTERIAL LINES – Adult/Pediatric Patients greater than 30 Kg A. Assisting with Insertion I. Preparing Pressure System II. Preparing Bedside Monitor III. Insertion B. Maintenance C. Dressing Change D. Withdrawal of Blood I. Open System II. Closed (or reservoir) System E. Removal of Peripheral and Femoral Arterial Lines
CATEGORY: RN – Special Nursing Procedure
To provide accurate invasive pressure monitoring. To maintain patency of arterial lines. To facilitate blood withdrawal for diagnostic and patient management purposes. To minimize risk of infection, damage, displacement and other complications associated with care and use of hemodynamic lines.
A. Assisting with Insertion
EQUIPMENT
PROCEDURE
I. Preparing Pressure System
4.1 Push reservoir plunger to closed position. 4.2 Ensure shut off valve is in open position (parallel to tubing), orient the kit so that reservoir inlet and outlet ports are in an upward vertical position. Hold sampling site above reservoir at a 45° angle. 4.3 Flush system by pulling Snap-tab of pressure transducer system. Slowly fill and de- bubble reservoir, sample site and stopcocks in succession. 4.4 Ensure removal of all air from system.
NOTE: Replace all vented caps on ports of stopcocks with non-vented caps.
NOTE: When pressure bag is inflated to 300 mmHg, pressure system will deliver 3 mL/hour and 4 mL/second when fast flush device is pulled.
II. Preparing Bedside Monitor
NOTE: Measurement labels are stored in the Multimeasurement Module (MMS).
NOTE: In case of label conflict or selecting additional labels please refer to IntelliVue Quick guide at bedside.
NOTE: Depending on pressure tubing length for some set-ups, transducers are unable to be secured at phlebostatic axis. In these circumstances, secure transducer as close to insertion site as the tubing allows.
14.1 Re-zero pressure line. 14.2 Adjust pressure scale as needed. 14.3 Adjust ABP alarm parameters as appropriate. 14.4 Ensure ABP monitoring alarm is activated.
B. Maintenance
For purposes of monitoring, ensure ABP alarms remain on. If limb distal to arterial catheter ever shows signs of circulatory compromise, physician must be notified immediately and catheter must be removed. Patients with femoral arterial lines must remain on strict bed-rest unless ordered otherwise by physician. The HOB may be elevated 30°.
NOTE: Depending on pressure tubing length for some set-ups, transducers are unable to be secured at phlebostatic axis. In these circumstances, secure transducer as close to insertion site as tubing allows.
C. Dressing Change
NOTE: Transparent semipermeable dressing to be changed every 7 days or PRN. For people with sensitivities to chlorhexidine, alcohol followed by povidone- iodine is an accepted alternative.
EQUIPMENT
PROCEDURE
4.1 Obtain swab for C&S, if indicated.
NOTE: Use of alternate dressings, or additional material such as steri-strips/gauze to be supported with documentation in Nursing Notes. Gauze dressings to be changed every 2 days or PRN.
12.1 Use syringe from ABG kit and set plunger to desired sample volume of 1 mL. 12.2 Attach syringe and turn stopcock off to transducer. 12.3 Allow syringe to fill with blood. 12.4 Turn stopcock off to vacutainer port. 12.5 Remove syringe from stopcock. 12.6 Eject any air bubbles from ABG syringe. 12.7 Cap with rubber stopper from package. 12.8 Label specimen. 12.9 Transport specimen to lab.
NOTE: Lactate specimens in grey top tube must be placed on ice. Cross Match blood tubes must include patient’s date of birth.
II. Closed (or reservoir) System (Blood Conservation System)
12.1 Use syringe from ABG kit and set plunger to desired sample volume of 1 mL. 12.2 Remove needle from syringe and attach VAMP Needleless Shielded Cannula. 12.3 Insert cannula into sampling site.
Edwards Lifesciences, 09/2000, VAMP® Venous/Arterial Blood Management Protection System Package Insert,; Irvine Ca.
19.1 Peripheral Site: 19.1.1 Apply direct manual pressure to insertion site. 19.1.2 Check site after 5 minutes, if oozing or bleeding persists, continue to apply manual pressure for 5 more minutes before checking again. 19.1.3 Continue with manual pressure for a minimum of 5 minutes after evidence of bleeding from site has stopped.
19.2 Femoral Site: 19.2.1 Apply manual pressure 1 – 2cm proximal to insertion site. 19.2.2 Check site after 10 minutes, if oozing or bleeding persists, continue to apply manual pressure for 5 more minutes before checking again. 19.2.3 Continue with manual pressure for a minimum of 5 minutes after evidence of bleeding from site has stopped.
NOTE: Prolonged and direct pressure is required to stop bleeding from an artery. Inadequate hemostasis can lead to bleeding, and hematomas may impair circulation distal to puncture site, as well as cause discomfort for patient.
Use of pressure dressings are not recommended. Pressure dressings do not provide adequate compression, can increase patient discomfort and delay detection of bleeding.
21.1 Peripheral Site: 21.1.1 Assess site q15min x 1 hour, then PRN 21.1.2 Apply direct pressure to site if bleeding noted at any time, as per step 19.
21.2 Femoral Site: 21.2.1 Assess site q 15min x 1hour, q 30min x 1hour, q 1hour x 2hours, then PRN 21.2.2 Apply direct pressure to site if bleeding noted at any time, as per step 19.
22.1 Femoral Lines: 22.1.1 Immobilize leg from hip flexion for a minimum of two hours. 22.1.2 HOB may be elevated up to 30°.
NOTE: Remove dressing from site within 24 – 48 hours.
Square Wave Test
Square wave test configuration Square wave test configuration Square wave test configuration
Figur Figure 16- 56 Square wave test. (A) Optimally damped system: Activation of the fast flush device generates a sharp vertical upstroke, horizontal line, and straight vertical downstroke ending with one or two oscillations (minimal ringing) and quick return to the baseline. (B) Overdamped system: Activation of the fast flush device generates a slurred upstroke and downstroke with no oscillations above or below the baseline. Causes of an overdamped system include system leaks, blood clots, or air bubbles in the tubing or transducer. (C) Underdamped system: Activation of the fast flush device generates a sharp vertical upstroke and downstroke and ends with numerous oscillations (more than three) above and below the baseline. Usually caused by small air bubbles in the system. From: Darovic GO: Hemodynamic Monitoring: Invasive and Noninvasive Clinical Application, p
Code: A. Date: March 2015 Author: Justin Rae, Teresa Vall, Lucia Parsons, Angela Kubiak
Blood Withdrawal from Arterial Line Using Syringe
If blood cultures are required, they must be drawn by syringe method and transferred into blood culture medium vials. The media within the blood culture tubes must never come into contact with the patient’s circulation.
Double female connector
Syringe with blood Male Leur Angel Wing® Blood culture vial
Reference: http://www.biomerieux-usa.com/upload/Worksafe-Blood-Culture-Collection-Procedure-1.pdf
Code: A. Date: March 2015 Author: Justin Rae, Teresa Vall, Lucia Parsons, Angela Kubiak