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Ipump Pain Management System Operator’s Manual
1-10
CD07-19-E4-766
! WARNING !
For infection control purposes, consider the set change interval recommended by the United
States Centers for Disease Control and Prevention (CDC), your institution's guidelines, and the
instructions provided with the administration set, using whichever is most appropriate.
! WARNING !
Only use sets manufactured by Baxter as specified in “Accessories, Disposables, and
Recommended Sets,” 8-1.
! WARNING !
To reduce the risk of stored fluid being infused after a downstream occlusion occurs, relieve the
pressure by disconnecting the system above the occlusion before freeing the occlusion.
! WARNING !
The tubing set MUST NOT be connected to the patient while priming.
! WARNING !
When the Upstream Occlusion Detection feature is enabled, and the automatic upstream
occlusion test is performed, the pump may withdraw up to 0.03 mL of fluid and subsequently
deliver up to 0.09 mL of fluid at the end of the test period. If these volumes are clinically
significant for the patient, please take appropriate measures. See "Upstream Occlusion Testing,"
5-18, for more details.
! WARNING !
When infusing at low flow rates (less than 0.5 mL/hr), the pump may not detect air in the tubing. In
addition, when infusing at low flow rates (less than 0.5 mL/hr), and there is an upstream
occlusion, it is possible for the pumping mechanism to pull air through the tubing wall and into
the fluid path of the set. For infusion routes where air in tubing may be clinically significant for the
patient, Baxter strongly recommends the use of administration sets containing an air eliminating
filter. See "Accessories, Disposables, and Recommended Sets," 8-1, for a list of air eliminating
administration sets available for this pump.
! WARNING !
Clamp tubing distal to the pump before opening the tubing door or troubleshooting any pump
connected to a patient.
Oct02_0719E4766.book Page 10 Friday, August 3, 2007 1:46 PM