Halyard ON-Q Instrucciones De Uso página 6

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• It is the responsibility of the healthcare provider to ensure
patient is educated on the proper use of the system.
• It is the responsibility of the healthcare provider to modify
Patient Guidelines provided with the pump as appropriate
for your patients' clinical status and medication prescribed.
CAUTIONS
Do not use if package is open, damaged or a
protector cap is missing.
Single use only. Do not resterilize, refill or reuse.
Reuse of the device could result in the following risks:
• Improper functioning of the device (i.e., inaccurate flow rate)
• Increased risk of infection
• Occlusion of the device (i.e., impedes or stops infusion)
• The pump is sterile and non-pyrogenic.
Product uses Di (2-ethylhexyl) phthalate (DEHP)
plasticized PVC:
• DEHP is a commonly used plasticizer in medical
devices. There is no conclusive scientific evidence
to date that exposure to DEHP has a harmful effect
on humans. However, the risk and benefit of using
medical devices with DEHP for pregnant women,
breastfeeding mothers, infants and children should be
evaluated prior to use.
• Certain solutions may be incompatible with the PVC
material used in the administration set. Consult
drug package insert and other available sources of
information for a more thorough understanding of
possible incompatibility problems.
• Do not underfill pump. Underfilling pump may
significantly increase the flow rate.
• Do not exceed maximum fill volume. (Table 1)
• Clamp is provided to stop the infusion. Do not remove or
break clamp. Do not use clamp as an intermittent
delivery device.
• Roll tubing between fingers to promote flow if clamped
for extended time.
• The fill volume, infusion rate, bolus dose and bolus
interval is labeled on the fill port.
• Avoid contact of cleansing agents (like soap and alcohol)
with the filter because leakage may occur from the air
eliminating vent.
• Do not tape over filter(s) as this could block the air vent
and impede the infusion.
• Do not immerse pump in water. Take care to protect the
pump during any activities, which could cause pump and
filter to get wet, such as showering.
4
• In the event of any leakage from pump or administration
set, close tubing clamp. Replace pump if necessary.
• Do not discard pump and contact I-Flow* for product
return instructions.
• Do not add unvented filter to end of the administration
set as this may impede or stop the flow rate.
• Do not remove the red tab until the tubing is completely
primed. Up to 5 ml bolus of air may be delivered if not
primed correctly.
• Flow rates may vary due to:
Fill volume
• Filling pump less than the labeled volume results in faster
flow rate.
• Filling pump greater than the labeled results in slower
flow rate.
• Viscosity and/or drug concentration
• Pump position - position pump at approximately the
same level as the catheter site:
• Positioning pump above this level increases flow rate.
• Positioning pump below this level decreases flow rate.
Temperature
• The ONDEMAND* device should be worn outside
clothing and kept at room temperature.
• To ensure flow rate accuracy, do not place heat or cold
therapy in close proximity to the flow controller.
• Temperature will affect solution viscosity, resulting in
faster or slower flow rate.
• ONDEMAND* device have been calibrated using
Normal Saline (NS) as the diluent and room
temperature (22°C, 72°F) as the operating
environment. Flow rate will increase approximately
1.4% per 1°F/0.6°C increase in temperature and will
decrease approximately 1.4% per 1°F/0.6°C decrease
in temperature.
• If refrigerated, allow pump to reach room temperature
before using.
• It may take approximately 12 or 15 hours (depending
on model) for a pump to reach room temperature. (See
table below.)
Fill Volume (ml)
Refrigerator to Room Temp (hr)
270
400
12
15

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