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Intrathecal Pump Implant ("Spinal Morphine Pump") FAQs
The following Frequently Asked Questions and the answers are for the Intrathecal Pump Implant ("Spinal Morphine Pump"). The following material is given as general information only, and is not to be considered as medical advice or consultation. The information was prepared by the TPM staff.
What is an Intrathecal Pump Implant
("Spinal Morphine Pump")?
An Intrathecal Pump is a specialized device, which delivers concentrated amounts of
medication(s) into spinal cord area via a small catheter (tubing). What is an Intrathecal Pump Implant
("Spinal Morphine Pump")?
An Intrathecal Pump is a specialized device, which delivers concentrated amounts of
medication(s) into spinal cord area via a small catheter (tubing).
Am I a candidate for Intrathecal Pump
Implant ("Spinal Morphine Pump")?
Currently at TPM, Intrathecal Pump is offered to patients with :
What is the purpose of it?
This device delivers concentrated amounts of medication into spinal cord area allowing the
patient to decrease or eliminate the need for oral medications. It delivers medication
around the clock, thus eliminating or minimizing breakthrough pain and/or other symptoms.
How long does the procedure take?
It is done in two stages. In the first stage, a single injection is made to assess
effectiveness and screen for unwanted side effects. If this trial is successful in
relieving symptoms, then the permanent device is placed under the skin. The patients have
to meet certain other screening criteria before implanting the pump.
Will the procedure hurt?
The procedure involves inserting a needle through skin and deeper tissues (like a
"tetanus shot"). So, there is some discomfort involved. However, we numb the
skin and deeper tissues with a local anesthetic using a very thin needle prior to
inserting the needle. Most of the patients also receive intravenous sedation and
analgesia, which makes the procedure easy to tolerate.
Will I be "put out" for this procedure?
The placement of the tubing is done under local anesthesia with patients mildly sedated.
The amount of sedation given generally depends upon the patient tolerance.
For the pump placement, patients are given stronger intravenous sedation and analgesia.
How is the procedure performed?
It is done with the patient lying on the side. Sometimes the tubing is placed with the
patient sitting up. The patients are monitored with EKG, blood pressure cuff and blood
oxygen-monitoring device. The skin is cleaned with antiseptic solution and then the
procedure is carried out. X-ray (fluoroscopy) is used to guide the needle for inserting
the tubing.
Where is the tubing inserted? Where is the pump placed?
Tubing is inserted in the midline at the lower back. The pump is then placed on the side
of the abdomen.
What should I expect after the procedure?
If the procedure is successful, you may feel that your pain may be controlled or quite
less. The pump is adjusted electronically to deliver adequate amount of medication.
What should I do after the procedure?
This procedure is normally a day-procedure and patients are kept overnight for observation
and pump adjustment.
How long will the pumps last?
The medication contained within the pump will last about 1 to 3 months depending upon the
concentration and amount infused. It is then refilled via a tiny needle inserted into the
pump chamber. This is done in the office or at your home and it takes only a few minutes.
The batteries in the pump may last 3 to 5 years depending upon the usage. The batteries can not be replaced or recharged. The pump is replaced at that time.
Will the Intrathecal Pump Implant ("Spinal Morphine Pump")
help me?
It is very difficult to predict if the procedure will indeed help you or not. For that
reason a trial is carried out to determine if a permanent device (pump) will be effective
to relieve your pain or not.
What are the risks and side effects?
Generally speaking, this procedure is safe. However, with any procedure there are risks,
side effects, and possibility of complications. Please discuss your concerns with your
physician.
Who should not have this procedure?
If you are on a blood thinning medication (e.g. Coumadin®), or if you have an
active infection going on, you should not have the procedure. The patients also have to
meet certain other screening criteria before implanting the pump.
Where can I get additional information?
More detailed information is available from the manufacturer of this device. At the time
of consultation you will receive a Synchromed™ Infusion System Patient Education Booklet.
Additional information is also available at the Medtronic™ Web Site @ http://www.medtronic.com
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Last Updated:
Tuesday, February 09, 2010