The following information is meant to be used as a guide to assist you post-implant with patients who have an intrathecal drug delivery system for chronic pain.
Follow-up care for intrathecal drug delivery is critical to ongoing patient management. Some patient management considerations continue throughout the course of the patient's treatment.
The refill procedure involves a specific set of steps that must be followed precisely to help ensure patient safety. Before clinicians perform refills, they must be trained in the correct procedures.
A typical refill appointment takes about 30 minutes. The pump is refilled by inserting a needle through the skin into the pump septum.
Medtronic recommends that clinicians refrain from depending solely on the pump alarm to determine refill intervals or remaining battery life. Some hearing-impaired patients may not hear the alarm or the pump may be implanted too deep to adequately hear the alarm. Always use the programmer to verify the battery life of the pump and the reservoir alarm status.
The goal of intrathecal drug delivery for pain is to determine for each patient the drug dose that achieves optimal pain control without intolerable adverse effects. It is important to observe patients for symptoms of drug overdose, tolerance, and ineffective dosing.
Drug dosage will vary with each patient. Encourage patients to notify their clinicians of unusual symptoms, drug overdose, or loss of drug effect. If drug tolerance, disease progression, or psychosocial issues that may impact therapeutic effect are ruled out, evaluate the infusion system for malfunction.
Some patients may require supplemental drugs for ongoing pain management and/or for episodic breakthough pain. Intraspinal preservative-free morphine sulfate and intraspinal preservative-free ziconotide sterile solution are indicated for use with the SynchroMed Infusion System for chronic pain management.
This reference manual contains information specifically regarding indications, drug stability, and emergency procedures for the SynchroMed and IsoMed Infusion Systems.
This is the user manual for the myPTM programmer model 8835.
This is the user manual for the Personal Therapy Manager (PTM) model 8832.
This is the user manual for the SynchroMed II model 8637 Programmable Drug Infusion system.
Whenever there is a change in drug concentration or solution, the remaining old drug in the pump tubing and catheter must be accounted for to prevent under- or overdosing the patient while the old drug concentration is being cleared from the fluid pathway. This reference card outlines how to calculate a bridge bolus.
The existing implanted pump internal pump tubing, reservoir and any unrevised catheter segment are full of drug following a catheter revision. All unrevised spinal catheter segments must be aspirated. A priming bolus is programmed to advance the drug to the tip of the catheter. Before executing a priming bolus it is important to know the location of drug.
Emergency procedure information for morphine/epidural overdose.
The existing implanted pump internal pump tubing and reservoir are full of drug following a catheter replacement. A priming bolus is programmed to advance drug to the tip of the catheter. Before executing a priming bolus it is important to know the location of drug.
This card offers a quick overview of how to use the myPTM programmer model 8835.
This card offers a quick overview of how to use the Personal Therapy Manager model 8832.
This reference guide offers in-depth information on programming the SynchroMed II programmable pump and intrathecal morphine for pain management.
This reference guide offers in-depth information on programming the SynchroMed II programmable pump with the myPTM Personal Therapy Manager.
This reference guide offers in-depth information on therapy maintenance, patient education, complications management, and more.