Targeted drug delivery
Cancer pain
Patient selection and clinical evidence
Targeted drug delivery is effective in reducing or eliminating the need for systemic opioids when used to treat cancer-related pain.1
The SynchroMed™ III implantable infusion system delivers prescribed medication directly into the intrathecal space, thereby bypassing the blood-brain barrier. As result, only a fraction of the oral dose is needed to sustain pain relief.2
For many cancer patients, oral analgesics may be adequate; however, those cancer patients with intractable pain who meet any of the criteria listed below may be appropriate for more advanced pain management techniques including targeted drug delivery (TDD) using intrathecal opioids. These patients may be candidates for targeted drug delivery (TDD) using intrathecal opioids to control pain.
Pending a successful intrathecal morphine trial, a permanent intrathecal catheter and Medtronic SynchroMed™ III programmable pump may help control your patients’ pain.
Cancer patients with intractable pain who meet any of the criteria below may be candidates targeted drug delivery with SynchroMed™ III
Consider patients on lower doses if opioid side effects are refractory to conservative treatment and severe enough to prevent upward titration3,8,9
Note: It is important to consider increased assessment and referral vigilance for women,5–7,10 minorities,5–7,11 and the elderly,5,6,11 who have been shown to be at increased risk for inadequate analgesia.
Randomized clinical trial of an implantable drug delivery system compared with comprehensive medical management for refractory cancer pain:3
Contraindications may include infection; implant depth greater than 2.5 cm below skin; insufficient body size; spinal anomalies; drugs with preservatives, drug contraindications, drug formulations with pH ≤3, use of catheter access port (CAP) kit for refills or of refill kit for catheter access, blood sampling through CAP in vascular applications, use of the personal therapy manager (PTM) to administer opioid to opioid-naïve patients. See SynchroMed™ product labeling for more information.
† 200 mg oral morphine or equivalent was used as enrollment criterion in a pivotal randomized clinical trial published in 2002,3 and has since been referenced as a criterion in additional clinical studies related to cancer pain and intrathecal drug delivery.8,9