Medicaid has a carve out for duragesic...a fairly expensive drug, approx 700/month...the intrathecal drug cost for a patient with a limited life expectancy would be substantially less....40 cc pump with 2-3 refills
additionally, the cost of the pump is artificially high.....
the technology is over 20 years old/and minimal design changes....I'm sure the manufacturing processes have paid for themselves by now. So, the company has to only worry about the variable costs of the pump components and the expenses of running the factory....so, why does it still cost 20, 000 dollars? I would wager that a price of 1000-1500/pump would still be profitable for the company; then factor in OR time....then compare these costs to untreated pain/repeat hospitalizations for standard opioids
so if costs were realistic, pumps could be competitively priced
as far as interventional pain for cancer, there is a widespread belief that some procedures may prolong life...there was a paper out of Hopkins by Lillemoe (intra-op celiac plexus) in the early 1990s...I believe in interventional pain for cancer./life prolongation (my bias out in the open)..but we must pay respect to arguably the best RCT in interventional pain by GY Wong, which debunks this myth....yet again, EBM is the party pooper. I will still offer the NCPB for this population of patients, barring contraindications.
Don't get depressed....but, if the holy grail (NCPB for pancreatic cancer) of interventional pain can't beat EBM...I don't know what will be in store for us
Vol. 291 No. 9, March 3, 2004 Featured Link
Effect of Neurolytic Celiac Plexus Block on Pain Relief, Quality of Life, and Survival in Patients With Unresectable Pancreatic Cancer
A Randomized Controlled Trial
Gilbert Y. Wong, MD; Darrell R. Schroeder, MS; Paul E. Carns, MD; Jack L. Wilson, MD; David P. Martin, MD, PhD; Michelle O. Kinney, MD; Carlos B. Mantilla, MD, PhD; David O. Warner, MD
JAMA. 2004;291:1092-1099.
Context Pancreatic cancer is an aggressive tumor associated with high mortality. Optimal pain control may improve quality of life (QOL) for these patients.
Objective To test the hypothesis that neurolytic celiac plexus block (NCPB) vs opioids alone improves pain relief, QOL, and survival in patients with unresectable pancreatic cancer.
Design, Setting, and Patients Double-blind, randomized clinical trial conducted at Mayo Clinic, Rochester, Minn. Enrolled (October 1997 and January 2001) were 100 eligible patients with unresectable pancreatic cancer experiencing pain. Patients were followed up for at least 1 year or until death.
Intervention Patients were randomly assigned to receive either NCPB or systemic analgesic therapy alone with a sham injection. All patients could receive additional opioids managed by a clinician blinded to the treatment assignment.
Main Outcome Measures Pain intensity (0-10 numerical rating scale), QOL, opioid consumption and related adverse effects, and survival time were assessed weekly by a blinded observer.
Results Mean (SD) baseline pain was 4.4 (1.7) for NCPB vs 4.1 (1.8) for opioids alone. The first week after randomization, pain intensity and QOL scores were improved (pain intensity, P.01 for both groups; QOL, P<.001 for both groups), with a larger decrease in pain for the NCPB group (P = .005). From repeated measures analysis, pain was also lower for NCPB over time (P = .01). However, opioid consumption (P = .93), frequency of opioid adverse effects (all P>.10), and QOL (P = .46) were not significantly different between groups. In the first 6 weeks, fewer NCPB patients reported moderate or severe pain (pain intensity rating of 5/10) vs opioid-only patients (14% vs 40%, P = .005). At 1 year, 16% of NCPB patients and 6% of opioid-only patients were alive. However, survival did not differ significantly between groups (P = .26, proportional hazards regression).
Conclusion Although NCPB improves pain relief in patients with pancreatic cancer vs optimized systemic analgesic therapy alone, it does not affect QOL or survival.