Access to the PPM Journal and newsletters is FREE for clinicians.
11 Articles in Volume 6, Issue #4
Assessing Secondary Gain In Chronic Pain Patients
Chronic Overuse Sports Injuries
Introducing Low Level Laser Therapy to Pain Management
Managing Diabetic Peripheral Neuropathic Pain (DPNP)
Moral Virtue and the Pain Physician
Non-pharmacologic Therapy for Chronic Opioid-dependent Sickle Cell Pain
Osteoarthritis of the Knee
Smoking and Low Back Pain
Temporal Tendinitis Migraine Mimic
The Underutilization of Intrathecal Treatment
Tumblin’ Dice–Why Does Random Matter?

The Underutilization of Intrathecal Treatment

Editor's Memo from May/June 2006

Despite significant, positive advances in opioid formulations ranging from long-acting tablets to lollipops, the most potent way to administer opioids is by the intrathecal route. Practical Pain Management has recently collected and published opioid blood levels from chronic pain patients throughout the country. One of the striking findings in this survey was that some patients demonstrated low opioid blood levels even though they were treated with high, oral dosages of opioids. No wonder. Opioids given by all non-intrathecal routes have a long, torturous road to reach the endogenous opioid receptors in the central nervous system. The saliva and gastric juices have the ability to knock out an oral opioid molecule in the opening round. If an opioid molecule makes it to the small intestine, all kinds of intraluminal enzymes and gut-wall opioid receptors are well equipped to finish off an oral opioid—Round 2. If an opioid molecule is lucky enough to reach Round 3, lots of blood enzymes and and the liver just can’t wait to floor opioid molecules and send them floating out the bile or urine. Just in case some molecule makes it past the liver, the goalie of the body, known as the “blood brain barrier,” will deflect would-be brain seekers “en masse.” All these barriers give credence to estimates that only one opioid molecule out of a few hundred given orally will reach the innards of the brain. That is why opioids, to be effective, have to be prescribed in large amounts. Also, this is the obvious rationale for intrathecal therapy in which essentially 100% of opioid molecules administered will reach brain targets.

Given that intrathecal administration has the best ability to relieve pain, why isn’t it more widely utilized? Cost is an obstacle, but so is bias and lack of knowledge. While no one likes the idea of an implant or its attendant, potential complications, the effectiveness of intrathecal administration must be recognized and recommended by all physicians.

From this editor’s position, the underutilization of intrathecal treatment, including the resistance of third party payors to foot the bill, is the current lack of a scientific, objective indication for intrathecal therapy. To date, about the only criteria to implant “the pump” has been a poor response to standard opioid therapy—whatever that is. It’s time to not only put an end to nebulous clinical indications, but also to any misdirected claims of unethical, financial gain.

As with all medical advances, science is paving the way. Since the 1950’s, research on severe pain relative to biologic markers, cardiovascular impacts, and adrenal hormone abnormalities show that a number of objective biologic assessments are available to physicians to identify patients who are legitimate, needy candidates for intrathecal administration. A beginning is to identify patients who state their pain is constant, unremitting, interferes with sleep and eating, and functionally impairs them without oral opioid therapy. Then see if the patient has what this editor calls the “cardiac-adrenal syndrome.” Severe pain is a potent stressor that stimulates the hypothalamic-pituitary-adrenal axis to increase output of catecholamines and the glucocorticoids, cortisol, and pregnenolone. These patients demonstrate high resting pulse rates, often over 100, and abnormal serum adrenal hormone levels which are easily and inexpensively demonstrated on a single, early morning blood specimen. Serum cortisol may be high due to the stress of pain but the adrenal gland may exhaust over time and later show low serum cortisol or low pregnenolone. While excess catecholamine excretion may cause hypertension, severe pain likely also triggers some central mechanism which raises blood pressure. Put another way, a simple measure of blood pressure, pulse rate, and serum pregnenolone and cortisol will demonstrate a “cardiac-adrenal syndrome” in many, if not, all severe, intractable pain patients. Given the potential hazardous complications of abnormal adrenal excretion including cardiac arrest, osteoporosis, depression, cerebral atrophy, and diabetes, among many others, the presence of this syndrome should compel aggressive pain treatment.

There are other important considerations regarding intrathecal treatment. Too often it has been billed by advocates as an alternative to oral opioid therapy. This is a fallacy. Intrathecal therapy should be considered additive and not a substitute for oral therapy. Seldom can all oral opioid drugs be completely stopped after intrathecal administration is initiated. There is even some scientific evidence that opioids exert a positive, pain relieving affect in the periphery. Second, the great pain relieving effect of ziconotide, which can only be given intrathecally, is a compelling reason to make this route available to severe pain patients. Ziconotide isn’t the only non-opioid that may be effective by the intrathecal route. Fortunately, the US has produced some outstanding companies that are expert in producing a number of opioid and non-opioid medications that are appropriate for intrathecal use.

How many patients are candidates for intrathecal administration? No one knows for sure, but epidemiologic surveys of pain incidence and prevalence in the US suggest that one to three million intractable pain patients may demonstrate a cardiac-adrenal syndrome and benefit from intrathecal treatment.

Last updated on: November 16, 2011
close X