Opioids - Appropriate Care for Chronic Pain
Medical Disclaimer
"Few things a doctor does are more
important than relieving pain, pain is soul destroying. No patient should
have to endure intense pain unnecessarily. The quality of mercy is essential
to the practice of medicine, here, of all places, it should not be
strained." Marcia Angell
"Pain must be regarded as a disease, and the physician's first duty is action,
heroic action, to fight disease.". Benjamin Rush
Opioid medications allow us to treat chronic pain as aggressively as we would
any pathogen, but we must first overcome ingrained misconceptions about
patients' motivations for seeking treatment and about the addictive properties
of the drugs. With controlled use, the newer sustained-release formulations
give real hope for safe and sustained pain relief.
Opioid medications were once withheld from suffering cancer patients because of
fear of addiction, exaggerated concern about side effects, or, in some cases,
doubt about the morality of treatment. Less than 50 years ago, some medical
textbooks discussed the need for patients to experience pain and suffering at
the end of life so that they would relate to the agony of Christ and prepare
for redemption. Although few physicians still hold these views, many continue
to imply that pain should be accepted without complaint, telling their
patients that "after all, pain is not going to kill you."
There is growing evidence, however, that too much pain can cause damage and
even death. When pain is controlled, medications for the underlying disease or
disorder tend to work better. Opioid analgesia is one of the most pro-life
therapies that we have to offer patients with cancer pain, and there is no
reason to think that patients with other diseases are any less deserving of
relief or that their pain is any less amenable to treatment. Although there is
currently no ideal analgesic for chronic pain, medications that act on µ-opioid
receptors are the closest thing that we have.
Assessment of Pain
One of the main problems in assessing patients with chronic pain is that the
physical examination and laboratory tests often do not provide the information
necessary to gauge severity and assess outcomes. Various survey instruments and
visual analogue scales that allow precise measurements of pain are available
but used only rarely. Pain is generally assessed indirectly, which why it is
so important to listen to--and believe--patients when they say that they are
in pain.
Some physicians apparently have difficulty with that. Many of my patients with
chronic pain have been refused treatment by previous caregivers who apparently
believed that their pain was not real. Even after undergoing painful
procedures and surgeries that failed to bring relief, some of these patients
were labeled as drug-seekers when they continued to ask for help. They had to
contend not only with the pain but also with feelings of frustration,
isolation, and abandonment by those on whom they had most relied.
In some cases, physicians may be well informed about pain mechanisms but lack
an organized approach to the individual assessment of pain. A comprehensive
evaluation of patients with chronic pain syndromes can be time-consuming and
often requires more data than can be obtained in a few brief clinic visits. I
have found the following operational format to be particularly useful, both in
gauging the severity of pain and in determining the degree of disability:
- The patient's perception. Asking the patient to keep a pain diary that includes
numerical scales can help to objectify the pain. If it is understood that the
physician will review the diary carefully, the patient will not have to act out
a month's worth of pain at every appointment. The diary can also be an important
aid in identifying exacerbating or ameliorating factors and developing more
effective strategies to cope with the pain such as behavioral changes or the
preemptive use of analgesics in certain situations.
- The patient's emotional state and somatic preoccupation. This relates to the
degree to which the patient remains focused on bodily symptoms to the
exclusion of other issues and often can be best assessed by interviewing a
close family member.
- Functional status at home. The first things that many patients in pain stop
doing are usually non-work-related activities such as going out with family
and friends, attending church, or engaging in hobbies. Some patients continue
to report pain or discomfort even though their condition has improved. By
keeping track of daily activities, both patient and physician have some measure
of how disabling the pain actually is.
- Functional status at work. The number of work days missed and the specific
work activities curtailed because of pain are also useful indices of pain
severity. Since these variables can be expected to change with analgesic
treatment, they provide a way to gauge the patient's response to different
therapies.
- Use of analgesic medications. If the patient is given an adequate supply of
effective short-acting rescue medications and told to take them as needed,
the number consumed can be a measure of pain. It can also be a way to assess
whether the patient is benefiting from other medications or nonpharmacologic
treatments. The physician should make it plain that the other treatments are
not designed to get the patient to stop using the pain medication but to stop
needing it.
Pain and the Brain
Setting Goals of Treatment
It is important that the physician and patient collaborate in developing the
goals to guide treatment and the means to assess progress. In many cases, there
is no realistic hope of cure, and patients must come to terms with the fact
that treatment will probably continue for a long time. At first, the goals may
be as simple as sleeping through the night, but as the patient's condition
improves, more ambitious goals, such as returning to work or participating in
recreational activities, may be attainable. In addition to reviewing the
patient's diary and keeping track of the various functional indicators, the
physician must take the time to discuss the patient's personal goals--what he
or she has been missing because of pain and most wants to be restored.
Treating Suffering as Well as Pain
The ultimate goal in treating chronic pain is for patients to reclaim control
of their lives, and, to do that, they must be relieved of suffering as well as
pain. Issues such as sadness over lost opportunities, guilt for being a burden
to others, and feelings of inadequacy or abandonment contribute to the
suffering of many patients with chronic pain and deserve attention. Ensuring
that the patient obtains good psychological care is just as important as
providing analgesic medications.
Unfortunately, many patients with chronic pain see referral to a psychologist
as an invalidation of the physical nature of their pain. After years of hearing
their disease or disorder referred to as functional or somatoform, they may
need to be convinced that it is common for chronic pain to have an impact on
many aspects of their lives, including their relationships with family and
friends. In referring my patients for psychological assessment, I encourage
them to recognize that psychological health is a vital aspect of well-being.
Initiation of Opioid Therapy
In the United States, up to 90% of the prescriptions written for opioids are
for noncancer pain. The efficacy and safety of these drugs in treating chronic
pain syndromes has been demonstrated many times over. Most patients with
chronic pain of moderate or greater severity who have not gotten good relief
with disease-specific treatments or nonopioid analgesics should at least have
a trial of an opioid medication, no matter what the cause of the pain. One of
the most important ground rules for such a trial, as well as for subsequent
treatment, is that a single physician must take full responsibility for
establishing the protocol and writing all prescriptions.
Opiate-naive patients are usually started with a short half-life drug (e.g.,
hydrocodone, hydromorphone, oxycodone, codeine, or morphine). Because of their
rapid clearance, these drugs must be taken every three to four hours. For
severe pain, the usual starting dose is 10 to 15 mg of hydrocodone or
oxycodone, 2 to 4 mg of hydromorphone, 30 to 60 mg of codeine, or 15 to 30
mg of morphine.
The common strategy in treating chronic pain with opioid analgesics is to rely
on "as-needed" intermittent dosing, but that does not usually provide
sufficient coverage. As a result, the patient is subjected to periods of
anxiety and pain that are not only unnecessary but also contribute to the
patient's distrust of the physician's instructions.
Posttrial Therapy - Sustained-Release Opioids
For patients with continuous pain who respond well to opioids, long-acting sustained-release agents are indicated. They can be started once a good response to a short half-life opioid has been obtained and any side effects have been managed. The initial daily dose should be roughly equivalent to the average daily amount of short-acting opioid that provided relief.
Oxycodone is available in an eight- to 12-hr formulation, morphine in both
eight- to 12- and 24-hr formulations, and fentanyl in a 72-hr controlled-release
skin patch. Hydromorphone formulations allowing once-a-day dosing are expected
to be on the market by next year, and several other sustained-release opioids
are in various stages of testing.
These drugs have many important advantages over their short half-life
counterparts. Because serum levels remain steady, mini withdrawals or
rebound reactions do not occur, as they sometimes do with long-term use of
short-acting opioids. Sleep patterns are also more normal; with careful
titration, the intermittent sedation that occurs with high-peaking,
short-acting drugs is largely avoided.
Furthermore, because dosing is more convenient, compliance increases. By
reducing the number of daily pills and eliminating fluctuations in serum
levels, sustained-release opioids may help patients to shift their focus away
from somatic concerns. Several studies have shown that patients using
sustained-release opioids for pain are more satisfied with outcomes and have a
measurably higher quality of life.
These drugs also provide less reinforcement of inappropriate use. Because they
are more difficult to convert into injectable forms, they have a lower
potential for diversion and a lower street price than short-acting opioids.
The vast majority of prescription opioid abuse or drug diversion cases
investigated by the Drug Enforcement Administration, state medical boards,
and other regulatory or law enforcement agencies involve short-acting
opioids, sustained-release opioids are rarely a problem. A recent study by
D.E. Joranson and colleagues showed that with increased use of
sustained-release opioids, medical emergencies related to abuse of prescription
opioids have decreased.
Drug Selection
A careful review of the patient's medical history is the first essential in
choosing a medication. Patients with chronic pain can often tell what has
worked in the past and what has not. In one study of cancer patients using
opioid analgesics, 44% required trials of two or more opioids, and 20% required
three or more, before achieving satisfactory pain relief without intolerable
side effects. As in selecting any drug, both adverse and beneficial effects
must be evaluated in the context of the individual patient's current physical
condition.
Morphine
Of the sustained-release opioids, morphine is considered by many to
be the gold standard, probably because it was the first sustained-release drug
that allowed adequate dosing. The designation is more historic than clinically
significant, however. In comparison to other opioids, morphine generally
causes more nausea and pruritus. It also has the disadvantage of being
relatively hydrophilic, which delays its transport across the blood-brain
barrier. In addition, morphine has several active metabolites whose levels
can vary with renal or hepatic function. The drug apparently induces its own
metabolism, which makes it difficult to maintain a steady serum level.
Fentanyl
Because of these problems, fentanyl, a derivative of meperidine, was
specifically designed to substitute for morphine in operative anesthesia.
It is lipophilic and therefore faster acting. Of greater import, however, is
that its potency is hundreds of times greater than morphine's. Microgram
amounts, administered by a transdermal patch, can provide pain relief for up to
72 hours. Because fentanyl does not traverse the gastrointestinal tract, it
causes less constipation than other sustained-release opioids and does not
induce liver metabolism through first-pass effects. It also does not appear to
have active metabolites.
Oxycodone
Oxycodone is sometimes thought of as a weak opioid, probably because it has
been formulated in low-dose pills. Like Fentanyl, however, it is more potent
than morphine and is associated with fewer adverse effects. A sustained-release
formulation, introduced about five years ago, has quickly become the most
popular opioid for treatment of chronic noncancer pain in the United States.
Oxycodone is actually a pro drug. The active metabolite, oxymorphone, is
produced in the liver by the enzymatic activity of cytochrome P450 2D6.
(This is the same enzyme responsible for activating two other pro drugs,
hydrocodone and codeine). Approximately 10% of the population have genetically
low levels of P450 2D6 and thus require higher than usual doses of the pro-drug
to obtain pain relief. Less than optimal effects may also be expected in
patients taking neuroleptics, quinine, or selective serotonin reuptake
inhibitors such as fluoxetine that inhibit P450 2D6 activity.
There have been sporadic reports of agitation, sleeplessness, and dysphoria in
patients taking high doses of oxycodone, which suggests that, in addition to
µ-opioid effects, the drug also has kappa-opioid effects. It may thus have
some added advantage for treatment of visceral pain, which appears to
respond to kappa-receptor agonists.
Hydromorphone
The clinical trials of sustained-release hydromorphone indicate that it has
analgesic effects similar to those of morphine but that it has fewer side
effects. None of hydromorphone's metabolites are pharmacologically active,
which will make this drug particularly useful for patients with renal failure.
Methadone and Levorphanol
By virtue of their intrinsically long half-lives, methadone and levorphanol
are also useful for treatment of chronic pain. Both have significant nonopioid
effects that may contribute to their utility as pain relievers, especially for
neuropathic pain. Methadone appears to be a potent N-methyl-D-aspartate
(NMDA)-receptor blocker. Levorphanol also has some NMDA inhibitory effect and
may, in addition, inhibit reuptake of serotonin and noradrenaline.
These drugs are generally reserved for second-line treatment, however, because
they are difficult to titrate and have delayed-onset side effects. To control
pain effectively, methadone must be administered at intervals (6-8 hr) shorter
than its metabolic half-life (15-90 hr). As serum levels of the drug increase,
so does the risk of toxicity, primarily sedation.
Many U.S. physicians are under the impression that it is illegal to prescribe
methadone without a license from the federal government, but that is the case
only if methadone is used in a maintenance program for treatment of drug
addiction. When prescribed for pain, methadone is subject to the same
regulations as other high-potency opioid medications. One practical advantage
of methadone and levorphanol is that they are both relatively inexpensive.
morphine fentanyl oxycodone oxycontin oxymorphone µ-opioid kappa-opioid hydromorphone methadone levorphanol rescue medication break through thru BT
Rescue Medication (also break-through or BT)
Most patients taking long-acting opioids should be supplied with a fast-acting
rescue opioid to treat pain that breaks through the regular medication
schedule. Oral rescue agents may be needed as often as every two to four hours.
The usual dose is the analgesic equivalent of 5% to 15% of the 24-hour baseline
dose of the long-acting opioid.
Clinical Opiology
Choosing the right opioid for a particular patient is usually a matter of
guesswork. Even though opioids have been in use as long as any other class of
medications, the base of knowledge on how to use them most effectively is
surprisingly small, particularly with regard to combining them with nonopioid
medications and with each other.
Much of the human research has involved patients who were not in pain or who
experienced limited episodes of acute pain. As a result, we often see
disparities between the guidance of the medical literature and empiric clinical
practice. That tables of drug equivalence are still published attests that many
clinicians think opioids are interchangeable. Imagine the reaction if someone
were to publish a conversion table for antibiotics showing how to convert
milligrams of ampicillin into milligrams of gentamicin!
The opioid medications currently in use act largely through the µ-opioid
receptor, but nearly all of them stimulate kappa- and delta-opioid receptors
and some nonopioid receptors as well. In addition to their inhibitory
functions, some opioid receptors appear to have stimulatory functions that may
be responsible for some adverse effects of opioids. According to recent
studies, these stimulatory effects can be inhibited by miniscule doses of
opioid antagonists such as naltrexone and nalmefene. As we get more
sophisticated in using these medications, we may be able to combine opioid
agonists and antagonists both to enhance pain relief and to attenuate
dependence and other side effects. This exciting field of analgesic research
has recently been reviewed by R. F. Crain and S. M. Shen.
While there is general agreement that µ-opioid receptors predominate in
mediating opioid-induced analgesia, we still do not know the consequences of
stimulating other opioid receptors, including how they affect different groups
of patients. Kappa-opioid agonists, for example, produce greater analgesia in
women than in men. Until recently, most clinical pain research was conducted
in men to reduce the variability caused by hormonal fluctuations.
There are also wide metabolic variabilities within groups of pain patients that
may be determined by genetics or influenced by interacting drugs. Yet we have
little information to guide the selection of dosages. For patients on chronic
opioid therapy, it may soon be reasonable to periodically assess serum levels
of the drugs and their metabolites to guide therapy, much as we do with
antiarrhythmics and other medications.
Titration Against Pain
The daily consumption of the rescue drug can be an indicator of how much the
sustained-release drug is falling short of providing adequate relief. By
titrating the sustained-release drug accordingly, the minimum dose needed to
ameliorate the pain can usually be quickly established. Patients sometimes do
well at the beginning of opioid therapy and then seem to lose ground within a
few weeks. In those who have been severely limited in their activities, the
recurrence of pain is not necessarily a sign of growing tolerance to the
medication--the patient may be experiencing more pain because of increased
activity and should be reassured that more medication is required to alleviate
the pain of someone with a busy schedule than of someone lying in bed all day.
Maintaining close communication with patients and families and explicitly
laying out the criteria for evaluating the effects of analgesic medications
can go a long way toward defusing the anxiety that often accompanies visits to
the physician.
Side Effects
The most feared side effect of opioid medications is respiratory depression.
This does not occur, however, when the drugs are titrated against the patient's
pain, probably because the pain signals activate respiratory centers in the
brain that counterbalance depressive effects (Figure 1). In the event of an
overdose, the activity of various brain centers is affected in an orderly,
progressive fashion, with the cortex affected before the brainstem. The patient will thus become
unresponsive and obtunded before the opioid level is high enough to suppress
the respiratory centers. One can be assured that a patient who is awake and
complaining of pain is not in any imminent danger of respiratory depression.
If the source of pain is abruptly removed, an opioid dose that is
well-tolerated can suddenly become sedating. That is clinically relevant when
sending a patient taking opioids for an anesthetic or neurolytic procedure.
Otherwise, respiratory depression rarely occurs. The main challenges of opioid
therapy have to do with managing such common side effects as nausea, vomiting,
itching, or somnolence. Although typically resolved within a few days to a
week, they can be temporarily incapacitating.
Nausea occurs in 10% to 40% of patients treated with opioids. If they are
getting good pain relief, there is no need to withdraw or reduce the
medication. Antiemetics such as promethazine or prochlorperazine, both of
which are available as pills and suppositories, are usually effective when
used three to four times a day for a few days. If the nausea is primarily
postprandial or related to bloating and early satiety, metoclopramide (10-20
mg tid) is the drug of choice. For some patients, antihistamines such as
hydroxyzine are also useful as antiemetics. In refractory cases, low doses of
haloperidol or olanzapine at bedtime can be very helpful.
Hives or itching may occur at the beginning of therapy with certain opioids as
a result of their direct effect on mast cells. These problems are more commonly
seen with the naturally occurring opiates (e.g., codeine or morphine) than
with synthetics. Although hives and itching are not generally considered
allergic reactions, relief can often be obtained with antihistamines. Patients
with a positive history of such symptoms can be preemptively given a
nonsedating antihistamine for the first week of opioid therapy.
Initiation or escalation of opioid medications can produce sedation or
somnolence in some patients. However, those with severe pain may feel more
alert or normal. If the patient is getting good pain relief but experiences
sedation, the patient and family should be counseled to find ways to limit
activities such as driving, working, meal preparation, and child care while the
opioid is being titrated. If the situation cannot be tolerated, the dose can be
reduced by 25% until the sedation lifts. Should it persist, other sedating
medications, including antihistamines and antiemetics used to counteract other
side effects, may have to be reduced in dose or eliminated.
A few patients experience myoclonus with opioid use. If discomforting, the
condition can be treated with a benzodiazepine. Clonazepam is a good choice,
because it is less sedating than other drugs in the same class. Opioids can
sometimes cause urinary retention and increased bladder capacity due to
increased sphincter tone. With high doses, peripheral edema may also occur as
a result of antidiuretic hormone release, in which case a short course of
diuretics is usually effective. There is no evidence of any organ toxicity
attributable to the prolonged use of sustained-release opioids.
The one common persistent side effect of opioid use is constipation, which is
mediated by opioid receptors in the bowel. More than half of patients on
sustained-release opioids experience constipation requiring specific therapy.
It is important to get patients on a good bowel regimen as soon as possible
and to teach them to adjust their bowel medications as needed. Many patients
start out with a stool softener (e.g., docusate) and a mild fiber-based
cathartic (e.g., senna). Osmotic laxatives such as milk of magnesia,
polyethylene glycol, magnesium citrate, or lactulose will probably also be
needed and may as well be started early. In contrast to stimulant laxatives,
osmotic diuretics are safe and non-habit-forming. Patients have to find the
dose that they can safely take nightly to produce a firm stool in the
morning. Persistent constipation can be a serious problem requiring emergency
treatment. I tell my patients to let me know if they have not had a bowel
movement for at least three days. At that point, oral magnesium citrate or a
sodium phosphate enema may be indicated.
Tolerance to Opioids
That most adverse side effects of opioids resolve on their own is an indication
of growing tolerance with continued use. Tolerance can also be conferred by
other factors. Severe pain, for example, allows patients to tolerate the
sedative effects of opioids. Whether tolerance develops to the pain-relieving
effects of opioids is a matter of controversy. Most of the data on opioid
tolerance and physical dependence in humans involves subjects who were not in
pain. Studies of patients with chronic pain who have taken opioids for a long
time indicate that once the dose required for pain relief is established, it
generally remains stable unless the underlying disease progresses.
Often, when a specific treatment or adjunctive therapy begins to work,
patients who have been taking opioids for some time will begin to feel
somnolent or sedated, or will not require rescue medications for long periods.
That is the time to consider slowly tapering the long-acting pain medication.
Physical Dependence on Opioids
With long-term use of opioids, patients will experience physical symptoms
(abdominal cramping, sweating, nausea, diarrhea, irritability) if the
medication is abruptly withdrawn or the dose is markedly reduced. This type of
physical dependence is not limited to opioids but can occur with other drugs
such as antihypertensives and steroids. It is a medical condition and should
not be taken as a sign of psychological or spiritual weakness. Withdrawal
symptoms are easily avoided by using a tapering regimen when lowering the
dose. This can nearly always be done, without discomfort, in an outpatient
setting. When necessary, however, withdrawal symptoms can usually be relieved
by slowing the taper or using small doses of clonidine or a benzodiazepine.
Appropriate Use Versus Abuse
"Nothing is intrinsically good or evil, but its manner of usage
may make it so." St. Thomas Aquinas
The fear of drug abuse and drug addiction is the major reason that physicians
are reluctant to prescribe opioid medications for patients in severe pain.
The inappropriate use of a medication for a nonmedicinal problem is drug
abuse. Using a pain medication to get high or euphoric is clearly
inappropriate, as is using drugs to escape family or other problems that
should be dealt with by other means. If a patient's physical pain has
prevented him or her from living life fully, using a medication that allows a
return to normal activities cannot be called drug abuse.
The appropriate role of medicine is to prolong and maintain life, promote
function, and provide comfort from symptoms of disease. It is up to the
physician to determine whether the prescribed medications are being used to
participate in life or to escape from it. The patient's mood and activities,
and the reports of family members, can be helpful indicators. Health care
facilities are beginning to use validated quality-of-life instruments that
should make the assessment of appropriate and inappropriate use easier.
Appropriate use of pain medications can significantly increase the quality of
life, inappropriate use invariably decreases it.
Addiction and Pseudoaddiction
Taken to the extreme, drug abuse can become drug addiction, a driving force
that leads to compulsive, socially inappropriate, or even dangerous behaviors.
The overwhelming majority of drug addicts report that their addiction began with
recreational drug use. Medical use of opioids is generally not associated with
addiction (less than 1%).
The most important predictor of continued abuse or addiction is previous
substance abuse. If a physician prescribes a pain medication in good faith,
anyone who leaves that physician's care with an addiction probably already
had a problem when the treatment began. That is not to say that addiction
disorders are not an important concern--they are serious health problems that
must be evaluated and treated. If substance abuse or addiction is strongly
suspected, the patient should be referred for evaluation by a psychologist or
psychiatrist who has had experience working with chronic pain patients.
Inappropriately labeling patients as addicts can alienate them from their
caregivers and family, deepen their isolation, and prolong their suffering.
Denied the pain treatment to which they are entitled, patients often say that
they feel isolated, anxious, and even desperate. The obsessive and manipulative
behaviors that these feelings engender, which can sometimes be confused with
addiction, are called pseudoaddiction. Russell Portenoy's tabulation of
drug-seeking behaviors is a useful reference for discriminating between
addiction and pseudoaddiction (Table 2). I go over this table with my patients
so that they are specifically aware of what I consider to be inappropriate
behaviors.
Behavioral Assessment of Drug Abuse or Addiction
Predictive Behaviors
- Selling prescription drugs
- Obtaining prescription drugs from a nonmedical source
- Stealing or borrowing drugs from others
- Using illicit drugs or abusing alcohol
- Injecting oral formulations
- Escalating dosage or otherwise not complying with therapy despite repeated
warnings
- Seeking prescriptions from other physicians without
informing the prescriber or after being warned to stop
- Demonstrating functional deterioration related to drug use
- Resisting changes in therapy repeatedly despite adverse
drug effects
Nonpredictive Behaviors
- Complaining aggressively about the need for more medicine
- Hoarding drugs during periods of reduced symptoms
- Requesting specific medications
- Escalating dosage or otherwise not complying with
therapy on only one or two occasions
- Using medication to treat unrelated symptoms
- Reporting psychic effects not intended by the physician
Adapted from Portenoy, 1994
Treating Chronic Pain - Healing the Incurable
Opioids are usually reserved as a last resort for the treatment of pain, but
it may be time to consider using them to rescue patients in severe pain who
have not responded to disease-specific treatments or mild analgesics. Once
some relief is achieved, adjuvant medications and nonpharmacologic or more
aggressive approaches can be tried. In my experience, most treatments work
better when there has been some initial pain relief.
Medical training places such a strong emphasis on curing disease that we
sometimes do not pay as much attention as we should to patients who cannot be
cured. This is particularly true of patients whose condition has not improved
despite years of traditional therapy. Even if they cannot be cured, however,
they can be healed. There may be no effective treatment for the underlying
illness, but there is almost always an effective treatment for the pain.
One thing that I learned in medical school that is still true today is that it
is very easy to become judgmental when faced with a patient whose suffering is
difficult to understand. Unfounded assumptions are harmful and can rob a
suffering patient of hope. With our current knowledge of how pain is generated
and alleviated, it is both disrespectful to the patient and a breach of medical
ethics not to provide what is clearly needed. When a patient in chronic pain
seeks our help, the first question we should ask ourselves is not whether we
should provide an analgesic but whether we can in good conscience leave that
person in pain.
Daniel Brookoff
University of Tennessee
Methodist Hospitals of Memphis
Copyright (C) 2000. The McGraw-Hill Companies