CLINICIAN’S CORNER Managing an Acute Pain Crisis in a Patient With Advanced Cancer “This Is as Much of a Crisis as a Code” The assessment and management of an acute pain crisis in the setting of advanced illness is challenging. Using the case of Mr X, a 33-year-old man with advanced metastatic mucinous adenocarcinoma of the appendix and “15 out of THE PATIENT’S STORY 10” pain, we explore the issues of acute pain and its man-
Mr X is a 33-year-old man with a 4-year history of meta-
agement. We define a pain crisis as an event in which the
static mucinous adenocarcinoma of the appendix. Over thecourse of his illness, Mr X completed several cycles of che-
patient reports pain that is severe, uncontrolled, and caus-
motherapy and had several percutaneous draining osto-
ing distress for the patient, family members, or both. Our
mies for small-bowel obstruction due to peritoneal carci-
management strategy focuses on making a pain diagno-
nomatosis. His most recent admissions were triggered by
sis, differentiating reversible from intractable causes of pain,
protracted nausea and vomiting and recurrent small-bowel
and making decisions about further workup; selecting the
obstructions associated with increasing abdominal pain. opioid and monitoring and treating opioid adverse effects;
In recent months, Mr X’s overall care had been managed
titrating and rotating opioid and coanalgesics; consulting
by his medical oncologist and the anesthesia pain service. In addition, on the admission prior to this, he had been briefly
experts to treat a pain crisis as quickly as possible to pre-
seen by a palliative care physician. His wife reported that
vent unnecessary suffering; and co-opting the available insti-
he had been “close to death” on several previous admis-
tutional resources. The timely intervention of a palliative
sions. Mr X and his family were aware of the extent of his
care team and its expertise can provide the staff, patients,
disease but wanted aggressive life-prolonging treatment to
and their families the benefit of an interdisciplinary approach
continue, including cardiopulmonary resuscitation. Mr X’s
and help the patients address goals of care; understand the
baseline chronic abdominal pain had nociceptive, visceral,
benefits and risks of treatment decisions; and meet the psy-
and neuropathic features and had been difficult to manage. chological, social, and existential needs of the patient and
After a variety of opioid trials, he had finally obtained someanalgesia on escalating doses of intravenous (IV) metha-
the family commonly seen in this setting.
done. His methadone dose at home after his last admission
was 800 mg over 24 hours (200 mg IV every 6 hours), withhis wife administering each 200-mg dose over a 20- to 30-
regimen was contraindicated because of the finding of a QTc
minute period. A visiting nurse service and a home care in-
prolongation on an electrocardiogram with the conse-
fusion company oversaw his methadone administration.
quent potential for an arrhythmia led to the decision to bring
One day before his final hospital admission, Mr X under-
went a celiac plexus block in an attempt to improve his pain
Author Affiliations: Department of Neurology, Pain and Palliative Care Service,
relief and decrease his opioid requirements. Two hours later
Memorial Sloan-Kettering Cancer Center, New York, New York.
he developed fever and severe abdominal pain, self-rated as
Corresponding Author: Kathleen M. Foley, MD, Weill Medical College of Cornell University, and Department of Neurology, Pain and Palliative Care Service, Me-
“15 out of 10” on a 0-to-10 scale. The patient’s unrelieved
morial Sloan-Kettering Cancer Center, 1275 York Ave, New York, NY 10021 (foleyk
pain and the visiting nurse’s concern that the methadone
@mskcc.org). Perspectives on Care at the Close of Life is produced and edited at the University of California, San Francisco, by Stephen J. McPhee, MD, Michael W. Rabow, MD, CME available online at www.jamaarchivescme.com
and Steven Z. Pantilat, MD; Amy J. Markowitz, JD, is managing editor. and questions on p 1487. Perspectives on Care at the Close of Life Section Editor: Margaret A. Winker, MD, Deputy Editor.
2008 American Medical Association. All rights reserved.
(Reprinted with Corrections) JAMA, March 26, 2008—Vol 299, No. 12 1457
PERSPECTIVES ON CARE AT THE CLOSE OF LIFE
Upon his arrival at the hospital, the patient’s tempera-
Mr X and his family, as homelike as possible, in which all
ture was 40.0°C, his blood pressure was 98/40 mm Hg, his
of the monitoring necessary to manage his pain and other
heart rate was 116/min, and his respiratory rate was 34/
symptoms was available. As he became more comfortable,
min. When examined by Dr P, the attending physician on
his methadone dose was stabilized, and Mr X made tele-
the medicine team, he was sitting up in bed in acute dis-
phone calls to say good-bye to family and friends.
tress. He was cachectic and jaundiced and complained of
Over the ensuing hours, his pain again started to esca-
severe abdominal pain. His abdominal examination re-
late and the doses of IV methadone were titrated up. Even-
vealed diffuse tenderness to palpation with rebound and
tually, he became sedated without evidence of distress, but
guarding. There was pus draining through the skin sites of
he developed myoclonic jerks. He was given a 60-mg dose
previous percutaneous draining ostomies.
of dantrolene intravenously and the myoclonus resolved.
The initial impression was that Mr X was in an acute pain
Approximately 36 hours after admission, Mr X died peace-
crisis superimposed on chronic abdominal pain. The pain
fully. His wife, their 2 dogs, and several family members and
exacerbation was thought to be associated with acute peri-
tonitis or bowel perforation due to the progressive meta-
Dr P and Dr S were interviewed by a Perspectives editor
static disease or the recent celiac plexus block. The main
priority of the medical team was pain crisis management andreestablishing the goals of care in the setting of the rapid
PERSPECTIVES
worsening of the patient’s condition. Despite the severity
DR P: I think as a primary medical team, we were becoming
of his pain, Mr X was alert and oriented with clear capacity
uncomfortable with the dosage and the amount of pain medi-
to engage in decision making about his care. cation the patient was requiring . . .
The medical team, in consultation with the anesthesia pain
DR S: The patient looked ashen and stressed. He was just
service, decided to transfer Mr X to the intensive care unit
holding his belly and he looked incredibly uncomfortable. He
(ICU) because of plans to control his pain with high-dose
was sweating and basically telling us that he really, really
IV opioids and ketamine. This would require a level of ob-
wanted us to do whatever it took to get his pain under control.
servation and monitoring not available on a medical ward. Mr X’s electrocardiogram again showed a prolonged QTc
Assessment and Management of an Acute Pain Crisis
interval. Because of the possibility that this was associated
The assessment and management of an acute pain crisis in
with the high dose of parenteral methadone, the decision
the setting of advanced illness are challenging.1,2 Using Mr
was made to discontinue the methadone and rotate to IV
X’s case, we outline a management strategy that focuses on
hydromorphone. Hydromorphone infusion was titrated from
(1) making a pain diagnosis, differentiating reversible from
30 mg/h to 80 mg/h with IV boluses of 80 mg every 10 min-
intractable causes of pain and making decisions about fur-
utes over the early morning hours without any improve-
ther workup, (2) selecting the opioid and monitoring and
ment in his pain. He was also given a racemic ketamine in-
treating adverse opioid effects, (3) titrating and rotating opi-
fusion titrated up to 7 mg/h. After almost 5 g of
oids and coanalgesics, (4) consulting experts to treat a pain
hydromorphone in a 10- to 12-hour period, the patient re-
crisis as quickly as possible to prevent unnecessary suffer-
ing, and (5) identifying and co-opting the available institu-
Dr S, the palliative care consultant, met with the family
and discussed the risks of restarting IV methadone despiteQTc interval prolongation. Mr X and his wife acknowl-
Definition of a Pain Crisis
edged that he was dying, requested use of any medications
We define a pain crisis as an event in which the patient re-
necessary to stop his pain, and declined further life-
ports severe, uncontrolled pain that is causing the patient,
prolonging measures such as cardiopulmonary resuscita-
family, or both severe distress. The pain may be acute in on-
tion. Pain relief, other symptom control, and facilitating the
set or may have progressed gradually to an intolerable thresh-
opportunity for him to say good-bye to family and friends
old (as determined by the patient), but requires immediate
became the focus of his care. The immediate goal was to man-
intervention. National Comprehensive Cancer Network pain
age the acute pain crisis as quickly as possible. The hydro-
management guidelines identify a pain emergency as an event
morphone was discontinued and the methadone was re-
in which patients have severe pain (a numerical estimate of
started with IV boluses of 40 mg every 15 minutes until pain
at least 7 on a 10-point scale) that requires rapid opioid ti-
relief was obtained. It had taken almost 12 hours to reduce
tration to provide analgesia.3 There are no epidemiological
his pain from 15 to 2 on a scale of 0 to 10. Within several
data to suggest how commonly pain crises occur. Our own
hours, a total dose of 1.59 g of methadone was adminis-
experience at Memorial Sloan-Kettering Cancer Center sug-
tered, and Mr X reported minimal and adequately con-
gests that of about 120 inpatient consultations a month, our
trolled pain of 2 on a 0-to-10 scale. His mental status re-
Pain and Palliative Care Service is called for what is iden-
mained intact. His wife stayed with him throughout. During
tified as a pain crisis by the referring physician as fre-
this period, the ICU staff created a private environment for
quently as 20 to 30 times a month—the message usually con-
1458 JAMA, March 26, 2008—Vol 299, No. 12 (Reprinted with Corrections)
2008 American Medical Association. All rights reserved.
PERSPECTIVES ON CARE AT THE CLOSE OF LIFE
veyed is that the patient needs to be seen “right now.” Thetreatment plan starts with a rapid clinical assessment, titra-
Box 1. Assessment of a Pain Crisis in a Patient
tion of analgesics, and direct supervision by a physician/
With Advanced Cancera
nurse team. When the medications or doses are not famil-
Believe the patient’s complaint of pain.
iar to the clinician providing direct patient care, appropriate
Take a careful history of each pain complaint and place it
experts and resources should be consulted to help outline
temporally in the patient’s cancer history (extent of dis-
a plan of care; guide medication titration; monitor the out-
ease, recent treatments, and interventions).
comes; and provide support to staff, patient, and family.3-5
Assess the characteristics of each pain, including its site, itspattern of referral, and its aggravating and relieving fac-
Pain Assessment During a Pain Crisis
DR S (THE PALLIATIVE CARE CONSULTANT): The first thing was
Clarify the temporal aspects of the pain (acute, subacute,
to understand what happened. Why was he saying that his pain
chronic, episodic, intermittent, breakthrough, or incident). was worse than it had ever been before? . . . I explained to them
Clarify the response to previous and current analgesic thera-
[patient and family] that something potentially catastrophichad happened since the celiac plexus block, and it might be aperforation. He very well might be dying of that, and then there
Evaluate the psychological state of the patient (eg, de-lirium, terminal agitation, existential crisis; all can contrib-
was the severe pain we had to deal with.
A thorough assessment of a pain crisis is just like the evalu-
ation of any other medical emergency. The basic pain as-
Ask whether the patient has a past history of alcohol or drugdependence (may influence the degree of opioid requirements).
sessment principles are outlined in BOX 1.6 Pain intensity, pain relief, and adverse effects of the therapy should be moni-
Perform a careful medical and neurological examination.
tored and recorded until the resolution of the pain crisis.
Define the goals of the pain intervention and be aware of
Based on Mr X’s description of severe abdominal pain and
the associated fever, which started approximately 2 hours
Order and personally review any appropriate diagnostic pro-
after receiving a celiac plexus block, bacterial peritonitis
cedures (diagnostic tests and interventions are dependent
caused by perforation of an underlying malignant bowel ob-
struction was considered to be a likely contributing cause
Treat the patient’s pain at the same time as determining the
of his pain crisis. High fever and hypotension due to bac-
terial peritonitis can be a terminal event in a patient with
Provide continuous monitoring and support of the patient
and family until the pain is brought under control.
In assessing both the pain experience and patients’ desired
Continuously reassess the patient’s response to pain therapy.
goals of care, clinicians should use a communication ap-
Continuously document drug doses administered, patient
proach that allows patients to lead the discussion, beginning
response, and reasons for dose escalation.
with their understanding of the nature of the pain, its mean-
Talk to the dying patient’s family about what to expect dur-
ing to them, and how they prioritize its management in es-
ing the dying process and availability of social work and chap-
tablishing treatment goals.7,8 Patients can often distinguish pain
from their experience of suffering, which frequently stems from
their multiple concerns about being a burden to their loved
ones, fear of dying, and concerns about their family.9 Anxi-ety, depression, existential distress, and delirium are com-mon psychological symptoms that can occur in a patient withsevere cancer pain and need to be addressed.10
and pain descriptors and takes only 15 seconds to com-
To assess Mr X’s pain, it was essential to establish a clear
plete, allowing for frequent repeated use.16 Studies using the
description of its onset, localization, pattern of referral, ex-
MPAC have demonstrated that the perception of pain in-
acerbating and relieving factors, and relationship to the re-
tensity contributes significantly to subjective distress, but
cent procedure and changes to his analgesic regimen (Box 1).6
the perception of inadequate pain relief was the more im-
Pain and symptom assessment tools that could be used to
portant factor. In Mr X’s case, a numeric scale provided a
define and quantify pain include the Brief Pain Inven-
useful outcome measure for the treating team, who ob-
tory,11 the McGill Pain Questionnaire,12 the Visual Analog
served the correlation of the scale representing decreased
Scale for the Management of Acute Pain,13 the Edmonton
pain with the patient’s appearance of improved comfort and
Symptom Assessment Scale,14 the Memorial Symptom As-
sessment Scale,15 and the Memorial Pain Assessment Card
This patient’s pain was thought to be mixed nociceptive,
(MPAC).16 Of these, the MPAC (FIGURE) provides a vali-
visceral, and neuropathic with inflammatory components.
dated method for rapid assessment of the patient; evalua-
This pain diagnosis was based on his previous pain history,
tion of the patient’s pain intensity; and degree of relief, mood,
his radiological studies consistent with malignant bowel ob-
2008 American Medical Association. All rights reserved.
(Reprinted with Corrections) JAMA, March 26, 2008—Vol 299, No. 12 1459
PERSPECTIVES ON CARE AT THE CLOSE OF LIFE
struction, his ascites, his multiple draining infected osto-
documentation should specify the plan and rationale for the
mies, and the high likelihood of perineural tumor infiltra-
workup, congruent with the goals of care and options con-
tion. These pain mechanisms can be inferred from animal
sidered. This is particularly important if a decision regard-
and human studies of malignant bowel obstruction and tu-
ing further workup and or management is focused on pro-
viding the patient with comfort.7 In a patient close to death,no further diagnostic studies should be ordered and “rou-
Diagnostic Studies and Treatment Strategy
tine” orders should be rewritten to focus on patient comfort.
Mr X presented as a medical emergency with severe intol-
Congruent to the goals of care, rapid titration of the an-
erable pain as his major symptom. Rapid assessment of his
algesias with close monitoring of the patient for pain and
medical status was necessary to establish a correct diagno-
adverse effects is paramount. The main principles of opi-
sis and develop a treatment plan. Although this patient re-
oid selection are outlined in BOX 2. Opioids should be ti-
fused further diagnostic studies, a flat plate of the abdo-
trated aggressively (BOX 3, TABLE 1, and TABLE 2). Nono-
men to assess for free air and bowel dilatation or a computed
pioids such as IV ketorolac or corticosteroids to address the
tomography scan to confirm bowel perforation to assess the
inflammatory components of pain may be combined with
severity of bowel obstruction may be appropriate diagnos-
opioids (TABLE 3).34-36 Spinal analgesia may be advanta-
tic studies in this situation.19 Broad-spectrum antibiotics were
geous because of the lower opioid dose needed, along with
a reasonable treatment option for one aspect of his pain ex-
the possibility of using a local anesthetic.
acerbation. The extent of the diagnostic workup to be done
In Mr X’s case, the medical team in consultation with an-
depends on the clinical situation (reversible crisis vs antici-
esthesia and palliative care services developed a treatment
pated worsening of a progressive disease that led to the cri-
strategy that reflected an end-of-life care pathway address-
sis), the goals of care, the patient’s wishes, and the risk-
ing the patient’s physical, psychological, social, and spiri-
benefit burden ratio of any diagnostic test considered. Clear
tual needs with the needs of his family.37,38
Figure. Memorial Pain Assessment Card Memorial Pain Assessment Card 4 Mood Scale 2 Pain Description Scale
Put a mark on the line to show your mood.
Circle the word that describes your pain. 1 Pain Scale 3 Relief Scale
Put a mark on the line to show how much pain there is.
Put a mark on the line to show how much relief you get.
Each numbered item is on a card and each card is presented to the patient separately in the numbered order: (1) visual analog scale for pain intensity, (2) modifiedTursky Pain descriptors scale, (3) visual analog scale for pain relief, and (4) visual analog scale for mood. 1460 JAMA, March 26, 2008—Vol 299, No. 12 (Reprinted with Corrections)
2008 American Medical Association. All rights reserved.
PERSPECTIVES ON CARE AT THE CLOSE OF LIFE
The Importance of Rapid Pain Control DR S: I feel that this is as much of a crisis as a code, and we Box 2. Principles of Opioid Selection have to be there by the bedside, supporting the primary team.for the Management of Pain
A rapid response to a pain crisis is essential for patients
Select the opioid drug based on the patient’s analgesic his-
both with early stage disease and those at the end of life.
tory, severity of the pain, and inferred pain mechanism(s).
Failure to adequately manage a pain crisis early in the dis-
Take into consideration the patient’s age, metabolic state,
ease course encumbers both the patient and family with the
presence of major organ failure (renal, hepatic, lung), and
fear that escalating pain and lack of effective treatment will
Consider pharmacologic issues (eg, potential accumula-
In cases of intractable pain refractory to rapid and expert
tion of active metabolites, effects of concurrent drugs, and
interventions such as opioid escalation or rotation, use of
coanalgesics, and anesthetic approaches, clinicians can con-
Know the drug class (eg, agonist, agonist/antagonist),
sider sedation as a temporary measure while other pain re-
duration of analgesic effects, and pharmacokinetic prop-
lief measures are being explored. It is helpful to ask the pa-
tient (with the family present) if it is acceptable to be sedated
Consider which of the available routes of administration for
if that is the only way to achieve adequate pain control. For
the opioid selected (eg, oral, rectal, transdermal, transmu-
some patients, sedation may be the treatment of choice. The
cosal, buccal, subcutaneous, intravenous, epidural, intra-
use of sedation in the imminently dying has been previ-
If nonparenteral administration is chosen, consider whichamong the various drug formulations available for the opi-
Use of Opioid Analgesics for a Pain Crisis
oid selected (eg, immediate release, controlled release, liq-
in an Inpatient Setting
uid, transmucosal, buccal) is most appropriate.
DR S: I was giving her [Mrs X] that bad news and also explain-ing that if we gave him the pain medication he needed, he wouldprobably go into a deep sleep and not wake up.Principles of Opioid Selection. In a patient who has not
be used with caution and consultation with a palliative care
been exposed to opioids in the past (opioid naı¨ve), mor-
or pain consultation team is recommended.
phine is generally considered the standard starting drug of
Opioid Route. Table 1 provides equianalgesic guidelines
choice (Box 2).41,42 Morphine should be avoided or used with
for commonly used opioid drugs to be converted from the
caution in patients with renal disease and hepatic insuffi-
oral or transdermal route of administration to IV or from
ciency. Morphine-6-glucoronide, an active metabolite of mor-
phine, contributes to analgesia and may worsen adverse ef-
Dose Escalation. Once an appropriate opioid has been
fects as it accumulates in patients with renal insufficiency.43,44
selected, the dose should be rapidly titrated until the pa-
Morphine-3-glucuronide, a nonactive metabolite, pro-
tient has relief of pain or excessive adverse effects develop
duces neuroexcitatory effects and the accumulation of both
(Box 3). Based on the pharmacokinetics of the specific opi-
of these metabolites is associated with confusion, sedation,
oids and current best practice identified in both the Na-
and myoclonus.45 For patients with hepatic or renal insuf-
tional Comprehensive Cancer Network Cancer Pain Guide-
ficiency, an opioid with a short half-life such as hydromor-
lines3 and the American Pain Society Guidelines,4 parenteral
phone or fentanyl are appropriate choices.
opioids are usually administered to the patient every 15 min-
Methadone has been found to provide effective analge-
utes as needed. This time interval is based on the approxi-
sia for patients whose pain is uncontrolled with other opi-
mate time to analgesic effect with IV opioid administration.
oids.46-49 In using methadone, the clinician must be aware
To achieve adequate analgesia in opioid-tolerant pa-
that the half-life of the drug is highly variable, ranging from
tients, it is recommended that the IV dose be incrementally
17 to 50 hours up to 190 hours in some patients with can-
increased by 50% (Box 3). Because the analgesic effect is a
cer.46,48 More importantly, if switching to methadone, the
logarithmic function of the dose of the opioid, a doubling
equianalgesic ratio dose depends on the patient’s degree of
of the dose in an opioid-tolerant patient may be needed.
tolerance to the previous opioid and can also vary over 10-
Opioid Rotation. For patients unable to tolerate escala-
fold (see Table 2).25-28 The significant reduction in opioid
tion of their current opioid dose because of adverse effects,
doses when switching is thought also to be related, in part,
an alternate opioid should be considered (opioid rotation;
to d-methadone being a noncompetitive antagonist at the
Box 3). Studies involving patients with cancer demon-
N-methyl D-aspartate (NMDA) receptor.49 The NMDA re-
strate wide interindividual variations in analgesic response
ceptor antagonists are analgesic in neuropathic pain and have
and adverse effects, and thus it may require a trial of 2 or 3
been shown to block the development of opioid toler-
opioid drugs to obtain effective analgesia with tolerable ad-
ance.49 In addition, methadone inhibits the uptake of sero-
verse effects.51 Tolerance to one opioid does not necessarily
tonin and norepinephrine.50 Therefore, methadone should
lead to complete tolerance to another (Table 2).25-28 This phe-
2008 American Medical Association. All rights reserved.
(Reprinted with Corrections) JAMA, March 26, 2008—Vol 299, No. 12 1461
PERSPECTIVES ON CARE AT THE CLOSE OF LIFE
Box 3. Managing a Pain Crisis With Parenteral Opioids in Patients Currently Receiving Opioid Therapy Group 1. Patients Who Have Inadequate Pain Relief and No Significant Opioid Adverse Effects
Continue the current opioid and use rescue doses for titration.
If taking an oral opioid, convert the patient’s rescue dose to an intravenous equivalent using relative potency tables (Table 1 andTable 2).
Administer double the rescue dose intravenously.
Repeat same dose in 15 minutes if there is no or minimal pain relief.
If pain persists at 7 or higher on a 10-point scale without adverse effects, increase the intravenous rescue dose by 50%.
Continue to administer this dose every 15 minutes until patient experiences more than 50% pain relief or adverse effects develop.
Consider intravenous adjuvants or coanalgesics (eg, a nonsteroidal anti-inflammatory drug or corticosteroids).
Once the patient has obtained adequate pain relief, calculate the new 24-hour opioid requirements including rescue doses andorder accordingly.
Decide route of opioid administration (eg, oral, intravenous, transdermal) best suited to the patient’s ongoing analgesic needsand adjust dose accordingly. Group 2. Patients Who Have Significant Opioid Adverse Effects
Discontinue the current opioid and rotate the patient to a different opioid (opioid rotation).
Refer to the equianalgesic tables (Table 1 and Table 2).
If the pain control is good but significant adverse effects are present, reduce the equianalgesic dose (Table 3) of the new opioidby 25% to 50% (accommodates for cross-tolerance); continue to monitor the patient for reduction in adverse effects and ad-equacy of pain relief; and provide for rescue doses for breakthrough pain.
If pain control is poor and significant adverse effects are present, rotate opioids without reduction in the equianalgesic dose;continue to monitor the patient for reduction in adverse effects and adequacy of pain relief; and provide for rescue doses.
For opioid-tolerant patients, estimate the safe starting dose of the new opioid depending on the patient’s tolerance (the higherthe previous opioid dose, the greater the level of tolerance; Table 2).
In all situations of opioid rotation, monitor the patient closely for adequacy of pain relief and reduction of adverse effects.
nomena of incomplete cross-tolerance, as evidenced by im-
Use of Adjuvant Coanalgesic Medications
proved pain relief or a reduction in adverse effects follow-
Adjuvant coanalgesic medications should be considered early
ing opioid rotation, is thought to be related, in part, to a range
in pain crisis management (Table 3).69 The term adjuvant
of interindividual pharmacogenetic factors including ge-
is used to describe different drugs and classes of drugs that
netic polymorphisms in the morphine gene and in drug
may enhance the effects of opioids or nonsteroidal
anti-inflammatory drugs.29 Adjuvants exert independent an-
When rotating from a short half-life opioid such as hy-
algesic activity in certain circumstances or counteract the
dromorphone or fentanyl to another opioid, calculate the
adverse effects of analgesics.3,5 Introducing adjuvant coan-
equianalgesic dose and estimate the safe starting dose (Table 1
algesic agents concurrently with opioid titration is recom-
and Table 2).20-25,27,55 In patients who have adequate anal-
mended based on the inferred mechanism of the pain crisis
gesia on their current opioid dose but intolerable or un-
and their known effectiveness in these situations. Table 3
manageable adverse effects, reduce the calculated equian-
lists some of the adjuvant coanalgesic medications that can
algesic dose by 25% to 50% or up to 90% in case of methadone
be administered through an IV when managing a pain
Opioid Adverse Effects. Nausea and vomiting, seda-
For Mr X, the anesthesia pain service recommended ket-
tion, delirium, respiratory depression, constipation, multi-
amine based on its reported efficacy in neuropathic and can-
focal myoclonus, and seizures are known adverse effects of
cer pain.30,31 Ketamine, an NMDA antagonist and an anes-
opioid drugs (TABLE 4).1,56,63,68 Tolerance develops to some
thetic that does not interfere with respiratory drive, has been
of these adverse effects, although at varying rates. For ex-
shown to be a potent analgesic in low doses.71 Multiple case
ample, tolerance may develop to nausea and vomiting, res-
series and small prospective studies using a double-blind,
piratory depression, and sedation but does not develop to
placebo-controlled approach suggest that very low-dose ket-
constipation. Each adverse effect requires a careful assess-
amine may potentiate opioid analgesia and reduce pain.30-32,34
The use of ketamine may not only provide greatly im-
1462 JAMA, March 26, 2008—Vol 299, No. 12 (Reprinted with Corrections)
2008 American Medical Association. All rights reserved.
PERSPECTIVES ON CARE AT THE CLOSE OF LIFE
proved pain relief but also allow for significant decreases
Table 1. Relative Single-Dose Potencies of Commonly Used Opioid
in the dose of current analgesics and sedatives. Some re-
Drugs for Pain and Their Oral-Intravenous Ratiosa
ports suggest that it is useful in visceral pain as well as neu-
Equianalgesic Intravenous or Oral-Intravenous
Ketamine should be started at a low dose of 0.02 to 0.05
Intramuscular Dose, mg
mg/kg per hour by continuous IV infusion and rapidly ti-
trated upward as needed, escalating the dose by up to 100%
every 4 to 6 hours, depending on the pain intensity and ad-
verse effect profile. In our experience, this dosing regimen
is both safe and well-tolerated. Cognitive adverse effects have
occurred infrequently at these doses. Because of the sever-
ity of his pain, Mr X eventually received 7 mg/h of IV ket-
amine, and because he was in a closely monitored setting,
a This table should be used as a guide only and not replace a more in-depth review.4
his dose could have been titrated upward even further in
Individual dosing and drug selection depend on each patient’s particular situation andcomprehensive assessment.
an attempt to increase his pain relief, had he desired, to al-
b Refer to Table 2 for rotation to methadone for long-term administration.
low for a decrease in his methadone requirements. How-ever, at doses of 10 to 20 mg/h, 30% to 50% of patients arereported to develop drowsiness, nightmares, and halluci-
Table 2. Variability in Dose Ratios When Switching Oral Morphine, Oral Hydromorphone, and Transdermal Fentanyl to Methadonea
nations.72 Due to few published data, a Cochrane review con-cluded that the role of ketamine is not yet established.33 To
Morphine→Methadone Ratio25
develop evidence-based guidelines for cancer patients, ad-
Use of Methadone in Pain Crisis Management
Dr S: I told him that if he wanted us to get the pain under con-trol and if the only way that we could do this was with IV metha-done, then we thought that it did not make sense to follow hisQT interval, or get EKGs, and we should just put that aside.He said he completely agreed, and his wife said she also
a To change from oral morphine to oral methadone for a patient taking 80 mg/d of
morphine orally, the equivalent methadone dose based on this study (4:1 ratio) willbe 20 mg of methadone orally every 24 hours. For a patient taking 800 mg/d oral
Prior to this admission, methadone was the only opioid that
morphine based on a 12:1 conversion ratio, the equivalent methadone dose will be67 mg/24 h. When changing from transdermal fentanyl to oral methadone the dose
was effective in at least partially controlling Mr X’s pain. He
ratio is reported to remain the same, independent of the fentanyl dose. Table 3. Adjuvant Drugs for Parenteral Use in Pain Crisis Managementa Category/Drug Indication Comments
Equianalgesic to morphine (10 mg IV morphine = 10 mg
Substantial GI and renal toxic effects may precipitate
Potential for GI bleed, hyperglycemia, psychosis
Inform patient/caregiver that sedation is common
If sedation is the goal, it can be given as IV infusion
but may cause agitation in elderly or delirious patients
Administer slowly over 2-3 min; monitor for sedation
If sedation is the goal, it can be given as an IV infusionTachyphylaxis is common
Opioid-sparing dissociative agent in higher doses
Abbreviations: GI, gastrointestinal; IV, intravenous; NSAID, nonsteroidal anti-inflammatory drug.
a Indications are based on clinical experience and are not necessarily supported by trial data or US Food and Drug Administration approval.
2008 American Medical Association. All rights reserved.
(Reprinted with Corrections) JAMA, March 26, 2008—Vol 299, No. 12 1463
PERSPECTIVES ON CARE AT THE CLOSE OF LIFE
had received 800 mg of parenteral methadone in the 24-hour
tant administration of CYP3A4 inhibitors such as erythro-
period prior to his admission to the hospital in a pain crisis.
mycin, dicumarol, and other drugs (which can inhibit the bio-
Based on published pain practice guidelines,3,4 a bolus dose
transformation of methadone), hypokalemia, hepatic failure,
of 80 to 160 mg (10% to 20% of the 24-hour dose) of metha-
and administration of other QT-prolonging agents such as
done should be repeated every 15 minutes until the patient
chlorobutanol, the preservative in parenteral methadone prepa-
experiences pain relief or dose-limiting toxicity. Because of
rations.80 Clearly, the benefit of methadone in the individual
the prolonged QTc interval, Mr X was rotated to parenteral
patient needs to be weighed against the potential for risk of
hydromorphone and obtained no relief despite using 80 mg
arrhythmia. Each of the associated factors that could con-
of hydromorphone per IV with boluses of 80 mg every 10 min-
tribute to methadone toxicity need to be evaluated in pa-
utes. After reestablishing the goals of care and declining life-
tients with a history of significant QTc prolongation.
prolonging therapy, methadone was restarted and titrated up
In Mr X, electrolyte correction and the use of preservative-
to analgesia over the next few hours.
free methadone would have been one approach to consider
This clinical predicament raises several questions:
to reduce risk and to allow continuation of methadone.75
What is the relationship between parenteral methadone and
Despite the potential risk and consequences of torsades de
pointes, his goals of care and lack of pain control with other
The relationship between methadone and QTc prolonga-
agents favored continuation of parenteral methadone.
tion is well described.73-79 Drug-induced long QT syndrome
Could the hydromorphone have been titrated up further?
is characterized by a prolonged corrected QT interval (QTc)
Abrupt discontinuation of methadone has been reported
and increased risk of a polymorphic ventricular tachycardia,
to cause pain escalation in 12 of 13 patients who were re-
also known as torsades de pointes. Published studies sug-
ceiving methadone as a third- or fourth-line opioid, de-
gest that QT prolongation is context-dependent and occurs
spite titration of the alternative opioid to the highest toler-
more frequently with high doses of methadone, concomi-
ated dose.81 If rotation from high-dose methadone to an
Table 4. Opioid-Related Adverse Effects During Rapid Opioid Escalation Management Influenced by Goals of Care1,27,28,51 More Likely to Be Seen in Patients Adverse Effects With the Following Conditions Treatment
Use benzodiazepinesReduce opioidRotate opioid57,58
Avoid sedating medications, unless essential
Rotate to opioid with short half-life and no active metabolites
Discontinue all medications that can contribute to the sedation
Rotate to opioid with short half-life and no active metabolite
Rotate opioid to short half-life drug without active metabolites
If no response to naloxone, consider intubation
Rotate opioid to another opioid with less histamine release potential64,65
Abbreviation: COPD, chronic obstructive pulmonary disease.
a Naloxone has the potential to increase pain in nearly all cases and should be administered with caution, understanding that only unacceptable and life-threatening opioid-induced
sedation and respiratory depression should be reversed by naloxone (respirations Ͻ8/min, shallow respirations, O2 saturation less than 92%, difficult to arouse). If a decision touse naloxone is made, 1 ampule (0.4 mg) needs to be diluted in 9 mL of normal saline and administered slowly, 0.1 to 0.2 mg (1- to 2-mL increments) every 2 to 3 minutes toachieve the desirable level of opioid-agonist respiratory depression reversal and alertness without pain flare. The half-life of naloxone is shorter than for many oral, long-actingopioids, so repeated doses of naloxone may be needed, and careful patient monitoring with continuous pulse oximetry and nasal cannula oxygen are recommended. If therespiratory depressant effects of a long half-life drug such as methadone is required, a naloxone infusion should be used (2 mg/50 mL of dextrose with water or normal saline [0.4mg]. Infuse 0.4 to 0.8 mg/h. Titrate infusion rate to desired effect). For opioid-induced respiratory depression and sedation caused by partial agonists/antagonists, much largerdoses of naloxone may be required. For patients taking buprenorphine, naloxone may be ineffective. If intravenous boluses (typically 0.4-2 mg) are effective, start naloxone dripif on fentanyl patch, methadone, or other long-acting medications/delivery systems. Monitor for pain escalation after administering naloxone. 1464 JAMA, March 26, 2008—Vol 299, No. 12 (Reprinted with Corrections)
2008 American Medical Association. All rights reserved.
PERSPECTIVES ON CARE AT THE CLOSE OF LIFE
alternate opioid is necessary, frequent monitoring of the pa-
nently dying and distinguishes it from physician-assisted
tient for pain escalation, withdrawal symptoms, or overse-
dation is essential. A step-wise approach is recommended,
The house officer’s intent in rapidly titrating Mr X’s opioid
decreasing the methadone dose by one-third daily while add-
dose was to reduce his pain and to improve his quality of life,
ing the new opioid in equianalgesic doses. This approach
albeit recognizing that this approach could potentially has-
helps to prevent symptoms of withdrawal from methadone
ten the patient’s death.94 Yet 2 studies involving terminally ill
as well as adverse effects from rapid up-titration of the al-
cancer patients receiving palliative care found no difference
ternate opioid. Mr X received almost 5 g of hydromor-
in the time to death when comparing patients sedated to con-
phone without evidence of analgesia or adverse effects, so
trol refractory symptoms with patients who were not se-
it could have been further escalated. Practically speaking,
dated.86,91 A study of survival following withdrawal of life-
using 80-mg boluses of a drug that comes in 2-mg and 10-mg
sustaining measures in ICU patients who were dying observed
vials is onerous for pharmacists to prepare, and often there
that the patients receiving morphine lived longer than those
who did not.92 Data from the National Hospice Outcomes
How difficult is it to rotate to methadone?
Project found opioid dosing to be associated with the time of
Any rotation to methadone requires frequent monitoring
death but it was only a minor factor in the variation in sur-
of the patient for undertreatment, withdrawal symptoms, or
vival.93 Despite these data, health care professionals com-
oversedation. Methadone is a unique opioid and an increas-
monly have concerns about their role in hastening a patient’s
ing number of case reports describe improved pain relief af-
death.94,95 These concerns can be addressed by institutions in
ter rotation to methadone.25-28,82,83 Patients rotated to paren-
the form of guidelines or pathways that make transparent the
teral methadone may have incomplete cross-tolerance. The
indications for opioid titration and symptom outcome end
ratio for calculating the safe initial continuous infusion metha-
points (eg, evidence of patient comfort) that allow for clear
done dose can be much lower than the published single-dose
documentation of goals of treatment.
equianalgesic dose ratios (Table 2).25,26,84,85
Methadone, therefore, should be used with caution, and
CONCLUSION
consultation with a palliative care or pain consultation team
DR P: The day after he [Mr X] passed away, the resident, themedical student, the interns, and I got together, and we spentalmost an hour debriefing about the experience. It was an ex-Pain Crisis Management and Institutional Resources perience that I hope was as helpful for them as it was for me.
DR P: One of the pearls of wisdom that we talked about as aWe talked about the medical aspects and what we learned. Weteam the next day is that in situations at the end of life, it’s reallytalked about pain management and what we learned from ourimportant to get people involved just as if someone was havingconsulting services. We really spent a lot of time just talkinga heart attack. In that case, you would call a cardiologist. Ifabout death and dying, communication at that stage, and whatsomeone had a dropped lung, you would call a surgeon. In ait was like to go home after an experience like that and to talksimilar way, you have to treat someone who is terminal, mean-ing death being imminent, as almost a code, in the sense that
The palliative care consultation team became actively in-
you have to get the people involved who can best provide care
volved with the patient when his goals of care changed to com-
fort care and when he was identified as dying. The stand-
Mr X presented a particular challenge because the dose
point that a palliative care team should only become “really
of parenteral opioids that he was receiving was clearly beyond
involved” if the patients has a “no code” status is contrary to
the house officer’s experience and the house officer needed
the current concept of palliative care for which the goal is to
expert consultation. This case illustrates the critical need
move palliative care upstream as part of comprehensive care.
for a clinical pathway for an acute pain crisis and other symp-
Although discussion of the management of this case has been
tom management in a dying patient.86,87 Such institutional
focused on the medical management of the pain crisis, ho-
guidelines are important for resource allocation both of staff
listic care of the patient and the family needs the expertise of
time and ICU bed allocation, enabling continuous moni-
the other team members providing psychological support and
toring of the high-dose opioid and ketamine infusions. Such
behavioral approaches as well as spiritual care.2,96-98 Most of
guidelines for management of an acute pain crisis frame a
palliative care in oncology is provided by oncological teams.
standard of care, informing both the patient and the health
Routine comprehensive symptom assessment and manage-
care professionals of a recommended approach, and help to
ment may help identify the areas for which palliative care spe-
distinguish the appropriate use of rapidly escalating high-
cialists may provide direct care to the patient; support the pri-
dose opioids and other agents in a dying patient from inap-
mary service; or facilitate communications between the patient,
propriate strategies of euthanasia and physician-assisted sui-
caregivers, and medical team.96,98-101 Institutional guidelines
cide (illegal in all states except Oregon).88-90 The Supreme
can provide structure for routine palliative care assessment
Court decision on physician-assisted suicide endorses aggres-
to identify and address unmet palliative care needs and to tran-
sive palliative care, even to the point of sedation, in the immi-
2008 American Medical Association. All rights reserved.
(Reprinted with Corrections) JAMA, March 26, 2008—Vol 299, No. 12 1465
PERSPECTIVES ON CARE AT THE CLOSE OF LIFE
Financial Disclosures: None reported.
the management of chronic cancer pain: safe and effective starting doses when
Funding/Support: The Perspectives on Care at the Close of Life section is made
substituting methadone for fentanyl. Cancer. 2001;92(7):1919-1925.
possible by a grant from the California HealthCare Foundation. 28. Mercadante S, Villari P, Ferrera P, Casuccio A, Gambaro V. Opioid plasma Role of the Sponsors: The funding source had no role in the preparation, review,
concentrations during a switch from transdermal fentanyl to methadone. J PalliatOther Resources: For a list of related references, see the JAMA Web site at http: 29. Mercadante SL, Berchovich M, Casuccio A, Fulfaro F, Mangione S. A pro-
spective randomized study of corticosteroids as adjuvant drugs to opioids in ad- vanced cancer patients. Am J Hosp Palliat Care. 2007;24(1):13-19. 30. Fine PG. Low-dose ketamine in the management of opioid nonresponsive ter- REFERENCES
minal cancer pain. J Pain Symptom Manage. 1999;17:296-300. 31. Ben-Ari A, Lewis MC, Davidson E. Chronic administration of ketamine for 1. Moryl N, Carver A, Foley KM. Pain and palliation. In: Holland JF, Frei E, eds.
analgesia. J Pain Palliat Care Pharmacother. 2007;21(1):7-14. Cancer Medicine. 7th ed. Hamilton, ON: BC Decker Inc; 2006:1113-1124. 32. Mercadante S. Ketamine in cancer pain an update. Palliat Med. 1996;10 2. Meyers FJ, Linder J, Beckett L, Christensen S, Blais J, Gandara DR. Simulta-
neous care: a model approach to the perceived conflict between investigational
33. Bell RF, Dahl JB, Moore RA, et al. Peri-operative ketamine for acute post-
therapy and palliative care. J Pain Symptom Manage. 2004;28(6):548-556.
operative pain: a quantitative and qualitative systematic review (Cochrane review). 3. NCCN Clinical Practice Guidelines in Oncology: Adult Cancer Pain; 2007. http: Acta Anaesthesiol Scand. 2005;49(10):1405-1428.
//www.nccn.org/professionals/physician_gls/PDF/pain.pdf. Accessed February 27,
34. Visser E, Schug SA. The role of ketamine in pain management. Biomed Pharmacother. 2006;60(7):341-348. 4. American Pain Society. Principles of Analgesic Use in the Treatment of Acute 35. Gutstein BH, Akil A. Opioid analgesics. In: Hardman JG, Limbird LE, eds. Good- Pain and Cancer Pain. 5th ed. Glenview, IL: American Pain Society; 2007. man and Gillman The Pharmacological Basis of Therapeutics. 10th ed. New York,
5. NCCN Clinical Practice Guidelines: Palliative Care; 2007. http://www.nccn.org
NY: McGraw-Hill Companies Inc North America; 2001:598-599.
/professionals/physician_gls/PDF/palliative.pdf. Accessed February 27, 2008. 36. Feuer DJ, Broadley KE. Corticosteroids for the Resolution of Malignant Bowel 6. Foley KM. Management of cancer pain. In: DeVita VT, Hellman S, Rosenberg Obstruction in Advanced Gynecological and Gastrointestinal Cancer. Chichester,
SA, eds. Cancer Principles and Practice of Oncology. 7th ed. Philadelphia, PA: Lip-
UK: The Cochrane Library, John Wiley & Sons Ltd; 2004.
pincott Williams & Wilkins; 2005:2615-2649. 37. Bookbinder M, Blank AE, Arney E, et al. Improving end-of-life care: develop- 7. Steinhauser KE, Christakis NA, Clipp EC, et al. Factors considered important at
ment and pilot-test of a clinical pathway. J Pain Symptom Manage. 2005;29
the end-of-life by patients, family, physicians and other care providers. JAMA. 2000;
38. Ellershaw JE, Murphy D. The Liverpool Care Pathway (LCP) influencing the 8. Coyle N. The hard work of living in the face of death. J Pain Symptom Manage.
UK national agenda on care of the dying. Int J Palliat Nurs. 2005;11(3):132-
9. Cherny NI, Foley KM. Suffering in the advanced cancer patient: a definition 39. Cherny NI. Sedation for the care of patients with advanced cancer. Nat Clin
and taxonomy. J Palliat Care. 1994;10(2):57-70. Pract Oncol. 2006;3(9):492-500. 10. Wilson KG, Chochinov HM, Skirko M, et al. Depression and anxiety disorders 40. Lo B, Rubenfeld G. Palliative sedation in dying patients: “we turn to it when
in palliative cancer care. J Pain Symptom Manage. 2007;33(2):118-129.
everything else hasn’t worked.” JAMA. 2005;294(14):1810-1816. 11. Daut RL, Cleeland CS, Flanery R. Development of the Wisconsin Brief Pain Inventory to assess pain in cancer and other diseases. 41. Klepstad P, Kaasa S, Skauge M, Borchgrevink PC. Pain intensity and side ef-
fects during titration of morphine to cancer patients using a fixed schedule dose
12. Melzak R. The McGill Pain Questionnaire. In: Melzak R, ed. Pain Measure-
escalation. Acta Anaesthesiol Scand. 2000;44(6):656-664. ment and Assessment. New York, NY: Raven Press; 1993. 42. Klepstad P, Kaasa S, Borchgrevink PC. Start of oral morphine to cancer pa- 13. Bijur PE, Silver W, Gallagher J. Reliability of the Visual Analog Scale for Mea-
tients: effective serum morphine concentrations and contribution from morphine-
surement of Acute Pain. Acad Emerg Med. 2001;8(12):1153-1157.
6-glucuronide to the analgesia produced by morphine. Eur J Clin Pharmacol. 2000;
14. Bruera E, Kuehn N, Miller MJ, et al. The Edmonton Symptom Assessment Sys-
tem (ESAS): a simple method for the assessment of palliative care patients. J Pal-43. Owen JA, Sitar DS, Berger L, Brownell L, Duke PC, Mitenko PA. Age-related
morphine kinetics. Clin Pharmacol Ther. 1983;34(3):364-368. 15. Portenoy RK, Thaler HT, Kornblith AB, et al. The Memorial Symptom Assess- 44. Portenoy RK, Foley KM, Stuhnan J, et al. Plasma morphine and morphine-6-
ment Scale: an instrument for the evaluation of symptom prevalence, character-
glucuronide during chronic morphine therapy for cancer pain: plasma profiles, steady-
istics and distress. Eur J Cancer. 1994;30A(9):1326-1336.
state concentrations and the consequences of renal failure. Pain. 1991;47(1):
16. Fishman B, Pasternak S, Wallenstein SL, Houde RW, Holland JC, Foley KM.
The Memorial Pain Assessment Card. A valid instrument for the evaluation of can-
45. Smith MT. Neuroexcitatory effects of morphine and hydromorphone: evi-
cer pain. Cancer. 1987;60(5):1151-1158.
dence implicating the 3-glucuronide metabolites. Clin Exp Pharmacol Physiol. 2000;
17. Sandner-Kiesling A, Bantel C. New models for visceral pain. Curr Opin Anaesthesiol. 2003;16(5):535-540. 46. Manfredi PL, Foley KM, Payne R, Houde R, Inturrisi CE. Parenteral metha- 18. Anthony T, Baron T, Mercandante S, et al. Report of the clinical protocol com-
done: an essential medication for the treatment of pain. J Pain Symptom Manage.
mittee: development of randomized trials for malignant bowel obstruction. J PainSymptom Manage. 2007;34(1 suppl):S49-S59. 47. Bruera E, Sweeney C. Methadone use in cancer patients with pain: a review. 19. Ripamonti C, Twycross R, Baines M, et al; Working Group of the European J Palliat Med. 2002;5(1):127-138.
Association for Palliative Care. Clinical practice recommendations for the man-
48. Davis MP, Walsh D. Methadone for relief of cancer pain a review of phar-
agement of bowel obstruction in patients with end-stage cancer. Support Care
macokinetics, pharmacodynamics, drug interactions and protocols of administration. Support Care Cancer. 2001;9(2):73-83. 20. Colucci RD, Swanton RE, Thomas GB, Kaiko RF. Relative variability in bio- 49. Gorman AL, Elliott KJ, Inturrisi CE. The D- and L-isomers of methadone bind
availability of oral controlled-release formulations of oxycodone and morphine.
to the non-competitive site on the N-methyl D-aspartate (NMDA) receptor in rat
Am J Ther. 2001;8(4):231-236.
forebrain and spinal cord. Neurosci Lett. 1997;223(1):5-8. 21. Ordo´n˜ez A, Gonza´lez BM, Espinosa AE. Oxycodone: a pharmacological and 50. Codd EE, Shank RP, Schupsky JJ, Raffa RB. Serotonin and norepinephrine up-
clinical review. Clin Transl Oncol. 2007;9(5):298-307.
take inhibiting activity of centrally acting analgesics: structural determinants and
22. Sarhill N, Walsh D, Nelson KA. Hydromorphone: pharmacology and clinical
role in antinociception. J Pharmacol Exp Ther. 1995;274(3):1263-1270.
applications in cancer patients. Support Care Cancer. 2001;9(2):84-96. 51. Cherny NI, Chang V, Frager G, et al. Opioid pharmacotherapy in the man- 23. Muijsers RB, Richard BR, et al. Transdermal fentanyl: an updated review of
agement of cancer pain: a survey of strategies used by pain physicians for the se-
its pharmacological properties and therapeutic efficacy in chronic cancer pain control.
lection of analgesic drugs and routes of administration. Cancer. 1995;76(7):1283-
Drugs. 2001;61(15):2289-2307. 24. Sopalski MA. Pain control with fentanyl patch. J Hospice Pall Nursing. 2007; 52. Pasternak GW. Molecular biology of opioid analgesia. J Pain Symptom Manage. 25. Bruera E, Pereira J, Wantanabe S, Belzile M, Kuehn N, Hanson J. Opioid ro- 53. Somogyi AA, Barratt DT, Coller JK. Pharmacogenetics of opioids. Clin Phar-
tation in patients with cancer pain: a retrospective comparison of dose ratios be-
macol Ther. 2007;81(3):429-444.
tween methadone, hydromorphone, and morphine. Cancer. 1996;78(4):852-
54. Tomalik-Scharte D, Lazar A, Fuhr U, Kirchheiner J. The clinical role of genetic
polymorphisms in drug-metabolizing enzymes. Pharmacogenomics. 2008;8(1):
26. Ripamonti C, Zecca E, Bruera E. An update on the clinical use of methadone
for cancer pain. Pain. 1997;70(2-3):109-115. 55. Foley KM. Changing concepts of tolerance to opioids: what the cancer pa- 27. Santiago-Palma J, Khojainova N, Kornick C, et al. Intravenous methadone in
tient has taught us. In: Chapman CR, Foley KM, eds. Current & Emerging Issues1466 JAMA, March 26, 2008—Vol 299, No. 12 (Reprinted with Corrections)
2008 American Medical Association. All rights reserved.
PERSPECTIVES ON CARE AT THE CLOSE OF LIFE
in Cancer Pain: Research & Practice. New York, NY: Raven Press; 1993:
79. Al-Khatib SM, LaPointe NM, Kramer JM, Califf RM. What clinicians should
know about the QT interval. JAMA. 2003;289(16):2120-2127. 56. Wilson RK, Weissman DE. Neuroexcitatory effects of opioids: patient assess- 80. Kornick CA, Kilborn MJ, Santiago-Palma J, et al. QTc interval prolongation
ment #57. J Palliat Med. 2004;7(4):579.
associated with intravenous methadone. Pain. 2003;105:499-506. 57. Marinella MA. Meperidine-induced generalized seizures with normal renal 81. Moryl N, Santiago-Palma J, Kornick C, et al. Pitfalls of opioid rotation: sub-
function. South Med J. 1997;90(5):556-558.
stitution another opioid for methadone in patients with cancer pain. Pain. 2002;
58. Challoner KR, McCarron MM, Newton EJ. Pentazocine (Talwin) intoxication:
report of 57 cases. J Emerg Med. 1990;8(1):67-74. 82. Crews JC, Sweeney NJ, Denson DD. Clinical efficacy of methadone in pa- 59. Breitbart W, Marotta R, Platt MM, et al. A double-blind trial of haloperidol,
tients refractory to other mu-opioid receptor agonist analgesics for management
chlorpromazine, and lorazepam in the treatment of delirium in hospitalized AIDS
of terminal cancer pain: case presentations and discussion of incomplete cross-
patients. Am J Psychiatry. 1996;153(2):231-237.
tolerance among opioid agonist analgesics. Cancer. 1993;72(7):2266-2272. 60. Boettger S, Breitbart W. Atypical antipsychotics in the management of de- 83. Nicholson AB. Methadone for cancer pain. Cochrane Database Syst Rev. 2004;
lirium: a review of the empirical literature. Palliat Support Care. 2005;3(3):227-
84. Kloke M, Rapp M, Bosse B, Kloke O. Toxicity and/or insufficient analgesia to 61. Prommer E. Modafinil: is it ready for prime time? J Opioid Manag. 2006;
opioid therapy risk factors and the impact of changing the opioid. A retrospective
analysis of 273 patients observed at a single center. Support Care Cancer. 2000;
62. Reissig JE, Rybarczyk AM. Pharmacologic treatment of opioid-induced seda-
tion in chronic pain. Ann Pharmacother. 2005;39(4):727-731. 85. Houde RW, Wallenstein SL, Beaver WT. Evaluation of analgesics in patients 63. Mercadante S. Pathophysiology and treatment of opioid-related myoclonus
with cancer pain. In: Lasagna L, ed. International Encyclopedia of Pharmacology
in cancer patients. Pain. 1998;74(1):5-9. and Therapeutics. Oxford, United Kingdom: Pergamon Press; 1966:59-98. 64. Tarcatu D, Tamasdan C, Moryl N, Obbens E. Are we still scratching the sur- 86. Ventafridda V, Ripamonti C, DeConno F, Tanburini M, Cassileth BR. Symp-
face? a case of intractable pruritus following systemic opioid analgesia. J Opioid
tom prevalence and control during cancer patient’s last days of life. J Palliat Care. 65. Katcher J, Walsh D. Opioid-induced itching: morphine sulfate and hydromor- 87. Foley KM, Gelband H, eds. Improving Palliative Care for Cancer. Washing-
phone hydrochloride. J Pain Symptom Manage. 1999;17(1):70-72.
ton, DC: Institute of Medicine Report, National Academies Press; 2001. 66. Barretto de Carvalho Fernandes MC, Vieira da Costa V, Saraiva RA. Postop- 88. Burt RA. The Supreme Court speaks: not assisted suicide but a constitutional
erative urinary retention: evaluation of patients using opioids analgesic. Rev Lat
right to palliative care. N Engl J Med. 1997;337(17):1234-1236. Am Enfermagem. 2007;15(2):318-322. 89. Sulmasy DP, Ury WA, Ahronheim JC, et al. Publication of papers on assisted 67. Bruera E, Belzile M, Neumann C, Harsanyi Z, Babul N, Darke A. A double-
suicide and terminal sedation. Ann Intern Med. 2000;133(7):564-565.
blind, crossover study of controlled-release metoclopramide and placebo for the
90. Cranford RE, Gensinger R. Hospital policy on terminal sedation and euthanasia.
chronic nausea and dyspepsia of advanced cancer. J Pain Symptom Manage. 2000;
HEC Forum. 2002;14(3):259-264. 91. Stone P, Phillips C, Spruyt O, Waight C. A comparison of the use of sedatives 68. McNicol E, Horowicz-Mehler N, Fisk RA, et al; American Pain Society. Man-
in a hospital support team and in a hospice. Palliat Med. 1997;11(2):140-144.
agement of opioid side effects in cancer-related and chronic non-cancer pain: a
92. Wilson WC, Smedira NG, Fink C, McDowell JA, Luce JM. Ordering and ad-
systematic review. J Pain. 2003;4(5):231-256.
ministration of sedatives and analgesics during the withholding and withdrawal
69. Lussier D, Huskey AG, Portenoy RK. Adjuvant analgesics in cancer pain
of life support from critically ill patients. JAMA. 1992;267(7):949-953.
management. Oncologist. 2004;9(5):571-591. 93. Portenoy RK, Sibireceva U, Smout R, et al. Opioid use and survival at the end 70. Wiffen P, Collins S, McQuay H, Carroll D, Jadad A, Moore A. Anticonvulsant
of life: a survey of hospice population. J Pain Symptom Manage. 2006;32(6):
drugs for acute and chronic pain. Cochrane Database Syst Rev. 2000;3(3):CD001133. 71. Edwards ND, Fletcher A, Cole JR, Peacock JE. Combined infusions of mor- 94. Kaldjian LC, Wu BJ, Kirkpatrick JN, Thomas-Geevarghese A, Vaughan-
phine and ketamine for postoperative pain in elderly patients. Anaesthesia. 1993;
Sarrazin M. Medical house officers’ attitudes toward vigorous analgesia, terminal
sedation, and physician-assisted suicide. Am J Hosp Palliat Care. 2004;21(5):
72. White PR, Way WL, Trevor AL. Ketamine—its pharmacology and therapeu-
tic uses. Anesthesiology. 1982;56:119-136. 95. Carver AC, Vickrey BG, Bernat JL, Keran C, Ringel SP, Foley KM. End-of-life 73. Wedam EF, Bigelow GE, Johnson RE, et al. QT-interval effects of methadone,
care: a survey of US neurologists’ attitudes, behavior, and knowledge. Neurology.
levomethadyl, and buprenorphine in a randomized trial. Arch Intern Med. 2007;
96. Berzoff J, Silverman P. Living With Dying. New York, NY: Columbia Univer- 74. Krantz MJ, Lowery CM, Martell BA, Gourevitch MN, Arnsten JH. Effects of
methadone on QT-interval dispersion. Pharmacotherapy. 2005;25(11):1523-
97. Sulmasy DP. A biopsychosocial-spiritual model for the care of patients at the
end of life. Gerontologist. 2002;42:24-33. 75. Sekine R, Obbens E, Coyle N, Inturrisi CE. The successful use of a parenteral 98. Murillo M, Holland JK. Clinical practice guidelines for the management
methadone in a patient with a prolonged QTc Interval. J Pain Symptom Manage.
of psychosocial disorders at the end-of-life. Palliat Support Care. 2004;2(1):65-
76. Katchman AN, Koerner J, Tosaka T, Woosley RL, Ebert SN. Comparative evalu- 99. Cohen MZ, Easley MK, Ellis C, et al. JCAHO. Cancer pain management and
ation of HERG currents and QT intervals following challenge with suspected tor-
the JCAHO’s pain standards an institutional challenge. J Pain Symptom Manage.
sadogenic and nontorsadogenic drugs. J Pharmacol Exp Ther. 2006;316(3):1098-
100. Redinbaugh EM, Sullivan AM, Block SD, et al. Doctors’ emotional reaction 77. Kornick CA, Kilborn MJ, Santiago-Palma J, et al. QTc interval prolongation
to recent death of a patient: cross sectional study of hospital doctors. BMJ. 2003;
associated with intravenous methadone. Pain. 2003;105(3):499-506. 78. Ehret GB, Desmeules JA, Broers B. Methadone-associated long QT syn- 101. Braiteh F, El Osta B, Palmer JL, Reddy SK, Bruera E. Characteristics, findings,
drome: improving pharmacotherapy for dependence on illegal opioids and les-
and outcomes of palliative care inpatient consultations at a comprehensive cancer
sons learned for pharmacology. Expert Opin Drug Saf. 2007;6(3):289-303.
center. J Palliat Med. 2007;10(4):948-955.
2008 American Medical Association. All rights reserved.
(Reprinted with Corrections) JAMA, March 26, 2008—Vol 299, No. 12 1467 Web Sites for End-of-Life Care Resources NATIONAL CONSENSUS END OF LIFE/PALLIATIVE PROJECT FOR QUALITY RESOURCE CENTER PALLIATIVE CARE CITY OF HOPE PAIN & PALLIATIVE CARE RESOURCE CENTER NATIONAL COMPREHENSIVE CANCER NETWORK GUIDELINES
related to pain and palliative care. PALLIATIVE CARE LEADERSHIP CENTERS EDUCATION FOR PHYSICIANS
h t t p : / / c a p c . o r g / p a l l i a t i v e - c a r e -
ON END-OF-LIFE CARE AMERICAN PAIN SOCIETY GUIDELINES FOR CANCER PAIN
2008 American Medical Association. All rights reserved.
(Reprinted) JAMA, March 26, 2008—Vol 299, No. 12 E1
Guidance for Primary Care on Commencement of Anti-Arrhythmic Therapy Background NSF Chapter 8 has made recommendations on the management of atrial fibrillation. These include the use of sotalol and flecainide, drugs that GPs may be unfamiliar with. The AGW Arrhythmia sub-group has drawn up a protocol for AF management, based on NSF Chapter 8 that includes commencement of sotalol an