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Methadone for Hospice Patients Part 1

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Introduction

Methadone is a potent synthetic opioid with unique characteristics that offer some distinct advantages over other opioid drugs. It was developed as an analgesic in Germany in the late 1940s. Despite its advantages, the level of Methadone prescribing for chronic pain has remained relatively low until recently. Primary reasons for the lack of widespread use of Methadone for chronic pain include:

  • The difficulty of titrating the dosage when initiating Methadone therapy
  • The fact that Methadone may carry some negative stigma since it is best known as a treatment of opioid drug addiction
  • Complex pharmacokinetics, potential drug interactions, and dynamic opioid conversion ratios

Methadone and Prescriptive Authority

Regulations restrict the prescribing of Methadone for treatment of addiction to FDA approved drug treatment programs. These restrictions do not apply when Methadone is prescribed to treat pain, however, some healthcare professionals have been reluctant to prescribe it due to fear of scrutiny by regulatory agencies (Baumrucker (2000). Amer. J. Hospice & Palliative Care; 17(3): 153-154). Methadone is a schedule II controlled substance that may be prescribed for treatment of pain by any physician with valid Drug Enforcement Agency registration.

Pharmacokinetics of Methadone

Methadone is a fat soluble drug which is widely distributed and bound to various tissues. The extensive distribution and tissue binding is responsible for the long half-life of the drug and extended duration of analgesic effect upon continuous chronic use. (Goodman and Gilman. The Pharmacological Basis of Therapeutics 11th Edition). The Methadone distribution phase is complete in 4 to 6 days at which time a "steady-state" condition is achieved between drug levels in the plasma and drug tissue levels. It is because of this extensive distribution phase that the drug may appear to have a shorter duration of analgesic action initially, then exhibit a longer half-life & extended duration of action once the distribution phase is complete. During the last few days of the distribution phase after Methadone therapy is initiated the clinician should be alert for signs of drug accumulation and possible adverse effects (somnolence, delirium, respiratory depression). Methadone is primarily eliminated by metabolism in the liver to inactive metabolites.(Eap, et al. (2002) Clin. Pharmacokinetics 41: 1153-93).

There is no need for dosage adjustment of Methadone in patients with renal impairment such as those often required with Morphine which has a potentially toxic metabolite that can accumulate and cause toxicity in these patients.

Methadone Dosage for Hospice Patients

For opioid naïve patients, a starting dose of 2.5mg orally every Q8hr has been suggested (The College of Physicians and Surgeons of Ontario (Nov 2000)). In frail, elderly patients the starting dose may need to be reduced to 2.5mg Q12h. The duration of analgesic effect of a single dose may be in the range of 4 to 6 hours for many patients during the initial distribution phase when starting Methadone treatment, therefore, a need for PRN doses should be expected in order to titrate to the therapeutic dose during this period.

Breakthrough pain can be managed by using Methadone doses equal to 25-50% of the total daily routine dose at intervals of every 4 hours as needed during the distribution phase. At the end of the distribution phase on approximately Day 5, the total amount of PRN Methadone required for the previous 24 hours is added to the routine total daily dosage and administered in divided doses at 8 or 12 hour intervals. Alternatively, oral morphine solution may be used on a PRN basis for management of breakthrough pain.

For patients who will be converted from another opioid to Methadone, there are a variety of published methodologies available. Outcome Resources pharmacists use  the following guidelines for conversion which were derived from Ayonrinde and Bridge (Med J Aust 2000) and Ripamonti (Cancer Pain & Palliative Care 1999):

Methadone Conversion Guide for Hospice

  • Convert current opioid dose to the total daily dose of oral Morphine
    equivalent (see Opioid Conversion Table below)
  • Convert the oral Morphine equivalent to the total daily dose
    of oral Methadone (see Morphine to Methadone ratio Table below)
  • Divide total daily Methadone dose into 3 or 2 doses and administer
    at 8 or 12 hour intervals
Opioid Conversion Table
DRUG   Equivalent Oral Dose  Equivalent Parenteral Dose
 Morphine  30 mg  10 mg
Hydromorphone   7.5 mg  1.5 mg
 Oxycodone  20 mg  -
 Methadone  See Methadone Conversion Guide  -
 Hydrocodone  30 mg  -
 Codeine  200 mg  -
 Propoxyphene  180 mg  -
 Meperidine  300 mg  75 mg
 Fentanyl Patch

 25mcg patch is approximately equivalent to 50 mg

 -

 

Morphine to Methadone Ratio Table

Total Daily Oral Morphine Dose  Morphine to Methadone Ratio 
 < 100 mg  5:1
 101 - 749 mg  10:1
 > 750 mg  12:1

 

Sample Methadone Conversion for hospice: 

We have a patient on Fentanyl patch 300mcg/hr that we want to convert to Methadone. Fentanyl is converted to an oral Morphine equivalent of 600mg/day using the opioid conversion table. The oral morphine equivalent is then converted to oral Methadone 60mg/day using the Morphine to Methadone ratio table. This total daily dose is then given in divided doses at 20mg Q8hr. This may be further converted to a Q12h regimen at 30mg Q12h for many patients allowing for greater convenience and compliance.

All equi-analgesic ratios are approximations and are intended to be used as tools to guide the clinician in the determination of an equivalent dosage. Final decisions regarding the appropriate conversion doses should be tempered by individual patient clinical factors including current level of pain, history of compliance with the previous regimen, renal and/or hepatic function, and potential drug interactions.

TO BE CONTINUED... See Part 2 for Advantages of Methadone, Indications for Use, and Drug Interactions.

Outcome Resources is dedicated to supporting hospices in the utilization of methadone and provides consultations and education programs for hospices geared toward this and other palliative appropriate medications. Call today to learn more or contact us for a Free Hospice Pharmacy Consultation.

Comments

exellent work, keep it up. for furthrt reading : 
 
www.SupportiveOncology.net THE JOURNAL OF SUPPORTIVE ONCOLOGY  
T  
Getting Comfortable with Methadone  
hree speakers addressed the top-  
ic of “Getting Comfortable with  
Methadone” during the recent  
meeting of The American Academy of  
Hospice and Palliative Medicine.  
“Methadone is a key drug in pallia-  
tive care, and knowledge of its use  
ought to be a core competency for pal-  
liative care physicians,” said David  
Schifeling, MD, of the Marshfield Clin-  
ic Regional Cancer Center, a viewpoint  
shared by his two co-speakers, Gail  
Gazelle, MD, of Harvard Medical  
School, and Susan LeGrand, MD, of  
the Cleveland Clinic Foundation.  
“It’s a good drug for neuropathic pain.  
It is, however, not just another opioid,”  
he said. “Methadone is important but also  
potentially dangerous. It can take some-  
one whose pain you could not control to  
someone whose pain is in control,” said  
Dr. LeGrand.  
She also cited its low cost as an ad-  
vantage that can be especially valuable  
in hospice settings. “It’s important to  
learn when and how to use the drug  
safely. Some people are scared of metha-  
done and don’t want to use it. It is a dif-  
ferent medication from all the others that  
you work with—it is unique among opi-  
oids.” She described its pharmacology as  
“highly lipophilic. It stores in fat and drug  
accumulation results.”  
In terms of its pharmacokinetics, it  
demonstrates “initial rapid tissue dis-  
tribution with a slow elimination phase  
(so if you overdose a patient, his return  
to normalcy can be slow). Unlike mor-  
phine, there is also significant individ-  
ual variability of half-life with  
methadone.”  
DRUG INTERACTIONS  
Dr. LeGrand and the other speak-  
ers strongly cautioned that patients tak-  
ing methadone and all physicians and  
nurses involved in their care need to  
understand the high degree to which  
the drug interacts with other medica-  
tions, so that dangerous combinations  
can be avoided. Dr. LeGrand gave a  
partial list of the medications with  
which it can interact and included car-  
bamazepine, the antibiotic rifampin,  
certain antiretrovirals, and risperidone,  
among those agents that decrease  
methadone levels. Among the agents  
that increase methadone levels, she  
included SSRI antidepressants, grape-  
fruit juice, other antibiotics such as  
erythromycin, and antifungals. “Pa-  
tients need to know to call the physi-  
cian who prescribed the methadone be-  
fore starting any other drug,” said Dr.  
Schifeling. Dr. LeGrand described her  
own approach: “I tell my patients,  
‘Don’t take anything that I don’t tell  
you to take.’”  
EQUIANALGESIA  
Physicians using methadone face real  
challenges in finding the right dosages for  
a patient previously using another opio-  
id. “The equianalgesia is not linear”, Dr.  
Gazelle said; “it’s quite complex, and  
many equianalgesia tables give informa-  
tion that you should not use.” The speak-  
ers suggest using the United Kingdom  
Hospice Model to calculate equianalge-  
sia. Using this formula (see box), the  
speakers find that patients adapt well,  
experience minimal side effects, and have  
excellent analgesia. Another advantage  
of the UK Hospice model, Dr. Gazelle  
said, is that it “safely allows conversion  
[to methadone use] on an outpatient  
basis.”  
UK Hospice Model for Equianalgesic Conversion to Methadone  
1. Calculate the 24-hour use of opioids, using oral morphine equivalents.  
2. Stop all other opioids.  
3. The initial methadone dose is 10% of the calculated 24-hour morphine dose  
(maximum starting dose, 30 mg), given every 3 hours prn. Therefore, any dose of  
morphine greater than 300 mg/24 h (or its equivalent) calls for a starting dose of  
methadone of 30 mg q3h prn.  
4. After 5–6 days, total the dose of methadone used in 48 hours, divide by 4, and  
then give the calculated dose every 12 hours.  
Example 1:  
Patient is receiving 60 mg sustained-release morphine bid with five extra doses of  
15 mg immediate-release morphine.  
24-hour dose = 60 mg × 2 = 120 mg + 15 mg × 5 = 195 mg morphine  
Start methadone at 10% of 195 mg, or 20 mg q3h prn.  
Example 2:  
Patient is receiving 40 mg OxyContin (oxycodone) bid with 10 mg immediate-release  
oxycodone qid.  
24-hour dose = 40 mg × 2 = 80 mg + 10 mg × 4 = 120 mg oxycodone  
Convert to morphine equivalents. We use 1:1, so it is still 120 mg.  
Start methadone at 10% of 120 mg, or 12 mg q3h prn (for dosing purposes, we  
probably would use 10 mg q3h prn).  
Example 3:  
Patient is receiving 200 mg sustained-release morphine bid and 60 mg immediate-  
release morphine tid.  
24-hour dose = 200 mg × 2 = 400 mg + 60 mg × 3 = 580 mg morphine  
Start methadone at 30 mg q3h prn (30 mg is maximum starting dose). 
 
supportiveoncology.net
Posted @ Saturday, April 03, 2010 12:38 PM by DR. KAZMI
Great reading thank you!!
Posted @ Sunday, August 22, 2010 10:07 AM by H.Thomas
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