VOLUME 18    NO.6                                                      JUNE 2003

PAIN MANAGEMENT:  PHARMACOLOGICAL APPROACHES TO TREATING PAIN

            There are three broad categories of pain:  acute, chronic and malignant or cancer pain.  Acute pain is the kind of pain that follows trauma, surgery, or self-limiting diseases.  In most cases, acute pain persists for a limited duration of time.  Chronic pain may be described as pain persisting for 3-6 months.  It may be episodic or persistent, and it may be associated with disabling physical  and emotional symptoms.  Cancer pain may include acute, chronic, or intermittent pain related to the malignancy and its treatment.

            The management of chronic and/or cancer pain is more challenging due to the duration of pain, its etiology, and the complexity of emotional and psychological components.  All pain experienced by patients should be routinely monitored, and a clinical approach to pain assessment and management should be followed.  This review will focus on the pharmacologic approach to pain management and available therapy options.

            In the pharmacologic management of pain, non-narcotic analgesics, narcotic analgesics, and adjuvant drugs may have a role in patient therapy.

NONSTEROIDAL ANTI-FLAMMATORY DRUGS (NSAIDS) AND ACETAMINOPHEN:

Non-narcotic analgesics such as the NSAIDS and acetaminophen are the most helpful for mild to moderate acute pain and acute exacerbations of chronic pain, or "flares."  NSAIDS are also helpful in painful conditions related to chronic inflammatory conditions (eg arthritis).  It is generally accepted that some patients respond better to one NSAID than others, and different agents may need to be given if results are unsatisfactory.  The most common adverse effects of NSAIDS are gastrointestinal irritation and ulceration.  The newer cyclooxygenase-2 (COX-2) selective NSAIDS (eg Rofecoxib [VIOXX]) may have less GI effects, and may be preferred if chronic therapy is anticipated.  Renal effects may also occur with high dose or long term use of NSAIDS.

            Acetaminophen is a very useful agent for acute pain, and it is used quite frequently.  It must be remembered that acetaminophen is also contained in many combination analgesic drugs.  If used alone or in conjunction with other drugs, total daily dose of acetaminophen should not generally exceed 4000mg.  The risk of hepatic damage due to high-dose or chronic use of acetaminophen is well established.  Greater risk is evident in patients with pre-existing liver disease or alcoholics.

NARCOTIC ANALGESICS:

            Narcotic analgesics or "opioid" drugs are used for moderate to severe pain and have become more accepted as management of many acute and chronic pain conditions.  Some of the concerns regarding narcotic analgesics use have stemmed from misconceptions or confusion regarding the risks of addiction, tolerance and physical dependence.  Addiction or psychological dependence is rare in patients receiving opioids for pain management.  Some degree of physical dependency will occur in patients who receive long-term therapy with opioids.  This should not be confused with addiction.  Gradual tapering of opioid therapy will ease withdrawal symptoms.  Tolerance occurs when a specific opioid dose not produce as much analgesia as it previously did.  There are various reasons for this, although it does not occur in all patients.  Many patients remain on stable doses of opioids for long periods without evidence of tolerance.

            Due to the inherent CNS depressant effects of opioids, clinicians and patients have feared that chronic opioid therapy may impair cognitive and psychomotor function.  Studies have shown, however, that opioids can be safely administered without impairment of daily activities, and in fact, tolerance to the CNS depressant effects of opioids develop rather quickly.

In order to minimize sedation and cognitive impairment, doses of opioids should be started low and gradually escalated to establish pain relief with minimal adverse effects. The most persistent adverse effect of opioid therapy is constipation.  It is best managed with a regular regimen of laxatives, hydration, and a high-fiber diet.  Nausea and vomiting, lightheadedness and dizziness also commonly occur with opioid use. 

Narcotic analgesics vary in their dosage and potency, and an effective analgesic dose varies considerably between patients.  Therefore, dosage titration is essential for each patient, with careful review of pain assessments by clinicians in the determination of the most appropriate dose and frequency.  In most cases, patients should receive regularly scheduled doses for persistent pain.  Exacerbations of pain (i.e. breakthrough pain) may receive additional intermittent doses of analgesics.

ADJUVANT ANALGESICS:

            Adjuvant analgesics represent a diverse group of drugs that are analgesic in specific circumstances.  Tricyclic antidepressants (eg amitriptyline, imipramine) and anti-convulsants (eg gabapentin) are used for neuropathic pain.  Other agents used to treat specific pain conditions include corticosteroids, mexiletine, and clonidine.

The following table describes medications used for pain management in JHMC, including dosage forms, usual effective dose and duration of action.  Narcotic analgesics are described in potency in relation to morphine, considered the standard for comparison, including approximate equi-analgesic doses to morphine 10mg.

PAIN MANAGEMENT

JAMAICA HOSPITAL MEDICAL CENTER

HOSPITAL FORMULARY


NON-NARCOTIC ANALGESICS

AGENT

SUPPLIED

DOSAGE

MAXIMUM DOSAGE

DURATION OF ACTION (hr)

COMMENTS

Aspirin

325mg

325-650mg PO q 4 h

3900mg

2-4

 

Acetaminophen

(TYLENOL®)

325mg

650mg/20.3ml ud

325-650mg PO q 4 h

3900mg

2-4

Do not exceed maximum dosage

Tramadol (ULTRAM®)

50mg

50-100mg PO q 4-6h

400mg

4-6

Narcotic-like agent with less tolerance/ withdrawal  effects than opioid agents

50mg = 30mg codeine

NSAIDS

Ibuprofen (MOTRIN®)

400mg, 600mg, 800mg

100mg/5ml

400-800mg PO q 6 h

3200mg

4-6

Administer with food or after meals

Indomethacin

(INDOCIN®)

25mg, 50mg

50mg suppos.

25-50mg  PO q

8 h

200mg

4-6

Administer with food or after meals

Ketorolac inj. (TORADOL®)

15mg/ml

30mg/ml

60mg/2ml

60mg IM/IV x 1

30mg IM/IV q 6h

120mg

4-6

Ketoralac injection orders are valid for 48 hours maximum

Naproxen (NAPROSYN®)

250mg, 375mg, 500mg

250-500mg  PO BID

1500mg

4-8

Administer with food or after meals

Rofecoxib

(VIOXX®)

12.5mg, 25mg

50mg

12.5mg-50mg PO daily

50mg

up to 24

50mg dose not recommended beyond 5 days

GI side effects less than other NSAIDS

 

NARCOTIC ANALGESICS

PARENTERAL/ORAL AGENTS

SUPPLIED

EQUIANALGESIC DOSE1

DURATION OF ACTION (hr)

COMMENTS

Morphine IM/IV/SC

            DURAMORPH®

4,8,10mg

PCA-30mg syr

5mg/10ml

10mg IM, IV, SC

IV

3-6

Standard for comparison

PCA-as per policy

DURAMORPH:             Anesthesia only

Morphine Oral

            M.S.I.R.

            Oral solution

            M.S. CONTIN®

30mg tab

10mg/5ml

20mg/10ml u/d

15,30,60mg SA tablet

60mg PO

60mg PO

30mg PO

3-6

3-6

8-12

Immediate release morphine

Sustained release morphine

1Based approximately on morphine 10mg IM/SC. Initial dose of a new drug may be given at 1/2 the calculated dose due to incomplete cross-tolerance among opioids. For patients without prior narcotic exposure, it is recommended to start at 1/2 the equianalgesic morphine dose.

NARCOTIC ANALGESICS

PARENTERAL/ORAL AGENTS

SUPPLIED

EQUIANALGESIC DOSE1

DURATION OF ACTION (hr)

COMMENTS

Merperide (DEMEROL®)

            IM/IV

            Oral

50, 75, 100mg

50mg tablet

75mg IM, IV

300mg PO

3-4

3-4

Short-term use, active metabolite (nor-meperidine) may accumulate with renal dysfunction

Hydromorphone (DILAUDID®)

            IM/IV

            Oral

2mg

2mg tablet

2mg IM, IV

8mg PO

4-6

4-6

Higher abuse potential

Oxycodone Oral

            Oral solution

            OXY-CONTIN®

5mg/5ml

10,20, 40mg SA tablet

20mg PO

20mg PO

4-6

8-12

Immediate release

Sustained release

ORAL AGENTS

 (in combination)

SUPPLIED

USUAL DOSAGE

DURATION OF ACTION (hr)

COMMENTS

Acetaminophen/Codeine

            TYLENOL #3, #4®

            Liquid

300mg/30mg (#3)

300mg/60mg (#4)

120/12mg/5ml

1-2 tabs PO q 4  h PRN

15ml PO q 4 h PRN

4-6

4-6

Maximum 12 tabs/day

(3600mg acetaminophen)

Lowest potency agent for mild/moderate pain

Hydrocodone/Acetamino-phen

VICODIN®

            LORTAB®

5/500mg

7.5/500mg

1-2 tabs PO q 4 h PRN

1-2 tabs PO q 4 h PRN

4-6

4-6

Maximum 8 tabs/day

(4000mg acetaminophen)

More potent than Codeine for moderate pain

Oxycodone/Acetaminophen

(PERCOCET 5/325®)

5/325mg

1-2 tabs PO q 4 h PRN

4-6

Max 12 tabs/day

(3900mg acetaminophen)

Highest potency agent for moderate to moderately-severe pain

Propoxyphene N/Acetamino-phen (DARVOCET N 100®)

100/650mg

1-2 tabs PO q 6 h PRN

4-6

Max 6 tabs/day

(3900mg acetaminophen)

TRANSDERMAL

       

Fentanyl Patch (DURAGESIC®)

25,50,75, 100

micrograms/hour

1 patch every 72 hours

72

Apply patch every 72 hours

100micrograms/hr = 10mg Morphine IV q 4 h

1Based approximately on morphine 10mg IM/SC. Initial dose of a new drug may be given at 1/2 the calculated dose due to incomplete cross-tolerance among opioids. For patients without prior narcotic exposure, it is recommended to start at 1/2 the equianalgesic morphine dose.

This publication is intended for information only.  Full product information should be consulted before prescribing, dispensing or administering

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