Pain Management Flashcards

1
Q

Features of selective COX2 inhibitors

A

Fewer GI side effects and toxicity
Higher CVS risk - MI and stroke
Addition of aspirin reverses GI benefits
Taken with meals

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2
Q

Features of paracetamol

A

Inhibits central prostaglandin production
Well tolerated at therapeutic dose
OD- toxic metabolite NAPQI causes liver failure
Can cause nephropathy with chronic use
Use with caution in renal and liver impairment
Normal adult dose is 1g 4-6 hourly, max 4g/day

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3
Q

Adverse effects of NSAIDs

A
Bronchoconstriction
Fluid retention
Nephropathy and ARF
Bleeding
Hypersensitivity
Dyspepsia and ulceration
Hepatotoxicity
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4
Q

Features of NSAIDs

A

For mild to moderate pain
Inhibit COX - decrease prostaglandin - less inflammation
Take with meals

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5
Q

Caution and contraindications of NSAIDs

A

Caution: renal or hepatic impairment, dyspepsia, cardiac failure, HPT, asthma, bleeding disorders
Contraindications: hypersensitivity, active PUD

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6
Q

Features of chronic pain

A

Pain lasting beyond term of injury or painful stimulu s, over 4-6/52
Can be somatic, visceral or neuropathic
Manage s per cancer pain, using WHO analgesic ladder
A. Non-opioid with or without adjuvant
B. Weak opioid with or without non-opioid with or without adjuvant
C. Strong opioid with or without non-opioid with or without adjuvant

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7
Q

Side effects of morphine

A

Nausea - resolves over few days, can give metoclopramide 10mg 8hourly
Sedation- resolves over a few days
Constipation - treat with stool softener and peristaltic stimulator eg senna solution

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8
Q

Caution and complications of morphine

A

Caution in renal and hepatic impairment, elderly, pregnant close to term, lactation, neonates, reduced pulmonary reserve
Complications: respiratory depression - reduces responsiveness of BS respiratory center to CO2 and rhythmicity; can develop tolerance, dependence, addiction

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9
Q

Features of morphine

A

Used for severe pain
Strong affinity for u-receptors
CNS effects: analgesia, euphoria, sedation
Causes histamine release: vasodilation, itching, bronchoconstriction
No ceiling dose- titrate upwards to effect, start 10mg 4 hourly for 24 hours increase 30-50%

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10
Q

Features of codeine

A

Weak opioid used for mild and moderate pain
Prodrug metabolized by CYP2D6 - can get variants : slow metabolizer (poor analgesia but still constipation), fast metabolizer (resp depression, coma and death)
Adverse effects as with morphine
Adult dose: 30-60mg 4-6 hourly

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11
Q

Features of tramadol

A

Used in conjunction with paracetamol
Weak opioid used for moderate to severe pain
Dual MOA: parent drug and active metabolite agonists of u-receptor, 5HT and NE reuptake inhibitors
Adverse effects similar to morphine but less abuse potential, resp depression and constipation
Interactions: risk of serotonin if used with SSRIs and MAOIs; metabolism induced by carbamazepine ; can drop seizure threshold
Dose: 50mg 4-6 hourly

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12
Q

Adjuvant therapy options

A

TCAs

Anticonvulsants

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13
Q

TCA used as adjuvant

A

Amitriptyline

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14
Q

Features of amitriptyline

A

Has antidepressant, analgesic, anxiolytic and sedative effect
Useful if pain associated with sleep and anxiety disorders
Useful in neuropathic pain
Dose: 10-25mg nocte, upped to 75

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15
Q

Anticonvulsants used as adjuvants and features of

A

Carbamazepine, valproate, lamotrigine, gabapentin
Useful for neuropathic pain
Start low, titrate up
Can be used alone or with TCAs

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16
Q

Pathophysiology of pain

A

Nociceptive- normal pain processing pathway, free nerve endings stimulated by damage or inflammation
Neuropathic- abnormal pain pathway, processing of stimuli from PNS or CNS, no useful purpose
Peripheral pain pathways- noxious stimuli activate nociceptors, nociceptors induce inflammation by releasing inflammatory peptides