Palliative Care Flashcards

1
Q

Pain management guidelines

A

if mild pain (1-3 out of 10 on scale), use step 1 non-opioid analgesics (aspirin, acetaminophen or NSAID)

if moderate pain (4-6 out of 10 on scale), use step 2 weak opioid analgesics (tramadol or low dose strong opioid)

if severe pain (7-10 out of 10 on scale), use step 3 strong opioid analgesics (morphine, hydromorphone, oxycodone, fentanyl, methadone or codeine)

1st line strong opioid is morphine, which is the gold standard for treating severe cancer pain

demerol (meperidine, pethidine) should not be given due to risk of neurotoxicity from its active metabolite

at any step, additional therapy such as palliative radiation therapy, palliative chemotherapy, palliative surgery and hormone therapy if indicated

if pain is significantly reduced, then step down to a lower step

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2
Q

Preferred route of opioid administration

A

Oral –> SC –> IV

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3
Q

Routes of administration for different opioids

A

opioids that can only be given orally (PO): tramadol and oxycodone

opioids that can be given orally (PO) or parenterally (IV, SC): morphine, hydromorphone, codeine

opioids that can only be given parenterally (IV, SC, transdermal): fentanyl

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4
Q

How often should breakthrough opioid dosing be prescribed

A

breakthrough opioid dose is Q2H PO PRN or Q1H SC/ IV PRN

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5
Q

How many breakthrough doses should a patient use in a day

A

patient should only be allowed no more than 5 breakthrough doses in a day, where need for >3 breakthrough doses should prompt reassessment and readjustment of treatment

if inadequate pain control or >3 breakthrough doses used per day, then increase regular dose by 25-50%

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6
Q

Write out a usual morphine prescription regimen for a palliative care patient requiring pain control

A

1) Morphine 5mg PO Q4H
2) Morphine 5mg PO Q2H PRN for breakthrough pain
3) Senna (stimulant) 1 tab PO OD + Lactulose (osmotic) 10mL PO OD + docusate (stool softener)
4) Metoclopramide 5-10mg PO/SC/IV Q4H PRN for nausea (preferred because it negates the mechanism through which opioids cause nausea - activation of dopamine chemoreceptor in brain stem)
5) PRN dose with dulcolax suppository or micro fleet enema

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7
Q

How should opioid prescribing change in patients with renal failure and why should it be changed?

A

in renal failure patients, opioid dose should be decreased but given more regularly to decrease active opioid metabolite level

all opioids (except for methadone or fentanyl) have active metabolite that tend to accumulate and cause neurotoxicity in renal failure

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8
Q

In what patients should the opioid dose be halved

A

in frail / weak patients

or patients with COPD

or patients with non-cancer pain due to organ failure

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9
Q

Nausea management in palliative care

A

1st line = Metoclopramide (if no bowel obstruction) or Haloperidol, because most common cause of nausea & vomiting due to chemoreceptor trigger zone

2nd line = adding Dexamethasone if nausea and vomiting still unresolved or if brain edema

if anti-emetic is not completely effective, reassess patient and either add another anti-emetic or replace with another anti-emetic

add other anti-emetic as per suspected aetiology of nausea & vomiting

if bowel obstruction, consider adding Dexamethasone, Octreotide and Buscopan

if chemotherapy or radiation induced, consider adding Ondansetron

if brain tumor, consider adding Dexamethasone

if vestibular related (e.g. motion sickness, vertigo), consider adding Dimenhydrinate

if anxiety or anticipatory nausea & vomiting, consider adding Benzodiazepine

prevent constipation, which may exacerbate nausea & vomiting

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10
Q

Bowel clearance regimen for established constipation

A

1st line = increase dose of laxative (stimulant (Senna) + osmotic (Lactulose))

2nd line = phosphosodium (Fleet) enema or bisacodyl suppository or other enema or other suppository

3rd line = oral Magnesium Citrate

last line = manual disimpaction

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11
Q

Agent to consider for opioid induced constipation

A

Methylnaltrexone

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12
Q

Palliative care dyspnea management

A
  1. Assess and address underlying cause
  2. Relieve symptom

oxygen if hypoxic or patient notes relief with use

1st line =
low dose opioids such as morphine (Morphine 2.5mg PO Q4H)
may consider adding benzodiazepine (Midazolam) if patient is anxious (Midazolam 0.5mg SC Q1H PRN)

non-pharmacological interventions include
fan directed toward face
relaxing and open environment
positioning for most comfortable breathing
cool humid air
pulmonary or palliative rehabilitation
optimize nutrition
non-invasive positive pressure ventilation (e.g. BiPAP) note that BiPAP is very uncomfortable and usually only used transiently to allow patient get through episode of dyspnea, BiPAP most commonly used for ALS patients

3) Re-evaluate

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13
Q

What is opioid induced neurotoxicity

A

OIN is a syndrome of neuropsychiatric side effects due to opioid therapy with ANY opioid caused by accumulation of metabolite and imbalance in CNS cholinergic and dopaminergic system

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14
Q

OIN presentation

A
sedation 
hallucination 
cognitive impairment 
delirium 
myoclonus 
seizure 
hyperalgesia and allodynia
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15
Q

OIN management

A

hydration (oral, IV or SC) and any of the following

A) opioid dose reduction, where an adjuvant analgesic / therapy may be added for pain to compensate for lower dose opioid

B) opioid rotation (switching to another opioid)

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16
Q

Palliative spinal cord compression management

A

1) high dose glucocorticoid Dexamethasone
2) urgent referral to neurosurgeon / orthopedic surgeon / radiation oncologist for surgery or radiation therapy

surgery or radiation therapy to remove / shrink spinal tumor is definitive treatment for spinal cord compression

decision of surgery or radiation therapy depend on stability of spine and type of neoplasm

17
Q

Status epilepticus treatment

A

1) ABCs

2) control seizure
all anti-convulsant medications should be administered parenterally

1st line seizure control is benzodiazepine with phenytoin

benzodiazepine IV (Midazolam or Lorazepam or Diazepam) as fast acting drug to control seizure
can develop abrupt respiratory depression or hypotension
Lorazepam 0.05mg/kg SC/IV/IM up to maximum of 8mg / 12 hours
usually 2mg dose Midazolam 0.15-0.3mg/kg SC/IV/IM, may repeat Q20 minutes X3
usually 5-10mg dose Diazepam 0.2-0.5mg/kg IV up to maximum of 20mg

usually 10mg dose Phenytoin (or Fosphenytoin) IV as long acting drug as maintenance
can develop hypotension and cardiac arrhythmias Phenytoin 15-20mg/kg IV maximum rate of 50mg/minute

if seizure still uncontrolled with benzodiazepine and phenytoin, escalate in the following order:

increase phenytoin dose

phenobarbital
Phenobarbital 100mg IM bolus followed by 200-400mg IM over 24 hours

general anesthesia: propofol, pentobarbital or midazolam

in any stage, intubate and ventilate if necessary
intubation and ventilation mandatory if phenobarbital or general anesthesia used

18
Q

Palliative chronic seizure control

A
Sodium Valproate usually effective for generalized seizures in palliative care setting 
Sodium Valproate (Epival) 15mg/kg/day PO maximum 60mg/kg/day 

Carbamazepine usually effective for partial seizure and generalized tonic-clonic seizure
Carbamazepine 200mg PO daily maximum 1600mg daily

if patient cannot take oral medication, then benzodiazepine Midazolam 20-30mg SC daily

19
Q

How to screen for delirium

A

CAM - may have delirium if all of the following

A) acute onset of confusion that is a change from patient’s normal mental status and has a fluctuating course

B) presentation of inattention attention can be tested in physical exam by patient performing simple tasks such as serial 7s (subtract 7s from 100), WORLD backwards, digit span, days of week backwards, months of year backwards

C) disorganized thinking or altered level of consciousness (fluctuate between hyper-alert to drowsiness)

20
Q

Management of delirium

A

1st line medication for delirium is typical antipsychotic haloperidol or methotrimeprazine

haloperidol can be delivered po, IM or IV usually in low doses (lower than psychiatric doses)
Haloperidol 0.5-1mg PO or SC Q8-12H and 1mg Q1H PRN low doses short term haloperidol have very low risk of EPS
if delirium not controlled, increase dose (maximum for haloperidol is 15-20mg / day) or change to more sedating antipsychotic (methotrimeprazine)

2nd line medication for delirium is atypical antipsychotic (olanzapine, risperidone, quetiapine)
for severe agitated delirium, give high dose haloperidol (2-2.5mg SC) or methotrimeprazine (25mg SC) stat followed by regular regimen

Always non pharmacological management (orienting patient, respectful, empathetic care)