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g. prior MI
h. prior coronary revascularization
6. Recommend appropriate medical treatment for a patient presenting with a NSTEMI.
a. SL nitroglycerin 0.3-0.4mg q5min x3 doses IV if persistent (0.6-1.2mg/h)
i. Symptomatic relief of chest pain
ii. If not having pains now dont need to give maybe just order prn
b. PO Aspirin 100mg OD
i. Clopidogrel
i. Loading 300mg maintenance 75mg OD for 3-12 months
ii. Ticagrelor
i. Loading 180mg maintenance 90mg BD for up to 12 months
c. PO beta blockers within 24h
i. Except if patient has heart failure, low-output state, risk of cardiogenic shock
or if beta blockade contraindicated
ii. For hypertension and tachycardia
iii. Prefer cardioselective agents:
i. Metoprolol 25-50mg BD
ii. Atenolol 50-100mg OD
d. Anti-thrombotic/anti-coagulant therapy
i. To prevent further thrombosis at site of injury
ii. SC enoxaparin 1mg/kg q12h (if CrCl <30 q24h)
iii. UFH Loading 60IU/kg (max 4000IU), maintenance 12IU/kg/h (max 1000IU/h)
iv. Or SC fondaparinux 2.5mg OD
v. For duration of hospitalization or until percutaneous coronary intervention is
done
i. In practice 3-5days
e. High intensity statin shown to be more beneficial for NSTEMI
i. Atorvastatin or Rosuvastatin
ii. Atorvastatin 40mg ON
f. ACEI or ARB
i. Beneficial for morbidity and mortality but not necessarily immediately post-MI
g. Note: specifically for this case sepsis, hypotension, preferably stop beta
blocker and ACEI to prevent lowering the bp further
7. Recommend appropriate monitoring parameters for efficacy and toxicity of the
drug therapy for a patient with HCAP or NSTEMI.
a. Vitals (T, RR), CRP, WBC back to baseline efficacy (HCAP)
b. Allergic reaction, diarrhea, renal function (more because pt already has CKD,
not because drug is nephrotoxic) toxicity (HCAP)
c. No recurrence of chest discomfort, reduced SOB efficacy
d. Symptoms of bleeding (anticoagulant),
e. Vomiting blood, heartburn, gastric bleeding, black tarry stools (Aspirin)
f. BP, Creatinine, K (ACEI)
g. BP, HR (beta blocker)
1. Does RMN meet the criteria for a diagnosis of sepsis? What is the difference
between SIRS and sepsis?
a. SIRS: T >38 or <36; HR > 90; RR > 20; WBC > 12 or < 4 (2 or more)
b. Sepsis: systemic response to infection = presence of documented/suspected
infection + SIRS
c. T: 39.2
d. Elevated WBC
e. Raised CRP
f. Suspected infection
g. Therefore meets criteria for diagnosis of sepsis
2.
3.
4.
5.
6.
7.
Bonus
Cefepime (cephalosporin) wide therapeutic index
No worries about accumulation and toxicity
So just start the new dose at 8am the next morning for convenience
Gentamicin or vancomycin narrower therapeutic index
May need to take levels of the drug first before deciding when to start the new dose
a. ADRs
b. DDIs
c. Hospitalisation
d. Being on inappropriate medications
2. Generally increased risk with increased number of drugs
3. Less adherence (with increased number of drugs)
3. Describe tools that can be used to optimize prescribing in the elderly and reduce
polypharmacy.
i. Med Reconciliation
ii. Identify all drugs that patient is taking
1. Including vitamins, supplements, OTC, herbal/TCM
2. Identify drugs by generic names
3. Check for compliance
4. Identify possible ADRs, DDIs
a. Discontinue if necessary
b. Helps to identify what drugs to avoid in the future
5. Look out for drugs with
a. No therapeutic benefit, no clear indication
b. Patient experiencing ADRs
c. Presence of safer alternative
6. Avoid treating ADRs with another drug increases number of drugs taken
(polypharmacy)
iii. Simplify medication regimen
1. Reduce risk of ADRs
2. Avoid non-compliance
3. While maintaining benefits
4. Define the concept of de-prescribing and describe the 5-step approach to deprescribing in the elderly.
i. Ascertain all drugs that patient is taking and indication for each drug
1. Check for non-compliance and reasons (eg financial, inconvenient, forget)
ii. Assess overall risk of drug therapy determines how aggressive de-prescribing
should be done
1. Number of drugs
2. Presence of high-risk drug (opioids, benzodiazepines, psychotropics, NSAIDs,
anticoagulants, digoxin, cardiovascular drugs, hypoglycemic agents, drugs
with anticholinergic effects)
1. Past or current toxicity
2. Age (>80yo)
3. Cognitive impairment
4. Substance abuse
5. Multiple comorbidities
6. Multiple prescribers
7. Past or current non-compliance
iii. For each drug, assess eligibility for discontinuation
1. No valid indication
2. Part of a prescribing cascade
3. Actual or potential harm outweighs potential benefit
4. Disease and/or symptom control is ineffective or symptoms have completely
resolved
5. Preventive drug unlikely to confer any important benefits over the patients
remaining lifespan
6. Drugs imposing unacceptable treatment burden
iv. Prioritise for discontinuation starting with drugs:
1. With the greatest harm and least benefit;
DDIs
o Omeprazole and Risedronate
o Proton Pump Inhibitors may diminish the therapeutic effect of Risedronate.
Increased risk of fractures when taking PPIs
o Proton Pump Inhibitors may increase the serum concentration of
Risedronate
Drugs that increase the pH in the stomach have the potential to
accelerate pH-sensitive dissolution of delayed-release risedronate
(enteric-coated)
o Consider switching or removing omeprazole
If possible, should investigate the reason why unable to eat and digest
food properly, and why nausea
Could be simple case of bloating, indigestion OTC products available
Could be ADR of levodopa nausea (3-30% incidence), can be relieved
by metoclopramide which she is already on
If acid-related cause of nausea, can switch to H2RA (eg ranitidine)
which does not have the same effect of diminishing therapeutic effect of
Risedronate
Monitoring: monitor for frequency and severity of episodes of nausea
after stopping/switching
o Risedronate should not be removed, important for osteoporosis.
ADRs
o Increased falls
Perhaps due to reduced mobility as a result of Parkinsons
Could also be due to orthostatic hypotension effect of
levodopa/carbidopa + worsened by antihypertensive agents (bisoprolol,
candesartan)
frequency and severity of episodes of orthostatic hypotension, frequency
of falls
o Hypotensive
Consider removing bisoprolol
Causing bradycardia (HR<60)
Causing hypotension
No indication no PMHx of HF, MI, AF
Can also remove candesartan
No indication no PMHx of HTN
Causing hypotension
Monitoring: BP
o Trazodone
May cause orthostatic hypotension and syncope
Not to be used in patients with glaucoma
Associated with higher risk of bone fractures (patient has osteoporosis)
Mood changes, suicidal thoughts (patient feels demoralized, to be safe,
stop before thoughts become suicidal)
Costs outweigh benefits consider removing
Monitoring: Insomnia
Betahistine
o Vertigo seems to be improved
o No important benefits if continued
o Should consider removing
o Monitoring: Any recurrence of vertigo episodes after removing
Watery and itchy eyes
o ADR of timolol
o Interferes with daily life.
o Should not remove timolol, important for glaucoma control
o Cetirizine tried but does not work
o Consider switching to another anti-histamine, eg: loratadine
o Monitoring: watery and itchy eyes, whether if it improves quality of life
Dimenhydrinate
o Strong anti-cholinergic activity (BEERS)
o Should avoid in elderly, glaucoma
Levodopa
o Use with caution with patients with narrow angle glaucoma
o However, levodopa necessary for parkinsons control
o Keep, but monitor intra-ocular pressure
Metoclopramide
o Dopamine receptor antagonists with potential to worsen parkinsonian
symptoms.
o BEERS criteria remove
Rosuvastatin
o Data on benefits of giving statins is for ischemic stroke
Not really for hemorrhagic strokes
o Low LDL levels (below ?)
o Should consider removing
Levodopa/carbidopa
o Possible ADRs experienced: nausea
o Not really causing falls or orthostatic hypotension
o Keep
o Perhaps after removing metoclopramide, may need to taper down dose
metoclopramide counteracts the action of levodopa if removed, may
become a levodopa overdose
Hypotension (77/50)
o Consider removing bisoprolol
Causing bradycardia (HR<60)
Causing hypotension
No indication no PMHx of HF, MI, AF
o Can also remove candesartan
No indication no PMHx of HTN
Causing hypotension
o Monitoring: HR, BP
Betahistine
o Vertigo seems to be improved
o Should consider removing or tapering off the dose
Risedronate
o Appropriate for osteoporosis
o On vitamin D but not on calcium should add calcium
Vitamin D
o Recommended daily dose 600-800IU
o Lower dose if possible
o Too high may cause nausea vomiting
Trazodone
o As a sedative: mirtazapine, escitalopram more used in elderly
o Should consider removing
Levothyroxine
o TSH is within normal range
o Continue same dose of levothyroxine
o Hypothyroidism signs and symptoms: fatigue may mask symptoms of
depression
If suspect depression, conduct thyroid function tests to confirm if
hypothyroidism
Omeprazole
o Nausea may be a ADR of other medications dont use drugs to treat side
effects of other drugs
o No PMHx of PUD, GERD, not on NSAIDs, antiplatelets no strong indications
for PPI
o Consider taking off
Metoclopramide
o Dopamine receptor antagonists with potential to worsen parkinsonian
symptoms. (BEERS)
o ADRs: Extrapyramidal symptoms
o If still needs a prokinetic can use domperidone (does not cross BBB into
CNS and cause EPS)
Timolol eye drops
o PMHx of glaucoma indication for timolol
o Used for 10 years
o Keep
Cetirizine
o Stop, because it may not be working against the watery and itchy eyes
o ADRs: dizziness, fatigue, dry mouth
Dimenhydrinate
o Used to treat nausea, which is a side effect of another drug
o ADRs: dry mouth, confusion, dizziness
o Stop
Non pharm
o Falls: refer to physiotherapist, occupational therapist to improve patients
balance
Vitamin B12
o Slightly low
o B12 supplements
Monitor diabetes
o Diabetes may cause gastroparesis
Monitor
o HR, BP
o Nausea vomiting
o ADRs
o Parkinsons disease
Walking: is it getting better or worsening