02 Geriatrics
02 Geriatrics
02 Geriatrics
Geriatrics
Jennifer P. Dugan, Pharm.D., BCPS
Kaiser Permanente Colorado Region
evergreen, Colorado
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tus, chronic low back pain caused by osteoarthritis (OA) A. MMSE score of 20/30.
of the spine, peripheral neuropathy, and benign pros- B. Neuropsychiatric Inventory (NPI) score of
tatic hypertrophy (BPH). W.G. weighs 72 kg and is 71″ 75/120.
tall, and his serum creatinine (SCr) is 1.4 mg/dL. W.G.’s C. MMSE score of 10/30.
medications include metoprolol extended release 50 mg D. NPI score of 20/120.
once daily, lisinopril 20 mg/day, metformin 1000 mg 2
times/day, gabapentin 900 mg 3 times/day, glipizide ex- 10. After initiation of a cholinesterase inhibitor, which
tended release 10 mg/day, citalopram 20 mg/day, acet- of the following screenings is most indicated?
aminophen 1000 mg 3 times/day, Tylenol PM as needed A. Watch for new or worsening hypertension.
at night, and hydrocodone-acetaminophen 5 mg/500 mg B. Watch for new or worsening depression.
1 tablet as needed for pain every 4–6 hours. C. Watch for new or worsening hallucinations.
D. Watch for new or worsening urge
5. Given the pharmacokinetic changes in W.G., dose incontinence.
reduction is most indicated for which of the follow-
ing medications? The following case on L.M. pertains to questions 11–14.
A. Metoprolol. L.M. is a 92-year-old woman who is admitted to a nurs-
B. Metformin. ing facility after treatment of urosepsis at the local hos-
C. Glipizide. pital. Her diagnoses include hypertension, generalized
D. Gabapentin. anxiety disorder, dementia, transient ischemic attacks,
frequent urinary tract infections, OA, and inconti-
6. For W.G., which one of the following is most nence. L.M.’s medications include aspirin 81 mg/day,
strongly linked to his likelihood of experiencing a a multivitamin daily, amlodipine 5 mg/day, omeprazole
medication adverse event? 20 mg at night, sertraline 100 mg/day, cranberry cap-
A. Advanced age. sules 4 times/day, donepezil 10 mg at night, lorazepam
B. Use of many medications. 0.5 mg every 8 hours as needed for anxiety, quetiapine
C. Diagnosis of lower back pain. 25 mg 3 times/day, and the house bowel regimen. L.M.
D. Renal insufficiency. weighs 62 kg; her laboratory parameters are within nor-
mal limits except for an SCr of 1.5 mg/dL and blood
7. For W.G., which one of the following interventions urea nitrogen of 22 mg/dL. Her Tinetti fall risk assess-
is most important to avoid liver toxicity? ment is 9/28 (high risk), MMSE is 21/30, and GDS is
A. Decrease the dose of gabapentin. 1/15 (low risk).
B. Decrease the dose of glipizide.
C. Decrease the dose of acetaminophen from all 11. Given this patient’s medication regimen, which one
sources. of the following is L.M. at most increased risk of?
D. Discontinue metformin. A. Agitation.
B. Weight loss.
8. For W.G., which one of the following interventions C. Death.
is best to avoid urinary symptoms from BPH? D. Pain.
A. Discontinue Tylenol PM.
B. Discontinue glipizide. 12. L.M. is somnolent for most of the day and unable
C. Discontinue citalopram. to participate in activities on the unit. Which one of
D. Discontinue hydrocodone with the following interventions is the best approach?
acetaminophen. A. Reduce the dose of quetiapine over 1 month
and discontinue.
9. A patient with a recent diagnosis of Alzheimer dis- B. Discontinue donepezil.
ease is considering treatment with a cholinesterase C. Add a 7-day course of levofloxacin.
inhibitor. Which one of the following parameters D. Discontinue the cranberry supplement.
best justifies therapy initiation?
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Table 1. Physiologic Changes with Age That May Change Drug Pharmacokinetics
Organ System Physiologic Change with Aging Resulting Effect on Pharmacokinetics
Gastrointestinal ↑ Stomach pH ↓ Absorption of some drugs and nutrients
↓ Gastrointestinal bloodflow ↓ In first-pass extraction/metabolism
Slowed gastric emptying Rate of absorption may be prolonged
Slowed gastrointestinal transit
Skin Thinning of dermis ↓ Or no change to drug reservoir formation with
Loss of subcutaneous fat transdermal formulation
Body composition ↓Total
body water ↑ Volume of distribution and accumulation of lipid-
↓ Lean body mass soluble drugs
↑ Body fat ↓ Volume of distribution of water-soluble drugs
↓ Or unchanged serum albumin
↑ a1-Acid glycoprotein
Liver ↓ Liver mass No change in phase II drug metabolism
↓ Bloodflow to the liver ↓ Or no change in phase I metabolism
↓ Or no change in cytochrome P450 ↑ Half-life and ↓ clearance of drugs with a high first-pass
enzymes extraction/metabolism
Renal ↓ Glomerular filtration rate ↓ Renal elimination of many medications
↓Renal bloodflow ↑ Half-life of renally eliminated drugs and metabolites
↓ Tubular secretion
↓ Renal mass
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a. Absorption
i. Iron, vitamin B12, and calcium are decreased with hypo- or achlorhydria.
ii. Slower gastric emptying can increase risk of ulceration from aspirin or nonsteroidal anti-
inflammatory drugs (NSAIDs).
iii Most drugs are absorbed by passive diffusion without significant changes with aging.
iv. Transdermal formulations usually require a subcutaneous fat layer to form a drug reservoir
for absorption. Use with caution in individuals who are thin or cachetic.
b. Distribution
i. Lipid-soluble benzodiazepines such as diazepam have an increased half-life in older people.
ii. Highly albumin-bound drugs such as phenytoin may have a larger fraction of free (active)
drug.
iii. P-glycoprotein, an efflux transporter for several organs including the brain, is decreased with
aging, which may lead to higher brain concentrations of medications.
c. Metabolism
i. Morphine and propranolol clearance are substantially reduced because of a reduction in first-
pass metabolism.
ii. Changes in metabolism through phase I (oxidative) and cytochrome P450 (CYP) enzymes are
variable and confounded by age, sex, concomitant drugs, and genetics.
iii. Lorazepam, oxazepam, and temazepam are dependent on phase II metabolism and are less
affected by age-related changes in metabolism.
d. Elimination
i. Drugs eliminated through glomerular filtration must be dosed on the basis of the patient’s
estimated renal function.
ii. The Cockcroft-Gault equation is the most widely accepted method to estimate creatinine
clearance in the elderly.
iii. The four-variable Modification of Diet in Renal Disease equation is the most accepted
method to estimate glomerular filtration rate for diagnosing chronic kidney disease.
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Patient Case
1. N.H. is an 85-year-old woman who resides in a nursing home. She weighs 65 kg. Her medical history is signifi-
cant for type 2 diabetes mellitus, hypertension, and moderate dementia, likely attributable to vascular changes.
Two years ago, she had a cerebrovascular accident, and 1 year ago, she sustained a right hip fracture after a
fall. Her regularly scheduled medications include glyburide 10 mg/day, lisinopril 10 mg/day, metformin 500
mg 2 times/day, donepezil 10 mg/day, aspirin 81 mg/day, and a multivitamin daily. Her as-needed medications
include zolpidem 5 mg/day as needed for sleep, meclizine 25 mg ½ tablet 3 times/day as needed for dizziness,
and the house bowel regimen. When recommending medication changes for this patient, which one of the fol-
lowing functional assessments is most important to evaluate?
A. IADLs.
B. Depression.
C. Gait and balance.
D. Pressure sores.
2. Your further evaluation of N.H. reveals that she has not used any of her as-needed medications in 2 months.
In addition, her laboratory results reveal the following: fasting plasma glucose 90 mg/dL, sodium 138
mEq/L, potassium 4.5 mEq/L, chloride 102 mEq/L, CO2 25 mEq/L, blood urea nitrogen 30 mg/dL, SCr 1.8
mg/dL, and TSH 4.0 mU/L. Which one of the following pharmacokinetic parameters is most likely to be
changed in N.H.?
A. Oral absorption.
B. Distribution.
C. Metabolism.
D. Renal excretion.
3. Based on your assessment of age- and disease-related changes in N.H., which one of the following areas of
pharmacotherapy is best to address first?
A. Diabetes treatment.
B. Alzheimer disease treatment.
C. Hypertension treatment.
D. Stroke prevention.
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8. Falls
a. Pharmacists are frequently consulted to review medication regimens for high-risk patients or
patients who have experienced a fall.
b. Psychoactive medications (sedative-hypnotics, anxiolytics, antipsychotics, antidepressants)
should be minimized or withdrawn if possible.
c. Polypharmacy by itself is a risk factor for falls; evaluate medications for indication and risks/
benefits.
d. Vitamin D deficiency should be assessed for and corrected, and vitamin D supplementation of
800 IU/day can be considered for all older adults at high risk of falls.
e. Orthostatic hypotension is associated with a greater risk of falls.
f. Hyponatremia is a risk factor for falls, and it may be worsened by diuretics, selective serotonin
reuptake inhibitors (SSRIs), and ACE inhibitors.
g. Vitamin B12 deficiency is also a risk factor falls. B12 absorption may be impaired by proton pump
inhibitors, histamine-2 blockers, and potassium supplements.
9. Creation of an optimal pharmacotherapy regimen
a. Use as few medications as possible.
b. Every drug used should have evidence-based literature to support treatment of the particular
indication.
c. All drugs should be screened to avoid drug interactions (e.g., drug, disease, food, and
supplements).
d. Evaluate the drug dose for possible adjustments caused by pharmacokinetic changes.
e. Evaluate the drug for proper therapy duration.
f. Avoid duplicate therapy.
g. Ensure it is affordable for patient.
h. Evaluate unexplained patient symptoms to rule out drug adverse effects.
i. Ensure that treatment goals are appropriate given patient age and frailty.
i. ACCF/AHA 2011 expert consensus document on hypertension in the elderly indicates a goal
systolic BP less than 140 mm Hg for those 79 years or younger is appropriate; but for those
80 years and older, 140–145 mm Hg, if tolerated, can be acceptable.
ii. The American Geriatrics Society and American Diabetes Association recommend that target
A1c levels be individualized for patients. For frail, older adults; people with a life expectancy
of less than 5 years; and others in whom the risks of intensive glycemic control appear to
outweigh the benefits, a less-stringent target such as less than 8% is appropriate.
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II. DEMENTIA
A. Epidemiology
1. Dementia affects 4–5 million people in the United States.
2. Disease is strongly associated with advanced age.
a. 2% prevalence in 65 year olds
b. Up to 30% prevalence in 85 year olds
B. Definitions
1. Mild cognitive impairment
a. Transitional stage between normal aging and early dementia
b. 5%–25% will progress to develop dementia.
2. Delirium
a. Mental status change with recent onset and fluctuation
b. Includes two of the following:
i. Misinterpretation, illusions, hallucinations
ii. Incoherent speech at times
iii. Disturbance in sleep-wake cycle
iv. Change in psychomotor activity
c. Usually related to medical illness or medications and is reversible
3. Dementia
a. Progressive, irreversible decline in mental function, marked by memory impairment
b. Not a normal part of aging
c. Symptoms include functional disability, cognitive impairments, and behavioral and psychological
symptoms.
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Patient Case
5. An 85-year-old woman is assessed at a memory loss clinic to determine the cause of her dementia. Her most
recent score on the MMSE is 24/30. Present diagnoses include Parkinson disease, hypothyroidism, and OA
of both knees. She has had these conditions for more than 10 years, is stable, and is independent in her ADLs.
Her present medications include carbidopa/levodopa continuous release, trihexyphenidyl, celecoxib, levothy-
roxine, docusate, and bisacodyl. Which one of the following medication changes is best to consider first?
A. Add donepezil 5 mg/day.
B. Slow dosage reduction of carbidopa/levodopa.
C. Slow dosage reduction and discontinue trihexyphenidyl.
D. Replace celecoxib with acetaminophen.
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G. Treatment
1. Goals
a. Maintain cognition or slow progression of decline.
b. Maintain function.
2. Nonpharmacologic therapy
a. Education, particularly directed toward the caregiver
b. Reduction in environmental triggers
c. Optimal management of comorbid diseases
3. Pharmacologic therapy
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Patient Case
6. An 87-year-old man with Alzheimer disease began therapy with rivastigmine. He has been titrated up to
rivastigmine 6 mg 2 times/day. His family notes improvement in his functional ability but reports that he is
experiencing nausea and vomiting that seem related to rivastigmine. Which one of the following is the best
course to take?
A. Advise the patient to take his drug with an antacid.
B. Add prochlorperazine 25 mg by rectal suppository with each rivastigmine dose.
C. Discontinue rivastigmine and initiate memantine 5 mg twice daily.
D. Change rivastigmine to the daily patch that delivers 9.5 mg/day.
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4. Review of consensus treatment guidelines from the American College of Physicians and American
Academy of Family Physicians, and a Guide to Dementia Diagnosis and Treatment the American
Geriatrics Society
a. Therapy initiation
i. For patients with mild-moderate Alzheimer disease, begin therapy with a cholinesterase
inhibitor when the benefits of treatment outweigh the risks and are consistent with individual
patient goals.
ii. Evidence from high-quality studies often shows statistically significant differences in
measures of cognition, global assessment, and, occasionally, ADL function.
iii. Often, the statistically significant differences found in the high-quality research are not
deemed clinically meaningful.
iv. Only 10%–25% of patients taking cholinesterase inhibitors may show modest global
improvement, but more patients may have less rapid cognitive decline. There is no way to
determine which individuals may show clinically meaningful improvement before initiating
therapy.
v. There is no evidence that any one cholinesterase inhibitor is better than another.
vi. Results for memantine are similar to those for cholinesterase inhibitors: Statistically
significant but questionable clinically meaningful changes. Memantine is labeled for use
in patients with moderate-severe Alzheimer disease. It has been studied in randomized
controlled trials as monotherapy and in combination with donepezil.
b. Therapy duration
i. Expected decline without treatment is about 4 points/year on MMSE/SLUMS/MOCA.
Evaluate 3–6 months after treatment initiation for stabilization (prevention of decline) or
improvement using repeat testing and caregiver input.
ii. Conflicting evidence exists regarding therapy discontinuation, should a patient decline or
become unresponsive to treatment.
iii. When prevention of decline is no longer a therapeutic goal for a patient, consider
discontinuing drug treatment.
iv. A taper is recommended if a patient is at a higher dose.
v. Rebound agitation may occur for the first 1–2 weeks.
Patient Case
7. R.A. is a 75-year-old woman with Alzheimer disease who has been treated with donepezil 10 mg/day for
about 3 years. When she initiated therapy, her MMSE was 21/30, and her present MMSE is 17/30. R.A. is
living at home with her husband. She cannot perform most IADLs but can perform most ADLs with cueing.
R.A.’s husband asks about changing her drug treatment to help maintain her function. Which one of the fol-
lowing is the best course of action?
A. Change her treatment from donepezil to rivastigmine.
B. Stop donepezil.
C. Add memantine 5 mg/day.
D. Add vitamin E 400 units 2 times/day.
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A. Epidemiology
1. More than 50% of people with dementia have significant behavioral and psychological symptoms.
2. These symptoms are associated with high rates of disability and functional decline, poor health
outcomes, physical injury, increased rates of nursing home placement, greater use of emergency
services, and difficulty with nurse retention.
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3. Nonpharmacologic interventions
a. Educate caregivers.
b. Patient interventions
i. Correct underlying factors that may contribute to agitation.
ii. Establish a routine.
iii. Orientation aids
iv. Segment task.
v. Music, pet, and other forms of behavioral therapy
c. Environmental interventions
i. Improve safety.
ii. Appropriate lighting
iii. Appropriate amount of sensory stimulation
iv. Increase in personal space
4. Pharmacologic interventions
a. Cholinesterase inhibitors
i. Cochrane comprehensive review showed a small improvement in the NPI with donepezil and
galantamine after several months.
ii. A more recent randomized controlled trial did not show improvement in the NPI with
donepezil treatment.
iii. An increase in agitation may occur with initiation of cholinesterase inhibitor treatment.
iv. Cholinesterase inhibitors are first line for psychosis in Lewy body dementia.
b. Atypical antipsychotics (APs)
i. No AP approved by the U.S. Food and Drug Administration (FDA) for the treatment of
dementia-related psychosis or agitation.
ii. No clear standard on when to use, but generally should be reserved for patients who are
aggressive, pose a danger to self or others, have symptoms that are interfering with function,
or experience delusions or hallucinations that are distressing to the patient. This should be
done only if the patient has not responded to a comprehensive nonpharmacologic plan or if
the patient requires emergency intervention for further workup.
iii. Cochrane comprehensive review and recent meta-analysis suggests olanzapine and
risperidone have the most evidence for use in psychosis and aggression.
iv. APs have a high rate of adverse effects such as sedation, orthostasis, dose-dependent
movement disorders, and increased risk of stroke and mortality.
v. Conventional APs do not appear to be any safer.
vi. Increased risk of death validated in several reviews (number need to harm =87)
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Patient Cases
8. You are evaluating the medication profile of an 87-year-old female nursing home resident. She resides in
a secure advanced dementia unit. Her medical history includes dementia probably caused by Alzheimer
disease, Parkinson disease, and OA. She requires assistance with all ADLs including total assistance with
bathing and dressing and help with feeding. She ambulates with the assistance of a four-wheeled walker.
Her medication regimen includes donepezil 10 mg/day, memantine 10 mg 2 times/day, carbidopa/levodopa
25/100 mg 4 times/day, oxybutynin extended release 5 mg/day, and a multivitamin supplement daily. The
patient’s MMSE score is 5/30, and her GDS is 4/15. When reviewing the nursing notes, there are several ref-
erences to the patient’s continuously crying out, “Help me, help me.” Which one of the following additional
assessment tools is most necessary in assessing this patient?
A. The Brief Psychiatric Rating Scale.
B. Functional Assessment Staging.
C. An evaluation of incontinence.
D. Framingham Risk Assessment.
9. Which one of the following changes would be best to reduce inappropriate medications?
A. Change carbidopa/levodopa to a continuous-release formulation.
B. Discontinue oxybutynin.
C. Discontinue memantine.
D. Reduce dose of donepezil.
10. This patient is medically assessed, and reversible causes of her hyper-vocalization are ruled out. Which one
of the following represents the best approach to treating her behavioral symptoms?
A. Implement a behavioral approach.
B. Add valproic acid.
C. Add quetiapine.
D. Add citalopram.
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A. Epidemiology
1. In community-dwelling elderly individuals, UIs affect about 38% of women and 17% of men.
2. More than half of nursing home residents suffer from UIs.
3. Although the prevalence of UIs is correlated with age, UIs are not part of normal aging.
4. UI is a costly condition, with estimates of more than $5 billion annually spent by long-term care
institutions.
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c. Urination results when the bladder intravesical pressure exceeds resistance from the urethra and
urethral sphincter.
2. Aging effects on the genitourinary system
a. Decrease in bladder elasticity
b. Reduction in bladder capacity
c. More frequent voiding
d. Genitourinary changes related to sex
i. Women have a decline in bladder outlet and urethral resistance because of a loss of estrogen,
which weakens the pelvic musculature.
ii. Men may experience a decrease in urine flow rate and instability of the detrusor muscle from
prostatic enlargement.
3. Causes/risk factors for UI: An evaluation of UIs is important to correct any reversible underlying
conditions. The following mnemonic is sometimes used, spelling the word DIAPERS: Delirium,
Infection, Atrophic vaginitis and urethritis, Psychiatric disorders, Excessive urine output, Restricted
mobility, and Stool impaction.
4. Types of UIs
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Patient Case
11. A 75-year-old woman reports urinary urgency, frequency, and loss of urine when she cannot make it to the
bathroom in time. She also wears a pad at night that she changes 2 or 3 times because of incontinence. Her
medical history is significant for Alzheimer disease (MMSE 23), osteoarthritis, and hypothyroidism. A
urinalysis is negative, her examination is normal, and postvoid residual (PVR) is normal (less than 100 mL).
Which one of the following interventions would be best at this time?
A. Bethanechol.
B. Pelvic floor exercises plus estrogen vaginal cream.
C. Darifenacin.
D. Oxybutynin.
A. Epidemiology
1. Prostatic hypertrophy usually develops after age 40.
2. By age 60, half of all men have BPH; by age 85, 90% have BPH.
3. Growth of the prostate gland leads to narrowing of the urethra and obstruction of urinary flow.
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C. Evaluation of BPH
1. All patients should undergo a medical history, digital rectal examination, and urinalysis.
2. Selected individuals should be further assessed with the prostate-specific antigen (PSA) test.
3. Patients with mild symptoms on the AUASI (total score of 0–7) should undergo watchful waiting.
4. Patients with moderate LUTS on the AUASI (8–19) can consider medical therapy.
5. Patients with severe LUTS (20 or higher on the AUASI) and those with the following problems should
be assessed for surgery.
a. Persistent gross hematuria
b. Bladder stones
c. Recurrent urinary tract infections
d. Renal insufficiency
6. Assess for medications that may exacerbate BPH symptoms.
a. Adrenergic agonists (decongestants) can stimulate smooth muscle contraction in the prostate and
urethra, obstructing urinary flow through the urethra.
b. Anticholinergic drugs (urinary and GI antispasmodics, antihistamines, TCAs, phenothiazines)
can reduce the ability of the bladder detrusor muscle to contract and empty the bladder.
c. Diuretics can increase urinary frequency and volume.
d. Testosterone replacement can stimulate prostate growth.
D. Treatment of BPH
1. α-Adrenergic blockers: Relieve LUTS in men with AUASI scores that are moderate or severe by
reducing smooth muscle contraction in the urethra and surrounding tissues.
a. Nonspecific α-adrenergic blockers such as doxazosin and terazosin also lower BP. They require
dose titration and are not usually effective at lower doses.
b. Newer agents are selective antagonists of α1-adrenergic receptors (tamsulosin, silodosin) and
selective antagonists of postsynaptic α1-adrenergic receptors (alfuzosin) in prostate, bladder base,
bladder neck, prostatic capsule, and prostatic urethra tissues.
c. All the α-blockers can cause hypotension.
d. Compared with placebo, the α-blockers have been shown to be effective in improving LUTS in
patients with BPH. A 4- to 6-point reduction in the AUASI can be expected.
e. Differences between the agents are related to their adverse effect profile. Although the newer
agents are more specific antagonists, all agents can cause hypotension.
f. All α-blockers are metabolized through the CYP3A4 pathway and have drug interactions with
strong 3A4 inhibitors and inducers.
g. Intraoperative floppy iris syndrome is a concern with α-blockers, especially tamsulosin. Men
with LUTS being offered α-blockers should be asked about planned cataract surgery. Men with
planned cataract surgery should avoid the initiation of α-blockers until their cataract surgery is
completed.
2. α-Reductase inhibitors
a. DHT is a hormone that stimulates prostate growth.
b. α-Reductase inhibitors prevent the conversion of testosterone to DHT; these agents have been
shown to modify the disease course and may reduce the risk of urinary retention and surgical
interventions.
i. Finasteride competitively inhibits type II 5-α-reductase and lowers prostatic DHT by 80%–90%.
ii. Dutasteride is a nonselective inhibitor of both type I and II 5-α-reductase. Prostatic DHT
production is quickly suppressed with this agent.
iii. Despite these pharmacologic differences, no differences between these two agents were
observed in trials; both reduce prostate size.
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c. α-Reductase inhibitors do not immediately reduce LUTS and should be reserved for use in men
with large prostate volume (more than 40 g). At least 6 months of therapy is usually needed to
achieve clinical benefit. Prostate size may be reduced by about 25% in this time frame.
d. PSA concentrations are used to monitor for prostate cancer. Because these agents lower PSA
concentrations, a baseline PSA test is recommended before initiating treatment with α-reductase
inhibitors.
e. Long-term therapy with an α-reductase inhibitor can increase the risk of high-grade tumors of the
prostate in healthy men without a history of prostate cancer.
3. Phosphodiesterase (PDE)-5 inhibitors
a. Tadalafil 5 mg once daily is approved for use in BPH.
b. Mechanism thought to be caused by PDE-induced smooth muscle relaxation in the bladder,
urethra, and prostate
c. Studied as monotherapy; FDA does not recommend in combination with α-blockers because
the combination has not been adequately studied for the treatment of BPH, and there is a risk
of lowering BP. However, this combination is sometimes used in practice to treat both BPH and
erectile dysfunction with a 4-hour separation of doses.
4. Combination therapy
a. May be needed in men with LUTS, a larger prostate size, and an elevated PSA
b. Finasteride and doxazosin most studied; dutasteride is FDA label approved for use with
tamsulosin in symptomatic men having an enlarged prostate
c. Two large clinical trials (MTOPS and CombAT) have evaluated monotherapy versus combination
therapy and have concluded that, in men with LUTS and an enlarged prostate, further benefit can
be achieved by the use of the two drugs in combination.
5. Supplements
a. Saw palmetto plant extract (Serenoa repens)
b. Conflicting evidence regarding the efficacy of saw palmetto in relieving LUTS; two recent trials
suggested no benefit over placebo
c. Use of this agent with 5-α-reductase inhibitors may reduce the efficacy of the reductase inhibitors.
6. Surgery is preferred in men with severe symptoms and in those with moderate symptoms who have
not adequately responded to medical options.
7. Anticholinergic agents can be appropriate and effective treatment alternatives in men without an
elevated PVR when LUTS are predominantly storage (irritative) symptoms.
Patient Case
12. A.W. is an 85-year-old man who presents to his physician with LUTS. A digital rectal examination confirms
the diagnosis of BPH, and the physician schedules a further workup including a prostate ultrasound, which
indicates his prostate volume is 31 g. A.W.’s score on the AUASI is 15. His BP is 118/70 sitting, 102/62 stand-
ing. Which one of the following therapies is best at this time?
A. Terazosin.
B. Finasteride.
C. Tamsulosin.
D. Finasteride plus tamsulosin.
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Table 10. Comparison of Drugs for the Treatment of Benign Prostatic Hypertrophy
Medication Dose Range Adverse Effects Comments
Terazosin/ 1–10 mg PO QHS Orthostatic hypotension Initiate at low dose; can titrate
Doxazosin 1–8 mg PO QHS up every 2–7 days
Alfuzosin 10 mg PO DAILY Orthostatic hypotension No need to titrate
Tamsulosin 0.4–0.8 mg PO QHS May cause less orthostasis, but has Recommended for patients who
higher rate of ejaculatory dysfunction cannot tolerate α1-blockers
Silodosin 8 mg PO daily Similar to tamsulosin in causing Contraindicated if CrCl < 30
4 mg PO daily if CrCl ejaculatory dysfunction; appears less mL/minute
30–50 mL/minute sedating
Finasteride/ 5 mg PO daily Decreased libido Onset of action is usually 6
Dutasteride 0.5 mg PO daily months
CrCl = creatinine clearance; PO = orally; QHS = every night at bedtime.
VI. Arthritis
A. Osteoarthritis
1. Epidemiology
a. OA is the most prevalent form of arthritis, affecting more than 46 million Americans.
b. Highly associated with aging
c. Women are afflicted more often than men and often live to old age with disability from OA.
d. Large weight-bearing joints, such as the hip and knee, are commonly affected.
2. Etiology and pathophysiology
a. Several concomitant conditions can greatly increase the likelihood of developing OA.
i. Obesity
ii. Joint damage from repetitive movements and certain sports
iii. Genetics and family history
b. Loss of cartilage occurs in the joint as the balance of chondrocyte function shifts from formation
to destruction.
c. Subchondral bone is damaged, and the joint space narrows.
d. Symptoms of pain result from activation of nociceptive nerve endings within the damaged joint.
B. Therapy goals are to relieve pain, maintain or improve joint function, prevent loss of function, and
maintain or improve quality of life.
C. Nonpharmacologic Treatment
1. Patients need education to understand the chronic nature of OA.
2. Weight loss will decrease the biomechanical load on large weight-bearing joints; even small amounts
of weight loss help decrease pain and disability.
3. Physical and occupational therapy
4. Exercise
5. Surgery
D. Drug Therapy (analgesics are summarized in a table at the end of the Rheumatoid Arthritis section)
1. Acetaminophen is the analgesic of choice to treat pain from OA. Early research in the treatment of OA
of the knee recommended 1 g taken 4 times/day.
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a. The FDA estimates 400 people die every year of liver failure related to unintentional
acetaminophen overdose.
b. Patients often take different combination products containing acetaminophen, leading to
excessive dosages.
c. The FDA has changed the available OTC products, so only 325-mg tablets are available.
d. The new recommended maximal daily dosage is 3000 mg/day.
e. Individuals with liver disease should receive doses of acetaminophen that are less than 2600 mg/day.
2. In older people with OA, NSAIDs should seldom be used.
a. In selected patients, cyclooxygenase-2 (COX-2) inhibitors and NSAIDs may be used with extreme
caution when other therapies have failed and when the benefit of treatment outweighs the risk.
b. For those using a nonselective NSAID such as ibuprofen, naproxen, indomethacin, and
diclofenac, some authorities recommend that a proton pump inhibitor be used for gastric
protection.
c. Histamine-2 blockers can be considered, but in studies, they have been shown to be inferior to
proton pump inhibitors in preventing ulcer formation and bleeding.
d. For patients taking any NSAID and aspirin (for cardiac disease), a proton pump inhibitor may be
recommended for gastric protection, provided the patient is not taking clopidogrel. Patients should
be educated to take their aspirin at least 30 minutes before their first daily dose of ibuprofen or
other NSAID in the morning to avoid any interaction and reduction in aspirin efficacy.
e. Older patients receiving treatment with NSAIDs or COX-2 inhibitors should be closely monitored
for gastric and renal toxic reactions, hypertension, heart failure, and drug-drug interactions.
3. Opioids
a. Patients with persistent pain from OA that is moderate or severe are candidates for treatment with
opioids. The American Geriatrics Society recommends treatment with opioids for OA when older
patients do not respond to initial therapy with acetaminophen.
b. Monitor and anticipate opioid adverse effects and treat accordingly.
c. Do not exceed acetaminophen daily dosage guidelines when using combination products.
d. Patients should be reassessed in an ongoing fashion to ensure that treatment goals are being met.
4. Adjuvant drug therapy
a. Use appropriate medications, such as gabapentin, in patients with neuropathic pain from OA.
b. Avoid the use of tricyclic antidepressants in older patients because of the increased risk of
anticholinergic adverse effects.
c. Avoid the use of skeletal muscle relaxants such as cyclobenzaprine and carisoprodol because
of the high risk of anticholinergic adverse effects and lack of efficacy. In patients with muscle
spasms related to OA, the use of baclofen could be considered.
d. There is limited efficacy for topical agents such as capsaicin, diclofenac gel, and lidocaine patch
5% for OA.
e. Short-term relief of pain may be achieved with intra-articular hyaluronic acid or
glucocorticosteroid injections.
5. Alternative dietary supplements: Glucosamine sulfate, 500 mg taken 3 times/day, with or without
chondroitin, may be considered for chronic therapy to prevent joint degradation and relieve pain.
a. Evidence to support treatment is contradictory.
b. The adverse effect profile of glucosamine is similar to that of placebo and includes
gastrointestinal complaints.
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Patient Case
13. W.F. is an 85-year-old man who presents to his physician with pain from hip OA. He also has hypertension,
coronary artery disease, and BPH. For his OA, W.F. has been taking acetaminophen 650 mg 3 times/day.
W.F. reports that acetaminophen helps, but he still experiences pain that limits his ability to walk. Which
one of the following is the best next step in analgesic therapy for W.F.?
A. Change the analgesic to celecoxib.
B. Add hydrocodone.
C. Change the analgesic to ibuprofen.
D. Add glucosamine.
A. Epidemiology
1. A systemic disease characterized by a bilateral inflammatory arthritis that usually affects the small
joints of the hands, wrists, and feet
2. The prevalence is estimated to be between 1% and 2%, with women afflicted 3 times more often than men.
3. Rheumatoid arthritis can occur at any age; it is often seen in younger people.
4. Rheumatoid arthritis is an autoimmune disease with a strong genetic predisposition.
C. Treatment
1. The treatment goal is to control the inflammatory process so that disease remission occurs. This should
lead to relief of pain, maintenance of function, and improved quality of life.
a. Measurement of treatment response:
i. Reduction in the number of affected joints and in joint tenderness and swelling
ii. Improvement in pain
iii. A decreased amount of morning stiffness
iv. Reduction in serologic markers such as RF
v. Improvement in quality-of-life scales
2. Disease-modifying antirheumatic drugs (DMARDs)
a. DMARD therapy should be initiated within the first few months of diagnosis.
i. Methotrexate, hydroxychloroquine, sulfasalazine, and leflunomide are commonly used as
first-line agents.
ii. Biologic agents that inhibit tumor necrosis factor and interleukin receptor antagonists are
often used in patients who do not respond to a first-line agent such as methotrexate.
iii. DMARDs generally require about 3 months of use before an effect is seen.
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b. NSAIDs and/or glucocorticosteroids should be used for the immediate treatment of pain and
inflammation.
i. NSAIDs do not affect disease progression in rheumatoid arthritis; their anti-inflammatory
effect is seen within 1–2 weeks of daily dosing, whereas the analgesic effect begins within
several hours of administration.
ii. Glucocorticosteroids are not recommended for long-term use because of their high number
of adverse effects and long-term complications. They are often used as bridge therapy to
provide anti-inflammatory effects while waiting for the DMARDs to take effect.
c. The order of use of disease-modifying therapy is unclear. Often, methotrexate is used as first-
line therapy. If the treatment response is not optimal, combination DMARDs may be tried, or a
biologic agent can be added to methotrexate.
d. Published guidelines provide summary information to help guide therapy. Patients are
categorized by their history of disease response and severity of disease indicators to determine
the appropriate use of biologic agents.
3. Nonpharmacologic treatment
a. Rest during periods of disease exacerbation
b. Occupational and physical therapy to support mobility and maintain function
c. Maintenance of a normal weight (avoid overweight and obesity) to reduce biomechanical stress
on joints
Patient Case
14. F.A. is a 55-year-old woman with rheumatoid arthritis. On diagnosis 1 year ago, F.A. had an RF titer of 1:64,
signs and symptoms of inflammation in the joints of both hands, and about 45 minutes of morning stiffness.
She began therapy with methotrexate, and she is presently receiving 15 mg every week, folic acid 2 mg/day,
ibuprofen 800 mg 3 times/day, and omeprazole 20 mg/day. At today’s clinic visit, F.A. reports a recurrence
of her symptoms. Radiographic evaluation of her hand joints shows progression of joint space narrowing
and bone erosion. Which one of the following is the best next step in therapy for F.A.?
A. Administer etanercept.
B. Switch to hydroxychloroquine.
C. Add prednisone bridge therapy.
D. Change to leflunomide.
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Table 11. Selected Drug Therapy for Osteoarthritis and Rheumatoid Arthritisa
Drug Starting Dose Comments
Preferred Nonopioid Analgesics for Osteoarthritis
Acetaminophen 650 mg every 6 hours First-line therapy. Maximal daily dose from all sources
should not exceed 3000 mg
Celecoxib 100 mg/day For patients also receiving antiplatelet therapy for cardiac
disease, gastric protection should be employed
Tramadol 25 mg every 4–6 hours An extended-release form is available; mixed opioid and
SSRI effects may lead to serotonin syndrome in patients
also receiving antidepressant therapy
Selected Opioid Analgesics for Osteoarthritis
Hydrocodone 2.5–5 mg every 4–6 hours Daily dose limited by the other analgesic components of
most products
Oxycodone 2.5–5 mg every 4–6 hours As above for the combination products; sustained-release
preparation is usually used every 12 hours, but dosing can
vary from every 8–24 hours
Morphine 2.5–10 mg every 4–6 hours A variety of dosage forms are available including extended-
and immediate-release forms
Hydromorphone 1–2 mg every 3–4 hours Short duration of action
Fentanyl 12- to 25-mcg/hour patch Not recommended in opioid-naive patients; peak effects
every 72 hours from the transdermal system usually occur 18–24 hours
after the first dose, with steady state achieved after 1–2
weeks of therapy
Selected NSAIDs for Rheumatoid Arthritis
Anti-inflammatory Dose
Ibuprofen 1.2–3.2 g/day Monitor for GI ulceration, bleeding, and renal toxicity;
Meloxicam 7.5–15 mg/day anti-inflammatory effect may take 1–2 weeks; should be
Nabumetone 1–2 g/day avoided in patients with chronic kidney disease or heart
Naproxen 0.5–1.5 g/day failure
Selected DMARDs for Rheumatoid Arthritis
Customary Dose
Methotrexate 7.5–15 mg every week Probably first-line DMARD; monitor for myelosuppression,
liver dysfunction, and pulmonary fibrosis; a teratogen
Leflunomide 10–20 mg/day Similar to methotrexate; an initial loading dose may give
(Arava) therapeutic response within the first month
Hydroxychloroquine 200–300 mg 2 times/day Must routinely monitor for ocular toxicity; however, this
(Plaquenil) agent has a better adverse effect profile overall
Sulfasalazine 500–1000 mg 2 times/day GI adverse effects often limit the use of this agent
Etanercept 50 mg SC weekly Binds to TNF, inactivating this cytokine; generally well
(Enbrel) tolerated; usually used in those whose methotrexate therapy
fails; monitor for infection; check baseline PPD
Infliximab 3 mg/kg IV at 0, 2, and 6 A mouse/human chimeric antibody to TNF; used in
(Remicade) weeks and then every 8 combination with methotrexate to prevent formation of
weeks thereafter antibodies to this protein; monitor for infection; check
baseline PPD
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Table 11. Selected Drug Therapy for Osteoarthritis and Rheumatoid Arthritisa (continued)
Drug Starting Dose Comments
Adalimumab 40 mg SC every 2 weeks Human antibody to TNF; less antigenic than other TNF
(Humira) antibodies; monitor for infection; check baseline PPD
Anakinra 100 mg SC daily IL-1 receptor antagonist; avoid combination therapy with
(Kineret) TNF agents because of increased risk of infection
Rituximab Two infusions of 1000 mg Chimeric antibody to CD20 protein on B lymphocytes;
(Rituxan) given 2 weeks apart corticosteroid infusions help reduce infusion reactions;
used in combination with methotrexate to improve response
Abatacept Weight-based dose every Inhibits interactions between antigens and T cells; may
(Orencia) 2 weeks for two doses and be useful in those who do not respond to TNF inhibitors;
then monthly (i.e., 750 mg for monitor for infusion reactions
those weighing 60–100 kg)
Golimumab 50 mg SC every month Monoclonal antibody against TNF. Intended for use in
(Simponi) combination with methotrexate. Monitor for infections
Certolizumab pegol 400 mg SC at 0, 2, and 4 Monoclonal antibody against TNF; may have best response
(Cimzia) weeks, then 200 mg every when used in combination with methotrexate. Monitor for
other week infections
Tocilizumab 4 mg/kg IV infusion every 4 Anti-human IL-6 receptor monoclonal antibody; indicated
(Actemra) weeks; can increase to 8 mg/ for patients who have not responded to TNF inhibitors.
kg based on clinical response Monitor for infections
a
Tofacitinib is an oral Janus kinase inhibitor that may be reviewed by the FDA in 2012.
DMARD = disease-modifying antirheumatic drug; GI = gastrointestinal; IL = interleukin; IV = intravenous(ly); NSAID = nonsteroidal anti-
inflammatory drug; PPD = purified protein derivative; SC = subcutaneously; SSRI = selective serotonin reuptake inhibitor; TNF = tumor
necrosis factor.
Acknowledgment: The contributions of the previous author, Dr. Norma Owens, are acknowledged.
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12. Answer A
Several medications can often increase sedation and
somnolence in older people. In L.M., lorazepam and
quetiapine have the greatest likelihood of causing seda-
tion. There is no indication for quetiapine, and an at-
tempt to titrate this drug down and discontinue it should
be made. In the future, the same attempt should be made
with lorazepam because the goal should be to treat
L.M.’s generalized anxiety disorder with citalopram.
13. Answer d
Patients should be assessed for reversible causes of be-
havior when a change in their status occurs. This evalu-
ation should include assessment of the patient for signs
and symptoms of hunger, dehydration, depression, pain,
delirium, sleep deprivation, infection, and drug adverse
effects. Any reversible causes for the combative behav-
ior should be corrected and a behavioral approach im-
plemented to achieve proper hygiene and personal care.
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