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C N
S D
AMIE TAGGART BLASZCZYK and LISA C. HUTCHISON
L O
1. Compare the prevalence of dementia across different age groups.
2. Contrast the different etiologies, symptoms, and therapies for mild cognitive impairment, Alzheimer disease
(AD), vascular dementia, dementia with Lewy bodies, and frontotemporal dementia.
3.
Develop a treatment plan for a patient with mild cognitive impairment or dementia.
4. Design a treatment plan for behavioral symptoms associated with dementia.
5. Distinguish the epidemiology and features of dementia and delirium in an elderly patient.
6. Devise a prevention and treatment plan for an elderly patient with delirium.
7. Recognize the impact of Parkinson disease (PD) and its treatment on the quality of life of patients and
caregivers.
8.
Recommend appropriate therapy for a senior individual with PD throughout the course of the disease.
9. Recommend nonpharmacologic and pharmacologic interventions for a person with PD experiencing depression
and constipation.
10. Recognize the different etiologies and clinical presentation of seizures in the senior population versus the
younger population with seizures.
11. Recommend appropriate therapy for a senior individual diagnosed with epilepsy, adjusting for pharmacokinetic
and pharmacodynamic changes.
12. Recommend an appropriate titration schedule for a senior to switch antiepileptic drugs.
12
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K T  D
BETA AMYLOID: Peptide of 39–43 amino acids formed after cleavage of the amyloid precursor protein. Beta-
amyloid is insoluble in the brain and forms plaques associated with AD.
CHEMICAL RESTRAINT: Use of psychoactive medications as a matter of convenience in order to prevent a
patient from moving about or to control behavior. No medical indication or safety issue, which would require
treatment for the patient’s best interest, is present for use of a psychoactive medication to be considered
inappropriate.
DYSKINESIAS: Uncontrollable, automatic, dance-like movements, commonly occurring when levodopa doses
are peaking or “peak-dose dyskinesias.”
EPILEPSY: Chronic neurologic condition characterized by recurrent unprovoked seizures.
HYPODERMOCLYSIS: Infusion of isotonic fluids into the subcutaneous tissue. This avoids the potential safety
issues of an intravenous infusion, therefore requiring less monitoring by nursing staff. However, the solution is
limited to normal saline or 5% dextrose with 0.45% sodium chloride without additives.
LEWY BODY: Abnormal collection of proteins, usually alpha-synuclein, ubiquitin, and others, that forms inside
nerve cells. In PD they are initially found in the substantia nigra, whereas in dementia with Lewy bodies (DLB)
they are found in the hippocampus. However, as disease progresses, Lewy bodies will extend to many other
parts of the brain, as observed at autopsy.
MOTOR COMPLICATIONS: Symptoms that include wearing off between doses and dyskinesias.
MOTOR SYMPTOMS: Collection of symptoms that commonly include tremor, bradykinesia, rigidity, and
postural instability.
NEUROLEPTIC SENSITIVITY: Excess sensitivity to agents with dopamine effects, resulting in increased extra-
pyramidal effects. This is most often described as an attribute of patients with DLB seen when treated with
antipsychotic agents.
NEUROPSYCHIATRIC SYMPTOMS: Noncognitive symptoms secondary to moderate-to-severe dementia,
including psychosis, agitation, aggression, wandering, crying out, hostility, suspiciousness, anxiety, or
depression.
NONMOTOR SYMPTOMS/COMPLICATIONS: Symptoms that commonly include swallowing difficulties, consti-
pation and other gastrointestinal (GI) transit slowing, autonomic dysfunction, shuffling gait, masked facies,
depression, dementia, anosmia, and others.
OFF: State in which medications are not working and the patient feels symptoms of PD.
ON: Symptom-free state, when PD medication is working.
REFRACTORY EPILEPSY: Although the definition is controversial, this term means the failure of two or more
drugs and occurrence of one or more seizures per month over 18 months.
WEARING OFF: Sensation that the effects of medications for PD, typically levodopa, are diminishing; typically
felt in between doses and occurring with increased frequency as PD progresses.
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12 - Central Nervous System Disorders |
335
I
T
he workings of the brain remain a mystery in
many respects. Some elderly patients main-
tain a quick wit, enthusiasm for learning, and
wisdom to share with the younger generations.
Yet others are plagued with neurologic abnor-
malities that are not normal with aging. Dementia,
delirium, PD, and epilepsy are more common in
older adults, and their exact causes and cures
are yet to be identified. This chapter reviews
these neurologic conditions in the elderly patient,
focusing on the optimal use of medications in this
population.
D
Etiology, Epidemiology, and
Clinical Presentation Specic to
Geriatrics
Dementia is a disease of the white matter of the
brain, with various etiologies. It is defined by
the Diagnostic and Statistical Manual of Mental
Disorders, 5th edition (DSM-5) as cognitive
decline in one or more domains (complex atten-
tion, executive function, learning and memory,
language, perceptual-motor, or social cogni-
tion).
1
In addition, the cognitive deficits must
interfere with social or work activities for the
diagnosis to be applied. Mild cognitive impair-
ment (MCI) is a term used when the patient has
memory or cognitive problems that do not qualify
for the definition of dementia. From 10% to 16%
of patients with MCI progress on to develop
a diagnosis of dementia each year, with the
remainder stable without clinically significant
decline.
2
Pharmacists may be the first to recog-
nize that a patient may have MCI or dementia
when problems with medication management
are identified. Table 12-1 provides information
related to the various subtypes of dementia
and related disorders. Dementia is estimated to
occur in 6% to 10% of individuals over 65 years
of age; however, prevalence increases from 1%
to 2% of the young-old (age 65–74 years) to 30%
of those over 85 and crests at 58% of individuals
older than 94.
3
When a patient presents with complaints of
memory impairment, reversible causes should
be identified and treated. These include hypo-
thyroidism, depression, electrolyte disturbances,
hepatic insufficiency, anemia, and vitamin B12
deficiency. In addition, if patient history indi-
cates, serologic testing for neurosyphilis is
performed. Many medications can cloud menta-
tion as part of their pharmacologic effect. The
most commonly associated medications are
benzodiazepines, medications with anticholin-
ergic properties, opioid analgesics, and anticon-
vulsants; however, amiodarone, digoxin, cortico-
steroids, nonsteroidal anti-inflammatory drugs,
H
2
blockers, and many other medications have
been reported to cause delirium. Dosage reduc-
tion or drug discontinuation is desirable to elimi-
nate iatrogenic memory loss.
Vitamin B12 deficiency is associated with
increasing age, atrophic gastritis, and acid-
suppression therapy. Anemia may occur with
vitamin B12 deficiency, but this effect may be
masked with the current level of folic acid supple-
mentation in cereals and breads consumed in
the United States.
4
The typically normal range
(150–900 pg/mL) for vitamin B12 serum concen-
trations, also named cobalamin, is not a good
marker of tissue vitamin B12 levels; measure-
ment of folic acid and methylmalonic acid are
required to clearly document vitamin B12 defi-
ciency when vitamin B12 serum concentrations
are in the low-normal range.
5
In many cases it
is easier and less expensive to replace vitamin
B12 in individuals to bring serum concentrations
above 300–500 pg/mL.
KEY POINT:
Reversible causes of
memory loss must be addressed, including
medication-related issues, before a
diagnosis of dementia can be applied.
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Table 12-1. Some Diseases of Cognition
Disease Prevalence Characteristics Risk Factors
Mild cognitive
impairment
5.4 million U.S. citizens
(10% to 22% of older
adults),
12% progress to
dementia annually, 8%
mortality rate
Varied, including prodromal AD,
medical conditions, vascular disease,
depression, or neurologic conditions
Age
Low educational
attainment
AD 2.5–5.1 million U.S.
citizens (10% of
individuals older than
71), 70% of dementias
Early symptoms include difficulty
remembering names and recent
events, apathy and depression; later
symptoms of impaired judgment,
confusion and behavior change
Age
APO ε-4 alleles
Vascular
dementia
2.4% of individuals
older than 71, 17% of
dementias
Symptoms overlap with AD, but
progression occurs in a stairstep
fashion with lower plateaus of
functional impairment and focal
neurological deficits
Hypertension
Diabetes
Age
Atherosclerosis
Male sex
Atrial fibrillation
Myocardial infarction
Heart disease
Smoking
History of stroke
DLB 15% to 20% of
dementias, 0.7% of
individuals older than
65
Symptoms overlap with AD, but
alertness and cognition fluctuate day
to day; visual hallucinations, muscle
rigidity and tremors occur
Duplicate or
triplicate copies of
α-synuclein gene
(familial cases only)
FTD 5% to 10% of
dementias
Personality and behavior changes,
difficulty with language and self-care,
onset at younger age (average 58
years old), rarely occurs after age 75
Family history
Tau protein genetic
mutation
Creutzfeldt-Jakob
disease
1 case per million
per year worldwide,
increased 30–100 fold
where familial cases
cluster
Rapidly progressive memory
impairment, incoordination, and
behavior changes; mortality within
1–2 years
Prion protein gene
on chromosome 20
(familial cases)
Medical history of
psychosis
Multiple surgeries
Live 10+ years on a
farm
Normal pressure
hydrocephalus
2–20 cases per million
per year worldwide
Symptoms include memory loss,
difficulty walking, and incontinence
Dementia of
advanced PD
In later stages of PD, dementia may
develop
AD, Alzheimer Disease; APO, Apolipoprotein; DLB, dementia with Lewy bodies; FTD, frontotemporal dementia;
PD, Parkinson Disease.
Source:
Compiled from references 2, 11, 126, and 127.
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