I. Dementia
A. About 5-8% of all people over the age of 65 have some
form of dementia, and this number doubles every five years above that
age.
Dementia is the loss of mental ability that is severe enough to
interfere with
people's every life and Alzheimer's disease is the most common type of
dementia
in aging people. American typical diet contains high amount of saturated
and trans fat, artificial ingredients with less fruits and vegetable
which can lead to dementia and other kind of diseases.
B. Dementia associated with Parkinson's disease
Parkinson disease (PD)
is a disabling, progressive condition. It is a cognitive deficits due
to the interruption of frontal-subcortical loops that facilitate
cognition and that parallel the motor loop. Contrary to common perception, many Non-motor symptoms (NMS) of PD occur early in PD and some may even predate the diagnosis
of PD that is based on motor signs. These include olfactory deficit,
sleep problems such as rapid eye movement behaviour disorder,
constipation and the more recently described male erectile dysfunction.(1).
II. Treatments of Dementia Associated with Parkinson's Disease
Treatments are depending to the degree of functional and cognitive impairment, but according to the suggestion of the Movement Disorder Society (MDS) Task Force on Evidence-Based Medicine (EBM)
1. Treatments for the non-motor symptoms of Parkinson's disease
The Movement Disorder Society (MDS) Task Force on Evidence-Based Medicine (EBM) Review of Treatments for Parkinson's Disease (PD) was first published in 2002 and was updated in 2005 to cover
clinical trial data up to January 2004 with the focus on motor symptoms
of PD, suggested the tricyclic antidepressants nortriptyline and desipramine for the
treatment of depression or depressive symptoms and macrogol for the
treatment of constipation.... The practice implications for these treatments
are possibly useful. Methylphenidate and modafinil for the treatment
of fatigue; amantadine for the treatment of pathological gambling;
donepezil, galantamine, and memantine for the treatment of dementia;
quetiapine for the treatment of psychosis; fludrocortisone and
domperidone for the treatment of orthostatic hypotension; sildenafil for
the treatment of erectile dysfunction, ipratropium bromide spray for
the treatment of sialorrhea; levodopa/carbidopa controlled release (CR),
pergolide, eszopiclone, melatonin 3 to 5 mg and melatonin 50 mg for the
treatment of insomnia and modafinil for the treatment of excessive
daytime sleepiness. There were no RCTs that met inclusion
criteria for the treatment of anxiety disorders, apathy,
medication-related impulse control disorders and related behaviors other
than pathological gambling, rapid eye movement (REM) sleep behavior
disorder (RBD), sweating, or urinary dysfunction. Therefore, there is
insufficient evidence for the treatment of these indications(2). Other researchers suggested that Sildenafil citrate (50 mg) may be considered to treat erectile
dysfunction in patients with Parkinson disease (PD) (Level
C). Macrogol (polyethylene glycol) may be
considered to treat constipation in patients with PD (Level C). The use
of levodopa/carbidopa
probably decreases the frequency of spontaneous
nighttime leg movements, and should be considered to treat periodic limb
movements
of sleep in patients with PD (Level B). There is
insufficient evidence to support or refute specific treatments for
urinary
incontinence, orthostatic hypotension, and anxiety
(Level U). Future research should include concerted and
interdisciplinary
efforts toward finding treatments for nonmotor
symptoms of PD(3).
2. Treatments for the motor symptoms of Parkinson's disease
The Movement Disorder Society (MDS) Task Force on Evidence-Based Medicine (EBM) Review of Treatments for Parkinson's Disease
(PD) was first published in 2002 and was updated in 2005 to cover
clinical trial data up to January 2004 with the focus on motor symptoms
of PD. Piribedil, pramipexole, pramipexole extended release, ropinirole,
rotigotine, cabergoline, and pergolide were all efficacious as
symptomatic monotherapy; ropinirole prolonged release was likely
efficacious. All were efficacious as a symptomatic adjunct except
pramipexole extended release, for which there is insufficient evidence.
For prevention/delay of motor fluctuations, pramipexole and cabergoline
were efficacious, and for prevention/delay of dyskinesia, pramipexole,
ropinirole, ropinirole prolonged release, and cabergoline were all
efficacious, whereas pergolide was likely efficacious. Duodenal infusion
of levodopa was likely efficacious in the treatment of motor
complications, but the practice implication is investigational.
Entacapone was nonefficacious as a symptomatic adjunct to levodopa in
nonfluctuating patients and nonefficacious in the prevention/delay of
motor complications. Rasagiline conclusions were revised to efficacious
as a symptomatic adjunct, and as treatment for motor fluctuations.
Clozapine was efficacious in dyskinesia, but because of safety issues,
the practice implication is possibly useful. Bilateral subthalamic
nucleus deep brain stimulation, bilateral globus pallidus stimulation,
and unilateral pallidotomy were updated to efficacious for motor
complications. Physical therapy was revised to likely efficacious as
symptomatic adjunct therapy(4)
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Sources
(1) http://www.helpguide.org/elder/parkinsons_disease.htm
(2) http://www.ncbi.nlm.nih.gov/pubmed/22021174
(3) http://www.neurology.org/content/74/11/924.full
(4) http://www.ncbi.nlm.nih.gov/pubmed/22021173
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