schizophrenia in old age
TRANSCRIPT
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Schizophrenia In Old Age
Dr Ayedh Alkhadem
Al-Amal Psychiatric Hospital
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Historical Background
Little research done compared to schiz.in young
In 1693 sir isaac newton experienced an episodeat age 51
Remitted after 18 months ,sym.includedpar.del.,social withdral,reference 2 convers.
That never ocuured Emil Kraepelin described dementia praecox as
an adolescent /early adult onset
Initail studies of LOS by Bleuler
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Martin Roth1952 applied the term Late Paraphrenia for pts.After age 60\ DSM-I , DSM-II didnt specify age of onset criteria for schiz
DSM-II used the term involutional paraphrenia
DSM-III restricted Dx of schiz.for those b4 age 45
DSM-III-R included a late onset category for pts. 45Yrold or
later. ICD-10, DSM-IV, and DSM-IV-TR dont include diagnoses for
late onset schiz,
DSM-IV-TR mention differences b/w Late and early onset
schiz. international late-onset schizophrenia group Reach consensus
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Epidemiology
Approx. 23% of schizophrenics have onset after40
About 13% in 5th
decade,7% in 6th,3% later the 1-year prevalence rate of schiz. between
ages 45 and 64 is 0.6% ,0.1-0.5%above 65
Late onset schiz. Affects women 2 to 10 timesmore (oestrogen-mediated dopaminergicinhibition)
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Etiology
Familial association 4 LOS similar to that ofearly-onset schizophrenia but not 4 VLO.
CT and MRI studies have found nonspecificstructural changes similar to those noted inearly-onset patients
No evidence it is neurobiologically d/f from
early
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Genetic factors Sex
Sensory deficits
Premorbid personality
Social Isolation
Demonstrable brain abnormality
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ClinicalFeatures
More similar than d/f w/ earlyonset schiz.
The most common features of LOS are per del., that
may be bizarre and aud hall. Partition delusions
less severe negative symptoms
lower daily doses of antipsychotics less frequent loose associations and inapp. Affect
mostly paranoid or undiff subtype
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low prevalence of thought disorder(abt 5% of pts )and affective blunting
Schneiderian first-rank syms are less prevalent
(eg,Thought insertion, block, and withdrawal
uncommon) higher prevalence of visual hallucinations
Sym. differences could be related to cohort
differences or age-associated (CNS) differencesthat are independent of the illness. Not necessarilyd/f in pathophys. or etiolgy
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Differential Diagnosis
Early onset schiz.
Mood disorder
Delusional disorder Psyc. Due to gen. med. Condition
Substance induced psychosis
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Course and Prognosis
usually chronic but may be interrupted by partialremissions and exacerbations
prognosis : better than that in early-onset
quite responsive to antipsychotics used in lower doses mortality (esp from suicide) probably comparable to
that in early-onset
factors assoc.with positive outcome : female gender,later onset, paranoid subtype, less severe negative
symptoms, and better premorbid functioning
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Treatment
better symp. improvement with antipsychotic than early-onsetillness .
substantially reduced doses of antipsychotics are necessary
Maintenance therapy is frequently required
Elderly pts are more susceptible to antipsychotic side effects
Atypical antipsy. have become the agents of choice
Lack of data for clozapine prevents its use in old pts.
augmentation of antipsychotic therapy :antidepressants Psychosocial treatment :CBT, social skills training
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Genetic Life time risk for schiz. In FDR is 10% ,holds
true for age onset upto 50 yrs.
FDR of pts with very-late-onset (> 59 years)schizophrenia-like psychoses do not have anelevated lifetime morbid risk
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Sex Females are at much higher risk in the late-life
population female-to-male ratios 2:1 to 10:1 Estrogens could have protective actions.
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Sensory deficits
Visual impairment is also more common inelderly paranoid pts than those with affectivedisorder
higher coincidence of visual and hearingimpairment in paranoid than affective patients.
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PremorbidPersonality
consistent presence of abnormal personalitytraits( schizoid or paranoid)
unsociability, reticence, suspiciousness, and
hostility Low marriage rate,less children if marreid educational and occupational adjustment
generally good
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Determining the onset insidious onset of symptoms
premorbid traits difficult to diff. from prodromalsymps.
Earlier onset are associated with more severe neg. anddisorganized symps. and greater cognitive deficits (esp.learning and abstraction)
late-onset : less severe symptoms with somewhat betterpreservation of affect and social functioning.
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mood disturbances common during the prodromal, active,and residual phases mood-congruent or mood-incongruent psychotic
features :H/O mood sym.
Mood symps. in schiz. have a brief duration, in prodormal& residual,dont meet criteria.
MD cPF:Affective sym. Precede psych. Shizoaffective: major episode in active phase,psych.
Present 4 2wks without prominent mood sym.
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lack of prominent aud or visual hall.
absence of deterioration in areas of functioningoutside the delusional scope
necessarily nonbizarre and involve situations
that may occur in real life
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thorough evaluation for underlying medical
disorders
1/3 of pts with a diagnosis of AD may present withpsychotic symptoms at some point
Delusions in AD : nonbizarre, episodic, andpreceded by cognitive decline
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amphetamines, cocaine, and phencyclidine, can
produce symps. Diff. from schizophrenia after a period of
abstinence
symptoms appear to be exacerbated by thesubstance and decrease when it has beendiscontinued
symptoms have been provoked and maintained
by the substance use Back