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8/8/2019 Recovery in Schizophrenia
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R ECOVERY IN
SCHIZOPHRENIA AND
AMISULPRIDE
Dr.Surabhi VermaDr. G. K. Vankar
B.J. Medical college, Ahmdabad
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ORGANIZATION
What is recovery?Evolution of recovery movement
Journey to recovery:rehabilitataionEvidence based treatmentsChanging role of psychiatrist
Additional issues
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S chizophrenia is one of the mostdevastating and challenging of mentalillnesses.Common disorder with prevalence of 1%S chizophrenia is associated with highlydeleterious effects on social and
occupational functioning, independenceand integrationRisk of suicide is much higher thangeneral population
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WHAT I S RECOVERY ?
Mental health recovery is a journeyof healing and transformation
enabling a person with a mentalhealth problem to live a meaningfullife in a community of his or herchoice while striving to achieve hisor her potential
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WHAT I S RECOVERY ?
S hifting focus from ´illnessµ alone
to ´personµ Advocating for quality of lifeS ubjective experience
Participation in treatment
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F U NDAMENTALCOMPONENT S OF RECOVERY
S elf directionLead ,control ,exercise choiceThemselves define goals
Individualized and person centreredRecovery based of persons strength,
resiliences,needs,preferences,experiences,cultural
backgroundEmpowerment Authority to choose among the options
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HolisticEncompasses various aspects:mind ,body,spirit andcommunity
Non linearContinual growth ,occasional setbacks, and learning fromexperience
S trengths basedRecovery based on capabilities,resiliences,talents,copingskills
Peer supportMutual support
Provide each other with supportive relationships
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RespectProtecting rights,eliminating
discrimination and stigma
ResponsibiltyPersonal responsibilty for their own
self care and recoveryIdentify coping strategies
HopeMotivating message of a better future
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A PPROACHE S TO S CHIZOPHRENIA
Degree to which persons with mentalillness can recover is uncertainNo recoveryS ome recoverF ully recover
Most relaible indicator of long termoutcome is is unremitting psychosis in thefirst 2 years following its onset
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VOL U TION O F RECOVERY MOVEMENT
1950·s ² introduction of antipsychotic treatment
1960 and 1970- civil rights movements among
the minoritiesrefused employment and educational
opportunitiesillness was embarssiningreintegration only by not revealing the fact
Anger against the ´psychiatric establishmentµ
Thomas S zasz - Antipsychiatry views
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NAMI -1979supportive of psychiatric treatmentnow focus also on issues other than
psychiatric treatment
Greater attention to non psychiatric problems
Consumers and family members as coequalparticipants
Recognise metabolic syndrome
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E VIDENCE BA S ED TREATMENT
Emerged in 1990 at McMaster U niversity inCanadaPORT funded to ´develop and disseminate
recommnedations for treatment of schizophrenia based on scientific eveidence...µconformance to psychosocial treatment was
lower than pharmacological recommendations
highlighting facilitators and barriers,including rules and regulationsEBT is integration of best research evidence
with clinical expertise and patient values
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E VIDENCE BA S ED TREATMENT (CONT .)
15-20 yrs lag between what we know and whatwe do
Apprehension- interefere with clinical judgement and specific consumerconsiderationChallenge was to facilitate widespread
adoption of research based practicesQuality and accountabilityF inancial issues are biggest obstacles
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Tool kits include introductoryvideos,practise demonstration videos, andworkbooks and manuals
Illness managemant and recovery
Assertive community treatmentF amily psychoeducationS upported employmentCo-occuring disorder :integrated dualdiagnosis treatment
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ILLNE SS MANAGEMENT AND RECOVERY
Recovery strategiesPractical facts about mental illnessThe stress ²vulnerability model andstrategies for treatmentBuilding social supportU sing medication effectivelyReducing relapses and coping with stressCoping with problems and symptomsGetting needs met in the mental healthsystem
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A SS ERTIVE COMM U NITY TREATMENT
S ymptom managementHousingF inances
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F AMILY P S YCHOED U CATION
Learn about mental illnessMaster new ways of managing their mentalillnessReduce tension and stress within the familyProvide social support and encouragement toeach other
F ocus on the futureF ind ways for families and supported to helpconsumers in their recovery
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S U PPORTED EMPLOYMENT
Eligibilty based on consumer choices andpreferencesS upported employment as an integrated
treatmentContinous follow-along supportsHelp with moving beyond the patient roleand developing new employment relatedroles
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CO-OCC U RING DI S ORDER S ;INTEGRATED D U ALDIAGNO S IS TREATMENT
Individualized treatmentEducation about the illness
Case managementHelp with housingMoney management
Relationships and social supportCounseling
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THE CHANGING ROLE S OF
P S YCHIATRI S TS
Recovery is possible and everyone has the potential to recover
Change from ´how can I relieve the symptoms ?µ to´How can I help you as a person in the world?µRemove obstacles to help consumer achieve his self-defined goals
Psychiatrist serves as the educatorMulti-disciplinary teamCommunication with primary care physicianPsychiatrist as an advocate
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´T ravel companion than a travel agentµ
Listening to recovery storiesMaintaining longterm relationshipEmpatheticlistening,clarification,awareness of changes in subjectsF rom patient to partner
Acknowledge strengths
Doctor in charge modelF lexible boundariesEthical issues
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S ide effectsS exual side effetcs
S hared decision making : ´Two experts ina room :The practioner and the clientµS igns of potential relapse
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A DDITIONAL I SSU E S
S pirituality and religionS ense of self esteem and coping response
Also contribute to negative affectsanger at god
discouragement with religious attendancedifficulty in making conversation
insults by religious leadersBeliefs of leaders which are anti medication
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Recovery
Experts(information)
Veterans(guidance)
Peers(emotionalsupport)
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Peer support
Wellness recovery action plan(WRAP)developed by Mary Ellen Copeland
greater sense of control over their dailylivesattention to qualitywritten action plan
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A MISULPRIDE
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D OPAMINE P ATHWAYS
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Dopaminepathways
From - To Controls Blockade of dopamine
receptors in this
pathway by Anti-psychotics
Mesolimbicdopamine pathway
Tegmentum toNAcc
Controls behavioralreactions such as
pleasure
sensations,rewards,
motivation,euphoria
Controls positivesymptoms like
delusions,
hallucinations &bizarre behavior.
Mesocorticaldopamine pathway
Tegmentum tofrontal cortex
Controls cognitionand normal mood
Worsens negativesymptoms,
depression andcognition
NAcc: Nucleus Accumbens ;
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Dopamine pathways From - To Controls Blockade of dopamine
receptors in thispathway by Anti-
psychotics
Nigrostriataldopamine pathway
Substantia nigrato dorsal striatum
Controlsmovements
Producesmovement
disorders like EPS-akathisia, tremor,slow movement,
dystonia
Tuberoinfundibulardopamine pathway
Hypothalamus toanterior pituitary
gland
Controls prolactinsecretion
Induces endocrineS/E e.g.
galactorrhoea,amenorrhoea,gynecomastia,
sexual dysfunction
EP S : Extra-pyramidal symptoms
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A MI SU LPRIDE - M E SOCORTICAL PATHWAY IMPROVE S NEGATIVE , DEPRE SS IVE AND COGNITIVES YMPTOM S
At low doses Amisulprideblocks the pre-synapticD3/D2 receptors in the mesocortical pathway.This increases the dopaminergic transmission.
Thus, improving the negative symptoms1,depressive 2 and cognitive symptoms.
1. Perrault et al. Encephale 1996 ;229spec issue 2):3-8
2. Gessa et al. Eur Psychiatry 1996 ;11(s3):123s-127s
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-PATHWAY
CONTROL S PO S ITIVE S YMPTOM S
At doses of 400-800 mg/d, amisulpride blocksboth the pre- and post-synaptic D3/D2 receptorsin the mesolimbic pathway.
This blocks the dopaminergic transmission.Thus, controlling the positive symptoms.
Peuch A et al. Acta Psychiatr Scand 1998 ;98(1):65-72
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RECEPTOR PRO F ILE
Lacks the combined antagonosm of 5HT2/D2receptors which usually defines ¶atypicality·Low doses : presynaptic
High dose : post synapticLittle affinity for other dopamine receptorsubtypesS erotonin
AdrenergicHistaminemuscarine
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A MI SU LPRIDE ² N IGRO S TRIATALPATHWAY
M INIMAL EP S
Amisulpride has more affinity for D3 > D2receptors.
D3 receptors are absent in the nigrostriatalpathway.
Doses >1200 mg are required to block the post-synaptic D2 receptors in this pathway.
Therefore, amisulpride at recommended dosages(up to 1200 mg) cause minimal EP S .
Xiberas X et al. J Clin Psychopharmacol 2001 ;21(2):207-214
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PHARMACOKINETIC S
Absorptionwithin 8-10 hours of oral administrationMetabolism
Minimal2 inactive metabolitesExcretion
Via urine
Elimination half-life -20 hours
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INDICATION S
Acute and chronic schizophrenia
S pecial population:
Hepatic impairement : S tandard doseRenal impairement : dose reduction when
creatinne clearance <60 ml/min
Plasma concentration : 150-250 g/l with minimalEP S
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A DVANTAGE S OF AMIL SU LPRIDE
Greater improvement in positive and negativesymptomsTorerabiltiy advantages
Less weight gainLow risk of drug ²drug interactionLess sedative effetcsDoes not increase BMI
F avourable lipid profileLower propensity to cause DM and metabolicsyndromes
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S IDE E FF ECT S
Increase in prolactin levelsWeight gain
Acute dystonia
EP STremorsRigidityHypokinesia
Hypersalivation
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A MI SU LPRIDE DO S AGE ALGORITHM
Acute episode:S evere and recurrent treated patients
Initial dose 800mg/d(upto 1200 mg/d for in-patients)
Mild-moderateOut-patient
Initial dose 400 mg/d
F irst episodeU ntreated patients
Initial dose 600mg/d
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S HORT TERM F OLLOW U P
According to symptom evolution
S evere pts.
Reduce dose by 200mg/d
Mild- moderateContinue patients at same dose
F irst episodeIncrease dose by 200mg/d
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M AINTENANCE
Modulation according to symptomsNo positive symptoms
Patients stable
Dose reduce by 100-200mg/d every 2-3 months
MAINTENANCE DO S E :200-400 mg/d(for predominantly negative symptoms: 200 mg/d)