SZ bio treatment: ANTIPSYCHOTICS Flashcards

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1
Q

Antipsychotics SZ

protocol of Antipsychotics

Krishna patel et al 2014

A

Krishna Patel et al. (2014)

in a review on the efficacy of medication for schizophrenia

they explain that it is important to start medication use quickly
– in order to be most effective in

the first seven days following a psychotic episode, the objectives are to decrease hostility
– and to attempt to return the client to normal functioning (e.g. sleeping ad eating).

The individual is carefully monitored for changes in symptoms and side effects

Once symptoms have began to subside,
– a maintenance dose will be prescribed to encourage socialisation, self-care ad improve mood and combat relapse,
– which occurs in 60-80% of people who do not take a maintenance dosage
– but only 18-32% of those who do

• This dosage should be maintained for at least 12 months after remission.

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2
Q

Antipsychotics SZ

additional conciderations when taking/ perscribing Antipsychotics

A

• Amphetamines, alcohol, caffeine and nicotine can all disrupt the effectiveness of antipsychotic medications

• Therefore, support for substance abuse may also be a consideration when treating a person with antipsychotics

• Drug treatments often fail to bring relief to people who have experienced symptoms for many years

– as it appears the first five years following an acute episode can lead to the most significant changes in the brain

~ (Patel et al., 2014).

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3
Q

Antipsychotics SZ

First Generation ‘Typical’ Antipsychotics

Chlorpromazine and Haloperidol

A

The first antipsychotic medications was called chloropromazine which was created 1953

this worked by blocking the uptake from D2 receptors

• and within 48 hours dampening dopamines effect throughout the brain

• it was taken 2-4 times per day in tablet form

• they mainly reduced positive symptoms such as hallucinations and delusions this was only successful in 60% of people

• they had many side effects such as major motor side effects
due to a lack of dopamine in the brain

• such as tardive dyskinesia which is involuntary lip and tongue movements
– which affected 30% of patients
– and was irreversible in 75% of cases even after medication had stopped (Hill 1986)

Other side effects included:
– slow, unusual, lack of and uncontrollable movements
– blurry vision

These side effects were continued in the next medication released Haloperidol in 1967

• this drug was stronger so there was less dosage needed and also slightly less of their side effects
– they were however still very present and very severe

– additional side effects of this drug included:
– dry mouth, dizziness, sleepiness and insomnia and constipation

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4
Q

Antipsychotics SZ

Second generation ‘Atypical’ Antipsychotics

Clozapine and Risperidone

A

The first of these drugs was closer paying which was developed in 1990.

which worked by blocking dopamine(D2), serotonin and glutamate (NMDA) receptors, and binded Dopamine and Seritonin Receptors also

• an imbalance of dopamine and serotonin levels further increases this difference therefore by blocking serotonin receptors as well as doping receptors it’s reduces the chances of this causing negative side effects such as depression

• glutamate regulates dopamine, and is involved in memory and problem solving this allows it to target negative symptoms

• it was taken in tablets 2-4 daily

• it reduces both positive and negative symptoms of schizophrenia such as hallucinations and poverty of speech

• Because this drug blocked many different kinds of receptors it didn’t 100% block every dope receptor

= less motor side effects

• however the worst still some side effects such as Clozapine in paticular:
– had a 2% risk of agrannlocytosis which is a reduction white blood cell efficiency this had a 10% risk of death
– to combat this regular blood tests needed to be done to patients to make sure they didn’t develop it

• risperidone was developed in 1993 to counteract this risk

– it’s also blocks the same receptors and treats positive and negative symptoms

– another thing this does is it binds serotonin and dopamine receptors more strongly than clozapine and therefore it is more effective in smaller doses

– other side effects that it has include:
– weight changes, appetite changes, sleepy, headaches and movement stiffness

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5
Q

Antipsychotics SZ

Olanzapine SGA

A

Olanzapine was developed in 1996 and has the same function as risperidone

However it is also highly effective in the earliest stages of schizophrenia

and therefore may be able to be used as a treatment before any major episodes have occurred in a patient

Side effects include blurry vision, dizziness and balance issues

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6
Q

Antipsychotics SZ

3rd generation antipsychotics

A

3rd generation antipsychotics have been recently developed to utilize being a partial agonist and therefore reduce the side effects of the drug

Some third generation antipsycotics may use partial glutamate agonists whereas others may use partial dopamine Agonists

One such example of a partial dopamine agonist is Aripriprizole

Developed in 2002 it is a partial dopamine agonist therefore it blocks some dope mean and replicate a dopamine effect in other places therefore reducing motor side effects

Side effects it does have however are:
– light-headedness, anxiousness, feeding sick, sleepiness, constipation and blurry vision

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7
Q

Antipsychotics SZ

support research

Leutcht et al 2012

A

A meta analysis of 65 studies between 1959-2011

6,000 patients all of which had been stabilized by antipsychotics

some will then put on a Placebo and within 12 months the Relapse late rates were as followed:

the placebo had a 64% Relapse rate

while antipsycotics had a 27% Relapse rate

meaning that the drugs are much more effective treatments compared to a placebo

Providing evidence to support the effectiveness of antipsychotics

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8
Q

Antipsychotics SZ

Research -

Krishna patel 2014

A

Notes that 20% of people show almost no improvement after multiple FGA use

48% experience inadequate improvement and unacceptable side effects

and reduced Relapse rates are important
but lots of people who are on drug therapy fail to function well in everyday life and are unemployed

showing that drug treatments are inadequate 65% of the time

and fail to incorpricate patients back into Society
only reducing their symptoms

therefore it criticizes drugs as an effective treatment as it shows drugs only reduce symptoms and don’t help patients every day

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9
Q

Antipsychotics SZ

research + Ying jiao zhao et al 2016

+ ma is ethical

A

Conducted a meta-analysis which is ethical as its full of secondary data

(which means that no negative ethical impacts can be done on a participant because there are no participants)

Comparing 18 anticyclotics and utilizing data from 56 randomized control trials

with over 10,000 people they

found that 17/18 of the antipsychotics tested significantly lowered the Relapse rates compared to placebo’s

showing their effectiveness reducing symptoms reoccurring

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10
Q

Antipsychotics SZ

research -

Kapur et al 2000

A

States that using an animals in clinical trials to give schizophrenic medication to

does not show the effects of such medication on humans and how they would also interfere with their everyday lives

providing a weakness of drug trials used for sz

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11
Q

Antipsychotics SZ

Availability

A

Drugs are widely available and are also used in almost all over treatments including act

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12
Q

Antipsychotics SZ

ethics (+/-) + side effects (-)

A

Antipsychotics can be considered ethical as they rapidly decrease symptoms and reduce the need for physical straight jackets

However they do not aid the reimplication of patients into Society as act does via its complex one to one program

Also due to the amounts of side effects of antipsychotics that could also be considered an ethical as more problems are created than resolved by them:

FGA:

Motor side effects, seizures, dry mouth, dizziness, blurry vision, sleepiness, Insomnia, constipation, tardive dyskinesia

SGA:

Agrannlocytosis, blurry vision, balance troubles, dizziness, lightheadness, constipation, sleepiness, clumsiness, walking changes, stomach pains, anxiousness and feeling sick

Where is alternatives such as act have no side effects other than possibly being distressing

this is because there is no physical changes within the patient there compared to in drug treatment

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13
Q

Antipsychotics SZ

time +

A

Daily doses of drugs forever May in the long term be a long time but for their effective use it is much shorter term

especialy shorter than act which also lasts until the patient dies or until they can live independently which rarely occurs

however for the effects to be achieved antipsychotics do this much faster

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14
Q

Antipsychotics SZ

cause -

A

Antipsychotics and act both do not tackle the root cause of schizophrenia

as one Focuses on the implementation of the patient back into Society

and the other one Focuses on reduction of symptoms of schizophrenia

neither permanently resolve to the issue

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15
Q

Antipsychotics SZ

symptoms +

A

Unlike act

anti psychotics actively decreased the prevalence of schizophrenic symptoms including positive symptoms

such as + hallucinations and later in second generation anticyclotics negative symptoms such as poverty of speech

in 1997 the American psychiatric Association claims that anticipotic drugs are effective for 60% of schizophrenic patients

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16
Q

Antipsychotics SZ

expense

A

Antipsychotics are far Far cheaper than act as they are prescribed and mass-produced cheaply

whereas act is expensive as it is a one-to-one treatment program for their entire life

17
Q

Antipsychotics

3GA

ARIPIPRIZOLE 2002

A

Aripiprizole is a 3GA developed in 2002

it is a partial Dopamine Agonist
aswell as a Dopmaine/ seretonin/ Glutamate Antagonist

it is an agonist in the presynaptic D2 receptors (in theory this means there is no detection of a dope issue so no symptoms or side effects but in reality there is still those things)

and an Antagonist at post psynaptic receptors

this is because SGA are antagonists at both and this leads to overexcitation induced depolarisation block leading ti a broad reduction in Dope neuron activity and responsivness which isnt good

Side effects:

– light-headedness, anxiousness, feeding sick, sleepiness, constipation and blurry vision

Rare ones:

– Increased impulses, blood clots, stiff muccless, tardive dyskinesa ect.

y is it a Glutamate Antagonist despite being after Carlssons reseach?

well Miller and Abercrombie (found within the literature review)
– identified that dopamine release is increased if glutamate is reduced (the blocking of the NMDA receptors).

– This will then help to combat the negative symptoms of SZ which are associated with low levels of dopamine.

– So by blocking the glutamate, this increases the dopamine and then improves negative symptoms.

• Low levels of glutamate in basal ganglia are responsible for the positive symptoms.

• NDMA receptors being blocked can lead to negative symptoms. in Cerebal Cortex (cuz low Lvls = - so less = even more -)

But all different receptors so it all works out right