Discuss biological therapies for schizophrenia. (8+16) Flashcards

1
Q

Drug treatment types

A

Conventional/typical antipsychotics (chlorpromazine) and Clozapine/atypical antipsychotics

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2
Q

Conventional/typical antipsychotics

A

Use - reduces the positive symptoms of schizophrenia, Rationale - based on the theory that schizophrenia results from an excess of dopamine activity at certain synaptic sites, Aim - to reduce dopamine activity at receptor sites, Process - works by blocking the D2 dopamine receptors, reducing the ability of dopamine to bind on the post-synaptic receptor, lessening the response

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3
Q

Clozapine/atypical antipsychotics

A

Use - to treat schizophrenia without the previous problems of side effects, Rationale - based on the theory that schizophrenia results from an excess of dopamine activity at certain synaptic sites, also based on the idea that an imbalance in other neurotransmitters, such as serotonin, are linked to schizophrenia, Aim - to target serotonin and dopamine receptors in the brain, Process - the precise biochemical mechanisms are unknown. They do appear to have a major impact on serotonin receptors, blocking these receptors

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4
Q

Taking antipsychotics

A

Usually taken orally, absorbed from the digestive tract, pass the blood/brain barrier and then make their way to synapses where they bind to post-synaptic receptors. However, they can also be injected. High potency typical antipsychotics and some atypical antipsychotics are available as depot injections. The interval between injections is usually between 2 and 4 weeks.

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5
Q

Appropriateness

A

side effects, compliance, ethics

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6
Q

Effectiveness

A

research findings, methodological evaluation, reduction of symptoms, relapse

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7
Q

Frude

A

before the 1950s, over half of those admitted to a mental hospital and diagnosed with schizophrenia remained in hospital for the rest of their days. For most patients, ‘treatment’ considered of little more than long-term care and custody - the management of such patients was revolutionised by these drugs; rapidly reduced many of the most disturbing symptoms and sharply decreased the average length of stay in hospital

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8
Q

Gross and Rolls

A

traditional drugs have little effect on negative symptoms, about 30% of patients with schizophrenia don’t respond favourably to these antipsychotics - even those on maintenance does may make only marginal adjustment to the community

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9
Q

Herz

A

tested the effectiveness of a new treatment which involved; education patients about relapse and recognising signs of relapse, monitoring early signs of relapse by staff, weekly supportive group sessions or individual therapy, family educational sessions, quick intervention, involving both increased doses of medication and crisis-orientated problem-solving therapy - over an 18-month period, the new treatment cut relapse rates in half and reduced hospitalisation rates by 44%

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10
Q

Bennett

A

antipsychotic drugs may be an important protective factor against relapse, relapse rates of 40% in the first year following the start of treatment, and 15% in successive years, are typical; overall, they appear to delay relapse rather than prevent it

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11
Q

Side effects of typical antipsychotics

A

Dry mouth, dizziness, blurred vision, restlessness, constipation, glaucoma and sexual dysfunction. Theres a group of particularly disturbing side effects, which stem from dysfunctions of the nerve tracts which resembles the symptoms of Parkinsons disease

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12
Q

Benefits of newer drug therapies

A

Clozapine can produce therapeutic gains in schizophrenic patients who don’t respond well to traditional antipsychotics and it has proven more effective in reducing positive symptoms than traditional antipsychotics. Also has the advantage of reducing negative symptoms

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13
Q

Side effects of clozapine

A

produces fewer motor side effects, those it does produce are serious. Agrancilocytosis involved an impairment to the functioning of the immune system in 1-2% of patients by lowering the number of white blood cells, making patients susceptible to infection and even death. Other side effects include seizures, fatigue, drooling and weight gain.

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14
Q

Cochrane review - chlorpromazine

A

meta-analysis of 302 studies of the effectiveness of chlorpromazine, all used placebo effect, all used random allocation to conditions. chlorpromazine reduces relapse rates in the short and medium term, though less so in the long term, it improves symptoms, functioning and the probability of leaving treatment. It leads to various side effects, movement disorders, sedation and lower blood pressure

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15
Q

Cochrane review - chlorpromazine evaluation

A

meta-analyses are more reliable than individual studies as results are much less likely to be a fluke. the only studies chosen for analyses were well-designed with appropriate control groups. they all involved use of placebos, so effects are not a result of participant reactivity. these also involve random allocation, so effects are not just due to patients who are likely to better choosing to undergo treatment

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16
Q

Cochrane review - clozapine

A

meta-analysis of 52 randomised controlled trials, 44 less than 13 weeks duration. no significant difference in the effects of clozapine and typical antipsychotics in terms of broad outcomes, including ability to work and suitability for discharge at the end of the study. clinical improvements (symptom reduction) were seen more frequently for those taking clozapine and fewer relapses. clozapine was more acceptable in long term treatment than conventional antipsychotic medication

17
Q

ECT

A

Use - originally developed to treat schizophrenia but now more commonly used to treat depression, Rationale - there is an abnormal activity of neurotransmitters and/or hormones, Aim - the shock disrupts/corrects the abnormal neurotransmitter activity in the brain, Process - anaesthetic and muscle relaxants are administered before, electrical current is applied via electrodes positioned on the head, current is either given bilaterally or unilaterally. When given unilaterally it is usually to the non-dominant cerebral hemisphere, small electric current (70-130mv) for 0.5 to 5 seconds, induces a mini-seizure by producing electrical convulsions in brain. Usually given 3 times a week from 3-4 to 12-15 treatments

18
Q

Tharayan and Adams

A

meta-analysis of 26 studies, inclusion of all randomised controlled clinical trials comparing ECT with ‘sham ECT, non-pharmacological interventions and antipsychotics’ - results - ECT compared with sham ECT - more patients improved in real ECT groups, ECT seemed to result in less relapses in the short term than sham ECT - when ECT was compared with antipsychotic drug treatment, drug treatment was favoured

19
Q

Side effects of ECT

A

‘adverse cognitive effects’ - global cognitive deficits, and memory loss, that persist for up to six months after treatment

20
Q

Ethical issues of ECT

A

possible that because we don’t know the precise mechanisms there may be some effects we are unaware of - minor side effects of memory loss may outweigh the side effects of schizophrenia

21
Q

When to get ECT treatment

A

possible to give treatment under mental health act - if they are a threat tot heir own or other’s health