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5 main steps to evidence based medicine
defining a clinically relevant question
searching for the best evidence
critically evaluate the evidence
applying the evidence
evaluating the performance of EBM
meta-analyses & systematic reviews
bringing together a number of separate studies and synthesizing their results
advantages: transparent, less bias, comprehensive, protocol driven, critical appraisal, resolve for conflicitng results, identifying gaps in current research, reliable basis for decision making
disadvantages: only published studies, quality of included studies, conflict of interest, findings may not be applicable to certain settings, language bias
randomised controlled trials (RCTs)
the gold standard in clinical trails - double blind and patients randomly assigned to treatment or placebo
active control: compare standard care to new treatment
placebo control: ‘sham treatment’ indistinguishable from active treatment
Pope & McNally (2002)
shows why RCTs are so important
cohort study (longitudinal)
recruit and follow participants with a common characteristic over time
case-control studies
study group is defined by the outcome (presence of disorder). identify group of cases and group of controls from same pop. questionnaires, interviews, medical records etc
advantages: cost effective, no long follow up, can be used to study outcomes or rare diseases, examining multiple exposures simultaneously
disadvantages: risk factors are collected retrospectively and can give rise to recall and observer bias, selecting a suitable control group
cross-sectional survery
data is collected on the whole study population a singe point in time to examine the relationship between disease and other variables of interest.
descriptive: frequency and distribution of a disorder in a defined population
analytical: investigate the correlation between a risk factor and a health outcome. cannot determine possible causality bc the risk factors and outcomes are measured at the same time
adv: quick, cheap, no long follow-up, multiple outcomes & exposured to be studied, data only collected once, measure prevalence of disorder
disadv: difficult to determine whether the exposure or outcome came first, bias, difficult to interpret correlation, can’t study rare conditions
hierarchy of evidence
systematic reviews and meta-analyses
randomised controlled trials
cohort (longitudinal) studies
case-control studies
cross-sectional surveys
case studies and case reports
mental health risk factors
conflict, discrimination, compromised environment, gender, economic adversity, socially marginalised groups
mental health and poverty
less financial resources to maintain living standards, fewer education and employment opportunities, less access to health care, stigma and discrimination
hedonistic view on wellbeing
subjective wellbeing: positive mood, avoidance of pain and negative mood, high life satisfaction (Ryan & Deci, 2001)
eudaimonic view on wellbeing
psychological wellbeing: self-actualisation, personal growth (Ryan & Deci, 2001)
wellbeing framework
dynamically contructed through circumstances, activies, psychological resources, interpersonal relations, and locality
individual, family, community, and society
Steel et al., 2014
females more likely to experience mood or anxiety condition. males more likely to experience alcohol or substance abuse
anxiety and depression in COVID
signfiicant increase of depression and anxiety. biggest pandemic countries = biggest disorder prevalence. greater increase in women and younger children
defining a mental health disorder
personal distress, maladaptive behaviour, statistical outlier, violation of social norms
classifying mental disorder advantages
provides us with common nomenclature, enables us to structure info, enables us to identify causes and treatments of disorders, insurance reimbursement, recognition and validation of problems
classifying mental disorder disadvantages
stigma of having a disorder, labelling change in self-concept
categorical classification
presence/absence of a symptom pattern. qualitative differences between normal and abnormal
dimensional classification
symptoms vary on a continuum, differences are quantitative rather than qualitative