Professional Documents
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CONTENTS
Introduction
Incidence and prevalence rates
Surveys across life span
Depression epidemiology
Biopolar epidemiology
Schizophrenia epidemiology
Anxiety disorders epidemiology
Suicidal ideas epidemiology
Adolescent suicides
Personality disorders
Unmet needs
Assessment instruments
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Introduction:
Psychiatric epidemiology deals with counting the frequency, risk factors and burden of
psychiatric diseases in specified human population in a specified period. The essence of
epidemiology is studying the distribution of disease using which causal attributions could be
drawn and health services could be organised. Descriptive epidemiology deals with
describing the pattern of diseases while analytical epidemiology attempts to make
associations of observed patterns in order to make inferences in a hypothesis driven manner.
A fast expanding branch of psychiatric epidemiology is genetic epidemiology. It is the
epidemiological evaluation of the role of inherited causes of disease in families and in
populations; Gene-gene and gene-environment interactions are also studied in genetic
epidemiology. Morton defined genetic epidemiology as ‗a science which deals with the
etiology, distribution, and control of disease in groups of relatives and with inherited causes
of disease in populations‘ (Morton NE. Outline of genetic epidemiology. Basel: S Karger,
1982.)
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Levels of prevention:
Most psychiatric disorders are thought to have a biological or sociological aetiology which
produces the ‗hit‘ for later development of the disorder. For a time after this insult, the patient
may exhibit prodromal disturbances which are usually not picked up clinically. This
prodrome later develops into full blown disorder which is diagnosed clinically. This disorder
can have various outcomes: disability, death or recovery. This natural course of a disease
provides us with various nodes of intervention;
1. insult to prodrome node - averting a clinical disorder (primary)
2. prodrome to diagnosis node – early diagnosis (secondary)
3. diagnosis to outcome node - prevention of disability (tertiary)
Primary Prevention
o Primary prevention is meant to reduce the incidence of the disease by preventing
the development of new cases.
o This is done through the elimination of aetiologic factors, increasing host
resistance, the reduction of risk factors, and blocking modes of disease
transmission. E.g vaccines
o The aetiologic factors in mental illnesses such as schizophrenia are not known
with sufficient certainty to make primary prevention possible
Secondary Prevention
o Early identification and prompt treatment of illness is the definition of secondary
prevention. The goal is to reduce the total number of existing cases by more rapid
effective intervention which shortens the duration of illness. This includes
screening programmes and early intervention, crisis support programmes.
Tertiary Prevention
o Tertiary prevention involves the reduction in the prevalence of residual defects or
disabilities that are consequences of the illness. It may not be possible to
eliminate fully the sequel of the illness, but the goal of tertiary prevention is for
individuals to reach their highest level of functioning.
o In the case of schizophrenia, tertiary prevention is rehabilitation.
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Risk factors:
Risk factors predate the associated disorder; while some are easily identifiable and
are malleable via a preventive intervention, some may not be changeable.
Biological risk factors include genetic vulnerability, adverse prenatal event
(traumatic, toxic, infectious)
Psychological/Psychosocial risk factors include family discord, parenting skill
deficits
Social/Environmental risk factors include availability of drugs and firearms, extreme
economic and social deprivation etc.
Protective factors:
Protective factors predate the associated disorder; while some are easily identifiable
and are promotable via a preventive intervention, some may not be. Examples include
support from caring adults, good school performance, conflict resolution skills,
positive role models clear and consistent discipline in the family.
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Incidence is a ratio measured against time. One month incidence will be invariably lower than
one year incidence. The most common measurement of incidence using the above formula is
also called as cumulative incidence. This is valid in cohort studies where attrition is low, but
not so useful when attrition is significant. This is because dropouts are excluded from being
counted as new cases, while the denominator population usually takes them into account. To
avoid this problem, incidence density (also called as incidence rate) is used. It expresses
number of new cases per person-year of observation. The unit of incidence rate is rather
bizarre, time-1. Hence incidence rate ratios are often used in reporting results that compare
two groups‘ incidence rates.
Prevalence:
Prevalence is defined as the number of ‗existing‘ cases in a specified population for a period
of observation (either cross-sectional observation – called point prevalence, or longitudinal
observation for a specified time – called period prevalence). The existing cases include all
new cases, all cases diagnosed before the observation but still suffering from the disease. But
existing cases exclude those who have been previously diagnosed but now cured or dead. The
essential criterion is that the cases must be found when observation is being carried out,
irrespective of when the diagnosis occurred. This is not possible if someone is dead or cured
well before the observation period.
For illnesses which are significantly chronic (e.g. schizophrenia), prevalence will be higher
compared to those illnesses which are acute and short-lived (e.g. influenza), even if the
incidence rates are comparable. Hence a simple expression
Prevalence = incidence X duration of illness explains the relationship between incidence
and prevalence.
Certain factors can influence incidence and prevalence differently. For example, if a new
vaccine is developed for preventing an illness both incidence and prevalence may come
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down. If a cure is developed for schizophrenia, incidence may not be affected, but prevalence
can drop. Similarly if interventions are introduced to reduce mortality in chronic
schizophrenia, then prevalence may paradoxically increase due to longevity of patients. This
may not affect incidence rates directly.
Lifetime prevalence is the proportion of individuals in the population who have ever
manifested a disorder, who are alive on a given day (ref: Saha). This is ascertained by
surveying a population cross-sectionally and finding out if they ever satisfied the criteria for a
disorder in the past or currently. As one can observe, this method though commonly used in
epidemiological surveys, is prone for recall bias.
Lifetime prevalence needs to be clearly distinguished from lifetime morbid risk (LMR).
LMR is the probability of a person developing the disorder during entire period (often a
specified period, defined by the life expectancy of the population studied) of their life. LMR
includes the entire lifetime of a birth cohort both past and future, and includes those deceased
at the time of the survey. For low-incidence disorders such as schizophrenia, summation of
age-specific incidence rates gives approximate LMR (Saha et al PLoSMed 2004)
Mortality rates:
Crude, specific and standardised rates: A crude rate is any rate applicable to whole
population e.g. crude birth rate, crude mortality rate etc. A specific rate is any rate applicable
to a subgroup of a population e.g. age specific mortality, disease specific mortality, cause
specific mortality rates etc. A standardized rate is a rate applicable to a hypothetical
population with an adjusted variable e.g. age. As population samples are heterogeneous, crude
rates from one population may not be comparable to another population. For example suicide
rates in inner London may not be comparable to rates in rural Yorkshire, as working age
population may be more in London, spuriously increasing suicide rates. Hence, standardized
hypothetical populations are used on which observed rates from a population are applied and
adjusted values are derived. These standardized values are easily comparable.
Crude mortality rate: Ratio between number of deaths due to all cause in a population and
total population size
Cause specific mortality rate: e.g. alcohol specific mortality. This refers to ratio between
number of deaths due to alcohol in a population and total population size.
Case fatality rate: Ratio between number of deaths due to a specific disease and number of
persons affected by the disease in a population. It is a measure of the fatal severity of the
disease studied. For example, 15 patients out of 100 with anorexia will die due to its
complications.
Proportionate mortality rate: It is a measure of contribution of a disease to societal mortality
burden. It is given by the ratio between deaths due to a specific cause and total number of
deaths in a population.
Years of Potential Life Lost (YPLL) is a measure of the impact of premature mortality on a
population. It is calculated as the sum of the differences between some predetermined end
point and the ages of death for those who died before that end point. The two most commonly
used end points are age 65 years and average life expectancy. Because of the way in which
YPLL is calculated, this measure gives more weight to a earlier deaths than later deaths.
Disability adjusted life years - The DALY is a health gap measure that extends the
concept of potential years of life lost due to premature death (PYLL) to include equivalent
years of 'healthy' life lost in states of less than full health, broadly termed disability. One
DALY represents the loss of one year of equivalent full health. Additionally, 3% time
discounting and non-uniform age weights which give less weight to years lived at young and
older ages were used in calculating DALYs.
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YLL = N x LE
Where N = number of deaths and
LE = standard life expectancy at age of death in years
YLD = I X DW x LD
I = number of incident cases
DW = weight given to the disability
LD = average duration of the case until remission or death (life until death in years)
For most of the above rates, total number of live births is the denominator.
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WHO used CIDI, more comprehensive structured instrument that includes elements of ICD
and DSM for second generation of cross national surveys from 1990. CIDI and DIS can
detect prevalence (frequency) but not severity of psychiatric conditions.
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Comorbidity data from ESEMED: Of all respondents with a mood disorder, 41.7% also
had an anxiety or alcohol disorder. Among those with an anxiety disorder, 28.3% also had a
disorder from another broad category, whereas for alcohol disorder this figure was 22.8%.
Thus, mood disorder is the broad category most likely to be comorbid with another broad
category. Of the separate mood disorders, dysthymia had higher rates of comorbidity than
major depression (73.3% vs. 53.1%). In general, anxiety disorders were highly comorbid.
Agoraphobia (81.0%), GAD (69.4%) and panic disorder (63.8%) were the most comorbid
anxiety disorders; specific phobia (28.6%) and social phobia (49.1%) were the least. Alcohol
dependence was more frequently comorbid with other disorders (27.7%) than alcohol abuse
(20.8%). Alcohol abuse was the least comorbid of all the separate disorders. There were no
significant country differences in these data but two significant gender differences were
found: GAD and alcohol dependence were significantly more often comorbid in women.
NEMESIS
The Netherlands Mental Health Survey and Incidence Study (NEMESIS study) is a large
general population study with three measurement points (baseline in 1996, first follow up in
1997 and subsequent follow up in 1999). Nearly 7000 individuals aged 18–64 years
participated in the baseline survey. Trained lay interviewers applied the Composite
International Diagnostic Interview for case ascertainment.
DEPRES Study
DEPRES (Depression Research in European Society) was the first large pan-European survey
of depression in the community. 78463 adults participated in screening interviews across six
countries and the 6-month prevalence of major depression was found to be nearly 7%. A
significant proportion of sufferers from depression (43%) failed to seek treatment for their
depressive symptoms. Of those who did seek help (57%), most consulted a primary care
physician, the frequency of consultation increasing with the severity of depression. Sufferers
from major depression made almost three times as many visits to their GP or family doctor as
non-sufferers, placing huge demands on the primary care. Only 31%of those who sought help
were given a drug therapy and among these, only 25% were given antidepressant drugs
(Lepine et al, International clinical psychopharmacology 1997 Jan;12(1):19-29).
Depression epidemiology:
Various studies including NCS and its replication NCS-R, NSEARC and ECA have
implicated that lifetime prevalence of depression is changing. But ECA was a subject of
differential recall bias as lifetime prevalence was recollected by subjects. NCS used DSMIIIR
(10.1% depression 12 month period prevalence) while its replication used DSMIV (8.7%
depression prevalence) with its clinical impairment and distress criteria making it possible
that less patients will be diagnosed with DSM IV. In fact it was later shown that if DSM IV
criteria were reapplied then prevalence of depression drops from 10.1% to 6.4% in NCS 1994.
Also NCS excluded all those above age 54 but included 15 to 17 age group (in contrast from
NCS-R), inadvertently choosing the most prevalent population that might have inflated the
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prevalence value. These flaws were absent in NSEARC which showed nearly doubled point
prevalence estimate of depression from 3.3 to 7% (1992 to 2002).
Interestingly, the Stirling county study (cross-sectional samples 1952, 1970 and 1992)
revisited in 2000 (Murphy et al, 2000), showed that vernacular changes in semantic use of
terms like dysphoria can affect results of epidemiological survey. It also showed that lifetime
recall using DIS resulted in spuriously increased prevalence. Using the same diagnostic
system (called DPAX-1) in 1952 and 1970, no increases in point prevalence of depression
were noted. But when same criteria were employed in 1992 a drop in prevalence was noted.
This was due to a change in the use of term dysphoria in the studied population. By increasing
number of questions exploring the mood state and changing the diagnostic system (DPAX2)
similar prevalence rates were detected. It was noted that women and younger people were at
greater risk in 1992 than in 1970. Any historical trend in depression was a matter of
redistribution by sex and age, with a higher rate among younger women being of recent origin.
Bipolar epidemiology:
Consistently in large epidemiological studies, 1.5% prevalence is quoted for bipolar disorders.
It is unclear if there is an elevated estimation of depressive disorders and under-diagnosis of
bipolar type 2 disorder in these surveys. Hypomania, being positively appraised by patients
themselves, is often missed in structured, non-clinician interviews. Angst et al (Eur Arch
Psychiatry Clin Neurosci 2003, 253:236-240) observed in a 20 year long prospective study
that patients with depression and clinically undiagnosed subsyndromal hypomania have
similar risk factors, course and outcome compared to bipolar disorder type 2.
The kappa agreement between structured and clinical diagnostic techniques for mood
disorders is poor, ranging from 0.23 to 0.49 in ESEMED study. In the IOWA Study (a
prospective investigation of the hereditary nature of schizophrenia and bipolar disorders) the
prevalence of mania among relatives of patients affected by bipolar disorders, calculated
solely on the basis of diagnostic interviews, was 1.9%; however, when additional sources of
information such as clinical records and cross-interviewing of relatives were considered, the
rate increased to 5.3%.
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Schizophrenia epidemiology:
Incidence:
In 1986, WHO published results from 7 countries; ICD 9 schizophrenia was 16 to 42 per
100,000. Using narrow criteria it was 7 to 14 per 100,000. It showed considerable between
sites variation. But in spite of that it was concluded that schizophrenia showed remarkably
similar incidence across various countries. This led to an undervaluation of the potential role
of environmental factors on schizophrenia. McGrath et al has showed a five fold difference in
the incidence rates of schizophrenia across various sites. Being urban born increases the risk
of schizophrenia two-fold compared to rural born individuals. Living in the city is also noted
to increase incidence of schizophrenia. The incidence of schizophrenia is 3 to 5 times more
common in migrants than native population; this becomes 1.8 when considering prevalence
rates. Winter/spring birth increases the risk of schizophrenia to a small extent (RR 1.11); but
as prevalence of birth itself is common in winter/spring, 10.5% of all schizophrenia
incidences can be attributed to the seasonal birth. The winter/spring excess is positively
associated with latitude. Fluctuations in schizophrenia incidence have been reported over
many decades. This may be related to changing structure of the population. Irrespective of
broad or narrow definition, the incidence of schizophrenia has definitely increased in certain
urban areas over last 40 years. Boydell et al (BJP, 2003; 182, 45 -49) demonstrated a large
increase in Camberwell between 1965 and 1997 using case record analyses. The male: a
female difference in incidence of schizophrenia is estimated to be around 1.4:1, with more
males being diagnosed with the disease. The male excess persists even when factors such as
age range and diagnostic criteria are taken into account.
Prevalence:
The median prevalence of schizophrenia is estimated 4.6/1,000 for point prevalence,
3.3/1,000 for period prevalence, 4.0/1000 for lifetime prevalence (not 1% as quoted in DSM
IV manual) , and 7.2/1000 for lifetime morbid risk (Saha , McGrath et al PLoS Medicine
2004). There were no significant differences between males and females, or between urban,
rural, and mixed sites, although migrants and homeless people had higher rates of
schizophrenia and, not surprisingly, developing countries had lower prevalence rates (as
previously documented). As it is well known that outcome is better in developing nations,
point prevalence must be low as a corollary, as it was shown by Saha et al. Of note, catatonia
was 10% in developing vs. 1% in developed nations; hebephrenia was 13% in developed vs.
4% in developing nations
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Determinants of DUP: AESOP also investigated the variables that determine long DUP. An
insidious mode of onset (psychotic symptoms appeared incrementally over a period of more
than 1 month since first noticeable behavioural change) was associated with a substantially
longer DUP compared with an acute onset, independent of other factors. Unemployment had a
similar, if less strong, effect. Conversely, family involvement in help-seeking was
independently associated with a shorter duration. There was a weak suggestion (not significant
on adjustment) that nonaffective psychosis was more associated with longer DUP than
affective psychosis.
MORGAN C et al., ―Clinical and social determinants of duration of untreated psychosis in the AeSOP first-
episode psychosis study,‖ The British Journal of Psychiatry 189, no. 5 (November 1, 2006): 446-452.
Outcome in schizophrenia:
In the Iowa 500 study, 186 persons with schizophrenia were followed for an average of 35
years. Excluding affective or schizoaffective disorder, 46% of those people with
schizophrenia had improved or recovered. The Bonn Hospital Study (Germany) followed 502
persons with schizophrenia for an average of 22.4 years. The results were that 22% of the
research participants had complete remission of symptoms, 43% had non-characteristic types
of remission (defined as involving non-psychotic symptoms only) and 35% experienced
characteristic schizophrenia residual syndromes. Therefore, 65% had a more favorable
outcome than would have been expected from clinical experience. With respect to social
functioning, 56% of all participants were judged to be ―fully recovered,‖ which was defined
in this study as full-time employment. At the last follow-up, 13.3% were permanently
hospitalized. In Chestnut Lodge study, 446 patients were followed for an average of 15 years.
One third (36%) were recovered (strict recovery criteria) or functioning adequately. In
Vermont longitudinal study, 68% of patients (n=269, follow up average 32 years) who
underwent a rehabilitation programme had good functioning as determined by GAF scale.
Males show more cognitive deficits while females have more depression at first episode.
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It is thought that the individuals at enhanced genetic risk of schizophrenia (family history)
inherit a state of vulnerability characterised by transient and partial psychosis like symptoms;
but not all of these develop florid schizophrenia.
Edinburgh High Risk Study:
According to Edinburgh High Risk Study, the 10% risk present in those with
high risk family history increases to nearly 50% in those subgroup who have
high score on schizotypal cognition and social withdrawal characterised by
introversion and anxiety.
The EHRS population composed of non-help seekers i.e. identified as high
risk but not presenting themselves with symptoms.
Measures of episodic memory are also proposed to be significantly
discriminating between those with high risk who develop schizophrenia from
those who do not; this is suggestive of temporal lobe dysfunction.
It is also shown that temporal lobe volume deteriorate with the passage of
time in those with psychotic symptoms (this is controversial).
Johnstone EC, et al. Predicting schizophrenia—findings from the Edinburgh High-Risk Study.
Br J Psychiatry. 2005;186:18-25
Klosterkötter J, et al. Diagnosing schizophrenia in the initial prodromal phase. Arch Gen
Psychiatry. 2001;58(2):158-164
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Cannon TD, et al. Prediction of psychosis in youth at high clinical risk: a multisite longitudinal
study in North America. Arch Gen Psychiatry. 2008;65(1):28-37.
The suicide rate in schizophrenia was thought to be 10% for a long time. But a recent
metaanalysis which included studies that were continued for at least 2 years with minimum
90% follow up rates concluded differently (Palmer, Arch Gen Psych 2005)
The estimate of lifetime suicide prevalence in those observed from first admission or illness
onset was 5.6% (95% confidence interval, 3.7%-8.5%). Mixed samples showed a rate of 1.8%
(95% confidence interval, 1.4%-2.3%). Case fatality rates showed no significant differences
when studies of patients diagnosed with the use of newer systems were compared with studies
of patients diagnosed under older criteria.
This concluded that 4.9% of schizophrenics will commit suicide during their lifetimes, usually
near illness onset.
In patients with schizophrenia, suicide is the major cause of death under the age of 35.
Suicide most commonly occurs in early stages or during exacerbations.
15% of adults in UK at any time have broadly defined neurosis according to National
Psychiatric Morbidity Survey. In NPMS 1995 UK prevalence of anxiety disorder was higher
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than depression (consistent with ECA and NCS USA), Phobic disorder the most common in
ECA & NCS but in NPMS – the most common anxiety disorder was mixed anxiety-
depression followed by GAD. 25% of all GP consultations are for anxiety related symptoms.
It is noted that with each generation, anxiety disorders are diagnosed at younger age than the
previous cohort. Considering the mean age of onset for various anxiety disorders, the
following pattern is noted; GAD – 30years, Panic disorder – 22 to 25 years, OCD – 20 years,
social phobia – 15 years, specific phobia – varies with individual categories – blood injury
injection or environmental types start around age 5 to 9 years while situational phobia starts
around 20 years of age.
The estimated lifetime prevalence of blood-injection-injury phobia is around 3.5%. The
median age of onset is around 5 to 6 years. Subjects with blood-injection-injury phobia have
higher lifetime histories of fainting and seizures. Prevalence was lower in the elderly and
higher in females and persons with less education. Patients with this phobia almost never seek
psychiatric help; but they have significantly higher than expected lifetime prevalences of
other psychiatric conditions, including substance use, depression, anxiety disorders and OCD.
Sex distribution of anxiety disorders is an important topic often tested by the College. As a
general rule, all anxiety disorders are common in women than men. Notable exceptions are
OCD which is more in boys than girls, but equally common in adult men and women. Also
men outnumber women in attending health care centres for social phobia.
PTSD epidemiology:
The incidence varies across the world. Resilience to trauma is a dynamic factor and so
individuals who may not develop PTSD after one trauma may develop after another.
Males are more likely than females to be exposed to traumatic events (60% males vs. 50%
females). But females develop PTSD two times more frequently (12% vs 6% in NCS) even
after controlling the type of trauma. It is unclear if this is due to higher exposure to trauma or
greater vulnerability to develop PTSD. Molestation is more common in females than males.
Mugging is more common in males than females. But in both instances women develop more
PTSD. The only trauma where men develop more PTSD may be rape. PTSD is more common
in younger than older individuals; more common in those with higher anxiety response to
initial event and in those who perceive external locus of control (as opposed to internal locus).
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Somatisation epidemiology:
Community surveys in the United States and Western Europe have found prevalence rates of
less than 1 per cent. Primary care surveys using structured interviews have found only a
slightly higher prevalence—typically 1 to 2 per cent. An analysis of follow-up data from the
World Health Organization multicentre primary care survey, however, indicates that recall
during structured interviews may significantly underestimate the lifetime prevalence of
somatization disorder and unexplained somatic symptoms. The prevalence of somatization
disorder and of less severe somatization syndromes is typically twice as high in women as
men. The survey also noted that approximately 20 per cent of primary care patients suffered
from persistent pain (one or more pain symptoms present for most of the last 6 months). Pain
syndromes are approximately twice as prevalent in women as in men
In a different study using ethnic census data, Four per cent of the White British sample
endorsed a hallucination question. Hallucinations were 2.5-fold higher in the Caribbean
sample and half as common in the South Asian sample. (Johns, LC et al, BJPsych 2002,
180:174-78)
Of NCS sample respondents, 13.5% reported lifetime ideation, 3.9% a plan, and 4.6% an
attempt. Cumulative probabilities were 34% for the transition from ideation to a plan, 72%
from a plan to an attempt, and 26% from ideation to an unplanned attempt. About 90% of
unplanned and 60% of planned first attempts occurred within 1 year of the onset of ideation.
All significant risk factors (female, previously married, age less than 25 years, in a recent
cohort, poorly educated, and having 1 or more of the DSM-III-R disorders assessed in the
survey) were more strongly related to ideation than to progression from ideation to a plan or
an attempt.
Kessler later concluded that despite a dramatic increase in treatment, no significant decrease
occurred in suicidal thoughts, plans, gestures, or attempts in the United States during the
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1990s, after analyzing NCS and NCS-R data between 1990-2000 (Kessler, JAMA. 2005; 293:
2487-2495.)
Note that males commit more suicides though females attempt more. Approximately 25
attempts of suicide are recorded for each recorded suicide. Diagnosis of any mental disorder
increases the risk of suicide. The most common method in UK is poisoning by overdose
(paracetamol or antidepressants). In US firearms top the list.
In depression risk factors such as panic attacks, anxiety symptoms, anhedonia, alcohol use,
and insomnia are regarded as short term modifiable risk factors for suicide. Long term factors
include hopelessness, suicidal attempt in the past and ongoing suicidal ideations. (Fawcett,
1990). No difference in suicide rates exist between melancholic and non-melancholic
depression.
♣ Highest suicide rates for both men and women – Eastern Europe (Estonia, Latvia,
Lithuania, Finland, Hungary and Russian Federation) followed by Sri Lanka and China.
♣ Island nations have higher suicide rates generally (Cuba, Japan, Mauritius and Sri Lanka)
♣ Lowest rates – Eastern Mediterranean Islamic nations and some central Asian (formerly
Soviet)
♣ Largest absolute number of suicides: Asia (due to population size)
♣ The male:female ratio is 3.5:1 for completed suicides globally. An exception is China
where females have higher or comparable rates to males. Number of suicides in China is
30% greater than that of whole Europe – due to the size of population.
♣ Globally suicide rates increase with age. In elderly, the rates are 6 – 8 times higher; but
in terms of absolute numbers, more young people are dying than the elderly. 55% of all
suicides fall within ages 5 and 44. (This was 40% in 1950 – the suicide rate in younger
people is increasing at faster pace than the elderly)
♣ Some Islamic countries have nearlyzero suicide rate – e.g. Kuwait. Predominantly Hindu
/ Christian nations have low to moderate rate (India: 10 per 100000 with male:female =
1.3:1 Italy 11.2 per 100000). Atheist nations have very high rates (China: 25.6 per
100000) and so does predominantly Buddhist countries (Sri Lanka, Japan 18 per 100000)
♣ WHO projection for 2020: nearly 1.53 million will die by suicide; 10-20times more will
attempt it. (i.e. one death every 20 seconds or one attempt every 1 -2 seconds)
Barraclough B, Bunch J, Nelson B, Sainsbury P. A hundred cases of suicide: clinical aspects. Br J Psychiatry.
1974;125:355-73.
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Suicide statistics:
Description Rates
1. Global annual suicide rate 1 in 6000/year
2. Male:female 2-4:1
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Adolescent suicides:
Suicidal ideation (without deliberate self harm) in the past year was reported by 15.0% of an
adolescent cohort in UK (school pupils – self report). This was more common in females
(22%) than males (8.5%) (Odds ratio 3.1).
FACT FIGURE
Most common methods Paracetamol overdose and
cutting
One year prevalence of self-harm among 5-10 year- = 0.8%
olds without any mental health issues
Meltzer, H., Gatward, R., Goodman, R and Ford, T. (2000) The mental health of children and adolescents in
Great Britain: Summary Report, London: The Stationery Office
Hawton K., Rodham K., Evans E., Weatherall R. (2002). Deliberate self harm in adolescents: self report
survey in schools in England. British Medical Journal, 325 (7374), 1207-1211.
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Homicide Statistics:
Around 50 homicides per year are committed by those in recent contact with mental health services;
this represents 9% of all homicides
5% of homicide perpetrators have a diagnosis of schizophrenia
Perpetrators with mental illness are less likely to kill strangers and the rate of ‘stranger homicides’ by
those with mental illness has not increased with national trends
Alcohol and drug misuse contribute to homicide in 61% of cases
People with personality disorders as a group are more likely to be separated, divorced, never
married, have more unemployment, frequent job changes, poorer social and interpersonal
functioning, and poorer occupational achievement. But as a group they are only rarely found
to be less well educated.
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Schizotypal 6 0.6 6
Antisocial 19 6 36
Borderline 16 7 93
Histrionic 20 12 10
Narcissistic 2 8 23
Anankastic 17 19 87
Avoidant 7 8 147
Dependent 7 1 14
Passive aggressive 17 - No data
Cluster A = 1.6% Cluster A = 6%
Cluster B = 1.2% Cluster B = 13%
Cluster C = 2.6% Cluster C = 22%
Any PD = 4.4% Any PD = 46%
Epidemiological studies report that the prevalence of personality disorder in primary care
lies between 10 and 30% (Dilling et al, 1989; Casey & Tyrer 1990). In the community,
approximately 1 in 20 community residents in Britain have a personality disorder. The highest
prevalence occurs among GP patients with conspicuous psychiatric illness, although this may
be due to abnormalities of mental state biasing the assessment of personality. Patients with
Cluster C personality disorders are the commonest personality disorders to be encountered
among primary care attenders (Moran et al, 2000). When ICD diagnoses are considered
individually, anankastic personality is the most common type in primary care, followed by
impulsive (emotionally unstable) type.
Dissocial personality is the most prevalent category of personality disorder in prison settings.
A survey of a randomly selected sample of one in six prisoners in England and Wales, found
that the prevalence of any personality disorder was 78% for male remand, 64% for male
sentenced and 50% for female prisoners (Singleton et al, 1998). Antisocial personality
disorder had the highest prevalence of any category of personality disorder, with 63% of male
remand prisoners, 49% of sentenced prisoners and 31% of female prisoners. In Great Britain,
the prevalence of antisocial PD in general population is estimated at 0.6% (See Coid et al –
above table), with the rate in men (1%) five times that in women (0.2%). Surveys conducted
in other countries report prevalence rates for ASPD ranging from 0.2% to 4.1%. Higher
prevalence rates for personality disorders appear to be found in urban populations and this
may account for some of the range in reported prevalence (from NICE: The
ASPD draft scope [Post consultation 29/01/07] Page 5).
Paranoid personality:
More in males , lower social class
Common among relatives of probands with schizophrenia than among relatives of
controls.
Schizoid
uncommon in clinical settings but is more prevalent in offender populations
more common in males
Demonstrate association with schizotypal personality disorder.
might be better classified as a neurodevelopmental disorder than a personality
disorder possibly within the autistic spectrum
Schizotypal
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** The 10 year follow up of McLean sample further clarified this. Affective instability, quasi-psychotic
thoughts, serious identity disturbance, specific impulsivity, substance abuse/dependence, promiscuity,
self-mutilation, and help-seeking suicide efforts, stormy relationships,
devaluation/manipulation/sadism, demandingness/entitlement, serious treatment regressions, and
countertransference problems/"special" treatment relationships remitted relatively rapidly. Chronic
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dysphoria, intense anger, nondelusional paranoia, general impulsivity (disordered eating, spending
sprees, or reckless driving) remained relatively common after 10 years of prospective follow-up.
** In the Collaborative Longitudinal Personality Disorders Study, abandonment fears and physically
self-destructive acts were found to be the least stable (rapidly remitting).
John G. Gunderson, ―Borderline Personality Disorder: Ontogeny of a Diagnosis,‖ Am J Psychiatry 166, no.
5 (May 1, 2009): 530-539.
Antisocial
Antisocial personality disorder has a prevalence of 2-3% in most Westernized
societies
4-5 times more common in men than in women.
The highest prevalence is in the 25- to 44-year age band.
Associated with school drop-out, homelessness and raised mortality in early
adulthood.
The prevalence is higher in inner-city populations and lower in rural areas.
Diminish in middle age, but 20% still meet the criteria at 45 years of age.
Specific reading disorders: In the UK (and the USA) it is generally recognized that between
4 to 7% of children have specific reading disorder - developmental dyslexia – at any given
time. However, it has been argued that dyslexia is far less prevalent in Japan or China because
these languages use logographic rather than alphabetic, phoneme based, scripts and do not
suffer the multiplicity of irregular spellings (such as yacht for ―yot‖) that characterize
English. Indeed some children have been found dyslexic in one language (often English) but
not in the other (Japanese), and in Kana, the Japanese phonetic script, but not in logographic
Kanji. But recent neurobiological studies have shown that developmental dyslexia results
from impaired development of auditory, visual, and motor aspects of basic brain function that
are likely to be as common in Japan as in the UK. Hence it is possible that the same brain
differences might manifest in rather different ways in children learning different languages.
The definitive review on cross-liguistic prevalence of dyslexia is the often quoted study of
Tarnapol & Tarnapol (1977). They reported surveys from 26 countries; the lowest prevalence
was in China and Japan (1%) while in Venezuela it was 33%. In Europe, Germany (5%) and
Italy reported lower rates than US.
Autism: The risk of autism was associated with breech presentation (risk ratio (RR) = 1.63),
low Apgar score at 5 minutes (RR = 1.89), gestational age at birth <35 weeks (RR = 2.45),
and parental psychiatric history (schizophrenia-like psychosis: RR = 3.44 & affective
disorder: RR = 2.91). Analyses showed no statistically significant association between risk of
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autism and weight for gestational age, parity, number of antenatal visits, parental age, or
socioeconomic status. Results suggest that prenatal environmental factors and parental
psychopathology are associated with the risk of autism. These factors seem to act
independently. Childrearing practices have no impact on development of autism – in contrary
to earlier opinion (i.e. refrigerator mothers don‘t exist).
American Journal of Epidemiology 2005 161(10):916-925
Paraphrenia: Howard suggested a prevalence rate of 1-2% over 65 (broadly 0.1 to 4%). It is
important to remember that in >65, 90% of those with schizophrenia are graduates i.e. have
onset before age 45 – only 10% constitute late onset group. The incidence of paraphrenia is
estimated to be 10-26 per 100 000 per year. People with late paraphrenia represent
approximately 10% of the elderly population of psychiatric hospitals. The point prevalence of
paranoid ideation in the general elderly population has been estimated to be 4%–6%, but most
of these patients will have dementia.
Dementia: The prevalence of dementia increases exponentially with age. About one third of
the population aged 85 and over has dementia, with prevalence ranging from 0.4% under 60
years to 45% at 95 years and over. The exponential doubling of prevalence rates after age 65
apparently slows down after age 90 in epidemiological studies, mostly due to reduced sample
size of observation in this age group. A 90+ study of n=911 reported 45% prevalence in
women and 28% prevalence in men with prevalence doubling every 5 years for women but
not men (Corrada et al).
Nearly 64% of those with dementia have Alzheimer‘s disease.
ADHD epidemiology:
The reported prevalence of ADHD in school age children worldwide varies from 1.7% to
17.8% depending on the criteria used. Most estimates lie between 5% and 10%. US estimates
have historically been higher than UK estimates, due presumably to the application of
narrower diagnostic criteria by UK authors. Three studies of English populations have shown
a prevalence rate of between 2% and 5%, depending on whether DSM-IV or ICD-10 criteria
were applied. A large sample of school children (n = 22,044) screened using DSM-IV teacher
rating scales showed a similar prevalence at school entry. The male to female ratio in ADHD
prevalence is at least 4 to 1.
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http://www.sign.ac.uk/guidelines/fulltext/52/references.html#15
Pathways to care:
Also called as filter model, this was developed by Goldberg and Huxley, to account for how
mental illness interacts with the healthcare system. Five levels of mental illness occurrence
were described: The community, the primary care attendees, the diagnosed primary care
attendees (in whom the mental illness has been recognised), the level of psychiatrist and that
at the level of psychiatric inpatient care.
Four filters explain the decreasing numbers of cases when going from the general population
to inpatient psychiatric care
1. At the level of the patient himself or herself (recognition)
2. At the level of the general practitioner (recognition, decision to treat, decision to refer),
3. At the outpatient level of the mental healthcare system and
4. At the inpatient admission level.
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Rating scales:
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Reynolds Child Depression Scale and the Children's Depression Inventory were developed
specifically for children and are written at lower reading levels.
Advantages of the BDI and CES-D include ease of scoring, low cost, and comparable
psychometric properties.
o Perinatal depression:
The BDI, CES-D, and Edinburgh Postnatal Depression Scale (EPDS) have been used
to screen for depression in women during the antepartum and postpartum periods.
o The BDI and CES-D tend to produce higher scores and more false-positive results in
symptomatic pregnant women.
o Edinburgh Postnatal Depression Scale was specifically developed for assessing
postpartum depression and relies much less on somatic questions.
o Questions on the Edinburgh scale (10 items, can be self or clinician rated) are framed
within the "past seven days" and the response format is frequency-based.
o Routine use of EPDS during the postpartum period has been shown to increase the
detection of postpartum depression compared with usual care.
Cox JL, et al. Validation of the Edinburgh Postnatal Depression Scale (EPDS) in postnatal
women. J Affect Disord 1996;39:185-9.
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Geriatric depression:
o The GDS – Geriatric depression scale was specifically developed for use in geriatric
patients, and it contains fewer somatic items.
o Questions pertain to symptoms within the past week and responses require only a
"yes" or ‗no‘.
o In patients who have cognitive deficits, interviewer-administered instruments such as
the Cornell Scale for Depression in Dementia or the Hamilton Rating Scale for
Depression are preferred.
o The Cornell measure should be administered to the patient's primary caregiver.
Sharp LK, Lipsky MS. Screening for depression across the lifespan: a review of measures for use
in primary care settings. Am Fam Physician 2002;66: 1001-8.
Achenbach, T. M. (1991). Manual for the Child Behavior Checklist/4-18 and 1991 Profile.
Burlington, VT: University of Vermont, Department of Psychiatry.
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Hamilton Rating Interviewer ated, 17- 17 items scored according to severity, producing
Scale for item rating scale for total score.
Depression (HAM- depressive illness.
D) Not a diagnostic
instrument; used to
measure changes
(e.g. as a result of
drug treatment).
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CAGE Brief screening test a score of 2 or more indicating the need for further
Questionnaire for alcohol problems assessment.
consisting of 4
yes/no questions,
Minnesota Results generate Self-report questionnaire consisting of 567
Multiphasic information useful questions covering 8 areas of psychopathology, 2
Personality for a broad range of additional areas of personality type, and 3 scales
Inventory (MMPI) clinical applications. assessing truthfulness. Results are compared with
normative data from non-clinical populations. NOT
A PROJECTIVE TEST.
International Semi-structured 67 standardised probe questions. 57-item true/false
Personality clinical interview for questionnaire also included for screening purposes.
Disorder use by clinicians
Examination producing ICD-10-
(IPDE) personality disorder
diagnosis.
References:
Brugha, T., Bebbington, P. E., Jenkins, R., et al (1999) Cross validation of a general population
survey diagnostic interview: a comparison of CIS-R with SCAN ICD-10 diagnostic categories.
Psychological Medicine, 5, 1029 -1042.
Johns, LC et al. Prevalence and correlates of self-reported psychotic symptoms in the British
population. The British Journal of Psychiatry 2004 185: 298-305
Bebbington, PE et al. Psychological Medicine (1997), 27: 821-834 Depression among older people
in Europe: the EURODEP studies
Kessler et al. Prevalence of and Risk Factors for Lifetime Suicide Attempts in the National
Comorbidity Survey. Arch Gen Psychiatry, 1999; 56: 617 - 626.
Murphy, JM., et al (2000) A 40-Year Perspective on the Prevalence of Depression: The Stirling
County Stud. Arch Gen Psychiatry.; 57:209-215.
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