The Child Bipolar Questionnaire (CBQ) A Screening Instrument For Juvenile-Onset Bipolar Disorder
The Child Bipolar Questionnaire (CBQ) A Screening Instrument For Juvenile-Onset Bipolar Disorder
Psychiatric Rating Scale Characteristics. The CBQ item data are obtained
as Likert scale data, with response range 1-4. For the purposes of the
analyses, we dichotomized these responses, with 1-2 recoded as zero and 3-4
recoded as 1. The CBQ instrument has an important subscale called the CBQ
Core Bipolar Symptoms Subscale, comprising 35 of the 65 CBQ items.
Scoring
Determination of a “probable” diagnosis of childhood-onset bipolar disorder is
based on positive endorsement of >40/65 general items at frequencies > 2,
or alternatively at least 20/33 core syndromal symptoms (see below).
Results
There were 827 subjects for whom both bipolar diagnostic and CBQ data
were obtained via the JBRF internet-based system. For 619 (74.8%) of
these subjects, it was reported that a diagnosis of bipolar disorder had
formally been assigned at some prior time by a clinician (pediatrician,
psychiatrist, or other clinician). Included in this group were 290 girls
(35.1%) and 537 boys; average age was 10.6 ± 3.6 years (range 2.2 – 20).
Among the CBQ items with the strongest correlations with BPD diagnosis are
several that have obvious face validity. For example, the three CBQ items
most strongly correlated with bipolar diagnostic status are: Item 62 “Has
acknowledged experiencing hallucinations,” Item 26 “Has many ideas at once,”
and Item 31 “Displays abrupt, rapid mood swings.” All of these have odds
ratios exceeding 2.0.
3. Papolos, D.F., & Papolos, J.D. The Bipolar Child: The Definitive and Reassuring
Guide to One of Childhood's Most Misunderstood Disorders. Broadway Books, N.Y.,
December, 2002.
The Bipolar Child Questionnaire Version 2.0
Core Syndromal Symptoms
The Bipolar Child Parent Questionnaire Version 2.0 (CBQ V.2.0), a 65 item
questionnaire, has been developed to serve as a rapid screening inventory of
common behavioral symptoms, and temperamental features associated with
PBD. The first version of the CBQ, version 1.2, contained 85 items, many
drawn from DSM-IV categories of childhood psychiatric illnesses. This
inventory, as a first iteration, was constructed as a method to determine
rates of positively endorsed symptoms for specific age epochs, and scored
retrospectively by parents of children diagnosed with PBD by DSM-IV criteria.
The most common positively endorsed symptoms were rank ordered
according to frequency of occurrence (scores > 60%), and of these, the 65
highest ranked symptoms and behaviors were included in the CBQ Version
2.0.
This CBQ 1.2 inventory was administered along with a survey that consisted
of 35 questions that assessed demographics, premorbid symptoms and
behaviors, family psychiatric and substance abuse history, treatment
response, as well as an 85 item checklist that recorded parents retrospective
reports of symptoms and behaviors in chronological two- year age epochs
from birth to age 20. 70 of 85 items from the behavioral checklist were
drawn from the DSM-IV diagnostic categories for childhood and adult
psychiatric disorders that define criteria for: separation anxiety disorder,
generalized anxiety disorder, phobias, obsessive compulsive disorder,
oppositional defiant disorder, conduct disorder, attention-deficit disorder,
major depression and bipolar disorder. Additionally, because several clinical
studies reported on juvenile-onset cases (Papolos et. al. 1996; Wozniack et
al, 1995; Geller et al,1998;) have found a predominance of rapid and ultra-
ultra rapid cycling variants, the frequency of mood cycles was evaluated by
additional items which asked parents to rate mood variations occurring at
hourly intervals (one and six hours and greater than six hours were
included), as well as through a visual display illustrating six different possible
cycling patterns. Follow-up telephone interviews were conducted with parents
to validate and enlarge upon the survey responses.
The sample comprised all children and adolescents (n=210), ages 5.4-18.8
yrs., consecutively referred over a 36 month period (11/1999 - 11/2002) to
the practice of one of the authors (DFP). The mean age 10.2 yrs. 61.6%
were male Each diagnostic evaluation involved separate interviews with
children and one or both parents. For every diagnosis, information was
gathered regarding ages of onset and offset, number of episodes and
treatment history. A full 82.9% of the sample had some psychiatric
symptoms by 6 years of age, 79% at or prior to the age of 4, and 54% by
age 2 or earlier. 52.1% had been seen at least once by a mental health
professional by the age of 5, 88% by age 11, and almost the entire sample
(99.1%) by age 16. 72% of the sample was diagnosed with bipolar disorder
– NOS, 15% with BP I and 13% BP II. 86.3% had at least one previous
DSM-IV diagnosis.
Diagnostic Criteria
To be given a lifetime diagnosis of mania, the child had to meet full DSM-IV
criteria for a manic episode with associated impairment. Thus a child must
have met criteria A for a period of extreme and persistently elevated or
irritable mood, plus criteria B; manifested by three (four if mood is irritable
only) of seven symptoms during the period of mood disturbance. To be
diagnosed with BP-NOS the child must have had distinct periods of
abnormally, elevated, expansive or irritable mood, most of the day, nearly
every day for repeated periods (a minimum of 5 such episodes) for at least 2
days as indicated by either subjective report or observations made by others,
and during the period of mood disturbance have 3 or more of the following
symptoms present to a significant degree (4 if the mood is only irritable);
inflated self esteem or grandiosity, decreased need for sleep, more talkative
than usual or pressure to keep talking, flight of ideas or subjective
experience that thoughts are racing, distractibility, increase in goal-directed
activity or psychomotor agitation, excessive involvement in pleasurable
activities that have a high potential for painful consequences.
In the BP-NOS group, marked variations in mood and energy were present
and were characterized by abrupt, rapidly alternating levels of excitability,
emotional lability, and motor activity. A large majority of cases experienced
chronic irritable mood states with a superimposed diurnal pattern of irritable
mood states in the morning on arising, associated with decreased energy and
low activity, followed by intense, rapid shifts of mood throughout the day
with intensification in the PM of irritable or elated/euphoric (silly, goofy,
giddy) mood states, as well as, early insomnia, and middle of the night
arousals. A majority of cases exhibited a low tolerance for frustration in
situations that required sustained attention, interest and effort which was
manifest by difficulties with postponement of immediate gratification, such as
waiting one’s turn, or denial of expressed needs, as well as, changes in
planned activities, established routines, or making required transitions from
one context to another. This deficit, combined with poorly regulated
attentional focus, often resulted in maladaptive responses, such as seeming
not to listen, interrupting or intruding on others, and disruptive,
oppositional/defiant, and provocative behaviors, or -- in the extreme --
temper tantrums and aggressive rage attacks, often followed by sullen
withdrawal and expressions of remorse. Episodes of anger dyscontrol, temper
tantrums, rages, often of more than half an hour in duration, occurred
spontaneously, but were most often precipitated by limit setting attempts by
parents or other authority figures, and were commonly associated with the
use of profane language and/or the expression of physical violence. The
typology of rapid cycling of fast frequency in these patients was of the type
described by Kramlinger and Post (1995), who performed extended in-
patient psychiatric evaluations that included longitudinal assessments,
retrospective life charting and prospective assessment of daily mood by self
and blinded observer ratings to describe this variant of the condition in
adults.
Results
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