Peds/Geri/Med Flashcards
mental retardation. M:F?
IQ of 70 or below. onset before age of 18. Males are affected 2x as much as females.
does most MR have an identifiable cause? 2 most common causes.
no. Downs and fragile X (M>F)
criteria for conduct disorder
at least 3 of the following within past year:
- aggression to people or animals
- destruction of property
- deceitfulness
- serious violation of rules
criteria for ODD
at least 6 months of negativistic, hostile, and defiant behavior, which 4 of the following have been present.
- frequent loss of temper
- arguments with adults
- defying adults rules
- deliberately annoying people
- easily annoyed
- anger and resentment
- spiteful
- blaming others for mistakes or behaviors
ADHD and ODD/conduct?
2/3 of children wit ADHD also have ODD or conduct
M:F in ODD? remission?
before puberty, more common in males. after puberty, M=F. remission in 25% of children. may progress to conduct
pharm for ADHD
CNS stimulants with TCAs as adjunctive
how to diagnose autism
- problems with social interaction
- impairments in communication
3 repetitive and stereotypes patterns of behavior and activities
what kind of problems with social interactions can autistic kids have
at least two.
- impairment in nonverbal relationships- facial expression, gestures
- failure to develop peer relationships
- failure to seek sharing of interests of enjoyment with others
- lack of social/emotional reciprocity
what kind of impairments in communication can autistic kids have
at least one
- lack of or delayed speech
- repetitive use of language
- lack of varied/spontaneous play
what kind of repetitive and stereotypes patterns of behavior and activity can autistic kids have
at least one
- inflexible rituals
- preoccupation with parts of objects
how to treat autism
no cure. treat sxs.
- remedial education
- behavioral therapy
- neuroleptics- to help control aggression, hyperactivity, and mood lability
- SSRIs- to help control stereotypes and repetitive behaviors
- some children benefit from stimulants
when does autism present. what percent are mentally retarded. is there genetic assn?
usually presents before age 3.
M»>F.
70% have MR
significant assn with fragile X syndrome, tuberous sclerosis, MR, and seziures
concordance of autism in biological twins
36%
diff b/w Aspergers and autistic
Aspergers have normal language and cognitive development. but they do have problems with relationships and with restricted or stereotyped behaviors, interests, or activities
what is mutation of Rett’s? M vs. F. what is treatment
MECP2 gene on X chromosome. Seen mostly in girls, but sometimes in boys
blood test of anoerxia? Bulimia?
AN: hypochloremic, hyperkalemic akalosis.
hypercholesterolemia
leukopenia
BN: hypochloremic hypokalemic alkalsosi, increased amylase, increase BUN, hypernatreamia, metabolic acidosis, elevated bicarbonate
primary vs secondary enuresis? when is it usually established? when is enuresis usually remitted?
usually establish continence at age 4.
primary: never established continence
secondary: 5-8 incontinence after having it.
usually spontaneously remits by age 7
how to treat enuresis
behavior modification- buzzer when child pees.
TCA- imipramine.
antidiuretics- DDAVP
when is bowel control obtained normally? what to rule out in encopresis? how long do you need to have it?
normally get it at 4. need encopresis for 1x a mo for 3 mo. rule out hypothyroidism.
what other diseases is encopresis associated with
ADHD, conduct disorder
dissociative amnesia vs dementia
amnesia: can’t really name but can remember obscure details. dementia: remember stuff fro past
dissociative amneisa vs. dissociative fugue
unlike dissociative amnesia, pts w/dissociative fugue are unaware that they have forgotten anything
depersonalization disorder? how to treat?
persistent or recurrent feelings of detachment from one’s self, environment, or social situation. reality testing remans intact during episode. treat with anti anxiety agents or SSRIs.
how to treat impulse control disorder
SSRI. low levels of serotonin have been associated with impulsiveness and aggression. anticonvulsants, lithium, propranolol. individual psychotherapy is difficult and/or family therapy may be useful
what is often comorbid with bulimia
kleptomania. 1/4 of BN patients
treatment for trichitolomania
SSRI, lithium, antipsychotics. hypnosis, relaxation techniques. behavioral therapy- substitites anoher habit
hypchondriasis vs factitious
hypo: anxiety is main thing- it doesnt really go away. they wouldn’t want aggressive stuff.
pathophys of ADHD
dopamine filters the noise. norepinephrine increases the volume.
when do you use clonidine
BP and ADHD and opiate withdrawal
what med to give if depressed w/heart disease
sertraline (or citalopram)
can you try ECT after MI?
after 2 months- yes. after 2 good trials, try it.
angelman syndrome sxs
chromosome 15-developmental delay, movement or balance disorder, happy demeanor, sometimes seizures, short
prader-willi syndrome sxs
chromosome 15- cog diabilities, low muscle tone, short stature, chronic feeling of hunger-> obesity, almond shaped eyes
signs of porphyra
depression. GI pain, romberg sign, decreased joint position sense
carbidopa vs levidopa
levodopa crosses the BBB, carbidopa does not. carbidopa presents conversion of levodopa in the periphery. Once levodopa crosses BBB, it is free to be converted to dopamine. levodopa can cause depression or mania.
pathology and pathophysio of parkinsons
loss of cells in the substantial nigra of the basal ganglia-> decrease in dopamine and loss of dopaminergic tracts
53 yr old woman with changes in personality over last 6 years. personality became irritable, sexually uninhibited, and loud. intermittent jerky movements. MRI will likely reveal..
caudate atrophy. this is huntingtons
Huntingtons. onset? path? diagnostic? MRI? treatment?
35-50.
trinucleotide repeat on short arm of chromosome 4. primarily affects basal ganglia.
MRI shows caudate atrophy and sometimes cortical atrophy. genetic test and MRI are diagnostic.
no effective treatment
Huntingtons sxs vs FTD sxs
both have personality changes but Huntingtons has more movement- bizarre choreiform, muscle hypertonicity, and depression and psychosis are common.. FTD has more aphasia, apraxia, agnosia.
cortical dementia vs. subcortical dementia
cortial: alzheimer, Pick’s, CJD: decline in intellectual functioning.
subcortical: huntingtons, parkinsons, NPH, multi-infarct dementia- more prominent affective and movement sxs
parent management therapy
aims to change parenting behaviors, positive reinforcement, used for disruptive behavior like ODD and Conduct Disorder
are related sleep changes in elderly.
sleep less at night and nap during the day. period of deep sleep (stage 4) becomes shorter and eventually disappears. they awaken more throughout the night. not a sleep disorder.
preferred treatment for narcolepsy
modanifil. amphetamine stimulant are second line because of their abuse potential.
brain changes seen in PTSD
decrease in size of hippocampus
brain changes seen in autism
increased total brain volume nd accelerated head growth during inancy
brain changes seen in OCD
structural abnormalities in orbitofrontal cortex and basal ganglia
how to qualify for insomnia
3x per week for at least one month. difficulty maintaining or initiating sleep. leads to difficulty in completing tasks.
how to qualify for primary hypersomnia
at least 1 month of daytime sleepiness or excessive sleep not attributable to medical conditions, medications, poor sleep hygiene, insufficient sleep or narcolepsy. usually begins in adolescence.