Child & Adolescent Psychiatry Flashcards
(546 cards)
What are mental health outcomes associated with cannabis use in adolescents?
Depression
Psychosis
What are the most common scales used to assess Pediatric delirium?
The Pediatric Confusion Assessment Method for the Intensive Care Unit (pCAM-ICU)
Cornell Assessment for Pediatric Delirium (CAPD/CAPD-R)
What are evidence-based means of non pharmacologic pediatric delirium prevention?
reduction of pain
sleep disturbance
physical restraint use
addressing sensory and communication difficulties
ensuring early mobilization
providing frequent reorientation, including the use of familiar items from home
consistent presence of the child’s caregivers
What are evidence-based pharmacologic treatment of Pediatric delirium?
antipsychotics
alpha-2 agonists
melatonin
“Antipsychotics have been the mainstay of delirium treatment, with haloperidol, risperidone, olanzapine, and quetiapine showing equivalent safety profiles and improvement in agitation, sleep-wake disturbance, and symptom severity.,”
Name 5 social impacts of cannabis use in youth.
- Decreased performance in school, leading to lower educational attainment
- Higher unemployment levels
- Involvement in criminal activity
- Greater social assistance requirements
- withdrawal from their usual peer groups and conflict with family
- Lower Levels of Life Satisfaction
- Reduction in social, occupational or recreational activities
- Unable to fulfill major role obligations – school, work, family, friends
- Financial problems (leading to possible criminality)
- “gateway” to other drug use *
What is the relationship between cannabis and psychosis?
- Half of pts who develop induced psychotic symptoms with cannabis will go on to develop ongoing psychotic disorder
- Cannabis increases risk of psychosis from 40-400% (linked to how much use)
- The prevalence of schizophrenia is about 1% in the adult population, risk doubled in heavy cannabis users
- Use of cannabis and other illicit substances was associated with an earlier age at onset of psychotic disorders
What would you say to provide psychoeducation to a youth who vapes?
- Impact on respiratory system (Vaping Associated lung injury (VALI), chronic cough, bronchitis, asthma exacerbation, and decreased exercise tolerance)*
- Acute risk of injury (ie: burns, explosion)
- Highly addictive, quick tolerance/ dependence due to high nicotine content of pods (1 pod = 1 pack)
- Problematic use associated with the substances within the vapes (cannabis, nicotine, occasionally opioid, stimulants)
- Due to high concentration - acute nicotine intoxication/Nicotine toxicity – N/V, dizziness, H/A, confusion
- Vaping has been associated with high-risk behaviours and adverse mental health outcomes, notably depression and suicidality *
- Expensive
- Withdrawal
Dx of Catatonia. What are organic causes to be ruled out?
Neuro: Head trauma, cerebrovascular disease, encephalitis (e.g., anti-NMDAr or viral)
- Cancer: Brain tumor, paraneoplastic syndrome
- Metabolic: Hypercalcemia, diabetic ketoacidosis, hepatic encephalopathy, cerebral folate deficiency, homocystinuria
First psychotic episode. Parents asking for brain imaging. Explain why not and also what indications for brain imaging would be.
- Neurological exam is sufficient, and neuroimaging is not routinely recommended for first-episode psychosis (Canadian Schizophrenia Guidelines)
- Routine brain imaging often delays treatment and findings generally not contributory/ do not alter management in any meaningful way.
- Consider imaging if:
(a) History and neurological exam reveal: new/worsening headaches, n/v, seizures, focal neurological deficits
(b) Features of autoimmune encephalitis: rapid progression over <3 months, new focal findings, seizures
4M with imaginary friend. What is going on? Other DDx for visual hallucinations? What are 2 classes of medication that could cause VH?
Normal development
- DDx – adjustment d/o (severe stress), depression/ anxiety, PTSD, ASD, ID, sleep d/o
- Secondary to GMC – tumor, seizures, delirium, encephalitis
- Medications – steroids, opiate analgesics, anticholinergics
VH x 2 months, no other psychotic sx, no mood issues or bipolarity.
- PTSD, delirium, (temporal lobe) epilepsy, ASD
What is the therapeutic approach for pre-psychotic patients? Evidence-based approaches to treatment.
Approach to treatment for Clinical High Risk (Canadian Schizophrenia Guideline):
- Psychological interventions and medications can prevent or delay a first episode
- Offer Individual CBT +/- Family Intervention
- Offer Social Skills Training
- Treat comorbid conditions (e.g., depression)
- Monitor regularly for 3 years using validated tools
- Treatment should be provided by a psychiatrist or psychologist
- Use a staged and least-restrictive approach to treatment (e.g., CBT first then low dose SGA if needed)
What are the criteria for SIPS?
- SIPS – structured interview for psychosis-risk syndromes, which includes:
- Attenuated Positive Symptom Prodromal Syndrome (APS);
- Brief Intermittent Psychosis Prodromal Syndrome (BIPS);
- Genetic Risk & Deterioration Prodromal Syndrome (GRDS)
- SIPS assess:
- FHx
- GAF
- Scale of prodromal sx
- Schizotypal personality assessment
4F in hospital, seeing spiders. DDx? Recommendations?
- Delirium
- Work-up to determine cause
- Assessment – scales such as CAP-D (0-21yo), SOS-PD (0-16yo) or PAED (1-17yo) [pCAM-ICU is for >5yo]
CAPD: Cornell Assessment of Pediatric Delirium (age 0-21)
PAED: Pediatric Anesthesia Emergence Delirium Scale (age 1-17)
pCAM-ICU: Pediatric Confusion Assessment Method – ICU (age >5)
PsCAM-ICU: Preschool Confusion Assessment Method – ICU (age <5)
SOS-PD: Sophia Observation Withdrawal Symptoms – Pediatric Delirium (age 0-16)
- Non-pharmacological – early mobilization; remove unneeded unused lines; reorientation; parents at bedside; familiar items; maintain day-night cycle with multiple cues; reassurance
- Pharmacological – avoid polypharmacy + opiates + benzodiazepines + anticholinergic medications; Risperidone or Haldol/ Loxapine if hyperactive delirium. Titrate dose based on PRN use.
Metabolic syndrome criteria. What populations are most at risk? What are common secondary medical dx?
3 or more of the following
- Abdominal circumference >102cm for men, 88cm for women. For children 10-16 yo: the 90th percentile for waist circumference or adult cut point (whichever was lower) should define abdominal obesity.
- BP >130/85
- TG >1.7mmol/L
- HDL < 1.00mmol/L in men, <1.3mmol/L in women
- Fasting BG >5.6mmol/L
- Ethnicity – indigenous, blacks
T2DM, hypertension, cardiac disease, fatty liver, polycystic ovarian syndrome (PCOS), and pro-inflammatory states
Young child with cancer. Hospitalized x6 days. How do you explain why he is « not himself »?
- Ddx – delirium?
- Developmental regression in the context of critical illness (normal)
Which drugs cause VH?
- LSD, PCP, Amphetamines, Cannabis, Psylocibin
Which AP to avoid hyperPL?
1 Aripiprazole
Distant 3rd Clozapine
Secretion of prolactin by the pituitary gland is inhibited by dopamine in the hypothalamus. D2 blockade by antipsychotics in the hypothalamus releases this inhibition and causes hyperprolactinemia. D2 partial AGONISTS are not associated with hyperprolactinemia and can even treat it = Aripiprazole, Brexpiprazole, Cariprazine
Quetiapine is a D2 antagonist (not a partial agonist) but it (and Clozapine) have the lowest D2 blockade.
16 year old with schizophrenia. Attends a Section 23 school. Struggling with hallucinations.
a) Name 2 things that the teacher can do in order to support this student.
b) Name 2 things the teacher could do to decrease social isolation.
c) Name one intervention that a guidance counsellor can apply.
(a) Quiet room for evaluations and additional time for completion = (tests, exams); Headphones (+/- music) and ear plugs; Access to resource room/ supports; Body breaks; Technology adaptations (ie : Chromebook); Relaxation techniques. Adapt the schedule, workload and expectation according to capacities and absences with realistic expectations. Help with increased visual support.
(b) Integrate activities and projects of pre-selected groups; vocational projects; work in dyads or groups. Social skills training, tutoring from other student.
(c) IEP; specialized educator and decrease ratio; promote vocational projects; quiet and calm environment; cognitive remediation; cognitive remediation; build on strengths; consider school placement.
List two mental health disorders associated with hallucinations in youth (other than a psychotic disorder, SUD and bipolar disorder):
Anxiety disorders
Borderline Personality Disorder
PTSD
Depression
ASD/DD (less so)
Clinical vignette of an adolescent admitted and treated with an antipsychotic for acute psychosis. He is now febrile, delirious, and displays muscle stiffness. List two mandatory laboratory investigations. List three important components to evaluate on physical exam.
- Investigations – blood work, (CK, Creatinine, CBC, blood cultures, liver enzymes, LDH, Ca, PO4, Serum iron, urine myoglobin, ABG, coag, serum and urine toxicology)
- Most important is to rule out Ddx (ex. infection)
- Physical examination - Worry about NMS – (FARM)
- Temp
- HR/BP
- Rigidity
- Most important/dangerous: hyperthermia
List three features to differentiate schizophrenia from ASD in a child.
Temporal evolution/ onset of symptoms
Those with ASD do not spontaneously orient to emotional information
Origin of bizarre behaviours – delusions/ hallucinations/ disorganization vs. sensory hyper/hypo-sensitivities, adherence to routine/ rigidity
Period of normal or quasi-normal development before onset of symptoms (in scz)
Told of a family doctor who placed a youth on an antipsychotic and is now asking you what will be important to monitor over time. Asked to list five things.
Weight, BMI (Height), WC
Vitals – BP
Blood work – glucose/ HbA1c, lipid profile, PL (and effects of hyper-PL)
EPS + neurological exam
Psychotic Symptoms
Adolescent on clozapine. More lethargic past 2 weeks. Given most concerning side effect, name 3 signs or symptoms to do on history or physical exam. What lab investigation is most important to monitor? How often to check bloodwork in the first 6 months?
- Agranulocytosis – low NT count
- Fever, mouth ulcers, sore throat (maybe also HR/BP)
- Weekly for the first 6 months and biweekly for the next 6 months. CBC/ NT count weekly x 6 months. TnI and ERP weekly x first 4 weeks.
Prior to initiating treatment, obtain a baseline ANC; the ANC must be ≥2,000/mm3 in order to initiate treatment. Initiate treatment in an inpatient setting or an outpatient setting with medical supervision and monitor of vital signs for at least 6 to 8 hours after the first few doses. During the first 6 months (26 weeks) of treatment, ANC should be obtained at baseline and at least weekly. If count remains acceptable (ANC ≥2,000/mm3) during this time period, then may be monitored every other week for the next 6 months (26 weeks). If ANC continues to remain within these acceptable limits after the second 6 months (26 weeks) of therapy, monitoring can be decreased to every 4 weeks.

