Professional Documents
Culture Documents
RANZCP
OSCE (usually station 1) examines medical aspects associated with psychiatric practice Resuscitation stations are revised regularly to reflect the latest ARC Guidelines
(ARC, 2011)
D (check for danger before starting) R (responsiveness is the person rousable or breathing normally) S ( send someone for help) A (airway; clear obstruction, head tilt / jaw thrust) B (is the person breathing effectively) C (start chest compressions; 30 then 2 breaths) D (attach defibrillator ASAP; follow AED prompts)
(ARC, 2011)
Non-shockable rhythms
sinus rhythm with insufficient output (PEA) Asystole Bradycardia (<60 bpm) with insufficient output
VT
Status epilepticus
Acute dystonia
Risk factors
Onset of AP, increase in dose, IM route of administration, cessation of DA agents, highpotency and typical APs Pre-existing structural brain lesions Genetic loading
Treatment
Cease DA-antagonist or re-start DA-agonist, lorazepam (agitation), correct fluid/electrolyte imbalances In HDU, dantrolene (mm relaxant) and bromocriptine (DA agonist) may be helpful
Serotonin Syndrome
Physiology
Excessive 5HT activity on 5HT1A and 5HT2 receptors; increased NAd activity also likely to be a factor
Risk factors
Serotonergic agents (incl SSRIs. Li, synthetic opioids, MAOIs, amphetamines, St Johns Wort), genetic predisposition, drugs with multiple serotonin-increasing actions often responsible
Serotonin Syndrome
Diagnosis
History, clonus, hypereflexia, autonomic disregulation, deterioration in mental state with pronounced agitation, headache May mimic encephalitis, meningitis, toxin exposure, anticholinergic delirium
Treatment
Mild cease agent, diazepam 10mg q1h and (debatably) stat dose 6mg cyproheptadine Severe cease agent, consider early ICU admission for sedation/intubation
Treatment
Convulsive SE treated with airway/circulatory support, IV lorazepam/diazepam, IV phenytoin and, if no resolution, intubation and inducedparalysis with midazolam/propofol
Acute dystonia
Pathpohysiology
Likely due to decreased DA in basal ganglia/motor cortex with decreased motor inhibition
Risks
Use of any D2- receptor antagonist (although typical APs much greater problem), Li, SSRIs Genetic predisposition significant risk factor Previous problem with other drugs in same class
Acute dystonia
Features
Typically affects 3-5% of all patients on APs and up to 10% on typical APs Most commonly in muscles of neck (30%), tongue (17%), jaw, occular movements
Treatment
Stat dose 2mg IVI benztropine, diazepam 10mg; symptoms usually resolve in 3-5 mins
Final thoughts
Attending an arrest is confronting, no matter how many times youve done it before You really cant make things worse, so doing something (even if youre unsure) will always be better than doing nothing If you cant remember anything else, good CPR with some ventilation will buy you the 10-15mins it generally takes for help to arrive