Sweatman: Syndromes Flashcards

(41 cards)

1
Q

who gets serotonin syndrome

A

those who overdose on SSRI’s

patients of all ages-newborn-elderly

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2
Q

how many doses of SSRI’s needed to precipitate the syndrome

A

only one

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3
Q

what precipitates serotonin syndrome at molecular level

A

concurrent CYP 2d6 and 3A4 INHIBITION BY OTHER DRUGS

WITHDRAWL OF CONCURRENT DRUG TREATMENT WHILE STILL TAKING SSRI

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4
Q

SEROTONERGIC NEURONS FOUND IN HIGH CONCENTRATIONS ON THE

A

BRAINSTEM

MIDLINE RAPHE NUCLEI
FROM MEDULLA TO MIDBRAIN

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5
Q

ROSTRAL (UPPER) END OF SEROTONERGIC MIDLINE RAPHE NUCLEI ASSISTS IN

A

REGULATION OF WAKEFULNESS, AFFECTIVE BEHAVIOR, FOOD INTAKE, THERMOREGULATION, MIGRAINE, EMESIS, AND SEXUAL BEHAVIOR

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6
Q

SEROTONERGIC MIDLINE RAPHE IN LOWER PONS AND MEDULLA PARTICIPATE IN

A

REGULATION OF VASCULAR TONE AND GI MOTILITY AND EVEN NOCIOCEPTION

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7
Q

AGONISM OF WHAT RECEPTOR CONTRIBUTES SUBSTANTIALLY TO SEROTONIN SYNDROME

A

5HT2

excess serotonin-impacts a variety of brain stem functions and thus disrupts autonomic functions on many levels-leading to the syndrome appearance

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8
Q

spectrum of findings in serotonin syndrome

*note not all present in a given patient and some may mask the presence of other

A

Akathisia (feeling of inner restlessness)
tremor
AMS
Clonus (inducible)-rhythmic muscle contraction
Clonus (sustained)
Muscular Hypertonicity
Hyperthermia

*muscular hypertonicity may overwhelm/mask tremor and hyperreflexia

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9
Q

critical in decision making for dx of serotonin syndrome

A

recent use of serotonergic agents and evidence of the classical clinical symptoms

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10
Q

signs that are highly diagnostic for serotonin syndrome in the historys etting of recent SSRI use

A

neuromuscular feature of clonus and hyperreflexia-their occurance established the diagnosis

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11
Q

management of serotonin syndrome

A

discontinue use of ALL potential precipitating drugs

supportive management

control agitation-may need additional drugs

cyproheptadine-serotonin antagonist

control autonomic instability-may need additional drugs

control hyperthermia-appropriate cooling measures

reassess need for serotonergic drug after stable

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12
Q

serotonin antagonist

A

cyproheptadine

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13
Q

drug classes associated with serotonin syndrome

A

SSRIS-duh
Antimigraine-sumatriptan
Antiemetics-setrons
MAOIs-inhibit serotonin breakdown-phenelzine and isocarboxazid
TCAs-inhibit serotonin reuptake-venlafaxine, trazodone, nefazodone, buspirone, clomipramine
st johns wort-inhibits serotonin reuptake
LI-CSF specific
tryptophan
AED-valproic acid
analgesics with serotonergic properties but are mainly opiate agonsits- meperidine, fentanyl, tramadol, pentazocine
metoclopramide

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14
Q

clasical symptoms of neuroleptic malignant syndrome

A

hyperthermia
autonomic dysfunction
muscle rigidity
extrapyramidal tremor

*possibility of a direct effect on skeletal muscle causing malignant hyperthermia

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15
Q

what processes bring about neuroleptic melignant syndrome

A

BLOCKADE OF DOPAMINERGIC D2 RECEPTORS IN THE HYPOTHALAMUS
-RESULTS IN HYPERTHERMIA

BLOCKADE OF INHIBITORY ACTIONS OF DOPAMINE ON THE SNS-AUTOMONIC DYSFUNCTION

BLOCKADE OF NIGROSTRIATAL DOPAMINE CAUSING INCREASED MUSCLE RIGIDITY/TREMOR VIA EXTRAPYRAMIDAL PATHWAYS
*POSSIBLY DIRECT MUSCLE TOXICITY VIA INCREASED CALCIUM RELEASE FROM SR

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16
Q

SUMMING UP NEUROLEPTIC MALIGNANT SYNDROME

A

BLOCKADE OF DOPAMINE IN THE HYPOTHALAMUS, ON THE SNS, NIGROSTRIATAL PATHWAY

LOSS OF THE STIMULATORY AND INHIBITORY FUNCTION OF DOPA AT DIFFERNT AREAS IN THE SNS

LEADS TO AUTONOMIC DYSFUNCITON, AND HYPERTHERMIA AND MOTOR DYSFUNCTION

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17
Q

MOST COMMON RISK FACTOR FOR NEUROLEPTIC MALIGNANT SYNDROME

A

HIGH-DOSE, HIGH POTENCY ANTIPSYCHOTIC AGENTS, DURING RAPID DOSE ESCALATION AND WITH DEPOT FORMS OF DRUG RELEASE

OTHER CAUSES

  • concurrent antidepresants, antiemetics,lithium
  • withdrawl of anti-parkinsonian agents
  • past hx of NMS
  • increased ambient temp or dehydration
  • catatonia
  • agitation
  • hx of affective disorders or physical disorders of the brian that cause decreased mental function
18
Q

USE OF IM PREPARATIONS OF ANTIPSYCHOTICS VARIES BETWEEN WHICH TWO IMPORTANT DRUGS

A

HALOPERIDIOL&raquo_space;» CLOZAPINE

19
Q

management of NMS

A

withdraw causative drug
initiate supportive care

acute symptoms=fever, rigidity, AMS
aid recovery by preventing rhabdomyolysis, renal and resp failure, prevent recurrence

dopa agonists= bromocriptine»>amantidine
dantrolene -muscle relaxant and for malignant hyperthermia

lorazepam -reduce psychosis, agitation, anxiety, and anticonvulsant

20
Q

drugs indicated in management of NMS

A

bromocriptine
dantrolene
lorazepam-ativan

21
Q

drugs associated with Neuroleptic Malignant syndrome

A

haloperidol and chlorpromazine (d2 antagonist)
*these are worse because they are high potency-avoid to rapid dose escalation
any antipsychotic can cause it

22
Q

management of malignant hyperthermia

A
IV dantrolene
correct metabolic acidosis-hyperventilate?
monotor serum potassium
-insulin and glucose
-calcium chloride or glucuronate
-IV lidocaine for arrhythmia
COOL BODY TO 38 DEGREES CELCIUS
MAINTINA URINARY OUTPUT
-COLD FLUIDS, FUROSEMIDE, AND MANNITOL IF NEEDED
23
Q

WHAT PRECIPITATES MALIGNANT HYPERTHERMIA

A

VOLITILE ANESTHETICS

  • DESFLURANE
  • N2O
  • SEVOFLURANE
  • XENON
  • ISOFLURANE

SUCCINYLCHOLINE-NMBAGENT

24
Q

MOA FOR MALIGNANT HYPERTHERMIA

A

UNCONTROLLED RELEASE OF CALCIUM FROM CR BY RYR RECEPTOR-MUSCLE CONTRACTION AND REVERSION TO INTERMEDIATE METABOLISM-METABOLIC ACIDOSIS

25
IN GENERAL-ANTICHOLINERGIC POISONING BROUGHT ABOUT BY
UNIMPEDED SYMPATHETIC ATIMULATION - DIMINISHED PANS ACTIVITY - CONSEQUENT CV CHANGES
26
MANAGEMENT OF ANTICHOLINERGIC POISONING
HYPERTHERMIA AND AGITATION-COOLING AND BENZODIAZEPINE PHYSOTIGIMINE-IN RARE SEQUENCE
27
WHEN IS PHYSOSTIGIMINE INDICATED NOT USED ROUTINELY EBCAUSE IT HAS ITS OWN TOXICITIES
SEVERE SELF HARMING PSYCHOSIS HEMODYNAMIC DYSFUNCTION SECONDARY TO TACHYDYSRHYTHMIAS-USE THIS ACETYLCHOLINSTERASE
28
PHYSOSTIGIMINE DRUG CLASS
ACETYLCHOLINESTERASE INHIBITOR PARASYMPATHOMIMETIC
29
PHYSOSTIGIMINE CONTRAINDICATED WITH TCA OVERDOSE BECAUSE OF
SEIZURES
30
SEVERE TCA POISONING AND PHYSOSTIGIMINE MAY CAUSE
SEIZURES AND BRADYSYTOLE
31
ACETYLCHOLINESTERASE INHIBITOR THAT CAN ACCESS BBB AND ACTS AS A PARAYMPATHOMIMETICS
PHYSOSTIGIMINE RARELY GIVEN BECAUSE OF IT SOWN TOXICICITIES NOT WITH TCA POISONING BRADYSYSTOLE AND SEIZURES
32
+ HX OF SEROTONERGIC DRUG HTN, tachycardia, tachypnea, hyperthermia mydriasis, sialorrhea, hyperactive bowel sounds tone increased in Lower ext, hyperreflexia, clonus (unless masked), agitation coma
serotonin syndrome cyproheptadine
33
Anticholingeric agent HTN, tachycardia, tachypnea, hyperthermia, mydriasis, dry erythema, hot and dry to touch decreased bowel sounds, normal muscle tone, normal reflexes, agitated and delirious
anticholinergic poinsing syndrome physostigimine if dangerous or tachydysrhythmia
34
< 12 hours
serotonin syndrome | anticholinergic toxidrome
35
tempoerature < 38.8
anticholinergic poisoning syndrome
36
temperature > 41.1
serotonin syndrome | neuroleptic malignant syndrome
37
temperature can be as high as 46
malignant hyperthermia
38
+ hx of dopa antagonist (haloperidol) 1-3 days, HTN, tachycardia, tahcypnea, normal pupil size, sialorrha, pallor, diaphoresis, normal or dec bowel sounds, lead pip rigidity, in all muscle groups, bradyreflexia, stupor, alert, coma
neuroleptic malignant syndrome
39
1-3 days
neuroleptic malignant syndrome
40
30 mins - one day
malignant hyperthermia
41
inhalatiuonal anesthtics or succinylcholine HTN, tachycardia, tachypnea, hyperthermia (46degress), normal pupils, normal salivation, mottled skin, diaphoresis, decreased bowel sounds, rigor mortis liek rigidity, hyporeflexia, agitiation
malignant hyperthermia dantrolene-cooling