Suits and Cases: Potential Pitfalls in the management of Poisoned Patients

Suits and Cases: Potential Pitfalls in the management of

Poisoned Patients

John Kashani DOSt. Josephs Regional Medical Center

New Jersey Poison Center

Case 1

• An 18 year old female, with a past medical history significant for asthma and depression, presents to the ED for shortness of breath

• She has a respiratory rate of 34, is diaphoretic, is actively vomiting and appears confused

Case 1

• Her blood pressure is 90/54, Heart rate is 150 and a rectal temperature is 102.

farenheit and pulse oximetry is 99% on supplemental oxygen

• Her mother states that this is the worst asthma attack she has ever had

• She is emergently intubated

Case 1

• Shortly after being intubated she seizes and develops ventricular fibrilation

• Despite your best efforts she dies• An autopsy is requested by the family• A post mortem salicylate level was

150mg/dL

Introduction

• Salicylates are the most widely used analgesic, anti-pyretic and anti-inflamatory and is the standard for the comparison and evaluation of others

• Because salicylates are so widely available the potential for misuse is often underappreciated

Introduction

• The physician taking care of the salicylate intoxicated patient must be familiar with the pathophysiology, pharmakokinetics, potential pitfalls, and treatment options

Sources of Salicylates• Found in Willow bark (Salix alba vulgaris)• Available in a multitude of

formulas/preparations– Over-the-counter (pepto-bismol)– Topical preparation (wart removal)– Combinations (excedrin, fiorinal,

percodan)– Other (oil of wintergreen)

Pharmakokinetics• Peak levels

– Regular preparations – Enteric coated– Liquids preparations– Overdose

• Distribution• Metabolism• Excretion

Distribution• Volume of distribution (Vd)

– Apparent volume the drug is dissolved in– Measured in Liters or Liters/Kg

• not a real volume

Salicylates: Toxic Dose

• Therapeutic Range: 10–20 mg/kg• Mild Toxicity: 150 mg/kg• Moderate Toxicity: 150-300 mg/kg• Severe Toxicity: > 300 mg/kg

Inflamatory Mediators

• Inhibits cyclooxygenase– Decrease in prostaglandins– Increase leukotrienes

• Increases microvascular permeability

acetyl-CoA

oxaloacetate citrate

isocitrate

-ketoglutarate

succinyl-CoAsuccinate

fumarate

malateNAD+

pyruvate

matrix

Glucose

Pyruvate Lactate2 ATP

Muscle

Alanine

Pyruvate

Glucose

Urea 6 ATP4 ATP

Respiration• Uncouples oxidative phosphorylation

– Disrupts hydrogen ion gradient– Unable to generate ATP using electron

transport• Increased oxygen consumption,

increased heat production, increased metabolic rate, decreased ATP production, increased CO2 production

R-COOH

matrix

intermembrane space

H+ H+ H+ H+ H+ H+ H+ H+

R-COOHR-COO-

R-COO-

matrix

intermembrane space

O2 H2O

succinate

NADH + H+

ATP + H2O

ADP + Pi + H+

R-0- + H+

Metabolic

• Increased lipolysis• Increased production of ketones

– Ketonuria present in almost all overdose patients

Ketone bodies

Acetyl CoA

Fatty Acids

Metabolic

• Hyperglycemia in acute setting– Glycogenolysis– May cause glucosuria

• Hypoglycemia may subsequently develop

Metabolic• Causes a respiratory alkalosis

– Due to respiratory center stimulation– Increase in respiratory rate and depth

Hematologic• Platelet dysfunction• Inhibition of Vitamin K dependent

clotting factors• II, VII, IX, X, Protein C, Protein S

• Hypoprothrombinemia

Gastrointestinal Effects

• Nausea• Vomiting• Gastritis• Pylorospasm

Neurologic• Occurs from metabolic derangements and

salicylate CNS levels– Agitation, irritability– Tinnitus

• Occurs at levels of 20-45 mg/dL– Lethargy

Laboratories

• Salicylate Level– An Level of 100 mg/dL is extremely

worrisome (impending doom)– Chronic Levels of > 30 mg/dL are

concerning• Difficulty in interpretation due to variable Vd

Laboratories• Levels should be obtained every 1 to 2

hours until downward trend is observed• Do not rely on a single level• Levels < 20mg/dl and a downward trend

can be medically cleared

Case 2• A 35 year old male presents to the

emergency department for profound weakness, bradycardia and emesis

• An I stat potassium is 8.5mg/dL and an EKG show a sine wave pattern

• IV Calcium chloride is administered and he develops ventricular fibrilitation shortly thereafter

Case 2

• Despite your best efforts he dies• The wife said he has no medical

problems, but was recently doing a “cleansing diet” that included herbal teas

Introduction

• Digitalis and digitalis like cardiac glycosides (DG’s) are found in a variety plants, toads and pharmaceutical agents

• Dried powders and extracts have been used for centuries for medicinal agents and as arrow poisons

Pharmacokinetics• Peak serum concentrations occur in

minutes with IV dosing and 1-2 hours after an oral dose

• The VD is initially small and increases following a two phase compartment model– Higher in infants and neonates and

lower in the elderly

Pharmacokinetics

• Tissue distribution takes 6-12 hours• Digoxin crosses the placenta with fetal

levels approaching that of the mother• Elimination

– Hepatic metabolism– Urinary excretion of unchanged drug

Pathophysiology

• Cardiac glycosides inhibit the sodium potassium atp-ase – Responsible for pumping two sodium

ions out of the cell for every two potassium ions in to the cell

Na-KATPase Na+

Ca++Ca++

ATPase

myocardium

-90 mv

Na-KATPase Na+

Ca++Ca++

ATPase

myocardium

-90 mv

Na+Na+

Na-KATPase Na+

Ca++Ca++

ATPase

myocardium

-90 mv

Na+Na+

Ca++Ca++

Na-KATPase Na+

Ca++Ca++

ATPase

myocardium

-90 mv

Na+Na+

Ca++Ca++

[Ca++]Ca++

Inhibition of Na-K-ATPase

[Nai+]

[Cai++]

contractility

Na-KATPase Na+

Ca++Ca++

ATPase

muscle

-90 mv

Na+Na+

Ca++Ca++

[Ca++]

[Nai+]

hyperkalemia

[Cai++]

skeletal muscleheart

contractility

Na-KATPase Na+

Ca++Ca++

ATPase

myocardium

-90 mv

Na-KATPase Na+

Ca++Ca++

ATPase

myocardium

-90 mv

Na+Na+

Ca++Ca++

Ca++ Ca++

Na-KATPase Na+

Ca++Ca++

ATPase

myocardium

-90 mv

Na+Na+

Ca++Ca++

Ca++ Ca++

-90 mv

premature beat or ectopic focus

increased automoticity

late afterdepolarizations

[Nai+]

hyperkalemia

[Cai++]

contractility

automoticity

premature beatsescape rhythmsV-tach, V-fib

rise in Nai+

and Cai++

BaroreceptorsCarotidsinus

receptorsCN IX Vagus Nerve

Aortic arch

receptors

Vagal Tone

Bradycardia AV blocksAsystole

Vagus Nerve

Increasedbaroreceptor

firing

CNSParasympathetic

Sympathetic

IncreasedArterial

Pressure

(-)(-)

Baroreceptors

[Nai+]

hyperkalemia

[Cai++]

contractility

premature beatsescape rhythmsV-tach, V-fib

firing

baroceptors

vagal tone

bradycardia, AV blocks, asystole

automoticity

rise in Nai+

and Cai++

rise in Nai+

and Cai++

Devils Advocate

• Treatment of Hyperkalemia in a patient with unrecognized digitalis toxicity– 80 yr old female presents to the ED

with AMS, hyperkalemia and bradycardia

– Treated with intravenous pacing and IV calcium chloride

J Toxicol Clin Toxicol. 2003;41(4):373-6

Devils Advocate

• A toxicological Surprise– A 42 year old man was admitted to a

medical service for CP, nausea and vomiting

– Heart rate was 35, EKG showed total AV block

– Potassium was 5.7mmol/LLancet. 2000 Oct 21;356(9239):1406.

Devils Advocate

• He was treated for a myocardial infarction

• A transvenous pacer was inserted with an increase in his heart rate to 70 BPM

• A serum digoxin level was 365ng/mL (therapeutic range 10-30)

Lancet. 2000 Oct 21;356(9239):1406.

Digoxin in herbal Supplements

• Digoxin Toxicity in a 26 year-old woman taking a herbal dietary supplement– Presented to an ED with chest pain– Initially her heart rate was 70 BPM

and BP was 112/59– Her heart rate dropped to 39 and BP

dropped to 59/36J Am Osteopath Assoc. 2001 Aug;101(8):444-6

• EKG showed the absence of P waves• She was given a NS fluid bolus and

placed in the trendelenberg position• Her BP and heart returned to her

original baseline• A digoxin level was 0.9ng/mL

J Am Osteopath Assoc. 2001 Aug;101(8):444-6

• She confessed to consuming a tea that contained:– Skullcap herb, wood betony herb,

black cohosh root, hops flowers, valerian root and cayenne pepper fruit

J Am Osteopath Assoc. 2001 Aug;101(8):444-6

Case 3• A 36 year old female, with a past

medical history for depression and chronic back pain, presents to the ED for back pain

• She states that Demerol is the only medication that relieves her pain

• Reluctantly, you write an order for Demerol

Case 3

• Two hours after the administration of Demerol she develops tachycardia, AMS and myoclonus

• You believe that she developed serotonin syndrome

• A NGT is placed in preparation for the administration of cyproheptadine

Case 3 • She has a self limited seizure, vomits

and has a decrease in her O2 sat• She is intubated using etomidate and

succinylcholine• A post intubation x-ray shows a right

upper lobe consolidation• She dies on hospital day 6 from

complications of aspiration pneumonia

Serotonin Syndrome• Drug Induced Disorder• Variable alterations in

– cognition-behavior– neuromuscular activity– autonomic nervous system function

• Increased CNS serotonin neurotransmission at 5-HT1A and 5-HT2A receptors

Serotonin Receptors• The largest and most diverse of all

neurotransmitter systems– 5HT1 – 5HT7

• Each receptor class may contain many subclasses

• 5HT1A - presynaptic and postsynaptic• 5HT1D - presynaptic and postynaptic 5HT2A

- postsynaptic

Serotonin Syndrome

• No gender predilection• Idiosyncratic in nature• Patients are not more likely to develop

SS following an overdose than they are while taking therapeutic doses

• SS is a diagnosis of exclusion

Precipitants

– Addition of second serotonergic drug usually at therapeutic doses

– Increasing primary drug• Inherited / Acquired

– Reduction in endothelial MAOA activity

– Genetic variation

Serotonergic Agents

• Inhibit 5-HT uptake• Enhances 5-HT release• Inhibits 5-HT breakdown• Metabolized to 5-HT• 5-HT1A agonist

• Enhances 5-HT receptor response to stimulation

L-tryptophan

5-hydroxytrytophan

5-HT receptors 1-7

5-HIAA

5-HT1A, D

Inhibit 5-HT Uptake• Specific SRIs• Non-specific SRIs - clomipramine, trazodone• TCAs• Meperidine• Dextromethorphan• Pentazocine• Tramadol• Dexfenfluramine

Enhance 5-HT Release

• Lithium• Levodopa, dopamine• MDMA• Cocaine• Amphetamines• Fenfluramine• Dexfenfluramine

5-HT1 Agonists

• LSD • Buspirone• Sumatriptan• Dihydroergotamine

Serotonergic Agents

• Inhibits 5-HT breakdown– MAOIs

• Metabolized to 5-HT– Tryptophan

• Enhances 5-HT1A receptor response to stimulation– Lithium

Drug Combinations

• All MAOI combinations• Dextromethorphan and SSRI• Lithium and SSRI• Trazodone and SSRI• Tramadol and SSRI• Trazodone and Buspirone• Selegiline and SSRIs or TCAs• Switching from 1 SSRI to another SSRI

Serotonin Syndrome Associated with Monotherapy

• Clomipramine• Fluvoxamine• Venlafaxine• MDMA• Sertraline

Clinical Manifestations

• Cognitive and behavioral– Confusion (54%)– Agitation (35%)– Coma (28%) – Hypomania (15%) – Seizures (14%)– Hallucinations (6%)

Mills K. Serotonin Syndrome A Clinical Update. Critical Care Clinics, Volume 13:4 Oct 1997

Clinical Manifestations

• Autonomic Dysfunction– Blood Pressure Lability (47%)– Hyperthermia (46%)– Diaphoresis (46%)– Tachycardia (41%)– Mydriasis (26%)– Diarrhea (12%)

Clinical Manifestations• Neuromuscular Abnormalities

– Myoclonus (57%) – Hyperreflexia (55%) – Rigidity (49%)– Tremor (49%) – Incoordination (38%) – Shivering (25%) – Nystagmus (13%)– Seizures (14%)

Sternbach’s Suggested Diagnostic Criteria

• Coincidental with the addition of or increase in known serotonergic agents to an established medications regimen - at least 3 of the following– agitation, diaphoresis, diarrhea, fever,

hyperreflexia, incoordination, MS changes, myoclonus, shivering, tremor

• Other etiologies (infections, metabolic, withdrawal) have been ruled out

• A neuroleptic agent has not been started or increased in dosage

Other Criteria

• Hegerl Criteria• Dursun Criteria• Randomski Criteria• Mills Criteria• Hunters Decision Rules• MOFO Criteria

Time course

• Usually abrupt• Occurring within hours after initiation of

new serotonergic agent• 2/3 of cases resolves within 24 hours

Treatment

• Five basic management principles– Supportive care– Discontinue serotinergic agents– Anticipate potential complications– Administer antiserotinergic agents– Reassess the need for reinstituting

pharmacotherapy

Treatment

• Antipyretics are generally ineffective• Benzodiazepines are the initial choice

for relieving muscle spasm• No specific antidotes for SS• Most symptoms resolve in 12 – 24

Cyproheptadiene

• Cyproheptadine (periactin)– Most consistently effective– Blocks postsynaptic 5HT1A and 5HT2

receptors– Only available orally (syrup, tablet)– Also has antimuscarinic and

antihistaminc properties

Case 4 • A 54 year old male presents to the ED

with a rash that has been getting progressively worse over that past week and a half

• He also offers complaints of chills, nausea, vomiting and diarrhea

• Past medical history is significant for seizure disorder and hypertension

Case 4

• His medications include phenytoin and lisinopril

• He is febrile with a temperature of 102.c, tachycardic at a ventricular rate of 130, hypotensive with a sys BP of 80, RR 24

• His white count is 28,000 with a left shift, HG: 19, HCT: 45, Platelets 52

Case 4

• Na+ 156, K+ 5.4, Cl- 92, NaHco3- 12,• BUN: 60, CR 5.2 and glucose is 220• His LFTS are markedly elevated and he

has a creatinine of 3.2• His phenytoin level 0.5mcg/mL• He is loaded with IV phenytoin in the ED

Case 4

• One hour after the administration of phenytoin he drops his blood pressure and becomes apneic

• He is subsequently intubated and is transferred to the ICU

• He dies on Hospital day 7 from multi-system organ failure

Introduction

• Anticonvulsant hypersensitivity syndrome (ACHS) is a rare, potentially fatal multisystem disorder that occurs after exposure to phenytoin, carbamazepine, phenobarbital, felbamate and lamotrigine

Signs and Symptoms

• ACHS commonly begins within one to four weeks after starting therapy, but may present as late as three months

• ACHS may occur within hours of a previously sensitized individual

• ACHS is not related to the dose or serum concentration

Signs and Symptoms

• Most commonly ACHS begins with a fever, followed by a rash and variable degrees of lymphadenopathy

• The fever usually ranges from 38 – 40.C • The Rash may develop concurrently or

shortly after the fever

Signs and Symptoms

• The Rash is commonly described as an exanthem with or without pruritus

• The upper extremities, face and trunk are usually first affected

• Periorbital edema, exudative tonsillitis, pharyngitis, oral ulcerations and conjunctivitis may be seen

Signs and Symptoms

• Rarely, more severe skin reactions may occur (SJS, TEN, EM)– Usually in the setting of repeated

exposures or continued use• Tender lymphadenopathy is commonly

Signs and Symptoms

• The Liver is the most common organ involved

• The CNS, heart, lungs, renal system and thyroid gland may be involved– Patients may present with elevated

transaminases, alkaline phosphatase, PT and bilirubin

• The hepatitis is usually mild and anicteric

Signs and Symptoms

• The degree of hepatitis is related to the time between the onset of symptoms and the discontinuation of the offending agent

• Liver biopsies reveal periportal inflammation with or without necrosis

• The majority of patients recover within a few weeks

Signs and Symptoms• Hematologic abnormalities

– Lymphocytosis – Leukocytosis– Eosinophilia– Anemia– Leukopenia – Thrombocytopenia– Aplastic anemia

Pathophysiology

• The anticonvulsants implicated in ACHS all have in common an aromatic benzene ring that is metabolized by cytochrome p450 to an arene oxide

• Arene oxides are highly electrophilic and covalently bind to macromolecules to disrupt cellular function

Pathophysiology

• Arene oxides may also form neoantigens that trigger an immunologic response

• These metabolites are highly unstable and under normal conditions can be detoxified by one of several routes

Diagnosis

• Usually based on history of drug exposure and clinical examination– Atypical lymphocytes – Eosinophilia– Elevated liver enzymes– hyperbilirubinemia

Treatment

• The mainstay of treatment is discontinuation of the offending agent and supportive care

• Severe skin reactions are best managed in a burn center

• Strict attention must be paid to maintaining fluid and electrolyte balance

Thank You

Suits and Cases: Potential Pitfalls in the management of Poisoned Patients

Documents

Transcript of Suits and Cases: Potential Pitfalls in the management of Poisoned Patients

Kazuo Ishiguro - Getting Poisoned (PDF)

Poisoned Speech

Management of Poisoned Patients

The Whole Country is Poisoned

Poisoned Stream Book

Approach to Poisoned Patient

Church of the Poisoned Mind

Approach to a poisoned child

POISONED WATER - media.bloomsbury.com

Who Poisoned Buzz Lightyear?

Poisoned Panem et Circenses - CanalBlog · 2020-01-09 · Poisoned Panem et Circenses. BtRE: IAEA International Atomic Energy Agency Atoms For Peace POISONED POWER dohn W- and Case

Approach to the critically ill poisoned patientindiachest.org/wp-content/uploads/2016/07/Approach-to... · 2018-10-07 · THE CRITICALLY ILL POISONED Most critically ill poisoned

Poisoned Apple

Suits and Cases: Potential Pitfalls in the management of Poisoned Patients John Kashani DO St. Josephs Regional Medical Center New Jersey Poison Center.

Suruchi Creations · range of Exclusive Fancy Ladies Suits. Our offered assortment of suits is comprises of Ladies Suits, Ladies Cotton Suits and Ladies Designer Suits. Offered suits

Poisoned ofl{ers Toxic exposure poisoned places kept secret - US Army … · 2015. 5. 29. · USA Today 9-6-00 Poisoned ofl{ers poisoned places Toxic exposure kept secret The U.S.

Church of the Poisoned Mind - Askadesignaskadesign.com/tchristensen1981/.../DF19-Church-of-the-Poisoned-Mind.pdf · DF19 Church of the Poisoned Mind Mik Calow Introduction This adventure

SCORCHED EARTH, POISONED AIR

Introduction to the Poisoned Patient

Poisoned RDP - Black Hat Briefings€¦ · Poisoned RDP He Said, She Said –Poisoned RDP Offense and Defense. Eyal Itkin Security Researcher Check Point Research @EyalItkin Who Are