pdp 406 clinical toxicologywebstor.srmist.edu.in/web_assets/srm_mainsite/files/... ·...
TRANSCRIPT
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PDP 406 CLINICAL TOXICOLOGY
Pharm.D
Fourth Year
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Management of overdose and poisoning
Mr.D.Raju.M.Pharm.,Lecturer
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General- evaluation
recognition of poisoningidentification of agents involved assessment of severity prediction of toxicity
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General- management
provision of supportive careprevention of poison absorptionenhancement of elimination of poisonadministration of antidotes
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Supportive care
ABCVital signs, mental status, and pupil size Pulse oximetry, cardiac monitoring, ECGProtect airwayIntravenous access cervical immobilization if suspect traumaRule out hypoglycaemiaNaloxone for suspected opiate poisoning
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History
Pill bottlesAlcoholDrug history including accessRemember OTC drugsSuicide noteNational Poisons Information Centre *
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Examination
Physiologic excitation –anticholinergic, sympathomimetic, or central hallucinogenic agents, drug withdrawal
Physiologic depression –cholinergic (parasympathomimetic), sympatholytic, opiate, or sedative-hypnotic agents, or alcohols Mixed state –polydrugs, hypoglycemic agents, tricyclic antidepressants, salicylates, cyanide
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Drug detection
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Drug levels
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Preventing absorption
Gastric lavage
Not in unconscious patient unless intubated (risk aspiration)
Flexible tube is inserted through the nose into the stomach
Stomach contents are then suctioned via the tube
A solution of saline is injected into the tube
Recommended for up to 2 hrs in TCA & up to 4hrs in Salicylate OD
Induced VomitingIpecac - Not routinely recommended Risk of aspiration
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Preventing absorption
Activated charcoalAdsorbs toxic substances or irritants, thus inhibiting GI absorption Addition of sorbitol →laxative effectOral: 25-100 g as a single dose repetitive doses useful to enhance the elimination of certain drugs (eg, theophylline, phenobarbital, carbamazepine, aspirin, sustained-release products)not effective for cyanide, mineral acids, caustic alkalis, organic solvents, iron, ethanol, methanol poisoning, lithium
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Elimination of poisons
Renal eliminationMedication to stimulate urination or defecation may be given to try to flush the excess drug out of the body faster.
Forced alkaline diuresisInfusion of large amount of NS+NAHCO3Used to eliminate acidic drug that mainly excreted by the kidney eg salicylatesSerious fluid and electrolytes disturbance may occurNeed expert monitoring
Hemodialysis or haemoperfusion: Reserved for severe poisoning Drug should be dialyzable i.e. protein bound with low volume of distributionmay also be used temporarily or as long term if the kidneys are damagdue to the overdose.
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Antidotes
Does an antidote exist?Does actual or predicted severity of poisoning warrant its use?Do expected benefits of therapy outweigh its associated risk?Are there contraindications?
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Specific overdoses
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OpiatesAntidote – naloxone
MOA: Pure opioid antagonist competes and displaces narcotics at opioid receptor sites
I.V. (preferred), I.M., intratracheal, SubQ: 0.4-2 mg every 2-3 minutes as needed
Lower doses in opiate dependence
Elimination half-life of naloxone is only 60 to 90 minutes
Repeated administration/infusion may be necessary
S/E BP changes; arrhythmias; seizures; withdrawal
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Benzodiazepines
Antidote – flumazenil
MOA: Benzodiazepine antagonist
IV administration 0.2 mg over 15 sec to max 3mg
S/E N&V; arrhythmias; convulsions
C/I concomitant TCAD; status epilepticus
Should not be used for making the diagnosis
Benzodiazepines may be masking/protecting against other drug effects
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Tricyclic antidepressants
PHARMACOLOGY —TCAs have several important cellular effects, including inhibition of:
Presynaptic neurotransmitter reuptake
Cardiac fast sodium channels
Central and peripheral muscarinic acetylcholine receptors
Peripheral alpha-1 adrenergic receptors
Histamine (H1) receptors
CNS GABA-A receptors
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TCAD overdoseclinical features
Arrhythmias
- widening of PR, QRS, and QT intervals;
heart block; VF/VT
Hypotension
Anticholinergic toxicity
- hyperthermia, flushing, dilated pupils,
intestinal ileus, urinary retention, sinus tachycardia
Confusion, delirium, hallucinations
Seizures
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Diagnosis
History
Blood/urine toxicology screen
Levels not clinically useful
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TCAD overdose -Treatment
ABC – many require intubationConsider gastric lavage if taken < 2hrsActivated charcoalTreatment of hypotension with isotonic salineSodium bicarbonate for cardiovascular toxicityAlpha adrenergic vasopressors (norepinephrine) for hypotension refractory to aggressive fluid resuscitation and bicarbonate infusion Benzodiazepines for seizures
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Sodium Bicarbonate in TCA overdose
Hypertonic sodium bicarbonate (NaHCO3)
- QRS widening >100 msec; ventricular
arrhythmias, and/or refractory hypotension
↑ serum pH promotes protein binding and ↓ free drug
concentrations; narrows the QRS complex, ↑ systolic blood
pressure, and controls ventricular arrhythmias
1 to 2 meq/kg (two to three 100 mL ampules of 8.4 percent
NaHCO3) rapid IV push large bore IV then infusion if working
reasonable goal pH is 7.50 to 7.55 then taper dose
S/E Volume overload, hypernatreamia, and metabolic alkalosis
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Special Cautions in TCAD overdose
Class IA and IC antiarrhythmic agents are
contraindicated eg quinidine;disopyramide,
flecainide; propafenone
Class IB Lignocaine, phenytoin used
Phenytoin may precipitate arrhythmias
Magnesium may be useful
Flumazenil must not be given
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Salicylate overdose
Aspirin (acetylsalicylic acid)Methyl salicylate (Oil of Wintergreen)5 ml = 7g salicylic acidHerbal remediesFatal intoxication can occur after the ingestion of 10 to 30 g by adults and as little as 3 g by children
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Salicylate levels
Plasma salicylate concentration
Rapidly absorbed; peak blood levels usually occur
within one hour but delayed in overdose 6-35 hrs
Measure @ 4 hrs post ingestion & every 2 hrs until
they are clearly falling
Most patients show signs of intoxication when the
plasma level exceeds 40 to 50 mg/dL (2.9 to 3.6
mmol/L)
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Salicylate overdose
Inhibition of cyclooxygenase results in decreased synthesis of prostaglandins, prostacyclin, and thromboxanesStimulation of the chemoreceptor trigger zone in the medulla causes nausea and vomitingDirect toxicity of salicylate species in the CNS, cerebral edema, and neuroglycopeniaActivation of the respiratory center of the medulla results in tachypnea, hyperventilation, respiratory alkalosisUncoupled oxidative phosphorylation in the mitochondria generates heat and may increase body temperature Interference with cellular metabolism leads to metabolic acidosis
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Clinical features
Early symptoms of aspirin toxicity include tinnitus,
fever, vertigo, nausea, hyperventilation, vomiting,
diarrhoea
More severe intoxication can cause altered mental
status, coma, non-cardiac pulmonary oedema and
death
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Metabolic abnormalities
Stimulate the respiratory center directly, early fall in the PCO2
and respiratory alkalosis
An anion-gap metabolic acidosis then follows, due to the
accumulation of organic acids, including lactic acid and ketoacids
Mixed respiratory alkalosis and metabolic acidosis with ↑ anion
gap
Arterial Ph variable depending on severity
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Metabolic abnormalities
Metabolic acidosis increases the plasma concentration of protonated salicylate
thus worsening toxicity by allowing easy diffusion of the drug across cell membranes
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Salicylate overdose - treatment
directed toward increasing systemic pH by the administration of sodium bicarbonate
IV fluids +/- vasopressors
Avoid intubation if at all possible (↑ acidosis)
Supplemental glucose (100 mL of 50 percent dextrose in adults) to patients with altered mental status regardless of serum glucose concentration to overcome neuroglycopaenia
Hemodialysis
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Alkalinization of plasma and urine
Alkalemia from a respiratory alkalosis is not a contraindication to sodium bicarbonate therapy
A urine pH of 7.5 to 8.0 is desirable
Blood gas analysis every two hours
Avoid severe alkalemia (arterial pH >7.60)
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Haemodialysis - indications
Altered mental status
Pulmonary or cerebral edema
Renal insufficiency that interferes with salicylate excretion
Fluid overload that prevents the administration of sodium bicarbonate
A plasma salicylate concentration >100 mg/dL (7.2 mmol/L)
Clinical deterioration despite aggressive and appropriate supportive care
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Paracetamol
Widely available
Potential toxicity underestimated
Toxicity unlikely to result from a single dose of less than 150
mg/kg in child or 7.5 to 10 g for adult
Toxicity is likely with single ingestions greater than 250 mg/kg
or those greater than 12 g over a 24-hour period
Virtually all patients who ingest doses in excess of 350 mg/kg
develop severe liver toxicity unless appropriately treated
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Factors influencing toxicity
Dose ingested
Excessive cytochrome P450 activity due to induction by
chronic alcohol or other drug use eg carbamazepine,
phenytoin, isoniazid, rifampin
Decreased capacity for glucuronidation or sulfation
Depletion of glutathione stores due to malnutrition or chronic
alcohol ingestion
Acute alcohol ingestion is not a risk factor for hepatotoxicity
and may even be protective by competing with
acetaminophen for CYP2E1
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Clinical featuresStage I (0.5 to 24 hours)
No symptoms; N&V Malaise
Stage II (24 to 72 hours)
Subclinical elevations of hepatic aminotransferases (AST, ALT)
right upper quadrant pain, with liver enlargement and tenderness. Elevations of prothrombin time (PT), total bilirubin, and oliguria and renal function abnormalities may become evident
Stage III (72 to 96 hours)
Jaundice, confusion (hepatic encephalopathy), a marked elevation in hepatic enzymes, hyperammonemia, and a bleeding diathesis hypoglycemia, lactic acidosis, renal failure 25%, death
Stage IV (4 days to 2 weeks)
Recovery phase that usually begins by day 4 and is complete by 7 days after overdose
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Paracetamol overdose
The risk of toxicity is best predicted by relating the time of ingestion to the serum paracetamol concentration
The dose history should not be used as studies have found no correlation
Peak serum concentrations reached within 4 hrs following overdose of immediate-release preparations
May be delayed with extended releases preparations or drugs that delay gastric emptying (eg, opiates, anticholinergic agents) are coingested
Check level at >= 4 hrs
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Paracetamol overdose treatment
Activated charcoal within four hours of
ingestion
May reduce absorption by 50 to 90 percent
Single oral dose of one gram per kilogram
Inhibits absorption of oral methionine
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N-acetylcysteine
Antidote – MOA: a glutathione precursor
Limits the formation and accumulation of NAPQI
Powerful anti-inflammatory and antioxidant effects
IV infusion or oral tablets (also oral methionine)
150mg/Kg over 15 min; 50mg/Kg over next 4 hrs; 100mg/kg over next 16 hrs up to 36hrs
Beyond 8 hours, NAC efficacy progressively decreases
S/Es nausea, flushing, urticaria, bronchospasm, angioedema, fever, chills, hypotension, hemolysis and rarely, cardiovascular collapse
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Paracetamol overdose treatment
At the end of NAC infusion, a blood sample should be taken for determination of the INR, plasma creatinine and ALT. If any is abnormal or the patient is symptomatic, further monitoring is required and advice sought from the NPIS
Patients with normal INR, plasma creatinine and ALT and who are asymptomatic may be discharged from medical care. They should be advised to return to hospital if vomiting or abdominal pain develop or recur
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Indications for liver transplantation
Liver transplantation is life-saving for fulminant hepatic necrosis The indications for liver transplantation are:1 - Acidosis (pH < 7.3), or 2 - PT > 100 sec 3 - Creatinine > 300 mcg/l 4 - Grade 3 encephalopathy (or worse)It is better to contact the local liver transplant centre earlier than this. Grossly abnormal prothrombin times should trigger referral:PT > 20 sec at 24 hr PT > 40 sec at 48 hr
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Alcohol poisoning
Clinical features of acute alcohol poisoning include:
Ataxia and anaesthesia leading to accidental injury
Dysarthria and nystagmus
Drowsiness which may progress to coma
Inhalation of vomit which can be fatal & should be prevented
Hypoglycaemia in children and some adults
Check BM stix and give 50% glucose i.v. if required
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Coma (alcohol induced)In cases of alcohol induced coma exclude:
1. Coincident head injury2. Hepatic failure 3. Meningitis4. Wernicke’s encephalopathy 5. Other associated drug ingestion
A blood test will confirm substantial levels of alcohol Rule out alcoholic hypoglycaemiaThe airway and circulation must be maintainedBut glucose- containing fluids may precipitate Wernicke's encephalopathyThiamine should given to allIntravenous naloxone has reversed coma in a proportion of cases
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