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Biochemistry and Clinical Toxicology Mike Hallworth Royal Shrewsbury Hospital ACB North West Region Autumn Meeting – 18 October 2005
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Page 1: Biochemistry and Clinical Toxicology

Biochemistry andClinical Toxicology

Mike HallworthRoyal Shrewsbury Hospital

ACB North West RegionAutumn Meeting – 18 October 2005

Page 2: Biochemistry and Clinical Toxicology

Poisoning - epidemiology

• Incidence approx. 3 per thousand pa

• Approx. 100 000 hospital admissions pa

• <5% unconscious• <0.5% die

Page 3: Biochemistry and Clinical Toxicology

Most frequent enquiries to Toxbase [relative to paracetamol]

1. Paracetamol 1.002. Diazepam 0.303. Aspirin 0.284. Ibuprofen 0.265. Zopiclone 0.256. Ecstasy 0.237. Amitriptyline 0.208. Dothiepin 0.209. Temazepam 0.1810. Coproxamol 0.17

(Camidge et al, 2003)

Page 4: Biochemistry and Clinical Toxicology

Commonest poisons on admission to hospital

(Watson and Proudfoot, 2002)

• Paracetamol 60%• Ethanol 35%• Salicylate 30%• Carbon monoxide 25%• Tricyclics & phenothiazines 12%• Others 30%

Page 5: Biochemistry and Clinical Toxicology

Laboratory support for drug-related emergencies:

• standard laboratory tests

• specific drug concentrations

• drug screens

Page 6: Biochemistry and Clinical Toxicology

Standard laboratory tests

• Arterial blood gases– Ventilation problems– Acid-base disturbances

• Urea & electrolytes (incl Cl, HCO3, creat)– Hyper/hypo kalaemia– Anion gap

• Osmolality– Alcohols

• Calcium, albumin, Mg– Oxalate/fluorides

Page 7: Biochemistry and Clinical Toxicology

Standard laboratory tests ii

• Glucose– Differential diagnosis of coma– Hypoglycaemic

agents/EtOH/salicylates

• LFTs– Paracetamol– Iron salts– Halogenated hydrocarbons

Page 8: Biochemistry and Clinical Toxicology

Standard laboratory tests iii

• Creatine kinase– Rhabdomyolysis

• FBC/INR– Paracetamol

• Urine tests– Colour– Hb, (myoglobin)– Crystals

Page 9: Biochemistry and Clinical Toxicology

Emergency measurement of plasma drug concentrations

• assessing severity of poisoning – if this is not possible clinically

• determining need for specific treatment

• monitoring efficacy of treatment

• guiding therapy in severely ill patients

in rapidly changing circumstances

Page 10: Biochemistry and Clinical Toxicology

Toxicological testing in overdose

1. Toxicity predictable based on serum levels. Drug-specific therapy can be instituted when levels dictate:

Salicylate Theophylline LithiumDigoxin ParacetamolMethanol Ethylene glycol

2. Toxicity correlates with serum level, but supportive care only required:

Ethanol Barbiturates Phenytoin

Page 11: Biochemistry and Clinical Toxicology

Toxicological testing in overdose

3. Toxicity and requirement for specific treatment depend on clinical parameters - testing only confirms:

Tricyclics Narcotics (naloxone)Cyanide OrganophosphatesBenzodiazepines (flumazenil)

4. Toxicity poor correlation with serum level - supportive care only required:

Neuroleptics CocaineHallucinogens PhenylpropanolamineAmphetamine Phencyclidine

(Mahoney, 1990)

Page 12: Biochemistry and Clinical Toxicology

Reducing absorption

• ((emesis))• (lavage)• ORAL CHARCOAL

Page 13: Biochemistry and Clinical Toxicology

Increasing elimination

• (forced diuresis)• Urine alkalinization• Dialysis• Charcoal/resin haemoperfusion• Multiple-dose oral charcoal

Page 14: Biochemistry and Clinical Toxicology

Specific antidotes

• Paracetamol:N-acetylcysteine Methionine

• Methanol/ ethylene glycol: Ethanol, fomepizole

• Opiates : Naloxone• Metals: Chelators

(DFO, EDTA, etc)

Page 15: Biochemistry and Clinical Toxicology

Laboratory analyses for poisoned patients:joint position paper

National Poisons Information Service and the Association of Clinical Biochemists

Ann Clin Biochem 2002; 39: 328-339

Page 16: Biochemistry and Clinical Toxicology

Concentration measurements required at

any time:(NPIS/ACB, 2002)

• Salicylate• Paracetamol• Iron• Lithium• Theophylline

• Ethanol• CoHb, MetHb• Digoxin• Paraquat (qual)

within 2h

Page 17: Biochemistry and Clinical Toxicology

Specialist assays that may be required urgently

(ACB/NPIS, 2002)

• Methanol• Ethylene glycol• Phenytoin• Carbamazepine • Phenobarbital• Methotrexate• Paraquat (quant.

plasma)

• AChE• As• Hg• Pb• Thyroxine

• Unknown screen

Page 18: Biochemistry and Clinical Toxicology

Drug screens

• Usually of very limited value

Page 19: Biochemistry and Clinical Toxicology

Mahoney et al., 1990 - Boston, USA

Impact of qualitative toxic screening in management of suspected OD

176 cases of drug OD164 screened by:

GC, HPLC x3, acid GCMS, basic GCMS

Page 20: Biochemistry and Clinical Toxicology

Mahoney et al., 1990 - Boston, USA

81% screens POSITIVE

19% screens NEGATIVE

Page 21: Biochemistry and Clinical Toxicology

Mahoney et al., 1990 - Boston, USA

Impact of screens on management:

Treatment: n %No impact 146 90 Initiated 2 1 theophylline, salicylate

Continued 12 7 salicylate x2, lithium x2

paracetamol x2,

digoxin x1, Hg x1

Discontinued 4 2 paracetamol x4

Page 22: Biochemistry and Clinical Toxicology

Mahoney et al., 1990 - Boston, USA

Impact of screens on disposition:

35/176 admitted to hospital:

20 because of clinical findings7 because of clinical findings + drug screen

(6 salicylate, 1 imipramine)8 because of drug screen alone

(3 paracetamol, 2 lithium, 1 salicylate, 1 carbamazepine,

1 diphenhydramine)

Page 23: Biochemistry and Clinical Toxicology

Utility of toxicology screening in paediatric ER

(Sugarman; Pediatr Emerg Care 1997; 15: 194-7)

• Full toxicological screens on 338 children

• Unexpected results in 7% of screens• Management altered as a result of

screening results in 3 patients (<1%)– All three had abnormal symptoms

Page 24: Biochemistry and Clinical Toxicology

Urgent drug screens

• Poisoned patient very ill – ? Nature of poison

• Deteriorating unconscious patient without

Page 25: Biochemistry and Clinical Toxicology

“Routine” toxicology

• Diagnosis of brain death• Suitability of organs for Tx• Medico-legal (e.g. “date rape”)• Forensic

Page 26: Biochemistry and Clinical Toxicology

Exposure to poisons

Toxin Age <5 Age >15

Drugs 50.9% 74.8%Household prods. 20.4% 7.3%Toiletries 7.4% 1.4%Petroleum distill. 5.7% 1.4%Chemicals 6.2% 10.1%

(SPIB, 1994)

Page 27: Biochemistry and Clinical Toxicology

Poisonings other than drugs

• “Detection of poisonings by substances other than drugs: a neglected art”

Badcock NR Ann Clin Biochem 2000; 37:

146-57

Page 28: Biochemistry and Clinical Toxicology

S.B., 40 years, F

• On admission (1600, 18.1.97):– Na 147, K 4.4, Cl 103, urea 1.5, creat

91

– pH 6.73, pO2 51.2 , pCO2 6.2, bicarb 6, glucose 16.9

– Anion Gap = 42 mmol/L (12-20)– Osmolality: calc: 320, meas: 470– Osmolar Gap = 150 mmol/L

Page 29: Biochemistry and Clinical Toxicology

Gaps

• ANION GAP:Raised in:

– lactic acidosis– ketoacidosis– salicylate

poisoning– methanol/ethylene

glycol poisoning– CRF

• OSMOLAR GAPRaised with:

– Unmeasured osmoles:

• ethanol/methanol• (ethylene glycol)• mannitol/glycine

– severe shock– high

lipid/protein

Page 30: Biochemistry and Clinical Toxicology

Methanol / ethylene glycol

• Usually latent period before symptoms (12-72h)

• Headache• Pale, restless• Sweating• Convulsions• Nausea/vomiting

• Visual symptoms• Severe metabolic

acidosis• Cardiorespirator

y failure• Crystalluria &

renal tubular necrosis (glycol)

Page 31: Biochemistry and Clinical Toxicology

Ethanol(intoxication)

Methanol(intoxication)

Ethylene glycol(intoxication)

Acetaldehyde(hangover, flushing)

Formaldehyde(blindness,

cerebral oedema)

Glycoaldehyde(CNS effects)

Acetic acid Formic acid(metabolic acidosis)

Glycolic acid(metabolic acidosis)

CO2 + H2O Glyoxylate(lactic acidosis)

Oxalate(cerebral and renal

damage, hypocalcaemia)

Alcoholdehydrogenase

Aldehydedehydrogenase

LDH or glycolic acid oxidase

LDH or aldehyde oxidase

Page 32: Biochemistry and Clinical Toxicology

Diagnosis of methanol poisoning

• Metabolic acidosis• High anion gap• High osmole gap• Eye signs

presumptive

Page 33: Biochemistry and Clinical Toxicology

Estimation of alcohol concentration

• Ethanol (mg/dL) / 4.6 = osmolalityi.e. 80 mg/dL = 17 mmol/kg

• Methanol (mg/dL) / 3.2 = osmolality

• Ethylene glycol (mg/dL) / 6.2 = osmolality

Page 34: Biochemistry and Clinical Toxicology

M.McG, age 28, female

• OD 20 tabs Theo-Dur (husband’s) + 7 cans strong lager

• Anxious ++, pulse 130-160/reg• SWO 1h after ingestion• at 11h, Fits ++, pH = 6.9 : xfer to ITU• K+ 2.3 mmol/L• Theophylline @ 16h = 138 mg/L (760

mol/L)• Start HD & CHP• CK 113,300 U/L, ARF developed (creat =

1355)

Page 35: Biochemistry and Clinical Toxicology

Key points (i)

• Laboratory support for drug-related emergencies consists of standard biochemical/haematological tests, measurement of specific substances and drug screens for unknown poisons.

• Standard laboratory tests are most important for determining immediate management in most patients.

• Emergency measurement of specific substances is indicated in a small number of cases where specific therapy may be instituted depending on the nature and quantity of the poison ingested.

Page 36: Biochemistry and Clinical Toxicology

Key points (ii)

• Laboratories in hospitals dealing with acute admissions need key toxicological analyses available 24/7

• Repeated measurement of specific substances may be used to guide therapy.

• Drug screens rarely of immediate value but may be necessary when the patient is critically ill, or when the patient is ill and not improving, and the diagnosis is uncertain.


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