Clinical Toxicology Testing Flashcards

1
Q

Impacts of substance abuse

A

Lost productivity
Increased health costs
Increased cost to the courts

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Specimens for Clinical Toxicology Testing

A

Urine
Blood/Plasma
Gastric fluids
Meconium
Oral fluids
Sweat
Hair
Placenta and cord blood/tissues

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Why urine is a preferred specimen

A

Easy collection
More concentrated than in blood
Screening assay compatibility
Metabolite detection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Limitations of urine as a clinical toxicology specimen

A

Can’t correlate ingestion time/amount/frequency nor degree of impairment
Misses certain drugs - Ritalin and oral hypoglycemics

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Drug detection time lines in urine

A

<24hrs - Alcohol, Heroin,
3 days - Opiates
4 days - MDMA, Amphetamines, Cocaine
Days to Weeks - the B’s Barbiturates and Benzodiazepines
3 weeks - Methadone
30 days - Marijuana

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Testing methods and associated issues

A

Immunoassays
LC/MS/MS - Opioid ID
GC/MS - Full scan

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Advantages and Limitations of Immunoassay testing

A

Advantages: improved TAT, detects broad class of drugs
Limitations: prone to cross-reactivity and false pos/negs
- pos immunaassay is anything form A to Z

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is KIMS and when do we use it?

A

Kinetic Interaction of Micro-particles in Solution

Used to detect benzodiazepines but interfered by oxaprozin (FP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Describe the principle of KIMS

A

Ab bound to microparticles
Drugs conj to aminodextran

No drugs: amino-dextran agglut with micro particles = increased absorbance

Drugs: drugs bind Ab on micro particles os amino-dextran cant agglutinate = low absorbance

ie more drug =less absorbance

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Advantages of GC/MS and LC/MS confirmatory testing

A

Very specific

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Limitations of GC/MS and LC/MS confirmatory testing

A
  • More expensive/resource driven
  • Limited by quality of extraction and chromatographic properties
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Specimen integrity issues

A
  1. Internal dilution - drinking lots of water
  2. External dilution - adding water to sample
  3. Tampering - adding adulterants or masking agents
  4. Substitution - submits sample thats not their own
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

How do we test for specimen integrity?

A

Temperature (baseline)
pH (adulterants)
Creatine and SG (dilution and substitution)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Non-clinical testing scenarios

A

Clinical tox is not used for
-employment
-insurance
-anything relating to the law
-determination of compliance or impairment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

STAT drug testing

A

Not recommended
- non-specific
- doesn’t meaningfully influence acute medical management

How well did you know this?
1
Not at all
2
3
4
5
Perfectly