George Floyd Autopsy (FULL REPORT)
George Floyd Autopsy (FULL REPORT)
George Floyd Autopsy (FULL REPORT)
ME NO.: 20-3700
CARDIOPULMONARY ARREST COMPLICATING LAW ENFORCEMENT
CASE TITLE:
SUBDUAL, RESTRAINT, AND NECK COMPRESSION
DECEASED: George Floyd aka Floyd Perry SEX: M AGE: 46
FINAL DIAGNOSES:
1. Fentanyl 11 ng/mL
4. Methamphetamine 19 ng/mL
6. Cotinine positive
7. Caffeine positive
X
Andrew M. Baker, M.D.
Chief Medical Examiner
Signed by: Andrew M. Baker MD
In accordance with HCME policy, this report was
reviewed by another board-certified forensic
pathologist prior to release.
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20-3700
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IDENTIFICATION:
EXTERNAL EXAMINATION:
TATTOOS:
The following clothing items are received with the body in the
body bag, in a hospital patient belongings bag, and examined
separate from the body at the start of the postmortem
examination:
MEDICAL INTERVENTION:
EVIDENCE OF INJURY:
INTERNAL EXAMINATION:
HEAD: The soft tissues of the scalp are free of injury. The
calvarium is intact, as is the dura mater beneath it. Clear
cerebrospinal fluid surrounds the 1380 g brain, which has
unremarkable gyri and sulci. Coronal sections demonstrate sharp
demarcation between white and gray matter, without hemorrhage or
contusive injury. The ventricles are of normal size. The basal
ganglia, brainstem, cerebellum, and arterial systems are free of
injury or other abnormalities. There are no skull fractures.
The atlanto-occipital joint is stable.
RESPIRATORY SYSTEM: The right and left lungs weigh 1085 and
1015 g, respectively. The external surfaces are pink only on the
most anterior aspects, and deep red-purple in all other areas.
The pulmonary parenchyma is diffusely congested and edematous.
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ADRENALS: The right and left adrenal glands are symmetric, with
bright yellow cortices and gray medullae. No masses or areas of
hemorrhage are identified.
1 Kitzman DW, Scholz DG, Hagen PT, et al. Age-related changes in normal human
hearts during the first 10 decades of life. Part II (maturity): a
quantitative anatomic study of 765 specimens from subjects 20 to 99 years
old. Mayo Clin Proc. 1988; 63: 137-146.
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SPECIAL PROCEDURES:
ADDITIONAL PROCEDURES:
AB/SB: 5/27/20
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MICROSCOPIC EXAMINATION:
LEFT PELVIC
MASS (1,2): Decalcified (1) and routinely fixed (2) sections
show a proliferation of generally bland appearing
cells with small to moderate amounts of
eosinophilic cytoplasm and generally uniform
nuclei with neuroendocrine features. Occasional
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Positive Findings:
Testing Requested:
Analysis Code Description
8050U Postmortem, Urine Screen Add-on (6-MAM Quantification only)
9096B Alcohol Screen, Blood (Forensic)
8210B Novel Psychoactive Substances (NPS) Screen 2, Blood
8052B Postmortem, Expanded, Blood (Forensic)
8756B Novel Psychoactive Substances (NPS) Screen 1, Blood
Specimens Received:
ID Tube/Container Volume/ Collection Matrix Source Miscellaneous
Mass Date/Time Information
001 Lavender Vial 2.8 mL 05/25/2020 21:00 Hospital Blood
002 Gray Vial 0.6 mL 05/25/2020 21:00 Hospital Blood
003 Lavender Vial 5.75 mL 05/25/2020 21:00 Hospital Blood
004 Light Blue Vial 2.5 mL 05/25/2020 21:00 Hospital Blood
005 Green Vial 1.3 mL 05/25/2020 21:00 Hospital Blood
006 Red Vial 0.75 mL 05/25/2020 21:00 Hospital Serum or Plasma
007 Gray Top Tube 8.8 mL 05/26/2020 12:20 Femoral Blood
008 Gray Top Tube 8.8 mL 05/26/2020 12:20 Femoral Blood
009 Gray Top Tube 8.8 mL 05/26/2020 12:20 Femoral Blood
NMS v.18.0
CONFIDENTIAL Workorder 20159963
Chain NMSCP59310
Patient ID 2020-3700
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Detailed Findings:
Rpt.
Analysis and Comments Result Units Limit Specimen Source Analysis By
Other than the above findings, examination of the specimen(s) submitted did not reveal any positive findings of
toxicological significance by procedures outlined in the accompanying Analysis Summary.
Reference Comments:
1. 11-Hydroxy Delta-9 THC (Active Metabolite) - Hospital Blood:
11-Hydroxy Delta-9 THC is an active intermediate metabolite of tetrahydrocannabinol (THC) the active
component of marijuana. Usual peak levels: Less than 10% of THC levels after smoking.
2. 4-ANPP (Despropionyl fentanyl) - Hospital Blood:
4-ANPP (despropionylfentanyl) is a precursor chemical used in the production of fentanyl and is also a fentanyl
metabolite. It may be used in the production of other related compounds such as acetyl fentanyl, butyryl
fentanyl and furanyl fentanyl and may be a metabolite of these and other fentanyl-related compounds. It is
considered to be pharmacologically weak.
3. Amphetamines - Urine:
Amphetamines are a class of central nervous system stimulant drugs, with some therapeutic uses, and a high
potential for abuse.
This result derives from a presumptive test, which may be subject to cross-reactivity with non-amphetamine
related compounds. A second test is necessary to confirm the presence of amphetamine related compounds.
NMS v.18.0
CONFIDENTIAL Workorder 20159963
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Patient ID 2020-3700
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Reference Comments:
4. Caffeine (No-Doz®) - Hospital Blood:
Caffeine is a xanthine-derived central nervous system stimulant. It also produces diuresis and cardiac and
respiratory stimulation. It can be readily found in such items as coffee, tea, soft drinks and chocolate. As a
reference, a typical cup of coffee or tea contains between 40 to 100 mg caffeine.
The reported qualitative result for this substance was based upon a single analysis only. If confirmation testing
is required please contact the laboratory.
5. Cannabinoids - Urine:
Cannabinoids are chemical compounds derived from the plant Cannabis sativa (marijuana), including active
components, chemical congeners and metabolites. Delta-9-Tetrahydrocannabinol (THC) is the principal active
component.
This result derives from a presumptive test, which may be subject to cross-reactivity with non-cannabinoid
related compounds. A second test is necessary to confirm the presence of cannabinoid related compounds.
6. Cotinine (Nicotine Metabolite) - Hospital Blood:
Cotinine is a metabolite of nicotine and may be encountered in the fluids and tissues of an individual as a result
of tobacco exposure.
Anabasine is a natural product occurring in tobacco, but not in pharmaceutical nicotine and a separate test for
anabasine in urine can be used to distinguish tobacco from pharmaceutical nicotine use.
The reported qualitative result for this substance was based upon a single analysis only. If confirmation testing
is required please contact the laboratory.
Delta-9-THC is the principle psychoactive ingredient of marijuana/hashish. It rapidly leaves the blood, even
during smoking, falling to below detectable levels within several hours. Delta-9-carboxy-THC (THCC) is the
inactive metabolite of THC and may be detected for up to one day or more in blood. Both delta-9-THC and
THCC may be present substantially longer in chronic users.
THC concentrations in blood are usually about one-half of serum/plasma concentrations. Usual peak levels in
serum for 1.75% or 3.55% THC marijuana cigarettes: 50 - 270 ng/mL at 6 to 9 minutes after beginning
smoking, decreasing to less than 5 ng/mL by 2 hrs.
9. Fentanyl (Duragesic®; Sublimaze®) - Hospital Blood:
Fentanyl is a DEA Schedule II synthetic morphine substitute anesthetic/analgesic. It is reported to be 80 to 200
times as potent as morphine and has a rapid onset of action as well as addictive properties.
It is reported that patients lost consciousness at mean plasma levels of fentanyl of 34 ng/mL when infused with
75 mcg/Kg over a 15 min period; peak plasma levels averaged 50 ng/mL.
After application of a fentanyl transdermal preparation (patch), serum fentanyl concentrations are reported to
be in the following ranges within 24 hours:
25 mcg/hour patch: 0.3 - 1.2 ng/mL
50 mcg/hour patch: 0.6 - 1.8 ng/mL
75 mcg/hour patch: 1.1 - 2.6 ng/mL
100 mcg/hour patch: 1.9 - 3.8 ng/mL
NMS v.18.0
CONFIDENTIAL Workorder 20159963
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Patient ID 2020-3700
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Reference Comments:
Following removal of the patch, serum fentanyl concentrations are reported to decrease with a mean
elimination half-life of 17 hours (range, 13 to 22 hours).
The mean peak plasma serum fentanyl concentration in adults given an 800 mcg oral transmucosal fentanyl
preparation over 15 minutes is reported at 2.1 ng/mL (range, 1.4 - 3.0 ng/mL) at approximately 0.4 hours.
Signs associated with fentanyl toxicity include severe respiratory depression, seizures, hypotension, coma and
death. In fatalities from fentanyl, blood concentrations are variable and have been reported as low as 3 ng/mL.
Substance(s) known to interfere with the identity and/or quantity of the reported result: 4-methylphenethyl
acetyl fentanyl
10. Fentanyl / Metabolite - Urine:
Fentanyl is a DEA Schedule II synthetic morphine substitute anesthetic/analgesic. It is reported to be 80 to 200
times as potent as morphine and has a rapid onset of action as well as addictive properties.
This result derives from a presumptive test, which may be subject to cross-reactivity with non-fentanyl related
compounds. A second test is necessary to confirm the presence of fentanyl related compounds.
11. Methamphetamine - Hospital Blood:
d-Methamphetamine is a DEA schedule II stimulant drug capable of causing hallucinations, aggressive
behavior and irrational reactions. Chemically, there are two forms (isomers) of methamphetamine: l- and d-
methamphetamine. The l-isomer is used in non-prescription inhalers as a decongestant and has weak CNS-
stimulatory activity. The d-isomer has been used therapeutically as an anorexigenic agent in the treatment of
obesity and has potent CNS-, cardiac- and circulatory-stimulatory activity. Amphetamine and norephedrine
(phenylpropanolamine) are metabolites of methamphetamine. d-Methamphetamine is an abused substance
because of its stimulatory effects and is also addictive.
A peak blood concentration of methamphetamine of 20 ng/mL was reported at 2.5 hr after an oral dosage of
12.5 mg. Blood levels of 200 - 600 ng/mL have been reported in methamphetamine abusers who exhibited
violent and irrational behavior. High doses of methamphetamine can also elicit restlessness, confusion,
hallucinations, circulatory collapse and convulsions.
*In this case, the level of methamphetamine determined has not been differentiated according to its isomeric
forms. Differentiation of the isomers of methamphetamine is available upon request.
12. Morphine - Free (Codeine Metabolite) - Urine:
Morphine is a DEA Schedule II narcotic analgesic. In analgesic therapy, it is usually encountered as the parent
compound, however, it is also commonly found as the metabolite of codeine and heroin. In illicit preparations
from which morphine may arise, codeine may be present as a contaminant. A large portion of the morphine is
bound to the blood proteins or is conjugated; that which is not bound or conjugated is termed 'free morphine'.
Hydromorphone is a reported metabolite of morphine.
In general, free morphine is the active biologic agent. Morphine has diverse effects that may include analgesia,
drowsiness, nausea and respiratory depression. 6-monoacetylmorphine (6-MAM) is the 6-monoacetylated form
of morphine, which is pharmacologically active. It is commonly found as the result of heroin use.
13. Norfentanyl (Fentanyl Metabolite) - Hospital Blood:
Norfentanyl is the primary inactive metabolite of the synthetic narcotic analgesic fentanyl.
Substance(s) known to interfere with the identity and/or quantity of the reported result: Benzyl Fentanyl
Sample Comments:
001 Physician/Pathologist Name: Dr. Andrew Baker
Unless alternate arrangements are made by you, the remainder of the submitted specimens will be discarded one (1) year
from the date of this report; and generated data will be discarded five (5) years from the date the analyses were
performed.
NMS v.18.0
CONFIDENTIAL Workorder 20159963
Chain NMSCP59310
Patient ID 2020-3700
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-Analysis by High Performance Liquid Chromatography/ Tandem Mass Spectrometry (LC-MS/MS) for:
-Analysis by High Performance Liquid Chromatography/ Tandem Mass Spectrometry (LC-MS/MS) for:
-Analysis by High Performance Liquid Chromatography/ Tandem Mass Spectrometry (LC-MS/MS) for:
-Analysis by High Performance Liquid Chromatography/ Tandem Mass Spectrometry (LC-MS/MS) for:
-Analysis by High Performance Liquid Chromatography/ Tandem Mass Spectrometry (LC-MS/MS) for:
NMS v.18.0
CONFIDENTIAL Workorder 20159963
Chain NMSCP59310
Patient ID 2020-3700
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-Analysis by High Performance Liquid Chromatography/Time of Flight-Mass Spectrometry (LC/TOF-MS) for: The
following is a general list of compound classes included in this screen. The detection of any specific analyte is
concentration-dependent. Note, not all known analytes in each specified compound class are included. Some
specific analytes outside these classes are also included. For a detailed list of all analytes and reporting limits,
please contact NMS Labs.
Amphetamines, Anticonvulsants, Antidepressants, Antihistamines, Antipsychotic Agents, Benzodiazepines, CNS
Stimulants, Cocaine and Metabolites, Hallucinogens, Hypnosedatives, Hypoglycemics, Muscle Relaxants, Non-
Steroidal Anti-Inflammatory Agents, Opiates and Opioids.
Acode 8210B - Novel Psychoactive Substances (NPS) Screen 2, Blood - Hospital Blood
-Analysis by Gas Chromatography/Mass Spectrometry (GC/MS) for: The following is a general list of compound
classes considered to be Novel Psychoactive Substances included in the Gas Chromatographic screen. The
detection of any particular compound is concentration-dependent. Please note that not all known compounds
included in each specified class or heading are included. Some specific compounds outside these classes are
also included. For a detailed list of all compounds and reporting limits included in this screen, please contact
NMS Labs.
Substituted Phenethylamines, Opioid Analgesics, Substituted Cathinones, Pyrrolidinophenones, Piperazines,
Tryptamines, Aminoindanes, and Benzofurans.
Acode 8756B - Novel Psychoactive Substances (NPS) Screen 1, Blood - Hospital Blood
NMS v.18.0
CONFIDENTIAL Workorder 20159963
Chain NMSCP59310
Patient ID 2020-3700
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NMS v.18.0