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Forensic Pathology for Police - Brainshare Public Online Library

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Death Certification 267<br />

blood via diffusion from adjacent structures (stomach, liver). It is generally agreed<br />

that the best blood sample to collect in order to minimize the effects of postmortem<br />

redistribution is femoral blood. Examples of drugs that are known to exhibit marked<br />

postmortem redistribution include tricyclic antidepressants and propoxyphene. In<br />

cases where postmortem redistribution has occurred, heart blood samples have drug<br />

levels that are much higher than femoral blood samples.<br />

Another issue of concern is the concept of “pharmacogenomics.” Different people<br />

have genetic variations in the enzymes used to metabolize certain drugs. As<br />

such, a given dose of a particular drug may cause certain, predictable results in many<br />

individuals, but have serious or even lethal effects in another individual. For example,<br />

many persons of Chinese, Vietnamese, and Japanese descent have a reduced<br />

activity of one of the enzymes involved in the metabolism of ethanol (drinking alcohol).<br />

When these individuals drink alcohol, they have a severe reaction with facial<br />

flushing.<br />

For some drugs, a generally accepted level <strong>for</strong> lethality is known. In other words,<br />

a death will not be considered due to the toxic effects of that drug unless the blood<br />

level is at or above the generally accepted lethal level. For other drugs, such a level<br />

does not exist, or the levels in cases reportedly due to the drug are so widely spread<br />

that a generally accepted lethal level is not agreed upon. Many factors contribute<br />

to this somewhat confusing situation regarding these drugs, including postmortem<br />

redistribution, postmortem metabolism, pharmacogenomics, short half-lives, tolerance,<br />

and the fact that with many such drugs a possible mechanism of death involves<br />

the initiation of a lethal cardiac arrhythmia or perhaps a seizure. With drugs that can<br />

induce a lethal arrhythmia or seizure, it can be argued that, in a given individual,<br />

an absolutely safe level of the drug may not exist. It is beyond the scope of this<br />

text to provide detailed in<strong>for</strong>mation regarding lethal levels of the drugs and toxins<br />

discussed. The reader is referred to an excellent reference book, Disposition of<br />

Toxic Drugs and Chemicals in Man, eighth edition, by Randall C. Baselt (copyright<br />

2008 by Biomedical <strong>Public</strong>ations, Foster City, CA), as an extremely useful resource<br />

regarding lethal drug levels.<br />

Death Certification<br />

If a death is caused exclusively by the acute toxic effects of a drug, the cause of<br />

death ruling can be written in several different ways. Examples include “toxic effects<br />

of cocaine,” “cocaine intoxication,” or “acute cocaine intoxication.” If more than<br />

one drug is involved, several options exist, <strong>for</strong> example, “mixed drug intoxication,”<br />

“combined toxic effects of multiple drugs,” or “combined intoxication with cocaine<br />

and heroin.” Occasionally, an underlying natural disease process or finding may<br />

be considered contributory to death. It is appropriate to list such a finding in part<br />

II of the death certificate. For example, part I – toxic effects of cocaine; part II –<br />

cardiomegaly. In other instances, a natural disease process may be considered the<br />

primary cause of death, but the presence of a drug intoxication is believed to have

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