Forensic Exam (2) PDF
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Jessenius Faculty of Medicine in Martin (JFMED CU)
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Summary
This document covers various aspects of estimating time since death in a forensic context, including the processes of algor mortis, rigor mortis, and livor mortis. It explores how these processes can be used to provide information for forensic investigations.
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23A - Time since death estimation (possibilities in the field practice, accuracy) Time of death terms - Time of death (ToD)= Exact moment of death estimation - Postmortem interval (PMI) = Time elapsed since death...
23A - Time since death estimation (possibilities in the field practice, accuracy) Time of death terms - Time of death (ToD)= Exact moment of death estimation - Postmortem interval (PMI) = Time elapsed since death - → Shorter PMI = More accurate estimation Crime scene - Police estimate times of death using body temp + Stiffness → Forensic pathologist conduct more accurate evaluations - Provide police with preliminary idea of time of assault + Verify if time since death matches suspect alibi Methods - Premortem changes= Wound age + Gastric content - Postmortem = Progressive changes at time scene → more commonly used - Algor mortis (cooling of body, normal 1°/h) - Livor mortis (pooling of blood to gravity, 30 min-12h) - Rigor mortis (stiffening to muscle, lack of ATP, 2-24h) - Drying of lips/genitals/Conjunctiva/Extremities - Supravital reaction + Putrefaction + Corpse fauna presence (insects) Purpose - Criminology = Helps to narrow down time frame related to crimes, to match alibi‘s - Civil proceedings = Legal contexts → Inheritance cases - Medicine = Organ transplantation viability Algor mortis - Body temperature →After death heat production stops → Cools gradually - Factors ↑ Cooling - ↓ environmental temp + minimal clothing + ↑ humidity + air movement + ↓ s.c fat - Estimation - Central core temp (Rectum + brain) → Most useful - Temp ↓ varies across body parts - Skin = Cools quickly + unpredictable - Rectum = Drops 0,5°C (first 3h) + 1°C (next 6h) + continues until it matches environment in 20-24h - Brain = Drops at consistent intervals → Measured w. Needle probe - Henssge Nomogram = based on calculation of Marshall → Calculates time of death based on: - Rectal temp + Environmental temp + Body weight + Covering of body - Adjustments are needed for non-standard cooling conditions Rigor mortis - Stiffening of muscles after death due to persistent actin-myosin attachment due to ↓ ATP - Timing - Occurs in 30min-2h after death → Lasts 8-36h (>36 h rigor disappears, muscle relax) - Nysten rule - Starts in mandibular joints and eyelids → Trunk → Lower extremities → Upper extremities - Can start in lower extremities in prolonged agony or glycogen depletion - Also affects smooth muscles = Visible as gooseflesh due to arrectores pilorum rigidity - Limitations = Rigor mortis as evidence diminishes significantly over time Livor mortis - Begins in 20-30 min PMI → Fully developed in 6-8h - Relocation - Occurs within 6h depending on body position - Partial relocation (6-12h PMI) + Permanent (12h PMI) - Blanching - Blanchable by moderate exertion within 20h PMI + by rigid object 36h PMI - Supravital reaction - refers to certain bodily functions that can continue briefly after death, during the period before all cellular activity stops. These signs are useful in estimating the post-mortem interval (PMI), which is the time since death. - Muscle excitability =Mechanical (1,5-2h PMI) + Electrical (1-5h PMI) - Pupillary reaction = Mydriasis (4-6h PMI) + Miosis (2-21h PMI) - Motile sperm cells = up to 80h PMI Malach criteria - Warm + Flaccid = Death occurred < 3h - Warm + Stiff = Death occured 3-8h - Cold + Stiff = Death occured 8-36h - Cold + Flaccid = Death occurred > 36h Putrification - breakdown of tissues, the production of gasses, and a strong odor - Development of putrefaction at 21°C → PMI - Greening of skin (48h) - Marbling of skin/green-gray color/Blisters (1 week) - Detachment of hair (2 weeks) - Drying of tissues (1-2 m) - Complete decomposition of soft tissues (6m) - Putrefaction of internal organs - Liquefaction of brain (10 days) - Loss of renal structure/Gastric + hepatic emphysema (3 weeks) - Mold on internal organs (2m) - Soft tissue decay/dry leaving skeleton exposed (1y) - Rate of decomposition rate = Casper‘s rule → Air:water:earth = 1:2:8 - Air is the fastest + Earth is the slowest Stages of - Greenish discoloration (lower abd) putrefaction - Marbling on skin (due to breakdown of blood vessels) - Bloating (swelling of body caused by gas production) - Purge fluids (release of body fluid from body opening) - Skin loosen and peels Stomach emptying - Location of meal in stomach since last eating stages - Recent meal (stomach + minimal duodenum) - 2-3h post meal (SI + minimal stomach) - 6h (LI) + >30h (GIT is completely empty) - hægt að nota mat til að sjá tímann - Insect activity → Sjá spurningu 10A 23B - Drug dependence: amphetamines, cath Addiction Definition - persistent use of drugs despite substantial harm and adverse consequences Drug dependence Definition - adaptive state ass. w. withdrawal symptoms upon cessation of repeated exposure to drugs - Receptors decrease in number due to adaptation after prolonged exposure CNS stimulant What is it - similar effects and risk (vary in usage pattern and cultural significance) - amphetamine (speed) - methamphetamine (meth) - MDMA (ecstasy / molly) - Cathinones (khat) Amphetamine MoA - ↑ release and ↓ reuptake of neurotransmitters (adrenaline + NE + serotonin + dopamine) → CNS stimulation Effect - Central - euphoria + ↑ energy + hallucinations + impaired judgment + agitation + confusion + sleep disturbances + psychosis - Peripheral - tachycardia + hypertension + arrhythmia + hyperthermia + mydriasis + nausea + weight loss + muscle weakness - hugsa allt öfugt við opioids Complications - Cardiac arrhythmias + cerebral hemorrhage + rhabdomyolysis + hyperthermia + memory impairment Withdrawal symptoms - Dysphoria + fatigue + depression + ↑ appetite + insomnia/hypersomnia + drug cravings + anxiety + aggression - Chronic use → psychosis Death - Death usually results from overdose → cardiovascular collapse or hyperthermia Management - symptoms based → BNZ for seizures or agitation Mechanism of overdose - Hypertensive crisis - vasoconstriction + SNS stimul.dangerously high BP - stroke, MI, aortic dissection - Arrhythmia - tachycardia and irregular heart beats → sudden cardiac arrest and death - Severe hyperthermia - can lead to multiorgan failure and can also cause rhabdomyolysis and kidney failure - Seizure - amphetamine overdose can lead to seizure and status epilepticus - Lethal dose - 150-500 mg in non tolerant users KHAT What is it - lauf af plöntu sem er tuggið (CATHIONINE → the potent stimulant found in the khat leaves) - can cause physical and psychological dependence - Stimulant and contains amphetamines. - Small amounts of khat might feel like drinking a lot of coffee, which opens the blood vessels in the brain to allow more oxygen to pass through and causes the heart to pump faster. Large dose of Khat - can lead to several cardiovascular effects effects - Positive - euphoria + excitement + mild hyperactivity - glaður kall að hoppa í grasinu - Negative - agitation + hallucination + paranoia + hypertension + tachycardia + mydriasis + constipation - svo kemur pirringur og paranoia - Long term - liver damage + permanent tooth darkening + ulcers + compromised self control Withdrawal - mild depression + irritability (occasional use) + lethargy + tremors (chronic use) Tests - blood, urine, saliva - Death: cardiovascular í bæði - Autopsy: MI, left ventricular hypertrophy, ats - Intracerebral hemorrhage and stroke - Brain edema - Git ulcers - Brain edema Comparison - commonalities = euphoria + ↑ energy + agitation + psychosis + withdrawal (depression + irritability) - differences - Amphetamines = stronger + faster onset effects → ↑ risk of severe complications - (hypernatremia + cardiovascular events) - Khat = more culturally embedded in some regions → more gradual intoxication but similar long term dependance risk