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Triage
General allocation strategies when demand is greater than supply
Traditional Triage
Prioritize who will survive without medical support, but not without
Savulescu’s Allocation Principles 1st Level
Support Autonomy
Assess urgency (delay non-urgent)
Consider resource availability
Save the most lives
Resource Adjusted Probability Ratio
Probability of Survival / Expected resource demand
Factors of RAPR
Age, frailty (health status), co-morbidity
Savulescu’s Allocation Principles 2nd Level
Lottery or FCFS (egalitarianism)
2nd triage (utilitarian)
Priority (utilitarian/desert-based)
Trial of treatment
Emanuel Fundamental Views
Maximize benefits (max life years)
Treating equally (lottery)
Promoting instrumental value (can/have saved others)
Priority to worst off
Disability Paradox
Gap between disabled persons self-assessment & how others view quality of life
Activist Alice Wong argument
Ethical framework for triage discriminates people with disabilities
Joe Stramondo critique
Priority based on quality of life (ableist)
Disability components
Physical/mental impairment and personal/social limitation
Statistical impairment
Regard to an average
Biological impairment
Theory of functioning
Normative impairment
View of flourishing
Impairment definition
Loss or abnormality
Disability definition
Restriction/lack of ability
Handicap definition
Disadvantage given
Goal of Human Research
Producing scientifically valid, generalizable knowledge
Therapeutic Misconception
Confuses aims of research and practice
Coercive Vaccine Enforcement
Conditional mandates, public or private businesses, medical/religious exemptions
Libertarianism
Primary role of state is protection of individual rights, maximize liberty
Millian Harm Principle
Only state-justified interference: coercively enforcing prohibitions on harming each other
Largent & Miller Argument
Vaccine must be recommended for & readily available
Public health threat must persist
Adequate evidence of safety & efficacy of vaccine
Effort for voluntary vaccine first
Nuremberg Code (1947)
Not legally binding, informed consent, international
Declaration of Helsinki (1964)
International ethical code, nuanced view of informed consent
Helsinki Points
Rights/interests over knowledge, importance/benefit must outweigh risks
Belmont Report (1979)
U.S. ethical code
Belmont Main Ideas
Distinction between research & practice, any research needs review
Belmont Applications
Respect for persons'
Beneficence
Justice
Health & Human Services Regulations
U.S. regulations, CFR
The Common Rule
Requires IRBs (additional protection for fetuses/neonates, prisoners, & children)
Preclinical Phase
In animals, cells, etc.
Phase 1
New drug tested on small group (find safe dosage)
Phase 2
Larger group, test effectiveness
Phase 3
Confirm effectiveness, compare, monitor, collect info
Phase 4
Gone to market, monitor, effects in population
Double-Blind Trials
Investigator & subjects don’t know who got what
Randomized Trials
Assigned to arms randomly
Control Arm
Placebo or Standard of care
Clinical Equipoise
Don’t know which arm is better
Makes randomization ethical
if Clinical Equipoise
If during trial one arm is superior
Move participants slowly to that arm
Emanuel, Wendler, Grady
Focus on informed consent is misguided (not necessary or sufficient)
Emanuel, Wendler, + Grady Proposal
Value, scientific validity, fair subject selection, favorable risk-benefit ratio, independent review, informed consent, respect for potential & enrolled subjects
Respect for Potential & Enrolled Subjects
Privacy, permit mind changes, provide new info as it arises, monitor welfare, recognize contribution (inform of results)
Kriegar Lead Paint Study Goal
Find cheap ways to reduce contamination
Krieger Lead Paint Study Problems
Not fully informed consent, long time till notified of lead ingestion
Kriegar Lead Paint Study Result
Parents can’t consent to children’s participation that poses more than minimal risk
Placebo
Inert substance/treatment with no pharmalogical effect