Access | |
Authorization burden |
Supply and quality Clinician Financial
|
Law and policy burden |
Federal Provincial Hospital policy
|
Patient burden |
Pragmatic use Conditional rights
|
Relationships and relational autonomy | |
Clinical communication |
Individualistic approach Data transparency Informed consent
|
Clinical support |
|
Nonclinical communication |
|
Medically appropriate use | |
Riskābenefit calculus |
Harms Balance risk and benefit
|
EvidenceĀbased treatment |
Considered option Not considered option
|
Consumption |
|
Research priorities | |
Necessary research |
|
Barriers to research |
Study design Institutional
|
Research ethics |
Ethical considerations Obligations
|