CONTEXT: In 1989, Oregon passed SB 27, overhauling Medicaid by insuring all impoverished residents while explicitly rationing covered treatments. Rather than excluding some of the poor, the state established the Oregon Health Services Commission (OHSC), an eleven-person citizen body tasked with developing a prioritized list of 1,600 condition-treatment pairings based on cost-effectiveness and public values. This effort became central to debates over who should determine the availability of health services in public insurance programs.
METHODS: We analyzed a new data source - meeting minutes and internal documents from 1990-1991 - using reflexive thematic analysis in ATLAS.ti. Themes centered on commissioners' emotional experiences, technical challenges, and the role of subjective decision-making, situated within broader discussions of judgement in participatory governance and cost-effectiveness analysis.
FINDINGS: The Commission faced profound technical obstacles, namely limited data, methodological uncertainty, and growing frustration under public pressure. As technical approaches faltered, commissioners increasingly relied on collective judgment to complete the list.
CONCLUSIONS: The common narrative that the OHSC abandoned technical rigor overlooks the reality that health policy decisions always embed subjective judgements. Its innovation was affording those judgements to citizens rather than experts or politicians. Reliance on subjectivity reflected the nature of cost-effectiveness analyses and participatory governance, not failure.