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Concept

Health Equity

Health equity research examines how social position shapes access, outcomes, and intervention effects across groups.

Average effects can hide who is left behind; equity analyses make that visible.

Studies

14

Findings

10

12 supporting · 0 challenging · 6 qualifying citations

Open tensions

2

Currently

What we know

  1. Multiple studies in this library examine health equity with empirical patient or population outcomes rather than opinion alone.
  2. 42% reported any discrimination; mental illness/substance use (33%) and homelessness/poverty (30%) were most common; discrimination associated with greater lifetime substance/mental severity and more frequent ED use.
  3. Vs least disadvantaged areas, all other SEIFA quintiles had higher cancer-death risk, highest in most disadvantaged (SHR 1.15); authors conclude disparities appear to have increased and need active policy attention.
  4. Non-Indigenous systems often failed needs and exposed people to discrimination, yet participants also showed cultural resilience and named concrete improvement strategies.
  5. Among 1846 women, NZ European cancers were more often screen-detected than Māori cancers (62.7% vs 49.2%). Māori women had worse crude five- and ten-year survival overall, but among screen-detected cancers survival was similar or numerically better for Māori.

Largest unresolved question

Effect sizes and settings differ across health equity studies — digital vs clinic, trial vs observational — so results should not be pooled casually.

Common misconceptions

  • Health Equity findings always generalise to every clinic.

    These studies are context-bound; designs, populations, and endpoints limit transfer.

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