Abstract
• Accurate data about Indigenous child health is vital to enable us to understand its current state, to acknowledge achievements, and to determine how to reduce inequalities between Indigenous and non-Indigenous children.
• We have identified a paucity of national, or nationally representative, data relating to Indigenous child health outcomes, and significant deficiencies in available data.
• A coordinated national approach will help address current data limitations, including lack of identification of Indigenous status, lack of currency, and lack of information about specific health disorders affecting Indigenous children.
• To ensure that health data collected are relevant and useful, Indigenous communities must have a role in data collection and management.
| Original language | English |
|---|---|
| Pages (from-to) | 588-591 |
| Number of pages | 4 |
| Journal | Medical Journal of Australia |
| Volume | 188 |
| Issue number | 10 |
| Publication status | Published - 19 May 2008 |
| Externally published | Yes |
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