Abstract
Background This study examines what proportion of families of recently diagnosed pediatric cancer patients are offered recommended psychosocial services, and if that proportion is linked to size of institution or number of psychosocial staff.
| Original language | English |
|---|---|
| Pages (from-to) | 435-440 |
| Number of pages | 6 |
| Journal | Pediatric Blood and Cancer |
| Volume | 58 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - Mar 2012 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- pediatric oncology
- psychosocial
- quality of life
- support care
- SIOP WORKING COMMITTEE
- PEDIATRIC ONCOLOGY
- CANCER SURVIVORS
- CHILDHOOD-CANCER
- SUPPORTIVE CARE
- CENTERS
- GUIDELINES
- FAMILIES
- ISSUES
- INTERVENTION
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