Rights of children to primary health care.
| Child Primary Care Rights Statement | Enabling Service Policy Statements (and Underpinning Source) |
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| Child Primary Care Rights Statement | Enabling Service Policy Statements (and Underpinning Source) |
All children in Europe have the | All children have the right to the enjoyment of the highest attainable standard of physical and mental health |
Primary Health Care is the basis and foundation for preventive and therapeutic health care | |
All children have the right to access appropriate facilities for the treatment of illness and rehabilitation of health | |
All children in Europe have the | Primary health care services for children should be appropriate, particularly with regard to their age |
Such provision should adhere to the principles of Availability, Accessibility, Affordability and Acceptability of services | |
Such services should be culturally and linguistically appropriate | |
Children are not the creators of their circumstances; services should be equally available to all children within a country, regardless of location, family circumstances, creed, ethnicity or civil status | |
Primary Health Care services, and the need for supporting and related services, should be the subject of specific plans, constructed with input from stakeholder representation including children and resourced appropriately | |
All children in Europe have the | Consultation should be in private |
The fact of seeking or receiving a consultation, or any form of follow-up, should itself be confidential | |
All children in Europe have the | Planning and provision of services for children should be focussed first and foremost on the child’s (or group of children’s) needs |
In the making of decisions about a treatment, or service provision, the interest of the child or children should be foremost, including their safety | |
All children in Europe have the | Information regarding children’s health and health behaviours should be available to parents and caregivers, in accessible form |
Parents and caregivers should be advised of the availability of appropriate information and how to access it | |
As appropriate, accessible child health-related education including health literacy should be available to parents and caregivers | |
All children in Europe, or parents acting as agents of younger children, have the | Choice of provider is important in engendering trust, as well as ensuring appropriateness |
Older children may wish to choose a provider other than the one selected by their parents, in order to ensure confidentiality and empathy | |
Ability to access specific types of primary care provision is important to maintaining the mental, reproductive and physical health of older children | |
All children in Europe have the | Primary health records, and health data, should always be subject to clinical confidentiality. |
Children, or parents acting on their behalf, should be advised when external parties have accessed their record – including hacking | |
Children who are old enough to understand, and parents acting on behalf of younger children, should have access to their health record and data in line with policy and good practice | |
All children in Europe have the | Appropriate to their age and maturity, children have the right to be informed about their health and related health care issues |
The views and perceptions of the child should be sought and taken into account in health care delivery decision-making | |
To the greatest extent possible, children should be co-producers and co-managers of their own health and health care | |
Where a longer-term condition necessitates care at home linked to primary care, all children in Europe and their informal care team have the | The need for ongoing health (and as appropriate related social or other) care should be communicated and documented |
Where necessary, a care coordinator should be designated | |
The overall plan, pathway and objectives of care should be agreed by all parties – child, family carers and professionals | |
Appropriate respite care, for the benefit of the child and informal carers, should be a part of the plan for children with long-term conditions or where necessitated by carers’ needs | |
When a child’s health condition necessitates hospital admission, all children in Europe have the | Discharge planning should commence at the time of admission (whether emergency or planned) |
Primary health care services, and community or specialised health and care support as needed, should be involved in planning and informed of the final plan, arrangements and date of discharge | |
The needs and views of the child, and of family and other informal carers, should be acknowledged, documented and accommodated as far as possible | |
Older children in Europe with a long-term health condition have the | Transition planning should be initiated by the lead specialist, linking with adult service partners and with primary care |
The child should be fully involved in preparation of the transition plan and should be considered a co-designer | |
Depending on the condition, and on local services, the transition may be before or after the 18th birthday | |
Where children’s primary care is provided by dedicated community paediatricians, the double transition of primary and specialist care to adult services should be planned carefully | |
All children in Europe have the | There should be defined standards for aspects of service structure (including professional skills), access and delivery |
All personnel treating children in primary care should be appropriately trained for their role with children | |
There should be open and transparent governance and quality assurance processes, ensuring efficacy and safety of services |
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