Handle Information in Health and Social Care Settings.

337 Words2 Pages
The Data Protection Act 1998 is a United Kingdom Act of Parliament which defines UK law on the Processing of data on identifiable living people. It is the main piece of legislation that governs the protection of personal data in the UK. Although the Act itself does not mention privacy, it was enacted to bring UK law into line with the European Directive of 1995 which required Member States to protect people’s fundamental rights and freedoms and in particular their right to privacy with respect to the processing of personal data. In practice it provides a way for individuals to control information about themselves. Care records are valuable because of the information they contain and that information is only usable if it is correctly and legibly recorded in the first place, is then kept up to date, and is easily accessible when needed. After a month records are collected and given into the office and stored in case they are needed. Making and keeping records is an essential and integral part of care the purpose of making record Provide accurate, current and concise information concerning the condition and care of the client or other associated observations. Provide a record of any problems that arise and the action taken in response to them. Medication will also be recorded so as not to give out the wrong dose. Provide evidence of care required, intervention by nurses or doctors and patient or client responses. Provide a baseline record against which improvement or deterioration may be judged. Show evidence of on-going assessment and treatment and reasons for carrying it out. Discuss and agree with service users what they are going to record about them. Records can be stored electronically on computers or as paper documents which can be typed or handwritten. Computers must be password protected and it is recommended that individual documents are also
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