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A Summary Care Record (SCR) is an electronic patient record, a summary of National Health Service patient data held on a central database covering England, part of the NHS National Programme for IT. The purpose of the database is to make patient data readily available anywhere that the patient seeks treatment, for example if they are staying ...
GPs are required from 2015 only to offer patients online access to the medication, allergies and adverse reactions in their summary care record, not to the complete record. [4] Jeremy Hunt announced in September 2015 that all patients will be entitled to read and write to all their NHS health records online by 2018. [5]
In 2019 only 10% of NHS trusts claimed to be fully digitised. The NHS Long Term Plan requires all hospitals to move to digital records by 2023, so clinicians can access and interact with patient records and care plans wherever they are. As of 2019, 62% of trusts have plans to digitise all their patient records.
the Summary Care Record which allows authorised NHS staff (such as hospital or ambulance staff) to see a summary of important information about a patient, to help give the best care. [11] the e-referral service which manages the booking of first time appointments with hospitals and specialists. [12]
The Summary Care Record (SCR). The Summary Care Record is a summary of patient's clinical information, such as allergies and adverse reactions to medicine. The Secondary Uses Service (SUS) , which uses data from patient records to provide anonymised and pseudonymised business reports and statistics for research, planning and public health delivery.
A personal health record (PHR) is a health record where health data and other information related to the care of a patient is maintained by the patient. [1] This stands in contrast to the more widely used electronic medical record, which is operated by institutions (such as hospitals) and contains data entered by clinicians (such as billing data) to support insurance claims.
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While GPs could record that patients had opted out of their data being used for any other purpose than their own personal care, that opt out wasn't passed on. The result is that data from 150,000 patients was disseminated by NHS Digital for audit and research purposes. [12] In August 2018 there were problems with the repeat prescription system.