A key aspect of delivering effective and appropriate health care
is the availability of robust data and information on which decisions
can be based. The introduction of clinical governance and evidence-based
practice requires improved access for all NHS staff to information
on effective clinical practice and service provision, investment
in clinical information systems and information support services
and the collection of comparative data from hospital and Primary
Care systems.
The National Service Frameworks
(NSFs) have set national standards for specific care groups and
each is supported by the requirement to implement an associated
information strategy. They will be supported by information systems
to enable the consistent and comprehensive recording of treatment
or care provided and the associated outcomes to support patient
care.
This information will be available
from a variety of sources and across a range of organisation's across
the NHS and Social Care. In order to provide a comprehensive health
needs assessment, data required will include: population estimates
and forecasts; birth and death statistics; public health data; hospital
statistics; social care data and other data sources.
The collation, analysis and presentation of this data will be facilitated
by the implementation of robust and fully integrated information
systems and the Electronic Patient Record, which underpins the Information
for Health Strategy.
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