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Abstract copyright UK Data Service and data collection copyright owner.The National Patient Survey Programme is one of the largest patient survey programmes in the world. It provides an opportunity to monitor experiences of health and provides data to assist with registration of trusts and monitoring on-going compliance. Understanding what people think about the care and treatment they receive is crucial to improving the quality of care being delivered by healthcare organisations. One way of doing this is by asking people who have recently used the health service to tell the Care Quality Commission (CQC) about their experiences.
The CQC will use the results from the surveys in the regulation, monitoring and inspection of NHS acute trusts (or, for community mental health service user surveys, providers of mental health services) in England. Data are used in CQC Insight, an intelligence tool which identifies potential changes in quality of care and then supports deciding on the right regulatory response. Survey data will also be used to support CQC inspections.
Each survey has a different focus. These include patients' experiences in outpatient and accident and emergency departments in Acute Trusts, and the experiences of people using mental health services in the community.
History of the programme
The National Patient Survey Programme began in 2002, and was then conducted by the Commission for Health Improvement (CHI), along with the Commission for Healthcare Audit and Inspection (CHAI). Administration of the programme was taken over by the Healthcare Commission in time for the 2004 series. On 1 April 2009, the CQC was formed, which replaced the Healthcare Commission.
Further information about the National Patient Survey Programme may be found on the CQC Patient Survey Programme web pages.
The Maternity Services Survey, 2010 was designed to provide actionable feedback to each participating trust on patients’ views of the care they had received in England, as...
Terminology used is generally based on DDI controlled vocabularies: Time Method, Analysis Unit, Sampling Procedure and Mode of Collection, available at CESSDA Vocabulary Service.
Methodology
Data collection period
01/04/2010 - 01/08/2010
Country
England
Time dimension
Repeated cross-sectional study
part of a wider NHS patient survey programme
Analysis unit
Individuals
National
Universe
Women patients of healthcare trusts in England who had given birth in February 2010.
Sampling procedure
Each healthcare trust identified women patients who had given birth in February 2010 (if the trust had had fewer than 250 births that month, January 2010 was also included). The sample size for each trust therefore varied. Women who had a stillbirth, whose baby had died since delivery, or those aged 16 years or under at the time of their baby's birth were not included.
Kind of data
Numeric
Data collection mode
Postal survey
Access
Publisher
UK Data Service
Publication year
2011
Terms of data access
The Data Collection is available to UK Data Service registered users subject to the End User Licence Agreement.
Commercial use of the data requires approval from the data owner or their nominee. The UK Data Service will contact you.