Summary information

Study title

National Surveys of NHS Patients: Coronary Heart Disease, 1999

Creator

Picker Institute Europe
National Centre for Social Research

Study number / PID

4477 (UKDA)

10.5255/UKDA-SN-4477-1 (DOI)

Data access

Restricted

Series

Not available

Abstract

Abstract copyright UK Data Service and data collection copyright owner.The National Surveys of NHS Patients programme comprises a series of surveys designed to contribute to monitoring the performance of the NHS as seen from the patient's perspective. The Government committed itself to this programme in 1997, in The New NHS - modern dependable White Paper, which proposed the introduction of annual surveys of patients and users to allow systematic comparisons of experiences over time and between different parts of the country. The first survey, covering general practice patients, was carried out in 1998. The second survey, covering Coronary Heart Disease (CHD) patients, took place in 1999. The third survey, covering Cancer patients, took place in 2000. The fourth survey, covering General Practice, took place in 2002. Further information about the series may be found on the Department of Health National Surveys of NHS Patients web page. The survey of Coronary Heart Disease (CHD) patients was the second in the National Surveys of NHS Patients series, and was designed to assess the quality of NHS patient care as seen by hospital in-patients and day patients diagnosed with CHD. The aim was to provide data which could be used to inform performance management by highlighting areas in need of improvement. The survey was also designed to give reliable results at Health Trust level so that individual Trusts could use the data to improve performance and so that comparisons could be made between Trusts, as well as providing a detailed national picture and the possibility of measuring future trends.Main Topics:The dataset addresses a number of issues relevant to all types of patients and some relevant only to patients with CHD. The main issues covered were access to care, physical comfort, the hospital environment, information and communication, patient involvement, co-ordination and continuity of care, discharge and transition. Question coverage was as follows: access to...
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Methodology

Data collection period

01/05/1999 - 01/09/1999

Country

England

Time dimension

Repeated cross-sectional study
These studies are part of a rolling programme of patient surveys - every year different patient groups are surveyed.

Analysis unit

Individuals
National
Adults

Universe

In-patients and day patients who had undergone an operational procedure at the hospital indicating CHD, or who had been diagnosed on discharge as having ischaemic heart disease or hypertension (using ICD code), between June and September 1998.

Sampling procedure

All Trusts in England where there were projected to be 200+ patients in the appropriate diagnosis categories in the sampling period were selected for survey - all agreed to take part. In smaller Trusts, all patients in appropriate diagnosis categories were included. Larger Trusts were asked to select a random sub-sample - the proportion selected varied according to Trust size, in order to yield a manageable sample size.

Kind of data

Numeric

Data collection mode

Postal survey

Access

Publisher

UK Data Service

Publication year

2002

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.

Related publications

Not available