AndreaBozzo/ceres-open-data-index huggingface dataset:
National Head and Neck Cancer Audit, Open data - 2014

Making clinical audit data transparent 
 
In his transparency and open data letter to Cabinet Ministers on 7 July 2011, the Prime Minister made a commitment to make clinical audit data available from the national audits within the National Clinical Audit and Patient Outcomes Programme. 
  
What information is being made available? 
 
Audit participation by NHS Trust and network, and data completeness for the key fields. 
 
Measures of aspects of the care given to patients. 
 
Information about care outcomes and treatment.

These data do not list individual patient information, nor do they contain any patient identifiable data. 
  
The National Head and Neck Cancer Audit focuses on cancer sites within the head and neck (excluding tumours of the brain and thyroid cancers).  It describes a group of cancers (larynx, oral cavity, oropharynx, hypopharynx, nasopharynx, major salivary gland nose and sinuses and cancer of the bones of the jaw) that have many common features but also important differences in biological behaviour. 

The Head and Neck Cancer Audit database contains a vast amount of information on more than 54,000 head and neck cancer cases, with 7,700 cases of cancer of the glottic larynx, more than 7,500 cases of oral tongue cancer, more than 14,000 cases of larynx cancer, and almost 17,500 cases of oral cavity cancer. 

The National Head and Neck Cancer Audit 2014, Tenth Annual Report provided information that represents 7875 cases of head and neck cancer from England and 554 cases from Wales. The report, therefore, represents a comprehensive overview of head and neck cancer care, and this supporting dataset contains those England indicators in the main report and supplementary report files. 

The National Head and Neck Cancer Audit was commissioned and sponsored by the Healthcare Quality Improvement Partnership (HQIP) and developed in partnership with the British Association of Head and Neck Oncologists (BAHNO). The Health and Social Care Information Centre provided project management and technical infrastructure.
 
Accessing the data

Each year data from the National Head and Neck Cancer Audit is made available in CSV format. The data are also being made available on the data.gov website. 

Which level of data is being reported?

Trusts and networks within England are included. 

Trusts and Strategic Clinical Networks / Integrated Cancer Systems are identified by name and their national code. 

What period does the data cover?

The National Head and Neck Cancer Audit 2013-2014 covered the time period from 1st November 2013 to 31st October 2014. 

Organization: Healthcare Quality Improvement Partnership
National Head and Neck Cancer Audit, Open data - 2013

Making clinical audit data transparent 
 
In his transparency and open data letter to Cabinet Ministers on 7 July 2011, the Prime Minister made a commitment to make clinical audit data available from the national audits within the National Clinical Audit and Patient Outcomes Programme. 
  
What information is being made available? 
 
Audit participation by NHS Trust and data completeness for the key fields. 
 
Measures of aspects of the care given to patients. 
 
Information about care outcomes and treatment.

These data do not list individual patient information, nor do they contain any patient identifiable data. 
  
The National Head and Neck Cancer Audit focuses on cancer sites within the head and neck (excluding tumours of the brain and thyroid cancers). The most common of which are the larynx, oropharynx and in the oral cavity.
 
The National Head and Neck Cancer Audit is commissioned and sponsored by the Healthcare Quality Improvement Partnership (HQIP) and developed in partnership with the British Association of Head and Neck Oncologists (BAHNO). The Health and Social Care Information Centre provides project management and technical infrastructure.
 
The National Head and Neck Cancer Audit 2013, Ninth Annual Report provided information that represents 7,817 cases of head and neck cancer from England and 541 cases from Wales. The report, therefore, represents a comprehensive overview of head and neck cancer care, and this supporting dataset contains those England indicators in the main report and supplementary report files. 

Accessing the data

Each year data from the National Head and Neck Cancer Audit will be made available in CSV format. The data are also being made available on the data.gov website. 

Which level of data is being reported?

Trusts and networks within England are included. 

Trusts and Networks are identified by name and their national code. 

What period does the data cover?

The National Head and Neck Cancer Audit 2012-2013 covers the time period from 1st November 2012 to 31st October 2013. 


Organization: Healthcare Quality Improvement Partnership
National Head and Neck Cancer Audit, Open data - 2011

Making clinical audit data transparent 

In his transparency and open data letter to Cabinet Ministers on 7 July 2011, the Prime Minister made a commitment to make clinical audit data available from the national audits within the National Clinical Audit and Patient Outcomes Programme. 

Each year data from the Head and Neck Cancer Audit will be made available in CSV format. The data are also being made available on the data.gov website. 

What information is being made available? 

Audit participation by NHS Trust and data completeness for the key fields. 

Measures about the process of care given to patients. 

Information about care outcomes and treatment. 

Trusts and Networks are identified by name and their national code. These data do not list individual patient information, nor do they contain any patient identifiable data. 

The National Head and Neck Cancer Audit focuses on cancer sites within the head and neck (excluding tumours of the brain and thyroid cancers). The most common of which being the larynx and in the oral cavity. 

The Head and Neck Cancer Audit Project is a high profile, collaborative, national clinical audit for bowel cancer run by The Health and Social Care Information Centre and developed in partnership with the British Association of Head and Neck Oncologists (BAHNO) 

The audit aims to improve the quality of care and survival of patients with Head and Neck cancer. It meets the requirements as set out in the NHS Cancer Plan and NICE guidelines. 

The Head and Neck Cancer Audit 2011 covers the time period from 1st November 2010 to 31st October 2011 and only Hospital sites within England are included in these csv files.

Organization: Healthcare Quality Improvement Partnership
National Diabetes Audit, Open data - 2010-2011

Making clinical audit data transparent 

In his transparency and open data letter to Cabinet Ministers on 7 July 2011, the Prime Minister made a commitment to make clinical audit data available from the national audits within the National Clinical Audit and Patient Outcomes Programme. 

Each year data from the National Diabetes Audit will be made available in CSV format. The data are also being made available on the data.gov website. 

What information is being made available? 

Audit participation by Primary Care Trusts (PCTs) 

Measures about the process of care given to patients. 

Information about care outcomes and treatment. 

Information about complications and mortality 

PCTs are identified by name and their national code. These data do not list individual patient information, nor do they contain any patient identifiable data. 

The National Diabetes Audit is a high profile, collaborative, national clinical audit for diabetes. The National Diabetes Audit was run by the NHS Information Centre with Diabetes UK and Yorkshire and Humber Public Heath Observatory, commissioned by HQIP. 

The audit aims to improve the quality of care in people with diabetes. It meets the requirements as set out in the NICE guidelines. 

The National Diabetes Audit 2010/11 covers the time period from 1 January 2010 up to 31 March 2011 with information from GP Practices and specialist diabetes units in England. 

Organization: Healthcare Quality Improvement Partnership
National Diabetes Inpatient Audit, Open data - 2011

Making clinical audit data transparent 

In his transparency and open data letter to Cabinet Ministers on 7 July 2011, the Prime Minister made a commitment to make clinical audit data available from the national audits within the National Clinical Audit and Patient Outcomes Programme. 

Each year data from the National Diabetes Inpatient Audit will be made available in CSV format. The data are also being made available on the data.gov website. 

What information is being made available? 

Audit participation by NHS Trust and data completeness for the key fields. 

Measures about the process of care given to patients. 

Information about care outcomes and treatment. 

Trusts and Networks are identified by name and their national code. These data do not list individual patient information, nor do they contain any patient identifiable data. 

The National Diabetes Inpatient Audit (NaDIA) is commissioned by the Healthcare Quality Improvement Partnership (HQIP) and delivered by the Health and Social Care Information Centre, working with Diabetes UK. 

The National Diabetes Inpatient Audit is a snapshot audit of diabetes inpatient care in England. The audit is set out to answer the following questions: 

Did diabetes management minimise the risk of avoidable complications? 

Did harm result from the inpatient stay? 

Was patient experience of the inpatient stay favourable? 

Has the quality of care and patient feedback changed since NaDIA 2010? 

The audit takes place every year in autumn. NaDIA 2011 was carried out by diabetes teams in acute hospitals in England on a nominated day in the first two weeks of October



Organization: Healthcare Quality Improvement Partnership
National Diabetes Inpatient Audit (NaDIA) - 2016

Making clinical audit data transparent 

In his transparency and open data letter to Cabinet Ministers on 7 July 2011, the Prime Minister made a commitment to make clinical audit data available from the national audits within the National Clinical Audit and Patient Outcomes Programme. 

The information available from this webpage comes from the National Diabetes Inpatient Audit. The National Diabetes Inpatient Audit is a snapshot audit of diabetes inpatient care. In September 2016 the National Diabetes Inpatient Audit was conducted in hospitals across England and Wales, collecting data on characteristics of the hospital including staffing structures, patient clinical data and patient experience information. 

What information is being made available? 

 Audit participation and data completeness for the key fields 

 Measures about the process of care given to patients 

 Information about care outcomes and treatment. 

These data do not list individual patient information nor do they contain any patient identifiable data. 

Using and interpreting the data 

Data from the National Diabetes Inpatient Audit should not be looked at in isolation when assessing standards of care. 

Accessing the data 

The data are being made available on the data.gov website. Each year a data file from the National Diabetes Inpatient Audit will be made available in CSV format. Hospitals are identified by name and their national code. 

What does the data cover? 

The audit looks at the following areas: 

• Did diabetes management minimise the risk of avoidable complications? 

• Did harm result from the inpatient stay? 

• Was patient experience of the inpatient stay favourable? 

• Has the quality of care and patient feedback changed? 

What period does the data cover? 

This data covers patients surveyed on a date between 26 and 30 September 2016. The audit report was published on 08 March 2017.

Organization: Healthcare Quality Improvement Partnership
National Diabetes Inpatient Audit (NaDIA) - 2015

Making clinical audit data transparent

In his transparency and open data letter to Cabinet Ministers on 7 July 2011, the Prime Minister made a commitment to make clinical audit data available from the national audits within the National Clinical Audit and Patient Outcomes Programme. 

The information available from this webpage comes from the National Diabetes Inpatient Audit. The National Diabetes Inpatient Audit is a snapshot audit of diabetes inpatient care. In September 2015 the National Diabetes Inpatient Audit was conducted in hospitals across England and Wales, collecting data on characteristics of the hospital including staffing structures, patient clinical data and patient experience information. 

What information is being made available? 

	Audit participation and data completeness for the key fields

	Measures about the process of care given to patients 

	Information about care outcomes and treatment. 

These data do not list individual patient information nor do they contain any patient identifiable data. 

Using and interpreting the data 

Data from the National Diabetes Inpatient Audit should not be looked at in isolation when assessing standards of care. 

Accessing the data 

The data are being made available on the data.gov website. Each year files of data from the National Diabetes Inpatient Audit will be made available in CSV format. Hospitals are identified by name and their national code. 

What does the data cover? 

The audit looks at the following areas: 

• Did diabetes management minimise the risk of avoidable complications? 

• Did harm result from the inpatient stay? 

• Was patient experience of the inpatient stay favourable? 

• Has the quality of care and patient feedback changed? 

What period does the data cover? 

This data covers patients surveyed on a date between 21 and 25 September 2015.

This publication was produced in two parts: the comparative hospital-level analysis was published on 08 March 2016 and the National Report was published on 23 June 2016.


Organization: Healthcare Quality Improvement Partnership
National Diabetes Foot Care Audit 2014-2016

Making clinical audit data transparent 

In his transparency and open data letter to Cabinet Ministers on 7 July 2011, the Prime Minister made a commitment to make clinical audit data available from the national audits within the National Clinical Audit and Patient Outcomes Programme. 

The National Diabetes Foot Care Audit (NDFA) is a continuous audit of diabetic foot disease in England and Wales. The audit enables all diabetes foot care services to measure their performance against NICE clinical guidelines and peer units, and to monitor adverse outcomes for people with diabetes who develop diabetic foot disease. 

What information is being made available?  

Trust, service, and clinical commissioning group (CCG) audit participation and data completeness for the key fields

Measures about the process of care given to patients  

Information about care outcomes and treatment. 

These data do not list individual patient information nor do they contain any patient identifiable data. 

Using and interpreting the data 

Data from the National Diabetes Foot Care Audit should not be looked at in isolation when assessing standards of care. 

Accessing the data 

The data are being made available on the data.gov website. Each year a data file from the National Diabetes Foot Care Audit will be made available in CSV format. Trusts, CCGs and Networks are identified by name and their national code. Foot care services are identified by name and locally derived code.

What does the data cover? 

The audit looks at the following areas: 

Structures: are the nationally recommended care structures in place for the management of diabetic foot disease? 

Processes: does the treatment of active diabetic foot disease comply with nationally recommended guidance? 

Outcomes: are the outcomes of diabetic foot disease optimised? 

What period does the data cover? 

This data covers patients first seen with a diabetic foot ulcer by a specialist foot team between 14 July 2014 and 8 April 2016. This National Report was published on 8 March 2017. 

Organization: Healthcare Quality Improvement Partnership
National Diabetes Foot Care Audit 2014-2015

Making clinical audit data transparent 

In his transparency and open data letter to Cabinet Ministers on 7 July 2011, the Prime Minister made a commitment to make clinical audit data available from the national audits within the National Clinical Audit and Patient Outcomes Programme. 

The National Diabetes Foot Care Audit (NDFA) is a continuous audit of diabetic foot disease in England and Wales. The audit enables all diabetes foot care services to measure their performance against NICE clinical guidelines and peer units, and to monitor adverse outcomes for people with diabetes who develop diabetic foot disease.

What information is being made available?  

Trust and clinical commissioning group (CCG) audit participation and data completeness for the key fields  

Measures about the process of care given to patients  

Information about care outcomes and treatment. 

These data do not list individual patient information nor do they contain any patient identifiable data. 

Using and interpreting the data 

Data from the National Diabetes Foot Care Audit should not be looked at in isolation when assessing standards of care. 

Accessing the data 

The data are being made available on the data.gov website. Each year files of data from the National Diabetes Foot Care Audit will be made available in CSV format. Trusts, CCGs and Networks are identified by name and their national code. 

What does the data cover? 

The audit looks at the following areas: 

Structures: are the nationally recommended care structures in place for the management of diabetic foot disease? 

Processes: does the treatment of active diabetic foot disease comply with nationally recommended guidance? 

Outcomes: are the outcomes of diabetic foot disease optimised? 

What period does the data cover? 

This data covers patients first seen with a diabetic foot ulcer by a specialist foot team between 14 July 2014 and 10 April 2015. This National Report was published on 31 March 2016. 

Organization: Healthcare Quality Improvement Partnership
National Bowel Cancer Audit, Open data – 2011-2012

Making clinical audit data transparent.

In his transparency and open data letter to Cabinet Ministers on 7 July 2011, the Prime Minister made a commitment to make clinical audit data available from the national audits within the National Clinical Audit and Patient Outcomes Programme. 

Each year data from the National Bowel Cancer Audit will be made available in CSV format. The data are also being made available on the data.gov website. 

What information is being made available? 

Audit participation by NHS Trust and data completeness for the key fields. 

Measures about the process of care given to patients. 

Information about care outcomes and treatment. 

Trusts and Networks are identified by name and their national code. These data do not list individual patient information, nor do they contain any patient identifiable data. 

The National Bowel Cancer Audit Project is a high profile, collaborative, national clinical audit for bowel cancer run jointly by The Health and Social Care Information Centre and the Association of Coloproctology of Great Britain and Ireland (ACPGBI). 

The NHS Information Centre's National Clinical Audit Support Programme (NCASP) provides project management and the technical infrastructure, while the ACPGBI provides clinical leadership and direction. 

The audit aims to improve the quality of care and survival of patients with bowel cancer. It meets the requirements as set out in the NHS Cancer Plan, NICE guidelines and the Report of the Bristol Royal Infirmary Inquiry. 

The National Bowel Cancer Audit 2011-2012 covers the time period from 1st April 2011 to 31st March 2012. Hospital sites within England are included.

Organization: Healthcare Quality Improvement Partnership
National Bowel Cancer Audit, Open data – 2010-2011

Making clinical audit data transparent 

In his transparency and open data letter to Cabinet Ministers on 7 July 2011, the Prime Minister made a commitment to make clinical audit data available from the national audits within the National Clinical Audit and Patient Outcomes Programme. 

Each year data from the National Bowel Cancer Audit will be made available in CSV format. The data are also being made available on the data.gov website. 

What information is being made available? 

Audit participation by NHS Trust and data completeness for the key fields. 

Measures about the process of care given to patients. 

Information about care outcomes and treatment. 

Trusts and Networks are identified by name and their national code. These data do not list individual patient information, nor do they contain any patient identifiable data. 

The National Bowel Cancer Audit Project is a high profile, collaborative, national clinical audit for bowel cancer run jointly by The Health and Social Care Information Centre and the Association of Coloproctology of Great Britain and Ireland (ACPGBI). 

The NHS Information Centre's National Clinical Audit Support Programme (NCASP) provides project management and the technical infrastructure, while the ACPGBI provides clinical leadership and direction. 

The audit aims to improve the quality of care and survival of patients with bowel cancer. It meets the requirements as set out in the NHS Cancer Plan, NICE guidelines and the Report of the Bristol Royal Infirmary Inquiry. 

The National Bowel Cancer Audit 2010-2011 covers the time period from 1st August 2010 to 31st July 2011, Hospital sites within England are included. 

Organization: Healthcare Quality Improvement Partnership
National Bowel Cancer Audit, Open data - 2009-2010

Making clinical audit data transparent 

In his transparency and open data letter to Cabinet Ministers on 7 July 2011, the Prime Minister made a commitment to make clinical audit data available from the national audits within the National Clinical Audit and Patient Outcomes Programme. 

Each year data from the National Bowel Cancer Audit will be made available in CSV format. The data are also being made available on the data.gov website. 

What information is being made available? 

Audit participation by NHS Trust and data completeness for the key fields. 

Measures about the process of care given to patients. 

Information about care outcomes and treatment. 

Trusts and Networks are identified by name and their national code. These data do not list individual patient information, nor do they contain any patient identifiable data. 

The National Bowel Cancer Audit Project is a high profile, collaborative, national clinical audit for bowel cancer run jointly by The Health and Social Care Information Centre and the Association of Coloproctology of Great Britain and Ireland (ACPGBI). 

The NHS Information Centre's National Clinical Audit Support Programme (NCASP) provides project management and the technical infrastructure, while the ACPGBI provides clinical leadership and direction. National Bowel Cancer Audit Consultation Document (pdf 92KB). 

The audit aims to improve the quality of care and survival of patients with bowel cancer. It meets the requirements as set out in the NHS Cancer Plan, NICE guidelines and the Report of the Bristol Royal Infirmary Inquiry. 

The National Bowel Cancer Audit 2009/10 covers the time period from 1st August 2009 to 31st July 2010 and only Hospital sites within England are included. 



Organization: Healthcare Quality Improvement Partnership