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Congenital Anomaly Statistics

Online Shop | Miscellaneous Print On Demand | Department of Health and Social Care |  Congenital Anomaly Statistics



National Congenital Anomaly and Rare Disease Registration Service. Congenital anomaly statistics 2017
National Congenital Anomaly and Rare Disease Registration Service. Congenital anomaly statistics 2017 is in stock now
Free UK delivery on National Congenital Anomaly and Rare Disease Registration Service. Congenital anomaly statistics 2017

In Paperback Format
National Congenital Anomaly and Rare Disease Registration Service. Congenital anomaly statistics 2017

£15.00
ISBN
9781787761506
Author
Public Health England
Published by
Dandy Booksellers Ltd
Publication Date
28 August 2019
Edition
2017
Format
Paperback
Extent
71 pages
Dimensions
A4 (210 x 297 mm)

This report is the National Congenital Anomaly and Rare Disease Registration Service’s (NCARDRS) third report on congenital anomalies. It describes the number of babies with 1 or more congenital anomalies delivered between 1 January and 31 December 2017.

This report is intended primarily as a useful resource for commissioners and providers of healthcare needed for the diagnosis and management of babies with congenital anomalies. It also provides high quality data for the use of researchers and those seeking detailed information about congenital anomaly prevalence in England. It is hoped that this annual public report will be of interest to healthcare professionals involved in the direct care of patients.

The ambition to provide a comprehensive national register relies on the commitment of healthcare professionals across the country to report babies diagnosed or suspected with congenital anomalies to NCARDRS. The multi source approach to data collection in NCARDRS is dependent on the dedication of healthcare staff in a range of settings including maternity units, neonatal units, diagnostic departments, genetic laboratories and many more. This collaborative approach enables high ascertainment and completeness of data and ensures consistency and standardisation across the country.

Thanks to the dedication of these notifying healthcare professionals, this important and reliable information is available for clinicians, researchers, patients and their families. 


National Congenital Anomaly and Rare Disease Registration Service. Congenital anomaly statistics 2016
National Congenital Anomaly and Rare Disease Registration Service. Congenital anomaly statistics 2016 is in stock now
Free UK delivery on National Congenital Anomaly and Rare Disease Registration Service. Congenital anomaly statistics 2016

In Paperback Format
National Congenital Anomaly and Rare Disease Registration Service. Congenital anomaly statistics 2016

£15.00
ISBN
9781787760516
Author
Public Health England
Published by
Dandy Booksellers Ltd
Publication Date
7 November 2018
Edition
2016
Format
Paperback
Extent
61 pages
Dimensions
A4 (210 x 297 mm)

This report is the National Congenital Anomaly and Rare Disease Registration Service’s (NCARDRS) second annual report. It primarily describes the number of cases with 1 or more congenital anomalies delivered between 1 January and 31 December 2016

This report is intended primarily as a useful resource for commissioners and providers of healthcare needed for the diagnosis and management of congenital anomalies. It also provides high quality data for the use of researchers and those seeking detailed information about congenital anomaly prevalence in England. It is hoped that this annual public report will be of interest to healthcare workers involved in the direct care of patients.

The ambition to provide a comprehensive national register relies on the commitment of healthcare professionals across the country to report cases to NCARDRS. The multiple source approach to data collection in NCARDRS relies on the dedication of healthcare staff in a range of settings including maternity units, neonatal units, diagnostic departments, genetic laboratories and many more. This multiple source approach enables high ascertainment and completeness of cases and ensures consistency and standardisation across the country. 



Online Shop | Miscellaneous Print On Demand | Department of Health and Social Care |  Congenital Anomaly Statistics

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