Request an accessible format
This information can be made available in alternative formats such as easy read or large print and may be available in different languages, upon request. If you use assistive technology (such as a screen reader) and need a version of this document in a more accessible format, please email firstname.lastname@example.org and tell us what you need
Please see below, important documents related to the work and function of the Congenital Heart Network
Risk And Governance Documents »
Document Management Process »
Patient & Public Voice Documents »
CHD Board Papers »
Risk And Governance Documents
This describes how the Network identifies, manages and controls risks across the Network
This document describes the process whereby Network Incidents and Mortalities will be discussed in a meeting to be held twice a year. Providers are requested to complete an incident reporting form Incident Report Form
This is a standardised mortality reporting form to be used by all providers within our Network. This can be used locally for M&M reporting within individual Trusts for patients. This form is to be used to report all deaths where a diagnosis of congenital heart disease is relevant.
Please send a copy to the Network securely via NHS.net email to:
Please remove all patient identifiable data prior to sending to the Network
Document Management Process
The Network has set up Ratification Task and Finish Groups who are responsible for signing off documents on behalf of the CHD Network Board. This is the Terms of Reference Document for these groups.
Describes how the Network ensures that documents are up to date and relevant and where possible evidenced based.
Patient & Public Voice Documents
Are you interested in becoming a Network Patient and Public Voice Partner? Please see below for more information
We are always looking for patients and families to join our Network Patient and Public Voice Group”. Please see advert on how to apply for this important role. Please print off and display this advert in wards and clinical areas.
This document describes what is involved in taking on the role of a Patient and Public Voice Partner for the Network.
The attached pathway describes the steps that need to be taken in order to become a Patient and Public Voice Partner for the Network.
CHD Board Papers
CHD Board Meeting Notes from 26th March 2021
CHD Board Meeting Notes from 27th January 2021
CHD Board Meeting Notes from 28th September 2020
CHD Board Meeting Notes from 19th June 2020
CHD Board Meeting Notes from 13th January 2020
Network Annual Reports
NW CHD Network Annual Report 2020
Read the latest news from across the NW CHD Network