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Please see below, important documents related to the work and function of the Congenital Heart Network
Risk And Governance Documents »
Network Documents »
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. Please be careful to ensure you follow data protection rules when sending confidential emails. The Alder Hey email address is accredited to DCB1596 standards: firstname.lastname@example.org
Please remove all patient identifiable data prior to sending to the Network
Describes how the Network ensures that documents are up to date and relevant and where possible evidenced based.
Attached is the Network Media Consent Form to be used by the Network when interviewing, filming or taking pictures of both staff and patients for Network publications only.
The Network Memorandum of Understanding describes the role and function of the North West, North Wales & the Isle of Man Congenital Heart Disease Network and the role and function of its interdependent organisations.
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.
The purpose of this document is to describe the approach that the North West, North Wales and the Isle of Man Operational Delivery Network intends to take to meet regularly with CHD providers within its footprint in order review progress against the delivery of nationally recognised CHD standards.
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.
Here is a competency based framework to support the development and role of the Nurse with a special interest in ACHD.
Here is a competency based framework to support the development and role of the paediatric nurse with a special interest in congenital heart disease.
This document outlines what is involved in becoming a nurse with a special interest in ACHD.
This document outlines what is involved in becoming a paediatric nurse with a special interest in CHD.
CHD Board Papers
CHD Board Meeting Notes from 17th October 2022
CHD Board Meeting Notes from 15th July 2022
CHD Board Meeting Notes from 24th January 2022
CHD Board Meeting Notes from 13th October 2021
CHD Board Meeting Notes from 28th June 2021
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 2021
NW CHD Network Annual Report 2020
Read the latest news from across the NW CHD Network