midwifery

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RCNi webinar series: From Niche to Necessity: Genomics in routine care

Online , United Kingdom

NHS England and NHS Improvement and Health Education England’s Genomics Education Programme have partnered with the RCNi and extend a warm invitation to you to join  an introductory series of 3 webinars exploring genomics, its use in healthcare and the opportunities it brings for nurses, midwives, and health visitors. With no prior knowledge of genomics […]

Recurring

Wellcome Trust Nursing Genomics & Healthcare Virtual Conference

Online , United Kingdom

Nurses comprise over 50% of the global healthcare workforce, and have an important role in bringing the benefits of genomics to patients. Despite this, genomics has not been systematically incorporated into nursing teaching curricula, and there have been no significant changes in nursing practice that bring genomics into day-to-day health care. The inaugural conference aims to […]

Recurring

Virtual Prenatal Genetics Short Course

Online , United Kingdom

This online course accredited by the Royal College of Midwives is designed to give midwives and other health professionals working in a prenatal testing setting, the tools to help them to enable patients to access appropriate onwards referral. This includes: obtaining a family history, identify high risk family histories, approaches to genetic testing, consent taking, […]

Niche to Necessity: The Northern Return

Online , United Kingdom

Following on from the highly successful ‘Niche to Necessity’ webinars in summer 2021, the North East and Yorkshire and North West Genomic Medicine Service Alliances, in collaboration with Health Education England North West have partnered with the RCNi and extend a warm invitation to you to join us for ‘Niche to Necessity: The Northern Return. This […]

RCOG: Genomics in perinatal medicine webinar

Online , United Kingdom

This free on-demand webinar from the Royal College of Obstetricians and Gynaecologists, will explore the use, potential and challenges of implementing genomics in perinatal medicine. Donna Kirwan, Midwifery Lead in NHS England and NHS Improvement’s Genomics Unit, will discuss midwives’ role in prenatal genetic testing. Who should attend: All clinicians in Obstetrics Allied Healthcare Professionals […]

Lunch and Learn: Think Patient Care, Think Genomics

Online , United Kingdom

Session One: Cystic Fibrosis screening and diagnosis Join us for our first edition of Lunch and learn, a session for nurses and midwives focused on Cystic Fibrosis. Speakers and topics covered:   Carrier testing Cathryn Moss, Principle Genetic Counsellor, St George’s Hospital This session will offer nurses and midwives a practical guide to Cystic Fibrosis […]

Lunch and Learn: Think Patient Care, Think Genomics

Online , United Kingdom

Session Two: Monogenic Diabetes in pregnancy Join us for our second edition of Lunch and learn, a session for nurses and midwives focused on Monogenic Diabetes.   Monogenic diabetes is a rare form of diabetes caused by a mutation in a single gene and can often be misdiagnosed as type 1 diabetes. Accurate diagnosis and […]

Lunch and Learn: Think Patient Care, Think Genomics

Online , United Kingdom

Session Three: Lynch Syndrome Join us for our third edition of Lunch and learn, a series of webinars for nurses and midwives to gain insight into how genomic testing is used across different areas of healthcare. Professionals will share their expertise of genomic tests available for patients through different patient pathways.   Speakers and topics […]

Lunch and Learn: Think Patient Care, Think Genomics

Online , United Kingdom

Session Fifth: Spinal Muscular Atrophy Spinal muscular atrophy (SMA) is a genetic condition affecting the central nervous system, peripheral nervous system, and voluntary muscle movement (skeletal muscle). During this session we will hear from professionals in the field on SMA management, genetic testing, and treatments available as well as hearing from a patient advocate. Agenda: […]

With any Whole Genome Sequencing (WGS) test ordered, a Record of Discussion (RoD) form will also need to be submitted. This document is to record the patient’s consent for genomic testing and their choice on taking part in research. Guidance on the patient choice conversation can be found here
 
This RoD form will be available for clinicians to download from this webpage. Once completed with the patient, it can be send to the lab with the corresponding test order form and sample.
Tests available to order will be listed in the National Genomic Test Directory. A test order form will soon be made available for clinicians on this webpage to download and complete. This form will include the address of the laboratory that the appropriate sample and completed form needs to be sent to.
 
Until the new Genomic Laboratory Service goes live, please continue to follow existing test order processes.
 
Later this year, the online test ordering tool for Whole Genome Sequencing will be integrated into the National Genomics Informatics System (NGIS) and clinicians will be able to search or filter to find a clinical indication, confirm eligibility criteria and start the test request process for their patient.