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Virtual Prenatal Genetics Short Course 2022

September 20 @ 9:30 AM - 12:45 PM

|Recurring Event (See all)

One event on September 20 2022 at 9:30 AM

One event on October 17 2022 at 9:30 AM

One event on October 18 2022 at 9:30 AM

One event on November 7 2022 at 9:30 AM

One event on November 8 2022 at 9:30 AM

This skills based course is designed to give midwives and other health professionals working in a prenatal testing setting tools to help them to enable patients to access appropriate onwards referral. These include obtaining a family history, identify high risk family histories, approaches to genetic testing, consent taking and counselling skills associated with providing information and results.

The course will provide the background scientific knowledge needed to understand the theory behind the application of genetics in a prenatal setting. The scientific content will be complemented with case based examples and practical exercises to connect the scientific theory to the application in your day to day practice.

Participants will be equipped with the basics of prenatal genetic counselling and managing complex scenarios as well as an update on new technologies. They will also gain skills in taking a family history and assessing when a referral on to clinical genetics is indicated.

 

All attendees will receive a certificate of attendance upon completion of the course. CPD accredited by Royal College of Midwives.

 

Format

6 half days on Zoom 19th September-8th November 2022

 

Agenda

Day 1:

  • Recognise basic inheritance patterns
  • Identify relevant family history and draw a family tree

Day 2:

  • Demonstrate the knowledge and communication skills to obtain informed consent for genetic testing in a prenatal setting

Day 3:

  • Compare types of genetic tests and recognise the situations that they might be used in

Day 4:

  • Discuss tools and procedures used to diagnose genetic conditions during or following pregnancy
  • Compare and contrast the role of different healthcare professionals in the prenatal setting

Day 5:

  • Demonstrate the use of knowledge about genetic testing gained to discuss a patient’s pathway involving genetic testing in pregnancy

Day 6:

  • Recognise the emotions that a patient undergoing genetic testing in a prenatal setting may experience and when further support might be needed
  • Recall how to refer to clinical genetics services and what information is useful to include in the referral

 

More information is available on the Guy’s and St Thomas’ website and don’t forget to book you place on Eventbrite.

Critical incident affecting genomics tests from Viapath

We have been experiencing issues with the IT systems at our Hub laboratory based at Guy’s Hospital as a result of recent extreme weather. We have been working hard to fix these issues and minimise the impact on our services. Please be aware that as a result of this critical incident you may experience some delays to receiving results and some test reports may look different. 

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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.