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Announcements and latest updates

Welcome to the Right Decision Service (RDS) newsletter for August 2024.

  1. Contingency planning for RDS outages

Following the recent RDS outages, Tactuum and the RDS team have been reviewing the learning from these incidents. We are committed to doing all we can to ensure a positive outcome by strengthening the RDS to make it fully robust and clinically resilient for the future.

We would like to invite you to a webinar on 26th September 3-4 pm on national and local contingency planning for future RDS outages.  Tactuum and the RDS team will speak about our business continuity plans and the national contingency arrangements we are putting in place. This will also be a space to share local contingency plans, ideas and existing good practice. We would also like to gather your views on who we should send communications to in the event of future outages.

I have sent a meeting request for this date to all editors – please accept or decline to indicate attendance, and please forward on to relevant contacts. You can also contact Olivia.graham@nhs.scot directly to register your interest in participating.

 

2.National  IV fluid prescribing  calculator

This UK CA marked calculator is now live at https://righdecisions.scot.nhs.uk/ivfluids  . It has been developed by a multiprofessional steering group of leads in IV fluids management, as part of the wider Modernising Patient Pathways Programme within the Centre for Sustainable Delivery.  It aims to address a known cause of clinical error in hospital settings, and we hope it will be especially useful to the new junior doctors who started in August.

Please do spread the word about this new calculator and get in touch with any questions.

 

  1. New toolkits

The following toolkits are now live;

  1. Updated guidance on current and future Medical Device Regulations

We have updated and simplified this guidance within our standard operating procedures. We have clarified the guidance on how to determine whether an RDS tool is a medical device, and have provided an interactive powerpoint slideset to steer you through the process.

 

  1. Guide to six stages of RDS toolkit development

We have developed a guide to support editors and toolkit leads through the process of scoping, designing, delivering, quality assuring and implementing a new RDS toolkit.  We hope this will help in project planning and in building shared understanding of responsibilities throughout the full development process.  The guide emphasises that the project does not end with launch of the new toolkit. Implementation, communication and evaluation are ongoing activities throughout the lifetime of the toolkit.

 

  1. Training sessions for new editors (also serve as refresher sessions for existing editors) will take place on the following dates:
  • Thursday 5 September 1-2 pm
  • Wednesday 24 September 4-5 pm
  • Friday 27 September 12-1 pm

To book a place, please contact Olivia.graham@nhs.scot, providing your name, organisation, job role, and level of experience with RDS editing (none, a little, moderate, extensive.)

7 Evaluation projects

Dr Stephen Biggart from NHS Lothian has kindly shared with us the results of a recent survey of use of the Edinburgh Royal Infirmary of Edinburgh Anaesthesia toolkit. This shows that the majority of consultants are using it weekly or monthly, mainly to access clinical protocols, with a secondary purpose being education and training purposes. They tend to find information by navigating by specialty rather than keyword searching, and had some useful recommendations for future development, such as access to quick reference guidance.

We’d really appreciate you sharing any other local evaluations of RDS in this way – it all helps to build the evidence base for impact.

If you have any questions about the content of this newsletter, please contact his.decisionsupport@nhs.scot  If you would prefer not to receive future newsletters, please email Olivia.graham@nhs.scot and ask to be removed from the circulation list.

 

With kind regards

 

Right Decision Service team

Healthcare Improvement Scotland

Fetal Tissue - handling and disposal (up to and including 23+6 weeks gestation) (340)

Warning

Objectives

This document provides guidance on the handling and disposal of tissue which contains, or potentially contains, fetal tissue of up to and including 23+6 weeks gestation.

Scope

All pregnancy tissue up to and including 23+6 weeks gestation

Audience

This guideline is intended for use by healthcare professionals working within GGC.  In particular this is relevant to Pathology Department Medical and BMS Staff, Mortuary MTO Staff Obstetrics and Gynaecology, Medical, Nursing, Midwifery and theatre staff in Obstetrics and Gynaecology, Medical and Nursing Staff working in Accident and Emergency.

Please report any inaccuracies or issues with this guideline using our online form

NHS GG&C Policy on the Handling and Disposal of Fetal Tissue (up to and including 23+6 weeks gestation) 

This document is to provide guidance on the handling and disposal of tissue which contains, or potentially contains, fetal tissue of up to and including 23+6 weeks gestation. 

This includes:

  • Medical Termination of Pregnancy tissue
  • Surgical Termination of Pregnancy tissue
  • Ectopic Pregnancy tissue
  • Any tissue from an Early Pregnancy Loss (including spontaneous loss, medically managed, surgically managed and MVA)
  • Fetuses of up to and including 23+6 weeks gestation where there has been a Post Mortem Examination
  • Retained products of conception specimens

Our aim is to ensure that all fetal tissue is handled appropriately and disposed of respectfully. This has been defined as Shared Cremation with agreement of the Department of Obstetrics and Gynaecology. The purpose of this document is to provide guidance and clarity as to the appropriate examination of tissue and the paperwork which is required to allow this examination and disposal. 

Specimen Flow

Medical Termination of Pregnancy

The majority of these specimens do not require histopathological assessment. If no histopathological examination is required then the tissue should be transferred directly to the Mortuary for sensitive disposal (cremation) along with a completed copy of Authorisation for burial or cremation following pregnancy loss up to 23 weeks and 6 days gestation (Form 2).

If the tissue is to be released directly to the family then a release of pregnancy tissue form should be completed by clinical staff. If the patient opts to take the specimen from the Pathology Department then the relevant section of Form 2 should be completed and submitted with the specimen. In addition, a completed PATH-COM-COMF-006 form accepting the associated risks of taking formalin fixed tissue from the pathology department requires to be completed. Pathology staff will complete this form with the family collecting the tissue.

If there are concerns about fetal anomalies and examination is required then appropriate Post Mortem Consent should be obtained.

Any specimen received without appropriate documentation will be stored in the Pathology Department and logged as a non-conformance. The specimen will not be processed until the correct paperwork is received and may be returned to the sender. If the correct paperwork has not been received within 12 weeks, the specimen will be sampled and processed to FFPE blocks and stored in the pathology archives. No glass slides or formal histopathology report will be prepared until a completed copy of Form 2 is received by the pathology department. Following receipt of a completed copy of Form 2, a replacement request form will be required in order to generate a report on Trak Care. The remainder of the specimen will be sensitively disposed of without further examination.

NB: If a molar pregnancy is suspected clinically, accurate details of the clinical team treating the patient must be included with the request form so that if an error is identified in Form 2, the clinical team can be contacted regarding the non-conformance in a timely manner.

A Datix will be raised by Pathology if an error is made in a Form 2 that is not rectified within 4 weeks of submitting the specimen. If a Form 2 is being resubmitted, then a replacement pathology request must be made via Trak Care to generate a pathology report on Trak Care.

Surgical Termination of Pregnancy

These specimens do not require histopathological assessment. They should be transferred directly to the Mortuary for sensitive disposal (cremation) along with a completed copy of Authorisation for burial or cremation following pregnancy loss up to 23 weeks and 6 days gestation (Form 2). If the patient opts to take the specimen from the Pathology Department then the appropriate section of Authorisation for burial or cremation following pregnancy loss up to 23 weeks and 6 days gestation (Form 2) should be completed and submitted with the specimen. In addition, a completed PATHCOM-COMF-006 form accepting the associated risks of taking formalin fixed tissue from the pathology department requires to be completed. Pathology staff will complete this form with the family collecting the tissue.

Any specimen received without appropriate documentation will be stored in the Pathology Department and logged as a non-conformance. The specimen will not be processed until the correct paperwork is received and may be returned to the sender. If the correct paperwork has not been received within 12 weeks, the specimen will be sensitively disposed of without further examination.

Ectopic Pregnancy Tissue

These specimens should be sent for histopathological examination for confirmation of ectopic pregnancy and assessment of associated pathology. These specimens should be submitted to the Pathology Department with a Pathology Request form (containing relevant clinical information) and with a completed Authorisation for burial or cremation following pregnancy loss up to 23 weeks and 6 days gestation (Form 2). Following reporting, any residual tissue will be transferred from the Pathology Department to the Mortuary for sensitive disposal (cremation). If the patient opts to take the specimen from the Pathology Department then the appropriate section of Authorisation for burial or cremation following pregnancy loss up to 23 weeks and 6 days gestation (Form 2) should be completed and submitted with the specimen. In addition, a completed PATH-COM-COMF-006 form accepting the associated risks of taking formalin fixed tissue from the pathology department requires to be completed. Pathology staff will complete this form with the family collecting the tissue.

Any specimen received without appropriate documentation will be stored in the Pathology Department and logged as a non-conformance. The specimen will not be processed until the correct paperwork is received and may be returned to the sender. If the correct paperwork has not been received within 12 weeks, the specimen will placed into FFPE blocks and processed for histology. The FFPE blocks to confirm the presence of an ectopic pregnancy will remain in the pathology archives and a histopathology report will be generated when a completed copy of Form 2 is received. If this is required, a replacement specimen request form will be required to generate a report on Trak Care.

Early Pregnancy Loss Tissue

This includes spontaneously passed tissue and surgically removed tissue. It is for the sender to decide whether histopathological examination is desirable.

Possible reasons for examination include

  • Confirmation of products of conception
  • Exclusion of gestational trophoblastic disease
  • Attempts at determining cause of recurrent miscarriage

If histopathological examination is required, then the specimen should be submitted to the Pathology Department with a Pathology Request form (containing relevant clinical information) and a completed Authorisation for burial or cremation following pregnancy loss up to 23 weeks and 6 days gestation (Form 2). Following reporting, any residual tissue will be transferred from the Pathology Department to the Mortuary for sensitive disposal (cremation). If the patient opts to take the specimen from the Pathology Department then the relevant section of Authorisation for burial or cremation following pregnancy loss up to 23 weeks and 6 days gestation (Form 2) should be completed and a completed PATH-COM-COMF-006 form accepting the associated risks of taking formalin fixed tissue from the pathology department requires to be completed. Pathology staff will complete this form with the family collecting the tissue.

If no histopathological examination is required and the patient opts for the hospital to sensitively dispose of the specimen, then the specimen should be transferred directly to the Mortuary for sensitive disposal (cremation) along with a completed Form 2. If no histopathological examination irequired and the patient opts to take the tissue from the hospital the relevant section of Form 2 should also be completed to provide an audit trail for the fetal tissue as well as a completed release of pregnancy tissue form. The tissue can be passed to the patient in a suitable container. The paperwork (Form 2) should be sent to the Mortuary for registration.

Any specimen received without appropriate documentation will be stored in the Pathology Department and logged as a non-conformance. The specimen will not be processed until the correct paperwork is received and may be returned to the sender. If the correct paperwork has not been received within 12 weeks, the specimen will be sampled to FFPE block but no glass slide or formal histopathology report will be available until a completed Form 2 is received. The remainder of the specimen will be sensitively disposed of without further examination. If a histopathology report is required following receipt of the completed form 2, then a replacement pathology request will be required to generate a report on Trak Care.

NB: If a molar pregnancy is suspected clinically, accurate details of the clinical team treating the patient must be included with the request form so that if an error is identified in Form 2, the clinical team can be contacted regarding the non-conformance in a timely manner. A Datix will be raised by Pathology if an error is made in a Form 2 that is not rectified within 4 weeks of submitting the specimen. If a Form 2 is being resubmitted, then a replacement pathology request must be made via Trak Care to generate a pathology report on Trak Care.

Recurrent Miscarriage or Suspected Underlying Cytogenetic Cause of Pregnancy Loss

RCOG Guidelines (GT17) recommend that cytogenetic analysis of the products of conception should be performed for all couples with a history of recurrent miscarriage, (loss of three or more pregnancies).

Previously this required division of tissue for both histological and cytogenetic analysis. With the centralization of laboratory services this is no longer necessary. Products of conception should be sent complete to Cytogenetics (in a dry sterile container – not in formalin) with the relevant request form giving a clear history and a completed Form 2. Please ensure that the sample container itself is also labelled with appropriate patient identifiers. Following examination within both Cytogenetics and Pathology, any residual tissue will be transferred from the Pathology Department to the Mortuary for sensitive disposal (cremation). The same applies to the examination of fetal and placental tissues where an underlying cytogenetic cause is suspected e.g. following detection of abnormality on early ultrasound scan or miscarriage associated with raised risk of aneuploidy on antenatal screening.

Fetuses up to and including 23+6 weeks gestation where there is to be a Post Mortem Examination

These specimens should be transferred directly to the mortuary along with any associated placental tissue and appropriately completed Post Mortem Consent Forms. The further handling of these requests is detailed elsewhere.

Retained Products of Conception Specimens in which there has been a separately identified fetus

This clinical scenario has been previously discussed at the Sensitive Disposal Committee. It has been agreed that there is no requirement to supply a Form 2. Surplus tissue will be disposed of as clinical waste.

Tissue Type

Tissue Flow

Sample and Paperwork Required

Medical Termination of Pregnancy tissue

Histopathology assessment not required and tissue for shared cremation/sensitive disposal

  • pathology/tissue specimen dry specimen -completed Form 2

Send to the mortuary, QEUH

Medical Termination of Pregnancy tissue

If specimen does not require Histopathology assessment and being released to family without further assessment

  • pathology/tissue specimen dry
  • completed Form 2 – send to pathology for registration -release of pregnancy tissue form
  • Tissue to be sent with parent

Medical Termination of Pregnancy tissue

If specimen requires histopathology assessment

  • pathology/tissue specimen in formalin
  • completed Form 2
  • pathology request form

Send to the pathology department, QEUH *

Medical Termination of Pregnancy tissue

If specimen requires cytogenetic and histopathology assessment

  • pathology/tissue specimen in sterile dry pot
  • completed Form 2
  • pathology request form
  • cytogenetics request form

Send to the Cytogenetics department, QEUH*

Medical Termination of Pregnancy tissue

If specimen requires postmortem assessment

  • pathology/tissue/fetal specimen
  • completed Form 2
  • pathology request form (for placenta)
  • completed PM authorisation form

Send fetus and placenta as dry sample to mortuary

Send to the pathology department, QEUH*

Surgical Termination of Pregnancy tissue

Histopathology assessment not required

  • pathology/tissue specimen dry specimen -completed Form 2

Send to the mortuary, QEUH*

Surgical Termination of Pregnancy tissue

If specimen requires histopathology assessment

  • pathology/tissue specimen in formalin
  • completed Form 2
  • pathology request form

Send to the pathology department, QEUH*

If suspected molar pregnancy please ensure clear documentation of lead clinician and contact details

Surgical Termination of Pregnancy tissue

If specimen requires cytogenetic and histopathology assessment

  • pathology/tissue specimen in dry sterile pot
  • completed Form 2
  • pathology request form
  • cytogenetic request form

Send to the Cytogenetics department, QEUH*

Ectopic Pregnancy tissue

Histopathology required

  • pathology specimen in formalin
  • completed Form 2
  • pathology request form

Send to Pathology Department, QEUH*

Tissue from an Early Pregnancy Loss (pregnancy loss up to 11+6 weeks gestation)

Histopathology required

  • pathology/tissue specimen in formalin
  • completed Form 2
  • pathology request form

Send to Pathology Department, QEUH *

Tissue from an Early Pregnancy Loss (pregnancy loss up to 11+6 weeks gestation)

Histopathology NOT required

  • pathology specimen (dry ) -completed Form 2

Send to the Mortuary, QEUH

Tissue after recurrent miscarriage (3 consecutive early losses)

Tissue for histopathology and cytogenetics

  • pathology specimen in dry sterile container -pathology request
  • cytogenetics request -completed Form 2

Send to Cytogenetics department QEUH*

Fetus of between 11 and 23+6 weeks gestation where there is a Post Mortem Examination (postmortem requests for less than 11 weeks gestation MUST be discussed with a pathologist)

Histopathology and Post

Mortem Examination required

  • pathology/tissue/fetal specimen
  • completed Form 2
  • pathology request form (for placenta)
  • completed PM authorisation form

Send fetus and placenta as dry sample to mortuary

Send to the mortuary department, QEUH*

Retained products of conception (RPOC) specimen in which there has been a separately identified fetus.

Histopathology required

  • Pathology/tissue specimen in formalin
  • Pathology request to confirm RPOC
  • No need for Form 2 for RPOC component

Send to Pathology Department QEUH*

Retained products of conception (RPOC) specimen with NO separately identified fetus

Histopathology required

  • Pathology/tissue specimen in formalin
  • Pathology request to confirm RPOC
  • Completed Form 2

Send to Pathology department QEUH*

*if parents want to take tissue home from mortuary following cytogenetics and histopathology, they will require to have a Form PATH-COM-COMF-006 completed at the time of collection from pathology. This form makes them aware of the risks of handling tissue that has been stored in formalin. Pathology staff will complete the form with the family collecting the tissue. Photographic Identification is required for collection of tissue. Please make the family aware that there may not be any tissue remaining after examination.

Editorial Information

Last reviewed: 14/06/2022

Next review date: 14/07/2025

Author(s): Dr Felicity Watson, Claire Higgins.

Version: 3

Approved By: Gynaecology Clinical Governance Group

Document Id: 340