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May 2025 RDS newsletter now available. Expand this announcement to view.

Welcome to the May 2025 update from the RDS team

1.     RDS deployments

Three small-scale releases took place during April and May, including the following fixes and improvements:

  • Applying moderate severity security patch to Umbraco.
  • Fixes to:
    • Random ordering of tiles on mobile app
    • Simultaneous issuing of multiple copies of content review alerts
    • Content display on mobile app for the left hand menu navigation option
  • Whitelisting of Jotforms outcomes pages so that recommendations for action can be displayed following completion of a form or calculation.

2.     RDS performance

Two short outages took place on the mornings of 12th and 22nd May. Tactuum is still investigating the root cause and will report on this shortly.

3.     Redesign of Gentamicin and Vancomycin calculator interfaces

New designs have been produced which make the health board name and calculator title clear to the user on these calculator pages, with a warning message and link to ensure users access the right calculator for their board. These designs have been implemented in a test environment and are now under review.

4.     RDS Redesign, archiving and version control

We now plan to release at end of July 2025 the following major enhancements:  redesigned Right Decision Service homepage, new search and browse interface, upgraded archiving and version control, and capability to edit content adopted from the Shared Content Library. We will provide slides and demos in advance of the release to introduce users and editors to the new functionality.

5. Training sessions for RDS editors

Introductory webinars for RDS editors will take place on:

  • Monday 16 June 12.30-1.30 pm
  • Tuesday 24 June 3.45-4.45 pm

Running usage statistics reports using Google analytics

  • Wednesday 11th June: 2-3pm

 To book a place on any of these webinars, please contact Olivia.graham@nhs.scot providing your name, role, organisation, title and date of the webinar you wish to attend.

6.New RDS toolkits

The following toolkits were launched during March 2025:

7.New RDS developments

Work is progressing on a number of decision support systems that are part of the wider Right Decision Service platform, beyond the web and mobile apps:

  • The Patient Reported Outcome Measures system. A minimum viable product version will be available for functional testing by key stakeholders at end of July.
  • Pharmacogenomics decision support as an extension of the current high risk prescribing decision support integrated with primary care electronic health record systems. This is part of a European research and innovation project.
  • Planned Date of Discharge decision support system to be tested in NHS Lanarkshire. Will undergo user acceptance testing in July with a view to piloting from November.

8. Implementation projects

Public library services in Inverclyde, East Renfrewshire, Glasgow Life, Angus, Falkirk and Stirling have come forward to work with the RDS team, the Scottish Library and Information Council and local Realistic Medicine leads, to develop their role in engaging citizens in Realistic Medicine. This includes promoting the Being a partner in my care app: Realistic Medicine Together. This provides tools and resources to support conversations about what matters to the person,  shared decision-making and self-management.

 

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.

 

 

 

Women Who Refuse Blood Products, Obstetrics (401)

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

Most women will accept blood transfusion if there is a clinical need and they are fully informed. Some women may refuse transfusion because of specific personal or religious beliefs. The main group of women, who refuse transfusion of allogenic blood or primary blood components (red cells, white cells, plasma and platelets), are practising Jehovah’s Witnesses.

Applicable Unit Policies

 

Antenatal Management

  • At booking Identify women who may decline blood transfusion and transfer to RED pathway. (Highlight in Alerts and Management plan on Badgernet.)
  • Women declining blood transfusion should be booked for hospital delivery in a Consultant led unit. All women should be seen antenatally by  their  Consultant  preferably  before  24+0 weeks,  and advised  about the risk of haemorrhage, including management options and the increased risk of hysterectomy. This must be carefully documented.
  • Complete the refusal of Blood Transfusion Consent Form in file in the base notes. A copy should be given to the woman.(Appendix A) Complete the Advanced Directive. (Appendix B) and again put copy in basenotes and give woman copy.. Ideally by 24+0 weeks.
  • Ensure that the woman’s wishes are documented, ensuring that blood and primary blood components that the woman would not accept, and treatments that she will accept, are clearly documented and consented to. (Appendix A)
  • Arrange anesthetic review antenatally.
  • Blood group and antibody status should be checked routinely and the haemoglobin and serum ferritin should be checked every 6 weeks. Haematinics  should  be  given  throughout  pregnancy  to maximise iron stores. If the ferritin remains low despite oral iron then intravenous iron should be considered.

Elective Delivery

If elective induction is indicated aim to achieve this Monday, Tuesday or Wednesday in order that completed in weekdays. Elective caesarean section must be on a Consultant list. (Appendix D) Cell Salvage should ideally be available.

Intrapartum / Delivery Management

  • Inform Consultant Obstetrician and Anaesthetist when a woman declining blood transfusion is admitted in labour.
  • The labour should be managed routinely, by the most senior medical and midwifery staff available. Student midwives and junior medical staff should not conduct these deliveries.
  • The third stage of labour should be actively managed and routine prophylactic oxytocin should be given.
  • A Consultant Obstetrician should be present at any operative delivery (vaginal or caesarean section) if this is possible.
  • Cell salvage should ideally be available for elective deliveries.

Postnatal Management

  • The woman should not be left alone for at least an hour after delivery – one to one midwifery care.
  • A postnatal MEWS chart should be commenced.
  • After discharge women should be advised to report promptly if they have concerns about bleeding during the puerperium. Haematinics should be continued.

Management of Haemorrhage

  • The principle of management of haemorrhage is to minimise blood loss and avoid delay. Rapid decision-making may be necessary, particularly with regard to surgical intervention.
  • If significant bleeding occurs at any time during pregnancy, labour or the puerperium, the Consultant Obstetrician, Anaesthetist and Haematologist should immediately be informed. A second Obstetric &  Gynaecology Consultant  should  be  contacted  if laparotomy required.  This surgeon must  be suitably  skilled  to aid major surgery.
  • Start the standard management promptly (pdf link to Appendix E). The threshold for intervention should be lower than in other patients. Extra vigilance should be exercised to quantify any abnormal bleeding and to detect complications, such as clotting abnormalities, as promptly as possible.
  • Intravenous crystalloid should be used. Do not use Dextran
  • If available cell salvage may be life-saving if there is substantial blood loss. A cell sa ver set with additional leucocyte depletion filter to remove amniotic fluid components (order code RS1VAE) together with separate suction has been reported as a potential life-saving technique during caesarean section.
  • The woman and her family should be kept fully informed about what is happening  by  an informed  member  of  Massive obstetric  haemorrhage  can rapidly  become life threatening.  If standard treatment is not controlling the bleeding, she should be advised that blood transfusion is strongly recommended.
  • Surgical management of bleeding should include use of a B-Lynch Suture, intrauterine balloon, interventional radiology techniques, internal iliac artery ligation and hysterectomy. The woman’s life may be saved by timely hysterectomy, though even this does not guarantee   If hysterectomy  is  performed  the  uterine arteries  should  be  clamped  as  early  as  possible  in the procedure. Subtotal hysterectomy can be just as effective as total hysterectomy, as well as being quicker and safer. The timing of hysterectomy is a decision for the consultant on site. A second Consultants presence is advised only if this does not cause undue delay in definitive treatment.
  • If the woman requires transferred to an intensive care unit, the management there should include erythropoetin, parenteral iron therapy and adequate protein for haemoglobin Hyperbaric oxygen therapy is an option in life threatening anaemia due to PPH but availability is limited.
  • If, in spite of all care, the woman dies, her relatives require support like any other bereaved family. It is very distressing for staff to have to watch a woman bleed to death while refusing effective treatment. Support should also be promptly available for staff in these circumstances. Early contact with the Perinatal Counselling Service.

Legal and Ethical Aspects

Any patient is entitled to change her mind about a previously agreed treatment plan.

  • The doctor  must be  satisfied  that the woman is  not being subjected to pressure from others (including staff). It is reasonable to ask the accompanying persons to leave the room so that the doctor (with a midwife or other colleague) can ask her whether she is making her decision of her own free will. If she maintains her refusal to accept blood or blood products, her wishes should be respected. The legal position is that any adult patient (i.e. 16 years old or over) who has the necessary mental capacity  to do  so is entitled to refuse treatment, even if it is likely that  refusal will result in the patient’s death. No other person is  legally able to consent to treatment for that adult or to refuse treatment on that person’s behalf.

Note: This document does not apply to the neonate.

 

HELP AND ADVICE

Further help and advice on the non-blood management of Jehovah’s Witnesses may be obtained from the Hospital Liaison Committee of Jehovah’s Witnesses. They operate a 24/7 assistance arrangement. Contacts are as shown below:

Harry Crawford

22 Loch Goil

East Kilbride

Glasgow

G74 2EJ

Tel 01355 220 674

Mobile 07711 367409

harry@harry-crawford.com

John Allum

110 Brownside Road Cambuslang

GLASGOW

G72 8AF

Tel 0141.641.6206

Mobile 07836.704774

johnallum@hlcglasgow.co.uk

John Flack

17 Croft Road Balmore

TORRANCE

G64 4AL

Tel 01360.621865

Mobile 07775.837513

Johnflack080238@aol.com

Editorial Information

Last reviewed: 13/03/2018

Next review date: 31/03/2023

Author(s): Ann Duncan.

Approved By: Obstetrics Clinical Guideline Group

Document Id: 401

References

Useful Publications

  1. Royal College of Surgeons. Code of Practice for the Surgical Management of Jehovah’s Witness . London: IBSA Press; 2002
  2. Association of Anaesthetists of Great Britain and Ireland. Management of Anaesthesia for Jehovah’s Witness. 2nd London:AAGBI;2005 [www.aagbi.org/publications/guidelines/docs/jehovah’.pdf]
  3. RCOG green-top guideline for Blood Transfusion in Obstetrics- 47; July 2008