There are CKS guidelines on management of Hypertension in Pregnancy (1) - includes advice on pre-eclampsia and post partum follow-up.
***Update June 2025** There is currently no local guidance or an established formulary position regarding the use of aspirin in pregnancy in BNSSG. The antenatal teams and midwives may advise on use of aspirin which is currently off label.
The BNSSG Formulary team are currently involved in a research project with the University of Bristol – the Medicines Adherence in Pregnancy Study – Aspirin (MAP-A), which aims to investigate the factors influencing adherence to low-dose aspirin in pregnancy. As part of this work, a formulary application through the Joint Formulary Group will be submitted to support a formal position on the off-label use of aspirin for this indication.
The CKS guidelines give advice on managing women at high risk of, or exhibiting clinical features of pre-eclampsia (1) which advises the following:
Prescribing aspirin for women assessed to be at high risk of pre-eclampsia:
Other trusts and ICBs have existing information for patients on use of aspirin in pregnancy that may also be useful (2,3).
Please see the Maternity Services section for advice on how to refer.
Please see the CKS guidelines below for advice on management during the postpartum period:
Postpartum follow-up | Management | Hypertension in pregnancy | CKS | NICE
The guideline gives the following advice about follow up of this group of patients:
The secondary care NBT Guideline Hypertension in Pregnancy includes pathways on management of pre-eclampsia and eclampsia.
(1) Hypertension in pregnancy | Health topics A to Z | CKS | NICE
(3) Low dose aspirin (150mg) in pregnancy - East Sussex.pdf
Efforts are made to ensure the accuracy and agreement of these guidelines, including any content uploaded, referred to or linked to from the system. However, BNSSG ICB cannot guarantee this. This guidance does not override the individual responsibility of healthcare professionals to make decisions appropriate to the circumstances of the individual patient, in consultation with the patient and/or guardian or carer, in accordance with the mental capacity act, and informed by the summary of product characteristics of any drugs they are considering. Practitioners are required to perform their duties in accordance with the law and their regulators and nothing in this guidance should be interpreted in a way that would be inconsistent with compliance with those duties.
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