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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.

 

 

 

Hypertension Eclampsia Management (402)

Warning

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

Eclampsia is a life threatening complication of pregnancy. 

UK incidence is about 1 per 2000 maternities.

Seizure incidence: 38% pre-labour, 18% during labour, 44% postnatal

Pathophysiology is thought to involve cerebral vasospasm leading to ischaemia, disruption of the blood brain barrier and cerebral oedema. 

Neurological complications may include coma, focal motor defects and cortical blindness. Cerebrovascular haemorrhage is a complicating factor in 1- 2 % of cases.

Eclampsia is usually part of a multisystem disorder. There may be little or no warning that a seizure is imminent and no evidence of existing "pre-eclampsia". All pregnant women regardless of parity are at risk. There is a significant increased risk in women in the 15-19 year age group and women with previous eclampsia. 

Acute management of eclampsia

A

AIRWAY

(Jaw thrust, High flow O2)

& LATERAL TILT & CALL FOR HELP 2222 

B

BREATHING

Assess, ventilate as required.

C

CIRCULATION

Assess (BP, pulse, O2 saturation) & Access

  • Site 2 large bore cannulae (14g ideally, minimum 16g)
  • Obtain blood FBC,U&E, LFT, urate, coagulation screen
  • G&S

C1: CONTROL SEIZURE

C2: CONTROL BLOOD PRESSURE

C3: CONTROL FLUID BALANCE

*** The “Eclampsia” box contains all the necessary drugs, antidotes and instructions ***

D

DELIVERY PLAN

E

EVALUATE

Reassess monitoring and Investigations

C1: CONTROL SEIZURE

Magnesium Sulphate is the drug of choice unless there are specific contra indications to its use.

Magnesium Sulphate:

Loading Dose (by hand):                      

  • 4 grams IV over 5 minutes
    (Add 4 grams (8 mls of 50%) Magnesium Sulphate to 12 mls Normal Saline)          

Maintenance Infusion Dose:

  • IV infusion 1 gram Magnesium Sulphate per hour                 

Maintenance Infusion Preparation:

  • 10 grams (20 mls of 50%) Magnesium Sulphate made up to 50 mls by adding to 30 mls normal saline in a 60 ml luer lock syringe
  • Infusion rate is 1 gram (5 mls) per hour via an syringe driver

Infusion is maintained at 1 gram/hr for 24 hours provided:

  • Respiratory rate > 14 per minute
  • Urine output > 25mls/hour, and
  • Patellar reflexes are present

NB:  The volume of the Magnesium Sulphate infusion must be included as part of  the total fluid maintenance infusion for the patient of 85ml/hour

Recurrent Seizures on Treatment:

  • Give a 2nd bolus dose of Magnesium Sulphate 2 grams over 5 minutes by hand (do not stop infusion)
  • add 2 grams (4 mls of 50%) Magnesium Sulphate to 6 mls of Normal Saline
  • One dose only

If further seizures despite 2nd bolus give Diazepam 10mg IV.  Intubation may be required to protect airway and ensure adequate oxygenation.

Magnesium Sulphate – Patient Monitoring:

Reflexes:

  • Patellar reflexes after completion of loading dose and hourly whilst on maintenance dose (use arm reflexes if functional regional anaesthesia).
  • If reflexes are absent stop infusion until reflexes return and check Magnesium level.

Oxygen Saturation / Respiratory Rate:

  • Continuous O2 saturation should be assessed.
  • Perform respiratory rate every 15 minutes
  • If O2 saturation < 94% or respiratory rate < 14 / min, administer O2 (4 L/min via Hudson mask), stop Magnesium Sulphate infusion and call anaesthetist. Check Magnesium level. Consider antidote

Urine Output:

Monitor hourly.

If >20 ml/h - continue Magnesium Sulphate infusion.

If 10 - 20 ml/h & creatinine <150mmol/l - continue as protocol and recheck Magnesium level every 2 hours.

If 10 - 20 ml/h & creatinine > 150mmol/l (or urea >10) - recheck Magnesium levels immediately and every 2 hours. Decrease infusion rate to 0.5gram/hour.

If < 10 ml/h - stop infusion and check Magnesium level.

Biochemical Monitoring (Magnesium levels):  This is not routine. If required then see below.

The Therapeutic range is 2-4 mmol/l.

Low If < 2 mmol/l - Maintain infusion at current rate.  Recheck in 2 hours.

Therapeutic If 2 -3.5 mmol/l - Continue infusion at current rate. Recheck in 2 hours if clinical indication remains.

High If 3.55 - 5 mmol/l - STOP INFUSION for 15 min and then recommence at half previous infusion rate and recheck in 1 hour.

Very High If > 5mmol/l - STOP INFUSION and consider antidote. See below for further details.

Magnesium Sulphate toxicity and management:

Clinical Features

   Mg level

Action

Loss of Patellar reflexes
Weakness
Nausea, Flushing
Double vision
Slurred speech
Somnolence 

circa 5 mmol/l

STOP INFUSION

GIVE ANTIDOTE
10 ml of 10% Calcium Gluconate (1gram)
Slow IV inject over 10 mins. 
CHECK Magnesium level.  

Muscle Paralysis

circa 6-7.5 mmol/l

STOP INFUSION

GIVE ANTIDOTEAS ABOVECHECK
Magnesium level
.  

Respiratory Arrest
Cardiac Arrest 

circa 12 mmol/l

STOP INFUSION

INSTITUTE CPR 
2222 CALL Obstetric and cardiac arrest team INTUBATE AND VENTILATE
GIVE ANTIDOTE AS ABOVE 
CHECK Magnesium level

C2: CONTROL BLOOD PRESSURE

  • MAP > 140 mm Hg is an obstetric emergency

  • No evidence that one particular drug is superior for treatment. Labetalol tends to be the first line drug of choice in this locality.

  • Continuous fetal monitoring is necessary because lowering of maternal BP may lead to fetal distress, particularly if there is associated IUGR

  • Automated oscillometric devices may underestimate BP

  • Commence MEWS chart (one large bold box per hour)

  • MAP >140 mm Hg - measure BP every 5 minutes

  • MAP 125 -140 mm Hg - measure BP every 15 minutes

  • Aim for gradual reduction in BP to around 130-140 / 90 - 100 mmHg (MAP < 125)

  • Site 2 x wide bore IV cannula & check BP bloods (U+E, LFT, urate, FBC +/- coagulation if platelet count is < 150 or previous abnormality) 6 hourly if patient stable, X-match 2 units blood

  • Foley catheter inserted and hourly urine volumes commenced

  • Continuous pulse oximetry

Antihypertensive treatment for hypertensive crisis (flowchart)

If Labetalol contraindicated or above labetalol regime has failed to control blood pressure - Second Line Agent (Hydralazine OR Nifedipine) (flowchart)

Antihypertensive drugs

Labetalol:

Contraindications including:

Asthma, Bronchospasm, Uncontrolled heart failure

IV bolus:    

50 mg over 5 minutes
i.e. 10 mls of 5 mg/ml
Can be repeated; and/or followed by infusion (see chart)

Infusion preparation: 

Prepare 5 mg/ml infusion
i.e.  300 mg Labetalol in 60mls
Commence infusion at 50 mg (10 mls) per hour.

Nifedipine:

Contraindications including: Hypersensitivity to nifedipine, or to other dihydropyridines because of the theoretical risk of cross-reactivity, or to any of the excipients, Angina, Recent MI, Aortic Stenosis
  (Care with Magnesium Sulphate – see note below*)
Preparation:  10 mg capsule orally (swallowed whole)Repeated doses of 10 mg can be given at 6 hourly intervals

Hydralazine:

Contraindications: Hypersensitivity to hydralazine or dihydralazine
Connective tissue disorders
Severe tachycardia and heart failure with high output cardiac failure (e.g. in thyrotoxicosis)
Myocardial insufficiency due to mechanical obstruction (e.g. in the presence of aortic or mitral stenosis or constructive pericarditis)
Isolated right ventricular failure due to pulmonary hypertension (cor pulmonale)
Dissecting aortic aneurysm
IV bolus: 5 mg slowly over 5 minutes
Boluses can be repeated at 20 minute intervals, but may be simpler to start infusion(
A 5 mg dose can be effective for 6 hours)
Infusion preparation:   Prepare 1 mg/ml infusion i.e.  40 mg Hydralazine made to 40mls with normal saline.
Infuse at 10 mg (10 mls) per hour

*Note

There are 2 case reports of neuromuscular blockade resulting from simultaneous use of Nifedipine and Magnesium Sulphate.  However, 1,469 women were assigned to receive Magnesium Sulphate and Nifedipine in the Magpie trial, and no such blockade was reported.  Similarly, no adverse events were reported in RCTs comparing Hydralazine with Nifedipine in which all, or some, women received magnesium sulphate.  The risk of neuromuscular blockade is therefore likely to below. MAP > 140 mm Hg is an obstetric emergency.

C3: CONTROL FLUID BALANCE

  • The main risk is of pulmonary oedema to iatrogenic fluid overload.
  • Patients should be fluid restricted (85mls per hour of total input).
  • Document hourly urine output on MEWS chart
  • Oliguria is common in severe pre-eclampsia.
  • The natural diuresis may not occur for at least 12 hours post delivery.
  • Renal failure is uncommon.

  • Furosemide should be reserved for pulmonary oedema and prescription must be discussed with consultant obstetrician.

  • In persisting oliguria U&Es should be checked 6 hourly.
  • In persisting oliguria: urine osmolality that is not concentrated, or high potassium levels indicates renal failure and renal physicians should be contacted.

  • CVP monitoring can be misleading.
  • Consultant obstetrician on-call must be informed if CVP line is considered.

Delivery

  • Delivery is the definitive treatment for severe pre-eclampsia/eclampsia
  • Mother MUST be stabilised prior to delivery irrespective of circumstances (e.g. fetal distress)
  • HDU support is required post delivery
  • ITU if ventilated

N.B.  Avoid ergometrine use. Skip to next medical treatment if uterine atony (PPH guideline). 

Editorial Information

Last reviewed: 22/12/2015

Next review date: 15/02/2021

Author(s): Janet Brennand.

Approved By: Obstetrics Clinical Governance Group

Document Id: 402