Limit acute treatment to less than 10 days per month (on average 2 days per week) to prevent development of medication overuse headache.
Welcome to the March 2025 update from the RDS team
1.1 Stability issues - Tactuum implemented a fix on 24th March which we believe has finally addressed the stability issues experienced over recent weeks. The issue seems to have been related to the new “Tool export” function making repeated calls for content when new toolkit nodes were opened in Umbraco. No outages have been reported since then, and no performance issues in the logs, so fingers crossed this is now resolved.
1.2 Toolkit URL redirects failing– these were restored manually for the antimicrobial calculators on the 13th March when the issue occurred, and by 15th March for the remainder. The root cause was traced to adding a new hostname for an app migrated from another health board and made live that day. This led to the content management system automatically creating internal duplicate redirects, reaching the maximum number of permitted redirects and most redirects therefore ceasing to function.
This issue should not happen again because:
1.3 Gentamicin calculators – Incidents have been reported incidents of people accessing the wrong gentamicin calculator for their health board. This occurs when clinicians are searching for the gentamicin calculator via an online search engine - e.g. Google - rather than via the health board directed policy route. When accessed via an external search engine, the calculator results are not listed by health board, and the start page for the calculator does not make it clearly visible which health board calculator has been selected.
The Scottish Antimicrobial Prescribing Group has asked health boards to provide targeted communication and education to ensure that clinicians know how to access their health board antimicrobial calculators via the RDS, local Intranet or other local policy route. In terms of RDS amendments, it is not currently possible to change the internet search output, so the following changes are now in progress:
We would encourage all editors and users to use the Help and Support standard operating procedure and the Editors’ Teams channel to highlight issues, even if you think they may be temporary or already noted. This helps the RDS team to get a full picture of concerns and issues across the service.
A new presentation illustrating how RDS supports all partners in the patient journey – multiple disciplines across secondary, primary, community and social care settings – as well as patients and carers through self-management and shared decision-making tools – is now available. You will find it in the Promotion and presentation resources for editors section of the Learning and support toolkit.
A new user guide is now available in the Guidance and tips section of Resources for providers within the Learning and Support area, explaining how to embed content from Google Calendar, Google Maps, Daily Motion, Twitter feeds, Microsoft Stream and Jotforms into RDS pages. A webinar for editors on using this new functionality is scheduled for 1 May 3-4 pm (booking information below.)
A new checklist to support editors in making all the checks required before making a new toolkit live is now available at the foot of the “Request a new toolkit” standard operating procedure. Completing this checklist is not a mandatory part of the governance process, but we would encourage you to use it to make sure all the critical issues are covered at point of launch – including organisational tags, use of Alias URLs and editorial information.
Introductory webinars for RDS editors will take place on:
Special webinar for RDS editors – 1 May 3-4 pm
This webinar will cover:
Running usage statistics reports using Google analytics
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.
The following toolkits were launched during March 2025:
SIGN guideline - Prevention and remission of type 2 diabetes
Valproate – easy read version for people with learning disabilities (Scottish Government Medicines Division)
Obstetrics and gynaecology induction toolkit (NHS Lothian) – password-protected, in pilot stage.
Oral care for care home and care at home services (Public Health Scotland)
Postural care in care homes (NHS Lothian)
Quit Your Way Pregnancy Service (NHS GGC)
Release of the redesign of RDS search and browse, archiving and version control functionality, and editing capability for shared content, is now provisionally scheduled for early June.
The Scottish Government Realistic Medicine Policy team is leading development of a national approach to implementation of Patient-Reported Outcome Measures (PROMs) as a key objective within the Value Based Health and Care Action Plan. The Right Decision Service has been commissioned to deliver an initial version of a platform for issuing PROMs questionnaires to patients, making the PROMs reports available from patient record systems, and providing an analytics dashboard to compare outcomes across services. This work is now underway and we will keep you updated on progress.
The RDS team has supported Scottish Government Effective Prescribing and Therapeutics Division, in partnership with Northern Ireland and Republic of Ireland, in a successful bid for EU funding to test develop, implement and assess new integrated care pathways for polypharmacy, including pharmacogenomics. As part of this project, the RDS will be working with NHS Tayside to test extending the current polypharmacy RDS decision support in the Vision primary care electronic health record system to include pharmacogenomics decision support.
We have just completed a series of three workshops consulting on proposed improvements to the Being a partner in my care: Realistic Medicine together app, following piloting on 10 sites in late 2024. This app has been commissioned by Scottish Government Realistic Medicine to support patients and citizens to become active partners in shared decision-making and encouraging personalised care based on outcomes that matter to the person. We are keen to gather more feedback on this app. Please forward any feedback to ann.wales3@nhs.scot
Limit acute treatment to less than 10 days per month (on average 2 days per week) to prevent development of medication overuse headache.
Please consider a prescription of a triptan, as per BNF. As a first option we recommend sumatriptan 50mg-100mg orally, as per SIGN 155.
Types of triptan
There are seven different triptans – almotriptan, eletriptan, frovatriptan, naratriptan, rizatriptan, sumatriptan, zolmitriptan. Response to different triptans is variable, and people who fail to respond to one triptan may respond to another. Therefore, if the patient does not respond to one triptan after use in three separate attacks, consider an alternative triptan. It can be worth trying triptans in sequence to find the most suitable of any individual patient. Note that naratriptan and frovatriptan have a slower onset but a longer half-life (approximately 5-6h for naratriptan; 25h for frovatriptan) and are therefore useful if patients describe recurrence of headache with a shorter acting triptan. All preparations come in tablet form. Sumatriptan also comes as a subcutaneous injection, sumatriptan and zolmitriptan come in nasal spray preparations (useful if prominent nausea) and rizatriptan and zolmitriptan also come in an orodispersible (melt) preparation.
Adverse effects
Patients should be warned that triptan sensations and/or sedation may occur. Symptoms may include tightness in the jaw, throat, or chest, or pins and needles in the face.
Cautions and contraindications
Triptans are contraindicated in coronary heart disease, peripheral vascular disease, or those with a history of stroke, and are cautioned in those with Raynaud’s phenomenon. They should not be used in patients with a history or moderate or severe hypertension. Do not prescribe if blood pressure measurements are consistently above 140/90mmHg. While triptans are not licensed for adults greater than 65 years, there is no reason they can’t be used. Vascular risk factors are more common and should be actively looked for in this age group.
How to Take Triptans
Triptans should be taken at the onset of the headache pain, and are more effective when taken early in an attack. Treatment frequency should be limited to two days per week (up to 2 doses can still be taken in any one day if needed) – more frequent use can result in medication overuse headache. If the first dose is ineffective, a second dose should not be taken for the same attack. If there is response to the first dose, but symptoms recur, a second dose may be taken provided there is a minimum of 2 hours between doses of almotriptan, eletriptan, frovatriptan, rizatriptan, sumatriptan, zolmitriptan, and 4 hours between doses for naratriptan.
Drug Interactions (not exhaustive)
Triptans should not be combined with monoamine oxidase inhibitors.
Triptans are not contra-indicated with Selective Serotonin Reuptake Inhibitors (SSRIs).
In patients taking propranolol, limit rizatriptan to the 5mg dose, and ensure a minimum separation of 2h between taking propranolol and rizatriptan. No more than 2 doses of rizatriptan should be taken in a 24h period.
Please check BNF for drug interactions in those taking antibiotics, antifungal agents, cimetidine, antiretroviral agents, and verapamil – interactions vary between triptans.
Although all UK summary of product characteristics caution against the concomitant use of triptans and selective serotonin reuptake inhibitor (SSRI) / serotonin – norepinephrine reuptake inhibitor (SNRI) anti-depressants due to the risk of serotonin syndrome, in practice this combination can be taken safely in most patients. It is the opinion of the authors that this combination is not contra-indicated. Nonetheless, patients should be monitored for signs of serotonin syndrome if this combination is used.
Rimegepant is an oral selective calcitonin gene-related peptide (CGRP) receptor antagonist. It is thought to relieve migraine by blocking CGRP-induced neurogenic vasodilation, returning dilated intracranial arteries to normal by halting the cascade of CGRP-induced neurogenic inflammation which leads to peripheral and central sensitisation and / or by inhibiting the central relay of pain signals from the trigeminal nerve to the caudal trigeminal nucleus.
For patients who have not responded to adequate trials of at least 2 triptans or triptans are contraindicated then Rimegepant 75mg can be considered.
The maximum dose is 75mg per day. If also on a CYP3A4 inhibitor (e.g., clarithromycin, itraconazole, ritonavir) then a second dose should be delayed for 48 hours. Rimegepant is generally well tolerated. Nausea is the main adverse effect. Hypersensitivity reactions have been reported but are uncommon occurring in <1%.
Before Rimegepant is considered patients should have had an adequate trial of at least 2 triptans
The European Headache Federation (EHF) consensus on the definition of effective treatment of a migraine attack by a triptan is adequate symptom relief in 3 out of 4 headaches. Triptan resistance as inadequate symptom relief after trials of at least two triptans, and triptan refractory is inadequate symptom relief after trials of at least three triptans.
Ensure adequate hydration
For patients in whom oral preparations have been ineffective, parenteral NSAIDs (such as intramuscular diclofenac 75mg) or subcutaneous sumatriptan 6mg should be considered.
Evidence also supports the use of parenteral antiemetics (intramuscular metoclopramide 10mg or prochlorperazine 10mg).
Opioids have not been shown to be significantly effective and should not be used.
Most patients should be able to be managed in the community. For patients, in whom standard treatment has not been effective and migraine is persisting, who attend the Emergency Department or are admitted to hospital, the following additional measures should be considered:
@NHSScotCfSD
Centre for Sustainable Delivery
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