Limit acute treatment to less than 10 days per month (on average 2 days per week) to prevent development of medication overuse headache.
We asked you in January to update to v4.7.2. After the deployment planned for 27th February, this new update will be needed to ensure that you are able to download RDS toolkits even when the RDS website is not available. We will wait until as many users as possible have downloaded the new version before switching off the old system for app downloads and moving entirely to the new approach.
To check your current RDS version, click on the three dots bottom right of the RDS app screen. This takes you to a “More” page where you will see the version number.
To update to the latest release:
On iPhones – go to the Apple store, click on your profile icon top right, scroll down to see the apps waiting to be updated and update the RDS app.
On Android phones – these can vary, but try going to the Google Play store, click on your profile icon top right, click on “Manage apps and device”, select and update the RDS app.
Welcome to the February 2025 update from the RDS team
A new release of RDS is planned (subject to outcomes of current testing) for week beginning 24th February. This will deliver:
The release will also incorporate a number of small fixes, including:
We will let you know when the date and time for the new release are confirmed.
There is now the capability to publish toolkits on the web with left hand side navigation rather than tiles on the homepage. To use this feature, turn on the “Toggle navigation panel” option at the top of the Page settings menu at toolkit homepage level – see below. Please note that publication to downloadable mobile app for this type of navigation is still under development.
The Benzodiazepine tapering tool is now available as part of the RDS toolkit for the national benzodiazepine prescribing guidance developed by the Scottish Government Effective Prescribing team. The tool uses this national guidance developed with a wide-ranging multidisciplinary group. This should be used in combination with professional judgement and an understanding of the needs of the individual patient.
Due to the intensive work Tactuum has had to undertake on the new technology infrastructure has pushed back the delivery dates again and some new requirements have come out of the recent user acceptance testing. It now looks likely to be an April release for the search and browse interface. The archiving and version control functionality may be released earlier. We’ll keep you posted.
At the end of January, Olivia completed the generation of the latest set of usage statistics for all RDS toolkits. If you would like a copy of the stats for your toolkit, please contact Olivia.graham@nhs.scot .
We have now generated reports of all RDS toolkit content that has exceeded its review date by 6 months or more. We will be in touch later this month with toolkit owners and editors to agree the plan for updating or withdrawing out of date content.
Some important toolkits in development by the RDS team include:
The RDS team and other information scientists in HIS have also been producing evidence summaries for the Scottish Government Realistic Medicine team, to inform development of national guidance around Procedures of Limited Clinical Value. This guidance will in due course be translated into an RDS toolkit.
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.)
To invite colleagues to sign up to receive this newsletter, please signpost them to the registration form - also available in End-user and Provider sections of the RDS Learning and Support area. 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
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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