👋 Happy Friday. It’s been a long week, hasn’t it?
Work, uni, exams, yadda yadda ya.
Life can feel like a never-ending all-you-can-eat smorgasbord of stress🤕
So time to relax, kick back and enjoy, there’s no scary NEWS of 8 in here, just your medical news at 8 instead 🤝 ☕
Here’s what we got:
💆♀ The Migraine Olympics: Saving The Best Meds For Last
📩 I Got Ninety-Nine Notifs, But a Murmur Ain’t One
🚢 WHO Assures It’s Not Time for World Pandemic Round 2
🧠 QuickBits: Other Top Stories of The Week
If you want to read any previous editions of The Handover, you can on our website.
RESEARCH UPDATE
💆♀ The Migraine Olympics: Saving The Best Meds For Last
Common things are common. And there is nothing common-er than a headache.
Usually, you can chalk it up to dehydration, stress, or mysteriously needing a sick note on a Monday morning 🤔
But when those headaches come in that one-sided, throbbing, please-turn-off-the-sun flavour, we need a more tailored approach.
You see, migraine management has a problem…
Treating a migraine attack is super straightforward.
Take a triptan.
Take an NSAID.
Take it easy.
But stopping it from coming back? Something curious happens. It takes the pain in your patient's head and makes it a pain in your arse.
How about propanolol? Oh… you’re asthmatic
How about toparimate? Oh… you’re trying to get pregnant
And acupuncture(NICE-recommended)? Oh… you’re traumatised by Final Destination 5
There are a load of wonderful ways to tackle migraine prophylaxis.
Contenders included heritage drugs, like propranolol, topiramate, and Botox(Botulinum Toxins). None of which has the primary job of treating migraines. It’s like a side-hustle for them.
And also, the new, sexy CGRP-targeted therapies. A class of drugs that finally treats migraines as a day job. TLDR: they block the chemical released during migraine attacks that causes inflammation.
But which is definitively the best? And which aren’t worth the hype? This meta-analysis and systematic review from the Annals of Internal Medicine has the answers.
This study is the Migraine Olympics.
A head-to-head comparison of the biggest names in chronic migraine prevention.
The review looked at 43 randomised controlled trials involving 14,725 patients with chronic migraine.
Researchers wanted to answer three big questions:
Which treatments reduced monthly migraine days and by how many?
Which drugs cause people to stop due to side effects?
Which drugs had weak studies backing them?
And after an industrial quantity of unpaid academic labour, these were the key findings:
Headline Finding = CGRP therapies on top.
The new-gen CGRP-targeted therapies were the most effective class overall. A load of them reducing monthly migraine days by about 2 days vs placebo
Erenumab vs placebo: MD -2.08 days per month (95% CI -2.82 to -1.33).
Eptinezumab vs placebo: MD -2.34 days per month (95% CI -2.76 to -1.92).
Atogepant vs placebo: MD -2.10 days per month (95% CI -3.06 to -1.14).
What about the old faithfuls? Well… they had an evidence quality problem
Bad studies: The review didn’t find a solid, dependable body of trials for topiramate, propranolol and valproate. The authors concluded that the studies were not robust enough to give them confidence that these drugs are any good.
Botox held its own: Migraine Days -1.34 (95% CI -2.27 to -0.41). BUT did have increased adverse-event-related discontinuation. RR 3.36 (95% CI 1.75 to 6.45).
This is fascinating because the CGRPs, according to NICE scripture(1.3.24), should only be recommended AFTER 3 of our old fathfuls had failed. Even though they have stronger evidence.
You would think these findings would lead to the Migraine Union boycotting NICE HQ, but the study found several shortcomings.
High risk of bias.
Short follow-up period(12 weeks only).
Conflicting interests(pharma-funded) are some of the big ones.
Overall, after years of treating migraines with meds that don’t quite fit the bill, we might finally have a class of meds that takes these “headaches” as seriously as patients do 🤝
RESEARCH UPDATE
📥 I Got Ninety-Nine Notifs, but A Murmur Ain't One
You slump into a seat at the M&S cafe and chow into your £6.90 chicken & stuffing sandwich.
Finally, lunch (it’s 4:30 pm).
A time to rest, ingest, and slog through the ever-growing pile of Outlook emails.
…99+ Notifications.🫠
Anything fun? A cheeky ST1 offer perchance?
Dream on, hun. It’s the usual lineup:
Subject: Staff Reminder - Theatre Equipment Is NOT Gym Equipment!
Orthopaedics, stop trying to ‘squeeze in a set or two’ with the intramedullary rods during surgery.
Subject: Poor Spelling Noted Frequently on Patients' Notes.
Some recently noted errors:
Heal Ulcer.
Well… I sure hope they did.Haemogoblin.
Those darned oxygen-stealing thieves strike again.Emergency C-sections for faecal distress.
Maybe try the toilet first.
And then, righttt at the bottom of your inbox: Subject: Urgent Results Available⚠
“Patient X’s Echocardiogram showed severe stenosis.”
Sh**. You should’ve been on this yesterday.

And that's the kicker.
An inconspicuous “results available”.
No mention of the ticking time bomb hiding within.
But, what if you were ALERTed instead?
Published in JACC, the ALERT trial set out to do just that.
Researchers conducted a multicentre RCT trial across 5 US health systems, involving 35 hospitals and 765 clinicians. They analysed over 1,900 patients with significant valvular heart disease identified on echo.
The clinicians were split into two groups:
Alert Group - pinged an automated EHR notification if the echo results showed significant Aortic Stenosis or Mitral Regurgitation (+ guideline-based management recommendations)
Control Group - business + care as usual.
The primary outcome?
Whether these alerts improved timely, guideline-based care, measured via:
Time to valve intervention (surgery or transcath)
If both groups tied for above → time to multidisciplinary heart team review
Let’s just say the results deserve a half-swipe at the minimum, because the study found a pretty significant difference between the groups:
Win ratio: 1.27 (95% CI 1.05–1.54), p=0.007
i.e., Patients seen by the Alert group were more likely to get care quicker

It’s a win for Team Alert⏰
But don’t forget to read the community notes for extra context on those results:
Short follow-up (90 days) → Misses longer-term decisions
Alert fatigue → Clinicians may ignore alerts (don’t we all) → limits real-world impact
Doesn’t address system capacity → Referrals ≠ guaranteed intervention
Design bias → Differences between clinicians/hospitals may affect results
Most notifications you get don’t matter. But don’t miss the ones that do.
Delete, ignore, and scroll may remain the default options for now.
But if you start getting big alerts reminding you that valve disease is severe, and even a guide on what to do, it's time to pay attention.
Let’s just hope no one misspells Aortic Stenosis as “ASS”, because an ASS valve replacement would be a very awkward consent procedure.
WORLD NEWS
WHO Swears It’s Not Time for World Pandemic Round 2
The Pandemic that Shall Not be Named of 2020 and its worldwide impact is permanently scarred into our collective consciousness.
And although the new virus on the block - Hantavirus, is not transmitted as easily as its predecessor, it’s little wonder the world is holding its breath over the 5 confirmed cases thus far.
The current alarm began aboard the MV Hondius, where passengers thought they were signing up for Antarctic views and cute penguins, but were instead faced with a bubonic plague-esque rodent-transmitted nightmare.

By the time the outbreak was confirmed, 29 passengers had already disembarked and dispersed across a dozen countries (this is generally considered less than ideal in infectious disease circles)
Three people have died thus far, and authorities are scrambling to trace all remaining passengers. The strain involved, Andes hantavirus, can spread between humans but usually only through close, intimate contact.
So it’s not quite giving Covid 2.0. The World Health Organisation desperately stresses that the overall risk to the public remains low.
Still, not easily transmissible is only mildly comforting when your fellow passengers spent weeks sharing buffet tongs, shot glasses and mics during karaoke renditions of My Heart Will Go On.
For now, there’s no cause for panic.
But just in case, best keep the hand sanny nearby 👀🧴
OTHER NEWS YOU SHOULD KNOW
Data governance has never been the NHS’s strong point 🥴
And now with a major US data analytics company, Palantir, lined up to process huge chunks of UK patient data, it’s not set to improve anytime soon.
Palantir is at the heart of the NHS’s £330 million Federated Data Platform, a decision that has faced huge controversy.
The reasons are many, including political concerns and worries over the lack of healthy competition.
Read all about the details here
IV Ketamine might not be your first thought when treatment of depression comes up, but given time, it just might be.
Turns out, the crazy spaced-out + dissociative feelings* from ket might be good for numbing the real bad stuff too.
*⚠️DISCLAIMER: NOT AUTHOR ANECDOTAL EVIDENCE. All creds to FRANK.
A meta-analysis published in JAMA looked at 26 RCTs totalling 1,166 patients, and found that intravenous ketamine reduced depressive symptoms within 4 hours, lasting up to a week after a single infusion.
AND suicidal symptoms were also significantly lower by 24 hours, with effects lasting up to a month. Repeated infusions showed similar benefits.
Common side effects (e.g. headache) were transient. A lot more research is needed, especially as longer-term outcomes remain uncertain.
But in the acute phase, ketamine might just give a quick boost to those who need it most📈
More than a million people in England are now using combination inhalers for their asthma, surpassing the few who still rely on the classic blue SABA alone.
New data shows 1.09 million patients on MART/AIR regimens, rising 63% in the past year.
This follows updated 2024 guidance from NICE, which pushed for earlier combo therapy as just bronchodilating temporarily via a SABA simply wasn’t doing anything to address inflammation.
Combination inhalers (usually ICS + formoterol) target both symptoms and underlying inflammation via the steroid, either as PRN (AIR) or as maintenance plus reliever (MART).
Despite a higher cost, NICE estimates fewer exacerbations, fewer ED trips, and overall fewer admissions.
It ain’t easy being wheezy, but it’s a sMART step in the right direction.
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Fun Fact: Botox is one of the most lethal substances known to science. An estimated 1–2 nanograms per kilogram could kill a human if inhaled.
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The Handover is intended for healthcare professionals and does not constitute medical advice.

