Brennan Kahan
@brennankahan.bsky.social
730 followers 310 following 36 posts
Principal Research Fellow in Medical Statistics at MRC Clinical Trials Unit at UCL. Clinical trials, estimands, estimation. https://scholar.google.co.uk/citations?user=Lf0jsXAAAAAJ&hl=en&oi=sra
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Reposted by Brennan Kahan
marionkcampbell.bsky.social
There has been a lot of debate recently about the promise of real world data - the routine (observational) data collected on patients eg  treatments received, clinical outcomes etc – for estimating treatment effects. But can they deliver? 1/9
#MethodologyMonday #123
Reposted by Brennan Kahan
marionkcampbell.bsky.social
We often now hear the term “Bayesian borrowing” in trials. But what is Bayesian borrowing and what are the pros and cons around its use? 1/6
#MethodologyMonday #122
Reposted by Brennan Kahan
gscollins.bsky.social
NEW PAPER in @bmj.com "Dealing with continuous variables and modelling non-linear associations in healthcare data: practical guide"

--> www.bmj.com/content/390/...

#methodologymatters #StatsSky #EpiSky
brennankahan.bsky.social
If outcome = "no. of antibiotic prescriptions" and more people in one arm get LT antibiotics (which presumably precludes further prescriptions?), this does seem like a challenge.

Could of course be good reasons for it - does highlight importance of estimands (along with justifications for choice)!
brennankahan.bsky.social
Think they've used a treatment policy strategy (ie were interested in the effect of Hiprex vs placebo whether or not people started on suppressive antibiotics later).

I don't know enough about the area to say if this is sensible, but if suppressive antibiotics are part of usual care, it may be?
Reposted by Brennan Kahan
jdwilko.bsky.social
What's that? The target trial emulation obtained the same answer as the RCT? Wow, I guess RCTs are generalisable after all! Perhaps we should perform them rather than using interventions on hundreds of thousands of people before we know whether or not they work, then doing a TTE?
Reposted by Brennan Kahan
timpmorris.bsky.social
Reckon I can submit this as a figure for a paper?
Goose chase meme. Goose asks "Unbiased for what estimand?" then yells "Unbiased for what!!"
Reposted by Brennan Kahan
timpmorris.bsky.social
New post: “Marginal” and “conditional” are relative descriptions of an estimand
Foreground text says “Marginal” and “conditional” are relative descriptions of an estimand
In the background is a smokey mollusc
Reposted by Brennan Kahan
ukcrc-ctu.org.uk
The CONSORT 2025 Statement is here. Essential reading for those involved in the reporting & reviewing of randomized trials.

We're proud to see so many #UKCTUNetwork units & individual researchers contributing to this crucial update!

🔗 tinyurl.com/yc3cbh33

#CONSORT2025 #ResearchTransparency
CONSORT 2025 Statement
This Special Communication introduces the updated Consolidated Standards of Reporting Trials (CONSORT) 2025 statement, which includes substantive and structural changes to account for recent methodolo...
jamanetwork.com
Reposted by Brennan Kahan
episconroy.bsky.social
Would like to add… there are guidelines for all types of studies… www.equator-network.org/reporting-gu...
Reposted by Brennan Kahan
statsepi.bsky.social
Please people. It's not hard. In fact, it makes your life easier. And when you don't use CONSORT, you look like a novice.
jama.com
JAMA @jama.com · Jun 15
Authors, editors, reviewers, and other potential users should use CONSORT 2025 when writing and evaluating manuscripts of randomized trials to ensure that trial reports are clear and transparent.

Learn more in this Special Communication.

https://ja.ma/3TlnKQe
CONSORT 2025 Statement
Updated Guideline for Reporting Randomized Trials
Reposted by Brennan Kahan
jama.com
JAMA @jama.com · Jun 15
Authors, editors, reviewers, and other potential users should use CONSORT 2025 when writing and evaluating manuscripts of randomized trials to ensure that trial reports are clear and transparent.

Learn more in this Special Communication.

https://ja.ma/3TlnKQe
CONSORT 2025 Statement
Updated Guideline for Reporting Randomized Trials
Reposted by Brennan Kahan
richardhooper.bsky.social
Stepped wedge devotees step up, and cluster enthusiasts get ready to cluster: it's conference time again.
steppedwedgehog.bsky.social
📢 The 11th annual meeting on Current Developments in Cluster Randomised Trials & Stepped Wedge Designs will take place 18/19 November 2025 in Birmingham UK.

Abstract submission is open, deadline for submission 11 July 2025 forms.gle/jS83TAKhs4U8.... Info on registration etc to follow!
Reposted by Brennan Kahan
mrcctu.bsky.social
🆕New CONSORT & SPIRIT 2025 Guidelines

Our colleagues helped shape these updates, making #ClinicalTrial reporting more transparent & useful for everyone.

Key changes:
✔️More open science
✔️Better reporting of harms & missing data
✔️Greater harmonisation between guidelines

More info: buff.ly/HC1rx31
New CONSORT & SPIRIT 2025 Guidelines Published | MRC Clinical Trials Unit at UCL
www.mrcctu.ucl.ac.uk
Reposted by Brennan Kahan
gscollins.bsky.social
NEW PAPER "Importance of sample size on the quality and utility of AI-based prediction models for healthcare"

www.thelancet.com/journals/lan...

We discuss seven reasons why inadequate sample size negatively affects model training, evaluation, and performance.

#StatsSky #machinelearning #AI
Reposted by Brennan Kahan
marionkcampbell.bsky.social
One of the trial designs that has been cropping up in my discussions recently is the cluster randomised crossover, or CRXO, design. But when is it best used & what are the key issues to look out for? 1/7
#MethodologyMonday #119
brennankahan.bsky.social
New 3-post for a research/senior research fellow to work on adaptive longitudinal cluster randomised trials in Melbourne.

Interesting work with a great research group.

careers.pageuppeople.com/513/cw/en/jo...
Job Search
careers.pageuppeople.com
Reposted by Brennan Kahan
rachpips.bsky.social
Next Thursday, June 5th at 1pm (BST) we host our 4th webinar in our adverse event special series. Rayan Taher & Jenny Yiend will present their work on developing a process for assessing the safety of a digital mental health intervention & gaining regulatory approval. Register here: lnkd.in/eaW3MQrB
Microsoft Forms
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Reposted by Brennan Kahan
rachpips.bsky.social
Next week (May 22nd) we host our third webinar in our adverse event special series. Regina Stegherr will be discussing the SAVVY project which aims to improve the analyses of AEs in clinical trials using survival methods to handle varying follow-up & competing events. Register here: lnkd.in/eaW3MQrB
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