Andrew Sharp

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Andrew Sharp

Andrew Sharp

@drandrewsharp

Interested in stuff. (This is my personal account only)

Ireland Katılım Mart 2014
2.8K Takip Edilen6.9K Takipçiler
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Jake Thornton 🇬🇧🇺🇸
“Tell him to enter the password he knows is correct. Inform him it is incorrect. Invite him to reset it. Watch as he enters the password he believed it to be all along. Then tell him he cannot use it… because it is his current password.”
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Andrew Sharp
Andrew Sharp@drandrewsharp·
Two minutes into Bayern-PSG and we have already had more entertainment than Arsenal-Athletico
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Samuel
Samuel@SamueILFC·
Bayern and PSG, please save football.
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Lester
Lester@Chen·
the best 3 minutes of video I've watched this year
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Bo Wang
Bo Wang@BoWang87·
Another huge medical achievement from our very own @UHN 🇨🇦🔥 A Toronto man lived with HIV for 27 years. Then he got leukemia and that diagnosis may have just cured him of both. His doctors found a bone marrow donor carrying CCR5-Δ32, a rare mutation in ~1% of people of European descent. HIV hijacks immune cells through the CCR5 receptor. If you don't have it, the virus has no door. The transplant replaced his entire immune system with one HIV can't infect. He stopped antiretroviral therapy in July 2025. As of today, HIV is undetectable by the most sensitive assays available. No viral reservoir. No immune response to HIV. Nine months clean. He would be the 11th person in history to possibly be cured of HIV. HIV cure is possible. We just proved it again at @UHN Proud of the team at @UHN and @UofT ! Source: uhn.ca/corporate/News…
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Anish Moonka
Anish Moonka@anishmoonka·
A parasite that has been eating people for 3,500 years is about to be wiped off the planet. It infected 3.5 million people in 1986. Last year, it infected 10. And I have not seen it make a single front page. It is called Guinea worm. You drink contaminated water from a pond in a poor village. A year later, a worm up to three feet long starts coming out of your leg through a burning blister. There is no pill that stops it and no surgery that works. You wrap the worm around a stick and pull it out slowly, over days or weeks, inch by inch. If you rush, the worm breaks inside you and causes a fresh infection. Guinea worm is ancient. Preserved worms have been pulled out of Egyptian mummies from around 1000 BCE. The Ebers Papyrus, an Egyptian medical scroll from 1550 BCE, describes pulling the worm out with a stick. For three and a half thousand years, that was the best humans could do. Then in 1986, public health workers decided to kill the parasite off. They had no vaccine and no drug. What they had was cheap cloth water filters and a small army of volunteers willing to walk from village to village for decades. The plan was simple. Give everyone who drinks from a pond a cloth filter to strain out the tiny water fleas that spread the parasite. Then send volunteers walking house to house, year after year, teaching people how to use the filters and keeping anyone with an emerging worm out of the water. It worked. From 3.5 million cases a year to 10. Four were in Chad, four in Ethiopia, two in South Sudan. The other four countries where the worm used to be common, Angola, Cameroon, the Central African Republic, and Mali, had zero human cases for the second year in a row. The World Health Organization has already certified 200 countries as Guinea worm free. Six are left. The last hurdle is dogs. Cameroon had 445 infected animals last year and Chad had 147, so a lot of the remaining work is on animals, not humans. Strays get leashed, and crews treat ponds to kill any remaining worms. The campaign keeps watching until the number hits zero. When Guinea worm hits zero, it becomes the second human disease ever erased from the planet. The first was smallpox. It will also be the first parasite humans have ever wiped out, and the first disease ever ended without a single dose of medicine. Volunteers walked village to village with cloth filters for 40 years. Now a plague from the age of the pharaohs is about to be gone.
ً@prinkasusa

Give me the kind of good news from around the world that nobody ever talks about... but should.

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NASA
NASA@NASA·
Welcome home Reid, Victor, Christina, and Jeremy! 🫶 The Artemis II astronauts have splashed down at 8:07pm ET (0007 UTC April 11), bringing their historic 10-day mission around the Moon to an end.
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Andrew Sharp@drandrewsharp·
Seen few comments of ‘we got it wrong on b-blocker use post MI’ Did we get it wrong? When patients had limited culprit revasc, no bystander revasc, bigger infarcts, more arrhythmia, ongoing smoking, limited HF drugs and minimal statin plaque stabilisation, needs were different.
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Andrew Sharp@drandrewsharp·
Some evolved primates dug some stuff out of the ground, pieced it together and are now riding the proceeds 250,000 miles away, further than any humans have ever travelled. 125 years ago we got across the oceans by steam power.
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Piotr Buszman MD, PhD
Piotr Buszman MD, PhD@piotr_buszmanMD·
With great pleasure we report metaanalysis of 5 trials including LEMANS at 10 year follow-up in @JACCJournals. There is no difference in mortality between PCI and CABG for left main disease. In fact its identical : 23.4% vs 23.3%, HR 1.02 (0.89–1.17), RMST difference of exactly 0.0 years. Those are outcomes still with BMS and rare IVUS. Not bad! Great news for the patients. @GreggWStone @Hragy @SerruysPatrick @ZSiudak @EAPCIPresident @AHP_PAKS @uniwersytet_afm Thank you David Koeckerling and Ahmad Yosif. jacc.org/doi/10.1016/j.…
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Andrew Sharp
Andrew Sharp@drandrewsharp·
@chamath Free AI personal tutoring for kids will help disadvantaged kids more than those from wealthier backgrounds. It seems unlikely that AI couldn’t teach any motivated kid maths. You and @Jason talk on the pod about giving back. Surely this is the lowest of low hanging fruit.
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Stefano Garzon, MD
Stefano Garzon, MD@stefano_garzon·
🧵 ORBITA-CTO Seeing a study like ORBITA-CTO being published — regardless of its results — is a beautiful thing. This level of commitment to producing high-quality, as-unbiased-as-possible evidence in interventional cardiology should be praised. It took 4 years to randomize 50 patients. That's dedication. Think about what this team had to do: Noise-cancelling headphones, deep sedation, clocks removed from every room, scripted handovers, overnight admission for both arms, dual-operator procedures lasting 3+ hours — all to protect the blinding. Bang blinding index ≈ 0. It worked. Design: 50 patients, single-vessel CTO, confirmed ischemia + viability, J-CTO ≤3, no bystander disease. 1:1 to CTO PCI or placebo after dual-injection angiography. All anti-anginals stopped at randomization. Daily symptom tracking via ORBITA-app for 6 months. Patient-initiated re-titration only. Primary endpoint: angina symptom score (Bayesian ordinal MOST model, daily repeated measures). CTO PCI vs placebo: OR 4.38 (95% CrI 1.57–12.69) Pr(Benefit) = 0.996 Driven by angina frequency: OR 4.38 (95% CrI 1.55–11.78) Pr(Benefit) = 0.997 In patient-centered terms: CTO PCI yielded ~31 additional angina-free days over 6 months vs placebo. 95% CrI: 11.1–50.7 Pr(Benefit) > 0.999 That's roughly 5 extra angina-free days per month. SAQ domains were consistent: Angina frequency: +10.7 (CrI 1.4–20.2) Physical limitation: +13.5 (CrI 4.5–22.3) Quality of life: +18.2 (CrI 5.4–30.5) Summary score: +13.7 (CrI 4.2–23.2) All Pr(Benefit) ≥ 0.988. CCS class also improved. Dyspnea and EQ-5D did not separate. Procedural quality was outstanding: 96% technical success, 92% IVUS-guided, experienced dual-operator teams. One failed PCI case — averaging 6 angina episodes/day — was included in ITT. This biased against the PCI arm. But the treatment effect survived it. Why does this matter so much? EuroCTO (Werner et al.) showed CTO PCI improved symptoms vs OMT at 1 year, sustained at 3 years. But it was open-label, with 17.5% crossover from OMT to PCI. Without blinding, the placebo contribution to symptom relief was unknown. ORBITA-CTO quantified it. Both arms improved — so yes, the placebo response was substantial. But the PCI effect was immediate and sustained. The placebo group progressively needed more anti-anginals. Now, what ORBITA-CTO does NOT prove: 1. Benefit in multivessel disease or high-complexity CTOs (J-CTO 4–5) 2. Prognostic benefit (not designed for hard endpoints) 3. Generalizability beyond expert centers with 96% success rates 4. Benefit on dyspnea or generic quality of life I know. N=50 is small. Credible intervals are wide. This was an expert-center study with carefully selected lesions. Noted. But 8,631 follow-up days of daily symptom data, a Bayesian framework designed for this exact scenario, and verified blinding give it far more inferential weight than sample size alone suggests. For years, CTO PCI skeptics had a legitimate point: no blinded evidence. That point is now addressed. CTO PCI relieves angina beyond placebo — in well-selected patients, at experienced centers. Agreed. Hats off to the ORBITA-CTO team for doing this the hard way. Our field is better for it. And by the way, this is not me celebrating the results. I don't do CTO. But it makes me happy to see good medical science being made. #ORBITACTO #CardiologyX #InterventionalCardiology #ACC26 @JACCJournals
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Andrew Sharp
Andrew Sharp@drandrewsharp·
PCRonline 🫀@PCRonline

Optimal minimal stent area and impact of stent underexpansion in left main up-front 2-stent strategy This study 📊aimed to revise the #IVUS-derived segmental MSA criteria for optimal stent expansion in patients undergoing an up-front 2-#stent strategy using the crush technique for LM #bifurcation lesions to predict the 5-year clinical outcomes. 🔗 pcronline.com/PCR-Publicatio… Read this #EAPCI/PCR #JournalClub review ✍️ by @sbrugaletta. Selected in @CircAHA (image source = graphical abstract)

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Andrew Sharp@drandrewsharp·
Lots to think about in these tables: 2.9 yr OPTIMAL and 3yr EXCEL results
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Andrew Sharp retweetledi
Saad Ur Rahman
Saad Ur Rahman@SaadUrRahman55·
Compilation of LBT’s into a single image for ease. Thank you @drhussnainsadiq for your work.
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Andrew Sharp
Andrew Sharp@drandrewsharp·
@djc795 @JAMarbach @NavinKapur4 Given that the active arm was no worse, despite ~ 47 mins of planned delay in reperfusion, perhaps it doesn’t end the hypothesis, just this mode of delivery.
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Jeffrey Marbach
Jeffrey Marbach@JAMarbach·
Criticism of STEMI-DTU is revisionist. Biologically grounded strategy supported by years of preclinical work. We cannot claim to value innovation, then ridicule a rigorously tested hypothesis because the trial was neutral. Hypocrisy deserves to be called out. @NavinKapur4
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Andrew Sharp@drandrewsharp·
Many thanks to the people who work so hard to bring us new clinical trial data. We’d be forced to argue about politics and war if we didn’t have trial designs to keep us busy.
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