Helen OConnell AO

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Helen OConnell AO

Helen OConnell AO

@OconnellProf

President USANZ Urologist Surgeon Researcher

Melbourne, Australia 가입일 Şubat 2019
969 팔로잉1.4K 팔로워
Helen OConnell AO 리트윗함
Imperial Prostate
Imperial Prostate@IP_London·
Using data from #IP8FLUORESCE and #LaserSAFE, @NikhilMayor presents our development and validation of a deep learning tool for detecting positive margins during RARP using fluorescence confocal microscopy - highly accurate results! #EAU26
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USANZ
USANZ@USANZUrology·
Are you the future of urology? Essay Competition. Submit on the topic of "Inclusion without Exclusion: Addressing Perceptions of Reverse Discrimination in Surgical Careers" Submissions Close 28 Nov25 An initiative of the USANZ DE&I Committee Find out more: bit.ly/USANZEssay
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Helen OConnell AO 리트윗함
USANZ
USANZ@USANZUrology·
MEET THE EXPERTS: Introducing Prof Christian Gratzke from Albert-Ludwigs-University, Germany who will present at #USANZ26. Specialty: Uro-oncology (Prostate cancer) and BPH/LUTS Read @cgratzke Profile and Research here: bit.ly/USANZ26MTE
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Helen OConnell AO 리트윗함
USANZ
USANZ@USANZUrology·
USANZ & ANZUNS 2026 ASM Melbourne Abstract Submissions Now Open! Don't leave it until the last minute to submit your abstract. Abstract Submissions will close on Monday 1st September. Find out more here: asm.usanz.org.au/abstracts-open/ @ANZUNS_Urology
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Ashish M. Kamat, MD, MBBS
Ashish M. Kamat, MD, MBBS@UroDocAsh·
Our recent publication in @EurUrolOncol demonstrates - for the first time -that an AI-powered histologic biomarker (CHAI) can predict response to intravesical BCG vs. gemcitabine/docetaxel in high-grade NMIBC. A critical step forward in precision intravesical therapy. doi.org/10.1016/j.euo.… 🧵1/6
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Helen OConnell AO 리트윗함
Chronic UTI Australia Inc.
Chronic UTI Australia Inc.@ChronicUTIAus·
This will be a good one 👉 July UTI Hour Paediatric UTIs: Characterising pathogenesis and immune responses Hosted by Australia's Arthika Manoharan @Arthiii_M with guest speakers Dr John David Spencer @kidneytweets and another Aussie, Dr Aniruddh (Ani) Deshpande. Friday 11th July 🗓️ mark it on your calendar
UTI Global Alliance@GlobalUti

#UTIs don't sleep, and neither do we! Our next #UTIhour is already on the books. The topic is, "Paediatric UTIs: Characterising pathogenesis and immune responses." 👶👩‍🍼 Please mark your calendars for July 11, 2025, at 9AM EDT/1100 UTC! UTIGA.org/upcoming

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ICS
ICS@icsoffice·
Renew your ICS membership for 2025 now to ensure full and uninterrupted access to your ICS member benefits including all educational content! For a reminder of the perks of being an ICS member, visit: ics.org/members #ICSMember #ICSMembership #ICS #JoinICS
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Steffi Yuen
Steffi Yuen@steffiyuen·
📏 measuring #IRP is important. 💡 knowing how to utilize devices is equally important (#IRP_FANS #IRPfURS #pressurewire) Freshly out! 📝Measuring, monitoring and reporting intrarenal pressure: a practical guide to endourologists from section of #EAUendourology journals.lww.com/co-urology/abs… 🤓more work has to be done! Let’s go @DocGauhar @endouro @Uroweb @naeembhojani7 @DrBenChew @bsc_urology @BSCEMEA_Urology #COMETII #ZSR #iMIMER #YiGaoElephantIII #Tidor
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Kari Tikkinen
Kari Tikkinen@KariTikkinen·
@MattBultitude Thanks @MattBultitude for your comments Prophylaxis likely works also for simple UTI: best guess is about 50% risk reduction (trial underpowered for the outcome) #APPEALtrial messages 1⃣ 1-dose cipro helps 2⃣ Not all need it 3⃣ Individualize: patient values & risk factors
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Chronic UTI Australia Inc.
Chronic UTI Australia Inc.@ChronicUTIAus·
This UTI research used nanogels combined with a special peptide to push gentamicin inside infected bladder wall cells to clear the infection. The researchers say nanogel delivers about 36% more antibiotic inside cells compared to standard antibiotic delivery methods. It is also quick releasing and exhibits low toxicity, causing minimal harm to cells. #chronicUTI #recurrentUTI #urinarytractinfection news.cuanschutz.edu/news-stories/p…
Chronic & Recurrent UTI Aus & NZ Support Group@cUTIrUTIAusNZ

Promising New Research Shows Potential to Cure Recurrent Urinary Tract Infections news.cuanschutz.edu/news-stories/p…

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Helen OConnell AO 리트윗함
Michael Hofman
Michael Hofman@DrMHofman·
Twenty cycles (that's right 20) of Lutetium-177 PSMA-617 for metastatic castration-resistant cancer!! Check our case report just published in @JournalofNucMed jnm.snmjournals.org/content/early/… Current randomized controlled data demonstrate the safety and efficacy of 6 cycles of [¹⁷⁷Lu]Lu-PSMA-617 therapy in men with metastatic castration-resistant prostate cancer. In our first phase 2 trial, 15 of 30 patients received additional cycles; 11 (73%) had a subsequent prostate-specific antigen (PSA) decline of 50% or more. A German multicenter study also supported extended therapy in 111 patients, with a median survival of 31.1 mo from the first administration and no increase in grade 3–4 toxicities. We describe safety and efficacy in a patient who received 20 cycles of [¹⁷⁷Lu]Lu-PSMA-617, receiving a total administered radioactivity of 129 GBq over 5 y. Initially diagnosed at age 59 with de novo bone-only metastatic prostate cancer and a PSA of 96 ug/L, he underwent intermittent androgen deprivation therapy for 13 y before requiring palliative radiotherapy for painful bone metastases. The following year, he was treated with 6 cycles of docetaxel, followed by 18 mo of enzalutamide. On progression with a PSA of 195 ug/L and a doubling time of 3.0 mo, the patient received 6 cycles of [¹⁷⁷Lu]Lu-PSMA-617, with a PSA nadir of 3.2 ug/L, as part of the TheraP trial. Paired PSMA PET/CT (SUVmax, 73; SUVmean, 10.7) and 18F-FDG PET/CT (metabolic tumor volume, 14 cm3) at enrollment had favorable characteristics. A second treatment block of 2 cycles of [¹⁷⁷Lu]Lu-PSMA-617 was given 266 d after cycle 6 (14 mo after cycle 1) on a clinical registry, resulting in a PSA decline of more than 90% (nadir, 14.2 ug/L) and a further treatment break of 229 d. The treatment-free interval remained similar between treatment blocks 2 and 3 at 216 d; however, this interval shortened to 75 and 78 d between blocks 4 and 5 and blocks 5 and 6, respectively (see Figure). After cycle 15, he continued to receive symptomatic benefit, but on-treatment biochemical and imaging progression emerged. The hemoglobin and platelet nadirs were 98 g/L and 115 × 109/L, respectively, occurring after cycle 18. Renal function remained normal, with an estimated glomerular filtration rate of 92 mL/min after cycle 20, compared with 117 mL/min at baseline, and an estimated cumulative kidney dose of 55.5 Gy. This exceeds the 23-Gy maximum tolerated dose defined by external-beam radiotherapy, highlighting the limitation of extrapolating external-beam radiotherapy normal-organ constraints to radiopharmaceutical therapy. Grade 1 xerostomia occurred from cycle 3 and remained mild and transient, usually lasting a few days after many, but not all, cycles. After cycle 20, he received 2 cycles of cabazitaxel and had a clinical response but subsequently progressed with new brain metastases and physical decline; he died 2 mo later at age 81, 4.9 y after the initiation of [¹⁷⁷Lu]Lu-PSMA-617. In conclusion, in selected patients, [¹⁷⁷Lu]Lu-PSMA-617 appears to have substantial benefits beyond 6 cycles. @DrKerryJewell @ButeauJames @EdmondMKwan @liz_medhurst @SandhuShahneen @AzadOncology
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