201. Vimseltinib versus placebo for tenosynovial giant cell tumour (MOTION): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial.
作者: Hans Gelderblom.;Vivek Bhadri.;Silvia Stacchiotti.;Sebastian Bauer.;Andrew J Wagner.;Michiel van de Sande.;Nicholas M Bernthal.;Antonio López Pousa.;Albiruni Abdul Razak.;Antoine Italiano.;Mahbubl Ahmed.;Axel Le Cesne.;Gabriel Tinoco.;Kjetil Boye.;Javier Martín-Broto.;Emanuela Palmerini.;Salvatore Tafuto.;Sarah Pratap.;Benjamin C Powers.;Peter Reichardt.;Antonio Casado Herráez.;Piotr Rutkowski.;Christopher Tait.;Fiona Zarins.;Brooke Harrow.;Maitreyi G Sharma.;Rodrigo Ruiz-Soto.;Matthew L Sherman.;Jean-Yves Blay.;William D Tap.; .
来源: Lancet. 2024年403卷10445期2709-2719页
Tenosynovial giant cell tumour (TGCT) is a locally aggressive neoplasm for which few systemic treatment options exist. This study evaluated the efficacy and safety of vimseltinib, an oral, switch-control, CSF1R inhibitor, in patients with symptomatic TGCT not amenable to surgery.
202. Induction-concurrent chemoradiotherapy with or without sintilimab in patients with locoregionally advanced nasopharyngeal carcinoma in China (CONTINUUM): a multicentre, open-label, parallel-group, randomised, controlled, phase 3 trial.
作者: Xu Liu.;Yuan Zhang.;Kun-Yu Yang.;Ning Zhang.;Feng Jin.;Guo-Rong Zou.;Xiao-Dong Zhu.;Fang-Yun Xie.;Xiao-Yu Liang.;Wen-Fei Li.;Zhen-Yu He.;Nian-Yong Chen.;Wei-Han Hu.;Hai-Jun Wu.;Mei Shi.;Guan-Qun Zhou.;Yan-Ping Mao.;Rui Guo.;Rui Sun.;Jing Huang.;Shao-Qiang Liang.;Wei-Li Wu.;Zhen Su.;Ling Li.;Ping Ai.;Yu-Xiang He.;Jian Zang.;Lei Chen.;Li Lin.;Shao Hui Huang.;Cheng Xu.;Jia-Wei Lv.;Ying-Qing Li.;Shu-Bin Hong.;Yu-Sheng Jie.;Hao Li.;Sai-Wei Huang.;Ye-Lin Liang.;Ya-Qin Wang.;Ying-Lin Peng.;Jin-Han Zhu.;Sheng-Bing Zang.;Song-Ran Liu.;Qing-Guang Lin.;Hao-Jiang Li.;Li Tian.;Li-Zhi Liu.;Hong-Yun Zhao.;Ai-Hua Lin.;Ji-Bin Li.;Na Liu.;Ling-Long Tang.;Yu-Pei Chen.;Ying Sun.;Jun Ma.
来源: Lancet. 2024年403卷10445期2720-2731页
Anti-PD-1 therapy and chemotherapy is a recommended first-line treatment for recurrent or metastatic nasopharyngeal carcinoma, but the role of PD-1 blockade remains unknown in patients with locoregionally advanced nasopharyngeal carcinoma. We assessed the addition of sintilimab, a PD-1 inhibitor, to standard chemoradiotherapy in this patient population.
203. Inflammatory risk and cardiovascular events in patients without obstructive coronary artery disease: the ORFAN multicentre, longitudinal cohort study.
作者: Kenneth Chan.;Elizabeth Wahome.;Apostolos Tsiachristas.;Alexios S Antonopoulos.;Parijat Patel.;Maria Lyasheva.;Lucy Kingham.;Henry West.;Evangelos K Oikonomou.;Lucrezia Volpe.;Michail C Mavrogiannis.;Edward Nicol.;Tarun K Mittal.;Thomas Halborg.;Rafail A Kotronias.;David Adlam.;Bhavik Modi.;Jonathan Rodrigues.;Nicholas Screaton.;Attila Kardos.;John P Greenwood.;Nikant Sabharwal.;Giovanni Luigi De Maria.;Shahzad Munir.;Elisa McAlindon.;Yogesh Sohan.;Pete Tomlins.;Muhammad Siddique.;Andrew Kelion.;Cheerag Shirodaria.;Francesca Pugliese.;Steffen E Petersen.;Ron Blankstein.;Milind Desai.;Bernard J Gersh.;Stephan Achenbach.;Peter Libby.;Stefan Neubauer.;Keith M Channon.;John Deanfield.;Charalambos Antoniades.; .
来源: Lancet. 2024年403卷10444期2606-2618页
Coronary computed tomography angiography (CCTA) is the first line investigation for chest pain, and it is used to guide revascularisation. However, the widespread adoption of CCTA has revealed a large group of individuals without obstructive coronary artery disease (CAD), with unclear prognosis and management. Measurement of coronary inflammation from CCTA using the perivascular fat attenuation index (FAI) Score could enable cardiovascular risk prediction and guide the management of individuals without obstructive CAD. The Oxford Risk Factors And Non-invasive imaging (ORFAN) study aimed to evaluate the risk profile and event rates among patients undergoing CCTA as part of routine clinical care in the UK National Health Service (NHS); to test the hypothesis that coronary arterial inflammation drives cardiac mortality or major adverse cardiac events (MACE) in patients with or without CAD; and to externally validate the performance of the previously trained artificial intelligence (AI)-Risk prognostic algorithm and the related AI-Risk classification system in a UK population.
204. Burden of bacterial antimicrobial resistance in low-income and middle-income countries avertible by existing interventions: an evidence review and modelling analysis.
作者: Joseph A Lewnard.;Esmita Charani.;Alec Gleason.;Li Yang Hsu.;Wasif Ali Khan.;Abhilasha Karkey.;Clare I R Chandler.;Tapfumanei Mashe.;Ejaz Ahmed Khan.;Andre N H Bulabula.;Pilar Donado-Godoy.;Ramanan Laxminarayan.
来源: Lancet. 2024年403卷10442期2439-2454页
National action plans enumerate many interventions as potential strategies to reduce the burden of bacterial antimicrobial resistance (AMR). However, knowledge of the benefits achievable by specific approaches is needed to inform policy making, especially in low-income and middle-income countries (LMICs) with substantial AMR burden and low health-care system capacity. In a modelling analysis, we estimated that improving infection prevention and control programmes in LMIC health-care settings could prevent at least 337 000 (95% CI 250 200-465 200) AMR-associated deaths annually. Ensuring universal access to high-quality water, sanitation, and hygiene services would prevent 247 800 (160 000-337 800) AMR-associated deaths and paediatric vaccines 181 500 (153 400-206 800) AMR-associated deaths, from both direct prevention of resistant infections and reductions in antibiotic consumption. These estimates translate to prevention of 7·8% (5·6-11·0) of all AMR-associated mortality in LMICs by infection prevention and control, 5·7% (3·7-8·0) by water, sanitation, and hygiene, and 4·2% (3·4-5·1) by vaccination interventions. Despite the continuing need for research and innovation to overcome limitations of existing approaches, our findings indicate that reducing global AMR burden by 10% by the year 2030 is achievable with existing interventions. Our results should guide investments in public health interventions with the greatest potential to reduce AMR burden.
205. Ensuring progress on sustainable access to effective antibiotics at the 2024 UN General Assembly: a target-based approach.
作者: Marc Mendelson.;Joseph A Lewnard.;Mike Sharland.;Aislinn Cook.;Koen B Pouwels.;Yewande Alimi.;Mirfin Mpundu.;Evelyn Wesangula.;Jeffrey Scott Weese.;John-Arne Røttingen.;Ramanan Laxminarayan.
来源: Lancet. 2024年403卷10443期2551-2564页
Rising antimicrobial resistance (AMR) is a global health crisis for countries of all economic levels, alongside the broader challenge of access to antibiotics. As a result, development goals for child survival, healthy ageing, poverty reduction, and food security are at risk. Preserving antimicrobial effectiveness, a global public good, requires political will, targets, accountability frameworks, and funding. The upcoming second high-level meeting on AMR at the UN General Assembly (UNGA) in September, 2024, is evidence of political interest in addressing the problem of AMR, but action on targets, accountability, and funding, absent from the 2016 UNGA resolution, is needed. We propose ambitious yet achievable global targets for 2030 (relative to a prepandemic 2019 baseline): a 10% reduction in mortality from AMR; a 20% reduction in inappropriate human antibiotic use; and a 30% reduction in inappropriate animal antibiotic use. Given national variation in current levels of antibiotic use, these goals (termed the 10-20-30 by 2030) should be met within a framework of universal access to effective antibiotics. The WHO Access, Watch, Reserve (AWARE) system can be used to define, monitor, and evaluate appropriate levels of antibiotic use and access. Some countries should increase access to narrow-spectrum, safe, and affordable (Access) antibiotics, whereas others should discourage the inappropriate use of broader-spectrum (Watch) and last-resort (Reserve) antibiotics; AWARE targets should use a risk-based, burden-adjusted approach. Improved infection prevention and control, access to clean water and sanitation, and vaccination coverage can offset the selection effects of increased antibiotic use in low-income settings. To ensure accountability and global scientific guidance and consensus, we call for the establishment of the Independent Panel on Antimicrobial Access and Resistance and the support of leaders from low-income and middle-income countries.
206. Expanding antibiotic, vaccine, and diagnostics development and access to tackle antimicrobial resistance.
作者: Ramanan Laxminarayan.;Isabella Impalli.;Radha Rangarajan.;Jennifer Cohn.;Kavi Ramjeet.;Betsy Wonderly Trainor.;Steffanie Strathdee.;Nithima Sumpradit.;Daniel Berman.;Heiman Wertheim.;Kevin Outterson.;Padmini Srikantiah.;Ursula Theuretzbacher.
来源: Lancet. 2024年403卷10443期2534-2550页
The increasing number of bacterial infections globally that do not respond to any available antibiotics indicates a need to invest in-and ensure access to-new antibiotics, vaccines, and diagnostics. The traditional model of drug development, which depends on substantial revenues to motivate investment, is no longer economically viable without push and pull incentives. Moreover, drugs developed through these mechanisms are unlikely to be affordable for all patients in need, particularly in low-income and middle-income countries. New, publicly funded models based on public-private partnerships could support investment in antibiotics and novel alternatives, and lower patients' out-of-pocket costs, making drugs more accessible. Cost reductions can be achieved with public goods, such as clinical trial networks and platform-based quality assurance, manufacturing, and product development support. Preserving antibiotic effectiveness relies on accurate and timely diagnosis; however scaling up diagnostics faces technological, economic, and behavioural challenges. New technologies appeared during the COVID-19 pandemic, but there is a need for a deeper understanding of market, physician, and consumer behaviour to improve the use of diagnostics in patient management. Ensuring sustainable access to antibiotics also requires infection prevention. Vaccines offer the potential to prevent infections from drug-resistant pathogens, but funding for vaccine development has been scarce in this context. The High-Level Meeting of the UN General Assembly in 2024 offers an opportunity to rethink how research and development can be reoriented to serve disease management, prevention, patient access, and antibiotic stewardship.
207. The scope of the antimicrobial resistance challenge.
作者: Iruka N Okeke.;Marlieke E A de Kraker.;Thomas P Van Boeckel.;Chirag K Kumar.;Heike Schmitt.;Ana C Gales.;Silvia Bertagnolio.;Mike Sharland.;Ramanan Laxminarayan.
来源: Lancet. 2024年403卷10442期2426-2438页
Each year, an estimated 7·7 million deaths are attributed to bacterial infections, of which 4.95 million are associated with drug-resistant pathogens, and 1·27 million are caused by bacterial pathogens resistant to the antibiotics available. Access to effective antibiotics when indicated prolongs life, reduces disability, reduces health-care expenses, and enables access to other life-saving medical innovations. Antimicrobial resistance undoes these benefits and is a major barrier to attainment of the Sustainable Development Goals, including targets for newborn survival, progress on healthy ageing, and alleviation of poverty. Adverse consequences from antimicrobial resistance are seen across the human life course in both health-care-associated and community-associated infections, as well as in animals and the food chain. The small set of effective antibiotics has narrowed, especially in resource-poor settings, and people who are very young, very old, and severely ill are particularly susceptible to resistant infections. This paper, the first in a Series on the challenge of antimicrobial resistance, considers the global scope of the problem and how it should be measured. Robust and actionable data are needed to drive changes and inform effective interventions to contain resistance. Surveillance must cover all geographical regions, minimise biases towards hospital-derived data, and include non-human niches.
208. LANDMARK comparison of early outcomes of newer-generation Myval transcatheter heart valve series with contemporary valves (Sapien and Evolut) in real-world individuals with severe symptomatic native aortic stenosis: a randomised non-inferiority trial.
作者: Andreas Baumbach.;Niels van Royen.;Ignacio J Amat-Santos.;Martin Hudec.;Matjaz Bunc.;Alexander Ijsselmuiden.;Peep Laanmets.;Daniel Unic.;Bela Merkely.;Renicus S Hermanides.;Vlasis Ninios.;Marcin Protasiewicz.;Benno J W M Rensing.;Pedro L Martin.;Fausto Feres.;Manuel De Sousa Almeida.;Eric van Belle.;Axel Linke.;Alfonso Ielasi.;Matteo Montorfano.;Mark Webster.;Konstantinos Toutouzas.;Emmanuel Teiger.;Francesco Bedogni.;Michiel Voskuil.;Manuel Pan.;Oskar Angerås.;Won-Keun Kim.;Jürgen Rothe.;Ivica Kristić.;Vicente Peral.;Scot Garg.;Hesham Elzomor.;Akihiro Tobe.;Marie-Claude Morice.;Yoshinobu Onuma.;Osama Soliman.;Patrick W Serruys.; .
来源: Lancet. 2024年403卷10445期2695-2708页
Transcatheter aortic valve implantation is an established, guideline-endorsed treatment for severe aortic stenosis. Precise sizing of the balloon-expandable Myval transcatheter heart valve (THV) series with the aortic annulus is facilitated by increasing its diameter in 1·5 mm increments, compared with the usual 3 mm increments in valve size. The LANDMARK trial aimed to show non-inferiority of the Myval THV series compared with the contemporary THVs Sapien Series (Edwards Lifesciences, Irvine, CA, USA) or Evolut Series (Medtronic, Minneapolis, MN, USA).
209. Efficacy and safety of bimekizumab in patients with moderate-to-severe hidradenitis suppurativa (BE HEARD I and BE HEARD II): two 48-week, randomised, double-blind, placebo-controlled, multicentre phase 3 trials.
作者: Alexa B Kimball.;Gregor B E Jemec.;Christopher J Sayed.;Joslyn S Kirby.;Errol Prens.;John R Ingram.;Amit Garg.;Alice B Gottlieb.;Jacek C Szepietowski.;Falk G Bechara.;Evangelos J Giamarellos-Bourboulis.;Hideki Fujita.;Robert Rolleri.;Paulatsya Joshi.;Pratiksha Dokhe.;Edward Muller.;Luke Peterson.;Cynthia Madden.;Muhammad Bari.;Christos C Zouboulis.
来源: Lancet. 2024年403卷10443期2504-2519页
Patients with hidradenitis suppurativa have substantial unmet clinical needs and scarce therapeutic options. We aimed to assess the efficacy and safety of bimekizumab, a monoclonal IgG1 antibody that selectively inhibits interleukin (IL)-17F and IL-17A, in patients with moderate-to-severe hidradenitis suppurativa.
210. Societal implications of the Dobbs v Jackson Women's Health Organization decision.
作者: Claire D Brindis.;Melissa H Laitner.;Ellen Wright Clayton.;Susan C Scrimshaw.;Barbara J Grosz.;Lisa A Simpson.;Sara Rosenbaum.;Corale L Brierley.;Melissa A Simon.;Yvette Roubideaux.;Bruce N Calonge.;Paula A Johnson.;Laura DeStefano.;Ashley Bear.;Kavita S Arora.;Victor J Dzau.
来源: Lancet. 2024年403卷10445期2751-2754页
On June 24, 2022, the US Supreme Court's decision in Dobbs v Jackson Women's Health Organization marked the removal of the constitutional right to abortion in the USA, introducing a complex ethical and legal landscape for patients and providers. This shift has had immediate health and equity repercussions, but it is also crucial to examine the broader impacts on states, health-care systems, and society as a whole. Restrictions on abortion access extend beyond immediate reproductive care concerns, necessitating a comprehensive understanding of the ruling's consequences across micro and macro levels. To mitigate potential harm, it is imperative to establish a research agenda that informs policy making and ensures effective long-term monitoring and reporting, addressing both immediate and future impacts.
211. Health-care workforce implications of the Dobbs v Jackson Women's Health Organization decision.
作者: Claire D Brindis.;Melissa H Laitner.;Ellen Wright Clayton.;Susan C Scrimshaw.;Barbara J Grosz.;Lisa A Simpson.;Sara Rosenbaum.;Corale L Brierley.;Melissa A Simon.;Yvette Roubideaux.;Bruce N Calonge.;Paula A Johnson.;Laura DeStefano.;Ashley Bear.;Kavita S Arora.;Victor J Dzau.
来源: Lancet. 2024年403卷10445期2747-2750页
The Dobbs v Jackson Women's Health Organization Supreme Court decision, which revoked the constitutional right to abortion in the USA, has impacted the national medical workforce. Impacts vary across states, but providers in states with restrictive abortion laws now must contend with evolving legal and ethical challenges that have the potential to affect workforce safety, mental health, education, and training opportunities, in addition to having serious impacts on patient health and far-reaching societal consequences. Moreover, Dobbs has consequences on almost every facet of the medical workforce, including on physicians, nurses, pharmacists, and others who work within the health-care system. Comprehensive research is urgently needed to understand the wide-ranging implications of Dobbs on the medical workforce, including legal, ethical, clinical, and psychological dimensions, to inform evidence-based policies and standards of care in abortion-restrictive settings. Lessons from the USA might also have global relevance for countries facing similar restrictions on reproductive care.
212. Bariatric surgery for spontaneous ovulation in women living with polycystic ovary syndrome: the BAMBINI multicentre, open-label, randomised controlled trial.
作者: Suhaniya N S Samarasinghe.;Bianca Leca.;Shahd Alabdulkader.;Georgios K Dimitriadis.;Allan Davasgaium.;Puja Thadani.;Kate Parry.;Migena Luli.;Karen O'Donnell.;Brett Johnson.;Ali Abbara.;Florian Seyfried.;Rachel Morman.;Ahmed R Ahmed.;Sherif Hakky.;Christos Tsironis.;Sanjay Purkayastha.;Carel W le Roux.;Stephen Franks.;Vinod Menon.;Harpal Randeva.;Alexander D Miras.
来源: Lancet. 2024年403卷10443期2489-2503页
Polycystic ovary syndrome (PCOS) is the most common cause of anovulatory infertility. Obesity exacerbates the reproductive complications of PCOS; however, the management of obesity in women with PCOS remains a large unmet clinical need. Observational studies have indicated that bariatric surgery could improve the rates of ovulatory cycles and prospects of fertility; however, the efficacy of surgery on ovulation rates has not yet been compared with behavioural modifications and medical therapy in a randomised trial. The aim of this study was to compare the safety and efficacy of bariatric surgery versus medical care on ovulation rates in women with PCOS, obesity, and oligomenorrhoea or amenorrhoea.
213. Post-trial monitoring of a randomised controlled trial of intensive glycaemic control in type 2 diabetes extended from 10 years to 24 years (UKPDS 91).
作者: Amanda I Adler.;Ruth L Coleman.;Jose Leal.;William N Whiteley.;Philip Clarke.;Rury R Holman.
来源: Lancet. 2024年404卷10448期145-155页
The 20-year UK Prospective Diabetes Study showed major clinical benefits for people with newly diagnosed type 2 diabetes randomly allocated to intensive glycaemic control with sulfonylurea or insulin therapy or metformin therapy, compared with conventional glycaemic control. 10-year post-trial follow-up identified enduring and emerging glycaemic and metformin legacy treatment effects. We aimed to determine whether these effects would wane by extending follow-up for another 14 years.
214. Tenecteplase versus standard of care for minor ischaemic stroke with proven occlusion (TEMPO-2): a randomised, open label, phase 3 superiority trial.
作者: Shelagh B Coutts.;Sandeep Ankolekar.;Ramana Appireddy.;Juan F Arenillas.;Zarina Assis.;Peter Bailey.;Philip A Barber.;Rodrigo Bazan.;Brian H Buck.;Ken S Butcher.;Marie-Christine Camden.;Bruce C V Campbell.;Leanne K Casaubon.;Luciana Catanese.;Kausik Chatterjee.;Philip M C Choi.;Brian Clarke.;Dar Dowlatshahi.;Julia Ferrari.;Thalia S Field.;Aravind Ganesh.;Darshan Ghia.;Mayank Goyal.;Stefan Greisenegger.;Omid Halse.;Mackenzie Horn.;Gary Hunter.;Oje Imoukhuede.;Peter J Kelly.;James Kennedy.;Carol Kenney.;Timothy J Kleinig.;Kailash Krishnan.;Fabricio Lima.;Jennifer L Mandzia.;Martha Marko.;Sheila O Martins.;George Medvedev.;Bijoy K Menon.;Sachin M Mishra.;Carlos Molina.;Aimen Moussaddy.;Keith W Muir.;Mark W Parsons.;Andrew M W Penn.;Arthur Pille.;Octávio M Pontes-Neto.;Christine Roffe.;Joaquin Serena.;Robert Simister.;Nishita Singh.;Neil Spratt.;Daniel Strbian.;Carol H Tham.;M Ivan Wiggam.;David J Williams.;Mark R Willmot.;Teddy Wu.;Amy Y X Yu.;George Zachariah.;Atif Zafar.;Charlotte Zerna.;Michael D Hill.; .
来源: Lancet. 2024年403卷10444期2597-2605页
Individuals with minor ischaemic stroke and intracranial occlusion are at increased risk of poor outcomes. Intravenous thrombolysis with tenecteplase might improve outcomes in this population. We aimed to test the superiority of intravenous tenecteplase over non-thrombolytic standard of care in patients with minor ischaemic stroke and intracranial occlusion or focal perfusion abnormality.
215. Adding 6 months of androgen deprivation therapy to postoperative radiotherapy for prostate cancer: a comparison of short-course versus no androgen deprivation therapy in the RADICALS-HD randomised controlled trial.
作者: Chris C Parker.;Noel W Clarke.;Adrian D Cook.;Howard Kynaston.;Charles N Catton.;William R Cross.;Peter M Petersen.;Rajendra A Persad.;Fred Saad.;Lorna C Bower.;John Logue.;Heather Payne.;Silvia Forcat.;Cindy Goldstein.;Claire Murphy.;Juliette Anderson.;Maroie Barkati.;David M Bottomley.;Jennifer Branagan.;Ananya Choudhury.;Peter W M Chung.;Lyn Cogley.;Chee L Goh.;Peter Hoskin.;Vincent Khoo.;Shawn C Malone.;Lindsey Masters.;Stephen L Morris.;Abdenour Nabid.;Aldrich D Ong.;Rakesh Raman.;Kathryn L Tarver.;Alison C Tree.;Jane Worlding.;James P Wylie.;Anjali M Zarkar.;Wendy R Parulekar.;Mahesh K B Parmar.;Matthew R Sydes.; .
来源: Lancet. 2024年403卷10442期2405-2415页
Previous evidence indicates that adjuvant, short-course androgen deprivation therapy (ADT) improves metastasis-free survival when given with primary radiotherapy for intermediate-risk and high-risk localised prostate cancer. However, the value of ADT with postoperative radiotherapy after radical prostatectomy is unclear.
216. Duration of androgen deprivation therapy with postoperative radiotherapy for prostate cancer: a comparison of long-course versus short-course androgen deprivation therapy in the RADICALS-HD randomised trial.
作者: Chris C Parker.;Howard Kynaston.;Adrian D Cook.;Noel W Clarke.;Charles N Catton.;William R Cross.;Peter M Petersen.;Rajendra A Persad.;Cheryl A Pugh.;Fred Saad.;John Logue.;Heather Payne.;Lorna C Bower.;Chris Brawley.;Mary Rauchenberger.;Maroie Barkati.;David M Bottomley.;Klaus Brasso.;Hans T Chung.;Peter W M Chung.;Ruth Conroy.;Alison Falconer.;Vicky Ford.;Chee L Goh.;Catherine M Heath.;Nicholas D James.;Charmaine Kim-Sing.;Ravi Kodavatiganti.;Shawn C Malone.;Stephen L Morris.;Abdenour Nabid.;Aldrich D Ong.;Rakesh Raman.;Sree Rodda.;Paula Wells.;Jane Worlding.;Wendy R Parulekar.;Mahesh K B Parmar.;Matthew R Sydes.; .
来源: Lancet. 2024年403卷10442期2416-2425页
Previous evidence supports androgen deprivation therapy (ADT) with primary radiotherapy as initial treatment for intermediate-risk and high-risk localised prostate cancer. However, the use and optimal duration of ADT with postoperative radiotherapy after radical prostatectomy remains uncertain.
217. Burden of disease scenarios for 204 countries and territories, 2022-2050: a forecasting analysis for the Global Burden of Disease Study 2021.
Future trends in disease burden and drivers of health are of great interest to policy makers and the public at large. This information can be used for policy and long-term health investment, planning, and prioritisation. We have expanded and improved upon previous forecasts produced as part of the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) and provide a reference forecast (the most likely future), and alternative scenarios assessing disease burden trajectories if selected sets of risk factors were eliminated from current levels by 2050.
218. Global burden and strength of evidence for 88 risk factors in 204 countries and 811 subnational locations, 1990-2021: a systematic analysis for the Global Burden of Disease Study 2021.
Understanding the health consequences associated with exposure to risk factors is necessary to inform public health policy and practice. To systematically quantify the contributions of risk factor exposures to specific health outcomes, the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2021 aims to provide comprehensive estimates of exposure levels, relative health risks, and attributable burden of disease for 88 risk factors in 204 countries and territories and 811 subnational locations, from 1990 to 2021.
219. Decompressive craniectomy plus best medical treatment versus best medical treatment alone for spontaneous severe deep supratentorial intracerebral haemorrhage: a randomised controlled clinical trial.
作者: Jürgen Beck.;Christian Fung.;Daniel Strbian.;Lukas Bütikofer.;Werner J Z'Graggen.;Matthias F Lang.;Seraina Beyeler.;Jan Gralla.;Florian Ringel.;Karl Schaller.;Nikolaus Plesnila.;Marcel Arnold.;Werner Hacke.;Peter Jüni.;Alexander David Mendelow.;Christian Stapf.;Rustam Al-Shahi Salman.;Jenny Bressan.;Stefanie Lerch.;Arsany Hakim.;Nicolas Martinez-Majander.;Anna Piippo-Karjalainen.;Peter Vajkoczy.;Stefan Wolf.;Gerrit A Schubert.;Anke Höllig.;Michael Veldeman.;Roland Roelz.;Andreas Gruber.;Philip Rauch.;Dorothee Mielke.;Veit Rohde.;Thomas Kerz.;Eberhard Uhl.;Enea Thanasi.;Hagen B Huttner.;Bernd Kallmünzer.;L Jaap Kappelle.;Wolfgang Deinsberger.;Christian Roth.;Robin Lemmens.;Jan Leppert.;Jose L Sanmillan.;Jonathan M Coutinho.;Katharina A M Hackenberg.;Gernot Reimann.;Mikael Mazighi.;Claudio L A Bassetti.;Heinrich P Mattle.;Andreas Raabe.;Urs Fischer.; .
来源: Lancet. 2024年403卷10442期2395-2404页
It is unknown whether decompressive craniectomy improves clinical outcome for people with spontaneous severe deep intracerebral haemorrhage. The SWITCH trial aimed to assess whether decompressive craniectomy plus best medical treatment in these patients improves outcome at 6 months compared to best medical treatment alone.
220. Stroke.
作者: Nina A Hilkens.;Barbara Casolla.;Thomas W Leung.;Frank-Erik de Leeuw.
来源: Lancet. 2024年403卷10446期2820-2836页
Stroke affects up to one in five people during their lifetime in some high-income countries, and up to almost one in two in low-income countries. Globally, it is the second leading cause of death. Clinically, the disease is characterised by sudden neurological deficits. Vascular aetiologies contribute to the most common causes of ischaemic stroke, including large artery disease, cardioembolism, and small vessel disease. Small vessel disease is also the most frequent cause of intracerebral haemorrhage, followed by macrovascular causes. For acute ischaemic stroke, multimodal CT or MRI reveal infarct core, ischaemic penumbra, and site of vascular occlusion. For intracerebral haemorrhage, neuroimaging identifies early radiological markers of haematoma expansion and probable underlying cause. For intravenous thrombolysis in ischaemic stroke, tenecteplase is now a safe and effective alternative to alteplase. In patients with strokes caused by large vessel occlusion, the indications for endovascular thrombectomy have been extended to include larger core infarcts and basilar artery occlusion, and the treatment time window has increased to up to 24 h from stroke onset. Regarding intracerebral haemorrhage, prompt delivery of bundled care consisting of immediate anticoagulation reversal, simultaneous blood pressure lowering, and prespecified stroke unit protocols can improve clinical outcomes. Guided by underlying stroke mechanisms, secondary prevention encompasses pharmacological, vascular, or endovascular interventions and lifestyle modifications.
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