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共有 145290 条符合本次的查询结果, 用时 9.2026425 秒

481. Weighing up causes of and risk factors for postpartum haemorrhage to improve its prevention.

作者: Anne-Sophie Ducloy-Bouthors.;Maria-Fernanda Escobar Vidarte.
来源: Lancet. 2025年405卷10488期1440-1441页

482. The promise and compromise of the WHO Pandemic Agreement for spillover prevention and One Health.

作者: Alexandra Finch.;Neil M Vora.;Latiffah Hassan.;Chris Walzer.;Raina K Plowright.;Robyn Alders.;Chyna Yong Suit-B.;John H Amuasi.;Moses Mulumba.;Ted Loch-Temzelides.;Sergio Guerrero-Sanchez.;Lawrence O Gostin.
来源: Lancet. 2025年405卷10492期1800-1802页

483. Loretta Ford.

作者: Georgina Ferry.
来源: Lancet. 2025年405卷10485期1138页

484. Pancreatic cancer.

作者: Thomas F Stoop.;Ammar A Javed.;Atsushi Oba.;Bas Groot Koerkamp.;Thomas Seufferlein.;Johanna W Wilmink.;Marc G Besselink.
来源: Lancet. 2025年405卷10485期1182-1202页
Pancreatic cancer is frequently a lethal disease with an aggressive tumour biology often presenting with non-specific symptoms. Median survival is approximately 4 months with a 5-year survival of 13%. Surveillance is recommended in individuals with familial pancreatic cancer, specific mutations, and high-risk intraductal papillary mucinous neoplasm, as they are at high risk of developing pancreatic cancer. Chemotherapy combined with surgical resection remains the cornerstone of treatment. However, only a small subset of patients are candidates for surgery. Multi-agent chemotherapy has improved survival in the palliative setting for patients with metastatic disease, as (neo)adjuvant and induction therapy have in patients with borderline resectable and locally advanced pancreatic. Given that pancreatic cancer is predicted to become the second leading cause of cancer-related death by 2030, novel therapies are urgently needed.

485. Response to treatment in the Multiple Symptoms Study 3 trial - Authors' reply.

作者: Christopher Burton.;Vincent Deary.;Cara Mooney.;Laura Sutton.;Cindy Cooper.
来源: Lancet. 2025年405卷10485期1146页

488. PET evaluation in Hodgkin lymphoma: when to change treatment - Authors' reply.

作者: Justin Ferdinandus.;Gundolf Schneider.;Peter Borchmann.
来源: Lancet. 2025年405卷10485期1145页

489. Response to treatment in the Multiple Symptoms Study 3 trial.

作者: Joan S Crawford.;David Tuller.
来源: Lancet. 2025年405卷10485期1145-1146页

490. The omission of Angola in mpox epidemiological reports.

作者: Hermenegildo Osvaldo Chitumba.;Mauer Alexandre da Ascensão Gonçalves.;Humberto Morais.;Howard Lopes Ribeiro Junior.
来源: Lancet. 2025年405卷10485期1144页

491. PET evaluation in Hodgkin lymphoma: when to change treatment.

作者: Yutaka Shimazu.
来源: Lancet. 2025年405卷10485期1144-1145页

492. Why all countries should adopt the term mpox.

作者: Clarissa R Damaso.;David Ulaeto.
来源: Lancet. 2025年405卷10485期1143-1144页

493. Long-acting HIV preventive treatments for remote rural communities.

作者: Justin T Okano.;Sally Blower.
来源: Lancet. 2025年405卷10485期1143页

494. Maternal and child health adaptation to declining fertility in China.

作者: Zhiming Dai.
来源: Lancet. 2025年405卷10485期1142页

495. Cardiovascular risk assessment in venous disease?

作者: Sarah Onida.;Alun H Davies.
来源: Lancet. 2025年405卷10485期1141-1142页

496. Adivasis of eastern India and the global planetary health crisis.

作者: Vinita Damodaran.
来源: Lancet. 2025年405卷10485期1136-1137页

497. Reducing postpartum haemorrhage.

作者: The Lancet.
来源: Lancet. 2025年405卷10485期1119页

498. Head-to-head comparison of balloon-expandable transcatheter heart valves.

作者: Mariama Akodad.
来源: Lancet. 2025年405卷10487期1316-1317页

499. SAPIEN 3 versus Myval transcatheter heart valves for transcatheter aortic valve implantation (COMPARE-TAVI 1): a multicentre, randomised, non-inferiority trial.

作者: Christian Juhl Terkelsen.;Philip Freeman.;Jordi Sanchez Dahl.;Troels Thim.;Bjarne Linde Nørgaard.;Nils Sofus Borg Mogensen.;Mariann Tang.;Ashkan Eftekhari.;Jonas Agerlund Povlsen.;Steen Hvitfeldt Poulsen.;Lars Pedersen.;Jakob Hjort.;Julia Ellert.;Evald Høj Christiansen.;Henrik Toft Sørensen.;Henrik Nissen.
来源: Lancet. 2025年405卷10487期1362-1372页
Transcatheter aortic valve implantation (TAVI) is a guideline-directed treatment for severe aortic stenosis and degenerated aortic bioprostheses. When new transcatheter heart valve (THV) platforms for TAVI are launched, they should be compared with best-in-practice contemporary THVs for their short-term and long-term performance. The COMPARE-TAVI 1 trial was designed to provide a head-to-head comparison of the SAPIEN 3 or SAPIEN 3 Ultra THVs and the Myval or Myval Octacor THVs.

500. The Lancet Commission on rethinking coronary artery disease: moving from ischaemia to atheroma.

作者: Sarah Zaman.;Jason H Wasfy.;Vikas Kapil.;Boback Ziaeian.;William A Parsonage.;Sira Sriswasdi.;Timothy J A Chico.;Davide Capodanno.;Róisín Colleran.;Nadia R Sutton.;Lei Song.;Nicole Karam.;Reecha Sofat.;Chiara Fraccaro.;Daniel Chamié.;Mirvat Alasnag.;Takayuki Warisawa.;Nieves Gonzalo.;Walid Jomaa.;Shamir R Mehta.;Elizabeth E S Cook.;Johan Sundström.;Stephen J Nicholls.;Leslee J Shaw.;Manesh R Patel.;Rasha K Al-Lamee.
来源: Lancet. 2025年405卷10486期1264-1312页
Coronary artery disease has long been understood through the paradigm of epicardial coronary artery obstruction, causing myocardial ischaemia (a mismatch between myocardial blood supply and demand). However, this model, which focuses on diagnosing and managing coronary artery disease based on ischaemia and cardiovascular events, is flawed. By the time ischaemia manifests, it is often too late for optimal intervention, limiting the effectiveness of treatment options. Despite decades of medical advances, coronary artery disease continues to be a leading cause of morbidity and mortality globally, highlighting the inadequacy of this traditional ischaemic-centric approach. The central limitation of current approaches is the focus on the temporary solutions of restoring myocardial blood flow after obstruction, rather than tackling the underlying disease. Coronary artery disease, caused by atherosclerosis, often results in myocardial infarction through mechanisms that emerge earlier in the progression of disease. The focus of medical care has predominantly been on the recognition of symptoms and treatment of acute events, missing opportunities for early detection and prevention of disease. Billions of dollars in health-care funding continue to be spent on identifying and managing coronary ischaemia; yet, the dominant mechanisms for myocardial infarction are atherosclerotic plaque rupture or erosion and, to a lesser extent, erupted calcified nodules that can emerge at a much earlier stage of the disease. This Commission advocates for a shift in the conceptual framework of coronary artery disease. We suggest reclassifying the condition as atherosclerotic coronary artery disease (ACAD), moving away from the traditional emphasis on ischaemia and acute cardiac events towards a more systematic understanding of atherosclerosis. This reframing will enable the identification and management of the disease much earlier in its course, potentially saving millions of lives worldwide. Risk of ACAD develops over a lifetime, beginning in utero, progressing through childhood and adolescence, and continuing into older age. The early stages of disease, which involve the formation of atherosclerotic plaques, are often undetected. A major shift is needed from acute event-centred care to strategies focused on early diagnosis, prevention, and management of atherosclerosis. In this new framework, ACAD should be recognised across all stages, from the earliest signs of atheroma formation to the advanced stages of disease. Our goals should not just to be to manage symptoms and events but to prevent the disease from developing in the first place and, where possible, reverse its course.
共有 145290 条符合本次的查询结果, 用时 9.2026425 秒