2766. Global incidence, prevalence, years lived with disability (YLDs), disability-adjusted life-years (DALYs), and healthy life expectancy (HALE) for 371 diseases and injuries in 204 countries and territories and 811 subnational locations, 1990-2021: a systematic analysis for the Global Burden of Disease Study 2021.
Detailed, comprehensive, and timely reporting on population health by underlying causes of disability and premature death is crucial to understanding and responding to complex patterns of disease and injury burden over time and across age groups, sexes, and locations. The availability of disease burden estimates can promote evidence-based interventions that enable public health researchers, policy makers, and other professionals to implement strategies that can mitigate diseases. It can also facilitate more rigorous monitoring of progress towards national and international health targets, such as the Sustainable Development Goals. For three decades, the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) has filled that need. A global network of collaborators contributed to the production of GBD 2021 by providing, reviewing, and analysing all available data. GBD estimates are updated routinely with additional data and refined analytical methods. GBD 2021 presents, for the first time, estimates of health loss due to the COVID-19 pandemic.
2767. Systemic lupus erythematosus.
Systemic lupus erythematosus (SLE) is a multisystemic autoimmune disease characterised by the presence of autoantibodies towards nuclear antigens, immune complex deposition, and chronic inflammation at classic target organs such as skin, joints, and kidneys. Despite substantial advances in the diagnosis and management of SLE, the burden of disease remains high. It is important to appreciate the typical presentations and the diagnostic process to facilitate early referral and diagnosis for patients. In most patients, constitutional, mucocutaneous, and musculoskeletal symptoms represent the earliest complaints; these symptoms can include fatigue, lupus-specific rash, mouth ulcers, alopecia, joint pain, and myalgia. In this Seminar we will discuss a diagnostic approach to symptoms in light of the latest classification criteria, which include a systematic evaluation of clinical manifestations (weighted within each domain) and autoantibody profiles (such as anti-double-stranded DNA, anti-Sm, hypocomplementaemia, or antiphospholipid antibodies). Non-pharmacotherapy management is tailored to the individual, with specific lifestyle interventions and patient education to improve quality of life and medication (such as hydroxychloroquine or immunosuppressant) adherence. In the last decade, there have been a few major breakthroughs in approved treatments for SLE and lupus nephritis, such as belimumab, anifrolumab, and voclosporin. However the disease course remains variable and mortality unacceptably high. Access to these expensive medications has also been restricted across different regions of the world. Nonetheless, understanding of treatment goals and strategies has improved. We recognise that the main goal of treatment is the achievement of remission or low disease activity. Comorbidities due to both disease activity and treatment adverse effects, especially infections, osteoporosis, and cardiovascular disease, necessitate vigilant prevention and management strategies. Tailoring treatment options to achieve remission, while balancing treatment-related comorbidities, are priority areas of SLE management.
2768. CAR T-cell therapy rescues adolescent with rapidly progressive lupus nephritis from haemodialysis.
作者: Tobias Krickau.;Nora Naumann-Bartsch.;Michael Aigner.;Soraya Kharboutli.;Sascha Kretschmann.;Silvia Spoerl.;Ingrid Vasova.;Simon Völkl.;Joachim Woelfle.;Andreas Mackensen.;Georg Schett.;Markus Metzler.;Fabian Müller.
来源: Lancet. 2024年403卷10437期1627-1630页 2771. The Lancet Breast Cancer Commission.
作者: Charlotte E Coles.;Helena Earl.;Benjamin O Anderson.;Carlos H Barrios.;Maya Bienz.;Judith M Bliss.;David A Cameron.;Fatima Cardoso.;Wanda Cui.;Prudence A Francis.;Reshma Jagsi.;Felicia Marie Knaul.;Stuart A McIntosh.;Kelly-Anne Phillips.;Lukas Radbruch.;Mareike K Thompson.;Fabrice André.;Jean E Abraham.;Indrani S Bhattacharya.;Maria Alice Franzoi.;Lynsey Drewett.;Alexander Fulton.;Farasat Kazmi.;Dharrnesha Inbah Rajah.;Miriam Mutebi.;Dianna Ng.;Szeyi Ng.;Olufunmilayo I Olopade.;William E Rosa.;Jeffrey Rubasingham.;Dingle Spence.;Hilary Stobart.;Valentina Vargas Enciso.;Ines Vaz-Luis.;Cynthia Villarreal-Garza.; .
来源: Lancet. 2024年403卷10439期1895-1950页 2773. Chronic suppurative otitis media.
作者: Mahmood F Bhutta.;Amanda J Leach.;Christopher G Brennan-Jones.
来源: Lancet. 2024年403卷10441期2339-2348页
Chronic suppurative otitis media (CSOM) is a leading global cause of potentially preventable hearing loss in children and adults, associated with socioeconomic deprivation. There is an absence of consensus on the definition of CSOM, which complicates efforts for prevention, treatment, and monitoring. CSOM occurs when perforation of the tympanic membrane is associated with severe or persistent inflammation in the middle ear, leading to hearing loss and recurrent or persistent ear discharge (otorrhoea). Cholesteatoma, caused by the inward growth of the squamous epithelium of the tympanic membrane into the middle ear, can also occur. The optimal treatment of discharge in CSOM is topical antibiotics. In resource-limited settings where topical antibiotics might not be available, topical antiseptics are an alternative. For persistent disease, surgery to repair the tympanic membrane or remove cholesteatoma might offer long-term resolution of otorrhoea and potential improvement to hearing. Recent developments in self-fitted air-conduction and bone-conduction hearing aids offer promise as new options for rehabilitation.
|