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Background: Anaemia causes widespread health and economic harm. Current international targets for reducing anaemia in women of reproductive age, including the Sustainable Development Goal of halving prevalence by 2030, are unlikely to be met by any signatory country. This outcome suggests that current targets were grounded in aspiration rather than a systematic assessment of what is achievable given current recommended interventions and national health-care priorities. We propose a novel method of target setting for global health goals, with reducing anaemia in women of reproductive age as an example.
Methods: In this modelling study, we developed a country-level health economic model to support feasible and ambitious target-setting for anaemia for women of reproductive age (aged 15-49 years) based on cost-effectiveness analysis and applied it to 191 signatory countries. Our model integrated country-specific data on the current prevalence of anaemia, the effectiveness and current and maximal coverage of recommended interventions available to each country, the local unit costs of these interventions, and country-specific cost-effectiveness threshold estimates, including Global Burden of Disease data and data from the Demographic and Health Survey Program. Interventions were applied to maximise health gains subject to country-level cost-effectiveness thresholds at 1 × gross domestic product per capita. We assessed parameter uncertainty through Monte Carlo simulations and scenarios that considered alternative thresholds, constraints on cost, and coverage.
Findings: Our results indicate that an ambitious, achievable, and cost-effective global target for anaemia reduction in women aged 15-49 years by 2030 is 17% (95% uncertainty interval [UI] 5-34). The maximum achievable target removing all cost constraints is a 22% (11-36) reduction. No scenario approached the current 50% global Sustainable Development Goal reduction target, indicating that this goal is unachievable with existing recommended interventions. Reduction targets for individual countries ranged from 0% to 29%, with substantial variation both between and within regions and income groups.
Interpretation: Our findings suggest that a value-based global target for anaemia reduction will be substantially lower than the existing international commitment. Value-based targets using evidence from available interventions and cost-effectiveness for what is achievable given countries' differing contexts can provide better incentives for progress and offer more realistic forecasts of human development.
Funding: Gates Foundation.
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http://dx.doi.org/10.1016/S2352-3026(25)00168-1 | DOI Listing |
Transplant Cell Ther
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Department of Hematology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Traditional Chinese Medicine); Hangzhou, China; The First School of Clinical Medicine, Zhejiang Chinese Medical University; Hangzhou, China. Electronic address: szyyblood@1
Aplastic anemia (AA) is a bone marrow failure disorder treated with allogeneic hematopoietic stem cell transplantation (allo-HSCT). Despite improvements in conditioning regimens and GVHD prophylaxis, graft failure and GVHD remain critical challenges. This study compared the efficacy of mesenchymal stem cells (MSCs) and umbilical cord blood cells (UCBs) as adjunctive therapies in 184 AA patients undergoing allo-HSCT.
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Daiichi Sankyo Inc., Basking Ridge, NJ, USA.
Valemetostat is a dual inhibitor of EZH2/1 approved in Japan for the treatment of relapsed/refractory (R/R) adult T-cell lymphoma/leukemia (ATLL) and R/R peripheral T-cell lymphoma (PTCL). It is administered orally once daily (QD) at 200 mg. Here, we present comprehensive population pharmacokinetic (PPK) and exposure-response (ER) analyses of valemetostat.
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Department of Microbiology & Biotechnology, University School of Sciences, Gujarat University, Ahmedabad 380009, Gujarat, India; Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, Victoria, Australia. Electronic addr
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View Article and Find Full Text PDFFront Med (Lausanne)
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Department of Infectious Diseases, Liaocheng People's Hospital, Liaocheng, China.
This article presents a case of a 15-year-old male with a 6-year history of aplastic anemia treated with long-term oral stanozolol to promote hematopoiesis. Throughout this period, he underwent regular outpatient follow-up assessments of blood and liver function parameters. While abnormal liver function was recorded on several occasions and treated with oral hepatoprotective drugs, no abdominal imaging test was conducted.
View Article and Find Full Text PDFClin Rheumatol
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Department of Rheumatology and Immunology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Number 197 Ruijin Second Road, Shanghai, 200025, China.
Objectives: Pulmonary hemorrhage (PH) represents a rare complication in systemic lupus erythematosus (SLE). In this study, we conducted a thorough investigation into the clinical features, diagnosis, treatment modalities, and outcomes of patients with SLE-associated PH at our medical center. Additionally, a comparative analysis of clinical and laboratory parameters before and after rituximab therapy were performed to assess its efficacy in the management of SLE-associated PH.
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