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The Changing Landscape of Sugar-Sweetened Beverage Taxes-Small Cities Have a Big Impact. 含糖饮料税的变化——小城市影响很大。
JAMA Pub Date : 2025-04-29 DOI: 10.1001/jama.2025.5377
John Maa,Sabrina Adler,Sarah de Guia,Laura Schmidt
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引用次数: 0
SPIRIT 2025 Statement SPIRIT 2025声明
JAMA Pub Date : 2025-04-28 DOI: 10.1001/jama.2025.4486
An-Wen Chan, Isabelle Boutron, Sally Hopewell, David Moher, Kenneth F. Schulz, Gary S. Collins, Ruth Tunn, Rakesh Aggarwal, Michael Berkwits, Jesse A. Berlin, Nita Bhandari, Nancy J. Butcher, Marion K. Campbell, Runcie C. W. Chidebe, Diana R. Elbourne, Andrew J. Farmer, Dean A. Fergusson, Robert M. Golub, Steven N. Goodman, Tammy C. Hoffmann, John P. A. Ioannidis, Brennan C. Kahan, Rachel L. Knowles, Sarah E. Lamb, Steff Lewis, Elizabeth Loder, Martin Offringa, Philippe Ravaud, Dawn P. Richards, Frank W. Rockhold, David L. Schriger, Nandi L. Siegfried, Sophie Staniszewska, Rod S. Taylor, Lehana Thabane, David J. Torgerson, Sunita Vohra, Ian R. White, Asbjørn Hróbjartsson
{"title":"SPIRIT 2025 Statement","authors":"An-Wen Chan, Isabelle Boutron, Sally Hopewell, David Moher, Kenneth F. Schulz, Gary S. Collins, Ruth Tunn, Rakesh Aggarwal, Michael Berkwits, Jesse A. Berlin, Nita Bhandari, Nancy J. Butcher, Marion K. Campbell, Runcie C. W. Chidebe, Diana R. Elbourne, Andrew J. Farmer, Dean A. Fergusson, Robert M. Golub, Steven N. Goodman, Tammy C. Hoffmann, John P. A. Ioannidis, Brennan C. Kahan, Rachel L. Knowles, Sarah E. Lamb, Steff Lewis, Elizabeth Loder, Martin Offringa, Philippe Ravaud, Dawn P. Richards, Frank W. Rockhold, David L. Schriger, Nandi L. Siegfried, Sophie Staniszewska, Rod S. Taylor, Lehana Thabane, David J. Torgerson, Sunita Vohra, Ian R. White, Asbjørn Hróbjartsson","doi":"10.1001/jama.2025.4486","DOIUrl":"https://doi.org/10.1001/jama.2025.4486","url":null,"abstract":"ImportanceThe protocol of a randomized trial is the foundation for study planning, conduct, reporting, and external review. However, trial protocols vary in their completeness and often do not address key elements of design and conduct. The SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) statement was first published in 2013 as guidance to improve the completeness of trial protocols. Periodic updates incorporating the latest evidence and best practices are needed to ensure that the guidance remains relevant to users. Herein, we systematically update the SPIRIT recommendations for minimum items to address in the protocol of a randomized trial.ObservationsWe completed a scoping review and developed a project specific database of empirical and theoretical evidence to generate a list of potential changes to the SPIRIT 2013 checklist. The list was enriched with recommendations provided by lead authors of existing SPIRIT/CONSORT (Consolidated Standards of Reporting Trials) extensions (harms, outcomes, nonpharmacological treatment) and other reporting guidelines (Template for Intervention Description and Replication [TIDieR]). The potential modifications were rated in a 3-round Delphi survey followed by a consensus meeting. Overall, 317 individuals participated in the Delphi consensus process and 30 experts attended the consensus meeting. The process led to the addition of 2 new protocol items, revision to 5 items, deletion/merger of 5 items, and integration of key items from other relevant reporting guidelines. Notable changes include a new open-science section, additional emphasis on the assessment of harms and description of interventions and comparators, and a new item on how patients and the public will be involved in trial design, conduct, and reporting. The updated SPIRIT 2025 statement consists of an evidence based checklist of 34 minimum items to address in a trial protocol, along with a diagram illustrating the schedule of enrollment, interventions, and assessments for trial participants. To facilitate implementation, we also developed an expanded version of the SPIRIT 2025 checklist and an accompanying explanation and elaboration document.Conclusions and RelevanceWidespread endorsement and adherence to the updated SPIRIT 2025 statement have the potential to enhance the transparency and completeness of trial protocols for the benefit of investigators, trial participants, patients, funders, research ethics committees, journals, trial registries, policy makers, regulators, and other reviewers.","PeriodicalId":518009,"journal":{"name":"JAMA","volume":"7 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143884287","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Non–Cystic Fibrosis Bronchiectasis in Adults 成人非囊性纤维化支气管扩张症
JAMA Pub Date : 2025-04-28 DOI: 10.1001/jama.2025.2680
Alan F. Barker, Elham Karamooz
{"title":"Non–Cystic Fibrosis Bronchiectasis in Adults","authors":"Alan F. Barker, Elham Karamooz","doi":"10.1001/jama.2025.2680","DOIUrl":"https://doi.org/10.1001/jama.2025.2680","url":null,"abstract":"ImportanceNon–cystic fibrosis (CF) bronchiectasis is a chronic lung condition caused by permanent bronchial dilatation and inflammation and is characterized by daily cough, sputum, and recurrent exacerbations. Approximately 500 000 people in the US have non-CF bronchiectasis.ObservationsNon-CF bronchiectasis may be associated with prior pneumonia, infection with nontuberculous mycobacteria or tuberculosis, genetic conditions (eg, α<jats:sub>1</jats:sub>-antitrypsin deficiency, primary ciliary dyskinesia), autoimmune diseases (eg, rheumatoid arthritis, inflammatory bowel disease), allergic bronchopulmonary aspergillosis, and immunodeficiency syndromes (eg, common variable immunodeficiency). Up to 38% of cases are idiopathic. According to US data, conditions associated with non-CF bronchiectasis include gastroesophageal reflux disease (47%), asthma (29%), and chronic obstructive pulmonary disease (20%). The prevalence of non-CF bronchiectasis increases substantially with age (7 per 100 000 in individuals 18-34 years vs 812 per 100 000 in those ≥75 years) and is more common in women than men (180 vs 95 per 100 000). Diagnosis is confirmed with noncontrast chest computed tomography showing dilated airways and often airway thickening and mucus plugging. Initial diagnostic evaluation involves blood testing (complete blood cell count with differential); immunoglobulin quantification testing (IgG, IgA, IgE, and IgM); sputum cultures for bacteria, mycobacteria, and fungi; and prebronchodilator and postbronchodilator spirometry. Treatment includes airway clearance techniques; nebulization of saline to loosen tenacious secretions; and regular exercise, participation in pulmonary rehabilitation, or both. Inhaled bronchodilators (β-agonists and antimuscarinic agents) and inhaled corticosteroids are indicated for patients with bronchiectasis who have asthma or chronic obstructive pulmonary disease. Exacerbations of bronchiectasis, which typically present with increased cough and sputum and worsened fatigue, are associated with progressive decline in lung function and decreased quality of life. Exacerbations should be treated with oral or intravenous antibiotics. Individuals with 3 or more exacerbations of bronchiectasis annually may benefit from long-term inhaled antibiotics (eg, colistin, gentamicin) or daily oral macrolides (eg, azithromycin). Lung transplant may be considered for patients with severely impaired pulmonary function, frequent exacerbations, or both. Among patients with non-CF bronchiectasis, mortality is higher for those with frequent and severe exacerbations, infection with <jats:italic>Pseudomonas aeruginosa,</jats:italic> and comorbidities, such as chronic obstructive pulmonary disease.Conclusions and RelevanceNon-CF bronchiectasis is a chronic lung condition that typically causes chronic cough and daily sputum production. Exacerbations are associated with progressive decline in lung function and decreased quality of life. Management involv","PeriodicalId":518009,"journal":{"name":"JAMA","volume":"35 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143884903","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Electronic Sepsis Screening Among Hospital Ward Patients. 医院病房病人败血症电子筛查
JAMA Pub Date : 2025-04-28 DOI: 10.1001/jama.2025.1616
Rinaldo Bellomo,Daryl Jones
{"title":"Electronic Sepsis Screening Among Hospital Ward Patients.","authors":"Rinaldo Bellomo,Daryl Jones","doi":"10.1001/jama.2025.1616","DOIUrl":"https://doi.org/10.1001/jama.2025.1616","url":null,"abstract":"","PeriodicalId":518009,"journal":{"name":"JAMA","volume":"83 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143889241","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Reflecting on 2 Decades of Medicare ACO Experience. 20年医疗ACO经验的反思。
JAMA Pub Date : 2025-04-28 DOI: 10.1001/jama.2025.6175
Mariétou H Ouayogodé,Carrie H Colla
{"title":"Reflecting on 2 Decades of Medicare ACO Experience.","authors":"Mariétou H Ouayogodé,Carrie H Colla","doi":"10.1001/jama.2025.6175","DOIUrl":"https://doi.org/10.1001/jama.2025.6175","url":null,"abstract":"","PeriodicalId":518009,"journal":{"name":"JAMA","volume":"42 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143889289","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Toward Defining Problematic Media Usage Patterns in Adolescents 定义青少年有问题的媒体使用模式
JAMA Pub Date : 2025-04-28 DOI: 10.1001/jama.2025.6113
Dimitri A. Christakis, Lauren Hale
{"title":"Toward Defining Problematic Media Usage Patterns in Adolescents","authors":"Dimitri A. Christakis, Lauren Hale","doi":"10.1001/jama.2025.6113","DOIUrl":"https://doi.org/10.1001/jama.2025.6113","url":null,"abstract":"This Viewpoint discusses the urgent need to form an analogous taxonomy for digital media use that identifies patterns of use, irrespective of content, that could be problematic, particularly for children and adolescents.","PeriodicalId":518009,"journal":{"name":"JAMA","volume":"37 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143884288","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Extended Caffeine for Apnea in Moderately Preterm Infants: The MoCHA Randomized Clinical Trial. 延长咖啡因治疗中度早产儿呼吸暂停:MoCHA随机临床试验。
JAMA Pub Date : 2025-04-28 DOI: 10.1001/jama.2025.5791
Waldemar A Carlo,Eric C Eichenwald,Benjamin A Carper,Edward F Bell,Martin Keszler,Ravi M Patel,Pablo J Sánchez,Ronald N Goldberg,Carl T D'Angio,Krisa P Van Meurs,Anna Maria Hibbs,Namasivayam Ambalavanan,Shirley S Cosby,Nancy S Newman,Betty R Vohr,Michele C Walsh,Abhik Das,Robin K Ohls,Janell Fuller,Matthew A Rysavy,Sarvin Ghavam,Luc P Brion,Karen M Puopolo,Ryan Moore,Michelle L Baack,Tarah T Colaizy,Mariana Baserga,Ahmed F Osman,Stephanie L Merhar,Brenda B Poindexter,Sara B DeMauro,Vasanth Kumar,C Michael Cotten,
{"title":"Extended Caffeine for Apnea in Moderately Preterm Infants: The MoCHA Randomized Clinical Trial.","authors":"Waldemar A Carlo,Eric C Eichenwald,Benjamin A Carper,Edward F Bell,Martin Keszler,Ravi M Patel,Pablo J Sánchez,Ronald N Goldberg,Carl T D'Angio,Krisa P Van Meurs,Anna Maria Hibbs,Namasivayam Ambalavanan,Shirley S Cosby,Nancy S Newman,Betty R Vohr,Michele C Walsh,Abhik Das,Robin K Ohls,Janell Fuller,Matthew A Rysavy,Sarvin Ghavam,Luc P Brion,Karen M Puopolo,Ryan Moore,Michelle L Baack,Tarah T Colaizy,Mariana Baserga,Ahmed F Osman,Stephanie L Merhar,Brenda B Poindexter,Sara B DeMauro,Vasanth Kumar,C Michael Cotten,","doi":"10.1001/jama.2025.5791","DOIUrl":"https://doi.org/10.1001/jama.2025.5791","url":null,"abstract":"ImportanceHospitalization of moderately preterm infants may be prolonged while waiting for apnea of prematurity to resolve after discontinuing caffeine.ObjectiveTo evaluate whether extending caffeine treatment reduces the duration of hospitalization.Design, Setting, and ParticipantsFrom February 2019 to December 2022, this randomized clinical trial in 29 US hospitals enrolled infants born at 29 to 33 weeks' gestation who at 33 to 35 weeks' postmenstrual age were receiving caffeine treatment with plans to discontinue it plus receiving full feeds (≥120 mL/kg/d). Follow-up was completed on March 20, 2023.InterventionsInfants were randomized to oral caffeine citrate (10 mg/kg/d) or placebo until 28 days after discharge.Main Outcomes and MeasuresThe primary outcome was days to discharge after randomization. Secondary outcomes included days to physiological maturity (apnea free for 5 consecutive days, receiving full oral feeds, and out of the incubator for at least 48 hours), postmenstrual age at discharge, all-cause hospital readmissions, all-cause sick and emergency department visits, safety outcomes, and death.ResultsA total of 827 infants (median gestational age, 31 weeks; 414 female [51%]) were randomized (416, caffeine; 411, placebo) out of the 878 planned before reaching the prespecified futility threshold. Days of hospitalization after randomization did not differ between groups (18.0 days [IQR, 10 to 30 days] for caffeine vs 16.5 [IQR, 10 to 27 days] for placebo; adjusted median difference, 0 days [95% CI, -1.7 to 1.7 days]), nor did days to physiological maturity differ (14.0 vs 15.0 days, adjusted median difference, -1 day [95% CI, -2.4 to 0.4 days]). Infants receiving caffeine were apnea free sooner (6.0 vs 10.0 days; adjusted median difference, -2.7 days [95% CI, -3.4 to -2.0 days ]) but had similar days to full oral feeding (7.5 vs 6.0 days, adjusted median difference, 0 days [95% CI, -0.1 to 0.1]). Rates of readmissions and sick visits did not differ between groups. There was no statistically significant difference in adverse events between the 2 groups.Conclusions and RelevanceIn moderately preterm infants, continuation of caffeine treatment compared with placebo did not shorten hospitalization.Trial RegistrationClinicalTrials.gov Identifier: NCT03340727.","PeriodicalId":518009,"journal":{"name":"JAMA","volume":"36 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143889288","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Preserving Research Ethics Oversight Amid Decimation of the Research Enterprise 在研究企业大量流失的情况下,保持研究伦理监督
JAMA Pub Date : 2025-04-28 DOI: 10.1001/jama.2025.6361
Holly Fernandez Lynch, Ivy Tillman, Elyse I. Summers, Eric Mah
{"title":"Preserving Research Ethics Oversight Amid Decimation of the Research Enterprise","authors":"Holly Fernandez Lynch, Ivy Tillman, Elyse I. Summers, Eric Mah","doi":"10.1001/jama.2025.6361","DOIUrl":"https://doi.org/10.1001/jama.2025.6361","url":null,"abstract":"This Viewpoint examines how research ethics oversight, particularly by institutional review boards, has been affected by expansive federal staffing and budget cuts.","PeriodicalId":518009,"journal":{"name":"JAMA","volume":"8 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143884286","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Long-Term Spending of Accountable Care Organizations in the Medicare Shared Savings Program 医疗保险共享储蓄计划中负责任的医疗机构的长期支出
JAMA Pub Date : 2025-04-28 DOI: 10.1001/jama.2025.3870
Amelia M. Bond, Yasin Civelek, William L. Schpero, Lawrence P. Casalino, Manyao Zhang, Reekarl Pierre, Dhruv Khullar
{"title":"Long-Term Spending of Accountable Care Organizations in the Medicare Shared Savings Program","authors":"Amelia M. Bond, Yasin Civelek, William L. Schpero, Lawrence P. Casalino, Manyao Zhang, Reekarl Pierre, Dhruv Khullar","doi":"10.1001/jama.2025.3870","DOIUrl":"https://doi.org/10.1001/jama.2025.3870","url":null,"abstract":"ImportanceEvidence from initial cohorts of accountable care organizations (ACOs) participating in the Medicare Shared Savings Program (MSSP) found modest reductions in health care spending. Little is known about whether these effects have changed over time.ObjectiveTo determine long-term changes in spending for MSSP ACO participants.Design, Setting, and ParticipantsUsing 2010 to 2019 traditional Medicare data, difference-in-differences analyses were performed to compare spending changes for patients attributed to ACOs relative to changes for patients at non-ACO organizations. Outcomes included total Medicare spending and spending by category. Three- and 6-year effects and estimated differential changes overall and by ACO characteristics were calculated, including size (small defined as <10 000 patients), rurality, and whether an ACO included a hospital (hospital-associated ACO) or not (physician-group ACO).ExposureAttribution to a medical group or clinic in an ACO during the first 2 years of ACO tenure.Main Outcomes and MeasuresTotal annual per-patient Medicare spending.ResultsThe sample included 41 973 272 Medicare patient-years. Baseline characteristics for 2 719 406 ACO patients and 5 523 652 control patients were similar (average age, 72 years; 58% female; and 82% to 84% White) prior to ACO formation in 2010 and 2011, and unadjusted annual per-patient spending was slightly lower in the ACO group vs control group ($12 147 vs $12 318; difference, −$171 [95% CI, −$223 to −$118]) in the 2 years prior to ACO formation. ACO formation was associated with a mean differential reduction of $142 (95% CI, −$193 to −$92) in annual per-patient spending over 3 years and $294 (95% CI, −$347 to −$241) over 6 years. Spending reductions associated with ACO formation increased over time: compared with control patients, ACO patients experienced a mean reduction of $234 (95% CI, −$298 to −$171) in year 3 and $584 (95% CI, −$680 to −$489) in year 6. Physician-group and small ACOs generated larger spending reductions. Spending changes resulted in $4.1 billion to $8.1 billion in savings to Medicare between 2012 and 2019.Conclusions and RelevanceDuring the MSSP’s first decade, ACOs generated meaningful reductions in spending, with larger effects over time.","PeriodicalId":518009,"journal":{"name":"JAMA","volume":"94 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143884847","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Electronic Sepsis Screening Among Hospital Ward Patients-Reply. 电子败血症筛查在医院病房患者中的应用。
JAMA Pub Date : 2025-04-28 DOI: 10.1001/jama.2025.1622
Yaseen M Arabi,Abdulmohsen Alsaawi,Ali M Al Khathaami
{"title":"Electronic Sepsis Screening Among Hospital Ward Patients-Reply.","authors":"Yaseen M Arabi,Abdulmohsen Alsaawi,Ali M Al Khathaami","doi":"10.1001/jama.2025.1622","DOIUrl":"https://doi.org/10.1001/jama.2025.1622","url":null,"abstract":"","PeriodicalId":518009,"journal":{"name":"JAMA","volume":"19 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143889230","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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