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Addressing visa inequities in health: a geopsychiatry perspective. 解决健康方面的签证不平等问题:地理精神病学视角。
IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-01-01 Epub Date: 2024-11-15 DOI: 10.1177/01410768241290726
Albert Persaud, Dinesh Bhugra, Antonio Ventriglio
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引用次数: 0
Using recruitment data instead of national population ethnicity proportions in clinical trial preparation may introduce bias. 在临床试验准备过程中,使用招募数据而不是全国人口种族比例可能会造成偏差。
IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-01-01 Epub Date: 2024-11-19 DOI: 10.1177/01410768241299529
H Logan Ellis, J Smith, A M Murtagh, M Al-Agil, M B Whyte
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引用次数: 0
Regulating reliably: building high-reliability regulators in healthcare.
IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-01-01 Epub Date: 2025-01-24 DOI: 10.1177/01410768241309191
Carl Macrae
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引用次数: 0
Trusting in lived experience. 相信生活经验
IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-01-01 Epub Date: 2024-11-19 DOI: 10.1177/01410768241288343
Donald A Redelmeier, Edward E Etchells, Umberin Najeeb
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引用次数: 0
John Keats: the mystery years. 约翰-济慈:神秘岁月
IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-12-01 Epub Date: 2024-09-20 DOI: 10.1177/01410768241279029
Nick Black
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引用次数: 0
Whether you are highly numerate, literate, or both, stay humble and read more poetry.
IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-12-01 DOI: 10.1177/01410768241308879
Kamran Abbasi
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引用次数: 0
Death Notices. 死亡通知。
IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-12-01 DOI: 10.1177/01410768241306260
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引用次数: 0
Whether you are highly numerate, literate, or both, stay humble and read more poetry. 无论你的计算能力很强,还是识字,或者两者兼而有之,保持谦虚,多读诗。
IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-12-01 DOI: 10.1177/01410768241308879
Kamran Abbasi
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引用次数: 0
Food in Daniel 1:1-16: the first report of a controlled experiment? 但以理书》1:1-16 中的食物:首次对照实验报告?
IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-12-01 Epub Date: 2024-11-15 DOI: 10.1177/01410768241294253
Susan Weingarten
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引用次数: 0
Deriving and validating a risk prediction model for long COVID: a population-based, retrospective cohort study in Scotland. 长 COVID 风险预测模型的得出与验证:苏格兰一项基于人群的回顾性队列研究。
IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-12-01 Epub Date: 2024-11-18 DOI: 10.1177/01410768241297833
Karen Jeffrey, Vicky Hammersley, Rishma Maini, Anna Crawford, Lana Woolford, Ashleigh Batchelor, David Weatherill, Chris White, Tristan Millington, Robin Kerr, Siddharth Basetti, Calum Macdonald, Jennifer K Quint, Steven Kerr, Syed Ahmar Shah, Amanj Kurdi, Colin R Simpson, Srinivasa Vittal Katikireddi, Igor Rudan, Chris Robertson, Lewis Ritchie, Aziz Sheikh, Luke Daines

Objectives: Using electronic health records, we derived and internally validated a prediction model to estimate risk factors for long COVID and predict individual risk of developing long COVID.

Design: Population-based, retrospective cohort study.

Setting: Scotland.

Participants: Adults (≥18 years) with a positive COVID-19 test, registered with a general medical practice between 1 March 2020 and 20 October 2022.

Main outcome measures: Adjusted odds ratios (aORs) with 95% confidence intervals (CIs) for predictors of long COVID, and patients' predicted probabilities of developing long COVID.

Results: A total of 68,486 (5.6%) patients were identified as having long COVID. Predictors of long COVID were increasing age (aOR: 3.84; 95% CI: 3.66-4.03 and aOR: 3.66; 95% CI: 3.27-4.09 in first and second splines), increasing body mass index (BMI) (aOR: 3.17; 95% CI: 2.78-3.61 and aOR: 3.09; 95% CI: 2.13-4.49 in first and second splines), severe COVID-19 (aOR: 1.78; 95% CI: 1.72-1.84); female sex (aOR: 1.56; 95% CI: 1.53-1.60), deprivation (most versus least deprived quintile, aOR: 1.40; 95% CI: 1.36-1.44), several existing health conditions. Predictors associated with reduced long COVID risk were testing positive while Delta or Omicron variants were dominant, relative to when the Wild-type variant was dominant (aOR: 0.85; 95% CI: 0.81-0.88 and aOR: 0.64; 95% CI: 0.61-0.67, respectively) having received one or two doses of COVID-19 vaccination, relative to unvaccinated (aOR: 0.90; 95% CI: 0.86-0.95 and aOR: 0.96; 95% CI: 0.93-1.00).

Conclusions: Older age, higher BMI, severe COVID-19 infection, female sex, deprivation and comorbidities were predictors of long COVID. Vaccination against COVID-19 and testing positive while Delta or Omicron variants were dominant predicted reduced risk.

目标:利用电子健康记录,我们得出了一个预测模型,并在内部进行了验证:利用电子健康记录,我们推导出一个预测模型,并在内部进行了验证,该模型可估算长COVID的风险因素,并预测个人罹患长COVID的风险:设计:基于人群的回顾性队列研究:环境:苏格兰:主要结果测量指标:长COVID预测因素的调整后几率比(aORs)及95%置信区间(CIs),以及患者患长COVID的预测概率:共有 68,486 名(5.6%)患者被确认为患有长 COVID。长COVID的预测因素包括年龄的增加(aOR:3.84;95% CI:3.66-4.03 和 aOR:3.66;95% CI:3.27-4.09,第一和第二斜线)、体重指数(BMI)的增加(aOR:3.17;95% CI:2.78-3.61 和 aOR:3.09;95% CI:2.13-4.49,第一和第二斜线)。49)、严重 COVID-19(aOR:1.78;95% CI:1.72-1.84)、女性(aOR:1.56;95% CI:1.53-1.60)、贫困(最贫困与最不贫困的五分位数,aOR:1.40;95% CI:1.36-1.44)、若干现有健康状况。与长 COVID 风险降低相关的预测因素是,当 Delta 或 Omicron 变体显性时,相对于野生型变体显性时,检测结果呈阳性(aOR:0.85;95% CI:0.81-0.88 和 aOR:0.64)。88和aOR:0.64;95% CI:0.61-0.67)接种过一或两剂COVID-19疫苗,相对于未接种者(aOR:0.90;95% CI:0.86-0.95和aOR:0.96;95% CI:0.93-1.00):结论:年龄越大、体重指数越高、COVID-19感染越严重、女性、贫困和合并症越多,这些因素都是预测长期COVID的因素。接种COVID-19疫苗以及在Delta或Omicron变体占优势时检测结果呈阳性可降低风险。
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引用次数: 0
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