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Into the Borderland. 进入边境之地。
IF 55 Q1 Medicine Pub Date : 2026-01-20 DOI: 10.1001/jama.2025.20836
Michael S Avidan
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引用次数: 0
Bones, Broken. 骨头,坏了。
IF 55 Q1 Medicine Pub Date : 2026-01-14 DOI: 10.1001/jama.2025.23668
Todd Boss
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引用次数: 0
Chronic Pain Linked to Hypertension. 慢性疼痛与高血压有关。
IF 55 Q1 Medicine Pub Date : 2026-01-13 DOI: 10.1001/jama.2025.20022
Shravya Pant
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引用次数: 0
Strides in Cervical Cancer Elimination. 消除子宫颈癌的进展。
IF 55 Q1 Medicine Pub Date : 2026-01-13 DOI: 10.1001/jama.2025.20021
Shravya Pant
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引用次数: 0
Use of Controls in Medical Research. 在医学研究中使用控制。
IF 55 Q1 Medicine Pub Date : 2026-01-13 DOI: 10.1001/jama.2025.15661
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引用次数: 0
CDC's Failure to Recommend COVID-19 Vaccination-"Shared Clinical Decision-Making" Is Abdication of Responsibility. 疾控中心未能推荐COVID-19疫苗接种-“共同临床决策”是放弃责任。
IF 55 Q1 Medicine Pub Date : 2026-01-13 DOI: 10.1001/jama.2025.22473
Thomas R Frieden, William Schaffner, Joshua M Sharfstein
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引用次数: 0
Acetaminophen (Paracetamol) or Opioid Analgesia Added to Ibuprofen for Children's Musculoskeletal Injury: Research Summary. 对乙酰氨基酚(扑热息痛)或阿片类镇痛加入布洛芬治疗儿童肌肉骨骼损伤:研究综述
IF 55 Q1 Medicine Pub Date : 2026-01-08 DOI: 10.1001/jama.2025.25146
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引用次数: 0
Acetaminophen (Paracetamol) or Opioid Analgesia Added to Ibuprofen for Children's Musculoskeletal Injury: Two Randomized Clinical Trials. 对乙酰氨基酚(扑热息痛)或阿片类镇痛加入布洛芬治疗儿童肌肉骨骼损伤:两项随机临床试验
IF 55 Q1 Medicine Pub Date : 2026-01-08 DOI: 10.1001/jama.2025.25033
Samina Ali, Terry P Klassen, Patricia Candelaria, Maala Bhatt, Scott Sawyer, Antonia Stang, Maryna Yaskina, Anna Heath, Petros Pechlivanoglou, Martin Offringa, Amy L Drendel, Serena Hickes, Naveen Poonai
<p><strong>Importance: </strong>Ibuprofen is first-line therapy for musculoskeletal pain. However, two-thirds of children experience inadequate pain relief with ibuprofen monotherapy, and the efficacy of additive medications for moderate to severe musculoskeletal pain is unclear.</p><p><strong>Objective: </strong>To determine whether treatment with an opioid (hydromorphone) plus ibuprofen or nonopioid (acetaminophen [paracetamol]) plus ibuprofen decreased pain scores compared with ibuprofen alone.</p><p><strong>Design, setting, and participants: </strong>Two randomized, double-masked, placebo-controlled trials were conducted from April 2019 to March 2023 in 6 university-affiliated, tertiary care Canadian pediatric emergency departments. Children aged 6 to 17 years presenting with a nonoperative acute limb injury (<24 hours) and a verbal numerical rating scale (vNRS) pain score of 5 or more out of 10 were enrolled. Date of final follow-up was March 22, 2023.</p><p><strong>Interventions: </strong>The opioid trial randomized participants to a single oral dose of ibuprofen plus hydromorphone, ibuprofen plus acetaminophen, or ibuprofen alone. The nonopioid trial randomized participants to a single oral dose of ibuprofen plus acetaminophen or ibuprofen alone. In all groups, ibuprofen was dosed at 10 mg/kg (maximum, 600 mg). The acetaminophen dose was 15 mg/kg (maximum, 1000 mg), and the hydromorphone dose was 0.05 mg/kg (maximum, 5 mg).</p><p><strong>Main outcomes and measures: </strong>The primary efficacy outcome was self-reported vNRS pain score at 60 minutes post medication administration (score range, 0 [no pain] to 10 [worst pain]; minimal clinically important difference, 1.5). The primary safety end point was the proportion of children with any adverse event related to study drug administration.</p><p><strong>Results: </strong>A total of 8098 children were screened for eligibility; 699 were randomized and 653 were included in the efficacy analyses. The opioid trial included 249 children: 110 randomized to ibuprofen plus hydromorphone, 70 to ibuprofen plus acetaminophen, and 69 to ibuprofen alone. The nonopioid trial included 450 children: 225 randomized to a single oral dose of ibuprofen plus acetaminophen and 225 randomized to ibuprofen alone. The mean (SD) age of children in the 2 trials was 11.5 (3.5) years and 47.4% were female. The mean (SD) vNRS score at recruitment was 6.4 (1.8). In pooled analyses, mean (SD) vNRS scores 60 minutes after drug administration were 4.8 (2.6) in the ibuprofen plus hydromorphone group, 4.6 (2.4) in the ibuprofen plus acetaminophen group, and 4.6 (2.3) in the ibuprofen alone group (P = .78). Any adverse event occurred at higher rates in the ibuprofen plus hydromorphone group (28.2%) compared with the ibuprofen plus acetaminophen (6.1%) or ibuprofen alone groups (5.8%). No serious adverse events occurred.</p><p><strong>Conclusions and relevance: </strong>For children with acute nonoperative musculoskeletal injur
重要性:布洛芬是治疗肌肉骨骼疼痛的一线药物。然而,三分之二的儿童在布洛芬单药治疗中疼痛缓解不足,并且加药治疗中度至重度肌肉骨骼疼痛的疗效尚不清楚。目的:确定阿片类药物(氢吗啡酮)加布洛芬或非阿片类药物(对乙酰氨基酚[扑热息痛])加布洛芬与单独布洛芬相比,是否能降低疼痛评分。设计、环境和参与者:2019年4月至2023年3月,在加拿大6所大学附属三级护理儿科急诊科进行了两项随机、双盲、安慰剂对照试验。干预措施:阿片类药物试验将参与者随机分为单次口服布洛芬加氢吗啡酮、布洛芬加对乙酰氨基酚或单独服用布洛芬。非阿片类药物试验将参与者随机分为单次口服布洛芬加对乙酰氨基酚或单独服用布洛芬。在所有组中,布洛芬的剂量为10mg /kg(最大600mg)。对乙酰氨基酚剂量为15 mg/kg(最大剂量为1000 mg),氢吗啡酮剂量为0.05 mg/kg(最大剂量为5 mg)。主要结局和测量指标:主要疗效结局为给药后60分钟自我报告的vNRS疼痛评分(评分范围:0[无疼痛]至10[最严重疼痛];最小临床重要差异为1.5)。主要安全性终点是与研究药物管理相关的任何不良事件的儿童比例。结果:共有8098名儿童被筛选为合格;699例随机化,653例纳入疗效分析。阿片类药物试验包括249名儿童:110名随机分配到布洛芬加氢吗啡酮组,70名布洛芬加对乙酰氨基酚组,69名布洛芬单独组。非阿片类药物试验包括450名儿童:225名随机分为单次口服布洛芬加对乙酰氨基酚组,225名随机分为单次口服布洛芬组。两项试验中儿童的平均(SD)年龄为11.5(3.5)岁,其中47.4%为女性。入组时vNRS平均(SD)评分为6.4分(1.8分)。合并分析显示,布洛芬联合氢吗啡酮组给药后60分钟vNRS平均评分(SD)为4.8分(2.6分),布洛芬联合对乙酰氨基酚组为4.6分(2.4分),布洛芬单独给药组为4.6分(2.3分)(P = 0.78)。与布洛芬加对乙酰氨基酚组(6.1%)或单独布洛芬组(5.8%)相比,布洛芬加氢吗啡酮组的不良事件发生率(28.2%)更高。未发生严重不良事件。结论及相关性:对于急性非手术性肌肉骨骼损伤的儿童,与单独使用布洛芬相比,布洛芬联合对乙酰氨基酚或布洛芬联合氢吗啡酮在给药后60分钟的疼痛评分没有改善。氢吗啡酮的不良事件发生率是前者的4倍。试验注册:Clinicaltrials.gov标识符:NCT03767933。
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引用次数: 0
What Is Prostatitis? 什么是前列腺炎?
IF 55 Q1 Medicine Pub Date : 2026-01-08 DOI: 10.1001/jama.2025.20559
Rebecca Voelker
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引用次数: 0
Safe and Sufficient-Ibuprofen for Pediatric Musculoskeletal Injuries. 安全充足的布洛芬治疗小儿肌肉骨骼损伤。
IF 55 Q1 Medicine Pub Date : 2026-01-08 DOI: 10.1001/jama.2025.25528
Jessica B Calihan, Tori N Sutherland, Scott E Hadland
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引用次数: 0
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