Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Botnar Research Centre, Oxford OX3 7LD, UK
NIHR Oxford Biomedical Research Centre, Oxford, UK.
BMJ. 2019 Feb 20;364:l298. doi: 10.1136/bmj.l298.
To provide accurate risk estimates of serious adverse events after elective shoulder replacement surgery for arthritis, including age and sex specific estimates of the lifetime risk of revision surgery.
Population based cohort study.
Hospital episode statistics for NHS England, including civil registration mortality data.
58 054 elective shoulder replacements in 51 895 adults (aged ≥50 years) between April 1998 and April 2017.
The lifetime risk of revision surgery, calculated using an actuarial life table approach and the cumulative probability method. Rates of serious adverse events at 30 and 90 days post-surgery: pulmonary embolism, myocardial infarction, lower respiratory tract infection, acute kidney injury, urinary tract infection, cerebrovascular events, and all cause death. Secondary outcome measures were the number of surgeries performed each year and Kaplan-Meier estimates of revision risk at 3, 5, 10, and 15 years.
The number of shoulder replacements performed each year increased 5.6-fold between 1998 and 2017. Lifetime risks of revision surgery ranged from 1 in 37 (2.7%, 95% confidence interval 2.6% to 2.8%) in women aged 85 years and older to 1 in 4 (23.6%, 23.2% to 24.0%) in men aged 55-59 years. The risks of revision were highest during the first five years after surgery. The risk of any serious adverse event at 30 days post-surgery was 1 in 28 (3.5%, 3.4% to 3.7%), and at 90 days post-surgery was 1 in 22 (4.6%, 4.4% to 4.8%). At 30 days, the relative risk of pulmonary embolism compared with baseline population risk was 61 (95% confidence interval 50 to 73) for women aged 50-64. Serious adverse events were associated with increasing age, comorbidity, and male sex. 1 in 5 (21.2%, 17.9% to 25.1%) men aged 85 years and older experienced at least one serious adverse event within 90 days.
Younger patients, particularly men, need to be aware of a higher likelihood of early failure of shoulder replacement and the need for further and more complex revision replacement surgery. All patients should be counselled about the risks of serious adverse events. These risks are higher than previously considered, and for some could outweigh any potential benefits. Our findings caution against unchecked expansion of shoulder replacement surgery in both younger and older patients. The more accurate age and sex specific estimates of risk from this study are long overdue and should improve shared decision making between patients and clinicians.
ClinicalTrials.gov NCT03573765.
提供关节炎择期肩关节置换术后严重不良事件的准确风险估计,包括修订手术终身风险的年龄和性别特异性估计。
基于人群的队列研究。
英格兰国民保健署的医院发病统计数据,包括公民登记死亡率数据。
1998 年 4 月至 2017 年 4 月期间,51895 名年龄≥50 岁的成年人中进行了 58054 例择期肩关节置换术。
使用 actuarial 寿命表方法和累积概率方法计算修订手术的终身风险。术后 30 天和 90 天的严重不良事件发生率:肺栓塞、心肌梗死、下呼吸道感染、急性肾损伤、尿路感染、脑血管事件和全因死亡。次要结局指标为每年进行的手术数量以及 3、5、10 和 15 年时修订风险的 Kaplan-Meier 估计。
1998 年至 2017 年间,每年进行的肩关节置换手术数量增加了 5.6 倍。修订手术的终身风险范围从 85 岁及以上女性的 1/37(2.7%,95%置信区间 2.6%至 2.8%)到 55-59 岁男性的 1/4(23.6%,23.2%至 24.0%)。手术五年内,风险最高。术后 30 天的任何严重不良事件风险为 1/28(3.5%,3.4%至 3.7%),术后 90 天的风险为 1/22(4.6%,4.4%至 4.8%)。在 30 天时,与基线人群风险相比,50-64 岁女性的肺栓塞相对风险为 61(95%置信区间 50 至 73)。严重不良事件与年龄增长、合并症和男性有关。85 岁及以上的男性中,1/5(21.2%,17.9%至 25.1%)在 90 天内至少发生一次严重不良事件。
年轻患者,尤其是男性,需要意识到肩关节置换早期失败的可能性更高,需要进一步和更复杂的翻修置换手术。所有患者都应接受关于严重不良事件风险的咨询。这些风险比以前认为的要高,对某些患者来说,可能超过任何潜在的益处。我们的研究结果告诫人们,在年轻和老年患者中,不应不加控制地扩大肩关节置换手术的范围。本研究中更准确的年龄和性别特异性风险估计长期以来一直被忽视,应能改善患者和临床医生之间的共同决策。
ClinicalTrials.gov NCT03573765。