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Vitamin D3 Supplementation Prior to Total Knee Arthroplasty: A Randomized Controlled Trial
The Journal of Arthroplasty ( IF 3.5 ) Pub Date : 2022-08-19 , DOI: 10.1016/j.arth.2022.08.020
Matthew T Weintraub 1 , Jonathan Guntin 1 , JaeWon Yang 1 , Anne DeBenedetti 1 , Vasili Karas 1 , Craig J Della Valle 1 , Denis Nam 1
Affiliation  

Background

The purpose of this randomized controlled trial was to determine if a one-time dose of vitamin D3 prior to total knee arthroplasty (TKA) improves function and patient-reported outcomes, while decreasing complications.

Methods

One hundred seven patients undergoing primary TKA were randomized to receive 50,000 international units (IU) vitamin D3 (57 patients) or placebo (50 patients) on the morning of surgery. Power analysis determined 45 patients were required in each cohort to detect a minimal clinically important difference of six points in the functional component of the 2011 version of the Knee Society Score (KSS), assuming an alpha of 0.05 and power of 80%. KSS and a Timed Up and Go Test (TUGT) were measured preoperatively and at three and six weeks postoperatively.

Results

There was no difference in improvement of KSS at three weeks (+4.8 points vitamin D3 vs. +3.0 points placebo; p= 0.6) or six weeks (+14.5 points vitamin D3 vs. +12.4 points placebo; p= 0.5) from baseline. There was no difference in change in TUGT at three weeks (+1.2 seconds vitamin D3 vs. +0.6 seconds placebo; p=0.6) or six weeks (-0.3 seconds vitamin D3 vs. -0.9 seconds placebo; p=0.6) from baseline. There were four complications in the placebo cohort within the first 90 days postoperatively and five complications in the vitamin D3 cohort (p=1.0).

Conclusion

Supplementation with 50,000 IU vitamin D3 on the day of surgery failed to demonstrate significant differences in functional KSS, TUGT times, or complications in the early postoperative period compared to placebo.



中文翻译:

全膝关节置换术前补充维生素 D3:一项随机对照试验

背景

这项随机对照试验的目的是确定在全膝关节置换术 (TKA) 之前一次性服用维生素 D 3是否可以改善功能和患者报告的结果,同时减少并发症。

方法

接受初次 TKA 的 107 名患者在手术当天被随机分配接受 50,000 国际单位 (IU) 维生素 D 3 (57 名患者)或安慰剂(50 名患者)。假设 alpha 为 0.05,功效为 80%,功效分析确定每个队列中需要 45 名患者才能检测到 2011 年版膝关节协会评分 (KSS) 功能成分中 6 分的最小临床重要差异。术前和术后三周和六周测量了 KSS 和定时起步测试 (TUGT)。

结果

三周(+4.8 点维生素 D 3与 +3.0 点安慰剂;p= 0.6)或六周(+14.5 点维生素 D 3与 +12.4 点安慰剂;p= 0.5)的 KSS 改善没有差异从基线。三周(+1.2 秒维生素 D 3对比 +0.6 秒安慰剂;p=0.6)或六周(-0.3 秒维生素 D 3对比 -0.9 秒安慰剂;p=0.6)时 TUGT 的变化没有差异从基线。术后前 90 天内安慰剂组有 4 例并发症,维生素 D 3组有 5 例并发症 (p=1.0)。

结论

与安慰剂相比,在手术当天补充 50,000 IU 维生素 D 3未能证明功能性 KSS、TUGT 时间或术后早期并发症有显着差异。

更新日期:2022-08-20
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