Riley Sean P, Cote Mark P, Swanson Brian, Tafuto Vincent, Sizer Phillip S, Brismée Jean-Michel
UCONN Health, Farmington, CT, USA; University of Connecticut Physical Therapy Program, Storrs, CT, USA.
UCONN Health, Farmington, CT, USA.
Man Ther. 2015 Jun;20(3):494-8. doi: 10.1016/j.math.2014.12.002. Epub 2014 Dec 20.
The Shoulder Pain and Disability Index (SPADI) is designed to detect changes in shoulder pain and disability after a one-week interval. With the new Medicare guideline, the SPADI may have to be employed for time frames of less than one week.
To determine if the SPADI or its subscales could detect immediate changes in pain and function after a thoracic manipulative intervention known to produce short-term improvement and by comparing it to changes on the numeric pain rating scale (NPRS).
Subjects with primary complaints of non-post-surgical shoulder pain completed the NPRS and the SPADI prior to and immediately following interventions.
The SPADI pain subscale detected statistically significant differences that were also detected using the NPRS. In addition, the SPADI pain score and the NPRS scores were moderately correlated between the pre-intervention SPADI and NPRS scores (r = 0.49-0.61, p < 0.001) and post-intervention SPADI and NPRS scores (r = 0.49-0.67, p < 0.001). These differences did not appear to be sensitive or responsive to immediate change.
Since the SPADI may have to be employed in durations of less than one week secondary to third party payer requirements, it is valuable to validate the SPADI for this particular use.
Although SPADI scores demonstrated low sensitivity and responsiveness to immediate changes, the SPADI pain scale was able to detect changes in durations of less than one week. This finding should be confirmed through further prospective experimentation.
肩痛与功能障碍指数(SPADI)旨在检测一周间隔后肩痛和功能障碍的变化。根据新的医疗保险指南,SPADI可能不得不用于少于一周的时间段。
通过将其与数字疼痛评分量表(NPRS)的变化进行比较,确定SPADI或其分量表是否能够检测出已知能产生短期改善效果的胸椎手法干预后疼痛和功能的即时变化。
以非手术性肩痛为主诉的受试者在干预前和干预后立即完成NPRS和SPADI评估。
SPADI疼痛分量表检测到的具有统计学意义的差异也能用NPRS检测到。此外,干预前SPADI与NPRS评分之间(r = 0.49 - 0.61,p < 0.001)以及干预后SPADI与NPRS评分之间(r = 0.49 - 0.67,p < 0.001),SPADI疼痛评分与NPRS评分呈中度相关。这些差异似乎对即时变化不敏感或无反应。
由于第三方支付方的要求,SPADI可能不得不用于少于一周的时间段,因此针对这一特定用途验证SPADI很有价值。
尽管SPADI评分对即时变化的敏感性和反应性较低,但SPADI疼痛量表能够检测出少于一周时间段内的变化。这一发现应通过进一步的前瞻性实验加以证实。