Purpose

The importance of interpreting clinical trial results in terms of the benefits a treatment may offer to individuals with chronic pain is becoming more widely recognized. The clinical meaningfulness of group differences can better be described by looking at the percentages of responders in each treatment group, rather than between group mean differences. We have reassessed the outcomes of a clinical trial for chronic low back pain (LBP) from this new perspective.

PURPOSE: A new device for intraoperative pedography was developed. The purpose of this study was to validate the introduced method with standard dynamic pedography, and to analyze the clinical benefit.

Methods: For an intraoperative introduction of standardized forces to the footsole, a device named Kraftsimulator Intraoperative Pedographie was developed.

The validation was performed in two steps: Step 1. Comparison of standard dynamic pedography (three trials, walking, third step, three trials, mid stance force pattern), static pedography in standing position (three trials) and pedography with KIOP in healthy volunteers (three trials, total force 400 N).. Step 2. Comparison between pedography in standing position, pedography with KIOP in awake and anaesthesized patients (three trials, total force 400 N).

A randomized prospective controlled study comparing treatment with and without intraoperative pedography has started on November 1, 2005. The subjects are randomized into two groups,

a) use of intraoperative pedography, versus

One-year-follow-up including standard dynamic pedography is planned. The following scores are used: American Orthopaedic Foot and Ankle Society (AOFAS), Visual-Analogue-Scale Foot and Ankle (VAS FA), Short-Form 36 (SF36, standardized to 100-point-maximum). Intraoperative consequences after the use of intraoperative pedography were recorded.

Results: Validation Step 1: 30 individuals were included (age, 26.1±8.6 years; gender, male: female = 24: 6). Step 2: 30 individuals were included (age, 55.3±30.3 years; gender, male: female = 24: 6). No significant differences between all measurements of step 1 and 2 were found for step 1 and 2 without the dynamic platform measurements of step 1.

Clinical use: 16 patients were included until January 31, 2006 (ankle correction arthrodesis, n=2; subtalar joint correction arthrodesis, n=4; arthrodesis midfoot, n=4, correction forefoot, 4; Lisfrcan-fracture-dislocation, n=2). 9 patients were randomized for the use of intraoperative pedography. The mean preoperative scores were: AOFAS: 49.6±23.7; VAS FA: 42.2±13.1; SF36: 48.1±23.2. The mean interruption of operative procedure for the intraoperative pedography was 359±34 seconds. In 4/9 cases changes were made after intraoperative pedography during the same operative procedure (correction modified, n=3; screw tightened, n=1). The follow-up has not been completed so far.

Conclusion: Since no statistical significant differences were found between the measurements of intraoperative pedography in anaesthesized individuals and the standard static pedography, the introduced method can be considered to be valid for intraoperative static pedography.

During the clinical use, in 44% of the cases a modification of the surgical correction were made after intraoperative pedography in the same surgical procedure.

Aims: The roentgenologic morphology of symptomatic calcified deposits of the rotator cuff can be classified according Gärtner (1993, Z Orthop Ihre Grenzgebiete 131: 461–469). This classification influences therapeutic procedures and prognosis of clinical outcome in these patients. In the present study intraoberserver-reproducibility and interobserver-reliability of Gärtner’s classification were tested. Methods: Plane radiographs of 100 patients with calcifications of the supraspinatus tendon were classified according the criteria of Gärtner by six independent observers twice within four months. Intrao-berserver-reproducibility and interobserver-reliability were calculated by means of Cohen’s-kappa-index. Results: Kappa-values of intraoberserver-reproducibility had a mean of 0.4208 (SD 0.1299), kappavalues of interobserver-reliability were 0.490 for the first and 0.474 for the second classification. Conclusions: Determination of intraoberserverreproducibility gave insufficient to satisfactory results, interobserver-reliability was sufficient. The clinical use of Gärtner’s classification to plan therapeutic procedures or to determine clinical prognosis in patients with calcifying tendinitis can be recommended only with limitations.