Subjects
The subjects were 30 ankles (24 patients) with or without a history of ankle sprain who complained of instability or pain. First, all patients underwent stress radiography, and ankle instability was defined using stress radiography. Second, all patients underwent manual ADT using two methods; the procedure was performed by a junior resident doctor (junior examiner: orthopedic surgeon with 2 years of experience) and senior foot and ankle surgeon (senior examiner: orthopedic surgeon with 23 years of experience) who were blinded.
Stress radiography
Lateral stress radiographs of the ankles were taken in two projections using the Telos stress device (Telos, Griesheim, Germany). Anterior drawer stress was applied with a magnitude of 150 N of posteriorly directed force to the tibia, which allowed the visualization of changes in the neutral position of the joint ends in the ankle joint under constant stress. The distance of anterior talar translation was measured from the posterior lip of the tibial plafond to the nearest articular surface of the talus (Figure 1). In comparison with the unstressed position, anterior subluxation of the talus of more than 3.5 mm was considered to be indicative of ankle instability [18, 19].
Manual anterior drawer test
To perform traditional ADT, the patient was seated on the edge of the examination bed with the calf hanging over (Figure 2a). The examiner pulled the calcaneus of the subject forward with one hand, while pushing the tibia backward with the other hand to reverse the direction of the forces. The examiner evaluated ankle instability using the sensation of the relative motion between the two hands.
Fixed ADT was performed in the supine position with the lower leg placed on a board with the hip and knee joints in 90-degree flexion and the ankle joint in 10- to 20-degree plantar flexion (Figure 2b). The examiner stabilized the lower leg on the board, pulled the calcaneus forward with one hand, and judged the ankle instability by the sensation of the movement of one hand.
The two methods of ADT were performed by a junior and senior examiner. The examiner graded the amount of posterior displacement of the talus using manual ADT, with a grade of 1 as stable joint, 2 as partially unstable, and 3 as completely unstable. Grades 2 and above were considered positive for excessive instability, whereas grade 1 was considered negative or normal [6].
Anterior drawer displacement measured by the sensor during manual anterior drawer test
To clarify the actual distance of anterior displacement in the manual ADT, we evaluated anterior translation measurements using a capacitance-type sensor device, as previously described [20]. Briefly, braces hold the foot and ankle, and allow freedom of movement between them. The sensor was fixed with a snap button to the lateral malleolus and talar part of the brace, and the anterior drawer distance was calculated from the lengthening measured by the sensor. Traditional and fixed ADTs were also performed by junior and senior examiners, as mentioned above, to measure the anterior drawer displacement.
Statistical analysis
Statistical significance was evaluated using Welch’s t-test for comparison using EZR, a graphical user interface for R (The R Foundation for Statistical Computing, Vienna, Austria) [21]. Pearson’s correlation coefficient was used to determine the linear relationship between the anterior drawer displacement of manual ADT between the senior and junior examiners. To assess the diagnostic performance of the tests, the sensitivity, specificity, and positive and negative predictive values were calculated for each examination. The correlation between junior and senior examiners in terms of the accuracy of each physical examination was assessed using the kappa statistic. Statistical significance was set at P less than 0.05.
Ethics and registration
This study was conducted in accordance with the principles of the Declaration of Helsinki and Good Clinical Practice guidelines. The study was approved by the Institutional Review Board for Clinical Research of our hospital (reference number 29-242), and informed consent was obtained from all study participants after providing patients with written and oral information before inclusion in the study.