Background: An estimated 4000 Anterior Cruciate Ligament Injuries (ACL) occur annually in Norway (Granan et al., 2004). 1630 primary ACL reconstructions were performed in Norway in 2008 (Norwegian Arthroplasty Register, 2009). Approximately 120 of these ACL reconstructions were performed at Haraldsplass Deaconess Hospital. Physical therapists at our hospital are responsible for postoperative outpatient controls of patients with a reconstructed anterior cruciate ligament. A clinical observation is that stair walking (especially downstairs) may be problematic up to 6 months after ACL reconstruction. One reason may be that the quadriceps muscle is unable to control the knee when the subject is walking downstairs, and that the knee is perceived to be unstable. Other contributing factors may be pain and swelling. It is of interest to know which pre and post operative factors can predict measured and patient reported function 6 months after ACL reconstruction. Previous research shows that predictive factors for clinical outcome after ACL reconstruction are anterior knee pain (Heijne et al., 2009), preoperative electromyography, early postoperative strength (McHugh et al., 2002), preoperative quadriceps muscle strength deficits, meniscus injury and pain (Eitzen et al., 2009), obesity, smoking and serious chondrosis (Kowalchuk et al., 2009). Purpose: 1. To analyse which pre and post operative factors can predict measured and patient reported function 6 months after Anterior Cruciate Ligament reconstruction. 2. To investigate if there is an asymmetry in step time between the affected and unaffected leg during down stairs walking, and if degree of asymmetry decreases during a 6 months period post operatively. Further we want to compare step time asymmetry with other established outcome measures to investigate sensitivity to change over the observation period and also compare the patient group in this study with a control group of healthy subjects to see if asymmetry in the patient group after 6 months is still higher than in healthy subjects.
Methods: The investigators wish to recruit 35 people scheduled for anterior cruciate ligament (ACL) reconstruction with hamstrings tendon graft. Patients will be asked to write a training diary. Data will be collected 1 day preoperatively, 2 days, 6 weeks, 3 months and 6 months post operatively. Ethics: All participants will have to give informed consent before inclusion. All information obtained through the surveys will be treated confidentially. Participation is completely voluntary. References: GRANAN, L., ENGEBRETSEN, L. \& BAHR, R. (2004) Kirurgi ved fremre korsbåndskader i Norge - sett fra et idrettsmedisinsk perspektiv. Tidsskr Nor Lægeforen, 124, 928-930. NASJONALT REGISTER FOR LEDDPROTESER (2009) Nasjonalt korsbåndregister. Ortopedisk klinikk Haukeland Universitets Sykehus.
Study Type
OBSERVATIONAL
Enrollment
35
Haraldsplass Deaconess hospital
Bergen, Norway
RECRUITINGAsymmetry in step time between the affected and unaffected leg during down stairs walking.
A triaxial kinematic sensor (XSens Mtx) positioned at the level of the lower trunk will be used to identify foot strike and separate left and right steps.
Time frame: 6 months postoperatively
Isokinetic muscle strength measured with a fixed dynamometer (isok BI con/con 60/60 240/240 BIODEX).
Time frame: 6 months postoperatively
Single leg hop test for distance, a 6-m timed hop test, a triple hop test for distance, a crossover hop test for distance (Noyes et al, 1991).
Time frame: 6 months postoperatively
Self reported function.
International Knee Documentation Committee 2000 subjective knee evaluation form.
Time frame: 6 months post operatively
Pain scores on a visual analog scale
Time frame: 1 day preoperatively
Degree of swelling measured with The Modified Stroke Test (Logerseth at al, 2010).
Time frame: 1 day preoperatively
The circumference around the center of the patella will be measured to assess for swelling around the knee joint.
Time frame: 1 day preoperatively
Passive range of movement compared to the healthy knee, measured with a goniometer.
Time frame: 1 day preoperatively
Isokinetic muscle strength measured with a fixed dynamometer (isok BI con/con 60/60 240/240 BIODEX)
Time frame: 1 day preoperatively
Asymmetry in step time between the affected and unaffected leg during down stairs walking.
A triaxial kinematic sensor (XSens Mtx) positioned at the level of the lower trunk will be used to identify foot strike and separate left and right steps.
Time frame: 1 day preoperatively
Self reported function
International Knee Documentation Committee 2000 subjective knee evaluation form
Time frame: 1 day preoperatively
Muscle atrophy in the quadriceps muscle will be measured 12 and 17 cm above the medial knee joint line.
Time frame: 1 day preoperatively
Passive range of movement compared to the healthy knee, measured with a goniometer.
Time frame: at discharge
Pain scores on a visual analog scale.
Time frame: at discharge
Difficulties with walking downstairs on a visual analog scale.
Time frame: 1 day preoperative
Pain scores on a visual analog scale.
Time frame: 6 weeks post operatively
Difficulties with walking down stairs on a visual analog scale.
Time frame: 6 weeks postoperatively
Degree of swelling measured with The Modified Stroke Test (Logerseth at al, 2010).
Time frame: 6 weeks postoperatively
The circumference around the center of the patella will be measured to assess for swelling around the knee joint.
Time frame: 6 weeks postoperatively
Passive range of movement compared to the healthy knee will be measured with a goniometer.
Time frame: 6 weeks postoperatively
Asymmetry in step time between the affected and unaffected leg during down stairs walking.
A triaxial kinematic sensor (XSens Mtx) positioned at the level of the lower trunk will be used to identify foot strike and separate left and right steps.
Time frame: 6 weeks postoperatively
Muscle atrophy in the quadriceps muscle will be measured 12 and 17 cm above the medial knee joint line.
Time frame: 6 weeks postoperatively
Knee joint laxity measured with knee laxity testing device (KT 1000).
Time frame: 6 weeks postoperatively
Asymmetry in step time between the affected and unaffected leg during down stairs walking.
A triaxial kinematic sensor (XSens Mtx) positioned at the level of the lower trunk will be used to identify foot strike and separate left and right steps.
Time frame: 3 months postoperatively
Pain scores on a visual analog scale.
Time frame: 3 months postoperatively
Difficulties with walking down stairs on a visual analog scale.
Time frame: 3 months postoperatively
Degree of swelling measured with The Modified Stroke Test (Logerseth at al, 2010).
Time frame: 3 months postoperatively
The circumference around the center of the patella will be measured to assess for swelling around the knee joint.
Time frame: 3 months postoperatively
Passive range of movement compared to the healthy knee, measured with a goniometer.
Time frame: 3 months postoperatively
Muscle atrophy in the quadriceps muscle will be measured 12 and 17 cm above the medial knee joint line.
Time frame: 3 months postoperatively
Knee joint laxity measured with a knee laxity testing device (KT 1000).
Time frame: 3 months postoperatively
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