Study design
This retrospective study was approved by the Biomedical Ethics Committee in the institute on March 9, 2020, with approval number 286. Additionally, the trial was registered on the clinical registry. This study was funded by the hospital. The case-report form (CRF) recorded patients aged less than 14 years of age with a diagnosis of DLM who underwent arthroscopic meniscoplasty from 2010 to 2021. All surgeries were performed by surgeons from the same institute who had rich clinical experience in arthroscopy. All participants provided written informed consent before surgery.
Patient selection
The hospital information system (HIS) of the institutional database of medical and operative records was retrieved, and the inclusion criteria were as follows: 1. Patients ≤14 years of age; 2. Patients were treated by arthroscopic meniscoplasty between January 1st 2010 and April 9th 2021; 3. Patients were diagnosed with bilateral DLM by MRI and arthroscopy and were found symptomatically on one side; 4. Patients who had at least 1 year of postoperative follow-up; 5. Patients who signed informed consent before participation.
The exclusion criteria were as follows: 1. Patients diagnosed with discoid medial meniscus (DMM); 2. Patients with other knee diseases, such as ligament injury, knee dislocation; 3. Patients unwilling or unable to complete the follow-up questionnaires; 4. The uninjured side had a history of knee surgery; 6. Patients with meniscus sutures; 7. Patients were diagnosed with bilateral DLM with symptoms on both sides.
Patients were categorized according to their injury type and surgical options. Based on their surgical options, the patients were divided into 2 groups: group 1 included patients diagnosed with bilateral DLM undergoing unilateral meniscoplasty on the symptomatic side and conservative management on the asymptomatic side. Group 2 included patients with bilateral DLM and to prevent predictable meniscus injury who had a strong willingness to undergo bilateral meniscopalsty concurrently on both the symptomatic and asymptomatic sides.
Surgical procedure
All arthroscopic surgeries were performed in one center, and all surgeons were experienced. Patients were under general anesthesia in the supine position. Arthroscopy was performed through the medial and lateral portal of the parapatellar region, and a knee diagnosis was performed anteromedially and anterolaterally to observe the intra-articular structures. Then, the lesion was found and measured, including the type of DLM, the type of lesion and the quality of meniscus tissue. The next step was to reshape the meniscus by performing meniscoplasty, trimming the meniscus to 6 to 8 mm in the periphery. After smoothening the edge, knee stability was tested, and only a stable meniscus was included in the study. The unstable meniscus was stabilized by the outside-in suture technique.
The postoperative rehabilitation was as follows. For the first 4 weeks, patients’ range of motion was restricted to no more than 90 degrees, and they performed partial weight-bearing (started at 2 weeks after surgery at 20% of full weight-bearing) no more than 50% of full weight-bearing. After 4 to 6 weeks, patients were asked to reach full range of motion and progressively perform full weight-bearing. After 6 months, patients were able to return to sports.
Conservative treatment for asymptomatic DLM
Patients with bilateral DLM operated on symptomatic side and chose conservative treatment on the asymptomatic side were suggested for protective training programs. Detailed trainings included quadriceps, hamstrings, lateral and internal muscle groups, triceps strengthening and core stability exercise. Each training required at least 3 days per week, 3 sessions per day, 10 sets per session, using a theraband for resistance training. Precautions and attentions were listed, such as avoidance of sudden position changes, and avoidance of reversing during weight-bearing.
Patients’ medical reports
Data collected included sex, age, body mass index (BMI), periods from symptom to surgery, Watanabe classification of injury types, length of follow-up, condition in most recent follow-up, activities and sports.
Patients were asked to complete two self-evaluated scales. Functional status was evaluated by the Ikeuchi scale and Lysholm scale. The Ikeuchi scale contained 4 stages: excellent, good, fair and poor, and for each stage, a detailed explanation was provided for better understanding[15]. The Lysholm scale contains 8 items: limp, support, locking, instability, pain, swelling, stair climbing, and squatting. The maximum score on the Lysholm scale was 100, and scores < 85 were considered fair or poor[16]. Additionally, the Lysholm scale was completed on both sides of the knee to compare functional status.
Descriptive symptoms before and after surgery were recorded. The criteria for pain severity were based on the visual analog scale (VAS). The “locking” symptom was described as a sudden stuck in the knee with no clear reason, and patients were unable to move freely. The criteria for limited range for motion were described as patients unable to reach full range of motion, including full knee flexion or extension. The criteria for knee swelling were measured by tape and were asked to perform comparisons to the other side. The “snapping” symptom was described as a sound in the knee being heard when patients moved.
Statistical analysis
Data management and statistical analysis were performed with Statistical Product Service Solutions (SPSS) 22.0. The quantitative variables were described as the means and standard deviations (SDs), and the descriptive variables were described as frequencies or percentages. The X2 test was applied for comparisons between the two groups. Continuous variables were analyzed by the independent t test. The survival analysis was applied by Kaplan‒Meier curves. The survival timepoint was defined as the occurrence time of symptoms (such as locking and pain with VAS score > 3) on the asymptomatic side of the knee[17]. A p value < 0.05 was set as a significant difference.