Subjects
A retrospective review of 50 patients who had undergone primary OWHTO between December 2011 to May 2017 at Tokyo Medical and Dental University Hospital of Medicine was conducted. The OWHTO had been undergone for younger and/or physically active unicompartmental knee osteoarthritis patients with patient demand. Patients were excluded during the course of the study if patients refused of consent or joined stem cell clinical trial, postoperative infection occurred, procedure was inadequate with the weight bearing line passed at less than 40% of the width of the tibial plateau postoperatively, questionnaire was incomplete, or follow-up lost in within 2 years. All patients gave their full written informed consent for participation in this clinical research prior to the operative procedure. Three patients were enrolled stem cell clinical trial (Figure 1). Four patients did not fill completely questionnaire before surgery. Four patients were excluded due to the weight bearing line passed at less than 40% of the width of the tibial plateau postoperatively. All the patients were followed up for 2 years or more, except for 3 who were lost to follow-up within 2 years. One patient did not fill completely questionnaire at 2 year after surgery. Consequently, a total of 35 patients were included in this study. Until 2014, OWHTO solely had been performed for 5 patients regardless of the condition of the medial meniscus. However, since 2014, OWHTO with arthroscopic centralization of the medial meniscus have been performed for 21 patients where extrusion of the midbody of the medial meniscus was confirmed preoperatively; and solely OWHTO have been performed for 9 patients without extrusion of the medial meniscus. The extrusion of the medial meniscus was defined as extension of the meniscal margin by at least 3 mm beyond the tibial margin, on a coronal magnetic resonance imaging (MRI) at the mid-point of the medial meniscus. Consequently, this study included 21 patients that underwent OWHTO and arthroscopic meniscal centralization (centralization group) and 14 patients that underwent only OWHTO (control group). Demographic data including age, sex, height, weight, and body mass index (BMI) had been recorded preoperatively. This study was approved by the institutional review board.
Operative procedures
All surgeries were performed by/under the supervision of two senior surgeons (more than 15 years of experience in orthopedic surgery). A standard arthroscopic evaluation was performed before OWHTO. Articular cartilage lesions were assessed by International Cartilage Repair Society (ICRS) grade. Any unstable meniscal tears were repaired if possible, by the all-inside suture technique using the Fast-Fix device (Smith & Nephew, Andover, MA, USA) and/or the inside-out suture technique using the Henning meniscal suture kit (Stryker, Kalamazoo, Michigan, USA). Three patients in centralization group and one patient in control group were undergone meniscus suture. If the torn menisci were difficult to repair, they were partially resected while trying to preserve as much volume as possible. Eight patients in centralization group and four patients in control group were undergone partially meniscus resection.
Arthroscopic meniscal centralization, as previously described, was performed for the extrusion of the medial meniscus in the centralization group (Figure 2).8 In brief, extrusion of the medial meniscus was confirmed by pushing the midbody of the meniscus out of the rim of the medial tibial plateau using a probe (Figure 2A, B). A mid-medial portal was made with an arthroscopic view from the anterolateral portal, 1 cm proximal to the medial meniscus and anterior to the medial femoral condyle. Any osteophytes were resected (if they existed) using a chisel. The meniscotibial capsule under the medial meniscus was then released from the medial tibial plateau for mobilization of the meniscus in order to ease reduction of the meniscal extrusion. The rim and distal part of the medial tibial plateau were rasped to prepare for adhesion of the tibia and meniscotibial capsule (Figure 2D, E). A JuggerKnot Soft Anchor loaded with a No. 1 MaxBraid (Biomet, Warsaw, IN) suture was inserted on to the medial edge of the medial tibial plateau as posterior as possible (Figure 2F, G). The tip of the Micro Suture Lasso Small Curve with nitinol wire loop (Arthrex, Naples, FL) penetrated the capsule from a superior to an inferior direction at the margin between the meniscus and the capsule (Figure 2H, I). A single strand of sutures was passed into the wire loop, and the other limb of the wire loop was pulled to pass the suture from an inferior to a superior direction (Figure 2J). The same procedure was repeated with another strand of the suture to create a mattress suture configuration. Another JuggerKnot Soft Anchor was inserted on to the medial edge of the medial tibial plateau, 1 cm anterior to the first anchor, and the same procedure was repeated. The passed sutures were then tied using a self-locking sliding knot (Figure 2K). The displaced meniscus was centralized after centralization of the midbody of the medial meniscus (Figure 2L).
The OWHTO procedure followed the method proposed by Staubli et al.11 In brief, the preoperative plan involved, shifting the mechanical axis to a point 57% lateral on the transverse diameter of the tibial plateau. The correction angle and opening width were measured. The osteotomy site was opened by a spreader while the limb alignment was simultaneously monitored by fluoroscopy to check the position of the alignment rod at the knee. Once the desired alignment (weight bearing line ratio at 57%) was obtained, wedge-shaped β- tricalcium phosphates (Osferion 60; Olympus Terumo Biomaterials, Tokyo, Japan) were inserted between the opened osteotomy site. Tris plate (Olympus Terumo Biomaterials, Tokyo, Japan) or Tomofix plates (DePuy Synthes Johnson & Johnson, Tokyo, Japan) were used to fix the osteotomy site with locking screws.
The postoperative rehabilitation followed our standard protocol, which did not vary with the meniscal procedure. The patients began to practice the range of motion and quadriceps setting exercises a day after surgery. One-third, two-third, and full weight-bearing with crutches were initiated 3, 10, and, 14 days respectively after surgery. Patients were allowed to start running exercises at 3 months after confirming bone union and patients progressed to full activity after six months postoperatively.
Clinical evaluations
Clinical evaluations for all patients were assessed by orthopedic doctors who were qualified by Japanese Board of Orthopaedic Surgery and were more than 10 years of experience in orthopedics.
Passive knee extension and flexion angles were measured in a supine position with a goniometer and described in 1° and 5° increments, respectively, pre-operatively and at the final follow-up. The Lysholm knee scale was used to determine the knee functional score at the final follow-up. The International Knee Documentation Committee (IKDC) subjective score, and KOOS were used to measure patient-reported outcomes at the final follow-up.12 Patient subjective satisfaction scores out of 100 points were also evaluated pre-operatively and at the final follow-up. Post-operative complications needing an additional surgery, such as loss of knee motion, infection at the operation site, a tear of the sutured meniscus, and conversion to total knee arthroplasty were recorded.
Radiological evaluations
A single orthopedic surgeon (HK), who had more than fifteen years of experience in orthopedic surgery and did not perform any surgery in this series, retrospectively reviewed the JSW and joint line congruence angle (JLCA) at pre-operative, 1 year, and 2 years after surgery intervals in a blinded manner. The medial joint space of the affected knee was measured on the Rosenberg view (standing, 45° flexion, posteroanterior view), since this is more sensitive and accurate to view narrowing of the joint space than the conventional extension weight bearing anteroposterior view.13 The JSW was measured at the narrowest point in the medial compartment. The JLCA was measured as the angle between joint orientation lines at the distal femur and the proximal tibia. The femoro-tibial angle (FTA), hip-knee-ankle angle (HKA angle), weight bearing line ratio, and Kellgren-Lawrence grade were also described using an anteroposterior long-leg weight-bearing radiograph preoperatively and 2 years after surgery. Intra-observer measurement reproducibility for JSW was assessed with the Intra-class correlation coefficient (ICC). The observer was blinded to the previous results. The intra-observer ICC for JSW was 0.97. Therefore, the results were considered to be excellent.14 Minimal detectable change at the 95% confidence level (MDC95) was 0.43mm for JSW.
Statistical analysis
Statistical analyses were performed using the GraphPad Prism 5 (GraphPad Software, Inc., La Jolla, CA, USA). Kellgren-Lawrence grade, ICRS grade for articular cartilage lesions, and postoperative follow up periods were compared between centralization group and control group using a Mann-Whitney test. Rest of items were compared between the two groups using a t-test, after confirming normality using a histogram, and equal variance using the F test. JSW, JLCA, and range of knee joint motion in both groups were compared between at pre-operation and at 2 year after operation by a paired t-test. P-values <0.05 were considered statistically significant. Data were expressed as mean with 95% CI or median with minimum and maximum values. A post hoc power analysis revealed that, with an alpha value of 0.05, the current study achieved a power of 66.4% for the difference in change of JSW between the groups.