This study highlights the clinical value of UKA as a surgical treatment option for end-stage unicompartmental knee OA in patients with Parkinson’s disease. The present study presents favorable implant survivorship, clinically relevant functional improvements, and a very low perioperative medical complication rate for UKA in this distinct patient population.
Patients with Parkinson’s disease are known to have an increased risk of perioperative medical complications following TKA. Large database studies have shown that PD patients undergoing TKA experience higher rates of postoperative delirium, pneumonia, urinary tract infection, need for blood transfusion, and increased 90-day readmission rates compared with non-PD controls [4, 24]. While previous reports have demonstrated lower medical complication rates after UKA compared with TKA in the general population, no separate analysis has been performed specifically for PD patients [9, 25]. In our series, the overall rate of medical complications after UKA was very low, and none of the commonly reported complications observed in PD patients after TKA occurred.
To date, there is only one study on the usage of medial UKA in 13 PD patients describing modest functional improvement and one revision due to disease progression at 10-year follow-up [13]. The present study expands on these findings based on a substantially larger cohort of medial and lateral UKA demonstrating an implant survivorship of 91% and a reoperation-free survivorship of 86% at 9 years. These results compare favorably to reported data on primary TKA in PD patients, with reported low implant survival rates of 88% at 5 years and 66% at 10 years follow-up [7, 8]. In another study, 90% implant survivorship of primary TKA was reported at 10 years [6]. Interestingly, failure mechanisms following knee arthroplasty in patients with PD appear to differ from those observed in the general population. Recent studies identified PD as an independent risk factor for periprosthetic joint infection (PPI) as well as periprosthetic fracture (PPF) following arthroplasty procedures [8, 24].
Considering these independent risk factor, UKA may provide distinct advantages over TKA. In our cohort, one early postoperative PPI occurred following lateral UKA, corresponding to an infection rate of 2%. The infection rates after primary UKA in the general population have consistently been described around 0.3–0.9% [26, 27]. The study is underpowered to compare PPI rates in PD patients with healthy individuals and cannot provide robust evidence on PPI rates for UKA in PD patients. However, in comparison to infection rates of up to 13% for TKA in PD patients, PPI rates in this study appear low [8]. Gait disorder associated with Parkinson’s disease significantly increases the risk of sustaining a fall, which increases to risk for periprosthetic fractures [8, 24]. Recent studies have reported a higher incidence of PPF, particularly in the early postoperative period, for cementless medial UKA compared to cemented medial UKA. This severe complication is typically surgery-related and has been associated to female sex, age > 70 years, BMI > 40, and valgus alignment of the tibial component (reduced keel–cortex distance posteriorly) [16, 28]. In our series, one periprosthetic fracture in a 75-year-old male patient was detected 13 days after cementless medial UKA without any reported fall. In this patient, severe medial-compartment OA with bone loss of the proximal tibia, a deep vertical cut combined with valgus orientation of the tibial component relative to the anatomy of the proximal tibia may have predisposed to the fracture.
OA progression is considered the most common reason for revision after UKA [29, 30]. In line with the current literature, disease progression was also the most frequent cause (3/6 cases) for additional surgery in this study. Overcorrection is a well described risk factor for early femorotibial disease progression [31]. In this study, overcorrection to 4° varus in a valgus knee resulted in medial-compartment OA four months postoperatively (Table 2, Case 5). In another case, a high BMI of 46 kg/m2 may have contributed to disease progression observed after 15 months (Table 2, Case 2) [32]. Due to the small numbers and the lack of a control group, this study cannot establish a causal link between PD and increased disease progression rates after UKA. The observed cases of disease progression (all within the first 2 postoperative years) appear rather surgery-related or must be interpreted in the context of a non-ideal indication. Our findings therefore do not suggest any reason to discourage the use of UKA in patients with PD, particularly given its potential advantages as a less invasive procedure.
Patients with Parkinson’s disease undergoing mobile-bearing UKA may theoretically face an increased risk of bearing dislocation in medial UKA due to tremor, impaired postural control and altered joint kinematics. Interestingly, none of these disease-specific neuromuscular impairments translated into a bearing dislocation. These findings therefore support the continued use of mobile-bearing implants in PD patients.
Achieving good functional results following knee arthroplasty in patients with PD remains a clinical challenge. Previous studies have reported inferior functional outcomes in PD patients compared to controls following TKA [5, 6]. Similarly, Goh et al. reported improvements in pain scores but only modest gains in knee function following UKA in a series of 13 PD patients, with relevant functional improvement observed in only half of the patients [13]. In contrast, the postoperative OKS scores in the present study were encouraging, showing a significant improvement to nearly 40 points at a mean follow-up of 5 years; 80% (26/32) of patients exceeded the PASS threshold, with only six patients falling below it. To optimize Parkinson’s disease control and enhance the functional outcome, we strongly encourage a multidisciplinary approach in close collaboration with a neurologist during surgical planning, perioperative management, and postoperative rehabilitation.
This study has several limitations that warrant consideration. First, its retrospective design may introduce selection and information bias. Second, although the study presents the largest cohort to date examining the outcome of UKA in PD patients, the sample size remains relatively small, which limits the study’s power. Third, only 76% of patients completed postoperative PROMs, as a substantial proportion had passed away at the time of follow-up. Additionally, preoperative PROMs were only available in a small subset of patients, limiting the assessment of functional change over time. Lastly, the severity of PD symptoms was not systematically assessed, which may have influenced the outcome and limits interpretation of the results.