Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Objective: To analyze the accuracy of prosthesis size selection in Naton robot-assisted medial unicondyle knee arthroplasty by comparing the actual prosthesis size used during operation and the preoperative planning.

Methods: The clinical data of 100 patients (110 knees) who underwent Naton robot-assisted medial unicondylar knee arthroplasty between June 2023 and July 2024 was retrospectively analyzed, including 47 knees on left side and 63 knees on right side. There were 37 males (40 knees) and 63 females (70 knees) with a mean age of 65.4 years (range, 59-71 years). Body mass index was 22.2-28.6 kg/m (mean, 25.4 kg/m ). The disease duration ranged from 1 to 8 years (mean, 3.4 years). Preoperative planning was performed by Naton robotic surgical system based on lower limb CT data. The final prosthesis size after osteotomy was recorded and compared with the preoperative plan to analyse whether it was consistent with the preoperative plan, as well as the situation of knee flexion and extension gaps (<0.5 mm, >2.0 mm) corresponding to the different models of prostheses.

Results: During operation, 5 patients (5 knees) were treated with traditional UKA due to mechanical arm failure, software obstacles, significant bone amputation bias, or loose reference frame, and were excluded from the final analysis. The remaining 95 patients (105 knees) successfully received Naton robot-assisted surgery, and no related complications occurred. The prosthesis size was consistent with the preoperative plan in 101 knees (96.2%) on the femur side, 100 knees (95.2%) on the tibia side, and 97 knees (92.4%) on both femur and tibia sides. The prosthesis size was inconsistent in 3 cases (2.86%) on the femur side alone, 4 cases (3.81%) on the tibial side alone, and 1 case (0.95%) on both femur and tibial sides. Among the prostheses with different models, the flexion and extension gaps were less than 0.5 mm in 3 knees, the flexion gap was less than 0.5 mm and the extension gap was more than 2.0 mm in 3 knees, and the flexion gap was more than 2.0 mm and the extension gap was less than 0.5 mm in 2 knees.

Conclusion: The accuracy of prosthesis size selection for Naton robot-assisted medial unicondylar knee arthroplasty is relatively high.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11563753PMC
http://dx.doi.org/10.7507/1002-1892.202406060DOI Listing

Publication Analysis

Top Keywords

prosthesis size
28
naton robot-assisted
20
robot-assisted medial
16
accuracy prosthesis
12
size selection
12
selection naton
12
medial unicondylar
12
unicondylar knee
12
knee arthroplasty
12
knees
12

Similar Publications

Purpose: To analyze the difference in objective and subjective photic phenomena following virtual implantation of three different presbyopia-correcting diffractive intraocular lens (IOL) designs.

Methods: The study was conducted at JENVIS Research Germany. A prospective cross-over and double-masked trial design was used.

View Article and Find Full Text PDF

Purpose: This study aimed to evaluate the inherent and after cyclic loading fracture strength of implant-supported cantilevered fixed prostheses fabricated from recently introduced additively manufactured (AM) and subtractively manufactured (SM) materials, considering variations in prosthesis height.

Materials And Methods: Three cylinder-shaped master files (20 mm long and 11 mm wide) with varying heights (7, 11, and 15 mm) and a titanium-base (Ti-base) abutment space were designed. These designs were used to fabricate a total of 144 specimens with two AM resins indicated for definitive use (Crowntec; AM-CT and Flexcera Smile Ultra+; AM-FS), one high-impact polymer composite (breCAM.

View Article and Find Full Text PDF

Purpose: To compare the accuracy of static guided surgery using a pilot drill guide and dynamic guided surgery for dental implant placement.

Materials And Methods: Partially edentulous adult patients requiring implant placement were randomly assigned to either the static guided surgery group using a pilot drill guide or the dynamic guided surgery group. Digital implant planning was conducted using intraoral scans and CBCT with planning software to determine the optimal prosthetic position.

View Article and Find Full Text PDF

Prospective Evaluation of Thrombotic Complications After Internal Jugular Vein Cannulation for External Bypass.

J Cardiothorac Vasc Anesth

August 2025

Goethe-University Frankfurt, University Hospital Frankfurt, Department of Anaesthesiology, Intensive Care Medicine and Pain Therapy, Frankfurt, Germany; Department of Anesthesiology and Intensive Care Medicine, Rheinische Friedrich-Wilhelms-University, University Hospital Bonn, Bonn, Germany.

Objectives: To determine the incidence and subsequent complications of internal jugular vein (IJV) thrombosis after cannulation performed during cardiopulmonary bypass (CPB) to ensure adequate venous drainage during minimally invasive cardiac surgery.

Design: Single-center observational trial SETTINGS: Intensive care postoperative monitoring of cardiac surgery patients and diagnosis of IJV thrombi at a university tertiary hospital during the 13-month study period from December 1, 2022, to January 11, 2024.

Participants: 44 patients undergoing catheterization of the IJV for total CPB.

View Article and Find Full Text PDF

Pharyngeal Bulb Reduction Program in Individuals with Cleft Palate.

Cleft Palate Craniofac J

September 2025

Graduation Program in Rehabilitation Sciences, Hospital for Rehabilitation of Craniofacial Anomalies, University of Sao Paulo, Bauru, Brazil.

ObjectivesTo describe a pharyngeal bulb reduction program (PBRP) aimed at decreasing the size of the velopharyngeal gap in individuals with repaired cleft palate presenting hypodynamic velopharynx, and to evaluate the effect of the PBRP on pharyngeal bulb dimensions.MethodsThirteen patients (6 females and 7 males; mean age = 28 years) with repaired cleft palate and hypodynamic velopharynx, who demonstrated normal speech using a pharyngeal bulb, participated in the study. The PBRP lasted two weeks and consisted of sequential pharyngeal bulb reductions during nasoendoscopy combined with intensive speech therapy.

View Article and Find Full Text PDF