Vol 32, No 1 (2026)
- Year: 2026
- Published: 24.03.2026
- Articles: 16
- URL: https://journal.rniito.org/jour/issue/view/76
- DOI: https://doi.org/10.17816/2311-2905-2026-1-1
CLINICAL STUDIES
Evaluation of functional outcomes and patient satisfaction after unicompartmental knee arthroplasty: a retrospective analysis from 2011 to 2022
Abstract
Background. Despite the proven advantages of unicompartmental knee arthroplasty (UKA) over total knee arthroplasty for isolated single-compartment pathology, the proportion of UKA in Russia remains extremely low (less than 6%), which is due to a lack of objective information about long-term functional outcomes and factors influencing patient satisfaction.
The aim of the study — to evaluate functional outcomes and patient satisfaction following unicompartmental knee arthroplasty, as well as to determine the impact of demographic factors and obesity on clinical outcomes and subjective pain perception during various activities of daily living.
Methods. A retrospective analysis was conducted on data from 302 patients who underwent UKA between 2011 and 2022. Patient satisfaction was assessed using a 5-point Rasch scale, and pain syndrome was measured using the Likert scale across 12 types of activities. Two integral indicators were calculated: the pain index (PI) and the pain-free percentage (PFP).
Results. Overall satisfaction was high across the sample (median score — 5). Women exhibited a higher PI (1.30±0.12) than men (0.74±0.17), although the differences were not significant. The most painful activities for women were rising from a low object, walking on uneven surfaces, and climbing stairs, while for men they were prolonged standing, household chores, and rising from a low object. No significant differences were found between age groups or BMI categories. The percentage of patients with high satisfaction (scores of 4-5) gradually increased with age, although these differences did not reach statistical significance.
Conclusion. Unicompartmental knee arthroplasty has demonstrated high effectiveness in achieving patient satisfaction (92.1%) and restoring functional mobility, regardless of sex, age, or BMI, over a 12-year observation period.
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Efficacy of intra-articular 3% polyacrylamide hydrogel in the treatment of knee osteoarthritis: findings from the 24-month follow-up
Abstract
Background. Osteoarthritis (OA) is among the most common chronic diseases and leading causes of disability globally. It places a significant burden on healthcare systems and adversely effects patients’ quality of life. The short-term efficacy of most therapies has driven the search for new treatment approaches in OA.
The aim of the study — to evaluate the duration of response to intra-articular injections of 3% polyacrylamide hydrogel in patients with knee osteoarthritis, factors influencing response duration, and the efficacy and safety of repeated treatment.
Methods. In a 6-month placebo-controlled randomized trial, patients with Kellgren-Lawrence (1957) grades II-III knee OA were randomly assigned to receive either intra-articular injections of 8.0 ml polyacrylamide hydrogel (PAAG) or placebo. Subjects from the PAAG group could roll over to the open-label extension (OLE) and if clinically indicated received the second course of PAAG. A survey of OLE participants was conducted at 24 months post-treatment. The efficacy of PAAG was assessed by the WOMAC index, a pain VAS, subjective evaluations of treatment outcomes by both the patient and the researcher, as well as by the daily requirement for paracetamol and nonsteroidal anti-inflammatory drugs. Safety was assessed by adverse events (AEs) monitoring.
Results. At month 6, PAAG was superior to placebo in reducing the WOMAC-T score (-604.44 versus -450.61, p = 0.011). Within 6-9 months of initial treatment, 26% of patients who had significantly higher baseline WOMAC scores and body weight required a repeat course of PAAG. In these patients, the mean reduction in WOMAC-T from baseline to month 12 was -361.33 and -795.64, respectively, compared to -688.53 with one course of PAAG (p = 0.107). At the end of the 24-month follow-up, the mean WOMAC-T reduction reached 714.13 versus -716.65 in the single-course group compared to two-course group. The majority of AEs were mild, and there were no serious AEs reported.
Conclusion. Polyacrylamide hydrogel has demonstrated a favorable safety profile and sustained symptomatic benefit over 2 years. In patients with risk factors for disease progression a repeated course is recommended.
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Potential use of a new fully porous multi-hole titanium acetabular component with cemented liner fixation
Abstract
Background. 3D printing technology has found widespread use in the production of custom-made and mass-produced acetabular components. Since the end of 2022, a new fully porous acetabular component with multiple screw holes and cemented liner fixation has been available.
Research questions. In which clinical scenarios were the fully porous acetabular components used, and with which friction units? Which additional elements were used to achieve reliable primary fixation? What are the short-term survival rates of these implants and the functional outcomes of patients?
Methods. The new component was used in 106 patients between October 2023 and December 2024. There were 55 (51.9%) women and 51 (48.1%) men. The average age was 60.7 years. In 11 (10.4%) cases, implantation was performed in complex cases of primary hip arthroplasty; in 48 (45.3%) cases, during aseptic revisions; and in 47 (44.3%) cases, during the second stage of infection-related revision. In all cases, screws were used for fixation, the number of which ranged from 2 to 10, with an average of 5.5. In 38 (35.8%) cases, acetabular components were combined with augments and/or cup-cage systems. In 47 (44.3%) cases, dual mobility cement fixation systems were used as a friction unit; in the remaining cases, cemented polyethylene liners were used.
Results. The mean follow-up period was 14.1 months (range, 9-23 months). There were 18 (17.0%) complications, 10 of which required repeat revisions. Complications included 6 (5.7%) cases of infection, 5 (4.7%) cases of recurrent dislocations, 3 patients developing sciatic neuropathy, 2 cases of femoral component loosening, and 2 cases of periprosthetic fractures. No aseptic loosening of the acetabular component was observed.
Conclusions. The advantages of the new acetabular component include the possibility of extended screw fixation and the use of different bearing surfaces, including dual mobility. This ensures reliable primary fixation and reduces the risk of recurrent dislocations. The use of a fully porous titanium acetabular cup with a cemented liner in complex primary and revision hip arthroplasty has demonstrated good radiographic results and early survival with a minimum follow-up of 9 months.
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How justified is simultaneous femoral head reduction osteotomy and triple pelvic osteotomy in children with perthes disease?
Abstract
Background. At the current stage of reconstructive orthopedics, femoral head reduction osteotomy in patients with severe aspherical deformation of the femoral head (Stulberg classes IV-V) remains the only effective surgical procedure capable of providing a favorable long-term outcome. However, in the vast majority of cases, secondary hip subluxation develops in the early postoperative period. In this context, simultaneous performance of femoral head reduction osteotomy and triple pelvic osteotomy appears to be a logical option.
The aim of the study — to perform a clinical and radiographic analysis of the outcomes of simultaneous femoral head reduction osteotomy and triple pelvic osteotomy in children with Perthes disease and Stulberg class IV-V femoral head deformity, as well as to assess the invasiveness of the procedure.
Methods. The study was based on the analysis of clinical, radiographic, and laboratory data from 25 patients (25 hip joints) aged 8 to 12 years with Stulberg class IV-V femoral head deformity due to Perthes disease. All patients were divided into two groups. Group I included 15 patients who underwent simultaneous femoral head reduction osteotomy and triple pelvic osteotomy. Group II consisted of 10 patients who underwent triple pelvic osteotomy as the second stage due to the development of secondary hip subluxation.
Results. A comprehensive assessment of surgical invasiveness revealed no statistically significant differences. At a follow-up period of at least 6 months after surgery, all patients in Group I demonstrated a marked improvement in the femoral head shape, as well as the restoration of the articular surface congruency with adequate hip joint stability. In Group II, hip subluxation was eliminated. However, some patients required a greater degree of acetabular fragment correction.
Conclusion. Simultaneous femoral head reduction osteotomy and triple pelvic osteotomy enables the restoration of the articular surface congruency while minimizing the risk of secondary hip subluxation. Moreover, this combined approach does not demonstrate excessive invasiveness compared with other surgical procedures performed via an anterolateral approach.
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Comparative evaluation of the antibacterial activity of bone allografts impregnated with various antibiotics
Abstract
Background. Radical surgical debridement is the most important condition for the successful treatment of patients with chronic osteomyelitis. However, since even the most meticulous debridement cannot guarantee complete eradication of the pathogen, local antibacterial therapy becomes of key importance. This underscores an urgent clinical need for the development of an osteoplastic biodegradable material with prolonged antimicrobial activity. One of the most promising options is a purified allogeneic bone-based material.
The aim of the study — to perform a comparative evaluation of the duration of the antibacterial activity of allografts impregnated with different antibiotics against Gram-positive and Gram-negative bacteria.
Methods. Purified and delipidized bone allografts measuring 5×5×5 mm were prepared according to the procedure developed by the authors. The bone blocks were impregnated with antibacterial agents with varying activity spectra: vancomycin, aztreonam, meropenem, and fosfomycin. The presence and duration of antibacterial activity of the obtained samples were determined against reference bacterial strains depending on the drug’s spectrum of activity by applying a 24-hour incubation solution containing the samples to the surface of a bacterial lawn. The data were analyzed using GraphPad Prism 9.0.
Results. Applied standard vacuum impregnation protocol ensured reproducible saturation of bone tissue with antibiotics. The greatest increase in mass was observed after impregnation with aztreonam, whereas the smallest increase was noted after impregnation with fosfomycin. Vancomycin-impregnated blocks were most active against methicillin-sensitive and methicillin-resistant S. aureus. Meropenem-impregnated blocks were effective for 4 days against K. pneumoniae. Impregnation with aztreonam provided antibacterial activity against K. pneumoniae for up to 6 days. Fosfomycin-impregnated blocks were active against Gram-negative pathogens for 6 days.
Conclusion. The developed technique was shown to ensure the antibiotic loading of the bone substitute material and drug release over several days, with the most prolonged effect observed following impregnation with vancomycin and fosfomycin. Further optimization of osteoplastic materials processing methods is needed, as well as testing other potential antimicrobial agents in combination with antibiotics to overcome potential pathogen resistance.
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Application of an accelerated rehabilitation protocol after surgical treatment of acquired hallux valgus
Abstract
Background. Hallux valgus (HV) is a common orthopedic deformity, and optimization of postoperative rehabilitation is considered one of the key factors in accelerating functional recovery after corrective osteotomies.
The aim of the study — to evaluate the effectiveness of the developed accelerated postoperative rehabilitation protocol for patients who underwent open or minimally invasive hallux valgus correction.
Methods. A prospective non-randomized comparative cohort study was conducted, including 120 patients older than 18 years with hallux valgus deformity. All patients underwent surgical treatment: open scarf osteotomy (n = 40) or minimally invasive MICA osteotomy (n = 80). After surgery, all patients were assigned an original accelerated rehabilitation protocol. Patients with pain intensity ≥ 6 points on the visual analog scale (VAS) at week 2 were transferred to the standard rehabilitation protocol. As a result, two groups were formed: accelerated protocol (AP, n = 74) and standard protocol (SP, n = 46). Pain intensity was assessed using the VAS at 4 and 8 weeks, 6 months, and 1 year; functional outcomes were evaluated using the AOFAS score at 8 weeks, 6 months, and 1 year; postoperative complication rates were also analyzed.
Results. Patients in the AP group demonstrated significantly lower VAS pain scores compared with the SP group at 4 weeks (median 3.00 vs 5.00 points; p < 0.001), 8 weeks (1.00 vs 3.00 points; p < 0.001), and 6 months (0.00 vs 1.00 point; p < 0.001). At 1 year, no significant difference in VAS scores between the groups was observed (p = 0.364). Functional outcomes assessed by the AOFAS score at 8 weeks were higher in the AP group (median 65.00 points) compared with the SP group (52.00 points); p < 0.001. At 6 months (88.00 vs 82.00 points; p = 0.183) and 1 year (95.00 vs 92.00 points; p = 0.353), no significant differences were noted. Complication rates were comparable between the groups: 8.1% in the AP group and 6.5% in the SP group (p = 1.000). The AP group predominantly included patients who underwent minimally invasive MICA osteotomy (89.2%), whereas scarf osteotomy was more frequently performed in the SP group (69.6%; p < 0.001).
Conclusion. The combination of a minimally invasive surgical technique and an accelerated rehabilitation protocol constituted an optimal treatment model, providing adequate deformity correction with minimal postoperative pain and reduced recovery time.
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Outcomes of surgical treatment for combined deformity of the first and fifth metatarsal bones in patients with cerebrovascular disorders of the lower extremities
Abstract
Background. At present, the issues surrounding the surgical treatment of combined deformity of the first and fifth metatarsal bones, particularly when accompanied by cerebrovascular disorders of the lower extremities, remain unresolved.
The aim of the study — to compare the outcomes of different surgical techniques used for the treatment of the fifth metatarsal bone in patients with combined deformity of the first and fifth metatarsal bones accompanied by cerebrovascular disorders of the lower extremities.
Methods. This prospective randomized monocentric cohort study enrolled 70 female patients with combined deformities of the first and fifth metatarsal bones accompanied by cerebrovascular disorders of the lower extremities. Correction of the fifth metatarsal deformity was achieved through minimally invasive closed osteotomies employing two different techniques. Group I included 33 (47.1%) patients treated with a minimally invasive free-hand burring technique. Group II, consisting of 37 (52.9%) patients, was treated using a specifically developed universal guiding device. In all patients, first metatarsal deformity correction was achieved through combined scarf and Akin osteotomy of the proximal phalanx of the hallux. The duration of surgery, as well as the number of intraoperative X-rays taken and the radiation exposure, were assessed. At 6 months post-surgery, we evaluated the type and incidence of postoperative complications, pain dynamics, functional outcomes, and the degree of deformity correction according to radiographic data.
Results. No statistically significant difference in operative time was found between the groups: 47.3±8.5 mins in Group I versus 51.5±9.1 mins in Group II. However, Group II demonstrated a significant reduction both in the number of intraoperative X-rays and radiation exposure: 6-8 X-rays per surgery with a mean radiation dose of 0.1-0.3 mGy, whereas Group I required up to 17-21 X-rays with a mean radiation dose of 0.4-0.6 mGy (p < 0.001). The 6-month follow-up revealed a significant reduction in pain intensity according to the VAS FA scale (scores: 8 [8; 9] in Group I versus 9 [8; 10] in Group II, p < 0.001) and enhanced functional status according to the AOFAS scale (scores: 72 [67; 85] in Group I versus 74 [62; 87] in Group II, p < 0.001) for both groups.
Conclusion. Minimally invasive osteotomies proved to be a highly effective and safe treatment modality for correcting combined deformities of the first and fifth metatarsal bones in patients with concomitant vascular and endocrine pathology. While the functional outcomes and postoperative complication rates were comparable between the two minimally invasive osteotomy techniques for the fifth metatarsal bone, the use of the developed universal guiding device significantly decreased the number of intraoperative X-rays taken and the radiation exposure.
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Surgical treatment of sacral chordomas: monocentric cohort analysis
Abstract
Background. Surgical treatment of sacral chordoma remains one of the most challenging areas of medicine. Despite advances in oncology, en-bloc resection continues to represent the gold standard of treatment. The absence of relevant cohort studies in the domestic literature prompted us to systematize and present our own experience.
The aim of the study — to analyze the short-term and long-term outcomes of surgical treatment of sacral chordomas using en-bloc resection.
Methods. A monocentric cohort study evaluated results of en-bloc sacral resection in 9 patients with histologically verified sacral chordomas. Follow-up period was evaluated 2 yrs 4 mos ± 5 mos. Comprehensive analysis included surgical technique, health-related quality of life, post-op complication rates, recurrence-free survival, and local tumor control. Diagnostic and therapeutic delay duration, intraoperative blood loss, and operative time were assessed.
Results. Follow-up duration: 2 yrs 4 mos ± 5 mos [1 yr 2 mos; 4 yrs 10 mos]. No significant differences identified between diagnostic and therapeutic delay durations. Intraoperative blood loss: 422±220 ml; operative duration: 3 hrs 11 mins ± 67 mins. All patients demonstrated significant reduction in low-back pain postoperatively (p = 0.003). Similar improvement trends in health-related quality of life according to Oswestry Disability Index (ODI) (p = 0.007) and SF-12 questionnaire (p = 0.003). Preoperative neurological deficit occurred in 33% of patients (Frankel D lower paraparesis); pelvic organ dysfunction noted in 77%. Postoperative complications (Clavien-Dindo III b) occurred in 4 cases. R0 resection margins confirmed in all cases. Overall and recurrence-free survival: 100%.
Conclusion. This cohort study demonstrates the efficacy and safety of en-bloc sacral chordoma resection. The procedure achieves 100% resectability, high local control rates, and improved postoperative quality of life.
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Theoretical and experimental studies
Influence of drill hole diameter for the long head of biceps tenodesis on the risk of pathological fractures of the proximal humerus
Abstract
Background. Pathology of the long head of the biceps tendon (LHBT) includes dislocation/subluxation, tendinitis, and tendon rupture and is frequently associated with rotator cuff injuries. Surgical treatment options include tenotomy or tenodesis. Although the choice of the tenodesis level for the LHBT is largely subjective, the tenodesis site affects not only functional outcomes but also the risk of pathological fracture of the humerus.
The aim of the study — to evaluate the influence of drill hole diameter for the suprapectoral tenodesis of the long head of the biceps on the risk of the pathological fractures of the proximal humerus using finite element analysis.
Methods. A three-dimensional model of the humerus, including cortical and trabecular bone components, was constructed based on CT data of a 64-year-old patient. Finite element analysis (ANSYS; SOLID185 elements, average element size ~0.7 mm) included the following scenarios: (1) a fall with the arm abducted at 45°, (2) external and internal rotational loading of the humerus with kinematic rotation of 3°-6° in both directions, and (3) comparative stress distribution analysis in intact bone (no drill hole) and after creation of through holes. An intact humerus was compared with humeri containing suprapectoral through holes of d = 5.0/1.5 mm (anchor fixation) and d = 7.0/2.4 mm (screw fixation).
Results. During a fall on an abducted arm, peak tensile stresses were localized in the region of the surgical neck on the medial surface of the humerus, while the bicipital groove and suprapectoral region remained outside the zone of critical stress. During rotational loading, the presence of a drill hole shifted the maximum shear stress toward the drilling zone. In intact bone, the critical external rotation angle decreased from 6° to 5° after drilling. In bone with reduced mineral density, it decreased from 6° to 3°. For internal rotation, the critical angle decreased from 5° to 4°. The influence of drill hole diameter was minimal, accounting for only a 1-2% increase in stress.
Conclusions. This study identified critical patterns in how bone perforation affects the stress–strain state of the humerus. Bone strength was primarily dependent on the presence of perforation rather than on the drill hole diameter within the investigated range, and increasing the diameter from 5 to 7 mm resulted in only a minor increase in stress (1-2%). These findings suggest that the optimal strategy is to place the drill hole in the proximal humerus, where critical shear stress concentrations are not initially present.
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Trauma and orthopedic care
Impact of an AI-assisted automated system on the clinical workload of orthopedic trauma surgeons and the quality of medical documentation
Abstract
Background. The increasing volume of clinical information under conditions of limited time and human resources places a substantial burden on medical personnel and increases the risk of errors in routine tasks, including the completion of medical records. Automation of medical documentation using artificial intelligence (AI) technologies represents a promising approach to reducing time costs and improving the quality of clinical data management.
The aim of the study — to evaluate the impact of an AI-assisted automated system on the clinical workload of an orthopedic trauma surgeon and the quality of medical documentation.
Methods. A retrospective comparative before-after study was conducted. An automated system integrating automatic speech recognition (ASR), natural language processing (NLP), and generative text modules was implemented in the clinical workflow. Three orthopedic trauma surgeons with more than 10 years of professional experience participated in the study. Data from 480 electronic medical records of patients hospitalized for primary total hip arthroplasty were analyzed (240 before and 240 after system implementation). The following parameters were evaluated: time required for completing medical records, frequency of record returns for correction by the quality control department, subjective workload assessed using the adapted Russian version of the NASA-TLX, and physician satisfaction assessed using a 5-point Likert scale.
Results. After system implementation, the average time required to complete a full medical record decreased from 92.4±14.7 to 48.1±11.2 minutes (p < 0.001). The proportion of records returned for revision decreased from 18.3% to 6.7% (p = 0.004). The mean NASA-TLX score reflecting subjective workload decreased from 67.5±8.2 to 48.9±7.1 (p = 0.002). Physician satisfaction with the system averaged 4.3 out of 5.0 points on the Likert scale.
Conclusion. Implementation of an automated system incorporating artificial intelligence technologies significantly reduces the time required for medical documentation, improves its quality, and decreases the cognitive workload of physicians. These findings support the potential of AI-based tools to optimize clinical workflows and improve efficiency in orthopedic practice.
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EXPERIENCE EXCHANGE
Augmented reality in the treatment of intra-articular distal tibial fractures
Abstract
Background. Augmented reality (AR) technology represents a fundamentally new visualization method in which computer-generated information (fracture imaging) is projected onto real-world objects (the patient’s limb). The potential use of AR methods may significantly improve the accuracy of surgical approach placement, the quality of reduction, and the overall safety of surgical interventions.
The aim of the study — to present our experience of using augmented reality in clinical practice in the treatment of intra-articular distal tibial fractures.
Methods. In this retrospective cohort study, we analyzed the use of AR technology with the MS HoloLens smart glasses and the Voka Trauma Surgery Assistant software. The technology was applied in the treatment of 20 patients (21 injured limbs) with intra-articular distal tibial fractures (types 43B and 43C according to the AO/OTA classification). We assessed the time required to use the system during preoperative planning and intraoperatively, the accuracy of surgical approach relative to the target fracture line, the quality of fracture reduction, the incidence of postoperative complications, and long-term treatment outcomes with a follow-up period of at least one year after surgery.
Results. The time required for data upload to the MS HoloLens headset and preoperative planning using the device comprised Me = 50.0 minutes [Q1 — 45.0; Q3 — 60.0], depending on model size and fracture complexity. The duration of the intraoperative use of the MS HoloLens ranged from 3 to 10 minutes (5.6±1.9). The accuracy of targeting the fracture line was rated as excellent or good in 86% of cases and satisfactory in 14%. The achieved quality of fracture reduction was assessed as good in 18 (86%) cases and satisfactory in three (14%) cases. There were no cases of deep infection; superficial infection was observed in 2 cases. Impaired bone union was identified in three cases: one case of delayed union and two cases of non-union requiring bone grafting and re-operation. Revision surgical procedures were required in four (19%) patients.
Conclusion. The clinical and radiological outcomes obtained in our study are generally consistent with the data reported in the literature regarding complication rates and functional treatment results, which allows us to draw a preliminary conclusion about the safety of augmented reality. Further direct comparative studies are required to determine the clinical efficacy of this technology.
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Registry reports
Modern trends in primary anterior cruciate ligament reconstruction: data from the local registry of the Vreden National Medical Research Center of Traumatology and Orthopedics for 2023-2024
Abstract
Background. Medical registries play an important role in modern evidence-based medicine, providing objective data on the comparative effectiveness of various treatment methods and their long-term outcomes. Since 2023, Vreden National Medical Research Center of Traumatology and Orthopedics has maintained a local registry of knee cruciate ligament reconstruction maintained, the performance of which requires a detailed study.
The aim of the study — to analyze main trends in primary anterior cruciate ligament reconstruction using data from the local registry of the Vreden National Medical Research Center of Traumatology and Orthopedics, and to compare the obtained results with those from foreign registries.
Methods. The study included data on 850 patients from the knee cruciate ligament registry who underwent primary anterior cruciate ligament (ACL) reconstruction. To compare the obtained results with global data, official reports and articles containing information on the work of leading foreign ACL reconstruction registries — Denmark, Sweden, Norway, the United Kingdom, the United States (Kaiser Permanente), and New Zealand — were reviewed.
Results. The mean patient age was 35±9 years [23.6; 35.1], with a pronounced predominance of males within the cohort (71.7%). Regarding the distribution of graft types, a slight preference for autografts was observed (52.9%). Among the allografts utilized, the tibialis posterior tendon was overwhelmingly preferred, accounting for 81.6% of all allografts. Concomitant meniscal injuries were diagnosed in 69.2% of cases. Concerning surgical technique, the transtibial approach was the most frequently employed, utilized in 34.6% of cases. The data on the surgical technique were missing from the registry for 16.8% of cases. An 8 mm graft diameter was the most commonly used size for drilling both the femoral (45.0%) and tibial (46.4%) tunnels. For both the transtibial and anteromedial techniques, the primary method of fixation was a “button — screw” combination, employed in 64.0% and 60.9% of cases, respectively.
Conclusion. The present study has demonstrated the potentially high informational value of the local registry as a tool for analyzing various aspects of primary anterior cruciate ligament reconstruction. However, a direct comparison with foreign data appears challenging due to the substantial difference in the sample size between our data and those of the large foreign anterior cruciate ligament reconstruction registries.
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Foreign and the first Russian shoulder arthroplasty registries: opportunities and prospects
Abstract
Shoulder arthroplasty is a surgical intervention aimed at restoring function and reducing pain in patients with various pathologies of the shoulder. Despite advances in surgical techniques and prosthetic components, various complications remain a significant issue requiring revision procedures. Arthroplasty registries, implemented in foreign countries, have proven valuable for monitoring long-term outcomes, identifying risk factors, and comparing surgical approaches. In 2024, the Vreden National Medical Research Center of Traumatology and Orthopedics has implemented a local shoulder arthroplasty registry designed to systematically collect and analyze data on performed interventions, used implant, and treatment outcomes. In 2024, data on 347 arthroplasties were entered into the register, including 321 (92.5%) primary procedures and 26 (7.5%) revisions. Registration of treatment results will enable early detection of complications, ensuring their timely treatment. Given that the Vreden National Medical Research Center of Traumatology and Orthopedics leads Russia in the number of shoulder arthroplasties performed, the data obtained from the registry analysis can be extrapolated to other healthcare facilities.
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Reviews
Comparative effectiveness of the Masquelet technique, the Ilizarov method, and vascularized bone flaps in the reconstruction of extensive long-bone defects of the limbs: a systematic review and meta-analysis
Abstract
The aim of this meta-analysis — to compare clinical outcomes and complications of the reconstruction of extensive long-bone defects of the limbs of various etiologies in patients older than 18 years using the Masquelet technique, the Ilizarov bone transport, and reconstructive procedures with vascularized bone flaps.
Methods. Publications were searched in the eLIBRARY, PubMed, Embase, Cochrane Central Register of Controlled Trials, and Google Scholar databases for the period 2015–2025. Randomized controlled trials and cohort studies addressing the reconstruction of extensive bone defects of the limbs using different techniques (the Masquelet technique (MT), bone transport (BT), and free vascularized flaps (FVF), particulary the fibular graft) were included in the analysis.
Results. Nine publications involving a total of 375 patients were included in the meta-analysis to assess the effectiveness and safety of the techniques. The majority of cases involved long bones of the lower limbs (n = 332; 87%), most commonly the tibia (n = 284; 74%), followed by the femur (n = 48; 13%). Among upper limb injuries, extensive bone defects of the forearm were reported in 44 cases (12%) and of the humerus in 4 cases (1%). The overall duration of fixation did not differ significantly between MT and FVF groups, nor between MT and BT groups (p = 0.76 and p = 0.40, respectively). The proportion of patients achieving complete bone union without additional surgical interventions was significantly higher with BT compared to MT (86% vs. 61%, p = 0.02). The analysis of surgical site infection (SSI) rates revealed the following patterns: the proportion of patients with superficial SSI was significantly lower with MT compared to BT (11% vs. 23%, p = 0.0004). Conversely, the incidence of deep SSI was significantly higher with MT compared to BT (15% vs. 8%, p = 0.04). No statistically significant differences were found regarding nonunion rates or the conversion of surgical treatment to amputation. The proportion of patients with excellent or good outcomes according to the ASAMI score was 85% for MT and 71% for BT; however, the difference was not statistically significant (p = 0.48).
Conclusion. The systematic literature review confirmed the effectiveness of all three methods: the Masquelet technique, the Ilizarov bone transport, and free vascularized flaps. The meta-analysis did not reveal a significant advantage of any single method in terms of fixation time or time to union; however, distinct safety profiles were identified and should be considered when selecting the surgical strategy. When choosing a technique for the reconstruction of large segmental bone defects, it is essential to take into account the defect location and length, soft tissue status, the presence and activity of infection, as well as individual patient characteristics, particularly treatment adherence and expectations regarding the quality of life.
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Surgical treatment of the sequelae of intra-articular injuries of the proximal interphalangeal joint of the fingers: an umbrella review
Abstract
The aim of the review — to systematize and critically evaluate evidence from systematic reviews on the surgical treatment of the sequelae of the intra-articular injuries of the proximal interphalangeal joint of the fingers in adults.
Methods. An umbrella review (review of systematic reviews) was performed in accordance with the PRIOR 2022 and PRISMA 2020 reporting guidelines. A comprehensive search was conducted in international and Russian databases for publications from 2000 to 2025. Systematic reviews and meta-analyses on proximal interphalangeal joint (PIPJ) surgery were included. The methodological quality was assessed using AMSTAR 2 and ROBIS tools. The degree of the overlap of primary studies across reviews was assessed using the Corrected Covered Area (CCA). Due to substantial heterogeneity in the data, conducting a new quantitative meta-analysis was considered inappropriate.
Results. Seventeen systematic reviews comprising 211 unique primary studies were included. The overall CCA was 4%; however, substantial overlap was observed within specific intervention categories (joint arthroplasty — 17.3%; hemi-hamate autograft arthroplasty — 31%; arthrodesis — 19%; denervation — 56%). According to AMSTAR 2, six reviews were rated as high quality, nine as moderate, and two as low. Based on ROBIS, the risk of bias was low in ten reviews, unclear in six, and high in one. Following PIPJ arthrodesis, repeated interventions are quite rare. Silicone implant arthroplasty offers the most predictable balance between restoration of motion (approximately 50-60°), pain reduction, and acceptable implant survival (85-94% at 3-5 years), although revision rates remain high. Pyrocarbon implants are associated with higher complication and revision rates compared with silicone implants, without convincing functional advantages. Hemi-hamate autograft arthroplasty achieves a high postoperative range of motion (74°), but is applicable only in carefully selected patients with narrowly defined indications. Denervation leads to significant pain reduction but does not address structural joint pathology and has no effect on joint function. Mobilizing procedures are effective in improving joint motion, but full restoration of flexion is rarely achieved.
Conclusions. Surgical treatment methods for the sequelae of the proximal interphalangeal joint injuries of the fingers yield heterogeneous clinical outcomes and are associated with different complication risks. Therefore, the choice of the optimal procedure depends on the specific clinical scenario. The low overall level of evidence, the absence of direct comparisons, and the heterogeneity of reported outcomes underscore the need for prospective comparative studies and standardized core outcome sets.
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FOR RESEARCHERS
Universal long bone defect classification: step by step from diagnosis to treatment strategy and outcome assessment. Part 1: diaphyseal defects
Abstract
This article presents the Universal Long Bone Defect Classification (ULBDC), developed for the standardized description of bone defects, selection of treatment strategy, and assessment of reconstructive outcomes. The current paper focuses on the part of the classification dedicated to diaphyseal defects. The system is based on AO/OTA principles and uses an alphanumeric hierarchical code reflecting localization (bone and segment) and defect morphology (type, group, subgroup, specification) according to the principle “from simple to complex.” To ensure standardized reporting, a unified terminology is proposed to provide precise morphological assessment of bone defects. The following terms are introduced: anticipated bone defect (BDa), cortical bone defect (BDc), and segmental bone defect (BDs). The classification is based on key morphological parameters, including bone integrity (Bi) and defect dimensions (length and width) relative to bone diameter (Bd). For segmental defects, particular attention is paid to shortening (Sh) and diastasis (D). Three types of diaphyseal defects are described: Type A — defects with preserved bone integrity (cortical and anticipated defects), Type B — non-segmental defects (cortical defects with disrupted bone integrity), and Type C — segmental bone defects. The hierarchical structure reflects increasing reconstructive complexity and prognostic severity. The possibility of transforming more complex defects into less complex ones through specific surgical strategies is demonstrated, highlighting the algorithmic value of the system. The ULBDC standardizes terminology, facilitates professional communication, and provides a foundation for the harmonization of clinical research. Despite its relative complexity, the classification demonstrates high reproducibility and practical relevance.
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