Purpose: The cumulative probability of a first-time dislocation (CPD) after total hip arthroplasties (THAs) with a 22-mm head was reported in 2004 to rise steadily to 7% at 25 years. Later reports employing larger heads indicated that dislocations were concentrated in shorter periods after THA. Therefore, dislocations may occur differently over time depending on head sizes, which has not been clearly demonstrated. The purpose was to examine this hypothesis.
Methods: With first-time dislocation as the endpoint, the Cox proportional-hazards regression model and the Kaplan-Meier analyses were applied to 6,339 THAs performed for nontraumatic osteonecrosis of the femoral head, considering all possible influencing variables. Follow-up was 6.5 years on average (range, 0 to 27).
Results: First-time dislocations occurred in 289 THAs (4.6%) at a mean of 2.9 years (range, 0 to 19) following THA, with head sizes of 22, 26, 28, 32, and ≧ 36 mm in 33, 76, 86, 58, and 36 THAs, respectively (dislocation rate: 13.5, 8.2, 5.7, 2.5, and 2.7%, respectively; p < 0.001 in χ2 test). CPD increased linearly after THA in the 22-mm group, while larger-head groups showed a steep early rise followed by a decline.
Conclusion: First-time dislocations occurred differently over time with different head sizes.
{"title":"Timing of first-time dislocation varied by head size after total hip arthroplasty for nontraumatic osteonecrosis.","authors":"Seneki Kobayashi, Nobuhiko Sugano, Wataru Ando, Wakaba Fukushima, Kyoko Kondo, Takashi Sakai","doi":"10.1007/s00264-025-06724-9","DOIUrl":"10.1007/s00264-025-06724-9","url":null,"abstract":"<p><strong>Purpose: </strong>The cumulative probability of a first-time dislocation (CPD) after total hip arthroplasties (THAs) with a 22-mm head was reported in 2004 to rise steadily to 7% at 25 years. Later reports employing larger heads indicated that dislocations were concentrated in shorter periods after THA. Therefore, dislocations may occur differently over time depending on head sizes, which has not been clearly demonstrated. The purpose was to examine this hypothesis.</p><p><strong>Methods: </strong>With first-time dislocation as the endpoint, the Cox proportional-hazards regression model and the Kaplan-Meier analyses were applied to 6,339 THAs performed for nontraumatic osteonecrosis of the femoral head, considering all possible influencing variables. Follow-up was 6.5 years on average (range, 0 to 27).</p><p><strong>Results: </strong>First-time dislocations occurred in 289 THAs (4.6%) at a mean of 2.9 years (range, 0 to 19) following THA, with head sizes of 22, 26, 28, 32, and ≧ 36 mm in 33, 76, 86, 58, and 36 THAs, respectively (dislocation rate: 13.5, 8.2, 5.7, 2.5, and 2.7%, respectively; p < 0.001 in χ2 test). CPD increased linearly after THA in the 22-mm group, while larger-head groups showed a steep early rise followed by a decline.</p><p><strong>Conclusion: </strong>First-time dislocations occurred differently over time with different head sizes.</p>","PeriodicalId":14450,"journal":{"name":"International Orthopaedics","volume":" ","pages":"453-461"},"PeriodicalIF":2.6,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145892579","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-11-25DOI: 10.1007/s00264-025-06703-0
Ernest Siret, Fabio Sammartino, Florent Bernard De Villeneuve, Bandar Nasser Al Maeen, Jean-Noel Argenson, Christophe Jacquet
Purpose: The aim of this study was to report the 10-year clinical and radiological outcomes, survivorship, and patient-reported results of the Persona posterior-stabilized (PS) total knee arthroplasty (TKA) performed in a single centre.
Methods: This retrospective cohort study was based on a prospectively institutional database. A total of 293 primary Persona PS TKAs performed between 2012 and 2015 were identified. After applying inclusion and exclusion criteria, 185 knees (168 patients) were available for analysis at a minimum follow-up of ten years. Clinical evaluation included the Knee injury and Osteoarthritis Outcome Score (KOOS) and the 2011 Knee Society Score (KSS). Radiological assessment consisted of the hip-knee-ankle (HKA) angle. Implant survivorship was analyzed using Kaplan-Meier methods.
Results: At 10 years, Kaplan-Meier survivorship for revision for any reason was 94.1% (95% CI 90.3-97.9%). Four revisions were performed (2 infections, 2 aseptic loosening). Mean KOOS scores improved significantly from preoperative to ten year follow-up (Pain 48→86; Symptoms 45→84; ADL 50→89; Sport 25→72; QoL 30→82; all p < 0.001). The KSS 2011 domains also significantly improved. The mean postoperative HKA angle was 179° ± 2°, with 7.8% of knees outside ± 3° from neutral. No radiographic evidence of radiolucent lines, osteolysis, or loosening was observed.
Conclusion: At ten years, the Persona PS knee system demonstrated excellent survivorship and durable functional results comparable to other contemporary TKA designs. Further comparative studies are required to determine whether its morphometric concept provides additional clinical benefit.
Level of evidence: IV Retrospective cohort study.
目的:本研究的目的是报告在单一中心进行的Persona后稳定(PS)全膝关节置换术(TKA)的10年临床和放射学结果、生存率和患者报告的结果。方法:本回顾性队列研究基于前瞻性机构数据库。在2012年至2015年期间,共有293个主要角色PS tka被确定。在应用纳入和排除标准后,在至少10年的随访中,185个膝关节(168例患者)可用于分析。临床评估包括膝关节损伤和骨关节炎结局评分(oos)和2011年膝关节社会评分(KSS)。放射学评估包括髋关节-膝关节-踝关节(HKA)角度。采用Kaplan-Meier法分析种植体成活率。结果:在10年时,Kaplan-Meier生存率为94.1% (95% CI 90.3-97.9%)。进行了4次翻修(2次感染,2次无菌松动)。需要进一步的比较研究来确定其形态计量概念是否提供额外的临床益处。证据水平:回顾性队列研究。
{"title":"Minimum ten years follow-up of total knee arthroplasty using morphometric implants in patients with osteoarthritis.","authors":"Ernest Siret, Fabio Sammartino, Florent Bernard De Villeneuve, Bandar Nasser Al Maeen, Jean-Noel Argenson, Christophe Jacquet","doi":"10.1007/s00264-025-06703-0","DOIUrl":"10.1007/s00264-025-06703-0","url":null,"abstract":"<p><strong>Purpose: </strong>The aim of this study was to report the 10-year clinical and radiological outcomes, survivorship, and patient-reported results of the Persona posterior-stabilized (PS) total knee arthroplasty (TKA) performed in a single centre.</p><p><strong>Methods: </strong>This retrospective cohort study was based on a prospectively institutional database. A total of 293 primary Persona PS TKAs performed between 2012 and 2015 were identified. After applying inclusion and exclusion criteria, 185 knees (168 patients) were available for analysis at a minimum follow-up of ten years. Clinical evaluation included the Knee injury and Osteoarthritis Outcome Score (KOOS) and the 2011 Knee Society Score (KSS). Radiological assessment consisted of the hip-knee-ankle (HKA) angle. Implant survivorship was analyzed using Kaplan-Meier methods.</p><p><strong>Results: </strong>At 10 years, Kaplan-Meier survivorship for revision for any reason was 94.1% (95% CI 90.3-97.9%). Four revisions were performed (2 infections, 2 aseptic loosening). Mean KOOS scores improved significantly from preoperative to ten year follow-up (Pain 48→86; Symptoms 45→84; ADL 50→89; Sport 25→72; QoL 30→82; all p < 0.001). The KSS 2011 domains also significantly improved. The mean postoperative HKA angle was 179° ± 2°, with 7.8% of knees outside ± 3° from neutral. No radiographic evidence of radiolucent lines, osteolysis, or loosening was observed.</p><p><strong>Conclusion: </strong>At ten years, the Persona PS knee system demonstrated excellent survivorship and durable functional results comparable to other contemporary TKA designs. Further comparative studies are required to determine whether its morphometric concept provides additional clinical benefit.</p><p><strong>Level of evidence: </strong>IV Retrospective cohort study.</p>","PeriodicalId":14450,"journal":{"name":"International Orthopaedics","volume":" ","pages":"393-400"},"PeriodicalIF":2.6,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145604107","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Purpose: Platelet-rich plasma (PRP) is a promising treatment for enhancing the outcomes of bone marrow stimulation for osteochondral lesions of the talus (OLT) and has demonstrated efficacy in alleviating symptoms due to its biological properties. However, the role of leukocyte concentration in PRP remains unclear, particularly regarding cartilage regeneration. This study aimed to compare the clinical outcomes and time to return to activity between leukocyte-poor PRP (LP-PRP) and leukocyte-rich PRP (LR-PRP) in OLT surgery.
Methods: Data from 29 patients with ≥ two year follow-up were retrospectively reviewed: 18 who received LP-PRP and 11 who received LR-PRP with OLT surgery. The study assessed the timeline of return to activity and Self-Managed Foot Evaluation Questionnaire (SAFE-Q) scores preoperatively and at three months, six months, and two years postoperatively.
Results: The LP-PRP group resumed jogging and sports significantly earlier than the LR-PRP group (P = 0.03, P < 0.01). No patients in either group experienced complications. Both groups showed improved SAFE-Q scores at six months, but at two years, the LP-PRP group maintained significantly higher scores compared to their preoperative levels, whereas the LR-PRP group showed declines in some domains.
Conclusion: LP-PRP enabled an earlier return to sports compared with LR-PRP. Additionally, LP-PRP maintained good clinical scores two years after surgery. In contrast, the LR-PRP group showed some decline from their early postoperative peak, although absolute scores remained above preoperative levels. These findings suggest that LP-PRP may be an effective adjuvant treatment for OLT surgery.
{"title":"Comparison of the effects of leukocyte-rich and leukocyte-poor platelet-rich plasma following bone marrow stimulation technique on osteochondral lesions of the talus in athletes: a retrospective cohort study.","authors":"Taihei Miura, Benny Ewe Boon Yeow, Yasuyuki Jujo, Kosui Iwashita, Parthiban Sivasamy, Kazuaki Okugura, Yukinori Mori, Kenta Komesu, Masato Takao","doi":"10.1007/s00264-025-06709-8","DOIUrl":"10.1007/s00264-025-06709-8","url":null,"abstract":"<p><strong>Purpose: </strong>Platelet-rich plasma (PRP) is a promising treatment for enhancing the outcomes of bone marrow stimulation for osteochondral lesions of the talus (OLT) and has demonstrated efficacy in alleviating symptoms due to its biological properties. However, the role of leukocyte concentration in PRP remains unclear, particularly regarding cartilage regeneration. This study aimed to compare the clinical outcomes and time to return to activity between leukocyte-poor PRP (LP-PRP) and leukocyte-rich PRP (LR-PRP) in OLT surgery.</p><p><strong>Methods: </strong>Data from 29 patients with ≥ two year follow-up were retrospectively reviewed: 18 who received LP-PRP and 11 who received LR-PRP with OLT surgery. The study assessed the timeline of return to activity and Self-Managed Foot Evaluation Questionnaire (SAFE-Q) scores preoperatively and at three months, six months, and two years postoperatively.</p><p><strong>Results: </strong>The LP-PRP group resumed jogging and sports significantly earlier than the LR-PRP group (P = 0.03, P < 0.01). No patients in either group experienced complications. Both groups showed improved SAFE-Q scores at six months, but at two years, the LP-PRP group maintained significantly higher scores compared to their preoperative levels, whereas the LR-PRP group showed declines in some domains.</p><p><strong>Conclusion: </strong>LP-PRP enabled an earlier return to sports compared with LR-PRP. Additionally, LP-PRP maintained good clinical scores two years after surgery. In contrast, the LR-PRP group showed some decline from their early postoperative peak, although absolute scores remained above preoperative levels. These findings suggest that LP-PRP may be an effective adjuvant treatment for OLT surgery.</p><p><strong>Level of evidence: </strong>III.</p>","PeriodicalId":14450,"journal":{"name":"International Orthopaedics","volume":" ","pages":"401-410"},"PeriodicalIF":2.6,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145633729","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2026-01-24DOI: 10.1007/s00264-025-06719-6
Joanna Wałecka, Paweł Bąkowski, Marta Jokiel, Rafał Trąbka, Monika Chaszczewska-Markowska, Daniel Ghete, Dorota Gurda-Woźna, Agnieszka Fedoruk-Wyszomirska, Przemyslaw Lubiatowski, Eliza Wyszko, Agata Tyczewska, Kamilla Bąkowska-Żywicka
Purpose: Degeneration at the common extensor origin leads to lateral elbow pain and reduced quality of life. We conducted a double-blind, randomized, placebo-controlled trial involving 71 patients treated with leukocyte-poor PRP (LP-PRP), leukocyte-rich PRP (LR-PRP), or saline.
Methods: PRP content was analyzed using flow cytometry, confocal microscopy, and holotomography. Clinical outcomes (Visual Analogue Scale, Oxford Elbow Score) were assessed at baseline and at three, six, 12, 24, and 55 weeks.
Results: LR-PRP contained 3.8 × more leukocytes and 2.7 × fewer platelets than LP-PRP. Imaging revealed distinct platelet morphology and activation patterns between PRP types. The LP-PRP group showed significantly greater pain reduction at six weeks and improved elbow function from three to six weeks onward.
Conclusion: LP-PRP produced superior and longer-lasting clinical outcomes compared to LR-PRP and saline.
Clinicaltrials: GOV: NCT06854666 (retrospectively registered on 2025-01-13).
{"title":"Molecular background behind lateral elbow pain reduction with Leukocyte-Rich and Leukocyte-Poor Platelet-Rich Plasma-randomized control trial and single-cell platelet analysis.","authors":"Joanna Wałecka, Paweł Bąkowski, Marta Jokiel, Rafał Trąbka, Monika Chaszczewska-Markowska, Daniel Ghete, Dorota Gurda-Woźna, Agnieszka Fedoruk-Wyszomirska, Przemyslaw Lubiatowski, Eliza Wyszko, Agata Tyczewska, Kamilla Bąkowska-Żywicka","doi":"10.1007/s00264-025-06719-6","DOIUrl":"10.1007/s00264-025-06719-6","url":null,"abstract":"<p><strong>Purpose: </strong>Degeneration at the common extensor origin leads to lateral elbow pain and reduced quality of life. We conducted a double-blind, randomized, placebo-controlled trial involving 71 patients treated with leukocyte-poor PRP (LP-PRP), leukocyte-rich PRP (LR-PRP), or saline.</p><p><strong>Methods: </strong>PRP content was analyzed using flow cytometry, confocal microscopy, and holotomography. Clinical outcomes (Visual Analogue Scale, Oxford Elbow Score) were assessed at baseline and at three, six, 12, 24, and 55 weeks.</p><p><strong>Results: </strong>LR-PRP contained 3.8 × more leukocytes and 2.7 × fewer platelets than LP-PRP. Imaging revealed distinct platelet morphology and activation patterns between PRP types. The LP-PRP group showed significantly greater pain reduction at six weeks and improved elbow function from three to six weeks onward.</p><p><strong>Conclusion: </strong>LP-PRP produced superior and longer-lasting clinical outcomes compared to LR-PRP and saline.</p><p><strong>Clinicaltrials: </strong>GOV: NCT06854666 (retrospectively registered on 2025-01-13).</p>","PeriodicalId":14450,"journal":{"name":"International Orthopaedics","volume":" ","pages":"495-508"},"PeriodicalIF":2.6,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146040828","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2026-01-05DOI: 10.1007/s00264-025-06731-w
Pascal Kouyoumdjian, Youssef Jamaleddine, Emeline Chapron, Ahmad Haj Hussein, Mohammad Al Suwaidi, Rémy Coulomb
Background: Modular dual mobility (MDM) cups are widely used in primary total hip arthroplasty (THA) to reduce dislocation, but their impact on range of motion (ROM) to impingement versus single-mobility (SM) cups remains uncertain.
Methods: In this paired robotic-simulation study, 108 primary robotic-assisted THAs were virtually planned twice with CT-based software, once with an SM cup and once with an MDM cup. Cup and stem orientation were optimised to restore intra-articular length and global offset within 5 mm of the contralateral hip and to avoid impingement. ROM to first impingement was measured in extension/external rotation (ER), flexion/internal rotation (IR) with physiological pelvic tilt, and flexion/IR with 20° adduction. The mode of first impingement (intra-articular, extra-articular, or mixed) was recorded.
Results: Compared with SM, MDM cups increased ROM to impingement in extension and ER but slightly reduced ROM in flexion and IR at several test positions. Maximal extension to impingement and ER in extension were higher with MDM, whereas flexion with pelvic anteversion and IR at 100° flexion were lower. ROM to impingement was not uniformly greater with MDM, and first contact often shifted from intra-articular implant-on-implant impingement toward extra-articular impingement.
Conclusion: In robotic THA, MDM cups provide selective gains in ROM to impingement and shift the impingement towards extra-articular structures rather than providing a global increase in safe ROM. Clinically, MDM may suit patients needing extension/ER reserve or with anterior instability risk, and planning should consider osteophytes and bony constraints. Further prospective clinical validation is warranted.
{"title":"Beyond jump distance: modular dual mobility versus single mobility cups in robotic total hip arthroplasty - simulation of hip kinematics and impingement.","authors":"Pascal Kouyoumdjian, Youssef Jamaleddine, Emeline Chapron, Ahmad Haj Hussein, Mohammad Al Suwaidi, Rémy Coulomb","doi":"10.1007/s00264-025-06731-w","DOIUrl":"10.1007/s00264-025-06731-w","url":null,"abstract":"<p><strong>Background: </strong>Modular dual mobility (MDM) cups are widely used in primary total hip arthroplasty (THA) to reduce dislocation, but their impact on range of motion (ROM) to impingement versus single-mobility (SM) cups remains uncertain.</p><p><strong>Methods: </strong>In this paired robotic-simulation study, 108 primary robotic-assisted THAs were virtually planned twice with CT-based software, once with an SM cup and once with an MDM cup. Cup and stem orientation were optimised to restore intra-articular length and global offset within 5 mm of the contralateral hip and to avoid impingement. ROM to first impingement was measured in extension/external rotation (ER), flexion/internal rotation (IR) with physiological pelvic tilt, and flexion/IR with 20° adduction. The mode of first impingement (intra-articular, extra-articular, or mixed) was recorded.</p><p><strong>Results: </strong>Compared with SM, MDM cups increased ROM to impingement in extension and ER but slightly reduced ROM in flexion and IR at several test positions. Maximal extension to impingement and ER in extension were higher with MDM, whereas flexion with pelvic anteversion and IR at 100° flexion were lower. ROM to impingement was not uniformly greater with MDM, and first contact often shifted from intra-articular implant-on-implant impingement toward extra-articular impingement.</p><p><strong>Conclusion: </strong>In robotic THA, MDM cups provide selective gains in ROM to impingement and shift the impingement towards extra-articular structures rather than providing a global increase in safe ROM. Clinically, MDM may suit patients needing extension/ER reserve or with anterior instability risk, and planning should consider osteophytes and bony constraints. Further prospective clinical validation is warranted.</p>","PeriodicalId":14450,"journal":{"name":"International Orthopaedics","volume":" ","pages":"469-477"},"PeriodicalIF":2.6,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145906008","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-12-02DOI: 10.1007/s00264-025-06695-x
Karim Abdallah, Alhassan M Abdelhamid, Ahmed M Bashendi, Ahmed Samir Barakt, Hazem Abd El-Hameed, Mohamed M Hegazy, Mohamed Tageldeen Mohamed
Purpose: Knee coronal angular deformities are a frequently encountered challenge in paediatric orthopaedic practice. When surgical treatment is indicated, guided growth techniques have many advantages in managing these conditions. The purpose of this study is to evaluate the outcome of a modification of the original Percutaneous Epiphysiodesis using Transphyseal Screw (PETS) technique described by Métaizeau as a minimally invasive surgical approach in the treatment of knee angular deformities.
Methods: In this prospective study, a total of 14 patients (comprising 25 limbs) with a coronal plane deformity of the knee underwent percutaneous transphyseal screw hemiepiphysiodesis. Operative time is assessed. The patients were subsequently monitored for an average duration of 28 months. The radiological assessment was conducted using the metrics of MAD (mechanical axis deviation), mLDFA (mechanical lateral distal femoral angle), and MPTA (medial proximal tibial angle). Clinical assessment included the intermalleolar distance (IMD) and intercondylar distance (ICD). The functional outcome evaluation was conducted using a modified version of the original Böstman score, taking into account the different age groups of the targeted cases.
Results: In the genu valgum group, the mean preoperative values were: intermalleolar distance (IMD) 16.9 cm, mechanical axis deviation (MAD) 2.6 cm, and mechanical lateral distal femoral angle (mLDFA) 84°. In the genu varum group, the mean preoperative values were: intercondylar distance (ICD) 8.4 cm, mechanical axis deviation (MAD) -3.0 cm, and medial proximal tibial angle (MPTA) 77.8°. The mean operative time was 15 min. All radiological and clinical outcome measures showed significant improvement (P ≤ 0.05). At 24 months, 96% of cases achieved an excellent Böstman knee score. One patient reached skeletal maturity before full correction could be achieved. No other complications were observed.
Conclusion: This modification of the Métaizeau technique retains the advantages of PETS and offers a simplified approach that may reduce operative time and fluoroscopy use. Our results suggest that it is a safe and effective option for correcting coronal angular knee deformities in children. Further comparative studies are needed to confirm these potential benefits.
{"title":"Treatment of coronal knee angular deformities in children by a modified métaizeau percutaneous transphyseal screw technique.","authors":"Karim Abdallah, Alhassan M Abdelhamid, Ahmed M Bashendi, Ahmed Samir Barakt, Hazem Abd El-Hameed, Mohamed M Hegazy, Mohamed Tageldeen Mohamed","doi":"10.1007/s00264-025-06695-x","DOIUrl":"10.1007/s00264-025-06695-x","url":null,"abstract":"<p><strong>Purpose: </strong>Knee coronal angular deformities are a frequently encountered challenge in paediatric orthopaedic practice. When surgical treatment is indicated, guided growth techniques have many advantages in managing these conditions. The purpose of this study is to evaluate the outcome of a modification of the original Percutaneous Epiphysiodesis using Transphyseal Screw (PETS) technique described by Métaizeau as a minimally invasive surgical approach in the treatment of knee angular deformities.</p><p><strong>Methods: </strong>In this prospective study, a total of 14 patients (comprising 25 limbs) with a coronal plane deformity of the knee underwent percutaneous transphyseal screw hemiepiphysiodesis. Operative time is assessed. The patients were subsequently monitored for an average duration of 28 months. The radiological assessment was conducted using the metrics of MAD (mechanical axis deviation), mLDFA (mechanical lateral distal femoral angle), and MPTA (medial proximal tibial angle). Clinical assessment included the intermalleolar distance (IMD) and intercondylar distance (ICD). The functional outcome evaluation was conducted using a modified version of the original Böstman score, taking into account the different age groups of the targeted cases.</p><p><strong>Results: </strong>In the genu valgum group, the mean preoperative values were: intermalleolar distance (IMD) 16.9 cm, mechanical axis deviation (MAD) 2.6 cm, and mechanical lateral distal femoral angle (mLDFA) 84°. In the genu varum group, the mean preoperative values were: intercondylar distance (ICD) 8.4 cm, mechanical axis deviation (MAD) -3.0 cm, and medial proximal tibial angle (MPTA) 77.8°. The mean operative time was 15 min. All radiological and clinical outcome measures showed significant improvement (P ≤ 0.05). At 24 months, 96% of cases achieved an excellent Böstman knee score. One patient reached skeletal maturity before full correction could be achieved. No other complications were observed.</p><p><strong>Conclusion: </strong>This modification of the Métaizeau technique retains the advantages of PETS and offers a simplified approach that may reduce operative time and fluoroscopy use. Our results suggest that it is a safe and effective option for correcting coronal angular knee deformities in children. Further comparative studies are needed to confirm these potential benefits.</p>","PeriodicalId":14450,"journal":{"name":"International Orthopaedics","volume":" ","pages":"517-523"},"PeriodicalIF":2.6,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12917006/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145653279","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-12-23DOI: 10.1007/s00264-025-06728-5
Xing Wang
{"title":"Letter to the editor on \"CT-based three-dimensional planning predicts cup size with near-perfect accuracy in robotic total hip arthroplasty\".","authors":"Xing Wang","doi":"10.1007/s00264-025-06728-5","DOIUrl":"10.1007/s00264-025-06728-5","url":null,"abstract":"","PeriodicalId":14450,"journal":{"name":"International Orthopaedics","volume":" ","pages":"533-534"},"PeriodicalIF":2.6,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145810111","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-12-29DOI: 10.1007/s00264-025-06730-x
Raghuraman M Sethuraman, Shruthi Vinothkumar
{"title":"Comment on: \"Perineural dexamethasone effectively prolongs anaesthesic block duration in total hip arthroplasty\".","authors":"Raghuraman M Sethuraman, Shruthi Vinothkumar","doi":"10.1007/s00264-025-06730-x","DOIUrl":"10.1007/s00264-025-06730-x","url":null,"abstract":"","PeriodicalId":14450,"journal":{"name":"International Orthopaedics","volume":" ","pages":"535-536"},"PeriodicalIF":2.6,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145849946","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-11-27DOI: 10.1007/s00264-025-06708-9
Pascal Kouyoumdjian, Thomas Grosso, Youssef Jamaleddine, Rémy Coulomb
Introduction: Accurate cup sizing is crucial in total hip arthroplasty (THA). Conventional templating and intra-operative head sizing show inconsistent accuracy, whereas CT-based planning in robotic-assisted THA may offer superior precision. We aimed to compare implanted cup size with both CT-based planning and intra-operative native head sizing, hypothesising that CT planning would provides greater accuracy and consistency.
Methods: This single-centre study included 619 consecutive robot-assisted primary THAs templated with pre-operative CT scans. Implanted cup size was compared with the pre-operative CT-planned size in all hips, and with the intra-operative measurement of the native femoral head in 299 hips.
Results: CT-based planning closely predicted the implanted cup (exact 94.3%; ±1 size 98.7%; mean difference 0.05 ± 0.67 mm; r = 0.984, p < 0.001). Implant-native head comparisons showed larger mismatches (3.14 ± 2.31 mm; exact 9.4%; ±1 size 40.5%; r = 0.817, p < 0.001). Plan-implant agreement was modestly better in females (p = 0.039) and in smaller head categories (< 50 and 50-54 mm) versus > 54 mm (p = 0.007). For implant versus head, mismatch magnitude varied by head size, smaller heads tended toward greater relative oversizing, without a sex effect (p = 0.76).
Conclusion: In robotic THA, CT-based 3-D planning provides near-perfect cup-size prediction and substantially outperforms using the native head as a sizing reference. Residual variation reflects patient-specific factors, chiefly native head size and, to a lesser extent, sex, which should be considered alongside the CT plan. Using native head diameter as a complementary check may further refine pre-operative algorithms and guide intra-operative choices, optimizing component selection for long-term stability and function.
准确的罩杯尺寸在全髋关节置换术(THA)中至关重要。传统的模板和术中头部尺寸显示不一致的准确性,而在机器人辅助THA中基于ct的计划可能提供更高的精度。我们的目的是比较植入罩杯大小与基于CT的计划和术中原始头部大小,假设CT计划可以提供更高的准确性和一致性。方法:这项单中心研究包括619个连续的机器人辅助原发性tha,并进行术前CT扫描。将所有髋关节的植入罩杯尺寸与术前ct计划的尺寸进行比较,并将299髋的植入罩杯尺寸与术中原股骨头尺寸进行比较。结果:ct规划与植入杯形吻合较好(正确率94.3%;±1尺寸98.7%;平均差0.05±0.67 mm; r = 0.984, p 54 mm (p = 0.007)。对于假体和头,不匹配程度随头的大小而变化,较小的头倾向于相对较大的尺寸,没有性别效应(p = 0.76)。结论:在机器人THA中,基于ct的三维规划提供了近乎完美的罩杯大小预测,并且大大优于使用原生头部作为尺寸参考。剩余变异反映了患者的特定因素,主要是原生头部大小,其次是性别,这些因素应与CT计划一起考虑。使用原始头部直径作为补充检查可以进一步完善术前算法并指导术中选择,优化组件选择以实现长期稳定性和功能。
{"title":"Computerised Tomography based three dimensional planning predicts cup size with near-perfect accuracy in robotic total hip arthroplasty: a study of six hundred and nineteen hips.","authors":"Pascal Kouyoumdjian, Thomas Grosso, Youssef Jamaleddine, Rémy Coulomb","doi":"10.1007/s00264-025-06708-9","DOIUrl":"10.1007/s00264-025-06708-9","url":null,"abstract":"<p><strong>Introduction: </strong>Accurate cup sizing is crucial in total hip arthroplasty (THA). Conventional templating and intra-operative head sizing show inconsistent accuracy, whereas CT-based planning in robotic-assisted THA may offer superior precision. We aimed to compare implanted cup size with both CT-based planning and intra-operative native head sizing, hypothesising that CT planning would provides greater accuracy and consistency.</p><p><strong>Methods: </strong>This single-centre study included 619 consecutive robot-assisted primary THAs templated with pre-operative CT scans. Implanted cup size was compared with the pre-operative CT-planned size in all hips, and with the intra-operative measurement of the native femoral head in 299 hips.</p><p><strong>Results: </strong>CT-based planning closely predicted the implanted cup (exact 94.3%; ±1 size 98.7%; mean difference 0.05 ± 0.67 mm; r = 0.984, p < 0.001). Implant-native head comparisons showed larger mismatches (3.14 ± 2.31 mm; exact 9.4%; ±1 size 40.5%; r = 0.817, p < 0.001). Plan-implant agreement was modestly better in females (p = 0.039) and in smaller head categories (< 50 and 50-54 mm) versus > 54 mm (p = 0.007). For implant versus head, mismatch magnitude varied by head size, smaller heads tended toward greater relative oversizing, without a sex effect (p = 0.76).</p><p><strong>Conclusion: </strong>In robotic THA, CT-based 3-D planning provides near-perfect cup-size prediction and substantially outperforms using the native head as a sizing reference. Residual variation reflects patient-specific factors, chiefly native head size and, to a lesser extent, sex, which should be considered alongside the CT plan. Using native head diameter as a complementary check may further refine pre-operative algorithms and guide intra-operative choices, optimizing component selection for long-term stability and function.</p>","PeriodicalId":14450,"journal":{"name":"International Orthopaedics","volume":" ","pages":"411-417"},"PeriodicalIF":2.6,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145633761","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-12-05DOI: 10.1007/s00264-025-06715-w
Farouk Khury, Garrett Ruff, Sophia Antonioli, Daniel Sherwood, Ran Schwarzkopf, Joshua Rozell
Purpose: To investigate the incidence and risk factors for dressing-induced allergic contact dermatitis (DIACD) following total hip and knee arthroplasty (THA and TKA, respectively) across different dressings and sealants.
Methods: A retrospective review was conducted of patients who underwent primary, elective THA or TKA between 2019 and 2024 with ≥ 90 days of follow-up. Incidences of DIACD were identified by reviewing medical records for "allergy" diagnoses and use of antihistamines or corticosteroids within 30 days postoperatively. Patient characteristics, prior exposure, treatment, dressing type, and allergy history were analyzed.
Results: A total of 61 (0.3%) of the 23,396 investigated patients developed a DIACD on average 12.2 ± 7.3 days postoperatively. Overall, 41% had a preoperative allergy (excluding seasonal), and 55.7% were treated with topical or low-dose oral antihistamines and corticosteroids. The majority (41%) of the DIACD involved mesh-adhesive dressings, and a liquid skin adhesive (2-octyl cyanoacrylate) was also used in 41% of cases, often in combination with the primary dressing. Of the 61 DIACD patients, 24 (39.3%) had previously undergone THA or TKA, and nearly half of these (n = 11, 45.8%) had been exposed to the same dressing without prior occurrence of DIACD. DIACD patients were significantly more likely to have undergone TKA (73.8 vs. 58.3%, p = 0.015) and to have never smoked (75.4 vs. 58.4%, p = 0.014). The effect sizes of these findings were negligible (Cramer's V = 0.016 and 0.019, respectively).
Conclusions: The incidence of DIACD following joint arthroplasty is low (0.3%) but remains a frustrating complication, primarily occurring two weeks postoperatively, with mesh-adhesive dressings most frequently implicated. Patients with prior exposure to dressings, those undergoing TKA, and non-smokers are at higher risk. Identifying at-risk patients can guide dressing selection and application.
目的:探讨不同敷料和密封剂在全髋关节和膝关节置换术(分别为THA和TKA)后敷料诱发的过敏性接触性皮炎(DIACD)的发生率和危险因素。方法:回顾性分析2019年至2024年间接受原发性、选择性THA或TKA的患者,随访≥90天。通过回顾“过敏”诊断和术后30天内使用抗组胺药或皮质类固醇的医疗记录,确定了DIACD的发生率。分析患者特征、既往暴露、治疗、敷料类型和过敏史。结果:在23,396例被调查的患者中,共有61例(0.3%)在术后平均12.2±7.3天发生DIACD。总体而言,41%的患者术前过敏(不包括季节性过敏),55.7%的患者接受了局部或低剂量口服抗组胺药和皮质类固醇治疗。大多数(41%)的DIACD涉及网状粘接剂敷料,41%的病例也使用液体皮肤粘接剂(2-辛基氰基丙烯酸酯),通常与初级敷料联合使用。在61例DIACD患者中,24例(39.3%)曾接受过THA或TKA,其中近一半(n = 11,45.8%)曾接触过相同的敷料,此前未发生DIACD。DIACD患者更有可能接受TKA (73.8 vs. 58.3%, p = 0.015)和从未吸烟(75.4 vs. 58.4%, p = 0.014)。这些发现的效应大小可以忽略不计(Cramer's V分别= 0.016和0.019)。结论:关节置换术后DIACD的发生率很低(0.3%),但仍然是一个令人沮丧的并发症,主要发生在术后两周,最常见的是网状粘接剂敷料。既往接触过敷料的患者、接受TKA的患者和非吸烟者的风险更高。识别高危患者可以指导敷料的选择和应用。
{"title":"Dressing-induced allergic contact dermatitis in total joint arthroplasty.","authors":"Farouk Khury, Garrett Ruff, Sophia Antonioli, Daniel Sherwood, Ran Schwarzkopf, Joshua Rozell","doi":"10.1007/s00264-025-06715-w","DOIUrl":"10.1007/s00264-025-06715-w","url":null,"abstract":"<p><strong>Purpose: </strong>To investigate the incidence and risk factors for dressing-induced allergic contact dermatitis (DIACD) following total hip and knee arthroplasty (THA and TKA, respectively) across different dressings and sealants.</p><p><strong>Methods: </strong>A retrospective review was conducted of patients who underwent primary, elective THA or TKA between 2019 and 2024 with ≥ 90 days of follow-up. Incidences of DIACD were identified by reviewing medical records for \"allergy\" diagnoses and use of antihistamines or corticosteroids within 30 days postoperatively. Patient characteristics, prior exposure, treatment, dressing type, and allergy history were analyzed.</p><p><strong>Results: </strong>A total of 61 (0.3%) of the 23,396 investigated patients developed a DIACD on average 12.2 ± 7.3 days postoperatively. Overall, 41% had a preoperative allergy (excluding seasonal), and 55.7% were treated with topical or low-dose oral antihistamines and corticosteroids. The majority (41%) of the DIACD involved mesh-adhesive dressings, and a liquid skin adhesive (2-octyl cyanoacrylate) was also used in 41% of cases, often in combination with the primary dressing. Of the 61 DIACD patients, 24 (39.3%) had previously undergone THA or TKA, and nearly half of these (n = 11, 45.8%) had been exposed to the same dressing without prior occurrence of DIACD. DIACD patients were significantly more likely to have undergone TKA (73.8 vs. 58.3%, p = 0.015) and to have never smoked (75.4 vs. 58.4%, p = 0.014). The effect sizes of these findings were negligible (Cramer's V = 0.016 and 0.019, respectively).</p><p><strong>Conclusions: </strong>The incidence of DIACD following joint arthroplasty is low (0.3%) but remains a frustrating complication, primarily occurring two weeks postoperatively, with mesh-adhesive dressings most frequently implicated. Patients with prior exposure to dressings, those undergoing TKA, and non-smokers are at higher risk. Identifying at-risk patients can guide dressing selection and application.</p>","PeriodicalId":14450,"journal":{"name":"International Orthopaedics","volume":" ","pages":"371-379"},"PeriodicalIF":2.6,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12917024/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145677155","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}