Aims: Frailty has recently been associated with postoperative complications and clinical outcomes in various fields. This study aimed to assess the relationships between frailty and surgical outcomes of palliative surgery for spinal metastases and assess the usefulness of the modified five-item frailty index (mFI-5) in this population.
Methods: We prospectively evaluated 273 patients who underwent spinal metastasis surgery from June 2015 to December 2021. The mFI-5 was used to assess frailty, with a score of 0 defined as non-frailty, 1 as pre-frailty, and 2 or more as frailty. The following variables were assessed: background characteristics, complications (Clavien-Dindo grade 2 or higher), postoperative clinical outcomes, and life expectancy. The clinical outcomes compared between the three groups were the performance status (PS), Barthel index, and EuroQoL five-dimension questionnaire (EQ-5D) at six months postoperatively. A multivariate stepwise logistic regression analysis was performed of variables with values of p < 0.1 on the univariate analysis.
Results: The overall complication rate was 19% (52/273). The complication rate was significantly higher in the frailty group (p = 0.005), and patients with a greater mFI-5 score tended to have a higher incidence of postoperative complications. The Kaplan-Meier curve showed that the non-frailty group had a significantly longer survival time than the pre-frailty and frailty groups (p < 0.001). Multivariate logistic regression analysis suggested that mFI-5 is not predictive of postoperative complications and improvement of the EQ-5D, while is predictive of improvement of the PS (odds ratio (OR) 4.22) and Barthel index (OR 4.49).
Conclusion: The current study suggested that mFI-5 is not predictive of postoperative complications and improvement of the EQ-5D, while is predictive of improvement of the PS and Barthel index. Furthermore, palliative surgery for spinal metastases improved the PS, Barthel index, and EQ-5D, even in patients with frailty.
{"title":"Relationships between frailty and surgical outcomes of palliative surgery for spinal metastases : a prospective cohort study.","authors":"Takeru Tsujimoto, Tomoya Matsuo, Takashi Yurube, Yoshiki Takeoka, Yutaro Kanda, Ryosuke Kuroda, Kenichiro Kakutani","doi":"10.1302/2633-1462.610.BJO-2024-0253.R1","DOIUrl":"10.1302/2633-1462.610.BJO-2024-0253.R1","url":null,"abstract":"<p><strong>Aims: </strong>Frailty has recently been associated with postoperative complications and clinical outcomes in various fields. This study aimed to assess the relationships between frailty and surgical outcomes of palliative surgery for spinal metastases and assess the usefulness of the modified five-item frailty index (mFI-5) in this population.</p><p><strong>Methods: </strong>We prospectively evaluated 273 patients who underwent spinal metastasis surgery from June 2015 to December 2021. The mFI-5 was used to assess frailty, with a score of 0 defined as non-frailty, 1 as pre-frailty, and 2 or more as frailty. The following variables were assessed: background characteristics, complications (Clavien-Dindo grade 2 or higher), postoperative clinical outcomes, and life expectancy. The clinical outcomes compared between the three groups were the performance status (PS), Barthel index, and EuroQoL five-dimension questionnaire (EQ-5D) at six months postoperatively. A multivariate stepwise logistic regression analysis was performed of variables with values of p < 0.1 on the univariate analysis.</p><p><strong>Results: </strong>The overall complication rate was 19% (52/273). The complication rate was significantly higher in the frailty group (p = 0.005), and patients with a greater mFI-5 score tended to have a higher incidence of postoperative complications. The Kaplan-Meier curve showed that the non-frailty group had a significantly longer survival time than the pre-frailty and frailty groups (p < 0.001). Multivariate logistic regression analysis suggested that mFI-5 is not predictive of postoperative complications and improvement of the EQ-5D, while is predictive of improvement of the PS (odds ratio (OR) 4.22) and Barthel index (OR 4.49).</p><p><strong>Conclusion: </strong>The current study suggested that mFI-5 is not predictive of postoperative complications and improvement of the EQ-5D, while is predictive of improvement of the PS and Barthel index. Furthermore, palliative surgery for spinal metastases improved the PS, Barthel index, and EQ-5D, even in patients with frailty.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 10","pages":"1199-1207"},"PeriodicalIF":3.1,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12500341/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145240003","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-06DOI: 10.1302/2633-1462.610.BJO-2025-0159.R1
Markus Luger, Alexander Bumberger, Constantin Cik, Christoph Böhler, Kevin Staats, Stephan E Puchner, Reinhard Windhager, Irene Katharina Sigmund
Aims: This study aims to evaluate the diagnostic performance of serum parameters, synovial fluid analysis, tissue and sonication fluid cultures, and histology to identify persistent infection, and to predict reinfection at reimplantation of two-stage exchange arthroplasty.
Methods: From January 2015 to January 2023, a total of 133 patients with completed two-stage exchange arthroplasty for periprosthetic joint infection (PJI) following total hip or knee arthroplasty were eligible for inclusion in this retrospective study. Diagnostic values of serum parameters (CRP, white blood cell count (WBC), differential, fibrinogen), synovial fluid WBC (SF-WBC), culture (synovial fluid, tissue, sonication fluid), and histology were evaluated prior to or at the second stage. Additionally, Kaplan-Meier curves were used to determine infection-free prosthesis survival rates for all parameters.
Results: Serum CRP showed the highest area under the receiver operating characteristic curve (AUC; 0.624) among all analyzed test methods (serum WBC: 0.501; serum % polymorphonuclear neutrophils (PMN): 0.605; fibrinogen: 0.533; SF-WBC: 0.601; SF culture: 0.566; tissue culture: 0.463; sonication fluid culture: 0.473; histology: 0.492). Sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of CRP were 51.7% (95% CI 35 to 69), 73.1% (95% CI 64 to 81), 34.9% (95% CI 21 to 49), and 84.4% (95% CI 77 to 92), respectively. In 35% (n = 15/43) of patients with an elevated serum CRP (≥ 10 mg/l), reinfection occurred, while the reinfection rate was only 16% (n = 14/90) in patients with a normal CRP (< 10 mg/l, p = 0.012). Reinfection rates in patients with all-negative cultures at 23% were not significantly different from cases with positive cultures at 13% (p = 0.352).
Conclusion: Although CRP showed the best diagnostic value among all analyzed test methods, none of them could reliably identify persistent infection or predict reinfection. Additionally, a positive culture may not justify a further intervention (spacer exchange, prolonged antibiotics). In case of positive culture or elevated CRP, a further thorough debridement at the second stage is recommended to increase the chance of infection eradication.
目的:本研究旨在评估血清参数、滑液分析、组织和超声液培养以及组织学的诊断性能,以识别持续感染,并预测两期置换术再植入术后的再感染。方法:2015年1月至2023年1月,共133例在全髋关节或膝关节置换术后完成两期假体周围关节感染(PJI)的患者纳入本回顾性研究。血清参数(CRP,白细胞计数(WBC),鉴别,纤维蛋白原),滑液WBC (SF-WBC),培养(滑液,组织,超声液)和组织学的诊断价值在之前或在第二阶段进行评估。此外,Kaplan-Meier曲线用于确定所有参数的无感染假体存活率。结果:血清CRP(血清WBC: 0.501,血清%多形核中性粒细胞(PMN): 0.605,血清多形核中性粒细胞(PMN): 0.605)在所有检测方法中显示出最高的受试者工作特征曲线下面积(AUC; 0.624)。纤维蛋白原:0.533;SF-WBC: 0.601;SF培养:0.566;组织培养:0.463;超声流体培养:0.473;组织学:0.492)。CRP的敏感性、特异性、阳性预测值(PPV)和阴性预测值(NPV)分别为51.7% (95% CI 35 ~ 69)、73.1% (95% CI 64 ~ 81)、34.9% (95% CI 21 ~ 49)和84.4% (95% CI 77 ~ 92)。血清CRP升高(≥10 mg/l)的患者中有35% (n = 15/43)发生再感染,而CRP正常(< 10 mg/l, p = 0.012)的患者中再感染率仅为16% (n = 14/90)。全阴性培养患者的再感染率为23%,与阳性培养患者的再感染率为13%无显著差异(p = 0.352)。结论:虽然CRP在所有检测方法中表现出最好的诊断价值,但没有一种检测方法能够可靠地识别持续感染或预测再感染。此外,培养阳性可能不证明进一步干预(间隔剂交换,延长抗生素)是合理的。如果培养阳性或CRP升高,建议在第二阶段进一步彻底清创,以增加根除感染的机会。
{"title":"Performance of established test methods in diagnosing persistent infection at the second stage of a two-stage procedure for periprosthetic hip and knee infections.","authors":"Markus Luger, Alexander Bumberger, Constantin Cik, Christoph Böhler, Kevin Staats, Stephan E Puchner, Reinhard Windhager, Irene Katharina Sigmund","doi":"10.1302/2633-1462.610.BJO-2025-0159.R1","DOIUrl":"10.1302/2633-1462.610.BJO-2025-0159.R1","url":null,"abstract":"<p><strong>Aims: </strong>This study aims to evaluate the diagnostic performance of serum parameters, synovial fluid analysis, tissue and sonication fluid cultures, and histology to identify persistent infection, and to predict reinfection at reimplantation of two-stage exchange arthroplasty.</p><p><strong>Methods: </strong>From January 2015 to January 2023, a total of 133 patients with completed two-stage exchange arthroplasty for periprosthetic joint infection (PJI) following total hip or knee arthroplasty were eligible for inclusion in this retrospective study. Diagnostic values of serum parameters (CRP, white blood cell count (WBC), differential, fibrinogen), synovial fluid WBC (SF-WBC), culture (synovial fluid, tissue, sonication fluid), and histology were evaluated prior to or at the second stage. Additionally, Kaplan-Meier curves were used to determine infection-free prosthesis survival rates for all parameters.</p><p><strong>Results: </strong>Serum CRP showed the highest area under the receiver operating characteristic curve (AUC; 0.624) among all analyzed test methods (serum WBC: 0.501; serum % polymorphonuclear neutrophils (PMN): 0.605; fibrinogen: 0.533; SF-WBC: 0.601; SF culture: 0.566; tissue culture: 0.463; sonication fluid culture: 0.473; histology: 0.492). Sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of CRP were 51.7% (95% CI 35 to 69), 73.1% (95% CI 64 to 81), 34.9% (95% CI 21 to 49), and 84.4% (95% CI 77 to 92), respectively. In 35% (n = 15/43) of patients with an elevated serum CRP (≥ 10 mg/l), reinfection occurred, while the reinfection rate was only 16% (n = 14/90) in patients with a normal CRP (< 10 mg/l, p = 0.012). Reinfection rates in patients with all-negative cultures at 23% were not significantly different from cases with positive cultures at 13% (p = 0.352).</p><p><strong>Conclusion: </strong>Although CRP showed the best diagnostic value among all analyzed test methods, none of them could reliably identify persistent infection or predict reinfection. Additionally, a positive culture may not justify a further intervention (spacer exchange, prolonged antibiotics). In case of positive culture or elevated CRP, a further thorough debridement at the second stage is recommended to increase the chance of infection eradication.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 10","pages":"1190-1198"},"PeriodicalIF":3.1,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12497500/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145233605","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-03DOI: 10.1302/2633-1462.610.BJO-2025-0107.R1
Nyashadzaishe Mafirakureva, Pauline Chido Ishumael, Tadios Manyanga, Prudance Mushayavanhu, Munyaradzi Ndekwere, Hannah Wilson, Anya Burton, Simon Graham, James Masters, Matthew L Costa, Rashida A Ferrand, Celia L Gregson, Sian M Noble
Aims: Hip fractures are a leading cause of morbidity and mortality worldwide, particularly among older people. While early surgical management improves outcomes compared to non-surgical approaches, high costs of surgery pose significant barriers in low- and middle-income countries. A cost-utility analysis of hip fracture management was undertaken in Zimbabwe, to guide resource allocation and policy.
Methods: Patient-level data were obtained from a prospective cohort of adults aged 40 years and above with acute hip fractures presenting to hospital in Harare (two public; five private) between October 2021 and October 2022. Healthcare resource use and costs in 2023 USD$ were assessed from individual billing data, with imputed values used for missing resources. Health outcomes were measured in quality-adjusted life-years (QALYs). Incremental cost-effectiveness ratios (ICERs), defined as the ratio of incremental costs to incremental QALYs, were estimated using a regression approach. Sensitivity analyses assessed the impact of different assumptions on cost-effectiveness.
Results: The cohort had 190 patients with an average age of 72 years (SD 14.3), and 51% (n = 97) were male; 61% (n = 116) had surgery for their hip fracture. Patients who underwent surgery had 0.17 (95% CI 0.10 to 0.25) additional QALYs and incurred substantially higher healthcare costs: $1,676 (95% CI 730 to 2,621) higher per patient. The ICER for the primary analysis was $9,647/QALY gained. Restricting the analysis to patients who did not experience extensive surgical delays resulted in smaller difference in costs and an ICER of $4,126/QALY gained. The results were sensitive to the exchange rate used to estimate costs.
Conclusion: Although patients who underwent surgery for hip fractures had higher costs, they had better health outcomes in terms of QALYs. Targeted improvements in provision of surgical care, particularly in minimizing surgical delays, could improve both patient outcomes and lower healthcare costs.
目的:髋部骨折是世界范围内发病率和死亡率的主要原因,特别是在老年人中。虽然与非手术方法相比,早期手术治疗可以改善结果,但在低收入和中等收入国家,高昂的手术费用构成了重大障碍。在津巴布韦进行了髋部骨折管理的成本效用分析,以指导资源分配和政策。方法:从2021年10月至2022年10月期间在哈拉雷医院就诊的40岁及以上急性髋部骨折成人(2名公立医院,5名私立医院)的前瞻性队列中获得患者水平的数据。根据个人账单数据评估了2023年医疗保健资源使用和成本(美元),并对缺失的资源使用了估算值。以质量调整生命年(QALYs)衡量健康结果。增量成本-效果比(ICERs),定义为增量成本与增量质量年的比率,使用回归方法估计。敏感性分析评估了不同假设对成本效益的影响。结果:该队列有190例患者,平均年龄72岁(SD 14.3),其中51% (n = 97)为男性;61% (n = 116)因髋部骨折接受手术治疗。接受手术的患者有0.17个额外的质量年(95% CI 0.10至0.25),并且产生了更高的医疗保健费用:每位患者增加1,676美元(95% CI 730至2,621)。初步分析的ICER为9,647美元/QALY。将分析限制在没有经历大量手术延误的患者身上,成本差异较小,ICER为4126美元/QALY。结果对用于估算成本的汇率很敏感。结论:尽管接受髋部骨折手术的患者成本较高,但就质量质量而言,他们的健康结果更好。有针对性地改进手术护理,特别是尽量减少手术延误,可以改善患者的预后并降低医疗保健费用。
{"title":"Hip fracture care in Zimbabwe : a cohort-based health economic analysis.","authors":"Nyashadzaishe Mafirakureva, Pauline Chido Ishumael, Tadios Manyanga, Prudance Mushayavanhu, Munyaradzi Ndekwere, Hannah Wilson, Anya Burton, Simon Graham, James Masters, Matthew L Costa, Rashida A Ferrand, Celia L Gregson, Sian M Noble","doi":"10.1302/2633-1462.610.BJO-2025-0107.R1","DOIUrl":"10.1302/2633-1462.610.BJO-2025-0107.R1","url":null,"abstract":"<p><strong>Aims: </strong>Hip fractures are a leading cause of morbidity and mortality worldwide, particularly among older people. While early surgical management improves outcomes compared to non-surgical approaches, high costs of surgery pose significant barriers in low- and middle-income countries. A cost-utility analysis of hip fracture management was undertaken in Zimbabwe, to guide resource allocation and policy.</p><p><strong>Methods: </strong>Patient-level data were obtained from a prospective cohort of adults aged 40 years and above with acute hip fractures presenting to hospital in Harare (two public; five private) between October 2021 and October 2022. Healthcare resource use and costs in 2023 USD$ were assessed from individual billing data, with imputed values used for missing resources. Health outcomes were measured in quality-adjusted life-years (QALYs). Incremental cost-effectiveness ratios (ICERs), defined as the ratio of incremental costs to incremental QALYs, were estimated using a regression approach. Sensitivity analyses assessed the impact of different assumptions on cost-effectiveness.</p><p><strong>Results: </strong>The cohort had 190 patients with an average age of 72 years (SD 14.3), and 51% (n = 97) were male; 61% (n = 116) had surgery for their hip fracture. Patients who underwent surgery had 0.17 (95% CI 0.10 to 0.25) additional QALYs and incurred substantially higher healthcare costs: $1,676 (95% CI 730 to 2,621) higher per patient. The ICER for the primary analysis was $9,647/QALY gained. Restricting the analysis to patients who did not experience extensive surgical delays resulted in smaller difference in costs and an ICER of $4,126/QALY gained. The results were sensitive to the exchange rate used to estimate costs.</p><p><strong>Conclusion: </strong>Although patients who underwent surgery for hip fractures had higher costs, they had better health outcomes in terms of QALYs. Targeted improvements in provision of surgical care, particularly in minimizing surgical delays, could improve both patient outcomes and lower healthcare costs.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 10","pages":"1179-1189"},"PeriodicalIF":3.1,"publicationDate":"2025-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12492040/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145213952","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-02DOI: 10.1302/2633-1462.610.BJO-2025-0147.R1
Shotaro Watanabe, Takuma Kaibara, Brian T Feeley, Alan L Zhang, Drew A Lansdown, C Benjamin Ma
Aims: There are few reports of outcomes after reverse total shoulder arthroplasty (RTSA) with over ten years of follow-up. Further, there is a lack of reports on RTSA with trabecular metal (TM) implants with ten-year follow-up. We aim to assess the ten-year survival and minimum ten-year outcomes of TM-RTSA.
Methods: All RTSA procedures were performed between October 2007 and July 2013 in a single institution. A consecutive series of 206 RTSAs in 194 patients were included in the Kaplan-Meier survival analysis using revision or removal for any reason as the endpoint. We also investigated the clinical and radiological outcomes at a minimum follow-up of ten years.
Results: Out of 206 RTSAs, there were a total of 13 failures. The median time from surgery was 1.6 years (IQR 0.08 to 7.5). The five-year implant survival rate was 94.7% (95% CI 89.9 to 97.2; 102 RTSAs at risk), and the ten-year rate was 90.5% (95% CI 82.9 to 94.8; 62 RTSAs at risk). Minimum ten-year outcomes were available for 60 RTSAs, including 57 with ASES scores and 40 RTSAs with radiographs with a mean follow-up period of 11.3 years. The ASES score was a median pain score of 50 (IQR 45 to 50) and a median functional score of 36.7 (IQR 23.3 to 41.7) on the ipsilateral side. In radiological analyses for 40 RTSAs, scapular notching was observed in 31 RTSAs (77.5%) and classified as grade III or IV, as described by Sirveaux et al, in five RTSAs (12.5%). Glenoid radiolucency was observed in 11 RTSAs (27.5%) and loosening in three RTSAs (7.5%).
Conclusion: TM RTSA demonstrated a high ten-year survival rate of 90.5%. Although radiological findings increased over time, clinical outcomes remained favourable.
{"title":"Survival rate and outcomes of reverse total shoulder arthroplasty with a minimum ten-year follow-up using a trabecular metal implant.","authors":"Shotaro Watanabe, Takuma Kaibara, Brian T Feeley, Alan L Zhang, Drew A Lansdown, C Benjamin Ma","doi":"10.1302/2633-1462.610.BJO-2025-0147.R1","DOIUrl":"10.1302/2633-1462.610.BJO-2025-0147.R1","url":null,"abstract":"<p><strong>Aims: </strong>There are few reports of outcomes after reverse total shoulder arthroplasty (RTSA) with over ten years of follow-up. Further, there is a lack of reports on RTSA with trabecular metal (TM) implants with ten-year follow-up. We aim to assess the ten-year survival and minimum ten-year outcomes of TM-RTSA.</p><p><strong>Methods: </strong>All RTSA procedures were performed between October 2007 and July 2013 in a single institution. A consecutive series of 206 RTSAs in 194 patients were included in the Kaplan-Meier survival analysis using revision or removal for any reason as the endpoint. We also investigated the clinical and radiological outcomes at a minimum follow-up of ten years.</p><p><strong>Results: </strong>Out of 206 RTSAs, there were a total of 13 failures. The median time from surgery was 1.6 years (IQR 0.08 to 7.5). The five-year implant survival rate was 94.7% (95% CI 89.9 to 97.2; 102 RTSAs at risk), and the ten-year rate was 90.5% (95% CI 82.9 to 94.8; 62 RTSAs at risk). Minimum ten-year outcomes were available for 60 RTSAs, including 57 with ASES scores and 40 RTSAs with radiographs with a mean follow-up period of 11.3 years. The ASES score was a median pain score of 50 (IQR 45 to 50) and a median functional score of 36.7 (IQR 23.3 to 41.7) on the ipsilateral side. In radiological analyses for 40 RTSAs, scapular notching was observed in 31 RTSAs (77.5%) and classified as grade III or IV, as described by Sirveaux et al, in five RTSAs (12.5%). Glenoid radiolucency was observed in 11 RTSAs (27.5%) and loosening in three RTSAs (7.5%).</p><p><strong>Conclusion: </strong>TM RTSA demonstrated a high ten-year survival rate of 90.5%. Although radiological findings increased over time, clinical outcomes remained favourable.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 10","pages":"1171-1178"},"PeriodicalIF":3.1,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12666477/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145207894","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-01DOI: 10.1302/2633-1462.610.BJO-2025-0140.R1
Kenney Ki Lee Lau, Kenny Yat Hong Kwan, Jason Pui Yin Cheung, Karlen Ka Pui Law, Arnold Yu Lok Wong, Daniel Hung Kay Chow, Kenneth Man Chee Cheung
Aims: Adolescent idiopathic scoliosis (AIS) is considered a multifactorial disease, and proprioceptive deficit (PD) is evident as a potential associated factor. However, existing studies have indicated that only a subgroup of scoliotic adolescents would display PD. The aim of this cross-sectional clinical trial was to investigate the prevalence of, and relationship between, AIS and PD in spinal and peripheral regions.
Methods: A total of 166 participants aged ten to 25 years with AIS were assessed using 3D motion analysis to evaluate their spinal and peripheral proprioceptive abilities. Six proprioceptive tests were used to determine the presence of PD in the trunk, neck, elbow, and knee. PD was characterized by test results that were inferior to the established normative values.
Results: We found that the prevalence of trunk PD was 30.1%, while that of the neck, elbow, and knee was 19.3%, 32.5%, and 32.5%, respectively. We also revealed a correlation between spinal PD and curve magnitudes, suggesting a significant association between trunk PD and the severity of AIS. However, the presence of PD in different body parts was not significantly correlated with one another, indicating that PD may occur in the spine in isolation.
Conclusion: Overall, 50 subjects (30%) with AIS have truncal PD without necessarily the presence of peripheral PD. Moreover, their presence was associated with a larger curve magnitude. Future longitudinal studies are warranted to examine the causal relationship between PD and curve progression in AIS and vice versa.
{"title":"A substantial proportion of subjects with adolescent idiopathic scoliosis display spinal and peripheral proprioceptive deficits.","authors":"Kenney Ki Lee Lau, Kenny Yat Hong Kwan, Jason Pui Yin Cheung, Karlen Ka Pui Law, Arnold Yu Lok Wong, Daniel Hung Kay Chow, Kenneth Man Chee Cheung","doi":"10.1302/2633-1462.610.BJO-2025-0140.R1","DOIUrl":"10.1302/2633-1462.610.BJO-2025-0140.R1","url":null,"abstract":"<p><strong>Aims: </strong>Adolescent idiopathic scoliosis (AIS) is considered a multifactorial disease, and proprioceptive deficit (PD) is evident as a potential associated factor. However, existing studies have indicated that only a subgroup of scoliotic adolescents would display PD. The aim of this cross-sectional clinical trial was to investigate the prevalence of, and relationship between, AIS and PD in spinal and peripheral regions.</p><p><strong>Methods: </strong>A total of 166 participants aged ten to 25 years with AIS were assessed using 3D motion analysis to evaluate their spinal and peripheral proprioceptive abilities. Six proprioceptive tests were used to determine the presence of PD in the trunk, neck, elbow, and knee. PD was characterized by test results that were inferior to the established normative values.</p><p><strong>Results: </strong>We found that the prevalence of trunk PD was 30.1%, while that of the neck, elbow, and knee was 19.3%, 32.5%, and 32.5%, respectively. We also revealed a correlation between spinal PD and curve magnitudes, suggesting a significant association between trunk PD and the severity of AIS. However, the presence of PD in different body parts was not significantly correlated with one another, indicating that PD may occur in the spine in isolation.</p><p><strong>Conclusion: </strong>Overall, 50 subjects (30%) with AIS have truncal PD without necessarily the presence of peripheral PD. Moreover, their presence was associated with a larger curve magnitude. Future longitudinal studies are warranted to examine the causal relationship between PD and curve progression in AIS and vice versa.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 10","pages":"1164-1170"},"PeriodicalIF":3.1,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12486178/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145201667","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-26DOI: 10.1302/2633-1462.69.BJO-2025-0109.R1
Oddrún Danielsen, Kirill Gromov, Claus Varnum, Thomas H Jakobsen, Mikkel R Andersen, Manuel J Bieder, Christoffer C Jørgensen, Henrik Kehlet, Martin Lindberg-Larsen
Aims: The limited documentation on patients' perspectives on undergoing discharge on the day of surgery impedes its adoption as a standard of care. Hence, the aim of this study was to investigate whether patients were willing to repeat being discharged on the day of surgery if having a future hip or knee arthroplasty procedure.
Methods: This multicentre, prospective consecutive cohort study spanned from 1 September 2022 to 31 January 2024, and was conducted at six public arthroplasty centres adhering to the same published protocol for discharge on the day of surgery following hip and knee arthroplasty. Patients undergoing primary total hip arthroplasty (THA), total knee arthroplasty (TKA), or medial unicompartmental knee arthroplasty (mUKA) were screened for eligibility and discharged when fulfilling predetermined discharge criteria. Patients discharged on the same calendar day of surgery were sent a questionnaire 30 days postoperatively.
Results: Of 9,542 primary hip and knee arthroplasties registered, 3,457 (36%) were eligible for discharge on day of surgery; 58% of eligible patients (n = 2,011) were discharged on day of surgery and therefore received the survey. Baseline characteristics were comparable across all arthroplasty groups. The survey response rate was 88% (n = 1,771). Overall, 90% (95% CI 88 to 91) were willing to repeat discharge on the day of surgery if having a future joint arthroplasty, with 91% (95% CI 88 to 93) after THA, 89% (95% CI 86 to 92) after TKA, and 90% (95% CI 86 to 92) after mUKA. The difference between centres ranged from 84% to 93%. Patients responding 'no' to repeat discharge on the day of surgery were more often female (55%, n = 95) compared to patients responding 'yes' (47%, n = 744); otherwise, the groups were comparable.
Conclusion: A total of 90% of patients (n = 1,590) discharged on the day of surgery following hip and knee arthroplasty expressed willingness to repeat discharge on the day of surgery. This supports further implementation efforts.
目的:关于患者在手术当天出院的观点的有限文献阻碍了其作为标准护理的采用。因此,本研究的目的是调查如果患者将来有髋关节或膝关节置换术,是否愿意在手术当天重复出院。方法:这项多中心前瞻性连续队列研究从2022年9月1日持续到2024年1月31日,在六个公共关节置换中心进行,遵循髋关节和膝关节置换术后手术当天出院的相同公布方案。接受原发性全髋关节置换术(THA)、全膝关节置换术(TKA)或内侧单室膝关节置换术(mUKA)的患者进行资格筛选,并在满足预定出院标准时出院。手术当天出院的患者在术后30天进行问卷调查。结果:在登记的9542例原发性髋关节和膝关节置换术中,3457例(36%)手术当天出院;58%符合条件的患者(n = 2011)在手术当天出院,因此接受了调查。所有关节置换术组的基线特征具有可比性。调查回复率为88% (n = 1771)。总体而言,90% (95% CI 88 - 91)的患者愿意在手术当天再次出院,其中THA术后91% (95% CI 88 - 93), TKA术后89% (95% CI 86 - 92), mUKA术后90% (95% CI 86 - 92)。中心之间的差异从84%到93%不等。在手术当天回答“否”的患者中,女性患者(55%,n = 95)多于回答“是”的患者(47%,n = 744);除此之外,两组具有可比性。结论:在髋关节置换术当日出院的患者中,有90% (n = 1590)表示愿意在手术当日再次出院。这支持进一步的实施工作。
{"title":"Willingness to repeat discharge on day of surgery after hip and knee arthroplasty.","authors":"Oddrún Danielsen, Kirill Gromov, Claus Varnum, Thomas H Jakobsen, Mikkel R Andersen, Manuel J Bieder, Christoffer C Jørgensen, Henrik Kehlet, Martin Lindberg-Larsen","doi":"10.1302/2633-1462.69.BJO-2025-0109.R1","DOIUrl":"10.1302/2633-1462.69.BJO-2025-0109.R1","url":null,"abstract":"<p><strong>Aims: </strong>The limited documentation on patients' perspectives on undergoing discharge on the day of surgery impedes its adoption as a standard of care. Hence, the aim of this study was to investigate whether patients were willing to repeat being discharged on the day of surgery if having a future hip or knee arthroplasty procedure.</p><p><strong>Methods: </strong>This multicentre, prospective consecutive cohort study spanned from 1 September 2022 to 31 January 2024, and was conducted at six public arthroplasty centres adhering to the same published protocol for discharge on the day of surgery following hip and knee arthroplasty. Patients undergoing primary total hip arthroplasty (THA), total knee arthroplasty (TKA), or medial unicompartmental knee arthroplasty (mUKA) were screened for eligibility and discharged when fulfilling predetermined discharge criteria. Patients discharged on the same calendar day of surgery were sent a questionnaire 30 days postoperatively.</p><p><strong>Results: </strong>Of 9,542 primary hip and knee arthroplasties registered, 3,457 (36%) were eligible for discharge on day of surgery; 58% of eligible patients (n = 2,011) were discharged on day of surgery and therefore received the survey. Baseline characteristics were comparable across all arthroplasty groups. The survey response rate was 88% (n = 1,771). Overall, 90% (95% CI 88 to 91) were willing to repeat discharge on the day of surgery if having a future joint arthroplasty, with 91% (95% CI 88 to 93) after THA, 89% (95% CI 86 to 92) after TKA, and 90% (95% CI 86 to 92) after mUKA. The difference between centres ranged from 84% to 93%. Patients responding 'no' to repeat discharge on the day of surgery were more often female (55%, n = 95) compared to patients responding 'yes' (47%, n = 744); otherwise, the groups were comparable.</p><p><strong>Conclusion: </strong>A total of 90% of patients (n = 1,590) discharged on the day of surgery following hip and knee arthroplasty expressed willingness to repeat discharge on the day of surgery. This supports further implementation efforts.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 9","pages":"1156-1163"},"PeriodicalIF":3.1,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12486177/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145151159","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-25DOI: 10.1302/2633-1462.69.BJO-2025-0086.R1
Thilo Khakzad, Sebastian Meller, Sebastian Hardt, Vincent J Leopold, Lukas Mödl, Carsten Perka, Michael Mueller, Tobias Winkler
Aims: The classic, widely accepted approach for one-stage hip revision arthroplasty in patients with periprosthetic joint infection (PJI) is the cemented exchange. This approach provides stable implant anchoring despite bone defects after removal of infected components, and facilitates local antibiotic delivery. This study aims to investigate the efficacy of cementless one-stage hip revision arthroplasty using a gentamicin-eluting bone graft substitute (GBGS) to address both bone defect filling and antibiotic elution.
Methods: We conducted a prospective analysis of 20 patients with confirmed PJI undergoing cementless one-stage hip revision arthroplasty using GBGS. The GBGS was used to fill femoral and acetabular defects during implantation. Clinical outcomes, radiographs, adverse events, and patient-reported outcome measures (PROMs) including Harris Hip Score (HHS) and EuroQol five-dimension five-level questionnaire (EQ-5D-5L) were assessed. Patients received 12 weeks of systemic antibiotics and were followed up for at least 24 months.
Results: The mean age of the cohort was 66.3 years (SD 8.4; 46 to 80), with ten female and ten male patients. On average, 13.2 ml (SD 3.9; 5 to 17) of GBGS was applied to bone defects. No reinfections occurred during the follow-up period of 3.3 years (SD 0.92; 2.1 to 4.8). We observed 15 serious adverse events (SAEs), none of which were associated with the product. All cases showed good bony consolidation and prosthesis integration at 12 months. Significant improvements were seen in HHS (preoperative mean: 47.7; final visit mean: 80.1; p < 0.001) and EQ-5D-5L score (preoperative mean: 0.43; 12-month mean: 0.88; p < 0.001).
Conclusion: This prospective pilot study is the first to demonstrate the safety and feasibility of single-stage cementless hip exchange arthroplasty using GBGS in managing PJI and associated bone defects. The technique resulted in significant improvements in functional outcomes and quality of life, with a good safety profile. Further studies with larger cohorts are warranted to validate these findings.
{"title":"Cementless one-stage hip revision arthroplasty with an injectable antibiotic bone graft substitute : a pilot study.","authors":"Thilo Khakzad, Sebastian Meller, Sebastian Hardt, Vincent J Leopold, Lukas Mödl, Carsten Perka, Michael Mueller, Tobias Winkler","doi":"10.1302/2633-1462.69.BJO-2025-0086.R1","DOIUrl":"10.1302/2633-1462.69.BJO-2025-0086.R1","url":null,"abstract":"<p><strong>Aims: </strong>The classic, widely accepted approach for one-stage hip revision arthroplasty in patients with periprosthetic joint infection (PJI) is the cemented exchange. This approach provides stable implant anchoring despite bone defects after removal of infected components, and facilitates local antibiotic delivery. This study aims to investigate the efficacy of cementless one-stage hip revision arthroplasty using a gentamicin-eluting bone graft substitute (GBGS) to address both bone defect filling and antibiotic elution.</p><p><strong>Methods: </strong>We conducted a prospective analysis of 20 patients with confirmed PJI undergoing cementless one-stage hip revision arthroplasty using GBGS. The GBGS was used to fill femoral and acetabular defects during implantation. Clinical outcomes, radiographs, adverse events, and patient-reported outcome measures (PROMs) including Harris Hip Score (HHS) and EuroQol five-dimension five-level questionnaire (EQ-5D-5L) were assessed. Patients received 12 weeks of systemic antibiotics and were followed up for at least 24 months.</p><p><strong>Results: </strong>The mean age of the cohort was 66.3 years (SD 8.4; 46 to 80), with ten female and ten male patients. On average, 13.2 ml (SD 3.9; 5 to 17) of GBGS was applied to bone defects. No reinfections occurred during the follow-up period of 3.3 years (SD 0.92; 2.1 to 4.8). We observed 15 serious adverse events (SAEs), none of which were associated with the product. All cases showed good bony consolidation and prosthesis integration at 12 months. Significant improvements were seen in HHS (preoperative mean: 47.7; final visit mean: 80.1; p < 0.001) and EQ-5D-5L score (preoperative mean: 0.43; 12-month mean: 0.88; p < 0.001).</p><p><strong>Conclusion: </strong>This prospective pilot study is the first to demonstrate the safety and feasibility of single-stage cementless hip exchange arthroplasty using GBGS in managing PJI and associated bone defects. The technique resulted in significant improvements in functional outcomes and quality of life, with a good safety profile. Further studies with larger cohorts are warranted to validate these findings.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 9","pages":"1146-1155"},"PeriodicalIF":3.1,"publicationDate":"2025-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12461155/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145138748","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-19DOI: 10.1302/2633-1462.69.BJO-2025-0028.R1
Yuan Yan, Chongquan Huang, Guoqing Zhong, Yao Mengyu, Shi Cheng, Wenhan Huang, Yu Zhang
Aims: Soft-tissue sarcoma (STS) is a rare, aggressive malignancy with a high risk of recurrence when invading surrounding structures, and the optimal treatment strategy for safe surgical margins is still unclear. This study aimed to evaluate the safety and efficacy of combined local inactivation by ablation in STS during limb-sparing surgery in high-risk STS patients.
Methods: A retrospective cohort study was conducted on 44 patients between 1 January 2018 and 31 December 2022, at a tertiary medical centre. The patients were divided into two groups based on whether combined microwave in situ ablation (MWA) was performed during surgery (MWA group, n = 24 vs Control group, n = 20). The two groups were compared for postoperative complications, local disease-free survival (DFS), overall survival (OS), and progression-free survival (PFS).
Results: At the last follow-up, 12 patients in the Control group and eight patients in the MWA group experienced local recurrence. The MWA group showed longer local DFS than the Control group (48.02 (SD 4.70), 95% CI 38.81 to 57.23 vs 33.91 (SD 6.54), 95% CI 21.10 to 46.71; p = 0.047). Postoperative complications showed no significant difference (MWA: 33.3% vs Control 25%, p = 0.143). No significant differences were observed in the median OS (MWA: 53.10 (SD 6.91), 95% CI 39.55 to 66.75) compared with Control (58.30 (SD 4.66), 95% CI 49.16 to 67.44; p = 0.512) and median PFS (MWA: 16.67 (SD 3.75), 95% CI 9.32 to 23.97) compared with Control (12.62 (SD 5.88), 95% CI 1.10 to 24.09; p = 0.691) between the two groups.
Conclusion: The combined in situ ablation inactivation in high-risk STS during limb-sparing surgery can improve local tumour control and prolong local disease-free survival.
目的:软组织肉瘤(STS)是一种罕见的侵袭性恶性肿瘤,侵袭周围结构时复发风险高,安全手术切缘的最佳治疗策略尚不清楚。本研究旨在评价高危STS患者保肢手术期间联合局部消融灭活STS的安全性和有效性。方法:对某三级医疗中心2018年1月1日至2022年12月31日期间的44例患者进行回顾性队列研究。根据术中是否进行联合微波原位消融(MWA)将患者分为两组(MWA组,n = 24,对照组,n = 20)。比较两组患者术后并发症、局部无病生存期(DFS)、总生存期(OS)和无进展生存期(PFS)。结果:末次随访时,对照组12例,MWA组8例局部复发。MWA组局部DFS较对照组长(48.02 (SD 4.70), 95% CI 38.81 ~ 57.23 vs 33.91 (SD 6.54), 95% CI 21.10 ~ 46.71;P = 0.047)。术后并发症无明显差异(MWA: 33.3% vs对照组25%,p = 0.143)。中位OS (MWA: 53.10 (SD 6.91), 95% CI 39.55 ~ 66.75)与对照组(58.30 (SD 4.66), 95% CI 49.16 ~ 67.44)相比无显著差异;p = 0.512)和中位PFS (MWA: 16.67 (SD 3.75), 95% CI 9.32至23.97)与对照组(12.62 (SD 5.88), 95% CI 1.10至24.09;P = 0.691)。结论:高危STS保肢手术中联合原位消融灭活可改善局部肿瘤控制,延长局部无病生存期。
{"title":"Limb-sparing surgery combined with local inactivation by ablation improves local control in soft-tissue sarcomas : a comparative study with long-term follow-up.","authors":"Yuan Yan, Chongquan Huang, Guoqing Zhong, Yao Mengyu, Shi Cheng, Wenhan Huang, Yu Zhang","doi":"10.1302/2633-1462.69.BJO-2025-0028.R1","DOIUrl":"10.1302/2633-1462.69.BJO-2025-0028.R1","url":null,"abstract":"<p><strong>Aims: </strong>Soft-tissue sarcoma (STS) is a rare, aggressive malignancy with a high risk of recurrence when invading surrounding structures, and the optimal treatment strategy for safe surgical margins is still unclear. This study aimed to evaluate the safety and efficacy of combined local inactivation by ablation in STS during limb-sparing surgery in high-risk STS patients.</p><p><strong>Methods: </strong>A retrospective cohort study was conducted on 44 patients between 1 January 2018 and 31 December 2022, at a tertiary medical centre. The patients were divided into two groups based on whether combined microwave in situ ablation (MWA) was performed during surgery (MWA group, n = 24 vs Control group, n = 20). The two groups were compared for postoperative complications, local disease-free survival (DFS), overall survival (OS), and progression-free survival (PFS).</p><p><strong>Results: </strong>At the last follow-up, 12 patients in the Control group and eight patients in the MWA group experienced local recurrence. The MWA group showed longer local DFS than the Control group (48.02 (SD 4.70), 95% CI 38.81 to 57.23 vs 33.91 (SD 6.54), 95% CI 21.10 to 46.71; p = 0.047). Postoperative complications showed no significant difference (MWA: 33.3% vs Control 25%, p = 0.143). No significant differences were observed in the median OS (MWA: 53.10 (SD 6.91), 95% CI 39.55 to 66.75) compared with Control (58.30 (SD 4.66), 95% CI 49.16 to 67.44; p = 0.512) and median PFS (MWA: 16.67 (SD 3.75), 95% CI 9.32 to 23.97) compared with Control (12.62 (SD 5.88), 95% CI 1.10 to 24.09; p = 0.691) between the two groups.</p><p><strong>Conclusion: </strong>The combined in situ ablation inactivation in high-risk STS during limb-sparing surgery can improve local tumour control and prolong local disease-free survival.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 9","pages":"1129-1137"},"PeriodicalIF":3.1,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12445939/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145087619","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-19DOI: 10.1302/2633-1462.69.BJO-2025-0125.R1
Lissa Pacheco-Brousseau, Paul E Beaulé, Sasha Carsen, Geoffrey Wilkin, George Grammatopoulos, Stephane Poitras
Aims: We aimed to determine if a home-based hip exercise programme, designed to use strength and flexibility exercises to modify pelvic positioning, is superior to usual care in reducing pain and improving function and quality of life in patients with symptomatic femoroacetabular impingement (FAI).
Methods: This was a single-blind parallel-group randomized controlled trial. Eligible participants were aged ≥ 16 years and diagnosed with symptomatic cam FAI. A sample size of 94 was needed to detect a clinically important difference. Participants were randomly allocated to: 1) an eight-week home-based exercise programme focused on posterior pelvic tilt supervised by a physiotherapist every two weeks in addition to usual care; and 2) usual care. The primary outcome measure was function (patient-reported 33-Item International Hip Outcome Tool (iHOT-33)) and secondary outcome measures were quality of life (EuroQol five-dimension five-level questionnaire (EQ-5D-5L)), and pain (visual analogue scale (VAS)) at baseline, nine weeks, and six months. The Mann-Whitney U test was used to test between-group differences in scores using a two-tailed level of significance of p < 0.05.
Results: A total of 95 participants were recruited (48 intervention, 47 control), 55 were males (57.9%), the mean age was 32 years (SD 8.5), and both groups were similar at baseline. There were no statistically significant differences in the primary outcome measure between groups at nine weeks and six months for function (nine weeks: p = 0.394, 95% CI -15.5 to 6.5; six months: p = 0.526, 95% CI -8.8 to 13.7). There were no statistically significant differences in the secondary outcome measures between groups: pain (nine weeks: p = 0.153, 95% CI -0.4 to 2.4; six months: p = 0.743, 95% CI -1.1 to 1.7), and quality of life (quality of life VAS nine weeks: p = 0.877, 95% CI -10.0 to 6.0; six months: p = 0.269, 95% CI -15.0 to 5.0; index value nine weeks: p = 0.815, 95% CI -0.067 to 0.052; six months: p = 0.217, 95% CI -0.099 to 0.020).
Conclusion: Our results demonstrated no statistical differences in pain, function, and quality of life for participants following an eight-week home-based exercised programme supervised by a physiotherapist compared to usual care.
{"title":"Efficacy of a home-based hip exercise programme for patients with symptomatic cam femoroacetabular impingement: a randomized controlled trial.","authors":"Lissa Pacheco-Brousseau, Paul E Beaulé, Sasha Carsen, Geoffrey Wilkin, George Grammatopoulos, Stephane Poitras","doi":"10.1302/2633-1462.69.BJO-2025-0125.R1","DOIUrl":"10.1302/2633-1462.69.BJO-2025-0125.R1","url":null,"abstract":"<p><strong>Aims: </strong>We aimed to determine if a home-based hip exercise programme, designed to use strength and flexibility exercises to modify pelvic positioning, is superior to usual care in reducing pain and improving function and quality of life in patients with symptomatic femoroacetabular impingement (FAI).</p><p><strong>Methods: </strong>This was a single-blind parallel-group randomized controlled trial. Eligible participants were aged ≥ 16 years and diagnosed with symptomatic cam FAI. A sample size of 94 was needed to detect a clinically important difference. Participants were randomly allocated to: 1) an eight-week home-based exercise programme focused on posterior pelvic tilt supervised by a physiotherapist every two weeks in addition to usual care; and 2) usual care. The primary outcome measure was function (patient-reported 33-Item International Hip Outcome Tool (iHOT-33)) and secondary outcome measures were quality of life (EuroQol five-dimension five-level questionnaire (EQ-5D-5L)), and pain (visual analogue scale (VAS)) at baseline, nine weeks, and six months. The Mann-Whitney U test was used to test between-group differences in scores using a two-tailed level of significance of p < 0.05.</p><p><strong>Results: </strong>A total of 95 participants were recruited (48 intervention, 47 control), 55 were males (57.9%), the mean age was 32 years (SD 8.5), and both groups were similar at baseline. There were no statistically significant differences in the primary outcome measure between groups at nine weeks and six months for function (nine weeks: p = 0.394, 95% CI -15.5 to 6.5; six months: p = 0.526, 95% CI -8.8 to 13.7). There were no statistically significant differences in the secondary outcome measures between groups: pain (nine weeks: p = 0.153, 95% CI -0.4 to 2.4; six months: p = 0.743, 95% CI -1.1 to 1.7), and quality of life (quality of life VAS nine weeks: p = 0.877, 95% CI -10.0 to 6.0; six months: p = 0.269, 95% CI -15.0 to 5.0; index value nine weeks: p = 0.815, 95% CI -0.067 to 0.052; six months: p = 0.217, 95% CI -0.099 to 0.020).</p><p><strong>Conclusion: </strong>Our results demonstrated no statistical differences in pain, function, and quality of life for participants following an eight-week home-based exercised programme supervised by a physiotherapist compared to usual care.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 9","pages":"1138-1145"},"PeriodicalIF":3.1,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12445941/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145087660","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-18DOI: 10.1302/2633-1462.69.BJO-2024-0235.R1
Jonathan Sterne, Andrew Crone, Gavin Baker, Niall Eames, Roslyn Cassidy, Janet Hill, David Beverland, Paul N Karayiannis
Aims: With the increasing burden of arthroplasty waiting lists within Northern Ireland, this study aims to evaluate the safety, efficacy, and postoperative outcomes following the introduction of a high-volume day-case arthroplasty unit in a district general hospital (South West Acute Hospital (SWAH)), with no previous routine orthopaedic service.
Methods: An independent company was contracted to provide high-volume, day-case arthroplasty. Standardization of care, enhanced recovery after surgery (ERAS) principles, and recruiting experienced staff were important steps in the set-up. This study includes the first 244 total hip arthroplasty (THA) cases performed. A matched cohort of 43 THA patients was compared with patients from the largest elective unit in Northern Ireland (Musgrave Park Hospital) to ensure satisfactory outcomes in the 90-day postoperative period.
Results: Same-day discharge was achieved in 83.7% of cases performed in SWAH which compared with 4.7% of MPH patients (p < 0.001). There was no significant difference in rates of attendance to an out of hours general practioner (7% vs 9.3%, p = 0.693) or emergency department (11.6% vs 16.3%, p = 0.757). Readmission rates (2.3% vs 11.6%) and reoperation rates (2.3% vs 0%) also did not show any significant difference (p = 0.202 and p = 0.500, respectively). No patient in either matched cohort had a venous thromboembolism diagnosed. Between the matched cohorts, there was a significantly higher number of American Society of Anesthesiologists grade I and II patients performed at SWAH (p = 0.003); however, this was likely due to the strict exclusion criteria necessary for the safe implementation of a day-case arthroplasty unit.
Conclusion: An arthroplasty day-case service was safely set up in a district general hospital without a previous orthopaedic unit. More than 80% of these patients were discharged on the same day of surgery. With the ever-increasing pressure, demand, and waiting lists for arthroplasty, this model could prove an important adjunct to existing services.
目的:随着北爱尔兰关节置换等待名单负担的增加,本研究旨在评估在没有常规骨科服务的地区综合医院(西南急性医院(SWAH))引入大容量日病例关节置换单元后的安全性、有效性和术后结果。方法:与一家独立公司签约,提供大容量、日间关节置换术。标准化护理、加强术后恢复(ERAS)原则和招募有经验的工作人员是建立的重要步骤。本研究包括244例全髋关节置换术。将43例THA患者与北爱尔兰最大的选择性医院(马斯格雷夫公园医院)的患者进行匹配队列比较,以确保术后90天的满意结果。结果:83.7%的swh患者当天出院,而4.7%的MPH患者当天出院(p < 0.001)。非工作时间全科医生的出勤率(7%对9.3%,p = 0.693)和急诊科的出勤率(11.6%对16.3%,p = 0.757)无显著差异。再入院率(2.3% vs 11.6%)和再手术率(2.3% vs 0%)也无显著差异(p = 0.202和p = 0.500)。两组患者均未被诊断为静脉血栓栓塞。在匹配的队列中,美国麻醉医师协会I级和II级患者在SWAH接受治疗的人数显著增加(p = 0.003);然而,这可能是由于严格的排除标准,必须安全实施一天的关节置换术单元。结论:在没有骨科的地区综合医院建立关节成形术日间服务是安全的。超过80%的患者在手术当天出院。随着关节成形术的压力、需求和等待名单的不断增加,这种模式可以证明是对现有服务的重要补充。
{"title":"High-volume day-case hip arthroplasty in a district general hospital.","authors":"Jonathan Sterne, Andrew Crone, Gavin Baker, Niall Eames, Roslyn Cassidy, Janet Hill, David Beverland, Paul N Karayiannis","doi":"10.1302/2633-1462.69.BJO-2024-0235.R1","DOIUrl":"10.1302/2633-1462.69.BJO-2024-0235.R1","url":null,"abstract":"<p><strong>Aims: </strong>With the increasing burden of arthroplasty waiting lists within Northern Ireland, this study aims to evaluate the safety, efficacy, and postoperative outcomes following the introduction of a high-volume day-case arthroplasty unit in a district general hospital (South West Acute Hospital (SWAH)), with no previous routine orthopaedic service.</p><p><strong>Methods: </strong>An independent company was contracted to provide high-volume, day-case arthroplasty. Standardization of care, enhanced recovery after surgery (ERAS) principles, and recruiting experienced staff were important steps in the set-up. This study includes the first 244 total hip arthroplasty (THA) cases performed. A matched cohort of 43 THA patients was compared with patients from the largest elective unit in Northern Ireland (Musgrave Park Hospital) to ensure satisfactory outcomes in the 90-day postoperative period.</p><p><strong>Results: </strong>Same-day discharge was achieved in 83.7% of cases performed in SWAH which compared with 4.7% of MPH patients (p < 0.001). There was no significant difference in rates of attendance to an out of hours general practioner (7% vs 9.3%, p = 0.693) or emergency department (11.6% vs 16.3%, p = 0.757). Readmission rates (2.3% vs 11.6%) and reoperation rates (2.3% vs 0%) also did not show any significant difference (p = 0.202 and p = 0.500, respectively). No patient in either matched cohort had a venous thromboembolism diagnosed. Between the matched cohorts, there was a significantly higher number of American Society of Anesthesiologists grade I and II patients performed at SWAH (p = 0.003); however, this was likely due to the strict exclusion criteria necessary for the safe implementation of a day-case arthroplasty unit.</p><p><strong>Conclusion: </strong>An arthroplasty day-case service was safely set up in a district general hospital without a previous orthopaedic unit. More than 80% of these patients were discharged on the same day of surgery. With the ever-increasing pressure, demand, and waiting lists for arthroplasty, this model could prove an important adjunct to existing services.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 9","pages":"1122-1128"},"PeriodicalIF":3.1,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12445311/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145081900","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}