Staged Management of Bone Defects in Chronic Osteomyelitis and Nonunions Using Antibiotic-Loaded Calcium Sulphate-Hydroxyapatite: A Multicenter Retrospective Analysis of 101 Cases.

IF 2.6 3区 医学 Q1 Pharmacology, Toxicology and Pharmaceutics
Therapeutics and Clinical Risk Management Pub Date : 2026-05-08 eCollection Date: 2026-01-01 DOI:10.2147/TCRM.S599996
Jonas Armbruster, Nick Mattern, Felix Lamadé-Dootz, Eva Simone Steinhausen, Gregor Reiter, Marcel Dudda, Paul Alfred Grützner, Holger Freischmidt
{"title":"Staged Management of Bone Defects in Chronic Osteomyelitis and Nonunions Using Antibiotic-Loaded Calcium Sulphate-Hydroxyapatite: A Multicenter Retrospective Analysis of 101 Cases.","authors":"Jonas Armbruster, Nick Mattern, Felix Lamadé-Dootz, Eva Simone Steinhausen, Gregor Reiter, Marcel Dudda, Paul Alfred Grützner, Holger Freischmidt","doi":"10.2147/TCRM.S599996","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate the clinical outcomes of an antibiotic-loaded calcium sulphate-hydroxyapatite biocomposite (ALB) used specifically in staged surgical protocols for chronic osteomyelitis and nonunions, including large bone defects resulting from the necessary debridement of necrotic bone.</p><p><strong>Patients and methods: </strong>This retrospective multicenter study analyzed 101 patients treated between 2013 and 2020. Inclusion criteria comprised adult patients with bone defects resulting from osteomyelitis, septic nonunion, or aseptic nonunion, treated with ALB (gentamicin or vancomycin) in a staged procedure. The primary outcome was treatment success, defined as infection eradication and stable bone consolidation without unplanned surgical revision. Secondary outcomes included revision rates, reinfection rates, and biomaterial-related side effects such as white drainage.</p><p><strong>Results: </strong>Treatment success was achieved in 30.7% of patients. The overall revision rate was 58.4%, and the reinfection rate was 45.5%. The mean defect size was 4.1 cm. Statistical analysis identified larger defect sizes and higher volumes of implanted ALB as significant risk factors for failure. \"White drainage\" was observed in 13.9% of patients and was significantly associated with the use of larger material volumes.</p><p><strong>Conclusion: </strong>The use of ALB in staged protocols for large bone defects is associated with high revision and reinfection rates. These findings identify the limits of the technique and sharpen its indication spectrum, standing alongside the favorable outcomes reported for single-stage procedures in smaller defects. In large defects, the resorption of the carrier may outpace bone ingrowth, leading to recurrence of infection. Consequently, the use of ALB in large defects cannot be recommended based on these data.</p>","PeriodicalId":22977,"journal":{"name":"Therapeutics and Clinical Risk Management","volume":"22 ","pages":"599996"},"PeriodicalIF":2.6000,"publicationDate":"2026-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13165491/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Therapeutics and Clinical Risk Management","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2147/TCRM.S599996","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: To evaluate the clinical outcomes of an antibiotic-loaded calcium sulphate-hydroxyapatite biocomposite (ALB) used specifically in staged surgical protocols for chronic osteomyelitis and nonunions, including large bone defects resulting from the necessary debridement of necrotic bone.

Patients and methods: This retrospective multicenter study analyzed 101 patients treated between 2013 and 2020. Inclusion criteria comprised adult patients with bone defects resulting from osteomyelitis, septic nonunion, or aseptic nonunion, treated with ALB (gentamicin or vancomycin) in a staged procedure. The primary outcome was treatment success, defined as infection eradication and stable bone consolidation without unplanned surgical revision. Secondary outcomes included revision rates, reinfection rates, and biomaterial-related side effects such as white drainage.

Results: Treatment success was achieved in 30.7% of patients. The overall revision rate was 58.4%, and the reinfection rate was 45.5%. The mean defect size was 4.1 cm. Statistical analysis identified larger defect sizes and higher volumes of implanted ALB as significant risk factors for failure. "White drainage" was observed in 13.9% of patients and was significantly associated with the use of larger material volumes.

Conclusion: The use of ALB in staged protocols for large bone defects is associated with high revision and reinfection rates. These findings identify the limits of the technique and sharpen its indication spectrum, standing alongside the favorable outcomes reported for single-stage procedures in smaller defects. In large defects, the resorption of the carrier may outpace bone ingrowth, leading to recurrence of infection. Consequently, the use of ALB in large defects cannot be recommended based on these data.

使用抗生素负载硫酸钙-羟基磷灰石分阶段治疗慢性骨髓炎和骨不连的骨缺损:101例多中心回顾性分析。
目的:评估抗生素负载硫酸钙-羟基磷灰石生物复合材料(ALB)在慢性骨髓炎和骨不连的分阶段手术方案中的临床效果,包括因坏死骨的必要清创术而导致的大面积骨缺损。患者和方法:这项回顾性多中心研究分析了2013年至2020年间接受治疗的101例患者。纳入标准包括由骨髓炎、脓毒性骨不连或无菌性骨不连引起的骨缺损的成年患者,并分阶段接受ALB(庆大霉素或万古霉素)治疗。主要结果是治疗成功,定义为感染根除和稳定的骨巩固,没有计划外的手术翻修。次要结局包括翻修率、再感染率和生物材料相关的副作用,如白色引流。结果:治疗成功率为30.7%。总翻修率为58.4%,再感染率为45.5%。平均缺陷尺寸为4.1 cm。统计分析表明,较大的缺陷尺寸和植入ALB的体积是导致失败的重要危险因素。13.9%的患者出现“白色引流”,这与使用更大的材料容量显著相关。结论:在大骨缺损分期治疗方案中使用白蛋白可提高翻修率和再感染率。这些发现确定了该技术的局限性,并明确了其适应症范围,与报道的小缺陷单阶段手术的有利结果并列。在较大的缺陷中,载体的吸收可能超过骨长入,导致感染复发。因此,基于这些数据,不能推荐在大缺陷中使用ALB。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Therapeutics and Clinical Risk Management
Therapeutics and Clinical Risk Management HEALTH CARE SCIENCES & SERVICES-
CiteScore
5.30
自引率
3.60%
发文量
139
审稿时长
16 weeks
期刊介绍: Therapeutics and Clinical Risk Management is an international, peer-reviewed journal of clinical therapeutics and risk management, focusing on concise rapid reporting of clinical studies in all therapeutic areas, outcomes, safety, and programs for the effective, safe, and sustained use of medicines, therapeutic and surgical interventions in all clinical areas. The journal welcomes submissions covering original research, clinical and epidemiological studies, reviews, guidelines, expert opinion and commentary. The journal will consider case reports but only if they make a valuable and original contribution to the literature. As of 18th March 2019, Therapeutics and Clinical Risk Management will no longer consider meta-analyses for publication. The journal does not accept study protocols, animal-based or cell line-based studies.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书