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      A systematic review on current osteosynthesis-associated infection animal fracture models

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          Abstract

          Objective

          Osteosynthesis-associated infection is a challenging complication post fracture fixation, burdening the patients and the orthopaedic surgeons alike. A clinically relevant animal model is critical in devising new therapeutic strategies. Our aim was to perform a systematic review to evaluate existing preclinical models and identify their applications in aspects of animal selection, bacterial induction, fracture fixation and complications.

          Methods

          A systematic literature research was conducted in PubMed and Embase up to February 2020. A total of 31 studies were included. Information on the animal, bacterial induction, fracture fixation, healing result and complications were extracted.

          Results

          Animals selected included murine (23), rabbit (6), ewe (1) and goat (1). Larger animals had enabled the use of human-sized implant, however small animals were more economical and easier in handling. Staphylococcus aureus (S. aureus) was the most frequently chosen bacteria for induction. Bacterial inoculation dose ranged from 10 2−8 ​CFU. Consistent and replicable infections were observed from 10 4 ​CFU in general. Methods of inoculation included injections of bacterial suspension (20), placement of foreign objects (8) and pretreatment of implants with established biofilm (3). Intramedullary implants (13), plates and screws (18) were used in most models. Radiological (29) and histological evaluations (24) in osseous healing were performed. Complications such as instability of fracture fixation (7), unexpected surgical death (5), sepsis (1) and persistent lameness (1) were encountered.

          Conclusion

          The most common animal model is the S. aureus infected open fracture internally fixated. Replicable infections were mainly from 10 4 ​CFU of bacteria. However, with the increase in antibiotic resistance, future directions should explore polymicrobial and antibiotic resistant strains, as these will no doubt play a major role in bone infection. Currently, there is also a lack of osteoporotic bone infection models and the pathophysiology is unexplored, which would be important with our aging population.

          The translational potential of this article

          This systematic review provides an updated overview and compares the currently available animal models of osteosynthesis-associated infections. A discussion on future research directions and suggestion of animal model settings were made, which is expected to advance the research in this field.

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          Most cited references93

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          CDC/NHSN surveillance definition of health care-associated infection and criteria for specific types of infections in the acute care setting.

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            Sex differences in autoimmune disease.

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              The challenge of treating biofilm-associated bacterial infections.

              Biofilm formation is a crucial step in the pathogenesis of many subacute and chronic bacterial infections, including foreign body-related infections. Biofilms are difficult to eradicate with conventional antimicrobial agents. Bacterial biofilms have several potential antimicrobial resistance mechanisms. Antimicrobial resistance mechanisms may act concurrently, and in some cases, synergistically. Persister cells play a major role in the tolerance of biofilm bacteria to antimicrobial agents. Understanding the mechanisms involved in biofilm-associated antimicrobial resistance is key to development of new therapeutic strategies.
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                Author and article information

                Contributors
                Journal
                J Orthop Translat
                J Orthop Translat
                Journal of Orthopaedic Translation
                Chinese Speaking Orthopaedic Society
                2214-031X
                2214-0328
                30 March 2020
                July 2020
                30 March 2020
                : 23
                : 8-20
                Affiliations
                [a ]Department of Orthopaedics and Traumatology, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong
                [b ]School of Pharmacy, The Chinese University of Hong Kong, Hong Kong
                [c ]Department of Microbiology, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong
                Author notes
                []Corresponding author. Department of Orthopaedics and Traumatology, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong. louischeung@ 123456cuhk.edu.hk
                Article
                S2214-031X(20)30032-2
                10.1016/j.jot.2020.03.002
                7231979
                32440511
                1b9ee1c4-e419-43df-a23d-ae7843a8d351
                © 2020 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 23 December 2019
                : 18 February 2020
                : 2 March 2020
                Categories
                Review Article

                animal models,fracture,infection models,osteosynthesis-associated infection,systematic review

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