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Open Access

Infographic

Fracture-related infection



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Cite this article: Bone Joint Res 2021;10(6):351–353.

Background

Fracture-related infection (FRI) carries a substantial burden of disease and socio-economic costs.1-3 The incidence of FRI is 1% to 2% in closed fractures and can reach 30% in open fractures.1 Until recently, amputation and recurrence rates remained high.2,4 With the publication of international consensus documents,4,5 an evidence-based overview of diagnosis and management has been provided, which should improve treatment outcomes.

Pathology

The pathology of FRI is multifactorial; bacterial infection and fracture instability are interdependent and fundamental in FRI.6,7 Biofilm formation, canalicular invasion,8 intracellular infection,9 and formation of staphylococcal abscess communities10 are the key niches occupied by bacteria. A vicious cycle between instability with ongoing soft-tissue trauma, compromised neovascularity, and osteolysis creates a supportive environment for bacteria, promoting the development of FRI or hindering its eradication.6

Diagnosis

Confirmatory criteria include fistula or sinus tract, purulent drainage or pus, microbial growth in two or more deep tissue samples, and histological evidence of pathogens and inflammation in peri-implant tissue.4,5 Suggestive criteria include clinical signs such as: erythema; swelling; persistent, increasing, or new-onset wound drainage; radiological or nuclear imaging signs; increased serum inflammatory markers; and microbial growth in a single deep tissue sample.5,7

Management

A consensus-derived management algorithm has been developed and should be led by a multidisciplinary team.5,7 Based on three basic principles, consisting of exchange, retention, or removal of the indwelling implant, the preferred strategy depends on host physiology, time interval between fracture fixation and FRI manifestation, anatomical localization, and causative pathogen. For implant retention, the stability of the construct and the ability to perform proper debridement are critical, considering the implant type and soft-tissue conditions.7

Prevention

Appropriate use of prophylactic antibiotics is crucial to prevent FRI. In closed injuries, perioperative antibiotic prophylaxis limited to a single dose is recommended. In open fractures, prophylactic antibiotic administration should not exceed 24 hours for Gustilo-Anderson types I and II and 72 hours for Gustilo-Anderson type III fractures.5,7 Early debridement, soft-tissue management, and stable fracture fixation are cornerstones of management.5

Follow-up of FRI should be planned in collaboration with a multidisciplinary team, for a minimum of 12 months after the cessation of surgical and antibiotic therapy.11

Future perspectives for prevention and management of FRI include: antimicrobial coated implants; osteoinductive antibiotic-loaded biomaterials; and bacteriophage and enzybiotic therapy. All these therapies consider the global threat of antibiotic resistance and target mechanisms of antimicrobial tolerance such as biofilm formation.1

Fig. 1

Fig. 1


Thomas Fintan Moriarty. E-mail:

References

1. Metsemakers WJ , Kuehl R , Moriarty TF , et al. Infection after fracture fixation: Current surgical and microbiological concepts . Injury . 2018 ; 49 ( 3 ): 511 522 . Crossref PubMed Google Scholar

2. Metsemakers W-. J , Smeets B , Nijs S , Hoekstra H . Infection after fracture fixation of the tibia: Analysis of healthcare utilization and related costs . Injury . 2017 ; 48 ( 6 ): 1204 1210 . Crossref PubMed Google Scholar

3. Bezstarosti H , Van Lieshout EMM , Voskamp LW , et al. Insights into treatment and outcome of fracture-related infection: A systematic literature review . Arch Orthop Trauma Surg . 2019 ; 139 ( 1 ): 61 72 . Crossref PubMed Google Scholar

4. Metsemakers WJ , Morgenstern M , McNally MA , et al. Fracture-related infection: A consensus on definition from an international expert group . Injury . 2018 ; 49 ( 3 ): 505 510 . Crossref PubMed Google Scholar

5. Obremskey WT , Metsemakers W-J , Schlatterer DR , et al. Musculoskeletal infection in orthopaedic trauma: Assessment of the 2018 international consensus meeting on musculoskeletal infection . J Bone Joint Surg Am . 2020 ; 102-A ( 10 ): e44 . Crossref PubMed Google Scholar

6. Foster AL , Moriarty TF , Zalavras C , Morgenstern M , Jaiprakash A , Crawford R . The influence of biomechanical stability on bone healing and fracture-related infection: the legacy of Stephan Perren . Injury . 2020 ; 52 ( 1 ): 43 52 . Crossref PubMed Google Scholar

7. Depypere M , Morgenstern M , Kuehl R , Senneville E , Moriarty TF , Obremskey WT . Pathogenesis and management of fracture-related infection . Clin Microbiol Infect . 2020 ; 26 ( 5 ): 572 578 . Crossref PubMed Google Scholar

8. de Mesy Bentley KL , Trombetta R , Nishitani K , et al. Evidence of staphylococcus aureus deformation, proliferation, and migration in canaliculi of live cortical bone in murine models of osteomyelitis . J Bone Miner Res . 2017 ; 32 ( 5 ): 985 990 . Crossref PubMed Google Scholar

9. Mohamed W , Sommer U , Sethi S , Domann E , Thormann U , Schütz I . Intracellular proliferation of S. aureus in osteoblasts and effects of rifampicin and gentamicin on S. aureus intracellular proliferation and survival . Eur Cell Mater . 2014 ; 28 : 258 268 . Crossref PubMed Google Scholar

10. Hofstee MI , Riool M , Terjajevs I , et al. Three-Dimensional In Vitro Staphylococcus aureus Abscess Communities Display Antibiotic Tolerance and Protection from Neutrophil Clearance . Infect Immun . 2020 ; 88 ( 11 ): e00293 - 20 . Crossref PubMed Google Scholar

11. Metsemakers W-J , Morgenstern M , Senneville E , et al. General treatment principles for fracture-related infection: Recommendations from an international expert group . Arch Orthop Trauma Surg . 2020 ; 140 ( 8 ): 1013 1027 . Crossref PubMed Google Scholar

Author contributions

S. Baertl: Designed, created, and revised the infographic.

W-J. Metsemakers: Designed and revised the infographic.

M. Morgenstern: Designed and revised the infographic.

V. Alt: Designed and revised the infographic.

R. G. Richards: Revised the infographic.

T. F. Moriarty: Conceptualized, designed, and revised the infographic.

K. Young: Designed and revised the infographic.

Funding statement

No benefits in any form have been received or will be received from a commercial party related directly or indirectly to the subject of this article.

Acknowledgements

We acknowledge the contribution of Medical Artist Louise Hinman in preparing the illustrations for this infographic.

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Follow T. F. Moriarty @fintan_moriarty

© 2021 Author(s) et al. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (CC BY-NC-ND 4.0) licence, which permits the copying and redistribution of the work only, and provided the original author and source are credited. See https://creativecommons.org/licenses/by-nc-nd/4.0/.