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Antibacterial hydrogel coating in joint mega-prosthesis: results of a comparative series.
Zoccali, Carmine; Scoccianti, Guido; Biagini, Roberto; Daolio, Primo Andrea; Giardina, Fabio Luca; Campanacci, Domenico Andrea.
Affiliation
  • Zoccali C; Oncological Orthopedics Department, IFO - Regina Elena National Cancer Institute, Via Elio Chianesi 53, 00144, Rome, Italy. carminezoccali@libero.it.
  • Scoccianti G; Department of Orthopaedic Oncology and Reconstructive Surgery, University of Florence, Azienda Ospedaliera Universitaria Careggi, Largo Brambilla, 3, 50134, Florence, Italy.
  • Biagini R; Oncological Orthopedics Department, IFO - Regina Elena National Cancer Institute, Via Elio Chianesi 53, 00144, Rome, Italy.
  • Daolio PA; Oncologic Surgery Centre, Gaetano Pini Orthopedic Institute, Via Quadronno, 25, 20122, Milan, Italy.
  • Giardina FL; Oncologic Surgery Centre, Gaetano Pini Orthopedic Institute, Via Quadronno, 25, 20122, Milan, Italy.
  • Campanacci DA; Department of Orthopaedic Oncology and Reconstructive Surgery, University of Florence, Azienda Ospedaliera Universitaria Careggi, Largo Brambilla, 3, 50134, Florence, Italy.
Eur J Orthop Surg Traumatol ; 31(8): 1647-1655, 2021 Dec.
Article in En | MEDLINE | ID: mdl-33547509
ABSTRACT

PURPOSE:

Joint mega-prosthesis after bone tumors, severe trauma or infection is associated with high rates of post-surgical septic complications. A fast-resorbable antibacterial hydrogel coating (DAC®, Defensive Antibacterial Coating) has previously been shown to be able to significantly reduce surgical site infection in various clinical settings. Aim of the present study was to evaluate the safety and efficacy of the DAC hydrogel coating to prevent early periprosthetic joint infection after joint mega-prosthesis.

METHODS:

In this three-centers, case-control study, 43 patients, treated with an antibacterial hydrogel coated mega-prosthesis for oncological (N = 39) or non-oncological conditions (N = 4), were retrospectively compared with 43 matched controls, treated with mega-implants without the coating. Clinical, laboratory and radiographic examinations were performed to evaluate the occurrence of post-surgical infection, complications and adverse events.

RESULTS:

At a mean follow-up of 2 years, no evidence of infection or adverse events were observed in the DAC-treated group, compared to six cases of post-surgical infection in the control group.

CONCLUSION:

This matched case-control study shows that a fast-resorbable, antibiotic-loaded coating can be safely used to protect joint mega-prosthesis, providing a reduction of early surgical site infections with no side effects. Larger prospective trials with longer follow-ups are warranted to confirm this report. TRIAL REGISTRATION RS1229/19 (Regina Elena National Cancer Institute Experimental Registry Number).
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prosthesis-Related Infections / Arthroplasty, Replacement, Hip / Joint Prosthesis / Anti-Bacterial Agents Type of study: Observational_studies / Risk_factors_studies Limits: Humans Language: En Journal: Eur J Orthop Surg Traumatol Year: 2021 Document type: Article Affiliation country: Italy

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prosthesis-Related Infections / Arthroplasty, Replacement, Hip / Joint Prosthesis / Anti-Bacterial Agents Type of study: Observational_studies / Risk_factors_studies Limits: Humans Language: En Journal: Eur J Orthop Surg Traumatol Year: 2021 Document type: Article Affiliation country: Italy