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Orthopaedic Proceedings
Vol. 104-B, Issue SUPP_10 | Pages 89 - 89
1 Oct 2022
FUNCTIONAL RESULTS AND COMPLICATIONS AT TWO AND FIVE YEARS IN PATIENTS WITH A REVERSE SHOULDER PROSTHESIS WITH CONTAMINATION BY C ACNES
Alier A Gasol B Pérez-Prieto D Santana F Torrens C
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Aim

A significant number of patients undergoing shoulder arthroplasty surgery have C acnes contamination at the end of the primary surgery. The objective of this study is to determine whether patients with C acnes contamination at the end of their primary shoulder surgery have a worse prognosis than those who end up without C. acnes contamination.

Method

Prospective study including all patients who underwent a reverse shoulder prosthesis from January 2015 to December 2018. In all of them, 5 to 12 cultures were performed during primary surgery. The patients underwent surgery for shoulder arthritis secondary to rotator cuff tears, acute fracture of the proximal humerus, and sequelae of fracture of the proximal humerus. Exclusion criteria included the existence of previous surgeries on the affected shoulder, the presence of signs of infection, having received infiltrations and / or complementary invasive examinations (Arthro-MRI and Arthro-CT). Follow-up from 2 to 5 years. Functional assessment according to the Constant Functional Scale. All complications were also recorded.

Orthopaedic Proceedings
Vol. 103-B, Issue SUPP_15 | Pages 17 - 17
1 Dec 2021
ARE CUTIBACTERIUM ACNES PRESENT AT THE END OF PRIMARY SHOULDER PROSTHETIC SURGERIES RESPONSIBLE FOR TOTAL SHOULDER ARTHROPLASTY INFECTION? A PROSPECTIVE STUDY
Alier A Torrens C Bellosillo B Gibert J Pérez-Prieto D Corvec S
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Aim

Cutibacterium acnes (C. acnes) is the most cultured organism implicated in periprosthetic shoulder infections. Nevertheless, the clinical significance of its persistence on the skin surface and in the deep layers during shoulder arthroplasty surgery remains still unknown. The purpose of this study was to know if the C. acnes isolate present in deep tissues at the end of a primary shoulder arthroplasty could be responsible for shoulder arthroplasty infection.

Method

Prospective study including 156 patients undergoing primary shoulder arthroplasty. In all the patients included 5 to 12 tissue samples were obtained and were specifically cultured to detect C. acnes presence. DNA was extracted from the C. acnes colonies selected with the QIAsymphony DSP Virus/Pathogen Midi Kit (Qiagen, Hilden, Germany). Libraries were prepared using Nextera XT kit (Illumina) and sequenced in an Illumina MiSeq sequencer. Sequencing files were pre-processed using The Microbial Genome Atlas pipeline. Samples that failed on QC analysis were discarded for further analysis. Isolate nucleotide distances were calculated using Genome-based distance matrix calculator from the enveomics collection. Comparative genomic analysis was performed between intra- and inter-patients’ isolates. Data analysis was performed using R 3.6.3.

Orthopaedic Proceedings
Vol. 98-B, Issue SUPP_23 | Pages 82 - 82
1 Dec 2016
LOW INCIDENCE OF P. ACNES ON THE SKIN OF PATIENTS UNDERGOING PRIMARY SHOULDER ARTHROPLASTY
Molina RM Suari AF Castellnou PG Puig L Torrens C
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Aim

Recent studies have indicated that the presence of P. acnes in the skin of the shoulder and around the acromion is higher than other body regions like the knee or the hip. The aim of this study was to estimate the presence of P. acnes in a real set of primary shoulder arthroplasty, after skin preparation with chlorhexidine and administration of empirical antibiotic therapy.

Method

A prospective observational study involving 63 patients undergoing primary shoulder arthroplasty was designed. In all patients two skin biopsies with a 3 mm dermal punch and one subcutaneous tissue sample after surgical incision were obtained. Skin biopsies were obtained at the most anterior part of the surgical wound in case of superior approach and at the upper part in the deltopectoral approach. All patients underwent preoperative antibiotic prophylaxis with cefazolin 2g ev and skin preparation with 2% chlorhexidine alcoholic tinted before the start of surgery twice. The aerobic cultures were incubated at 37ºC for 7 days whereas the anaerobic ones incubated for 14 days.