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1.
Int. braz. j. urol ; 42(6): 1183-1189, Nov.-Dec. 2016. tab
Artigo em Inglês | LILACS | ID: biblio-828943

RESUMO

ABSTRACT Introduction: Aim of this study is to investigate bacterial growth on non-infected devices and compare antibiotic-coated and non-coated implants. Materials and methods: The charts of 71 patients who underwent revision surgeries for penile prosthesis between 1995 and 2013 were reviewed. Of those, 31 devices were antibiotic-coated prostheses, while 40 of the implants were non-coated. Swab cultures were routinely obtained from corporal, pump or reservoir site during the operation. If a bacterial biofilm was determined on the prosthesis, it was also cultured. Results: A total of 5 different organisms were cultured from 18 patients. Of them, 4 devices were antibiotic-coated and the other 14 were non-coated devices. Staphylococcus epidermidis was the most common organism, while Staphylococcus hominis, beta hemolitic streptococcus, Escherichia coli and Proteus mirabilis were also cultured. All patients who had positive cultures were treated with appropriate antibiotics for four weeks postoperatively. Median follow-up time was 41 months, ranging between 8 and 82 months. One prosthesis (non-coated) became clinically infected in the follow-up period with a totally different organism. Culture positivity rates of antibiotic-coated and non-coated devices were 13% and 35% respectively and the result was significant (p=0.00254). Conclusions: Positive bacterial cultures are present on non-infected penile prostheses at revision surgeries in some of the patients. Antibiotic coated prostheses have much less positive cultures than non-coated devices.


Assuntos
Humanos , Staphylococcus epidermidis/crescimento & desenvolvimento , Prótese de Pênis/microbiologia , Infecções Relacionadas à Prótese/prevenção & controle , Antibacterianos/administração & dosagem , Staphylococcus epidermidis/efeitos dos fármacos , Fatores de Tempo , Contagem de Colônia Microbiana , Testes de Sensibilidade Microbiana , Prótese de Pênis/efeitos adversos , Células Cultivadas , Estudos Prospectivos , Estudos Retrospectivos , Infecções Relacionadas à Prótese/etiologia , Sistemas de Liberação de Medicamentos , Pessoa de Meia-Idade
2.
Int. braz. j. urol ; 40(5): 613-619, 12/2014. tab, graf
Artigo em Inglês | LILACS | ID: lil-731122

RESUMO

Introduction We aimed to assess the relationship between prostate volume (PV) and high grade prostate carcinoma (HGPCa) in patients with benign and suspicious digital rectal examination (DRE) in our prostate biopsy cohort. Materials and methods Between 2009-2012, 759 consecutive initial transrectal systematic 12 cores prostate biopsies were included. PVs were calculated with transrectal ultrasound. Only prostate adenocarcinomas (PCa) were included into the study. For standardization, patients with missing data, and who have been exposed to any form of hormonal or radiation therapy were excluded. Patients were categorized with DRE (negative or positive) and Gleason sum [<7: low grade PCa(LGPCa), ≥7: HGPCa]. Results Median PV was significantly lower in patients with HGPCa. There was a significantly increased risk of HGPCa with PV according to all groups in univariate logistic regression (LR). The significant relationship continued in multivariate LR with PSA and age. We found a PV cut-off value of 47.9cc for HGPCa. HGPCa was significantly higher in <47.9 volume, both in DRE positive and negative patients and in the whole cohort, although LGPCa did not differ significantly. Conclusions There is a significant relationship between HGPCa and decreasing PV. The continued significant relationship both in DRE negative and positive patients reinforces this relation. .


Assuntos
Idoso , Humanos , Masculino , Pessoa de Meia-Idade , Carcinoma/patologia , Exame Retal Digital/métodos , Próstata/patologia , Neoplasias da Próstata/patologia , Biópsia , Carcinoma , Modelos Logísticos , Gradação de Tumores , Antígeno Prostático Específico/sangue , Próstata , Neoplasias da Próstata , Padrões de Referência , Estudos Retrospectivos , Fatores de Risco , Curva ROC , Carga Tumoral
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