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1.
Int. braz. j. urol ; 33(6): 746-751, Nov.-Dec. 2007. tab
Artigo em Inglês | LILACS | ID: lil-476638

RESUMO

OBJECTIVE: To determine if intraoperative frozen sections of the bladder neck during radical prostatectomy (RP) could decrease the incidence of final positive surgical margins at the bladder neck. MATERIALS AND METHODS: This prospective cohort study included 51 consecutive men who underwent anatomic RP at University of Florida & Shands Jacksonville. All patients had intraoperative frozen section of bladder neck sent for analysis. Preoperative, operative, and postoperative data were collected and analyzed. Main Outcome Measures: Outcome measures were intraoperative bladder neck margin status, final pathologic bladder neck margin status, and postoperative urinary complications. Median follow-up for the 51 patients was 22 months. RESULTS: The final positive surgical margin rate was 20 percent (10 patients). An additional three patients had positive surgical margins at the bladder neck intraoperatively. These patients then had a wider resection of the affected bladder neck until the frozen sections were negative for cancer or prostatic tissue. Final pathologic evaluation of bladder neck margin was negative for tumor or persistent prostatic tissue in all 51 men. CONCLUSION: With intra-operative frozen sections, we were able to obtain a negligible positive bladder neck margin rate. Surgeons who are still on the learning curve for RP should consider intra-operative frozen section of the bladder neck.


Assuntos
Idoso , Humanos , Masculino , Pessoa de Meia-Idade , Secções Congeladas , Excisão de Linfonodo , Próstata/patologia , Prostatectomia/métodos , Neoplasias da Próstata/cirurgia , Bexiga Urinária/patologia , Seguimentos , Cuidados Intraoperatórios , Laparoscopia , Invasividade Neoplásica , Estadiamento de Neoplasias , Período Pós-Operatório , Estudos Prospectivos , Pelve/patologia , Antígeno Prostático Específico/sangue , Próstata/cirurgia , Neoplasias da Próstata/patologia , Bexiga Urinária/cirurgia
2.
Int. braz. j. urol ; 33(3): 347-354, May-June 2007. tab
Artigo em Inglês | LILACS | ID: lil-459857

RESUMO

OBJECTIVE: To assess the utility of enoxaparin in prevention of venous thromboembolism (VTE) in men poorly compliant with pneumatic compression stockings (PCS) in the immediate postoperative period after a radical retropubic prostatectomy (RP). MATERIALS AND METHODS: This retrospective study included 47 men who underwent RP at an inner-city tertiary care hospital. All patients were started on enoxaparin 40 mg subcutaneously 6-8 hours postoperatively and daily while hospitalized. Preoperative, operative, and postoperative data were collected and analyzed. Median follow-up was 18 months. RESULTS: Median patient age was 64 ± 7 years, median prostate-specific antigen level was 4.9 ng/mL and median prostate biopsy-determined Gleason score was 6. Forty-one men (87 percent) underwent a pelvic lymph node dissection. Median operative time was 181 minutes (range 164-450 minutes). Median estimated blood loss was 700 mL. Approximately 36 percent of the men wore PCS the recommended > 19 hours/day. On average PCS were worn 10.3 ± 7.5 hours/day. Postoperative complications were not increased in this cohort. Two patients developed pulmonary embolism requiring long-term anticoagulation. There were no mortalities. CONCLUSIONS: In men non-compliant with PCS, initiation of enoxaparin in the immediate postoperative setting was well-tolerated and maintained a low (4 percent) rate of VTE. Thus, enoxaparin may be useful in adjunct with PCS in these patients.


Assuntos
Idoso , Humanos , Masculino , Pessoa de Meia-Idade , Anticoagulantes/uso terapêutico , Enoxaparina/uso terapêutico , Excisão de Linfonodo/efeitos adversos , Prostatectomia/métodos , Neoplasias da Próstata/cirurgia , Tromboembolia Venosa/prevenção & controle , Anticoagulantes/administração & dosagem , Enoxaparina/administração & dosagem , Estudos de Viabilidade , Seguimentos , Dispositivos de Compressão Pneumática Intermitente , Complicações Pós-Operatórias , Prostatectomia/efeitos adversos , Estudos Retrospectivos , Resultado do Tratamento , Tromboembolia Venosa/etiologia
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