15 research outputs found

    Adjuvant Radiation Therapy Following Radical Prostatectomy for Pathologic T3 or Margin-positive Prostate Cancer: Are the EAU Guidelines Correct?

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    Objective: To present a critical review of the published data as to whether adjuvant radiation therapy (RT) is the preferred first line of management for pathologic T3 or margin-positive prostate cancer (PCa) after radical prostatectomy (RP), which has level 1B evidence in the European Association of Urology (EAU) guidelines. Methods: Three randomised studies have been published comparing immediate adjuvant RT and salvage treatment in patients with pT3 and/or margin-positive PCa. The concept of these trials was critically evaluated, and the translation of the outcome of these trials to daily clinical practice is discussed. Results: Current evidence is insufficient to subject all patients with pT3 and/or margin-positive PCa to adjuvant RT after RP, and it should be reserved for a subset of patients with adverse prognostic factors after RP, such as seminal vesicle invasion. Conclusions: The data that can be retrieved from the trials exploring the benefit of adjuvant RT following RP cannot be translated to routine clinical urologic practice, because the field of PCa is changing rapidly and the patients present at an earlier stage. A trial evaluating immediate versus salvage RT should answer the question of who needs adjuvant treatment and when. The recommendation concerning adjuvant RT should thus be adapted in the EAU guidelines. (C) 2011 European Association of Urology. Published by Elsevier B.V. All rights reserve

    A Randomized Control Trial Evaluating Efficacy of Nephrostomy Tract Infiltration with Bupivacaine After Tubeless Percutaneous Nephrolithotomy

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    Purpose: We conducted a randomized controlled trial to assess the efficacy of nephrostomy tract infiltration with bupivacaine in tubeless percutaneous nephrolithotomy (PCNL). Patients and Methods: All adult patients undergoing unilateral tubeless PCNL from July 1, 2007 to October 31, 2007 were included in the study. Patients were randomized to receive infiltration of bupivacaine in the nephrostomy tract at the end of the procedure or not to receive bupivacaine. To show a 10% difference in postoperative pain, a sample size of 30 persons per group would be needed. Postoperatively, the pain score were obtained at 4 and 24 hours by a nurse who was blinded to the protocol. The perioperative outcome of these patients (study group) was compared with those undergoing tubeless PCNL without nephrostomy tract infiltration of bupivacaine (control group). Results: Patient demographics and intraoperative parameters in both groups were comparable. Supracostal access was needed in 65.7% and 72.7% patients in the study and control group, respectively. The nephrostomy tract were infiltrated with bupivacaine in 31 patients. The visual analogue pain score at 4 hours and 24 hours for the study group was 2.66±1.07 & 2.23±0.50 respectively, while in control group was 5.15±1.52 and 3.22±1.11, respectively ( P =0.000). There was a trend toward lesser analgesia requirement in the study group (94.8 vs 124.2 mg of diclofenac sodium). There was no difference in the duration of postoperative catheterization, hospital stay, stone-free rates, and complication between both groups. Conclusions: Nephrostomy tract infiltration of bupivacaine in tubeless PCNL is associated with less postoperative pain and analgesia requirement

    A Plea for Centralized Care for Ureteroscopy: Results from a Comparative Study Under Different Conditions Within the Same Center

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    Purpose: We stratified factors that affect treatment morbidity, compared the outcomes of ureteroscopy procedures from a single department under different conditions, and provided evidence of treatment benefits when ureteroscopy is performed in an expert setting. Patients and Methods: Since the department became a dedicated endourologic center in 2002, we grouped all ureteroscopy procedures into those performed before 2002 (group A) and after 2002 (group B). The modified Clavien classification was used to score morbidity. Independent variables with an influence on postoperative outcomes were studied, including operative time, intraoperative and postoperative complications, and hospitalization time. Results: Of the 248 ureteroscopy procedures performed, 62 comprised group A and 186 comprised group B. Statistical preoperative differences were in the American Society of Anesthesiologists score, patients with diabetes mellitus, cardiovascular disease, and the use of anticoagulants; and the perioperative differences were seen in operative time, hospital stay, and the number of eventful procedures. Group A had a significantly longer operative time and a longer hospital stay compared with group B. The number of failed and eventful procedures are also higher in group A compared with group B. Stone-free rates were similar in both groups. Conclusions: The dedicated setting for ureteroscopy at our center resulted in decreased operative time, more uneventful procedures, and decreased hospitalization time. The modified Clavien morbidity score is a reliable tool for more objective comparisons of morbidity after ureteroscopic stone treatmen
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