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1.
World J Urol ; 39(10): 3875-3880, 2021 Oct.
Article in English | MEDLINE | ID: mdl-33787986

ABSTRACT

PURPOSE: Rezum is the latest developed minimally invasive treatment for benign prostatic hyperplasia (BPH). We aimed to carefully assess the functional outcomes of patients treated with Rezum for BPH. METHODS: We prospectively followed 135 consecutive patients treated by Rezum at 5 institutions from June 2019 to August 2020. The International Prostate Symptom Score (IPSS), International Consultation on Incontinence Questionnaire-Short Form (ICIQ-UI SF), the Overactive Bladder Questionnaire-Short Form (OAB-q SF) score, the International Index of Erectile Function (IIEF-5) and questions 9 and 10 to assess ejaculatory dysfunction were recorded. Election criteria were age > 18, no prior prostate interventions, IPSS ≥ 13, post-void residual ≤ 250 mL, prostate volume between 30 and 120 cc. RESULTS: The median operative time was 10.5 (IQR 8.7-15) min. All patients were dismissed few hours after surgery with indwelling urinary catheter that was removed after a median of 7 (IQR 7-10) days. A significantly decrease of IPSS from baseline at first (p = 0.001) and third (p < 0.0001) month after surgery was reported. No difference was reported in terms of ICIQ-UI SF score postoperatively. A mild reduction of the OAB-q SF score was reported at 1 month from surgery (p = 0.06) that turned significant at 3 months postoperatively (p < 0.0001). A slight but statistically significant increase of the IIEF-5 score was reported from baseline at 6 months (p = 0.04). Postoperatively, patients reported a significantly decrease of ejaculatory dysfunction after alpha-blocker interruption. CONCLUSION: Rezum treatment is a feasible minimally invasive option for patients with BPH symptoms and showed optimal early functional outcomes.


Subject(s)
Hyperthermia, Induced/instrumentation , Lower Urinary Tract Symptoms/therapy , Prostatic Hyperplasia/complications , Steam , Aged , Follow-Up Studies , Humans , Italy , Lower Urinary Tract Symptoms/etiology , Male , Middle Aged , Prospective Studies , Recovery of Function , Surveys and Questionnaires , Treatment Outcome
2.
Ann Oncol ; 16(1): 152-7, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15598953

ABSTRACT

BACKGROUND: The role of selected macronutrients, fatty acids and cholesterol in the etiology of prostate cancer was analyzed using data from a case-control study carried out in five Italian areas between 1991 and 2002. PATIENTS AND METHODS: Cases were 1294 men with incident, histologically confirmed prostate cancer, and admitted to the major teaching and general hospitals of study areas. Controls were 1451 men admitted for acute, non-neoplastic conditions to the same hospital network. Information on dietary habits was elicited using a validated food frequency questionnaire including 78 food groups and recipes. Odds ratios (OR) and 95% confidence intervals (CI) were estimated for increasing levels of nutrient intake. RESULTS: A direct association with prostate cancer was found for starch intake (OR = 1.4 in the highest versus the lowest quintile of intake; 95% CI: 1.1-1.8), whereas an inverse association emerged for polyunsaturated fatty acids (OR = 0.8; 95% CI: 0.6-1.0). Among polyunsaturated fatty acids, linolenic acid (OR = 0.7; 95% CI: 0.6-0.9) and linoleic acid (OR = 0.8; 95% CI: 0.6-1.0) were inversely related to prostate cancer. When the six major macronutrients were included in the same model, the adverse effect of high intake of starch and monounsaturated fatty acids was statistically significant together with the protective effect of polyunsaturated fatty acids. Results were consistent in separate strata of age, body mass index and family history of prostate cancer. CONCLUSIONS: Starch and monounsaturated fatty acids were directly associated with prostate cancer risk and polyunsaturated fatty acids were inversely associated.


Subject(s)
Cholesterol/blood , Cholesterol/pharmacology , Dietary Fats/pharmacology , Fatty Acids/pharmacology , Nutritional Status , Prostatic Neoplasms/etiology , Aged , Case-Control Studies , Humans , Male , Middle Aged , Prostatic Neoplasms/epidemiology , Risk Factors
3.
Arch Ital Urol Androl ; 72(4): 174-81, 2000 Dec.
Article in Italian | MEDLINE | ID: mdl-11221032

ABSTRACT

The diagnosis of prostate neoplasm is still limited today by the variable power of prediction of the three main surveys used: prostate-specific antigen (PSA), digito rectal exploration (DRE) and ultrasound transrectal (TRUS). The study aimed to estimate the benefits and the diagnostic impact of the color Doppler ultrasonography on the diagnosis of prostate neoplasm through biopsies targeted on areas with abnormal flow. With this purpose, 222 biopsies performed on 71 patients between 1997 and 1999 were considered, which led to a diagnosis of neoplasm in 36 patients. Of the 84 biopsies that revealed prostate adenocarcinoma, 74 (64.3%) were correlated to hypoechoic lesions with abnormal flow signals while 41 (35.6%) showed a benign pathology (prostatitis or benign prostatic hyperplasia) (p < 0.0011). In five patients (13%) who did not present any evident lesions at a first transrectal ultrasound, the diagnosis of neoplasm was made only through biopsies targeted on areas with abnormal flow. Therefore, the color Doppler exam can be used during prostate ultrasonography either to consolidate the diagnosis or to give a useful target in case of isoechoic lesions.


Subject(s)
Adenocarcinoma/diagnostic imaging , Adenocarcinoma/pathology , Prostatic Hyperplasia/diagnostic imaging , Prostatic Hyperplasia/pathology , Prostatic Neoplasms/diagnostic imaging , Prostatic Neoplasms/pathology , Ultrasonography, Doppler, Color , Aged , Aged, 80 and over , Biopsy/methods , Humans , Male , Middle Aged , Sensitivity and Specificity
4.
Urol Int ; 48(2): 154-6, 1992.
Article in English | MEDLINE | ID: mdl-1585510

ABSTRACT

At the Institute of Urology, University of Padova, 125 patients with multifocal superficial bladder cancer underwent treatment with intravesical Mitomycin C (MMC; 1 weekly instillation of 40 mg for 8 consecutive weeks) between January 1982 and December 1988. Eighty-four patients had multifocal papillary tumors (stages Ta-T1) and 41 patients had carcinoma in situ of the bladder. At 6 and 36 months the tumor free percentage in the group with papillary tumors was 69 and 36%, respectively; for carcinoma in situ the complete response percentage at the same intervals was 80 and 36%. Thirty-one patients previously unsuccessfully treated with adriamycin did not show any difference compared to untreated ones. The authors emphasize the efficacy and low toxicity of intravesical MMC in multiple superficial bladder cancer. The possibility of long-term relapse suggests maintenance therapy.


Subject(s)
Carcinoma in Situ/drug therapy , Carcinoma, Transitional Cell/drug therapy , Mitomycin/therapeutic use , Urinary Bladder Neoplasms/drug therapy , Administration, Intravesical , Carcinoma in Situ/epidemiology , Carcinoma, Transitional Cell/epidemiology , Drug Administration Schedule , Female , Humans , Male , Mitomycin/administration & dosage , Retrospective Studies , Time Factors , Urinary Bladder Neoplasms/epidemiology
5.
J Urol ; 146(1): 32-5, 1991 Jul.
Article in English | MEDLINE | ID: mdl-2056600

ABSTRACT

Bacillus Calmette-Guerin (BCG) intravesical therapy represents a major advance in the treatment of superficial transitional cell carcinoma of the bladder. To date, however, the optimal treatment schedule must be defined and the toxicity related to the treatment is significant. The preliminary results of a randomized ongoing study performed to evaluate the effectiveness and relative toxicity of a low dose (75 mg.) BCG regimen in the treatment of superficial bladder cancer therapy are reported. A total of 126 patients (70 for prophylaxis of recurrent stages Ta and T1 papillary tumors and 56 for treatment of carcinoma in situ or with microinfiltration of the subepithelial connective tissue) underwent a 6-week course of 75 mg. BCG (Pasteur vaccine). An additional course was given in patients who failed to respond to the induction course. Maintenance therapy was administered in complete responders monthly for 1 year and then quarterly for 1 year. The prophylaxis group (transurethral resection plus BCG) was randomized versus transurethral resection alone (63 patients, control group). A complete response in the prophylaxis, control and therapy groups was observed in 74, 17 and 57% of the patients, respectively, while 4, 17 and 12.5%, respectively, experienced tumor progression. The additional course of therapy increased the response rate. On the contrary, previous unsuccessful intravesical chemotherapy did not affect the response rate. In regard to toxicity, irritative disturbances (27%) and fever (17%) appeared to be significantly decreased compared with the rates reported in the literature. No major complications were experienced. In conclusion, a low dose (75 mg.) Pasteur strain BCG regimen was effective as prophylaxis against recurrent superficial papillary tumors and as treatment of carcinoma in situ or with microinfiltration of the subepithelial connective tissue. Toxicity related to the treatment appeared to be low.


Subject(s)
BCG Vaccine/administration & dosage , Carcinoma in Situ/therapy , Carcinoma, Transitional Cell/therapy , Neoplasms, Multiple Primary/therapy , Urinary Bladder Neoplasms/therapy , BCG Vaccine/adverse effects , Carcinoma in Situ/complications , Carcinoma in Situ/epidemiology , Carcinoma, Transitional Cell/complications , Carcinoma, Transitional Cell/epidemiology , Combined Modality Therapy , Female , Follow-Up Studies , Humans , Male , Middle Aged , Neoplasm Recurrence, Local/complications , Neoplasm Recurrence, Local/epidemiology , Neoplasm Recurrence, Local/prevention & control , Neoplasm Recurrence, Local/therapy , Neoplasms, Multiple Primary/complications , Neoplasms, Multiple Primary/epidemiology , Postoperative Care , Prospective Studies , Remission Induction , Urinary Bladder Neoplasms/complications , Urinary Bladder Neoplasms/epidemiology
6.
J Urol (Paris) ; 97(1): 15-8, 1991.
Article in French | MEDLINE | ID: mdl-2016547

ABSTRACT

Conservative treatment of ureteral stenoses has been possible since the evolution in materials and methods available. We report our experience in 49 cases of ureteral stenoses (1 case with bilateral lesion). The etiology was as follows: 3 cases of tuberculous strictures, 10 late complications of endourological treatment of ureteral stones, 16 stenoses of ureteroenteric anastomoses or bladder reimplantation, 16 after radical pelvic surgery, 5 after external beam radiation therapy. Forty-two cases were treated with balloon dilation or by means of a coaxial dilator; in 7 cases a cold-knife treatment was performed. All patients had a ureteral stent for 40 days. The results were evaluated by IVP, sonography and DTPA renal scan, 6 to 20 months after stent removal. Overall success rate was 56%: it was lower than the 100% rate obtained in a 13 patients group surgically treated. In selected cases of ureteral stenoses, endourological approach should be the first choice treatment because of low morbidity and reduced hospitalization time.


Subject(s)
Catheterization/methods , Ureteral Diseases/therapy , Adolescent , Adult , Aged , Anastomosis, Surgical/adverse effects , Child , Female , Humans , Male , Middle Aged , Pelvis/surgery , Postoperative Complications , Ureteral Calculi/surgery , Ureteral Diseases/etiology , Ureteral Diseases/surgery , Urinary Catheterization
7.
Arch Esp Urol ; 43(5): 503-7, 1990 Jun.
Article in Spanish | MEDLINE | ID: mdl-2202264

ABSTRACT

The preliminary results of a randomized ongoing study performed in order to evaluate the efficacy and the relative toxicity of a low dose (75 mg). BCG regimen in the treatment of superficial bladder cancer were considered. Ninety-eight patients (58 patients for prophylaxis of the recurrences of Ta-T1 papillary tumors; 40 patients for therapy of carcinoma in situ) received a 6-weeks course of 75 mg. BCG Pasteur vaccine. An additional course was given to non-responders. A maintenance therapy was administered in complete responders monthly for the first year and quarterly for the second. The prophylaxis group (TUR + BCG) was randomized vs TUR alone (40 patients = control group). Complete response in evaluated patients of the prophylaxis, control and therapy groups achieved 86%, 17% and 78%, respectively, after 18 months; 5%, 20% and 9% of patients, respectively, experienced tumor progression. As regards the toxicity, irritative disturbances (27%) and fever (16%) appeared significantly decreased in comparison with those reported in the literature. No major complications were experienced. In conclusion, the low dose (75 mg.) Pasteur BCG regimen used in our trial was effective as a prophylaxis against recurrent superficial papillary tumors and as a treatment of carcinoma in situ, with a significant decrease in toxicity.


Subject(s)
BCG Vaccine/therapeutic use , Carcinoma in Situ/therapy , Carcinoma, Papillary/therapy , Urinary Bladder Neoplasms/therapy , BCG Vaccine/administration & dosage , BCG Vaccine/adverse effects , Carcinoma in Situ/pathology , Carcinoma, Papillary/pathology , Female , Humans , Male , Middle Aged , Neoplasm Staging , Prospective Studies , Randomized Controlled Trials as Topic , Urinary Bladder Neoplasms/pathology
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