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1.
World J Urol ; 38(2): 343-350, 2020 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-31062122

RESUMEN

OBJECTIVES: To evaluate the effect of intensified treatment parameters on safety, functional outcomes, and PSA after MR-Guided Transurethral Ultrasound Ablation (TULSA) of prostatic tissue. PATIENTS AND METHODS: Baseline and 6-month follow-up data were collected for a single-center cohort of the multicenter Phase I (n = 14/30 at 3 sites) and Pivotal (n = 15/115 at 13 sites) trials of TULSA in men with localized prostate cancer. The Pivotal study used intensified treatment parameters (increased temperature and spatial extent of ablation coverage). The reporting site recruited the most patients to both trials, minimizing the influence of physician experience on this comparison of adverse events, urinary symptoms, continence, and erectile function between subgroups of both studies. RESULTS: For Phase I and TACT patients, median age was 71.0 and 67.0 years, prostate volume 41.0 and 44.5 ml, and PSA 6.7 and 6.7 ng/ml, respectively. All 14 Phase I patients had low-risk prostate cancer, whereas 7 of 15 TACT patients had intermediate-risk disease. Baseline IIEF, IPSS, quality of life, and pad use were similar between groups. Pad use at 1 month and quality of life at 3 months favored Phase I patients. At 6 months, there were no significant differences in functional outcomes or adverse events. CONCLUSION: TULSA demonstrated acceptable clinical safety in Phase I trial. Intensified treatment parameters in the TACT Pivotal trial increased ablation coverage from 90 to 98% of the prostate without affecting 6-month adverse events or functional outcomes. Long-term follow-up and 12-month biopsies are needed to evaluate oncological safety.


Asunto(s)
Próstata/diagnóstico por imagen , Próstata/cirugía , Neoplasias de la Próstata/diagnóstico por imagen , Neoplasias de la Próstata/cirugía , Resección Transuretral de la Próstata/métodos , Anciano , Ensayos Clínicos Fase I como Asunto , Endosonografía , Estudios de Factibilidad , Humanos , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Estudios Multicéntricos como Asunto , Cirugía Asistida por Computador , Resultado del Tratamiento , Ultrasonografía Intervencional
2.
Urol Int ; 90(4): 439-42, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23296396

RESUMEN

OBJECTIVE: Evaluation of the true incidence of balanitis xerotica obliterans (BXO) among boys younger than 10 years. METHODS: In a period of 13 months, 75 boys younger than 10 years were treated for phimosis. Suspicion of BXO was raised in phimosis grade 2 or 3 (classification by Kikiros). Patients were offered primarily either circumcision or conservative therapy and circumcision secondarily (if treatment failed in the conservative group). Each circumcision specimen was examined histopathologically. RESULTS: Circumcision was primarily performed in 29 and secondarily in 17 patients. The mean age was 3.7 years (range 1-10). BXO, chronic inflammation, and normal histological results were found in 8/26/12 (17.4/56.5/26.1%) cases, respectively. The mean follow-up was 8.1 months. No recurrences were reported. CONCLUSIONS: The incidence of BXO appears to be higher than previously reported. The clinical appearance in children may be confusing. The preoperative BXO suspicion did not correlate with the final histopathological results.


Asunto(s)
Balanitis Xerótica Obliterante/epidemiología , Fimosis/epidemiología , Factores de Edad , Austria/epidemiología , Balanitis Xerótica Obliterante/diagnóstico , Balanitis Xerótica Obliterante/terapia , Niño , Preescolar , Circuncisión Masculina , Humanos , Incidencia , Lactante , Masculino , Fimosis/diagnóstico , Fimosis/terapia , Factores de Tiempo , Resultado del Tratamiento
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