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1.
Actas Urol Esp (Engl Ed) ; 45(5): 366-372, 2021 Jun.
Artículo en Inglés, Español | MEDLINE | ID: mdl-34088436

RESUMEN

INTRODUCTION: The placement of a ureteral stent is one of the most widely performed procedures in urology. It can have a negative impact on the patients' quality of life, requiring a cystoscopy for its removal. The objective of this study is to evaluate the symptoms and impact on quality of life derived from the use of a magnetic double-J stent (Black Star®) and compare them to those presented in patients with a traditional double-J stent (OptiMed®). MATERIAL AND METHODS: We conducted a comparative, prospective, randomized study in 46 patients who underwent ureterorenoscopy with double-J stent placement between August 2019 and June 2020. Of all patients included, 23 had a traditional double-J stent placed (group A) and 23 had a magnetic double-J stent (group B) placed. We evaluated the results of the Ureteral Stent Symptom Questionnaire (USSQ) in both groups, assessed the technical difficulty related to stent removal and the pain during the procedure using the Visual Analogue Scale (VAS). We also reviewed the need for medical attention due to problems related to the stent or after its removal. RESULTS: There were no statistically significant differences between groups regarding the answers in the USSQ and the complications related to the use of the stent. Group B showed less pain (1.52 vs. 4, VAS, p = 0.001) and less difficulty during removal (1.61 vs. 3, p < 0.001) associated with a shorter procedure duration (11.65 min vs. 22.17 min p < 0.001). CONCLUSIONS: The tolerance shown by the use of magnetic double-J is comparable to the tolerance of traditional stent, since it does not cause an increase in urinary symptoms nor worsens the quality of life of patients during its use.


Asunto(s)
Calidad de Vida , Uréter , Humanos , Fenómenos Magnéticos , Estudios Prospectivos , Stents , Uréter/cirugía
2.
Actas Urol Esp (Engl Ed) ; 45(5): 398-405, 2021 Jun.
Artículo en Inglés, Español | MEDLINE | ID: mdl-34088440

RESUMEN

INTRODUCTION: Rectal injury is a rare complication after extraperitoneal laparoscopic radical prostatectomy. The development of rectourethral fistulas (URF) from rectal injuries is one of the most feared and of more complex resolution in urology. MATERIAL AND METHODS: Between 2013 and 2020 we have operated on a total of 5 patients with URF after extraperitoneal endoscopic radical prostatectomy through a perineal access using the interposition of biological material. All fistulas had a diameter of less than 6 mm at endoscopy and were less than 6 cm apart from the anal margin. RESULTS: The mean age of the patients was 64 years old. All patients had a previous bowel and urinary diversion for at least 3 months. Under general anesthesia and with the patient in a forced lithotomy position, fistulorraphy and interposition of biological material of porcine origin (lyophilized porcine dermis [Permacol®]) were performed through a perineal access. Mean operative time was 174 min (140-210). Most patients were discharged on the third postoperative day. The bladder catheter was left in place for a mean of 40 days (30-60). Prior to its removal, cystography and a Gastrografin® barium enema were performed, showing resolution of the fistula in all cases. CONCLUSIONS: The interposition of biological material from porcine dermis through perineal approach is a safe alternative with good results in patients submitted to urethrorectal fistulorraphy after radical prostatectomy.


Asunto(s)
Fístula Rectal , Enfermedades Uretrales , Fístula Urinaria , Animales , Humanos , Masculino , Persona de Mediana Edad , Próstata , Prostatectomía/efectos adversos , Fístula Rectal/etiología , Porcinos , Enfermedades Uretrales/etiología , Fístula Urinaria/etiología
3.
Actas Urol Esp (Engl Ed) ; 43(9): 488-494, 2019 Nov.
Artículo en Inglés, Español | MEDLINE | ID: mdl-31160158

RESUMEN

INTRODUCTION: The treatment for lower urinary tract symptoms secondary to benign prostatic hyperplasia with the Urolift® system has been carried out since 2005 with good results in the medium term. In this work, we present our experience performing this technique under local anaesthesia and sedation in 2 Spanish centres. MATERIAL AND METHODS: A prospective study was conducted with 20 patients treated with Urolift® under local anaesthesia and sedation between April 2017 and April 2018. The anaesthesia protocol consisted in the placement of 2 lubricants with cold lidocaine (the first one, 10min before the intervention, and the second one, just before introducing the cystoscopy). A prostate block (similar to the one employed in prostate biopsies) was administered to one third of the patients and 1mg of intravenous midazolam was added if required during the procedure. Our primary objective is to evaluate the tolerability of this procedure under local anaesthesia using the validated Visual Analogue Scale measurement instrument. RESULTS: The procedure has been performed under the same anaesthetic protocol to 20 patients from 2 different centres. The average pain scores on the Visual Analogue Scale were 1.37 for the cystoscopy procedure and 1.19 for the placement of the implants. When asked whether the pain sensations had been higher, lower or the same during the procedure or at the preoperative cystoscopy, only 18% of the patients responded it was higher. In all cases there was a good tolerance to the procedure, and changes to the anaesthesia protocols were never required. CONCLUSIONS: We consider that the Urolift® system under local anaesthesia and sedation is a well-tolerated, safe and effective method for the treatment of lower urinary tract symptoms secondary to benign prostatic hyperplasia.


Asunto(s)
Anestesia Local , Cistoscopía , Sedación Profunda , Síntomas del Sistema Urinario Inferior/etiología , Síntomas del Sistema Urinario Inferior/cirugía , Hiperplasia Prostática/complicaciones , Adulto , Anciano , Anciano de 80 o más Años , Humanos , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Procedimientos Quirúrgicos Urológicos Masculinos/métodos
4.
Otolaryngol Head Neck Surg ; 88(4): 486-90, 1980.
Artículo en Inglés | MEDLINE | ID: mdl-6821437

RESUMEN

The surgical technique for vestibular neurectomy through the middle fossa approach is described. Surgical details, including the use of a new middle fossa retractor, are discussed. A variety of technical refinements have been made to improve and shorten the operation. The main surgical indication is for Meniere's disease. It has, however, also been used in other peripheral vestibular problems such as traumatic vertigo and vertigo secondary to previous ear surgery. Long-term hearing and vestibular results using this approach for Meniere's disease have been encouraging. These results, in addition to the small incidence of postoperative complications, have made the operation extremely useful.


Asunto(s)
Enfermedad de Meniere/cirugía , Nervio Vestibular/cirugía , Humanos , Métodos , Neurocirugia/instrumentación , Complicaciones Posoperatorias/etiología , Cráneo/cirugía , Vértigo/cirugía
5.
Audiology ; 18(2): 145-56, 1979.
Artículo en Inglés | MEDLINE | ID: mdl-435175

RESUMEN

After a general review of the actual histopathological concept of Menière's disease, a review of the results, as concerns hearing, of the selective section of the vestibular fibers by the suboccipital approach, and of vestibular neurectomy by the middle fossa approach is made. From our personal experience in performing 247 neurectomies from November, 1969 to July, 1976 as treatment for peripheral vertigos of different etiologies, auditory function was followed-up in 78 cases of Menière's disease, with a postoperative control, between 2 and 6 1/2 years. In 51% of these cases the preoperative threshold was preserved, hearing improved in 32%, and deteriorated in 17%. Possible mechanisms by which vestibular neurectomy can favorably influence hearing are considered, with special mention of the neurovegetative theory.


Asunto(s)
Enfermedad de Meniere/terapia , Nervio Vestibular/cirugía , Adulto , Umbral Auditivo/fisiología , Estudios de Seguimiento , Pruebas Auditivas , Humanos , Masculino , Enfermedad de Meniere/diagnóstico , Enfermedad de Meniere/fisiopatología
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