As reported to coloplast, though not verified, the patient with this device experienced urinary tract infection, therefore, the competitor's devices were removed.He continued to have urinary frequency, change in urinary flow, change in urinary flow, the patient was urinating over her leg.Additionally, this patient continued to experience urinary incontinence, urinary frequency, urgency.A new coloplast device was implanted.Subsequently,.
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According to additional available information, the patient with this device experienced dyspareunia, stress urinary incontinence, recurrent urinary tract infections, cystocele with rectocele, vaginal mesh exposures, and severe atrophy.Partial excision of surgical mesh was performed along with anterior/posterior enterocele repair and vaginal colpopexy and cystoscopy.Surgical mesh exposures were located along the distal urethra midline and right vaginal sulcus.
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