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1.
Am J Med ; 132(11): e786-e790, 2019 11.
Article in English | MEDLINE | ID: mdl-31103644

ABSTRACT

BACKGROUND: This prospective study assessed the efficacy of prostate artery embolization after failure of a trial without catheter in patients suffering a first episode of acute urinary retention as a result of benign prostatic hyperplasia (BPH). METHODS: Patients with failure of a trial without catheter despite alpha-blocker therapy were invited to participate in this protocol. Twenty patients were included in the study, and all underwent prostate artery embolization with calibrated polyvinyl alcohol (PVA) microspheres (Bead Block, BTG Ltd., Farnham, UK). RESULTS: Successful removal of the indwelling bladder catheter and spontaneous voiding was achieved in 15 of 20 (75%) patients, and the overall clinical success at 6 months after prostate embolization was 14 of 20 (70%). No patient experienced severe adverse events. CONCLUSIONS: Prostate artery embolization might be a valuable treatment after a failure of a trial without catheter. Further studies are needed to better define its place in this setting.


Subject(s)
Embolization, Therapeutic/methods , Prostate/blood supply , Prostatic Hyperplasia/therapy , Urinary Retention/therapy , Aged , Aged, 80 and over , Humans , Male , Middle Aged , Prospective Studies , Prostatic Hyperplasia/complications , Urinary Catheterization , Urinary Retention/etiology
3.
N Engl J Med ; 346(25): 1963-9, 2002 Jun 20.
Article in English | MEDLINE | ID: mdl-12075057

ABSTRACT

BACKGROUND: Intestinal microsporidiosis due to Enterocytozoon bieneusi is a cause of chronic diarrhea, malabsorption, and wasting in immunocompromised patients. Currently, there is no effective treatment. METHODS: We conducted a randomized, double-blind, placebo-controlled trial of fumagillin (60 mg per day orally for two weeks) in patients with chronic E. bieneusi infection. Efficacy was assessed primarily by the clearance of microsporidia, as evidenced by analysis of stool specimens. Patients in whom microsporidia were not cleared received treatment for two weeks with open-label fumagillin. After clearance of the parasite, follow-up stool examinations were performed monthly to detect relapses. RESULTS: Twelve patients were enrolled in this study, 10 with the acquired immunodeficiency syndrome and 2 who had received organ transplants. Clearance of microsporidia occurred in all six of the patients in the fumagillin group, as compared with none of the six in the placebo group (P=0.002). Treatment with fumagillin was also associated with increases in absorption of D-xylose (P=0.003) and in Karnofsky performance scores (P<0.001) and with decreases in loperamide use (P=0.01) and total stool weight (P=0.04). There were serious adverse events (neutropenia and thrombocytopenia) in three patients in the fumagillin group; one patient in the placebo group had severe diarrhea. All six controls subsequently had clearance of microsporidia after open-label treatment with fumagillin. Relapses of the infection were identified in two patients during follow-up (median follow-up, 10 months). CONCLUSIONS: Fumagillin is an effective treatment for chronic E. bieneusi infection in immunocompromised patients.


Subject(s)
Antiprotozoal Agents/therapeutic use , Enterocytozoon , Fatty Acids, Unsaturated/therapeutic use , Intestinal Diseases, Parasitic/drug therapy , Microsporidiosis/drug therapy , Opportunistic Infections/drug therapy , Adult , Antiprotozoal Agents/adverse effects , Chronic Disease , Cyclohexanes , Double-Blind Method , Enterocytozoon/isolation & purification , Fatty Acids, Unsaturated/adverse effects , Feces/parasitology , Humans , Immunocompromised Host , Intestinal Diseases, Parasitic/diagnosis , Male , Microsporidiosis/diagnosis , Sesquiterpenes
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