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Prostaglandin E1 in the medical management of erectile dysfunction in a genito-urinary medicine clinic.

Fifty consecutive patients with erectile failure who had previously proved refractory to papaverine and phentolamine intracavernosal therapy or were inappropriate candidates for such treatment were treated with intracavernosal prostaglandin E1. Forty patients (80%) achieved an erection sufficient fo...

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Detalles Bibliográficos
Autores principales: Armstrong, D. K., Convery, A., Dinsmore, W. W.
Formato: Texto
Lenguaje:English
Publicado: Ulster Medical Society 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2449095/
https://www.ncbi.nlm.nih.gov/pubmed/8658990
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author Armstrong, D. K.
Convery, A.
Dinsmore, W. W.
author_facet Armstrong, D. K.
Convery, A.
Dinsmore, W. W.
author_sort Armstrong, D. K.
collection PubMed
description Fifty consecutive patients with erectile failure who had previously proved refractory to papaverine and phentolamine intracavernosal therapy or were inappropriate candidates for such treatment were treated with intracavernosal prostaglandin E1. Forty patients (80%) achieved an erection sufficient for sexual intercourse and after a mean follow-up period of 5.9 months, 32 patients were continuing to use treatment successfully. The average dose was 14 micrograms (range 2.5 to 30 micrograms). There were no cases of priapism or cavernosal fibrosis and no systemic side effects. A low incidence (8%) of local discomfort was reported. We conclude that prostaglandin is a safe and effective vasoactive agent for the treatment of erectile failure in a genito-urinary outpatient clinic.
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spelling pubmed-24490952008-07-10 Prostaglandin E1 in the medical management of erectile dysfunction in a genito-urinary medicine clinic. Armstrong, D. K. Convery, A. Dinsmore, W. W. Ulster Med J Research Article Fifty consecutive patients with erectile failure who had previously proved refractory to papaverine and phentolamine intracavernosal therapy or were inappropriate candidates for such treatment were treated with intracavernosal prostaglandin E1. Forty patients (80%) achieved an erection sufficient for sexual intercourse and after a mean follow-up period of 5.9 months, 32 patients were continuing to use treatment successfully. The average dose was 14 micrograms (range 2.5 to 30 micrograms). There were no cases of priapism or cavernosal fibrosis and no systemic side effects. A low incidence (8%) of local discomfort was reported. We conclude that prostaglandin is a safe and effective vasoactive agent for the treatment of erectile failure in a genito-urinary outpatient clinic. Ulster Medical Society 1994-04 /pmc/articles/PMC2449095/ /pubmed/8658990 Text en
spellingShingle Research Article
Armstrong, D. K.
Convery, A.
Dinsmore, W. W.
Prostaglandin E1 in the medical management of erectile dysfunction in a genito-urinary medicine clinic.
title Prostaglandin E1 in the medical management of erectile dysfunction in a genito-urinary medicine clinic.
title_full Prostaglandin E1 in the medical management of erectile dysfunction in a genito-urinary medicine clinic.
title_fullStr Prostaglandin E1 in the medical management of erectile dysfunction in a genito-urinary medicine clinic.
title_full_unstemmed Prostaglandin E1 in the medical management of erectile dysfunction in a genito-urinary medicine clinic.
title_short Prostaglandin E1 in the medical management of erectile dysfunction in a genito-urinary medicine clinic.
title_sort prostaglandin e1 in the medical management of erectile dysfunction in a genito-urinary medicine clinic.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2449095/
https://www.ncbi.nlm.nih.gov/pubmed/8658990
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