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1.
Nagoya J Med Sci ; 86(1): 104-109, 2024 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-38505715

RESUMO

Prostaglandin E1 intracavernous injection test is an established method for diagnosing erectile dysfunction. However, the evaluation is non-objective and often influenced by the evaluator's subjectivity. Herein, we measured and objectively evaluated shear wave elastography results of the corpus cavernosum before and after injection in 16 patients who underwent prostaglandin E1 testing. The response score of prostaglandin E1 tests were "1" in 2 cases, "2" in 2 cases, and "3" in 12 cases. The average transmission velocity before the injection and at the time of maximum erection after the injection were 2.21 m/s and 1.57 m/s, respectively. Transmission velocity decreased during erection in 14 of 16 cases (87.5%). The overall rate of change in transmission velocity due to injection was -26.7% and was significantly different between the poor (responses 1 and 2: -16.1%) and good erection (response 3: -30.2%) groups. To the best of our knowledge, this is the first attempt to evaluate erectile phenomenon using percutaneous ultrasonic elastography in Japan. Rate of change in shear wave transmission velocity due to prostaglandin E1 injection in the corpus cavernosum penis was associated with the degree of erection. Therefore, the rate of change in shear wave transmission velocity in the corpus cavernosum penis could be used as an objective index of erectile phenomenon. Percutaneous ultrasonic elastography is a non-invasive and useful test method for diagnosing erectile dysfunction, determining the therapeutic effect, and predicting prognosis.


Assuntos
Técnicas de Imagem por Elasticidade , Disfunção Erétil , Masculino , Humanos , Disfunção Erétil/diagnóstico por imagem , Disfunção Erétil/tratamento farmacológico , Alprostadil/uso terapêutico , Técnicas de Imagem por Elasticidade/métodos , Ereção Peniana/fisiologia , Pênis/diagnóstico por imagem
2.
Womens Health (Lond) ; 17: 17455065211009103, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-33866884

RESUMO

OBJECTIVES: Female sexual dysfunction is an underestimated problem that negatively affects women's quality of life. Although the overall prevalence of sexual dysfunction in women is high, only a few studies have focused on this problem. In Japan, an index of female sexual function has not been clearly defined. Hence, this study aimed to investigate the sexual function of normal Japanese women and the temporal changes they experienced using the Female Sexual Function Index administered online in 2012 and 2019. METHODS: The subjects were Japanese women aged 20-79 years registered in an Internet research company. We collected data of 1034 and 2031 women in 2012 and 2019, respectively, based on Japan's population distribution according to age. Subsequently, we analyzed the collected data using a Japanese version of the Female Sexual Function Index. We investigated the temporal changes in the Female Sexual Function Index total score, the ratio of women who did not engage in sexual activities and women having "no sexual activity" with their partners, and the total Female Sexual Function Index scores according to age. RESULTS: The average Female Sexual Function Index total score decreased from 14.6 in 2012 to 12.5 in 2019 (p < 0.001). No significant difference was observed in the average Female Sexual Function Index score of the group with sexual activity between 2012 (22.2) and 2019 (22.4). The ratio of women not engaging in sexual activities increased from 42.2% in 2012 to 54.0% in 2019. The ratio of women having "no sexual activity" with their partners increased by 10%. CONCLUSION: Comparison of data between 2012 and 2019 indicated that Japanese women have become less sexually active. The average Female Sexual Function Index total score of 22 may be useful as a reference value for diagnosing female sexual dysfunction in Japan.


Assuntos
Qualidade de Vida , Disfunções Sexuais Fisiológicas , Feminino , Humanos , Internet , Japão/epidemiologia , Comportamento Sexual , Disfunções Sexuais Fisiológicas/diagnóstico , Disfunções Sexuais Fisiológicas/epidemiologia , Inquéritos e Questionários
3.
Reprod Med Biol ; 18(4): 331-343, 2019 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-31607793

RESUMO

BACKGROUND: Ejaculatory dysfunction (EjD) is a complex pathological condition compared to erectile dysfunction (ED). A definitive classification of EjD is not established, and treatment is often delayed. Owing to its association with infertility, EjD is a serious concern, particularly in men of reproductive age. METHODS: The authors performed a literature search to identify the latest articles and overseas guidelines for review. RESULTS: Our new classification categorizes men into two groups as follows: (1) men with inability to ejaculate (retrograde ejaculation, anejaculation, intravaginal ejaculatory dysfunction) and (2) men requiring an abnormal time for ejaculation (premature ejaculation, delayed ejaculation). In Japan, the number of men presenting with an inability to ejaculate is greater than those presenting with premature ejaculation. Pharmacotherapy is the first-line treatment for the management of these EjD patients. Behavioral therapy is added to pharmacotherapy depending on the case. Penile vibratory stimulation or electroejaculation is indicated in some men with retrograde ejaculation and anejaculation. In cases who hope for a baby, assisted reproductive technology should be simultaneously considered not to waste time. CONCLUSION: It is important to distinguish between EjD and ED and accurately diagnose the type of EjD for optimal treatment of this condition.

4.
Int J Urol ; 24(8): 626-631, 2017 08.
Artigo em Inglês | MEDLINE | ID: mdl-28627033

RESUMO

OBJECTIVES: To determine the efficacy of two α1-adrenoceptor antagonists with different affinities for α1-adrenoceptor subtypes, silodosin and naftopidil, in the treatment of premature ejaculation. METHODS: This was a prospective, open-label, multicenter trial. A total of 26 patients with untreated acquired premature ejaculation were enrolled. Premature ejaculation was defined based on the International Society for Sexual Medicine recommendation. Patients self-administered on demand silodosin 4 mg or naftopidil 25 mg 1 h before intercourse, alternating drugs at least three times each. Clinical global impression change for premature ejaculation, premature ejaculation profile, and intravaginal ejaculation latency time were evaluated at baseline and during treatment. RESULTS: Due to clinical global impression change, 24 patients (92%) and 12 patients (46%) reported improvement in their own premature ejaculation problems under silodosin and nafitopidil administration, respectively. Silodosin treatment produced a significantly higher improvement rate compared with naftopidil (P = 0.0002). Objectively, silodosin significantly prolonged intravaginal ejaculation latency time compared with baseline and naftopidil (P < 0.01). Mean intravaginal ejaculation latency times were 1.9, 4.1, and 7.6 min at baseline, control and with silodosin, respectively. The rate of reduced semen volume during silodosin treatment was higher than during naftopidil treatment. There were no adverse systemic effects in either group. CONCLUSIONS: Silodosin, a highly selective α1A-adrenoceptor antagonist, produces greater improvements in premature ejaculation profiles and related symptoms along with intravaginal ejaculation latency time in acquired premature ejaculation patients with or without erectile dysfunction. This result supports the clinical use of silodosin as an alternative treatment for premature ejaculation.


Assuntos
Antagonistas de Receptores Adrenérgicos alfa 1/uso terapêutico , Indóis/uso terapêutico , Naftalenos/uso terapêutico , Piperazinas/uso terapêutico , Ejaculação Precoce/tratamento farmacológico , Agentes Urológicos/uso terapêutico , Adulto , Idoso , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Autoadministração , Fatores de Tempo , Resultado do Tratamento , Adulto Jovem
6.
Int J Urol ; 13(11): 1428-33, 2006 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-17083398

RESUMO

AIM: Vardenafil is a highly selective phosphodiesterase type-5 inhibitor for the treatment of erectile dysfunction (ED). Efficacy of vardenafil has been demonstrated in various ED populations, but that in Japanese patients with spinal cord injury (SCI) has not been assessed. METHODS: This was an open-label, multicenter, flexible dose, 12-week study in patients with ED due to SCI. Following a 4-week observation period, patients received vardenafil 10 mg for 4 weeks, and based on efficacy, tolerability and patient preference, doses for the remaining 8 weeks were decided by investigators. The primary efficacy parameter was erectile function domain score of the International Index of Erectile Function. RESULTS: Ten patients took 10 mg all through the study, while 22 patients took 20 mg after completing 4 weeks' treatment with 10 mg. The erectile function domain score increased from 12.2 at baseline to 25.0 at Last Observation Carried Forward (LOCF) in the former group and from 10.3 to 22.5 in the latter group, respectively. Importantly, there was a 5.0 point increase in erectile function domain score after up-titration in the latter group. Drug-related adverse events were observed in 22% of patients including hot flushes (9%) and headache (6%), but these were transient and mild in intensity. Serious adverse events and adverse events leading to discontinuation of the study drug were not reported. CONCLUSIONS: Vardenafil 10 and 20 mg was well tolerated and improved erectile function in patients with SCI. Of interest, erectile function was further improved by 20 mg in patients who were not sufficiently treated with 10 mg.


Assuntos
Disfunção Erétil/tratamento farmacológico , Imidazóis/uso terapêutico , Ereção Peniana/efeitos dos fármacos , Piperazinas/uso terapêutico , Traumatismos da Medula Espinal/complicações , Adulto , Relação Dose-Resposta a Droga , Esquema de Medicação , Disfunção Erétil/etiologia , Disfunção Erétil/fisiopatologia , Cefaleia/induzido quimicamente , Fogachos/induzido quimicamente , Humanos , Imidazóis/administração & dosagem , Imidazóis/efeitos adversos , Japão , Masculino , Pessoa de Meia-Idade , Ereção Peniana/fisiologia , Inibidores de Fosfodiesterase/administração & dosagem , Inibidores de Fosfodiesterase/efeitos adversos , Inibidores de Fosfodiesterase/uso terapêutico , Piperazinas/administração & dosagem , Piperazinas/efeitos adversos , Sulfonas/administração & dosagem , Sulfonas/efeitos adversos , Sulfonas/uso terapêutico , Fatores de Tempo , Resultado do Tratamento , Triazinas/administração & dosagem , Triazinas/efeitos adversos , Triazinas/uso terapêutico , Dicloridrato de Vardenafila
7.
Hinyokika Kiyo ; 52(8): 629-32, 2006 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16972626

RESUMO

The patient was a 66-year-old man who had undergone implantation of a penile prosthesis for organic erectile dysfunction 7 years prior to consulting our hospital with a complaint of gross hematuria. Since a pedunculated, superficial tumor 1 cm in diameter was noted lateral to the left ureteral orifice, transurethral resection of the bladder tumor (TURBT) was performed. In this patient, we were able to insert the sheath with no difficulty, and the surgical procedure was done smoothly, resulting in complete resection of the tumor. However, the location of the tumor in the anterior or posterior wall of the bladder predicted difficulty of the tumor resection. Therefore, we consider it important to sufficiently evaluate the feasibility of complete TURBT before surgery and to thoroughly examine the patient for benign prostatic hyperplasia and bladder cancer, which can cause difficulty with post-implantation ransurethral procedures, and to perform transurethral surgery before implantation, if prosthesis implantation is planned.


Assuntos
Carcinoma de Células de Transição/cirurgia , Neoplasias da Bexiga Urinária/cirurgia , Idoso , Disfunção Erétil/terapia , Humanos , Masculino , Prótese de Pênis , Procedimentos Cirúrgicos Urológicos Masculinos/métodos
14.
Nihon Hinyokika Gakkai Zasshi ; 93(4): 568-72, 2002 May.
Artigo em Japonês | MEDLINE | ID: mdl-12056042

RESUMO

We report two cases of priapism with metastases to the penis. The first case was a 52-year old man, diagnosed as suffering from gastric cancer by endoscopic biopsy five years previously, but for whom no treatment was performed. He visited our office due to priapism with a duration of 11 days. Physical examination showed two palpable mass lesions on the glans. A glansocavernosum shunt (Winter shunt) was performed, but this was not effective. Radiotherapy was also ineffective. Pathological analysis revealed gastric cancer metastasis to the penis and this was diagnosed as the cause of the priapism. He died of respiratory failure on postoperation day 28. The second case was a 64-year old man with kidney cancer. Hemodialysis had been performed due to chronic renal failure for 20 years and visited our office due to priapism from which he had suffered for 30 days. Computed tomography (CT) demonstrated a left renal cell cancer and metastasized to the retroperitoneal lymph nodes. A Winter shunt was performed on the penis and then a cavernosospongiosum anastomosis was done. The priapism improved about 40%. Pathological analysis confirmed that the renal cell cancer had metastasized to the penis and this was concluded to be responsible for the priapism.


Assuntos
Carcinoma de Células Renais/secundário , Carcinoma de Células Pequenas/secundário , Neoplasias Penianas/secundário , Priapismo/etiologia , Carcinoma de Células Renais/complicações , Carcinoma de Células Pequenas/complicações , Humanos , Neoplasias Renais/patologia , Metástase Linfática , Masculino , Pessoa de Meia-Idade , Neoplasias Penianas/complicações , Neoplasias Gástricas/patologia
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