Satisfaction assessment study in patients (and their partners) with/without Peyronie’s disease and penile prosthesis implantation

E. Lledó García , F.J. González García , J. Jara Rascón , J. García Muñoz , E. Lledó Graell , M.A. Sánchez Ochoa , C. Hernández Fernández
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引用次数: 0

Abstract

Introduction and objective

Among the many treatments for erectile dysfunction, implantation of a penile prosthesis has been associated with high patient satisfaction rates. However, patients with coexistent Peyronie’s disease (PD) and refractory erectile dysfunction and/or severe deformities may show different results. The aim of our study was to assess and to compare the level of satisfaction, with an inflatable penile prosthesis (IPP), in men with/without coexistent PD.

Material and methods

A survey study based on a five-item satisfaction questionnaire was submitted to all those live patients implanted in the period 1992–2022 at our center (n = 570) and their partners. Ninety-two percent of implants were inflatable devices. Surgeries were mainly performed by two surgeons. The main outcome measure used was the level of patient and partner satisfaction with sexual intercourse after IPP.

Results

Of the 570 eligible patients, 479 (84%) completed the survey (393 Non-PD: GROUP 1; 70 non-complex PD-Group 2; 16 complex PD). Eighty-six per cent of patients in Group 1 reported satisfactory sexual intercourse (very or moderately satisfied). Non-complex PD implanted patients (Group 2) reported a global 81% satisfactory sexual intercourse (very or moderately satisfied) (p > 0.05). However, when we evaluated the PD subgroup of patients with severe PD who require incision/excision/grafting at the time of implant (Group 3: n = 20), only 61% reported satisfactory sexual intercourse (p < 0.01) with predominance of moderately satisfied patients over very satisfied: 78% vs. 22%). Additionally, 84% (Group 1), 80% (Group 2) and 54% (Group 3) of partners reported satisfactory intercourses, respectively (p < 0.01). Overall, 84% of Group 1 implants and 79% of Group 2 reported that they would undergo the procedure again if the IPP failed (p > 0.05; ns). Only 50% of Group 3 patients would do it again. With regard to cosmetic aspects, 48% of the Group 3 implant reported penile shortness or soft glans as the main causes of their dissatisfaction. Only 2.4% of total PP patients expressed difficulty in manipulating the device.

Conclusion

The presence of PD alone may not impact PP patient and partner satisfaction, but patients with more severe baseline deformity who require incision/grafting may be less satisfied with outcomes including penile length and glans sensation.

对患有/未患有佩罗尼氏病和植入阴茎假体的患者(及其伴侣)进行满意度评估研究
简介和目的在众多治疗勃起功能障碍的方法中,植入阴茎假体的患者满意度较高。然而,同时患有佩罗尼氏病(PD)、难治性勃起功能障碍和/或严重畸形的患者可能会显示出不同的结果。我们的研究旨在评估和比较同时患有/未患有佩罗尼氏病的男性对充气阴茎假体(IPP)的满意度。材料和方法我们向 1992-2022 年期间在本中心植入假体的所有活体患者(570 人)及其伴侣发放了五项满意度调查问卷。92%的植入物为充气装置。手术主要由两名外科医生进行。结果 在 570 名符合条件的患者中,479 人(84%)完成了调查(393 名非复杂性前列腺增生症患者:第 1 组;70 名非复杂性前列腺增生症患者-第 2 组;16 名复杂性前列腺增生症患者)。在第 1 组中,86% 的患者表示性交满意(非常满意或中度满意)。非复杂性前列腺增生症植入患者(第 2 组)的总体满意度为 81%(非常满意或基本满意)(p > 0.05)。然而,当我们对需要在植入时进行切口/切除/移植手术的重度假体植入患者(第 3 组:n = 20)的假体植入亚组进行评估时,只有 61% 的患者报告了满意的性生活(p <0.01),其中中度满意的患者多于非常满意的患者:78%对22%)。此外,84%(第 1 组)、80%(第 2 组)和 54%(第 3 组)的伴侣对性交表示满意(p < 0.01)。总体而言,84% 的第一组植入者和 79% 的第二组植入者表示,如果 IPP 失败,他们会再次接受手术(p > 0.05; ns)。只有 50%的第 3 组患者会再次接受手术。在外观方面,第 3 组植入者中有 48% 表示阴茎短小或龟头软是他们不满意的主要原因。结论单纯的阴茎短小症可能不会影响阴茎短小症患者和伴侣的满意度,但基线畸形较严重且需要切开/移植的患者可能对阴茎长度和龟头感觉等结果不太满意。
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