Gamé X, Ruffion A, Cornu J-N, Phé V, Peyronnet B, Perrouin-Verbe M-A, Aublant C, Adé A, Chartier-Kastler E
Département d'urologie, transplantation rénale et andrologie, CHU Rangueil, TSA50032, 31059 Toulouse, France.
Équipe 2, service d'urologie, Centre d'innovation en cancérologie de Lyon (EA 3738 CICLY), faculté de médecine Lyon Sud, hospices civils de Lyon, université Lyon 1, centre hospitalier Lyon Sud, Pierre Bénite, France.
Prog Urol. 2022 Sep;32(10):672-680. doi: 10.1016/j.purol.2022.04.011. Epub 2022 Jun 22.
Sacral neuromodulation (SNM) is a minimally invasive technique that provides effective treatment for the management of refractory overactive bladder (OAB), non-obstructive urinary retention (NOUR), and fecal incontinence (FI). This study assessed patient preferences between the currently available non-rechargeable SNM device and a new, full-body magnetic resonance imaging (MRI)-safe, smaller, rechargeable device.
An online cross-sectional survey was conducted among French OAB, NOUR, FI patients, recruited via a market research vendor. To assess their preferences, patients were asked to indicate their level of agreement with 10 statements regarding the size of the device, its rechargeability, and the role of MRI using a 6-item Likert scale. A descriptive statistical analysis was performed.
In all, 95 patients (68% women), mean age 50 years, were included in the study: 51% were treated for OAB; 44% received an oral treatment and 28% had SNM. Overall, 71% of the 95 patients indicated a preference for the new device; 75% considered that recharging the device would not impact their lifestyle; 74% believed that the smaller size of the rechargeable device would facilitate their choice to be treated with SNM; 80% found full-body MRI compatibility important.
Most patients may prefer the new rechargeable SNM device over the current "standard". Compatibility with full-body MRI and the smaller device size seemed the key features of the newer device that would influence their choice of being treated with SNM. Future national and international recommendations should consider a shared decision-making process between the physician and the patient.
骶神经调节(SNM)是一种微创技术,可有效治疗难治性膀胱过度活动症(OAB)、非梗阻性尿潴留(NOUR)和大便失禁(FI)。本研究评估了患者对目前可用的不可充电SNM设备与一种新型、全身磁共振成像(MRI)安全、体积更小的可充电设备的偏好。
通过市场研究供应商招募法国OAB、NOUR、FI患者,进行在线横断面调查。为评估他们的偏好,要求患者使用6项李克特量表表明他们对关于设备尺寸、可充电性以及MRI作用的10条陈述的同意程度。进行描述性统计分析。
本研究共纳入95例患者(68%为女性),平均年龄50岁:51%接受OAB治疗;44%接受口服治疗,28%接受SNM治疗。总体而言,95例患者中有71%表示更喜欢新设备;75%认为设备充电不会影响他们的生活方式;74%认为可充电设备体积更小会促使他们选择接受SNM治疗;80%认为全身MRI兼容性很重要。
大多数患者可能更喜欢新型可充电SNM设备而非当前的“标准”设备。与全身MRI的兼容性和更小的设备尺寸似乎是新设备的关键特征,这会影响他们选择接受SNM治疗。未来国家和国际指南应考虑医生与患者之间的共同决策过程。