Sacral Neuromodulation with the InterStim System for Overactive Bladder: 3-Year Results from the French Prospective, Multicenter, Observational SOUNDS Study

SOUNDS strengthens the evidence basis of sacral neuromodulation (SNM) for overactive bladder (OAB) through real-world data. To analyze diary-based effectiveness, quality of life (QoL), disease severity, symptom bother, and safety data for SNM with the InterStim system up to 3 yr after implantation....

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Veröffentlicht in:European urology focus 2022-09, Vol.8 (5), p.1399-1407
Hauptverfasser: Chartier-Kastler, Emmanuel, Normand, Loïc Le, Ruffion, Alain, Saussine, Christian, Braguet, Raïssa, Rabut, Bertrand, Ragni, Evelyne, Perrouin-Verbe, Marie-Aimée, Pierrevelcin, Jean, Rousseau, Thierry, Gamé, Xavier, Tanneau, Yves, Dargent, François, Biardeau, Xavier, Graziana, Jean Pierre, Stoica, Gabriel, Brassart, Elena, Fourmarier, Marc, Yaghi, Najdat, Capon, Gregoire, Ferchaud, Jérôme, Berrogain, Nathalie, Peyrat, Laurence, Pecoux, François, Bryckaert, Pierre-Emmanuel, Melotti, Alice, Abouihia, Abdallah, Keller, David Urs Josef, Cornu, Jean-Nicolas
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container_end_page 1407
container_issue 5
container_start_page 1399
container_title European urology focus
container_volume 8
creator Chartier-Kastler, Emmanuel
Normand, Loïc Le
Ruffion, Alain
Saussine, Christian
Braguet, Raïssa
Rabut, Bertrand
Ragni, Evelyne
Perrouin-Verbe, Marie-Aimée
Pierrevelcin, Jean
Rousseau, Thierry
Gamé, Xavier
Tanneau, Yves
Dargent, François
Biardeau, Xavier
Graziana, Jean Pierre
Stoica, Gabriel
Brassart, Elena
Fourmarier, Marc
Yaghi, Najdat
Capon, Gregoire
Ferchaud, Jérôme
Berrogain, Nathalie
Peyrat, Laurence
Pecoux, François
Bryckaert, Pierre-Emmanuel
Melotti, Alice
Abouihia, Abdallah
Keller, David Urs Josef
Cornu, Jean-Nicolas
description SOUNDS strengthens the evidence basis of sacral neuromodulation (SNM) for overactive bladder (OAB) through real-world data. To analyze diary-based effectiveness, quality of life (QoL), disease severity, symptom bother, and safety data for SNM with the InterStim system up to 3 yr after implantation. Twenty-five representative French sites enrolled 291 patients with OAB followed according to the local standard of care. Overall, 229 patients received a de novo or replacement InterStim implant and had four follow-up visits, two within the first yr and annually thereafter. A total of 190 patients completed the fourth follow-up visit after a mean of 33.7 ± 3.7 mo. The effectiveness outcomes measured were changes in daily voids and leaks and the therapy responder rates. Other outcomes included validated QoL data (Ditrovie and EuroQol 5-dimension 5-level questionnaires), disease severity (Urinary Symptom Profile [USP]), symptom bother rated using a numeric rating scale (NRS), and safety data. Follow-up data were compared to baseline results using the Wilcoxon signed-rank test. Average daily voids and leaks were significantly reduced at all time points up to 3 yr after implantation (p < 0.05) except for voids at 21 mo in the group receiving a replacement device. The therapeutic response for urinary urge incontinence at the fourth follow-up was 72% for the de novo group and 86% for the replacement group. Disease-specific QoL (Ditrovie), OAB-specific symptom severity (USP domain 2), and NRS-rated disease bother were significantly improved at all visits (p < 0.001). Device- or procedure-related adverse events occurred in 49% of patients, with 68% of the events classified as minor (Clavien-Dindo grade I or II). Surgical revisions were performed in 33% of patients, including permanent removal in 13%, over a mean exposure time of 44.4 ± 15.3 mo. This study confirms the safety and effectiveness of SNM for OAB and improvements in QoL and disease bother in real life. Our study in French patients with overactive bladder showed that disease symptoms and bother were significantly reduced and quality of life was significantly improved over a study duration of approximately 3 yr after implantation of a device to stimulate nerves that control the bladder. This trial is registered at ClinicalTrials.gov as NCT02186041. This large, observational study confirmed that sacral neuromodulation confers significant symptom and quality-of-life improvements in patients with overactive bladde
doi_str_mv 10.1016/j.euf.2021.06.013
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Average daily voids and leaks were significantly reduced at all time points up to 3 yr after implantation (p &lt; 0.05) except for voids at 21 mo in the group receiving a replacement device. The therapeutic response for urinary urge incontinence at the fourth follow-up was 72% for the de novo group and 86% for the replacement group. Disease-specific QoL (Ditrovie), OAB-specific symptom severity (USP domain 2), and NRS-rated disease bother were significantly improved at all visits (p &lt; 0.001). Device- or procedure-related adverse events occurred in 49% of patients, with 68% of the events classified as minor (Clavien-Dindo grade I or II). Surgical revisions were performed in 33% of patients, including permanent removal in 13%, over a mean exposure time of 44.4 ± 15.3 mo. This study confirms the safety and effectiveness of SNM for OAB and improvements in QoL and disease bother in real life. Our study in French patients with overactive bladder showed that disease symptoms and bother were significantly reduced and quality of life was significantly improved over a study duration of approximately 3 yr after implantation of a device to stimulate nerves that control the bladder. This trial is registered at ClinicalTrials.gov as NCT02186041. 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Average daily voids and leaks were significantly reduced at all time points up to 3 yr after implantation (p &lt; 0.05) except for voids at 21 mo in the group receiving a replacement device. The therapeutic response for urinary urge incontinence at the fourth follow-up was 72% for the de novo group and 86% for the replacement group. Disease-specific QoL (Ditrovie), OAB-specific symptom severity (USP domain 2), and NRS-rated disease bother were significantly improved at all visits (p &lt; 0.001). Device- or procedure-related adverse events occurred in 49% of patients, with 68% of the events classified as minor (Clavien-Dindo grade I or II). Surgical revisions were performed in 33% of patients, including permanent removal in 13%, over a mean exposure time of 44.4 ± 15.3 mo. This study confirms the safety and effectiveness of SNM for OAB and improvements in QoL and disease bother in real life. Our study in French patients with overactive bladder showed that disease symptoms and bother were significantly reduced and quality of life was significantly improved over a study duration of approximately 3 yr after implantation of a device to stimulate nerves that control the bladder. This trial is registered at ClinicalTrials.gov as NCT02186041. 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To analyze diary-based effectiveness, quality of life (QoL), disease severity, symptom bother, and safety data for SNM with the InterStim system up to 3 yr after implantation. Twenty-five representative French sites enrolled 291 patients with OAB followed according to the local standard of care. Overall, 229 patients received a de novo or replacement InterStim implant and had four follow-up visits, two within the first yr and annually thereafter. A total of 190 patients completed the fourth follow-up visit after a mean of 33.7 ± 3.7 mo. The effectiveness outcomes measured were changes in daily voids and leaks and the therapy responder rates. Other outcomes included validated QoL data (Ditrovie and EuroQol 5-dimension 5-level questionnaires), disease severity (Urinary Symptom Profile [USP]), symptom bother rated using a numeric rating scale (NRS), and safety data. Follow-up data were compared to baseline results using the Wilcoxon signed-rank test. Average daily voids and leaks were significantly reduced at all time points up to 3 yr after implantation (p &lt; 0.05) except for voids at 21 mo in the group receiving a replacement device. The therapeutic response for urinary urge incontinence at the fourth follow-up was 72% for the de novo group and 86% for the replacement group. Disease-specific QoL (Ditrovie), OAB-specific symptom severity (USP domain 2), and NRS-rated disease bother were significantly improved at all visits (p &lt; 0.001). Device- or procedure-related adverse events occurred in 49% of patients, with 68% of the events classified as minor (Clavien-Dindo grade I or II). Surgical revisions were performed in 33% of patients, including permanent removal in 13%, over a mean exposure time of 44.4 ± 15.3 mo. This study confirms the safety and effectiveness of SNM for OAB and improvements in QoL and disease bother in real life. Our study in French patients with overactive bladder showed that disease symptoms and bother were significantly reduced and quality of life was significantly improved over a study duration of approximately 3 yr after implantation of a device to stimulate nerves that control the bladder. This trial is registered at ClinicalTrials.gov as NCT02186041. This large, observational study confirmed that sacral neuromodulation confers significant symptom and quality-of-life improvements in patients with overactive bladder after 3 yr in a standard care setting that are similar in magnitude to previously published results.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.euf.2021.06.013</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-8224-1195</orcidid><orcidid>https://orcid.org/0000-0003-4241-8125</orcidid><orcidid>https://orcid.org/0000-0003-1270-7401</orcidid><orcidid>https://orcid.org/0000-0003-0512-3459</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 2405-4569
ispartof European urology focus, 2022-09, Vol.8 (5), p.1399-1407
issn 2405-4569
2405-4569
language eng
recordid cdi_hal_primary_oai_HAL_hal_03457285v1
source Alma/SFX Local Collection
subjects Double incontinence
Human health and pathology
Life Sciences
Overactive bladder
Real-world data
Sacral neuromodulation
Tissues and Organs
title Sacral Neuromodulation with the InterStim System for Overactive Bladder: 3-Year Results from the French Prospective, Multicenter, Observational SOUNDS Study
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