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Sacral neuromodulation for neurogenic lower urinary tract dysfunction: systematic review and meta-analysis

cris.virtual.author-orcid0000-0002-8162-8910
cris.virtualsource.author-orcidf3def9ad-2068-403c-8f3f-80eecdb88337
cris.virtualsource.author-orcid3b12b088-ef2b-4665-b7a5-265aa75ade43
datacite.rightsrestricted
dc.contributor.authorKessler, Thomas M.
dc.contributor.authorLa Framboise, David
dc.contributor.authorTrelle, Sven
dc.contributor.authorFowler, Clare J
dc.contributor.authorKiss, Gustav
dc.contributor.authorPannek, Jürgen
dc.contributor.authorSchurch, Brigitte
dc.contributor.authorSievert, Karl-Dietrich
dc.contributor.authorEngeler, Daniel S
dc.date.accessioned2024-10-10T20:51:32Z
dc.date.available2024-10-10T20:51:32Z
dc.date.issued2010
dc.description.abstractContext Treatment of neurogenic lower urinary tract dysfunction (LUTD) is a challenge, because conventional therapies often fail. Sacral neuromodulation (SNM) has become a well-established therapy for refractory non-neurogenic LUTD, but its value in patients with a neurologic cause is unclear. Objective To assess the efficacy and safety of SNM for neurogenic LUTD. Evidence acquisition Studies were identified by electronic search of PubMed, EMBASE, and ScienceDirect (on 15 April 2010) and hand search of reference lists and review articles. SNM articles were included if they reported on efficacy and/or safety of tested and/or permanently implanted patients suffering from neurogenic LUTD. Two reviewers independently selected studies and extracted data. Study estimates were pooled using Bayesian random-effects meta-analysis. Evidence synthesis Of the 26 independent studies (357 patients) included, the evidence level ranged from 2b to 4 according to the Oxford Centre for Evidence-Based Medicine. Half (n = 13) of the included studies reported data on both test phase and permanent SNM; the remaining studies were confined to test phase (n = 4) or permanent SNM (n = 9). The pooled success rate was 68% for the test phase (95% credibility interval [CrI], 50–87) and 92% (95% CrI, 81–98%) for permanent SNM, with a mean follow-up of 26 mo. The pooled adverse event rate was 0% (95% CrI, 0–2%) for the test phase and 24% (95% CrI, 6–48%) for permanent SNM. Conclusions There is evidence indicating that SNM may be effective and safe for the treatment of patients with neurogenic LUTD. However, the number of investigated patients is low with high between-study heterogeneity, and there is a lack of randomised, controlled trials. Thus, well-designed, adequately powered studies are urgently needed before more widespread use of SNM for neurogenic LUTD can be recommended.
dc.description.numberOfPages10
dc.description.sponsorshipUniversitätsklinik für Urologie
dc.description.sponsorshipInstitut für Sozial- und Präventivmedizin (ISPM)
dc.identifier.doi10.7892/boris.2228
dc.identifier.isi000283646600011
dc.identifier.pmid20934242
dc.identifier.publisherDOI10.1016/j.eururo.2010.09.024
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/72935
dc.language.isoen
dc.publisherElsevier
dc.publisher.placeAmsterdam
dc.relation.ispartofEuropean urology
dc.relation.issn0302-2838
dc.relation.organizationDCD5A442C238E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BECFE17DE0405C82790C4DE2
dc.titleSacral neuromodulation for neurogenic lower urinary tract dysfunction: systematic review and meta-analysis
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage874
oaire.citation.issue6
oaire.citation.startPage865
oaire.citation.volume58
oairecerif.author.affiliationUniversitätsklinik für Urologie
oairecerif.author.affiliationInstitut für Sozial- und Präventivmedizin (ISPM)
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unibe.date.licenseChanged2017-09-11 17:44:24
unibe.description.ispublishedpub
unibe.eprints.legacyId2228
unibe.journal.abbrevTitleEUR UROL
unibe.refereedtrue
unibe.subtype.articlejournal

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