Systematic review and meta-analysis comparing Adjustable Transobturator Male System (ATOMS) and Adjustable Continence Therapy (ProACT) for male stress incontinence

dc.contributor.authorAngulo Cuesta, Javier
dc.contributor.authorSchönburg, Sandra
dc.contributor.authorGiammò, Alessandro
dc.contributor.authorAbellán, Francisco J.
dc.contributor.authorArance Gil, José Ignacio
dc.contributor.authorLora, David
dc.date.accessioned2021-08-05T10:33:49Z
dc.date.available2021-08-05T10:33:49Z
dc.date.issued2019
dc.description.abstractBackground and purpose: Urinary incontinence is one of the most serious complications of prostate cancer treatment. The objective of this study was to assess efficacy and safety of Adjustable Transobturator Male System (ATOMS) compared to Adjustable Continence Therapy (proACT) for male stress urinary incotinence according to literature findings. Material and methods: A systematic review and meta-analysis on adjustable devices ATOMS and ProACT is presented. Studies on female or neurogenic incontinence were excluded. Differences between ATOMS and proACT in primary objective: dryness status (no-pad or one safety pad/day) after initial device adjustment, and in secondary objectives: improvement, satisfaction, complications and device durability, were estimated using random-effect model. Statistical heterogeneity among studies included in the meta-analysis was assessed using tau2, Higgins´s I2 statistics and Cochran´s Q test. Results: Combined data of 41 observational studies with 3059 patients showed higher dryness (68 vs. 55%; p = .01) and improvement (91 vs. 80%; p = .007) rate for ATOMS than ProACT. Mean pad-count (-4 vs. -2.5 pads/day; p = .005) and pad-test decrease (-425.7 vs. -211.4 cc; p < .0001) were also significantly lower. Satisfaction was higher for ATOMS (87 vs. 56%; p = .002) and explant rate was higher for proACT (5 vs. 24%; p < .0001). Complication rate for ProACT was also higher, but not statistically significant (17 vs. 26%; p = .07). Mean follow-up was 25.7 months, lower for ATOMS than ProACT (20.8 vs. 30.6 months; p = .02). The rate of working devices favoured ATOMS at 1-year (92 vs. 76; p < .0001), 2-years (85 vs. 61%; p = .0008) and 3-years (81 vs. 58%; p = .0001). Significant heterogeneity was evidenced, due to variable incontinence severity baseline, difficulties for a common reporting of complications, different number of adjustments and time of follow-up and absence of randomized studies. Conclusions: Despite the limitations that studies available are exclusively descriptive and the follow-up is limited, literature findings confirm ATOMS is more efficacious, with higher patient satisfaction and better durability than ProACT to treat male stress incontinence.spa
dc.description.filiationUEMspa
dc.description.impact2.740 JCR (2019) Q2, 27/71 Multidisciplinary Sciencesspa
dc.description.impact1.023 SJR (2019) Q1, 10/148 Multidisciplinaryspa
dc.description.impactNo data IDR 2019spa
dc.description.sponsorshipSin financiaciónspa
dc.identifier.citationAngulo, J., Schönburg, S., Giammò, A., Abellán, F. J., Arance, I., & Lora, D. (2019). Systematic review and meta-analysis comparing Adjustable Transobturator Male System (ATOMS) and Adjustable Continence Therapy (ProACT) for male stress incontinence. PloS One, 14(12), e0225762. https://doi.org/10.1371/journal.pone.0225762spa
dc.identifier.doi10.1371/journal.pone.0225762
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/11268/10291
dc.language.isoengspa
dc.peerreviewedSispa
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.accessRightsopen accessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.otherNeoplasias de la próstataspa
dc.subject.otherIncontinencia urinariaspa
dc.subject.unescoCáncerspa
dc.subject.unescoUrologíaspa
dc.subject.unescoTecnología médicaspa
dc.titleSystematic review and meta-analysis comparing Adjustable Transobturator Male System (ATOMS) and Adjustable Continence Therapy (ProACT) for male stress incontinencespa
dc.typejournal articlespa
dspace.entity.typePublication
relation.isAuthorOfPublicationeaadbb3a-67c4-43f5-b477-5fb2318b809a
relation.isAuthorOfPublication25289cfb-2724-4dbd-929c-fd92cf10943f
relation.isAuthorOfPublication.latestForDiscoveryeaadbb3a-67c4-43f5-b477-5fb2318b809a

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