Voiding recovery after radical parametrectomy in cervical cancer patients: An international prospective multicentre trial – SENTIX

dc.contributor.authorZapardiel, Ignacio
dc.contributor.authorCoronado Martín, Pluvio Jesús
dc.contributor.authorCibula, David
dc.date.accessioned2025-12-15T08:41:42Z
dc.date.available2025-12-15T08:41:42Z
dc.date.issued2021-03-13
dc.description.abstractObjective: Voiding dysfunctions represent a leading morbidity after radical hysterectomy performed in patients with early-stage cervical cancer. The aim of this study was to perform ad hoc analysis of factors influencing voiding recovery in SENTIX (SENTinel lymph node biopsy in cervIX cancer) trial. Methods: The SENTIX trial (47 sites, 18 countries) is a prospective study on sentinel lymph node biopsy without pelvic lymphadenectomy in patients with early-stage cervical cancer. Overall, the data of 300 patients were analysed. Voiding recovery was defined as the number of days from surgery to bladder catheter/epicystostomy removal or to post-voiding urine residuum ≤50 mL. Results: The median voiding recovery time was three days (5th-95th percentile: 0-21): 235 (78.3%) patients recovered in <7 days and 293 (97.7%) in <30 days. Only seven (2.3%) patients recovered after >30 days. In the multivariate analysis, only previous pregnancy (p = 0.033) and type of parametrectomy (p < 0.001) significantly influenced voiding recovery >7 days post-surgery. Type-B parametrectomy was associated with a higher risk of delayed voiding recovery than type-C1 (OR = 4.69; p = 0.023 vs. OR = 3.62; p = 0.052, respectively), followed by type-C2 (OR = 5.84; p = 0.011). Both previous pregnancy and type C2 parametrectomy independently prolonged time to voiding recovery by two days. Conclusions: Time to voiding recovery is significantly related to previous pregnancy and type of parametrectomy but it is not influenced by surgical approach (open vs minimally invasive), age, or BMI. Type B parametrectomy, without direct visualisation of nerves, was associated with longer recovery than nerve-sparing type C1. Importantly, voiding dysfunctions after radical surgery are temporary, and the majority of the patients recover in less than 30 days, including patients after C2 parametrectomy.
dc.description.departmentDepto. de Salud Pública y Materno - Infantil
dc.description.facultyFac. de Medicina
dc.description.refereedTRUE
dc.description.statuspub
dc.identifier.citationZapardiel I, Kocian R, Köhler C, Klat J, Germanova A, Jacob A, Bajsova S, Böhmer G, Lay L, Gil-Ibañez B, Havelka P, Kipp B, Szewczyk G, Toth R, Staringer JC, De Santiago J, Coronado PJ, Poka R, Laky R, Luyckx M, Fastrez M, Dusek L, Hernandez A, Cibula D. Voiding recovery after radical parametrectomy in cervical cancer patients: An international prospective multicentre trial - SENTIX. Gynecol Oncol. 2021 Mar;160(3):729-734. doi: 10.1016/j.ygyno.2020.12.018. Epub 2021 Jan 6. PMID: 33419610.
dc.identifier.doi10.1016/j.ygyno.2020.12.018.
dc.identifier.essn1095-6859
dc.identifier.issn0090-8258
dc.identifier.officialurlhttps://doi.org/10.1016/j.ygyno.2020.12.018
dc.identifier.pmid33419610
dc.identifier.relatedurlhttps://www.sciencedirect.com/science/article/pii/S0090825820342219?via%3Dihub
dc.identifier.relatedurlhttps://pubmed.ncbi.nlm.nih.gov/33419610/
dc.identifier.urihttps://hdl.handle.net/20.500.14352/128900
dc.issue.number3
dc.journal.titleGynecologic Oncology
dc.language.isoeng
dc.page.final734
dc.page.initial729
dc.publisherElsevier
dc.relation.projectIDCzech Health Research Council (Czech Republic)
dc.rights.accessRightsrestricted access
dc.subject.cdu618.1:616-006.04
dc.subject.keywordCervical cancer
dc.subject.keywordNerve-sparing techniques
dc.subject.keywordParametrectomy
dc.subject.keywordRadical hysterectomy
dc.subject.keywordVoiding recovery
dc.subject.ucmCiencias Biomédicas
dc.subject.ucmGinecología y obstetricia
dc.subject.ucmOncología
dc.subject.unesco32 Ciencias Médicas
dc.subject.unesco3201.08 Ginecología
dc.subject.unesco3201.01 Oncología
dc.titleVoiding recovery after radical parametrectomy in cervical cancer patients: An international prospective multicentre trial – SENTIX
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number160
dspace.entity.typePublication
relation.isAuthorOfPublication30d02479-92c3-4435-a066-b282a5f6d2b0
relation.isAuthorOfPublication.latestForDiscovery30d02479-92c3-4435-a066-b282a5f6d2b0

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