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Voiding recovery after radical parametrectomy in cervical cancer patients: An international prospective multicentre trial - SENTIX.
Zapardiel, Ignacio; Kocian, Roman; Köhler, Cristhardt; Klat, Jaroslav; Germanova, Anna; Jacob, Anna; Bajsova, Sylva; Böhmer, Gerd; Lay, Laura; Gil-Ibañez, Blanca; Havelka, Pavel; Kipp, Barbara; Szewczyk, Grzegorz; Toth, Robert; Staringer, Juan Carlos; De Santiago, Javier; Coronado, Pluvio J; Poka, Robert; Laky, Rene; Luyckx, Mathieu; Fastrez, Maxime; Dusek, Ladislav; Hernandez, Alicia; Cibula, David.
  • Zapardiel I; Gynaecologic Oncology Unit, La Paz University Hospital-IdiPAZ, Madrid, Spain. Electronic address: ignaciozapardiel@hotmail.com.
  • Kocian R; Gynaecologic Oncology Centre, Department of Obstetrics and Gynaecology, First Faculty of Medicine, Charles University and General University Hospital, CEEGOG, Prague, Czech Republic.
  • Köhler C; Department of Special Operative and Oncologic Gynaecology, Asklepios-Clinic Hamburg, Hamburg, Germany.
  • Klat J; Department of Obstetrics and Gynaecology, University Hospital Ostrava, Ostrava, Poruba, Czech Republic.
  • Germanova A; Gynaecologic Oncology Centre, Department of Obstetrics and Gynaecology, First Faculty of Medicine, Charles University and General University Hospital, CEEGOG, Prague, Czech Republic.
  • Jacob A; Department of Special Operative and Oncologic Gynaecology, Asklepios-Clinic Hamburg, Hamburg, Germany.
  • Bajsova S; Department of Obstetrics and Gynaecology, University Hospital Ostrava, Ostrava, Poruba, Czech Republic.
  • Böhmer G; Department of Special Operative and Oncologic Gynaecology, Asklepios-Clinic Hamburg, Hamburg, Germany.
  • Lay L; Department of Gynaecology, Institute of Oncology Angel H Roffo University of Bueno s Aires, Buenos Aires, Argentina.
  • Gil-Ibañez B; Unit of Gynaecological Oncology, Institute Clinic of Gynaecology, Obstetrics and Neonatology (ICGON), Hospital Clinic of Barcelona, Barcelona, Spain.
  • Havelka P; Department of Obstetrics and Gynaecology, Bata Hospital Zlin, Czech Republic, CEEGOG, Zlin, Czech Republic.
  • Kipp B; Department of Obstetrics and Gynaecology, Cantonal Hospital of Lucerne, Lucerne, Switzerland.
  • Szewczyk G; Department of Obstetrics and Gynaecology, Institute of Mother and Child, Warsaw, Poland.
  • Toth R; Oncology Institute of East Slovakia, Kosice, Slovakia.
  • Staringer JC; Department of Gynaecology and Obstetrics, Hospital Español de Buenos Aires, Buenos Aires, Argentina.
  • De Santiago J; Gynecologic Oncology Unit, MD Anderson Cancer Centre, Madrid, Spain.
  • Coronado PJ; Departamento de Obstetricia y Ginecología, Hospital Clínico San Carlos, Madrid, Spain.
  • Poka R; Institute of Obstetrics and Gynaecology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
  • Laky R; Gynaecology, Medical University of Graz, Graz, Austria.
  • Luyckx M; Department of Gynaecology, Universite catholique de Louvain, Cliniques Universitaires St Luc, 1200, Brussels, Belgium.
  • Fastrez M; Department of Obstetrics and Gynaecology, St Pierre University Hospital, Université Libre de Bruxelles, Brussels, Belgium.
  • Dusek L; Institute of Biostatistics and Analyses, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
  • Hernandez A; Gynaecologic Oncology Unit, La Paz University Hospital-IdiPAZ, Madrid, Spain.
  • Cibula D; Gynaecologic Oncology Centre, Department of Obstetrics and Gynaecology, First Faculty of Medicine, Charles University and General University Hospital, CEEGOG, Prague, Czech Republic.
Gynecol Oncol ; 160(3): 729-734, 2021 03.
Article en En | MEDLINE | ID: mdl-33419610
OBJECTIVE: 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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias del Cuello Uterino / Histerectomía Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Middle aged Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias del Cuello Uterino / Histerectomía Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Middle aged Idioma: En Año: 2021 Tipo del documento: Article