TY - JOUR

T1 - Клиническое исследование нового поколения синтетических имплантов для коррекции апикального пролапса тазовых органов

AU - Кубин, Никита Дмитриевич

AU - Шульгин, Андрей Сергеевич

AU - Шахалиев, Рустам Алигисмет оглы

AU - Шкарупа, Дмитрий Дмитриевич

PY - 2025/6/25

Y1 - 2025/6/25

N2 - Introduction. Pelvic organ prolapse (POP) is a common condition that significantly impairs women's quality of life. Despite the effectiveness of synthetic implants, their use is limited due to the high risk of complications. In recent years, partially absorbable suture delivery systems have been actively developed to reduce implant-associated complications. Objective. To evaluate the clinical efficacy and safety of unilateral hybrid pelvic floor reconstruction using a partially absorbable suture delivery system. Materials and Methods. The study included 30 patients with stage 2–4 apical POP (POP-Q classification). Unilateral hybrid pelvic floor reconstruction was performed using the suture delivery system. Anatomical efficacy was assessed using the POP-Q system 12 months postoperatively. Additional assessments included quality of life (PFDI-20, ICIQ-SF) and patient satisfaction (IMPSS, PGI-I). MRI of the pelvic organs with intravenous contrast was performed in two patients. Results. At 12 months, anatomical efficacy was achieved in 96.7% of patients (p

AB - Introduction. Pelvic organ prolapse (POP) is a common condition that significantly impairs women's quality of life. Despite the effectiveness of synthetic implants, their use is limited due to the high risk of complications. In recent years, partially absorbable suture delivery systems have been actively developed to reduce implant-associated complications. Objective. To evaluate the clinical efficacy and safety of unilateral hybrid pelvic floor reconstruction using a partially absorbable suture delivery system. Materials and Methods. The study included 30 patients with stage 2–4 apical POP (POP-Q classification). Unilateral hybrid pelvic floor reconstruction was performed using the suture delivery system. Anatomical efficacy was assessed using the POP-Q system 12 months postoperatively. Additional assessments included quality of life (PFDI-20, ICIQ-SF) and patient satisfaction (IMPSS, PGI-I). MRI of the pelvic organs with intravenous contrast was performed in two patients. Results. At 12 months, anatomical efficacy was achieved in 96.7% of patients (p

UR - https://www.mendeley.com/catalogue/14c32aad-9309-39b8-bbee-2ec402ddee66/

U2 - 10.29188/2222-8543-2025-18-2-144-151

DO - 10.29188/2222-8543-2025-18-2-144-151

M3 - статья

VL - 18

SP - 144

EP - 151

JO - Экспериментальная и клиническая урология

JF - Экспериментальная и клиническая урология

SN - 2222-8543

IS - 2

ER -