Hypothesis / aims of study
Millions of women have pelvic organ prolapse (POP) worldwide, and it is a health problem associated with quality of life more than half of parous women aged over 50 years (1). POP is one of the most prevalent gynecological conditions requiring surgical treatment. Pectopexy using minimal invasive surgery was developed to reduce the short-term morbidity and recurrence associated with the open abdominal approach, providing the same results. We recently successfully performed prolapse surgery in POP patients, using a new laparoscopic and robotic pectopexy technique. The aim of this study is to evaluate the feasibility and safety of laparoscopic and robotic pectopexy in POP.
Study design, materials and methods
Data were retrospectively collected from database at Dong-san Medical Center, for POP patients who underwent laparoscopic or robotics pectopexy from January 2019 to September 2019. Laparoscopic pectopexy was performed through a standard multi-port (4 port) platform and robotic pectopexy was performed using the da Vinci Xi or X Surgical System (Intuitive Surgical, Sunnyvale, CA). The surgical procedure is retroperitoneum space from the isthmic portion of cervix to the iliopectineal ligament is exposed using unipolar. After completion of dissections, a polyvinylidene fluoride monofilament mesh was inserted into the abdominal cavity. The ends of the mesh were sutured to both iliopectineal ligaments via the intracorporeal suture technique, using nonabsorbable sutures. And mesh in the tension-free position was fixed to the cervicoisthmic portion of uterus with nonabsorbable sutures. Finally, the peritoneum dissected was sutured with an absorbable continuous suture.
Interpretation of results
Overall, laparoscopic and robotic pectopexy were performed successfully without complication in terms of the surgical outcomes.