Retrospective Data Analysis PelviGYNious/EndoGYNious

Exclusion Criteria

• •Patients who rule out subsequent contact by the hospital will be excluded.
• •The use of the products is contraindicated in case of:
• •pregnancy and/or patients who consider future pregnancies
• •adolescent/ pubescent patients
• •existence of a known sensitivity/ allergy against plastic materials such as polypropylene, polyester, etc.
• •any pathology, including known or suspected uterine pathology, which would compromise placement of the implant/mesh (e.g. anatomical distortion or abnormalities)
• •known anticoagulation disorder
• •anticoagulant therapy
• •autoimmune connective tissue disease
• •renal insufficiency and upper urinary tract obstruction
• •cancer illnesses of the vagina / cervix / rectum
• •undergone radiation therapy on the vagina, cervix, rectum
• •planned or emergency opening of the gastro-intestinal tract, as this could cause a risk of product contamination that could lead to infection that would require removal of the implant/device
• •active or latent infection especially of the genital system and/or urinary tract