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Updated: Jan 20, 2026

OP-IVM: Combining In vitro Maturation after Oocyte Retrieval with Gynecological Surgery
Published on: May 9, 2021
Experience with TachoSil in obstetric and gynecologic surgery
Pietro Santulli1, Louis Marcellin, Cyril Touboul
1Department of Obstetrics and Gynecology, Hôpital Tenon, Assistance Publique des Hôpitaux de Paris, CancerEst, Université Pierre et Marie Curie (UPMC), Paris, France.
TachoSil is effective and well-tolerated for controlling bleeding in obstetric and gynecologic surgeries. Improved documentation of TachoSil use is recommended for better traceability.
Area of Science:
- Gynecologic Surgery
- Obstetric Surgery
- Hemostatic Agents
Background:
- Perioperative bleeding is a significant risk in gynecologic and obstetric procedures.
- TachoSil, a hemostatic sealant, offers a potential solution for managing surgical bleeding.
- Evaluating its use in these specific surgical fields is crucial.
Purpose of the Study:
- To assess the feasibility and effectiveness of TachoSil in obstetric and gynecologic surgeries.
- To identify common indications and outcomes associated with TachoSil application.
- To evaluate the traceability of TachoSil usage in clinical practice.
Main Methods:
- Retrospective cohort study at a French university hospital (2007-2009).
- Inclusion of 84 women experiencing perioperative bleeding requiring TachoSil.
- Data collection included patient demographics, surgical details, transfusion needs, and postoperative course.
Main Results:
- TachoSil was utilized in 84 women, with indications including ovarian malignancy, fibroma, and breast cancer.
- Application sites included uterine serosa (n=16) and major vascular axis (n=7).
- 24 women received blood transfusions, and 3 required repeat surgery; TachoSil use was unrecorded in 51% of cases.
Conclusions:
- TachoSil demonstrates effectiveness and good tolerability in obstetric and gynecologic surgeries.
- The study highlights the need for enhanced measures to improve the traceability of TachoSil application.
- Further research into standardized documentation practices for hemostatic agents is warranted.
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