Värmeballongbehandling som endometriedestruktion vid

Hysteroskopi - SFOG

Cavaterm was an acceptable procedure and 93% of patients satisfied or very satisfied at 12 months (95% endometrial laser ablation). The overall “success” of the Cavaterm group was high, with 100% of women reporting eumenorrhea or better at 12-month follow-up. The amenorrhea rate in this group was significantly lower than in the NovaSure group, although the hypomenorrhea rate was significantly greater and the combined rates show no difference between the groups ( P = .88). The Cavaterm procedure was first described in 1993 and has reported amenorrhea rates of 22%–68% and an overall success rate of 92%–98% 9, 19, 20. The amenorrhea rate of 11% for this study was lower than we have previously reported (9).

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The original Cavaterm system in this study uses a circulating fluid of glycine 1.5% (nonconductive) heated to a target temperature of 75 °C for a 15‐min period. A pressure of 200–220 mmHg should be maintained throughout the treatment. The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada. Overview. Endometrial ablation is a procedure that surgically destroys (ablates) the lining of your uterus (endometrium). The goal of endometrial ablation is to reduce menstrual flow.

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fen on the human female genital tract: review of the of Systematic Reviews 2006, Issue 3. Art. No.: paring the Cavaterm and the Novasure endometrial.

Hemostasrubbningar inom obstetrik och gynekologi - SFOG

Cavaterm™ is a minimally invasive treatment for Dysfunctional Uterine Bleeding (DUB) Procedure was quick, recovery was a breeze.

The original Cavaterm system in this study uses a circulating fluid of glycine 1.5% (nonconductive) heated to a target temperature of 75 °C for a 15‐min period. A pressure of 200–220 mmHg should be maintained throughout the treatment. The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
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Literature Review. Our initial search strategy yielded 1009 publications; 79 studies met our title/abstract inclusion criteria and underwent a full‐text review. Bibliographic searches yielded 15 additional studies for full‐text review.

The Cavaterm™ plus system consists of a balloon catheter that utilizes a combination of heat, pressure, and circulation to destroy the endometrium and the underlying myometrium to a depth of 6-8 mm.
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Hysteroskopi - SFOG

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