2022
DOI: 10.1016/j.jmig.2022.06.006
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Postoperative Uterine Necrosis and Peritonitis Following Laparoscopic Radiofrequency Myoma Ablation

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Cited by 8 publications
(4 citation statements)
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“…21 22 Though total adverse events are low (1.78%), a case report of postoperative necrosis and peritonitis in a treated fibroid of > 10 cm dimension has been described. 23 Serosal bowel injury and postoperative pelvic abscess due to ultrasound probe use were also noted in the pivotal HALT trial. The average length of stay is 10.7 hours with mean return to work after 4.3 days.…”
Section: Short- and Long-term Outcomesmentioning
confidence: 95%
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“…21 22 Though total adverse events are low (1.78%), a case report of postoperative necrosis and peritonitis in a treated fibroid of > 10 cm dimension has been described. 23 Serosal bowel injury and postoperative pelvic abscess due to ultrasound probe use were also noted in the pivotal HALT trial. The average length of stay is 10.7 hours with mean return to work after 4.3 days.…”
Section: Short- and Long-term Outcomesmentioning
confidence: 95%
“…24 In the pivotal HALT trial, menstrual blood loss reduction was measured via alkaline hematin. 23 This reduced within 3 months of treatment by 31.8% (95% confidence interval [CI]: À40.3% to À20.3%) and decreased to 38.3% (95% CI: À45.2% to À31.4%) at 12 months (p < 0.001). Similarly, within 3 months, the total mean fibroid volume reduced by 39.8% (95% CI: À44% to À35.6%) with continued decrease at 12 months to 45.1% (95% CI: À51.6% to À38.6%, p ¼ 0.001).…”
Section: Short-and Long-term Outcomesmentioning
confidence: 99%
“…15 A case report describes postoperative necrosis and peritonitis requiring hysterectomy after treatment of a 10×12-cm leiomyoma with laparoscopic RFA, possibly related to a large amount of residual necrotic tissue. 16 Several studies have demonstrated safe use of laparoscopic RFA for leiomyomas up to 10 cm despite the initial trial exclusion of leiomyomas larger than 7 cm. However, the described complication represents evidence for caution with RFA use in significantly large leiomyomas larger than 10 cm.…”
Section: Short-term Outcomesmentioning
confidence: 99%
“…Though a growing body of literature has demonstrated its clinical effectiveness [2][3][4][5][6] and short learning curve, 7 there remains a paucity of information regarding adverse events and device malfunctions encountered during RFA procedures. 8,9 We studied RFA device-related events reported to the FDA's Manufacturer and User Facility Device Experience (MAUDE) database to determine whether there are emerging devicerelated issues.…”
mentioning
confidence: 99%