Pain Associated With Hysteroscopic Sterilization
نویسندگان
چکیده
BACKGROUND AND OBJECTIVES The safety and efficacy of female hysteroscopic sterilization using the Essure system has been well documented. Given the marked differences in the execution of hysteroscopic and laparoscopic sterilization, the objective of this study was to assess the experience of pain postprocedure between the 2. Secondary end-points included postoperative pain medication, time to return to normal activities, postprocedure bleeding, and patient satisfaction. METHODS Twenty cases each of laparoscopic sterilization (LS) and hysteroscopic sterilization (HS) were performed. Patients were surveyed regarding their experience of pain immediately postoperatively, 1 week, and 4 weeks postprocedure. RESULTS The average pain score immediately postprocedure was significantly lower among HS patients than among LS patients (t=-8.17, P<.0001). One-week postprocedure, none of the patients in the HS group reported any pain, while the average pain score among the LS patients was 2.65 (t=-9.67, P<.0001). Four weeks postprocedure, women in the HS group continued to report no pain, 35% of the LS group continued to report some pain (t=-3.04, P=.004). CONCLUSIONS Hysteroscopic sterilization offers a minimally invasive, less painful, equally efficacious modality for sterilization than laparoscopic sterilization and should be available to all women seeking permanent birth control.
منابع مشابه
Analysis of adverse events with Essure hysteroscopic sterilization reported to the Manufacturer and User Facility Device Experience database.
STUDY OBJECTIVE The Manufacturer and User Facility Device Experience database may be useful for clinicians using a Food and Drug Administration-approved medical device to identify the occurrence of adverse events and complications. We sought to analyze and investigate reports associated with the Essure hysteroscopic sterilization system (Conceptus Inc., Mountain View, CA) using this database. ...
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