TY - JOUR
T1 - Tolerance of Chlorhexidine Gluconate Vaginal Cleansing Solution
T2 - A Randomized Controlled Trial
AU - Rastogi, Supriya
AU - Glaser, Laura
AU - Friedman, Jaclyn
AU - Carter, Isabelle V.
AU - Milad, Magdy P.
N1 - Publisher Copyright:
© Copyright 2020, Mary Ann Liebert, Inc., publishers 2020.
PY - 2020/2
Y1 - 2020/2
N2 - Objective: The aim of this research was to compare the tolerance of 4% chlorhexidine gluconate (CHG)/isopropyl alcohol versus 7.5% povidone-iodine (PI) vaginal cleansing solutions in patients undergoing hysteroscopic procedures. Materials and Methods: For this randomized controlled trial at a university hospital, women at least 18 years old, who were undergoing diagnostic or operative hysteroscopy procedures, were randomized to either PI or CHG antiseptic as a vaginal preparation in a single-blinded fashion. The primary outcome was the presence and severity of vaginal dryness, vaginal burning, vaginal itching, unusual vaginal discharge, and burning or pain with urination. Patients completed a standardized survey at 3 timepoints: preoperatively (T0); immediately postoperatively (T1); and 24-48 hours postoperatively (T2). Results: Of 134 patients recruited and randomized, 123 (63 = PI, 60 = CHG) were analyzed at T0 and 97 patients completed all follow-up surveys. When controlling for age, menopause, catheterization, and T0 scores, patients treated with CHG had significantly higher rates of vaginal dryness (adjusted odds ratio (aOR): 4.38; 95% confidence interval (CI): 1.06-17.96; p = 0.042), vaginal burning (aOR: 6.45; 95% CI: 2.33-17.86; p < 0.001), and burning or pain with urination (aOR: 3.30; 95% CI: 1.18-9.19; p = 0.022). At T1, 54.2% of CHG versus 34.9% of PI patients had adverse symptoms. At T2, patients receiving CHG noted significantly more vaginal burning (aOR: 5.05; 95% CI: 1.85-13.78; p = 0.002), unusual discharge (aOR: 3.56; 95% CI: 1.13-11.26; p = 0.030), and burning or pain with urination (aOR: 4.78; 95% CI: 1.66-13.78; p = 0.004). At T2, 68.8% CHG versus 43.8% PI patients experienced adverse symptoms. Conclusions: Use of CHG vaginal preparation was associated with significantly worse vaginal and urinary symptoms, compared with PI, both in the immediate postoperative period and 24-48 hours postoperatively. Patients treated with CHG vaginal antiseptic for clean-contaminated gynecologic surgeries should be warned about the potential adverse side-effects.
AB - Objective: The aim of this research was to compare the tolerance of 4% chlorhexidine gluconate (CHG)/isopropyl alcohol versus 7.5% povidone-iodine (PI) vaginal cleansing solutions in patients undergoing hysteroscopic procedures. Materials and Methods: For this randomized controlled trial at a university hospital, women at least 18 years old, who were undergoing diagnostic or operative hysteroscopy procedures, were randomized to either PI or CHG antiseptic as a vaginal preparation in a single-blinded fashion. The primary outcome was the presence and severity of vaginal dryness, vaginal burning, vaginal itching, unusual vaginal discharge, and burning or pain with urination. Patients completed a standardized survey at 3 timepoints: preoperatively (T0); immediately postoperatively (T1); and 24-48 hours postoperatively (T2). Results: Of 134 patients recruited and randomized, 123 (63 = PI, 60 = CHG) were analyzed at T0 and 97 patients completed all follow-up surveys. When controlling for age, menopause, catheterization, and T0 scores, patients treated with CHG had significantly higher rates of vaginal dryness (adjusted odds ratio (aOR): 4.38; 95% confidence interval (CI): 1.06-17.96; p = 0.042), vaginal burning (aOR: 6.45; 95% CI: 2.33-17.86; p < 0.001), and burning or pain with urination (aOR: 3.30; 95% CI: 1.18-9.19; p = 0.022). At T1, 54.2% of CHG versus 34.9% of PI patients had adverse symptoms. At T2, patients receiving CHG noted significantly more vaginal burning (aOR: 5.05; 95% CI: 1.85-13.78; p = 0.002), unusual discharge (aOR: 3.56; 95% CI: 1.13-11.26; p = 0.030), and burning or pain with urination (aOR: 4.78; 95% CI: 1.66-13.78; p = 0.004). At T2, 68.8% CHG versus 43.8% PI patients experienced adverse symptoms. Conclusions: Use of CHG vaginal preparation was associated with significantly worse vaginal and urinary symptoms, compared with PI, both in the immediate postoperative period and 24-48 hours postoperatively. Patients treated with CHG vaginal antiseptic for clean-contaminated gynecologic surgeries should be warned about the potential adverse side-effects.
KW - gynecology
KW - laparoscopy
KW - surgery
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U2 - 10.1089/gyn.2019.0066
DO - 10.1089/gyn.2019.0066
M3 - Article
AN - SCOPUS:85079136268
SN - 1042-4067
VL - 36
SP - 13
EP - 19
JO - Journal of Gynecologic Surgery
JF - Journal of Gynecologic Surgery
IS - 1
ER -