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Impact of antibiotic therapy on the rate of negative test results for chronic endometritis: a prospective randomized control trial

D. Song, Yan-Fei He, Yixuan Wang, Ziyu Liu, En-lan Xia, Xiao-Wu Huang, Yu Xiao, Tin C. Li

Fertility and Sterility, 2021

132 participants · 72 citations

Abstract

OBJECTIVE

To compare the rates of negative test results for chronic endometritis (CE) between subjects who did and did not receive antibiotic treatment.

DESIGN

Prospective, single-blind randomized controlled trial.

SETTING

Tertiary hysteroscopic center in a university teaching hospital.

PATIENT(S)

A total of 132 women with CE confirmed with immunohistochemical study with CD138 epitope.

INTERVENTION(S)

Women randomized to antibiotic therapy received oral levofloxacin 500 mg and tinidazole 1,000 mg daily for 14 days. Women randomized to the control group did not receive any treatment. A repeated endometrial biopsy was performed 4 to 8 weeks after the initial biopsy to determine whether CE was still present.

MAIN OUTCOME MEASURE(S)

The rate of negative test results for CE (from positive to negative).

RESULT(S)

The CE rate of negative test results in the treatment group (89.3%) after one course of antibiotic treatment was significantly higher than that in the control group (12.7%). Among subjects who attempted pregnancy, there was no significant difference in ongoing pregnancy rates and miscarriage rates between the treatment arm (43.2%, 5.4%) and the control arm (25.7%, 14.3%). Among subjects randomized, there was also no significant difference in ongoing pregnancy rates and miscarriage rates between the treatment arm (27.1%, 3.4%) and the control arm (16.4%, 9.1%).

CONCLUSION

A course of broad-spectrum oral antibiotic therapy for 14 days is effective in the treatment of CE in…

How strong is the evidence?

Evidence Hub reads this as a randomized trial, done in people. Its evidence level is 2 of 5 (High · randomized trial). Randomized trials of a reasonable size are the strongest single-study design. Reported size: 132 participants or records.

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