eTable 1. Current randomized controlled trials (RCTs) and meta-analyses on local estrogenization, pessary therapy, and pelvic floor conditioning.
n | Comparison | Study design | Primary endpoint | Results [95% confidence interval] | Adverse events |
Study: Verghese et al. (2020) (e7) | |||||
325 | pre- and postoperative administration of local estradiol vs. no application | randomized pilot study | Compliance > 75 % Applikation secondary urinary tract infections symptom questionnaires |
preoperatively 79 % (34/43), 83 % (35/42) 6 weeks postoperatively 8/42 (19 %) vs. 4/42 (10 %)* no differences |
no serious complications related to estrogeni‧zation |
Study: Chiengthong et al. (2022) (e8) | |||||
78 | postmenopausal pessary therapy with estriol 0.03 mg intravaginally + Lactobacillus vs. without | randomized controlled trial (RCT) | bacterial vaginosis normal flora index ICIQ-VS questionnaire |
2/35 (6%) vs. 2/32 (6%) after 14 weeks 8/37 (6%) vs. 5/35 (6%)* 4.5 vs. 7.0 |
vaginal bleeding in a single patient in the control group |
Study: Lillemon et al. (2022) (e9) | |||||
39 | vaginaler Estrogenring vs. Placebo-Vaginalring | RCT | changes in the microbiome and urogenital symptoms | no significant changes in Lactobacilli or the microbiome | unclear |
Study: Probst et al. (2020) (e10) | |||||
130 | continuous pessary therapy for 24 vs. 12 weeks (= standard) | RCT | frequency of occurrence of vaginal epithelial lesions/erosionsnon-inferiority margin 7.5 percentage points | group differences –5.7 percentage points [-7, 4; 4.0] = longer duration of use non-inferior | none |
Study: Boyd et al. (2021) (e11) | |||||
132 | effect of pessary therapy on size of genital hiatus and degree of prolapse | Cohort study | mean change of genital hiatus (GH) and POPQ stage | −0.47 ± 1.02 cm* anterior compartment –0.47 ± 0.76* posterior compartment –0.47 ± 1.02* middle compartment –0.32 ± 1.33* |
not reported |
Study: Nekkanti et al. (2022) (e12) | |||||
50 | urethral pessary vs. disposable continence tampon | RCT | improvement of stress incontinence (Patient Global Impression of Improvement-[PGI]-I) | 80 % (8/10) vs. 75 % (9/12)study underpowered because of low patient recruitment | none |
Study: Stafne et al. (2022) (e13) | |||||
855 | targeted vs. no pelvic floor exercises during pregnancy | RCT | rate of urinary incontinence 7 years postpartum | 78 (51 %) vs. 63 (57 %) | none |
Study: Luginbuehl (2022) (e14) | |||||
96 | pelvic floor training with vs. without reflex contraction exercises | RCT | changes in the ICIQ short-form questionnaire | 2.9 vs. 3.0 | none |
Study: De Marco et al. (2022) (e15) | |||||
52 | pelvic floor exercises with or without manual therapy | RCT | changes in the ICIQ short-form questionnaire | 10,6 (± 4,9) vs. 11,2 (± 5,7) | none |
Study: Leonardo et al. (2022) (e16) | |||||
562 | pelvic floor exercises with or without biofeedback, and pelvic floor exercises vs. electrostimulation | systematic review and meta-analysis of RCTs | changes (mean differences) in two symptom questionnaires: King´s Health (KHQ) + Incontinence Impact Questionnaire (IIQ) | KHQ: –2.8 [-17.1; 11.5] IIQ: –2.5 [-0.5; 5.5] KHQ: 16.5 [6.1; 26.9]* IIQ: 5.3 [1.6; 9.1]* for electrostimulation |
none |
Study: Wang (2022) (e17) | |||||
pelvic floor exercises vs. no intervention in women with prolapse | meta-analysis | changes of the mean Prolapse Symptom Score POP-SS and POPQ stage | changes –1.7 [-2.4; 0.9]*RR 1.5 [1.1; 2.0]* long-term data without significant change | none |
*p ≤ 0.05
ICIQ, International Consultation on Incontinence Questionnaire; POPQ, pelvic organ prolapse quantification; RR, risk ratio