Prolapse, Stress Urinary Incontinence
Conditions
Brief summary
The ability to determine the postmenopausal vaginal environment and the impact of pessary use could help to maximize pessary therapy and non-surgical treatment for such a prevalent problem.
Detailed description
The study will advance the care of elderly patients through providing data to maximize non-surgical options to those at high risk for having surgery and its attending morbidity. In characterizing substantive differences in the vaginal environment of successful and unsuccessful pessary users, the investigators can identify elderly patients at higher risk of adverse events with pessary use as well as novel targets for the pharmacologic treatment of the altered vaginal microbiota and endogenous AMP levels, potentially allowing patients to continue with non-surgical therapies rather than pursuing surgical intervention.
Interventions
DEVICEContinued Pessary Use
Pessary Fitting
Sponsors
Loyola University
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
FEMALE
Age
51 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* must be English speaking * appropriate for pessary treatment * pelvic floor conditions such as POP (with or without the presence of a uterus), stress urinary incontinence, urge urinary incontinence, or any combination of the above.
Exclusion criteria
* a history of current, symptomatic vaginal stricture * a history of current, radiation therapy, * or current treatment with auto-immune suppression agents. * if they have eroded mesh in the vagina from prior pelvic floor surgery
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Predominant vaginal microorganisms of older women with and without a pessary | Baseline | The investigator will collect a vaginal swab specimen in an aerobic and anaerobic preservative tube. Specimens will be sent to the clinical microbiology lab for quantitative culture. Expanded quantitative vaginal culture techniques and matrix assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Vaginal antimicrobial peptide (AMP) profile of older women with and without a pessary. | Baseline | The investigator will collect vaginal lavage fluid (VLF) prior to pessary placement and after vaginal swabs are obtained. Assessing AMP activity using high pressure liquid chromatography fractionation and radial diffusion assay to assess for AMP activity and abundance of candidate AMPs (cathelicidin, beta defensisn (hBD1 and hBD2) psoriasin, lactoferrin). |
| Vaginal microbiome and AMP profile between those women that choose to continue pessary use and those that do not by correlating the data from Aim 1 and Aim 2 with the clinical characteristic of continued pessary use. | 3 month visit, 6 month visit | The investigator will collect vaginal swabs and the Vaginal Lavage Fluid for those subjects who decide to NOT have their pessaries replaced by correlating the data from outcome 1 and outcome 2 with the clinical characteristic of continued pessary use. |
Countries
United States
Outcome results
None listed