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- ProVate
- provate makes it your decision
- you decide WHEN to USE the device
- you decide WHEN to REMOVE the device
- You decides when to be spontaneous: sexual activity, swiming etz
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Pelvic Organ Prolapse (POP)
Empowering Women
Are you suffering from Pelvic Organ Prolapse (POP)?
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What causes POP?
Can I prevent having POP?
There are many causes for POP, mainly related to vaginal birth. However, other factors, such as constipation, chronic cough, obesity, aging and decline in hormones level, also contribute to the formation of POP.
Avoidance of some of the causes, such as constipation, chronic cough and obesity may reduce the incidence of POP.
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What are the treatment options for POP?
Treatment of POP is divided into either surgical or non-surgical management.
Surgery is indicated in more severe cases of POP, or in cases where women are not able or not willing to use pessaries or are wishing to try and have a one-time procedure. Surgery may have various complications, and there is a certain amount of failure involved, which may require more surgical procedures.
Most women need only the non-surgical options which may include
- Pelvic Floor Physiotherapy (PFP) which is associated with relief of some POP symptoms but does elevate the prolapsed organs
- Use of pessaries -vaginal inserts made of silicone or plastics are inserted into the vagina and lift the prolapsed organs. Pessaries are reusable only, and in most cases, insertion and removal are done by an HCP at the office, usually every 3 months, hence there is a dependency upon office appointments. Insertion and removal may be associated with discomfort or pain, and usage if frequently associated with discharge, spotting, foul-smell, infections, and hampered intercourse. This is why management dropout rate is high, usually within the initial 2 years.
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What steps will be taken at the HCP's office?
Woman arrives at the provider’s office
1. Vaginal digital size assessment of pessary ring
2. Provider inserts the appropriate ProVate size into the vagina and assesses adequacy
3. If needed – a larger or a smaller size may be used
Provider instructs patient how to insert ProVate according to the IFU
1. Patient inserts a ProVate device into her vagina and also removes the device
2. Patient inserts another ProVate device into the vagina and goes home with a device in-situ
Patient also takes home a larger size ProVate device and a smaller one
In case of expulsion – she inserts a larger size device, and if uncomfortable – a smaller size device
A TeleHealth visit is conducted within 5-7 days
1. Patient receives a prescription for 3 months via the EMR
2. Patient will receive every 3 months a package of 20 devices via Specialty Pharma
ProVate users study
ProVate USERS
After ProVate Use
of subjects achieved a substantial reduction in prolapse to POP-Q Stage 0/1†
other products users
Before ProVate Use
of users had POP Stage 3
had Stage 2
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POP FUCTS
pop fucts
Several facts about pop in the USA
- 57 million womens affected in the USA
- >90% of woman's undiagnosed
- Most women (>80%) need non-surgical management only
- A lack of satisfactory non-invasive management drives more patients to have various surgical procedures
It's so easy to manage pop in 2024
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