Varithena® (polidocanol) Injectable Foam
Varithena® (polidocanol) Injectable Foam
We are happy to announce the addition of Varithena® to our treatment armamentarium in the management of Varicose veins, venous insufficiency and chronic venous disease. We have successfully treated multiple patients with Varithena® since September 26th 2018. This procedure is minimally invasive and involves injection of a non-compounded foam (Varithena®) to treat the diseased refluxing superficial vein and eliminate the reflux in that vein which results in significant improvement in symptoms and in severe cases help heal venous ulcers in addition to the cosmetic improvement in the appearance of varicose veins.
INDICATIONS for Varithena®
Polidocanol injectable foam is a prescription medicine used to treat varicose veins caused by problems with the incompetent great saphenous veins (GSV), accessory saphenous veins, and visible varicosities of the great saphenous vein system above and below the knee. Varithena® improves symptoms related to or caused by varicose veins, and the appearance of varicose veins.
Common side effects of Varithena Injectable Foam include:
- pain or discomfort in the extremities
- numbness or tingling
- injection site reactions (pain, tenderness, warmth, itching, or bruising)
- increased hair growth on the treated leg
Varithena is for intravenous use under ultrasound guidance only. A dose of up to 5 ml per injection and 15 ml per treatment session is used. Treatment sessions should be separated by a minimum of 5 days. Varithena may interact with other drugs. Tell your doctor about all medications and supplements you use. Varithena is not recommended for use during pregnancy. It is unknown if this drug passes into breast milk.
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Mechanism of Action
Varithena® (polidocanol injectable foam) is a non-ionic surfactant sclerosing agent. The hydrophobic pole of the polidocanol molecule attaches to the lipid cell membrane of the venous endothelium, resulting in disruption of the osmotic barrier, destruction of the venous endothelium, and vasospasm. Following exposure to polidocanol, the interior surface of the vein becomes thrombogenic, which leads to thrombus formation and venous occlusion. The occluded vein is eventually replaced by fibrous connective tissue. Polidocanol is deactivated upon contact with blood, thus limiting the sclerosant action to the endothelium near the site of injection.
Common Patient Questions about Treatment with Varithena®
1. What are varicose veins?
Varicose veins are enlarged, bulging veins usually found in the legs; they can cause uncomfortable symptoms such as swelling and achiness. Common risk factors include family history, aging, being overweight or obese, and working at jobs requiring prolonged standing. Varithena® (polidocanol injectable foam) does not treat all types and all symptoms of varicose veins.
2. What is Varithena®? Varithena® (polidocanol injectable foam) is a prescription medicine used to treat varicose veins caused by problems with the great saphenous vein (GSV) and other related veins in the leg’s GSV system. Varithena® improves symptoms related to or caused by varicose veins, and the appearance of varicose veins. Varithena® is administered by the doctor into the malfunctioning veins. The minimally invasive, nonsurgical treatment doesn’t require incisions. The doctor usually numbs the injection site, but no additional anesthesia is required.
3. What results might I expect with Varithena®?
In clinical trials, Varithena® reduced patients’ varicose vein symptoms including heaviness, achiness, swelling, throbbing, and itching (HASTITM Symptoms). Varithena® also improved vein appearance in assessments by both patients and doctors.
4. How does Varithena® work?
Your doctor administers Varithena® through a catheter or by direct injection into your malfunctioning vein. The foam fills the desired section of the vein, and the diseased vein collapses. Blood flow shifts to healthier veins nearby.
5. What happens to Varithena® after it’s injected?
The foam is deactivated when it comes in contact with blood.
6. How long does treatment take?
It usually takes the doctor less than an hour to administer Varithena®, and you go home the same day.
7. Are there side effects to treatment with Varithena®?
The most common side effect seen with Varithena® is leg pain or discomfort. In the majority of cases, leg pain stops within one week. The other most common side effects are injection site bruising or pain, and potentially serious blood clots in the leg veins. These are not all of the possible side effects of Varithena®. Tell your doctor about any side effect that bothers you or that does not go away.
8. How many treatments might I need?
You may see results with as little as one treatment, depending on the number and size of your varicose veins. Additional treatment may be necessary if the size and extent of the veins to be treated require more than the maximum dose of Varithena® per session. Treatment sessions are separated by a minimum of 5 days.
9. How soon can I get back to normal activities?
You may resume some activities the same day as treatment. You will need to keep your post-treatment bandages dry and in place for 48 hours and to wear compression stockings on your treated leg for 2 weeks. You should avoid heavy exercise for one week. For a month, you should walk at least 10 minutes per waking hour and avoid long periods of inactivity.
10. How long do I have to wear my compression stockings after the procedure?
Compression stockings should be worn on the treated leg continuously for 2 weeks (14 days total) after treatment. Your doctor will recommend either thigh-high or knee-high stockings, depending on the location of the treated
11. Do I need to wear my compression stockings while I shower or bathe?
Your doctor will apply bandages and a compression stocking to the treated area, which should remain dry. You should not shower or bathe during the first 48 hours after treatment. After the initial 48-hour time period, your compression stockings must be worn day and night, including in the bath or shower, for the next 12 days. Replace the wet stocking with a dry one immediately after bathing or showering.
12. Is Varithena® covered by my insurance carrier?
Your insurance carrier may cover treatment. Your doctor’s office will contact your insurance provider to determine if you are eligible for treatment. Coverage may depend on the severity of your varicose veins and your symptoms.
IMPORTANT SAFETY INFORMATION
You should not be treated with Varithena® if you are allergic to polidocanol or have clots in your blood vessels. See back side for additional safety information. See Full Prescribing Information for Varithena® at VarithenaProfessional.com.
Severe allergic reactions have been reported in people treated with liquid forms of polidocanol and some patients have died from these reactions. Varithena® is a foam made from polidocanol. A healthcare professional will observe you for signs of allergic reactions for at least 10 minutes after you are treated with Varithena®.
Tell your doctor about all of your medical conditions, including if you • have arterial disease (a disease of the blood vessels) • have reduced mobility • have a history of blood clots in the veins or lungs • have had major surgery in the past 3 months • have recently had a long hospital stay • are pregnant or have recently been pregnant.
The most common side effects seen with Varithena® are leg pain or discomfort, injection site bruising or pain, and potentially serious blood clots in the leg veins. These are not all of the possible side effects of Varithena®. Tell your healthcare provider about any side effect that bothers you or that does not go away. You can also report side effects to the FDA at 1-800-FDA-1088. Varithena® is administered by your doctor. Doctors using Varithena® must be experienced in vein procedures and trained in using Varithena®.
See Full Prescribing Information for Varithena® at VarithenaProfessional.com © 2014 Biocompatibles, Inc., a BTG International group company All rights reserved US-VAR-2014-0134(1) 08/14 Varithena and HASTI are trademarks of Provensis Ltd, a BTG International group company BTG and the BTG roundel logo are registered trademarks of BTG International Ltd