Using Latisse for Eyelash Loss

FDA Approved Latisse is an Option for Eyelash Loss Caused by Chemotherapy

For those who have lost their eyelashes to chemotherapy, a drug called Latisse may be a solution for lash regrowth. The prescription drug is the first and only to be approved by FDA for eyelash growth and darkening. While Latisse is not marketed specifically for people with cancer, it may be a possible treatment for eyelash loss or shortening caused by chemotherapy.

It is also important to note that Latisse has not been evaluated in those with chemotherapy-induced eyelash loss. Side effects concerning people undergoing treatment are unknown. Ask your oncologist if Latisse is right for you, or if you have finished treatment, make sure the prescribing doctor is aware of your prior treatment.

How Do You Use Latisse?

Latisse is a topical treatment that is applied to the base of the eyelashes each evening. Before applying it, you must first remove all makeup and contact lenses. Latisse is packed as a kit with a small bottle of solution and applicators that look like small paintbrushes. Squeeze one drop of solution onto the applicator brush tip and apply to base of lashes. Blot excess solution with tissue and dispose of the applicator. To prevent cross contamination of bacteria, you should always use a new applicator for each eye.

How Long Before You See Eyelash Growth with Latisse

Most people begin to see initial results at 8 weeks after the first application. Full results can be expected at 12 to 16 weeks. Latisse was successful in clinical trials, with 78% of participants experiencing significant lash growth, thickening, and darkening.

Side Effects of Latisse

Eye redness and itchiness are the most common side effect of using Latisse. Properly applying the product can decrease the side effects. During clinical trials, these side effects did subside with use.

Latisse may also cause hyperpigmentation of the skin. Hyperpigmnetation is a condition where an increased amount of melanin is present in the skin, producing brown freckle-like spots. It is harmless and in most cases, temporary. Again, following application directions will greatly reduce the risk of hyperprigmentation. Once Latisse is discontinued, the hyperpigmentation usually goes away. However, your doctor may be able to prescribe a topical steroid if needed.

Because ingredients in Latisse are also used to in treatments for glaucoma, there is a rare risk that the iris of the eyes may develop a permanent brown pigmentation. (This side effect was not seen in any clinical trials, but may be a rare possibility.)

Will My Insurance Cover Latisse

Insurance companies see Latisse a cosmetic treatment, not a medical treatment. Your insurance company may or may not cover it if you have lost your eyelashes to chemotherapy. It may take a detailed letter from your doctor explaining why this Latisse is medically necessary. This situation is similar to insurance companies covering the cost of hair pieces and wigs for cancer patients. It may take a lot of letters and phone calls to get your provider to pay for Latisse.

If you choose to go the out-of-pocket route, Latisse costs about $4 a day. That equals to $450 for the 16-week course of treatment. To maintain lash growth, you must use Latisse about twice a week. Once discontinued, lashes return to their normal state.

_Sources:

Allergan. Lattise: What to Expect.
http://www.latisse.com/WhattoExpect.aspx?state=13

American Cancer Society. What are the Possible Side Effects of Chemotherapy? August 8, 2008.
http://www.cancer.org/docroot/ETO/content/ETO_1_4X_What_Are_The_Side_Effects_of_Chemotherapy.asp?sitearea=ETO