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Archive for the ‘Crosslinking’ Category

HOLCOMB C3-R® Corneal Collagen Crosslinking with Riboflavin (CXL or crosslinking): Fighting Keratoconus

Tuesday, June 1st, 2010

Corneal Collagen Cross-linking With Riboflavin (HOLCOMB C3-R®) is an increasingly popular treatment option for vision disorders including Keratoconus. This is the only treatment to stop the progression of Keratoconus, preserve vision, and avoid the need for the invasive long recovery cornea transplant surgery.

HOLCOMB C3-R® improves corneal structuring that has been weakened. It strengthens and stops the advanced symptoms of Keratoconus. In many cases vision distortions are decreased and effectively alleviated. HOLCOMB C3-R® treatments increase the amount of collagen cross-linking within the cornea. These cross links are natural anchors and provide stability to the shape of the cornea. The affects of Keratoconus cause corneas to thin out. As they thin, shape is compromised due to the intraocular pressure beneath. The pressure causes the cornea to bulge outward distorting the surface and causing light rays to enter the eyeball at improper angles. Without medical intervention, as Keratoconus progresses, it can seriously disrupt the quality of an individual’s lifestyle. Additionally, central cornea scarring may also develop.

Keratoconus changes refractive errors of the cornea and causes differing degrees of blurriness to occur. For certain patients, advanced Keratoconus may only be non-surgically treated by RGP (rigid gas-preamble) corrective lenses. HOLCOMB C3-R® collagen crosslinking with riboflavin restores the integrity of the corneas shape by creating more anchoring devices within the structure of the cornea itself. Taking only 30 minutes per eye, HOLCOMB C3-R® treatments utilize eye drops containing modified riboflavin. These drops are activated by a source of ultraviolet light. As the riboflavin becomes active, collagen cross-linking is increased and quality of vision is improved and preserved.

HOLCOMB C3-R® collagen crosslinking techniques may also be implemented in conjunction with Intacs® cornea inserts to more effectively battle the chronic symptoms of keratoconus. Intacs® cornea inserts are super-thin medical-grade plastic inserts that are inserted, via very small incisions, into sub-corneal regions in order to reverse the corneal bulging associated with keratoconus. Intacs® are FDA-approved. They are also the only refractive surgery technique that actually adds corneal structural integrity to an eye with Keratoconus.

Modern vision enhancement techniques and products, including HOLCOMB C3-R® collagen crosslinking with riboflavin and Intacs® corneal inserts, are reversing and eliminating the serious vision loss of keratoconus for Americans everywhere. Begin preserving your vision by learning more today.

View a free information webinar: www.FixesYourKC.com

Learn more about keratoconus treatments today: www.KeratoconusInserts.com

Fast Facts about C3-R (Cornea Collagen Crosslinking with Riboflavin and UV light)

Tuesday, June 1st, 2010

Previously patients told they have keratoconus had no option but to wait for their vision to deteriorate until they no longer could achieve good vision and then undergo the invasive cornea transplant procedure.

 

C3-R® (cornea collagen crosslinking), aka CXL or UV Crosslinking, is a simplistic, minimally invasive procedure that:

*Treats keratoconus and various similar conditions such as post LASIK Ectasia, Pellucid Marginal Degeneration, irregular cornea after RK;

*Helps to reverse some of the distortion of the cornea;

*Prevent further corneal distortion from occurring;

*Preserves vision and decreases the need for corneal transplants;

The cornea collagen crosslinking procedure:

*Drops of liquid riboflavin are applied to saturate the cornea 10-15 minutes prior to the application of UV light;

*Riboflavin is activated by a small amount of UV light;

*This strengthens and stabilizes the weakened links between the corneal fibers;

*The majority of patients to not require more than one treatment;

*Has very few postoperative complications associated;

*Can be completed in about 30 minutes per eye;

Explore the cost efficiency, simplicity and effectiveness of CR-3 cornea collagen crosslinking more today and begin looking forward to a future of clearer vision!

 

View a free information webinar: www.FixesYourKC.com

Learn more about keratoconus treatments today: www.KeratoconusInserts.com

 

 

 

 

 

 

 

 

 

Facts about CR-3: Cornea Collagen Crosslinking, CXL, UV Crosslinking

Tuesday, May 18th, 2010

The cornea is the transparent membrane (window like) that covers the front of the eyeball. It is comprised of millions of corneal fibers that are linked together for strength. This maintains the cornea’s natural shape. Certain medical conditions, including keratoconus, act to weaken the individual links between the corneal fibers. This in turn alters the shape of the cornea. With misshaped corneas, an individual will develop distorted vision, and the condition will worsen as time progresses.

Individuals with keratoconus have a bulging (like a hernia) of the cornea structure. This can make it difficult to fit the contacts due to the irregular cornea shape.

Those with poor vision use a variety of products and procedures to correct it. Eyeglasses, contact lenses, corneal implant procedures and more are used. However, in many cases, the weakening of the cornea progresses to the point where the cornea itself must be replaced with a procedure called a cornea transplant. The hope is that a new cornea will help to restore vision quality. Corneal transplants are invasive medical procedures that require lengthy periods for healing, up to one year for each eye. They are also expensive, cause individuals to lose time at work and are known to present considerable risks for postoperative complications. Usually patients will have to have a cornea transplant repeated every 10-20 years.

C3-R® (cornea collagen crosslinking with Riboflavin), aka CXL or UV Crosslinking, is a simplistic, minimally invasive procedure that has been effective for stabilizing corneas and avoiding the need for cornea transplant for patients with:

• Keratoconus
• Post- LASIK Ectasia
• Pellucid Marginal Degeneration
• Irregular cornea after RK;
• Helps to reverse some of the distortion of the cornea;
• Prevent further corneal distortion from occurring;
• Preserves vision and decreases the need for corneal transplants;

The cornea collagen crosslinking procedure is a one time office based procedure that takes approximately 45 minutes.

Explore the cost efficiency, simplicity and effectiveness of CR-3 cornea collagen crosslinking more today and begin looking forward to a future of clearer vision!

View a free information webinar: http://www.FixesYourKC.com

Learn more about keratoconus treatments today: http://www.KeratoconusInserts.com

Keratoconus Treatment Expectations

Saturday, April 17th, 2010

Keratoconus or Pellucid Marginal Degeneration are progressive non-inflammatory disorders that causes a characteristic thinning and cone-like steepening of the cornea. This steepening results in distortion of vision, increased sensitivity to glare and light and an associated reduction in visual acuity. 

 

 

Historically patients were told that they would have to endure painful RGP (rigid gas perm or hard) contacts until the point they could no longer wear contacts or obtain good vision in contacts.  At this point the patient was referred for a cornea transplant.

 

 

In 1998, Dr. Brian Boxer Wachler began exploring alternatives to avoid a cornea transplant and restore good vision for patients with keratoconus

 

 

Today there are 3 primary treatments for keratconusto avoid the need for a cornea transplant; Cornea Collage Crosslinking (C3-R), INTACS, and Conductive Keratoplasty (CK).

 

 

C3-R(cornea collagen crosslinking)treatment is the first line defense for keratoconus. This is a 45-minute in office treatment that consists of an application of a special riboflavin solution to the cornea which is activated by a UV light source; this treatment strenghtens the cornea.  C3-R(cornea collagen crosslinking)is the only known treatment that halts the progression of keratoconus.  The youngest patient treated to date has been 9 years old.  

 

If a patient is has begun to experience decrease quality of vision from keratoconus, INTACS can be combined with C3-R(cornea collagen crosslinking)to improve the quality of vision.  INTACS strengthens the cornea and decrease the cone-like shape from keratoconus. It is similar to added a beam to a building to increase structural support.   This aids in improving the fit and comfort of contact lenses as well as improve the quality of vision. INTACS are designed to remain inserted for a lifetime.  However, if technology changes they can be removed so a patient can proceed with a different technology to help improve the cornea. 

 

The goal of CK is to help reduce astigmatism. When combined with C3R (cornea collagen crosslinking) the CK treatment can effectively reduce astigmatism for a period of several years.  Due to the nature of the cornea in Keratoconus patients the effect of CK can diminish with time.  Patients may elect to have future CK to reduce astigmatism, if needed.

 

 

You can learn more about these treatments at: www.KeratoconusInserts.com

 

 

You can watch an informative video at: www.FixesYourKC.com  

Holcomb C3-R®- Cornea Collagen Crosslinking with Riboflavin for the Treatment of Keratoconus

Saturday, April 10th, 2010

Keratoconus

Keratoconus or Pellucid Marginal Degeneration is a progressive non-inflammatory disorder that causes a characteristic thinning and cone-like steepening of the cornea. This steepening results in distortion of vision, increased sensitivity to glare and light and an associated reduction in visual acuity. These symptoms usually appear in the late teens and early twenties. Keratoconus may progress for 10-20 years and then can slow or even stabilize. Each eye can be affected differently. This can result in a dramatic decrease in the ability to see clearly even with corrective lenses. (Note:  as keratoconus and pellucid are the same disease process, any reference to “keratoconus” also applies to “pellucid” as well.)

 

Why consider Holcomb C3-R® (Cornea Collagen Crosslinking) procedure for treatment of Keratoconus?

A non–surgical procedure Holcomb C3-R® (corneal collagen cross-linking riboflavin) procedure can strengthen the weak corneal structure in keratoconus. This method works by increasing collagen cross-linking, which are the natural “anchors” within the cornea. Essentially the Holcomb C3-R® cause new links to build between the weakened layers of the cornea creating a stronger cornea. These anchors are responsible for preventing the cornea from bulging out and becoming steep and irregular (which is the cause of keratoconus).

 

What do chicken wire and Keratoconus have in common?

In keratoconus, the cornea has weakened structural support; fewer collagen cross-links or like a fence that has become weakened. This weakened structure allows the cornea to bulge outwards. The Holcomb C3-R® (cornea collagen crosslinking with riboflavin) procedure is like placing chicken wire over a fence or crosslinking to the cornea, making it more stable and reinforced.  Chicken wire keeps the animals from getting out through a weakened fence; much like Holcomb C3-R® keeps the cornea from bulging out.

 

Will my vision improve after Holcomb C3-R®?

Holcomb C3-R® is vision preserving and stabilizing treatment.  Although it is not considered a vision correction procedure, many patients note that their vision has less fluctuation, less ghosting and appears crisper/sharper.  The full effect of Holcomb C3-R® occurs around 3-6 months after the procedure. A recent study that followed patients after Holcomb C3-R® reported that patients continued to have decreased astigmatism over a 5 year period of time.[1]

 

Can I wear contacts after Holcomb C3-R®?  Will I need new glasses or contact lens prescription?

Patients can return to wearing contact lenses the day after the Holcomb C3-R®procedure.  Patients who have had Holcomb C3-R®combined with INTACS or CK (conductive keratoplasty) will need to be re-fitted for contacts 10-14 days after the procedure and can resume wear 14 days after the procedures.

 


Most patients undergoing the Holcomb C3-R® will have new glasses or contact lenses prescribed 3-6 months after the procedure.  Patients who have a combination procedure, Holcomb C3-R® with INTACS or CK, will need a new glasses prescription 3-4 days after procedure and can obtain a new contact lens prescription 10-14 days after the procedure.

 

View a free information webinar: www.FixesYourKC.com

 

Learn more about keratoconus treatments today: www.KeratoconusInserts.com

[1] Wollensak G, Spoerl E, Seiler T.; Riboflavin/ultraviolet-a-induced collagen cross-linking for the treatment of keratoconus.  AJO 2003 May;135(5):620-7

 


Referring Keratoconus Patients for Surgical Management

Tuesday, March 16th, 2010

Referral criteria

While 80% to 85% of patients with keratoconus can be managed with spectacles, soft and rigid contact lenses to correct for visual acuity and astigmatism, in 15% to 20% of the keratoconic population, a corneal transplant is eventually required unless the patient undergoes Cornea Collagen Crosslinking (C3-R) and/or INTACS to halt the progression of disease.

Many surgeons are not aware of the less invasive Cornea Collagen Crosslinking (C3-R) developed in Dresden in the 1990s as a less invasive alternative to halt the progression of keratoconus . Patients who are referred for Cornea Collagen Crosslinking (C3-R) avoid the need for a cornea transplant in 99.0% of all referred cases.

The following are the considerations that should be made to referral for surgical management:

Cornea Collagen Crosslinking (C3-R) Referral

1) Diagnosed with keratoconus

Cornea Collagen Crosslinking (C3-R)  and INTACS Referral

1) Contact lens intolerance especially with recurrent abrasions;
2) Inability to fit the patient with a contact lens (including frequent lens loss);
3) Decreased vision (generally from scarring) which prevents the patient from doing necessary visual tasks; and
4) Large cone with progressive thinning in the periphery 

Cornea Transplant Referral

1) The danger of perforation, though rare in keratoconus.

Outcomes with Less Invasive Treatment INTACS

In most cases, the patients’ uncorrected visual acuity and best-corrected visual acuity show marked improvements.  A high percentage of these patients were candidates for an imminent transplant. The reshaped cornea, after the INTACS procedure, is typically aided by the use of glasses or soft contact lenses in order to provide improved functional vision to the patient and reduce the eye irritation previously experienced with the RGP contact lenses. 

Studies have shown that INTACS placements can restore functional vision by allowing most patients to be effectively corrected with contact lenses or glasses, if needed.  Specifically, Boxer Wachler, et. al. found that (1) the mean improvement was 4 lines UCVA and 2 lines BCVA, (2) those with less than two lines of improvement in BSCVA still improved UCVA by 2 lines or better in 60 percent of cases, (3) irregular astigmatism was reduced across the board, and (4) the number of lines of correction ranged from up to ten lines BSVCA and from counting fingers UCVA. These results were replicated by Colin, et. al., whose prospective study of 10 patients found that both BCVA and UCVA improved in more than 50% of those patients.

Researchers concluded that use of INTACS in patients with keratoconus is an effective way to manage the condition and restore functional acuity to patients.  Boxer Wachler goes farther, to say, “INTACS is to be a logical addition to the stepwise treatment of keratoconus that improves visual acuity and, in a number of patients, has negated the need for corneal transplantation, thus far.”

Surgical Treatment with Cornea Transplant

Penetrating keratoplasty (full cornea transplant) is the most common. In this procedure, the keratoconic cornea is prepared by removing the central area of the cornea, and a full-thickness corneal button is sutured in its place. An alternative is lamellar keratoplasty (partial corneal transplant); it should be noted that this alternative is used in less than 5% of cases. The cornea is removed to the depth of posterior stroma, and the donor button is sutured in place. This technique is technically difficult, and visual acuity is inferior to that obtained after penetrating keratoplasty. Its disadvantages include vascularization and haziness of the graft.

Clinical Challenges of Cornea Transplant

The eye-care practitioner must decide when to recommend keratoplasty for the keratoconic patient. This is often not a simple, straightforward decision. Keratoplasty for keratoconus is highly successful; however, there is a long recovery period and a risk of severe ocular complications. A number of factors must be considered in deciding when to do a keratoplasty. One of the most important factors is the patient’s functional vision. If the best acuity with their contact lenses prevents them from doing their job or carrying out their normal activities, or when the contact lenses cannot be worn more than a few hours a day, a transplant must be considered. The actual measured visual acuity may be quite different for different patients. One patient may find that he/she cannot do their job with 20/30 acuity while another patient may be very satisfied with 20/60 acuity.

Very careful contact lens fittings are necessary before recommending a corneal transplant. Prior to transplant every effort should be made to optimally fit the patient with contact lenses, especially if there is not significant corneal scarring affecting vision. Also, referral for less invasive procedures such as Cornea Collagen Crosslinking (C3-R) and/or INTACS.

However, a minority of patients becomes intolerant to contact lenses, and requires a transplant earlier than otherwise would be necessary. If the patient has a large area of thinning, a very decentered cone or significant blood vessel growth into the usually clear cornea, called neovascularization, a transplant may be performed earlier than otherwise indicated by the visual performance, as these factors may require a larger than normal transplant button size and/or increase the chance of rejection if allowed to advance too far.
The healing process following transplant is long, often taking a year or longer. The time from surgery to the removal of the stitches is commonly 6 to 17 months. The patient may be on steroids for months. Initially following surgery the donor button is swollen and even following healing the button is usually thicker than the corneal bed in which it rests.

Large amounts of astigmatism are common following keratoplasty. One such study found an average of 5.56 diopters of correction (DC) with a range from 0 to 17 diopters following suture removal . The patient’s spectacle prescription may fluctuate for some months following surgery. Refractive changes and keratometry or corneal topography can be used to follow the healing process.

Graft rejection reactions occur in 18% to 20% of the patients. Signs of graft rejection include ciliary flush, anterior chamber flare, keratic precipitates, Khodaoust line and Krachmer’s spots. Signs of graft rejection are reported to occur from 1 month to 5 years following surgery. The rejection rate for bilateral grafts is higher than if only one eye is grafted. In the bilateral cases, when a rejection reaction occurs it is commonly in both eyes. If the second eye is to be grafted, there is usually a period of at least a year between grafts. If signs of rejection occur, aggressive treatment with steroids is begun. Usually the reaction is overcome and the graft remains clear. A high percentage of the corneal grafts are successful. However, visual rehabilitation is slow (6 months to 1 year), and keratoconus may recur 15-20 years later in the corneal transplant. As significant, and of particular concern to younger patients, it is commonly understood and addressed in peer-reviewed literature that corneal grafts have a limited life, and that subsequent attempts to graft are less successful than the first.

View a free information webinar: www.FixesYourKC.com

Learn more about keratoconus treatments today: www.KeratoconusInserts.com

Historic Olympic Gold for Someone Once going Blind

Saturday, February 27th, 2010

Three years ago I shook hands with Steve Holcomb who was forced to retire as the top U.S. Olympic bobsled driver due to becoming legally blind from a degenerative eye disease known as Keratoconus where the cornea (outer lens) herniates out.  Today, February 27,2010 at the Winter Olympics in Vancouver, Steve walked away with a Gold medal, the first for the U.S. in bobsled in 62 years (last time that happened was when Harry Truman was president!)  An incredible, miracle comeback of all comebacks.

Learn more about Steve’s amazing story at: www.KeratoconusInserts.com

Being A Part of the Olympic Experience

Thursday, February 25th, 2010

Dr. Brian Boxer Wachler reported, “It is amazing to be in the Olympic arena, live, watching these talented athletes compete, and knowing that across the globe, there are three-billion other people watching too.   Being surrounded by such a strong force; makes you realize we are truly part of something huge.”

Dr. Brian Boxer Wachler is at the Olympics to cheer on Steve Holcomb as he goes for Olympic Gold in the 4-man bobsled competition.  Holcomb’s keratoconus was halted almost 2 years ago with the ground-breaking C3-R procedure.   

Go Team Night Train

Wednesday, February 24th, 2010

The track is slick and ready for Steve Holcomb’s Team, “Night-Train”, to steer towards the gold. 

Only a short time left until Steve Holcomb and his U.S. bobsled team compete.  Holcomb’s story has taken world stage after his miraculous vision saving procedure C3-R with Dr. Brian Boxer Wachler.  Only two years ago, Holcomb thought his dreams of Olympic Gold were fading away. Now with Holcomb’s vision restored he has his sight set for Gold.

Team Night-Train races tomorrow, Thursday, February 25th.  Be sure to support!

Feeling Alright About Improving Vision

Tuesday, February 23rd, 2010

It has been an immensely rewarding to have been a part of the Olympic experience.  I am so happy to have helped an individual with as much talent and honor as Steve.   It is amazing to think that only a year ago, he was legally blind and facing an early retirement from his bobsled career.  Luckily, after undergoing the C3-R procedure his vision is clearer than ever, and he’s ready to win Olympic gold!

Only two more days until Steve will take the track towards Olympic Gold on February 25th.  Tonight I am packing my bags to head up to Vancouver on Wednesday.