Surgery – Body protecting or restraining devices for patients or infants – Nonabsorbent body opening occluders – seals – or supporters
Reexamination Certificate
2000-06-20
2002-04-16
Brown, Michael A. (Department: 3764)
Surgery
Body protecting or restraining devices for patients or infants
Nonabsorbent body opening occluders, seals, or supporters
C604S008000
Reexamination Certificate
active
06371122
ABSTRACT:
FIELD OF THE INVENTION
The present invention is related to the field of keratoconjunctivitis sicca, and specifically to an apparatus for determining the proper size of a punctum plug to be used in treating dry eye.
BACKGROUND OF THE INVENTION
Keratoconjunctivitis sicca (commonly known as “dry eye”) is a chronic, bilateral dryness of the conjunctiva and cornea, marked by hyperemia of the conjunctiva, lacrimal deficiency, thickening of the corneal epithelium, itching and burning of the eye, and often reduced visual acuity(Saunders, W. B.,
Dorland's Illustrated Medical Dictionary
, 27
th
Edition, Harcourt Brace Jovanovich, Inc., Philadelphia, Pa., 1988, page 874). As an isolated phenomenon or in association with systemic diseases, dryness of the eyes occurs when the moisture level in the eye is not maintained by the balance of tear production and tear loss through drainage and evaporation.
Causes of dry eye include aging, hormonal change, a disease state, a medication, a contact lens, or a change in the environment.
In treating dry eye, it is desirable to determine a long term solution which provides for retention of a patient's lacrimal fluid using minimally invasive means. Several methods of treatment are available.
For example, one method of treatment replaces the natural tears using artificial tears. Artificial tears provide temporary relief for dry eyes, but with prolonged use can actually disrupt the eye's natural production of tears and lead to further aggravation of the dry eye condition by washing away the natural infection fighting tear film on the eye. (Berkow, R. and Fletcher, A. J.,
The Merck Manual
, 16
th
Edition, Merck Research Laboratories, Rahway, N.J., 1992, page 2374).
Another method of treatment involves permanent occlusion of the lacrimal punctum (also referred to as “punctum opening”). The occlusion prevents the lacrimal fluid from draining, thereby allowing the eyes to remain moist. Occlusion of the lacrimal punctum has been achieved using non-reversible cautery or laser closure to block lacrimal fluid drainage to the lacrimal canaliculi (tear drainage duct) and in severe cases partial tarsorrhapy is used to reduce loss of tears through evaporation.
Yet another method of treatment involves blocking drainage of lacrimal fluid by temporary non-surgical means, e.g., by use of a punctum plug.
U.S. Pat. No. 3,949,750 to Freeman (issued 1976), incorporated herein by reference, describes a removable rod-like plug for blocking lacrimal fluid flow through the punctum and associated canaliculus of the eye. Insertion of the plug is achieved by first dilating the punctal opening and canaliculus to about three times normal size followed by plug insertion.
Various removable punctum plugs and their use are also described in a number of patents, including: U.S. Pat. No. 5,283,063 to Freeman, issued 1994; U.S. Pat. No. 5,423,777 to Tajiri, issued 1995; U.S. Pat. No. 5,741,292 to Mendius, issued 1998; U.S. Pat. No. 5,318,513 to Lieb, et al., issued 1994; U.S. Pat. No. 5,417,651 to Guena, et al., issued 1995; U.S. Pat. No. 5,723,005 to Herrick, issued 1998; U.S. Pat. No. 6,016,806 to Webb, issued 2000; U.S. Pat. No. 6,041,785 to Webb, issued 2000; and U.S. Pat. No. 6,027,470 to Mendius, issued 2000. Each of the above patents are hereby incorporated by reference.
The punctum plugs can be utilized to close the upper as well as the lower punctal opening. The plugs were meant to firmly seat in the lacrimal punctum, being held in place by the punctal sphincter. In practice, however, they are known to fall out from the punctal opening or pass downward through the canaliculus, causing impassable canalicular stenoses. This occurs when the plug used is too small. On the other hand, too large a plug causes discomfort. Accordingly, determining the right size of the punctum plug to be used for occlusion of the punctum opening is important for successful treatment of dry eye.
SUMMARY OF THE INVENTION
It is an object of the present invention to provide an apparatus for determining the appropriate size of a punctum plug to be used in blocking a lacrimal punctum.
It is an object of the present invention to provide an apparatus for measuring a lacrimal punctum and canaliculus.
It is a further object of the present invention to provide an apparatus for controlled dilation of a punctum and a canaliculus to facilitate insertion of a punctum plug into the lacrimal punctum.
It is a further object of the present invention to provide a method for determining the appropriate size of a punctum plug to be used in blocking a lacrimal punctum.
In accordance with the above-identified objects and others, the present invention is related to an apparatus comprising a handle and a tip positioned at one end of the handle, said tip comprising a gauge (also referred to as “gauge portion”) having a shape and size that allows measurement of a lacrimal punctum as well as the canaliculus associated with said lacrimal punctum.
The gauge may be used to make an accurate measurement of the size (e.g., diameter) of the lacrimal punctum and canaliculus, which in turn allows one to determine what size punctum plug to be used. When a punctum plug is inserted into a lacrimal punctum, at least a portion of it rests on the canaliculus. By measuring the size of the canaliculus, in addition to the lacrimal punctum, and selecting for a plug which at will rest within the lacrimal punctum and the canaliculus and has approximately the same size diameter as the lacrimal punctum and the canaliculus, one can select a better fitting plug. For example, if the canaliculus measured is about 0.7 mm in diameter, a punctum plug of 0.7 mm diameter would be appropriate.
In an embodiment of the invention, the gauge has a plurality of graduating diameters each diameter corresponding to a respective lacrimal punctum and a canaliculus. The gauge can be conical in shape with the gauge gradually increasing in diameter from 0.1 to 1.0 mm and is at least 1.5-2.0 mm in length. One may use the apparatus of the present invention as follows. Insert the tip into the punctal opening slowly inserting apparatus into punctal opening until the sphincter seats flush around the smallest diameter of the handle. Read the marked graduation at this point. At this point, it is recommended that the tip not be inserted farther into the canaliculus, as doing so may cause premature or over-dilation of the sphincter.
In an embodiment, the gauge portion of the apparatus is of cylindrical shape. In an embodiment the gauge has a diameter of about 0.1 mm to about 1.0 mm and a length of 2 mm to 10 cm. In preferred embodiments, the gauge is at least 0.5-2 mm in length and about 0.4-0.9 mm in diameter. Preferably, the tip further comprises a tapered end, located at the end of the gauge, which may facilitate the insertion of the gauge into the punctum opening.
In preferred embodiments of the invention, the tip portion of the apparatus further comprises a dilator (also referred to as “dilator portion”) disposed between the gauge and the handle. After the lacrimal punctum and the canaliculus are measured using the gauge, the dilator portion is inserted into the puncture to dilate it to facilitate the insertion of the plug. Preferably, the dilator is of cylindrical shape and have a diameter that is about 0.1 mm larger than the diameter of the gauge.
In certain embodiments, the apparatus of the present invention further comprises a second tip on the other end of the handle. Accordingly, the apparatus comprises a handle, with a first tip having a first gauge disposed on one end of the handle and a second tip having a second gauge being disposed on the other end of the handle.
In addition, the apparatus may further comprise a first dilator located between the first gauge and the handle, and a second dilator located between the second gauge and the handle. A tapered tip may be provided at the end of the first and the second gauge to facilitate the insertion of the gauge. For example, one handle may contain the first gauge of about 0.4 mm in diameter and the second gau
Brown Michael A.
Davidson Davidson & Kappel LLC
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