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Anatomy and Pathophysiology for ICD-10 Module 10

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Page 1: Module 10 - Amazon Web Servicesaapcperfect.s3.amazonaws.com/3f227f64-019f-488a-b5a2-e... · 2014-08-12 · in understanding how to prepare for ICD-10-CM. Although every reasonable

Anatomy and Pathophysiology

for ICD-10

Module 10

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ii Anatomy and Pathophysiology for ICD-10 © 2014 AAPC. All rights reserved.

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DisclaimerThis course was current at the time it was published. This course was prepared as a tool to assist the participant in understanding how to prepare for ICD-10-CM. Although every reasonable effort has been made to assure the accuracy of the information within these pages, the ultimate responsibility of the use of this information lies with the student. AAPC does not accept responsibility or liability with regard to errors, omissions, misuse, and misinterpretation. AAPC employees, agents, and staff make no representation, warranty, or guarantee that this compilation of information is error-free and will bear no responsibility, or liability for the results or consequences of the use of this course.

AAPC does not accept responsibility or liability for any adverse outcome from using this study program for any reason including undetected inaccuracy, opinion, and analysis that might prove erroneous or amended, or the coder’s misunderstanding or misapplication of topics. Application of the information in this text does not imply or guarantee claims payment. Inquiries of your local carrier(s)’ bulletins, policy announcements, etc., should be made to resolve local billing requirements. Payers’ interpretations may vary from those in this program. Finally, the law, applicable regulations, payers’ instructions, interpretations, enforcement, etc., may change at any time in any particular area.

This manual may not be copied, reproduced, dismantled, quoted, or presented without the expressed written approval of the AAPC and the sources contained within. No part of this publication covered by the copyright herein may be reproduced, stored in a retrieval system or transmitted in any form or by any means (graphically, electronically, or mechanically, including photocopying, recording, or taping) without the expressed written permission from AAPC and the sources contained within.

ICD-10 ExpertsRhonda Buckholtz, CPC, CPMA, CPC-I, CGSC, CPEDC, CENTC, COBGC VP, ICD-10 Training and Education

Betty Hovey, CPC, CPMA, CPC-I, CPC-H, CPB, CPCD Director, ICD-10 Development and Training

Jackie Stack, CPC, CPB, CPC-I, CEMC, CFPC, CIMC, CPEDC Director, ICD-10 Development and Training

Peggy Stilley, CPC, CPB, CPMA, CPC-I, COBGC Director, ICD-10 Development and Training

Illustration copyright © OptumInsight. All rights reserved.

©2014 AAPC2480 South 3850 West, Suite B, Salt Lake City, Utah 84120

800-626-2633, Fax 801-236-2258, www.aapc.comRevised 061914. All rights reserved.

CPC®, CPC-H®, CPC-P®, CPMA®, CPCO™, and CPPM® are trademarks of AAPC.

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Contents

Module 10 Eye and Adnexa . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1

Terminology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1Adnexa Structure and Function . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3Diseases and Disorders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3ICD-10-PCS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10

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TerminologyAccommodation—The ability of the lens to focus clearly on objects at various distances.

Amblyopia—Reduced vision that is not correctable by lenses and has no pathological cause.

Aphakia—Absence of the lens of the eye.

Blepharoptosis—Drooping of the upper eyelid.

Blepharospasm—A condition causing the eyelid muscles to twitch.

Corneal Topography—Process for mapping the surface curvature of the cornea.

Diplopia—Double vision caused by each eye focusing separately.

Esotropia—An obvious inward turning of one eye in relation to the opposite eye.

Exotropia—An obvious outward turning of one eye in relation to the opposite eye.

Gonioscopy—A diagnostic test used to view the ante-rior chamber angle of the eye to determine if abnormal angle structure is present.

Keratoconjunctivitis—Inflammation of the cornea and the conjunctiva of the eye.

Optician—A healthcare professional (not an M.D.) who specializes in filling prescriptions for glasses or contact lenses.

Optometrist—A doctor of optometry (O.D.) who exam-ines the eye to determine problems and writes prescrip-tions for glasses or contact lenses.

Pseudophakia—Indicates the natural lens of an eye has been replaced with an intraocular lens.

Refraction—A test performed by an eye doctor to deter-mine the prescription required to correct one’s vision.

Slit-lamp exam—A low powered microscope combined with a high-intensity light source used to examine the internal and external structures of the eye.

Strabismus—Failure of the eyes to gaze in the same direction due to weakness in the muscles controlling the position of one eye.

IntroductionThe eyes are the most complex of all the sensory organs involving a much larger area of the brain than other senses. The cells of the eye that support vision are typi-cally activated by a stimulus, such as light. They collect light waves and transmit them as nerve impulses along the visual pathways to the brain, which translates them to images.

The eye is often compared to a camera. Each gathers light and then transforms that light into a “picture.” Both also have lenses to focus the incoming light. A camera uses the film to create a picture, whereas the eye uses a specialized layer of cells, called the retina, to produce an image.

Eye Anatomy and FunctionSeveral structures compose the eye. Among the most important anatomical components are the cornea, conjunctiva, iris, crystalline lens, vitreous humor, retina, macula, optic nerve, and extraocular muscles.

Globe(Eyeball)

Sclera

Cornea

Iris

Pupil

Anteriorchamber

Posteriorchamber

Ciliarybody

Conjunctiva

Retina

Lens

Hyaloidcanal

Vitreousbody

Fovea

Opticdisk

Opticnerve

Laminacribosa

Choroid (uvea)

Copyright OptumInsight. All rights reserved

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There are three layers of tissue that compose the spher-ical structure of the eye—the sclera (the outermost layer), the choroid (the middle layer), and the retina (the innermost layer). Within each of these layers are further subdivided regions that entail more specific functions.

Sclera and cornea—the sclera, which is the outermost layer, consists of tough fibrous tissue to protect it from the external environment. It is visible as the white part of the eye and it assists in maintaining the “globe” shape. The sclera includes two episcleral layers called Schlemm’s canal and trabecular meshwork.

Schlemm’s canal, also known as the scleral venous sinus, is a “tube” (resembling that of a lymphatic vessel) in the eye that collects aqueous humor from the anterior chamber and delivers it into the blood stream via the anterior ciliary veins.

Trabecular meshwork is an area of tissue in the eye located around the base of the cornea, near the ciliary body. It is made up of spongy tissue, lined by trabecu-locytes, and allows fluid to drain from the eye into Schlemm’s canal via the anterior chamber.

The anterior cornea is also located in the outermost layer of the eye. It is made up of a transparent fibrous coat covering the front of the eye including the iris, pupil, and anterior chamber. The cornea works with the lens to refract light, accounting for approximately two-thirds of the eye’s total optical power. Initially, the light waves are converged (bent) by the cornea. The crystalline lens further bends the waves and the image becomes backwards and upside down. Lacrimal glands keep the surface of the cornea moist and free from foreign bodies.

The choroid is the middle layer of tissue next to the sclera. There are three regions in this middle layer: choroid, ciliary body, and iris. The choroid is a highly vascularized area that surrounds most of the eye to provide oxygen and nutrients to the outer layers of the retina. Together the choroid, ciliary body, and the iris form the uveal tract.

The ciliary body produces aqueous humor, which is important to the function of the eye as it provides not only optical power to the cornea, but also assists in maintaining intraocular pressure, shape to the globe, and assists in the delivery of nutrients to tissues. Suspen-sory ligaments attach the lens to the ciliary muscle.

When the ciliary body contracts, the suspensory liga-ments relax causing the lens to thicken, allowing the ability to focus up close. Viewing distant objects causes the ciliary body to relax and the suspensory ligaments to contract. The lens becomes thinner, allowing the ability to focus far away.

Light waves from an object enter the eye through the cornea. The iris is the colored portion of the eye, which helps to regulate the amount of light entering the eye by controlling the size of the pupil. The pupil is seen from the outside as the black innermost circle of the eye within the iris. Bright lights cause the pupil to constrict (get smaller), while dim lighting causes the pupil to dilate (get larger). Often, the ophthalmologist will put drops in the eyes to dilate them so he or she can perform a comprehensive exam of the eye. The external object is seen like the camera takes a picture of an object. Light enters through the pupil and is focused on the retina, much like camera film.

The retina is the inner layer of the eye consisting mainly of nervous tissue. Its inner, transparent neural layer contains photoreceptors (rods and cones) for processing of external images. The retina of the eye contains about 137 million light-sensitive cells in an area of about 650 sq. mm/1 sq. in. There are 130 million rod cells for black and white vision and 7 million cone cells for color vision. The focusing muscles of the eye adjust about 100,000 times a day. In the center of the retina is the optic nerve, a circular to oval white area. Major blood vessels radiate from the center of the optic nerve, which contains about 1 million nerve fibers.

Light rays enter the eye and converge on the retina, where an upside-down image is created. The retina of each eye relays impulses to the brain through the optic nerves, which cross paths at a junction call the optic chiasm; half the nerve fibers from the right eye cross to the left, and vice versa, before passing on to the brain. In the visual cortex the image is turned upright.

Near the center of the retina is an oval-shaped highly pigmented yellow spot called the macula. Due to the yellow color of the macula it absorbs excess blue and ultraviolet light that enter the eye, and acts as a natural sunblock for this area of the retina. Within the macula is the fovea, a small pit that contains the largest concen-tration of cone cells in the eye and is responsible for

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central, high-resolution vision. If the macula begins to degenerate, central vision begins to diminish.

The anterior chamber is the space in the eye that is behind the cornea and in front of the iris. The poste-rior chamber is the space in the eye that is behind the iris and in front of the lens. The anterior and posterior chambers contain aqueous humor, a clear, watery fluid similar in composition to blood plasma. The posterior cavity contains vitreous humor, a thick, clear, gelatinous fluid making up about 80 percent of the eye’s volume.

Adnexa Structure and FunctionThe eyeball is set in a protective cone-shaped cavity in the skull called the “orbit” or “socket.” Layers of soft, fatty tissue to add additional protection, and allow the eye to turn easily surround the orbit. The acces-sory visual structures or adnexa of the eye include the eyelids, eyebrow, and eyelashes. All help to protect the eye, along with the lacrimal glands that lubricate the eye to reduce the risk of injury and remove small particles of material from the surface of the eye. Eyebrows and eyelashes filter out large materials that could cause inju-ries to the eye, keeping the surface of the eye as clean as possible to reduce the risks of irritation and infection. They also protect from very bright lights that may cause damage to the eye.

The conjunctiva lubricates the eye by producing mucus and tears. It is typically divided into three parts:

• Palpebral or tarsal conjunctiva lines the eyelids.• Bulbar or ocular conjunctiva covers the outer surface

of the eye and moves with the eyeball. It is tightly bound to the underlying sclera by Tenon’s capsule.

• Fornix conjunctiva are loose arching folds that connect the bulbar and palpebral conjunctivae, allowing independent movement of the lids and eyeballs.

There are six small muscles located in the orbit that are responsible for the movements on the eye. These are known as the extraocular muscles due to the fact that they are outside of the eyeball. The actions of the extraocular muscles depend on the position of the eye at the time of muscle contraction. Five of these muscles

originate in the back of the orbit in a fibrous ring called the annulus of Zinn. The functions of the muscles are:

• Superior rectus—elevation, intorsion (rotation towards the center of the body) and adduction.

• Inferior rectus—depression, adduction, and lateral rotation of the eye.

• Lateral rectus—abduction or moving the pupil away from the midline of the body.

• Medical rectus—adduction or moving the pupil towards the midline of the body.

• Superior oblique—abduction, depression, and internal rotation of the eye.

• Inferior oblique—lateral rotation, elevation, and abduction of the eye.

Iris

Cornea

Lens

Ciliarysuspensoryfibers

Trebeculae

Sclera

Posteriorpolar cataract

Anterior polarcataract

Corticalcataract

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Diseases and DisordersCataracts A cataract is a clouding that develops on the lens of the eye, which can obstruct the amount of light that comes through. There are varying degrees of opacity. Cata-racts typically progress slowly causing loss of vision. Left untreated they can potentially lead to blindness. The condition usually affects both eyes, but most often,

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one eye becomes affected earlier than the other. There are three different types of age related (senile) cataracts, which are characterized by their location on the lens:

• Nuclear sclerotic cataracts affect the center of the lens and are known to be the most common types of cataracts resulting from advancing age. They interfere with the ability to see far away.

• Cortical cataracts begin at the outer rim of the lens and gradually go to the center, resembling the spokes of a bicycle wheel and are most commonly found in people with diabetes.

• Posterior subcapsular cataracts affect the back of the lens causing glare and blurriness. These are considered the most rapidly progressive types of cataracts.

Cataracts are treated in various ways. Initially, they may be treated by a change in the eyeglass prescription. However, as they progress, surgery is the most common way to remove the cataract. There are three different types of surgery available:

• Phacoemulcification or photoemulcification is a type of extracapsular surgery in which the lens is softened with sound waves and then removed through a needle. A tiny probe is inserted through a very small incision on the side of the cornea producing a vibration at an extremely high rate of speed caused by high frequency sound waves. The ultrasonic vibration breaks the cataract into fine pieces, which are suctioned out of the eye through the needle. After all the cataract material is removed, the back half of the lens is left behind and the artificial lens is placed inside. The small incision closes on its own.

• Extracapsular surgery involves removing the eye’s natural lens through a large incision, while leaving the back of the lens in place (which holds the lens in place).

• Intracapsular surgery is the removal of the lens and the surrounding lens capsule all in one piece. It is rarely used any longer due to the relatively high rate of complication due the large size if the incision required for this procedure.

The ICD-10-CM code range for cataracts is H25.011–H28.

To code a cataract in ICD-10-CM the following is necessary:• Type of cataract• Laterality

Cortical age-related cataract, right eye H25.011

Cortical age-related cataract, left eye H25.012

Cortical age-related cataract, bilateral H25.013

Cortical age-related cataract, unspecified eye H25.019

Anterior subcapsular polar age-related cataract, right eye H25.031

Anterior subcapsular polar age-related cataract, left eye H25.032

Anterior subcapsular polar age-related cataract, bilateral H25.033

Anterior subcapsular polar age-related cataract, unspecified eye H25.039

Posterior subcapsular polar age-related cataract, right eye H25.041

Posterior subcapsular polar age-related cataract, left eye H25.042

Posterior subcapsular polar age-related cataract, bilateral H25.043

Posterior subcapsular polar age-related cataract, unspecified eye H25.049

In the above table, the laterality issue is shown. Note the fifth digits in the codes. The fifth digit of 1 denotes the right eye, the fifth digit of 2 denotes the left eye, the fifth digit of 3 denotes bilateral eyes, and the fifth digit of 9 denotes unspecified eye.

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Module 10 Eye and Adnexa

There are no ICD-10-CM guidelines related to this disease.

GlaucomaGlaucoma refers to a group of eye conditions that lead to damage to the optic nerve, the nerve that carries visual information from the eye to the brain. In many cases, damage to the optic nerve is due to increased pressure in the eye, also known as intraocular pressure (IOP). Glau-coma is the second most common cause of blindness in the United States.

The front part of the eye is filled with aqueous humor. This fluid is always being made in the back of the eye. It leaves the eye through channels in the front of the eye in an area called the anterior chamber angle, or simply the angle. Anything that slows or blocks the flow of this fluid out of the eye will cause pressure to build up in the eye.

Glaucoma can be divided roughly into two main categories, “open angle” and “closed angle” glaucoma. Closed angle glaucoma can appear suddenly and is often painful; visual loss can progress quickly but the discomfort often leads patients to seek medical attention before permanent damage occurs. Open angle, chronic glaucoma tends to progress at a slower rate and the patient may not notice that they have lost vision until the disease has progressed significantly.

There are two other types of glaucoma as well, congen-ital and secondary. Congenital glaucoma is hereditary so it is present at birth, resulting from abnormal develop-ment of the fluid outflow channels in the eye. Secondary glaucoma is the result of other conditions such as use of certain drugs (corticosteroids, some eye conditions, or systemic diseases).

Source: AAPC

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The ICD-10-CM code range for glaucoma is H40.10–H42.

To code glaucoma in ICD-10-CM the following is necessary:

• Type of glaucoma• Laterality

Acute angle-closure glaucoma, right eye H40.211

Acute angle-closure glaucoma, left eye H40.212

Acute angle-closure glaucoma, bilateral H40.213

Acute angle-closure glaucoma, unspecified eye H40.219

Chronic angle-closure glaucoma, right eye H40.221

Chronic angle-closure glaucoma, left eye H40.222

Chronic angle-closure glaucoma, bilateral H40.223

Chronic angle-closure glaucoma, unspecified eye H40.229

One of the following 7th characters is to be assigned to each code in subcategory H40.22 to designate the stage of glaucoma.

0 stage unspecified1 mild stage2 moderate stage3 severe stage 4 indeterminate stage

Intermittent angle-closure glaucoma, right eye H40.231

Intermittent angle-closure glaucoma, left eye H40.232

Intermittent angle-closure glaucoma, bilateral H40.233

Intermittent angle-closure glaucoma, unspecified eye H40.239

In the previous table, the laterality issue is shown. Note the fifth digits in the codes. The fifth digit of 1 denotes the right eye, the fifth digit of 2 denotes the left eye, the fifth digit of 3 denotes bilateral eyes, and the fifth digit of 9 denotes unspecified eye.

Currently there are no ICD-10-CM guidelines related to this disease.

Retinal DetachmentsRetinal detachments are often associated with a tear or hole in the retina through which eye fluids may leak. This causes separation of the retina from the underlying tissues. Once the retina has torn, liquid from the vitreous gel can then pass through the tear and accumulate behind the retina. The buildup of fluid behind the retina is what separates (detaches) the retina from the back of the eye.

As more of the liquid vitreous collects behind the retina, the extent of the retinal detachment can progress and involve the entire retina, leading to a total retinal detachment. A retinal detachment almost always affects only one eye at a time. The second eye, however, must be checked thoroughly for any signs of predisposing factors that may lead to detachment in the future.

Retinal detachment often occurs on its own without an underlying cause. However, it may also be caused by trauma, diabetes, or an inflammatory disorder. It is most often caused by a related condition called posterior vitreous detachment.

During a retinal detachment, bleeding from small retinal blood vessels may cloud the interior of the eye, which is normally filled with vitreous fluid. Central vision becomes severely affected if the macula, the part of the retina responsible for fine vision, becomes detached.

Some symptoms associated with retinal detachment include bright flashes of light in the peripheral vision, blurred vision, and floaters in the eye. Most patients with a retinal detachment will need surgery, either immediately or after a short period of time.

Types of surgery include:

• Cryopexy (intense cold applied to the area with an ice probe) to help a scar form, which holds the retina to the underlying layer

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• Laser surgery to seal the tears or holes in the retina• Pneumatic retinopexy (placing a gas bubble in the

eye) to help the retina float back into place

Vitreous

Retina

Choroid

Sclera

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More extensive detachments may require surgery in an operating room. Such procedures include:

• Scleral buckle to indent the wall of the eye• Vitrectomy to remove gel or scar tissue pulling on

the retina

The ICD-10-CM code range for retinal detachment is H33.001–H33.8.

To code retinal detachments in ICD-10-CM the following is necessary:

• Type of detachment• Laterality

Retinal detachment with single break, right eye H33.011

Retinal detachment with single break, left eye H33.012

Retinal detachment with single break, bilateral H33.013

Retinal detachment with single break, unspecified eye H33.019

Retinal detachment with multiple breaks, right eye H33.021

Retinal detachment with multiple breaks, left eye H33.022

Retinal detachment with multiple breaks, bilateral H33.023

Retinal detachment with multiple breaks, unspecified eye H33.029

Retinal detachment with giant retinal tear, right eye H33.031

Retinal detachment with giant retinal tear, left eye H33.032

Retinal detachment with giant retinal tear, bilateral H33.033

Retinal detachment with giant retinal tear, unspecified eye H33.039

In the above table, the laterality issue is shown. Note the fifth digits in the codes. The fifth digit of 1 denotes the right eye, the fifth digit of 2 denotes the left eye, the fifth digit of 3 denotes bilateral eyes, and the fifth digit of 9 denotes unspecified eye.

Diabetic RetinopathyDiabetic retinopathy is a condition that develops in patients with long-term diabetes causing damage to the blood vessels in the retina. It is the leading cause of blindness in the United States as over time the damage to the blood vessels causes a permanent decrease in the sharpness of vision. There are four stages of diabetic retinopathy:

• Mild nonproliferative retinopathy—This is the earliest stage where small balloon-like swelling occurs in the small vessels

• Moderate nonproliferative retinopathy—Indicates progression of the disease where the swelling turns into blockage

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• Severe nonproliferative retinopathy—Condition has progressed so that the retina is being deprived of the necessary amount of blood supply to keep it healthy so signals are sent to the body to grow new vessels to replace the blocked ones

• Proliferative retinopathy—This is the advanced stage of diabetic retinopathy where the new vessels have grown, but they have very fragile and thin walls so they are at risk for leaking, which would cause the retina to be blocked resulting in complete blindness

In severe cases a surgical procedure called a vitrectomy may be required. A vitrectomy is a procedure to remove vitreous humor from the center of the eye. Prior to a vitrectomy, laser procedures may be performed to slow the leakage and reduce the amount of fluid in the retina.

Source: AAPC

To code for diabetic retinopathy in ICD-10-CM the following is necessary:

• Type of diabetes • Severity of nonproliferative condition• Proliferative or nonproliferative• With or without macular edema

Type 1 diabetes mellitus with unspecified diabetic retinopathy with macular edema

E10.311

Type 1 diabetes mellitus with unspecified diabetic retinopathy without macular edema

E10.319

Type 1 diabetes mellitus with mild nonpro-liferative diabetic retinopathy with macular edema

E10.321

Type 1 diabetes mellitus with mild nonpro-liferative diabetic retinopathy without macu-lar edema

E10.329

Type 1 diabetes mellitus with moderate nonproliferative diabetic retinopathy with macular edema

E10.331

Type 1 diabetes mellitus with moderate nonproliferative diabetic retinopathy with-out macular edema

E10.339

Type 1 diabetes mellitus with severe non-proliferative diabetic retinopathy with macular edema

E10.341

Type 1 diabetes mellitus with severe non-proliferative diabetic retinopathy without macular edema

E10.349

Type 1 diabetes mellitus with proliferative diabetic retinopathy with macular edema

E10.351

Type 1 diabetes mellitus with proliferative diabetic retinopathy without macular edema

E10.359

Type 2 diabetes mellitus with unspecified diabetic retinopathy with macular edema

E11.311

Type 2 diabetes mellitus with unspecified diabetic retinopathy without macular edema

E11.319

Type 2 diabetes mellitus with mild nonpro-liferative diabetic retinopathy with macular edema

E11.321

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Type 2 diabetes mellitus with mild nonpro-liferative diabetic retinopathy without macu-lar edema

E11.329

Type 2 diabetes mellitus with moderate nonproliferative diabetic retinopathy with macular edema

E11.331

Type 2 diabetes mellitus with moderate nonproliferative diabetic retinopathy with-out macular edema

E11.339

Type 2 diabetes mellitus with severe non-proliferative diabetic retinopathy with macular edema

E11.341

Type 2 diabetes mellitus with severe non-proliferative diabetic retinopathy without macular edema

E11.349

Type 2 diabetes mellitus with proliferative diabetic retinopathy with macular edema

E11.351

Type 2 diabetes mellitus with proliferative diabetic retinopathy without macular edema

E11.359

Disorders of the ConjunctivaConjunctivitis refers to any inflammatory condition of the membrane that lines the eyelids and covers the exposed surface of the sclera, and is caused by either a virus or bacteria. Viruses are usually benign and self-limited, but tend to last longer than a bacterial type. Mucopurulent conjunctivitis is often characterized by the discharge of pus in the eye causing morning crusting, which makes it difficult to open the eyes.

The ICD-10-CM code range for disorders of the conjunctiva is H10–H11.

To code for disorders of the conjunctiva in ICD-10-CM the following is necessary:

• Type of conjunctivitis• Laterality• Acute or chronic

Acute follicular conjunctivitis, right eye H10.011

Acute follicular conjunctivitis, left eye H10.012

Acute follicular conjunctivitis, bilateral H10.013

Acute follicular conjunctivitis, unspecified eye

H10.019

Other mucopurulent conjunctivitis, right eye

H10.021

Other mucopurulent conjunctivitis, left eye H10.022

Other mucopurulent conjunctivitis, bilateral

H10.023

Other mucopurulent conjunctivitis, unspecified eye

H10.029

Acute atopic conjunctivitis, unspecified eye H10.10

Acute atopic conjunctivitis, right eye H10.11

Acute atopic conjunctivitis, left eye H10.12

Acute atopic conjunctivitis, bilateral H10.13

Acute toxic conjunctivitis, right eye H10.211

Acute toxic conjunctivitis, left eye H10.212

Acute toxic conjunctivitis, bilateral H10.213

Acute toxic conjunctivitis, unspecified eye H10.219

Pseudomembranous conjunctivitis, right eye H10.221

Pseudomembranous conjunctivitis, left eye H10.222

Pseudomembranous conjunctivitis, bilateral H10.223

Pseudomembranous conjunctivitis, unspeci-fied eye

H10.229

Serous conjunctivitis, except viral, right eye H10.231

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Serous conjunctivitis, except viral, left eye H10.232

Serous conjunctivitis, except viral, bilateral H10.233

Serous conjunctivitis, except viral, unspeci-fied eye

H10.239

Unspecified acute conjunctivitis, unspecified eye

H10.30

Unspecified acute conjunctivitis, right eye H10.31

Unspecified acute conjunctivitis, left eye H10.32

Unspecified acute conjunctivitis, bilateral H10.33

Unspecified chronic conjunctivitis, right eye

H10.401

Unspecified chronic conjunctivitis, left eye H10.402

Unspecified chronic conjunctivitis, bilateral H10.403

Unspecified chronic conjunctivitis, unspecified eye

H10.409

Chronic giant papillary conjunctivitis, right eye

H10.411

Chronic giant papillary conjunctivitis, left eye

H10.412

Chronic giant papillary conjunctivitis, bilateral

H10.413

Chronic giant papillary conjunctivitis, unspecified eye

H10.419

Simple chronic conjunctivitis, right eye H10.421

Simple chronic conjunctivitis, left eye H10.422

Simple chronic conjunctivitis, bilateral H10.423

Simple chronic conjunctivitis, unspecified eye

H10.429

Chronic follicular conjunctivitis, right eye H10.431

Chronic follicular conjunctivitis, left eye H10.432

Chronic follicular conjunctivitis, bilateral H10.433

Chronic follicular conjunctivitis, unspecified eye

H10.439

Vernal conjunctivitis H10.44

Other chronic allergic conjunctivitis H10.45

Currently there are no ICD-10-CM guidelines related to this disease.

ICD-10-PCS TerminologyAlteration—Modifying the natural anatomic structure of a body part without affecting the function of the body part. Principal purpose is to improve appearance.

Change—Taking out or off a device from a body part and putting back an identical or similar device in or on the same body part without cutting or puncturing the skin or mucous membrane. All CHANGE procedures are coded using the approach EXTERNAL.

Drainage—Taking or letting out fluids and/or gases from a body part, such as an incision and drainage.

Destruction—Physical eradication of all or a portion of a body part by direct use of energy, force, or a destruc-tion agent. None of the body part is physically taken out, such a biopsy or fulguration of a polyp.

Dilation—Expanding an orifice or the lumen of a tubular body part. The orifice can be a natural orifice or an artificially created orifice. Accomplished by stretching a tubular body part using intraluminal pressure or by cutting part of the orifice or wall of the tubular body part.

Excision—Cutting out or off, without replacement, a portion of a body part. The qualifier diagnostic is used to identify excision procedures that are biopsies.

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Extraction—Pulling or stripping out or off all or part of a body part by the use of force. The qualifier diagnostic is used to identify extractions that are biopsies.

Fragmentation—Breaking solid matter in a body part into pieces. Physical force (eg, manual, ultrasonic) applied directly through intervening body parts are used to break the solid matter into pieces. The pieces of solid matter are not taken out but are eliminated or absorbed through normal biological functions.

Extirpation—Taking or cutting out solid matter from a body part. The solid matter may be an abnormal byproduct of a biological function or a foreign body; it may be imbedded in a body part or in the lumen of a tubular body part. The solid matter may or may not have been broken into pieces.

Inspection—Visually or manually exploring a body part. Visual exploration may be performed with or without optical instrumentation. Manual exploration may be performed directly or through intervening body layers.

Insertion—Putting in a biological appliance that monitors, assists, performs, or prevents a physiological function that does not physically take the place of the body part.

Occlusion—Completely closing an orifice or lumen of a tubular part. The orifice can be a natural or artificially created orifice.

Repair—Restoring, to the extent possible, a body part to its normal anatomic structure and function. Use only when the method to accomplish the repair is not one of the other root operations.

Reposition—Moving to its normal location or other suitable location all or part of the body part. The body part is moved to a new location from an abnormal location, or from a normal location where it is not functioning correctly. The body part may or may not be cut out or off to be moved to the new location.

Removal—Taking out or off a device from a body part. If a device is taken out and a similar device put in without cutting or puncturing the skin or mucous membrane, the procedure is coded to the root operation of CHANGE. Otherwise, the procedure for taking out a device is coded to the root operation REMOVAL, and the procedure for putting in a new device is coded to the root operation performed.

Drainage—Taking or letting out fluids and/or gases from a body part, such as an incision and drainage.

Irrigation—Putting In or on a cleansing substance. Substance given is a cleansing substance or dialysate.

Reattachment—Putting back in or on all or a portion of a separated body part to its normal location or other suitable location.

0 Medical and Surgical 8 EyeS Reposition

Body Part Character 4

Approach Character 5

Device Character 6

Qualifier Character 7

C Iris, Right

D Iris, Left

G Retinal Vessel, Right

H Retinal Vessel, Left

J Lens, Right

K Lens, Left

3 Percutaneous Z No Device Z No Qualifier

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Body Part Character 4

Approach Character 5

Device Character 6

Qualifier Character 7

L Extraocular Muscle, Right

M Extraocular Muscle, Left

V Lacrimal Gland, Right

W Lacrimal gland, Left

0 Open

3 Percutaneous

Z No Device Z No Qualifier

N Upper Eyelid, Right

P Upper Eyelid, Left

Q Lower Eyelid, Right

R Lower Eyelid, Left

0 Open

3 Percutaneous

X External

Z No Device Z No Qualifier

X Lacrimal Duct, Right

Y Lacrimal Duct, Left

0 Open

3 Percutaneous

7 Via Natural or Artificial Opening

8 Via Natural or Artificial Opening Endoscopic

Z No Device Z No Qualifier

Example

Pre-op Diagnosis: Ptosis and Dermatochalasis Upper lids

Post-op Diagnosis: Ptosis and Dermatochalasis Upper lids

Procedure: Ptosis Repair and Blepharoplasty Upper lids

Anest: MAC Complications:None.

Justification for Procedure:

The patient was complaining of a progressive drooping of the upper lids with excess skin hanging down over the lashes. The skin was casting a shadow over the vision making it difficult to see. Visual field testing was performed which demonstrated a loss of the superior visual field in the primacy position. By taping the excess skin up, there was a marked improvement in the visual field.

Procedure description: After informed consent was obtained, the patient was brought to the operating room. A lid crease was marked at 9–10 mm above the lid margin. Excess skin was outlined with a Green’s forceps. A 50/50 mixture of xylocaine 1% with epinephrine mixed with .75% marcaine with epinephrine was then injected into the upper lids. The face was prepped and draped in the usual sterile fashion. An incision was

then made over the previously marked lines with a #15 Barde-Parker blade. A skin-muscle flap was then excised with a Bovie cutting cautery. Hemostasis was achieved with the bovie. The septum was then opened with the bovie. Excess medial fat was excised with the hot cautery. A segment of levator aponeurosis was excised from the anterior border of the tarsus. The newly cut edge of aponeurosis was then advanced and hooked to the distal aponeurosis with three 6-0 Vicryl sutures. These were adjusted until proper lid height and contour were achieved. The sutures were then passed through the subcutaneous tissue of the inferior wound margin to recreate the lid crease. The skin was then closed with interrupted and a running 6-0 plain suture. The patient tolerated the procedure well and left the operating room in good condition.

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ICD-10-PCS Coding: 08SN0ZZ 08SP0ZZ

Medical and Surgical Eye Reposition Upper Eyelid, Right Open No Device No Qualifier

0 8 S N 0 Z Z

Medical and Surgical Eye Reposition Upper Eyelid, Left Open No Device No Qualifier

0 8 S P 0 Z Z

In this case documentation supports this as medically necessary and meets the definition of a reposition, instead of cosmetic (alteration). Two codes are reported since this is bilateral and a bilateral code is not available.

0 Medical and Surgical

8 Eye

W Revision

Body Part Character 4

Approach Character 5

Device Character 6

Qualifier Character 7

0 Eye, Right

1 Eye, Left

0 Open

3 Percutaneous

7 Via Natural or Artificial Opening

8 Via Natural or Artificial Opening Endoscopic

X External

0 Drainage Device

3 Infusion device

7 Autologous Tissue Substitution

C Extraluminal Device

D Intraluminal Device

J Synthetic Substitute

K Nonautologous Tissue Substitute

Z No Qualifier

J Lens, Right

K Lens, Left

3 Percutaneous

X External

J Synthetic Substitute Z No Qualifier

L Extraocular Muscle, Right

M Extraocular Muscle, Left

0 Open

3 Percutaneous

0 Drainage Device

7 Autologous Tissue Substitute

J Synthetic Substitute

K Nonautologous Tissue Substitute

Z No Qualifier

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Example

Pre-operative diagnosis: Malpositioned corneal implant, Left Eye

Post-operative diagnosis: same

Procedure: Repair of graft of corneal implant operative wound

Procedure: The patient was brought to the operating room. Topical tetracaine and quinolone antibiotic drops were applied to the operative eye. The patient was prepped and draped in the usual manner for sterile ophthalmic surgery. A lid speculum was placed in the interpalpebral space. Using a 30 gauge needle, aqueous was removed from the anterior chamber. Using a 30 gauge needle, the anterior chamber was filled with air beneath the displaced corneal graft. The graft was centered and well approximated to the recipient corneal bed. Interface fluid was drained by use of the four previously placed perforations A patch was applied. The patient tolerated the procedure well and left the operating room in good condition.

ICD-10-PCS Coding: 08W13KZ

Medical and Surgical Eye Revision Eye, Left Percutaneous Nonautologous Tissue Substitute

No Qualifier

0 8 W 1 3 K Z

In this example the repair meets the definition of a revi-sion for correcting a misplaced device (corneal implant). Corneal implants come from another human and are considered nonautologous.

SourcesComprehensive Medical Terminology (Fourth Edition) by Betty Davis Jones.

Stedman’s Medical Dictionary, 28th edition

Bates’ Pocket Guide to Physical Examination and History Taking, Third Edition (Lynn S. Bickley-Lippincott)