Understanding Decreased Visual Acuity, Low Vision, and Vision Loss: This resource provides information on the diagnosis, clinical documentation, and medical coding of visual impairment for healthcare professionals. Learn about causes, symptoms, and treatment options related to Decreased Visual Acuity. Find essential information for accurate medical coding and improved patient care.
Also known as
Blindness and low vision
Covers various types of vision loss, including low vision and legal blindness.
Visual disturbances
Includes unspecified visual disturbances and abnormalities of spatial perception.
Persons encountering health services
Can be used for follow-up encounters related to decreased visual acuity if no other diagnosis applies.
Follow this step-by-step guide to choose the correct ICD-10 code.
Is the decreased visual acuity due to refractive error?
Yes, correctable with refractive lenses
Code the refractive error (e.g., H52.0, H52.1). Do NOT code decreased visual acuity separately.
No, or partially correctable
Is the decreased visual acuity in one eye?
When to use each related code
| Description |
|---|
| Reduced sharpness of vision. |
| Blurred vision, near or far. |
| Complete or partial absence of vision. |
Missing or incorrect laterality (right, left, both) can lead to claim denials and inaccurate data reporting for decreased visual acuity.
Lack of documentation specifying mild, moderate, or severe visual impairment may cause coding errors impacting reimbursement and quality metrics.
Failure to code the underlying etiology (e.g., macular degeneration, diabetic retinopathy) with decreased visual acuity can affect risk adjustment and statistical analysis.
Q: What are the most effective differential diagnosis strategies for sudden decreased visual acuity in adults, considering both common and rare etiologies?
A: Sudden decreased visual acuity in adults warrants a prompt and thorough evaluation to identify the underlying cause. Common etiologies to consider include retinal detachment, vitreous hemorrhage, central retinal artery occlusion, acute angle-closure glaucoma, optic neuritis, and ischemic optic neuropathy. Rarer, but crucial to consider, are giant cell arteritis, posterior scleritis, and intracranial masses compressing the optic pathways. Differential diagnosis strategies involve a detailed history focusing on symptom onset, associated symptoms (e.g., pain, floaters, halos), and relevant medical history (e.g., diabetes, hypertension, autoimmune disease). A comprehensive eye exam, including visual acuity assessment, pupillary examination, slit-lamp biomicroscopy, and dilated fundus examination, is paramount. Further investigations like optical coherence tomography (OCT), fluorescein angiography, and neuroimaging may be indicated depending on initial findings. Consider implementing a standardized diagnostic algorithm to ensure all potential causes are systematically evaluated. Learn more about evidence-based diagnostic approaches for sudden vision loss in adults by exploring the latest clinical guidelines.
Q: How can I differentiate between transient visual obscurations and permanent decreased visual acuity when evaluating a patient complaining of vision changes?
A: Differentiating between transient visual obscurations (TVOs) and permanent decreased visual acuity hinges on understanding the nature and duration of the vision changes. TVOs are typically brief episodes of vision loss, often described as a graying out, blurring, or curtain coming down over the visual field, which resolve spontaneously within seconds to minutes. They can be associated with conditions like migraine, carotid artery stenosis, or papilledema. Permanent decreased visual acuity, on the other hand, represents a sustained reduction in vision that doesn't improve on its own. Causes include macular degeneration, cataracts, glaucoma, and optic nerve damage. Clinicians should gather a detailed history, including the frequency, duration, and characteristics of the visual disturbances, as well as associated symptoms like headache, neurological deficits, or eye pain. A comprehensive eye examination, including visual field testing, is essential. Further investigations, like carotid Doppler ultrasound or neuroimaging, may be necessary to pinpoint the etiology. Explore how a comprehensive approach, combining thorough history taking and targeted investigations, can help distinguish between TVOs and permanent vision loss to guide appropriate management.
Patient presents with decreased visual acuity, also documented as low vision, visual impairment, or vision loss. Onset of [Specify onset - e.g., gradual, sudden] blurred vision, difficulty seeing at [Specify - e.g., distance, near, night], andor [Specify other symptoms - e.g., eye pain, halos, floaters] was noted [Specify timeframe - e.g., one week ago, three months prior]. Best-corrected visual acuity measured [Specify right eye VA] in the right eye and [Specify left eye VA] in the left eye using [Specify chart - e.g., Snellen chart, ETDRS chart] at [Specify distance - e.g., 20 feet, 1 meter]. Refraction revealed [Specify refractive error if applicable - e.g., myopia, hyperopia, astigmatism]. Ocular examination revealed [Document pertinent findings - e.g., normal anterior segment, clear lens, presence of cataracts, macular degeneration, optic nerve abnormalities]. Assessment suggests possible etiologies including [List differential diagnoses - e.g., refractive error, cataracts, macular degeneration, diabetic retinopathy, glaucoma, optic neuritis]. Plan includes [Outline plan - e.g., further diagnostic testing such as OCT, visual field testing, referral to ophthalmology, low vision rehabilitation, prescription for corrective lenses]. Patient education provided regarding diagnosis, management, and prognosis. ICD-10 code [Specify appropriate ICD-10 code - e.g., H54.2, H54.1, H54.3] is considered. Return to clinic scheduled for [Specify timeframe - e.g., 2 weeks, 1 month] for follow-up and reassessment of visual acuity. Medical decision making complexity is [Specify level - e.g., low, moderate, high] based on patient presentation and diagnostic uncertainty.