icd 10 cm code for sjogren's syndrome

by Kadin Swaniawski 6 min read

Sjögren syndrome, unspecified
M35. 00 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM M35. 00 became effective on October 1, 2021.

What is Sjogren's disease syndrome?

Sjogren's (SHOW-grins) syndrome is a disorder of your immune system identified by its two most common symptoms — dry eyes and a dry mouth. The condition often accompanies other immune system disorders, such as rheumatoid arthritis and lupus.Jul 22, 2020

Is Sjogren's syndrome the same as rheumatoid arthritis?

Rheumatoid arthritis (RA) is frustrating enough on its own. But about 15 percent of people with RA develop a complication that affects the tear and saliva glands, causing dry mouth, dry eyes, dry skin, and additional symptoms that further aggravate their arthritis. It's called Sjögren's syndrome (SS).Mar 16, 2017

What is the classification of Sjögren's syndrome?

ACR-EULAR Classification Criteria for primary Sjögren's syndrome (pSS)
ItemWeight / Score
Labial salivary gland with focal lymphocytic sialadenitis and focus score ≥ 1.33
Anti-SSA (Ro) +3
Ocular staining score ≥ 5 (or van Bijsterfeld score ≥ 4) on at least one eye41
Schirmer ≤ 5 mm/5min on at least one eye1
1 more row
Jan 1, 2018

What is another name for Sjogren's syndrome?

Sicca syndrome: An autoimmune disease, also known as Sjogren syndrome, that classically combines dry eyes, dry mouth, and another disease of connective tissue such as rheumatoid arthritis (most common), lupus, scleroderma or polymyositis.Jun 3, 2021

What type of doctor treats Sjogren's syndrome?

Depending on your symptoms, you might start by seeing your family doctor, dentist or eye doctor. But you might eventually be referred to a doctor who specializes in the treatment of arthritis and other inflammatory conditions (rheumatologist).Jul 22, 2020

What are two types of Sjogren's syndrome?

There are two types of Sjogren's syndrome. Primary Sjogren's syndrome occurs on its own and is not associated with another illness. Secondary Sjogren's syndrome develops in a person who has another autoimmune disease, usually rheumatoid arthritis or lupus.

How is primary Sjogren's syndrome diagnosed?

The diagnosis of primary Sjögren syndrome is strongly suggested in patients who present with signs and symptoms of oral and ocular dryness and who test positive for antibodies to the anti-SS-A or anti-SS-B antigen, or who have a positive salivary gland biopsy.Mar 15, 2009

What is a positive Sjogren's test?

Blood and urine tests, to look for the presence of antibodies common in Sjögren's syndrome. The results of an ANA (antinuclear antibody) test will determine if you have an autoimmune disorder. Schirmer's test, to see if your tear glands are producing enough tears to keep your eyes moist.

Who has Sjögren's syndrome?

Age: Most people who are diagnosed with Sjögren's syndrome are 40 or older, but it can affect younger individuals, including children. Gender: Women are as much as 10 times more likely to develop Sjögren's syndrome than men. This imbalance may be related to the effect of sex hormones on a woman's immune system.

Is Sjogren's lupus?

Sjogren's syndrome is a rare autoimmune condition that often accompanies other autoimmune conditions. Some of these include lupus or rheumatoid arthritis. It is estimated that up to 15 to 18 percent of people living with lupus also have Sjogren's syndrome.Feb 21, 2020

Is Sjögren's syndrome fatal?

Although life expectancy is not typically affected, patients' quality of life is, and considerably. Secretory glands don't work, resulting in dryness in the eyes, mouth, throat, and other organs, along with complications such as pain, fatigue, and digestive problems.Nov 8, 2019

Is Sjögren's syndrome serious?

Sjogren's is a serious condition, but timely treatment can mean that complications are less likely to develop, and tissue damage is less likely to occur. Once treated, an individual can usually manage the condition well. Sjogren's can develop at any age, but most diagnoses occur after the age of 40 years.