Home

ICD 10 code for ANCA associated vasculitis

ANCA vasculitis ICD 10 — icd-10-cm diagnosis code m0

ICD-10-CM Diagnosis Code H35.069 Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a group of diseases (granulomatosis with polyangiitis, eosinophilic granulomatosis with polyangiitis and microscopic polyangiitis), characterized by destruction and inflammation of small vessel AHA Coding Clinic ® for ICD-10-CM and ICD-10-PCS - 2021 Issue 1; Ask the Editor Anti-Neutrophil Cytoplasmic Autoantibody Vasculitis and Nephritic Syndrome. What is the appropriate diagnosis code assignment for anti-neutrophil cytoplasmic autoantibody (ANCA) vasculitis with nephritic syndrome?. Arteritis, unspecified 2016 2017 2018 2019 2020 2021 Billable/Specific Code I77.6 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2021 edition of ICD-10-CM I77.6 became effective on October 1, 2020

Anti-Neutrophil Cytoplasmic Autoantibody Vasculitis and

ANCA-associated vasculitis. ANCA - associated systemic vasculitis a subgroup of small vessel vasculitis in which there are circulating antineutrophil cytoplasmic autoantibodies ( ANCA ), including microscopic polyangiitis, Wegener granulomatosis, and some types of Churg - Strauss syndrome . Medical dictionary. 2011 M31.7 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2021 edition of ICD-10-CM M31.7 became effective on October 1, 2020. This is the American ICD-10-CM version of M31.7 - other international versions of ICD-10 M31.7 may differ

2021 ICD-10-CM Diagnosis Code I77

ANCA-associated vasculitis Genetic and Rare Diseases

  1. Positive results for MPO ANCA and pANCA are consistent with the diagnosis of autoimmune vasculitis including microscopic polyangiitis (MPA) or pauci-immune necrotizing glomerulonephritis. A positive result for PR3 ANCA or MPO ANCA has been shown to detect 89% of patients with active WG or MPA (with or without renal involvement) with fewer than.
  2. Vasculitis, ANCA-associated (AAV)for any of the following conditions Microscopic polyangiitis- when creatinine is 5.7 mg/dl or greater; Granulomatosis with polyangiitis- when creatinine is 5.7 mg/dl or greater; Renal- limited vasculitis- when creatinine is 5.7 mg/dl or greater; Voltage-gated potassium channel (VGKC) antibody related disease
  3. Vasculitis ICD-10-CM Alphabetical Index. Vasculitis. The ICD-10-CM Alphabetical Index is designed to allow medical coders to look up various medical terms and connect them with the appropriate ICD codes. There are 11 terms under the parent term 'Vasculitis' in the ICD-10-CM Alphabetical Index
  4. If a patient has ANCA-associated vasculitis, he or she may have one of three different vasculitis conditions: 1. granulomatosis with polyangiitis (GPA), previously known as Wegener's granulomatosis, 2. Microscopic polyangiitis (MPA) and 3. eosinophilic granulomatosis with polyangiitis (EGPA), previously known as Churg-Strauss syndrome (1)
  5. ANCA vasculitis has an associated autoimmune response that produces ANCAs that induce distinct pathologic lesions. Pauci-immune necrotizing and crescentic GN is a frequent component of ANCA vasculitis. ANCA vasculitis is associated with ANCA specific for myeloperoxidase (MPO-ANCA) or proteinase 3 (PR3-ANCA). A diagnosis of ANCA vasculitis should always specify the serotype as MPO-ANCA positive.

Vasculitis limited to the skin, unspecified L95.9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2019 edition of ICD-10-CM L95.9 became effective on October 1, 2018. Secondly, what causes granulomatosis with Polyangiitis Short description: Arteritis NOS. ICD-9-CM 447.6 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 447.6 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or.

Acute on chronic renal failure 2 2 ANCA vasculitis ICD 10 code. Pulmonary-renal syndrome refers to patients with DAH (or pathologic pulmonary purpura on physical examination implies a small-vessel, cutaneous vasculitis ( 10).. The ANCA-associated vasculitides, WG, CSS, and MPA, are grouped. . The syndrome is characterized by a triad of (1. In several studies, the relapse rate of ANCA-associated vasculitis on chronic dialysis was lower compared with that among patients with preserved renal function [31, 32]. Lionaki et al. estimated relapse rates of ANCA-associated vasculitis before and after initiation of chronic dialysis. In patients who reached ESRD, relapses occurred at a rate. The code I67.7 is valid during the fiscal year 2021 from October 01, 2020 through September 30, 2021 for the submission of HIPAA-covered transactions. The ICD-10-CM code I67.7 might also be used to specify conditions or terms like cerebral arteritis, cerebral arteritis in giant cell arteritis, cerebral arteritis in systemic vasculitis, cerebral.

2021 ICD-10-CM Diagnosis Code N05

The following ICD10 Codes match 'Vasculitis'. Quickly lookup the latest ICD-10 CM medical diagnosis codes or browse a complete list sorted by chapter or section The ICD-10-CM code M31.7 might also be used to specify conditions or terms like microscopic polyarteritis nodosa, microscopic polyarteritis nodosa with multi-organ involvement, microscopic polyarteritis nodosa with single organ involvement, necrosis of artery, polyarteritis nodosa , primary necrotizing systemic vasculitis, etc - Antineutrophil cytoplasmic antibody (ANCA) positive vasculitis Hide descriptions. Concept ID: 722191003 Read Codes: ICD-10 Codes: I776 + Glomerulonephritis co-occurrent and due to antineutrophil cytoplasmic antibody positive vasculitis; Powered by X-Lab. This tool allows you to search SNOMED CT and is designed for educational use only.. Medical billing and coding can be challenging for this auto-immune disorder as it involves using several codes. ICD-10 diagnosis codes for vasculitis include -. L95 Vasculitis limited to skin, not elsewhere classified. L95.0 Livedoid vasculitis. L95.1 Erythema elevatum diutinum

The frequency of ANCA-associated vasculitis in a national database of hospitalized patients in China Jiannan Li1, (ICD)-10 codes and free text. Variables from the front page of inpatient records were vasculitis (relevant ICD-10 coding in Appendix 1). The definition of AAV had to exclude large vesse ChiroCode.com for Chiropractors CMS 1500 Claim Form Code-A-Note - Computer Assisted Coding Codapedia.com - Coding Forum Q&A CPT Codes DRGs & APCs DRG Grouper E/M Guidelines HCPCS Codes HCC Coding, Risk Adjustment ICD-10-CM Diagnosis Codes ICD-10-PCS Procedure Codes Medicare Guidelines NCCI Edits Validator NDC National Drug Codes NPI Look-Up. ANCA Vasculitides - Testing for anti-neutrophil cytoplasmic antibodies (P-ANCA and/or C-ANCA) has been found to be useful in establishing the diagnosis of suspected vascular diseases (e.g., crescentic glomerulonephritis, microscopic polyarteritis and Churg-Strauss syndrome), bowel disease (Crohn's Disease, ulcerative colitis, primary sclerosing cholangitis, and autoimmune hepatitis) as well as.

Background: Anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (AAV) is a group of life-threatening autoimmune diseases. The epidemiological data on AAV in China are limited. The aim of the present study is to investigate the frequency, geographical distribution, and ethnic distribution of AAV in hospitalized patients in China, and its association with environmental pollution Anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (AAV) is a group of autoimmune diseases characterized by inflammation and damage to small blood vessels. This inflammation is typically caused by ANCAs, self-reactive antibodies that bind to certain cells of the immune system — called neutrophils — and overly activate them. . Researchers believe that a combination of. Background/Purpose: The management of ANCA-associated vasculitis (AAV) evolved substantially in recent years because of evidence supporting the efficacy of various treatment regimens. As such, treatment approaches may vary across physicians. Understanding current practice can guide the design of pragmatic trials, inform cost-effectiveness research, and establish benchmarks. We sought to.

Background/Purpose: ANCA-associated vasculitis (AAV) is often studied in the Caucasian population with few studies looking at the disease in other races. Disease presentation and treatment implications of autoimmune conditions vary by ethnicity, as seen in systemic lupus erythematous. A 2014 study of the Chicago area compared AAV in Hispanic and Caucasian patients and found increased [ ANCA vasculitis ICD 10 — icd-10-cm diagnosis code m0 . It is a form of vasculitis (inflammation of blood vessels) that affects smalland. If the person has TEENney failure or cutaneous vasculitis, a biopsy is obtained . Sep 25, 2015. Enter the ICD-10-CM code for the primary cause of failure on Field #15 of the. CMS-2728 Form.

Video: ICD-10 Codes, 'Really Important - ANCA Vasculitis New

What is ANCA associated vasculitis? ANCA associated vasculitis (AAV) is an umbrella term for a group of multi-system autoimmune small vessel vasculitides that can present at any age and affect 20-25 people per million per year in Europe.1 A typical GP practice with 8000 patients can expect to see one new case approximately every five years. AAV diseases include microscopic polyangiitis. Microscopic polyangiitis is the most common ANCA-associated small-vessel vasculitis, and is characterized by the presence of ANCA and few or no immune deposits in the involved vessels.1, 3, 7, 9. ICD-10-CM Code. I67.7. Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis. I67.7 is a billable ICD code used to specify a diagnosis of cerebral arteritis, not elsewhere classified. A 'billable code' is detailed enough to be used to specify a medical diagnosis Background/Purpose: ANCA-associated vasculitis (AAV) has a high rate of complications, both from disease itself and treatments. Hospital mortality rates for AAV range between 10-20%. There is a lack of information regarding reasons for hospitalization and outcomes of these hospitalizations. It is important to characterize the current state of treatment and outcomes in AAV in order [

management of ANCA-associated vasculitis. Ann Rheum Dis. 2016 Sep;75(9):1583-94. doi: 10.1136/annrheumdis-2016-209133. 9. Groh M, Panoux C, Baldini C, et al. Eosinophilic granulomatosis with polyangiitis (Churg- Strauss) (EGPA) Consensus Task Force recommendations for evaluation andmanagement. European Journal of Internal Medicine 26 (2015. The ICD-10-CM code L95.8 might also be used to specify conditions or terms like cutaneous gonorrhea, drug-induced lymphocytic vasculitis, eosinophilic vasculitis of skin, erythema induratum, familial pigmented purpuric eruption , gonococcal bacteremia-induced pustular vasculitis, etc ANCA-associated vasculitis (AAV) comprises three different disease entities, in particular granulomatosis with polyangiitis (WHO) mortality database for each disease, based on ICD-10 codes. We. Anti-neutrophil cytoplasmic antibodies (ANCAs) are a group of autoantibodies, mainly of the IgG type, against antigens in the cytoplasm of neutrophil granulocytes (the most common type of white blood cell) and monocytes.They are detected as a blood test in a number of autoimmune disorders, but are particularly associated with systemic vasculitis, so called ANCA-associated vasculitides (AAV)

M31. 6 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2020 edition of ICD-10-CM M31. 6 became effective on October 1, 2019. ANCA vasculitis, or antineutrophil cytoplasmic antibody-associated vasculitis, is the name of a group of autoimmune conditions characterized by the. ILD was observed in 2.7% (n = 14) of our patients with ANCA-associated vasculitis (n = 510); all had MPO-ANCA and a clinical diagnosis of MPA, giving a prevalence of 7.2% in patients with MPA (n = 194). There was no significant difference in survival between patients with MPA and ILD and those with MPA alone ICD-10-CM Alphabetical Index References for 'N01.7 - Rapidly progressive nephritic syndrome with diffuse crescentic glomerulonephritis' The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code N01.7. Click on any term below to browse the alphabetical index

Coding Vasculitis, a Common Autoimmune Disease in ICD-1

ANCA vasculitis, or antineutrophil cytoplasmic antibody-associated vasculitis, is the name of a group of autoimmune conditions characterized by the inflammation of the blood vessels caused by the immune system mistakenly attacking them. There is currently no cure for ANCA vasculitis, but there are treatments available to manage the condition The anti-MPO-ANCA EIA is useful for confirming positive ANCA results by IFA, particularly with the P-ANCA pattern. Presence of anti-MPO antibodies is highly specific for idiopathic and vasculitis-associated crescentic glomerulonephritis, classic polyarteritis nodosa, Churg-Strauss syndrome, and polyangiitis overlap syndrome without renal. Vasculitis is a group of disorders that destroy blood vessels by inflammation. Both arteries and veins are affected. Lymphangitis (inflammation of lymphatic vessels) is sometimes considered a type of vasculitis. Vasculitis is primarily caused by leukocyte migration and resultant damage. Although both occur in vasculitis, inflammation of veins or arteries on their own are separate entities - +ve ANCA by indirect immunofluorescence but -ve PR3/MPO is of doubtful significance and does not support a diagnosis of AAV - not all AVV has a +ve ANCA 2 aims of treatment for vasculitis Valid for Submission. N01.7 is a billable diagnosis code used to specify a medical diagnosis of rapidly progressive nephritic syndrome with diffuse crescentic glomerulonephritis. The code N01.7 is valid during the fiscal year 2021 from October 01, 2020 through September 30, 2021 for the submission of HIPAA-covered transactions

Creating ways to speed the process of getting an accurate diagnosis would help the health outcomes of patients with ANCA-associated vasculitis and other types of vasculitis, a study says. Delays in obtaining an accurate diagnosis are linked to unemployment, the need to travel long distances to a medical center,. Read more Vasculitis (Leukocytoclastic Vasculitis) Leukocytoclastic vasculitis, also known as hypersensitivity vasculitis, is an inflammation of blood vessels that forms small lesions on the skin. The direct cause is unknown, but vasculitis is often linked to autoimmune disorders. It could also be triggered by allergies, medication, or an infection Approximately 90% of patients have autoantibodies either to myeloperoxidase (MPO-ANCA) or to proteinase 3 (PR3-ANCA). The clinical manifestations of ANCA-small vessel vasculitis are protean. These can be limited to the kidney alone, or may involve the upper respiratory tract, the lungs, the skin, or a number of other organs in various combinations COVID-19-associated vasculitis and vasculopathy J Thromb Thrombolysis. 2020 Oct;50(3):499-511. doi: 10.1007/s11239-020-02230-4. Author Richard C Becker 1 Affiliation 1 University of Cincinnati Heart, Lung.

(ANCA)-associated vasculitis mention rituximab in combination with low-dose corticosteroids as specific HCPCS or ICD-10 code in a chart or companion article to an LCD is not by itself sufficient to approve coverage. Similarly, the absence of such a code does not necessarily mean that the applicabl Pain and swelling in the testes, in rare cases, may be the first symptoms of ANCA-associated vasculitis, even among patients without other symptoms associated with this disease, researchers reported, noting that testicular vasculitis is often misdiagnosed. ICD-10 Codes, 'Really Important' to Rare Disease Patients, Soon Up for Fresh. ANCA Screen with MPO and PR3, with Reflex to ANCA Titer. This test is used in the differential diagnosis of systemic vasculitis and for monitoring patients with the disorder. This test is used in the differential diagnosis of systemic vasculitis and for monitoring patients with the disorder. Reference ranges are provided as general guidance only Vasculitis-related costs were recorded as true costs charged. A total of 317 patients fulfilled the study criteria. The diagnoses were grouped into three clinically relevant groups: IgA vasculitis and other small-vessel vasculitis (n = 64), ANCA-associated vasculitis (AAV) (n = 112), and large-vessel vasculitis (LVV) (n = 141)

Local Coverage Determination for Rituximab (L35026

It is a type of antineutrophil cytoplasmic antibody (ANCA) associated vasculitis, most commonly affecting the upper and lower respiratory tract, the kidneys, and the eyes . The incidence in the United States is three per one million population, with peak incidences at 64 to 75 years of age, and recent studies have shown no sex predilection [ 2 ] Abstract. Objectives. Rituximab is effective in inducing remission in ANCA-associated vasculitis (AAV), with randomized evidence to support its use as four infusions of 375 mg/m 2 (the conventional lymphoma dosing schedule). As B cell depletion (BCD) appears to occur very rapidly after the first dose, we questioned the need for repeat dosing and adopted a standard single-dose protocol of 375.

Some studies of ANCA-associated vasculitis have suggested that pulmonary involvement is associated with a poor outcome [3, 4]. Diagnosis. The diagnosis of ANCA-associated vasculitis is made on the basis of the clinical findings, by biopsy of a relevant involved organ and the presence of ANCA antibody (ANCA)-associated vasculitis (AAV) with the rate in the background population, and to identify predictors of severe infections among patients with AAV. Methods. The study cohort was 186 patients with AAV diagnosed from 1998 to 2010, consisting of all known cases in a defined population in southern Sweden ANCA-associated renal vasculitis has an annual incidence of 10 to 15 per million population and occurs in the context of a systemic vasculitis, such as Wegener granulomatosis or microscopic polyangiitis, or as an isolated entity (renal limited vasculitis) . Confusingly, approximately 5% of pauci-immune, crescentic glomerulonephritis is ANCA.

C-anca vasculitis Medical Billing and Coding Forum - AAP

Diseases ICD-10 Codes Ischemic heart diseases* I20-I25 Cerebrovascular diseases* I60-I69 Hypertensive diseases I10-I15 Diabetes mellitus E10-E14 Disorders of the lipoprotein metabolism E78 Venous thromboembolism* I80.0-I80.9 and/or I26.0-I26.9 Thyroid diseases E00-E07 cytoplasmic antibody-associated vasculitis | ICD-10 from 2011 - 2016 ICD Code M31.3 is a non-billable code. To code a diagnosis of this type, you must use one of the two child codes of M31.3 that describes the diagnosis 'wegener's granulomatosis' in more detail Keywords: Administrative Data, ANCA associated vasculitis, Economics AV were identified by having ≥1 inpatient claim or ≥2 non-inpatient claims at least 7 days apart in 2016 with an ICD-10 code for granulomatosis with polyangiitis, microscopic polyangiitis, or eosinophilic granulomatosis with polyangiitis, with no AV claims in the year. A claim submitted without a valid ICD-10-CM diagnosis code will be returned to the provider as an incomplete claim under Section 1833(e) of the Social Security Act. The diagnosis code(s) must best describe the patient's condition for which the service was performed • ANCA [antineutrophil cytoplasmic antibody]-associated vasculitis (e.g., Wegener's granulomatosis [also known as granulomatosis with polyangitis (GPA)] with associated renal failure) ICD-10 Diagnosis Codes ICD-10-CM Diagnosis codes: Code Descriptio

2021 ICD-10-CM Index > 'Vasculitis

The following ICD-10 codes for MPO are listed as a convenience for the ordering physician. The ordering physician should report the diagnosis code that best describes the reason for performing the test. Myeloperoxidase (MPO) CPT Code 83876 Sample Type EDTA Plasma Order Code C133 Tube Type Lavender Top MPO levels are associated with an increased. Vasculitis is a term used to describe inflammation of blood vessels, which can develop as a result of infection or from one of several other causes. In anti-neutrophil cytoplasmic autoantibody (ANCA) vasculitis, the inflammation is caused by the body's own immune system. A disease of this kind is called an autoimmune disease Cutaneous vasculitis is a group of disorders in which there are inflamed blood vessels in the skin. These may include capillaries, venules, arterioles and lymphatics. Cutaneous vasculitis has several different causes. There are a wide variety of clinical presentations. It is associated with systemic vasculitis in a minority of patients The ordering physician must provide an ICD-10 diagnosis code or narrative description, if required by the fiscal intermediary or carrier. 4. Organ- or disease-related panels should be billed only when all components of the panel are medically ANCA-Associated Vasculitis Profile (ANCA/MPO/PR3) with Reflex to ANCA Titer x 11 2012232 Angelman. Autoimmune Disease-Anti-Neutrophil Cytoplasmic Autoantibody (ANCA) Vasculitis is an autoimmune disease that results in vascular tissue inflammation and systemic vasculitis.Antibodies-Autoimmune response by the body is triggered by autoantibodies.Antibodies react against the antigen present in the wall of neutrophils granulocytes and blood vessels.

ANCA-associated vasculiti

Aim: To describe changes in the 2001-2014 mortality of 6 autoimmune systemic diseases (AISDs), namely Systemic Lupus Erythematosus (SLE), Systemic Sclerosis (SSc), Idiopathic Inflammatory Myopathies (IIM), Sjögren's Syndrome (SS), Mixed Connective Tissue Disease (MCTD) and ANCA-associated vasculitis (AAV) at the country-, continent-, and world-levels management of ANCA-associated vasculitis. Ann Rheum Dis. 2016 Sep;75(9):1583-94. doi: 10.1136/annrheumdis-2016-209133. 9. Groh M, Panoux C, Baldini C, et al. Eosinophilic granulomatosis with polyangiitis (Churg- Strauss) (EGPA) Consensus Task Force recommendations for evaluation and management

2021 ICD-10-CM Diagnosis Code M31

Granulomatosis with polyangiitis (Wegener's) (GPA) is an antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis syndrome characterized by granulomatous inflammation and necrotizing vasculitis predominantly affecting small- to medium-sized blood vessels. Tenth Revision [ICD-10] code M31.3) ICD-10-CM Code Changes for Consideration. The second day of the meeting is dedicated to diagnosis code discussions and is led by CDC NCHS. There are currently 25 items on the list of topics to be covered. They are: Acute and chronic metabolic acidosis; ANCA vasculitis; Apnea related conditions of newbor On 1 July 2016, our dataset found 8,040 people in England were living with ANCA associated vasculitis. We estimate the prevalence was 14.55 (95% CI: 14.23-14.87)/100,000 adult population F. Proteinuria [ICD-9 Code: 791.0] [ICD-10: R80.9] Hematuria [ICD-9 Code: 599.70] [ICD-10 Code: R31.9] Possible Diagnosis Pre-Referral Evaluation When to refer to Rheumatology Pre-Referral Workup • Systemic Lupus Erythematosus (SLE) • ANCA - associated Vasculitis

Anti-neutrophil cytoplasm antibody (ANCA)-associated vasculitis (AAV) is a rare multi-system autoimmune disease, characterised by a pauci-immune necrotising small-vessel vasculitis, with a relapsing and remitting course. identified by screening computerised medical records for ICD-10 codes M30, M31, N01 and N05 We aimed to validate the accurate identification of patients treated with rituximab for ANCA-associated vasculitis (AAV) using HES data. Among patients identified only by the specific ICD-10.

2021 ICD-10-CM Code I77

Objective. To evaluate the consultation rates of selected comorbidities in patients with antineutrophil cytoplasmic antibody-associated vasculitis (AAV) compared with the general population in southern Sweden. Methods. We used data from a population-based cohort of patients with AAV diagnosed between 1998 and 2010 in Southern Sweden (701,000 inhabitants) Henoch-Schönlein purpura (HSP), also known as IgA vasculitis, is a disease of the skin, mucous membranes, and sometimes other organs that most commonly affects children.In the skin, the disease causes palpable purpura (small, raised areas of bleeding underneath the skin), often with joint pain and abdominal pain.With kidney involvement, there may be a loss of small amounts of blood and.

outcome in ANCA-associated vasculitis: a prospective analysis of 100 patients w ith severe renal. involvement. J Am Soc Nephrol. 2006, Based on ICD-10 code categories, the top five reasons for. 2. LIST DIAGNOSES: ICD-10: Type II diabetes for blood glucose control Heart Failure Type II diabetes with established cardiovascular disease and/or with additional cardiovascular risk Chronic kidney disease Other Diagnosis_____ICD-10 Code(s):_____ 3 All vasculitis relapses in the belimumab group (n = 6) occurred in patients who had PR3-ANCA-associated vasculitis with cyclophosphamide-induced disease remission; AEs occurred in 49 (92.5 %) of 53 patients receiving belimumab and 43 (82.7 %) of 52 patients receiving placebo, with no new safety concerns To extract the data, the hospital records were searched using the International Classification of Diseases (ICD)-10- codes (German modification 2019) of patients admitted to the medical ICU (A39.x-A41.x for sepsis and M31.x for the different vasculitis entities) ICD-9-CM 530.13 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 530.13 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes)