ICD-10-CM · Multi-region

M60.09

Infective myositis affecting skeletal muscle at multiple anatomic sites simultaneously, caused by a bacterial, viral, fungal, or parasitic organism.

Verified May 8, 2026 · 6 sources ↓

Status
Billable
Chapter
13
Related CPT
9
Region
Multi-region
Drawn from CDCICD10DataAAPCIcd10coded

Documentation tips

What should appear in the chart to support M60.09.

Source · Editorial brief grounded in 6 cited references ↓

  • Explicitly name each affected muscle or muscle group and its anatomic location — 'multiple sites' must be supported by discrete clinical findings at more than one region.
  • Document the suspected or confirmed causative organism (bacterial species, virus, fungus, or parasite) to support the required B95–B97 companion code.
  • Record diagnostic workup results — cultures, MRI findings showing muscle edema or abscess, elevated CK or ESR — to substantiate an infectious etiology rather than inflammatory or traumatic myositis.
  • Note any underlying immunocompromising conditions (HIV, diabetes, steroid use) that increase pyomyositis risk; these may qualify as MCCs affecting DRG weight.
  • Distinguish tropical pyomyositis from other infective myositis in the note if relevant — it is an Applicable To inclusion under M60.0 and supports M60.09 when multiple muscles are involved.

Related CPT procedures

Procedure codes commonly billed with M60.09. Linking the right diagnosis to the right procedure is what establishes medical necessity.

Source · CMS LCDs · AAOS specialty guidance · claims-pattern analysis

Common coding pitfalls

The recurring mistakes coders make with M60.09 and adjacent codes.

Source · Editorial brief grounded in CDC ICD-10-CM tabular guidance, AAOS coding references, and cited references ↓

  • Using M60.09 without appending a B95–B97 organism code violates the parent-level 'Use Additional Code' instruction and risks claim rejection or audit findings.
  • Defaulting to M60.09 when only one body region is documented — the correct code is the site-specific M60.0xx child code; M60.09 requires clinically documented multiple sites.
  • Confusing M60.09 with M60.08 (other site) — 'other site' applies to a single non-listed anatomic location, not to multiple concurrent sites.
  • Coding M60.09 for inclusion body myositis (IBM) — IBM is excluded from M60 entirely and must be coded G72.41.
  • Sequencing M60.09 as a secondary code when it is the principal diagnosis driving the encounter — infective myositis is the etiology, not a manifestation, so it sequences first with the organism code following.

Clinical context

Source · Editorial summary grounded in 6 cited references ↓

M60.09 is the correct billable code when an infectious process has been documented in skeletal muscle at more than one distinct body region in the same encounter. Classic presentations include tropical pyomyositis spreading across multiple muscle groups, hematogenous bacterial seeding of muscles at several sites, or viral myositis with diffuse multi-site involvement. The key differentiator from sibling codes under M60.0x is the 'multiple sites' qualifier — if the infection is confined to a single named region, use the site-specific code (e.g., M60.011 right shoulder, M60.061 right lower leg).

The parent code M60.0 carries a 'Use Additional Code' instruction: always append a code from B95–B97 to identify the causative infectious agent (e.g., B95.62 for MRSA, B96.89 for other specified bacteria). Failing to add the organism code is a documentation and compliance gap, not a coding shortcut. M60.09 groups into MS-DRG 557 (Tendonitis, Myositis and Bursitis with MCC) or 558 (without MCC), so secondary diagnoses that qualify as MCCs directly affect reimbursement.

Exclude inclusion body myositis (IBM) entirely — it routes to G72.41, not M60. Also confirm that the condition is not better described by dermatopolymyositis (M33.-) or a myopathy linked to a systemic disease such as SLE (M32.-) or rheumatoid arthritis (M05.32), all of which carry Type 1 or Type 2 Excludes notes at the M60–M63 section level.

Sibling codes

Other billable codes under M60.0 (laterality / anatomic variants).

Frequently asked questions

Source · Generated from the editorial pipeline, verified against 6 cited references ↓

01What makes M60.09 different from M60.08?
M60.08 covers infective myositis at a single anatomic site that doesn't fit any of the named site-specific codes (e.g., paraspinal muscle). M60.09 is reserved exclusively for concurrent infection documented at more than one distinct anatomic site in the same patient encounter.
02Do I always need to add a B95–B97 code with M60.09?
Yes. The M60.0 parent carries a mandatory 'Use Additional Code' note requiring a B95–B97 code to identify the infectious agent. If the organism is still pending culture, code the condition and add a note — but submit the organism code as soon as it is confirmed.
03Can M60.09 be used for tropical pyomyositis at multiple sites?
Yes. Tropical pyomyositis is listed as an Applicable To inclusion term under M60.0. When it involves multiple muscle groups, M60.09 is the correct billable code, paired with the appropriate organism code from B95–B97.
04Is inclusion body myositis (IBM) coded under M60.09?
No. IBM is explicitly excluded from the entire M60 category via a Type 2 Excludes note and must be coded G72.41, regardless of how many sites are affected.
05Which MS-DRGs does M60.09 map to?
M60.09 groups to MS-DRG 557 (Tendonitis, Myositis and Bursitis with MCC) or MS-DRG 558 (without MCC) under MS-DRG v43.0. Documenting qualifying MCCs — such as septicemia, respiratory failure, or severe immune compromise — directly affects which DRG is assigned.
06If myositis is secondary to a systemic autoimmune disease, should I still use M60.09?
Only if the etiology is genuinely infectious. Myopathy associated with SLE, rheumatoid arthritis, scleroderma, or Sjögren's syndrome routes to disease-specific codes (M32.-, M05.32, M34.-, M35.03) per the Type 1 and Type 2 Excludes notes at the M60–M63 section level — not to M60.09.
07What documentation distinguishes infective myositis from inflammatory myositis for coding purposes?
Infective myositis (M60.0x) requires documented evidence of an infectious process — positive culture, serologic confirmation, or imaging/clinical findings consistent with pyomyositis or abscess. Inflammatory myositis without a documented infectious agent codes to M60.80–M60.89 or, if autoimmune in origin, to the appropriate condition-specific code.

Mira AI Scribe

Mira's AI scribe captures the affected muscle groups and their laterality, the documented infectious organism or pending culture status, abnormal lab values (elevated CK, WBC, ESR/CRP), and any imaging findings (MRI signal changes, abscess formation) — everything needed to support M60.09 and the mandatory B95–B97 organism companion code. This prevents the two most common audit triggers: missing organism code and unsubstantiated 'multiple sites' designation.

See how Mira captures M60.09 documentation

Related ICD-10 codes

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