Summary & Overview
HCPCS M1195: Surgical Pathology Report Missing MMR/MSI Impression or Recommendation
HCPCS Level II code M1195 captures surgical pathology reports that omit an impression or conclusion, or omit recommendations regarding testing for mismatch repair (MMR) by immunohistochemistry or microsatellite instability (MSI) by DNA-based testing, with no reason documented. This code highlights gaps in reporting completeness for tumor testing that can affect downstream clinical decision-making and quality measurement.
Key national payers in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise explanation of what the code represents, the clinical context for reporting MMR/MSI testing status in surgical pathology, and why clear documentation matters for quality programs and claims processing. The publication provides benchmarking context where available, summaries of payer coverage themes, and identification of reporting and coding considerations related to pathology documentation standards.
The content addresses how the code is used in pathology workflows and common service settings, summarizes payer presence, and outlines where data is not available. This national-level overview is intended for revenue cycle, pathology, and compliance professionals seeking clarity on the clinical and billing meaning of HCPCS Level II code M1195.
Billing Code Overview
HCPCS Level II code M1195 describes surgical pathology reports that do not contain an impression or conclusion, or a recommendation for testing of MMR by immunohistochemistry, MSI by DNA-based testing status, or both, with no reason provided. The service type is surgical pathology reporting and documentation of tumor testing status. The typical site of service is pathology laboratory or hospital outpatient/inpatient pathology service where surgical specimens are examined and reports are issued.
Data not available in the input.
Clinical & Coding Specifications
Clinical Context
A surgical pathology report is generated after resection or biopsy of a tumor specimen from sites such as the colon, endometrium, ovary, or other organs. In this scenario a patient undergoes surgical excision of a suspected malignancy (for example, a segmental colectomy for a suspicious colonic mass). The specimen is submitted to the pathology laboratory for grossing, histologic processing, and microscopic interpretation. The pathologist issues a surgical pathology report describing tissue type, tumor grade, margins, lymphovascular invasion, and ancillary testing performed. The report, however, does not contain an explicit impression or conclusion addressing mismatch repair (MMR) status by immunohistochemistry or microsatellite instability (MSI) status by DNA-based testing, and no reason for omission is documented. Billing for this situation is captured by M1195.
Typical workflow steps:
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Surgeon obtains specimen and directs submission to pathology.
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Pathology performs gross examination, tissue fixation, embedding, sectioning, and staining (H&E).
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Pathologist reviews slides and documents morphologic findings in a descriptive report.
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Ancillary testing (IHC for MMR proteins or MSI DNA testing) may be considered but is not reported or concluded in the final report; no justification for omission is provided.
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The laboratory bills
M1195when the surgical pathology report lacks an impression/conclusion or recommendation regarding MMR by IHC or MSI by DNA testing status and no reason is given.
Typical site of service: hospital-based pathology laboratory or independent clinical pathology/laboratory facility associated with inpatient or outpatient surgical services.