Summary & Overview
HCPCS Level II M1407: Patients Who Died During Follow-Up
HCPCS Level II code M1407 denotes patients who died during the follow-up period and is used to capture mortality outcomes in clinical follow-up, registries, and administrative reporting. Nationally, consistent capture of mortality outcomes is important for quality measurement, clinical research, and longitudinal program evaluation. This code provides a standardized mechanism to flag deaths that occur after an index encounter or during a defined follow-up interval.
Key payers covered in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find an overview of how M1407 is applied in clinical and administrative workflows, descriptions of typical sites of service where the code is recorded, and a summary of common modifiers used with HCPCS Level II codes (modifiers listed in input). The publication addresses benchmarking and reporting implications relevant to national quality measurement and registry reporting, and highlights clinical context for why accurate mortality coding matters to longitudinal care coordination and outcomes assessment.
Data not available in the input for associated taxonomies, ICD-10 diagnoses, related codes, and service line.
Billing Code Overview
HCPCS Level II code M1407 describes patients who died during the follow-up period. This code is used to record the outcome of patient mortality observed during a study, registry, or follow-up interval.
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Service type: Outcome/status reporting derived from patient follow-up
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Typical site of service: Administrative or clinical follow-up settings, including hospitals, outpatient clinics, registries, and research follow-up contacts
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Clinical & Coding Specifications
Clinical Context
A typical patient scenario involves a patient enrolled in a clinical registry or longitudinal outcomes study who passes away during the study follow-up period. For example, a 78-year-old man with advanced congestive heart failure enrolled in a heart-failure outcomes registry is followed with scheduled clinic visits, telephone checks, and periodic mortality ascertainment. During routine follow-up, registry staff confirm date and cause of death from hospital records and death certificate. The clinical workflow includes documentation of the death in the patient record, abstraction of the date and cause of death, notification of the treating clinicians, closure of active study interventions, and coding the outcome event for billing and registry reporting. Typical stakeholders include primary care physicians, treating specialists (e.g., cardiology, oncology), medical records staff, clinical research coordinators, and billing offices. The service type is an outcome/status report related to cohort follow-up and mortality ascertainment. The typical site of service is administrative/registry services coordinated from outpatient clinic or health system data management; confirmation may occur at hospital inpatient service or via medical examiner/coroner records.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
22 | Increased procedural services | Use when services required substantially greater work than typical for the activity (e.g., extensive death-certification documentation due to complications). |