MedicaidDocumentationMedium impact
MMP 26-19: Additions to Standards of Coverage and Documentation Requirements for High Frequency Chest Wall Oscillation (HFCWO) Devices
Michigan Medicaid - MDHHS·MI · Pulmonology, Pediatrics, Critical Care·Medical Policy
Effective date
Aug 1, 2026
We identified it
Jul 2, 2026
Summary
Michigan Medicaid is adding new coverage standards and documentation requirements for High Frequency Chest Wall Oscillation (HFCWO) devices effective August 1, 2026. All initial HFCWO devices must now include an equipment usage meter, and DME providers must document the device serial number, delivery date, and meter readings (start/end) at delivery and at four-month intervals. Continuation of therapy requires ongoing meter documentation showing prescribed treatment compliance.
Action Required
By July 15, 2026: DME billing and clinical teams must implement the following changes: (1) Update supplier contracts and device specifications to ensure all HFCWO devices ordered include equipment usage meters (daily or cumulative hour capable); (2) Modify delivery documentation templates to capture device serial number, delivery date, and initial meter readings (photographs are acceptable); (3) Create a 4-month follow-up process to obtain and document end-date meter readings; (4) Establish ongoing meter documentation collection procedures for continuation of service beyond initial four months, including downloadable meter data where available; (5) Update prior authorization submission workflows to include all required meter documentation. Billing team must ensure all supporting documentation is retained in beneficiary files and immediately available upon request. For patients enrolled in Managed Care Organizations (MCOs), verify specific coverage and documentation requirements with each plan as MCOs may have differing standards. Failure to provide required documentation will result in claim denials and potential recoupment.