2026 OIG Audit Survival Guide
23 must-have items that saved our clients millions.
Download free →RTM is built for non-physiologic, therapeutic data--adherence, pain and function scores, inhaler use, CBT homework, post-op recovery--not just vitals. Data can be self-reported inside an FDA-defined medical device, including qualified software as a medical device (SaMD), then used to support RTM billing.
Calculate Your RTM Revenue RTM Essentials ↓RTM is the remote-care pathway designed for Physical Therapists, Occupational Therapists, Orthopedists, Pulmonologists, pain clinics, and CBT-focused behavioral health teams.
Where RPM tracks vital signs, RTM tracks therapy adherence, symptom and function scores, inhaler use, and digital CBT engagement--captured through an RTM-eligible app or device.
RTM gives you structured visibility into what patients are actually doing between encounters, and creates a compliant path to be reimbursed for that work instead of absorbing it as uncompensated care.
RTM CBT device supply (CPT 98978) is contractor-priced by Medicare; coverage and rates for CBT-focused RTM vary by MAC and commercial payer.
One-time per episode of care. Covers initial configuration and patient education. Critical 2026 Update: You no longer need to wait 16 days. This code can be billed as soon as the patient has successfully transmitted data for 2 days.
Monthly device supply. For the full reimbursement rate, 98976 (respiratory) and 98977 (MSK) require 16+ days of data. However, new "rescue codes" (98984–98986) now allow you to bill for 2–15 days of monitoring if the full threshold is missed.
Monthly RTM treatment-management time. 98980 covers the first 20+ minutes in a calendar month (with at least one real-time interaction), and 98981 covers each additional 20 minutes. The 16-day device rule does not apply to these management codes, but you still need legitimate RTM data and documented interaction.
RTM cannot be billed in the same period as RPM for the same patient. It can be billed alongside CCM/PCM/TCM/BHI/APCM when time and work are not double-counted.
Beginning January 1, 2026, RTM becomes more flexible. CPT and CMS introduce new codes for shorter monitoring periods and shorter management time, instead of a single “16 days or nothing” device threshold and a single 20-minute management bucket.
New codes for shorter episodes of respiratory, musculoskeletal, and CBT RTM. Financial Insight: These "rescue codes" are priced at near-parity with the full 16-day codes (approx. $40), meaning you protect revenue even if a patient only monitors for a partial month.
98979 covers 10–19 minutes of RTM management (with one live interaction). Note: You cannot bill 98979 and 98980 in the same month. Use 98979 for "maintenance" patients who require brief check-ins, and 98980 for patients requiring standard 20+ minute review.
In 2026, 98976/98977/98978 are updated to represent 16–30 days of monitoring; 98984/98985/98986 represent 2–15 days. The 16-day requirement does not “go away”--it is joined by a short-duration option.
FairPath and our agents prompt patients to record therapy adherence, symptom scores, and other RTM data inside a medical-device-qualified app. Prompts may be delivered by SMS or voice, but the clinical system of record is an RTM-eligible device or SaMD, maintaining alignment with RTM device rules.
We count RTM “days” and treatment-management minutes in the background. New for 2026: FairPath identifies when a patient hits the new 2-day threshold, allowing you to bill Setup (98975) and the new short-duration device codes immediately--weeks earlier than previous rules allowed.
Our compliance engine encodes RTM-specific rules: day thresholds for device codes, one-practitioner-per-period limits, incident-to rules for physician practices, therapy plan-of-care and de minimis rules for PT/OT/SLP teams, and coordination with RPM and care-management codes to prevent double-counted time. The result is a clear, exportable audit trail for every RTM claim.
RTM isn't one-size-fits-all. The data captured must be therapeutic and specific to the condition treated.
Target: Post-op joint replacement, chronic back pain.
Data Signals: Range of motion (ROM), exercise repetition counts, and pain scores.
Goal: Identify under-performance due to pain or over-activity that risks injury.
Target: Asthma, COPD.
Data Signals: Inhaler usage frequency (adherence), rescue inhaler spikes, and environmental triggers.
Goal: Detect "rescue" overuse early to prevent exacerbations and ER visits.
Target: Depression, Anxiety, Insomnia.
Data Signals: Homework completion, mood scoring, sleep logs.
Compliance Alert: Not all health apps qualify. To bill 98978 (or 98986), the software must meet the FDA definition of a medical device (SaMD). Generic "wellness" apps do not qualify.
Avoid the common pitfalls that trigger OIG scrutiny.
Use the calculator for current, payer-specific estimates. As a reference point, 2025 national, non-facility Medicare payments are approximately in the high-teens to low-$20s for 98975, low-to-mid-$40s for 98976/98977, around $50 for 98980, and around $40 for 98981. Local Medicare Administrative Contractors and commercial plans set their own rates, and 98978 (CBT device supply) is contractor-priced.
$9,000 based on current RTM reimbursement assumptions for 2025 Medicare non-facility rates.
Values shown are illustrative and based on national Medicare averages; your locality, payer contracts, and program design will affect actual results.
Calculate Your RevenueYes. RTM is “sometimes therapy.” Physical Therapists, Occupational Therapists, and Speech-Language Pathologists can bill RTM within their scope when it is delivered under a therapy plan of care. Physicians and other qualified health care professionals can also bill RTM. Use GP/GO/GN modifiers when RTM is provided as therapy under a plan of care, and follow your MAC’s supervision and documentation rules for the setting.
RTM requires that data be captured and transmitted by a medical device as defined by the FDA. That can include software as a medical device (SaMD), such as a qualified RTM app, but generic wellness apps or informal text messages are not sufficient. You can use SMS or voice to nudge patients, but the data of record must be entered into, or generated by, an RTM-eligible device or app that your billing team can name and document.
For 2025 device-supply codes 98976/98977 (and 98978 where covered), you generally need at least 16 days of RTM data in a 30-day period to bill. Management codes 98980/98981 do not have a 16-day requirement, but you still need legitimate RTM data and documented interaction.
Beginning in 2026, new codes 98984/98985/98986 allow you to bill for 2–15 days of monitoring, while 98976/98977/98978 are updated to explicitly cover 16–30 days.
You must have at least one synchronous, real-time conversation (audio-only telephone or audio-video). Crucial Update: Automated nudges, text messages, AI chat, or portal messages do not count toward the interactive requirement or the clinical labor time.
No. Only one practitioner can bill RTM (or RPM) services for a patient in a given 30-day period, even if multiple clinicians are involved and multiple devices are used. Practices should designate a single billing provider for each patient’s RTM episode and coordinate internally.
In many cases, yes. CMS allows RTM or RPM to be billed in the same month as CCM, PCM, TCM, BHI, chronic pain management, and APCM when the time and services are distinct and not counted twice. The key is that you do not use the same minutes or identical activities to support more than one code family. Your documentation should make the dividing lines clear.
No. CMS requires an established relationship for RPM, but not for RTM. RTM services still must be medically reasonable and necessary, and you must be able to show how RTM data is used in the context of the patient’s care, but there is no explicit “established patient” requirement in RTM policy.
CPT 98978 (and, beginning in 2026, 98986 for 2–15 days) support RTM device supply for cognitive-behavioral therapy–oriented digital therapeutics. These codes are contractor-priced and payer adoption is still evolving. If you provide CBT-aligned digital therapy, confirm your MAC and commercial payer policies before relying on RTM CBT codes in your financial planning.
Yes. In 2026, CMS finalized a policy allowing General Supervision for Physical Therapist Assistants (PTAs) and Occupational Therapy Assistants (OTAs) in private practice. This means the supervising therapist does not need to be in the same building, allowing for centralized remote monitoring teams.
Auditors look for: documented patient consent; the specific RTM device or app (and its status as a medical device); the plan of care or episode definition; day-counts for device-supply codes; cumulative treatment-management time logs; dates, times, and modes of interactive communication; and notes showing how RTM data influenced clinical decisions. The more explicitly you connect RTM data to care-plan changes, the stronger your position in an audit.
For dates of service on or after January 1, 2026, RTM gains new device-supply codes for 2–15 days of monitoring (98984–98986) and a new 10–19 minute treatment-management code (98979). Existing device codes 98976/98977/98978 are revised to clearly represent 16–30 days of RTM in a 30-day period, and 98980/98981 continue to cover longer management time buckets. These changes give you more granular options for short episodes and shorter management engagements, while preserving the ability to bill longer, ongoing programs.
Yes, with caveats. You can bill multiple device codes (e.g., 98976 for respiratory and 98977 for MSK) if the patient has distinct medical needs for both. However, you can still only bill one set of management codes (98980/98981) per month, as management time is per-patient, not per-condition. Coordination is key to avoid "duplicate service" denials.
23 must-have items that saved our clients millions.
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