Introduction

The use of remote monitoring to evaluate and manage patients with chronic illness has become even more important in the wake of COVID-19. Remote monitoring, which uses digital health technologies to monitor patient data from anywhere, allows patients and providers to manage the chronic disease without relying on in-person appointments. With remote monitoring, patients can self-manage their condition from home, and providers can leverage data on the patient’s condition to inform their clinical decision-making.

Prior to the COVID-19 pandemic, remote monitoring was gaining traction across several disease states, most notably heart disease, mental health, lung disease, and diabetes. COVID-19 accelerated the adoption of remote monitoring dramatically. With patients unable to see their providers in person, remote monitoring, telemedicine, telehealth, and virtual care saw a 20-fold increase in use1, and reimbursement for these services became a focal point for the Centers for Medicare and Medicaid Services (CMS). Remote monitoring is related but distinct from telemedicine by definition and modality in that it involves the interpretation of medical information without a direct, synchronous interaction between the practitioner and beneficiary.

Despite growing interest in the use of remote monitoring, ambiguity2 around reimbursement is still creating barriers to adoption3 and preventing the delivery of effective, socially distanced care for multiple conditions, which could exacerbate inequitable access to digital tools.

In the past several years, CMS has created multiple Current Procedural Terminology (CPT®) codes for remote monitoring services. Four CPT® codes now exist for the provision of “remote physiologic monitoring” services, but CMS has failed to define what it means by “physiologic”, causing providers and payers to question which technologies qualify for reimbursement.

Without clarity on whether a technology qualifies for reimbursement, providers are less able to implement tools that could significantly benefit patient care, lower cost, and increase access for underserved populations. While this is a problem during COVID-19 because of the need for social distancing, it will persist after the pandemic as well.

The current gaps in coding and reimbursement pose a particular problem for the remote treatment of respiratory disease. There are ~16 million people with chronic obstructive pulmonary disease (COPD) in the USA4 and just under 25 million with asthma5, accounting for $130 billion in direct and indirect costs annually for both COPD6 and asthma7. Acute and chronic lower respiratory diseases combined are the third leading cause of death8 in the USA. Furthermore, the social burden of asthma9 and COPD10 is demonstrated by the millions of days absent from work and school by both patients and caregivers.

In this analysis, we explore the history and use of remote monitoring codes for reimbursement, present several examples highlighting existing gaps in coding and reimbursement both in respiratory disease and other chronic conditions, and make recommendations for further clarifying and broadening coverage to enhance equitable access to remote monitoring.

Overview of CPT® and remote monitoring coding

The American Medical Association (AMA) maintains and develops the CPT® code set. CPT® codes are descriptive terms used in reporting medical, surgical, and diagnostic procedures and services that are performed by physicians and other qualified healthcare professionals in the USA. CPT® codes form the basis for reimbursement, research, and tracking medical utilization. Although CPT® codes have existed for numerous remote medical services, until recently, codes to describe general remote monitoring of physiologic data did not exist.

In the 2018 Physician Fee Schedule final rule, CMS concluded that “remote patient monitoring” services could be a significant part of ongoing medical care and that recognition and separate payment for “these services” was to be done “as soon as practicable”.

CPT® collection and interpretation of physiologic data (i.e., “remote patient monitoring”)

CMS chose to activate, cover, and pay for CPT® Code 99091—a code predicated on collection and interpretation of physiologic data, which CMS referred to as remote patient monitoring. Around the same time, CPT® approved three “remote physiologic monitoring” codes (CPT® 99453, 99454, and 99457), which went into effect on January 1, 2019 (Table 1). In September 2018, CPT® created a fourth “remote physiologic monitoring” code (CPT® 99458) that went into effect on January 1, 2020. It is important to note that these codes represent remote physiological monitoring, but also (and arguably more importantly) treatment management services that go well beyond the review of medical device data. However, CMS still had not defined “physiologic”, as reflected in Table 1.

Table 1 Description of current remote monitoring CPT® codes.

“Physiologic” limitations: the challenge of reimbursement given general terms

The lack of definition of “physiologic” has created confusion within the reimbursement community, causing providers and payers to question which technologies and physiologic markers qualify for remote “physiologic” monitoring reimbursement, therefore limiting adoption.

The term “physiologic” appears nearly 80 times throughout the AMA CPT® 2020 Professional Edition codebook. The CPT® Editorial Panel publishes the annual codebook to report the rules and guidelines surrounding CPT® codes and descriptors. Despite urgings by stakeholders for clarity, “physiologic” is not formally defined in the CPT® manual, the CPT® Coding Assistant, a coding “Resource and Coverage Guide”, AMA’s Digital Health Implementation Playbook, nor on any associated website.

CMS coverage and payment of remote physiologic monitoring

In November 2018, CMS extended coverage and payment for CPT® remote physiologic monitoring codes 99453, 99454, and remote physiologic monitoring treatment management services code 99457. In November 2019, CMS announced that it would adopt, cover, and pay CPT® code 99458 for each “additional 20 min”, beginning January 1, 2020. In the Final Rule commentary11, CMS acknowledged the need for clarification of the term physiologic and indicated they would consider these issues in future rulemaking. However, as of September 2020, CMS has not issued regulatory, sub-regulatory, or clarifying policy specific to the entire suite of remote physiologic (9945X) monitoring codes. More broadly, the term physiologic does not have a formal definition by CMS within rule, policy, or even in its listing of chronic diseases and associated terms.

“Physiologic” ambiguity: a respiratory disease case study

There exist a multitude of examples where a narrow definition of physiologic limits the application of remote monitoring, which we describe briefly below. Here, we describe examples in respiratory disease that demonstrate the need for a broadened, clarified definition of physiologic. This respiratory exploration is proposed due to the prevalence and social and economic burden of COPD and asthma, prior published research in this area, provider confusion about coverage, and the relevance of the topic given COVID-19.

Propeller digital therapeutic

Propeller is a Food and Drug Administration-cleared, digital therapeutic that combines inhaler sensors, companion mobile apps, predictive analytics, and monitoring and feedback to support self-management and clinical care for asthma and COPD12,13. Sensors passively monitor the use of inhaled medications, capturing the date and time of each usage, and approximate geographic location (when paired with a smartphone). These signals provide an assessment of daily adherence to controller medication therapy and changes in the use of rescue medications, or short-acting beta-agonists (SABA), which are used for acute relief of asthma and COPD symptoms. Patients have access to these data through web dashboards and smartphone applications. Clinical teams can also access sensor-collected data through a web dashboard to inform clinical decisions such as medication adjustments and receive notifications about patients whose status may be declining.

SABA use as a physiologic measure

Determination of a patient’s respiratory status is made with a combination of clinical input, including physical examination focused on the work of breathing and chest auscultation, patient-reported outcomes and measures including spirometry, heart rate, respiratory rate, oxygen saturation, and exercise testing. We propose that the signals collected by the inhaler sensor provide an objective assessment of SABA use, providing physiological indicators of stable, worsening, or improving lung health.

SABA use is an important marker of respiratory disease status, specifically level of control, disease burden, and risk14,15. Studies have shown that exacerbations—events characterized by a sudden worsening in symptoms requiring an oral corticosteroid, emergency department (ED) visit or hospitalization—may also be identified through increased use of SABA medication. In COPD, SABA overuse is associated with greater disease burden16, and upward trends in use have been associated with an increased risk of moderate-to-severe exacerbations17. Similar outcomes have been observed in asthma18, where increased SABA use has been associated with worsening symptoms and acute exacerbations. Studies have shown that clinically validated asthma and COPD self-reported instruments, such as the Asthma Control Test (ACT)19, Asthma Control Questionnaire (ACQ)20, and COPD Assessment Test (CAT)21, are significantly correlated with SABA use. Lastly, SABA has also been incorporated into the Asthma Medication Ratio22, which is a specific HEDIS criteria measure23, and is a commonly tracked outcome reported in 68% of studies of exacerbations24.

Previously, SABA use could only be captured based on medication pharmacy fill records, patient-reported history, or patients remembering to bring in their medications with a dose counter, making this component of respiratory status require record-keeping and/or presentation to a clinician for assessment. Passive monitoring of SABA with sensors provides a more real-time and objective component of evaluating respiratory status remotely, enabling early intervention to avoid unnecessary exacerbations.

Clinical benefit of respiratory monitoring

Respiratory digital therapeutics have been studied in multiple randomized controlled trials and observational studies. Across these studies, significant improvements in asthma and COPD outcomes have been demonstrated in association with their use, including reduction in daytime and night-time self-reported symptoms15, reduction in SABA use13,25, increase in the number of SABA-free days12,13, improvement in asthma control as measured by the ACT26,27, and improvement in adherence to controller medications28,29,30,31. These benefits have been observed in diverse participants, including underserved patients with both asthma and COPD13,26. Significant reduction in acute healthcare utilization, including ED visits and hospitalization events, has been demonstrated for both asthma and COPD27,29,32.

Ambiguity in multiple disease states

In other disease states, a similar promise yet ambiguity exists. In mental health, codes to support remote cognitive behavioral therapy33 are being developed; however, they do not necessarily cover other emerging signals, such as monitoring of smartphone usage or activity patterns, which may provide early indicators of depressive, anxious, or other pathologic behaviors34. For Parkinson’s disease, wearable sensors offer promise in remotely monitoring motor fluctuations, immobility, and tremors35, which can identify treatable symptoms such as dyskinesia and bradykinesia, but may not be covered by traditional physiologic monitoring codes.

These signals from multiple disease states demonstrate that digital health deployed for remote monitoring can serve as an important tool for medical practitioners, specialists, and clinicians to assist patients living with a multitude of conditions. It is therefore in the interest of those medical professionals who employ the use of remote monitoring technologies to accurately understand medical diagnostic and therapeutic services, particularly in the context of coding, coverage, and payment.

Regulatory clarity is needed

Without any definition or clarification by AMA/CPT, CMS, or a medical society that formally excludes digital health technologies as a valid mechanism by which to capture physiologic markers for purposes of remote physiologic monitoring, there is no conclusive exclusion to the broad use of the term “physiologic”.

CMS may at any given time produce regulatory or sub-regulatory policy guidance clarifying their position. In the absence of authorities limiting their power, such as national coverage determinations, the contractors in any one of the 12 Medicare Parts A and B and four Durable Medical Equipment Medicare Administrative Contractors regions, acting under their specific geographic jurisdiction, may at their discretion deny claims based on their particular opinion or other arbitrary factors. CPT® code reimbursements are therefore vulnerable given the lack of clear definitions.

As digital health innovation proliferates, CPT® should continue to explore code gaps and create additional remote monitoring codes that describe other ways to evaluate patient status. As announced publicly by CPT® in anticipation of the CPT® Editorial Panel Meeting in October 202036, several applications to create new codes have been submitted for consideration, including one submitted by Propeller Health for Remote Respiratory Status Monitoring Services.

Conclusion

Based on all of the foregoing, including medical practice and evidence, “physiologic”, as used by CPT® codes for “Remote Physiologic Monitoring” should encompass these services. Inhaler sensors, used in conjunction with medicines and provider services, satisfy the professional and technical requirements11 for remote patient monitoring and remote physiologic monitoring CPT® codes.

As the US progresses through the COVID-19 pandemic, remote monitoring and other forms of virtual care will become increasingly critical to delivering effective healthcare while reducing infection risk and patient access to these tools should be equitable. An important step in addressing equity is to ensure that systemic reimbursement barriers, like the ambiguity of the definition of “physiologic”, do not disproportionately affect beneficiaries of public insurance more than those with commercial insurance or who are paying cash. In addition, temporary waivers, such as lifting geographic care site restrictions or administrative sanctions for providers who reduce or waive cost-sharing obligations, could temporarily incentivize providers.

Increased utilization of virtual care in healthcare, which has been implemented on an emergency basis during the COVID-19 pandemic, now needs to be integrated permanently. Chronic respiratory disease care is just one example of the many conditions that could benefit from expanded access to remote monitoring.