Abstract
Background:
Telehealth for outpatient palliative care has grown rapidly since the COVID-19 pandemic, yet there remain important questions about the use of telehealth for underserved patient populations in a “postpandemic” society.
Objective:
To examine current perspectives from interdisciplinary providers on the use of telehealth and in-person care for outpatient palliative care among underserved patients.
Methods:
We conducted semi-structured interviews with outpatient palliative care providers and clinic staff (n = 17) from one health system in the United States.
Results:
Providers endorsed tele-palliative care for underserved patients because it enhanced patient-centered care and increased equity. However, providers noted two main challenges to the use of telehealth: technological issues on the part of patients and policies around prescribing controlled substances.
Conclusions:
Future efforts to improve tele-palliative care for underserved patients may focus on technological and institutional infrastructure to support telehealth and consider policies around prescribing controlled substances for palliative care patients.
Key Message
This study highlights current provider perspectives on the use of tele-palliative care for underserved patients in a “postpandemic” society.
Introduction
Patients from underserved communities, or those with low socioeconomic status, rural residents, who belong to a minoritized racial/ethnic group and/or have limited English proficiency (LEP), have historically experienced disparities in palliative care access and quality.1–6 Telehealth may expand access to palliative care for underserved populations but may also pose challenges for building the trust-based relationship intrinsic to high-quality palliative care,7–9 particularly for underserved patients who are less likely to receive goal-concordant care for life-limiting illnesses.4,10,11 As telehealth continues to be widely used in a “postpandemic” world, little is known about the persistent or emerging challenges and benefits of telehealth as a standard modality of care, particularly for underserved patients. The purpose of this study was to examine “postpandemic” perspectives on outpatient tele-palliative care from interdisciplinary providers and clinic staff who provide care to underserved patients.
Methods
We conducted interviews with providers and staff at a large academic health system serving rural, urban, and underserved populations in the southern United States from June to July 2024. The site PI (principal investigator) sent a recruitment email to 19 eligible participants, including attending physicians, nurse practitioners, pharmacists, social workers, chaplains, and administrative support staff. Interviews were conducted using a virtual platform and were facilitated using a semi-structured protocol about providing tele-palliative care (visits conducted by video or phone) to underserved patients. Interviews were conducted by two researchers (J.I.B. and J.T.) trained in qualitative methods and with a background in palliative care and telehealth. The interviews focused on experiences using telehealth to provide palliative care to patients from historically underserved communities, including perceived challenges and benefits of telehealth use, as well as strategies to improve the delivery of care via telehealth. Interviews ranged from 28 to 47 minutes and were audio recorded and transcribed. Interviewees received a $50 e-gift card for participation. The study was approved by the institutional review boards at the authors’ institutions.
Interview transcripts were uploaded to Dedoose to facilitate rigorous thematic coding using an inductive approach. 12 Transcripts were coded by two team members simultaneously during data collection using a codebook that was refined during the process. A codebook was developed, and the first five transcripts were coded to test the codebook. Following further refinement of the codebook, the remaining transcripts were coded. Two team members coded the data, and interrater reliability was established following the achievement of a 0.75 kappa score, indicating strong agreement between coders. 13 Team members, including coders and members of the larger research team, discussed findings throughout the data collection and analysis processes.
Results
We interviewed 17 providers (response rate 89.5%) (see Table 1 for demographics of interviewees). Providers varied widely in the proportion of visits they conducted via telehealth, from a couple of visits a month to 100% telehealth. This variation was mainly due to institutional reasons (e.g., scheduling) and provider preferences. Below we report on themes around challenges to telehealth and benefits of telehealth (see Table 2 for quotes for these two themes). We also report on communication strategies and goals of care (GOC) conversations (see Table 3 for quotes for this theme) and strategies to improve palliative care via telehealth.
Demographics of Interview Participants
This question did not apply to the clinic administrator.
Challenges and Benefits to Telehealth: Additional Quotes
Communication and Goals of Care Additional Quotes
GOC, goals of care.
Challenges to telehealth
Technological challenges
Providers felt that access to a device was not typically an issue for underserved patients but described challenges if the patient did not have a working phone number. For example, one physician described having to call the patient’s landlord to reach the patient if their video platform did not work. Patients often had difficulties navigating the virtual platform or lacked access to quality internet service.
Prescribing controlled substances
Providers reported that state policies for prescribing controlled substances have continued to evolve since the COVID-19 pandemic, and these policies present a barrier to conducting visits via telehealth for many of their patients who are prescribed opioids for pain management. Providers noted the current policy in their state requires an in-person visit every 90 days for patients receiving controlled substances; the policy makes an exception for patients with a “terminal diagnosis” but does not define terminal diagnosis. Providers expressed that these policies are not well-defined and not patient-centered, especially for underserved patients with advanced illnesses who face greater barriers coming to the clinic.
Benefits of telehealth
Telehealth promotes patient-centered care for underserved patients
Providers described how telehealth promotes patient-centered care for underserved patients by offering a virtual option for palliative care, which they noted was preferred by most patients. Providers articulated reasons that patients preferred telehealth, namely transportation challenges and the “hassle” of getting to the clinic while managing a serious illness. While a few providers expressed a preference for in-person visits, they also recognized that patient preference for telehealth carries important value for underserved patients.
Telehealth increases access for underserved patients
Providers expressed that telehealth increases equity and access to palliative care by allowing patients and their caregivers to have a visit without having to miss work or arrange transportation. Providers also noted that “no show” visits or cancelations have decreased following the introduction of telehealth, which may be related to socioeconomic factors such as limited transportation and resources, particularly for underserved patients.
Telehealth provides a holistic view into patients’ lives
Providers described how telehealth offers a holistic view of patients’ lives, in terms of their home surroundings and other aspects of their life beyond their illness. Providers were able to assess if patients’ living situations were “less than ideal” (e.g., bedroom on a third floor only accessible by stairs) and make appropriate referrals if needed (e.g., home health referrals). Telehealth also enables providers to “break the ice” by engaging in short conversations about their surroundings to start the visit. In addition, providers noted that telehealth can level the power dynamic by allowing patients to be comfortable in their own environment.
Communication strategies and GOC conversations
Providers described the pros and cons of communicating via telehealth, particularly for GOC conversations (see Table 3). Some providers preferred to have GOC conversations in-person because they found it easier to establish rapport and be attuned to nonverbal cues. Others felt GOC conversations may be better done by telehealth where the patient is comfortable in their home, surrounded by family members who may not otherwise be able to attend. Some providers perceived no difference in how they communicated between in-person and telehealth visits.
Providers discussed communication strategies for engaging with patients and their family members via telehealth. Many providers noted the importance of maintaining eye contact and proactive communication when they need to look away from the camera (e.g., to view the patient’s medical record or take notes).
Strategies to improve palliative care delivery via telehealth
Providers recommended proactive strategies to address technology issues during telehealth visits. Several providers recommended that clinic staff reach out to new patients in advance to ensure they are ready to use the virtual platform. Other suggestions included having medical assistants virtually “room” the patient or having support staff in a breakout room to troubleshoot patient technology issues. Several providers recommended that clinic staff who schedule visits help triage patients into telehealth or in-person visits based on the reason for a visit.
Providers noted that some of their patients face communication barriers that can make virtual visits challenging, but there are opportunities for telehealth platforms to improve accessibility. For example, patients who cannot vocalize can use the chat feature, and closed captioning can be useful for patients with hearing impairment or LEP. Several providers suggested the need to improve the functionality of the telehealth platform to address communication barriers, such as improving the chat feature, improving closed captioning, and making it easier to include a medical interpreter in virtual visits.
Several providers suggested that for patients living in rural or remote areas, health systems should ideally partner with local providers who could see patients in-person more regularly. Suggestions included dispatching a local nurse to assess patient vitals prior to telehealth visits and having patients’ local providers teleconference with the palliative care team. Providers also suggested alternative delivery models to better meet the needs of patients with serious illnesses who live far from the health system, such as offering a hybrid of home-based visits and telehealth.
Discussion
Providers emphasized the importance of tele-palliative care to enhance patient-centered care and increase equity and access to care in a “postpandemic” society. In Table 4, we outline key findings from interviews with providers and actionable recommendations for improving tele-palliative care.
Opportunities and Actionable Recommendations to Improve Tele-Palliative Care
One of the main challenges providers described was restrictions on opioid prescribing, specifically state policy requiring an in-person visit every 90 days for patients receiving controlled substances. Many providers found this requirement to be an arbitrary and unnecessary challenge to efficiently deliver care. Providers noted that state regulations do not clearly define the criteria for a “terminal diagnosis” that exempts patients from the in-person visit requirement. Opioid prescribing policies that require in-person visits posed greater challenges for the most vulnerable patients, including those who are underserved because of financial reasons, rurality, and challenges coming to the clinic. Though we only spoke to providers in Georgia, this issue is not unique to Georgia; evolving laws and regulations concerning opioid prescribing through telehealth have posed barriers to tele-palliative care in other states. 14 In addition to resources for palliative care providers regarding safe opioid prescribing in telehealth, standard policies and practices around opioid prescribing and telehealth are needed. State policies around opioid prescribing via telehealth should more clearly define “palliative care” and criteria for exemption from in-person visit requirements. Better guidance around how to prescribe controlled substances safely via telehealth is important to create a standard of care for tele-palliative care. These types of practice guidelines would be useful in measuring quality and safety for outpatient palliative care delivered via telehealth, particularly for vulnerable communities with limited access to palliative care.
Providers noted that access to a device was not typically a barrier to telehealth for underserved patients, but challenges with telehealth platforms remained an issue. A “virtual waiting room” may also help to ensure that patients are ready when the visit starts. 15 Investing in these resources may ultimately reduce provider burnout and increase access to care, while also improving organizational efficiencies such as decreasing “no show” visits and cancellations. Health systems may also consider partnering with nonprofit organizations or government initiatives to provide broadband access in rural or underserved areas.
This study represents the perspectives of providers and staff (mainly physicians) at one large health system in the South. Results may not be generalizable to all palliative care programs across the United States, for example, policies for prescribing controlled substances via telehealth vary across states.
Conclusion
This study highlights provider and clinic staff perspectives on tele-palliative care for underserved patients in a “postpandemic” period. Providers were overwhelmingly positive about the use of tele-palliative care to promote patient-centeredness and increase equity and access to care for the most vulnerable patients.
Footnotes
Author Disclosure Statement
D.K. serves on the Board of Directors of the American Academy of Hospice and Palliative Medicine. The views presented herein do not necessarily reflect those of the Academy or its members.
Funding Information
This work was supported by a grant from the National Institute of Nursing Research (1R01NR020788-01).
