key: cord-0735066-10um0953 authors: Solomon, George M.; Bailey, Julianna; Lawlor, James; Scalia, Peter; Sawicki, Gregory S.; Dowd, Christopher; Sabadosa, Kathryn A.; Van Citters, Aricca title: Patient and family experience of telehealth care delivery as part of the CF chronic care model early in the COVID-19 pandemic() date: 2021-12-18 journal: J Cyst Fibros DOI: 10.1016/j.jcf.2021.09.005 sha: 1630f7745ab170c417b5e234cc4c561e856fbac2 doc_id: 735066 cord_uid: 10um0953 BACKGROUND: During the COVID-19 pandemic, CF centers shifted to a telehealth delivery model. Our study aimed to determine how people with CF (PwCF) and their families experienced telehealth and assessed its quality and acceptability for future CF care. METHODS: The CF Patient and Family State of Care Survey (PFSoC) was fielded from August 31-October 30, 2020. The PFSoC explored themes of overall telehealth quality, ease of use, desirability, and preference for a future mix of in-person and telehealth care. Demographic covariates considered included: gender, age, CFTR modulator status, and region of residence. RESULTS: 424 PwCF and parents of PwCF responded (47% parents). Most (81%) reported a telehealth visit which included a MD/APP and nurse team members. 91% found telehealth easy to use, and 66% reported similar/higher quality than in-person care. One-third (34%) reported the highest desire for future telehealth care, with 45% (n =212) desiring 50% or more of visits conducted via telehealth. Adults were more likely than parents to report highest desire for future telehealth (64% vs. 36%). Respondents who perceived telehealth as similar/higher quality were more likely to desire future telehealth compared to those who perceived telehealth as lower quality (96% vs. 50%). Mixed methods analysis revealed themes affecting perceptions of telehealth. CONCLUSIONS: PwCF desire for future telehealth was influenced by perception of quality and age. Several themes emerged that need to be explored as telehealth is adapted into the CF chronic care model, especially when thinking about integration into pediatric care. Cystic fibrosis (CF) is a chronic genetic disease that involves multiple organ systems but primarily impairs the lungs and gastrointestinal tract [1] . Survival has increased rapidly over the past 3 E-mail address: gsolomon@uabmc.edu (G.M. Solomon). # Indicates authors Contributed equally decades, largely due to development of highly effective novel drug therapies and advancements in the robust clinical care provided by CF Foundation (CFF) accredited care centers [ 2 , 3 ] . The CF care model prioritizes regular quarterly visits with an interdisciplinary CF care team where treatment plans are updated and maintained in collaboration with people with CF (PwCF) and families. During the COVID-19 pandemic, routine in-person CF clinic visits were interrupted, necessitating a rapid shift to providing multidisciplinary telehealth care. Prior to the COVID-19 pandemic, limited evidence supported the efficacy of telehealth in the CF care model although several pilot studies explored introduction of outpatient CF telehealth [4] [5] [6] [7] [8] [9] [10] . Small single center studies of feasibility of telehealth in CF found improved access to clinical care for adults living in rural settings [6] , large potential cost savings [4] , and high levels of patient [ 5 , 6 ] . However, another study raised concerns with poor patient acceptance of the virtual model and noted no impact on pulmonary function after five years of telehealth interventions [11] . This study also highlighted legal and regulatory barriers to widespread implementation of telehealth practices after completing a 10-year study of telehealth in CF [11] . At the onset of the pandemic in early 2020, a large-scale shift to virtual care occurred to facilitate social distancing, to permit clinics to redistribute resources to meet other healthcare demands, and to promote infection control. These system changes coupled with regulatory and payer changes enabled a rapid adoption of telehealth in CF centers across the world [12] . Two adult CF programs demonstrated successful implementation of a multidisciplinary telehealth model of CF care with PwCF expressing positive regard for telehealth at the beginning of the pandemic [ 13 , 14 ] . Given the rapid and unexpected integration of telehealth into the CF care model, Davis and colleagues designed cross sectional surveys to explore pediatric and adult patient and family experience of telehealth care in the context of the COVID-19 pandemic [15] . Surveys were deployed at 11 CF centers and results indicated that most PwCF and families were highly satisfied with telehealth [15] . This work suggests that multidisciplinary telehealth care in CF was convenient and well accepted by PwCF and their families at the beginning of the pandemic [15] . However, there were several limitations of this work. The CF care centers surveyed were early adopters of telehealth and therefore, may have viewed it more favorably. The surveys were also cross-sectional and may only be representative of when telehealth was mandated due to social distancing. To more broadly understand telehealth experiences of PwCF and families, the CFF developed a Patient and Family State of Care (PFSoC) Survey. The objective of this study was to explore patient and family perceptions on different facets of the use of telehealth in the CF care model. The PFSoC was distributed to PwCF and families via CF care programs, CFF Community Voice newsletter, and the CFF Facebook page between August 31 and October 30, 2020. It included questions about the care experience and perceptions on the quality of telehealth, access to interdisciplinary care, and the desire for telehealth care as part of the CF care model. It also included open-end questions inviting comments regarding the quality of telehealth care, reasons for their assessment of quality, reasons for higher or lower desire for telehealth care in the future, and suggestions for improving delivery of future telehealth care. A detailed description of survey methods and respondent characteristics compared to a national sample is provided by Dowd and colleagues [16] . Telehealth use was surveyed by questions related to receipt of telehealth and mode of telehealth. Telehealth perceptions were surveyed by questions related to ease of use, overall quality of telehealth relative to in-person care, participation of care team members in the telehealth visit, proportion of top-box responses (those reporting scores of 9/9) to questions asking about care quality and ease of participation, and benefits and limitations of telehealth. Additional questions assessed desire for future telehealth in the CF care model; preferred mix between in-person and telehealth services; and recommendations for care model components to continue or change in the future. Independent variables included self-reported respondent type (adult with CF/parent of a child with CF), use of a modulator (yes/no), gender (male/female), or region of the US (Midwest, Northeast, Southeast, Southwest, and West). Data were summarized with descriptive statistics. Relationships between dependent and independent variables were determined with chi-square ( χ 2 ) analyses. We used two-sided significance tests and a P -value threshold of < 0.05 to identify significant differences. Analyses were conducted with SPSS (version 26.0). Qualitative analyses for free-text responses were conducted with Atlas.ti (version 8.4.5). We used inductive thematic analysis to identify themes and sub-themes. Qualitative data were independently coded by two reviewers (AVC and PS). Responses between reviewers were evaluated for consensus, and discrepancies were resolved via conversation. Human-subjects approval was granted by Advarra.com (Marshall, Pro0 0 045302). The PFSoC was completed by 424 participants, including 222 adults with CF (52.5%) and 201 parents of a child with CF (47.5%). A majority of respondents were female (59%) and most reported taking a CFTR modulator (71.5%). Respondents were distributed throughout the United States, with roughly one-fifth in the Midwest, Northeast, and Southeast, 28% in the West, and 10% in the Southwest. Respondent characteristics are described in detail by Dowd and colleagues [16] . Four-fifths (81%, n = 328) of PwCF indicated that they had a telehealth visit, either by phone or video connection, since the start of the COVID-19 pandemic. Among the 76 PwCF that had not had a telehealth visit, the most common reasons were the absence of health concerns (n = 30), participation in an in-person visit (n = 22), or preference to not receive telehealth services (n = 19). Less common reasons included the lack of a request by the care team to schedule a telehealth visit (n = 8), concerns regarding co-pays or insurance (n = 5), cross-state restrictions on telehealth (n = 3), and technical difficulties with telehealth (n = 3). PwCF who received telehealth services most often reported having a video component to their visit (n = 287, 88%). Among those that reported receiving a "phone only" telehealth visit (n = 40), this approach was chosen based on PwCF preference (n = 18) or care team preferences (n = 11). Less common reasons included challenges with the video technology (n = 5) or a lack of reliable internet (n = 3). Ninety-one percent (n = 294) of PwCF found the telehealth technology easy to use. Those who did not find it easy to use (n = 31) cited difficulty using the telehealth platform (n = 15, e.g., a need for a more reliable, user-friendly platform; a need to download applications; multiple layers of security), poor sound or video quality (n = 7), or poor internet connection (n = 6). These data are summarized in Fig. 1 A and B. PwCF were more likely (66%, n = 205) to feel that telehealth services were of equal or higher quality than in-person services. Overall quality data are summarized in Fig. 1 C. There were no differences in perceptions of quality among PwCF by respondent type, receipt of a modulator, gender, or region of the country. These data are summarized in Supplemental Figure 1 . Most PwCF (95%) reported that they interacted with a provider (MD/APP) during their last telehealth visit or during an additional phone or video visit. Over half of PwCF reported interacting with a nurse (63%) or dietitian (54%) during their telehealth visit or in an additional phone or video visit. Less than half of patients reported interacting with other members of the multidisciplinary team, including the social worker (44%), respiratory therapist (34%), physical therapist (8%), pharmacist (24%), or mental health coordinator (16%). See Supplemental Figure 2A . Most PwCF provided a top-box score indicating that every effort was made to ask about topics or concerns that patients wanted to discuss (75%, n = 231), help them understand their health issues (73%, n = 224), listen to the things that matter most (74%, n = 227), include what matters most in choosing what to do next (69%, n = 214), provide adequate time with team members (71%, n = 219), and schedule the visit at a time that works for the PwCF (73%, n = 225). See Supplemental Figure 2B . Among PwCF who perceived telehealth as somewhat or much better than in-person care (n = 25), the greatest benefit of telehealth was the savings in time spent traveling to the CF clinic, followed by not needing to take time off from work or school. Other benefits are shown in Fig. 2 A. Among PwCF who perceived telehealth as somewhat or much worse than in-person care (n = 106), more than three-quarters of individuals noted limitations associated with the lack of physical examination (81%, n = 86), the lack of a sputum or throat culture (81%, n = 86), and the lack of a pulmonary function test (69%, n = 73). One-third (29%, n = 31) found it difficult to connect with the care team on a personal level, and 18% (n = 19) felt that the telehealth connection was unstable. Other limitations are outlined in Fig. 2 B. One-third (34%, n = 104) of PwCF provided the highest level of desire for telehealth. Overall desire is illustrated in Fig. 3 A. PwCF with the highest desire for future telehealth, were more likely to think that the quality of telehealth care was the same or better than in-person care (96.2%; 100/104) compared to those with lower desire (50%; 102/203). See Figure 3B . Telehealth was more desired by adults with CF (40%, n = 66 of 166) than parents of children with CF (26%; n = 37 of 141), p = .021. See Supplemental Figure 3A . There were no differences among PwCF who expressed strongest desire for telehealth when compared by modulator status of the respondent (yes/no), gender (male/female), or region of the country. These data are summarized in Supplemental Figure 3 B-D . PwCF who rated their desire for telehealth as an 8 or lower on a 0-9 rating scale identified a number of changes needed to provide a higher rating for telehealth. The most frequently identified changes included issues related to measurement and testing, the model of care (emphasizing preference for in-person care), and issues of care quality and access. These themes are presented in Table 1 . When asked about the mix of telehealth, approximately equal proportions of PwCF preferred all or mostly telehealth (20%, n = 62); half and half telehealth and in-person (25%, n = 76); or all or mostly in-person care (24%, n = 73). The remainder were unsure or had other preferences (31%, n = 93). These data are summarized in Fig. 3 C. There were no differences in preferred mix of in-person and telehealth visits by age, gender, modulator status, or region of residence in the country. The qualitative observations of PwCF regarding the CF care model and changes implemented since the pandemic began are delineated in Table 2 . PwCF would like to see continued availability of telehealth and would like to see changes or improvements in measurement and testing associated with telehealth visits. We analyzed a large, nationwide dataset of the experiences of PwCF and families with telehealth from early in the COVID-19 pandemic. This mixed-method analysis was clustered around overall experience of telehealth, perception of quality of telehealth, and desire for future telehealth in the CF care model. We found that the majority of survey respondents felt that telehealth was easy to use (usually limited by technology concerns), and greater than two-thirds of patients felt telehealth was of similar or greater quality than in-person visits. It should be noted, however, that only a small proportion of respondents felt telehealth was of greater quality than in-person care, signaling. that telehealth is not the sole preference of CF care. Most visits involved physician and advance practice providers and some other members of the multidisciplinary team. The majority of PwCF or families of PwCF felt that their needs were met in telehealth visits. Convenience factors were most commonly cited amongst those who felt telehealth was superior to in-person care, and lack of key assessments (PFTs, etc.) were commonly cited by the one third of patients who felt that telehealth was of poorer quality than in-person visits. Subgroup analyses did not suggest key demographics differences in assessment of quality. These subgroup data suggest that telehealth is viewed similarly across a broad spectrum of PwCF. This assessment of quality overall compares to themes and quantitative assessment of quality from previously published limited samples [15] . However, this sample did assess a significant number of patients who had not experienced telehealth and this may have influenced perception of telehealth. This survey also includes data regarding PwCF and family perception of telehealth in those who a Responses are limited to PwCF that responded with an 8 or lower to the following question: "On a scale from 0-9, please indicate your desire for future telehealth visits?" (n = 204 of 308 respondents). The sample size was further reduced by 1 PwCF that did not respond to the question regarding quality of telehealth. had not experienced this mode of care delivery, which is unique compared to other recent publications of telehealth experience of care [15] . Respondents were more mixed on their desire for future telehealth, in contrast to previously published work [15] ; although, we also found that families of children with CF were less likely to de-sire telehealth than adults, indicating a perception gap between ages that compares similarly to survey data from providers [17] . In contrast, other key demographics did not influence desire for future telehealth. Importantly, the perception of quality is a strong, independent predictor of desire of future telehealth. Respondents were equally distributed in their preference for mix of telehealth and in-person care in the future of CF care. These demographics differences will need further exploration as the optimum population of PwCF for telehealth care is examined in future research. The study has some noted limitations. It is a relatively small sample size with 20% having not experienced telehealth at the time of the survey, but it adds a larger, national sample to the existing data available on PwCF and family perception. While this data will be helpful to determine the optimal conditions for future telehealth, it will not answer questions about perception after more frequent utilization of telehealth. There is work underway to repeat these analyses to determine the ongoing strength of perception both by the CFF and other smaller networks of CF centers. Finally, analyses regarding perceptions of quality were only differentiated on the basis of respondents' overall assessment of quality of telehealth. Therefore, additional work will be needed to understand if suggested improvements to telehealth are similar in respondents with differing views on the quality of telehealth. This summary data adds confidence to a growing body of literature of an overall positive perception of telehealth in CF and a desire to use telehealth in the future, especially for visits involving physician and advance practice providers. More research is needed to determine the optimal process for multi-disciplinary telehealth visits, including potential blend of in-person and telehealth models. Further, age differences will require attention in planning for the frequency and mix of telehealth and in-person visits in pediatric versus adult care centers. Finally, establishment of effective at-home monitoring and alleviation of technical issues will need special attention (see companion manuscripts) to adopt telehealth in the CF care model after COVID-19. There are no conflicts of interest. New and emerging targeted therapies for cystic fibrosis Cystic Fibrosis Foundation Patient Registry: 2019 Annual Data Report. 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Funding provided by NIH (1K08HL138153-01A1 and 2P30DK072482-12) and CFF (Solomon 20Y0 and NELSON20QI0). Supplementary material associated with this article can be found, in the online version, at doi:10.1016/j.jcf.2021.09.005 .