key: cord-0943088-s0lo3ech
authors: Roberts, Jordan E.; Halyabar, Olha; Petty, Carter R.; Son, Mary Beth
title: Assessing preparation for care transition among adolescents with rheumatologic disease: a single-center assessment with patient survey
date: 2021-05-01
journal: Pediatr Rheumatol Online J
DOI: 10.1186/s12969-021-00544-y
sha: 9019386be0d07194caafed7dfb7d07c7f1cfa647
doc_id: 943088
cord_uid: s0lo3ech

BACKGROUND: Despite the risk for poor outcomes and gaps in care in the transfer from pediatric to adult care, most pediatric rheumatology centers lack formal transition pathways. As a first step in designing a pathway, we evaluated preparation for transition in a single-center cohort of adolescents and young adults (AYA) with rheumatologic conditions using the ADolescent Assessment of Preparation for Transition (ADAPT) survey. FINDINGS: AYA most frequently endorsed receiving counseling on taking charge of their health and remembering to take medications. Less than half reported receiving specific counseling about transferring to an adult provider. AYA with lower education attainment compared with those who had attended some college or higher had lower scores in self-management (1.51 vs 2.52, p = 0.0002), prescription medication counseling (1.96 vs 2.41, p = 0.029), and transfer planning (0.27 vs 1.62, p < 0.001). AYA with a diagnosis of MCTD, Sjögren’s or SLE had higher self-management scores than those with other diagnoses (2.6 vs 1.9; p = 0.048). Non-white youth indicated receiving more thorough medication counseling than white youth (2.71 vs 2.07, p = 0.027). When adjusting for age, educational attainment remained an independent predictor of transfer planning (p = 0.037). AYA with longer duration of seeing their physician had higher transition preparation scores (p = 0.021). CONCLUSION: Few AYA endorsed receiving comprehensive transition counseling, including discussion of transfer planning. Those who were younger and with lower levels of education had lower preparation scores. A long-term relationship with providers was associated with higher scores. Further research, including longitudinal assessment of transition preparation, is needed to evaluate effective processes to assist vulnerable populations.

The transfer from pediatric to adult care is a highrisk period for poor outcomes [1, 2] . National data show that few adolescents receive comprehensive services to prepare them adequately for the transition to adult care [3] , and many adolescents and young adults (AYA) with rheumatologic conditions experience gaps in care and disease flares around the time they are transferring care [ 4, 5] . Despite these risks, most pediatric rheumatology centers lack formal pathways for transition [6] , and the majority of pediatric and adult rheumatologists feel preparation for transition to adult care is inadequate [7, 8] .

While there is increasing recognition of the need to develop and evaluate transition pathways in rheumatology, few studies have directly evaluated AYAs' preparation for transition in pediatric rheumatology [9, 10] . Most recent work has assessed patient satisfaction with transition interventions [11, 12] , rather than specifically evaluating the content of transition counseling delivered, or assessed rate of successful transfer [13, 14] , which is a crucial metric, but may be impacted by many factors other than a transition intervention. We evaluated the content of transitional care preparation in a single pediatric rheumatology center using a validated quality measure in order to identify areas for improvement.

AYA ages 16 and older with a confirmed rheumatologic diagnosis by ICD9 or ICD10 code, at least 3 prior visits at our rheumatology practice, and email addresses on file were identified by an electronic medical records search. Eligible AYA were emailed a version of the ADolescent Assessment of Preparation for Transition (ADAPT) survey, a validated tool developed to assess patient perception of preparation for transition in adolescents and young adults with chronic diseases [15] . At the time of this baseline survey, no written transition policy was in place and individual provider practices and counseling around the transition process were known to vary substantially. Thus, we sought to evaluate the rate of counseling on specific transition topics to identify gaps and areas for quality improvement. The ADAPT quality measure assesses transition preparation in three domains: (1) self-management, (2) prescription medications, and (3) transfer planning, using specific questions about counseling received and preparatory steps taken, such as receiving a written plan specifying transition to an adult provider. We selected the ADAPT over the TRAQ and other instruments due to its focus on patient perception of provider counseling, rather than assessing baseline transition skills. We felt this would provide the most useful information about patient education in our transition process, including giving a baseline assessment of provider counseling in our division. The survey was adapted for online completion using REDCap (Research Electronic Data Capture) [16, 17] . The tool was modified to expand the age (up to 23) and education (up to college graduate) categories, as our pediatric rheumatology program sees patients until age 22 or college graduation. AYA received an invitation email in October or November 2019, and two reminder emails were sent to nonrespondents. Respondents were offered a $15 gift card for completing the survey. Responses were converted to domain composite scores (self-management, prescription medications, and transfer planning) and analyzed using descriptive statistics. A total transition composite score was computed using the percent of affirmative responses out of all transition items assessed. The association of patient illness and demographic factors with composite transition scores was performed using t-tests and analysis of variance tests. Linear and logistic regression were used to evaluate for independent predictors of transition preparation.

Results 337 eligible AYA were identified and sent a survey invitation via email. 78 patients responded (response rate of 23%), of whom 77 had a visit within the past year and were eligible to complete the assessment tool. Mean age was 18.9 (range 16-23), 83% were female, and 86% were white. Full demographic and disease characteristics of respondents are reported in Table 1 . Compared to respondents, non-respondents were 67% female, and of same age (mean 18.8 years, range 16-23). Self-identified race and ethnicity were available only for respondents. Race recorded in the electronic medical record was compared between groups and was similar, with respondents 78% white, 6% Black, 3% Asian, and 1% American Indian or Alaskan Native versus non-respondents 71% white, 7% Black, 3% Asian, and 1% American Indian or Alaskan Native. Non-respondents had a similar distribution of diagnosis to respondents, with 66% having diagnosis codes for JIA, and 17% for SLE, MCTD and/or Sjögren's. Clinical Juvenile Arthritis Disease Activity Scores (cJA-DAS) were available for a visit within the past year for 65% of JIA patients who responded to the survey, with median score 2 (range 0-26), which was not significantly different from non-responders (median 1, range 0-23).

Respondents most frequently endorsed receiving counseling on taking charge of their health and remembering to take medications, but fewer than half reported receiving specific counseling about transfer to an adult provider (Table 2) .

AYA ages 16-18 had significantly lower scores in all domains compared to those 19 years and older. Those with lower education attainment compared with those who had attended some college or higher had lower scores in self-management (1.51 vs 2.52, p < 0.001), prescription medication counseling (1.96 vs 2.41, p = 0.029), and transfer planning (0.27 vs 1.62, p < 0.001). AYA with longer duration of seeing their rheumatologist had higher transition preparation scores (p = 0.021). When controlling for age, educational attainment remained an independent predictor of higher transfer planning scores (p = 0.037), but not of other measures.

AYA with a diagnosis of mixed connective tissue disease, Sjögren's syndrome or systemic lupus erythematosus had higher self-management scores than those with other diagnoses (2.6 vs 1.9; p = 0.048). Non-white respondents indicated they had received more thorough medication counseling than white respondents (2.71 vs 2.07, p = 0.027).

Survey respondents with diagnosis of JIA (n = 52) reported attending 1 (23%), 2(35%), 3 (17%) or 4 (21%) rheumatology visit with their rheumatologist in the year prior to survey completion; only 4% had 5 or more visits. Those with mixed connective tissue disease, Sjögren's syndrome or systemic lupus erythematosus (n = 15) reported 2 (27%), 3 (53%) or 4 (13%) visits over the same period.

Despite growing awareness of the importance of the pediatric to adult care transition for AYA with chronic illnesses, few youth in our cohort endorsed receiving comprehensive transition counseling, including discussion of transfer planning. This is similar to national data, with the National Survey of Children's Health reporting that just 18% of youth ages 12-17 received comprehensive services for care transition, defined as meeting with their pediatrician alone, addressing skill-building for transition, and receiving counseling about transfer to adult care if needed [3] .

We observed demographic and disease-related differences in transition preparation in our cohort. Non-white patients and those with lupus and related conditions had significantly higher domain scores, possibly reflecting greater provider awareness of these risk factors for poor transfer outcomes, or more frequent contact with their rheumatologist.

Consistent with prior work showing increased transition readiness with older age [18] [19] [20] , we found that transition preparation scores in all domains were highly correlated with age. Our study included older AYA than have typically been assessed in transition program evaluations in pediatric rheumatology, and therefore we were able to show significant gains in the 19 and up age group, which aligns with recent work in youth with inflammatory bowel disease showing that self-management skills may not be achieved until age 18 and after [21] . Therefore, it may be important to frame the young adult years as a time of continued transition skill-building, including support following a first visit with an adult provider [22] .

We also found that AYA with less formal education had lower transfer planning scores even when adjusting for age. This disparity may reflect differences in selfmanagement skills among AYA with less formal education [23] . In our program, many providers have traditionally seen young adults through their graduation from college, and therefore have used this as a milestone to counsel patients regarding transfer timelines. However, this may be less relevant for young adults not enrolled in post-secondary education, and could be a cause of lower preparedness for transfer among those with less formal education. In contrast, a longer-term relationship with a provider was associated with higher transition preparation scores. Our study had several limitations, including a low response rate, though age, race, and diagnosis of respondents were similar to non-respondents. As this was a single-center evaluation, our results may not be generalizable to other centers with different patient populations, referral patterns, and baseline transition processes.

Following closure of the survey, our clinic began distributing a newly created written transition policy to all patients 14 and older at follow-up visits. The importance of a written transition policy has been highlighted in the Six Core Elements of Transition developed by collaborative transition workgroup of the American Academy of Pediatrics, American Academy of Family Physicians, and American College of Physicians, and promoted by the American College of Rheumatology's Transition Toolkit [24, 25] . A written policy was selected as the first step in improving our transition process, as drafting and revising the policy afforded an opportunity for providers with diverse transition counseling practices to build consensus around priority areas for counseling and timelines for transfer, and to communicate this to families in our practice. This transition policy incorporated parent and patient input and addressed expectations for increasing patient responsibility and transition timelines. Additional initiatives were designed to distribute the policy during the COVID19 pandemic, including sending information about the transition policy via email prior to telemedicine encounters and posting the policy to the clinic's patient information website. A repeat survey following full electronic and in-person adoption of the policy is planned to assess improvement from this intervention.

Further research including longitudinal assessment of transition preparation is needed to evaluate effective processes to improve transition outcomes. Assessment of specific transition counseling gaps using tools such as the ADAPT, and evaluation of preparation in those with different demographic characteristics and disease features may help to effectively customize transition initiatives for vulnerable patient populations.

Abbreviations ICD: International classification of diseases; ADAPT: Adolescent assessment of preparation for transition; REDCap: Research electronic data capture; GED: General education development Acknowledgements Thank you to Dr. Sara Toomey for advising on our email version of the ADAP T survey, and to the ADAPT survey team for allowing use of this tool.

Authors' contributions JER conceptualized and designed the study, adapted the survey instrument, drafted the transition policy and initial manuscript, created tables, and reviewed and revised the manuscript. OH contributed to the design of the study, critically revised and led patient and parent review of the transition policy, and reviewed and revised the manuscript. CP assisted in design of analysis plan and carried out the analyses, created tables, and reviewed and revised the manuscript. MBS conceptualized and designed the study, supervised revision and implementation of the transition policy, and reviewed and revised the manuscript. All authors read and approved the final manuscript.

Dr. Roberts was supported by NIH grant 5T32AI007512-34, and a Fred Lovejoy House-staff Research and Education Fund grant. This work was conducted with support from Harvard Catalyst | The Harvard Clinical and Translational Science Center (National Center for Advancing Translational Sciences, National Institutes of Health Award UL 1TR002541). The NIH, Fred Lovejoy Fund, and the Harvard Catalyst had no role in the design and conduct of the study.

Yes n (%)

In the last 12 months, did you talk with this provider without your parent or guardian in the room? 46 (59.7%) 31 (40.3%)

In the last 12 months, did you and this provider talk about you being more in charge of your health? 53 (68.8%) 24 (31.2%)

In the last 12 months, did you and this provider talk about whether you may need to change to a new provider who treats mostly adults? 31 (40.8%) 45 (59.2%)

In the last 12 months, did this provider ask if you had any questions or concerns about changing to a new provider who treats mostly adults?

22 (71.0%) 9 (29.0%)

In the last 12 months, did you and this provider talk about a specific plan for changing to a new provider who treats mostly adults? 

Supporting the health care transition from adolescence to adulthood in the medical home

Current status of transition preparation among youth with special needs in the United States

National Survey of Children's Health (NSCH) data query. Data Resource Center for Child and Adolescent Health supported by the U.S. Department of Health and Human Services, Health Resources and Services Administration (HRSA), Maternal and Child Health Bureau (MCHB)

Accessed 21

Disease activity and transition outcomes in a childhood-onset systemic lupus erythematosus cohort

The challenges of transferring chronic illness patients to adult care: reflections from pediatric and adult rheumatology at a US academic center

Transitional care for rheumatic conditions in Europe: current clinical practice and available resources

Transitioning youth with rheumatic conditions: perspectives of pediatric rheumatology providers in the United States and Canada

US Adult Rheumatologists' Perspective on the Transition Process for Young Adults with Rheumatic Conditions

Pediatric rheumatology: addressing the transition to adult-orientated health care

Transitions in rheumatic disease: pediatric to adult care

Evaluation of a rheumatology transition clinic

British Society of Paediatric and Adolescent Rheumatology. The impact of a coordinated transitional care programme on adolescents with juvenile idiopathic arthritis

Quantitative evaluation of a pediatric rheumatology

Successful implementation of a clinical transition pathway for adolescents with juvenile-onset rheumatic and musculoskeletal diseases

Development and validation of the Adolescent assessment of preparation for transition: a novel patient experience measure

Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support

REDCap Consortium The REDCap consortium: Building an international community of software platform partners

Parents' perception of self-advocacy of children with myositis: an anonymous online survey

Self-management skills in adolescents with chronic rheumatic disease: a cross-sectional survey

An assessment of variables affecting transition readiness in pediatric rheumatology patients

Chronological age when healthcare transition skills are mastered in adolescents/young adults with inflammatory bowel disease

Practical steps to help transition pediatric patients to adult care

Can patient self-management help explain the SES health gradient?

Transitions clinical report authoring group

Supporting the Health Care Transition From Adolescence to Adulthood in the Medical Home

Pediatric to Adult Rheumatology Care Transition

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations

The datasets generated and analyzed during the current study are available from the corresponding author on reasonable request.

Ethics approval and consent to participate This study was approved by the Boston Children's Hospital Institutional Review Board (IRB-P00031635). All eligible patients received an email describing the study and were informed that completing the survey constituted consent to participate.

Not applicable.

The authors declare that they have no competing interests.