Abstract
We aimed to investigate (1) student-led clinics and (2) electronic patient-reported outcomes (ePROs) to accelerate diagnosis and treatment of patients with axial spondyloarthritis (axSpA). Patients with suspected axSpA completed an initial student-led clinic visit (T-1) prior to their planned actual rheumatologist visit (T0). Acceleration of patient appointment and NSAID therapy start, availability of diagnostic findings, and treatment response at T0 were evaluated. Beginning at T-1, patients completed electronic BASDAI questionnaires every 2 weeks. Concordance of paper-based and electronic BASDAI was evaluated. Patient acceptance of ePRO reporting and student-led clinics was measured using the net promoter score (NPS). 17/36 (47.2%) included patients were diagnosed with axSpA. Student-led clinics (T-1) significantly accelerated patient appointments by more than 2 months (T0, T-1, p < 0.0001) and axSpA guideline-conform NSAID treatment (p < 0.0001). At T0, diagnostic workup was completed for all patients and 7/17 (41.2%) axSpA patients presented with a clinically important improvement or were in remission. 34/36 (94.4%) patients completed at least 80% of the ePROs between T-1 and T0. Electronic and paper-administered BASDAI correlated well (r = 0.8 p < 0.0001). Student-led clinics and ePROs were well accepted by patients with NPS scores of + 62.0% (mean ± SD 9.2/10.0 ± 0.9) and + 30.5% (mean ± SD 8.0/10.0 ± 1.7), respectively. In conclusion, student-led clinics and ePRO monitoring were well accepted, accelerated diagnostic workup and treatment in patients with axSpA.
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Introduction
Axial Spondyloarthritis (axSpA) is one of the more common inflammatory rheumatic diseases with an estimated prevalence of 0.3–1.4% [1, 2]. Despite the availability of improved diagnostic aids and various health service strategies [3], the diagnostic delay of axSpA patients does not decline with around 7 years in Europe [4, 5]. This diagnostic delay often results in irreversible damage, worse treatment, and overall worse prognosis [6] and quality [7] of life. The increasing shortage of rheumatologists is likely to create an even greater diagnostic delay [8].
As a rapid expansion of the rheumatology workforce seems unlikely, innovative new health care strategies are needed. Delegation of tasks and implementation of telehealth are being increasingly discussed and adopted as two main methods to counteract the workforce shortage [9]. Delegation of tasks to specialized rheumatology assistants is increasing, and studies report high patient acceptance [10] and non-inferiority compared to standard care [11]. In other disciplines, e.g., diabetology and hypertensiology, student-led clinics also relieved the health care system and improved patient health outcomes [12]. The added value of student-led clinics in rheumatology is currently unclear.
Electronic patient-reported outcomes (ePROs) enable a flexible and yet standardized disease monitoring. A recent study reported a higher adherence in axSpA patients with high disease activity and a decline after time, suggesting that especially newly diagnosed patients would be motivated to adhere. With regard to the recommended initial therapy with NSAIDS [13], ePRO monitoring could be used to actually guide therapeutic decisions, i.e., switch to another NSAID or escalation of treatment.
Our study aimed to investigate two innovative health services, including (1) the implementation of student-led clinics and (2) electronic patient-reported outcomes to accelerate diagnosis and treatment of patients with axial spondyloarthritis (axSpA).
Methods
Study design
This prospective study was approved by the institutional review board (IRB) of the Medical Faculty of the University of Erlangen-Nürnberg, Germany (21–357-B) and conducted in compliance with the Declaration of Helsinki. During the recruitment period (October 2021–July 2022), patients referred by their (primary care) physician for rheumatologic evaluation due to the leading symptom chronic low back pain for at least 3 months and suspected axSpA were recruited. Further inclusion criteria were a minimum age of 18 years, sufficient language skills, and regular usage of a smartphone. Exclusion criteria were a known diagnosis, a previous rheumatologist appointment and unwillingness or inability to comply with the protocol. All study patients provided written informed consent prior to study participation.
Patients completed the student-led appointment (T-1) with one medical student trained for this purpose, prior to the routine rheumatology appointment (T0). Availability of medical findings was assessed at T-1 and at the actual visit with the rheumatologist (T0). Additionally, patients installed a medical app to answer disease activity questionnaires and answered a questionnaire regarding diagnostic delay. Patient acceptance was measured using the net promoter score [14] (NPS), which is based on an 11-point numeric rating scale (0–10). Answers between 0 and 6 are categorized as detractors, 7 and 8 as passives, and 9 and 10 as promoters. The NPS is equal to the percentage of promoters subtracting the percentage of detractors.
Student-led clinics (T-1)
A medical student independently studied axSpA disease and shadowed rheumatology residents in dedicated axSpA clinics to learn how to carry out a standardized evaluation and axSpA diagnosis. The student then documented the medical history in a standardized fashion, performed a standardized physical examination at T-1, and was given access to laboratory and imaging results once available. After each diagnostic step, the student had to state if axSpA was present or not (yes/no). Results were compared to the final diagnosis reported on the discharge summary report. A rheumatology resident reviewed the results and discussed next steps (start of therapy, further diagnostics) with the patient and student.
Electronic Patient-Reported Outcomes (ePRO)
At T-1, a medical app (ABATON) was installed on the patient’s smartphone and patients were asked to complete the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) [15] electronically and on paper at T-1 and hence electronically every 2 weeks. If the patient forgot to answer the questionnaire, he was reminded to answer on 3 consecutive days. Concordance of electronic and paper BASDAI results and adherence were analyzed. At T0, the physician was given access to BASDAI results, enabling a standardized evaluation of NSAID treatment response started at T-1.
Statistical analysis
No formal sample size calculation was performed due to the exploratory character of the trial. Following recommendations for pilot studies [16], the number of patients was set at 40. Statistical analysis was performed using Microsoft Excel 2019 and GraphPad Prism 8. P values less than 0.05 were considered significant. Patient-to-patient comparisons were summarized by median and interquartile range (IQR, interquartile range 25th and 75th percentiles) for interval data and as absolute (n) and relative frequency (percent) for nominal data. Statistical differences were assessed by Mann–Whitney U test, Kruskal–Wallis test with Dunn’s test for multiple comparisons, Spearman correlation analysis (rs), and Fisher's exact test for categorial variables. Results were reported following the STAndards for the Reporting of Diagnostic accuracy studies guideline [17]. Diagnostic accuracy of the medical student was evaluated referring to sensitivity, specificity, and overall accuracy.
Results
17/36 (47.2%) of patients were diagnosed with axSpA. Three patients were lost to follow up due to missed appointments and one patient refused to participate. Baseline patient characteristics are shown in Table 1. Median age was 37.2 years; 21/36 (58.3%) were female.
At T-1, CRP level had not been assessed in 19/36 (53%) patients, and no sacroiliac joint X-ray and lumbar/sacroiliac MRI scan was available in 31/36 (86%) and 16/36 (44%) patients, respectively (Fig. 1). Due to the student-led clinics, all diagnostic workup had been completed at T0.
Symptom onset preceded T0 by a median of 889 (1507) days (IQR); see Table 2. 14/36 (39%) of patients checked their symptoms on the internet prior to their appointment, 273 (449) days before T0. Time until first presentation could be reduced significantly from an average of 92 days (T0) to 25 days (T-1); p < 0.0001. Student-led clinics also significantly reduced the time interval from the suspected diagnosis to the first on-site presentation appointment.
Only a minority of patients (4/17, 23.5%, Fig. 2A) had already undergone guideline-conform therapeutic steps of axSpA with two different NSAIDs, each for at least 2 weeks, before first presentation at T-1. NSAID treatment/NSAID rotation, physiotherapy, or app-based physical therapy could be initiated already before T0, as soon as the diagnostics were completed. On average, this allowed guidelines-based NSAID therapy to be initiated significantly earlier with 22 days before T0 in axSpA patients; see Table 2. At T0, 2/17 (11.8%) axSpA patients presented with a clinically important improvement (reduction of ASDAS-CRP ≥ 1.1) and 5/17 (29.4%) patients were in remission (ASDAS-CRP < 1.3); see Fig. 2B. The majority of the 7 NSAID-treated patients at T-1 clinically improved (1/7, 14.3%) or reached remission (4/7, 57.1%) until T0 (Fig. 2C). The student's diagnostic accuracy slightly decreased with physical examination but gradually increased after review of laboratory results and imaging, respectively, to 86.1% (sensitivity 76.5%, specificity 94.7%), online supplemental material S1.
Early initiation of axSpA therapy. A The therapies of the 17 axSpA patients at the time before T-1 and before T0 are shown. B ASDAS-CRP scores of all axSpA patients and C of all newly NSAID-treated axSpA patients at T-1 and T0 are demonstrated. Statistical significance was assessed using the Mann–Whitney U test
34/36 (94.4%) patients completed at least 80% of the ePROs between T-1 and T0 enabling remote monitoring of disease activity and therapeutic response. Electronic and paper-administered BASDAI correlated well at T0 (r = 0.8 p < 0.0001, online supplemental material S2).
Patient acceptance was high for the student-led clinic and ePRO monitoring with a NPS of + 62% (mean ± SD 9.2 ± 0.9) and + 30.5% (mean ± SD 8.0 ± 1.7), respectively, online supplemental material S3.
Discussion
To our knowledge, this is the first study to examine the added value of student-led clinics and ePROs to accelerate diagnostic workup and treatment in patients with suspected axSpA. Due to the implementation of student-led clinics, patient appointments could be accelerated by more than 2 months, so that all diagnostic workup was complete at the actual rheumatologist visit and some patients already reached the goal of clinical remission. Importantly, patients showed great acceptance and also rheumatologists enjoyed the concept as student-led clinics also drastically reduced their consultation workload. Importantly, the medical student gained valuable clinical experience. The task of a sequential diagnosis (axSpA; yes/no) further supported critical diagnostic thinking. The general increase in diagnostic accuracy with additional information available supports a previous study by Ehrenstein et al. [18], that also examined relative contributions of sequential diagnostic steps. Being limited to medical history data only, they could show that even experienced rheumatologists only reach a diagnostic accuracy of 27%.
Early implementation of ePROs enabled remote, yet standardized assessment of a therapeutic response and importantly timely change of treatment. The concordance of paper-based and electronic BASDAI and high adherence of ePRO monitoring in patients with high disease activity is in line with the previous work [19]. To ensure monitoring adherence also in patients in remission, we believe that there needs to be a clear benefit for patients, such as the optional elimination of a physical appointment. In a large survey, we could previously show that patients generally embrace this concept [20]. Importantly, de Thurah et al. could previously demonstrate in a large randomized-controlled trial (RCT) that ePRO-based monitoring is safe in patients with rheumatoid arthritis [21]. Two large RCTs [22, 23] are currently ongoing and exploring, whether this ePRO-based monitoring is also safe in axSpA patients. In a different study (in review), we could demonstrate that the gold standard for disease activity monitoring, the ASDAS-CRP can be completely carried out at home by patients using a medical app and self-collecting capillary blood for CRP analysis, similar to the previous studies [24, 25].
Limitations
The small sample size and monocentric nature of the study are clear limitations. The individual student and app used for ePROs likely had a great impact on patient acceptance. The results should, therefore, be confirmed in larger studies at other centers, with different personnel and apps. The general concept could be rolled out to other diseases.
Conclusion
The need for innovative rheumatology health service strategies is imminent. Implementation of student-led clinics and asynchronous telehealth services, such as ePROs, could contribute to accelerate diagnosis and more efficient use of limited healthcare resources. Analysis of cost-effectiveness and safety will be essential for wider implementation. Additionally, work load reduction and acceptance of physicians should be evaluated in future studies.
Availability of data and materials
Data analyzed during the current study are available from the corresponding author on reasonable request.
References
Sieper J, Poddubnyy D (2017) Axial spondyloarthritis. Lancet 390(10089):73–84. https://doi.org/10.1016/S0140-6736(16)31591-4
Bohn R, Cooney M, Deodhar A, Curtis JR, Golembesky A (2018) Incidence and prevalence of axial spondyloarthritis: methodologic challenges and gaps in the literature. Clin Exp Rheumatol 36(2):263–274
Abawi O, van den Berg R, van der Heijde D, van Gaalen FA (2017) Evaluation of multiple referral strategies for axial spondyloarthritis in the SPondyloArthritis Caught Early (SPACE) cohort. RMD Open 3(1):e000389. https://doi.org/10.1136/rmdopen-2016-000389
Redeker I, Callhoff J, Hoffmann F, Haibel H, Sieper J, Zink A, Poddubnyy D (2019) Determinants of diagnostic delay in axial spondyloarthritis: an analysis based on linked claims and patient-reported survey data. Rheumatology (Oxford) 58(9):1634–1638. https://doi.org/10.1093/rheumatology/kez090
Garrido-Cumbrera M, Navarro-Compan V, Bundy C, Mahapatra R, Makri S, Correa-Fernandez J, Christen L, Delgado-Dominguez CJ, Poddubnyy D, Group EW (2022) Identifying parameters associated with delayed diagnosis in axial spondyloarthritis: data from the European map of axial spondyloarthritis. Rheumatology (Oxford) 61(2):705–712. https://doi.org/10.1093/rheumatology/keab369
Seo MR, Baek HL, Yoon HH, Ryu HJ, Choi HJ, Baek HJ, Ko KP (2015) Delayed diagnosis is linked to worse outcomes and unfavourable treatment responses in patients with axial spondyloarthritis. Clin Rheumatol 34(8):1397–1405. https://doi.org/10.1007/s10067-014-2768-y
Poddubnyy D, Sieper J (2021) Diagnostic delay in axial spondyloarthritis - a past or current problem? Curr Opin Rheumatol 33(4):307–312. https://doi.org/10.1097/BOR.0000000000000802
Knitza J, Krusche M, Leipe J (2021) Digital diagnostic support in rheumatology. Z Rheumatol 80(10):909–913. https://doi.org/10.1007/s00393-021-01097-x
Miloslavsky EM, Bolster MB (2020) Addressing the rheumatology workforce shortage: A multifaceted approach. Semin Arthritis Rheum 50(4):791–796. https://doi.org/10.1016/j.semarthrit.2020.05.009
Mai A, Abrantes Diaz S, Stein M, Denz R, Klaassen-Mielke R, Timmesfeld N, Krause D, Braun J (2022) Positive experiences of specialist assistants and physicians with respect to the delegation research project StaerkeR : evaluation of the training and experiences within the framework of this project. Z Rheumatol. https://doi.org/10.1007/s00393-022-01298-y
Krause D, Mai A, Denz R, Johow J, Reese JP, Westerhoff B, Klaassen-Mielke R, Timmesfeld N, Rittstieg A, Saracbasi-Zender E, Gunzel J, Klink C, Schmitz E, Fendler C, Raub W, Boddeker S, Dybowski F, Hubner G, Menne HJ, Lakomek HJ, Sarholz M, Trampisch U, Trampisch HJ, Braun J (2022) The structured delegation of medical care services for patients with inflammatory rheumatic diseases. Dtsch Arztebl Int 119(10):157–164. https://doi.org/10.3238/arztebl.m2022.0109
Broman P, Tokolahi E, Wilson OWA, Haggie M, Andersen P, Brownie S (2022) Patient outcomes from student-run health services: an integrative review. J Multidiscip Healthc 15:641–665. https://doi.org/10.2147/JMDH.S348411
Ramiro S, Nikiphorou E, Sepriano A, Ortolan A, Webers C, Baraliakos X, Landewe RBM, Van den Bosch FE, Boteva B, Bremander A, Carron P, Ciurea A, van Gaalen FA, Geher P, Gensler L, Hermann J, de Hooge M, Husakova M, Kiltz U, Lopez-Medina C, Machado PM, Marzo-Ortega H, Molto A, Navarro-Compan V, Nissen MJ, Pimentel-Santos FM, Poddubnyy D, Proft F, Rudwaleit M, Telkman M, Zhao SS, Ziade N, van der Heijde D (2023) ASAS-EULAR recommendations for the management of axial spondyloarthritis: 2022 update. Ann Rheum Dis 82(1):19–34. https://doi.org/10.1136/ard-2022-223296
Reichheld FF (2003) The one number you need to grow. Harv Bus Rev 81(12):46–54 (124)
Garrett S, Jenkinson T, Kennedy LG, Whitelock H, Gaisford P, Calin A (1994) A new approach to defining disease status in ankylosing spondylitis: the Bath Ankylosing Spondylitis Disease Activity Index. J Rheumatol 21(12):2286–2291
Browne RH (1995) On the use of a pilot sample for sample size determination. Stat Med 14(17):1933–1940. https://doi.org/10.1002/sim.4780141709
Cohen JF, Korevaar DA, Altman DG, Bruns DE, Gatsonis CA, Hooft L, Irwig L, Levine D, Reitsma JB, de Vet HC, Bossuyt PM (2016) STARD 2015 guidelines for reporting diagnostic accuracy studies: explanation and elaboration. BMJ Open 6(11):e012799. https://doi.org/10.1136/bmjopen-2016-012799
Ehrenstein B, Pongratz G, Fleck M, Hartung W (2018) The ability of rheumatologists blinded to prior workup to diagnose rheumatoid arthritis only by clinical assessment: a cross-sectional study. Rheumatology (Oxford) 57(9):1592–1601. https://doi.org/10.1093/rheumatology/key127
Kempin R, Richter JG, Schlegel A, Baraliakos X, Tsiami S, Buehring B, Kiefer D, Braun J, Kiltz U (2022) Monitoring of Disease Activity With a Smartphone App in Routine Clinical Care in Patients With Axial Spondyloarthritis. J Rheumatol 49(8):878–884. https://doi.org/10.3899/jrheum.211116
Kernder A, Morf H, Klemm P, Vossen D, Haase I, Mucke J, Meyer M, Kleyer A, Sewerin P, Bendzuck G, Eis S, Knitza J, Krusche M (2021) Digital rheumatology in the era of COVID-19: results of a national patient and physician survey. RMD Open. https://doi.org/10.1136/rmdopen-2020-001548
de Thurah A, Stengaard-Pedersen K, Axelsen M, Fredberg U, Schougaard LMV, Hjollund NHI, Pfeiffer-Jensen M, Laurberg TB, Tarp U, Lomborg K, Maribo T (2018) Tele-health followup strategy for tight control of disease activity in rheumatoid arthritis: results of a randomized controlled trial. Arthritis Care Res (Hoboken) 70(3):353–360. https://doi.org/10.1002/acr.23280
Hermans K, Boonen A, Vonkeman HE, van Tubergen A (2023) Effectiveness and cost-effectiveness of combined asynchronous telemonitoring and patient-initiated care for spondyloarthritis: protocol for a pragmatic multicentre randomised controlled trial (TeleSpA Study). BMJ Open 13(2):e067445. https://doi.org/10.1136/bmjopen-2022-067445
Osteras N DH (2021) Remote Monitoring of Axial Spondyloarthritis in Specialist Healthcare Services. https://clinicaltrials.gov/ct2/show/NCT05031767.
Zarbl J, Eimer E, Gigg C, Bendzuck G, Korinth M, Elling-Audersch C, Kleyer A, Simon D, Boeltz S, Krusche M, Mucke J, Muehlensiepen F, Vuillerme N, Kronke G, Schett G, Knitza J (2022) Remote self-collection of capillary blood using upper arm devices for autoantibody analysis in patients with immune-mediated inflammatory rheumatic diseases. RMD Open. https://doi.org/10.1136/rmdopen-2022-002641
Knitza J, Tascilar K, Vuillerme N, Eimer E, Matusewicz P, Corte G, Schuster L, Aubourg T, Bendzuck G, Korinth M, Elling-Audersch C, Kleyer A, Boeltz S, Hueber AJ, Kronke G, Schett G, Simon D (2022) Accuracy and tolerability of self-sampling of capillary blood for analysis of inflammation and autoantibodies in rheumatoid arthritis patients-results from a randomized controlled trial. Arthritis Res Ther 24(1):125. https://doi.org/10.1186/s13075-022-02809-7
Acknowledgements
The authors would like to thank all patients for their participation in this study. The present work was performed to fulfill the requirements for obtaining the degree “Dr. med.” for S. von Rohr.
Funding
Open Access funding enabled and organized by Projekt DEAL. The study was partially supported by Novartis Pharma GmbH, Nürnberg, Germany and the Deutsche Forschungsgemeinschaft FOR 2886 PANDORA.
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Conceptualization, JK, HL, SR, and MG; acquisition of data for the work, HL and SR; supervision, JK, SK, GS, AR, and MS; data curation, HL, SR, and JK; data analysis, HL, SR, and JK; data interpretation, HL, SR, and JK; manuscript drafting, HL, SR, and JK; critical reviewing, SK, GS, AR, and MS. All authors read and approved the final manuscript. According to the ICMJE authorship criteria, the authors have fulfilled the requirements of providing the final approval for the version to be published and agreed to be accountable for all aspects of the work, including the investigation and resolution of any questions regarding the accuracy or integrity of the manuscript.
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JK has received research support from and has received consulting/speaker’s fees from Novartis Pharma GmbH and ABATON. MG is founder and shareholder of ABATON GmbH. SK is founder and shareholder of MED.digital GmbH. The other authors have disclosed no conflicts of interest.
Ethical
The study was approved by the regional ethics review board in Erlangen, Germany (Reg no. 21–357-B). All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Informed consent was obtained from all individual respondents included in the study.
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von Rohr, S., Knitza, J., Grahammer, M. et al. Student-led clinics and ePROs to accelerate diagnosis and treatment of patients with axial spondyloarthritis: results from a prospective pilot study. Rheumatol Int 43, 1905–1911 (2023). https://doi.org/10.1007/s00296-023-05392-5
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DOI: https://doi.org/10.1007/s00296-023-05392-5