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POS1164 (2021)
USE OF TELEMEDICINE FOR FOLLOW-UP OF SLE PATIENTS WITH NEPHRITIS IN THE COVID-19 OUTBREAK (“TeleSLE”): THE 6-MONTH RESULTS OF A RANDOMIZED CONTROLLED TRIAL
H. So1, E. Chow1, T. K. LI1, S. L. Lau1, I. T. Cheng1, C. C. Szeto1, L. S. Tam1
1The Chinese University of Hong Kong, Medicine and Therapeutics, Hong Kong, Hong Kong (SAR)

Background: Patients with lupus nephritis (LN) might be more susceptible to COVID-19 due to the underlying disease, co-morbidities and use of immunosuppressants. We hypothesized that telemedicine (TM) could be a well-accepted mode of health-care delivery minimizing the risk of exposure to the severe acute respiratory syndrome coronavirus 2 ( SARS - CoV - 2 ), while maintaining disease control in these patients.


Objectives: To evaluate the short-term patient satisfaction, compliance, disease control and infection risk of TM compared with standard in-person follow-up (FU) for patients with LN during COVID-19.


Methods: This was a single-center randomized-controlled study. Consecutive patients followed at the LN clinic were randomized to either TM (TM group) or standard FU (SF group) in a 1:1 ratio. Patients in the TM group received scheduled follow-ups via videoconferencing. SF group patients continued conventional in-person outpatient care. The 6-month data were compared.


Results: From June to December 2020, 122 patients were randomized (TM: 60, SF: 62) and had attended at least 2 FU visits. There were no baseline differences, including SLEDAI-2k and proportion of patients in lupus low disease activity state (LLDAS), between the 2 groups except a higher physician global assessment score (PGA) in the TM group (mean 0.67±0.69 vs 0.45±0.60, p=0.003) ( Table 1 ). The mean FU duration was 19.8±4.5 weeks. When comparing the most recent visit, the mean waiting time between entering the clinic waiting room (virtual or real) and seeing a rheumatologist (virtual or in-person) was significantly shorter in the TM group (22.5±28.6 vs 68.9±40.7 minutes, p< 0.001) ( Figure 1A ). The mean overall patient satisfaction score was higher in the TM group (mean 2.19±0.61 vs 1.89±0.78, p=0.042). The results of the post-consultation satisfaction questionnaire are shown in Figure 1B . The number of visits was similar in the two groups (TM: 3.1±1.3 vs SF: 3.0±1.2, p=0.981). However, there was a trend suggesting that alternative mode of FU was requested more frequently in the TM group than the SF group (TM: 12/60, 20.0% and SF: 5/62, 8.1%; p=0.057). More patients in the TM group had hospitalization (15/60, 25.0% vs 7/62, 11.3%; p=0.049) within the FU period, which was no longer statistically significant after adjusting for the baseline PGA. The proportions of patients remained in LLDAS were similar in the 2 groups (TM: 75.0% vs SF: 74.2%, p=0.919). None of the patients had COVID-19.


Conclusion: TM resulted in better patient satisfaction and could achieve similar disease control in patients with LN in the short-term when compared to standard care.

Baseline clinical data of the recruited patients and comparison between the telemedicine/standard follow-up groups

Overall (n=122) Telemedicine group (n=60) Standard follow-up group (n=62) P-value
Age in years 44.4±11.5 44.1±11.7 44.7±11.5 0.779
Gender: Female 111 (91.0) 55 (91.7) 56 (90.3) 0.796
Disease duration in years 15.1±9.0 16.2±8.7 14.0±9.1 0.115
Nephritis class III, IV or V 108 (88.5) 54 (90.0) 54 (87.1) 0.427
24 hour urine proteinuria in gram 0.51±0.63 0.53±0.60 0.50±0.65 0.712
Current use of prednisolone 112 (91.8) 57 (95.0) 55 (88.7) 0.323
Daily prednisolone dose in mg 5.51±4.21 5.69±4.17 5.34±4.29 0.570
Use of immunosuppressant 90 (73.8) 46 (76.7) 44 (71.0) 0.474
SLEDAI-2K 3.65±2.33 4.00±2.34 3.30±2.29 0.097
PGA 0.56±0.65 0.67±0.69 0.45±0.60 0.003
LLDAS 78 (63.9) 36 (60.0) 42(67.7) 0.251
Remission 0 (0) 0 (0) 0 (0) n/a
Presence of comorbidity 87 (71.3) 40 (66.7) 47 (75.8) 0.264
SDI 0.93±1.15 1.08±1.28 0.78±0.98 0.243
HAQ-DI 0.23±0.46 0.25±0.47 0.21±0.44 0.571
HADS: Anxiety scale Depression scale 6.07±4.12 5.72±4.31 6.20±4.19 5.73±3.93 5.93±4.09 5.70±4.68 0.720 0.724

Data are reported as mean ± SD or number (%). LLDAS: lupus low disease activity state; SDI: Systemic Lupus International Collaborating Clinics/American College of Rheumatology (SLICC/ACR) Damage Index; HAQ-DI: Health Assessment Questionnaire Disability Index; and HADS: Hospital Anxiety and Depression Scale.


Disclosure of Interests: Ho SO: None declared, Evelyn Chow: None declared, Tena K. Li: None declared, Sze-Lok Lau: None declared, Isaac T. Cheng: None declared, Cheuk-Chun Szeto: None declared, Lai-Shan Tam Grant/research support from: Grants from Novartis and Pfizer.


Citation: Ann Rheum Dis, volume 80, supplement 1, year 2021, page 860
Session: COVID-19 (POSTERS only)