Coronavirus disease (COVID-19), first reported in December 2019 in Wuhan, China, is caused by infection with the novel betacoronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) . Since then, it has spread rapidly, and a worldwide outbreak was noted in a few months. The World Health Organization (WHO) declared the COVID-19 outbreak a global pandemic on March 11, 2020 . As of May 17, 2020, the WHO reported that the cumulative number of COVID-19 cases in the world was 4.6 million and that more than 310,000 patients had died . In Korea, the first case of COVID-19 was identified on January 20, 2020; subsequently, a substantial outbreak was noted in Korea . The outbreak has been relatively well-regulated by the implementation of appropriate preventive measures by the government and active participation of the public and medical professionals. However, new cases continue to be reported in Korea, and the COVID-19 pandemic has been scattered worldwide. Vaccines or therapeutic drugs for COVID-19 have not been developed to date.
Patients with systemic rheumatic diseases (SRD), such as rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE) are prone to infection because the immune system dysfunction is noted in patients with SRD and immunosuppressive medications are usually used for these patients [5-10]. In addition, patients with SRD often present with several comorbidities  that are known to be risk factors for COVID-19 [12,13]. Therefore, patients with SRD are a vulnerable population during the COVID-19 pandemic, which should be considered as one of the major threats to public health worldwide.
The Korean College of Rheumatology (KCR) recognized the urgent need to develop recommendations for rheumatologists and other physicians caring for patients with SRD during the COVID-19 pandemic. The working group was organized to review the evidence and draft preliminary statements of recommendation. The final statements were determined by expert panel consensus using a modified Delphi approach and approved by the KCR. The recommendations consist of general principles and individual items of recommendation for the management of SRD during the COVID-19 outbreak. These recommendations were based on the evidence available in literature at that time and the consensus of experts.
The working group comprised 11 rheumatologists and 3 infectious disease specialists. They participated in establishing the recommendation development plan, deciding the purpose and scope, selecting key questions, searching and reviewing the literature, and drafting the preliminary statements.
The recommendations were developed for the management of adult patients with SRD during the COVID-19 pandemic. Provision of recommendations for the treatment of COVID-19 was beyond our study scope. SRD refer to autoimmune or immune-mediated rheumatic diseases, including RA, SLE, spondyloarthritis, and other such diseases. The recommendations were intended for rheumatologists and other physicians who manage patients with SRD. The health questions for developing the recommendations included general principles, preventive measures against COVID-19, treatment of stable or active SRD patients without COVID-19, treatment of SRD patients with COVID-19, and assessment and monitoring of SRD. The medications used for patients with SRD were classified, as follows: 1) nonsteroidal anti-inflammatory drugs (NSAIDs), 2) glucocorticoids, 3) conventional synthetic disease-modifying antirheumatic drugs (csDMARDs), 4) biological DMARDs (bDMARDs), 5) targeted synthetic DMARDs (tsDMARDs), and 6) denosumab.
The working group searched for and reviewed the relevant literature archived in the MEDLINE database (via PubMed) as of April 23, 2020, for the following domains: 1) general principles, 2) preventive measures and monitoring, 3) NSAIDs, 4) glucocorticoids, 5) csDMARDs, 6) bDMARDs, 7) tsDMARDs, and 8) denosumab. We limited our search to publications in the English or Korean language. The clinical guidelines or recommendations for managing patients with COVID-19 or SRD that were developed by international or national medical societies were included. The working group selected literature relevant to health questions, reviewed and summarized the contents, and evaluated the evidence level according to the Oxford Centre for Evidence-Based Medicine .
The working group formulated the preliminary statements consisting of four general principles and thirteen recommendations. The consensus of the final statements was established using the modified Delphi approach as described in the RAND/University of California, Los Angeles (UCLA) Appropriateness Method . The voting panel comprised 27 rheumatologists and 3 infectious disease specialists, which included members of the working group. The survey was performed online with internet-based software. The voting panel members were asked to rate their level of agreement for the appropriateness of seventeen preliminary statements using a 9-point numeric scale (1 [strongly disagree] to 9 [strongly agree]). The statements were classified into three levels of appropriateness, using the following definitions: appropriate (median rating of 7∼9, without disagreement), uncertain (median rating of 4∼6 or any median with disagreement), and inappropriate (median rating of 1∼3, without disagreement). The definition of disagreement was based on the Interpercentile Range Adjusted for Symmetry (IPRAS) method described in the RAND/ UCLA appropriateness method . All draft statements were agreed to be appropriate by the panel, and then these final statements were officially endorsed as recommendations for the management of patients with SRD during the COVID-19 pandemic by the KCR (Table 1).
Among COVID-19 patients, elderly patients and patients with heart or lung disease have higher morbidity and mortality rates [12,13,16-19]. Although precise data are not available, patients with SRD may have a high risk for developing severe COVID-19 owing to immune dysfunction noted in SRD and common cardiovascular and lung disease comorbidities. Immunosuppressive therapies, including glucocorticoids and DMARDs can make them more prone to severe or fatal disease [7,8,10,20-28]. Therefore, patients with SRD should be considered a high-risk group for severe COVID-19 and preferred for evaluation and examination.2)Immediate diagnostic testing is required for patients with SRD with suspected COVID-19 (LoE: 5)
Early detection is essential for treating and preventing the spread of COVID-19 [29-32]. In the area of COVID-19 outbreak, any patient with acute onset of fever, respiratory symptoms, such as cough, phlegm, and dyspnea, and/or other constitutional symptoms, including arthralgia and myalgia, should be suspected of experiencing COVID-19 . In patients with SRD, however, the symptoms of infection can be masked by the effects of the anti-inflammatory drugs or glucocorticoids that they are receiving. In up to 20% of the patients with SRD who had COVID-19, fever did not appear as an initial symptom [17,18,33]. In addition, some manifestations of COVID-19, like arthralgia and cytokine storm, are similar to those of SRD . Therefore, the diagnosis of COVID-19 in patients with SRD is challenging when only symptoms and signs are considered. A diagnostic test, such as polymerase chain reaction (PCR) for COVID-19, is immediately required when COVID-19 is clinically suspected in a patient with SRD.3)Shared decision-making is fundamental, and the disease status, comorbidities, and presence or absence of COVID-19 should be considered when treating patients with SRD (LoE: 5)
Shared decision-making with patients is fundamental during the COVID-19 pandemic partly because of the current insufficient evidence on COVID-19 and inevitable uncertainty in medical decisions. Patients should be able to obtain appropriate medical advice and are encouraged to participate in treatment decision-making. When treating patients with SRD, the current status of underlying SRD and their comorbidities and the presence or absence of COVID-19 should be considered [35-38]. Patients with COVID-19 should be treated in cooperation with the relevant infectious disease specialists or considered to be referred to them [29,39-42].4)Patients should be provided with information regarding public preventive measures against COVID-19, such as washing hands, wearing a face mask, and social distancing (LoE: 2 [washing hands], 4 [wearing a mask], 5 [social distancing])
The transmission of COVID-19 mainly occurs by close contact through respiratory droplets, by direct contact with infected persons, or by contact with contaminated objects and surfaces . Therefore, in order to prevent infection and transmission of the virus, it is essential to keep strict hand hygiene [44-46], wear a face mask [47-52], and practice social distancing . The systematic review has shown that respiratory virus spread can be prevented by hygiene measures such as handwashing . Although wearing face masks in non-pandemic settings did not show a statistically significant reduction of acute respiratory viral infection cases , it is now considered a reasonable measure to reduce virus transmission during the COVID-19 pandemic [48,51,52]. In a randomized controlled trial, coronavirus was detected in the exhaled breath of 30%∼40% of participants without face masks, while it was not detected in participants wearing face masks . Social distancing is one of the best ways to reduce close contact and to prevent the spread of the virus . Patients should be provided with information on public precautionary measures and encouraged to comply with them for protecting themselves and their societies from COVID-19 [54-59].
Exercise may lower the disease activity of SRD and improve the function and the participation of patients with SRD . International societies have strongly recommended exercise for patients with SRD, such as RA and spondyloarthritis [36,61]. Considering that exercise is effective, safe, and can be easily performed, it is also recommended appropriately for public health [62,63]. However, prolonged high-intensity exercise is not advisable because it can lead to immunosuppression for hours . A well-ventilated personal space is suitable for exercise, considering the risk of COVID-19 transmission. Performing exercise outdoor while maintaining appropriate physical distance from other people may also be suitable [65,66].
Generally, smoking is a risk factor for acute respiratory disease . Regarding COVID-19, smoking has been reported to be associated with an increased risk of infection and worse outcomes [68-70]. Smoking can cause or worsen comorbidities such as cardiovascular disease, respiratory diseases, and diabetes mellitus [71,72]. Therefore, smoking cessation has been proposed as a major public health measure in response to the COVID-19 pandemic . Smoking reportedly has harmful effects on the human immune system . In terms of SRD, smoking is the most potent environmental risk factor for the development of RA  and is also associated with the development of SLE . Smoking may decrease the therapeutic responsiveness of DMARDs, such as antimalarial agents [77,78]. As patients with SRD also have a high risk of cardiovascular disease, smoking cessation is generally recommended by international societies [36,61,79].
Influenza infection may concurrently develop in COVID-19 patients , and one or more other pathogenic infections have been detected in 21% of the COVID-19 patients . Data from China showed that secondary bacterial infections were detected in 50% of the patients with COVID-19 who died [12,82]. Therefore, a co-infection may be a potential risk factor that may lead to fatal consequences . In addition, the severity of COVID-19 was reportedly low in patients who were vaccinated against influenza . In general, administration of influenza and pneumococcal vaccines is strongly recommended for patients with SRD . Prevention of respiratory diseases through vaccination can reduce not only fatality rates associated with COVID-19 but also the burden on the medical system during the COVID-19 pandemic.Recommendation 2. For stable SRD patients without COVID-19, current medication, including glucocorticoids, DMARDs, and other immunosuppressants, may be continued (LoE: 4)
High disease activity in patients with SRD may act as a risk factor for infection , and strict control of SRD activity, in general, is more important even if the infection risk may increase with the use of immunosuppressive medications, including glucocorticoids and DMARDs. Sudden drug withdrawal may exacerbate SRD. This can result in the requirement of an increased dose of immunosuppressive agents such as glucocorticoids, which may increase the risk of infection with COVID-19 [86,87]. As long-term use of glucocorticoids may lead to inhibition of the hypothalamic-pituitary-adrenal axis, the sudden cessation of glucocorticoids can cause adrenal crisis [88-90]. Thus, current medications for SRD, including glucocorticoids, DMARDs, and other immunosuppressive drugs, may be continued in stable SRD patients without evidence of COVID-19, and these medications should not be abruptly terminated.Recommendation 3. NSAIDs may be used, if indicated, for SRD patients, except for patients with severe COVID-19 (LoE: 4)
NSAIDs are used in patients with SRD for controlling symptoms or some disease activity or both. The WHO initially warned that the use of NSAIDs in patients with COVID-19 might be risky, based on a French study on the use of ibuprofen in patients with chickenpox and pneumonia . Paracetamol was suggested as the primary drug for controlling the symptoms of COVID-19 [92-95]. However, owing to the lack of further studies supporting it, this suggestion was withdrawn [96-98]. Discontinuation of NSAIDs in patients with SRD may aggravate disease activity, leading to an increase in the risk of infection . Thus, NSAIDs may be used if indicated in SRD patients with COVID-19, except for in cases of severe disease. NSAIDs may have a deleterious effect on patients presenting with severe COVID-19 with multi-organ dysfunction .Recommendation 4. A. Glucocorticoids, at the minimum effective dose required, can be used to control disease activity in active SRD patients without COVID-19 (LoE: 5). B. Even in patients with COVID-19, current treatment with glucocorticoids for SRD should not be abruptly terminated (LoE: 5)
Even during the COVID-19 pandemic, glucocorticoids can be used to control disease activity in SRD patients without COVID-19. However, systemic glucocorticoid therapy may increase the risk of infection in a dose-dependent manner. It is associated with an increased risk of reactivation of herpes zoster virus, severe bacterial infections, and opportunistic infections [10,27,100]. As glucocorticoids can cause several harmful side effects, besides infection, the minimum effective dose should be used.
There are controversies regarding the effects of systemic glucocorticoids on patients with respiratory viral diseases. Systemic glucocorticoid use was associated with increased mortality in patients with influenza  and delayed viral clearance in patients with Middle Eastern Respiratory Syndrome Coronavirus (MERS-CoV) . Although evidence regarding the benefits of glucocorticoid use is not available, systemic glucocorticoid therapy has been widely used for the treatment of SARS-CoV infection . COVID-19 can cause an explosive immune response, such as a cytokine storm, leading to immune-mediated tissue injury. Systemic glucocorticoids have been used in these patients, although the therapeutic effects of systemic glucocorticoids are not clear . A recent meta-analysis reported that glucocorticoids do not affect the mortality among patients with COVID-19 . In addition, systemic glucocorticoids currently used for SRD should not be terminated abruptly because the risk of adrenal crisis, flare of SRD or both may outweigh the potential advantages associated with glucocorticoid withdrawal. High doses of glucocorticoids may be permitted for SRD patients who have a severe or vital organ-threatening disease even when they are experiencing COVID-19.Recommendation 5. A. csDMARDs can be initiated or used for active SRD patients without COVID-19 (LoE: 5). B. In patients with COVID-19, treatment with csDMARDs, except for hydroxychloroquine and sulfasalazine, should be temporarily terminated (LoE: 4 [hydroxychloroquine], 5 [sulfasalazine])
csDMARDs, including methotrexate, leflunomide, chloroquine (CQ)/hydroxychloroquine (HCQ), and sulfasalazine (SSZ), are usually used for controlling disease activity and preventing structural damage in patients with SRD. It has been reported that csDMARDs are not associated with an increased risk of infection , and high disease activity is a risk factor of infection in patients with RA [6,106]. It is reasonable to use csDMARDs to control the disease in active SRD patients without COVID-19.
As both SRD and the use of immunosuppressant drugs are risk factors for infection in patients with SRD [7,25,106,107], the temporary discontinuation of immunosuppressant drugs is generally recommended in SRD patients with severe infection . In cancer patients with repeated cycles of chemotherapy, the clinical outcome of COVID-19 was significantly worse [109,110], and the hazard ratio of chemotherapy within 14 days prior to the documentation of COVID-19 for severe complications was 4.079 (95% confidence intervals [CIs] 1.086∼15.322) . These findings indicate that immuno-suppressive therapy may worsen the clinical outcome of COVID-19. Thus, it is recommended to temporarily discontinue csDMARDs with immunosuppressive potential in SRD patients infected with COVID-19. Since CQ/HCQ and SSZ may not have an immunosuppressive effect, they may be used in SRD patients with COVID-19.Recommendation 6. A. bDMARDs can be initiated or used for active SRD patients without COVID-19 (LoE: 5). B. In patients with COVID-19, treatment with bDMARDs, except for interleukin-6 inhibitors, should be temporarily terminated (LoE: 5)
bDMARDs, inhibiting tumor necrosis factor (TNF) or other proinflammatory cytokines, have a significant effect on improving disease activity, symptoms, and functions of patients with SRD refractory to first-line therapy [35,36,38,111,112]. However, incidental infection is a major concern for patients undergoing bDMARD therapy. bDMARDs are associated with an increased, but variable, risk of infection with
As in the case of csDMARD therapy, bDMARDs can be used for patients with newly diagnosed or active SRD patients, if indicated according to the current guidelines for patients without COVID-19, because uncontrolled disease activity poses a high risk of infection. In SRD patients with COVID-19, it is reasonable to discontinue bDMARDs temporarily except for interleukin-6 (IL-6) inhibitors. IL-6 inhibitors have been shown to be effective in the treatment of severe COVID-19 patients in several studies [117-120]. Patients with severe COVID-19 have sometimes deteriorated into cytokine syndromes, in which IL-6 is the primary cytokine in cytokine storm syndrome, so IL-6 inhibitors are assumed effective in inflammatory conditions caused by COVID-19 [121,122]. IL-6 inhibitors may also be considered in COVID-19 cases with respiratory failure, rapid exacerbation, or high serum levels of IL-6 . Thus, IL-6 inhibitors may be continued in active SRD patients with COVID-19.Recommendation 7. A. The initiation of tsDMARDs may be postponed until the cessation of the COVID-19 pandemic if an alternative therapy is available (LoE: 5). B. In patients with COVID-19, treatment with tsDMARDs should be temporarily discontinued (LoE: 5)
tsDMARDs that are currently used for patients with SRD include tofacitinib, baricitinib, and upadacitinib. Among them, baricitinib, an inhibitor of both Janus kinase 1 (JAK1) and Janus kinase 2 (JAK2), was proposed as a therapeutic agent for COVID-19, especially for patients with severe disease because it inhibits adaptor-associated protein kinase 1 (AAK1), a regulator of SARS-CoV-2 endocytosis [124,125]. However, the JAK inhibitors may not be safe for use because inhibition of JAK and the subsequent activator of the transcription protein signaling pathway can affect the activity of interferon-α, resulting in a decrease in the immune response to viral infection [126-129]. In early or asymptomatic patients with COVID-19, interferon-α may play an important role in overcoming the disease .
According to clinical data, tofacitinib has a serious risk of infection when compared to bDMARDs and is associated with a two-fold higher risk of herpes zoster versus all bDMARDs . In particular, older patients (>65 years of age) treated with tofacitinib had a significantly higher risk of severe and fatal infections than those who were treated with TNF inhibitors .
Considering the possible risk associated with the use of the JAK inhibitor for the viral disease, we suggest that beginning with tsDMARD therapy in active SRD patients be postponed until the cessation of the COVID-19 pandemic and an alternative therapy other than tsDMARDs be preferred. If a patient is infected with COVID-19, tsDMARDs should be temporarily discontinued.Recommendation 8. Continuing the use of denosumab is suggested for patients with osteoporosis (LoE: 5)
Denosumab is a human monoclonal antibody that binds to the receptor activator of nuclear factor kappa-B ligand (RANKL). Denosumab is used for treating osteoporosis and preventing fractures. Some effects of RANKL inhibition on immune function have been reported in animal models, and RANKL-RANK interaction might modify immune responses in the skin through an effect on the intensity of the inflammatory response [132-135]. Serious adverse events of infections have been noted in subjects receiving denosumab in some clinical trials [136-138]. However, an analysis of the serious infection events in a large clinical trial showed no clear clinical pattern to suggest a relationship with time or duration of exposure to denosumab . There are some emerging data that discontinuation of denosumab leads to a rebound increase in the risk of multiple vertebral fractures [139-141]. Fractures occurred 8 to 16 months after the last dose . Considering the risk of fractures, we suggest that the use of denosumab for SRD patients with osteoporosis be continued and the dosing intervals of denosumab do not exceed 8 months.Recommendation 9. The intervals for and methods of monitoring the disease status and drug toxicities may be appropriately adjusted for patients with stable SRD (LoE: 5)
Patients with newly diagnosed or active SRD should be evaluated for their disease status and drug toxicities periodically based on the current recommendations [35,36,38,111]. Frequent visits to hospitals might expose the patients to a risk of infection during the COVID-19 pandemic. For patients with stable SRD, the intervals and methods for monitoring the disease status and the safety of the patients can be adjusted appropriately to minimize unnecessary hospital visits .
COVID-19, an infectious disease that has turned into a global pandemic, is causing unprecedented damage to humans and societies. It poses a substantial threat to not only global public health but also vulnerable populations. Infection often leads to morbidity and mortality in patients with SRD; thus, the COVID-19 pandemic is a major concern for physicians treating SRD and for patients with SRD.
We have developed treatment recommendations for rheumatologists and other physicians who manage patients with SRD during the COVID-19 pandemic. Four general principles and thirteen recommendations, including the preventive measures against COVID-19, medicinal treatment for SRD, and patient evaluation and monitoring, were established.
Patients with SRD are vulnerable for COVID-19. Elderly patients and patients with underlying medical conditions are at higher risk of severe COVID-19 . The hospitalization and mortality rates associated with COVID-19 increase with older age [13,21]. The US CDC (Centers for Disease Control and Prevention) has stated that chronic kidney disease, chronic obstructive pulmonary disease, immunocompromised state, obesity, severe heart condition, sickle cell disease, and type 2 diabetes mellitus are related to an increased risk of severe COVID-19 . Although SRD is not stated to be clearly associated with an increased risk of COVID-19 by the US CDC, evidence has indicated that patients with SRD are associated with an increased risk of infection [7,142-144]. This may be because of the substantial dysfunction of the innate and adaptive immunity in SRD pathogenesis [143,145,146]. In addition, patients with SRD are prescribed immunosuppressive agents, including glucocorticoids and DMARDs, which increase the risk of infection [24,147]. Lymphocytopenia and corticosteroid therapy (>10 mg prednisolone equivalent per day) have been reported as predictive factors of infection requiring hospitalization in patients receiving chronic immunosuppressive therapy . With respect to COVID-19, immunosuppression and lymphocytopenia were associated with critical disease [22,148].
Most recent studies confirmed an increased risk of severe COVID-19 in patients with SRD. From the results of the COVID-19 Global Rheumatology Alliance Registry, the mortality rate of rheumatic patients with COVID-19 (9%) was higher than that of the general population with COVID-19 (5.7% according to the WHO on June 12, 2020), and glucocorticoid exposure (≥10 mg prednisolone equivalent per day) was associated with hospitalization . A large-scale study from the UK showed that common autoimmune diseases such as RA and SLE were risk factors for COVID-19 related death . Moreover, compared with the reference population, COVID-19 has occurred more frequently in patients with rheumatic diseases (odds ratio 1.32, 95% CIs 1.15∼1.52), especially in patients receiving bDMARDs or tsDMARDs as reported in a Spanish retrospective study conducted in seven hospitals .
COVID-19 is a highly infectious disease, especially during the early stage, and is associated with significant morbidity and fatality rates. Thus, early diagnosis and patient isolation are essential for the management of patients with COVID-19 and for preventing viral spread. However, during the early stages of the COVID-19 pandemic, the strategies for diagnostic testing differed among the nations, depending on the capacities of the medical system, availability of diagnostic kits, and perspective of health policies. For example, the use of diagnostic tests was limited to severely ill patients in Italy and the UK, while aggressive testing was performed in Korea for early disease diagnosis [152,153]. Diagnostic testing for COVID-19 is usually indicated for patients suspected to have been exposed to COVID-19 and presenting with fever or respiratory symptoms, such as cough, phlegm, and sore throat. However, in Korea, physicians can order COVID-19 diagnostic testing for patients with suspected COVID-19 even when they do not present with all the aforementioned symptoms . Owing to active testing, tracing, and implementation of an isolation strategy for patients with COVID-19, the COVID-19 outbreak has been relatively well-controlled in Korea.
The diagnosis of COVID-19 is challenging in patients with SRD. In SRD patients, systemic and respiratory symptoms of viral infections can be mistaken for those of underlying diseases or associated lung disease. In addition, the effects of anti-inflammatory drugs may mask symptoms, such as fever . Delay in the diagnosis may lead to worse outcomes in SRD patients vulnerable for COVID-19. COVID-19 cannot be excluded based on symptoms in patients with SRD. Testing for early diagnosis of COVID-19 should not be delayed for SRD patients with suspected viral infection.
Public preventive measures against COVID-19, such as washing hands, wearing a mask, and social distancing, are critical for preventing infection and the spread of the virus. There were controversies on the effectiveness of wearing a face mask in the early days of the COVID-19 pandemic. However, a recent systematic literature review showed that wearing a mask can significantly reduce the risk of COVID-19 . We recommend wearing a face mask, washing hands frequently, and social distancing to prevent the development of COVID-19 in vulnerable patients.
In these recommendations, medicinal treatments are categorized according to the states of both COVID-19 and SRD. In the absence of COVID-19, it is recommended to maintain current treatment in patients with stable SRD. In active SRD patients without COVID-19, medications except for tsDMARDs may be started or used if indicated. In the case of tsDMARDs, we suggest using alternative treatment options considering the risks of JAK inhibitors during the COVID-19 outbreak. However, tsDMARDs may be used for active SRD patients, if options other than tsDMARDs are not available. If SRD patients are infected with COVID-19, immunosuppressive drugs, except for glucocorticoids, CQ/HCQ, SSZ, and IL-6 inhibitors, should be discontinued temporarily because of the risk to exacerbate the viral disease. According to these recommendations, early diagnosis or exclusion of COVID-19 is crucial because the presence or absence of COVID-19 determines the initial clinical pathway for drug therapy.
Patients may have difficulty in visiting hospitals during the outbreak of COVID-19. Hospital visits can increase the risk of exposure to COVID-19. Therefore, during the COVID-19 pandemic, it may be necessary to extend the monitoring intervals or introduce the means of seeing the patients in a non-face-to-face way. Telemedicine was partly performed over the phone in Daegu, Korea, while the city was on near lockdown due to the COVID-19 outbreak.
Although increasing evidence is available regarding COVID-19, high-quality evidence is currently lacking. There is marked uncertainty on the management strategy for patients with COVID-19. Most of the evidence supporting these recommendations is low-level and indirect. Some recommendations have been formulated based mainly on expert opinions and precautionary principles. As considerable scientific evidence on COVID-19 is now emerging, these recommendations will require an appropriate revision in the not too distant future. Until then, we hope that these recommendations will serve as a helpful reference for the individualized management of patients with SRD.
The authors would like to thank all members of the voting panel: Wan-Uk Kim, Seoul St. Mary’s Hospital, The Catholic University of Korea; Tae-Hwan Kim, Hanyang University Hospital for Rheumatic Diseases; Hyun Ah Kim, Hallym University Sacred Heart Hospital; Namgyu Park, Dr. Park’s Clinic; Sung-Hwan Park, Seoul St. Mary’s Hospital, Catholic University Medical College; Jung-Soo Song, Chung-Ang University Hospital; Seung-Cheol Shim, Chungnam National University Hospital; Sang-Il Lee, Gyeongsang National University and Gyeongsang University Hospital; Sang-Heon Lee, Konkuk University Hospital Sung Won Lee, Dong-A University College of Medicine; Shin-Seok Lee, Chonnam National University Medical School & Hospital; Young Ho Lee, Korea University Medical Center; Eun Bong Lee, Seoul National University College of Medicine; Chang Keun Lee, University of Ulsan, College of Medicine, Asan Medical Center; Hoon-Suk Cha, Samsung Medical Center, Sungkyunkwan University; Seung-Jae Hong, Kyung Hee University Medical Center, Kyung Hee University.
No potential conflict of interest relevant to this article was reported.
Among the authors, M.R.S. and H.J.B. were in charge of conception and design of study, acquisition of data, analysis and/or interpretation of data, drafting and revising the manuscript. J.W.K., E.J.P., S.M.J., Y.K.S., H.K., H.S.K., and J.L. were responsible for design of study, acquisition of data, analysis and/or interpretation of data, and drafting the manuscript. G.K., M.S.L., J.A.H., B.S.C., and J.S.E contributed conception and design of study, and revising the manuscript critically for important intellectual content.