SciELO - Scientific Electronic Library Online

 
vol.31 issue3ASIA syndrome (autoimmune/inflammatory syndrome induced by adjuvants): Narrative literature reviewInterstitial lung disease in patients with idiopathic inflammatory myopathy (IIM-ILD): Definitions, epidemiology, pathophysiology, clinical manifestations, complications, risk, and mortality factors (narrative review) author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • On index processCited by Google
  • Have no similar articlesSimilars in SciELO
  • On index processSimilars in Google

Share


Revista Colombiana de Reumatología

Print version ISSN 0121-8123

Rev.Colomb.Reumatol. vol.31 no.3 Bogotá July/Sept. 2024  Epub Feb 01, 2025

https://doi.org/10.1016/j.rcreu.2023.04.001 

Review article

Clinical relationship between reactive arthritis and SARS-CoV-2 infection: A scoping review

Eduardo Tuta-Quinteroa  * 

Juan C. Santacruza 

Julián Camachoa 

Juan Olivellaa 

Estefanía Collazosa 

Juan C. Gómeza 

Damián A. Ochoab 

Jilmar Salazar-Villab 

José E. Rodríguezc 

Daniela F. Pérezd 

Julia Gutiérrezd 

Rodrigo Sanabria-Sarmientoe 

Camilo E. Herreraf 

a Department of Internal Medicine, Faculty of Medicine, Universidad de La Sabana, Chía, Cundinamarca, Colombia

b Department of Internal Medicine, Faculty of Medicine, Universidad Libre, Barranquilla, Atlántico, Colombia

c Department of Internal Medicine, Faculty of Medicine, Universidad de Cartagena, Cartagena, Bolívar, Colombia

d Department of Internal Medicine, Faculty of Medicine, Universidad El Bosque, Bogotá, Cundinamarca, Colombia

e Department of Internal Medicine, Faculty of Medicine, Universidad de Santander, Bucaramanga, Santander, Colombia

f Department of Internal Medicine, Faculty of Medicine, Fundación Universitaria Juan N. Corpas, Bogotá, Cundinamarca, Colombia


ABSTRACT

Introduction:

Reactive arthritis (ReA) is a monoarthritis or oligoarthritis that mainly affects the extremities, it can be related to bacterial or viral infections. Currently, COVID-19 has been linked to the development of arthropathies due to its inflammatory component.

Objective:

A scoping review of the literature that describes the clinical characteristics of ReA in survivors of SARS-CoV-2 infection.

Materials and methods:

A systematic review based on the guidelines for reporting systematic reviews adapted for Prisma-P exploratory reviews and steps proposed by Arksey and adjusted by Levan. Experimental and observational studies published in PubMed and Scopus, English and Spanish, which answered the research questions posed, were included.

Results:

Twenty-five documents were included describing the main clinical manifestations of ReA in 27 patients with a history of SARS-Cov-2 infection. The time from the onset of symptoms or microbiological diagnosis of COVID-19 to the development of articular and/or extra-articular manifestations compatible with ReA ranged from 7 days to 120 days. The clinical joint manifestations described were arthralgia and oedema, predominantly in knee, ankle, elbow, interphalangeal, metatarsophalangeal, and metacarpophalangeal joints.

Conclusions:

Arthralgias in the extremities are the main symptom of ReA in patients with a history of COVID-19, whose symptoms can present in a period of days to weeks from the onset of clinical symptoms or microbiological diagnosis of SARS-CoV-2 infection.

Keywords: COVID-19; Reactive arthritis; Clinical manifestations; Systematic review

RESUMEN

Introducción:

La artritis reactiva (ReA) es una monoartritis u oligoartritis que compromete principalmente las extremidades, y se puede relacionar con infecciones bacterianas o virales. En la actualidad, la COVID-19 se ha relacionado con el desarrollo de artropatías debido a su componente inflamatorio.

Objetivo:

Llevar a cabo una revisión exploratoria de la literatura que describa las características clínicas de la ReA en pacientes sobrevivientes a la infección por SARS-CoV-2.

Materiales y métodos:

Revisión sistemática exploratoria basada en las guías para comunicar revisiones sistemáticas adaptadas para las revisiones exploratorias Prisma-P y pasos propuestos por Arksey y ajustados por Levan. Se incluyeron estudios de tipo experimental y observacional publicados en PubMed y Scopus, en inglés y español, que respondieran las preguntas de investigación planteadas.

Resultados:

Se incluyeron 25 documentos que describen las principales manifestaciones clínicas de la ReA en 27 pacientes con antecedente de infección por SARS-CoV-2. El tiempo desde el inicio de los síntomas o diagnóstico microbiológico de la COVID-19 hasta el desarrollo de manifestaciones articulares o extraarticulares compatibles con ReA osciló entre 7 y 120 días. Las manifestaciones articulares clínicas descritas fueron las artralgias y el edema de predominio en articulaciones de las rodillas, los tobillos, los codos, las interfalángicas, las metatarsofalángicas y las metacarpofalángicas.

Conclusiones:

Las artralgias en las extremidades son el principal síntoma de la ReA en pacientes con antecedente de COVID-19. Sus síntomas se pueden presentar en un periodo de días a semanas, desde el inicio de los síntomas clínicos o el diagnóstico microbiológico de la infección por SARS-CoV-2.

Palabras clave: COVID-19; Artritis reactiva; Manifestaciones clínicas; Revisión sistemática

Introduction

Infection by the new coronavirus type 2, which causes the severe acute respiratory syndrome (SARS-CoV-2), is responsible for the coronavirus disease 2019 (COVID-19) pandemic. (1,2) The pathophysiological mechanisms of COVID-19 are related to immune-mediated processes and tissue damage that generate from mild symptoms to severe cases of the disease, due to complications such as acute respiratory distress syndrome or multiple organ failure, among others.2,3 SARS-CoV-2 infection can trigger a wide number of physical or mental sequelae (dyspnea, fatigue, headache, myalgia, arthralgia, anxiety), whose onset time varies from days to weeks after diagnosis, and last even for more than 12 weeks. (4,5 Osteomuscular symptoms in patients who survive COVID-19 are a topic of medical interest, due to the increasing number of cases and the absence of criteria or clinical practice guidelines that facilitate a diagnostic and therapeutic approach. (4,6

Spondyloarthritis (SpA) are a group of diseases that compromise the axial skeleton (sacroiliitis) or the peripheral skeleton (arthritis, tenosynovitis and enthesitis). (7-9 Reactive arthritis (ReA) is a type of SpA that can present as monoarthritis or oligoarthritis (mainly in the extremities), positive for HLA-B27 in 50 to 70% of cases, enthesitis, dactylitis and extra-articular manifestations (urethritis, psoriasis and conjunctivitis). (6,8,9 ReA can be related to bacterial (Chlamydia psittaci, Chlamydia pneumoniae, Staphylococcus aureus, Streptococcus pneumoniae) or viral infections. (8,9 Currently, SARS-CoV-2 infection is an important trigger of this rheumatological disease. (10

The pathophysiological processes of ReA in surviving patients could be related to COVID-19 due to the over-activation of the innate immune system and a molecular mimicry generated by the epitopes present at the tissue level, (11 whose osteomuscular clinical manifestations are similar to those described before the current pandemic. (5,12,13) However, there is no complete clarity regarding the main characteristics and temporality of the symptoms. (14-16 The objective of the manuscript is to perform an exploratory review of the literature that describes the clinical characteristics of ReA in patients who survived the SARS-CoV-2 infection.

Methods

Exploratory systematic review based on the steps proposed by Arksey17 and adjusted by Levan18: 1) define the research question; 2) search for relevant studies; 3) selection of studies; 4) data extraction, and 5) summarize the report of the results. The review adhered to the aspects recommended in the guide-lines for reporting systematic reviews adapted for Prisma-P scoping reviews. (19 (Supplementary material 1).

The research questions were: how can the available medical evidence about the relationship between ReA secondary to COVID-19 be described? and, how can be described the main osteomuscular clinical manifestations in patients with ReA who survive COVID-19?

The PICOT question is described to identify in the literature patients diagnosed with ReA duringor after SARS-CoV-2 infection, with a diagnosis by polymerase chain reaction, ELISA test or high clinical suspicion. This, in order to describe the course of the disease and identify differences between ReA patients with COVID-19 (Supplementary material 2).

Eligibility criteria

This review includes experimental and observational studies published in English and Spanish that answered the research question posed. For all potentially eligible publications, authors must have access to titles, abstracts, and full documents. Theoretical publications such as literature reviews, systematic reviews, position articles, clinical management guidelines, and letters to the editor are excluded. In addition, articles about patients with osteomuscular symptoms related to vaccination against SARS-CoV-2 infection were not taken into account.

Information sources and search strategy

PubMed and Scopus were used as databases, while the search strategies were structured with Boolean operators, and the appropriate keywords of each platform were guided by a librarian (Supplementary material 3). The documents obtained as a result of the search strategies were evaluated by 3 of the authors (ETQ, JO, JCG). References cited in the included papers, if they met the inclusion criteria and had not been previously identified, were also included in the exploratory review.

Data extraction and synthesis

The review of the titles and abstracts of the publications found in the databases was carried out by the authors (ETQ, JO, JCG), according to the eligibility criteria in the Rayyan free access web application for the management of systematic reviews. (20) For the publications in which there was some doubt about their inclusion, the remaining authors met to decide their usefulness in the review. The articles included were reviewed in full text by all authors, and the following information was extracted: authors, characteristics of the population, objective, duration of the onset of symptoms since the clinical or microbiological diagnosis of the infection, and main clinical manifestations. Regular meetings were held to discuss and adjust these synthesis formats.

The results are presented following the categories proposed by Grudniewicz et al.21: a) a summary of the characteristics and distribution of the publications included, and b) a narrative synthesis of the results.

Results

Of 148 documents identified by the search, 25 that describe the main clinical manifestations of ReA related to COVID-19 were included (Fig. 1).

Fig. 1 Prisma flow diagram. 

In all the included documents, 27 patients with a history of SARS-CoV-2 infection are described. The time elapsed between the onset of symptoms related to the active infection or the microbiological diagnosis of COVID-19 and the development of articular or extra-articular manifestations compatible with ReA generally ranges between 7 and 120 days. The clinical joint manifestations described were arthralgias and edema predominantly in the knees, ankles, elbows, interphalangeal, metatarsophalangeal and metacarpophalangeal joints. The general characteristics of the publications included are described in Table 1.

Table 1 Characteristics of the publications included. 

Ouedraogo et al. (13 reported the case of a 45-year-old male patient with a history of arterial hypertension, prostate cancer and chronic low back pain, who was hospitalized for 45 days due to COVID-19, requiring invasive mechanical ventilation, extracorporeal membrane oxygenation and renal replacement therapy. It was described that 7 days after hospital discharge, the patient was readmitted due to severe pain, erythema and edema in the left knee, associated with fever and tachycardia. Despite having elevated inflammatory markers, the left knee arthrocentesis showed no evidence of crystals or microorganisms in the synovial fluid compatible with septic arthritis, while antigenic and serological tests against the most common pathogens were negative.

Shimoyama et al. (23 reported the case of a 37-year-old man with a history of right ankle fracture and hyperuricemia, who 6 days after the diagnosis of SARS-CoV-2 infection developed pain in the right ankle, without improvement after the administration of non-steroidal anti-inflammatory drugs. The synovial fluid aspirate revealed inflammatory cells, while the MRI of the affected joint revealed synovitis without cartilage wear. The patient underwent arthroscopic synovectomy, finding bone damage in the medial malleolus; and days after the surgical intervention, resolution of clinical symptoms was observed. Due to the relationship with the recent diagnosis of COVID-19, it was considered the first report of ReA with bone erosion after the viral infection.

Kuschner et al. (28 presented the case of a 73-year-old man with a history of systemic arterial hypertension and chronic intermittent pain in the right metacarpophalangeal joint, who consulted due to worsening of the joint pain, associated with diarrheal stools without mucus or blood, dry cough and fever of 15 days of evolution. Pain treatment was started with non-steroidal anti-inflammatory drugs and it was decided to perform diagnostic arthrocentesis to rule out septic arthritis, whose synovial fluid was cloudy, without crystals, Gram stain without microorganisms and negative cultures at 48 h. Likewise, it was decided to perform reverse transcription polymerase chain reaction for COVID-19 of the synovial fluid and an antigen testfor COVID-19, which were positive. The authors concluded that this was the first case that demonstrated the presence of disseminated COVID-19 in a joint and its possible correlation as a trigger of ReA.

Santacruz et al. (43 described the clinical case of a 30-year-old woman with a history of SARS-CoV-2 infection 4 months earlier, without requiring ventilatory support, who consulted with a clinical picture of odynophagia associated with anosmia, dysgeusia, bilateral conjunctival injection, fever and dyspnea of 6 days of evolution. Painful ulcers on the labia majora, skin lesions with psoriasiform characteristics on the soles of the feet, subungual hyperkeratosis, and dactylitis of the fourth toe of the left foot were documented during the physical examination. The patient presented a report of an antigen test positive for COVID-19, and received treatment according to the Recovery protocol, without progression of the disease to lung involvement, for which she was discharged from the hospital.

Santacruz et al. (44 described the clinical case of a 27-year-old man who was admitted with a clinical picture of 5 days of evolution consisting of additive, symmetrical polyarticular pain, located in the metacarpophalangeal joints, the knees and the left shoulder, which caused limitation of the movement. The patient reported SARS-CoV-2 infection, confirmed by reverse transcription polymerase chain reaction one month before the onset of symptoms. The findings described in the MRI showed bursitis of the lateral collateral ligament of the left lower limb and a peritendinous inflammatory process of the triangular fibrocartilage in the right wrist. Among the differential diagnoses, a fourth-generation enzyme-linked immunosorbent assay for the detection of the human immunodeficiency virus was performed, which was positive with a subsequent CD4 count of 98 cells/mm3 and a viral load of 459,000 copies/mL. Treatment with prednisolone and sulfasalazine was started, without significant improvement in joint symptoms, and, simultaneously, antiretroviral therapy (abacavir, dolutegravir/lamivudine) achieved gradual improvement in symptoms.

Discussion

Within the clinical characteristics of ReA in patients who survive COVID-19, pain and edema in the joints of the extremities, including the knee and the ankle, after a period of days to weeks from the onset of clinical symptoms or the microbiological diagnosis of SARS-CoV-2 infection are mainly described13,22-45; extra-articular manifestations without joint involvement are infrequent in patients with a history of COVID-19. (35,43 Treatments with glucocorticoids with significant improvement in associated symptoms are described in a high percentage of patients22,23,29,31,34,41,44,45; and to a lesser extent, pharmacological treatment with non-glucocorticoid anti-inflammatory drugs was used. (13,24,26,32,35-37,40

The articular clinical manifestations in ReA are erythema, edema and inflammatory pain, which may or may not occur together with extra-articular symptoms, (23,38,39 with oligoarticular and monoarticular involvement being the most frequent forms of presentation of the disease. (46-48 Despite the fact that there is variety and poor performance in the criteria established for the diagnosis of ReA associated with COVID-19, it is proposed to use the term of clinical pictures with osteomuscular symptoms and signs related to the viral infection and laboratory tests. (6-8,43,46 The most frequent extra-articular manifestations in patients with ReA are urethritis, cervicitis, salpingo-oophoritis, cystitis, prostatitis, conjunctivitis, and aphthous ulcers, among others. (48 Even though the described cases of ReA after COVID-19 are mostly characterized by arthritis and dactylitis, 2 cases with involvement at the cutaneous and genitourinary levels are reported in this exploratory review. (35,43

The diagnosis of ReA related to COVID-19 is limited, due to the variety of musculoskeletal symptoms present in the convalescence period or post-COVID syndrome, the poor performance of the current classification criteria and the history of rheumatological diseases with joint involvement. (49,50 On the other hand, the use of medications such as corticosteroids or non-steroidal anti-inflammatory drugs during moderate or severe active infection could potentially reduce the occurrence of musculoskeletal symptoms and extra-articular manifestations. (7,8,23,35,45 Given the high number of patients who survive SARS-CoV-2 infection, studies are needed that allow us to understand the pathogenesis of COVID-19 in the different clinical phenotypes of joint involvement, the incidence and evolution of inflammatory manifestations, with a favorable impact on the diagnosis, treatment and prognosis of the disease. (46,50

The treatment of ReA aims to reduce clinical symptoms and the articular and extra-articular inflammatory process; non-glucocorticoid anti-inflammatory drugs are the first line, while systemic glucocorticoids are an option in refractory disease. (5,6,13,22 A surgical treatment such as synovectomy, used in patients who do not respond to pharmacological treatment, is useful to improve pain and prevent bone erosion in patients with rheumatoid arthritis or Reiter's syndrome, because the hypertrophic synovial membrane with infectious agents is removed23,48,49; however, the impact that this procedure may have on patients with ReA is unknown. (50 Treatment for extra-articular manifestations has been indicated only focused on the control of symptoms, or with topical gluco-corticoids, due to the low evidence available and the fact that in most cases they are self-limiting. (43,50

The immune system in patients with ReA is characterized by molecular mimicry events, as a consequence of the high load of microorganism antigens, which generates an autoimmune cross-reaction with specific human proteins and an inflammatory response by B cells, CD4+ T cells and inter-leukins at the intraarticular level. (5,7,13 Patients with COVID-19 present an inflammatory response with a marked elevation of Th17 cells, tumor necrosis factor, interferon-^ and interleukin-17, the latter related to the pathophysiology of ReA. (43,51 Even though the development of ReA in patients diagnosed with COVID-19 is related to a process of inflammatory response and tissue injury triggered by exposure to the virus, the development of this arthropathy can occur in mild, moderate and severe cases of the disease. (13,22-45

The presentation and musculoskeletal sequelae of SARS-CoV-2 are mainly related to a post-infectious multisystem inflammatory syndrome and inflammatory reactions after the virus has been eliminated. (5,9,13,45,52 The clinical symptoms described in post-COVID syndrome were also observed in previous infectious diseases, such as Middle East respiratory syndrome and severe acute respiratory syndrome, due to the extensive tissue damage in organs and systems.4,5,53,54 The joint pain can usually last from 6 weeks to 3-6 months after the SARS-CoV-2 infection, and the duration may be related to the anti-inflammatory medical treatment established and the severity of the disease. (6,48

The viral agents with capacity to cause joint damage most frequently are, in general, parvovirus, alphavirus, hepatitis B, hepatitis C virus, Epstein-Barr, Zika, and chikungunya, which trigger symptoms such as fever, rash, and lymphadenopathy. (52,53,55,56 The diagnostic definition of ost-seomuscular symptoms related to ReA in patients who survive COVID-19 is similar to viral-mediated arthritis, which is characterized by being self-limiting, as well as by the presence of synovial fluid positive for the infectious agent and patients who respond to treatment with nonsteroidal antiinflammatory drugs. However, it is necessary to establish criteria and definitions for a timely clinical diagnosis of these 2 diseases with a high incidence today. (4,13,53,54

Limitations

In the vast majority of the studies included in this review, there was a lack in the definition of the osteomuscular symptoms characteristic of ReA, as well as their differences with other rheumatological or infectious diseases that affect the joints. (21,43,45 On the other hand, all of the included studies were purely descriptive observational studies, without taking into account the age and other variables that worsened symptoms, such as sleeping habits, employment and physical activity.

The evidence was extracted only from PubMed and Scopus, in Spanish and English; nevertheless, the members of the research team are experienced in properly extracting and synthesizing this type of data. Being an exploratory review, the quality of the evidence was not evaluated, in accordance with the recommendations made by the Prisma-ScR guideline. (17-19

Conclusion

The medical literature describes pain in the joints of the extremities as one of the main clinical manifestations of ReA in patients with a history of COVID-19, whose symptoms can occur within a period of days to weeks, from the onset of the clinical symptoms or the microbiological diagnosis of the SARS-CoV-2 infection. However, for a timely diagnosis and therapeutic approach, it is necessary to establish criteria and definitions of ReA in patients who survived COVID-19.

REFERENCES

1. World Health Organization. Coronavirus disease 2019 dashboard. November 2, 2022>. Available from: https://covid19.who.int/. [ Links ]

2. Singh SP, Pritam M, Pandey B, Yadav TP. Microstructure, pathophysiology, and potential therapeutics of covid-19: a comprehensive review. J Med Virol. 2021;93:275-99, http://dx.doi.org/10.1002/jmv.26254. [ Links ]

3. Hu B, Guo H, Zhou P, Shi ZL. Characteristics of SARS-CoV-2 and covid-19. Nat Rev Microbiol. 2021;19:141-54, http://dx.doi.org/10.1038/s41579-020-00459-7. [ Links ]

4. Yong SJ. Long covid or post-covid-19 syndrome: putative pathophysiology, risk factors, and treatments. Infect Dis (Londres). 2021;53:737-54, http://dx.doi.org/10.1080/23744235.2021. [ Links ]

5. Tuta E, Hernández E, Toro SM, Bahamon EC, Vigles KO, Acuüa DA, et al. Posttraumatic stress disorder after covid-19: a scoping review. Gac Med Caracas. 2022;130:404-20, http://dx.doi.org/10.47307/GMC.2022.130.2.18. [ Links ]

6. Bekaryssova D, Yessirkepov M, Zimba O, Gasparyan AY, Ahmed S. Reactive arthritis before and after the onset of the COVID-19 pandemic. Clin Rheumatol. 2022;41:1641-52, http://dx.doi.org/10.1007/s10067-022-06120-3. [ Links ]

7. Taniguchi Y, Nishikawa H, Yoshida T, Terada Y, Tada K, Tamura N, et al. Expanding the spectrum of reactive arthritis (ReA): classic ReA and infection-related arthritis including poststreptococcal ReA, Poncet's disease, and iBCG-induced ReA. Rheumatol Int. 2021;41:1387-98, http://dx.doi.org/10.1007/s00296-021-04879-3. [ Links ]

8. Walsh JA, Magrey M. Clinical manifestations and diagnosis of axial spondyloarthritis. J Clin Rheumatol. 2021;27:e547-60, http://dx.doi.org/10.1097/RHU.0000000000001575. [ Links ]

9. Lucchino B, Spinelli FR, Perricone C, Valesini G, Di Franco M. Reactive arthritis: current treatment challenges and future perspectives. Clin Exp Rheumatol. 2019;37:1065-76. [ Links ]

10. Banicioiu-Covei S, Vreju AF, Rosu A, Ciurea PL. The importance of HLA-B27 in the evolution of reactive arthritis. Curr Health Sci J. 2019;45:345-52, http://dx.doi.org/10.12865/CHSJ.45.04.01. [ Links ]

11. Ahmed S, Zimba O, Gasparyan AY. Covid-19 and the clinical course of rheumatic manifestations. Clin Rheumatol. 2021;40:2611-9, http://dx.doi.org/10.1007/s10067-021-05691-x. [ Links ]

12. Zeidler H, Hudson AP. Reactive arthritis update: spotlight on new and rare infectious agents implicated as pathogens. Curr Rheumatol Rep. 2021;23:53, http://dx.doi.org/10.1007/s11926-021-01018-6. [ Links ]

13. Ouedraogo F, Navara R, Thapa R, Patel KG. Reactive arthritis post-SARS-CoV-2. Cureus. 2021;13:e18139, http://dx.doi.org/10.7759/cureus.18139. [ Links ]

14. Gustine JN, Jones D. Immunopathology of hyperinflammation in covid-19. Am J Pathol. 2021;191:4-17, http://dx.doi.org/10.1016/j.ajpath.2020.08.009. [ Links ]

15. Wendling D, Verhoeven F, Chouk M, Prati C. Can SARS-CoV-2 trigger reactive arthritis? Joint Bone Spine. 2021;88:105086, http://dx.doi.org/10.1016/j.jbspin.2020.105086. [ Links ]

16. An QJ, Qin DA, Pei JX. Reactive arthritis after covid-19 vaccination. Hum Vaccin Immunother. 2021;17:2954-6, http://dx.doi.org/10.1080/21645515.2021.1920274. [ Links ]

17. Arksey H, O'Malley L. Scoping studies: towards a methodological framework. Int J Soc Res Methodol. 2005;8:19-32, http://dx.doi.org/10.1080/1364557032000119616. [ Links ]

18. Levac D, Colquhoun H, O'Brien KK. Scoping studies: advancing the methodology. Implement Sci. 2010;5:69, http://dx.doi.org/10.1186/1748-5908-5-69. [ Links ]

19. Tricco AC, Lillie E, Zarin W, O'Brien KK, Colquhoun H, Levac D, et al. Prisma extension for scoping reviews (Prisma-ScR): checklist and explanation. Ann Intern Med. 2018;169:467-73, http://dx.doi.org/10.7326/M18-0850. [ Links ]

20. Ouzzani M, Hammady H, Fedorowicz Z, Elmagarmid A. Rayyan-a web and mobile app for systematic reviews. Syst Rev. 2016;5:210, http://dx.doi.org/10.1186/s13643-016-0384-4. [ Links ]

21. Grudniewicz A, Nelson M, Kuluski K, Lui V, Cunningham HV, X Nie J, et al. Treatment goal setting for complex patients: protocol for a scoping review. BMJ Open. 2016;6:e011869, http://dx.doi.org/10.1136/bmjopen-2016-011869. [ Links ]

22. Quaytman J, Gollamudi U, Bass N, Suresh S. Reactive arthritis and silent thyroiditis following SARS-CoV-2 infection: case report and review of the literature. Clin Case Rep. 2022;10:e05430, http://dx.doi.org/10.1002/ccr3.5430. [ Links ]

23. Shimoyama K, Teramoto A, Murahashi Y, Takahashi K, Watanabe K, Iba K, et al. Surgically treated reactive arthritis of the ankle after covid-19 infection: a case report. J Infect Chemother. 2022;28:587-90, http://dx.doi.org/10.1016/j.jiac.2021.12.028. [ Links ]

24. Ono K, Kishimoto M, Shimasaki T, Uchida H, Kurai D, Deshpande GA, et al. Reactive arthritis after covid-19 infection. RMD Open. 2020;6:e001350, http://dx.doi.org/10.1136/rmdopen-2020-001350. [ Links ]

25. Kocyigit BF, Akyol A. Reactive arthritis after covid-19: a case-based review. Rheumatol Int. 2021;41:2031-9, http://dx.doi.org/10.1007/s00296-021-04998-x. [ Links ]

26. Saricaoglu EM, Hasanoglu I, Guner R. The first reactive arthritis case associated with covid-19. J Med Virol. 2021;93:192-3, http://dx.doi.org/10.1002/jmv.26296. [ Links ]

27. Schenker HM, Hagen M, Simon D, Schett G, Manger B. Reactive arthritis and cutaneous vasculitis after SARS-CoV-2 infection. Rheumatology (Oxford). 2021;60:479-80, http://dx.doi.org/10.1093/rheumatology/keaa689. [ Links ]

28. Kuschner Z, Ortega A, Mukherji P. A case of SARS-CoV-2-associated arthritis with detection of viral RNA in synovial fluid. J Am Coll Emerg Phys Open. 2021;2:e12452, http://dx.doi.org/10.1002/emp2.12452. [ Links ]

29. Dutta S, Dey S, Poddar A, Pal P. Post-covid reactive arthritis. Indian J Pediatr. 2022;89:103, http://dx.doi.org/10.1007/s12098-021-03992-2. [ Links ]

30. H0nge BL, Hermansen MF, Storgaard M. Reactive arthritis after covid-19. BMJ Case Rep. 2021;14:e241375, http://dx.doi.org/10.1136/bcr-2020-241375. [ Links ]

31. Liew IY, Mak TM, Cui L, Vasoo S, Lim XR. A case of reactive arthritis secondary to coronavirus disease 2019 infection. J Clin Rheumatol. 2020;26:233, http://dx.doi.org/10.1097/RHU.0000000000001560. [ Links ]

32. Coath FL, Mackay J, Gaffney JK. Axial presentation of reactive arthritis secondary to covid-19 infection. Rheumatology (Oxford). 2021;60:e232-3, http://dx.doi.org/10.1093/rheumatology/keab009. [ Links ]

33. Jali I. Reactive arthritis after covid-19 infection. Cureus. 2020;12:e11761, http://dx.doi.org/10.7759/cureus.11761. [ Links ]

34. Fragata I, Mourão AF. Coronavirus disease 19 (covid-19) complicated with post-viral arthritis. Acta Reumatol Port. 2020;45:278-80. [ Links ]

35. De Stefano L, Rossi S, Montecucco C, Bugatti S. Transient monoarthritis and psoriatic skin lesions following covid-19. Ann Rheum Dis. 2020, http://dx.doi.org/10.1136/annrheumdis-2020-218520, in press. [ Links ]

36. Danssaert Z, Raum G, Hemtasilpa S. Reactive arthritis in a 37-year-old female with SARS-CoV2 infection. Cureus. 2020;12:e9698, http://dx.doi.org/10.7759/cureus.9698. [ Links ]

37. Gasparotto M, Framba V, Piovella C, Doria A, Iaccarino L. Post-covid-19 arthritis: a case report and literature review. Clin Rheumatol. 2021;40:3357-62, http://dx.doi.org/10.1007/s10067-020-05550-1. [ Links ]

38. Parisi S, Borrelli R, Bianchi S, Fusaro E. Viral arthritis and covid-19. Lancet Rheumatol. 2020;2:e655-7, http://dx.doi.org/10.1016/S2665-9913(20)30348-9. [ Links ]

39. Yokogawa N, Minematsu N, Katano H, Suzuki T. Case of acute arthritis following SARS-CoV-2 infection. Ann Rheum Dis. 2020;80:e101, http://dx.doi.org/10.1136/annrheumdis-2020-218281. [ Links ]

40. López-González MD, Peral-Garrido ML, Calabuig I, Jovani V, Bernabeu P, García-Sevila R, et al. Case series of acute arthritis during covid-19 admission. Ann Rheum Dis. 2020;80:e58, http://dx.doi.org/10.1136/annrheumdis-2020-217914. [ Links ]

41. Di Carlo M, Tardella M, Salaffi F. Can SARS-CoV-2 induce reactive arthritis? Clin Exp Rheumatol. 2021;39 Supl 128:25-6. [ Links ]

42. Sureja NP, Nandamuri D. Reactive arthritis after SARS-CoV-2 infection. Rheumatol Adv Pract. 2021;5:rkab001, http://dx.doi.org/10.1093/rap/rkab001. [ Links ]

43. Santacruz JC, Londoiio J, Santos AM, Arzuaga A, Mantilla MJ. Extra-articular manifestations in reactive arthritis due to covid-19. Cureus. 2021;13:e18620, http://dx.doi.org/10.7759/cureus.18620. [ Links ]

44. Santacruz JC, Mantilla MJ, Pulido S, Arzuaga A, Bello JM, Londono J. HIV and covid-19 coinfection: a synergism that results in more severe forms of reactive arthritis. Cureus. 2021;13:e19396, http://dx.doi.org/10.7759/cureus.19396. [ Links ]

45. Ruiz-Del-Valle V, Sarabia de Ardanaz L, Navidad-Fuentes M, Martín-Martín I, Lobato-Cano R. Reactive arthritis with SARS-COV-2 as a trigger. Reumatol Clin (Engl Ed). 2022;18:490-2, http://dx.doi.org/10.1016/j.reumae.2021.11.002. [ Links ]

46. Baimukhamedov C, Dossybayeva G, Makhmudov S, Botabekova A. Arthritis after SARS-CoV-2 infection: reactive arthritis or virally mediated arthritis? Infection. 2022:1-2, http://dx.doi.org/10.1007/s15010-022-01936-2. [ Links ]

47. Kobayashi S, Taniguchi Y, Kida I, Tamura N. SARS-CoV2-triggered acute arthritis: viral arthritis rather than reactive arthritis. J Med Virol. 2021;93:6458-9, http://dx.doi.org/10.1002/jmv.27229. [ Links ]

48. Bojovic J, Strelic N, Pavlica L. Reiter's syndrome-disease of young men- analysis of 312 patients. Med Pregl. 2014;67:222-30, http://dx.doi.org/10.2298/mpns1408222b. [ Links ]

49. Lipina M, Makarov M, Mukhanov V, Karpashevich A, Maglevaniy S, AmirdjanOva V, et al. Arthroscopic synovectomy of the knee joint for rheumatoid arthritis. Int Orthop. 2019;43:1859-63, http://dx.doi.org/10.1007/s00264-018-4160-z. [ Links ]

50. Bentaleb I, Abdelghani KB, Rostom S, Amine B, Laatar A, Bahiri R. Reactive arthritis: update. Curr Clin Microbiol Rep. 2020;7:124-32, http://dx.doi.org/10.1007/s40588-020-00152-6. [ Links ]

51. García LF. Immune response, inflammation, and the clinical spectrum of covid-19. Front Immunol. 2020;11:1441, http://dx.doi.org/10.3389/fimmu.2020.01441. [ Links ]

52. Chen Y, Xu Z, Wang P, Li XM, Shuai ZW, Ye DQ, et al. New-onset autoimmune phenomena post-covid-19 vaccination. Immunology. 2022;165:386-401, http://dx.doi.org/10.1111/imm.13443. [ Links ]

53. Beretta A, Cranage M, Zipeto D. Is cross-reactive immunity triggering covid-19 immunopathogenesis? Front Immunol. 2020;11:567710, http://dx.doi.org/10.3389/fimmu.2020.567710. [ Links ]

54. Lyons-Weiler J. Pathogenic priming likely contributes to serious and critical illness and mortality in covid-19 via autoimmunity. J Transl Autoimmun. 2020;3:100051, http://dx.doi.org/10.1016/j.jtauto.2020.100051. [ Links ]

55. Tiwari V, Bergman MJ. Viral arthritis. Treasure Island, FL: StatPearls Publishing; 2020. [ Links ]

56. Toussirot É, Bereau M. Vaccination and induction of autoimmune diseases. Inflamm Allergy Drug Targets. 2015;14:94-8, http://dx.doi.org/10.2174/1871528114666160105113046. [ Links ]

Funding None.

Appendix A. Supplementary data

Supplementary material related to this article can be found, in the online version, at doi: https://doi.org/10.1016 /j.rcreue.2023.04.001.

Received: January 06, 2023; Accepted: April 27, 2023; other: August 01, 2024

* Corresponding author. E-mail address:eduardotuqu@unisabana.edu.co(E. Tuta-Quintero).

Conflict of interest

The authors declare that they have no conflict of interest.

Creative Commons License This is an open-access article distributed under the terms of the Creative Commons Attribution License