Literature DB >> 33878606

Impact of the COVID-19 pandemic on therapeutic management of rheumatoid arthritis in Brittany (France).

Baptiste Queré1, Alain Saraux2, Thierry Marhadour1, Sandrine Jousse-Joulin1, Divi Cornec3, Camille Houssais1, Guillermo Carvajal Alegria3, Maxime Quiviger1, Margot Le Guillou1, Valérie Devauchelle-Pensec3, Dewi Guellec4.   

Abstract

Entities:  

Year:  2021        PMID: 33878606      PMCID: PMC7999690          DOI: 10.1016/j.jbspin.2021.105179

Source DB:  PubMed          Journal:  Joint Bone Spine        ISSN: 1297-319X            Impact factor:   4.929


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Early during the SARS-CoV-2 sanitary crisis, the vulnerability of patients treated with immunomodulatory agents or non-steroidal anti-inflammatory drugs (NSAIDS) with regards to the most severe forms of the disease have been suggested [1], [2]. Despite rapid clarifications from health authorities and expert societies regarding the indication to continue ongoing therapy in most situations, the usual immunosuppressive treatment of several clinical conditions, including inflammatory rheumatic diseases, may have been impacted by these scientific data and their media relay [3], [4], [5], [6]. In the present work, our objectives were to evaluate the impact of COVID-19 pandemic on therapeutic management of rheumatoid arthritis (RA) and to identify factors associated with patient's choice to reduce or stop Disease-modifying anti-rheumatic drugs regimen (DMARD). For this, we conducted a cross-sectional single-center study in Brittany (France) between April 23, 2020 and July 28, 2020. The study received approval from the Brest University Hospital Ethics committee (29BRC20.0110). A questionnaire was administered to patients with a diagnosis of RA satisfying ACR/EULAR criteria, receiving DMARD or having a prescription to initiate such treatment, during face-to-face or remote consultations. The primary outcome was DMARD treatment modification in relation to the pandemic. Logistic regression was performed in order to identify factors associated with patient's decision to modify DMARD treatment. The explanatory variables included in the multivariate regression model were those showing P-value < 0.20 in univariate analysis. Significance was defined as P  < 0.05 for variables in the final model. Data analyses were performed using Statistical package for the social sciences version 23.0 (IBM, Armonk, NY, USA). Two hundred and fifty two patients participated in this survey, of which 75.8% (191/252) were women. Detailed characteristics of participants, including those related to medical background, RA characteristics and ongoing immunomodulatory therapy at last visit are provided in Table 1 .
Table 1

Characteristics of overall population and results of logistic regression analyses comparing participants according to the personal decision to modify DMARD treatment in relation to the context of sanitary crisis.

Overall participants (n = 252)Personal decision to reduce or stop DMARD treatment (n = 24)No personal decision to reduce or stop DMARD treatment (n = 225)Univariate analysis odds ratiosMultivariate analysis odds ratios
General characteristics
 Age (years)61.3 (12.7)53.8 (13.3)62.2 (12.5)0.95 (0.92 to 0.98)***
 Age categories
  18 to 44 years32 (12.7%)6 (25.0%)26 (11.6%)1 (referent)1 (referent)
  45 to 64 years110 (43.9%)15 (62.5%)93 (41.5%)0.70 (0.25 to 1.98)0.77 (0.27 to 2.22)
  65 years and older109 (43.4%)3 (12.5%)105 (46.9%)0.12 (0.03 to 0.52)***0.15 (0.03 to 0.64)**
 Female191 (75.8%)20 (83.3%)169 (75.1%)1.66 (0.54 to 5.05)
 BMI (kg/m2)25.3 (5.0)25.2 (4.8)25.3 (5.1)1.00 (0.91 to 1.10)
 Urban residency80 (32.7%)10 (43.5%)69 (31.5%)1.67 (0.70 to 4.00)
 Active smoking51 (20.2%)4 (16.7%)47 (20.9%)0.76 (0.25 to 2.32)
Medical history
 High blood pressure69 (27.5%)3 (12.5%)66 (29.5%)0.34 (0.10 to 1.19)*0.44 (0.12 to 1.58)
 Diabetes11 (4.4%)0 (0.0%)11 (4.9%)Not applicable
 MACE32 (12.7%)2 (8.3%)30 (13.3%)0.59 (0.13 to 2.64)
 Chronic lung disease68 (28.1%)5 (21.7%)63 (29.0%)0.68 (0.24 to 1.91)
 Severe infection47 (18.8%)4 (16.7%)42 (18.7%)0.87 (0.28 to 2.67)
 Malignancy28 (11.2%)1 (4.2%)27 (12.1%)0.32 (0.04 to 2.44)
RA characteristics
 Disease duration (years)14.9 (10.8)13.2 (10.8)15.1 (10.8)0.98 (0.94 to 1.02)
 RF positivity194 (79.5%)18 (75.0%)175 (80.3%)0.74 (0.28 to 1.97)
 ACPA positivity200 (83.0%)18 (75.0%)181 (84.2%)0.56 (0.21 to 1.52)
 Erosive disease162 (66.4%)16 (66.7%)145 (65.9%)1.38 (0.52 to 3.67)
 Past glucocorticoid exposure (≥ 5 mg per day for more than 3 months)151 (62.9%)14 (58.3%)135 (63.1%)0.82 (0.35 to 1.93)
RA treatments
 Methotrexate164 (65.6%)15 (62.5%)149 (66.2%)0.85 (0.36 to 2.03)
 Hydroxychloroquine8 (3.2%)1 (4.2%)7 (3.1%)1.35 (0.16 to 11.4)
 Other synthetic DMARD23 (9.2%)3 (12.5%)20 (8.9%)1.46 (0.40 to 5.31)
 Biological DMARD140 (56.0%)13 (54.2%)126 (56.0%)0.93 (0.40 to 2.16)
 Targeted synthetic DMARD10 (4.0%)1 (4.2%)9 (4.0%)1.04 (0.03 to 8.57)
 Glucocorticoids62 (24.8%)8 (33.3%)53 (23.6%)1.62 (0.66 to 4.00)
 NSAIDs45 (18.1%)5 (20.8%)40 (17.9%)1.20 (0.42 to 3.42)

Reported values are mean (standard deviation) for continuous variables, numbers (percentage) for dichotomous variables. ACPA: anti–citrullinated protein antibody; BMI: body mass index; CI: confidence interval; DMARD: disease modifying anti-rheumatic drug; MACE: major adverse cardiac events; NSAID: non-steroidal anti-inflammatory drug; PGA: patient global assessment; RF: rheumatoid factor. * P-value < 0.20 (P-values < 0.20 in univariate analysis were included in the multivariate model); ** P-value < 0.05; *** P-value < 0.001.

Characteristics of overall population and results of logistic regression analyses comparing participants according to the personal decision to modify DMARD treatment in relation to the context of sanitary crisis. Reported values are mean (standard deviation) for continuous variables, numbers (percentage) for dichotomous variables. ACPA: anti–citrullinated protein antibody; BMI: body mass index; CI: confidence interval; DMARD: disease modifying anti-rheumatic drug; MACE: major adverse cardiac events; NSAID: non-steroidal anti-inflammatory drug; PGA: patient global assessment; RF: rheumatoid factor. * P-value < 0.20 (P-values < 0.20 in univariate analysis were included in the multivariate model); ** P-value < 0.05; *** P-value < 0.001. Of the patients, 2.8% (7/252) reported a history of SARS-CoV-2 infection at the time of the survey. Among them, only one case was further confirmed with RT-PCR. Overall, 11.2% of patients (28/249) reported that their DMARD treatment have been transiently reduced or stopped in relation to the context of sanitary crisis. Modification of the DMARD treatment was the result of a patient's choice in 85.7% of cases (24/28). Within the same period, DMARD treatment was reduced or stopped for other reasons in 7.6% (19/249) of participants. Logistic regression analyses showed that patient's decision to modify DMARD treatment was less frequent among participants aged 65 years or over (Table 1). This study shows that in a French area of low viral circulation, the sanitary crisis led to DMARD treatment modification in around 10% of RA patients, a result of the same order as what has been observed elsewhere in comparable contexts [7], [8], [9], [10]. Our results describe the therapeutic modifications that can be highlighted during a classic interview with patients but do not take into account the more complex problematic of non-compliance. In most cases, treatment modification was the consequence of a patient's decision rather than a decision driven by a healthcare professional. Future studies will have to determine the longitudinal impact of COVID-19 pandemic on RA optimal management.

Disclosure of interest

The authors declare that they have no competing interest.
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