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POS0703 (2021)
CARDIAC ADVERSE EFFECTS OF LONG-TERM USE OF HYDROXYCHLOROQUINE IN SYSTEMIC LUPUS ERYTHEMATOSUS. SINGLE UNIVERSITY CENTER STUDY OF 109 PATIENTS
A. Herrero-Morant1, A. Margarida-de Castro1, R. Pérez-Barquín1, J. Zubiaur-Zamacola1, M. Á. González-Gay1, R. Blanco1
1Hospital Universitario Marqués de Valdecilla, Rheumatology and Cardiology, Santander, Spain

Background: Hydroxychloroquine (HCQ) is a widely used drug especially in connective tissue disorders such as Systemic Lupus Erythematosus (SLE). Cardiac adverse effects of long-term use of HCQ remains controversial.


Objectives: To assess cardiac adverse effects of long-term use of HCQ in SLE.


Methods: Observational single center study of 109 patients with SLE treated with HCQ for more than 3 months. The main outcomes were cardiac structural and conduction disorders in a 12-lead electrocardiogram and/or echocardiogram at baseline and during HCQ treatment.


Results: We studied 109 patients (95 women/14 men; mean age 66.9±14.7 years). Main cardiovascular history was hypertension (n=61, 56.0%), diabetes mellitus (n=16, 14.7%) and renal impairment (n=11, 10.1%). HCQ was used for 11.7±8.9 years. Initial median SLE Disease Activity Index 2000 (SLEDAI-2K) was 7 [3.75-11]. At baseline, 27 (24.8%) patients had conduction disorders and 15 (13.7%) had structural abnormalities: Most prevalent cardiac alterations were Left Anterior Fascicular Block (LAFB) (n=9, 8.3%), left ventricular hypertrophy (n=9, 8.3%) and right bundle branch block (n=8, 7.3%). After 11.7±8.9 years of follow-up (mean HCQ cumulative dose: 1042.2±267.5 g; median SLEDAI-2K 1 [0-4]), there was a significant increase in conductions disorders (n=41, 37.6%, p=0.011) and in LAFB (n=16, 14.7%, p=0.021). There was no statistically significant increase in structural abnormalities (n=21, 19.7%, p=0.629).

Main cardiac abnormalities at baseline and after 11.7±8.9 years of follow-up are summarized in Table 1 . Time of occurrence of cardiac adverse effect in relation to HCQ cumulative dose is shown in Figure 1 .

Main cardiac abnormalities at baseline and after follow-up.

Baseline After follow-up p
Conduction disorders, n (%) 27 (24.8) 41 (37.6) 0.011
Left anterior fascicular block 9 (8.3) 16 (14.7) 0.021
Right bundle branch block 7 (6.4) 8 (7.3) 1.0
Atrioventricular block 4 (3.6) 11 (10.1) 0.092
Incomplete right bundle branch block 4 (3.6) 5 (4.6) 1.0
Short PR interval 2 (1.8) 4 (3.7) 0.5
Prolonged QT corrected interval 2 (1.8) 4 (3.7) 0.625
Left bundle branch block 1 (0.9) 5 (4.6) 0.125
Atrial Fibrillation 1 (0.9) 5 (4.6) 0.219
Structural abnormalities, n (%) 15 (13.7) 21 (19.7) 0.629
Ventricular hypertrophy 9 (8.3) 9 (8.3) 1.0
Atrial enlargement 6 (5.5) 13 (11.9) 0.096

Time of occurrence of cardiac adverse effect in relation to hydroxychloroquine cumulative dose.


Conclusion: Conduction disorders were more prevalent than structural abnormalities. Patients with SLE treated with HCQ had a significant increase in LAFB. Use of electrocardiogram and/or echocardiogram may be helpful in monitoring cardiac adverse effects.


Disclosure of Interests: Alba Herrero-Morant: None declared, Adrián Margarida-de Castro: None declared, Raquel Pérez-Barquín: None declared, Jon Zubiaur-Zamacola: None declared, Miguel Á. González-Gay Speakers bureau: AbbVie, Pfizer, Roche, Sanofi, Lilly, Celgene and MSD, Grant/research support from: AbbVie, MSD, Jansen and Roche, Ricardo Blanco Speakers bureau: AbbVie, Pfizer, Roche, Bristol-Myers, Janssen, Sanofi, Lilly and MSD, Grant/research support from: AbbVie, MSD, and Roche


Citation: Ann Rheum Dis, volume 80, supplement 1, year 2021, page 601
Session: SLE, Sjögren’s and APS – treatment (POSTERS only)