TY - JOUR
T1 - Anakinra for corticosteroid-dependent and colchicine-resistant pericarditis
T2 - The IRAP (International Registry of Anakinra for Pericarditis) study
AU - Imazio, Massimo
AU - Andreis, Alessandro
AU - De Ferrari, Gaetano Maria
AU - Cremer, Paul C.
AU - Mardigyan, Vartan
AU - Maestroni, Silvia
AU - Luis, Sushil Allen
AU - Lopalco, Giuseppe
AU - Emmi, Giacomo
AU - Lotan, Dor
AU - Marcolongo, Renzo
AU - Lazaros, George
AU - De Biasio, Marzia
AU - Cantarini, Luca
AU - Dagna, Lorenzo
AU - Cercek, Andreja Cerne
AU - Pivetta, Emanuele
AU - Varma, Beni
AU - Berkson, Laeora
AU - Tombetti, Enrico
AU - Iannone, Florenzo
AU - Prisco, Domenico
AU - Caforio, Alida Linda P.
AU - Vassilopoulos, Dimitrios
AU - Tousoulis, Dimitrios
AU - De Luca, Giacomo
AU - Giustetto, Carla
AU - Rinaldi, Mauro
AU - Oh, Jae K.
AU - Klein, Allan L.
AU - Brucato, Antonio
AU - Adler, Yehuda
N1 - Publisher Copyright:
© The European Society of Cardiology 2019.
PY - 2020/6/1
Y1 - 2020/6/1
N2 - Aims: Novel therapies are needed for recurrent pericarditis, particularly when corticosteroid dependent and colchicine resistant. Based on limited data, interleukin-1 blockade with anakinra may be beneficial. The aim of this multicentre registry was to evaluate the broader effectiveness and safety of anakinra in a ‘real world’ population. Methods and results: This registry enrolled consecutive patients with recurrent pericarditis who were corticosteroid dependent and colchicine resistant and treated with anakinra. The primary outcome was the pericarditis recurrence rate after treatment. Secondary outcomes included emergency department visits, hospitalisations, corticosteroid use and adverse events. Among 224 patients (46 ± 14 years old, 63% women, 75% idiopathic), the median duration of disease was 17 months (interquartile range 9–33). Most patients had elevated C-reactive protein (91%) and pericardial effusion (88%). After a median treatment of 6 months (3–12), pericarditis recurrences were reduced six-fold (2.33–0.39 per patient per year), emergency department admissions were reduced 11-fold (1.08–0.10 per patient per year), hospitalisations were reduced seven-fold (0.99–0.13 per patient per year). Corticosteroid use was decreased by anakinra (respectively from 80% to 27%; P < 0.001). No serious adverse events occurred; adverse events consisted mostly of transient skin reactions (38%) at the injection site. Adverse events led to discontinuation in 3%. A full-dose treatment duration of over 3 months followed by a tapering period of over 3 months were the therapeutic schemes associated with a lower risk of recurrence. Conclusion: In patients with recurrent pericarditis, anakinra appears efficacious and safe in reducing recurrences, emergency department admissions and hospitalisations.
AB - Aims: Novel therapies are needed for recurrent pericarditis, particularly when corticosteroid dependent and colchicine resistant. Based on limited data, interleukin-1 blockade with anakinra may be beneficial. The aim of this multicentre registry was to evaluate the broader effectiveness and safety of anakinra in a ‘real world’ population. Methods and results: This registry enrolled consecutive patients with recurrent pericarditis who were corticosteroid dependent and colchicine resistant and treated with anakinra. The primary outcome was the pericarditis recurrence rate after treatment. Secondary outcomes included emergency department visits, hospitalisations, corticosteroid use and adverse events. Among 224 patients (46 ± 14 years old, 63% women, 75% idiopathic), the median duration of disease was 17 months (interquartile range 9–33). Most patients had elevated C-reactive protein (91%) and pericardial effusion (88%). After a median treatment of 6 months (3–12), pericarditis recurrences were reduced six-fold (2.33–0.39 per patient per year), emergency department admissions were reduced 11-fold (1.08–0.10 per patient per year), hospitalisations were reduced seven-fold (0.99–0.13 per patient per year). Corticosteroid use was decreased by anakinra (respectively from 80% to 27%; P < 0.001). No serious adverse events occurred; adverse events consisted mostly of transient skin reactions (38%) at the injection site. Adverse events led to discontinuation in 3%. A full-dose treatment duration of over 3 months followed by a tapering period of over 3 months were the therapeutic schemes associated with a lower risk of recurrence. Conclusion: In patients with recurrent pericarditis, anakinra appears efficacious and safe in reducing recurrences, emergency department admissions and hospitalisations.
KW - Anakinra
KW - colchicine
KW - interleukin-1 inhibition
KW - interleukin-1 receptor antagonist
KW - recurrent pericarditis
UR - http://www.scopus.com/inward/record.url?scp=85074365752&partnerID=8YFLogxK
U2 - 10.1177/2047487319879534
DO - 10.1177/2047487319879534
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C2 - 31610707
AN - SCOPUS:85074365752
SN - 2047-4873
VL - 27
SP - 956
EP - 964
JO - European Journal of Preventive Cardiology
JF - European Journal of Preventive Cardiology
IS - 9
ER -