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Effectiveness of myocarditis therapy depending on the diagnosis approach (with or without myocardial biopsy)

https://doi.org/10.15829/1728-8800-2021-2637

Abstract

Aim. To evaluate the effectiveness of myocarditis therapy depending on the diagnosis approach (with or without myocardial biopsy).

Material and methods. The study included 83 patients ≥18 years old with severe and moderate myocarditis (25 women and 58 men; mean age, 45,7±11,7 years), established by myocardial biopsy (group 1, n=36) or by a non-invasive diagnostic algorithm (group 2, n=47), for which immunosuppressive therapy (IST) was carried out. Inclusion criteria were left ventricular (LV) end-diastolic dimension >5,5 cm and ejection fraction (EF) <50%. An endomyocardial (n=31) or intraoperative (n=5) biopsy with a study of the viral genome and level of anticardiac antibodies were performed. Coronary angiography (29%), cardiac multislice computed tomography (75%), cardiac magnetic resonance imaging (41%), and 99mTc-MIBI scintigraphy (35%) were also carried out. The mean follow-up period was 3 years (36 [12; 65] months). The study was approved by the Intercollegiate Ethics Committee.

Results. The groups were completely comparable in age, baseline parameters (class III [2,25; 3] and III [2; 3] heart failure (HF); end-diastolic LV dimension, 6,7±0,7 and 6,4±0,7 cm; EF, 29,9±8,7 and 31,4±9,3%), the extent of cardiac therapy (excluding the administration rate of в-blockers — 94,4 and 78,7%, p<0,05) and 1ST (methylprednisolone in 91,7 and 89,4% of patients at a mean dose of 24 [16; 32] and 20 [15; 32] mg/day, azathioprine in 50,0 and 46,8% of patients at a mean dose of 150 mg/day or mycophenolate mofetil 2,0 g/day in 30,6% in group 1, hydroxychloroquine 0,2 g/day in 27,8 and 23,4%). Biopsy in group 1 revealed active/borderline (61/39%) myocarditis, in 8 patients — viral genome in the myocardium, including parvovirus B19 in 7 of them. Both groups showed a comparable significant increase in EF after 6 months up to 37,6±8,1 and 42,6±11,5% (p<0,001) and after 27 [12; 54] months up to 43,4±9,6 and 45,5±12,3% (p<0,001), as well as a significant decrease in HF class to 2 [1; 2] in both groups. An increase in EF by ≥10% was recorded in 70 and 72% of patients, respectively. The mortality rate was 13,9 and 12,8%. Taking into account the only transplantation in group 2, the death+transplantation endpoints reached 13,9 and 14,9% of patients (without significant differences between the groups).

Conclusion. In patients with severe and moderate myocarditis diagnosed with and without myocardial biopsy, the effectiveness of combined therapy, including IST, was comparable. If it is impossible to perform a biopsy, complex non-invasive strategy makes it possible to diagnose myocarditis with different probability rate and conduct an effective IST, the refusal of which mostly is not justified.

About the Authors

O. V. Blagova
I.M. Sechenov First Moscow State Medical University
Russian Federation

Moscow.



A. V. Nedostup
I.M. Sechenov First Moscow State Medical University
Russian Federation

Moscow.



V. P. Sedov
I.M. Sechenov First Moscow State Medical University
Russian Federation

Moscow.



A. Yu. Zaitsev
I.M. Sechenov First Moscow State Medical University
Russian Federation

Moscow.



V. M. Novosadov
I.M. Sechenov First Moscow State Medical University
Russian Federation

Moscow.



E. A. Kogan
I.M. Sechenov First Moscow State Medical University
Russian Federation

Moscow.



References

1. Caforio AL, Pankuweit S, Arbustini E et al.; European Society of Cardiology Working Group on Myocardial and Pericardial Diseases. Current state of knowledge on aetiology, diagnosis, management, and therapy of myocarditis: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases. Eur Heart J. 2013; 34(33):2636-48, 2648a-2648d. doi:10.1093/eurheartj/eht210.

2. Bozkurt B, Colvin M, Cook J et al. Current Diagnostic and Treatment Strategies for Specific Dilated Cardiomyopathies: A Scientific Statement From the American Heart Association. Circulation. 2016;134(23):e579-e646. doi:10.1161/CIR.0000000000000455.

3. Blagova OV, Osipova YV, Nedostup AV, et al. Clinical, laboratory and instrumental criteria for myocarditis, established in comparison with myocardial biopsy: A non-invasive diagnostic algorithm. Ter Arkh. 2017;89(9):30-40. (In Russ)

4. Blagova O, Osipova Y, Nedostup A, et al. Diagnostic Value of Different Noninvasive Criteria of Latent Myocarditis in Comparison with Myocardial Biopsy. Cardiology. 2019;142(3):167-74. doi:10.1159/000499865.

5. Blagova OV, Nedostup AV, Kogan EA. Myocardial and pericardial diseases: from syndromes to diagnosis and treatment. M., “GEOTAR-Media”, 2019/ p. 884. (In Russ)

6. Frustaci A, Russo MA, Chimenti C. Randomized study on the efficacy of immunosuppressive therapy in patients with virusnegative inflammatory cardiomyopathy: the TIMIC study. Eur Heart J. 2009;30(16):1995-2002. doi:10.1093/eurheartj/ehp249.

7. Escher F, Kuhl U, Lassner D, et al. Long-term outcome of patients with virus-negative chronic myocarditis or inflammatory cardiomyopathy after immunosuppressive therapy. Clin Res Cardiol. 2016; 105(12):1011-20. doi:10.1007/s00392-016-1011-z.

8. Merken J, Hazebroek M, Van Paassen P, et al. Immunosuppressive Therapy Improves Both Short- and Long-Term Prognosis in Patients With Virus-Negative Nonfulminant Inflammatory Cardiomyopathy. Circ Heart Fail. 2018;11(2):e004228. doi:10.1161/CIRCHEARTFAILURE.117.004228.

9. Frustaci A, Chimenti C, Calabrese F, et al. Immunosuppressive therapy for active lymphocytic myocarditis: virological and immunologic profile of responders versus nonresponders. Circulation. 2003;107(6):857-63. doi:10.1161/01.cir.0000048147.15962.31.

10. Mlejnek D, Krejci J, Hude P, et al. Viral genome changes and the impact of viral genome persistence in myocardium of patients with inflammatory cardiomyopathy. Arch Med Sci. 2018;14(6):1245-53. doi:10.5114/aoms.2018.79002.

11. Tschope C, Elsanhoury A, Schlieker S, et al. Immunosuppression in inflammatory cardiomyopathy and parvovirus B19 persistence. Eur J Heart Fail. 2019;21(11):1468-9. doi:10.1002/ejhf.1560.

12. Kuhl U, Pauschinger M, Noutsias M, et al. High prevalence of viral genomes and multiple viral infections in the myocardium of adults with “idiopathic” left ventricular dysfunction. Circulation. 2005;111(7):887-93. doi:10.1161/01.CIR.0000155616.07901.35.

13. Verdonschot J, Hazebroek M, Merken J, et al. Relevance of cardiac parvovirus B19 in myocarditis and dilated cardiomyopathy: review of the literature. Eur J Heart Fail. 2016;18(12):1430-41. doi:10.1002/ejhf.665.


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For citations:


Blagova O.V., Nedostup A.V., Sedov V.P., Zaitsev A.Yu., Novosadov V.M., Kogan E.A. Effectiveness of myocarditis therapy depending on the diagnosis approach (with or without myocardial biopsy). Cardiovascular Therapy and Prevention. 2021;20(3):2637. (In Russ.) https://doi.org/10.15829/1728-8800-2021-2637

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ISSN 1728-8800 (Print)
ISSN 2619-0125 (Online)