Inflammatory Cardiomyopathy: A Current View on the Pathophysiology, Diagnosis, and Treatment
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, přehledy
PubMed
27382566
PubMed Central
PMC4921131
DOI
10.1155/2016/4087632
Knihovny.cz E-zdroje
- MeSH
- antibakteriální látky terapeutické užití MeSH
- antiflogistika terapeutické užití MeSH
- biopsie metody MeSH
- kardiomyopatie diagnóza terapie MeSH
- lidé MeSH
- medicína založená na důkazech MeSH
- myokarditida diagnóza terapie MeSH
- srdeční resynchronizační terapie metody MeSH
- výsledek terapie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- antibakteriální látky MeSH
- antiflogistika MeSH
Inflammatory cardiomyopathy is defined as inflammation of the heart muscle associated with impaired function of the myocardium. In our region, its etiology is most often viral. Viral infection is a possible trigger of immune and autoimmune mechanisms which contributed to the damage of myocardial function. Myocarditis is considered the most common cause of dilated cardiomyopathy. Typical manifestation of this disease is heart failure, chest pain, or arrhythmias. The most important noninvasive diagnostic method is magnetic resonance imaging, but the gold standard of diagnostics is invasive examination, endomyocardial biopsy. In a significant proportion of cases with impaired left ventricular systolic function, recovery occurs spontaneously in several weeks and therefore it is appropriate to postpone critical therapeutic decisions about 3-6 months after start of the treatment. Therapy is based on standard heart failure treatment; immunosuppressive or antimicrobial treatment may be considered in some cases depending on the results of endomyocardial biopsy. If severe dysfunction of the left ventricle persists, device therapy may be needed.
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Elevated Sera sST2 Is Associated With Heart Failure in Men ≤50 Years Old With Myocarditis