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DOI 10.1007/s00392-022-02114-y

Медицинская библиотека · Clinical research in cardiology : official journal of the German Cardiac Society · 2022

Epidemiology of cardiac amyloidosis in Germany: a retrospective analysis from 2009 to 2018.

Ney Svenja, Ihle Peter, Ruhnke Thomas, Günster Christian, Michels Guido, Seuthe Katharina, Hellmich Martin, Pfister Roman

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Аннотация

BACKGROUND

Improved imaging modalities contributed to increasing awareness of cardiac amyloidosis. Contemporary data on frequency trends in Germany are lacking.

METHODS

In a retrospective study using health claims data of a German statutory health insurance, patients with diagnostic codes of amyloidosis and concomitant heart failure between 2009 and 2018 were identified.

RESULTS

Prevalence increased from 15.5 to 47.6 per 100,000 person-years, and incidence increased from 4.8 to 11.6 per 100,000 person-years, with a continuous steepening in the slope of incidence trend. In patients with amyloidosis and heart failure age and proportion of men significantly increased, whereas the frequency of myeloma and nephrotic syndrome significantly decreased over time. Median (IQR) survival time after first diagnosis was 2.5 years (0.5-6 years), with a 9% (95% CI 2-15%, p = 0.008) reduced risk of death in the second compared to the first 5 years of observation. In the 2 years prior and 1 year after diagnosis, mean total health care costs were 6568 €, 11,872 € and 21,955 € per person and year.

CONCLUSION

The rise in cardiac amyloidosis has continuously accelerated in the last decade. Considering the adverse outcome and high health care burden, further effort should be put on early detection of the disease to implement available treatment.

Для цитирования: Ney Svenja, Ihle Peter, Ruhnke Thomas, Günster Christian, Michels Guido, Seuthe Katharina, Hellmich Martin, Pfister Roman. Epidemiology of cardiac amyloidosis in Germany: a retrospective analysis from 2009 to 2018.. Clinical research in cardiology : official journal of the German Cardiac Society. 2022. DOI: 10.1007/s00392-022-02114-y.

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