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. 2019 Oct 7;59(3):339–343. doi: 10.2169/internalmedicine.3675-19

Table 2.

The Clinical Status in Eight Consecutive Transthyretin Amyloid Cardiomyopathy Patients at the Time of Pimobendan Administration and Their Clinical Course (Present Case Is Patient 1).

No Diagnosis Age NYHA class Clinical status Pimobendan dose EF (%) BNP (pg/mL) eGFR (mL/
min/1.73 m2)
Clinical course
1 ATTRwt 71 4 In hospital and dobutamine dependent, 3 times HF hospitalization 2.5 mg 43 479.2 49.0 Free hospitalization and alive for 4 months
2 ATTRwt 78 3 In hospital, 10 times HF hospitalization 2.5 mg 35 630.5 30.1 3 times HF hospoitalization and HF death after 8 months
3 ATTRwt 76 3 Outpatient clinic, 3 times HF hospitalization 1.25 mg 35 220.9 23.1 3 times HF hospoitalization and alive for 2 years
4 ATTRwt 78 4 In hospital, 3 times HF hospitalization 1.25 mg 50 1,450.8 23.6 Discharged and HF death after 2 months
5 ATTRwt 78 4 In hospital, 3 times HF hospitalization 2.5 mg 34 NA NA 2 times HF hospoitalization and HF death after 8 months
6 ATTRwt 85 4 In hospital and dobutamine dependent, 5 times HF hospitalization 1.25 mg 33 NA NA Temporary going home for 1 day and HF death after 1 week
7 *ATTR 84 3 Outpatient clinic, 2 times HF hospitalization 1.25 mg 38 NA NA Free hospitalization and alive for 4 months
8 ATTRv 66 3 Outpatient clinic, 3 times HF hospitalization 1.25 mg 32 573.2 25.2 Free hospitalization and alive for 1 year

*ATTR: no genetic testing.

ATTRwt: wild-type transthyretin amyloid cardiomyopathy, ATTRv: variant (familial) transthyretin amyloid cardiomyopathy, NYHA class: New York Heart Association class, HF: heart failure, EF: ejection fraction, BNP: brain natiriuretic peptide, eGFR: estimated glomerular filtration rate, NA: not available