Skip to main content
. Author manuscript; available in PMC: 2023 Oct 1.
Published in final edited form as: J Card Fail. 2022 Jul 25;28(10):1500–1508. doi: 10.1016/j.cardfail.2022.07.047

Table 2.

Use of Guideline-Directed Medical Therapy in the First Year After HFrEF Diagnosis

Medication Group Overall (n=1160) Seen in HF Clinic in 1st Year P value
No (n=780) Yes (n=380)
Beta blocker
 Prior to HFrEF 345 (29.7%) 236 (30.3%) 109 (28.7%) <0.001
 Not eligible 148 (12.8%) 106 (13.6%) 42 (11.1%)
 Initiated in first year 592 (51.0%) 370 (47.4%) 222 (58.4%)
 Eligible, did not receive in first year 75 (6.5%) 68 (8.7%) 7 (1.8%)
HF beta blocker
 Prior to HFrEF 133 (11.5%) 84 (10.8%) 49 (12.9%) <0.001
 Not eligible 178 (15.3%) 130 (16.7%) 48 (12.6%)
 Initiated in first year 494 (42.6%) 268 (34.4%) 226 (59.5%)
 Eligible, did not receive in first year 355 (30.6%) 298 (38.2%) 57 (15.0%)
ACEi/ARB/ARNI
 Prior to HFrEF 342 (29.5%) 232 (29.7%) 110 (29.0%) <0.001
 Not eligible 142 (12.2%) 102 (13.1%) 40 (10.5%)
 Initiated in first year* 544 (46.9%) 328 (42.1%) 216 (56.8%)
 Eligible, did not receive in first year 132 (11.4%) 118 (15.1%) 14 (3.7%)
MRA
 Prior to HFrEF 24 (2.1%) 14 (1.8%) 10 (2.6%) <0.001
 Not eligible 135 (11.6%) 95 (12.2%) 40 (10.5%)
 Initiated in first year 156 (13.5%) 68 (8.7%) 88 (23.2%)
 Eligible, did not receive in first year 845 (72.8%) 603 (77.3%) 242 (63.7%)

ACEi= angiotensin converting enzyme inhibitor; ARB= angiotensin receptor blocker; ARNI= angiotensin receptor neprilysin inhibitor; MRA= mineralocorticoid receptor antagonist

*

A total of 13 patients diagnosed with HFrEF after July 2015 (sacubitril valsartan FDA approval date) were initiated on ARNI in the first year