Effect of Implantable Cardioverter-defibrillators in Nonischemic Heart Failure According to Background Medical Therapy: Extended Follow-up of the DANISH Trial
•In an extended follow-up study of the DANISH trial, lower dosages of pharmacological therapy (as assessed by the modified Heart Failure Collaboratory medical therapy score) were associated with higher rates of all-cause death, cardiovascular death and sudden cardiovascular death.•ICD implantation d...
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Published in | Journal of cardiac failure Vol. 30; no. 11; pp. 1411 - 1420 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.11.2024
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Online Access | Get full text |
ISSN | 1071-9164 1532-8414 1532-8414 |
DOI | 10.1016/j.cardfail.2024.04.017 |
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Abstract | •In an extended follow-up study of the DANISH trial, lower dosages of pharmacological therapy (as assessed by the modified Heart Failure Collaboratory medical therapy score) were associated with higher rates of all-cause death, cardiovascular death and sudden cardiovascular death.•ICD implantation did not reduce all-cause mortality rates, but it did reduce sudden cardiovascular death in patients with nonischemic HFrEF, regardless of pharmacological therapy at baseline.•Our results underline the potential patient-related effects of underuse of guideline-recommended medical therapies in patients with nonischemic HFrEF.
The Heart Failure Collaboratory (HFC) score integrates types and dosages of guideline-directed pharmacotherapies for heart failure (HF) with reduced ejection fraction (HFrEF). We examined the effects of cardioverter-defibrillator (ICD) implantation according to the modified HFC (mHFC) score in 1116 patients with nonischemic HFrEF from the Danish Study to Assess the Efficacy of ICDs in Patients with Nonischemic Systolic HF on Mortality (DANISH).
Patients were assigned scores for renin-angiotensin-system inhibitors, beta-blockers and mineralocorticoid receptor antagonists (0, no use; 1, < 50% of maximum dosage; 2, ≥ 50% of maximum dosage). The maximum score was 6, corresponding to ≥ 50% of maximum dosage for all therapies. The median baseline mHFC score was 4, and the median follow-up was 9.5 years. Compared with an mHFC score of 3–4, an mHFC score of 1–2 was associated with a higher rate of all-cause death (mHFC = 1–2: adjusted HR 1.67 [95% CI, 1.23–2.28]; mHFC = 3–4, reference; mHFC = 5–6: adjusted HR 1.07 [95% CI, 0.87–1.31]). ICD implantation did not reduce all-cause death compared with control (reference) (HR 0.89 [95% CI, 0.74–1.08]), regardless of mHFC score (mHFC = 1–2: HR 0.98 [95% CI, 0.56–1.71]; mHFC = 3-4: HR 0.89 [95% CI,0.66–1.20]; mHFC = 5–6: HR 0.85 [95% CI, 0.64–1.12]; Pinteraction, 0.65). Similarly, ICD implantation did not reduce cardiovascular death (HR 0.87 [95% CI, 0.70–1.09]), regardless of mHFC score (Pinteraction, 0.59). The ICD group had a lower rate of sudden cardiovascular death (HR, 0.60 [95% CI,0.40–0.92]); this association was not modified by mHFC score (Pinteraction, 0.35).
Lower mHFC scores were associated with higher rates of all-cause death. ICD implantation did not result in an overall survival benefit in patients with nonischemic HFrEF, regardless of mHFC score.
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AbstractList | •In an extended follow-up study of the DANISH trial, lower dosages of pharmacological therapy (as assessed by the modified Heart Failure Collaboratory medical therapy score) were associated with higher rates of all-cause death, cardiovascular death and sudden cardiovascular death.•ICD implantation did not reduce all-cause mortality rates, but it did reduce sudden cardiovascular death in patients with nonischemic HFrEF, regardless of pharmacological therapy at baseline.•Our results underline the potential patient-related effects of underuse of guideline-recommended medical therapies in patients with nonischemic HFrEF.
The Heart Failure Collaboratory (HFC) score integrates types and dosages of guideline-directed pharmacotherapies for heart failure (HF) with reduced ejection fraction (HFrEF). We examined the effects of cardioverter-defibrillator (ICD) implantation according to the modified HFC (mHFC) score in 1116 patients with nonischemic HFrEF from the Danish Study to Assess the Efficacy of ICDs in Patients with Nonischemic Systolic HF on Mortality (DANISH).
Patients were assigned scores for renin-angiotensin-system inhibitors, beta-blockers and mineralocorticoid receptor antagonists (0, no use; 1, < 50% of maximum dosage; 2, ≥ 50% of maximum dosage). The maximum score was 6, corresponding to ≥ 50% of maximum dosage for all therapies. The median baseline mHFC score was 4, and the median follow-up was 9.5 years. Compared with an mHFC score of 3–4, an mHFC score of 1–2 was associated with a higher rate of all-cause death (mHFC = 1–2: adjusted HR 1.67 [95% CI, 1.23–2.28]; mHFC = 3–4, reference; mHFC = 5–6: adjusted HR 1.07 [95% CI, 0.87–1.31]). ICD implantation did not reduce all-cause death compared with control (reference) (HR 0.89 [95% CI, 0.74–1.08]), regardless of mHFC score (mHFC = 1–2: HR 0.98 [95% CI, 0.56–1.71]; mHFC = 3-4: HR 0.89 [95% CI,0.66–1.20]; mHFC = 5–6: HR 0.85 [95% CI, 0.64–1.12]; Pinteraction, 0.65). Similarly, ICD implantation did not reduce cardiovascular death (HR 0.87 [95% CI, 0.70–1.09]), regardless of mHFC score (Pinteraction, 0.59). The ICD group had a lower rate of sudden cardiovascular death (HR, 0.60 [95% CI,0.40–0.92]); this association was not modified by mHFC score (Pinteraction, 0.35).
Lower mHFC scores were associated with higher rates of all-cause death. ICD implantation did not result in an overall survival benefit in patients with nonischemic HFrEF, regardless of mHFC score.
[Display omitted] The Heart Failure Collaboratory (HFC) score integrates types and dosages of guideline-directed pharmacotherapies for heart failure (HF) with reduced ejection fraction (HFrEF). We examined the effects of cardioverter-defibrillator (ICD) implantation according to the modified HFC (mHFC) score in 1116 patients with nonischemic HFrEF from the Danish Study to Assess the Efficacy of ICDs in Patients with Nonischemic Systolic HF on Mortality (DANISH).BACKGROUNDThe Heart Failure Collaboratory (HFC) score integrates types and dosages of guideline-directed pharmacotherapies for heart failure (HF) with reduced ejection fraction (HFrEF). We examined the effects of cardioverter-defibrillator (ICD) implantation according to the modified HFC (mHFC) score in 1116 patients with nonischemic HFrEF from the Danish Study to Assess the Efficacy of ICDs in Patients with Nonischemic Systolic HF on Mortality (DANISH).Patients were assigned scores for renin-angiotensin-system inhibitors, beta-blockers and mineralocorticoid receptor antagonists (0, no use; 1, < 50% of maximum dosage; 2, ≥ 50% of maximum dosage). The maximum score was 6, corresponding to ≥ 50% of maximum dosage for all therapies. The median baseline mHFC score was 4, and the median follow-up was 9.5 years. Compared with an mHFC score of 3-4, an mHFC score of 1-2 was associated with a higher rate of all-cause death (mHFC = 1-2: adjusted HR 1.67 [95% CI, 1.23-2.28]; mHFC = 3-4, reference; mHFC = 5-6: adjusted HR 1.07 [95% CI, 0.87-1.31]). ICD implantation did not reduce all-cause death compared with control (reference) (HR 0.89 [95% CI, 0.74-1.08]), regardless of mHFC score (mHFC = 1-2: HR 0.98 [95% CI, 0.56-1.71]; mHFC = 3-4: HR 0.89 [95% CI,0.66-1.20]; mHFC = 5-6: HR 0.85 [95% CI, 0.64-1.12]; Pinteraction, 0.65). Similarly, ICD implantation did not reduce cardiovascular death (HR 0.87 [95% CI, 0.70-1.09]), regardless of mHFC score (Pinteraction, 0.59). The ICD group had a lower rate of sudden cardiovascular death (HR, 0.60 [95% CI,0.40-0.92]); this association was not modified by mHFC score (Pinteraction, 0.35).METHODS AND RESULTSPatients were assigned scores for renin-angiotensin-system inhibitors, beta-blockers and mineralocorticoid receptor antagonists (0, no use; 1, < 50% of maximum dosage; 2, ≥ 50% of maximum dosage). The maximum score was 6, corresponding to ≥ 50% of maximum dosage for all therapies. The median baseline mHFC score was 4, and the median follow-up was 9.5 years. Compared with an mHFC score of 3-4, an mHFC score of 1-2 was associated with a higher rate of all-cause death (mHFC = 1-2: adjusted HR 1.67 [95% CI, 1.23-2.28]; mHFC = 3-4, reference; mHFC = 5-6: adjusted HR 1.07 [95% CI, 0.87-1.31]). ICD implantation did not reduce all-cause death compared with control (reference) (HR 0.89 [95% CI, 0.74-1.08]), regardless of mHFC score (mHFC = 1-2: HR 0.98 [95% CI, 0.56-1.71]; mHFC = 3-4: HR 0.89 [95% CI,0.66-1.20]; mHFC = 5-6: HR 0.85 [95% CI, 0.64-1.12]; Pinteraction, 0.65). Similarly, ICD implantation did not reduce cardiovascular death (HR 0.87 [95% CI, 0.70-1.09]), regardless of mHFC score (Pinteraction, 0.59). The ICD group had a lower rate of sudden cardiovascular death (HR, 0.60 [95% CI,0.40-0.92]); this association was not modified by mHFC score (Pinteraction, 0.35).Lower mHFC scores were associated with higher rates of all-cause death. ICD implantation did not result in an overall survival benefit in patients with nonischemic HFrEF, regardless of mHFC score.CONCLUSIONSLower mHFC scores were associated with higher rates of all-cause death. ICD implantation did not result in an overall survival benefit in patients with nonischemic HFrEF, regardless of mHFC score. The Heart Failure Collaboratory (HFC) score integrates types and dosages of guideline-directed pharmacotherapies for heart failure (HF) with reduced ejection fraction (HFrEF). We examined the effects of cardioverter-defibrillator (ICD) implantation according to the modified HFC (mHFC) score in 1116 patients with nonischemic HFrEF from the Danish Study to Assess the Efficacy of ICDs in Patients with Nonischemic Systolic HF on Mortality (DANISH). Patients were assigned scores for renin-angiotensin-system inhibitors, beta-blockers and mineralocorticoid receptor antagonists (0, no use; 1, < 50% of maximum dosage; 2, ≥ 50% of maximum dosage). The maximum score was 6, corresponding to ≥ 50% of maximum dosage for all therapies. The median baseline mHFC score was 4, and the median follow-up was 9.5 years. Compared with an mHFC score of 3-4, an mHFC score of 1-2 was associated with a higher rate of all-cause death (mHFC = 1-2: adjusted HR 1.67 [95% CI, 1.23-2.28]; mHFC = 3-4, reference; mHFC = 5-6: adjusted HR 1.07 [95% CI, 0.87-1.31]). ICD implantation did not reduce all-cause death compared with control (reference) (HR 0.89 [95% CI, 0.74-1.08]), regardless of mHFC score (mHFC = 1-2: HR 0.98 [95% CI, 0.56-1.71]; mHFC = 3-4: HR 0.89 [95% CI,0.66-1.20]; mHFC = 5-6: HR 0.85 [95% CI, 0.64-1.12]; P , 0.65). Similarly, ICD implantation did not reduce cardiovascular death (HR 0.87 [95% CI, 0.70-1.09]), regardless of mHFC score (P , 0.59). The ICD group had a lower rate of sudden cardiovascular death (HR, 0.60 [95% CI,0.40-0.92]); this association was not modified by mHFC score (P , 0.35). Lower mHFC scores were associated with higher rates of all-cause death. ICD implantation did not result in an overall survival benefit in patients with nonischemic HFrEF, regardless of mHFC score. |
Author | BRUUN, NIELS E. EISKJÆR, HANS PEHRSON, STEEN KØBER, LARS SVENDSEN, JESPER H. HAARBO, JENS THUNE, JENS JAKOB BUTT, JAWAD H. NIELSEN, JENS C. YAFASOVA, ADELINA HASSAGER, CHRISTIAN HØFSTEN, DAN E. DOI, SEIKO N. TORP-PEDERSEN, CHRISTIAN GUSTAFSSON, FINN |
Author_xml | – sequence: 1 givenname: ADELINA orcidid: 0000-0003-3889-0080 surname: YAFASOVA fullname: YAFASOVA, ADELINA email: adelinay@hotmail.com organization: Department of Cardiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark – sequence: 2 givenname: SEIKO N. surname: DOI fullname: DOI, SEIKO N. organization: Department of Cardiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark – sequence: 3 givenname: JENS JAKOB surname: THUNE fullname: THUNE, JENS JAKOB organization: Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark – sequence: 4 givenname: JENS C. surname: NIELSEN fullname: NIELSEN, JENS C. organization: Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark – sequence: 5 givenname: JENS surname: HAARBO fullname: HAARBO, JENS organization: Department of Cardiology, Copenhagen University Hospital, Herlev and Gentofte, Herlev, Denmark – sequence: 6 givenname: NIELS E. surname: BRUUN fullname: BRUUN, NIELS E. organization: Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark – sequence: 7 givenname: FINN surname: GUSTAFSSON fullname: GUSTAFSSON, FINN organization: Department of Cardiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark – sequence: 8 givenname: HANS surname: EISKJÆR fullname: EISKJÆR, HANS organization: Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark – sequence: 9 givenname: CHRISTIAN surname: HASSAGER fullname: HASSAGER, CHRISTIAN organization: Department of Cardiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark – sequence: 10 givenname: JESPER H. surname: SVENDSEN fullname: SVENDSEN, JESPER H. organization: Department of Cardiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark – sequence: 11 givenname: DAN E. surname: HØFSTEN fullname: HØFSTEN, DAN E. organization: Department of Cardiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark – sequence: 12 givenname: CHRISTIAN surname: TORP-PEDERSEN fullname: TORP-PEDERSEN, CHRISTIAN organization: Department of Cardiology, Copenhagen University Hospital, North Zealand, Hilleroed, Denmark – sequence: 13 givenname: STEEN surname: PEHRSON fullname: PEHRSON, STEEN organization: Department of Cardiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark – sequence: 14 givenname: LARS surname: KØBER fullname: KØBER, LARS organization: Department of Cardiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark – sequence: 15 givenname: JAWAD H. surname: BUTT fullname: BUTT, JAWAD H. organization: Department of Cardiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38750689$$D View this record in MEDLINE/PubMed |
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Keywords | HFC DAPA-HF pharmacotherapy mHFC nonischemic heart failure Implantable cardioverter-defibrillator DANISH |
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SubjectTerms | Adrenergic beta-Antagonists - therapeutic use Aged Angiotensin-Converting Enzyme Inhibitors - therapeutic use DANISH Defibrillators, Implantable Denmark - epidemiology Female Follow-Up Studies Heart Failure - drug therapy Heart Failure - mortality Heart Failure - therapy Humans Implantable cardioverter-defibrillator Male Middle Aged Mineralocorticoid Receptor Antagonists - therapeutic use nonischemic heart failure pharmacotherapy Stroke Volume - physiology Treatment Outcome |
Title | Effect of Implantable Cardioverter-defibrillators in Nonischemic Heart Failure According to Background Medical Therapy: Extended Follow-up of the DANISH Trial |
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