Medical Therapy and Clinical Outcomes in Cardiac Sarcoidosis Patients With Systolic Heart Failure.

Cardiac sarcoidosis Guideline-directed medical therapy Heart failure Immunosuppression

Journal

Circulation journal : official journal of the Japanese Circulation Society
ISSN: 1347-4820
Titre abrégé: Circ J
Pays: Japan
ID NLM: 101137683

Informations de publication

Date de publication:
03 Sep 2024
Historique:
medline: 5 9 2024
pubmed: 5 9 2024
entrez: 4 9 2024
Statut: aheadofprint

Résumé

Cardiac sarcoidosis (CS) may result in systolic heart failure (heart failure with reduced ejection fraction [HFrEF]), but its response to guideline-directed medical therapy (GDMT) remains uncertain. We investigated 881 patients evaluated for CS to identify those with diagnosed CS, left ventricular ejection fraction (LVEF) ≤40% at diagnosis, and follow-up echocardiogram within 11-24 months. Demographics, LVEF, GDMT as quantified by Kansas City Medical Optimization (KCMO) score, and immunosuppressive treatment were recorded. The primary outcome was a composite of event-free survival (unplanned heart failure hospitalization, left ventricular assist device [LVAD]/heart transplant, or death). Seventy-nine (9%) CS patients met the inclusion criteria (35% female, median age 57 years, mean LVEF 30.9%, median New York Heart Association class II [46%], mean number of GDMT agents 1.7, and mean KCMO score 31.8). Most (87%) were treated with immunosuppressive treatment. At follow-up (median 16 months), the mean number of GDMT agents increased to 2.2 (P=0.02), and the mean KCMO score to 70.1 (P<0.001). Mean LVEF improved to 39.9% (excluding LVAD/transplant; P<0.001) and the change in LVEF was correlated with follow-up KCMO score (P<0.001). The primary outcome occurred in 13 (16%) patients and differed by KCMO score (log-rank P<0.001), but not by immunosuppressive treatment (log-rank P=0.36). GDMT optimization is associated with better cardiac remodeling and clinical outcomes in CS patients with HFrEF.

Sections du résumé

BACKGROUND BACKGROUND
Cardiac sarcoidosis (CS) may result in systolic heart failure (heart failure with reduced ejection fraction [HFrEF]), but its response to guideline-directed medical therapy (GDMT) remains uncertain.
METHODS AND RESULTS RESULTS
We investigated 881 patients evaluated for CS to identify those with diagnosed CS, left ventricular ejection fraction (LVEF) ≤40% at diagnosis, and follow-up echocardiogram within 11-24 months. Demographics, LVEF, GDMT as quantified by Kansas City Medical Optimization (KCMO) score, and immunosuppressive treatment were recorded. The primary outcome was a composite of event-free survival (unplanned heart failure hospitalization, left ventricular assist device [LVAD]/heart transplant, or death). Seventy-nine (9%) CS patients met the inclusion criteria (35% female, median age 57 years, mean LVEF 30.9%, median New York Heart Association class II [46%], mean number of GDMT agents 1.7, and mean KCMO score 31.8). Most (87%) were treated with immunosuppressive treatment. At follow-up (median 16 months), the mean number of GDMT agents increased to 2.2 (P=0.02), and the mean KCMO score to 70.1 (P<0.001). Mean LVEF improved to 39.9% (excluding LVAD/transplant; P<0.001) and the change in LVEF was correlated with follow-up KCMO score (P<0.001). The primary outcome occurred in 13 (16%) patients and differed by KCMO score (log-rank P<0.001), but not by immunosuppressive treatment (log-rank P=0.36).
CONCLUSIONS CONCLUSIONS
GDMT optimization is associated with better cardiac remodeling and clinical outcomes in CS patients with HFrEF.

Identifiants

pubmed: 39231722
doi: 10.1253/circj.CJ-24-0205
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Daniel Sykora (D)

Mayo Clinic School of Graduate Medical Education.

Melanie Bratcher (M)

Department of Cardiovascular Diseases, Mayo Clinic Rochester.

Robert Churchill (R)

Mayo Clinic Alix School of Medicine.

B Michelle Kim (BM)

Mayo Clinic Alix School of Medicine.

Mohamed Elwazir (M)

Department of Cardiovascular Diseases, Mayo Clinic Rochester.

Kathleen Young (K)

Department of Cardiovascular Diseases, Mayo Clinic Rochester.

Sami Ryan (S)

Department of Cardiovascular Diseases, Mayo Clinic Rochester.

Nikhil Kolluri (N)

Department of Cardiovascular Diseases, Mayo Clinic Rochester.

Omar Abou Ezzeddine (O)

Department of Cardiovascular Diseases, Mayo Clinic Rochester.

John Bois (J)

Department of Cardiovascular Diseases, Mayo Clinic Rochester.
Department of Diagnostic Radiology, Mayo Clinic Rochester.

John Giudicessi (J)

Department of Cardiovascular Diseases, Mayo Clinic Rochester.

Leslie Cooper (L)

Department of Cardiovascular Diseases, Mayo Clinic Florida.

Andrew Rosenbaum (A)

Department of Cardiovascular Diseases, Mayo Clinic Rochester.

Classifications MeSH