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Systemic immune-inflammation index: A novel marker for predicting response to cardiac resynchronization therapy in patients with heart failure

dc.contributor.authorKarakus, Alper
dc.contributor.authorTopal, Dursun
dc.contributor.authorZengin, İsmet
dc.contributor.authorUguz, Berat
dc.contributor.authorÖztaş, Selvi
dc.contributor.authorTiryakioglu, Selma Kenar
dc.contributor.authorGünay, Tufan
dc.date.accessioned2026-10-09T21:17:22Z
dc.date.issued2022
dc.departmentYüksek İhtisas Üniversitesi
dc.description.abstractAim: To investigate the utility of systemic immune-inflammation index (SII) in predicting response to cardiac resynchronization therapy (CRT) among patients with heart failure (HF). Method: A total of 78 patients with HF who underwent CRT device implantation were included in this 6-month follow up study. Data on laboratory findings including complete blood count, blood biochemistry and SII as well as the transthoracic echocardiography findings were recorded at baseline prior to CRT device implantation and 6 months after CRT. Results: The criteria for response to CRT including improvements in New York Heart Association (NYHA), left ventricular end-systolic volume (LVESV) (decreased by ?15%) and ejection fraction (EF)(increased by?10%) were met by 73.1%, 65.4% and 69.2% of patients, respectively. In patients with decreased vs. increased SII values during 6-month therapy, the likelihood of meeting LVESV (84.3 vs. 15.7%, p<0.001), EF (81.5 vs. 18.5%, p<0.001) and NYHA (77.2 vs. 22.8%, p<0.001) response criteria for successful CRT were significantly higher. Multivariate analysis revealed that decrease in SII (OR 0.982, 95% CI: 0.970 to 0.995, p=0.006) and TAPSE (OR 0.602, 95% CI. 0.396 to 0.916, p=0.018) during treatment as the only significant determinants of presence of response to CRT in heart failure (HF) patients. Conclusions: Our findings seem to indicate the favorable utility of SII, as a non-invasive readily available marker, in predicting response to CRT and thus enabling a beneficial reverse remodeling process via timely implementation of advanced treatments in HF patients.
dc.identifier.doi10.30714/j-ebr.2022.157
dc.identifier.endpage391
dc.identifier.issn2618-6454
dc.identifier.issue4
dc.identifier.startpage377
dc.identifier.trdizinid1134122
dc.identifier.urihttps://doi.org/10.30714/j-ebr.2022.157
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/1134122
dc.identifier.urihttps://hdl.handle.net/20.500.12794/927
dc.identifier.volume5
dc.indekslendigikaynakTR-Dizin
dc.language.isoen
dc.relation.ispartofExperimental Biomedical Research
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_TR-Dizin_20260922
dc.subjectTıbbi İnformatik
dc.subjectPatoloji
dc.subjectTemel Sağlık Hizmetleri
dc.subjectKalp ve Kalp Damar Sistemi
dc.titleSystemic immune-inflammation index: A novel marker for predicting response to cardiac resynchronization therapy in patients with heart failure
dc.typeArticle

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