Российский кардиологический журнал (Dec 2017)
PREDICTIVE VALUE OF ERYTHROCYTE ANISOTROPY COEFFICIENT IN PATIENTS HOSPITALIZED FOR ACUTELY DECOMPENSATED CHRONIC HEART FAILURE
Abstract
Aim. To evaluate the role of erythrocyte anisotropy (RDW) coefficient as a predictor of adverse outcome in acutely decompensated chronic heart failure (ADCHF).Material and methods. Totally, 422 patients, age 37-82 y. o. (mean 66,8±2,3 y. o.) investigated, who had been hospitalized for ADCHF of ischemic origin with decreased ejection fraction (EFLV). All participants underwent routine tests, including the coefficient of erythrocyte anisotropy variation (RDW-CV, RDW-SD), C-reactive peptide (CRP) and brain natriuretic peptide (BNP). Instrumental methods included echocardiography in Mand B-regimens with EFLV measurement. Follow-up in 24 months was done via phone calls with the patient or relatives, and original questionnaire.Results. At admittance, mean values of RDW-CV were 16,3±2,9%, at discharge — 16,7±3,3%; RDW-SD — 48,7±7,3 fL and 53,6±8,7 fL, respectively. T-test for the relation of these two parameters with fatal outcome showed that only RDW-SD is significantly (p=0,045) relevant, for the period 24 months post discharge. Main group was separated to two subgroups — А (RDW-SD <46,5 fL (n=173)), and B (RDW-SD ≥46,5 fL (n=249)). In aspect of the adverse outcome, group comparison with T-criteria by Student was 6,9 (p=0,0001). There was direct correlation of average strength between hemoglobin contents (r=0,53, р<0,05), creatinine (r=0,55, р<0,05) and С-reactive protein (CRP) (r=0,35; р>0,05), negative correlation for EFLV (r=-0,54, p<0,05) with RDW-SD.Conclusion. In ADCHF patients the RDW-SD parameter seems to be more significant than RDW-CV in relevance to prediction, and its values correlate with CRP, hemoglobin, creatinine, as negatively also correlate with EFLV. The RDW-SD value higher than 46,5 fL, regardless the other factors, significantly predicts the increase of patients mortality after ADCHF.Russ J Cardiol 2017, 12 (152): 26–30 http://dx.doi.org/10.15829/1560-4071-2017-12-26-30
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