scholarly journals P1301CLINICAL OUTCOMES OF ORAL ANTICOAGULATION AND NO ANTICOAGULATION AMONG END-STAGE RENAL DISEASE PATIENTS ON MAINTENANCE HEMODIALYSIS WITH ATRIAL FIBRILLATION: A SINGLE-CENTER PROSPECTIVE COHORT STUDY

2020 ◽  
Vol 35 (Supplement_3) ◽  
Author(s):  
Eratosthenes Polito ◽  
Grecia Darunday

Abstract Background and Aims Progress has been made over the past six decades in the world of hemodialysis, however it still remained as an ongoing challenge for clinicians since it is coupled with an increasing incidence of dysrhythmia that brings a high cardiac mortality in the first year. Many of these patients will have a risk profile lending to oral anticoagulation with warfarin as the traditionally mainstay of therapy for this indication or a non-vitamin K oral anticoagulants (NOACs) in some because of ease of administration and comparable efficacy. There may be convincing as well as contrasting arguments regarding its use, but without well-conducted clinical trials, it is definitely impossible to consider the indication of oral anticoagulation therapy in this special group of population. This study aims to determine the difference in clinical outcomes between oral anticoagulation and no anticoagulation therapy among End-Stage Renal Disease patients on maintenance hemodialysis with atrial fibrillation in Perpetual Succour Hospital, and to provide local data on the prevalence and frequency of oral anticoagulation and no anticoagulation therapy in this group of patients. Method This is a single-center, prospective, observational cohort study conducted in a tertiary hospital in Cebu City, Cebu. All diagnosed End-Stage Renal Disease patients with chronic atrial fibrillation on maintenance hemodialysis for at least 3 months. Results A total of 188 ESRD patients on maintenance hemodialysis at The Kidney Service-Perpetual Succour Hospital were identified from May 1, 2017 through October 31, 2018, of which 74 (39.4%) subjects had a documented coexisting chronic atrial fibrillation at the time of recruitment but only 69 individuals were included in the analysis. At enrollment, 59 (85.5%) patients were identified to have no oral anticoagulation therapy and 10 (14.5%) were already receiving oral anticoagulation. Ischemic strokes was more prevalent (80%, p=<0.0001) among patients who were on oral anticoagulant. Likewise, patient differ significantly in terms of intracranial hemorrhage (30%, p= 0.0004) and gastrointestinal bleeding (50%, p= <0.00001) were noted among patients receiving oral anticoagulation therapy. In relation to over-all mortality, acute myocardial infarction, peripheral arterial occlusive disease and caciphylaxis, there was no sufficient evidence to show significant difference between two groups. Conclusion This study suggests that the use of oral anticoagulation did not prevent ischemic strokes in ESRD patients on maintenance hemodialysis with chronic atrial fibrillation. Further, it was associated with increased risk for intracranial hemorrhage and gastrointestinal bleeding. Lastly, there was no significant difference in relation to all-cause mortality, acute myocardial infarction, peripheral arterial occlusive disease and calciphylaxis between the two study groups.

2020 ◽  
Vol 75 (11) ◽  
pp. 1299-1308 ◽  
Author(s):  
Sean D. Pokorney ◽  
Eric Black-Maier ◽  
Anne S. Hellkamp ◽  
Daniel J. Friedman ◽  
Sreekanth Vemulapalli ◽  
...  

2020 ◽  
Vol 35 (Supplement_3) ◽  
Author(s):  
Sonja Golubović ◽  
Tijana Azasevac ◽  
Siniša Živković ◽  
Bojana Ljubiäiä‡ ◽  
Violeta Knezevic ◽  
...  

Abstract Background and Aims Neutrophil/Lymphocyte Ratio (NLR) and Platelet/Lymphocyte Ratio (PLR) are closely associated with increased inflammation in end-stage renal disease, which often contributes to the severity of anemia in these patients. Erythropoiesis stimulating agents (ESA) have become a standard treatment of anemia in hemodialysis patients. Since some patients do not respond well to erythropoietin therapy (EPO) the aim of this study is to investigate if NLR and PLR as markers of increased inflammation, could be associated with resistance to EPO therapy. Method A total of 90 patients (36 females, 54 males; mean age 60,45 ±11,58) undergoing maintenance hemodialysis and who received recombinant human EPO therapy were examined. Patients' clinical characteristics, laboratory data, dialysis adequacy and the applied doses os EPO were examined in a period of 3 months. EPO hyporesponsiveness index (EHRI) was calculated as the weekly dose of EPO divided by kilograms of body weight divided by the hemoglobin level. Results Obtained results show a statistically significant correlation of moderate-intensity between EHRI and NLR ( r = 0.497, p < 0.01) as well as a negative correlation of moderate-intensity between EHRI and hemoglobin levels (Hgb) (r = -0.403, p < 0.01). When it comes to the connection of NLR and PLR with logarithmically converted EHRI values, the results show that there is no statistically significant correlation between NLR and EHRI. Comparison of PLR among 25th, 50th and 75th percentile of EHRI showed that PLR levels increased going from the 25th towards the 75th percentile (p < 0.01). Post hoc analysis indicated that there is also a statistically strong connection for the 25th i 50th percentile (<0 .05) and furthermore for the 50th and 75th percentile (< 0.05). Conclusion PLR was found to be superior to NLR in terms of evaluating ESA therapy resistance. PLR could be used as a predictor of ESA therapy response.


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