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Hemostatic Abnormalities in Severe Renal Failure: Do They Bark or Bite?

Abnormal primary hemostasis is believed to be the most significant contributor to uremic bleeding. This study aimed to describe the prevalence and profile of primary and secondary hemostatic disorders in patients with chronic kidney disease (CKD) Stages 4 and 5 and to determine their association if...

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Autores principales: Mohapatra, A., Valson, A. T., Gopal, B., Singh, S., Nair, S. C., Viswabandya, A., Varughese, S., Tamilarasi, V., John, G. T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952452/
https://www.ncbi.nlm.nih.gov/pubmed/29861564
http://dx.doi.org/10.4103/ijn.IJN_104_17
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author Mohapatra, A.
Valson, A. T.
Gopal, B.
Singh, S.
Nair, S. C.
Viswabandya, A.
Varughese, S.
Tamilarasi, V.
John, G. T.
author_facet Mohapatra, A.
Valson, A. T.
Gopal, B.
Singh, S.
Nair, S. C.
Viswabandya, A.
Varughese, S.
Tamilarasi, V.
John, G. T.
author_sort Mohapatra, A.
collection PubMed
description Abnormal primary hemostasis is believed to be the most significant contributor to uremic bleeding. This study aimed to describe the prevalence and profile of primary and secondary hemostatic disorders in patients with chronic kidney disease (CKD) Stages 4 and 5 and to determine their association if any, with degree of uremia. Stages 4 and 5 predialysis CKD patients attending nephrology outpatient clinic were prospectively recruited and the following bleeding parameters were measured in all patients: platelet count, bleeding time (BT), Factor VIII assay, von Willebrand factor antigen (vWF:Ag), vWF:ristocetin cofactor activity (vWF:RCo), ratio of vWF:ristocetin cofactor activity to vWF antigen (vWF:RCo/vWF:Ag), prothrombin time (PT), and activated partial thromboplastin time (aPTT). Forty-five patients (80%, males) with a mean age of 39.4 years, 82% (n = 37) in Stage 5 CKD, were recruited for the study. The prevalence of thrombocytopenia was significantly higher among patients from West Bengal (15/26, 57.7%) compared to other study patients (2/19, 10.5%; P = 0.001); however, all had macrothrombocytes with normal BT, suggestive of the Harris syndrome. Factor VIII, vWF:Ag, vWF:RCo, vWF:RCo/vWF:Ag ratio, BT, PT, and aPTT were abnormal in 0 (0%), 0 (0%), 0 (0%), 4 (8.8%), 1 (2.2%), 7 (15.6%), and 5 (11.1%) patients, respectively. Except for thrombocytopenia, the prevalence of hemostatic abnormalities did not differ between CKD Stages 4 and 5. Hemostatic abnormalities are uncommon in Stages 4–5 CKD and except for thrombocytopenia, are not associated with degree of uremia. Constitutional macrothrombocytopenia is associated with normal BT even in CKD.
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spelling pubmed-59524522018-06-01 Hemostatic Abnormalities in Severe Renal Failure: Do They Bark or Bite? Mohapatra, A. Valson, A. T. Gopal, B. Singh, S. Nair, S. C. Viswabandya, A. Varughese, S. Tamilarasi, V. John, G. T. Indian J Nephrol Original Article Abnormal primary hemostasis is believed to be the most significant contributor to uremic bleeding. This study aimed to describe the prevalence and profile of primary and secondary hemostatic disorders in patients with chronic kidney disease (CKD) Stages 4 and 5 and to determine their association if any, with degree of uremia. Stages 4 and 5 predialysis CKD patients attending nephrology outpatient clinic were prospectively recruited and the following bleeding parameters were measured in all patients: platelet count, bleeding time (BT), Factor VIII assay, von Willebrand factor antigen (vWF:Ag), vWF:ristocetin cofactor activity (vWF:RCo), ratio of vWF:ristocetin cofactor activity to vWF antigen (vWF:RCo/vWF:Ag), prothrombin time (PT), and activated partial thromboplastin time (aPTT). Forty-five patients (80%, males) with a mean age of 39.4 years, 82% (n = 37) in Stage 5 CKD, were recruited for the study. The prevalence of thrombocytopenia was significantly higher among patients from West Bengal (15/26, 57.7%) compared to other study patients (2/19, 10.5%; P = 0.001); however, all had macrothrombocytes with normal BT, suggestive of the Harris syndrome. Factor VIII, vWF:Ag, vWF:RCo, vWF:RCo/vWF:Ag ratio, BT, PT, and aPTT were abnormal in 0 (0%), 0 (0%), 0 (0%), 4 (8.8%), 1 (2.2%), 7 (15.6%), and 5 (11.1%) patients, respectively. Except for thrombocytopenia, the prevalence of hemostatic abnormalities did not differ between CKD Stages 4 and 5. Hemostatic abnormalities are uncommon in Stages 4–5 CKD and except for thrombocytopenia, are not associated with degree of uremia. Constitutional macrothrombocytopenia is associated with normal BT even in CKD. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC5952452/ /pubmed/29861564 http://dx.doi.org/10.4103/ijn.IJN_104_17 Text en Copyright: © 2018 Indian Journal of Nephrology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Mohapatra, A.
Valson, A. T.
Gopal, B.
Singh, S.
Nair, S. C.
Viswabandya, A.
Varughese, S.
Tamilarasi, V.
John, G. T.
Hemostatic Abnormalities in Severe Renal Failure: Do They Bark or Bite?
title Hemostatic Abnormalities in Severe Renal Failure: Do They Bark or Bite?
title_full Hemostatic Abnormalities in Severe Renal Failure: Do They Bark or Bite?
title_fullStr Hemostatic Abnormalities in Severe Renal Failure: Do They Bark or Bite?
title_full_unstemmed Hemostatic Abnormalities in Severe Renal Failure: Do They Bark or Bite?
title_short Hemostatic Abnormalities in Severe Renal Failure: Do They Bark or Bite?
title_sort hemostatic abnormalities in severe renal failure: do they bark or bite?
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952452/
https://www.ncbi.nlm.nih.gov/pubmed/29861564
http://dx.doi.org/10.4103/ijn.IJN_104_17
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