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Factors contributing to poor outcome in patients on warfarin receiving 4-factor prothrombin complex concentrate in critically ill

AIM: To compare the demographical profile, indications, efficacy, and contributors to adverse outcome following administration of 4F-PCC in patients on warfarin with supratherapeutic INR. METHODOLOGY: Retrospective cross-sectional study was performed in a community-based teaching hospital. All patie...

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Autores principales: Mishra, Ajay Kumar, Sahu, Kamal Kant, Lal, Amos, George, Susan V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8689313/
https://www.ncbi.nlm.nih.gov/pubmed/34738603
http://dx.doi.org/10.23750/abm.v92i5.9601
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author Mishra, Ajay Kumar
Sahu, Kamal Kant
Lal, Amos
George, Susan V
author_facet Mishra, Ajay Kumar
Sahu, Kamal Kant
Lal, Amos
George, Susan V
author_sort Mishra, Ajay Kumar
collection PubMed
description AIM: To compare the demographical profile, indications, efficacy, and contributors to adverse outcome following administration of 4F-PCC in patients on warfarin with supratherapeutic INR. METHODOLOGY: Retrospective cross-sectional study was performed in a community-based teaching hospital. All patients 18 years and older on warfarin with supratherapeutic INR, who had received 4F-PCC between January 2014 and December 2018 were eligible and included in the study. RESULTS: 44 patients were included in the analysis. The mean age of the patients was 79.5 years. The male to female ratio was 1:1. Patients were on warfarin for atrial fibrillation, thromboembolism in 79.5% (N-35), and 20.5% (N-9) respectively. Indications for use of 4F-PCC were active bleeding in 93% (N-41) of patients. The common sites of bleeding were gastrointestinal, intracranial, and musculoskeletal which were seen in 54.5% (N-24), 29.5% (N-13) and 6.8% (N-3) respectively. The median number of doses of 4F-PCC administered was 1 per patient. The mean dose administered was 2,883u. Clinical improvement was documented in 84% (N-37) of patients. Mortality was seen in 16% (N-7) of patients. BMI greater than 30, anemia, hypotension, presence of intracranial bleed, the requirement of blood products, and mechanical ventilation were associated with higher odds for mortality. Hypotension and requirement of mechanical ventilation were statistically significant. CONCLUSION: 4F-PCC continues to be an effective agent in the rapid reversal of warfarin therapy in patients with supratherapeutic INR presenting with major bleeding events. Most patients have clinical improvement with a single, weight-adjusted dose.
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spelling pubmed-86893132022-01-06 Factors contributing to poor outcome in patients on warfarin receiving 4-factor prothrombin complex concentrate in critically ill Mishra, Ajay Kumar Sahu, Kamal Kant Lal, Amos George, Susan V Acta Biomed Original Article AIM: To compare the demographical profile, indications, efficacy, and contributors to adverse outcome following administration of 4F-PCC in patients on warfarin with supratherapeutic INR. METHODOLOGY: Retrospective cross-sectional study was performed in a community-based teaching hospital. All patients 18 years and older on warfarin with supratherapeutic INR, who had received 4F-PCC between January 2014 and December 2018 were eligible and included in the study. RESULTS: 44 patients were included in the analysis. The mean age of the patients was 79.5 years. The male to female ratio was 1:1. Patients were on warfarin for atrial fibrillation, thromboembolism in 79.5% (N-35), and 20.5% (N-9) respectively. Indications for use of 4F-PCC were active bleeding in 93% (N-41) of patients. The common sites of bleeding were gastrointestinal, intracranial, and musculoskeletal which were seen in 54.5% (N-24), 29.5% (N-13) and 6.8% (N-3) respectively. The median number of doses of 4F-PCC administered was 1 per patient. The mean dose administered was 2,883u. Clinical improvement was documented in 84% (N-37) of patients. Mortality was seen in 16% (N-7) of patients. BMI greater than 30, anemia, hypotension, presence of intracranial bleed, the requirement of blood products, and mechanical ventilation were associated with higher odds for mortality. Hypotension and requirement of mechanical ventilation were statistically significant. CONCLUSION: 4F-PCC continues to be an effective agent in the rapid reversal of warfarin therapy in patients with supratherapeutic INR presenting with major bleeding events. Most patients have clinical improvement with a single, weight-adjusted dose. Mattioli 1885 2021 2021-11-03 /pmc/articles/PMC8689313/ /pubmed/34738603 http://dx.doi.org/10.23750/abm.v92i5.9601 Text en Copyright: © 2021 ACTA BIO MEDICA SOCIETY OF MEDICINE AND NATURAL SCIENCES OF PARMA https://creativecommons.org/licenses/by-nc-sa/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License
spellingShingle Original Article
Mishra, Ajay Kumar
Sahu, Kamal Kant
Lal, Amos
George, Susan V
Factors contributing to poor outcome in patients on warfarin receiving 4-factor prothrombin complex concentrate in critically ill
title Factors contributing to poor outcome in patients on warfarin receiving 4-factor prothrombin complex concentrate in critically ill
title_full Factors contributing to poor outcome in patients on warfarin receiving 4-factor prothrombin complex concentrate in critically ill
title_fullStr Factors contributing to poor outcome in patients on warfarin receiving 4-factor prothrombin complex concentrate in critically ill
title_full_unstemmed Factors contributing to poor outcome in patients on warfarin receiving 4-factor prothrombin complex concentrate in critically ill
title_short Factors contributing to poor outcome in patients on warfarin receiving 4-factor prothrombin complex concentrate in critically ill
title_sort factors contributing to poor outcome in patients on warfarin receiving 4-factor prothrombin complex concentrate in critically ill
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8689313/
https://www.ncbi.nlm.nih.gov/pubmed/34738603
http://dx.doi.org/10.23750/abm.v92i5.9601
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