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Fatal right ventricular failure and pulmonary hypertension after protamine administration during cardiac transplantation

Protamine sulfate is the only Food and Drug administration approved medication for reversal of intraoperative heparin-induced anticoagulation during cardiac and vascular surgeries. One of the rare side effects of protamine sulfate is an idiosyncratic reaction resulting in acute pulmonary hypertensio...

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Autores principales: Pannu, Bibek S., Sanghavi, Devang K., Guru, Pramod K., Reddy, Dereddi Raja, Iyer, Vivek N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810899/
https://www.ncbi.nlm.nih.gov/pubmed/27076733
http://dx.doi.org/10.4103/0972-5229.178185
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author Pannu, Bibek S.
Sanghavi, Devang K.
Guru, Pramod K.
Reddy, Dereddi Raja
Iyer, Vivek N.
author_facet Pannu, Bibek S.
Sanghavi, Devang K.
Guru, Pramod K.
Reddy, Dereddi Raja
Iyer, Vivek N.
author_sort Pannu, Bibek S.
collection PubMed
description Protamine sulfate is the only Food and Drug administration approved medication for reversal of intraoperative heparin-induced anticoagulation during cardiac and vascular surgeries. One of the rare side effects of protamine sulfate is an idiosyncratic reaction resulting in acute pulmonary hypertension (APH) and right ventricular (RV) failure occurring after protamine administration. These reactions are rare but catastrophic with high mortality. A 36-year-old female with severe congestive heart failure was undergoing cardiac transplant surgery. After successful implantation of the donor heart, the patient was weaned off cardiopulmonary bypass. Protamine was then administered to reverse the heparin anticoagulation. She immediately developed APH and RV failure immediately after protamine infusion. The patient required immediate administration of inotropic agents, nitric oxide (NO), and subsequently required a number of mechanical support devices including an RV assist device (RVAD) and ultimately full veno-arterial extracorporeal membrane oxygenation (VA-ECMO). Despite heroic efforts, the patient developed refractory multi-organ failure in the Intensive Care Unit and died after family requested discontinuation of resuscitative efforts. This case probably represents the first reported occurrence of fatal protamine-induced APH and ventricular failure in the setting of cardiac transplantation surgery. A number of interventions including inhaled NO, systemic vasopressors, RVAD, and ultimately VA-ECMO failed to reverse the situation, and the patient died of multi-organ failure.
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spelling pubmed-48108992016-04-13 Fatal right ventricular failure and pulmonary hypertension after protamine administration during cardiac transplantation Pannu, Bibek S. Sanghavi, Devang K. Guru, Pramod K. Reddy, Dereddi Raja Iyer, Vivek N. Indian J Crit Care Med Case Report Protamine sulfate is the only Food and Drug administration approved medication for reversal of intraoperative heparin-induced anticoagulation during cardiac and vascular surgeries. One of the rare side effects of protamine sulfate is an idiosyncratic reaction resulting in acute pulmonary hypertension (APH) and right ventricular (RV) failure occurring after protamine administration. These reactions are rare but catastrophic with high mortality. A 36-year-old female with severe congestive heart failure was undergoing cardiac transplant surgery. After successful implantation of the donor heart, the patient was weaned off cardiopulmonary bypass. Protamine was then administered to reverse the heparin anticoagulation. She immediately developed APH and RV failure immediately after protamine infusion. The patient required immediate administration of inotropic agents, nitric oxide (NO), and subsequently required a number of mechanical support devices including an RV assist device (RVAD) and ultimately full veno-arterial extracorporeal membrane oxygenation (VA-ECMO). Despite heroic efforts, the patient developed refractory multi-organ failure in the Intensive Care Unit and died after family requested discontinuation of resuscitative efforts. This case probably represents the first reported occurrence of fatal protamine-induced APH and ventricular failure in the setting of cardiac transplantation surgery. A number of interventions including inhaled NO, systemic vasopressors, RVAD, and ultimately VA-ECMO failed to reverse the situation, and the patient died of multi-organ failure. Medknow Publications & Media Pvt Ltd 2016-03 /pmc/articles/PMC4810899/ /pubmed/27076733 http://dx.doi.org/10.4103/0972-5229.178185 Text en Copyright: © Indian Journal of Critical Care Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Pannu, Bibek S.
Sanghavi, Devang K.
Guru, Pramod K.
Reddy, Dereddi Raja
Iyer, Vivek N.
Fatal right ventricular failure and pulmonary hypertension after protamine administration during cardiac transplantation
title Fatal right ventricular failure and pulmonary hypertension after protamine administration during cardiac transplantation
title_full Fatal right ventricular failure and pulmonary hypertension after protamine administration during cardiac transplantation
title_fullStr Fatal right ventricular failure and pulmonary hypertension after protamine administration during cardiac transplantation
title_full_unstemmed Fatal right ventricular failure and pulmonary hypertension after protamine administration during cardiac transplantation
title_short Fatal right ventricular failure and pulmonary hypertension after protamine administration during cardiac transplantation
title_sort fatal right ventricular failure and pulmonary hypertension after protamine administration during cardiac transplantation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810899/
https://www.ncbi.nlm.nih.gov/pubmed/27076733
http://dx.doi.org/10.4103/0972-5229.178185
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