scholarly journals Platelet consumption during neonatal extracorporeal life support (ECLS)

Perfusion ◽  
1992 ◽  
Vol 7 (1) ◽  
pp. 27-33 ◽  
Author(s):  
Franz B Plötz ◽  
Walter R Wildevuur ◽  
Charles RH Wildevuur ◽  
Ralph E Delius ◽  
Robert H Bartlett

This paper reports the results of a retrospective study of blood use and blood loss in 40 neonates during extracorporeal life support (ECLS). Immediately after onset of bypass 39±2.5ml platelets, 59.4±6.5ml packed red blood cells (PRBC) and 15.0±5.4ml fresh frozen plasma (FFP) per patient were needed. The average daily amount given per patient was 49.0±3.0ml of platelets and 48.0±3.4ml and 9.6±3.9ml of PRBC and FFP respectively. The 10 patients who had bleeding complications received 50.0±6.3ml/day of platelets compared to 49.0±3.4ml in the other patients. The majority of blood loss during the entire period of ECLS was from samples, averaging 43.0 ± 1.5ml/day. Neck wound drainage, 6.7±2.5ml/day per patient, lasted for the entire period.

Perfusion ◽  
2009 ◽  
Vol 24 (3) ◽  
pp. 191-197 ◽  
Author(s):  
Kathryn Nardell ◽  
Gail M Annich ◽  
Jennifer C Hirsch ◽  
Cathe Fahrner ◽  
Pat Brownlee ◽  
...  

Background/Objective: There is limited literature documenting bleeding patterns in pediatric post-cardiotomy patients on extracorporeal life support (ECLS). This retrospective review details bleeding complications and identifies risk factors for bleeding in these patients. Methods: Records from 145 patients were reviewed. Patients were divided into excessive (E) and non-excessive (NE) bleeding groups based on blood loss. Results: Excessive bleeding occurred predominantly from 0-6h. Longer CPB duration (NE=174±8min; E=212±16; p=0.02) and lower platelet counts (NE=104.8±50K; E=84.3±41K; p=0.01) were associated with excessive bleeding during the first 6h (p=0.005). Use of intraoperative protamine with normal platelets was associated with decreased bleeding from 7-12h post-ECLS (p=0.002). Most mediastinal exploration occurred >49h post-ECLS, with decreased bleeding post-exploration in E patients. Conclusions: The majority of pediatric post-cardiotomy ECLS bleeding occurs early after support initiation. Longer CPB time and thrombocytopenia increased bleeding 0-6h post-ECLS. Since early bleeding may be coagulopathic in origin, an approach to minimize bleeding includes protamine administration and aggressive blood product replacement with target platelet counts of 100-120K. Surgical exploration should follow if additional hemostasis is necessary.


Blood ◽  
2020 ◽  
Vol 136 (Supplement 1) ◽  
pp. 4-5
Author(s):  
Lisa N Boggio ◽  
Mindy L. Simpson

Background: Extracorporeal membrane oxygenation (ECMO) is a salvage therapy for critically ill children and adults. Hematologic complications, such as hemorrhage and thrombosis, are the major complications in ECMO. The contact of blood with the tubing of the circuit, lines, blood pump, and oxygenator all contribute to the process. Most patients require anticoagulation while on ECMO. According to the international summary of Extracorporeal Life Support Organization (ELSO) registry in 2017, patients on ECMO consist of 69% neonate and pediatric patients (Neo 44.8%, Peds 24.1%, Adult 31.1%). Contributors to the risk of bleeding include excessive heparin use for systemic anticoagulation, consumption of coagulation factors, low fibrinogen levels, thrombocytopenia, platelet dysfunction, and hyperfibrinolysis, among others. This gives the appearance of a consumptive coagulopathy, the hallmark of which is hypofibrinogenemia. Fibrinogen replacement is most efficiently done with cryoprecipitate (cryo) or fibrinogen concentrate, while fresh frozen plasma (FFP) has a low and variable fibrinogen content. Cryo and FFP may contribute to volume expansion and have other prothrombotic factors which could contribute to thrombotic complications. We performed a retrospective analysis of pediatric and adult patients who presented for ECMO to evaluate management of low fibrinogen and bleeding and thrombotic complications. Methods: Data was reviewed for 11 adult and 12 pediatric consecutive patients who received ECMO prior to June 1st, 2019. Time on ECMO (hours), type of ECMO, indication, presence of bleeding or thrombotic complications during ECMO, and use of therapeutic anticoagulation was collected. Laboratory data included platelet counts, hemoglobin, fibrinogen activity, antithrombin activity, prothrombin time, and partial thromboplastin time. Transfusion data was also collected for amount of packed red blood cells (PRBC), platelets, FFP, and cryo transfused. Data were analyzed to evaluate when fibrinogen was low and if cryo was given. According to our institutional guideline, the fibrinogen activity goal is >100 mg/dL and >200 mg/dL if bleeding. Bleeding and/or clotting complications were also noted. Data: There were 24 runs of ECMO evaluated (11 adults, 12 children), including VA and VV, lasting from 65-1343 hours. One child had 2 runs of ECMO. The majority were VA (13/24; 54%) with 33% (8/24) VV and 13% (3/24) combined VA/VV (all occurred in children). Therapeutic anticoagulation was given in 17/24 (71%) overall, but 92% (12/13) of pediatric cases. Bleeding and/or clotting complicated 17 (71%) runs. Overall, bleeding occurred in 13 (54%) runs and thrombosis in 12 (50%). Of these events, 8 (33%) runs had both bleeding and thrombosis. Bleeding occurred in 8/11 (73%) adults and 5/12 (42%) children. Bleeding and/or thrombus occurred more often with longer ECMO runs, but affected all runs longer than 250 hours (12/24, 50%). While on ECMO, the fibrinogen activity was below 100 mg/dL at some point in 11/24 (46%) of runs. Of those 11, only 6 (55%) received cryo in response to the fibrinogen activity. Cryo was more likely to be given if both a low fibrinogen and bleeding were present. Even with bleeding episodes and fibrinogen activities <200 mg/dL, cryo was not given in the majority of cases (70% adults, 40% children), but FFP was given preferentially. Conclusions: Almost half (45%) of the patients evaluated had low fibrinogen levels at some point while on ECMO. Despite cryoprecipitate being standard replacement at our institution for low fibrinogen, only 55% of those patients received cryo in response to the low level. Therefore, 21% (5/24) of all cases were not specifically treated for their low fibrinogen value. Bleeding and/or thrombotic complications are common with ECMO. Further study to determine if fibrinogen replacement or lack thereof contributes to these complications and guide management of fibrinogen deficiency in ECMO patients is warranted. Figure Disclosures No relevant conflicts of interest to declare.


Author(s):  
Anne Craig ◽  
Anthea Hatfield

Part one of this chapter tells you about the physiology of blood and oxygen supply, about anaemia and tissue hypoxia, and the physiology of coagulation. Drugs that interfere with clotting are discussed. Bleeding, coagulation, and platelet disorders are covered as well as disseminated intravascular coagulation. Part two is concerned with bleeding in the recovery room: how to cope with rapid blood loss, managing ongoing blood loss, and how to use clotting profiles to guide treatment. There is also a section covering blood transfusion, blood groups and typing. Massive blood transfusion is clearly described, there are guidelines about when to use fresh frozen plasma, when to use platelets, and when to use cryoprecipitate. The final section of the chapter is about problems with blood transfusions.


Author(s):  
Jay Berger

Massive transfusion is defined as transfusion of 3 units of packed red blood cells in less than 1 hour in an adult, replacement of more than 1 blood volume in 24 hours, or replacement of more than 50% of blood volume in 3 hours. Massive transfusion protocols are implemented in cases of life-threatening hemorrhage after trauma, during a surgical procedure, or during childbirth. These protocols are intended to minimize the adverse effects of hypovolemia, dilutional anemia, metabolic complications, and coagulopathy with early empiric replacement of blood products and transfusion of fresh frozen plasma, platelets, and packed red blood cells in a composition that approximates that of whole blood.


2015 ◽  
Vol 81 (3) ◽  
pp. 245-251 ◽  
Author(s):  
Michael R. Phillips ◽  
Amal L. Khoury ◽  
Briana J. K. Stephenson ◽  
Lloyd J. Edwards ◽  
Anthony G. Charles ◽  
...  

No study describes the use of extracorporeal membrane oxygenation (ECMO) in pediatric patients with abdominal sepsis (AS) requiring surgery. A description of outcomes in this patient population would assist clinical decision-making and provide a context for discussions with patients and families. The Extracorporeal Life Support Organization database was queried for pediatric patients (30 days to 18 years) with AS requiring surgery. Forty-five of 61 patients survived (73.8%). Reported bleeding complications (57.1 vs 48.8%), the number of pre-ECMO ventilator hours (208.1 vs 178.9), and the timing of surgery before (50 vs 66.7%) and on-ECMO (50 vs 26.7%) were similar in survivors and nonsurvivors. Decreased pre-ECMO mean pH (7.1 vs 7.3) was associated with increased mortality (odds ratio, 1.49; 95% confidence interval, 1.04 to 2.14). ECMO use for pediatric patients with AS requiring surgery is associated with increased mortality and an increased rate of bleeding complications compared with all pediatric patients receiving ECMO support. Acidemia predicts mortality and provides a potential target of examination for future studies.


Blood ◽  
2020 ◽  
Author(s):  
Corentin Orvain ◽  
Marie Balsat ◽  
Emmanuelle Tavernier ◽  
Jean-Pierre Marolleau ◽  
Thomas Pabst ◽  
...  

Patients undergoing treatment for acute lymphoblastic leukemia (ALL) are at risk for thrombosis, in part due to the use of L-asparaginase (L-ASP). Antithrombin (AT) replacement has been suggested to prevent VTE and thus might increase exposure to ASP. We report herein the results of the prophylactic replacement strategy in the pediatric-inspired prospective GRAALL-2005 study. Between 2006 and 2014, 784 adult patients with newly diagnosed Philadelphia-negative ALL were included. The incidence rate of VTE was 16% with 69% of them occurring during induction therapy. Most patients received AT supplementation (87%). After excluding patients who did not receive L-ASP or developed thrombosis before L-ASP, AT supplementation did not have a significant impact on VTE (8% versus 14%, OR: 0.6, p=0.1). Fibrinogen concentrates administration was associated with an increased risk of VTE (17% versus 9%, OR 2.2, p=0.02) whereas transfusion of fresh-frozen plasma had no effect. Heparin prophylaxis was associated with an increased risk of VTE (13% versus 7%, OR 1.9, p=0.04). Prophylactic measures were not associated with an increased risk of grade 3-4 bleeding complications. The rate of VTE recurrence after L-ASP reintroduction was 3% (1/34). In ALL patients receiving L-ASP therapy, the use of fibrinogen concentrates may increase the risk of thrombosis and should be restricted to rare patients with hypofibrinogenemia-induced hemorrhage. Patients developed VTE despite extensive AT supplementation which advocates for additional prophylactic measures. While this large descriptive study was not powered to demonstrate the efficacy of these prophylactic measures, it provides important insight to guide future trial design. NCT00327678.


1981 ◽  
Author(s):  
D C Case

A 25-year old male was admitted for an episode of right sided headache and subsequent generalized seizure. On admission his temperature was 37.6°. He had generalized petechiae and conjunctival hemorrhages. Organomegaly and lymphadenopathy were absent. There was mild left sided weakness. The Hgb. was 6.9 g/dl., reticulocyte count 10%, WBC 11,500/mm3, and platelet count 10,000/mm3. There were numerous schistocytes on the peripheral smear; bone marrow revealed panhyperplasia. Coagulation studies were normal. The BUN was 30, and the creatinine 1.7 mg/dl. Plasma was positive for Hgb. CT scan was negative for gross intracranial bleeding. The diagnosis of T.T.P. was made. On admission, the patient received 10 units of platelets and 2 units of packed red blood cells. He did not require further red cell or platelet transfusions during the rest of his hospital course. He was then started on infusions of fresh-frozen plasma. He then received one unit every 3 hours for 6 days, one unit every 6 hours for 2 days, then one unit every 12 hours for 2 days and finally 1 unit daily for 5 days. The response was immediate. After the infusions were started, the hematologic parameters steadily improved. The patient’s hematuria rapidly improved. Further CNS symptoms did not appear. The patient’s Hgb. was 12 g/dl, and reticulocyte count was 2.5% by the 9th day. His platelet count was normal by the 4th day. The patient was discharged on the 15th day. Infusions of plasma were discontinued at the time of discharge. The patient required plasma therapy 4 weeks later for recurrent thrombocytopenia (50,000/mm3). The patient has remained normal for 9 months since therapy and further plasma has not been required. Primary plasma therapy for T.T.P. as sole treatment should be further studied.


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