scholarly journals Effect of amniotic fluid on blood coagulation

Critical Care ◽  
2009 ◽  
Vol 13 (Suppl 1) ◽  
pp. P440
Author(s):  
H Hayami ◽  
S Ohama ◽  
A Sakurai ◽  
J Yamada ◽  
O Yamaguchi ◽  
...  
1961 ◽  
Vol 06 (01) ◽  
pp. 025-036 ◽  
Author(s):  
James W. Hampton ◽  
William E. Jaques ◽  
Robert M. Bird ◽  
David M. Selby

Summary1. Infusions containing particulate matter, viz. whole amniotic fluid, amniotic fluid sediment, and glass beads, produce in dogs changes in both early and late phases of the clotting reaction. These changes are associated with the development of pulmonary hypertension.2. When dogs were given an active fibrinolysin followed by an infusion of whole amniotic fluid, the alterations in the clotting mechanism were either delayed or did not appear. No pulmonary hypertension developed in these animals.3. We infer that infusions containing particulate matter will produce in dogs both pulmonary hypertension and changes in the clotting mechanism. Although these are independent changes, both are as closely related to the damage to the pulmonary vessels as they are to the biological nature of the infusions.


2018 ◽  
Vol 172 ◽  
pp. 142-149 ◽  
Author(s):  
Tomoaki Oda ◽  
Naoaki Tamura ◽  
Yi Shen ◽  
Yukiko Kohmura-Kobayashi ◽  
Naomi Furuta-Isomura ◽  
...  

Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 4961-4961
Author(s):  
Johannes Thaler ◽  
Lena Hell ◽  
Lukas Wisgrill ◽  
Andreas Spittler ◽  
Michael Schwameis ◽  
...  

Abstract Background: The pathomechanisms underlying disseminated intravascular coagulation (DIC) following amniotic fluid (AF) embolism remain to be fully elucidated. Highly procoagulant phosphatidylserine (PS)- and tissue factor (TF) expressing extracellular vesicles (EVs) might play a central role. Objective: To perform extensive analyses of the procoagulant properties of AF with a panel of functional coagulation assays and flow cytometry to investigate the pathogenesis of AF induced DIC. Methods: A prothrombinase assay, an EV-TF dependent factor Xa (FXa) generation assay, a modified thrombin- and fibrin-generation assay, a whole blood clotting model and flow cytometry were applied in AF- and control plasma. Results: Phosphatidylserine expression was 21-fold increased in AF compared to plasma. Factor Xa generation was extremely high when TF-expressing EVs from AF were co-incubated with recombinant FVIIa. In the thrombin- and fibrin generation assay AF-derived EVs strongly activated the blood coagulation cascade via PS and TF. In a whole blood clotting model AF-derived TF-expressing EVs significantly shortened the clotting time from 734 ± 139 seconds in the presence- to 232 ± 139 seconds in the absence of an anti-TF antibody. The contact activation pathway via factor FXII was not affected. Applying flow cytometry, a sub-population of PS- and TF co-expressing EVs was clearly identified in AF. Conclusions: We thoroughly investigated the effect of AF on blood coagulation and found that PS+ and TF+ EVs determine its procoagulant potential. Taken together our data further delineate the pathomechanisms underlying AF-induced coagulopathy, which could improve diagnostic- and treatment modalities. Disclosures No relevant conflicts of interest to declare.


1972 ◽  
Vol 22 (3) ◽  
pp. 353-355 ◽  
Author(s):  
L. D. Courtney ◽  
M. Allington

1997 ◽  
Vol 9 (1) ◽  
pp. 35-47 ◽  
Author(s):  
Gary DV Hankins ◽  
Steven Leigh Clark

Attwood traces the earliest possible description of a case of amniotic fluid embolism (AFE) to 1825. The next case was described by Meyer some 101 years later. Not until 1941 was this obstetric catastrophe recognised as constituting a true syndrome with its own clinical and pathological characteristics. Any combination of sudden and profound shock, dyspnoea, cyanosis, apprehension, seizures, and the failure of rapid blood coagulation may herald the clinical onset of an AFE. Liban was the first to report the detection of squamous cells throughout the systemic circulation, an observation which was not explained at the time. Many have commented upon the ominous fetal heart pattern that almost invariably accompanies AFE if the fetus is in-utero at the time of the embolus.


Sign in / Sign up

Export Citation Format

Share Document