1977
DOI: 10.1016/0049-3848(77)90053-6
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Estimation and characterization of soluble fibrin monomer complexes during endotoxin-induced intravascular coagulation

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Cited by 15 publications
(16 citation statements)
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“…Yet, in the present series of patients with hypercoagulability no covalently linked fibrin derivatives were found. This could well be in agreement with the observations during the generalized Shwartzman reaction that hypercoagulability (before the second endotoxin injection) was accompanied by an elevated level of SFMC dissociable in SDS and urea, whereas intravascular coagulation (4 h after the second endotoxin injection) was evidenced by the occurrence of SDS-and urearesistant oligomers of fibrin containing y-y dimers [14].…”
Section: Discussionsupporting
confidence: 80%
“…Yet, in the present series of patients with hypercoagulability no covalently linked fibrin derivatives were found. This could well be in agreement with the observations during the generalized Shwartzman reaction that hypercoagulability (before the second endotoxin injection) was accompanied by an elevated level of SFMC dissociable in SDS and urea, whereas intravascular coagulation (4 h after the second endotoxin injection) was evidenced by the occurrence of SDS-and urearesistant oligomers of fibrin containing y-y dimers [14].…”
Section: Discussionsupporting
confidence: 80%
“…In some reports of experimental DIC in animals, fibrin deposits have been histologically observed in the capillaries of different organs, demonstrating that fibrin deposition is one of the consequences of DIC. 6,7,11,12 During DIC, the massive fibrin deposition that occurs in the microcirculation may occlude or restrict blood flow, and the resulting ischemia may lead to necrosis and potentially MOF. [31][32][33] DIC is thought to be a common complication in horses with colic, especially in those with ischemic and inflammatory processes.…”
Section: Discussionmentioning
confidence: 99%
“…[6][7][8][9][10] Other histologic studies in people with DIC have shown that excessive production and massive deposition of fibrin can be observed in capillaries from several organs, such as the kidneys, lungs, liver, spleen, heart, and brain. 6,7,11,12 The organs most frequently affected by microthrombi deposition in patients with DIC are lungs, kidneys, and liver. 4,7,9,13,14 In veterinary medicine, the detection of microvascular fibrin deposition in 1 or more organs also is considered essential for a histopathologic diagnosis of DIC.…”
mentioning
confidence: 99%
“…As a result of the increased thrombin action on fibrinogen, fibrin monomer and crosslinked fibrin is formed in the circulation [13]. Polymerisation of fibrin monomer is inhibited to a certain extent by complex formation with fibrinogen and fibrin degradation products [10,20] resulting in the so called soluble fibrin monomer complexes (SFMC).…”
Section: Pathological Findingsmentioning
confidence: 99%