scholarly journals 173: NOVEL COAGULATION TEST SUCCESSFULLY DETECTS ANTICOAGULATION RESISTANCE IN PATIENTS WITH COVID-19

2021 ◽  
Vol 50 (1) ◽  
pp. 70-70
Author(s):  
Galit Frydman ◽  
Rachel Rosovsky ◽  
Jarone Lee ◽  
Barry Berger ◽  
Dimitrios Papageorgiou ◽  
...  
Keyword(s):  
1977 ◽  
Author(s):  
J.G. Sharnoff

From 1960 through 1975, 337 patients with surgically treated acute fracture of the hip received subcutaneously administered aqueous heparin sodium to prevent thromboembolic episodes. Four hundred and three patients received no heparin. Their incidence of fatal pulmonary embolism was 3.5 percent. Ninety-five patients receiving the original “small dose” heparin regimen from August 1960 to November 1967 had a 4.2 percent incidence of fatal thromboembolism. These had been administered heparin 8-10 hours or less before surgery. Beginning November 1967 the “small dose” heparin schedule was altered in hip fracture patients to start heparin prophylaxis immediately following hospital admission. One hundred and forty-seven patients treated with the latter schedule had 0.0 percent fatal thromboembolism with the dose modified according to a coagulation time test. The patients received 2,500 units on admission and every 6 hours until the day before operation. Then they were given 5,000 to 10,000 units. 8 to 10 hours before surgery and 2,500 units every 6 hours after surgery until they were fully mobilized. The altered “small dose” heparin regimen adequately monitored by the blood coagulation test, the Dale and Laidlaw Coagulometer, proved highly effective as measured by fatality rates.


1996 ◽  
Vol 10 (2) ◽  
pp. 82-84 ◽  
Author(s):  
Jeff W. Tyler ◽  
Thomas E. Besser ◽  
Leilani Wilson ◽  
Dale D. Hancock ◽  
Sean Sanders ◽  
...  

PEDIATRICS ◽  
1988 ◽  
Vol 82 (5) ◽  
pp. 763-765
Author(s):  
Edward R. Burns ◽  
Ben-Zion Krieger ◽  
Larry Bernstein ◽  
Arye Rubinstein

The mechanism underlying the prolonged activated partial thromboplastin time (APTT) seen in some pediatric patients with acquired immunodeficiency syndrome (AIDS) and opportunistic infections was studied. A circulating inhibitor of coagulation was demonstrated in three patients. The inhibitor appears to be an immunoglobulin that interferes with some of the phospolipid-dependent coagulation reactions of the intrinsic pathway. This "AIDS anticoagulant" does not predispose the patient to clinical bleeding despite its ability to cause a marked prolongation of the APTT. As such, careful laboratory diagnosis of the cause of abnormal coagulation test results is necessary for children with AIDS.


Author(s):  
Fatma Demet İnce ◽  
Pınar Bilgi ◽  
Neşe Doğan ◽  
Elif Merve Arı ◽  
Lale Aldemir

Medicine ◽  
2018 ◽  
Vol 97 (45) ◽  
pp. e13104 ◽  
Author(s):  
Zikai Song ◽  
Haidi Wu ◽  
Hongyan Cao ◽  
Shuo Yang ◽  
Minglong Tang ◽  
...  

2018 ◽  
Vol 66 (4) ◽  
pp. 573-586
Author(s):  
Luca Laura Kummer ◽  
Jan Govaere ◽  
Borisz Egri

Twenty-eight warmblood mares were monitored during their late pregnancy in the Teaching Hospital of Ghent University. The reliability of two commercial assays (enzyme immunoassay and glutaraldehyde coagulation test) used for determining the IgG concentrations of their newborn foals was tested. Mammary secretions were examined at the time of foaling (T0), and then 4 (T1) and 8 (T2) hours after foaling by refractometry and electrophoresis. The foals’ blood IgG levels were measured at T1 and T2 as a routine clinical diagnostic examination using two different commercial test kits (SNAP Foal Ig and Gamma-Check E) and T0, T1 and T2 samples were stored (at −18 °C) for immunoglobulin (Ig) determination by electrophoresis. Differences between the results of refractometry and electrophoresis occurred in 27.8% of the colostrum analyses. Some serum IgG could be detected immediately post partum (T0) in 75% of the foals, and 42.82% of the newborn foals acquired a serum concentration of more than 800 mg/dl IgG within 8 h of birth. Compared to the electrophoresis, the glutaraldehyde test scored better (85%) than the enzyme immunoassay (74%), although both are accurate and safe to use since they clearly distinguish between safe and unsafe IgG concentrations.


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