Effect of aprotinin on activated clotting time, whole blood and plasma heparin measurements

1995 ◽  
Vol 9 (4) ◽  
pp. 473
1995 ◽  
Vol 59 (1) ◽  
pp. 106-111 ◽  
Author(s):  
George J. Despotis ◽  
J. Heinrich Joist ◽  
Diane Joiner-Maier ◽  
Alexander L. Alsoufiev ◽  
Anastasios N. Triantafillou ◽  
...  

1977 ◽  
Author(s):  
R.D. Hamstra ◽  
G.E. Ens ◽  
S. Simons

A new coagulation instrument (Sonoclot) has been evaluated in the laboratory, at the bedside, and in surgery. It was compared to the prothrombin time, activated partial thromboplastin time, activated clotting time, Lee-White clotting time, fibrinogen and thrombelastograph. Most coagulation tests are reported as time to a clot end point while the Sonoclot records a continuous thrombokinetic pattern by measuring the energy required to maintain axial vibration of a hollow plastic probe in 0.4 ml of whole blood while it clots. Disposable plastic probes and non-siliconized glass cuvettes are rapidly changed after testing. Results are a line pattern which has been analysed for Clot Onset (C0) and Clot Formation Rate (CFR). Native whole blood from normal adults (54 studied) has a C0 of 2-4.5 minutes and CFR of 4-8 chart units/minute. The only similar clotting instrument is the thrombelastograph (TEG). Sonoclot and TEG patterns correlate, the Sonoclot sensing change before the TEG. Whole blood clotting measured with the Sonoclot is a new method which distinguishes hypercoagulation, various levels of heparin, and severe bleeding problems from normal. The device is durable, stable, easy to operate, and portable, providing a permanent record in a few minutes.


2013 ◽  
Vol 179 (2) ◽  
pp. 199
Author(s):  
M.P. Chapman ◽  
E.E. Moore ◽  
T.L. Chin ◽  
A. Ghasabyan ◽  
C.R. Ramos ◽  
...  

1998 ◽  
Vol 12 (3) ◽  
Author(s):  
Masakazu Mori ◽  
Shigenori Yoshitake ◽  
Takaaki Kitano ◽  
Shunsuke Oda ◽  
Takayuki Noguchi

1981 ◽  
Vol 193 (1) ◽  
pp. 105-111 ◽  
Author(s):  
ALFRED T. CULLIFORD ◽  
SANFORD N. GITEL ◽  
NORMAN STARR ◽  
STEPHEN T. THOMAS ◽  
FRANCIS G. BAUMANN ◽  
...  

2018 ◽  
Vol 20 (1) ◽  
pp. 79-86 ◽  
Author(s):  
Sheng Zhang ◽  
Amanda R Guido ◽  
Richard G Jones ◽  
Benjamin J Curry ◽  
Angela S Burke ◽  
...  

Purpose: The use of cyanoacrylate for intravenous catheter securement is of interest to clinicians and patients, because of the superior adhesive strength and hemostatic effect of cyanoacrylate compared to current securement devices. The purpose of this study is to use novel in vitro and in vivo testing methods to analyze the hemostatic effect of a catheter securement cyanoacrylate (cyanoacrylate). Methods: An unprecedented in vitro method was performed to determine the effects of a cyanoacrylate on a customized modified activated clotting time assay and blood flow inhibition assay by exposing blood or plasma to either one or three drops of cyanoacrylate. For the in vivo testing, full-thickness incisions were made on swine, and the bleeding was scored prior to treatment and at 3, 6, 9, and 12 min after treatment. Results: The cyanoacrylate rapidly achieved hemostasis in the presence of anticoagulated whole blood, platelet-poor plasma, and non-anticoagulated whole blood, in vitro. The cyanoacrylate achieved hemostasis 12-fold faster than thromboplastin in the modified activated clotting time assay. The cyanoacrylate does not alter normal blood clotting, as measured by prothrombin time. In vivo, the bleeding score of cyanoacrylate prior to treatment and at 3, 6, 9, and 12 min after treatment were 2.3 ± 1.0, 0.3 ± 0.5, 0.2 ± 0.5, 0.2 ± 0.4, and 0.2 ± 0.4, respectively. Conclusion: This study indicates that cyanoacrylate demonstrates a potent mechanical hemostatic effect and cyanoacrylate in the presence of anticoagulated whole blood has an activated clotting time that is 12 times quicker than thromboplastin. The cyanoacrylate was found to be significantly equivalent to two known hemostatic agents, in vivo.


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