Elevated Fibrin D-Dimer Fragment in Sickle Cell Anemia: Evidence for Activation of Coagulation during the Steady State as well as in Painful Crisis

RB Francis - Pathophysiology of Haemostasis and Thrombosis, 1989 - karger.com
The fibrin D-dimer degradation fragment is produced by plasmin degradation of cross-linked
fibrin. Elevated plasma D-dimer levels indicate increased plasmin degradation of cross …

[HTML][HTML] Fragment D-dimer levels: an objective marker of vaso-occlusive crisis and other complications of sickle cell disease

DV Devine, TR Kinney, PF Thomas, WF Rosse… - Blood, 1986 - Elsevier
Although abnormalities in coagulation tests have been reported during vaso-occlusive
crises in patients with sickle cell disease, objective, readily performed laboratory tests that …

Plasma factor VII and thrombin–antithrombin III levels indicate increased tissue factor activity in sickle cell patients

J Kurantsin‐Mills, FA Ofosu, TK Safa… - British journal of …, 1992 - Wiley Online Library
Although the mechanisms involved in the persistent clinical complications of sickle cell
disease have not yet been fully delineated, previous studies suggest that sickle cell (HbSS) …

Effect of low‐dose warfarin on D‐dimer levels during sickle cell vaso‐occlusive crisis: a brief report

S Ahmed, AK Siddiqui, U Iqbal… - European journal of …, 2004 - Wiley Online Library
Objective: To evaluate the activation of clotting systems in patients with sickle cell disease
(SCD) by measuring the plasma D‐dimer level and to determine the effect of low‐dose …

Changes in coagulation and fibrinolysis in patients with sickle cell disease compared with healthy black controls

D Hagger, S Wolff, J Owen… - Blood coagulation & …, 1995 - journals.lww.com
Seventeen parameters of coagulation and fibrinolysis were measured in 33 patients with
sickle cell disease; 30 were tested in steady state (SS) and 19 in crisis (Cr). There were 16 …

Abnormalities of coagulation and fibrinolysis in homozygous sickle cell disease

B Nsiri, N Gritli, F Bayoudh, T Messaoud… - Hematology and cell …, 1996 - Springer
Abnormalities of coagulation and fibrinolysis were studied in a group of 28 children and
young adults with homozygous sickle cell disease (SCD), either in the steady state (n= 12) …

Thrombogenesis in sickle cell disease

A Tomer, LA Harker, S Kasey, JR Eckman - Journal of Laboratory and …, 2001 - Elsevier
Thirty-three subjects with sickle cell disease (SCD), 11 during episodes of pain and 22
during periods without pain, were evaluated for in vivo thrombogenic activities as compared …

Hemostatic alterations accompanying sickle cell pain crises

N Alkjaersig, A Fletcher, H Joist… - The Journal of …, 1976 - translationalres.com
Three patients with sickle-cell disease (SSD) were followed, weekly, for 112 to 2 years,
years, during which time they experienced one or more episodes of crisis. Crisis was …

Is sickle cell crisis a thrombotic event?

D Green, JP Scott - American journal of hematology, 1986 - Wiley Online Library
Although large vessel thrombi are occasionally reported in patients with homozygous sickle
cell disease, the role of intravascular coagulation in typical pain crises is controversial …

Elevated plasma levels of fibrinopeptide A during sickle cell anemia pain crisis–evidence for intravascular coagulation

DA Leichtman, GJ Brewer - American journal of hematology, 1978 - Wiley Online Library
A role for coagulation in the pathogenesis of sickle cell anemia (SCA) pain crisis has long
been suspected. We have observed evidence for in vivo coagulation in patients with SCA …