Low-affinity heparin potentiates the action of high-affinity heparin oligosaccharides

Previous studies have shown that high-affinity (HA) heparin oligosaccharides, with molecular weights of 3,000-5,000, were less effective than unfractionated heparin in preventing serum-induced venous thrombosis in rabbits, using a Wessler stasis model. In the present study, a larger high-affinity fragment (M.Wt. 6,000-6,500) was also found to be less effective than unfractionated heparin as an antithrombotic agent. However, addition of 80 micrograms/kg low affinity (LA) heparin to 80 micrograms/kg of this HA fragment significantly potentiated its antithrombotic activity, and the antithrombotic action of the mixture was equivalent to that of unfractionated heparin. Significant potentiation of antithrombotic activity was also observed on the addition of LA heparin to a HA decasaccharide (M.Wt. 3,000-3,500) with anticoagulant activity only against Factor Xa. The LA heparin content of low molecular weight heparin fractions appears to be an important determinant of their antithrombotic activity.     

Correction for displacement artifacts in 3D phase contrast imaging

PURPOSE: To correct for displacement artifacts in 3D phase contrast imaging. MATERIALS AND METHODS: A 3D phase contrast pulse sequence was modified so that displacements of velocity measurements were restricted to one direction. By applying a postprocessing method, displaced measurements could be traced back to their accurate positions. Flow studies were performed using a phantom that generated flow through a stenosis, directed oblique relative to the phase and frequency encoding directions. Velocity profiles and streamline visualization were used to compare displaced and corrected velocity data to a reference. RESULTS: Velocity profiles obtained from the original measurement showed skewed profiles due to the displacement artifact, both at close proximity to the orifice as well as further downstream. After correction, concordance with the reference improved considerably. CONCLUSION: The displacement artifact, which restricts the accuracy of phase contrast measurements, can be corrected for using the proposed method. Correction of the phase contrast velocity data may improve the accuracy of subsequent flow analysis and visualization.     

Comparison between angiographic right coronary artery motion and echocardiographic tricuspid annulus motion

Objective—To compare echocardiographic M‐mode measurements of tricuspid annulus motion (TAM) with angiographic M‐mode measurements of right coronary artery motion (RAM).

Design—Twenty‐four patients were included and examined by echocardiography before the angiographic examination. The amplitudes and the velocities of TAM and the atrial contribution to the total amplitude of TAM were measured. The obtained values were compared with angiographic M‐mode measurements of RAM at a proximal and a distal site of the second segment of the right coronary artery.

Results—There was no significant difference between several of the echocardiographic M‐mode measurements of TAM and the angiographic M‐mode measurements of RAM. However, the agreement was rather poor for some variables.

Conclusion—Different parameters obtained from echocardiographic TAM are not interchangeable with values from angiographic RAM. If measurements of RAM are to be used in the assessment of right ventricular (RV) function further studies are needed to examine the correlation and agreement between RAM and different methods of measuring RV function, i.e. radionuclide angiography or magnetic resonance imaging.     

Calculation of right ventricular stroke volume in short-axis MR images using the equation of the tricuspid plane

Short-axis (SA) magnetic resonance (MR) images are commonly planned parallel to the left atrioventricular valve. This orientation leads to oblique slices of the right ventricle (RV) with subsequent difficulties in separating the RV from the right atrium in the SA images. The insertion points of the tricuspid valve (TV) in the myocardium can be clearly identified in the right ventricle long axis (RVLA) and four-chamber (4CH) views. The purpose of this study was to develop a method that transfers the position of the tricuspid plane, as seen in the RVLA and 4CH views, to the SA images to facilitate the separation of the RV from the atrium. This methodology, termed Dissociating the Right Atrium from the Ventricle Volume (DRAW), was applied in 20 patients for calculations of right ventricular stroke volume (RVSV). The RVSV using DRAW (RVSV(DRAW)) was compared to left ventricular stroke volumes (LVSV) obtained from flow measurements in the ascending aorta. The RVSV was also determined using the conventional method (RVSV(CONV)) where the stack of images from the SA views are summarized, and a visual decision is made of the most basal slice to be included in the RV. The mean difference between RVSV(DRAW) and LVSV was 0·1 ± 12·7 ml, while the mean difference between RVSV(CONV) and LVSV was 0·33 ± 14·3 ml. Both the intra- and interobserver variability were small using the DRAW methodology, 0·6 ± 3·5 and 1·7 ± 2·7 ml, respectively. In conclusion, the DRAW method can be used to facilitate the separation of the RV and the atrium.     

Telomere length and correlation with histopathogenesis in B-cell leukemias/lymphomas

Telomere length was recently reported to correlate with cellular origin of B-cell malignancies in relation to the germinal center (GC). In this report, we measured telomere length by quantitative-PCR in 223 B-cell lymphomas/leukemias and correlated results with immunoglobulin (Ig) mutation status and immunostainings for GC/non-GC subtypes of diffuse large B-cell lymphoma (DLBCL). Shortest telomeres were found in Ig-unmutated chronic lymphocytic leukemia (CLL) [median telomere to single copy gene value (T/S) 0.33], differing significantly to Ig-mutated CLL (0.63). Contrary to this, mantle cell lymphomas (MCLs) exhibited similar telomere lengths regardless of Ig mutation status (0.47). Telomere length differed significantly between GC-like (0.73) and non-GC-like DLBCLs (0.43), and follicular lymphomas (FLs) had shorter telomeres (0.53) than GC-DLBCL. Hairy cell leukemias, which display Ig gene intraclonal heterogeneity, had longer telomeres (0.62) than FLs and non-GC-DLBCL, but shorter than GC-DLBCL. We conclude that although DLBCL and CLL subsets can be clearly distinguished, telomere length reflects many parameters and may not simply correlate with GC-related origin.