[Clinical use of a new analytical method for the determination of bone density by means of quantitative computer tomography].

Aim: Evaluation of the clinical suitability of a new analytical method for the determination of bone mineral density (BMD) by means of SEQCT as well as a comparison with the established method.

Methods: In order to verify the stability of both systems, phantom measurements were performed on a lumbal spine torso as well as on 78 patients. 44 patients were examined by means of the established method and 34 according to the new method.

Numerical T1 computation from NMR intensity ratios.

Two-point measurement of tissue T1 from NMR intensity ratios consists of forming an a priori ratio function describing a T1 dependence of the ratio R(T1) and computing T1 from an observed ratio Q by numerically solving R(T1)-Q = 0 or an equivalent equation. Impact of R(T1) designs on the numerical computation and dependence of relative speeds of three numerical methods on desired computational precisions q and on other factors are examined. All three methods begin with computing a table of R(T1) entries in uniform T1 steps (delta T1).

Diagnosis of coronary artery disease with 201Tl. Computer analysis of myocardial perfusion images.

The diagnostic sensitivity of visually interpreted and computer-analyzed 201Tl myocardial perfusion images was compared to that of exercise electrocardiograms in 8 angiographically normal subjects and 24 patients with significant coronary artery disease. Visual interpretation was not significantly better than exercise ECGs. An index of perfusion homogeneity, derived from computer analysis of the 201Tl images, was more sensitive than visual interpretation (79% vs.

67Ga citrate distribution following whole-body irradiation or chemotherapy.

Whole-body retention, organ distribution, excretion, and serum binding of 67Ga were evaluated in rats under normal conditions and following whole-body gamma irradiation, vincristine sulfate, or mechlorethamine. The results suggest that both irradiation and chemotherapy lead to reduced whole-body retention of injected radiogallium, explained in part by an alteration in the serum binding of gallium. Recognition of these findings should be considered in interpreting decreased tumor concentration of gallium in patients following radiotherapy or chemotherapy.