Biomedical subjects
Publications and source records attributed to M Kormano.
Preoperatively and postoperatively, patellar motion in 11 knees with chondromalacia was analyzed by MRI at 0 degrees, 10 degrees, 20 degrees, and 30 degrees of knee flexion. The preoperative patellar position clearly deviated from normal at 0 degrees-10 degrees of knee flexion. The lateral release operation corrected this deviation.
Negative gastrointestinal contrast enhancement can be achieved by oral administration of superparamagnetic particles. Their feasibility for the MR imaging of the female pelvis and lower abdomen was evaluated in studies on 32 follow-up patients with treated gynaecologic cancer. All the applied doses (0.2-1.0 mg particles/ml given in a volume of 600-800 ml) of contrast medium decreased the intraluminal signal. However, there was unpredictable individual variation in segmental distribution, and in some cases only a limited contrast effect was obtained. Image distortion was detected when the applied particle concentration exceeded 0.5 mg/ml, especially of the sagittal sections.
Intramuscular hemorrhage was induced by injecting autologous blood into the paraspinal muscle of 8 rabbits. In order to evaluate the time-dependent changes of hemorrhage observed on MRI, the animals were imaged at different stages of blood resolution at 0.02 tesla (T), and control examined with ultrasound using a 7.5 MHz linear transducer. Six inversion recovery sequences (TR = 1,000 ms. TE = 30 ms, and TI = 18, 48, 148, 201, 302, and 398 ms) were used for the in vivo calculation of T1 relaxation times. IR 1,000 (398)/30 imaging was performed before and after the Gd-DOTA administration. The hemorrhage was evident on MR images throughout the study, especially on the T2 weighted (SE 1,000/100) images. MRI showed the healing lesion longer than ultrasound. The T1 relaxation time increased during the time of resolution. Lesions on days 4 to 7 enhanced in intensity after the injection of Gd-DOTA.
Blood echogenicity was measured in four patient groups with circulatory disturbances (myocardial infarction, stroke, claudication, and deep venous thrombosis) at hospital admission and one week later. The recording was done by an A-mode ultrasonic method at three shear rates down to 4.1 s-1. The rheological effects of adding an anti-aggregatory drug, naftidrofuryl, was tested in vitro at concentrations ranging from 10(-8)-10(-6) M. Echogenicity was lowest in blood from healthy volunteers and significantly greater in blood from patients with claudication. The in vitro addition of naftidrofuryl significantly lowered the echogenicity of blood samples taken from patients with venous thrombosis in the lower extremities. The authors suggest that increased blood echogenicity, which can be pharmacologically manipulated, may be a nonspecific indicator of disease.
We investigated the effect of radiographic contrast media (RCM) on red blood cell (RBC) aggregation by analyzing echogenicity of flowing blood before and after the addition of 2%, 20%, 50% or 95% volume of undiluted meglumine diatrizoate, iohexol, sodium meglumine ioxaglate, or iopamidol and equiosmolar volume concentration of saline. This was done both by stepwise increasing the concentration with minimal mixing and by stepwise decreasing the concentrations with more efficient mixing. All contrast media caused a drop in blood echogenicity after a proper mixing when compared with saline addition. After minimal stirring, both meglumine diatrozoate and iohexol caused a significant increase in blood echogenicity at volume concentrations over 50%. The paper demonstrates that earlier findings of both increased and decreased RBC aggregation following exposure to RCM can be reproduced and that the result depends on experimental setup. In diatrizoate and iohexol RBC aggregates disappear after mixing (increasing the shear rate) or when the RCM/blood mixture is diluted. After dispersement, the abnormal RBC aggregates will not reform.
The correlation of roentgenographic findings, clinical history, and incipient disc degeneration (DD), diagnosed with magnetic resonance imaging, was analyzed in young patients with low-back pain (LBP). One or more lumbar discs were abnormal in 57% of the 20-year-old LBP patients (n = 75) and in 35% of the asymptomatic controls (n = 34) in MRI. Narrowed disc spaces and alterations attributed to lumbar Scheuermann's disease, shown on the radiographs, were always associated with DD in MRI. Such a strong relationship was not observed with transitional vertebrae, spondylolisthesis, spina bifida, or postural abnormalities. However, an increased weight, a positive straight leg raising test, and a reduced lumbar mobility was consistent with an increase in frequency of DD. Magnetic resonance imaging is a safe and sensitive method for studying the presence and etiologic factors of DD.
Magnetic resonance imaging was used to analyse the patellofemoral relationships during the first 30 degrees of knee flexion in women with recurrent patellar dislocation. The patellofemoral joints were imaged both sagittally and axially with the knee flexed 0 degrees, 10 degrees, 20 degrees, and 30 degrees. At the beginning of knee flexion the sulcus angle was greater than in unaffected women, the lateral patellofemoral angle was smaller, the patella displaced further laterally, tilted more laterally and the congruence angle was directed more laterally. At 30 degrees of knee flexion these differences were less marked than at 0 degree to 10 degrees. Logistic regression analysis showed that the sulcus angle at 10 degrees of knee flexion was the most diagnostic feature, indicating that there is an anatomical predisposition to recurrent dislocation and that pathological patellar tracking starts from the beginning of flexion. Traditional sunrise radiographic films taken at 25 degrees to 30 degrees knee flexion clearly miss diagnostically important information.
Conventional plain radiography, with or without flexion and extension images, is still the primary imaging modality of the lumbosacral spine despite the modern imaging methods. This is due to the simplicity of the technique and the good anatomical detail of the bone structure. Despite the limited information content of the plain radiographs, they are needed to serve as anatomical maps in connection with computed tomography or magnetic resonance imaging. In some institutions magnetic resonance imaging is now the primary modality for the evaluation of the lumbosacral spine, in others computed tomography and myelography still have a primary role, often depending on the availability of the devices. Magnetic resonance imaging clearly shows the anatomy of the discs, spinal nerves and dural sac. The diagnostic precision achieved with computed tomography in the evaluation of a herniated disc may also be achieved with magnetic resonance imaging. Differentiation of epidural scar from recurrent or residual disc herniation in patients with previous laminectomy, which with computed tomography myelography has been unreliable, can be evaluated by using magnetic resonance imaging enhanced with gadolinium-DTPA. The identification of facet joint disease is, however, less efficient with magnetic resonance imaging. Computed tomography and magnetic resonance imaging are probably nearly comparable in their accuracy in the evaluation of patients with sciatica. If cost and availability were not limiting factors, magnetic resonance imaging could provide an excellent screening technique for identifying individuals who would benefit from the identification of risks or preclinical disease or from institution of preventive measures.(ABSTRACT TRUNCATED AT 250 WORDS)
Flexion and extension radiographs of 75 young males with low back pain disclosed abnormal segmental motion of the lumbar spine in 16 patients with translational movements in 20 intervertebral segments. These 16 patients were further investigated by magnetic resonance imaging to assess disc degeneration in the unstable segments. On T2-weighted images of the 20 segments, the disc was normal in 13 and degenerated in only 7 patients. Thus, the initial factor in lumbar instability in young patients with low back pain is not always degeneration of the disc.
We have analyzed the normal patellar motion during the first 30 degrees of knee flexion by magnetic resonance imaging (MRI). Ten males and 10 females without knee symptoms were examined. The patellar articulation was imaged both sagittaly and axially with the knee flexed 0, 10, 20, and 30 degrees. The axial images were produced through the middle of the patellar articular cartilage. When the knee was in extension compared to 30 degrees flexion, the sulcus angle was greater, the lateral patellofemoral angle was smaller, there was more lateral patellar displacement, the patella tilted more laterally, and the congruence angle was directed more laterally. Differences between males and females were found.
Both normal and experimentally hydronephrotic rabbits were imaged at 0.02 T using partial saturation (PS 160/30) and inversion recovery (IR 1000/200/40) sequences. The signal intensity of normal renal medulla and cortex markedly increased after the injection of 0.1 mmol/kg of Gd-DOTA. In the unilateral total hydronephrosis the dilated renal pelvis did not contrast enhance after 15 and 35 min of Gd-DOTA injection. The enhancement pattern was similar in 1- and 3-week-old hydronephrosis. The effect of Gd-DOTA on renal T1 times at 0.02 T was studied using rats. Fifteen minutes after the Gd-DOTA injection (0.1 mmol/kg) the T1 times of excised rat kidneys decreased from 311 to 90 ms. The authors conclude that the enhancement of the MR signal of the kidney by Gd-DOTA at an ultralow magnetic field (0.02 T) is similar to its enhancement at higher fields (greater than 0.15 T).
The effect of contrast media (CM) dilution on contrast enhancement was studied using CM representing four structurally different molecular types at osmolalities ranging from 135 to 1340 mosm/kg. Diatrizoate (ionic monomer), iopamidol (nonionic monomer), ioxaglate (ionic dimer), and iodecol (nonionic dimer) were each given at a dose of 500 mgI/kg and at concentrations of both 300 and 150 mgI/mL. Contrast media concentrations were measured using iodine 125I. Tissue blood volumes were determined using human serum albumin labeled with 131I. For each of the four CM at each of the two concentrations and after each of five time intervals following injection (0, 15, 40, 120, and 300 seconds), five rats were killed (total = 200 rats). Blood and 14 other tissues were studied. Dilution of the CM did not lead to any lower iodine tissue concentrations, iodine distribution volumes, plasma volumes, or hematocrit. The authors conclude that lowering CM osmolality by dilution with water should improve tolerance without affecting CT contrast enhancement.
The effect of radiographic contrast media on zymosan-induced phagocytic activity of human blood samples was studied with an automatic luminometer. At iodine concentration of 0.2% biliary contrast media almost totally inhibited leukocyte phagocytosis. The effects of iohexol and iopamidol were nearly identical, eg, negligible inhibition at 0.05% and about 65% inhibition at 1%. Metrizamide, iodixanol, and iopentol cause no or little inhibition at concentrations 0.05% and 0.2% and about 50% inhibition at the concentration of 1% iodine. Among ionic contrast media, sodium salts inhibited leukocyte phagocytosis in vitro less than methylglucamine salts. Because the chemiluminometric method is rapid and easily reproducible even in large series, it may be useful in toxicity surveys of potential contrast media.
An intravenous injection of 153Gd-labeled gadolinium-DTPA or gadolinium chloride was given to 60 rats, which were killed either 15, 40, 120, 300, 900, or 3600 seconds later. Tissue concentrations of gadolinium in the blood, liver, spleen, stomach, pancreas, renal cortex, renal medulla, lungs, heart, adrenals, gluteal muscle, fat, skin, thymus, brain, thyroid, and parathyroids were measured. Five animals were killed at each time interval with gadolinium-DTPA, and at each of the latter four time intervals (15 and 40 seconds excluded) with gadolinium chloride. The pharmacokinetics of gadolinium-DTPA and chloride differ markedly in terms of tissue concentration, distribution volumes, and the time course of these parameters. Gadolinium, when injected as a chloride, evidently forms insoluble carbonate and phosphate precipitates in the blood, which are taken up by the reticuloendothelial system. The distribution of gadolinium-DTPA on dynamic MRI should closely parallel the distribution of iodinated contrast media on dynamic computed tomography.
The effect of 0.1 mmol gadolinium-DTPA on ultralow field magnetic resonance (MR) images of intracranial neoplasms was studied on 20 patients. Tumors that characteristically were enhanced markedly on computed tomography (CT) (meningiomas, acoustic neuromas) demonstrated moderate to marked contrast enhancement with inversion recovery sequences and with saturation recovery sequences with a short repetition time. Standard spin-echo sequences failed to show any contrast effect. The enhancement of gliomas and metastases was weak and often absent. Contrast enhancement, when present, was helpful in delineating the tumor from surrounding edema but the differentiation of living from necrotic tumor was not successful because of low signal intensity. The low effect of gadolinium-DTPA at 0.02 T may be due to a relatively higher T2 weighting of available pulse sequences. The relaxing effect of macromolecules may also change the proportional effect of paramagnetic substances in an ultralow magnetic field.
The brains of 42 newborn infants were examined with MRI at 0.02 T field, and regional variations of T1 relaxation time were measured from the images. There were three groups: 1. full term infants (9), 2. preterm infants (10) and 3. SGA (= small for gestational age) infants (20). Relaxation times showed a correlation to myelination of the brain. The brain of SGA infants showed a large variation in their T1 values.
Particulate iodipamide ethyl ester, a new hepatolienographic x-ray contrast agent, was intravenously injected into rats. Lung and kidney biopsies taken at various intervals after the injection were examined by light and electron microscopy. IDE particles could be found in the lung capillaries phagocytized by polymorphonuclear neutrophils (PMNs). There were also free particles in the alveolar capillaries in the samples taken 5 min to 4 hours after the injection. No aggregates or emboli were seen. Two days or more after the injection no intra- and extracellular particles were present. The PMNs underwent transient local hydropic degeneration; the lung cells were morphologically intact. In the kidneys, the particles first appeared in both cortical and medullary capillaries. No emboli were observed. The kidney cells did not ingest IDE, but polymorphonuclear neutrophils (PMNs) with ingested IDE were often seen loosely attached to the glomerular capillary walls. In addition, free particles were evident in the capillaries in the samples taken up to 1 hour after injection. All particles in subsequent kidney samples were located in PMNs in the glomeruli. After three or more days the renal tissue was totally devoid of particulate IDE. No morphological evidence of kidney cell injury was observed.
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