Biomedical subjects
H Johansen
Publications and source records attributed to H Johansen.
[Pendulum nystagmography].
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Absorption and dissolution characteristics of 14 different oral chloramphenicol preparations tested on healthy human male subjects.
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[Telemetric monitoring of rumen activity in cattle. 1. Material and experimental method].
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[Telemetric monitoring of rumen activity in cattle. 2. Full-day monitoring after 2 different types of ration].
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[Intraruminal pressures in a cow with rumen indigestion].
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Osteogenesis imperfecta. Light and electron microscopic studies of the stapes.
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Electrnic structure of the proflavine cation.
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The electronic spectra of the isomers of reduced l-alkyl-nicotinamide.
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Calculation of the electric structures and spectra for corrin and related compounds.
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[Some of the recent advances in the field of radiotherapy].
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The independent radiotherapy center.
From the beginning of this century radiology has embraced two widely different medical fields: diagnosis and therapy. The fundamental differences between these have grown ever more obvious with radiotherapy's playing such an important factor in the treatment of malignant diseases; the specialty has now been recognized as an independent therapeutic discipline at several medical schools. The development of the Radium Center in Copenhagen into an independent radiotherapy center is discussed and the importance of centralized radiotherapy is emphasized.
Cander risk in intraductal papilloma and papillomatosis.
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[Otosclerosis operation using the Shea method].
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Results of 200 otosclerosis operations a.m. Shea.
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Bioavailability of digoxin tablets.
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Does simple mastectomy followed by irradiation offer survival comparable to radical procedures?
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Differentiation of myocardial ischemia and necrosis by technetium 99m glucaric acid kinetics.
BACKGROUND: Current clinical approaches may not always be helpful in the early differentiation of necrotic tissue from ischemic viable myocardium in patients with acute myocardial infarction. Tc-99m-glucaric acid is a carbohydrate ligand that may permit differentiation of necrosis from ischemia. However, the myocardial kinetics of Tc-99m-glucaric acid have not been well defined early after myocardial injury. The aim of this study was to evaluate the effect of necrosis in comparison to postischemic injury alone on the kinetics of Tc-99m-glucaric acid with the use of an isolated perfused rat heart model. METHODS AND RESULTS: Three groups of hearts were studied: group I: control (n = 6); group II: postischemia (15 minutes of no flow with complete reperfusion, n = 6); and group III: necrosis (90 minutes of no flow to induce necrosis with complete reperfusion, n = 6). Tc-99m-glucaric acid (1.3 +/- 0.6 mCi/L of buffer) was perfused for 30 minutes to evaluate tracer accumulation. Then tracer-free buffer was perfused for 45 minutes to evaluate clearance. The peak accumulation relative to the control group mean was significantly increased (p < 0.01) in group III (necrosis) (254% +/- 75%) compared with control (100% +/- 10%) and compared with postischemia (108% +/- 26%). On kinetic data analysis, the monoexponential clearance rate constant: (kc) was significantly reduced with necrosis (control: kc = 20.2 +/- 14.0 x 10(-4) sec-1; postischemia: kc = 22.3 +/- 15.2 x 10(-4) sec-1; and necrosis: kc = 1.2 +/- 0.3 x 10(-4) sec-1; p < 0.05). A retention fraction was calculated from the activity after 45 minutes of clearance corrected for the peak activity for each group. The necrotic group had significant myocardial retention in comparison to control and postischemia (control: 12% +/- 8%; postischemia: 14% +/- 16%; necrosis: 64% +/- 10%; p < 0.01). CONCLUSIONS: The accumulation and retention of Tc-99m-glucaric acid is markedly increased in the presence of myocardial necrosis in comparison to control and postischemic myocardial injury. In this model, Tc-99m-glucaric acid is capable of defining the presence of necrotic myocardial injury in comparison to postischemic injury alone. This agent may have potential application for the early differentiation of ischemic from necrotic myocardium in acute myocardial infarction.