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23. Computertomographie zur Beurteilung des Beckenrings und des Acetabulums (1983)

Rath, M. ; Dittmer, H. ; Lissner, J.

Springer

Langenbeck's archives of surgery 361 (1983), S. 169-172

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ISSN: 1435-2451

Keywords: Computed tomography ; Pelvic injuries ; Computertomographie ; knöcherne Beckenverletzungen

Source: Springer Online Journal Archives 1860-2000

Topics: Medicine

Description / Table of Contents: Zusammenfassung Wegen der komplexen anatomischen Verhältnisse im Beckenbereich ist die exakte Beurteilung von Frakturen mittels konventioneller röntgenologischer Methoden oft schwierig. Durch die computertomographische axiale Ebene ergibt sich ein wesentlich anschaulicheres und genaueres Bild der Ausdehnung und des Verlaufs der Fraktur, der Gelenkverhältnisse und der Anzahl, Lage und Größe der Fragmente. Stufenbildungen und Interpositionen kleiner knöcherner Fragmente der Hüftpfanne sind sicher nachzuweisen. Weiterhin werden die biomechanisch wichtigen Verletzungen des hinteren Beckenrings sicher erfaßt.

Notes: Summary Pelvic fractures are often difficult to evaluate by conventional tomography due to the complex bony structures of the pelvis. Axial CT scans clearly show the extent of the fracture, location and size of fragments. Abnormalities of the hip joint space, like loose bone fragments are easy to demonstrate. Furthermore the biomechanically important injuries of the sacroiliac joint and sacrum are more often detected by computed tomography.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1007/BF01275848

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Pharmacokinetic data of propranolol enantiomers in a comparative human study with (S)- and (R,S)-propranolol (1989)

Lindner, W. ; Rath, M. ; Stoschitzky, K. ; [et al.]

New York, NY [u.a.] : Wiley-Blackwell

Chirality 1 (1989), S. 10-13

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ISSN: 0899-0042

Keywords: (S)-, (R,S)-propranolol ; pharmacokinetic ; human study ; Chemistry ; Organic Chemistry

Source: Wiley InterScience Backfile Collection 1832-2000

Topics: Chemistry and Pharmacology

Notes: The pharmacokinetics of (S)-propranolol were compared after the oral administration of a 40 mg dose of the pure enantiomer and an 80 mg dose of a racemic mixture of (R,S)-propranolol. The results of this study indicate that the bioavailability of (S)-propranolol, as expressed by the mean area uner the concentration-time curve (AUC) and maximum serum concentration, is lower after 40mg of the optically pure drug than after the racemic drug.

Additional Material: 2 Ill.