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  • 1
    ISSN: 1471-0528
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Objective To investigate the magnitude and pattern of the changes in bone mass during five years of continuous and cyclic sequential oestrogen/progestin treatment.Design Prospective study of normal, early postmenopausal women, initially a double-blind, placebo controlled trial, subsequently an open, controlled investigation.Setting Clinical physiology unit of a general hospital.Subjects Sixty-eight normal, early postmenopausal women.Results 1. Continuous treatment resulted in significantly higher lumbar spine bone density than did sequential treatment (P 〈 0.001). Lumbar spine bone density was 19% and 15%, respectively, above that of untreated women after three years and onwards, and 10% and 6%, respectively, above the initial value; 2. Both regimens induced a more pronounced rise in lumbar spine bone density than in forearm bone mineral content (P 〈 0.001); 3. The spontaneous decline (without treatment) in lumbar spine bone density and forearm bone mineral content averaged 1.86% and 1.90% per year, respectively. 4. There was a significant bone loss from the lumbar spine during the last year of active treatment (P 〈 0.001). This would suggest that lumbar spine bone density rises to a certain level and subsequently declines. However, neither data pooled before computation nor data processed individually for each patient over five years allowed for any definite conclusions regarding the pattern of the long term skeletal response to combined oestrogen/progestin treatment.Conclusion Five years treatment with oestradiol/norethisterone resulted in a substantial gain in bone mass. The highest values were found in the axial skeleton with daily administration of 2 mg oestradiol and 1 mg norethisterone. It is likely that bone mass after an absolute rise begins to decline after about four years of treatment.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Osteoporosis international 3 (1993), S. 276-282 
    ISSN: 1433-2965
    Keywords: Bone mineral content ; Bone mineral density ; Fracture risk ; Osteodensitometry ; Osteoporosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Identification of postmenopausal women at risk of developing osteoporotic fractures is a major clinical problem. In this study the use of projected planar lumbar bone density values for individual fracture risk assessment was questioned. Osteodensitometry (DXA) results from 415 normal women, 62 women with previous vertebral compressions, and 76 women with previous low-energy fractures were analyzed, together with their body size and lumbar vertebral body size variables. The following were found: (1) Lumbar vertebral projected bone mineral areal density (BMD) and bone mineral content (BMC) of normal women correlated with body size variables (p〈0.001). (2) Lumbar vertebral body size variables also correlated with body size variables (p〈0.001). Logistic regression analysis of measured and derived physical variables from women without and with vertebral compression fractures (n=477) showed: (3) The best compression fracture discriminator, significantly better than BMD, was BMC divided by (Hmax/165 cm)15×(D/4.35 cm)1.5, where Hmax is the body height (cm) at the menopause, and D the mean lumbar vertebral diameter of the three mid-lumbar vertebral bodies (cm). This parameter was termed BMCcorr.. ROC analysis showed: (4) At a BMCcoor. true positive ratio of 80% the corresponding uncorrected BMC or BMD true positive ratio was only 60%. The corresponding false positive ratio was 6%. Lumbar osteodensitometry could not be used to identify women with a history of peripheral low-energy fractures. (5) BMCcoor. did not, unlike BMC and BMD, correlate with body size and vertebral size variables. (6) Likewise, an observed correlation between BMC and lean body mass in a subpopulation of 116 normal women was abolished when BMCcorr. replaced BMC. We suggest that vertebral compression fracture risk limits based on BMC, corrected for individual differences in body size and vertebral body size, replace the commonly used BMD fracture risk limits. The discriminatory ability of BMCcorr. for low-energy fractures needs to be tested in a different population.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Medical & biological engineering & computing 14 (1976), S. 461-464 
    ISSN: 1741-0444
    Keywords: Whole-body monitor ; Background index ; Spectrum stabiliser
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Description / Table of Contents: Sommaire Il s'agit d'un moniteur de radioactivité du corps intégral. Le moniteur a trois cristaux d'iodure de sodium (T1) mesurant 153 mm de diamètre et 102 mm d'épaisseur. Les détecteurs sont montés sur un chariot en acier, le balayage étant effectué effectué le long d'un axe longitudinal. L'appareil électronique comporte un stabilisateur de spectre qui a réduit au minimum le temps nécessaire au réglage des détecteurs. Grâce à l'indice de fond très faible du compteur, 00.202 compte/min par cm3, ainsi qu à la résolution spectrométrique de 7.1% pour40K, on peut prendre des mesures précises du potassium total du corps à partir de40K en moins de 30 minutes.
    Abstract: Zusammenfassung Es wird ein neues Überwachungsgerät für den ganzen Körper beschrieben, das für den klinischen Einsatz vorgesehen ist. Das Überwachungsgerät hat drei Natriumiodid-Kristalle (T1) von 153 mm Durchmesser und 102 mm Stärke. Die Strahlungs-empfänger sind auf einem Stahlwagen angebracht, und die Abtastung erfolgt über eine Längsachse. Die Elektronik enthält u.a. einen Spektrumsstabilisator, durch den die Zeit zur Einstellung der Strahlungsempfänger sehr reduziert wird. Durch den sehr geringen Störpegelindex des Zählers von 0.202 Zahlen/min pro cm3 sowie die Spektrometerauflösung von 8.1% für40K ergibt sich ein genaues Meßinstrument, das den Gesamt-Kaliumgehalt des Körpers ab40K innerhalb von 30 Minuten messen kann.
    Notes: Abstract A new whole-body monitor for clinical use is described. The monitor has three sodium iodide (TI) crystals, 153 mm in diameter and 102 mm thick. The detectors are mounted on a steel carriage, and scanning is performed along a longitudinal axis. The electronic equipment includes a spectrum stabiliser, which has minimised the time used for adjustment of the detectors. The very low background index of the counter of 0·202 counts/min per cm3, together with the spectrometric resolution of 7·1% for40K, permits precise measurements of total body potassium from40K within 30 min.
    Type of Medium: Electronic Resource
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