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Träfflista för sökning "WFRF:(Axelsson Bertil) srt2:(2000-2004)"

Sökning: WFRF:(Axelsson Bertil) > (2000-2004)

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1.
  • Axelsson, Bertil (författare)
  • The incurable cancer patient at the end of life : Medical care utilization, quality of life and the additive analgesic effect of paracetamol in concurrent morphine therapy
  • 2001
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • Only 12% of the patients died at home. When the period between diagnosis and death was less than one month, every patient died in an institution. Younger patients, marriedpatients, and those living within the 40 km radius of the hospital utilized more hospital days. The "length of terminal hospitalisation" and the "proportion of days at home/ total inclusion days" seemed to be feasible outcome varibles when evaluating a palliative support service. The hospital-based palliative support service in this study defrayed its own costs due to a median saving of 10 hospital days/patient, compared with matched historical controls.A 19-item quality of life questionnaire (AQEL) was developed which evidenced good signs of reliability and validity. The item most closely correlated to global quality of life was the sense of meaningfulness. This was true for both patients and their spouses. Patients´ levels of pain and anxiety did not increase at the end of life. In this study we could not find convincing evidence for an additive analgesic effect of paracetamol in morphine therapy of pain in cancer patients.
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2.
  • Gustafsson, Agnetha (författare)
  • Evaluation of attenuation and scatter corrections in lung and brain SPECT
  • 2001
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • Single Photon Emission Computed Tomography (SPECT) is used to image functional processes in the human body. The image process is affected by physical effects such as attenuation, scatter, spatial resolution and statistical noise. The aim of this work was to investigate how attenuation and scatter effects and their associated correction methods affect the image quality in lung and brain SPECT.The effects of attenuation and scattering on the image of a uniform activity distribution in the lungs was investigated using Monte Carlo simulated data and the attenuation effect was evaluated in healthy volunteers. The homogeneity was measured as the CV inside a well-defined lung contour. The attenuation effect in lung SPECT was estimated to be about 13-14% expressed as the CV. The homogeneity improved with increasing accuracy of the attenuation correction method. After attenuation correction the remaining inhomogeneity in healthy subjects was considerable and could not be explained by statistical noise and camera non-uniformity. A non-uniform attenuation correction was thus required and a TCT-based density map was found to be adequate in most instances.The accuracy of the attenuation correction methods was studied in Monte Carlo simulated brain SPECT using the normalised mean square error, NMSE. The different degrees of accuracy in the methods were also reflected in the absolute deviation of the relative regional cerebral blood flow (rCBF) according to the min-max method. The NMSE value improved with the accuracy of the attenuationcorrection method. The difference in relative rCBF value was generally less than 5%. Therefore, it is unlikely that the choice of attenuation correction method will affect the diagnostic accuracy.The detectability, expressed as the contrast-to-noise-ratio dependence on the choice of energy window, was evaluated using SPECT studies of a thorax phantom containing cold lesions inside the lungs and a realistic brain phantom. The effects of subtractive scatter correction methods such as the dual-window method (DW), the triple-energy-window method (TEW) and the Klein-Nishina method (KN) were also evaluated. An optimal photopeak window setting was found to be 128-154 keV in lung SPECT for a gamma camera with 10% energy resolution, and 130-154 keV in rCBF SPECT for a gamma camera with 9% energy resolution. The detection limit for lung SPECT for spherical lesions is about 2 cm in diameter when normal variations in the lungs are relatively small compared with the statistical noise level. Under these conditions the detectability is degraded by using scatter correction, except when the TEW scatter correction is used for small lesions (<3 cm in diameter), when about the same detectability is achieved.
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4.
  • Johansson, Bertil, et al. (författare)
  • Isodicentric 7p, idic(7)(q11.2), in acute myeloid
  • 2001
  • Ingår i: Genes, Chromosomes and Cancer. - 1045-2257. ; 30:3, s. 261-266
  • Tidskriftsartikel (refereegranskat)abstract
    • Three adult de novo acute myeloid leukemias (AML M1, M2, and M4) with an isochromosome 7p are presented. No additional abnormalities were deterred by G-band and multicolor, using combined binary ratio labeling, fluorescence in situ hybridization (FISH) analyses, indicating that the i(7p) was the sole. i.e., the primary, chromosomal aberration. Although the patients were elderly-68, 72, and 78 years old-they all responded very well to chemotherapy, achieving complete remission lasting more than a year. Further FISH analyses, using painting, centromeric, as well as 7q11.2-specific YAC probes, revealed that the i(7p) contained two centromeres and that the breakpoints were located in 7q11.2. Thus, the abnormality should formally be designated idic(7)(q11.2). The detailed mapping disclosed a breakpoint heterogeneity, with the breaks in 7q11.2 varying among the cases, being at least 1,310 kb apart. Furthermore, the breakpoints also differed within one of the cases, being located on both the proximal and the distal side of the most centromeric probe used. Based on our three patients, as well as on a previously reported 82-year-old patient with AML M2 and idic(7)(q11) as the only chromosomal change, we suggest that this abnormality, as the sole anomaly, is associated with AML in elderly patients who display a good response to induction chemotherapy and. hence, have a favorable prognosis. Furthermore, the heterogeneous breakpoints in 7q11.2 suggest that the important functional outcome of the idic(7)(q11.2) is the genomic imbalance incurred, i.e., gain of 7p and loss of 7q material, rather than a rearrangement of a specific gene.
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