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1.
Nucl Med Commun ; 23(6): 537-44, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12029208

ABSTRACT

A detailed assessment of intra- and inter-reader variation in the interpretation of brain SPECT scans has been performed. A random sample was selected from scans performed at a community/teaching hospital in Seattle. Scans were interpreted independently by three experienced readers who were blinded to all patient information. Forty-eight scans were interpreted twice by each reader, for a total of 288 readings. Readers recorded detailed assessments of individual lesions and overall impressions using a standardized reporting form. Intra-observer agreement as reflected in per cent agreement for severity scores ranged from 65% to 100%. Intra-observer agreement on the 'overall impression' was very good for Alzheimer's pattern (kappa=0.73-1.00), and fair to good for the 'heterogeneous pattern' (kappa=0.30-0.63). Inter-observer agreement, as reflected in per cent agreement, ranged from 29% to 100%. Inter-observer agreement about the 'overall impression' was fair to moderate for Alzheimer's pattern (kappa=0.24-0.54) and was poor for the descriptors 'heterogeneous' and 'normal'. It is concluded that brain SPECT has great potential value in many important conditions. This study demonstrates a need for further work in the areas of pattern definition and reduction of observer variation.


Subject(s)
Brain Diseases/diagnostic imaging , Brain/diagnostic imaging , Nuclear Medicine/standards , Tomography, Emission-Computed, Single-Photon/methods , Tomography, Emission-Computed, Single-Photon/statistics & numerical data , Adult , Aged , Aged, 80 and over , Alzheimer Disease/diagnostic imaging , Cognition Disorders/diagnostic imaging , Dementia/diagnostic imaging , Dementia, Multi-Infarct/diagnostic imaging , Double-Blind Method , Female , Humans , Male , Middle Aged , Observer Variation , Reproducibility of Results , Retrospective Studies , Sensitivity and Specificity
2.
Environ Health Perspect ; 105 Suppl 1: 37-53, 1997 Feb.
Article in English | MEDLINE | ID: mdl-9114276

ABSTRACT

Porphyrias are relatively uncommon inherited or acquired disorders in which clinical manifestations are attributable to a disturbance of heme synthesis (porphyrin metabolism), usually in association with endogenous or exogenous stressors. Porphyrias are characterized by elevations of heme precursors in blood, urine, and/or stool. A number of chemicals, particularly metals and halogenated hydrocarbons, induce disturbances of heme synthesis in experimental animals. Certain chemicals have also been linked to porphyria or porphyrinuria in humans, generally involving chronic industrial exposures or environmental exposures much higher than those usually encountered. A noteworthy example is the Turkish epidemic of porphyria cutanea tarda produced by accidental ingestion of wheat treated with the fungicide hexachlorobenzene. Measurements of excreted heme precursors have the potential to serve as biological markers for harmful but preclinical effects of certain chemical exposures; this potential warrants further research and applied field studies. It has been hypothesized that several otherwise unexplained chemical-associated illnesses, such as multiple chemical sensitivity syndrome, may represent mild chronic cases of porphyria or other acquired abnormalities in heme synthesis. This review concludes that, although it is reasonable to consider such hypotheses, there is currently no convincing evidence that these illnesses are mediated by a disturbance of heme synthesis; it is premature or unfounded to base clinical management on such explanations unless laboratory data are diagnostic for porphyria. This review discusses the limitations of laboratory measures of heme synthesis, and diagnostic guidelines are provided to assist in evaluating the symptomatic individual suspected of having a porphyria.


Subject(s)
Heme/biosynthesis , Porphyrias/etiology , Environmental Exposure , Environmental Health , Humans , Hydrocarbons, Halogenated/toxicity , Lead/toxicity , Metals/toxicity , Porphyrias/diagnosis , Porphyrias/metabolism , Porphyrins/metabolism , Porphyrins/urine
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