Admission level of Gc-globulin predicts outcome after multiple trauma
Background: Actin is the dominating protein in mammalian cells. Release of excessive amounts of actin into the circulation may result in a condition resembling multiple organ failure. The purpose of this study was to determine if admission levels of Gc-globulin can predict survival after multiple tr...
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Published in | Injury Vol. 30; no. 4; pp. 275 - 281 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford
Elsevier Ltd
01.05.1999
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Background: Actin is the dominating protein in mammalian cells. Release of excessive amounts of actin into the circulation may result in a condition resembling multiple organ failure. The purpose of this study was to determine if admission levels of Gc-globulin can predict survival after multiple trauma. Also, we wanted to compare the predictive ability of Gc-globulin with that of the TRISS–Like scoring system.
Methods: Fifty-seven patients with a median ISS 18 (16–75) were included. All patients had a blood sample taken median 42 min after the injury (19–110 min). Serum Gc-globulin was measured by rocket immunoelectrophoresis.
Results: On admission, all patients had significantly reduced levels of Gc-globulin compared with normal controls. Gc-globulin was significantly higher in the group of survivors (
n=41), compared with non-survivors (
n=16). Median 237 mg/l vs. 188 mg/l (
P<0.01). The predictive ability of Gc-globulin regarding death was similar to that of TRISS–Like with positive predictive values of 69%, a negative predictive value of 84%, a sensitivity of 56% and a specificity of 90%.
Conclusions: The predictive value of Gc-globulin regarding survival was similar to that of an established scoring system. Gc-globulin, alone or in combination with other parameters, may serve as a routine tool for early identification of patients at risk after severe injury, increasing the possibility of early intervention. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0020-1383 1879-0267 |
DOI: | 10.1016/S0020-1383(99)00080-7 |