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OBJECT Cranial CT (CCT) scans and hospital admission are increasingly performed to rule out intracranial hemorrhage in patients after minor head injury (MHI), particularly in older patients and in those receiving antiplatelet therapy. This leads to high radiation exposure and a growing financial burden. The aim of this study was to determine whether the astroglial-derived protein S100B that is released into blood can be used as a reliable negative predictive tool for intracranial bleeding in patients after MHI, when they are older than 65 years or being treated with antiplatelet drugs (low-dose aspirin, clopidogrel). METHODS The authors conducted a prospective observational study in 2 trauma hospitals. A total of 782 patients with MHI (Glasgow Coma Scale Score 13–15) who were on medication with platelet aggregation inhibitors (PAIs) or were age 65 years and older, independent of antiplatelet therapy, were included. Clinical examination, bloodwork, observation, and CCT were performed in the traumatology emergency departments. When necessary, patients were admitted and observation took place on the ward; in these patients, CCT was performed during their hospital stay. Patients with severe trauma, focal neurological deficits, posttraumatic seizures, anticoagulant therapy, alcohol intoxication, coagulation disorder, blood sampling more than 3 hours after trauma, and unknown time of the trauma were excluded from the study. The median age of the patients was 83 years, and 69% were female. Sensitivity, specificity, and positive and negative predictive values of S100B with reference to CCT findings were calculated. The cutoff of S100B was set at 0.105 μg/L. RESULTS Of the 782 patients, 50 (6.4%) had intracranial bleeding. One patient with positive results on CCT scan showed an S100B level below 0.105 μg/L. Of all patients, 33.1% were below the cutoff. S100B showed a sensitivity of 98.0% (CI 89.5%–99.7%), a negative predictive value of 99.6% (CI 97.9%–99.9%), a specificity of 35.3% (CI 31.9%– 38.8%), and a positive predictive value of 9.4% (CI 7.2%–12.2%). CONCLUSIONS Levels of S100B below 0.105 μg/L can accurately predict normal CCT findings after MHI in older patients and in those treated with PAIs. Combining conventional decision criteria with measurement of S100B can reduce the CCT scan and hospital admission rates by approximately 30%.

Irradiation in the presence of a dye applied to the extracellular space was found to trigger neuronal degeneration in fly photoreceptor neurones. This phenomenon endowed the selected cells with a dark and fine-grained label such that they could be traced and scrutinized for synaptic specializations. It also initiated their phagocytotic removal from the neural network. Various states of degeneration fitting classical descriptions could be achieved by acting upon the light dose. The phenomenon seems to rely on photosensitization of the cell by the dye. The simplicity and precision with which this phenomenon can be induced makes “photo-degeneration” an exciting prospective tool for combined anatomical and physiological studies on (natural) neural networks and may provide a new line of medical applications.