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Introduction: Adult respiratory distress syndrome (ARDS) is a well-described complication of critical illness. We hy-pothesized that rates of comorbid diseases in a population may influence the risk for developing ARDS in trauma pa-tients. This can help plan medical responses., Methods: Patients from the 2017 National Trauma Databank were analyzed. Inclusion criteria were an injury sever-ity score (ISS) of ≥ 2 and 1 or more documented days of mechanical ventilation. Data were analyzed using χ 2 , Student's t test, Mann-Whitney U test, or logistic regression as indicated., Results: Diabetes (odds ratio [OR] 1.33, 95 percent confidence interval [CI] 1.17-1.52), smoking (OR 1.26, 95 per-cent CI 1.13-1.40), transfusion (OR 1.20, 95 percent CI 1.09-1.32), ISS (OR 1.02, 95 percent CI 1.02-1.03), male gen-der (OR 1.22, 95 percent CI 1.10-1.35), decreasing Glasgow coma score (OR 1.04, 95 percent CI 1.03-1.05), and in-creasing abbreviated injury score of the thorax (OR 1.12, 95 percent CI 1.09-1.16) were associated with an increase in risk for developing ARDS., Conclusion: Diabetes and smoking are risk factors for developing ARDS after trauma. Medical response planning in countries with high rates of diabetes mellitus or smoking should take into account a greater need for intensive care and longer patient admissions to field hospitals.

Tuning forks and electronic vibrometers have been used to quantify vibration sensation thresholds, which are thought to be affected early in carpal tunnel syndrome (CTS). The purpose of this study was to identify a reliable testing procedure for a newly designed, computer-controlled vibrometer (PCV50; Ztech, Salt Lake City, UT). Fifty-two patients (mean age 48+/-8 years) with electromyographically confirmed CTS were tested on one occasion. The computer-controlled vibrometer, with a fixed frequency of 50 Hz, used stepwise changes in amplitude to determine vibration sensation threshold. Each patient had three vibrometer measures (trials) taken on the pulp of the third digit of their right and left hands during the first test session and were retested by a single repetition 40 to 60 minutes later (retest). Intraclass correlation coefficients (ICCs) were used to examine several data analysis strategies. The strategy that generated the highest ICCs for both the right and left hands assumed that the first trial was a learning or practice attempt, and compared the average of the second and third trials with the score from the second session (ICC=0.86 and 0.89, respectively). The computer-controlled vibrometer offered an easily administered, quantitative, and comfortable means to assess median nerve function. Using this reliable testing procedure will allow for additional investigations to determine its usefulness in the early detection and accurate quantification of CTS-related impairment.

A hybrid nonlinear regression (NLR) model and a neural network (NN) model, each designed to forecast next-day maximum 1-hr average ground-level O3 concentrations in Louisville, KY, were compared for two O3 seasons--1998 and 1999. The model predictions were compared for the forecast mode, using forecasted meteorological data as input, and for the hindcast mode, using observed meteorological data as input. The two models performed nearly the same in the forecast mode. For the two seasons combined, the mean absolute forecast error was 12.5 ppb for the NLR model and 12.3 ppb for the NN model. The detection rate of 120 ppb threshold exceedances was 42% for each model in the forecast mode. In the hindcast mode, the NLR model performed marginally better than the NN model. The mean absolute hindcast error was 11.1 ppb for the NLR model and 12.9 ppb for the NN model. The hindcast detection rate was 92% for the NLR model and 75% for the NN model.

Freezing lymphocytes in microtest plates instead of vials for the purpose of screening sera for HLA or other cytotoxic antibodies offers the same technical advantages as freezing sera in microtest plates for tissue typing. Plate-loading errors and cell wastage are minimized, and time required for serum screening is greatly reduced. A method for freezing lymphocytes in large numbers of microtest plates for use in serum screening that is simple, reproducible, and inexpensive is described. Cryoprotected lymphocytes dispensed into microtest plates are placed on a metal table that is lowered onto a tray containing 1 cm of liquid nitrogen in a Styrofoam box. The amount of liquid nitrogen in the tray and the height of the metal table above the tray determine the freezing rate of the lymphocytes. Over 100 microtest plates can be frozen per cycle with total cooling uniformity. The materials required for this freezing device can be assembled for less than $400. Commercial freezing units typically cost over $4,000.