Compression depth estimation for CPR quality assessment using DSP on accelerometer signals

Chest compression is a vital part of cardiopulmonary resuscitation (CPR). This paper demonstrates how the compression depth can be estimated using the principles of inertia navigation. The proposed method uses accelerometer sensors, one placed on the patient's chest, the other beside the patient. The acceleration-to-position conversion is performed using discrete-time digital signal processing (DSP). Instability problems due to integration are combated using a set of boundary conditions. The proposed algorithm is tested on a mannequin in harsh environments, where the patient is exposed to external forces as in a boat or car, as well as improper sensor/patient alignment. The overall performance is an estimation depth error of 4.3 mm in these environments, which is reduced to 1.6 mm in a regular, flat-floor controlled environment.     

Arbitrary spot location diffractive beam-splitting elements

Diffractive beam-splitting elements are typically designed for replicating beams on positions belonging to an equidistant grid in the spatial spectrum. The parameter of the output grid follows directly from the period of the beam-splitter transmission through the grating equation. Our objective is to develop design strategies allowing a more accurate positioning of the replicated beams. Issues occurring when the output grid parameter is decreased below the output beam width are discussed and shown to be avoidable. Furthermore, a design algorithm is introduced, which permits an arbitrary positioning of the replicated beams. This algorithm is constructed for high computational efficiency by utilizing fast Fourier transform operations in the major part of its iterations.     

Exploring Problems with Function Analysis. Experimental Insights for Team Management

Problem analysis is an important, but mainly neglected part of the problem‐solving process. The theory of inventive problem solving (TRIZ) offers an instrument called function analysis to conduct problem analysis, which is especially useful for exploring a problem. This process is based on an idea applied in different creativity techniques, saying that behind one problem statement many problem formulations may occur, which allows for evaluation and selection of those problem formulations before looking for problem solutions. The application of function analysis as a tool for teams is recommended for a number of reasons. In so doing so, two main questions arise: (i) Should function analysis be used with the help of an external moderator? and: (ii) Should it be applied with currently available special software? After introducing the basics of function analysis this article provides key findings deducted from an experiment addressing these questions. An important result is the remarkable learning effect, which occurs while using function analysis in teams. By applying function analysis in R&D, companies will be able to get deeper and team‐based problem explorations, which may lead to maturing problem solutions.     

On Scheduling in a Semi-Ordered Flow Shop Without Intermediate Queues

The dynamic programming solution offered is of complexity O(n²) and is a significant improvement over the implicit enumeration procedure previously suggested by Arora and Rana in an article in the September 1980 issue of TRANSACTIONS.     

Identification of the Sex Pheromone of the Currant Shoot Borer Lampronia capitella

Under an artificial light:dark cycle, females of Lampronia capitella were observed calling, with extended terminal abdominal segments, during the first 2 hr of the photoperiod. Extracts of terminal abdominal segments from females elicited large electroantennographic responses from male antennae. Gas chromatography with electroantennographic detection revealed three active peaks. Based on comparison of retention times and mass spectra of synthetic standards, these compounds were identified as (Z,Z)-9,11-tetradecadienol and the corresponding acetate and aldehyde. The electroantennographic activity of the four geometric isomers of all three compounds was investigated, and the respective (Z,Z)-isomer was found to be the most active in all cases. Aldehydes generally elicited larger antennal responses than alcohols, whereas acetates were the least active compounds. A subtractive trapping assay in the field, based on a 13:26:100 micrograms mixture of (Z,Z)-9,11-tetradecadienal, (Z,Z)-9,11-tetradecadienyl acetate, and (Z,Z)-9,11-tetradecadienol confirmed that all three compounds are pheromone components. Subtraction of (Z,Z)-9,11-tetradecadienol from the blend completely eliminated its attractiveness, whereas the other two-component blends showed reduced activity. This is the first pheromone identification from the monotrysian superfamily Incurvarioidea, confirming that the common pheromones among ditrysian moths (long-chain fatty acid derivatives comprising alcohols, acetates, and aldehydes with one or more double bonds) is not an autapomorphy of Ditrysia, but a synapomorphy of the more advanced heteroneuran lineages.     

A setup for the coupling of a thin-layer electrochemical flow cell to electrospray mass spectrometry

A novel setup for the coupling of a commercially available thin-layer cell to electrospray mass spectrometry (ESI-MS) which allows the electrochemical reactions at the counter electrode to be straightforwardly separated from the flow into the mass spectrometer has been developed. In this way, interferences from reaction products formed at the counter electrode can be minimized. This reduces the risk of changes in the mass spectra as a result of electrochemical reactions in the solution. The described setup also enables the working electrode to be positioned close to the electrospray (ESI) emitter without the need for a grounding point or a long transfer line between the electrochemical cell and the electrospray emitter. By decoupling the electrochemical reactions in the flow cell and those in the electrospray emitter, improved facilities for studies of electrochemical reactions are obtained through a better control of the potential of the working electrode. The setup has been used to study the oxidation of a drug (Olsalazine), which previously has been found to involve chemical follow-up reactions. It is also demonstrated that uncharged thiols can be detected in ESI-MS after spontaneous adsorption on a gold working electrode, followed by oxidative desorption to yield sulfinates or sulfonates. This adsorption and potential-controlled desorption has been used for the preconcentration of micromolar concentrations of 1-hexanethiol as well as for desalting of solutions containing micromolar concentrations of thiols. The results indicate that the present on-line coupling of an electrochemical cell to ESI-MS provides promising possibilities for sample preconcentration, matrix exchange (including desalting), and ionization of neutral compounds, such as thiols.