Role of Error-Recovery Process in Projects

To reduce errors in projects, knowledge about their causes, through examining their chain of events, and costs should be made available. With this in mind, this paper examines the role of the error recovery process in detecting human-related errors with reference to seven Swedish building construction projects. A total of 2,879 human errors were identified, and those that were found to be the most costly were examined in detail. Industry practitioners’ opinions as to how the identified errors could have been prevented were solicited. It was revealed that the major areas of error reduction lay with improving communication between participants, introducing incentives, improving resourcing levels in projects particularly during design, and the encouragement of individual and organizational learning. The paper concludes by suggesting that the most effective learning takes place in projects when the entire error-recovery process is performed (i.e., detection, indication, and correction) and not parts thereof.     

Use of magnetic nanoparticles as nanosensors to probe for molecular interactions

Biocompatible magnetic nanosensors have been designed to detect molecular interactions in biological media. Upon target binding, these nanosensors cause changes in the spin-spin relaxation times of neighboring water molecules, which can be detected by magnetic resonance (NMR/MRI) techniques. These magnetic nanosensors have been designed to detect specific mRNA, proteins, enzymatic activity, and pathogens (e.g., virus) with sensitivity in the low femtomole range (0.5-30 fmol).     

Surface-functionalized nanoparticle library yields probes for apoptotic cells

We have developed techniques for the efficient synthesis and screening of small libraries of surface-functionalized nanoparticles for the recognition of specific types of cells. To illustrate this concept we describe the development of a nanoparticle that preferentially recognizes apoptotic Jurkat cells in a manner similar to the apoptosis-recognizing protein annexin V. The nanoparticle, which is detectable by fluorescence or NMR relaxometry, was analyzed for the ability to recognize normal and apoptotic cells by fluorescence-activated cell sorting (FACS) analysis and fluorescence microscopy. The capability to develop nanoparticles which interact with specific target cells could be applied to the design of materials for diverse applications including quantum dots, which serve as fluorescence tracers, colloidal gold, which serves as a tracer for electron micrographs, or the crystalline forms of drugs.     

Transnasal endoscopic repair of congenital choanal atresia: long-term results

Somatic mutations in the RET proto-oncogene are involved in the pathogenesis of an important subset (40-60%) of sporadic medullary thyroid carcinomas (MTCs) and less frequently (0-31%) in benign, sporadic phaeochromocytomas. Since limited data exist regarding the significance of somatic RET mutations in malignant phaeochromocytomas, we analysed a multicentre series of proven malignant (i.e., metastasised) phaeochromocytomas. Analogous with MTCs, where RET mutations lead to an aggressive behaviour, we hypothesised that somatic mutations would occur more frequently in malignant than in benign phaeochromocytomas. Paraffin-embedded tissue was available from 29 malignant and 27 benign phaeochromocytomas. Exons 10, 11 and 16 were analysed by non-radioactive single-strand conformation polymorphism, heteroduplex gel electrophoresis, restriction enzyme digestion and aberrant band patterns by non-isotopic sequencing. In only 1 of 29 malignant phaeochromocytomas was a mis-sense mutation found (at codon 634 of exon 11), whereas in 15% (4/27) of the benign tumours a point mutation was detected (in 3 tumours in exon 16 at codon 918 and in 1 tumour in exon 10 at codon 618). Absence of these mutations in non-tumourous DNA proved their somatic origin. Contrary to what has been reported for MTCs, oncogenic RET mutations are not associated with an aggressive tumour behaviour in sporadic phaeochromocytomas.     

Procainamide induced change of the width of the zone of entrainment and its relation to the inducibility of reentrant ventricular tachycardia

Procainamide depresses conduction velocity and prolongs refractoriness in myocardium responsible for reentrant VT, but the mechanism by which the induction of VT is suppressed after procainamide administration remains to be determined. In the present study, the relationship between electrophysiological parameters and the noninducibility of VT was assessed during procainamide therapy with a special reference to the change of an excitable gap. Clinically documented monomorphic sustained VT was induced in 30 patients and, utilizing the phenomenon of transient entrainment, the zone of entrainment was measured as the difference between the cycle length of VT and the longest paced cycle length interrupting VT (block cycle length) which was determined as the paced cycle length decreased in steps of 10 ms, and used as an index of the excitable gap. The effective refractory period was measured at the pacing site and the paced QRS duration was used as an index of the global conduction time in the ventricle. The cycle length of VT, the block cycle length, and the width of the zone of entrainment were determined and compared between the responders and nonresponders. In 15 patients, these parameters were determined at the intermediate dose and related to subsequent noninducibility at the final dose. At the final doses of procainamide, VT was suppressed in 8 (26.7%) of 30 patients. However, the cycle length of VT, the block cycle length, and the width of the zone of entrainment were unable to predict the drug efficacy, i.e., noninducibility. The change in the effective refractory period at the pacing site or the width of the paced QRS duration was not different between the responders and nonresponders. Among the variables, only the width of the zone of entrainment showed a significant narrowing in the responders at the intermediate dose of procainamide, and it was smaller than that of the nonresponders. The significant narrowing of the width of the zone of entrainment was associated with the subsequent noninducibility of VT at the final dose. The present study showed that the baseline cycle length of VT, the block cycle length, the drug induced change of the effective refractory period, or the paced QRS duration was not a predictor of the noninducibility after procainamide administration. However, a significant narrowing of the width of the zone of entrainment at the intermediate dose was associated with the noninducibility of VT at the final dose.     

Synthesis and Preliminary Evaluation of [11C]GNE-1023 as a Potent PET Probe for Imaging Leucine-Rich Repeat Kinase 2 (LRRK2) in Parkinson's Disease

Leucine-rich repeat kinase 2 (LRRK2) is a large protein involved in the pathogenesis of Parkinson's disease (PD). It has been demonstrated that PD is mainly conferred by LRRK2 mutations that bring about increased kinase activity. As a consequence, selective inhibition of LRRK2 may help to recover the normal functions of LRRK2, thereby serving as a promising alternative therapeutic target for PD treatment. The mapping of LRRK2 by positron emission tomography (PET) studies allows a thorough understanding of PD and other LRRK2-related disorders; it also helps to validate and translate novel LRRK2 inhibitors. However, no LRRK2 PET probes have yet been reported in the primary literature. Herein we present a facile synthesis and preliminary evaluation of [¹¹C]GNE-1023 as a novel potent PET probe for LRRK2 imaging in PD. [¹¹C]GNE-1023 was synthesized in good radiochemical yield (10 % non-decay-corrected RCY), excellent radiochemical purity (>99 %), and high molar activity (>37 GBq μmol⁻¹). Excellent in vitro binding specificity of [¹¹C]GNE-1023 toward LRRK2 was demonstrated in cross-species studies, including rat and nonhuman primate brain tissues by autoradiography experiments. Subsequent whole-body biodistribution studies indicated limited brain uptake and urinary and hepatobiliary elimination of this radioligand. This study may pave the way for further development of a new generation of LRRK2 PET probes.     

Identifying management research priorities

An agenda for management research can be set by the academic community with more or less input from practising managers. The purpose of this note is to describe a model for collecting, structuring and analysing practitioner views of what should be the priorities for construction management research. A meeting with construction sector participants gave rise to proposals that were consolidated into 20 management themes. Next, a questionnaire sent to 260 individuals received 140 responses where these themes had been ranked and the strength of recent industry development for each theme assessed. Results show that high priority was assigned to leadership issues and identification of customer needs. The process should be possible to replicate abroad, although cultural differences are expected to influence priorities.     

A smart manufacturing methodology for real time chemical process diagnosis using causal link assessment

Industrial chemical plant diagnosis is the task of analyzing process data to sufficiently pinpoint the causes of abnormal events as fast and as accurately as possible so corrective action can be taken in a timely manner. The need to identify failures explicitly and support human centered decision making becomes pronounced for enterprises. Qualitative diagnostic models offer robustness in capturing diagnostic behaviors when there is little or no data on fault conditions. This article develops, analyzes, and demonstrates a qualitative diagnostic methodology called Causal Link Assessment (CLA). CLA avoids the drawbacks of other methodologies while leveraging several new concepts that include dynamic pattern generation, single time step modeling with multitime step interpretation, and discretized, low granularity dynamic modeling. CLA is demonstrated for an existing ethylene production facility. Model building, robustness, reusability, unaccounted for faults and failures and alignment with emerging Smart Manufacturing infrastructure concepts are discussed. © 2016 American Institute of Chemical Engineers AIChE J, 62: 3420–3431, 2016     

Production of synthesis gas by partial oxidation and steam reforming of biomass pyrolysis oils

As the lowest cost biomass-derived liquids, pyrolysis oils (also called bio-oils) represent a promising vector for biomass to fuels conversion. However, bio-oils require upgrading to interface with existing infrastructure. A potential pathway for producing fuels from pyrolysis oils proceeds through gasification, the conversion to synthesis gas. In this work, the conversion of bio-oils to syngas via catalytic partial oxidation over Rh–Ce is evaluated using two reactor configurations. In one instance, pyrolysis oils are oxidized in excess steam in a freeboard and passed over the catalyst in a second zone. In the second instance, bio-oils are introduced directly to the catalyst. Coke formation is avoided in both configurations due to rapid oxidation. H₂ and CO can be produced autothermally over Rh–Ce catalysts with millisecond contact times. Co-processing of bio-oil with methane or methanol improved the reactor operation stability.