Embedded indexing with Word. Part 2 - editing entries and making work easier by using macros

In this second article in a series on the under-exploited potential for using Microsoft Word as a tool for embedded indexing, the focus is on editing entries and using macros while the index is being created. This article covers the index entry window, XE fields, separate document templates and exported UI files. It also includes step-by-step instructions for using macros. The first article in the series can be found in The Indexer 38(2), 207-18.

Performance of pirimiphos-methyl based Indoor Residual Spraying on entomological parameters of malaria transmission in the pyrethroid resistance region of Koulikoro, Mali.

Background: Following mosquito vector resistance to both pyrethroid and carbamates, organophosphate (pirimiphos-methyl) was used for the Indoor Residual Spray campaigns performed in 2015 to 2016 in the district of Koulikoro. In this context, we assessed the effect of IRS on malaria transmission by comparing entomological indices in two localities: Koulikoro (LLINs+IRS), and Banamba (LLINs -only) districts. Methods: The study was conducted in two villages of each district (Koulikoro and Banamba). Pyrethrum spray catches and entry window trapping were used to collect mosquitoes on a monthly basis. WHO tube tests were carried out to assess mosquito susceptibility to insecticides. Mosquitoes were identified to species level by PCR and their infection to P. falciparum was detected by ELISA. Results: An. coluzii was the most frequent species. Its density was rainfall dependent in the no-IRS area, and almost independent in the IRS area. The infection rate (IR) in the no-IRS area was 0.96%, while it was null in the IRS area. In the no-IRS area, the entomological inoculation rates (EIR) was 0.21 infective bites /person month with a peak in September. High resistance to pyrethroids and carbamates and susceptibility to organophosphates was observed at all sites. Conclusion: The introduction of pirimiphos-methyl based IRS in the area resulted to a significant decrease in malaria transmission. An.gambiae s.l., the main malaria vector of the area, was resistant to pyrethroids and carbamates, and remained susceptible to the organophosphates.

Performance of Indoor Residual Spray on entomological parameters of malaria transmission using pirimiphos-methyl in the context of pyrethroids resistance in Koulikoro region, Mali.

Background: Following vectors resistance to both pyrethroid and carbamates, organophosphate (pirimiphos-methyl) was used in the Indoor Residual Spray campaigns of 2015 to 2016 in the district of Koulikoro. In this context, we assessed the effect of IRS on malaria transmission by comparing entomological indices in two localities: Koulikoro (LLINs+IRS), and Banamba (LLINs -only) districts. Methods: The study was conducted in two villages of each of Koulikoro and Banamba in 2016. Pyrethroid spray catch and entry window trapping where used to collect mosquitoes monthly WHO bioassay test was used to assess mosquito’s susceptibility to insecticides. Mosquitoes were identified into species by PCR and the infection rate using ELISA. Results: An. coluzii was by far the most frequent species. Its density was rainfall dependent in no-IRS area, and almost independent in IRS area. The IR in the no-IRS area was 1.24%, while in the IRS area, we could not detect infection. In the no-IRS area, the EIR was 0.21 infective bites /person month with the peak in September. High resistance to pyrethroids and carbamates and susceptibility to organophosphates was observed in all sites. Conclusion: A big randomized study is needed to better estimate the added value of the IRS in an integrated malaria control strategy. Key words: Mali, IRS, Long-lasting insecticidal nets, insecticide resistance, transmission.

Abstract WP257: Accuracy of Pre-enrollment Last Known Well Time in a Large Prehospital Stroke Clinical Trial

Background: Clinical trials of stroke therapies require accurate documentation of last known well time (LKWT) to account for injury accumulation prior to treatment start. For prehospital studies, this requirement is particularly challenging, as paramedic-determined and final-determined LKWTs in routine practice are concordant (within 15 mins) in only half of cases. We sought to determine the accuracy of LKWT obtained in the field by a two-tier enrollment system of study-trained paramedics and cellphone-connected physician-investigators. Methods: Paramedics screened consecutive transports for participation in the NIH Field Administration of Stroke Therapy-Magnesium (FAST-MAG) clinical trial. Paramedic screening criteria included LKWT <2 hours. Physician-investigators by cellphone confirmed or refined the LKWT after conversation with paramedics and patients or legally authorized representative. Prehospital LKWT was compared with post-arrival LKWT determined by trained study nurses after ED arrival by speaking with patients, family and other sources. We describe the number of enrollment calls with inaccurate LKWT at the paramedic-screening level and at the post paramedic plus physician-investigator telephone screening level. Results: A total of 4458 post-screening enrollment calls were made by paramedics from January 2005 to December 2012 of which 539 (12%) were determined by physician-instigators to have inaccurate LKWT leading to non-enrollment. Of the remaining 3919 calls, 1700 led to enrollments in the study and 2219 were not enrolled for a reason other than inaccurate LKWT. Among enrolled cases, exact congruence between prehospital and post-arrival LKWTs occurred 72% (n=1220), concordance within 15 minutes in 87%, within 30 minutes in 93%, and within 1 hour in 97%. Among enrolled cases, final-determined LKWT was within the study entry window of 2h in 96.3%. Conclusions: A 2-tiered system of paramedic screening followed by physician-investigator cellphone assessment led to high congruence between prehospital-determined and post-arrival-determined of LKWT. This system can be used in future trials of prehospital, paramedic-in initiated stroke therapy when accuracy of LKWT is important for intervention evaluation.

Bag-1 Internal Ribosome Entry Segment Activity Is Promoted by Structural Changes Mediated by Poly(rC) Binding Protein 1 and Recruitment of Polypyrimidine Tract Binding Protein 1

ABSTRACT We have shown previously that an internal ribosome entry segment (IRES) directs the synthesis of the p36 isoform of Bag-1 and that polypyrimidine tract binding protein 1 (PTB-1) and poly(rC) binding protein 1 (PCBP1) stimulate IRES-mediated translation initiation in vitro and in vivo. Here, a secondary structural model of the Bag-1 IRES has been derived by using chemical and enzymatic probing data as constraints on the RNA folding algorithm Mfold. The ribosome entry window has been identified within this structural model and is located in a region in which many residues are involved in base-pairing interactions. The interactions of PTB-1 and PCBP1 with their cognate binding sites on the IRES disrupt many of the RNA-RNA interactions, and this creates a largely unstructured region of approximately 40 nucleotides that could permit ribosome binding. Mutational analysis of the PTB-1 and PCBP1 binding sites suggests that PCBP1 acts as an RNA chaperone to open the RNA in the vicinity of the ribosome entry window while PTB-1 is probably an essential part of the preinitiation complex.

Faraday Cup for Electron Flux Measurements on the Microtron MT 25

The basic criteria for constructing of an evacuated Faraday cup for precise measurement of 5 to 25 MeV electron beam currents in air from a microtron are established. The Faraday cup, built in the microtron laboratory of the Faculty of Nuclear Sciences and Physical Engineering of CTU Prague, is described together with the electronic chain and its incorporation in the measuring line on the beam. Measures to reduce the backward escape of electrons are explained. The range of currents is from 10–5 to 10–10 A. The diameter of the Al entry window of the Faraday cup is 1.8 cm, and its area is 2.54 cm2. The thickness of the entry window is 0.1 mm.