PubMed HealthSearch

PubMed · 7920674

Fiberoptic microtransducer pressure technology: urodynamic implications.

Abstract

The FST 200 is a novel commercially available pressure measurement system that combines microtechnology and fiberoptics and is particularly well suited for invasive urodynamic studies. Pressure recording with this system is highly accurate and reproducible. The pressure curves obtained parallel those from standard water cystometry. Being small and portable, the system lends itself to invasive transurethral monitoring in the privacy of an examination room. Additionally, the 5F catheter size allows the performance of leak point pressures and pressure/flow voiding studies with minimal urethral stenting artifact often seen with larger catheters. The technical aspects of this system are presented.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

W D Belville, S J Swierzewski, G Wedemeyer, E J McGuire. 1993. Fiberoptic microtransducer pressure technology: urodynamic implications.. https://doi.org/10.1002/nau.1930120211

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Adaptive calibration of imaging array detectors.

We present two methods for nonuniformity correlation of imaging array detectors based on neural networks; both exploit image properties to supply lack of calibrations and maximize the entropy of the output. The first method uses a self-organizing net that produces a linear correction of the raw data with coefficients that adapt continuously. The second method employs a kind of contrast equalization curve to match pixel distributions. Our work originates from silicon detectors, but the treatment is general enough to be applicable to many kinds of array detectors like those used in infrared imaging or in high-energy physics.

Calibration

Informatic selection of a neural crest-melanocyte cDNA set for microarray analysis.

With cDNA microarrays, it is now possible to compare the expression of many genes simultaneously. To maximize the likelihood of finding genes whose expression is altered under the experimental conditions, it would be advantageous to be able to select clones for tissue-appropriate cDNA sets. We have taken advantage of the extensive sequence information in the dbEST expressed sequence tag (EST) database to identify a neural crest-derived melanocyte cDNA set for microarray analysis. Analysis of characterized genes with dbEST identified one library that contained ESTs representing 21 neural crest-expressed genes (library 198). The distribution of the ESTs corresponding to these genes was biased toward being derived from library 198. This is in contrast to the EST distribution profile for a set of control genes, characterized to be more ubiquitously expressed in multiple tissues (P < 1 x 10(-9)). From library 198, a subset of 852 clustered ESTs were selected that have a library distribution profile similar to that of the 21 neural crest-expressed genes. Microarray analysis demonstrated the majority of the neural crest-selected 852 ESTs (Mel1 array) were differentially expressed in melanoma cell lines compared with a non-neural crest kidney epithelial cell line (P < 1 x 10(-8)). This was not observed with an array of 1,238 ESTs that was selected without library origin bias (P = 0.204). This study presents an approach for selecting tissue-appropriate cDNAs that can be used to examine the expression profiles of developmental processes and diseases.

Calibration

Determination of chlorate at low microgram/l levels by ion-chromatography with postcolumn reaction.

A new method for the determination of low concentrations of chlorate in natural waters is described. Chlorate is analyzed by ion-chromatography followed by an osmate-catalyzed postcolumn reaction of chlorate with iodide and UV-detection of triiodide. The new osmate catalysis allows to carry out the oxidation of iodide by chlorate at pH 3 instead of 6 M HCl for the uncatalyzed reaction. A detection limit of 5 nM (0.4 microgram/l) chlorate is achieved. The method also allows the simultaneous determination of chlorite, bromate, and nitrite at the low microgram/l level.

Calibration