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G Koning

Publications and source records attributed to G Koning.

11 recordsLinked to original sources

Angiographic assessment of dimensions of 6F and 7F Mallinckrodt Softouch coronary contrast catheters from digital and cine arteriograms.

Coronary contrast catheters are almost exclusively used for calibration purposes in quantitative coronary arteriography. In this study we have assessed the suitability of new 6F and 7F Mallinckrodt nylon catheter with Softouch tip with improved imaging specifications for such calibration purposes both from digital and cinefilm images using new analytical QCA-software packages (Philips DCI/ACA and Medis CMS). The average signed differences between the angiographically measured dimensions at 100% contrast fillings and acquired at 3 different kV-levels (60, 75 and 90 kV) were -3.3% and 0.6% for the 6F and 7F catheter tips, respectively as measured with the ACA-package on digital images, and -0.4% and 2.1%, respectively, as measured with the CMS-system on cinefilm images. The pooled standard deviations were 0.102 mm and 0.107 mm for the 6F and 7F catheter tips, respectively, as measured with the ACA-package, and 0.080 mm and 0.083 mm, as measured with the CMS-system. The deviations for the nylon shafts were much larger. It became also clear that neither the filling of the catheters, nor the kV-level used, had any appreciable effect on the measurement accuracy for the Softouch tips, which facilitates the frame selection in QCA-studies. From these data it can be concluded that the nontapering parts of the 6F and 7F Mallinckrodt Softouch tips are very well suitable for QCA calibration purposes, but that the nylon shafts are not.

Calibration

Advantages and limitations of two software calipers in quantitative coronary arteriography.

Software calipers allowing the measurement of the distances between pairs of manually defined picture elements in digitized images may be useful tools for a rapid assessment of the morphology of coronary vessels, e.g. for choosing the appropriate balloon or stent sizes before or during cardiac intervention procedures. In this paper we have studied extensively the advantages and limitations of two manual software calipers--one developed for a PC-based cinefilm analysis workstation, the other for the Philips DCI system. Based on analyses of a perspex vessel phantom with 17 sectors of known size filled with different concentrations (50 and 100%) of the contrast agent and acquired at two kV-levels (68 and 92 kV), it was found that the cinefilm approach is characterized by a very small overall (averaged over te data from three observers) systematic overestimation of 0.03 mm, and the DCI system by a systematic underestimation of 0.07 mm; the worst case accuracy value for an individual observer on frames with 100% contrast dye concentration was 0.20 mm for cinefilm, and -0.34 mm for the DCI, respectively. The overall variabilities in the measurements (precision) were almost identical for the two approaches (overall 0.07 and 0.08 mm for the cinefilm and digital approaches, respectively, and worst case for individual observers on the 100% contrast frames, 0.16 and 0.13 mm, respectively. Inverting the images (bright or dark contrast containing structures) of the phantom at 100% contrast concentration and acquired at 62 kV had no significant effect on the results obtained with the cinefilm analysis system (overall accurary -0.12 mm for both situations), whereas it had on the results from the DCI system (overall accuracies -0.29 (dark vessels on bright background) and -0.08 mm (bright vessels on dark background), respectively). Enhancing the digital images on the DCI with unsharp masking techniques did not significantly influence the measurement accuracy and precision. Finally, it was found that woven dacron, polyurethane and polyvinylchloride catheters filled with 100% contrast dye can be measured with an overall accuracy of better than 0.13 mm on the DCI system. On the PC-based system the woven dacron and polyvinylchloride catheters would result in an overall accuracy better than 0.17 mm, and the polyurethane catheter better than 0.30 mm. The evaluation study has made clear that the nylon catheter should not be applied in QCA-studies.(ABSTRACT TRUNCATED AT 250 WORDS)

Cardiac Catheterization

Usefulness of digital angiography in the assessment of left ventricular ejection fraction.

With modern digital cardiac systems the image data are digitized on-line and in real-time, allowing the replay and subsequent interpretation and analysis during or directly after the cardiac catheterization procedure. In this study we have evaluated the advantages and limitations of a manual tracing technique for left ventricular digital angiograms on the Phillips DCI system. Thirty-three patients who were catheterized for suspected coronary artery disease were studied. The manual tracings were performed by a senior cardiologist and an experienced function-analyst. It was found that the short- and long-term intraobserver variabilities in the assessment of the global ejection fraction were very small; short-term mean difference +/- standard deviation (correlation coefficient): 0.5 +/- 2.7 (r = 0.97) global EF%-units; long term; 0.7 +/- 2.7 (r = 0.96) EF%-units. The interobserver variabilities (5.1 +/- 4.8 (r = 0.93) EF%-units) were slightly higher than the intraobserver variabilities. A decrease by 25% in the amount of contrast medium administered did not significantly influence the variabilities in the contour tracings, which would suggest the use of smaller doses. At the average, the cardiologist and the function-analyst required 6 and 11 min of analysis time for a left ventricular study, respectively, emphasizing the need for further developments towards automated contour detection. Finally, an excellent correlation was found with a standard off-line cinefilm analysis procedure. Thus, it may be concluded that quantitative digital left ventricular angiography based on manual tracing of the outlines performed immediately following the cardiac catheterization (post-processing) is feasible as a routine procedure for the assessment of left ventricular function.

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