Biomedical subjects

W M Ivie

Publications and source records attributed to W M Ivie.

4 recordsLinked to original sources

PubMed1989

Multicenter evaluation of TDx test for assessing fetal lung maturity.

"TDx Fetal Lung Maturity," an automated assay that measures the relative concentrations of surfactant and albumin in amniotic fluid, was compared with the lecithin/sphingomyelin (L/S) ratio and phosphatidylglycerol determination at five clinical sites. A total of 695 amniotic fluid samples were analyzed, of which 312 were followed by delivery of the infant within three days of sample collection. Of these 312, 24 developed respiratory distress syndrome and seven developed transient tachypnea. With the cutoff for maturity set at a surfactant/albumin value of 50 mg/g, the assay showed a sensitivity of 0.96 and a specificity of 0.88 for all samples, compared with a sensitivity of 0.96 and a specificity of 0.83 for the L/S ratio. The combination of rapid assay (30 min), accurate results, and uniformity among testing centers makes the TDx assay a very promising method.

Albumins↗

PubMed1987

Effect of albumin and lamellar bodies on fluorescence polarization of amniotic fluid.

Using a probe and procedure developed for the Abbott TDx analyzer, we investigated the influence of albumin on fluorescence polarization of amniotic fluid. Polarization readings increased when albumin was added to either "mature" or "immature" amniotic fluids. Albumin added to a fraction rich in lamellar bodies (10,000 X g pellet) greatly increased polarization readings, but albumin added to the lamellar-body-free fraction resulted in only small increases. Adding increasing amounts of the lamellar-body-rich fraction from mature and immature pools to a constant amount of albumin decreased the polarization readings. We saw no correlation between amniotic fluid polarization and albumin concentration but found a significant correlation between polarization values and either total extractable phospholipids (r = 0.725, P less than 0.001) or the ratio albumin/total extractable phospholipids (r = 0.784, P less than 0.001). The concentration of albumin in amniotic fluid was variable and correlated poorly with gestational age.

Albumins↗

PubMed1987

Modified lamellar body phospholipid assay compared with L/S ratio and phosphatidylglycerol assay for assessment of fetal pulmonary status.

We used a modified lamellar body phospholipid (LB-PL) assay to evaluate the effect of sample processing and to evaluate the clinical efficacy of LB-PL determinations. Within-run and between-run CVs for the modified LB-PL assay respectively ranged from 2.9 to 6.7% and from 3.4 to 14.3%. Freezing and storage at -20 degrees C did not affect results for LB-PL (n = 12). Statistically significant amounts of lamellar bodies were lost on centrifugation, ranging from 20% at 150 X g to 54% at 1000 X g for 5 min. The LB-PL content, lecithin/sphingomyelin ratio, and phosphatidylglycerol content of 194 samples of amniotic fluid obtained within three days of delivery were compared for the assessment of fetal pulmonary maturity. Twenty-three neonates developed respiratory problems at or shortly after birth. With uncontaminated samples (n = 160), the LB-PL assay exhibited better specificity than the lecithin/sphingomyelin ratio (p less than 0.01, Chi square) or the phosphatidylglycerol assay (p less than 0.001, Chi square) for samples obtained after 36 weeks of gestation. Assay sensitivities did not differ significantly. Differences among assay predictive values were not significant.

Amniotic Fluid↗

PubMed1986

Mid-molecule parathyroid hormone assay comparison.

Parathyroid hormone (PTH) assays are becoming available to clinical chemistry laboratories for in-house use. We evaluated the clinical utility of two mid-molecule PTH assays in comparison to a sensitive but technically demanding component assay. A normal reference population, and an abnormal population including cases of primary and secondary hyperparathyroidism, hypoparathyroidism, and humoral hypercalcemia of malignancy were tested. PTH determinations with each assay system and total serum calcium determinations were done on all specimens. The Endocrine Metabolic Center (EMC) kit assay and the Immuno Nuclear Corp. (INC) kit assay demonstrated adequate standard curve reproducibility and precision for clinical use. With the aid of calcium determinations each assay performed well in the separation of abnormal patient groups, and in the separation of abnormal from normal PTH-calcium homeostasis. PTH values for the reference population differed among the three assays. The component assay and the EMC assay had a negative correlation with serum calcium, but the INC assay had a positive correlation with serum calcium.

Calcium↗