Multi-site reliability and validity of a diagnostic pattern-recognition knowledge-assessment instrument.
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Biomedical subjects
Publications and source records attributed to J Swaney.
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The concentrations of prostaglandin F (PGF) and its major metabolite, 13,14-dihydro-15-keto prostaglandin F-2 alpha (PGFM), were measured in caruncular and intercaruncular endometrium of pregnant and non-pregnant ewes on Days 9, 11, 13 and 15 after mating (Day 0) and related to the content of PGF and PGFM in the uterine flushings. The tissue concentrations of PGF and PGFM increased with time after mating particularly on Days 13 and 15 and to a greater extent in pregnancy. However, the ratio of PGF to PGFM remained constant at 0.7, except on Day 15 in non-pregnant endometrium when it fell to 0.3 (P less than 0.05), suggesting that synthesis rather than metabolism was limiting tissue concentrations of PGs. The changes in tissue concentrations of PGF and PGFM were reflected in the contents of PGF and PGFM in the uterine flushings of non-pregnant, but not pregnant ewes. Pregnant ewes had relatively more PGF and less PGFM than did non-pregnant ewes on Day 15. Moreover, there was always 5-10-fold less PGFM than PGF in the uterine flushings. It is concluded that the increase in PG in the uterine lumen in pregnancy has its origin in the blastocyst, and that pregnancy may be associated with an increase in the synthesis and retention of PGs in the endometrium, rather than a redistribution towards the uterine lumen away from the uterine venous drainage.
The rate of protein synthesis was higher in caruncular (P less than 0.05) and intercaruncular endometrium (P less than 0.01) of pregnant compared to non-pregnant ewes on Day 11 (Day 0 = day of oestrus), but not on Days 9, 13 and 15. Cytosolic oestrogen receptor concentrations (nmol/mg protein) were lower in caruncular endometrium of pregnant ewes than in non-pregnant ewes on Days 9 (P less than 0.02), 13 (P less than 0.05) and 15 (P less than 0.001) but not on Day 11. In intercaruncular endometrium, the receptor values were lower on Day 15 (P less than 0.02) of pregnancy compared to non-pregnancy, but not on the other days. The dissociation constant (0.75-2.55 x 10(-10) M) of oestradiol-17 beta for cytosolic receptors was similar in both tissues, regardless of pregnancy status or day of sampling. The rate of protein synthesis was generally higher in intercaruncular endometrium whereas cytosol receptor concentrations were higher in caruncular endometrium. When the blastocyst was confined to one uterine horn on Day 2 in another group of ewes, there was a decrease in nuclear (P less than 0.05), cytosolic (P less than 0.05) and total (P less than 0.05) oestrogen receptors only in caruncular endometrium in the pregnant horn on Day 15. There were no difference in the proportions of receptors localized in nuclear fractions or in the rate of protein synthesis in either endometrial tissue from the pregnant or the non-pregnant horn. We conclude that the ovine blastocyst is capable of influencing oestrogen receptors levels in caruncular and intercaruncular endometrium by a local action as early as Day 9, well before endocrine recognition of pregnancy on Day 12 and attachment on Day 15.
The pharmacokinetics of tobramycin were evaluated in 50 pediatric patients (two to 18 years of age) with malignancies and normal renal function. Patients receiving either 240 or 300 mg/m2 per 24 hr (8 or 10 mg/kg per 24 hr) divided into doses given every 4 hr had peak serum concentrations (mean +/- standard error) of 3.10 +/- 0.23 microgram/ml and 4.23 +/- 0.25 microgram/ml, respectively, at the end of a 1-hr infusion. Serum concentrations at 4 hr were 0.82 +/- 0.15 and 1.05 +/- 0.15 microgram/ml, respectively. The half-life of the drug was 96.6 min and was inversely correlated with age of the patients. The total clearance rate of tobramycin was 164 +/- 15 mg/min per 1.73 m2 and was directly correlated with age. The mean volume of distribution was 0.42 +/- 0.038 liter/kg and was inversely correlated with age. No accumulation of tobramycin was noted, and no side effects occurred. If therapeutic serum concentrations of tobramycin are to be achieved and maintained in children, the currently recommended dose and frequency of administration should be changed to 300 mg/m2 per 24 hr given in divided doses every 4 hr.