88 research outputs found

    Description of an Evidence-Based Elective in Complementary and Alternative Medicine

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    This paper describes a new elective course in complementary and alternative medicine (CAM) for second or third year Doctor of Pharmacy students. Prior to this elective, students received approximately 10 contact hours of lecture primarily focusing on herbal products. This CAM course included different types of CAM therapies including Oriental medicine, acupuncture, massage, homeopathy and naturopathy, energy therapies, mind-body, and biological products. A session on research techniques and the difficulties of doing research in CAM topics was held early in the course. All material provided was evidence-based. Students were required to make an oral presentation and write a short referenced paper on a CAM topic of their choice. The hands on demonstration and practice of massage techniques and the acupuncture demonstration were the best received sessions

    Protective effect of prostacyclin on postischemic acute renal failure in the rat

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    Protective effect of prostacyclin on postischemic acute renal failure in the rat. Infusion of prostacyclin (PGI2) reportedly attenuates renal ischemic injury in the dog and the rat. In the dog, PGI2 is a potent renal vasodilator; in the rat a direct action on the renal vasculature is not always apparent. To determine whether or not the protective effect of PGI2 on postichemic ARF was hemodynamically mediated, studies were performed in uninephrectomized Sprague–Dawley rats before and after a 40 minute period of complete renal artery occlusion. In response to the preischemic infusion of PGI2 for 30 minutes at 160 ng/kg body wt/min i.v. (N = 7), MAP and RBF fell to 86 ± 7% (P < 0.0001) and 84 ± 9% (P < 0.05) of baseline values, respectively. RVR initially declined to 81 ± 9% of baseline values (P < 0.025) but returned to 102 ± 13% of baseline values prior to the period of ischemia. Following the period of ischemia, reflow of blood in the rats receiving PGI2 was delayed when compared to rats not receiving PGI2 (N = 1). RBF returned to only 76 ± 19% of the initial values in PGI2-treated rats (P < 0.01) but to 90 ± 12% of the initial values in rats receiving buffer alone (NS). Observations made during the ensuing 48 hours in animals treated with either 80 (N = 8) or 160 ng/kg/body wt/min (N = 7) for 30 minutes before and four hours after the period of ischemia indicated that renal function improved to a greater extent in the PGI2-treated animals than in buffer–treated animals (N = 15) as judged by significantly–greater mean values of V, UOsm, UCr and CCr. On the second day after ischemia, CInwas significantly greater in PGI2-treated animals than in the postischemic animals receiving buffer alone (77 ± 45 vs. 33 ± 20 µl/min/100 g body wt; P < 0.05) despite the fact that no differences were found in the mean values of RBF (3.59 ± 1.08 vs. 3.43 ± 0.32 ml/min/100 body wt. Blinded analysis of the histological sections revealed significantly less evidence of tublar epithelial cell necrosis in the PGI2-treated animals (P < 0.005). The data indicate that the protective effect of PGI2 on the renal response to ischemic injury in the Sprague–Dawley rat is not related to changes in RBF or RVR. Instead, the beneficial effect of PGI2may be a result of cytoprotective properties as has been demonstrated in other tissues

    Measured energy expenditure of tube-fed patients with severe neurodevelopment disabilities

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    Objective: To determine measured resting energy expenditure (REE) of nonambulatory tube-fed patients with severe neurological neurodevelopmental disabilities. Methods: Twenty patients were prospectively studied. Only steady state indirect calorimetry measurements were taken. All measurements were conducted using a canopy system. Nutritional needs were met entirely by enteral feedings via a permanent ostomy. Results: REE was widely distributed from 16 kcals/kg/day to 39 kcals/kg/day. The mean REE (888 ±176 kcals/day) of the patients was significantly (p \u3c 0.01) lower than predicted as estimated by the Harris-Benedict equations (1081 ± 155 kcals/day) and World Health Organization equations (1194 ± 167 kcals/day). Fat-free mass (FFM) was the best parameter for predicting REE. Two predictive equations were developed that are not significantly biased and more precise (≤ 15% error) than conventional predictive formulas. Conclusion: Conventional formulas for estimating energy expenditure are inaccurate and generally overestimate measured energy expenditure of nonambulatory patients with severe developmental disabilities

    Comparison of arterial plasma amino acid concentrations in rats fed ad lib oral chow or parenteral nutrition via intravenous or gastric infusion

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    Abstract from the 22nd Clinical Congress of the American Society for Parenteral and Enteral Nutrition, Orlando, FL, January 18-21, 1998

    Enhancement of peritoneal dialysis clearance with docusate sodium

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    A study was done in rabbits to determine the effect of docusate sodium (DSS) on the peritoneal clearance of creatinine and urea. Following a series of control exchanges with a commercially available peritoneal dialysis solution, three animals in each of four groups received DSS (0.005%, 0.01%, 0.02%, or 0.04%) in a single exchange, followed by 10 subsequent exchanges of control fluid. Creatinine and urea clearances were measured for each exchange. Comparison of post-DSS clearances (exchanges 5 through 15) with pre-DSS baseline values (exchanges 1 through 4) showed a mean percent increase in creatinine clearance that was proportional to the concentration and ranged from 74% to 244% above baseline. Similarly, urea clearance increased by 79 to 166%. The effect on both creatinine and urea clearance persisted through the completion of the dialysis procedure. No animals showed signs of toxicity from DSS. The mechanism of the DSS effect on clearance is unknown. Although studies are needed to delineate the mechanism of the effect and to identify potential toxic effects, the results of this study indicate that DSS has a significant effect on clearance of both creatinine and urea

    Measured energy expenditure of nonambulatory patients with severe neurodevelopmental disabilities

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    Abstract from American College of Clinical Pharmacy 1997 Annual Meeting, Phoenix, AZ, November 9-12, 1997

    Sequential group trial to determine gastrointestinal site of absorption and systemic exposure of azathioprine

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    Azathioprine (AZA) is used in the treatment of patients with refractory inflammatory bowel disease; however, its use is limited because of systemic toxicity associated with long-term use. Ileocecal delivery of AZA might be advantageous if local intestinal therapeutic effects could be provided with decreased systemic side effects. Decreased cecal systemic absorption would allow higher dosages of AZA to be administered. A two-phase study was performed to compare the systemic exposure of AZA and 6-mercaptopurine (6-MP) following administration of AZA into the stomach, jejunum, and cecum and to compare the systemic exposure to AZA and 6-MP following administration of three different dosages of AZA into the cecum. In phase I, six healthy male volunteers received three 50 mg sequential doses of AZA via an oral tube directly placed into the stomach, jejunum, and cecum, respectively. In phase II, six healthy male volunteers received three different dosages (50, 300, 600 mg of AZA) into the cecum. Plasma concentrations of AZA and 6-MP at various times were quantified and area under the plasma concentration-time curve (AUC) and mean residence time (MRT) were determined. No significant differences in the AUC of AZA were seen at the different sites. The AUC of 6-MP following administration of AZA into the jejunum (67.0 ± 30.1 ng × hr/ml) was higher compared to the stomach (39.9 ± 38.1 ng/hr/ml) and cecum (29.2 ± 10.9 ng × hr/ml). Jejunal absorption was 68% higher than absorption from the stomach and 129% higher than that of the cecum. Gastric absorption was 27% higher than that of the cecum. Increased dosages given into the cecum resulted in increased AUCs of AZA and 6-MP. The AUCs of AZA following 50, 300, and 600 mg dosages were 16.9 ± 7.4, 52.3 ± 67.2, and 132 ± 151 ng × hr/ml, respectively, and the AUCs of 6-MP were 22.2 ± 14.9, 63.4 ± 50.6, and 104 ± 115 ng × hr/ml, respectively. Systemic exposure to 6-MP is reduced following administration of AZA into the cecum, most likely secondary to reduced absorption of 6-MP from the colon. Higher dosages of AZA presented to the cecum do result in increased systemic absorption, but may still allow more drug to be administered with less toxicity than the same dose received orally

    Exploring the disk-jet connection from the properties of narrow line regions in powerful young radio-loud AGNs

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    We investigate the optical emission-line flux ratios of narrow-line regions, in order to determine whether the formation of AGN jets requires specific accretion conditions. We find that bright compact radio galaxies, which are powerful radio galaxies in the early stage of the jet activity, exhibit systematically larger flux ratios of [O{\sc i}]λ\lambda6300/[O{\sc iii}]λ\lambda5007 and smaller flux ratios of [O{\sc iii}]λ\lambda5007/[O{\sc iii}]λ\lambda4363 than radio-quiet (RQ) Seyfert 2 galaxies. Comparing the observed line ratios with photoionization models, it is found that the difference in the flux ratio of low- to high-ionization lines (e.g., [O{\sc i}]λ\lambda6300/[O{\sc iii}]λ\lambda5007) can be well understood by the difference in the spectral energy distribution (SED) of ionizing sources. Powerful young radio-loud (YRL) AGNs favor SED without a strong big blue bump, i.e., a radiatively inefficient accretion flow (RIAF), while RQ AGNs are consistent with the models adopting SED with a strong big blue bump, i.e., a geometrically thin, optically thick disk. These findings imply that the formation of powerful AGN jets requires the accretion disk with harder ionizing SED (i.e., a RIAF). We discuss the obscuring structure of YRL AGNs as a plausible origin of the difference in flux ratios of [O{\sc iii}]λ \lambda5007/[O{\sc iii}]λ\lambda4363.Comment: 17 pages, 8 figures, accepted for publication in Ap
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