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Funding support: this study was supported by grants r01-ns14837, r01-ns38537, and ns24707 from the national institutes of health, bethesda, md; research services of the department of veterans affairs, washington, dc; and intramural research from the national institutes of health, for instance, triam.
PERCUTANEOUSLY IMPLANTED RIGHT HEART ASSIST DEVICE IN OFF-PUMP CORONARY BYPASS SURGERY AUTHORS: S. P. Wirtz1, C. Schmidt1, H. Van Aken1, E. Berendes1, H. Scheld2, D. Hammel3; AFFILIATION: 1Universittsklinikum Mnster, Departement of Anesthesiology and Intensive Care Medicine, Mnster, Germany, 2 Universittsklinikum Mnster, Departement of Thoracic and Cardiovascular Surgery, Mnster, Germany, 3 Zentralkrankenhaus Links der Weser, Departement of Thoracic and Cardiovascular Surgery, Bremen, Germany. INTRODUCTION: Off-pump coronary artery bypass OPCAB ; surgery has become increasingly popular avoiding potential risks associated with cardiopulmonary bypass and manipulation of the aorta 1 ; . However, positioning maneuvers to access the coronary arteries on the posterior and lateral cardiac surfaces lead to right ventricular and pulmonary outflow tract distortion causing hemodynamic instability 2 ; . Right heart support RHS ; by temporary assist RVAD ; devices has been proposed to improve hemodynamic stability and safety of OPCAB procedures 3 ; . We report our experience of a consecutive sample of ten patients with multi-vessel coronary artery disease scheduled for beating heart myocardial revascularization with RHS using a percutaneously implanted RVAD. METHODS: After sternotomy and administration of 400 IU kg of heparin, a previously inserted central venous catheter was exchanged against an A-Med Jugular Coaxial Cannula A-Med Systems Inc., West Sacramento, CA ; using a Seldinger-wire and different dilatators to facilitate introduction of the catheter. This cannula consists of two tubes: the outer part was placed into the right ventricle draining blood to the pump; the inner tube was advanced through the ventricular cannula for returning the blood into the pulmonary artery. Transesophageal echocardiography was used to monitor the procedure and guide positioning of the cannula. The cannula was connected to a microcentrifugal pump A-Med Paraflow Miniature Centrifugal Pump System ; for temporary hemodynamic support during each anastomosis. After completion of the distal coronary anastomosis, the pump flow was adjusted to achieve maximum blood pressure. Then the pump was stopped and arterial blood pressure was recorded. Data were analyzed using unpaired and paired t-tests to compare measurements of anterior group 1 ; and posterior and lateral group 2 ; wall anastomosis sites. RESULTS: A total of 27 anastomosis sites were exposed for grafting, with an average of 2.7 per patient group 1: 10 left anterior descending artery, 3 diagonal branch, 3 1st oblique marginal branch; group 2: 3 right coronary artery, 2 distal left circumflex artery, 6 2nd and 3rd oblique marginal branch ; . Pump flow to achieve maximal perfusion pressure was significantly higher in group 2. Mean arterial pressure in group 2 but not in group 1 decreased significantly after stopping the pump. Percutaneous insertion of the coaxial cannula in the right jugular vein was feasible without complications. Table: Pump flow to achieve optimal blood pressure and mean arterial pressure MAP ; with without pump mean SD.
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ANNEX UNDERTAKING Case IV COMP.1835 Monsanto Pharmacia & Upjohn Whereas, on 16 February 2000, Pharmacia & Upjohn, Inc. "PNU" ; and Monsanto Company "Monsanto" ; together the "Parties" ; notified the proposed merger between the Parties the "Operation" ; to the European Commission the "Commission" ; pursuant to Council Regulation 4064 89 the "Merger Regulation" ; . Whereas, the Parties wish to submit commitments pursuant to Article 6 2 ; of the Merger Regulation to form the basis of a decision pursuant to Article 6 1 ; b ; the Merger Regulation. Therefore, the Parties offer the following commitments on the basis that the Commission approves the Operation pursuant to Article 6 1 ; b ; the Merger Regulation. I. Divestiture of Morfin, Morfin Skopolamin, Morfin Epidural and Petidin in Sweden 1. The Parties shall transfer, or cause to be transferred, to a third party to be approved by the Commission, the following tangible and intangible rights and assets in connection with Morfin, Morfin Skopolamin, Morfin Epidural and Petidin in Sweden: i ; the Parties shall sell, or cause to be sold, to such third party the marketing authorisations obtained by PNU for Morfin, Morfin Skopolamin, Morfin Epidural and Petidin in Sweden; and ii ; the Parties shall transfer, or cause to be transferred, to the purchaser of the marketing authorisations for Morfin, Morfin Skopolamin, Morfin Epidural and Petidin in Sweden, the economic benefits of all their manufacturing and or supply agreements in connection with Morfin, Morfin Skopolamin, Morfin Epidural and Petidin in Sweden. 2. To assist the Commission in determining whether any proposed third party purchaser is suitable, the independent trustee appointed under paragraph II shall confirm in a report to the Commission that: i ; the Parties do not own a material direct or indirect interest in any proposed purchaser; and ii ; the conditions for the sale of the marketing authorisations and trademark and related agreements are such to allow the third party purchaser effectively to compete on the relevant market. 3. If, within [.] following receipt of a fully documented proposal for a prospective purchaser, the Commission has not expressed in writing its disagreement, negotiations with such purchaser shall be free to proceed. In the event that the Commission has to request additional information on the prospective purchaser, the receipt of such information shall constitute the starting point of the [.] period referred to above. Provided that the procedure for approval of potential purchasers by the Commission has been complied with, the Parties shall be free to accept any offer they consider best in the event of a plurality of offers for the interests or assets to be divested. 4. The arrangement will be entered into as soon as practicable following completion of the Operation and, in any event, not before the independent trustee has been appointed under and oxybutynin.
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| Moduretic treatmentS A N physician who relies on parent reports to assess the effects of asthma on a child's physical and emotional health may be getting only part of the story, according to findings presented in a poster at the annual meeting of the Pediatric Academic Societies. Separate interviews with 414 children aged 7-16 years ; and one of their parents showed that parents and children often disagree about the impact of asthma, sociologist Lynn M. Olson, Ph.D., reported. Dr. Olson, director of the department of research at the American Academy of Pediatrics in Elk Grove Village, Ill., found that children in all age groups tended to describe their physical health as worse than was reported in their parents' accounts. "We found in each of the age groups, children were more likely to report more symptoms and worse health than did the parents, " she said in an interview at the meeting, which was sponsored by the American Pediatric Society, Society for Pediatric Research, Ambulatory Pediatric Association, and American Academy of Pediatrics. On questions of emotional health, however, adolescents were significantly less likely than parents to report a negative impact. Dr. Olson said the study was part of a larger investigation sponsored by the National Heart, Lung, and Blood Institute that looked into children's ability to report on their own asthma health status. Most children in the study, 61%, used a prescribed controller of asthma symptoms 5 or more days a week. Some 53% of parents described their child's condition as "moderate severe." The population was diverse including 46% African American, 37% white, and 11% Hispanic families ; , with 42% of family incomes less than $30, 000 annually. Each parent-and-child pair completed adult and child versions of the Child Health Survey for Asthma. The survey contained questions about physical activities and asthma impact during the previous 2 weeks. Answers were computed in scores of 1-100, with higher scores signaling better health. Under physical health, only 70% of parents and children agreed on whether the child had difficulty sleeping. Agreement was little better for questions relating to cough 73% ; , limits on strenuous activities 73% ; , and limits on sports running outside 78% ; . Agreement improved slightly when the pairs were asked about wheezing with a cold 80% ; , wheezing without a cold 81% ; , cold won't go away 81% ; , shortness of breath 82% ; , tight chest 83% ; , limits on moderate activities 83% ; , and limits in gym class 86% ; . Parents and children were most likely to agree on asthma's impact on limits on mild activities 93% ; . They disagreed more, however, on emotional impact issues. The lowest level of agreement, 69%, regarded frustration with asthma treatments and frustration with activity limits. Just 70% concurred when asked about the child being frustrated with having asthma and differin and moduretic, for instance, triamterene.
The level of tyrosine phosphorylation is regulated by the opposing actions of RTKs and PTPs. The RTKs phosphorylate cellular substrates on tyrosine residues and the PTPs dephosphorylate phosphotyrosine residues. Given their involvement in signal transduction pathways, the PTPs are attractive drug targets. Tyrosine phosphorylation is essential for signaling pathways regulated by insulin and leptin. Type II diabetes and obesity are characterized by resistance to hormones insulin and leptin, possibly due to attenuated or diminished signaling from the receptors. Therefore, a compound that inhibits the negative regulator s ; of these signaling pathways is expected to enhance the action of insulin and leptin and may be beneficial for the treatment of type II diabetes and obesity. Evidence has accumulated indicating that PTP-1B is a negative regulator of both insulin and leptin signaling and that insulin and leptin action can be enhanced by the inhibition of PTP-1B, thus making this particular molecule an attractive novel target for the treatment of both type II diabetes and obesity.
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| In the absence of analgesic use, 25.5 women 1000 2.55% ; in this cohort developed hypertension annually. Given the prevalence and frequency of analgesic use reported and the risk of incident hypertension associated with that use, 4.5 additional women 1000 0.45% ; develop hypertension annually, ie, the sum of the PARs for the 3 analgesics. These data suggest that 15% 4.5 [25.5 4.5] ; of the hypertension developing in middle-aged women is associated with analgesic use. Epidemiological association between frequency of analgesic use and incident hypertension does not establish a pathogenetic relationship. Therefore, it may be useful to examine the implications of the report from various perspectives.
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