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Accelerated Stability Studies Polypyrrole-coated sensors with no further treatment were shown to be stable at 37C over a 4-month period. Polypyrrole sensors coated with streptavidin and treated with a simple sucrose stabilisation layer were also stable at 37 C for 4 months. A calibration curve for a quality control QC ; assay based on the capture of biotinylated-HRP was performed once a week for first seven weeks, and then once every two weeks for the next ten weeks. Any deterioration would be indicated by changes in the shape of the calibration curve over time.
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Anderson and colleagues abstract 182 ; reported on the results of a double-blind, placebo-controlled trial of ruboxistaurin, a selective protein kinase C PKC ; inhibitor in 123 Type 2 diabetic patients with established albuminuria on stable doses of ACE-Is or ARBs. At one year, the mean albumin: creatinine ratio decreased significantly with ruboxistaurin -24%, p 0.05 ; , whereas no change was seen with placebo -9%, p 0.33 ; . Additionally, no significant change in GFR was detected in the ruboxistaurin-treated patients -2.5 1.9 ml min; p 0.185 ; , whereas placebo patients did experience a small but significant decrement -4.8 1.8 ml min; p 0.009 ; . Importantly, the PKC inhibitor was not associated with any increased reporting of adverse events. The presenters concluded that ruboxistaurin may prove a useful addition to established therapies for diabetic nephropathy.
Licorice has also been associated with inhibition of platelet aggregation145 and should therefore be avoided in patients with bleeding and or hemostatic disorders. It should be used with caution in patients receiving anticoagulants or drugs with antiplatelet activity and phenytoin.
Massachusetts Memorial Medical Center, medical records and radiographs of patients 18 years old or younger at the time of IVC filter placement were reviewed. Follow-up data were obtained by interview, physical examination, and venous duplex ultrasound scanning. Results: A total of 15 IVC filters were placed in children 18 years old or younger between 1983 and 1999. In 10 patients the indications for IVC filter placement were lower-extremity deep venous thrombosis DVT ; and or pulmonary embolism. In five patients, prophylactic filters were placed in the absence of DVT because of a high risk for the development of pulmonary embolism. Surgical exposure of the right internal jugular vein was used to place the first eight filters. The remainder were inserted percutaneously through the right internal jugular vein or the right common femoral vein. There were no complications or mortality related to filter insertion. Follow-up of the surviving 14 patients ranged from 19 months to 16 years. During long-term follow-up, no patient had a pulmonary embolus. Of the nine patients who had lower-extremity DVT, three developed mild common femoral venous reflux documented by duplex scan. Of the five patients who had prophylactic filters, four had no symptoms or duplex evidence of reflux. The other patient, who was paraplegic, had bilateral leg edema but no venous varicosities and no reflux on duplex scan 11 years after filter placement. No patient in either group had chronic venous obstruction. Conclusion: In long-term follow-up there were no instances of pulmonary embolism, IVC thrombosis, significant post-phlebitic symptoms, or significant filter migration among 14 pediatric patients with Greenfield IVC filters. This suggests a safety profile and efficacy similar to that seen in adults. Authors' Abstract.
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For this reason it was not possible to calculate accurate pA2 or KM values with phenylephrine as the agonist. Using norepinephrine. the K for the alpha receptor-piperoxan complex was 1.24 10 7M and pA2 was 7.06. The pA2 and KM values are important parameters in the characterization of a receptor, because they should be the same irrespective of the agonist used for a particular antagonist acting on a specific receptor: also, for a given antagonist acting on the same type of receptor, they should be equal for various tissues 39 ; . The presently obtained value of pA2 for the feline middle cerebral artery is lower and hence the KM higher ; than that for the ovarian follicular wall tested under similar conditions 40 ; . and the pA2 value is higher Kn lower ; than that reported for the vas deferens of the rat and the intestine of the rabbit, although in the latter study 41 ; the precautions necessary for quantitative analysis of adrenoceptors were not taken. These discrepancies together with the high ED60 values and the finding that the specific alpha stimulant, phenylephrine. only acted as a partial agonist being less potent than isoproterenol and having a potency ratio to norepinephrine about ten times lower 17 ; than it is in other tissues ; suggest the presence of an unusual type of alpha receptor in pial arteries. Isoproterenol contracted the middle cerebral artery but only at high doses. There is now reason to believe that this action is not mediated by beta receptors as previously assumed 12 ; and that the inhibitor ' effect of certain beta antagonists on cerebral vasoconstriction is nonspecific 42-44 ; . On the other hand, it is not yet clear whether the isoproterenol contraction is an alpha-adrenergic effect; although the antagonism by piperoxan was reversible, it appeared to be noncompetitive. The competitive alpha antagonists, dibenamine and phenoxybenzamine. are for practical purposes irreversible because of the very slow recovery following inactivation of the receptor 28 ; . Based on the contractile responses before and after inactivation of a fraction of the receptors with phenoxybenzamine, it was possible to quantify 21 ; the effects of the sympathetic transmitter, norepinephrine, on the alpha receptors in pial vessels. The dissociation constant KA ; was 1.73 10 8.\i, which means that the affinity of norepinephrine for the receptors is similar to that found for the rat portal vein 24 ; but lower than that found for the rabbit aortic strip 17 ; . Furthermore, the relation between the actual response obtained on the middle cerebral artery with norepinephrine and the alpha.
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Plasma sensitivity 99%, specificity 89% ; or urinary Sens 97%, spec 69% ; fractionated metanephrines are most sensitive 2 ; For tumor localization, CT or MRI with and without contrast but iodine can precipitate hypertensive crisis 3 ; MIBG I-metaiodobenzylguanidine ; scanning has greater specificity v ; Treatment for pheochromocytoma-associated hypertensive crisis? 1 ; Nitroprusside a ; Rapid onset and short duration b ; 0.5-5.0 mcg kg 2 ; Phentolamine a ; Short-acting nonselective alpha blocker b ; Initial test dose of 1 mg followed by repeat 5 mg boluses or continuous infusion c ; Maximal response 2-3 minutes after bolus d ; Duration of action 10-15 minutes 3 ; Nicardipine a ; Calcium channel blocker dihydropyridine ; b ; Infusion of 5 mg hour titrated to BP i ; Increase infusion by 2.5 mg hr every 15 minutes to maximum of 15 mg hour 4 ; Alpha blockade a ; Phenodybenzamine i ; Irreversible, long-acting, nonspecific alpha-adrenergic blocker b ; Doxazosin, prazosin, terazosin for long-term management but blockade incomplete so suboptimal acutely 5 ; Beta-blockade a ; To be started ONLY AFTER adequate alpha blockade achieved due to potential for unopposed alpha stimulation if peripheral vasodilatory beta receptors are blocked vi ; What is the definitive treatment and outcome? 1 ; 10% are malignant and can't be differentiated from benign ones. Created on 4 19 2007 00 PM.
Q: Does the Alliance Provider Services Department have forms and other resources that providers can use to help their offices meet facility site review compliance standards? A: Yes. The Alliance Provider Services Department has a variety of forms that can be used to assist with medical record documentation and maintaining equipment and logs. In addition, other referral and resource information is available to assist providers in accessing services for members including health promotion and disease prevention. For more information call the Provider Services Department at 510 ; 747-4510 and ask to speak with a Provider Services Representative and videx.
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Recent evidence from our laboratory has demonstrated that 1-adrenoceptor antagonists doxazosin and terazosin induced apoptosis in prostate epithelial and smooth muscle cells in patients with benign prostatic hypertrophy BPH; J. Urol., 159: 1810 1815, J. Urol., 161: 2002 2007, ; . In this study, we investigated the biological action of three 1-adrenoceptor antagonists, doxazosin, terazosin, and tamsulosin, against prostate cancer cell growth. The antigrowth effect of the three 1-adrenoceptor antagonists was examined in two human prostate cancer cell lines, PC-3 and DU-145, and a prostate smooth muscle cell primary culture, SMC-1, on the basis of: a ; cell viability assay; b ; rate of DNA synthesis; and c ; induction of apoptosis. Our results indicate that treatment of prostate cancer cells with doxazosin or terazosin results in a significant loss of cell viability, via induction of apoptosis in a dosedependent manner, whereas tamsulosin had no effect on prostate cell growth. Neither doxazosin nor terazosin exerted a significant effect on the rate of cell proliferation in prostate cancer cells. Exposure to phenoxybenzamine, an irreversible inhibitor of 1-adrenoceptors, does not abrogate the apoptotic effect of doxazosin or terazosin against human prostate cancer or smooth muscle cells. This suggests that the apoptotic activity of doxazosin and terazosin against prostate cells is independent of their capacity to antagonize 1-adrenoceptors. Furthermore, an in vivo efficacy trial demonstrated that doxazosin administration at tolerated pharmacologically relevant doses ; in SCID mice bearing PC-3 prostate cancer xenografts resulted in a significant inhibition of tumor growth. These findings demonstrate the ability of doxazosin and terazosin but not tamsulosin ; to suppress prostate cancer cell growth in vitro and in vivo by inducing apoptosis without affecting cell proliferation. This evidence provides the rationale for targeting both drugs, already in clinical use and with established adverse-effect profiles, against prostatic tumors for the treatment of advanced prostate cancer.
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Male albino rats Sprague-Dawley strain ; , 180 to 220 gm, previously fasted for 16 hours were used. Epinephrine, l 2 mg per kg, was injected subcutaneously and the animals killed by decapitation 15 minutes later. The adrenergic blocking agents were administered under light ether anesthesia 30 minutes prior to the time of death. Phentolamine, 15 mg per kg, was injected into the tail vein and simultaneously a t the same dose subcutaneously; NDC, 40 mg per kg, or phenoxybenzamine, 8 mg per kg, was injected intravenously.
From the Valley Cancer Pain Treatment Center, Scottsdale, Arizona; Gunderson Lutheran Medical Center, LaCrosse, Wisconsin; Overlake Pain Medical Clinics, Bellevue, Washington; Department of Neurosurgery, Brown University Medical School, Providence, Rhode Island; University of Arizona Cancer Center, Tucson; Mayo Clinic, Scottsdale, Arizona; and the University of California, San Diego Hospice, San Diego, California. Acknowledgment: The multidisciplinary workshop on intrathecal drug delivery for the management of cancer pain was supported through an unrestricted grant to Valley Cancer Pain Foundation from Medtronic, Inc., Minneapolis, Minnesota. Manuscript received November 12, 2004; accepted April 1, 2005. Correspondence to: Lisa Stearns, MD, Valley Cancer Pain Treatment Center, 10460 N 92nd St., Suite 300, Scottsdale, AZ 85258; telephone: 480 ; 889-0180; fax: 480 ; 889-0186; e-mail: vcptc aol and dipyridamole.
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Nation showed normetanephrine to be 2.80 nmol L; the metanephrine level was obscured by interfering substances. Treatment with phenoxybenzamine was stopped, and the patient was discharged receiving a regimen of amlodipine, 10 mg twice a day; metoprolol, 100 mg every morning and 150 mg every evening; and hydralazine, 25 mg 3 times a day. Three months postoperatively she had persistent hypertension that required treatment with medication, although the hypertension was no longer paroxysmal. Repeat plasma normetanephrine determination showed a concentration of 2.28 nmol L, and metanephrine was again obscured by an interfering substance and persantine.
This probably depends on inhibition of compensatory cardiovascular reflexes, and not on a direct sensitizing effect on blood vessel elements. Although the pressor response to octapressin was augmented by the pithing procedure, pretreatment with the autonomic blocking agents phenoxybenzamine or chlorpromazine further potentiated the response, indicating a direct sensitizing effect on the vascular effector cells. This is substantiated by mlcrocirculation experiments o f Altura 1967 ; who showed that in the rat, p h e n and chlorpromazine prevent the vasoconstriction due to topical or intravenous administration o f catecholamines, and even potentmte the effect o f octapressin. In the present experiments a direct peripheral effect on vascular effector cells was found in the pithed rats for phenoxybenzamlne and chlorpromazine, both a-adrenerglc blocking agents. This effect may be related to their t~-adrenerglc receptor blocking capacity. Bartelstone and Nasmyth 1965 ; have implicated cyclic 3', 5'-AMP in the pressor response to vasopressin and catecholamines. It is suggested that an a-adrenerglc receptor block as induced by phenoxybenzamine and chlorpromazine may eliminate the stimulating influence o f catecholamines on cyclic 3', 5'-AMP production and subsequently increase the amount o f substrate available, probably resulting in a more sensitive effector system for vasopressin. However, Bartelstone and Nasmyth 1965 ; have shown that infusions of non-pressor doses of arginine-vasopressln potentiated the pressor responses to catecholamines. Such an effect obtained by non-pressor doses of vasopressin requires only a small amount o f available substrate and may differ from the effects o f high doses of octapressin as used m the present study. Therefore, this finding does not necessarily contradict our hypothesis.
Its empirical formula is c 26 and its molecular weight is 45 6 pharmacodynamics the secretion of prolactin by the anterior pituitary is mainly under hypothalamic inhibitory control, likely exerted through release of dopamine by tuberoinfundibular neurons and disopyramide and phenoxybenzamine, for instance, phenoxybenzamine pharmacology.
Lower extremity, 522531 mechanisms, 436448 orthotic management, 471472, 492, 495 pain management, 474479 penetrating, 446448, 491493 Persian Gulf War, 1114, 420, 422, pharmacological intervention, 475479 prognosis, 459462 range-of-motion maintenance, 465467 rehabilitative management, 465481 reinnervation following, 431432, 434, 436, secondary injury prevention, 435, 465 sensory reeducation, 473474 severity determination, 459462 in spinal cord injured patients, 192193 strength maintenance and improvement, 467470 stretch, 440443 surgical repair postponement, 465 upper extremity, 496522 Vietnam War, 447, 497 during World Wars, 420422, 447 See also Causalgia; specific injury Peripheral nerves anatomy, 422423, 426427 axonal transport, 425426 causalgia-associated changes in, 484 degeneration, 431434 effect of immobility on, 749 fascicular composition, 426427, 435, 438439, impulse propagation, 423425 neuroanatomy, 422423 physiology, 423426, 448450 regeneration, 431432, 434, 436, vascular system, 427428 Peroneal nerve, 527528 deep, 538 functional electrical stimulation, 725726 superficial, 540 Peroneal neuropathy, 527531 anatomic considerations, 527528 in burn patients, 689 case scenario, 493496 clinical presentation, 529 dislocation-associated, 440441 electrodiagnosis, 529530 etiology, 528529 fracture-associated, 441442 superficial, 540542 treatment, 530531 PERSCOM See Total Army Personnel Command PERSCOM ; Pershing, John J., 11 Persian Gulf War, 23 amputations, 1215, 4647, 80 Army Physical Therapy Registry, 2728 brain injuries, 15 burn injuries, 1415 causalgia, 482, 491 disability case statistics, 879880, 883 functional impairments, 15 hand rehabilitation, 38 immobility complications, 742, 745, 756 musculoskeletal injuries, 1113 nerve injuries, 1114, 38, 80, physical therapy, 2528 rehabilitation services, 1016 rehabilitation teams, 7 wrist-hand orthoses use, 709 Personality after traumatic brain injury, 217, 223, 238239 premorbid, 195196 Personnel Management Officers PMOs ; , 865, 877 PFTs See Pulmonary function tests PFTs ; Phalangization, 3637 Phalen's test, 511 Phantom limb pattern recognition system using, 66 Phantom limb pain, 14, 143147, 475 definition, 143 differential diagnosis, 148 duration and frequency, 144 incidence, 143144 in lower extremity amputees, 88 pathophysiology, 126, 144145 prevention, 147 treatment, 145148 in upper extremity amputees, 61 See also Residual limb pain Phantom limb sensation after lower extremity amputation, 126, 143 classification, 143 definition, 143 explanation, 126, 143 fading, 143 management, 126, 143 telescoping, 88, 143 Pharmacologic therapy and alcohol use, 240 auditory complications, 323 for burn patients, 599600 debilitating side effects, 851 for immobilization osteoporosis, 748 ocular complications, 296 for peripheral nerve injuries, 475479 for phantom limb pain, 126, 145146, 148 for traumatic brain injury, 214222, 232233 See also specific drug or drug class Pharyngeal phase of swallowing, 328 Pharyngeal reflex, 327 Phenobarbital, 221 Phenoxybenzamine, 490 Phenytoin, 477, 490 for cranial neuropathies, 308 for traumatic brain injury, 216, 221 Phosphagen system, 787788 Phosphorylation oxidative, 786787 Photographs in burn wound management, 599, 655 Photoreceptors, 285286 Phthalazinol, 217 Physiatrist definition, 4, 6, 229, duties beyond physical rehabilitation, 8 role in interdisciplinary team, 832 role in surgical decision process, 83, 96 role in traumatic brain injury care, 226, 229 Physiatry history, 46, 831 See also Interdisciplinary team Physical activity as risk factor for injury, 817 Physical capacity for exercise, 799803 aerobic, 803806.
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Dihydroergotamine phentolamine a-ergocryptine phehoxybenzamine p-bromo a-ergocryptine * i-isoxsuprine k ; -nylidrin azapetine naphazoline tj-cc-34 clonidine oxyfedrine oxymetazoline - + xc-25 - ; -ephedrine serotonin * i-metaraminol salbutamol dopamine ' values obtained at 37.
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Mentioned investigations. While determining the extent of structural heart disease, it is important to remember that heart failure results not only because of structural heart disease but also because of maladaptations of the neuroendocrine system with resultant fluid overload. Where there is mild or little detectable structural heart disease, it may be possible to pharmacologically control the renin angiotensin system with greater ease than if there is severe structural heart disease, although this is not always the case. Where an objective assessment of left ventricular function by echocardiography is required, this can usually be done qualitatively [21]. Measurement of ejection fraction may not always be necessary and M-mode measurements can be misleading if there is asymmetry of the left ventricle [22]. Where a detailed quantitative measurement of left ventricular function is required, this may be obtained by radionuclide ventriculography or cardiac catheterization for appropriate patients, such as those undergoing additional treatments such as coronary by-pass surgery. Attempts continue to be made to improve the access to echocardiography for those patients with suspected heart failure [23]. The introduction of more portable echocardiography may make this more achievable in practice [24]. While all the above mentioned investigations may be appropriate to an extent in the assessment of the older patient with heart failure, not every patient will require all of these investigations before treatment is commenced. Additional simple blood tests such as a FBC and serum electrolytes should be performed regularly in the older patient with a confirmed diagnosis of heart failure. Table 3 summarizes the initial investigations for an older patient with chronic heart failure!
Tendency, including intraoperative pretreatment of the graft with topical -adrenergic antagonist solutions such as phenoxxybenzamine ; or pharmacologic prophylaxis with calcium channel blockers 20 22 ; . The latest generation of multidetector CT scanners shows promise in the demonstration of luminal narrowing in radial artery spasm Fig 17 ; 23.
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Usually smoked as a cigarette or joint, or in a pipe or bong, marijuana has appeared in "blunts" in recent years. These are cigars that have been emptied of tobacco and re-filled with marijuana, sometimes in combination with another drug, such as crack. Some users also mix marijuana into foods or use it to brew tea. The main active chemical in marijuana is THC delta-9-tetrahydrocannabinol ; . Short-term effects of marijuana use include problems with memory and learning; distorted perception; difficulty in thinking and problem-solving; loss of coordination; and increased heart rate, anxiety, and panic attacks. Health Hazards Effects of Marijuana on the Brain. Researchers have found that THC changes the way in which sensory information gets into and is acted on by the hippocampus. This is a component of the brain's limbic system that is crucial for learning, memory, and the integration of sensory experiences with emotions and motivations. Investigations have shown that THC suppresses neurons in the information-processing system of the hippocampus. In addition, researchers have discovered that learned behaviors, which depend on the hippocampus, also deteriorate. Effects on the Lungs. Someone who smokes marijuana regularly may have many of the same respiratory problems that tobacco smokers have. These individuals may have daily cough and phlegm, symptoms of chronic bronchitis, and more frequent chest colds. Continuing to smoke marijuana can lead to abnormal functioning of lung tissue injured or destroyed by marijuana smoke. Regardless of the THC content, the amount of tar inhaled by marijuana smokers and the level of carbon monoxide absorbed are three to five times greater than among tobacco smokers. This may be due to marijuana users inhaling more deeply and holding the smoke in the lungs. Effects of Heavy Marijuana Use on Learning and Social Behavior. A study of college students has shown that critical skills related to attention, memory, and learning are impaired among people who use marijuana heavily, even after discontinuing its use for at least 24 hours. Researchers compared 65 "heavy users, " who had smoked marijuana a median of 29 of the past 30 days, and 64 "light users, " who had smoked a median of 1 of the past 30 days. After a closely monitored 19to 24-hour period of abstinence from marijuana and other illicit drugs and alcohol, the undergraduates were given several standard tests measuring aspects of attention, memory, and learning. Compared to the light users, heavy marijuana users made more errors and had more difficulty sustaining attention, shifting attention to meet the demands of changes in the environment, and in registering, processing, and using information. The findings suggest that the greater impairment among heavy users is likely due to an alteration of brain activity produced by marijuana. Longitudinal research on marijuana use among young people below college age indicates those who used have lower achievement than the non-users, more acceptance of deviant behavior, more delinquent behavior and aggression, greater rebelliousness, poorer relationships with parents, and more associations with delinquent and drug-using friends.
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Divisions, Albert Einstein College of Medicine, Hospital Center, Bronx, New York. tFellow in Pulmonary Medicine. lAssociate Professor, Division of Cardiology.
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Practice] or the Emergency Department [in] 2003. Peers would view this advice and subsequent lack of documentation with moderate disapproval. Despite other clinical pressures faced by [Ms E] on that shift and her feelings of intimidation by the [medical officer] on duty regarding the appropriateness of [Mr A's] presentation to the emergency department, his abnormal vital signs, repeated calls to the Ambulance Service and deteriorating condition should have raised concerns. 11. Are there any aspects of the care provided by [Ms E] that you consider warrant additional comment? [Ms E's] statement highlights the difficulties nurses face when working in rural hospitals with emergency department services. They are required to perform various tasks and roles internal and external to the immediate emergency setting but judged by emergency medicine and nursing standards. Larger emergency departments have dedicated roles, such as triage, that are supported by appropriate resources, systems, training and supervision that smaller hospitals cannot always provide. It is important that the licensee of the Public Hospital provides appropriate resources and training to ensure staff provide an acceptable standard of care to the community it serves. References 1. ACEM. 2002 ; . Policy Document: The Australasian Triage Scale. Retrieved 26 11 04: Retrieved: 26th November 2004. : acem .au open documents triage 2. ACEM. 2002 ; . Guidelines for implementation of the Australasian Triage Scale in Emergency Departments. Retrieved: 26th November 2004. : acem .au open documents triageguide 3. Couch, R., Patel, A. & Dale, J. 1996 ; . Paediatric calls to an inner city Accident and Emergency department: service demand and advice given. Accident and Emergency Nursing. 4, 17174. 4. Edmonds, E. 1997 ; . Telephone triage: 5 years' experience. Accident and Emergency Nursing. 5, 813. 5. Manchester Triage Group. 1997 ; . Emergency Triage. London. British Medical Journal Publishing Group. 6. Nursing Council of New Zealand 2000 ; . Professional Standards for Telenursing Practice. Standards New Zealand, for example, phenoxybenzamine hydrochloride.
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Subsequent 3 months. Knowledge and body weight improved over the course of the 5-month study in the individualized group. At the time of the 2-month follow-up in the classroom group, there were significant decreases in fasting plasma glucose and glycosylated hemoglobin levels and an increase in behavior scores compared with baseline. Behavior correlated with glycemic control. Glycosylated hemoglobin and behavior scores improved over the course of the 5-month study. Change in knowledge was the only variable that differed significantly between the two groups. Increases in knowledge did not correlate with improved glycemic control or body weight. The results of the study suggest that an individualized method of education is as effective as traditional classroom instruction in educating patients with diabetes. The individualized method may be more costeffective, particularly for patients who live a long distance from the classroom site or for whom the classroom schedule is inconvenient e.g., employed patients with inflexible work schedules ; . Choice of an education method for patients with diabetes might take into consideration various patient factors. Nurse case management to improve glycemic control in diabetic patients in a health maintenance organization. Aubert RE, Herman WH, Waters J, Moore W, Sutton D, Peterson BL, Bailey CM, Koplan JP. Ann Intern Med. 1998; 129: 60512. A 12-month randomized, controlled trial was conducted to compare diabetes control in patients receiving nurse case management with that in patients receiving usual care at primary care clinics in a group-model health maintenance organization. Patients were identified from pharmacy records and a database of patients who had visited a physician for diabetes care, been hospitalized for diabetes, been seen by a utilization management nurse, or been referred to an ophthalmologist for a diabetic retinal examination. Seventeen patients with type 1 diabetes and 121 patients with type 2 disease were randomized to the nurse case management group or the usual care group. The nurse case manager a registered nurse and certified diabetes educator ; was trained to follow detailed management algorithms under the direction of a board-certified family medicine physician and an endocrinologist. The algorithms were designed to improve glycemic control by adjusting drug therapy, planning meals, and reinforcing exercise recommendations. Patients assigned to the nurse case management group were instructed about blood glucose monitoring at an initial visit with the nurse case manager and returned for a follow-up visit 2 weeks later for reevaluation and adjustment of the treatment plan. Patients also were referred to a 5-week, 12-hour diabetes education program that addressed diet and exercise among other topics. Patients received weekly or biweekly follow-up telephone calls to discuss blood glucose values, adjust drug therapy, and reinforce dietary and exercise recommendations. Patients in the usual care group received diabetes care from their primary care physicians. They were provided with blood glucose monitoring equipment and encouraged to participate in the 5-week diabetes education program attended by the nurse case management group. The nurse case management group had a greater decrease in glycosylated hemoglobin values than did the usual care group 1.7% versus 0.6%, respectively ; over the course of the 12-month study. The difference between the two groups was evident after 6 months and was maintained for the subsequent 6 months. The reduction in glycosylated hemoglobin was greater with nurse case management than with usual care in the subset of patients with type 1 diabetes and in the subset of patients with type 2 disease. There was no significant difference between the two groups in blood pressure, serum cholesterol and triglyceride levels, body weight, insulin requirements, hospital admissions, emergency department visits, or frequency of severe hypoglycemic episodes. Self-reported health status improved significantly in the nurse case management group. A diabetes control program in a public health care setting. Baker SB, Vallbona C, Pavlik V, Fasser CE, Armbruster M, McCray R, Baker RL. Public Health Rep. 1993; 108 5 ; : 595604. Protocols for the prevention and care of diabetes-related complications of the eyes, lower extremities, and cardiovascular system were developed and implemented in nine community health centers. These facilities were located in urban low-income neighborhoods in Houston, Texas, and served approximately 4, 300 patients. A culturally sensitive patient education curriculum was provided in four 2-hour sessions by a diabetes nurse educator and a nutritionist. Health care professionals received continuing medical education, and there was financial incentive for nurses to become certified diabetes educators. These efforts are part of a program that is ongoing, although some results are available after 5 years of experience. There was an increase in eye examinations from 8% to 26% of the patient population. A reduction in the incidence of legal blindness from 9.5 to 2.7 per 1, 000 patients was observed after 4 years. A cost-benefit analysis of providing 12 months of screening and preventive treatment for diabetic eye disease suggests a benefit-tocost ratio of at least 2.77 for such a program. The percentage of the population with annual foot examinations increased from 18% to 44%. Control of blood pressure was achieved in 77% of patients. However, there were no significant improvements in body weight or blood glucose control. The average percentage of correct responses to test questions about diabetes increased from 65% to 85% in patients. The rate at which proliferative retinopathy and nonproliferative retinopathy or fundus abnormalities ; were correctly identified by physicians in slides or photographs was 79% and 77%, respectively, in 1990 and 95% and 86%, respectively, in 1991. In retrospective chart.
| Phenoxybenzamine reviewThere are a number of uptake processes in the body involving important mediators which can be manipulated pharmacologically. Commonly, the uptake process uses Na + and Cl as counter ions. Noradrenaline is transported by two uptake systems that have been extensively studied. On release of noradrenaline from sympathetic nerve varicosities in the peripheral nervous system, it is subject to two uptake systems. Uptake 1 U1 ; is reuptake process where the noradrenaline is recovered by the nerve via a process that has a high affinity but relatively low maximum rate, whereas a second process, uptake 2 U2 ; , clears noradrenaline from the tissues into extraneuronal sites by a low affinity, but fast, process which is inhibited by glucocorticoids, phenoxybenzamine and normetanephrine ; . The first neuronal system has been studied in detail, and is essentially the same process as used for dopamine and 5-hydroxytryptamine in the central nervous system. The U1 transport protein has now been cloned, and is one of a family of transporter proteins which act as cotransporters for Na + , Cl and the amine, driven by the ATP-generated electrochemical gradient for Na + . This U1 noradrenaline reuptake process is inhibited by cocaine and amphetamine thus accounting for some of their actions, particularly within the CNS ; , phenoxybenzamine, and the extensive class of tricyclic and related compounds that are used as antidepressants e.g. desipramine ; . See ANTIDEPRESSANTS. The dopamine uptake and the 5-hydroxytrypamine uptake systems are very similar to the noradrenaline uptake system. This is shown by the fact that nerves readily take up the `wrong' neurotransmitter, and by the difficulty in devising uptake-blockers that have some selectivity for one amine over the other. The older tricyclic agents show less than a ten-fold selectivity in inhibiting noradrenaline uptake over that for 5-HT e.g. desipramine, imipramine, nortriptyline ; to members such as amitryptyline which shows virtually no selectivity, through to members such as zimelidine, trazodone and chlorimipramine which are somewhat 5-HT selective ; . The newer `Serotonin-Selective Reuptake Inhibitors' SSRIs ; show a higher selectivity for inhibition of 5-HT reuptake in the brain, and have a different pharmacology. Examples clinically used include; fluoxetine, paroxetine, sertraline, and fluvoxamine. Experimental agents include: citalipram, 6-nitroquipazine, alaproclate, venlafaxine, nefazodone, litoxetine, indatraline, -CIT 2-carbomethoxy-3- 4iodophenyl ; tropane ; and trazodone. The dopamine uptake system or dopamine transporter system is inhibited by the following: GBR 12909, GBR 12935, indatraline, bupropion, amfonelic acid, BTCP, mazindol, nomifensine, -CFT 2-carbomethoxy-3- 4-fluorophenyl ; tropane ; , -CIT-FP N- 3.
McCabe et al19 of 74 women and 37 men with MS, only 20.4% of the men and 35.4% of the women reported no sexual difficulties, however over half of those surveyed were not overly concerned about this. In identifying patients' sexual concerns, and determining appropriate interventions, nurses can be guided by assessment guidelines based on the work of Szasz.20 This involves consideration, where relevant, of patients' sexual knowledge, self-view, activity, response, interest and behaviour. It is essential that assumptions are not made about any of these, and that the nurse appreciates the considerable variability not only between individual patients, but also in the broader community. This further highlights the need for neutral language, with word such as `partner' avoiding interpretations that judgements are being made regarding marital status or sexual orientation. MS is frequently diagnosed at a time in people's lives when intimacy, sexual identity and relationships are being explored, or becoming established. McCabe19 reports a strong association between sexual satisfaction and relationship satisfaction, but observes that there is limited research into sexuality and relationships of people with MS. There is a lower level of relationship satisfaction among people with MS and levels of disability are apparently not implicated. McCabe points out, however, that partners' perceptions may well differ from those of patients, and further studies into this are warranted. When dealing with sexual issues, the PLISSIT model can assist nurses in deciding the level of intervention needed for a particular patient. These components of the acronym form the levels of the pyramid shown above. Permission, at the base of the pyramid, applies to the majority of patients while intensive therapy, at the top of the pyramid, applies to relatively few patients.21 Each of these levels is described below in detail.
Instruct patient to report these symptoms to health care provider: dizziness, visual changes, palpitations.
| She complained of uncomfortable eye movements.
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