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Träfflista för sökning "L773:0012 6667 OR L773:1179 1950 srt2:(2005-2009)"

Search: L773:0012 6667 OR L773:1179 1950 > (2005-2009)

  • Result 1-9 of 9
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1.
  • Ambrosioni, E (author)
  • Delapril/manidipine: viewpoints
  • 2006
  • In: Drugs. - : Springer Science and Business Media LLC. - 0012-6667. ; 66:7, s. 970-971
  • Journal article (peer-reviewed)
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2.
  • Andersson, Roland, et al. (author)
  • Treatment of acute pancreatitis: focus on medical care.
  • 2009
  • In: Drugs. - 0012-6667. ; 69:5, s. 505-514
  • Journal article (peer-reviewed)abstract
    • Acute pancreatitis has an incidence of about 300 per 1 million individuals per year, of which 10-15% of patients develop the severe form of the disease. Novel management options, which have the potential to improve outcome, include initial proper fluid resuscitation, which maintains microcirculation and thereby potentially decreases ischaemia and reperfusion injury. The traditional treatment concept in acute pancreatitis, fasting and parenteral nutrition, has been challenged and early initiation of enteral feeding in severe pancreatitis and oral intake in mild acute pancreatitis is both feasible and provides some benefits. There are at present no data supporting immunonutritional supplements and probiotics should be avoided in patients with acute pancreatitis. There is also no evidence of any benefits provided by prophylactic antibacterials in patients with predicted severe acute pancreatitis. A variety of specific medical interventions have been investigated (e.g. intense blood glucose monitoring by insulin) but none has become clinically useful. Lessons can probably be learned from critical care in general, but studies are needed to verify these interventions in acute pancreatitis.
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3.
  • Battino, D, et al. (author)
  • Management of epilepsy during pregnancy
  • 2007
  • In: Drugs. - : Springer Science and Business Media LLC. - 0012-6667. ; 67:18, s. 2727-2746
  • Journal article (peer-reviewed)
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5.
  • Eriksson, Bengt I., 1946, et al. (author)
  • Oral anticoagulants in development: focus on thromboprophylaxis in patients undergoing orthopaedic surgery
  • 2006
  • In: Drugs. - 0012-6667. ; 66:11, s. 1411-29
  • Journal article (peer-reviewed)abstract
    • Current anticoagulant provision is dominated by parenteral heparin and oral warfarin, which act by inhibiting several steps of the coagulation pathway indirectly. Recent research efforts have focused on the identification of small molecule inhibitors of the coagulation enzymes as novel therapies for thrombotic disorders. There has been particular success in developing nonpeptidic, orally available, small molecules to directly inhibit the key proteases, factor IIa and factor Xa.Of the new oral anticoagulants in development, the two agents in the most advanced stage are dabigatran etexilate (BIBR 1048) and rivaroxaban (BAY 59-7939), which inhibit factor IIa and factor Xa, respectively. Other agents in the early stages of development include several Xa inhibitors (LY-517717, YM150, DU-176b and apixaban [BMS-562247]), a factor IXa inhibitor (TTP889), and an orally active glycosaminoglycan enhancer (odiparcil [SB-424323]), which indirectly enhances thrombin inhibition via heparin cofactor II. Results have been reported from important, phase II dose-finding studies, and a number of registration-track phase III studies have been initiated, reflecting the drive towards potentially more effective, but primarily safer and more convenient therapies for the prevention and treatment of venous and arterial thrombosis. Indeed, two unmet needs for anticoagulation that can be easily identified are safety and ease of use. Safety relates primarily to the incidence of major bleeding and this remains the key concern of orthopaedic surgeons, over and above any efficacy advantage, and convenience of use, which centres on oral administration replacing the need for injections.The clinical development of these new anticoagulants is following the well tested strategy of dose-ranging and registration studies in major orthopaedic surgery, prior to development in arterial indications. There are a number of subtle issues, including the timing of the first perioperative dose, duration of prophylactic treatment and definition/assessment of study endpoints that can influence study outcome and require careful consideration when evaluating study results with new agents and in the comparison with established agents, and which are considered in this review.It is anticipated that over the next 3 years, at least one of these agents will be successfully licensed for the prevention of venous thromboembolism after major orthopaedic surgery, which will act as a springboard for the gradual replacement of current anticoagulants.
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6.
  • Johannessen, Svein I, et al. (author)
  • Management of focal-onset seizures: an update on drug treatment.
  • 2006
  • In: Drugs. - 0012-6667. ; 66:13, s. 1701-25
  • Research review (peer-reviewed)abstract
    • Focal-onset seizures are manifestations of abnormal epileptic firing of brain cells in a localised area or areas of the brain. The diagnosis of focal-onset seizures initially entails an EEG, a detailed history from the patient and eyewitnesses, as well as computer tomographic or, preferably, magnetic resonance imaging scans. Video EEG to record ictal events may be necessary to establish the correct diagnosis.Focal seizures are classified according to the International Classification of Epileptic Seizures and International Classification of Epilepsies and Epilepsy Syndromes. It is important to try to decide how the seizure event fits into this system in order to successfully evaluate and optimise treatment, as well as to give detailed information to the patient about their seizures and prognosis.Once the decision to treat the seizures has been made, the physician must choose which medication is the most appropriate to begin with. Carbamazepine, phenytoin or valproic acid (sodium valproate) are often rated as first-line drugs, but factors such as adverse-effect profiles, age, possibility of pregnancy, and concomitant diseases and medication also need to be considered. Most of the newer antiepileptic drugs (AEDs) appear to have good efficacy and better tolerability than the older agents, but evidence to support their superiority is scarce and has led to conflicting advice in several guidelines. Among the newer AEDs, lamotrigine, gabapentin, topiramate and oxcarbazepine have obtained monotherapy indication in many countries. The higher costs of the newer AEDs may inhibit their wider use, especially in poorer countries.
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7.
  • Kahan, T (author)
  • Delapril/manidipine
  • 2006
  • In: DRUGS. - : Springer Science and Business Media LLC. - 0012-6667. ; 66:7, s. 970-970
  • Journal article (other academic/artistic)
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  • Result 1-9 of 9

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