Der Anaesthesist
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The laryngeal mask (LM) was developed by A. Brain to overcome the disadvantages of the face mask (impractical) and the tracheal tube (invasive). Today this new instrument is applied on a broad scale in Great Britain and with growing interest in continental Europe. ⋯ Apart from anaesthesia, the LM can be used for bronchoscopy in children, for difficult intubations and as a preliminary airway in cases of resuscitation. Two studies performed in Great Britain have evaluated the LM for resuscitation. The investigations should be confirmed in German-speaking countries.
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The duration of spinal anaesthesia in infants is short compared to adult patients. When tetracaine is used, the addition of epinephrine significantly prolongs the duration. For bupivacaine, however, the influence of epinephrine on the duration is not clear. ⋯ CONCLUSIONS. Epinephrine 1:200,000 significantly prolongs the duration of spinal anaesthesia in former preterm infants. Haemodynamic parameters in this age group remain unchanged during spinal anaesthesia and are not influenced by the addition of epinephrine.
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The rapid sequence induction of anaesthesia in patients with an increased risk of pulmonary aspiration is a quite involved procedure associated with many potential dangers. A new nasogastric balloon tube has been developed, which will prevent the reflux of gastric contents by blocking the cardia with a balloon. It was the aim of this initial study to assess the efficiency of the tube in animals, healthy volunteers and patients. ⋯ The average time from loss of consciousness to tracheal intubation was 164 +/- 8 s. CONCLUSIONS. It is concluded from the present results, with further clinical studies pending, that the gastric balloon probe permits low-risk conventional induction sequence of anaesthesia in patients with an increased risk for pulmonary aspiration and that the device may also be safely used during the extubation phase.
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It is the purpose of this review to outline the principles of biometric methods in clinical research. Several study designs such as cohort studies, case-control studies or randomized controlled trials are explained in detail, and their problems and their interpretation are discussed. It is demonstrated that observational studies may yield valuable information about associations between exposure and outcome variables but that only properly designed randomized clinical trials of adequate sample size make it possible to answer research questions about causal relationships. It is emphasized that good clinical research depends on properly designed studies more than on complicated statistical procedures.
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The primary goals of scoring in emergency medicine are grading of the severity of the patient's condition, measurement of diagnostic and therapeutic efforts, forecasting the outcome, and support in decision making on triage and therapy. Scores can also be used as tools for measuring efficacy and controlling quality. There has been less experience with use of scoring systems to estimate quality of life. ⋯ Scores for use in emergency medicine should be based on physiological parameters, universally applicable and suitable for use throughout the course of diseases. Appropriate score systems are the Glasgow Coma Scale, the Rapid Acute Physiology Score, and the Mainz Emergency Evaluation Score, Trauma Score and Injury Severity Score. Scores suitable for estimation of quality of life following emergencies are the Glasgow Outcome Scale and the Glasgow-Pittsburgh Scale.