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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Anaesthesia 48 (1993), S. 0 
    ISSN: 1365-2044
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: A randomised, double-blind study was undertaken to investigate the suitability of intranasally administered fentanyl for postoperative pain management under routine conditions in an unselected population. For postoperative pain relief, patients received either 0.027 mg fentanyl intranasally and sodium chloride 0.9% intravenously (intranasal group, n = 53) or sodium chloride 0.9% intranasally and 0.027 mg fentanyl intravenously (intravenous group, n = 59). These doses were repeated every 5 min until the patients were free of pain or refused further analgesia. Pain severity was evaluated before beginning opioid titration and 5, 10, 15, 20, 30, 40, 50, 60, 70 and 80 min thereafter. Adequate pain relief was achieved in 52 of 53 patients in the intranasal and in all patients in the intravenous group. Pain intensities evaluated on a 101-point numerical rating scale as well as on a verbal rating scale decreased significantly in both study groups within 5 min. At the 15 min measurement point, numerical rating scale pain intensity and at the 10 and 20 min point, verbal rating scale pain intensity was significantly lower in the intravenous group. The incidence of side effects was low in both groups and no patient complained of intranasal pain. Intranasally administered fentanyl would appear to be suitable for the management of postoperative pain.
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  • 2
    ISSN: 0378-1119
    Keywords: N^6-methyladenine inhibition ; Recombinant DNA ; blunt-ended fragments ; interrupted hexanucleotide palindrome ; relaxed sequence specifity
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 15 (1959), S. 487-488 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Zeitschrift für angewandte Mathematik und Physik 26 (1975), S. 501-504 
    ISSN: 1420-9039
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics , Physics
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 4-isothiocyanato-4′-nitrodiphenylamine was found to possess activity against intestinal nematodes in mice, against schistosomes in various hosts including primates and against two filarial species in the mongolian jird. Upon administration in a single oral dose it is equally effective againstS. haematobium, S. mansoni andS. japonicum.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Der Anaesthesist 44 (1995), S. 186-188 
    ISSN: 1432-055X
    Keywords: Schlüsselwörter Trachealruptur ; Intubationskomplikationen ; Exzessive Manschettenblockung ; Key words Tracheal rupture ; Problems of intubation ; Excessive inflation of endotracheal tube cuff
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Abstract The authors report a tracheal rupture in a 34-year-old patient who was primarily intubated following generalised seizures and loss of consciousness (Rüsch endotracheal tube). Some hours later, she developed high ventilatory airway pressures and subcutaneous and mediastinal emphysema were noted. Reintubation with a high-volume, low-pressure endotracheal tube was planned when it was noted that the ballon of the Rüsch tube was grossly overinflated. Endotracheal tube cuff pressure was measured and found to be greater than 120 cm H2O (the maximum measurement possible with the manometer). The diagnosis of tracheal rupture was confirmed by fiberoptic bronchoscopy. The patient immediately underwent a throacotomy and a 3-cm tear of the pars membranacea of the trachea was sutured with a dural patch. To maintain low airway pressures post-operatively, she remained sedated for 2 days and received a muscle relaxant to permit pressure-controlled ventilation. In this case, it can be concluded that excessive inflation of the endotracheal tube cuff resulted in the tracheal rupture. Other possible causes and results of tracheal rupture are discussed.
    Notes: Zusammenfassung Es wird über eine 34jährige Patientin berichtet, bei der es vermutlich aufgrund einer übermäßigen Blockung der Manschette des Endotrachealtubus (Firma Rüsch) zu einer Trachealruptur kam. Die Patientin wurde wegen zerebraler Krampfanfälle und Bewußtlosigkeit vom Notarzt intubiert. Stunden später fielen hohe Beatmungsdrücke auf. Die klinische Verdachtsdiagnose einer Trachealruptur wurde fiberbronchoskopisch bestätigt. In einer sofort durchgeführten rechtsseitigen Thorakotomie wurde ein ca. 3 cm langer Riß in der Pars membranacea der Trachea mit einem Durapatch übernäht. Am 4. postoperativen Tag konnte die Patientin problemlos extubiert werden. In dem vorliegenden Fall muß davon ausgegangen werden, daß die exzessive Manschettenblockung ursächlich für die Trachealruptur ist.
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  • 7
    ISSN: 1432-055X
    Keywords: Schlüsselwörter Patientenkontrollierte intranasale Analgesie ; PCINA ; Patientenakzeptanz ; Key words Patient-controlled intranasal analgesia ; PCINA ; Patients' acceptance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Abstract Patient-controlled intravenous analgesia (i.v.-PCA) represents the gold standard in the management of acute postoperative pain. However, in many countries i.v.-PCA is rarely used. Recent clinical studies demonstrated that intranasal fentanyl titration provides a rapid and safe form and pain management. In the present study we investigated patients' acceptance and assessment of patient-controlled intranasal analgesia (PCINA) and compared it to intravenous PCA and the customarily prescribed pain therapy. Material and Methods. After approval by the local ethics committee and written informed consent, 79 ASA physical status I or II patients were investigated on the first postoperative day following orthopaedic surgery. The patients were allocated either to the PCINA group (a maximum of 0.025 mg fentanyl over 6 min), to the i.v.-PCA group (0.025 mg fentanyl bolus, lockout interval 6 min) or to a group of patients who received the customarily prescribed pain management. Following the 8-h investigation period, the patients were questioned regarding their satisfaction with the pain therapy using a 6-point rating scale (ranging from 1=very good to 6=not acceptable). The patients were furthermore asked to name the advantages and disadvantages of their pain management. Results. Three patients in the i.v.-PCA group had to be excluded due to pain at the injection site and one patient in the PCINA group because of a surgical complication. Seventy-five patients were finally included, 25 patients per group. No statistically significant intergroup differences regarding age, weight, height and initial pain intensity (evaluated by a 101-point numeric rating scale) were demonstrated. The patients' satisfaction with the mode of pain management was significantly higher in the PCINA (median “good”) and in the i.v.-PCA group (median “good”) than in the group who received the customarily prescribed pain management (median “satisfactory”). This difference was statistically significant (P=0.0001). No statistically significant difference was demonstrated between the PCINA and i.v.-PCA groups. The patients in the PCINA and in the i.v.-PCA group stated as main advantages the rapid onset of action and good pain relief (n=25 and n=25, respectively), as well as their independence from the doctor or nurse (n=12 and n=13). The main disadvantages were pain on injection in the i.v.-PCA group and too frequent fentanyl administrations in the PCINA group (n=6). Discussion. The results demonstrate that the patients' satisfaction with PCINA is comparable to that with i.v.-PCA. Both PCINA and i.v.-PCA were assessed as superior to the customarily prescribed pain management (P=0.0001). Patients' acceptance of a given form of pain management is mainly related to its efficiency. However, side effects such as pain on injection with i.v.-PCA, or frequent opioid administration with PCINA, must be considered when assessing a method of pain control. Patients' global assessment includes both efficiency and side effects. PCINA represents an interesting alternative non-invasive method for postoperative pain management.
    Notes: Zusammenfassung In einer prospektiven, randomisierten Untersuchung wurden nach Genehmigung durch die zuständige Ethikkommission und schriftlicher Einverständniserklärung durch die Patienten am ersten Tag nach traumatologischen Operationen entweder eine patientenkontrollierte intravenöse Analgesie (i.v.-PCA, n=28), eine patientenkontrollierte intranasale Analgesie (PCINA, n=26) bzw. eine stationsübliche Schmerztherapie (SÜT, n=25) durchgeführt. Es werden die Ergebnisse zur Patientenakzeptanz gegenüber diesen Analgesieverfahren vorgestellt. Sowohl die Patienten der PCINA-Gruppe als auch die Patienten der i.v.-PCA-Gruppe konnten sich maximal 0,025 mg Fentanyl pro 6 min selbst intranasal bzw. intravenös verabreichen. Die stationsübliche Therapie sollte vom Untersucher unbeeinflußt bleiben und wurde vom zuständigen Stationsarzt bzw. der zuständigen Stationsschwester festgelegt. Am Ende des 8stündigen Untersuchungszeitraums wurden die Patienten zu ihrer globalen Zufriedenheit mit der durchgeführten Schmerztherapie befragt. Weiterhin sollten die Patienten Vor- und Nachteile der jeweiligen Verfahren frei formulieren. Die globale Zufriedenheit war in der Gruppe PCINA (Median: gut) und in der Gruppe i.v.-PCA (Median: gut) signifikant besser als in der Gruppe mit stationsüblicher Therapie (Median: zufriedenstellend). Als wesentliche Vorteile nannten die Patienten der PCINA- bzw. der i.v.-PCA-Gruppe die gute Schmerzlinderung (n=25 bzw. n=25) und die Unabhängigkeit von Arzt oder Pflegekraft (n=12 bzw. n=13). Nachteilig wurde von den Patienten der PCINA-Gruppe die häufig notwendige intranasale Applikation (n=6) und von den Patienten der i.v.-PCA-Gruppe Injektionsschmerz (n=4) und Bewegungseinschränkung (n=5) genannt. Die vorliegenden Ergebnisse zeigen, daß die Patientenakzeptanz gegenüber der PCINA vergleichbar gut ist wie bei der konventionellen i.v.-PCA.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Der Anaesthesist 44 (1995), S. 809-817 
    ISSN: 1432-055X
    Keywords: Schlüsselwörter Endotracheale Intubation ; Propofol ; Fentanyl ; Keine Relaxierung ; Key words Endotracheal intubation ; Propofol ; Fentanyl ; No relaxation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Abstract The routine use of succinylcholine for endotracheal intubation is being increasingly questioned. Initial studies have suggested that a combination of propofol and alfentanil without a muscle relaxant can provide good intubating conditions. However, most of these initial studies either did not have a double-blind design or did not include a control group with muscle relaxants. In this study, intubation conditions using fentanyl/propofol without a muscle relaxant were compared with the combinations of fentanyl/propofol/succinylcholine and sodium thiopental/succinylcholine. Material and methods. Following approval from the local ethics committee and written consent, 100 gynaecological patients (ASA I, II) were included in this study. The study was carried out in a double blind, randomized and prospective manner. Black perfusor syringes and extension sets were used, and the drugs administered were diluted to equal volumes. For induction, group 1 (n=25) received 0.1 mg fentanyl, 1 mg vecuronium, sodium thiopental (demand-adapted) and succinylcholine 1 mg/kg; group 2 (n=25) received 0.1 mg fentanyl and propofol (demand-adapted); group 3 (n=25) received 0.2 mg fentanyl and propofol (demand-adapted); group 4 (n=25) received 0.1 mg fentanyl, 1 mg vecuronium, propofol (demand-adapted) and succinylcholine 1 mg/kg. Each patient was assessed prior to induction with regard to visualization of the pharynx (grade I–IV). Following induction, jaw relaxation (grade I–IV) and the laryngoscopic visualization of the glottis (grade I-IV) were assessed. During the intubation, the position and movements of the vocal cords (grade I-IV) and patient movement during and 1 min following the intubation were assessed. The overall assessment of the intubation was graded (grade I–IV) by the anaesthetist and the anaesthetic nurse. Postoperatively the patients were questioned regarding muscle pain (grade I–IV). Before, during and after endotracheal intubation arterial haemoglobin oxygen saturation, heart rate and arterial blood pressure were monitored. Results. There were no intergroup differences with regard to age, height, weight and preanaesthetic visualization of the pharynx. In group 1 an average of 5.5±1.2 mg/kg sodium thiopental was required. There were no significant differences in group 2, 3 and 4 with respect to the dose of propofol (2.4, 2.2 and 2.2 mg/kg). No intergroup differences were noted with regard to jaw relaxation, laryngoscopic visualization of the glottis and patients' movements during intubation. Statistically significant intergroup differences occurred with regard to the position and movements of vocal cords during intubation (group 3 worse than groups 1, 2, 4) and the patients' movements 1 min after intubation (group 2 worse than group 3). Significant intergroup differences also occurred with regard to the overall assessment of the intubation by the anaesthetist (group 3 worse than groups 2, 4) and the anaesthetic nurse (group 3 wourse than group 4) and the postoperative muscle pain (group 1 worse than groups 2, 3). Conclusion. The use of 0.1 mg fentanyl/sodium thiopental/succinylcholine results in no better intubating conditions than 0.1 mg fentanyl plus propofol. Under these conditions, without the use of a muscle relaxant, it is possible to carry out safe endotracheal intubation in cases where no complications are anticipated.
    Notes: Zusammenfassung Es wurden die Intubationsbedingungen unter Fentanyl/Propofol (ohne Relaxansgabe) mit denen unter Fentanyl/Einleitungshypnotikum (Propofol bzw. Thiopental)/Succinylcholin verglichen. 100 gynäkologische Patientinnen (ASA I, II) wurden in die doppelblind, randomisiert und prospektiv durchgeführte Studie eingeschlossen. Als Einleitungsregimes wurden 0,1 mg Fentanyl, 1 mg Vecuronium, Thiopental (bedarfsadaptiert) plus Succinylcholin (1 mg/kg KG) (Gruppe 1, n=25), 0,1 mg Fentanyl plus Propofol (bedarfsadaptiert) (Gr. 2, n=25), 0,2 mg Fentanyl plus Propofol (bedarfsadaptiert) (Gr. 3, n=25) oder 0,1 mg Fentanyl, 1 mg Vecuronium, Propofol (bedarfsadaptiert) plus Succinylcholin (1 mg/kg KG) (Gr. 4, n=25) verabreicht. Einsehbarkeit des Rachens (Grad I–IV) bei den wachen Patientinnen, Relaxierung der Unterkiefermuskulatur (Grad I–IV) und laryngoskopische Einstellbarkeit der Glottis (Grad I–IV) nach Narkoseinduktion, Verhalten der Glottisöffnung während der Intubation (Grad I–VI) und Abwehrbewegungen bei und 1 min nach Intubation (Grad I–VI) wurden vom intubierenden Arzt beurteilt. Vom Intubierenden wurde eine abschließende globale Beurteilung der endotrachealen Intubation (Grad I–VI) vorgenommen. Bezüglich der pränarkotischen Einsehbarkeit des Rachens bestanden keine signifikanten Gruppenunterschiede. In Gruppe 1 wurden im Mittel 5,5±1,2 mg/kg KG Thiopental benötigt. Die in den Gruppen 2, 3 und 4 benötigten Propofoldosierungen (2,4± 0,63; 2,22±0,48; 2,24±0,48 mg/kg KG) waren nicht signifikant unterschiedlich. Auch bezüglich Relaxierung der Unterkiefermuskulatur, Einstellbarkeit der Glottis sowie Abwehrbewegungen bei der Intubation bestanden keine signifikanten Gruppenunterschiede. Dagegen waren betreffs des Verhaltens der Glottisöffnung während der Intubation (Gr. 3 schlechter als Gr. 1, 2, 4) und der Abwehrbewegungen 1 min nach Intubation (Gr. 2 schlechter als Gr. 3) sowie der Beurteilung der Intubation durch den Intubierenden (Gr. 3 schlechter als Gr. 2, 4) statistisch signifikante Gruppenunterschiede nachweisbar. Die durch Verwendung von 0,1 mg Fentanyl plus Thiopental/Succinylcholin erzielten Intubationsbedingungen waren nicht signifikant besser als die unter Propofol in Kombination mit 0,1 mg Fentanyl erzielten Intubationsbedingungen.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 15 (1959), S. 474-475 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Resumé Le développement embryonnaire du termiteKalotermes flavicollis dure 54 jours à une température de 26°C. Le germe appartient au «type court» (Kurzkeimtyp) selon la classification deKrause 2, mais se distingue de celui-ci par le fait qu'avant la blastocinèse il ne s'enfonce pas dans le vitellus, mais reste en position superficielle. A partir du 31e jour, il effectue d'importants déplacements (voir Fig. 2) qui mènent vers le 35e jour à son orientation définitive dans l'œuf.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 20 (1964), S. 452-453 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 5-[nitro-thiazolyl-(2)]-2-oxo-tetrahydroimidazole was found to possess schistosomicidal and amoebicidal properties. In mice this substance exhibited a curative effect in experimental infections withS. mansoni andS. japonicum. Preliminary clinical trials indicated that the compound is effective and well tolerated in the treatment of vesical bilharziasis.
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