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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 22 (1950), S. 486-488 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-055X
    Keywords: Schlüsselwörter TIVA ; Propofol/Remifentanil ; Balancierte Anästhesie ; Sevofluran/Fentanyl ; Laparoskopie ; Gynäkologie ; Key words TIVA ; Propofol/Remifentanil ; Balanced anaesthesia ; Sevoflurane/Fentanyl ; Laparoskopy ; Gynaecology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Abstract Objective: This study was designed to investigate the differences between TIVA with propofol/remifentanil (P/R) and balanced anaesthesia with sevoflurane/fentanyl (S/F) in gynaecological laparoscopic surgery. Emphasis was put on haemodynamic reaction, recovery profile, postoperative side effects and patient satisfaction. Methods: Sixty patients were randomly assigned to receive either total intravenous anaesthesia with propofol/remifentanil or anaesthesia with sevoflurane/fentanyl. After premedication (midazolam) and induction of anesthesia (propofol, atracurium) in both groups, either 1 µg/kg fentanyl (S/F) or 1 µg/kg remifentanil (P/R) was injected. Anaesthesia was maintained with 0.5 µg/kg/min remifentanil (reduced to 50% after 5 min) and 0.06 µg/kg/min propofol (P/R) or 1.7 vol % sevoflurane (S/F). Both groups were mechanically ventilated with 30% oxygen in air. The administration of sevoflurane and the infusion of the anaesthetics were adjusted to maintain a surgical depth of anaesthesia. For postoperative analgesia 1 g paracetamol was administered rectally prior to surgery. After recovery 20 mg/kg metamizol was given intravenously. At the end of surgery the anaesthetics were discontinued and haemodynamics, early emergence from anaesthesia, pain level, frequency of analgesic demand, incidence of PONV, shivering and patient satisfaction were assessed. Parameters were recorded for 24 h postoperatively. Results: Recovery time after propofol-remifentanil anaesthesia was significantly shorter than after administration of sevoflurane and fentanyl (spontaneous ventilation 4.1 vs. 6.3 min, extubation 4.3 vs. 9.3 min, eye opening 4.4 vs 8.2 min, stating name 5.3 vs. 13.2 min, stating date of birth 5.4 vs. 13.3 min). There were no significant differences between the groups in shivering, pain score, analgesic demand and PONV. The S/F group responded to tracheal intubation with significantly higher blood pressure than the P/R group. During maintenance of anaesthesia heart rate in patients with S/F was significantly higher (P/R: HR max +16/–10; S/F: HR max +24/–0.). Measured on a scale from very satisfied to very dissatisfied, 73% of the patients in the P/R group were ”very satisfied” (S/F 23%) and 23% were ”satisfied” (S/F 62%). Conclusion: Compared with patients given balanced anaesthesia with sevoflurane and fentanyl, TIVA with propofol and remifentanil proved to be particularly suited for gynaecological laparoscopic surgery. Its major advantages are haemodynamic stability, significantly shorter times of emergence, and the exceptional acceptance by the patients.
    Notes: Zusammenfassung Fragestellung: Unterscheidet sich eine TIVA mit Remifentanil/Propofol (P/R) von einer balancierten Anästhesie mit Sevofluran/Fentanyl (S/F) hinsichtlich der Hämodynamik, des Aufwachverhaltens, postoperativer Nebenwirkungen und der Patientenzufriedenheit? Methodik: 60 Patientinnen wurden randomisiert einer Anästhesie mit (P/R) oder (S/F) zugeteilt. Nach oraler Prämedikation mit Midazolam wurde die Narkose mit Propofol eingeleitet, die Relaxierung erfolgte mit Atracurium. Gemäß randomisierter Gruppenzuteilung wurde 1 µg/kg Fentanyl oder 1 µg/kg Remifentanil i.v. injiziert und die Narkose bis zum OP-Ende entweder mit 0,5 µg/kg/h Remifentanil (Reduktion auf 50% nach 5 min) und mit 0,06 mg/kg/min Propofol oder mit 1,7 Vol.-% Sevofluran aufrechterhalten. Beide Gruppen wurden mit 30% O2 in Luft beatmet. Die Dosierung von Sevofluran, Propofol und Remifentanil wurden bei Bedarf der jeweiligen Intensität chirurgischer Stimuli angepaßt. Zur postoperativen Analgesie erhielten alle Patientinnen zu OP-Beginn 1 g Paracetamol rektal, nach Erwachen Metamizol 20 mg/kg i.v.. Bei OP-Ende wurde die Anästhetikazufuhr unterbrochen und folgende Parameter erfaßt: mittlerer arterieller Blutdruck, Herzfrequenz, Aufwachverhalten, Schmerzintensität, Analgetikabedarf, PONV, Muskelzittern und die Patientenzufriedenheit mit dem Anästhesieverfahren. Der Beobachtungszeitraum betrug 24 h. Ergebnisse: Die Patientinnen waren nach einer P/R Narkose signifikant eher wach und orientiert als nach einer Anästhesie mit S/F (Spontanatmung 4,1 vs. 6,3 min, Extubation 4,3 vs. 9,3 min, Augenöffnen 4,4 vs. 8,2 min, Namen nennen 5,3 vs. 13,2 min, Geburtsdatum 5,4 vs. 13,3 min). Die Inzidenz von PONV (43% vs. 43%) und Muskelzittern (56% vs. 37%) sowie die Schmerzintensität und die Anzahl der Schmerzmittelanforderungen (67 vs. 52) waren in beiden Gruppen vergleichbar. Der MAP war in der S/F-Gruppe nach der Intubation signifikant höher, die HF im gesamten Verlauf signifikant höher als in der P/R Gruppe (P/R: HF max. +16/–10; S/F: HF max. +24/–0). Auf einer Skala von „sehr zufrieden–sehr unzufrieden” waren 73% (P/R) der Patientinnen mit dem Anästhesieverfahren „sehr zufrieden” (S/F 23%), 23% „zufrieden” (S/F 62%). Schlußfolgerung: Verglichen mit einer balancierten Anästhesie mit Sevofluran und Fentanyl erwies sich die TIVA mit Remifentanil und Propofol als besonders vorteilhaft für laparoskopische Operationen in der Gynäkologie. Wesentliche Vorteile waren signifikant schnellere Aufwachzeiten, die hämodynamische Stabilität und die große Akzeptanz des Anästhesieverfahrens durch die Patientinnen.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 144 (1986), S. 532-538 
    ISSN: 1432-1076
    Keywords: Cephalosporins ; Specific uses ; Pharmacokinetics ; Microbiologic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The cephalosporins have been available for clinical use for nearly 20 years and a large number is presently marketed, including drugs with a wide range of different pharmaokinetic and microbiologic properties. While some of these agents have certain specific uses in which they excel, the cephalosporins have not replaced older antibiotics but do provide the physician with a broader range of choices for the treatment of many infections, allowing greater individualization of therapy.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1076
    Keywords: Key wordsHaemophilus influenzae type b ; Acellular pertussis ; Vaccination ; PRP-tetanus ; Diphtheria
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract With an increasing number of new vaccines available for routine childhood immunization, combination vaccines are needed in order to maintain or achieve a high compliance with recommended immunization programmes. In a prospective, randomized, comparative, multi-centre study, 822 healthy infants were enrolled to receive three doses of either a candidate or a commercially available Haemophilus influenzae type b (Hib) vaccine concomitantly with diphtheria-, tetanus- acellular pertussis (DTaP) vaccine. Study subjects were randomly allocated to one of the following groups: (1) separate, or (2) mixed injection of DTaP and candidate Hib vaccine, or (3) separate injection of DTaP and commercial Hib vaccine. One year later the first 189 study subjects received either separate or mixed injections of the same Hib and DTaP vaccines as booster doses. Evaluation of reactogenicity was based on diary cards completed by parents. Immunogenicity was documented by measuring IgG antibody concentrations in serum samples taken before and 4 weeks after primary and booster vaccination. No serious adverse events occurred and most local and systemic reactions were mild to moderate. Booster doses were more reactogenic than primary doses with all groups. Antibody concentrations against pertussis antigens were similar to those seen with DTaP alone. All but one subject had protective antibody concentrations against diphtheria and tetanus. Primary immune response to the Hib vaccine was significantly lower in the group receiving the mixed Hib-DTaP vaccine, however, ≥95% of vaccinees had anti-Hib antibody concentrations ≥0.15 μg/ml and there was a marked booster response (〉100-fold) in all groups. Conclusions Mixing DTaP and Hib vaccines for primary immunization caused a decrease in anti-Hib antibody response, although after primary immunization as after booster doses, all subjects showed antibody concentrations considered to be protective for invasive Hib disease. Mixing of the vaccines did not result in increased reactogenicity.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1076
    Keywords: Key words pertussis ; attack rate ; household ; adult ; erythromycin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The objective of this study was to compare the spread of pertussis in children and adults being secondary contacts after household exposure. The study was nested in an efficacy trial of an acellular pertussis vaccine. The spread of the disease was also monitored with respect to gender and antibiotic therapy. A total of 453 index cases, of which 133 were monitored for adult disease, fulfilled the WHO definition of pertussis. They had contacts to 173 unvaccinated children aged 6–47 months, and a total of 101 adults with pertussis were followed. Detection of the bacteria, or a significant increase of specific antibodies confirmed the diagnosis. Secondary spread of the disease was assumed, when a household member coughed for 7 days or more and had laboratory evidence for pertussis. Crude attack rates (AR) were 69% in children and 31% in adults (P 〈 0.05). AR in children were independent of gender but more women than men (P = 0.02) were affected in those households where the index case was a child. Erythromycin treatment of the index case reduced the AR in exposed toddlers from 80% to 57% (P = 0.06), and in exposed adults from 40% to 21% (P= 0.2). Erythromycin therapy in contacts did not alter the clinical course of the disease significantly. Conclusions In a household study of pertussis, 69% of children and 31% of adults (more women than men) contracted the disease. Erythromycin reduced the number of infections in household contacts, but did not alter the clinical course in those who contracted pertussis.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 152 (1993), S. 387-388 
    ISSN: 1432-1076
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 152 (1993), S. 462-466 
    ISSN: 1432-1076
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 155 (1996), S. 74-76 
    ISSN: 1432-1076
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 143 (1984), S. 73-73 
    ISSN: 1432-1076
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 143 (1984), S. 74-74 
    ISSN: 1432-1076
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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