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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Anaesthesia 45 (1990), S. 0 
    ISSN: 1365-2044
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Postmortem specimens of 10 patients who had received continuous epidural anaesthesia postoperatively (ranging from 2–21 days) were examined. Slight epidural haemorrhage was observed in six patients and a macroscopically visible haematoma in a thrombocytopenic patient. Nonspecific epidural inflammatory reactions were observed microscopically in all patients. Specimens from seven patients with systemic infection showed signs of epidural infection. No similar pathology was found in a control group without epidural catheters. The aetiology and risk factors of the above findings are discussed, and recommendations given to prevent such sequelae after epidural anaesthesia.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Anaesthesia 45 (1990), S. 0 
    ISSN: 1365-2044
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 592 (1990), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Der Anaesthesist 43 (1994), S. 385-397 
    ISSN: 1432-055X
    Keywords: Schlüsselwörter: Postoperativer Schmerz – Allgemeine Krankenpflegestation – Akutschmerzdienst – PCA – Epiduralanalgesie – Komplikationen – Atemdepression – Hypotension ; Key words: Postoperative pain therapy – Acute pain service – Epidural analgesia – Patient-controlled analgesia – Respiratory depression – Hypotension – Normal ward
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Abstract. Despite major advances in knowledge and development of efficient techniques for pain control, many patients on surgical wards suffer from modest to severe pain following surgery or trauma. Therefore, in the University Hospital of Kiel, Germany, an anaesthesiology-based acute pain service (APS) was started in 1985 to improve this situation. Organization of an APS. The anaesthesiologist in training who manages the recovery unit serves as an APS for surgical wards and is supervised by a consultant. The anaesthesists on call are responsible after regular working hours. The activities of the APS are as follows: 1. Induction of sufficient postoperative analgesia in the recovery unit for all surgical patients. 2. Clinical rounds on all patients receiving epidural analgesia (EA), other forms of regional analgesia, or patient-controlled analgesia (PCA) every morning and throughout the day if necessary. 3. Additional consultations for postoperative pain management for other patients on request. 4. Assessment and documentation of the clinical status of the patient, quality of analgesia, and side effects. 5. Writing orders for further treatment. 6. Continuing consultations and informal education for ward nurses, physiotherapists, and surgical staff; formal medical training for ward nurses in postoperative pain management. Activity of the APS. From 1985 to 1992, 1947 patients on normal wards were treated (EA: 1736, PCA: 183). Epidural analgesia was performed using a standard protocol with bupivacaine 0.175% – 0.25% infused continuously with top-ups if needed (mean 240 mg/day, range 75 – 600 mg; median duration 7 days, range 1 – 53, Table 1). Demand for further treatment was proved by day-to-day withdrawal. Since the introduction of an APS, complications of EA such as hypotension (1985/1986: 5.1%; 1987/1992: 0.5%, Table 3) and insufficient analgesia due to dislocation or other technical complications could be reduced significantly (Table 3). Dermal infections were seen in 2.6% of patients, with a significantly higher incidence in patients with arteriosclerotic diseases (4.1%). Epidural opioids were used in only 46 selected cases on surgical wards. Nevertheless, 2 cases of marked respiratory depression occurred. The overall risk of complications during postoperative EA could be reduced from 1 : 11 cases in the first 2 years to 1 : 20 in the last 6 years since introducing the APS. For other regional procedures (e.g., interpleural analgesia) no complications were recorded. PCA was performed using a standard protocol with tramadol or piritramide without background infusion (Table 6). The loading dose was titrated in the recovery unit. The median duration of PCA was 4 days (range 1 – 23); the median dose of piritramide was 45 mg/day (range 3 – 226 mg). Two cases of somnolence and respiratory depression occurred. In this period there were 8 potential life-threatening complications due to postoperative pain therapy; 4 occurred during standard surgical pain management (3 cases of severe respiratory depression after i.m. and i.v. piritramide (unsuccessfull resuscitation), tramadol, and buprenorphine; 1 small child with multiorgan failure after paracetamol intoxication). In those cases the APS was not involved. Conclusions. There are insufficient data for comparison of the incidence of complications following standard management of postoperative pain relief without an APS, i.e., i.m. injections of opioids on request, but severe and sometimes lethal complications have been reported. Since the majority of patients used EA or PCA for several days, it is again emphasised that these techniques should not be restricted to high-dependency areas such as intensive care or recovery units. The introduction of an APS is an adequate approach to more efficient and safer pain management on surgical wards. This requires standard protocols (Table 7), standardised monitoring and trained ward nurses. Based on our experience, most complications develop slowly, and risk factors can be recognised early enough to avoid severe sequelae. The routine use of epidural opioids on surgical wards is not recommended unless special monitoring (e.g., pulse oximetry) is provided. Establishing an APS is a major future challenge for anaesthesiologists. Nevertheless, surgeons should also participate to improve the standard of pain management. We should be aware that this service can not be run efficiently during simultaneous activity in the operating room.
    Notes: Zusammenfassung. Seit 1985 wurden 1947 Patienten durch einen Anästhesiologischen Schmerzdienst auf Allgemeinen Krankenpflegestationen an insgesamt 13 971 Tagen betreut. Bei den 1736 Patienten mit Epiduralanalgesie (EA) mit 0,175 – 0,25% Bupivacain betrug die mittlere Behandlungsdauer 7 (1 – 53) Tage, bei 50% der Patienten länger als eine, bei 11% mehr als 2 Wochen. 183 Patienten mit PCA (Tramadol, Piritramid) wurden im Mittel an 4 (1 – 23) Tagen, hiervon 21,4% länger als eine Woche behandelt. Seit Einführung des Schmerzdienstes sank die Häufigkeit therapiebedingter Komplikationen unter der EA von 10,4% signifikant auf 6% in den letzten beiden Jahren, z. B. traten gravierende Hypotensionen in den letzten Jahren nicht mehr auf. Obwohl nur in Ausnahmefällen eingesetzt, traten zwei Fälle einer schweren Atemdepression nach epiduralem Morphin auf. Unter der PCA wurden ebenfalls zwei Fälle (1% der Anwendungen) beobachtet. Außerdem wurden vier schwere Komplikationen mit einem Todesfall im Rahmen der nicht vom Schmerzdienst betreuten Standardschmerztherapie dokumentiert. Die Anbindung des Schmerzdienstes an den Aufwachraum hat sich bewährt, da hier die Wirksamkeit und Verträglichkeit der auf den Allgemeinstationen vorgesehenen Therapie geprüft werden kann. Auf den Stationen muß mittels täglicher Visiten anhand standardisierter Protokolle der weitere Verlauf systematisch überwacht werden. Unter diesen Rahmenbedingungen ist die Schmerztherapie auch mittels spezieller Verfahren (EA, PCA) auf Allgemeinen Pflegestationen praktikabel und vertretbar.
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  • 5
    ISSN: 1432-069X
    Keywords: UV-photocarcinogenesis ; hairless mice ; UVA hazards
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The carcinogenic effect of three UVA tanning sources was studied in lightly pigmented hairless mice. The three tanning sources (Bellarium-S SA-1-12, Philips TL 09R and Philips TL 10R) have different emission spectra, and emit different amounts of UVB. Radiation from the tanning sources was administered for 20 min/day, 5 day/week in daily doses equivalent to those used in suntan salons. The radiation was given alone or after 12 weeks of exposure to solar-simulated UV radiation (SOLAR UV) (10min/day, 4 day/week; daily dose, 19.5 kJ/m2 UVA and 3.9 kJ/m2 UVB). Irradiation with Bellarium-S SA-1-12 for 47 weeks and Philips TL 09R for 74 weeks induced skin tumours in 20/20 and 13/20 of the animals, respectively. When irradiation with Bellarium-S SA-1-12 and Philips TL 09R was administered after 12 weeks of SOLAR-UV exposure, a strong enhancement of SOLAR-UV-induced photocarcinogenesis was observed (p〈0.001). Irradiation with Philips TL 10R was only slightly carcinogenic, and during 85 weeks of irradiation only one skin tumor appeared in a group of 20 mice. However, when irradiation with Philips TL 10R was administered after 12 weeks of exposure to SOLAR UV, an enhancement of SOLAR-UV-induced carcinogenesis was observed (p〈0.001). Our results suggest that the hazards of exposure to commercial tanning devices are increased when they are used after a period of natural sun exposure. Even tanning sources with a low carcinogenic potential are able to increase SOLAR-UV-induced carcinogenesis significantly.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Molecular Reproduction and Development 27 (1990), S. 93-101 
    ISSN: 1040-452X
    Keywords: Somatomedin ; sis protooncogene ; Menstrual cycle ; Endometrium ; Myometrium ; Leiomyoma ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The human uterus repeatedly exhibits cyclic biochemical and cytological changes during the reproductive period of life. These changes are the result of a well-characterized endocrine network involving the hypothalamus, pituitary, and ovary. The exact nature of the mechanism(s) by which the sex steroids act on the uterus remains to be elucidated. Possible local mediators of hormonal action on the uterus include polypeptide growth factors. Using the method of RNA transfer blot hybridization, we have analyzed tissue samples from the cycling human endometrium and tissue samples of human myometrium and myometrial benign tumor (leiomyoma) for the presence of platelet-derived growth factor (PDGF) and insulin-like growth factor (IGF) RNA. All the uterine tissues examined possessed RNA for PDGF-B chain and IGF-I and -II. Two transcripts were observed for PDGF-B chain, four were observed for IGF-I, and eight were observed for IGF-II. Overall, the relative abundance of PDGF-B chain RNA was consistent in all of the uterine tissues examined. In contrast, IGF RNA relative abundance varied. IGF-I RNA was highest in late proliferative stage endometrium, and IGF-II RNA was highest in early proliferative stage endometrium. Both IGF-I and IGF-II RNAs were greater in amount in leiomyoma than in myometrium. The increased IGF-I RNA in late proliferative-stage human endometrium correlates with the known elevation of estradiol secretion by the ovary and the increased concentration of uterine estradiol receptors during this stage of the menstrual cycle. Furthermore, these data are consistent with reports of increased IGF-I RNA in the rat uterus in response to administration of estradiol. Elevated levels of IGF RNA in leiomyomas may be related to the genesis and/or progression of these myometrial tumors.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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