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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 5 (1966), S. 2744-2755 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 37 (1965), S. 1225-1227 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1420-908X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract These experimental studies were conducted to obtain information about the antinociceptive action of flupirtine within the central nervous system. Flupirtine dose-dependently increased pain threshold in the electrostimulated pain test in mice. Its antinociceptive activity was attenuated by simultaneous administration of the noradrenergica 1/a 2-antagonist yohimbine anda 2-antagonist idazoxane. By contrast, the analgesia induced by codeine or morphine was not influenced bya 2-adrenergic antagonists at all. A striking resemblance could be observed in the pharmaco-EEG of freely moving rats treated with clonidine and flupirtine, respectively. The present results are consistent with the hypothesis that the noradrenergic descending pain-modulating system might be involved in the antinociceptive mode of action of flupirtine.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-055X
    Keywords: Schlüsselwörter Immobilisation ; Kopfschmerz ; Spinalanästhesie ; Spinalnadel ; Key words Headache ; Needle ; Recumbency ; Spinal anaesthesia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Abstract Post-dural puncture headache (PDPH) is a significant complication of spinal anaesthesia. Diameter and tip of the needle as well as the patient′s age have been proven to be important determinants. The question of whether post-operative recumbency can reduce the risk of PDPH has not been answered uniformly. And besides, some studies referring to this subject reveal methodical failures, for example, as to clear definition and exact documentation of post-operative immobilization. Furthermore, fine-gauge needles (26G or more) have not been investigated yet. The first aim of our study was therefore to examine the role of recumbency in the prevention of PDPH under controlled conditions using thin needles. Secondly, we wanted to confirm the reported prophylactic effect of needles with a modified, atraumatic tip (Whitacre and Atraucan) by comparing them to Quincke needles of identical diameter. Most of the former investigators compared Quincke with atraumatic needles of different size regardless of the known influence of the diameter on PDPH. Patients and methods: In a prospective study we included 481 consecutive patients undergoing a total of 500 orthopaedic operations under spinal anaesthesia. The latter was performed in a standardized manner (patient sitting, midline approach, needle with parallel bevel direction), using four different needles allocated randomly (26-gauge and 27-gauge needles with Quincke tip, 26-gauge Atraucan and 27-gauge Whitacre cannula). Half of the patients were instructed to stay in bed for 24 h (horizontal position without raising head), the others to get up as early as possible. An anaesthesiologist visited the patients on the fourth postoperative day or later and questioned them about headache and duration of recumbency. Additionally, the patients had to fill out a questionnaire 1 week after surgery. Any postural headache was considered as PDPH. Results: The four groups of different needles had homogeneous demographic characteristics (see Table 1). A total of 47 patients (9.4%) developed PDPH. The incidence was highest after puncture with a 26-gauge Quincke cannula (17.6%) with a significant difference compared to the other needles (see Table 2). PDPH incidence correlated well with increasing age and number of dural punctures, but showed no relation to sex, patient´s history of headache or experience of the anaesthesiologist. Only about half of the patients (60.5%) followed the instructions regarding mobilization or recumbency. The duration of strict bed rest did not influence the development of PDPH: The overall incidence was 9.4% in the recumbency group and 8.8% in the group of early ambulation. In all, 45 patients suffered from ordinary not posture-related headache. Conclusions: The significantly higher incidence of PDPH after spinal anaesthesia with 26-gauge Quincke needles compared to the 27-gauge Quincke and the 26-gauge Atraucan group confirmed the importance of both needle diameter and design of its tip. The Atraucan cannula has not been examined in a controlled study (in comparison with Quincke needle of the same diameter) before. In accordance with other investigators we found patient′s age and number of puncture attempts as additional predictors of PDPH. Consequent bed rest, however, was not able to reduce its incidence. Our studies reveal the poor compliance of patients with regard to mobilization/immobilization, a problem which possibly has not been considered enough in former studies examining the influence of bed rest on PDPH. Based on the literature and the present findings, we recommend using thin needles with atraumatic tips for spinal anaesthesia if possible. Recumbency presents an avoidable stress for patients as well as medical staff and should no longer be ordered.
    Notes: Zusammenfassung Patienten und Methoden: Bei 481 orthopädischen Patienten wurden prospektiv insgesamt 500 Spinalanästhesien randomisiert mit vier unterschiedlichen Kanülen durchgeführt (Spinocan® 26G und 27G mit Quincke-Schliff, Atraucan® 26G und Whitacre 27G mit atraumatischer Spitze). Ergebnisse: 47 Patienten (9,4%) litten anschließend unter postspinalen Kopfschmerzen. Das geringste Kopfschmerzrisiko bestand nach Punktion mit der Whitacre-Nadel (4,8%). Signifikante Unterschiede zwischen Spinocan® 26G (Kopfschmerzinzidenz 17,6%) einerseits und Spinocan® 27G (6,4%; p 〈 0,01) bzw. Atraucan® 26G (8,8%; p 〈 0,05) andererseits konnten die Bedeutung von Durchmesser bzw. Spitzenkonfiguration der Kanüle verifizieren. Weitere Prädiktoren waren niedriges Lebensalter (p 〈 0,0005) und mehrmalige Punktion (p 〈 0,05). Die Dauer der postoperativen Flachlagerung hatte dagegen keinen Einfluß auf die Kopfschmerzgenese. Schlußfolgerungen: Um das Risiko des postspinalen Kopfschmerzes zu minimieren, sollten nach Möglichkeit grundsätzlich dünne, atraumatische Spinalnadeln verwendet werden. Die postoperative Immobilisation dagegen ist als Prophylaxe ungeeignet und stellt eine vermeidbare Belastung für Patient und Personal dar.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-055X
    Keywords: Schlüsselwörter Atemarbeit ; Beatmung ; Pressure Support Ventilation ; COPD ; Key words Pressure support ventilation ; Work of breathing ; Chronic obstructive pulmonary disease ; Mechanical ventilation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Abstract During pressure support ventilation (PSV), the timing of the breathing cycle is mainly controlled by the patient. Therefore, the delivered flow pattern during PSV might be better synchronised with the patient's demands than during volume-assisted ventilation. In several modern ventilators, inspiration is terminated when the inspiratory flow decreases to 25% of the initial peak value. However, this timing algorithm might cause premature inspiration termination if the initial peak flow is high. This could result not only in an increased risk of dyssynchronization between the patient and the ventilator, but also in reduced ventilatory support. On the other hand, a decreased peak flow might inappropriately increase the patient's inspiratory effort. The aim of our study was to evaluate the influence of the variation of the initial peak-flow rate during PSV on respiratory pattern and mechanical work of breathing. Patients. Six patients with chronic obstructive pulmonary disease (COPD) and six patients with no or minor nonobstructive lung pathology (control) were studied during PSV with different inspiratory flow rates by variations of the pressurisation time (Evita I, Drägerwerke, Lübeck, Germany). During the study period all patients were in stable circulatory conditions and in the weaning phase. Method. Patients were studied in a 45° semirecumbent position. Using the medium pressurization time (1 s) during PSV the inspiratory pressure was individually adjusted to obtain a tidal volume of about 8 ml/kg body weight. Thereafter, measurements were performed during five pressurization times (〈0.1, 0.5, 1, 1.5, 2 s defined as T 0.1, T 0.5, T 1, T 1.5 and T 2) in random order, while maintaining the pressure support setting at the ventilator. Between each measurement steady-state was attained. Positive end-exspiratory pressure (PEEP) and FIO2 were maintained at prestudy levels and remained constant during the study period. Informed consent was obtained from each patient or his next of kin. The study protocol was approved by the ethics committee of our medical faculty. Gas flow was measured at the proximal end of the endotracheal tube with a pneumotachometer (Fleisch no. 2, Fleisch, Lausanne, Switzerland) and a differential pressure transducer. Tracheal pressure (Paw) was determined in the same position with a second differential pressure transducer (Dr. Fenyves & Gut, Basel, Switzerland). Esophageal pressure (Pes) was obtained by a nasogastric balloon-catheter (Mallinckrodt, Argyle, NY, USA) connected to a further differential pressure transducer of the same type as described above. The balloon was positioned 2–3 cm above the dome of the diaphragm. The correct balloon position was verified by an occlusion test as described elsewhere. The data were sampled after A/D conversion with a frequency of 20 Hz and processed on an IBM-compatible PC. Software for data collection and processing was self-programmed using a commercially available software program (Asyst 4.0, Asyst Software Technologies, Rochester, NY, USA). Patient's inspiratory work of breathing Wpi (mJ/l) was calculated from Pes/volume plots according to the modified Campbell's diagram. Dynamic intrinsic PEEP (PEEPidyn) was obtained from esophageal pressure tracings relative to airway pressure as the deflection in Pes before the initiation of inspiratory flow Patient's additive work of breathing (Wadd) against ventilator system resistance was calculated directly from Paw/V tracings when Paw was lower than the pressure on the compliance curve. Two-way analysis of variance (ANOVA) was used for statistical analysis, followed by post hoc testing of the least significant difference between means for multiple comparisons. Probability values less than 0.05 were considered as significant. Results. COPD patients had significantly higher pressure support than control patients. With decreasing inspiratory flow, Wpi increased significantly in COPD patients. Additionally, the duct cycle (Ti/Ttot) significantly increased with decreased flow rates which resulted in a higher PEEPidyn compared to the baseline. At T 1.5 and T 2 with lower flow rates, the pre-set pressure support level was not achieved within inspiration in the COPD patients. Wadd increased significantly at T 1, T 1.5 and T 2 in COPD patients and at T 1.5 and T 2 in the control group. In one patient, premature termination of inspiration owing to high initial peak flow was corrected by adjustment of the inspiratory flow. Conclusion. Our results demonstrate that a decreased peak flow during PSV resulted in increased patient's work of breathing in COPD patients. During lower flow, the pre-set pressure support level was not attained and additional work had to be done on the ventilator system. Furthermore, the higher PEEPidyn during lower flow rates indicates a higher risk of dynamic pulmonary hyperinflation in patients with COPD. We conclude that the use of pressurization times ≥1 s to decrease inspiratory peak flow during PSV is of no benefit and should be avoided, particularly in COPD patients. However, in selected cases, slight decrease of inappropriately high peak flows might be useful for optimization of PSV setting to avoid premature termination of inspiration.
    Notes: Zusammenfassung Bei einigen Respiratoren kann unter Pressure Support Ventilation (PSV) der Inspirationsfluß (V˙ i ) durch Veränderung der Druckanstiegszeit variiert werden. Über den Einfluß des Inspirationsflußprofils unter PSV auf die Atemarbeit ist besonders bei Patienten mit chronischer Atemwegsobstruktion (COPD) kaum etwas bekannt. Wir untersuchten an 6 COPD-Patienten und 6 Patienten ohne Lungenerkrankung (Kontrollgruppe) die Effekte einer Variation von V˙ i unter PSV auf atemmechanische Variablen und die mechanische Atemarbeit. Unter individuell eingestellter Druckunterstützung wurde die Druckanstiegszeit in 5 Stufen verändert. Die Verlängerung der Druckanstiegszeit verminderte den initialen V˙ i in beiden Patientengruppen. Gleichzeitig stieg die Atemarbeit in der COPD-Gruppe bei verringertem V˙ i signifikant an. Eine Ursache hierfür war, daß bei den COPD-Patienten bei langsamen Druckanstiegszeiten die eingestellte Druckunterstützung nicht mehr erreicht wurde. Der langsamere V˙ i führte zu einer Verlängerung der Inspiration auf Kosten der Exspirationszeit. Dies verursachte bei COPD-Patienten eine unerwünschte Erhöhung des intrinsischen PEEP. Die Auswirkungen eines niedrigeren V˙ i unter PSV in der Kontrollgruppe waren klinisch nur wenig relevant. Unsere Ergebnisse zeigen, daß besonders bei Patienten mit COPD unter PSV hohe initiale Inspirationsflüsse zu bevorzugen sind, da ein niedriger Fluß die Patientenatemarbeit erhöht und eine dynamische Lungenüberblähung verstärkt. Allerdings konnte bei einem Patienten ein vorzeitiger Inspirationsabbruch aufgrund eines hohen Initialflusses durch Anpassung des Flußprofils korrigiert werden. In Einzelfällen kann daher eine Verlängerung der Druckanstiegszeit bis auf maximal 1 s sinnvoll sein.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-055X
    Keywords: Schlüsselwörter Ropivacain ; Clonidin ; Epiduralanästhesie ; Analgesie ; Key words Ropivacaine ; Clonidine ; Epidural analgesia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Abstract Objective: The aim of this study was to in- vestigate preliminarydose-range effects of clonidine added to ropivacaine for epidural analgesia in elective orthopedic surgery of the lower limbs with doses, causing a minimum of cardiovascular side effects. Methods: 60 patients were randomly assigned to receive in a double-blind fashion a mixture of 1 mg/cm height ropivacaine plus saline or 1 mg/cm ropivacaine plus 25 µg, 50 µg, 75 µg, 100 µg or 150 µg clonidine for epidural analgesia. The sensory and motor function were determined at defined time intervalls for 30 minutes. Heart rate and blood pressure were controlled and sedation score was judged. The postoperative 2-segment-regression of pin-prick and the onset of pain were recorded. Results: The six groups were comparable in demographic datas and in term of onset time. The prolongation of analgesia reached 513 ± 92 min (p = 0,002) for 150 µg clonidine, 460 ± 148 min (p = 0,073) for 100 µg clonidine, 440 ± 86 min (p = 0,057) for 75 µg clonidine compared with 347 ± 114 min for saline. In an equal manner, 2-segment- regression for pin-prick was extended to 251 ± 47 min (p = 0,018) for 150 µg clonidine, 238 ± 33 min (p = 0,034) for 100 µg clonidine, 229 ± 29 min (p = 0,027) for 75 µg clonidine and 178 ± 43 min for saline. Heart rate dropped down in all groups. Mean arterial pressure decreased significantly in the groups with 75, 100 and 150 µg clonidine. Sedation score increased continously from 0,6 ± 0,5 (saline) to 1,8 ± 0,8 (150 µg clonidine). Conclusion: We conclude that 150 µg clonidine significantly enhances the duration of analgesia of epidurally administered ropivacaine in a mean of 171 mg. This time intervall is longer than the one with 200 mg ropi-vacaine alone. But, there are side effects in form of decrease of arterial pressure. Cardiovascular monitoring seems to be essential. Because of the enhanced analgesia duration, the time interval for reloading epidural anaesthesia are increased.
    Notes: Zusammenfassung Fragestellung: Es sollte bei elektiven orthopädischen Eingriffen an der unteren Extremität eine erste Dosis-Wirkungsbeziehung von Clonidin zu epidural appliziertem Ropivacain untersucht werden in einem Bereich, in dem am wenigsten mit kardiovaskuklären Nebenwirkungen zu rechnen ist. Methodik: Es wurden sechs Gruppen à 10 Patienten gebildet. Gruppe 1 bekam 1 mg/cm Körpergröße Ropivacain mit einem Zusatz von 25 µg Clonidin, die zweite Gruppe 50 µg Clonidin, die dritte Gruppe 75 µg Clonidin, die vierte Gruppe 100 µg Clonidin und die fünfte Gruppe 150 µg Clonidin als Zusatz. Als Kontrolle diente eine Gruppe mit NaCl 0,9% als Adjuvans. Der sensible und motorische Wirkungseintritt wurde ab der 5. min im Abstand von 5 min bis zur 20. min und dann in der 30. min bestimmt. Weiterhin wurde das Kreislaufverhalten dokumentiert und die Sedierung nach 45 min anhand eines Scores beurteilt. Nach Operationsende untersuchten wir die Rückkehr des „Spitz-Stumpf-Empfindens” bis zur 2-Segment-Regression und den Zeitpunkt des Einsetzens von Schmerzen. Ergebnisse: Die Gruppen waren hinsichtlich demographischer Daten und der Anschlagzeit vergleichbar. Die Analgesiezeit war mit dem Zusatz von 150 µg Clonidin auf 513 ± 92 min (p = 0,002) verlängert, mit 100 µg Clonidin auf 460 ± 148 min (p = 0,073), mit 75 µg Clonidin auf 440 ± 86 min (p = 0,057) gegenüber 347 ± 114 min in der Kontrollgruppe. Die 2-Segment-Regression betrug mit 150 µg Clonidin 251 ± 47 min (p = 0,018), mit 100 µg Clonidin 238 ± 33 min (p = 0,034), mit 75 µg Clonidin 229 ± 29 min (p = 0,027) und ohne Zusatz 178 ± 43 min. Die Herzfrequenz fiel in allen Gruppen ohne Gruppenunterschiede innerhalb von 60 min signifikant zum Ausgangswert ab. Der mittlere arterielle Druck (MAP) sank in allen Gruppen mit Ausnahme der Kontrollgruppe signifikant zwischen der 20. und der 40. min zum Ausgangswert. Im Gruppenvergleich zur reinen Substanz fanden sich mit 75 µg Clonidin signifikante Unterschiede des MAP von der 20. min an, mit 100 µg Clonidin von der 50. min an und mit 150 µg Clonidin in der 40. min. Der mittlere Sedationsscore lag nach 45 min in der Kontrollgruppe bei 0,6 ± 0,5, mit 75 µg Clonidin bei 1,3 ± 1,0, mit 100 µg Clonidin bei 1,7 ± 0,8 (p = 0,022) und mit 150 µg Clonidin bei 1,8 ± 0,8 (p = 0,007). Schlußfolgerung: Wir konnten in dieser Untersuchung zeigen, daß 150 µg Clonidin die analgetische Wirkung des Ropivacains signifikant steigert. Das schmerzfreie Intervall lag bei einer mittleren Ropivacainmenge von 171 mg mit Clonidin deutlich über den Zeiten, die mit 200 mg Lokalanästhetikum gefunden wurden. Parallel fanden sich signifikante Blutdruckunterschiede. Ein engmaschiges Herz-Kreislauf-Monitoring des Patienten ist dazu in jedem Fall notwendig. Durch den Clonidinzusatz können die Nachspritzintervalle verlängert werden.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-055X
    Keywords: Schlüsselwörter Kolloidale Volumenersatzmittel ; Neutrophile Granulozyten ; Phagozytose ; Oxidativer Burst ; Komplementrezeptoren ; Key words Kolloids ; Neutrophils ; Phagocytosis ; Oxidative burst ; Complement receptor expression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Abstract Introduction: The influence of kolloids on the immune system is not well documented. In this study we investigated the effects of gelatine, hydroxyethylstarch (HES), human albumine, and dextrane on neutrophil function and receptor expression by flow cytometry. Methods: Whole blood of healthy volunteers was incubated for 30 minutes with either gelatine, HES (6% and 10%), dextrane 40 and 60, or human albumin 20%. Phagocytic capacity was determined by uptake of fluorescein-isothiocyanate labeled bacteria, the conversion of dihydrorhodamine 123 into fluorescent rhodamine 123 was used for oxidative burst measurements. Expression of complement receptors CD 11b and CD35 was investigated using fluorescein-isothiocyanate labeled antibodies. Results: Incubation with gelatine significantly increased expression of complement receptors and oxidative burst. Dextranes and HES had no influence on neutrophil function. Human albumin reduced the oxidative burst, whereas CD 35 expression was increased. Conclusion: The physiological significance of these changes in a range of 10% has to be clarified in further investigations.
    Notes: Zusammenfassung Fragestellung: Der Einfluss kolloidaler Volumenersatzmittel auf die Immunfunktion ist unzureichend belegt. In dieser Studie wurden die Auswirkungen von Gelatinelösungen, Hydroxyäthylstärke (HAES), Humanalbumin und Dextranen auf Expression von Oberflächenrezeptoren und Funktion polymorphkerniger neutrophiler Granulozyten durchflusszytometrisch untersucht. Methodik: Vollblut von gesunden Probanden wurde 30 min mit folgenden Volumenersatzmitteln inkubiert: HAES (6% und 10%), Dextran 40, Dextran 60, Gelatinelösung (3%), Humanalbumin 20%. Die Phagozytoseleistung wurde mittels Fluoreszeinisothiozyanat-markierten Bakterien ermittelt. Der Oxidative Burst wurde anhand der Umwandlung von Dihydrorhodamin 123 in grün-fluoreszierendes Rhodamin 123 bestimmt. Die Expression der Komplementrezeptoren CD11b und CD 35 wurde mit Fluoreszeinisothiozyanat-markierten Antikörpern untersucht. Ergebnisse: Nach Inkubation mit Gelatinelösung waren Expression von Komplementrezeptoren und Oxidativer Burst signifikant erhöht. Der Median der Fluoreszenzintensität stieg für CD35 von 531±42 auf 565±51, für CD 11b von 416±24 auf 446±19 und für den Oxidativen Burst von 490±52 auf 516±51. HAES und Dextrane beeinflussten die Granulozytenfunktion nicht. Humanalbumin 20% steigerte die Expression von CD 35, reduzierte jedoch den Oxidativen Burst. Schlussfolgerung: Die klinische Bedeutung dieser in vitro-Veränderungen in einer Größenordnung von maximal 10% des Ausgangswerts sollte in in vivo-Studien näher untersucht werden.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Der Anaesthesist 47 (1998), S. 520-521 
    ISSN: 1432-055X
    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 clinical pharmacology 8 (1975), S. 223-226 
    ISSN: 1432-1041
    Keywords: Parkinson's syndrome ; dopamine receptor stimulating agent ; clinical trial ; piribedil ; L-DOPA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The effect of a new dopamine receptor stimulating agent, piribedil (ET 495), was studied in 10 patients with Parkinson's syndrome, who had had no or a poor response to previous L-DOPA treatment, or had displayed marked side effects during L-DOPA administration. Piribedil produced significant improvement of the functions of activity of daily living (ADL), and appeared to have a preferential effect on parkinsonian tremor. However, treatment was difficult to control primarily because of severe psychiatric side effects.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    European biophysics journal 7 (1981), S. 223-224 
    ISSN: 1432-1017
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Physics
    Type of Medium: Electronic Resource
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