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Trotz des breiten, klinischen Einsatzes des Propofols haben sich aufgrund bestehender Nebenwirkungen zunehmend Bestrebung entwickelt, alternative Formulierungen zur Lipidemulsion zu finden. In dieser Arbeit wurden die Substanzen Propofol/HPβCD und Na-Propofolat/HPβCD als alternative Formulierungen des Propofols mittels 1H-NMR-Spektroskopie, molekularer Modellierungen, DSC-Messungen, Zytotoxizitätstests (MTT-Test, LDH-Assay, EZ4U-Test) und dem Comet-Assay als Genotoxizitätstest auf biologische, chemische und physikalische Eigenschaften untersucht. Die Frage nach der Komplexbildung zwischen Propofol und HPβCD lässt sich nicht allein auf Basis des 1D-1H-NMR-Spektrums beantworten. Allerdings lässt sich mit Hilfe der 1H-NMR-Spektroskopie für Na-Propofolat/HPβCD das Vorliegen als deprotonierte Form nachweisen. Anderseits legen aber die DSC-Messungen eine Komplexbildung zwischen Propofol und HPβCD nahe. Zum einen ergibt sich das aus den unterschiedlichen Glasübergangstemperaturen der Substanzen. Zum anderen zeigt der Kurvenverlauf für HPβCD als auch für Na-Propofolat/HPβCD und Propofol/HPβCD keinen Verdampfungspeak bis zu der untersuchten maximalen Temperatur von 280 °C trotz des Propofol-Siedepunktes von 256 °C. Die molekularen Modellierungen legen nahe, dass die Bindung zwischen Propofol und Cyclodextrin über die Isopropylgruppen des Propofols erfolgt, wobei der aromatische Ring nicht in die Cavität des Cyclodextrinringes eindringt. Aus den molekularen Modellierungen ergeben sich Enthalpiewerte, die in ihrer Größenordnung schwachen Wasserstoffbrückenbindungen entsprechen. Für das Na-Propofolat/HPβCD lässt sich eine leichtere Abspaltung des Propofols aus dem Komplex voraussagen, wohingegen für Propofol/HPβCD die Abspaltung langsamer, aber über einen längeren Zeitraum erfolgen dürfte. Im Vergleich zu der hohen Zytotoxizität des Propofols als Lipidemulsion ergibt sich aus den an der CerebEND-Zelllinie durchgeführten Zyotoxizitätstests für HPβCD, Propofol/HPβCD und Na-Propofolat/HPβCD kein Nachweis einer Zytotoxizität nach 24-stündiger Exposition. Die Resultate zeigen für die drei Testverfahren die jeweils gleiche Reihenfolge mit der höchsten Zellvitalität für die mit Na-Propofolat/HPβCD behandelten Zellen und der niedrigsten Zellvitalität für HPβCD. In dem Comet-Assay zeigt sich nach 24-stündiger Exposition bei 37 °C für HPβCD, Propofol/HPβCD und Na-Propofolat/HPβCD keine genotoxische Wirkung an der HL-60-Zelllinie. Die Ergebnisse dieser Arbeit sprechen für die Fortsetzung der Untersuchungen von Propofol/HPβCD und Na-Propofolat/HPβCD als aussichtsreiche Option der Propofol-Formulierungen. / Despite the widespread clinical use of propofol, efforts to find alternative formulations to the lipid emulsion have increasingly developed due to existing side effects. In this study, the substances propofol/HPβCD and Na-propofolate/HPβCD were investigated as alternative formulations of propofol using 1H-NMR spectroscopy, molecular modelling, DSC measurements, cytotoxicity tests (MTT test, LDH assay, EZ4U test) and the Comet assay as a genotoxicity test for biological, chemical and physical properties. The question of complex formation between propofol and HPβCD cannot be answered solely on the basis of the 1D-1H NMR spectrum. However, the presence of Na-propofolate/HPβCD as a deprotonated form can be demonstrated with the aid of 1H NMR spectroscopy. On the other hand, the DSC measurements suggest a complex formation between propofol and HPβCD. On the one hand, this results from the different glass transition temperatures of the substances. On the other hand, the curve for HPβCD as well as for Na-propofolate/HPβCD and propofol/HPβCD shows no evaporation peak up to the analysed maximum temperature of 280 °C despite the propofol boiling point of 256 °C. The molecular modelling suggests that the bond between propofol and cyclodextrin takes place via the isopropyl groups of propofol, whereby the aromatic ring does not penetrate into the cavity of the cyclodextrin ring. The molecular modelling results in enthalpy values that correspond in their order of magnitude to weak hydrogen bonds. For Na-propofolate/HPβCD, easier cleavage of propofol from the complex can be predicted, whereas for propofol/HPβCD, cleavage is likely to occur more slowly but over a longer period of time. In comparison to the high cytotoxicity of propofol as a lipid emulsion, the cytotoxicity tests carried out on the CerebEND cell line for HPβCD, propofol/HPβCD and Na-propofolate/HPβCD do not provide any evidence of cytotoxicity after 24-hour exposure. The results show the same order for the three test methods with the highest cell viability for the cells treated with Na-propofolate/HPβCD and the lowest cell viability for HPβCD. The comet assay showed no genotoxic effect on the HL-60 cell line after 24-hour exposure at 37 °C for HPβCD, propofol/HPβCD and Na-propofolate/HPβCD. The results of this work speak in favour of continuing the investigations of propofol/HPβCD and Na-propofolate/HPβCD as a promising option for propofol formulations.

L’effet neuroprotecteur des agents anesthésiques est maintenant établi depuis plus de 30ans. Cependant, les mécanismes impliqués restent imparfaitement élucidés. A cours de cetravail nous avons étudié deux volets de leur protection :La première partie porte sur l’implication de la transmission glutaminergique dans leurseffets neuroprotecteurs directs, c'est-à-dire lorsqu’ils sont utilisés au cours d’une l’ischémiecérébrale. Nous avons étudié deux agents anesthésiques de classe distincte: le propofol et lesévoflurane sur des co-cultures de neurones et d’astrocytes corticaux de rat soumis à uneprivation en oxygène et en glucose transitoire (POG). Nous avons ainsi observé que laprésence de propofol ou de sévoflurane pendant la POG prévenait la mort neuronale,l’accumulation de glutamate extracellulaire et la diminution de la capture du glutamateinduites par l’ischémie. Nous avons également montré que cette restauration partielle del’activité de capture du glutamate impliquait des transporteurs distincts entre le propofol et lesévoflurane.La deuxième partie a porté sur la neuroprotection obtenue par un préconditionnement (PC)pharmacologique liée à l’utilisation avant l’ischémie d’agents anesthésique volatils. Nousavons tout d’abord confirmé in vitro l’existence d’une telle protection avec le sévoflurane etmis en évidence le rôle primordial, au cours de cette protection, des canaux potassiques ATPdépendantset des radicaux libres. Puis sur un modèle in vivo d’occlusion transitoire del’artère cérébrale moyenne, le PC par sévoflurane a induit une neuroprotection supérieure àcelle obtenue avec l’utilisation de sévoflurane uniquement pendant l’ischémie. Cependantcette protection est transitoire et ne perdure pas dans le temps. Le sévoflurane ne fait queretarder, sans l’empêcher, la mort neuronale liée à l’apoptose. Il offre cependant une fenêtrethérapeutique intéressante. / The neuroprotective effect of anesthetic agents is now established for over 30 years.However, the mechanisms involved remains to be fully explored. This work focuses on twoneuroprotective strategies:The first part is on the involvement of glutamatergic transmission in their directneuroprotective effects. We studied the effect of two separate classes of anesthetic agents:propofol and sevoflurane on co-cultures of cortical neurons and astrocytes from rats subjectedto a transient oxygen and glucose deprivation (OGD) mimicking cerebral ischemia. Weobserved that the presence of propofol or sevoflurane during OGD prevented neuronal death,accumulation of extracellular glutamate and decreased uptake of glutamate induced byischemia. We also demonstrated that this partial restoration of glutamate uptake mediated bypropofol and sevoflurane involved differential transporters.The second part deals with the neuroprotection achieved by pharmacologicalpreconditioning with regard to the use of volatile anesthetic agents before ischemia. We firstconfirmed in vitro the existence of such protection with sevoflurane. We also highlighted therole of ATP-dependent potassium channels and reactive oxygen species in sevofluranepreconditioning-induced neuroprotection. Then, using an in vivo model of focal transientischemia, we showed that sevoflurane preconditioning significantly improved functionaloutcome and reduced infarct volume. However, this protection was transient. Sevofluraneonly delayed the neuronal death associated with apoptosis but offers an interesting therapeuticwindow.

Propofol is an intravenously administered, hypnotic and short- acting pharmaceutical. One common sideeffect (>1:10) and therefore a disadvantage with propofol is the local pain that arise when the initial injection is given. Why the pain arise is not clearly understood. A majority of different pharmacological treatments, different doses and combinations, alternative administrations methods and physical interventions have been tried to reduce the pain when injection of propofol is given. One important task for the nurse is to relieve pain for patients. It is important for all patients to be painless and not experience discomfort caused by procedure in health care. The purpose of this study was to examine if administration of lidocaine and/ or remifentanil could in connection with injection of propofol reduce pain incidence and intensity at the injection. A literature study based on twenty-eight scientific articles was conducted. The result shows that a combination of lidocaine andremifentanil give the best pain relief. Howewer there is no difference in propofolinduced injection pain when lidocaine or remifentanil alone is compared. Other factors that could affect injection pain are use of a tourniquet which enhances the pain reduction, but the time that the tourniquet is applied is not decisive. The placement of the iv-catheter should be in the largest vein possible. By using this knowledge the incidence and intensity of pain could be reduced with drugs commonly used in Swedish aneasthetic care. Thereby patients' suffering could also be reduced.

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / Ao longo dos últimos anos, apesar de todo desenvolvimento e pesquisa, a mortalidade na sepse permanece elevada. Na área de microcirculação foram realizados estudos em modelos experimentais de sepse ao longo das últimas duas décadas, quando se observou, através de técnicas invasivas, alterações como redução expressiva da densidade capilar funcional. A técnica denominada sidestream dark field (SDF) imaging, recentemente desenvolvida, permite a avaliação da microcirculação de forma transcutânea. A utilização desta técnica permitiu evidenciar a redução da densidade capilar funcional em pacientes com sepse grave quando comparado a um indivíduo saudável. Posteriormente, foi demonstrado que alterações persistentes na microcirculação de pacientes sépticos, mesmo com sinais vitais estabilizados, estão associadas com pior prognóstico.Evidentemente, os pacientes com sepse grave ou choque séptico sofrem uma grande quantidade de intervenções terapêuticas, aonde muitas delas alteram a microcirculação. Estudos analisando a microcirculação em pacientes em uso de nitroglicerina, corticóide, recebendo hemotransfusão ou ainda infusão de noradrenalina foram publicados recentemente.Entretanto, até o presente momento, não existem publicações que descrevam a influência dos sedativos na microcirculação de pacientes com choque séptico. As drogas mais comumente utilizadas para sedação de pacientes em ventilação mecânica são o sedativo midazolam e o anestésico propofol. Os objetivos do estudo foram: avaliar o efeito dos principais agentes sedativos utilizados na prática clínica na microcirculação de pacientes com choque séptico utilizando a técnica de sidestream dark field imaging, comparar os efeitos na microcirculação do midazolam com o propofol em pacientes com choque séptico e verificar se existe relação das alterações microcirculatórias provocadas pelos sedativos com as variações de diferentes parâmetros hemodinâmicos, gasométricos ou metabólicos como pressão arterial, índice cardíaco, lactato e saturação venosa central de oxigênio. Foram estudados (estudo prospectivo) 16 pacientes internados no Centro de Terapia Intensiva da Casa de Saúde São José. Os pacientes internados com diagnóstico de choque séptico e que possuíam indicação clínica de ventilação mecânica e de suspensão diária da sedação foram submetidos ao estudo da microcirculação na mucosa sublingual utilizando a técnica de sidestream dark field imaging. Estes pacientes foram sedados conforme orientação do protocolo já existente de sedação, inicialmente com propofol e posteriormente com midazolam. Os principais resultados observados foram:a macrohemodinâmica não diferiu nos 2 momentos do exame, o BIS (bispectral índex of sedation) se manteve na faixa recomendada nos 2 momentos do exame, tendo aumentado quando o paciente acordava, conforme esperado, e a proporção de vasos pequenos perfundidos e o índice de fluxo da microcirculação foram significativamente menores, enquanto o índice de heterogeneidade foi significativamente maior quando os pacientes estavam recebendo infusão de propofol quando comparados com a infusão de midazolam. Concluímos que, em pacientes com choque séptico, a administração de midazolam resulta em uma melhora dos parâmetros microcirculatórios quando comparada com a administração de propofol. Essa diferença não pode ser atribuída a alterações de variáveis hemodinâmicas sistêmicas. / Over the past few years, despite all research and development, mortality from sepsis remains high. In microcirculatory studies using experimental models of sepsis, and invasive techniques, significant reduction in functional capillary density were observed. The recently developed technique called sidestream dark field (SDF) imaging, allows transcutaneously evaluation of the microcirculation. This technique has demonstrated reduction on functional capillary density in patients with severe sepsis, when compared to healthy individuals. Subsequently, it was shown that even in septic patients with stabilized vital signs, persistent alterations in the microcirculation are associated with worse prognosis. Obviously, patients with severe sepsis or septic shock suffer a lot of therapeutic interventions, many of them affecting the microvasculature. Studies analyzing the microcirculation in patients using nitroglycerin, corticosteroids, receiving blood transfusion or infusion of norepinephrine were recently published. However, to date, no publications have described the influence of sedatives in the microcirculation of these patients. The most commonly drugs used for sedation of mechanically ventilated patients are midazolam and propofol. The main objectives of this study were to observe the effects of two sedative agents used in clinical practice in the microcirculation of patients with septic shock. The sidestream dark field imaging technique was used to compare the effects on microcirculation of midazolam with propofol in patients with septic shock and verify a relationship between microcirculatory changes caused by sedatives and different variations of hemodynamic parameters such as blood pressure, heart rate, lactate and central venous oxygen saturation.We have prospectively studied 16 patients admitted to the Intensive Care Unit of Casa de Saúde São José. Patients admitted with a diagnosis of septic shock and in need of mechanical ventilation were submitted to microcirculation analysis in the sublingual mucosa using sidestream dark field imaging technique. These patients were sedated according to the sedation protocol, initially with propofol, and later on with midazolam. The main results were: the macrohemodynamics did not differ during the two moments of examination; BIS (bispectral index of sedation) remained in the range recommended during both exams and increased when patients woke up, as expected, and finally, the proportion of small vessels perfused and microcirculatory flow index were significantly lower, while the heterogeneity index was higher, when patients were receiving propofol infusion in comparison with the midazolam one. We concluded that in patients with septic shock, midazolam administration results in an improvement of the microcirculation when compared with the administration of propofol and this difference could not be attributed to changes in systemic hemodynamic.

<p>Propofol is an intravenously administered, hypnotic and short- acting pharmaceutical. One common sideeffect (>1:10) and therefore a disadvantage with propofol is the local pain that arise when the initial injection is given. Why the pain arise is not clearly understood. A majority of different pharmacological treatments, different doses and combinations, alternative administrations methods and physical interventions have been tried to reduce the pain when injection of propofol is given. One important task for the nurse is to relieve pain for patients. It is important for all patients to be painless and not experience discomfort caused by procedure in health care. The purpose of this study was to examine if administration of lidocaine and/ or remifentanil could in connection with injection of propofol reduce pain incidence and intensity at the injection. A literature study based on twenty-eight scientific articles was conducted. The result shows that a combination of lidocaine andremifentanil give the best pain relief. Howewer there is no difference in propofolinduced injection pain when lidocaine or remifentanil alone is compared. Other factors that could affect injection pain are use of a tourniquet which enhances the pain reduction, but the time that the tourniquet is applied is not decisive. The placement of the iv-catheter should be in the largest vein possible. By using this knowledge the incidence and intensity of pain could be reduced with drugs commonly used in Swedish aneasthetic care. Thereby patients' suffering could also be reduced.</p>

Thèse d'exercice : Médecine. Anesthésie-réanimation : Paris 12 : 2007. / Titre provenant de l'écran-titre. 61 f. : ill. Bibliogr. f. 58-61.

Tyrimo darbo tikslas - įvertinti ir palyginti propofolio, ketamino ir jų derinio farmakologinį poveikį eksperimentiniame izoliuotų aortos ir trachėjos žiedų modelyje in vitro. Bandymui atlikti naudojama vienos kameros organų vonelė. Rezultatai fiksuojami programine įranga LabChart 7. Pasirinkti laboratoriniai gyvūnai – 6 Jūrų kiaulyčių patinėliai. Vaistų poveikis vertinimas izoliuotiems aortos ir trahėjos segmentams. Segmentų kontrakcija sukeliama Krebso tirpalu, kuriame yra ištirpintas KCl (80 mmol/l). Pasiekus maksimalų susitraukimą, kumuliuojančiomis koncentracijomis (10-5 M, 10-4 M, 10-3 M), į vonelę pilamas ketamino, propofolio ir jų derinio tirpalas ir kiekvienu atveju fiksuojamas jėgos pokytis. Ketaminas aortos žiedą atpalaiduoja esant didelėms (10-3 M) ir vidutinėms (10-4 M) koncentracijoms, o propofolis ir ketamino/propofolio derinys tik esant didelėms koncentracijoms (p<0,05). Ketaminas, propofolis ir jų derinys atpalaiduoja trachėjos žiedą esant vidutinėms ir didelėms koncentracijoms (p<0,05). Ketamino vidutinė koncentracija turi didesnį poveikį aortos, o vidutinė ir didelė koncentracija – trachėjos žiedo atsipalaidavimui nei propofolis (p<0,05). Ketamino/propofolio derinys santykiu 1:1 esant 10-4 M koncentracijai mažiau veikia aortos atsipalaidavimą nei ketaminas (p<0,05), o 10-4 M ir 10-3 M derinio koncentracijos mažiau veikia trachėjos atsipalaidavimą nei vartojant ketaminą ir propofolį ne derinyje (p<0,05). Didėjant vaistų koncentracijai, didėja jų dilatacinis... [toliau žr. visą tekstą] / The aim of the study was to investigate and compare propofol, ketamine and ketamine/propofol combination pharmacological effects of isolated aortic and tracheal rings in vitro. Single-chamber organ bath was used for the experiment. The results were recorded by LabChart software. Selected laboratory animals – 6 guinea pig males. The influence of medicine over isolated aorta and trachea rings was evaluated. Pre-contraction was induced by Krebs solution containing dissolved KCl (80 mmol/l). After reaching the maximum contraction of the preparation, propofol, ketamine and ketamine/propofol mixture solution was separately added to the bath in a cumulative concentrations (10-5 M, 10-4 M, 10-3 M) and in each case the force change was recorded. Ketamine relaxed aortic rings at medium and large concentrations, while propofol and ketamine/propofol mixtures only in large concentrations (p<0,05). Medium concentration of ketamine showed a greater effect on aortic rings than propofol and medium and large concentrations showed a greater effect on trachea ring than equal concentration of propofol (p<0,05). An average concentration of a 1:1 ratio of ketamine/propofol mixture, had a lower impact on aortic ring relaxation than an equal concentration of ketamine (p <0.05). A high concentration of 1:1 ratio of ketamine/propofol had a lower impact on the trachea ring relaxation than equal concentration of ketamine and propofol used separately (p <0.05). In conclusion, contractions of aorta and... [to full text]

A cirurgia laparoscópica requer a criação de um espaço de trabalho intraabdominal, através do pneumoperitônio, e para isto utiliza-se o dióxido de carbono (CO2). As alterações sistêmicas relacionadas ao sistema respiratório ocorrem pelo aumento da pressão intra-abdominal, resultando em diminuição da complacência pulmonar, atelectasia, hipercarbia e hipóxia. A insuflação de CO2 com pressões intraabdominais acima de 8 mmHg produz alterações hemodinâmicas significantes, caracterizadas por decréscimo do débito cardíaco, elevação da pressão arterial. Para que a homeostase hemodinâmica e respiratória seja mantida são necessários protocolos anestésicos adequados e métodos de ventilação mecânica como, por exemplo, a pressão expiratória final positiva final (PEEP). O presente trabalho teve por objetivo avaliar e comparar quatro protocolos anestésicos e ventilatórios distintos em cadelas submetidas à ovariohisterectomia videolaparoscópica eletiva, com uso de pneumoperitônio com CO2 e 12 mmHg de pressão intra-abdominal, sob anestesia geral total intravenosa. Para isso, 16 caninos foram distribuídos em quatro grupos: no grupo 1 (Zeepbloq) os animais receberam atracúrio (0,5 mg.kg-1), propofol (5 mg.kg-1) e fentanil (2 mcg.kg-1), todos em bolus, por via intravenosa, e seguiu-se com infusão contínua de atracúrio (0,5 mg.kg-1/hora), propofol (0,4 mg.kg-1/minuto) e fentanil (2 mcg.kg-1/hora) por bomba de infusão, e não foi realizada PEEP; no grupo 2 (Peepbloq) administrou-se o mesmo protocolo anestésico, porém realizou-se a PEEP de 10 cm de água; no grupo 3 (Zeep) os animais receberam o mesmo protocolo anestésico, com exceção bloqueador neuromuscular, e não foi realizada PEEP; no grupo 4 (PEEP) os indivíduos receberam o mesmo protocolo do grupo 3, porém realizou-se PEEP. Para o procedimento cirúrgico foi realizado pneumoperitônio de 12 mmHg com CO2 com duração variável. Foram avaliadas as seguintes variáveis: pressão arterial média, freqüência respiratória, saturação de oxigênio na hemoglobina, pressão parcial de dióxido de carbono expirado, freqüência cardíaca, eletrocardiografia e tempo do procedimento anestésico, do pneumoperitônio. Para hemogasometria foi realizada a coleta de sangue arterial, sendo obtidas variáveis de pH, pressão parcial de O2 e CO2, bicarbonato, CO2 total, excesso/déficit de bases e saturação arterial de oxigênio na hemoglobina. Não foram observados valores que representassem diferença estatística significativa entre os grupos (p<0,05). No entanto, houve diferença significativa (p<0,05) entre momentos avaliados a para pressão arterial de oxigênio, a pressão arterial média e a temperatura, independente do protocolo empregado. Ambos os protocolos empregados, anestésico e de ventilação, foram satisfatórios e, de acordo com a metodologia empregada, pode-se concluir que animais submetidos à ventilação com PEEP não apresentaram benefícios significativos quando comparados com animais ventilados com ZEEP, independente do uso ou não de bloqueador neuromuscular. / The laparoscopic surgery requires the creation of a space in the abdominal cavity through pneumoperitoneum and that using the carbon dioxide (CO2). The systemic changes related to the respiratory system occur by increased intra-abdominal pressure, resulting in decreased lung compliance, atelectasis, hypercarbia and hypoxia. The CO2 insufflation with intra-abdominal pressure over 8 mmHg produces significant hemodynamic changes, characterized by decreased cardiac output, blood pressure elevation. For the hemodynamic and respiratory homeostasis is maintained anesthetic protocols are necessary and appropriate methods of mechanical ventilation, such as the positive end-expiratory pressure (PEEP). This study aimed to evaluate and compare four different protocols anesthetics and ventilatory in female dogs submitted to ovariohysterectomy videolaparoscopic elective, with the use of pneumoperitoneum with CO2 and 12 mmHg of intra-abdominal pressure, under general anesthesia total intravenous. A total of 16 dogs were distributed into four groups: in group 1 (Zeepbloq) the animals received atracurium (0.5 mg.kg-1), propofol (5 mg.kg-1) and fentanyl (2 mcg . kg-1), all bolus, intravenously, and followed up with continuous infusion of atracurium (0.5 mg.kg-1/hour), propofol (0.4 mg.kg-1/minute) and fentanyl (2 mcg.kg-1/hour) by infusion pump, and was not held PEEP, in group 2 (Peepbloq) administered to the same protocol anesthetic, but was held on PEEP of 10 cm of water, in group 3 (Zeep) the animals received the same protocol anesthetic, except neuromuscular blocker, and was not held PEEP, and in group 4 (PEEP) individuals received the same protocol as the group 3, but was held PEEP. For the surgical procedure was performed abdominal pressure of 12 mmHg with CO2. We evaluated the following variables: mean arterial pressure, respiratory rate, oxygen saturation in hemoglobin, end tidal of carbon dioxide expired, heart rate, electrocardiography and time of the anesthetic procedure and of the pneumoperitoneum. Arterial blood was sampled for arterial blood gas analyses, and variables obtained from pH, arterial pressure of CO2 and O2, bicarbonate, CO2 total, balance of bases and arterial oxygen saturation in hemoglobin. There were no evaluate parameters that represented statistically significant difference between groups (p <0.05). However, there was a significant difference (p <0.05) between moments evaluated for the blood pressure of oxygen, the mean blood pressure and temperature, independent of protocol employee. Both protocols employees, anaesthetic and ventilation, were satisfactory and in accordance with the methodology employed, we can conclude that animals treated with ventilation PEEP did not show significant benefits when compared with animals ventilated with ZEEP, regardless of whether or not to use atracurium.

Made available in DSpace on 2014-06-11T19:35:04Z (GMT). No. of bitstreams: 0 Previous issue date: 2008-02-29Bitstream added on 2014-06-13T21:07:06Z : No. of bitstreams: 1 castro_vb_dr_botfm.pdf: 811446 bytes, checksum: c21c255ab07d1f8809f7e545477272d8 (MD5) / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) / O emprego de procedimentos de anestesia intravenosa total em cães tem sido mais freqüente, devido ao melhor conhecimento do perfil farmacocinético dos fármacos empregados. Como ainda não existe um único fármaco que produza todas as características desejáveis em uma anestesia geral, há a necessidade de se associar ao hipnótico, agentes com propriedades analgésicas. O objetivo desse estudo foi avaliar os efeitos hemodinâmicos causados pela associação do cloridrato de dexmedetomidina, nas doses de 1 e 2 μg/kg/h, e propofol na dose de 0,3 mg/kg/min, administrada em infusão intravenosa contínua em cães, bem como o tempo de recuperação anestésica após duas horas de infusão. Seis cães, clinicamente sadios, sem raça definida, pesando 17,6±1,8 kg, foram submetidos a três tratamentos com intervalo de uma semana e em seqüência aleatória. Todos os animais foram inicialmente anestesiados com isofluorano a 5V% com fluxo de 3 l/min de O2. Após a indução e intubação, os animais foram posicionados em decúbito lateral esquerdo e mantidos com isofluorano na concentração de 1,8V%. As veias cefálicas e a artéria dorsal podal foram cateterizadas e um cateter de Swan Ganz 5F foi introduzido pela veia jugular. Após fixação dos cateteres na pele, a administração do isofluorano foi interrompida. Os cães permaneceram despertos por 1 hora, e após esse período, foi realizada a avaliação das variáveis hemodinâmicas. Em seguida os cães receberam um dos seguintes tratamentos: Controle: indução com propofol (6 mg/kg/30s) e solução de NaCl 0,9% (5 ml/10min) seguida de manutenção com propofol (0.3 mg/kg/min) e NaCl 0,9% (4 ml/h); Dex 1: indução com propofol (6 mg/kg/30s) e cloridrato de dexmedetomidina (1 μg/kg/10min) seguida de manutenção com propofol (0.3 mg/kg/min)... / Total intravenous anesthesia in dogs has been more frequently used, the pharmacokinetic profile of the new drugs is better understood. No injectable anesthetic produces all of the components of a general anesthesia, it is required to associate additional analgesics with hypnotic. The aim of this study was to evaluate the hemodynamic effects caused by the association of 1 and 2 μg/kg/h of dexmedetomidine and 0,3 mg/kg/min of propofol, administered by continuous intravenous infusion, as well time of anesthetic recovery after 2 hours of infusion. Six healthy dogs weighting 17,6±1,8 kg were randomly allocated to 3 treatments with at least one week intervals between each treatment. All animals were initially anesthetized with 5V% of isoflurane and 3 l/min of oxygen. After induction and intubation, the animals were posicionated in left lateral recumbence and maintained with 1.8% end tidal. All animals were instrumented with a cephalic veins and arterial catheter and a Swan Ganz catheter in order to a monitor hemodynamic parameters. After instrumentation isoflurane was interrupted and animals were awake and remained awake for one hour. After that, baselines parameters were taken. Dogs received each one of these treatments: Control: was induced with propofol (6 mg/kg/30s) and saline (5 ml/10 min), maintenance was with propofol (0.3 mg/kg/min) and saline (4 ml/h). Dex 1 was induced with propofol (6 mg/kg30s) and dexmedetomidine (1 μg/kg10 min), maintenance with propofol (0.3 mg/kg/min) and dexmedetomidine (1 μg/kg/h). Dex 2 was induced with propofol (6 mg/kg30s) and dexmedetomidine (2 μg/kg/10min), maintenance with propofol (0.3 mg/kg/min) and dexmedetomidine (2 μg/kg/h) during 120 minutes. The parameters (HR, SBP, MAP, DAP, CI, SI, CVP, PAP, POPA, SVRI, PVRI, RR, ETCO2, SaO2, pHa, PaO2, PaCO2, HCO3, Hb, CaO2, IDO2, temperature) were taken at 15, 30, 60, 90 e 120 minutes after induction... (Complete abstract click electronic access below)