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Objective The angle of the C-MAC D-Blade ® videolaryngoscope, which is used for difficult airway interventions, is not compatible with routinely used endotracheal tubes. Methods A prospective randomized crossover study was performed comparing five intubation methods for use with standardized airways, including using different stylets or no stylet: Group HS, hockey-stick stylet; Group DS, D-blade type stylet; Group CS, CoPilot ® videolaryngoscope rigid stylet ® ; Group GEB, gum elastic bougie; and Group NS, no stylet. A manikin was used to simulate difficult intubation with a Storz C-MAC D-Blade ® videolaryngoscope. The duration of each intubation stage was evaluated. Results Participants in this study (33 anesthesiology residents and 20 anesthesiology experts) completed a total of 265 intubations. The number of attempts made using no stylet was significantly greater than those made for the other groups ( p p p p Conclusion Use of the correct stylet leads to a more efficient use of the Storz C-MAC D-Blade ® . In our study, the use of the D-blade stylet, the CoPilot stylet and the hockey stick stylet provided quicker intubation, allowed easier passage of the vocal cords, and decreased the total intubation duration. To confirm the findings of our study, randomized controlled human studies are needed.

Introduction We investigated the liver transplantation literature since 1975 and found the most frequently cited 100 articles and assessed the distribution of authors and journals of these articles. Method Using the advanced mode of the Institute for Scientific Information (ISI) Web of Science (WOS) search engine, the words “SU = transplantation AND TI = liver OR SU = transplantation AND TS = liver” were used to scan articles and determine the most-cited 100 articles on July 18, 2016. Results From 1975 to date, it appears a total of 43,369 articles were published in the field of liver transplantation in the WOS. Although the most cited article had 677 citations, the least cited article had 180 citations. The mean citation number for the 100 articles was 252.31 ± 96.75. The mean annual citation number for the articles varied from 61.55 to 5 and the mean was 15.31 ± 8.63. The most cited article was by Feng et al “Characteristics Associated With Liver Graft Failure: The Concept of a Donor Risk Index” published in the American Journal of Transplantation (677 citations). Conclusion Bibliometric analysis highlights the key topics and publications that have shaped the understanding and management of liver transplantation. According to our research, this is the first study to investigate articles with most citations in the field of liver transplantation. In our study the article with the most citations was cited 677 times, whereas the 100th article was cited 180 times with a mean citation number for the 100 articles of 252.31 ± 96.75.

ResumoJustificativa e objetivosComparar os efeitos de sugamadex e neostigmina, usados para o antagonismo do bloqueio neuromuscular em náusea e vômito no pós‐operatório (NVPO).MétodosO estudo foi concluído com 98 pacientes de risco ASA I‐II, submetidos à intubação traqueal sob anestesia geral. No fim da cirurgia, os pacientes foram aleatoriamente alocados em dois grupos que receberam 2mgkg−1 de sugamadex (Grupo A) ou 50μgkg−1 de neostigmina mais 0,2mgkg−1 de atropina (Grupo N). Os tempos de monitoração e registro foram definidos como uma hora de pós‐operatório e de 1‐6, 6‐12 e 12‐24 horas. As quantidades administradas de antieméticos foram registradas.ResultadosNa primeira hora de pós‐operatório, 13 pacientes do Grupo N (27%) e quatro do Grupo S (8%) apresentaram náusea e/ou vômito e a diferença foi estatisticamente significativa (p=0,0016). Não houve diferença significativa na incidência e gravidade de NVPO (p>0,05) durante as 24 horas de monitoração, porém o número de pacientes que receberam ondansetron para o tratamento de NVPO no Grupo N foi significativamente maior do que o número de pacientes no Grupo S (16 e seis, respectivamente, p0.05), however the number of patients given ondansetron for PONV treatment in Group N was significantly higher than the number in Group S (16 in Group N, 6 in Group S, p

Aim: To evaluate the effects of three different doses of gabapentin pretreatment on the incidence and severity of myoclonic movements linked to etomidate injection. Method: One hundered patients, between 18 and 60 years of age and risk category American Society of Anesthesiologists I–II, with planned elective surgery under general anesthetic were included in the study. The patients were randomly divided into four groups and 2 h before the operation were given oral capsules of placebo (Group P, n = 25), 400 mg gabapentin (Group G400, n = 25), 800 mg gabapentin (Group G800, n = 25) or 1200 mg gabapentin (Group G1200, n = 25). Side effects before the operation were recorded. After preoxygenation for anesthesia induction 0.3 mg kg−1 etomidate was administered for 10 s. A single anesthetist with no knowledge of the study medication evaluated sedation and myoclonic movements on a scale between 0 and 3. Two minutes after induction, 2 μg kg−1 fentanyl and 0.8 mg kg−1 rocuronium were administered for tracheal intubation. Results: Demographic data were similar. Incidence and severity of myoclonus in Group G1200 and Group G800 were significantly lower than in Group P; sedation incidence and level were appreciably higher compared to Group P and Group G400. While there was no difference in the incidence of myoclonus between Group P and Group G400, the severity of myoclonus in Group G400 was lower than in the placebo group. In the two-hour period before induction other than sedation none of the side effects related to gabapentin were observed in any patient. Conclusion: Pretreatment with 800 mg and 1200 mg gabapentin 2 h before the operation increased the level of sedation and reduced the incidence and severity of myoclonic movements due to etomidate. Resumo: Objetivo: Avaliar os efeitos de três doses diferentes de gabapentina como pré-tratamento sobre a incidência e gravidade dos movimentos mioclônicos associados à injeção de etomidato. Método: Cem pacientes, com idades entre 18-60 anos, estado físico ASA I-II, programados para cirurgia eletiva sob anestesia geral foram incluídos no estudo. Os pacientes foram randomicamente divididos em quatro grupos e, 2 horas antes da operação, receberam cápsulas orais de placebo (Grupo P, n = 25), 400 mg de gabapentina (Grupo G400, n = 25), 800 mg de gabapentina (Grupo G800, n = 25) ou 1200 mg de gabapentina (Grupo G1200, n = 25). Os efeitos colaterais antes da cirurgia foram registados. Após pré-oxigenação para a indução da anestesia, etomidate (0,3 mg.kg−1) foi administrado por 10 segundos. Um único anestesista, cego para a medicação do estudo, avaliou a sedação e os movimentos mioclônicos usando uma escala de 0 a 3. Dois minutos após a indução, fentanil (2 μgr.kg−1) e rocurônio (0,8 mg.kg−1) foram administrados para a intubação traqueal. Resultados: Os dados demográficos foram semelhantes. A incidência e gravidade da mioclonia nos grupos G1200 e G800 foram significativamente menores que no Grupo P; a incidência e o nível de sedação foram consideravelmente maiores comparados ao Grupo P e Grupo G400. Enquanto não houve diferença na incidência de mioclonia entre os grupos P e G400, a gravidade da mioclonia no Grupo G400 foi menor que no grupo placebo. No período de 2 horas antes da indução, nenhum dos efeitos colaterais relacionados à gabapentina, exceto sedação, foi observado em qualquer paciente. Conclusão: O pré-tratamento com 800 mg e 1200 mg de gabapentina 2 horas antes da operação aumentou o nível de sedação e reduziu a incidência e gravidade dos movimentos mioclônicos associados ao etomidato. Keywords: Etomidate, Injection pain, Myoclonus, Gabapentin, Palavras-chave: Etomidato, Dor à injeção, Mioclonia, Gabapentina

Cerebral ischemia may cause permanent brain damage and behavioral dysfunction. The efficacy and mechanisms of pharmacological treatments administered immediately after cerebral damage are not fully known. Sugammadex is a licensed medication. As other cyclodextrins have not passed the necessary phase tests, trade preparations are not available, whereas sugammadex is frequently used in clinical anesthetic practice. Previous studies have not clearly described the effects of the cyclodextrin family on cerebral ischemia/reperfusion (I/R) damage. The aim of this study was to determine whether sugammadex had a neuroprotective effect against transient global cerebral ischemia. Animals were assigned to control, sham-operated, S 16 and S 100 groups. Transient global cerebral ischemia was induced by 10-minute occlusion of the bilateral common carotid artery, followed by 24-hour reperfusion. At the end of the experiment, neurological behavior scoring was performed on the rats, followed by evaluation of histomorphological and biochemical measurements. Sugammadex 16 mg/kg and 100 mg/kg improved neurological outcome, which was associated with reductions in both histological and neurological scores. The hippocampus TUNEL (terminal deoxynucleotidyl transferase dUTP nick end labeling) and caspase results in the S 16 and S 100 treatment groups were significantly lower than those of the I/R group. Neurological scores in the treated groups were significantly higher than those of the I/R group. The study showed that treatment with 16 mg/kg and 100 mg/kg sugammadex had a neuroprotective effect in a transient global cerebral I/R rat model. However, 100 mg/kg sugammadex was more neuroprotective in rats. Copyright (C) 2016, Kaohsiung Medical University. Published by Elsevier Taiwan LLC.

BACKGROUND AND OBJECTIVES: The aim of the study was to compare the block characteristics and clinical effects of dextrose added to levobupivacaine solutions at different concentrations to provide unilateral spinal anaesthesia in lower extremity surgery. METHODS: This prospective, randomised, double-blind study comprised 75 ASA I-II risk patients for whom unilateral total knee arthroscopy was planned. The patients were assigned to three groups: in Group I, 60 mg dextrose was added to 7.5 mg of 0.5% levobupivacaine, in Group II, 80 mg and in Group III, 100 mg. Spinal anaesthesia was applied to the patient in the lateral decubitus position with the operated side below and the patient was kept in position for 10 min. RESULTS: The time for the sensorial block to achieve T12 level was slower in Group I than in Groups II and III (p < 0.05, p< 0.00). The time to full recovery of the sensorial block was 136 min in Group I, 154 min in Group II and 170 min in Group III. The differences were statistically significant (p < 0.05). The mean duration of the motor block was 88 min in Group I, 105 min in Group II, and 139 min in Group III and the differences were statistically significant (p < 0.05). The time to urination in Group I was statistically significantly shorter than in the other groups (p < 0.00). CONCLUSIONS: The results of the study showed that together with an increase in density, the sensory and motor block duration was lengthened. It can be concluded that 30 mg mL-1 concentration of dextrose added to 7.5 mg levobupivacaine is sufficient to provide unilateral spinal anaesthesia in day-case arthroscopic knee surgery. RESUMO JUSTIFICATIVA E OBJETIVOS: Comparar as características do bloqueio e os efeitos clínicos da adição de dextrose às soluções de levobupivacaína em diferentes concentrações para proporcionar raquianestesia unilateral em cirurgia de extremidade inferior. MÉTODOS: Estudo prospectivo, randômico e duplo-cego conduzido com 75 pacientes, estado físico ASA I-II, programados para artroplastia unilateral total do joelho. Os pacientes foram divididos em três grupos: no Grupo-I, 60 mg de dextrose foram adicionados a 7,5 mg de levobupivacaína a 0,5%; no Grupo II, 80 mg e no Grupo III, 100 mg. A raquianestesia foi aplicada ao paciente posicionado em decúbito lateral, com o lado operado abaixo, e o paciente foi mantido em posição durante 10 minutos. RESULTADOS: O tempo para o bloqueio sensorial atingir o nível T12 foi mais lento no Grupo-I do que nos grupos II e III (p < 0,05,p < 0,00). O tempo de recuperação total do bloqueio sensorial foi de 136 minutos no Grupo-I, 154 minutos no Grupo-II e 170 minutos no Grupo III. As diferenças foram estatisticamente significativas (p < 0,05). A média da duração do bloqueio motor foi de 88 minutos no Grupo-I, 105 minutos no Grupo-II e 139 minutos no Grupo-III e as diferenças foram estatisticamente significativas (p< 0,05). O tempo de micção foi significativamente menor no Grupo-I do que nos outros grupos (p < 0,00). CONCLUSÕES: Os resultados do estudo mostraram que, junto com um aumento da densidade, a duração dos bloqueios sensorial e motor foi prolongada. Pode-se concluir que uma concentração 30 mg mL-1 de dextrose adicionada a 7,5 mg de levobupivacaína é suficiente para proporcionar raquianestesia unilateral para artroscopia do joelho em regime ambulatorial.

During surgery, changes in intraocular pressure (IOP) can be observed resulting from several factors, such as airway manipulations and drugs used. We aimed to investigate the effects of sugammadex and neostigmine on IOP, hemodynamic parameters, and complications after extubation. Our study comprised 60 patients, aged 18-65 years, with a risk status of the American Society of Anesthesiologists I-II who underwent arthroscopic surgery under general anesthesia. The patients were randomly assigned into two groups. At the end of the surgery, the neuromuscular block was reversed using neostigmine (50 mu g/kg) plus atropine (15 mu g/kg) in Group 1, and sugammadex (4 mg/kg) in Group 2. Neuromuscular blockade was monitored using acceleromyography and a train-of-four mode of stimulation. IOP was measured before induction and at 30 seconds, 2 minutes, and 10 minutes after extubation. A Tono-Pen XL applanation tonometer was used to measure IOP. This showed that elevation in IOP of patients reversed using sugammadex was similar to that recorded in patients reversed using neostigmine-atropine. When heart rate was compared, there was a significant difference between basal values and those obtained at 30 seconds and 10 minutes after extubation in the neostigmine-atropine group. Extubation time (time from withdrawal of anesthetic gas to extubation) was significantly shorter in the sugammadex group (p = 0.003) than in the neostigmine -atropine group. The postextubation IOP values of the sugammadex group were similar to the neostigmine-atropine group. Extubation time (time from withdrawal of anesthetic gas to extubation) was significantly shorter in the sugammadex group (p = 0.003) than in the neostigmine-atropine group. Copyright (C) 2016, Kaohsiung Medical University. Published by Elsevier Taiwan LLC.

WOS: 000367513200005, PubMed: 26614141, Objective: We have planned to evaluate the laryngeal mask cuff pressures (LMcp) inflated by anesthesia workers of several seniority, without using manometer. Methods: 180 patients scheduled to have short duration surgery with laryngeal mask were included in the study. Five anesthesia specialists (Group S), 10 residents (Group R) and 6 technicians (Group T) inflated the LMc; thereafter LMcp were measured with pressure manometer. Participants have repeated this practice in at least five different cases. LMcp higher than 60 cm H2O at the initial placement or intraoperative period were adjusted to normal range. Sore throat was questioned postoperatively. Groups were compared in terms of mean LMcp and occupational experience. Results: At the settlement of LM, LMcp pressures within the normal range were determined in 26 (14.4%) cases. Mean LMcp after LM placement in Group S, R and T were 101.2 +/- 14.0, 104.3+/-20.5 cm H2O and 105.2 18.4 cm H2O respectively (p >0.05). Mean LMcp values in all measurement time periods within the groups were above the normal limit (60 cm H2O). When groups were compared in terms of LMcp, no difference has been found among pressure values. Occupational experience was 14.2 3.9; 3.3 1.1 and 6.6 3.8 years for specialists, residents and technicians respectively and measured pressure values were not different in regard of occupational experience. Seven (3.9%) patients had sore throat at the 24th hour interview. Conclusion: Considering lower possibility of normal adjustment of LMcp and ineffectiveness of occupational experience to obtain normal pressure values, it is suitable that all anesthesia practitioners should adjust LMcp with manometer. (C) 2013 Sociedade Brasileira de Anestesiologia. Published by Elsevier Editora Ltda. All rights reserved.

ResumoObjetivoPlanejamos avaliar as pressões do manguito de máscara laríngea (PMML) inflado por profissionais da área de anestesiologia com tempos de serviço variados, sem o uso de manômetro.Métodos180 pacientes agendados para cirurgia de curta duração com máscara laríngea foram incluídos no estudo. Cinco especialistas em anestesia (Grupo E), 10 residentes (Grupo R) e seis técnicos (Grupo T) inflaram os manguitos das máscaras laríngeas; subsequentemente, as PMML foram medidas com manômetro de pressão. Os participantes repetiram essa prática em pelo menos cinco casos diferentes. As PMML superiores a 60cm H2O na colocação inicial ou no intraoperatório foram ajustadas para valores normais. Os pacientes foram questionados sobre a presença de dor de garganta no período pós‐operatório. Os grupos foram comparados quanto à média das PMML e experiência profissional.ResultadosAo inserirem a ML, as pressões do manguito dentro da faixa normal foram determinadas em 26 (14,4%) casos. As médias das PMML após a inserção da ML pelos grupos E, R e T foram 101,2±14,0, 104,3±20,5cm e 105,2±18,4cm H2O, respectivamente, (p>0,05). A média dos valores das PMML em todos os períodos de mensuração entre os grupos estava acima do limite normal (60cm H2O). Quando os grupos foram comparados quanto às PMML, nenhuma diferença foi encontrada entre os valores das pressões. A experiência profissional era de 14,2±3,9; 3,3±1,1 e 6,6±3,8 anos para especialistas, residentes e técnicos, respectivamente, e os valores das pressões mensuradas não foram diferentes em relação à experiência profissional. Sete pacientes (3,9%) apresentaram dor de garganta durante a entrevista realizada na 24a hora.ConclusãoLevando‐se em consideração uma possibilidade menor de ajuste da pressão do manguito da máscara laríngea (PMML) e da ineficácia da experiência profissional para a obtenção de valores normais das pressões, é adequado que todos os profissionais de anestesia ajustem as PMML com manômetro.AbstractObjectiveWe have planned to evaluate the laryngeal mask cuff pressures (LMcp) inflated by anesthesia workers of several seniority, without using manometer.Methods180 patients scheduled to have short duration surgery with laryngeal mask were included in the study. Five anesthesia specialists (Group S), 10 residents (Group R) and 6 technicians (Group T) inflated the LMc; thereafter LMcp were measured with pressure manometer. Participants have repeated this practice in at least five different cases. LMcp higher than 60cm H2O at the initial placement or intraoperative period were adjusted to normal range. Sore throat was questioned postoperatively. Groups were compared in terms of mean LMcp and occupational experience.ResultsAt the settlement of LM, LMcp pressures within the normal range were determined in 26 (14.4%) cases. Mean LMcp after LM placement in Group S, R and T were 101.2±14.0, 104.3±20.5cm H2O and 105.2±18.4cm H2O respectively (p>0.05). Mean LMcp values in all measurement time periods within the groups were above the normal limit (60cm H2O). When groups were compared in terms of LMcp, no difference has been found among pressure values. Occupational experience was 14.2±3.9; 3.3±1.1 and 6.6±3.8 years for specialists, residents and technicians respectively and measured pressure values were not different in regard of occupational experience. Seven (3.9%) patients had sore throat at the 24th hour interview.ConclusionConsidering lower possibility of normal adjustment of LMcp and ineffectiveness of occupational experience to obtain normal pressure values, it is suitable that all anesthesia practitioners should adjust LMcp with manometer.

BACKGROUND AND OBJECTIVES: It has been demonstrated that smoking increases pain perception; however the effect of smoking on perception of pain during venous cannulation is not known. The purpose of this study is to determine whether or not smoking has an effect on pain perception due to peripheral venous cannulation. METHODS: 220 patients scheduled to have elective surgery were enrolled in the study and were divided into two groups (Group S and C, n = 110 for each) according to their smoking habits. Numerical rating scale was introduced to the patients and then peripheral venous cannulation at the dorsum of the hand was made with a 20 G intracath. Pain perception of the patients was scored by subsequent numerical rating scale questioning. RESULTS: The demographic characteristics of the groups were identical. Numerical rating scale scores in Group S and C were 3.31 ± 1.56 and 1.65 ± 1.23, respectively (p < 0.001). CONCLUSION: Pain perception due to peripheral venous cannulation is higher in smokers. Future studies on pain treatment should consider the smoking habits of patients. JUSTIFICATIVA E OBJETIVOS: Sabe-se que o tabagismo aumenta a percepção de dor; porém, o efeito do tabagismo sobre a percepção da dor durante o cateterismo venoso não é conhecido. O objetivo deste estudo foi determinar se o tabagismo tem ou não algum efeito sobre a percepção da dor durante a punção venosa periférica. MÉTODOS: Foram incluídos no estudo 220 pacientes agendados para cirurgia eletiva randomicamente alocados em dois grupos: Grupo S (n = 110) e Grupo C (n = 110), de acordo com seus hábitos tabagísticos. Os pacientes foram instruídos sobre o uso da escala numérica de classificação da dor e, em seguida, a punção venosa periférica foi feita no dorso da mão com um cateter de calibre 20G (Intracath(r)). A percepção de dor dos pacientes foi posteriormente registrada de acordo com os escores da escala numérica. RESULTADOS: As características demográficas dos grupos eram idênticas. Os escores da escala numérica de dor dos grupos S e C foram 3,31 ± 1,56 e 1,65 ± 1,23, respectivamente (p < 0,001). CONCLUSÃO: A percepção da dor por causa da punção venosa periférica é maior em fumantes. Estudos futuros sobre o tratamento da dor devem considerar os hábitos tabagísticos dos pacientes. JUSTIFICACIÓN Y OBJETIVOS: Se sabe que el tabaquismo aumenta la percepción de dolor; sin embargo, el efecto del tabaquismo sobre la percepción del dolor durante el cateterismo venoso no se conoce. El objetivo de este estudio fue determinar si el tabaquismo tiene o no algún efecto sobre la percepción del dolor durante la punción venosa periférica. MÉTODOS: Fueron incluidos en el estudio 220 pacientes programados para cirugía electiva aleatoriamente ubicados en 2 grupos: grupo S (n = 110) y grupo C (n = 110), de acuerdo con sus hábitos tabáquicos. A los pacientes se les informó sobre el uso de la escala numérica de clasificación del dolor y a continuación se realizó la punción venosa periférica en el dorso de la mano con un catéter de calibre 20 G (Intracath(r)). La percepción de dolor de los pacientes fue posteriormente registrada de acuerdo con las puntuaciones de la escala numérica. RESULTADOS: Las características demográficas de los grupos eran idénticas. Las puntuaciones de la escala numérica de dolor de los grupos S y C fueron 3,31 ± 1,56 y 1,65 ± 1,23 respectivamente (p < 0,001). CONCLUSIÓN: La percepción del dolor por punción venosa periférica es mayor en los fumadores. Estudios futuros sobre el tratamiento del dolor deben tener en cuenta los hábitos tabáquicos de los pacientes.

ResumenJustificación y objetivosEn este estudio investigamos los efectos anestésicos y sobre la mucosa de la aplicación rectal de la dexmedetomidina en los ratones.MétodosRatones machos albinos Wistar, con un peso de 250-300g, fueron divididos en 4 grupos: el grupo S (n=8) fue un grupo simulado que sirvió de base para los valores basales normales; el grupo C(n=8) consistió en ratones que recibieron aplicación rectal solamente de suero fisiológico; el grupo IPDex (n=8) estaba formado por en ratones que recibieron aplicación intraperitoneal de dexmedetomidina (100μg/kg−1); y el grupo RecDex (n=8) consistió en ratones que recibieron la aplicación rectal de dexmedetomidina (100μg/kg−1). Para la administración de los fármacos por vía rectal usamos cánulas intravenosas de calibre 22 sin estiletes. La administración consistió en avanzar la cánula 1cm en el recto y el volumen de administración rectal fue de 1mL para todos los ratones. Los tiempos (min) de latencia y de anestesia fueron registrados. Dos horas después de la administración por vía rectal, fueron administrados 75mg/kg−1 de ketamina a todos los grupos para la anestesia intraperitoneal, seguido de la retirada de los rectos de los ratones a una distancia 3cm distal por medio de un procedimiento quirúrgico abdominoperineal. Los rectos fueron histopatológicamente examinados y clasificados.ResultadosLa anestesia fue realizada en todos los ratones del grupo RecDex después de la administración de dexmedetomidina. El inicio de la anestesia en el grupo RecDex fue significativamente más tarde y con una duración más corta que en el grupo IPDEx (p

ResumoJustificativa e objetivosInvestigar os efeitos da manutenção de sevoflurano, desflurano e propofol sobre nos níveis séricos de selênio, cobre, zinco, ferro e malondialdeído, as mensurações de glutationa peroxidase e a capacidade antioxidante.MétodosForam alocados em três grupos 60 pacientes agendados para cirurgia unilateral de membros inferiores, feita com torniquete sob anestesia geral. Amostras de sangue foram coletadas para determinar os níveis séricos basais de selênio, cobre, zinco, ferro, malondialdeído e glutationa peroxidase. A anestesia foi induzida com 2‐2,5mgkg−1 de propofol, 1mgkg−1 de lidocaína e 0,6mgkg−1 de rocurônio. Na manutenção da anestesia, sob gás de transporte de 50% O2 e 50% N2O (4Lmin−1), sevoflurano a 1CAM foi administrado ao Grupo S e desflurano a 1CAM ao Grupo D e, sob gás de transporte em mistura de 50% O2 e 50% ar (4Lmin−1), 6mgkgh−1 de propofol e 1mgkgh−1 de fentanil foram administrados ao Grupo P. No pós‐operatório, amostras de sangue foram novamente coletadas.ResultadosApenas nos grupos S e P os níveis de MDA diminuíram em 48 horas de pós‐operatório; os níveis de glutationa peroxidase aumentaram em comparação com os valores basais. Os níveis de selênio diminuíram no Grupo S e no Grupo P, os níveis de zinco diminuíram no Grupo P, os níveis de ferro diminuíram em todos os grupos e não houve alteração nos níveis de cobre em nenhum grupo no período pós‐operatório.ConclusãoDe acordo com os marcadores de malondialdeído e glutationa peroxidase, concluímos que a manutenção da anestesia geral com propofol e sevoflurano ativou o sistema antioxidante contra o estresse oxidativo e o uso de desflurano não teve efeitos sobre o estresse oxidativo e o sistema antioxidante.AbstractBackground and objectivesIn this study, we aimed to investigate the effects of sevoflurane, desflurane and propofol maintenances on serum levels of selenium, copper, zinc, iron, malondialdehyde, and glutathion peroxidase measurements, and antioxidant capacity.Methods60 patients scheduled for unilateral lower extremity surgery which would be performed with tourniquet under general anesthesia were divided into three groups. Blood samples were collected to determine the baseline serum levels of selenium, copper, zinc, iron, malondialdehyde and glutathion peroxidase. Anesthesia was induced using 2–2.5mgkg−1 propofol, 1mgkg−1 lidocaine and 0.6mgkg−1 rocuronium. In the maintenance of anesthesia, under carrier gas of 50:50% O2:N2O 4Lmin−1, 1 MAC sevoflorane was administered to Group S and 1 MAC desflurane to Group D; and under carrier gas of 50:50% O2:air 4Lmin−1 6mgkgh−1 propofol and 1μgkgh−1 fentanyl infusion were administered to Group P. At postoperative blood specimens were collected again.ResultsIt was observed that only in Group S and P, levels of MDA decreased at postoperative 48th hour; levels of glutathion peroxidase increased in comparison to the baseline values. Selenium levels decreased in Group S and Group P, zinc levels decreased in Group P, and iron levels decreased in all three groups, and copper levels did not change in any groups in the postoperative period.ConclusionAccording to the markers of malondialdehyde and glutathion peroxidase, it was concluded that maintenance of general anesthesia using propofol and sevoflurane activated the antioxidant system against oxidative stress and using desflurane had no effects on oxidative stress and antioxidant system.

ResumenJustificación y objetivosInvestigar los efectos del mantenimiento de sevoflurano, desflurano y propofol sobre los niveles séricos de selenio, cobre, cinc, hierro y malondialdehído, las medidas de glutatión peroxidasa y la capacidad antioxidante.MétodosFueron ubicados en 3 grupos 60 pacientes programados para cirugía unilateral de miembros inferiores, realizada con torniquete bajo anestesia general. Fueron recogidas muestras de sangre para determinar los niveles séricos basales de selenio, cobre, cinc, hierro, malondialdehído y glutatión peroxidasa. La anestesia fue inducida con 2-2,5mg/kg−1 de propofol, 1mg/kg−1 de lidocaína y 0,6mg/kg−1 de rocuronio. En el mantenimiento de la anestesia, bajo gas portador de 50% de O2 y 50% de N2O (4L/min−1), sevoflurano a 1CAM fue administrado al grupo S; y desflurano a 1CAM al grupo D y bajo gas portador en mezcla de 50% O2 y 50% aire (4L/min−1), 6mg/kg/h−1 de propofol y 1μg/kg/h−1 de fentanilo fueron administrados al grupo P. En el postoperatorio se recogieron de nuevo muestras de sangre.ResultadosSolamente en los grupos S y P los niveles de malondialdehído disminuyeron en las 48h del postoperatorio; los niveles de glutatión peroxidasa aumentaron en comparación con los valores basales. Los niveles de selenio disminuyeron en el grupo S y en el grupo P, los niveles de cinc disminuyeron en el grupo P, los de hierro disminuyeron en todos los grupos y no hubo alteración en los niveles de cobre en ningún grupo en el período postoperatorio.ConclusiónDe acuerdo con los marcadores de malondialdehído y glutatión peroxidasa, llegamos a la conclusión de que el mantenimiento de la anestesia general con propofol y sevoflurano activó el sistema antioxidante contra el estrés oxidativo y el uso de desflurano no tuvo efectos sobre el estrés oxidativo y el sistema antioxidante.AbstractBackground and objectivesIn this study, we aimed to investigate the effects of sevoflurane, desflurane and propofol maintenances on serum levels of selenium, copper, zinc, iron, malondialdehyde, and glutathion peroxidase measurements, and antioxidant capacity.Methods60 patients scheduled for unilateral lower extremity surgery which would be performed with tourniquet under general anesthesia were divided into three groups. Blood samples were collected to determine the baseline serum levels of selenium, copper, zinc, iron, malondialdehyde and glutathion peroxidase. Anesthesia was induced using 2-2.5mg/kg−1 propofol, 1mg/kg−1 lidocaine and 0.6mg/kg−1 rocuronium. In the maintenance of anesthesia, under carrier gas of 50:50% O2:N2O 4L/min−1, 1MAC sevoflorane was administered to group S and 1MAC desflurane to group D; and under carrier gas of 50:50% O2:air 4L/min−1 6mg/kg/h−1 propofol and 1μg/kg/h−1 fentanyl infusion were administered to group P. At postoperative blood specimens were collected again.ResultsIt was observed that only in group S and P, levels of malondialdehyde decreased at postoperative 48th hour; levels of glutathion peroxidase increased in comparison to the baseline values. Selenium levels decreased in group S and group P, zinc levels decreased in group P, and iron levels decreased in all three groups, and copper levels did not change in any groups in the postoperative period.ConclusionAccording to the markers of malondialdehyde and glutathion peroxidase, it was concluded that maintenance of general anesthesia using propofol and sevoflurane activated the antioxidant system against oxidative stress and using desflurane had no effects on oxidative stress and antioxidant system.

ResumenJustificación y objetivosLas alteraciones en la perfusión ocular desempeñan un rol importante en la patogénesis de la neuropatía óptica isquémica. La presión de perfusión ocular es igual a la presión arterial media menos la presión intraocular. El objetivo de este estudio fue evaluar las alteraciones de la presión intraocular y del espesor de la capa de fibras nerviosas de la retina en pacientes sometidos a cirugía de la columna vertebral en pronación.MétodosEste estudio prospectivo incluyó a 30 pacientes sometidos a cirugía de la columna vertebral. El espesor de la capa de fibras nerviosas de la retina se midió un día antes y uno después de la cirugía, con la tomografía de coherencia óptica. La presión intraocular se midió 6 veces con tonopen y el tiempo de duración en posiciones diferentes: en supinación (basal), 10min después de la intubación (supinación 1); después de la pronación a los 10min (pronación 1), 60min (pronación 2) y 120min (pronación 3), y justo después de la supinación en el período postoperatorio (supinación 2).ResultadosNuestro estudio contó con la participación de 10 pacientes del sexo masculino y 20 del femenino, con un promedio de edad de 57 años. En el postoperatorio, cuando las medidas del espesor de la capa de fibras nerviosas de la retina fueron comparadas con los valores del preoperatorio, se observó un adelgazamiento estadísticamente significativo de la retina en los cuadrantes nasales e inferiores (p=0,009 y p=0,003, respectivamente). Observamos una disminución de la presión intraocular estadísticamente significativa en supinación 1 y un aumento en pronación 2 y 3, en comparación con los valores basales. La presión arterial media y la presión de perfusión ocular fueron significativamente más bajas en pronación 1, pronación 2 y pronación 3, en comparación con los valores basales.ConclusionesNuestro estudio mostró un aumento de la presión intraocular durante la cirugía de la columna vertebral en pronación. Se observó un adelgazamiento estadísticamente significativo del espesor de la capa de fibras nerviosas de la retina en los cuadrantes nasales e inferiores un día después de la cirugía de columna vertebral.AbstractBackground and objectivesChanges in ocular perfusion play an important role in the pathogenesis of ischemic optic neuropathy. Ocular perfusion pressure is equal to mean arterial pressure minus intraocular pressure. The aim of this study was to evaluate the changes in the intraocular pressure and the retinal nerve fiber layer thickness in patients undergoing spinal surgery in the prone position.MethodsThis prospective study included 30 patients undergoing spinal surgery. Retinal nerve fiber layer thickness were measured one day before and after the surgery by using optical coherence tomography. Intraocular pressure was measured by tonopen six times at different position and time-duration: supine position (baseline); 10min after intubation (supine 1); 10min (prone 1), 60min (prone 2), 120min (prone 3) after prone position; and just after postoperative supine position (supine 2).ResultsOur study involved 10 male and 20 female patients with the median age of 57 years. When postoperative retinal nerve fiber layer thickness measurements were compared with preoperative values, a statistically significant thinning was observed in inferior and nasal quadrants (P=.009 and P=.003, respectively). We observed a statistically significant intraocular pressure decrease in Supine 1 and an increase in both Prone 2 and Prone 3 when compared to the baseline. Mean arterial pressure and ocular perfusion pressure were found to be significantly lower in prone 1, prone 2 and prone 3, when compared with the baseline.ConclusionsOur study has shown increase in intraocular pressure during spinal surgery in prone position. A statistically significant retinal nerve fiber layer thickness thinning was seen in inferior and nasal quadrants one day after the spinal surgery.

Stiff Person Syndrome (SPS), typified by rigidity in muscles of the torso and extremities and painful episodic spasms, is a rare autoimmune-based neurological disease. Here we present the successful endotracheal intubation and application of TIVA without muscle relaxants on an SPS patient. A 46 years old male patient was operated with ASA-II physical status because of lumber vertebral compression fracture. After induction of anesthesia using lidocaine, propofol and remifentanil tracheal intubation was completed easily without neuromuscular blockage. Anesthesia was maintained with propofol, remifentanil and O2/air mixture. After a problem-free intraoperative period the patient was extubated and seven days later was discharged walking with aid. Though the mechanism is not clear neuromuscular blockers and volatile anesthetics may cause prolonged hypotonia in patients with SPS. We think the TIVA technique, a general anesthetic practice which does not require neuromuscular blockage, is suitable for these patients. Resumo A síndrome da pessoa rígida (SPR), caracterizada pela rigidez dos músculos do tronco e das extremidades e por episódios de espasmos dolorosos, é uma doença neurológica autoimune rara. Apresentamos o ocaso de intubação endotraqueal bem-sucedida e aplicação de AVT sem relaxantes musculares em um paciente com SPR. Paciente do sexo masculino, 46 anos, estado físico ASA-II, submetido à cirurgia devido à fratura por compressão da coluna lombar. Após a indução da anestesia com lidocaína, propofol e remifentanil, a intubação traqueal foi concluída com facilidade, sem bloqueio neuromuscular. A anestesia foi mantida com propofol, remifentanil e mistura de ar/O2. Após o período intraoperatório, que transcorreu sem intercorrências, o paciente foi extubado e, sete dias depois, recebeu alta, deambulando com ajuda. Embora o mecanismo não esteja claro, bloqueadores neuromusculares e anestésicos voláteis podem causar hipotonia prolongada em pacientes com SPR. Acreditamos que a técnica de AVT, uma prática de anestesia geral que não requer bloqueio neuromuscular, é adequada para esses pacientes.

ResumoVentilação não invasiva é uma modalidade de tratamento aceita tanto em exacerbações agudas de doenças respiratórias quanto em doença pulmonar obstrutiva crônica. É comumente usada em unidades de terapia intensiva ou para suporte respiratório pós‐cirúrgico em salas de recuperação pós‐anestesia. Este relato descreve o suporte intraoperatório em ventilação não invasiva para bloqueio do neuroeixo em cirurgia abdominal alta de emergência.AbstractNon‐invasive ventilation is an accepted treatment modality in both acute exacerbations of respiratory diseases and chronic obstructive lung disease. It is commonly utilized in the intensive care units, or for postoperative respiratory support in post‐anesthesia care units. This report describes intraoperative support in non‐invasive ventilation to neuroaxial anesthesia for an emergency upper abdominal surgery.

ResumenJustificación y objetivosel síndrome de Guillain-Barré es una de las causas más comunes de polineuropatía aguda en adultos. Recientemente, la aparición del síndrome de Guillain-Barré después de cirugías mayores o menores se ha convertido en objeto de debate cada vez mayor. En el síndrome de Guillain-Barré, generalmente se observan síndrome de secreción inapropiada de hormona antidiurética y disautonomía después de un déficit motor máximo.Relato de casopaciente de sexo masculino, 44 años, sometido a colecistectomía laparoscópica por colecistitis aguda. Después de comenzar con un fuerte dolor de cabeza, náuseas, diplopía y ataques de hipertensión en el período postoperatorio inmediato, una tomografía computadorizada del cerebro del paciente se reveló normal. Las pruebas de laboratorio revelaron hiponatremia asociada con el síndrome de secreción inadecuada de hormona antidiurética; los líquidos se restringieron y se inició tratamiento con furosemida y NaCl al 3%. En el segundo día del postoperatorio, el paciente presentó adormecimiento que se propagaba desde las manos y los pies, pérdida de fuerza, dificultad para tragar y para respirar. Se sospechó síndrome de Guillain-Barré y el paciente fue derivado a la unidad de cuidados intensivos. El examen del líquido cefalorraquídeo reveló 320mg/dL de proteína y mediante electromiografía se identificó neuropatía axonal sensorial y motora aguda. Se diagnosticó síndrome de Guillain-Barré y se inició el tratamiento intravenoso con inmunoglobulina (0,4g/kg/día, durante 5 días). Después de 10 días en la unidad de cuidados intensivos, durante los cuales los parámetros respiratorio, hemodinámico, neurológico y de laboratorio volvieron a la normalidad, el paciente fue derivado al servicio de neurología.Conclusionesnuestro relato de caso indica que, aunque el síndrome de secreción inapropiada de hormona antidiurética y la disfunción autonómica rara vez son características iniciales del síndrome de Guillain-Barré, debe tenerse en cuenta la posibilidad de que en el postoperatorio aparezca el síndrome de secreción inadecuada de hormona antidiurética. La presencia de hiponatremia secundaria en ese tipo de presentación clínica puede retrasar el diagnóstico.

Resumen Justificacion y objetivo el objetivo de este estudio fue comparar la eficacia de la levobupivacaina en la induccion de la raquianestesia continua (RAC) versus dosis unica (RADU) en pacientes programados para la reseccion transuretral de prostata. Metodos cincuenta pacientes, ≥ 60 anos de edad, ASA I-II o III, fueron incluidos en el estudio. La levobupivacaina al 0,5% (12,5 mg) se administro via intratecal en el grupo RADU. En el grupo RAC, la levobupivacaina al 0,25% (2 mL) fue inicialmente administrada a traves de un cateter espinal. Para que el nivel de bloqueo sensorial alcanzase el dermatoma T10, se administro 1 mL adicional de levobupivacaina al 0,25% a traves del cateter cada 10 min. Los parametros hemodinamicos y las caracteristicas del bloqueo fueron registrados. Las muestras de sangre de los pacientes fueron extraidas en los periodos pre y postoperatorios para determinar los niveles plasmaticos de cortisona y adrenalina. Resultados la tecnica RAC proporciono una mejor estabilidad hemodinamica en comparacion con la tecnica RADU, particularmente a los 90 min despues de la administracion intratecal. El aumento del nivel de bloqueo sensorial fue rapido y el tiempo para alcanzar la anestesia quirurgica fue menor en el grupo RADU. El desarrollo del bloqueo motor fue mas rapido en el grupo RADU. En el grupo RAC, un nivel parecido de anestesia se obtuvo con una dosis mas baja de levobupivacaina que fue relacionada con la recuperacion mas rapida. Aunque ambas tecnicas hayan sido eficaces en la prevencion de la respuesta al estres quirurgico, los niveles de cortisona en el postoperatorio fueron mejor suprimidos en el grupo RADU. Conclusion la tecnica RAC con levobupivacaina al 0,25% puede ser usada como un metodo de anestesia regional en pacientes ancianos programados para la cirugia de reseccion transuretral de prostata.

Resumen Justificacion y objetivo Los medicamentos administrados por via intravenosa pueden ser contaminados durante las diversas fases de produccion o preparacion. El sugammadex es una gamaciclodextrina modificada. Aunque esten disponibles muchas investigaciones sobre los efectos antibacterianos de una variedad de ciclodextrinas, no existen estudios de los efectos antibacterianos del sugammadex. Este estudio investigo la actividad antimicrobiana in vitro del sugammadex. Materiales y metodos La actividad antimicrobiana in vitro del sugammadex fue investigada por el metodo de microdilucion en medio de cultivo. El pH de la solucion de ensayo fue determinado usando un medidor de pH. Los microorganismos testados analizados incluyeron Staphylococcus aureus (S. aureus) (ATCC 29213), Enterococcus faecalis (E. faecalis) (ATCC 29212), Escherichia coli (E. coli) (ATCC 25922) y Pseudomonas aeruginosa (P. aeruginosa) (ATCC 27853). En la segunda fase del estudio, se contaminaron 100 mg/mL de sugammadex (50 μg) con microorganismos testados (50 μg), incluyendo S. aureus (ATCC 29213), E. faecalis (ATCC 29212), E. coli (ATCC 25922) y P. aeruginosa (ATCC 27853), incubados durante 24 h e inmediatamente se calculo la produccion bacteriana. Resultados El pH de las soluciones del analisis vario entre 7,25 y 6,97. Usando el metodo de microdilucion, el sugammadex no tuvo ningun efecto antibacteriano contra S. aureus , E. faecalis , E. coli y P. aeruginosa en ninguna concentracion. En la segunda fase del estudio, la produccion bacteriana fue observada despues de 24 h en 100 mg/mL de sugammadex contaminados con los microorganismos testados S. aureus, E. faecalis, E. coli y P. aeruginosa . Conclusiones El sugammadex no presento ningun efecto antimicrobiano sobre los microorganismos testados S. aureus, E. faecalis, E. coli y P. aeruginosa. Se debe tener cuidado de que las condiciones esteriles se mantengan en la preparacion del sugammadex, de que la misma preparacion de sugammadex no se use en mas de un paciente y de que las condiciones de almacenaje se respeten despues de la colocacion del sugammadex en un inyector.

Justificativa e objetivo: comparar a eficácia de levobupivacaína na indução de raquianestesia contínua (RAC) versus dose única (Radu) em pacientes programados para ressecção transuretral de próstata (RTUP). Métodos: foram incluídos no estudo 50 pacientes, ≥ 60 anos, ASA I-II ou III. Levobupivacaína a 0,5% (12,5 mg) foi administrada por via intratecal no grupo Radu. No grupo RAC, levobupivacaína a 0,25% (2 mL) foi inicialmente administrada através de cateter espinhal. Para o nível de bloqueio sensorial atingir o dermátomo T10, 1 mL adicional de levobupivacaína a 0,25% foi administrado através do cateter a cada 10 minutos. Os parâmetros hemodinâmicos e as características do bloqueio foram registrados. Amostras de sangue dos pacientes foram coletadas nos períodos pré- e pós-operatórios para determinar os níveis plasmáticos de cortisona e adrenalina. Resultados: a RAC proporcionou melhor estabilidade hemodinâmica em comparação com a Radu, particularmente aos 90 minutos após a administração intratecal. O aumento do nível de bloqueio sensorial foi rápido e o tempo para atingir a anestesia cirúrgica foi menor no grupo Radu. O desenvolvimento do bloqueio motor foi mais rápido no grupo Radu. No grupo RAC, um nível semelhante de anestesia foi obtido com o uso de uma dose mais baixa de levobupivacaína, que foi relacionada à recuperação mais rápida. Embora ambas as técnicas tenham sido eficazes na prevenção da resposta ao estresse cirúrgico, os níveis de cortisona no pós-operatório foram mais suprimidos no grupo Radu. Conclusão: a técnica RAC com levobupivacaína a 0,25% pode ser usada como um método de anestesia regional em pacientes idosos programados para RTUP. Background: The aim of the study is to compare the efficacy of levobupivacaine induced continuous spinal anesthesia (CSA) versus single dose spinal anesthesia (SDSA) in patients who are planned to undergo transurethral prostate resection. Methods: Sixty years or older, ASA I-II or III, 50 patients were included in the study. 12.5 mg 0.5% levobupivacaine were administered intrathecally in SDSA group. In CSA group, initially 2 mL of 0.25% levobupivacaine were administered through spinal catheter. In order to achieve sensory block level at T10 dermatome, additional 1 mL of 0.25% levobupivacaine were administered through the catheter in every 10 min. Hemodynamic parameters and block characteristics were recorded. Preoperative and postoperative blood samples of the patients were drawn to determine plasma cortisone and plasma epinephrine levels. Results: CSA technique provided better hemodynamic stability compared to SDSA technique particularly 90 min after intrathecal administration. The rise in sensory block level was rapid and the time to reach surgical anesthesia was shorter in SDSA group. Motor block developed faster in SDSA group. In CSA group, similar anesthesia level was achieved by using lower levobupivacaine dose and which was related to faster recovery. Although, both techniques were effective in preventing surgical stress respond, postoperative cortisone levels were suppressed more in SDSA group. Conclusion: CSA technique with 0.25% levobupivacaine can be used as a regional anesthesia method for elderly patients planned to have TUR-P operation. Justificación y objetivo: el objetivo de este estudio fue comparar la eficacia de la levobupivacaína en la inducción de la raquianestesia continua (RAC) versus dosis única (RADU) en pacientes programados para la resección transuretral de próstata. Métodos: cincuenta pacientes, ≥ 60 años de edad, ASA I-II o III, fueron incluidos en el estudio. La levobupivacaína al 0,5% (12,5 mg) se administró vía intratecal en el grupo RADU. En el grupo RAC, la levobupivacaína al 0,25% (2 mL) fue inicialmente administrada a través de un catéter espinal. Para que el nivel de bloqueo sensorial alcanzase el dermatoma T10, se administró 1 mL adicional de levobupivacaína al 0,25% a través del catéter cada 10 min. Los parámetros hemodinámicos y las características del bloqueo fueron registrados. Las muestras de sangre de los pacientes fueron extraídas en los períodos pre y postoperatorios para determinar los niveles plasmáticos de cortisona y adrenalina. Resultados: la técnica RAC proporcionó una mejor estabilidad hemodinámica en comparación con la técnica RADU, particularmente a los 90 min después de la administración intratecal. El aumento del nivel de bloqueo sensorial fue rápido y el tiempo para alcanzar la anestesia quirúrgica fue menor en el grupo RADU. El desarrollo del bloqueo motor fue más rápido en el grupo RADU. En el grupo RAC, un nivel parecido de anestesia se obtuvo con una dosis más baja de levobupivacaína que fue relacionada con la recuperación más rápida. Aunque ambas técnicas hayan sido eficaces en la prevención de la respuesta al estrés quirúrgico, los niveles de cortisona en el postoperatorio fueron mejor suprimidos en el grupo RADU.

Justificativa e objetivo: os medicamentos administrados como perfusão intravenosa podem ser contaminados durante as várias etapas de produção ou preparação. No entanto, estudos sobre os efeitos antibacterianos de vasopressores são muito raros. Este estudo investiga a atividade antimicrobiana in vitro das formas de vasopressores usados clinicamente. Materiais e métodos: atividades antimicrobianas in vitro de substâncias vasopressoras de diferentes concentrações foram investigadas com o uso da técnica de microdiluição. Os microrganismos empregados no teste foram: Escherichia coli ATCC 25922, Yersinia pseudotuberculosis ATCC 911, Pseudomonas aeruginosa ATCC 10145, Listeria monocytogenes ATCC 43251, Enterococcus faecalis ATCC 29212, Staphylococcus aureus ATCC 25923, Bacillus cereus 702 Roma, Mycobacterium smegmatis ATCC607, Candida albicans ATCC 60193 e Saccharomyces cerevisiae RSKK 251. Os ensaios antibacterianos foram feitos em caldo de cultura Mueller-Hinton (pH 7,3) e os ensaios antifúngicos em solução tampão de base nitrogenada para levedura (pH 7,0). Resultados: duas preparações diferentes de dopamina mostraram atividade antimicrobiana. Nenhuma outra substância do estudo mostrou qualquer atividade antimicrobiana. Conclusões: em nossa opinião, os efeitos antibacterianos da dopamina podem ser vantajosos para inibir a propagação de contaminação bacteriana durante a preparação das soluções para perfusão. Contudo, salientamos a importância do seguimento rigoroso das diretrizes de esterilização dos equipamentos e de assepsia durante todos os procedimentos feitos em unidades de terapia intensiva.

Resumen Justificativa y objetivo Los medicamentos administrados como perfusion intravenosa pueden ser contaminados durante las diversas etapas de produccion o preparacion. Sin embargo, son muy raros los estudios existentes sobre los efectos antibacterianos de los vasopresores. Este estudio investiga la actividad antimicrobiana in vitro de las formas de vasopresores usados clinicamente. Materiales y metodos Actividades antimicrobianas in vitro de sustancias vasopresoras de diferentes concentraciones fueron investigadas con el uso de la tecnica de microdilucion. Los microrganismos usados en el test fueron: Escherichia coli ATCC 25922, Yersinia pseudotuberculosis ATCC 911, Pseudomonas aeruginosa ATCC 10145, Listeria monocytogenes ATCC 43251, Enterococcus faecalis ATCC 29212, Staphylococcus aureus ATCC 25923, Bacillus cereus 702 Roma, Mycobacterium smegmatis ATCC607, Candida albicans ATCC 60193 y Saccharomyces cerevisiae RSKK 251. Los ensayos antibacterianos se hicieron en un caldo de cultivo Mueller-Hinton (pH 7,3) y los ensayos antifungicos en una solucion tapon de base nitrogenada para levadura (pH 7,0). Resultados Dos preparaciones diferentes de dopamina mostraron actividad antimicrobiana. Ninguna otra sustancia del estudio mostro alguna actividad antimicrobiana. Conclusiones En nuestra opinion, los efectos antibacterianos de la dopamina pueden ser ventajosos para inhibir la propagacion de la contaminacion bacteriana durante la preparacion de las soluciones para perfusion. Sin embargo, destacamos la importancia del seguimiento riguroso de las directrices de esterilizacion de los equipos y de asepsia durante todos los procedimientos realizados en las unidades de cuidados intensivos.

Background and objectives: The aim of our study is to compare the effects of sugammadex and neostigmine, used for neuromuscular blockage antagonism, on postoperative nausea and vomiting (PONV). Methods: Our study was completed with 98 ASA I-II risk patients undergoing endotracheal intubation under general anesthesia. At the end of the surgery patients were randomly divided into two groups given 2 mg kg−1 sugammadex (Group S) or 50 μg kg−1 neostigmine plus 0.2 mg kg−1 atropine (Group N). Monitoring and recording times were set as 1 hour postoperative and from 1–6, 6–12, and 12–24 hours. The anti-emetic amounts administered were recorded. Results: In the first hour postoperative 13 patients in Group N (27%) and 4 in Group S (8%) were observed to have nausea and/or vomiting and the difference was statistically significant (p = 0.0016). During the 24 hours of monitoring there was no significant difference in the incidence and severity of PONV (p > 0.05), however the number of patients given ondansetron for PONV treatment in Group N was statistically significantly higher than the number in Group S (16 in Group N, 6 in Group S, p 0,05) durante as 24 horas de monitoração, porém o número de pacientes que recebeu ondansetron para o tratamento de NVPO no Grupo N foi estatística e significativamente maior que o número de pacientes no Grupo S (16 e 6, respectivamente, p

WOS: 000277766100003, PubMed: 20466334, The aim of this study was to compare the effects of fentanyl or dexmedetomidine when used in combination with propofol and lidocaine for tracheal intubation without using muscle relaxants. Sixty patients with American Society of Anesthesiologists stage I risk were randomized to receive 1 mu g/kg dexmedetomidine (Group D, n = 30) or 2 mu g/kg fentanyl (Group F, n = 30), both in combination with 1.5 mg/kg lidocaine and 3 mg/kg propofol. The requirement for intubation was determined based on mask ventilation capability, jaw motility, position of the vocal cords and the patient's response to intubation and inflation of the endotracheal tube cuff. Systolic arterial pressure, mean arterial pressure, heart rate and peripheral oxygen saturation values were also recorded. Rate pressure products were calculated. Jaw relaxation, position of the vocal cords and patient's response to intubation and inflation of the endotracheal tube cuff were significantly better in Group D than in Group F (p < 0.05). The intubation conditions were significantly more satisfactory in Group D than in Group F (p = 0.01). Heart rate was significantly lower in Group D than in Group F after the administration of the study drugs and intubation (p < 0.05). Mean arterial pressure was significantly lower in Group F than in Group D after propofol injection and at 3 and 5 minutes after intubation (p < 0.05). After intubation, the rate pressure product values were significantly lower in Group D than in Group F (p < 0.05). We conclude that endotracheal intubation was better with the dexmedetomidine lidocaine propofol combination than with the fentanyl lidocaine propofol combination. However, side effects such as bradycardia should be considered when using dexmedetomidine.

The present study aimed to investigate the neuroprotective efficacy of dexmedetomidine in a rat experimental spinal cord injury model. The rats (n = 40) were equally divided into four groups: G1, G2, G3, and G4. Rats in the Cl group underwent a laminectomy only. For the rats in the G2, G3, and G4 groups, spinal cord injury was induced by placing an aneurysm clip extradurally for 60 Sat T10. The rats in G2 did not receive any post-injury treatment. Immediately after trauma was induced, rats in G3 were given methylprednisolone (30 mg/kg) and in G4, dexmedetomidine (10 mu g/kg), both intraperitoneally. The rats were sacrificed under anesthesia 24 hours later and 1.5 cm lengths of injured spinal cord were obtained. Malonyldialdehyde values were significantly increased in G2 compared to G1, G3 and G4 (p < 0.05). The neuronal cell count in G1 was significantly higher than in G2 and G3 (p = 0.0001; p = 0.007). G4 had higher cell counts compared to G2 and G3 (p = 0.0001; p = 0.05). These findings indicated that dexmedetomidine might have neuroprotective effects in spinal cord injury. (C) 2009 Elsevier Ltd. All rights reserved.

Objective: To compare 3 kinds of topical hemostatic agents in terms of adhesive strength, control of hemorrhage, and postoperative intra-abdominal adhesions in an experimental partial nephrectomy (PN) model. Methods: A total of 27 Wistar rats were divided into 5 groups. PN was performed in 6 rats (control group) with the conventional technique, in which the lower pole of the kidney was excised and sutured after hilar control. In 5 rats, oxidized cellulose was placed over the excised part of the kidney following conventional technique. In 6 rats, the hemostatic plant extract was used without hilar control. In 5 rats, the hemostatic agent chitosan was used without hilar control. As a sham group, 5 rats underwent a laparotomy and handling of the renal pedicle without the removal of renal pole. On the tenth day after the operation, the degree of adhesions to the operated kidney were evaluated. Histopathological evaluation was also performed by a blinded pathologist. Results: Mean warm ischemia times for control and oxidized cellulose groups were 4.85 ± 0.75 and 4.28 ± 1.28 minutes, respectively (P =.662). Wound healing was excellent in all groups except in 1 rat in the chitosan group. Chitosan was associated with significantly higher intestinal and peritoneal adhesion scores, although histopathologically comparable scores were revealed. Conclusion: In our rat model, chitosan and the hemostatic plant extract were as effective as conventional suturing in achieving hemostasis even without hilar control. Warm ischemia was eliminated and PN time was significantly decreased. The use of oxidized cellulose was not associated with higher scores of adhesion, suppuration, or hematoma. © 2011 Elsevier Inc. All Rights Reserved.