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Dive into the research topics where José Otávio Costa Auler is active.

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Featured researches published by José Otávio Costa Auler.


JAMA | 2010

Transfusion requirements after cardiac surgery: the TRACS randomized controlled trial.

Ludhmila Abrahão Hajjar; Jean Louis Vincent; Filomena Regina Barbosa Gomes Galas; Rosana Ely Nakamura; Carolina Silva; Marília Harumi Higuchi dos Santos; J Fukushima; Roberto Kalil Filho; Denise B. Sierra; Neuza Lopes; Thais Mauad; A Roquim; M Sundin; Wanderson C Leão; José Paulo Almeida; Pablo Maria Alberto Pomerantzeff; Luis Oliveira Dallan; Fabio Biscegli Jatene; Noedir A. G Stolf; José Otávio Costa Auler

CONTEXT Perioperative red blood cell transfusion is commonly used to address anemia, an independent risk factor for morbidity and mortality after cardiac operations; however, evidence regarding optimal blood transfusion practice in patients undergoing cardiac surgery is lacking. OBJECTIVE To define whether a restrictive perioperative red blood cell transfusion strategy is as safe as a liberal strategy in patients undergoing elective cardiac surgery. DESIGN, SETTING, AND PATIENTS The Transfusion Requirements After Cardiac Surgery (TRACS) study, a prospective, randomized, controlled clinical noninferiority trial conducted between February 2009 and February 2010 in an intensive care unit at a university hospital cardiac surgery referral center in Brazil. Consecutive adult patients (n = 502) who underwent cardiac surgery with cardiopulmonary bypass were eligible; analysis was by intention-to-treat. INTERVENTION Patients were randomly assigned to a liberal strategy of blood transfusion (to maintain a hematocrit ≥30%) or to a restrictive strategy (hematocrit ≥24%). MAIN OUTCOME MEASURE Composite end point of 30-day all-cause mortality and severe morbidity (cardiogenic shock, acute respiratory distress syndrome, or acute renal injury requiring dialysis or hemofiltration) occurring during the hospital stay. The noninferiority margin was predefined at -8% (ie, 8% minimal clinically important increase in occurrence of the composite end point). RESULTS Hemoglobin concentrations were maintained at a mean of 10.5 g/dL (95% confidence interval [CI], 10.4-10.6) in the liberal-strategy group and 9.1 g/dL (95% CI, 9.0-9.2) in the restrictive-strategy group (P < .001). A total of 198 of 253 patients (78%) in the liberal-strategy group and 118 of 249 (47%) in the restrictive-strategy group received a blood transfusion (P < .001). Occurrence of the primary end point was similar between groups (10% liberal vs 11% restrictive; between-group difference, 1% [95% CI, -6% to 4%]; P = .85). Independent of transfusion strategy, the number of transfused red blood cell units was an independent risk factor for clinical complications or death at 30 days (hazard ratio for each additional unit transfused, 1.2 [95% CI, 1.1-1.4]; P = .002). CONCLUSION Among patients undergoing cardiac surgery, the use of a restrictive perioperative transfusion strategy compared with a more liberal strategy resulted in noninferior rates of the combined outcome of 30-day all-cause mortality and severe morbidity. TRIAL REGISTRATION clinicaltrials.gov Identifier: NCT01021631.


American Journal of Respiratory and Critical Care Medicine | 2010

Lung Pathology in Fatal Novel Human Influenza A (H1N1) Infection

Thais Mauad; Ludhmila Abrahão Hajjar; Giovanna D. Callegari; Luiz Fernando Ferraz da Silva; Denise Schout; Filomena Regina Barbosa Gomes Galas; Venancio Avancini Ferreira Alves; Denise M. A. C. Malheiros; José Otávio Costa Auler; Aurea F. Ferreira; Marcela R. L. Borsato; Stephania M. Bezerra; Paulo Sampaio Gutierrez; Elia Garcia Caldini; Carlos Augusto Pasqualucci; Marisa Dolhnikoff; Paulo Hilário Nascimento Saldiva

RATIONALE There are no reports of the systemic human pathology of the novel swine H1N1 influenza (S-OIV) infection. OBJECTIVES The autopsy findings of 21 Brazilian patients with confirmed S-OIV infection are presented. These patients died in the winter of the southern hemisphere 2009 pandemic, with acute respiratory failure. METHODS Lung tissue was submitted to virologic and bacteriologic analysis with real-time reverse transcriptase polymerase chain reaction and electron microscopy. Expression of toll-like receptor (TLR)-3, IFN-gamma, tumor necrosis factor-alpha, CD8(+) T cells and granzyme B(+) cells in the lungs was investigated by immunohistochemistry. MEASUREMENTS AND MAIN RESULTS Patients were aged from 1 to 68 years (72% between 30 and 59 yr) and 12 were male. Sixteen patients had preexisting medical conditions. Diffuse alveolar damage was present in 20 individuals. In six patients, diffuse alveolar damage was associated with necrotizing bronchiolitis and in five with extensive hemorrhage. There was also a cytopathic effect in the bronchial and alveolar epithelial cells, as well as necrosis, epithelial hyperplasia, and squamous metaplasia of the large airways. There was marked expression of TLR-3 and IFN-gamma and a large number of CD8(+) T cells and granzyme B(+) cells within the lung tissue. Changes in other organs were mainly secondary to multiple organ failure. CONCLUSIONS Autopsies have shown that the main pathological changes associated with S-OIV infection are localized to the lungs, where three distinct histological patterns can be identified. We also show evidence of ongoing pulmonary aberrant immune response. Our results reinforce the usefulness of autopsy in increasing the understanding of the novel human influenza A (H1N1) infection.


Critical Care | 2007

Goal-directed fluid management based on pulse pressure variation monitoring during high-risk surgery: a pilot randomized controlled trial

Marcel Rezende Lopes; Marcos Antonio de Oliveira; Vanessa Oliveira S Pereira; Ivaneide Paula B Lemos; José Otávio Costa Auler; Frédéric Michard

IntroductionSeveral studies have shown that maximizing stroke volume (or increasing it until a plateau is reached) by volume loading during high-risk surgery may improve post-operative outcome. This goal could be achieved simply by minimizing the variation in arterial pulse pressure (ΔPP) induced by mechanical ventilation. We tested this hypothesis in a prospective, randomized, single-centre study. The primary endpoint was the length of postoperative stay in hospital.MethodsThirty-three patients undergoing high-risk surgery were randomized either to a control group (group C, n = 16) or to an intervention group (group I, n = 17). In group I, ΔPP was continuously monitored during surgery by a multiparameter bedside monitor and minimized to 10% or less by volume loading.ResultsBoth groups were comparable in terms of demographic data, American Society of Anesthesiology score, type, and duration of surgery. During surgery, group I received more fluid than group C (4,618 ± 1,557 versus 1,694 ± 705 ml (mean ± SD), P < 0.0001), and ΔPP decreased from 22 ± 75 to 9 ± 1% (P < 0.05) in group I. The median duration of postoperative stay in hospital (7 versus 17 days, P < 0.01) was lower in group I than in group C. The number of postoperative complications per patient (1.4 ± 2.1 versus 3.9 ± 2.8, P < 0.05), as well as the median duration of mechanical ventilation (1 versus 5 days, P < 0.05) and stay in the intensive care unit (3 versus 9 days, P < 0.01) was also lower in group I.ConclusionMonitoring and minimizing ΔPP by volume loading during high-risk surgery improves postoperative outcome and decreases the length of stay in hospital.Trial registrationNCT00479011


Anesthesia & Analgesia | 2008

Online monitoring of pulse pressure variation to guide fluid therapy after cardiac surgery.

José Otávio Costa Auler; Filomena Regina Barbosa Gomes Galas; Ludhmila Abrahão Hajjar; Luciana Santos; Thiago Carvalho; Frédéric Michard

BACKGROUND: The arterial pulse pressure variation induced by mechanical ventilation (&Dgr;PP) has been shown to be a predictor of fluid responsiveness. Until now, &Dgr;PP has had to be calculated offline (from a computer recording or a paper printing of the arterial pressure curve), or to be derived from specific cardiac output monitors, limiting the widespread use of this parameter. Recently, a method has been developed for the automatic calculation and real-time monitoring of &Dgr;PP using standard bedside monitors. Whether this method is to predict reliable predictor of fluid responsiveness remains to be determined. METHODS: We conducted a prospective clinical study in 59 mechanically ventilated patients in the postoperative period of cardiac surgery. Patients studied were considered at low risk for complications related to fluid administration (pulmonary artery occlusion pressure <20 mm Hg, left ventricular ejection fraction ≥40%). All patients were instrumented with an arterial line and a pulmonary artery catheter. Cardiac filling pressures and cardiac output were measured before and after intravascular fluid administration (20 mL/kg of lactated Ringer’s solution over 20 min), whereas &Dgr;PP was automatically calculated and continuously monitored. RESULTS: Fluid administration increased cardiac output by at least 15% in 39 patients (66% = responders). Before fluid administration, responders and nonresponders were comparable with regard to right atrial and pulmonary artery occlusion pressures. In contrast, &Dgr;PP was significantly greater in responders than in nonresponders (17% ± 3% vs 9% ± 2%, P < 0.001). The &Dgr;PP cut-off value of 12% allowed identification of responders with a sensitivity of 97% and a specificity of 95%. CONCLUSION: Automatic real-time monitoring of &Dgr;PP is possible using a standard bedside monitor and was found to be a reliable method to predict fluid responsiveness after cardiac surgery. Additional studies are needed to determine if this technique can be used to avoid the complications of fluid administration in high-risk patients.


Anesthesiology | 2015

Transfusion Requirements in Surgical Oncology Patients A Prospective, Randomized Controlled Trial

Juliano Pinheiro de Almeida; Jean Louis Vincent; Filomena Regina Barbosa Gomes Galas; Elisangela Pinto Marinho de Almeida; J Fukushima; E Osawa; F Bergamin; C Park; Rosana Ely Nakamura; Silvia Moulin Ribeiro Fonseca; Guilherme Cutait; Joseane Inacio Alves; Mellik Bazan; Silvia Vieira; Ana C. Vieira Sandrini; Henrique Palomba; Ulysses Ribeiro; Alexandre Crippa; Marcos F. Dall'Oglio; Maria Del Pilar Estevez Diz; Roberto Kalil Filho; José Otávio Costa Auler; Andrew Rhodes; Ludhmila Abrahão Hajjar

Background:Several studies have indicated that a restrictive erythrocyte transfusion strategy is as safe as a liberal one in critically ill patients, but there is no clear evidence to support the superiority of any perioperative transfusion strategy in patients with cancer. Methods:In a randomized, controlled, parallel-group, double-blind (patients and outcome assessors) superiority trial in the intensive care unit of a tertiary oncology hospital, the authors evaluated whether a restrictive strategy of erythrocyte transfusion (transfusion when hemoglobin concentration <7 g/dl) was superior to a liberal one (transfusion when hemoglobin concentration <9 g/dl) for reducing mortality and severe clinical complications among patients having major cancer surgery. All adult patients with cancer having major abdominal surgery who required postoperative intensive care were included and randomly allocated to treatment with the liberal or the restrictive erythrocyte transfusion strategy. The primary outcome was a composite endpoint of mortality and morbidity. Results:A total of 198 patients were included as follows: 101 in the restrictive group and 97 in the liberal group. The primary composite endpoint occurred in 19.6% (95% CI, 12.9 to 28.6%) of patients in the liberal-strategy group and in 35.6% (27.0 to 45.4%) of patients in the restrictive-strategy group (P = 0.012). Compared with the restrictive strategy, the liberal transfusion strategy was associated with an absolute risk reduction for the composite outcome of 16% (3.8 to 28.2%) and a number needed to treat of 6.2 (3.5 to 26.5). Conclusion:A liberal erythrocyte transfusion strategy with a hemoglobin trigger of 9 g/dl was associated with fewer major postoperative complications in patients having major cancer surgery compared with a restrictive strategy.


Pediatric Anesthesia | 2007

Effects of preanesthetic administration of midazolam, clonidine, or dexmedetomidine on postoperative pain and anxiety in children

André P. Schmidt; Emília Aparecida Valinetti; Denise Ruschel Bandeira; Maria Isabel Ferreira Bertacchi; Claudia Marquez Simões; José Otávio Costa Auler

Background:  A growing interest in the possible influences of pre‐ and postoperative anxiety and pain scores as outcomes of surgical treatment and benefits of anxiety or pain‐reducing interventions has emerged. The aim of this study was to evaluate the influence of three different premedication regimens on postoperative pain and anxiety in children.


Veterinary Anaesthesia and Analgesia | 2002

A new brachial plexus block technique in dogs

Fábio Futema; Denise Tabacchi Fantoni; José Otávio Costa Auler; Silvia Renata Gaido Cortopassi; Andrea Acaui; Angelo João Stopiglia

OBJECTIVE To evaluate the feasibility and efficacy of a new technique of brachial plexus anesthesia in dogs. STUDY DESIGN Prospective, experimental study. ANIMALS Twelve adult mongrel dogs, six males and six females weighing 14.8 ± 1.75 kg. METHODS The animals were sedated with acepromazine 0.05 mg kg-1 and anesthetized with propofol (6 mg kg-1, IV bolus) followed by an infusion of 212 μg kg-1 minute-1. The brachial plexus block technique was performed utilizing the brachial artery as an anatomic landmark, the needle was inserted from the axilla and a nerve stimulator was used to ensure the accuracy of needle placement. Bupivacaine (0.375% with 5 μg mL-1 epinephrine) was used at a dose rate of 4 mg kg-1. Dogs underwent mid-diaphyseal osteotomies of the humerus followed by intramedullary pin fixation. RESULTS Onset time to motor and sensory block were 9.70 ± 5.52 and 26.20 ± 8.86 minutes, respectively. Analgesia lasted for 11.11 ± 0.47 hours. The block was effective in 91.6% of the animals, being verified by anesthesia of the whole front limb distal to the shoulder. One animal became hypotensive after the block and did not undergo the surgery at that time. In the remaining 10 animals the heart and respiratory rates, blood pressure, blood gas parameters and plasma bicarbonate concentration did not show any statistically significant alterations during the surgical procedure. CONCLUSIONS This brachial plexus block technique is effective in most cases to provide surgical analgesia for the front limb distal to the shoulder. CLINICAL RELEVANCE Various surgical procedures in the front limb can be performed with a regional anesthetic technique without the use and concomitant risks of general anesthesia in dogs. Long-lasting analgesia associated with this technique may also provide a valuable tool for the management of pain in the forelimb.


Clinics | 2009

INtENSIvE pErIopErAtIvE gLuCoSE CoNtroL doES Not ImprovE outComES of pAtIENtS SubmIttEd to opEN-hEArt SurgEry: A rANdomIzEd CoNtroLLEd trIAL

Raquel Pei Chen Chan; Filomena Regina Barbosa Gomes Galas; Ludhmila Abrahão Hajjar; Carmen Narvaes Bello; Marilde de Albuquerque Piccioni; José Otávio Costa Auler

BACKGROUND: The objective of this study was to investigate the relationship between different target levels of glucose and the clinical outcomes of patients undergoing cardiac surgery with cardiopulmonary bypass. METHODS: We designed a prospective study in a university hospital where 109 consecutive patients were enrolled during a six-month period. All patients were scheduled for open-heart surgery requiring cardiopulmonary bypass. Patients were randomly allocated into two groups. One group consisted of 55 patients and had a target glucose level of 80–130 mg/dl, while the other contained 54 patients and had a target glucose level of 160–200 mg/dl. These parameters were controlled during surgery and for 36 hours after surgery in the intensive care unit. Primary outcomes were clinical outcomes, including time of mechanical ventilation, length of stay in the intensive care unit, infection, hypoglycemia, renal or neurological dysfunction, blood transfusion and length of stay in the hospital. The secondary outcome was a combined end-point (mortality at 30 days, infection or length of stay in the intensive care unit of more than 3 days). A p-value of <0.05 was considered significant. RESULTS: The anthropometric and clinical characteristics of the patients from each group were similar, except for weight and body mass index. The mean glucose level during the protocol period was 126.69 mg/dl in the treated group and 168.21 mg/dl in the control group (p<0.0016). There were no differences between groups regarding clinical outcomes, including the duration of mechanical ventilation, length of stay in the intensive care unit, blood transfusion, postoperative infection, hypoglycemic event, neurological dysfunction or 30-day mortality (p>0.05). CONCLUSIONS: In 109 patients undergoing cardiac surgery with cardiopulmonary bypass, both protocols of glycemic control in an intraoperative setting and in the intensive care unit were found to be safe, easily achieved and not to differentially affect clinical outcomes.


Anesthesia & Analgesia | 2002

The Effects of Abdominal Opening on Respiratory Mechanics During General Anesthesia in Normal and Morbidly Obese Patients: A Comparative Study

José Otávio Costa Auler; Erika Miyoshi; Cláudia Regina Fernandes; Fábio Ely Martins Benseñor; Luciana Elias; Jorge Bonassa

Morbid obesity has a profound effect on respiratory mechanics and gas exchange. However, most studies were performed in morbidly obese patients before or after anesthesia. We tested the hypothesis that anesthesia and abdominal opening could modify the elastic and resistive properties of the respiratory system. Eleven morbidly obese and eight normal-weight patients scheduled for gastric binding and cancer treatment, respectively, under laparotomy were studied. Respiratory mechanics, partitioned into its lung and chest wall components, were investigated during surgery by means of the end-inspiratory inflation occlusion method and esophageal balloon at five time points. Static respiratory and lung compliance were markedly reduced in obese patients; on the contrary, static compliance of chest wall presented comparable values in both groups. Obese patients also presented higher resistances of the total respiratory system, lung and chest wall, as well as “additional” lung resistance. Mainly in obese patients, laparotomy provoked a significant increase in lung compliance and decrease in “additional” lung resistance 1 h after the peritoneum was opened, which returned to original values after the peritoneum had been closed (P < 0.005). In obese patients, low respiratory compliance and higher airway resistance were mainly determined by the lung component.


Anesthesiology | 2017

Vasopressin versus Norepinephrine in Patients with Vasoplegic Shock After Cardiac Surgery: The VANCS Randomized Controlled Trial.

Ludhmila Abrahão Hajjar; Jean Louis Vincent; Filomena Regina Barbosa Gomes Galas; Andrew Rhodes; Giovanni Landoni; E Osawa; Renato Rosa Melo; M Sundin; Solimar Miranda Grande; Fábio Antônio Gaiotto; Pablo Maria Alberto Pomerantzeff; Luis Oliveira Dallan; Rafael Alves Franco; Rosana Ely Nakamura; Luiz Augusto Ferreira Lisboa; Juliano Pinheiro de Almeida; Aline Muller Gerent; Dayenne Hianae Souza; Maria Alice Gaiane; J Fukushima; C Park; Cristiane Zambolim; Graziela Santos Rocha Ferreira; Tânia Mara Varejão Strabelli; Felipe Lourenço Fernandes; L Camara; S Zeferino; Valter Garcia Santos; Marilde de Albuquerque Piccioni; Fabio Biscegli Jatene

Background: Vasoplegic syndrome is a common complication after cardiac surgery and impacts negatively on patient outcomes. The objective of this study was to evaluate whether vasopressin is superior to norepinephrine in reducing postoperative complications in patients with vasoplegic syndrome. Methods: This prospective, randomized, double-blind trial was conducted at the Heart Institute, University of Sao Paulo, Sao Paulo, Brazil, between January 2012 and March 2014. Patients with vasoplegic shock (defined as mean arterial pressure less than 65 mmHg resistant to fluid challenge and cardiac index greater than 2.2 l · min−1 · m−2) after cardiac surgery were randomized to receive vasopressin (0.01 to 0.06 U/min) or norepinephrine (10 to 60 &mgr;g/min) to maintain arterial pressure. The primary endpoint was a composite of mortality or severe complications (stroke, requirement for mechanical ventilation for longer than 48 h, deep sternal wound infection, reoperation, or acute renal failure) within 30 days. Results: A total of 330 patients were randomized, and 300 were infused with one of the study drugs (vasopressin, 149; norepinephrine, 151). The primary outcome occurred in 32% of the vasopressin patients and in 49% of the norepinephrine patients (unadjusted hazard ratio, 0.55; 95% CI, 0.38 to 0.80; P = 0.0014). Regarding adverse events, the authors found a lower occurrence of atrial fibrillation in the vasopressin group (63.8% vs. 82.1%; P = 0.0004) and no difference between groups in the rates of digital ischemia, mesenteric ischemia, hyponatremia, and myocardial infarction. Conclusions: The authors’ results suggest that vasopressin can be used as a first-line vasopressor agent in postcardiac surgery vasoplegic shock and improves clinical outcomes.

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J Fukushima

University of São Paulo

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Jean Louis Vincent

Université libre de Bruxelles

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E Osawa

University of São Paulo

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