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The TELE-critical Care verSus usual Care On ICU PErformance (TELESCOPE) trial aims to assess whether a complex telemedicine intervention in intensive care units, which focuses on daily multidisciplinary rounds performed by remote intensivists, will reduce intensive care unit length of stay compared to usual care.The TELESCOPE trial is a national, multicenter, controlled, open label, cluster randomized trial. The study tests the effectiveness of daily multidisciplinary rounds conducted by an intensivist through telemedicine in Brazilian intensive care units. The protocol was approved by the local Research Ethics Committee of the coordinating study center and by the local Research Ethics Committee from each of the 30 intensive care units, following Brazilian legislation. The trial is registered with ClinicalTrials. gov (NCT03920501). The primary outcome is intensive care unit length of stay, which will be analyzed accounting for the baseline period and cluster structure of the data and adjusted by prespecified covariates. Secondary exploratory outcomes included intensive care unit performance classification, in-hospital mortality, incidence of nosocomial infections, ventilator-free days at 28 days, rate of patients receiving oral or enteral feeding, rate of patients under light sedation or alert and calm, and rate of patients under normoxemia.According to the trial's best practice, we report our statistical analysis prior to locking the database and beginning analyses. We anticipate that this reporting practice will prevent analysis bias and improve the interpretation of the reported results.ClinicalTrials.gov registration: NCT03920501.O ensaio TELE-critical Care verSus usual Care On ICU PErformance (TELESCOPE) visa avaliar se uma intervenção complexa por telemedicina em unidades de terapia intensiva, que se concentra em rondas multidisciplinares diárias realizadas por intensivistas a distância, reduzirá o tempo de permanência na unidade de terapia intensiva em comparação com os cuidados habituais.O TELESCOPE é um ensaio nacional, multicêntrico, controlado, aberto, randomizado em cluster. O estudo testa a eficácia de rondas multidisciplinares diárias realizadas por um intensivista por meio de telemedicina em unidades de terapia intensiva brasileiras. O protocolo foi aprovado pelo Comitê de Ética em Pesquisa local do centro coordenador do estudo e pelo Comitê de Ética em Pesquisa local de cada uma das 30 unidades de terapia intensiva, de acordo com a legislação brasileira. O ensaio está registado no ClinicalTrials.gov (NCT03920501). O desfecho primário é o tempo de internação na unidade de terapia intensiva, que será analisado considerando o período basal e a estrutura dos dados em cluster, sendo ajustado por covariáveis predefinidas. Os desfechos exploratórios secundários incluem a classificação de desempenho da unidade de terapia intensiva, a mortalidade hospitalar, a incidência de infecções nosocomiais, o número de dias sem ventilação mecânica aos 28 dias, a taxa de pacientes que recebem alimentação oral ou enteral, a taxa de pacientes sob sedação leve ou em alerta e calmos e a taxa de pacientes sob normoxemia.De acordo com as melhores práticas do ensaio, divulgamos nossa análise estatística antes de bloquear a base de dados e iniciar as análises. Esperamos que essa prática de notificação evite o viés das análises e aprimore a interpretação dos resultados apresentados.Registro no ClinicalTrials.gov: NCT03920501.

Made available in DSpace on 2022-04-29T08:30:53Z (GMT). No. of bitstreams: 0 Previous issue date: 2021-04-01 National Health and Medical Research Council Objective: To describe fluid resuscitation practices in Brazilian intensive care units and to compare them with those of other countries participating in the Fluid-TRIPS. Methods: This was a prospective, international, cross-sectional, observational study in a convenience sample of intensive care units in 27 countries (including Brazil) using the Fluid-TRIPS database compiled in 2014. We described the patterns of fluid resuscitation use in Brazil compared with those in other countries and identified the factors associated with fluid choice. Results: On the study day, 3,214 patients in Brazil and 3,493 patients in other countries were included, of whom 16.1% and 26.8% (p < 0.001) received fluids, respectively. The main indication for fluid resuscitation was impaired perfusion and/or low cardiac output (Brazil: 71.7% versus other countries: 56.4%, p < 0.001). In Brazil, the percentage of patients receiving crystalloid solutions was higher (97.7% versus 76.8%, p < 0.001), and 0.9% sodium chloride was the most commonly used crystalloid (62.5% versus 27.1%, p < 0.001). The multivariable analysis suggested that the albumin levels were associated with the use of both crystalloids and colloids, whereas the type of fluid prescriber was associated with crystalloid use only. Conclusion: Our results suggest that crystalloids are more frequently used than colloids for fluid resuscitation in Brazil, and this discrepancy in frequencies is higher than that in other countries. Sodium chloride (0.9%) was the crystalloid most commonly prescribed. Serum albumin levels and the type of fluid prescriber were the factors associated with the choice of crystalloids or colloids for fluid resuscitation. Discipline of Anesthesiology Pain and Intensive Care Universidade Federal de São Paulo, Rua Napoleão de Barros, 737, 6ºandar Critical Care and Trauma Division George Institute for Global Health Hospital Sírio-Libanês Hospital das Clínicas Faculdade de Medicina Universidade de São Paulo Instituto de Pesquisa HCor - Hospital do Coração Instituto de Pesquisa Clínica Evandro Chagas Fundação Oswaldo Cruz Hospital de Clínicas Mário Lioni Hospital do Rim e Hipertensão Fundação Oswaldo Ramos Hospital Samaritano Hospital Paulistano Hospital São José Instituto D’Or de Ensino e Pesquisa Hospital Municipal São José Hospital Israelita Albert Einstein Hospital Santa Rita Hospital de Base Faculdade de Medicina de São Jose do Rio Preto Hospital Unimed de Belo Horizonte Hospital Santa Lúcia Hospital Evangélico de Sorocaba Hospital PIO XII Hospital São Camilo Pompéia Hospital Alvorada Brasília Hospital Ecoville Hospital do Trabalhador Hospital Vita Batel Hospital das Clínicas Faculdade de Medicina de Botucatu Universidade Estadual “Júlio de Mesquita Filho” Hospital Geral Dr. César Cals Hospital Copa D’Or Associação Beneficente Hospital Unimar Hospital Casa de Saúde de Santos Hospital Estadual Getúlio Vargas Hospital e Maternidade Otaviano Neves Instituto Estadual do Cérebro Paulo Niemeyer Hospital Universitário Universidade Federal de Juiz de Fora Lifecenter Hospital Geral de Fortaleza Hospital Municipal Dr. Moysés Deutsch (M’Boi Mirim) Santa Casa de Misericórdia de Presidente Prudente Hospital 9 de julho Hospital Estadual Rocha Faria Hospital Municipal Santa Isabel Hospital e Maternidade Municipal Dr. Odelmo Leão Carneiro Hospital Evangélico de Londrina Universidade Estadual de Londrina Hospital Samaritano João Pessoa Hospital de Caridade Astrogildo de Azevedo Vitória Apart Hospital Instituto de Ortopedia e Traumatologia Hospital do Subúrbio Hospital Renascentista Hospital Felício Rocho Hospital Municipal Irmã Dulce Hospital Universitário Júlio Müller Universidade Federal do Mato Grosso Hospital de Urgência Hospital Geral de Goiânia Fundação Doutor Amaral Carvalho Hospital Adventista de Belém Hospital Santa Juliana Hospital Dom Vicente Scherer Hospital Primavera Hospital Carlos da Silva Lacaz Hospital Escola Faculdade de Medicina de Jundiaí Hospital Sepaco Hospital Professor Edmundo Vasconcelos Hospital Paulo Sacramento Clínica Dom Rodrigo Complexo Hospitalar Ortotrauma de Mangabeira Hospital Nossa Senhora da Conceição Hospital Regional de Samambaia Hospital São Camilo Ipiranga Hospital da Restauração Instituto do Coração Hospital das Clínicas Faculdade de Medicina Universidade de São Paulo Hospital Estadual Jayme Santos Neves Hospital SOS Cárdio Hospital da Luz Vila Mariana Hospital Maternidade e Pronto-Socorro Santa Luci Santa Casa de Misericórdia de Vitória da Conquista Santa Casa de Misericórdia de Porto Alegre Hospital São Francisco de Assis Hospital Memorial São José Hospital Regional de Jundiaí Hospital Universitário Faculdade de Medicina de Jundiaí Hospital Regional de Presidente Prudente Santa Casa de Misericórdia de Assis Hospital de Clínicas Gaspar Vianna Hospital do Coração do Brasil Hospital Hélio Anjos Ortiz Hospital Vila da Serra Hospital Nereu Ramos Hospital Santa Maria Intensibarra Santa Casa de Misericórdia de Santo Amaro Santa Casa de Caridade de Don Pedrito Santa Casa de Misericórdia de Santana do Livramento Hospital Unimed de Macaé Hospital Municipal Pedro II Hospital Federal dos Servidores do Estado Hospital São Mateus Hospital IBR Hospital Uniclinic Santa Casa de Misericórdia de Paraguaçu Paulista Associação Hospitalar Beneficente São Vicente de Paulo Hospital do Servidor Público Municipal de São Paulo Hospital Santa Isabel Hospital Municipal Dr Jose Soares Hungria Hospital Fernandes Távora Hospital Distrital Evandro Ayres de Moura Hospital Saúde da Mulher Hospital Estadual de Urgência e Emergência de Vitória Samur Hospital e Pronto-Socorro 28 de Agosto Hospital Assunção Hospital Universitário de Santa Maria Hospital Universitário Cajuru Instituto do Câncer do Estado de São Paulo Hospital Unimed de Limeira Hospital Amecor Santa Casa de Caridade de Diamantina Hospital das Clínicas Faculdade Ribeirão Preto Universidade de São Paulo HCor - Hospital do Coração Hospital Goiânia Leste Hospital Ortopédico Hospital Santa Maria Hospital Municipal Dr. Munir Rafful Hospital Jardim Amália Hospital Madre Regina Prottman Hospital Universitário São Francisco de Paula Universidade Católica de Pelotas Hospital São Joao de Deus Hospital Nossa Senhora Monte Serrat Hospital Unimed Salto Hospital Moinhos de Vento Hospital Geral de Vitória da Conquista Hospital Marcelino Champagnat Hospital São Lucas Pontifícia Universidade Católica do Rio Grande do Sul Hospital Universitário Universidade Federal da Grande Dourados Hospital Português Hospital Brigadeiro Hospital Regional de Sousa Hospital das Clínicas Universidade Federal do Espírito Santo Santa Casa de Misericórdia de Ribeirão Preto Hospital Universitário Lauro Wanderley Santa Casa de Belo Horizonte Hospital Adventista de Manaus Santa Casa Maringá Universidade Estadual Maringá Hospital Total Cor Hospital Universitário Universidade de Santa Cruz do Sul Hospital Dom Hélder Hospital das Clínicas de Porto Alegre Universidade Federal do Rio Grande do Sul Hospital Anis Rassi Instituto de Infectologia Emílio Ribas II Hospital Unimed Rio de Janeiro Hospital Alemão Oswaldo Cruz Hospital Samaritano Rio de Janeiro São Bernardo Apart Hospital Hospital Nossa Senhora dos Prazeres Hospital Unimed ABC Hospital Municipal de Paracatu Hospital Municipal Padre Germano Lauck Hospital Santa Helena Hospital Santa Izabel Santa Casa de Misericórdia de São Paulo Hospital Tereza Ramos Hospital Alvorada Taguatinga Hospital Maternidade São José Hospital Universitário Ciências Médicas Fundação Educacional Lucas Machado Santa Casa de Belém do Pará Instituto Nacional de Cardiologia Hospital Novo Atibaia BP - A Beneficência Portuguesa de São Paulo Hospital Universitário Maria Aparecida Pedrossian Universidade Federal de Mato Grosso do Sul Hospital do Servidor Público Estadual “Francisco Morato de Oliveira” Hospital Norte D’Or Hospital Estadual Ipiranga Hospital Universitário de Maringá Universidade Estadual de Maringá Albert Sabin Hospital e Maternidade Casa de Caridade de Carangola Irmandade de Misericórdia de Guaxupé Disciplina de Emergências Clínicas Universidade Estadual de Campinas Hospital São Lucas Fundação Pio XII- Hospital de Câncer de Barretos Clínica Campo Grande Hospital das Clínicas Universidade Federal de Minas Gerais Casa de Saúde Santa Lúcia Hospital Regional de Itapetininga São Camilo Santa Casa de Angra dos Reis Grupo Hospitalar Nossa Senhora da Conceição Irmandade Misericórdia Hospital Santa Casa de Monte Alto Hospital São Marcos Hospital Unimed de Manaus Hospital Universitário Getúlio Vargas Universidade Federal do Amazonas Casa de Saúde Campinas Hospital e Maternidade Galileo Hospital das Clínicas Faculdade de Medicina de Botucatu Universidade Estadual “Júlio de Mesquita Filho” National Health and Medical Research Council: APP1039312

Metabolic disturbances are quite common in critically ill patients. Glycemic control appears to be an important adjuvant therapy in such patients. In addition, disorders of lipid metabolism are associated with worse prognoses. The purpose of this study was to investigate the effects that two different glycemic control protocols have on lipid profile and metabolism. We evaluated 63 patients hospitalized for severe sepsis or septic shock, over the first 72 h of intensive care. Patients were randomly allocated to receive conservative glycemic control (target range 140–180 mg/dl) or intensive glycemic control (target range 80–110 mg/dl). Serum levels of low-density lipoprotein, high-density lipoprotein, triglycerides, total cholesterol, free fatty acids, and oxidized low-density lipoprotein were determined. In both groups, serum levels of low-density lipoprotein, high-density lipoprotein, and total cholesterol were below normal, whereas those of free fatty acids, triglycerides, and oxidized low-density lipoprotein were above normal. At 4 h after admission, free fatty acid levels were higher in the conservative group than in the intensive group, progressively decreasing in both groups until hour 48 and continuing to decrease until hour 72 only in the intensive group. Oxidized low-density lipoprotein levels were elevated in both groups throughout the study period. Free fatty acids respond to intensive glycemic control and, because of their high toxicity, can be a therapeutic target in patients with sepsis.

Metabolic acid–base disorders, especially metabolic acidosis, are common in critically ill patients who require renal replacement therapy. Continuous veno-venous hemodiafiltration (CVVHDF) achieves profound changes in acid–base status, but metabolic acidosis can remain unchanged or even deteriorate in some patients. The objective of this study is to understand the changes of acid–base variables in critically ill patients with septic associated acute kidney injury (SA-AKI) during CVVHDF and to determine how they relate to clinical outcome. Observational study of 200 subjects with SA-AKI treated with CVVHDF for at least 72 hours. Arterial blood gases and electrolytes and other relevant acid–base variables were analyzed using quantitative acid–base chemistry. Survivors and nonsurvivors had similar demographic characteristics and acid–base variables on day one of CVVHDF. However, during the next 48 hours, the resolution of acidosis was significantly different between the 2 groups, with an area under the ROC curve for standard base excess (SBE) and mortality of 0.62 (0.54–0.70), this was better than APACHE II score prediction power. Quantitative physicochemical analysis revealed that the majority of the change in SBE was due to changes in Cl and Na concentrations. Survivors of SA-AKI treated with CVVHDF recover hyperchloremic metabolic acidosis more rapidly than nonsurvivors. Further study is needed to determine if survival can be improved by measures to correct acidosis more rapidly. Abbreviations: AG = anion gap, APACHE = Acute Physiology and Chronic Health Evaluation, CVVHDF = continuous venovenous hemodiafiltration, ROC = receiver operator characteristics, SA-AKI = sepsis associated acute kidney injury, SIDa, SIDe = strong ion difference, SIG = strong ion gap.

The use of echocardiography in the intensive care unit for patients in shock allows the accurate measurement of several hemodynamic variables in a noninvasive way. By using echocardiography as a hemodynamic monitoring tool, the clinician can evaluate several aspects of shock states, such as cardiac output and fluid responsiveness, myocardial contractility, intracavitary pressures, and biventricular interactions. However, to date, there have been few guidelines suggesting an objective hemodynamic-based examination in the intensive care unit, and most intensivists are usually not familiar with this tool. In this review, we describe some of the most important hemodynamic parameters that can be obtained at the bedside with transthoracic echocardiography.

Objective: To evaluate the cost-effectiveness, from the funding body's point of view, of real-time ultrasound-guided central venous catheter insertion compared to the traditional method, which is based on the external anatomical landmark technique. Methods: A theoretical simulation based on international literature data was applied to the Brazilian context, i.e., the Unified Health System (Sistema Unico de Saude - SUS). A decision tree was constructed that showed the two central venous catheter insertion techniques: real-time ultrasonography versus external anatomical landmarks. The probabilities of failure and complications were extracted from a search on the PubMed and Embase databases, and values associated with the procedure and with complications were taken from market research and the Department of Information Technology of the Unified Health System (DATASUS). Each central venous catheter insertion alternative had a cost that could be calculated by following each of the possible paths on the decision tree. The incremental cost-effectiveness ratio was calculated by dividing the mean incremental cost of real-time ultrasound compared to the external anatomical landmark technique by the mean incremental benefit, in terms of avoided complications. Results: When considering the incorporation of real-time ultrasound and the concomitant lower cost due to the reduced number of complications, the decision tree revealed a final mean cost for the external anatomical landmark technique of 262.27 Brazilian reals (R$) and for real-time ultrasound of R$187.94. The final incremental cost of the real-time ultrasound-guided technique was -R$74.33 per central venous catheter. The incremental cost-effectiveness ratio was -R$2,494.34 due to the pneumothorax avoided. Conclusion: Real-time ultrasound-guided central venous catheter insertion was associated with decreased failure and complication rates and hypothetically reduced costs from the view of the funding body, which in this case was the SUS.

JUSTIFICATIVA E OBJETIVOS: A contusão miocárdica está freqüentemente associada ao trauma torácico fechado. Seu correto diagnóstico é um constante desafio aos profissionais que trabalham em unidades de emergência, devido aos seus sintomas inespecíficos e a ausência de exames subsidiários com precisão para fazer o diagnóstico. Dentre os diversos métodos diagnósticos estudados, tem-se destacado nos últimos anos o papel dos indicadores de necrose miocárdica troponina I e troponina T. Por serem proteínas constituintes do aparelho de regulação contrátil celular, são liberadas na corrente sanguínea somente após a perda da integridade de membrana dos miócitos e, portanto, são altamente específicas para detectar lesão miocárdica. CONTEUDO: Foi realizada uma revisão de estudos clínicos nas bases eletrônicas de dados MedLine e LILACS, no período de janeiro de 1980 a novembro de 2006, sobre a importância da dosagem seriada de troponina como instrumento diagnóstico e preditor de evolução clínica desfavorável nos pacientes com contusão miocárdica. CONCLUSÕES: Embora exista maior especificidade das troponinas I e T quando comparadas aos indicadores tradicionais, CKMB massa e CPK total, esses dois indicadores apresentarem sensibilidade e valor preditivo positivo baixos para diagnosticar contusão miocárdica. Pacientes que apresentam alterações eletrocardiográficas, elevação de troponinas, ou ambas, devem permanecer em observação em unidade de terapia intensiva (UTI), por no mínimo 24 horas, período em que se desenvolve a maioria das complicações decorrentes da contusão miocárdica. BACKGROUND AND OBJECTIVES: Myocardial contusion is often associated with blunt chest trauma. Its diagnosis is challenging to the professionals who work in emergency department due to nonspecific symptoms and the lack of auxiliary exams with enough accuracy to diagnose. Among the available diagnostic tools, the biomarkers of myocardial injury troponin I and troponin T have stood out. Troponins are proteins of the citocellular apparatus, released into the bloodstream only after the disruption of myocytes cellular membrane. Therefore they are highly specific to detect myocardial injuries. CONTENTS: We performed a clinical review using the electronic databases MedLine and LILACS from January 1980 to November 2006 about the importance of a serial measurement of troponin I and T as a diagnostic tool as well as predictor of unfavorable clinical outcome in patients with myocardial contusion after a blunt chest trauma. CONCLUSIONS: Although troponins I and T are more specific than usual biomarkers CKMB and CK, these two first biomarkers show a low sensitivity and positive predictive value to diagnosis myocardial contusion. Patients with ECG abnormalities, troponins elevations or both should remain in an intensive care unit (ICU) for at least 24 hours, period in which they cam develop most of the complications related to myocardial contusion.

esta restrito a alguns poucos grupos, e o uso da ECMO, na maioria dos servicos, e apenas eventual.A incorporacao de novas modalidades terapeuticas, especialmente quando sao invasivas ou incorrem em risco significativo ao paciente, torna-se um dilema na decisao da equipe assistencial. Mesmo quando existem dados sobre sua eficacia em estudos controlados, e natural que o medico e a equipe multidisciplinar hesi-tem em tomar uma atitude ainda pouco difundida em seu meio.

We present a case of central nervous system (CNS) infection by a member of the Penicillium genera in a HIV-negative man in Brazil. The patient was admitted complaining of loss of visual fields and speech disturbances. CT scan revealed multiple brain abscesses. Stereothacic biopsies revealed fungal infection and amphotericin B treatment begun with initial improvement. The patient died few days later as a consequence of massive gastrointestinal bleeding due to ruptured esophageal varices. The necropsy and final microbiologic analyses disclosed infection by Penicillium sp. There are thousands of fungal species of the Penicillium genera. Systemic penicilliosis is caused by the P. marneffei and was formerly a rare disease, but now is one of the most common opportunistic infection of AIDS patients in Southeast Asia. The clinical presentation usually involves the respiratory system and the skin, besides general symptoms like fever and weight loss. Penicillium spp infection caused by species other than P. marneffei normally cause only superficial or allergic disease but rare cases of invasive disease do occur. We report the fourth case of Penicillium spp CNS infection. Apresentamos um caso de infecção do sistema nervoso central (SNC) por Penicillium spp em paciente do sexo masculino, HIV-negativo no Brasil. O paciente apresentou-se ao Serviço de Urgência do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo queixando-se de alteração visual e dificuldade na fala. Exames de neuroimagem mostraram lesões múltiplas, compatíveis com abscessos. A biópsia esterotáxica revelou infecção fúngica, iniciando-se o tratamento com anfotericina B com sucesso inicial. O paciente morreu poucos dias depois, vítima de uma hemorragia digestiva maciça devido a varizes de esôfago. A necropsia e a análise microbiológica final da biópsia cerebral revelaram infecção por Penicillium spp. Exixtem centenas de espécies de fungos do gênero Penicillium. A peniciliose sistêmica é causada pelo P. marneffei e costumava ser uma doença rara, mas atualmente é uma das infecções oportunistas mais comuns em associação com AIDS no Sudeste Asiático. Infecção pelo Penicillium spp de espécie diferente do P. marneffei normalmente causa apenas doenças superficiais ou alérgicas mas doenças invasivas também ocorrem raramente. Nós relatamos o quarto caso de infecção do SNC por Penicillium spp.

To evaluate whether a multifaceted, centrally coordinated quality improvement program in a network of hospitals can increase compliance with the resuscitation bundle and improve clinical and economic outcomes in an emerging country setting. This was a pre- and post-intervention study in ten private hospitals (1,650 beds) in Brazil (from May 2010 to January 2012), enrolling 2,120 patients with severe sepsis or septic shock. The program used a multifaceted approach: screening strategies, multidisciplinary educational sessions, case management, and continuous performance assessment. The network administration and an external consultant provided performance feedback and benchmarking within the network. The primary outcome was compliance with the resuscitation bundle. The secondary outcomes were hospital mortality, hospital and ICU length of stay, quality-adjusted life year (QALY) gain, and cost-effectiveness. The proportion of patients who received all the required items for the resuscitation bundle improved from 13 % [95 % confidence interval (CI) 8–18 %] at baseline to 62 % (95 % CI 54–69 %) in the last trimester (p

Objective: The current definition of severe sepsis and septic shock includes a heterogeneous profile of patients. Although the prognostic value of hyperlactatemia is well established, hyperlactatemia is observed in patients with and without shock. The present study aimed to compare the prognosis of septic patients by stratifying them according to two factors: hyperlactatemia and persistent hypotension. Methods: The present study is a secondary analysis of an observational study conducted in ten hospitals in Brazil (Rede Amil - SP). Septic patients with initial lactate measurements in the first 6 hours of diagnosis were included and divided into 4 groups according to hyperlactatemia (lactate >4mmol/L) and persistent hypotension: (1) severe sepsis (without both criteria); (2) cryptic shock (hyperlactatemia without persistent hypotension); (3) vasoplegic shock (persistent hypotension without hyperlactatemia); and (4) dysoxic shock (both criteria). ABSTRACT Results: In total, 1,948 patients were analyzed, and the sepsis group represented 52% of the patients, followed by 28% with vasoplegic shock, 12% with dysoxic shock and 8% with cryptic shock. Survival at 28 days differed among the groups (p

Acidose metabólica é um fenômeno comum e clinicamente significativo em pacientes com sepse grave ou choque séptico. Entretanto, sua composição não é bem estabelecida. Neste estudo, descrevemos a composição da acidose metabólica em pacientes com sepse grave ou choque séptico desde sua internação em unidade de terapia intensiva (UTI) até os quinto dia de internação em unidade de terapia intensiva (UTI). Na admissão à UTI, a acidose metabólica foi um fenômeno muito freqüente. Ela era composta principalmente pelo componente derivado dos íons inorgânicos (dado principalmente pela diferença sódio cloro), seguido em magnitude pelo componentes decorrentes de ânions não mensuráveis e lactato e atenuada por hipoalbuminemia. A magnitude da acidose metabólica e hipercloremia foram maiores entre os pacientes não-sobreviventes (considerando a mortalidade hospitalar). Em análise multivariada o grau de acidose por íons inorgânicos, além do escore de gravidade APACHE II e nível inicial de creatinina sérica, esteve associada a mortalidade hospitalar. Ao longo do período de estudo, os pacientes sobreviventes apresentaram melhora da acidose metabólica por diminuição dos níveis de ânions não-mensuráveis e lactato. Os não sobreviventes mantiveram a mesma magnitude de acidose metabólica e apresentaram queda do pH por aumento da PCO2 Metabolic acidosis is frequently found in patients with severe sepsis and septic shock. Several studies have shown that the amount of metabolic acidosis measured by the standard base excess (SBE) at hospital admission and its evolution throughout the first days of intensive care unit (ICU) stay are correlated with clinical outcome. However, the precise composition of the metabolic acidosis in patients with severe sepsis and septic shock is not well known. In this study, we have described the composition of metabolic acidosis in patients with severe sepsis or septic shock at ICU admission and throughout the first five days of ICU stay, by applying the quantitative physicochemical methodology. Metabolic acidosis was extremely frequent at admission to the ICU. Its main component was attributable to the inorganic ion difference disturbance (mainly determined by the Na Cl difference), followed in magnitude by unmeasured anions and lactate´s components. Hypoalbuminemia represented the most frequent and important alkalinizing component. The degree of metabolic acidosis and hyperchloremia was more pronounced in the non-survivors group (according to hospital mortality). In a multivariate analysis the degree of metabolic acidosis due to disturbances in innorganic ion difference was associated to hospital mortality. Acidosis in survivors was corrected during the study period due to a decrease in lactate and SIG levels, whereas non-survivors did not correct their metabolic acidosis and suffered a decrease in the pH due to an increase in PCO2 levels

BACKGROUND AND OBJECTIVES: The amount of metabolic acidosis measured through the standard base excess (SBE) has been shown to be an outcome marker and its improvement has been associated with better survival. We studied the mechanism of standard base excess variation in the first three days of intensive care unit (ICU) stay through the evaluation of independent variables of physico-chemical approach. METHODS: Data were retrieved from our prospective collected data base from patients with diagnosis of septic shock, daily up to the third day after the ICU admission. Single correlations between SBE and independent variables were performed as well as a mathematical multilinear model was built to disclose the SBE variation determinants. RESULTS: We have shown that in septic shock patients the standard base excess variation during the first three days of ICU stay is weakly correlated to strong ion gap (SIG), lactate, creatinin and PaCO2 when individually analyzed. Analyzing concomitantly those independent variables, we built a mathematical model with a stepwise multilinear regression composed by apparent strong ion difference (SIDa), SIG, PaCO2, albumin and diuresis that resulted in a R² coefficient of 0.866 to determine SBE variation. CONCLUSIONS: Variations of metabolic acidosis measured through the standard base excess in septic shock patients when analyzed until the third day after intensive care unit admission, is resultant of interaction of several independent determinants as PaCO2, diuresis, SIG, SIDa and albumin. JUSTIFICATIVA E OBJETIVOS: A acidose metabólica diagnosticada pela mensuração do standard base excess (SBE) é indicadora de maior mortalidade e sua melhora temporal é associada à maior sobrevida em pacientes críticos. O objetivo deste estudo foi esclarecer o mecanismo de variação do SBE, em pacientes com choque séptico, durante os três primeiros dias de internação na unidade de terapia intensiva (UTI), através da avaliação físico-química do equilíbrio ácido básico. MÉTODO: Os dados foram coletados de pacientes com choque séptico a partir de um banco de dados, prospectivamente, diariamente até o terceiro dia de internação na UTI. Correlações entre o SBE e outras variáveis físico-químicas independentes foram realizadas, assim como um modelo matemático multilinear foi desenhado para revelar os determinantes independentes da variação do SBE. RESULTADOS: A variação do SBE em pacientes sépticos nos primeiros três dias de internação na UTI foi fracamente correlacionado ao strong ion gap (SIG), lactato, albumina, creatinina e PaCO2 quando analisados individualmente. Quando analisados de forma concomitante, as variáveis albumina, strong ion difference (SIDa), SIG, PaCO2 e diurese foram independentemente associados à variação do SBE com um coeficiente de determinação de 0,866. CONCLUSÔES: A variação do SBE durante os três primeiros dias de internação na UTI foi resultante da interação de alguns fatores independentes como PaCO2, diurese, SIG, SIDa e albumina.

Many factors are involved in the progression of secondary hyperparathyroidism, including acidosis. Stewart's approach has made it possible to identify real determinants of acid-base status, making chloride a real etiological factor of acid-base disturbances. In addition, it has allowed the quantification of the components of these disturbances, especially the unmeasured anions. We performed a cross-sectional study to quantify each component of acidosis in hemodialysis patients and correlate them with renal bone disease biochemical markers.Sixty maintenance hemodialysis patients and 14 controls were enrolled in this study. Each acid-base determinant was quantified and correlated in multivariate regression with intact serum parathormone and bone-specific alkaline phosphatase, adjusting to other variables.Hemodialysis patients were more acidotic than controls, mainly due to the retention of unmeasured anions, hyperchloremia and hyperphosphatemia. In multivariate regression analysis, the only acid-base determinants independently correlated with bone markers were chloride, calcium and phosphorus (beta=0.537, beta=-0.256 and beta=-0.242, respectively). Although unmeasured anions were a major component of acidosis, they had no correlation with these markers.Although unmeasured anions are considered the main component of acidosis in hemodialysis patients, serum chloride was the only acid-base determinant correlated with bone markers.

PURPOSE: Pathophysiological studies in humans regarding sepsis are difficult to perform due to ethical and methodological concerns. In this context, animal models of sepsis can be useful to better understand this condition and to test therapeutic strategies. The purpose of this study was to characterize a feasible and clinically relevant model of sepsis in pigs that could be useful for testing different therapeutic interventions. METHODS: 5 White Large pigs were anesthetized, arterial and pulmonary catheters were introduced, and sepsis was induced by fecal peritonitis. Several biochemical indicators of organ dysfunction and infectious parameters were measured. The pigs were monitored until death, when fragments of organs were removed for pathology. Three animals without peritonitis served as controls and were sacrificed 24 hours after surgery without developing significant changes in organ function. RESULTS: Septic pigs survived 17 hours on average (range, 16-18 h), and Escherichia coli was recovered from blood cultures. They developed a significant decrease in left ventricular work and a nonsignificant reduction in mixed venous oxygen saturation. Respiratory dysfunction was characterized by a decrease in the PaO2/FiO2 ratio and respiratory compliance. Pathology of the lungs revealed areas of pulmonary collapse, hemorrhage, pulmonary congestion, and discrete neutrophil infiltrate. CONCLUSIONS: Fecal peritonitis in pigs is a clinically relevant model of sepsis associated with acute lung injury without direct pulmonary insult. This model may prove to be useful for studying pathogenic aspects of secondary lung injury as well as for validating ventilatory or pharmacologic interventions.PROPOSTA: Estudos sobre sepse envolvendo sua fisiopatologia são difíceis de serem realizados devido a razões éticas e metodológicas. Neste sentido, modelos animais criam oportunidades de estudos para entender a fisiopatologia e testar estratégias terapêuticas. O objetivo deste estudo foi criar um modelo relevante de choque séptico em porcos para testar e entender diferentes intervenções. MÉTODOS: 5 porcos da raça "White Large" foram anestesiados e monitorizados com uma linha arterial e um cateter de artéria pulmonar. Uma peritonite fecal foi induzida através de laparotomia. Marcadores de disfunções orgânicas e infecciosos foram mensurados. Todos porcos evoluíram até a morte e amostras de órgãos foram coletadas para exame anátomo patológico. Três animais controles com o mesmo preparo cirúrgico e sem peritonite foram sacrificados após 24 horas de evolução, sem desenvolver mudanças significativas nas funções orgânicas. RESULTADOS: Os animais séptico sobreviveram na média 17 horas (16 - 18h), e Escherichia coli foi cultivada nas amostras de sangue. Os animais sépticos evoluíram com redução do trabalho de ventrículo esquerdo. A disfunção respiratória foi caracterizada por uma redução na relação PaO2/FiO2 e na complacência respiratória. A anatomia patológica dos pulmões revelou colapso pulmonar, hemorragia, congestão e infiltrado neutrofílico. CONCLUSÕES: A peritonite fecal em porcos é um modelo de choque séptico clinicamente relevante e associada a uma lesão pulmonar sem um insulto direto. Este é um modelo que pode ser utilizado para estudar aspectos fisiopatológicos das lesões pulmonares secundárias, assim como para estudar intervenções ventilatórias ou farmacológicas.

Myocardial contusion is often associated with blunt chest trauma. Its diagnosis is challenging to the professionals who work in emergency department due to nonspecific symptoms and the lack of auxiliary exams with enough accuracy to diagnose. Among the available diagnostic tools, the biomarkers of myocardial injury troponin I and troponin T have stood out. Troponins are proteins of the citocellular apparatus, released into the bloodstream only after the disruption of myocytes cellular membrane. Therefore they are highly specific to detect myocardial injuries.We performed a clinical review using the electronic databases MedLine and LILACS from January 1980 to November 2006 about the importance of a serial measurement of troponin I and T as a diagnostic tool as well as predictor of unfavorable clinical outcome in patients with myocardial contusion after a blunt chest trauma.Although troponins I and T are more specific than usual biomarkers CKMB and CK, these two first biomarkers show a low sensitivity and positive predictive value to diagnosis myocardial contusion. Patients with ECG abnormalities, troponins elevations or both should remain in an intensive care unit (ICU) for at least 24 hours, period in which they cam develop most of the complications related to myocardial contusion.

BACKGROUND AND OBJECTIVES: To correlate standard base excess (SBE) with serum lactate level and demonstrate the independent prognostic significance of each one. METHODS: In a retrospective study, we retrieved data from 333 patients of our prospectively collected database of 7-bed medical intensive care unit of a 1800-bed university hospital. RESULTS: The results have shown a poor correlation between SBE and lactate, r = - 0.358, p < 0.001, and an independent prognostic significance of each one when analyzed concomitantly, odds ratio (95% Confidence interval) = 0.996 (0.992 - 0.999) to standard base excess and 1.000 (1.000 - 1.002) to lactate at entrance; and odds ratio (95% Confidence interval ) = 0.990 (0.985 - 0.994) to standard base excess and 1.003 (1.001 - 1.005) to lactate after 24 hours. The accuracy of standard base excess was close to lactate to determine in-intensive care unit death. CONCLUSIONS: The lactic component of the metabolic acidosis is not the major determinant of standard base excess. Serum lactate and SBE are independent outcome predictors in critically ill patients. JUSTIFICATIVA E OBJETIVOS: Correlacionar o excesso de bases padronizado com o nível sérico de lactato e demonstrar a independência entre eles em relação a significância prognóstica. MÉTODO: Em uma avaliação retrospectiva,nós recuperamos os dados de 333 pacientes de nosso banco de dados prospectivamente coletado em uma unidade de terapia intensiva clínica de 7 leitos de um hospital universitário terciário de 1800 leitos. RESULTADOS: Nos resultados, achamos uma pobre correlação entre o excesso de bases padronizado e lactato, r = - 0,358, p < 0,001, e uma independente significância prognóstica de cada um quando analisados concomitantemente, odds ratio (Intervalo de confiança 95%) = 0,996 (0,992 - 0,999) para o excesso de bases padronizado e 1,000 (1,000 - 1,002) para o lactato na admissão; e odds ratio (Intervalo de confiança 95%) = 0,990 (0,985 - 0,994) para o excesso de bases padronizado e 1,003 (1,001 - 1,005) para o lactato após 24 horas da admissão. A acurácia do excesso de bases padronizado foi semelhante à do lactato em prever morte na internação na unidade de terapia intensiva. CONCLUSÕES: O componente láctico do excesso de bases padronizado não é o maior determinante deste. O nível de lactato sérico e o excesso de bases padronizado são preditore independentes de mortalidade em pacientes críticos.

PURPOSE: To compare the evolution of standard base excess and serum lactate level between surviving and non surviving patients with severe sepsis and septic shock resuscitated with early goal-directed therapy. METHODS: This is a retrospective study in an intensive care unit of a university tertiary hospital where 65 consecutive severe sepsis and septic shock patients were observed without any intervention in the treatment by the authors of this report. RESULTS: In our study, the mortality of severe sepsis and septic shock patients was 38%. The central venous oxygen saturation of both groups was above 70% after the resuscitative period, excluding the second day of the non survivors group (69.8%). After the second day, the central venous oxygen saturation was significantly higher in the survivors group (P < .001). Standard base excess was initially low in both groups, but from the second day on, the correction of standard base excess was significantly more successful and linear in the survivor group (P < .001). Lactate levels were similar during the evolution of both groups. CONCLUSIONS: Although evolutive standard base excess and serum lactate level are still outcome markers in severe sepsis and septic shock patients resuscitated with early goal-directed therapy, other studies must be performed to clarify if hemodynamic interventions based on standard base excess and serum lactate level could be reliable to improve clinical outcomes in severe sepsis and septic shock patients. OBJETIVO: Comparar a evolução do "standard base excess" e o nível de lactato sérico entre pacientes sobreviventes e não sobreviventes com sepse grave ou choque séptico reanimados com o "early goal directed therapy". MÉTODOS: Estudo retrospectivo em uma unidade de terapia intensiva de um hospital escola onde sessenta e cinco pacientes com sepse grave e choque séptico foram observados sem intervenções. RESULTADOS: Em nosso estudo, a mortalidade na sepse grave e choque séptico foi de 38%. A saturação venosa central de oxigênio nos dois grupos foi maior que 70% depois da reanimação, exceto no segundo dia no grupo dos pacientes não sobreviventes (69,8%). Depois do segundo dia, a saturação venosa central foi significantemente maior no grupo dos sobreviventes (p

The performance of hand disinfection by staff in a 31-bed department of intensive care was monitored. During 32 hours of observation, 727 opportunities for hand disinfection were observed, and the compliance rate was 27.9%. The level of work experience was not correlated with hand disinfection compliance rates.

The use of echocardiogram performed by intensivists, as a modality of hemodynamic monitoring, is becoming increasingly frequent in ICUs worldwide. Several training programs and curriculums have been proposed to avoid the misuse and misinterpretation of this tool. However, until now, there have been few reports validating this type of training. The aim of the present study is to compare these measurements in order to evaluate the efficacy of our institutional training program.

Applying a quantitative methodology, we described the acid – base status of severe septic patients in the first 5 days after admission to the ICU.

Intensive glycemic control has been widely discussed in critical care patients. It remains unclear whether intensive insulin therapy also improves the prognosis of patients in a medical ICU, who often are more severely ill than are patients in a surgical ICU and have a higher risk of death. Recently, medical patients have been investigated, as a special group. We decided to study possible differences in lipid profile in septic shock patients during the first 72 hours and correlate it with different organ dysfunctions.

The widening of the QTc is a mortality predictor in acute coronary syndromes and cerebral vascular accident.

Pathophysiological human studies in sepsis are difficult to perform due to ethical and methodological concerns. In this context, animal models of severe sepsis can be useful to better understand this condition and to test new therapeutic interventions.

A 41-year-old man, with chronic liver disease caused by long-term HBV infection (Child–Pugh C), presented to the Emergency Department complaining of bilateral loss of visual fields and dysphasia for 3 days. CT scan and MRI revealed multiple brain abscesses. Stereothacic biopsies revealed fungal infection and amphotericin B treatment was begun with initial improvement. The patient died a few days later as a consequence of massive gastrointestinal bleeding due to ruptured esophageal varices. The final microbiologic analyses disclosed infection by Penicillium spp.

Base excess (BE) and lactate (LAC) have been used to monitor ICU patients. Each results from different pathophysiological derangements in perfusion, inflammation and renal function. The individual significance of BE or LAC to predict the outcome of the critically ill patients is still uncertain and was the focus of this retrospective study.

Introduction Oversedation frequently occurs in ICUs. We aimed to evaluate a minimal sedation policy, using sedative consumption as a monitoring tool, in a network of ICUs targeting decrement of oversedation and mechanical ventilation (MV) duration. Methods A prospective quality improvement project was conducted in ten ICUs within a network of nonteaching hospitals in Brazil during a 2-year period (2010 to 2012). In the first 12 months (the preintervention period), we conducted an audit to identify sedation practice and barriers to current guideline-based practice regarding sedation. In the postintervention period, we implemented a multifaceted program, including multidisciplinary daily rounds, and monthly audits focusing on sedative consumption, feedback and benchmarking purposes. To analyze the effect of the campaign, we fit an interrupted time series (ITS). To account for variability among the network ICUs, we fit a hierarchical model. Results During the study period, 21% of patients received MV (4,851/22,963). In the postintervention period, the length of MV was lower (3.91 ± 6.2 days versus 3.15 ± 4.6 days; mean difference, −0.76 (95% CI, −1.10; −0.43), P

Introdução: Triagem para admissão em unidades de terapia intensiva (UTIs) é realizada rotineiramente e é comumente baseada somente no julgamento clínico, o que pode mascarar vieses e preconceitos. Neste estudo, foram avaliadas a reprodutibilidade e validade de um algoritmo de apoio a decisões de triagem em UTI. Também foi avaliado o efeito da implementação de um instrumento de auxílio à tomada de decisão para a priorização de vagas de UTI nas decisões de admissão em UTI. Foi avaliada, ainda, a acurácia da predição prognóstica dos médicos na população de pacientes em deterioração clínica aguda. Métodos: Para o primeiro objetivo do estudo, um algoritmo computadorizado para auxiliar as decisões de priorização de vagas em UTI foi desenvolvido para classificar pacientes nas categorias do sistema de priorização da \"Society of Critical Care Medicine (SCCM)\". Nove médicos experientes (experts) avaliaram quarenta vinhetas clínicas baseadas em pacientes reais. A referência foi definida como as prioridades classificadas por dois investigadores com acesso ao prontuário completo dos pacientes. As concordâncias entre as prioridades do algoritmo com as prioridades da referência e com as prioridades dos experts foram avaliadas. As correlações entre a prioridade do algoritmo e o julgamento clínico de adequação da admissão na UTI em contexto com e sem escassez de vagas também foram avaliadas. A validade foi ainda avaliada através da aplicação do algoritmo, retrospectivamente em uma coorte de 603 pacientes com solicitação de vagas de UTI, para correlação com desfechos clínicos. Para o segundo objetivo do estudo, um estudo prospectivo, quaseexperimental foi conduzido, antes (maio/2014 a novembro/2014, fase 1) e após (novembro/2014 a maio/2015, fase 2) a implementação de um instrumento de auxílio à tomada de decisão, que foi baseado no algoritmo descrito acima. Foi avaliado o impacto da implementação do instrumento de auxílio à tomada de decisão na ocorrência de admissões potencialmente inapropriadas na UTI em uma coorte de pacientes com solicitações urgentes de vaga de UTI. O desfecho primário foi a proporção de solicitações de vaga potencialmente inapropriadas que foram admitidas na UTI em até 48 horas após a solicitação. Solicitações de vaga potencialmente inapropriadas foram definidas como pacientes prioridade 4B, conforme diretrizes da SCCM de 1999, ou prioridade 5, conforme diretrizes da SCCM de 2016. Foram realizadas análises multivariadas com teste de interação entre fase e prioridades para avaliação dos efeitos diferenciados em cada estrato de prioridade. Para o terceiro objetivo do estudo, a predição prognóstica realizada pelo médico solicitante foi registrada no momento da solicitação de vaga de UTI. Resultados: No primeiro objetivo do estudo, a concordância entre as prioridades do algoritmo e as prioridades da referência foi substancial, com uma mediana de kappa de 0,72 (IQR 0,52-0,77). As prioridades do algoritmo evidenciaram uma maior reprodutibilidade entre os pares [kappa = 0,61 (IC95% 0,57-0,65) e mediana de percentagem de concordância = 0,64 (IQR 0,59-0,70)], quando comparada à reprodutibilidade entre os pares das prioridades dos experts [kappa = 0,51 (IC95% 0,47-0,55) e mediana de percentagem de concordância = 0,49 (IQR 0,44-0,56)], p=0,001. As prioridades do algoritmo também foram associadas ao julgamento clínico de adequação da admissão na UTI (vinhetas com prioridades 1, 2, 3 e 4 seriam admitidas no último leito de UTI em 83,7%, 61,2%, 45,2% e 16,8% dos cenários, respectivamente, p < 0,001) e com desfechos clínicos reais na coorte retrospectiva, como admissão na UTI, consultas com equipe de cuidados paliativos e mortalidade hospitalar. No segundo objetivo do estudo, 2374 solicitações urgentes de vaga de UTI foram avaliadas, das quais 1184 (53,8%) pacientes foram admitidos na UTI. A implementação do instrumento de auxílio à tomada de decisão foi associada com uma redução de admissões potencialmente inapropriadas na UTI, tanto utilizando a classificação de 1999 [adjOR (IC95%) = 0,36 (0,13-0,97), p = 0,043], quanto utilizando a classificação de 2016 [adjOR (IC95%) = 0,35 (0,13-0,96, p = 0,041)]. Não houve diferença em mortalidade entre as fases 1 e 2 do estudo. No terceiro objetivo do estudo, a predição prognóstica do médico solicitante foi associada com mortalidade. Ocorreram 593 (34,4%), 215 (66,4%) e 51 (94,4%) óbitos nos grupos com prognóstico de sobrevivência sem sequelas graves, sobrevivência com sequelas graves e nãosobrevivência, respectivamente (p < 0,001). Sensibilidade foi 31%, especificidade foi 91% e a área sob a curva ROC foi de 0,61 para predição de mortalidade hospitalar. Após análise multivariada, a gravidade da doença aguda, funcionalidade prévia e admissão na UTI foram associadas com uma maior chance de erro prognóstico, enquanto que uma predição de pior prognóstico foi associada a uma menor chance de erro prognóstico. O grau de expertise do médico solicitante não teve efeito na predição prognóstica. Discussão/Conclusão: Neste estudo, um algoritmo de apoio a decisões de triagem em UTI demonstrou boa reprodutibilidade e validade. Além disso, a implementação de um instrumento de auxílio à tomada de decisões para priorização de vagas de UTI foi associada a uma redução de admissões potencialmente inapropriadas na UTI. Também foi encontrado que a predição prognóstica dos médicos solicitantes foi associada a mortalidade hospitalar, porém a acurácia foi pobre, principalmente devido a uma baixa sensibilidade para detectar risco de morte Introduction: Intensive care unit (ICU) admission triage is performed routinely and is often based solely on clinical judgment, which could mask biases. In this study, we sought to evaluate the reliability and validity of an algorithm to aid ICU triage decisions. We also aimed to evaluate the effect of implementing a decision-aid tool for ICU triage on ICU admission decisions. We also evaluated the accuracy of physician\'s prediction of hospital mortality in in acutely deteriorating patients. Methods: For the first objective of the study, a computerized algorithm to aid ICU triage decisions was developed to classify patients into the Society of Critical Care Medicine\'s prioritization system. Nine senior physicians evaluated forty clinical vignettes based on real patients. Reference standard was defined as the priorities ascribed by two investigators with full access to patient\'s records. Agreement of algorithm-based priorities with the reference standard and with intuitive priorities provided by the physicians were evaluated. Correlations between algorithm prioritization and physician\'s judgment of appropriateness of ICU admission in scarcity and non-scarcity settings were also evaluated. Validity was further assessed by retrospectively applying this algorithm to 603 patients with requests for ICU admission for association with clinical outcomes. For the second objective of the study, a prospective, quasi-experimental study was conducted, before (May 2014 to November 2014, phase 1) and after (November 2014 to May 2015, phase 2) the implementation of a decision-aid tool for ICU admission triage, which was based on the aforementioned algorithm. We assessed the impact of the implementation of the decision-aid tool in potentially inappropriate ICU admissions in a cohort of patients referred for urgent ICU admission. Primary outcome was the proportion of potentially inappropriate ICU referrals that were admitted to the ICU in 48 hours following referral. Potentially inappropriate ICU referrals were defined as priority 4B patients, as described by the 1999 Society of Critical Care Medicine (SCCM) guidelines and as priority 5 patients, as described by the 2016 SCCM guidelines. We conducted multivariate analyses and evaluated the interaction between phase and triage priorities to assess for differential effects in each priority strata. For the third objective of the study, physicians\' prognosis and other variables were recorded at the moment of ICU referral. Results: On the first objective of the study, agreement between algorithm-based priorities and the reference standard was substantial, with a median kappa of 0.72 (IQR 0.52-0.77). Algorithm-based priorities demonstrated higher interrater reliability [overall kappa of 0.61 (95%CI 0.57-0.65) and median percent agreement of 0.64 (IQR 0.59-0.70)] than physician\'s intuitive prioritization [overall kappa of 0.51 (95%CI 0.47-0.55) and median percent agreement of 0.49 (IQR 0.44-0.56)], p=0.001. Algorithm-based priorities were also associated with physicians\' judgment of appropriateness of ICU admission (priorities 1, 2, 3 and 4 vignettes would be admitted to the last ICU bed in 83.7%, 61.2%, 45.2% and 16.8% of the scenarios, respectively, p < 0.001) and with actual ICU admission, palliative care consultation and hospital mortality in the retrospective cohort. On the second objective of the study, of 2374 urgent ICU referrals, 1184 (53.8%) patients were admitted to the ICU. Implementation of the decision-aid tool was associated with a reduction of potentially inappropriate ICU admissions using the 1999 [adjOR (95% CI) = 0.36 (0.13-0.97), p = 0.043] or 2016 [adjOR (95%CI) = 0.35 (0.13-0.96, p = 0.041)] definitions. There was no difference on mortality between phases 1 and 2. On the third objective of the study, physician\'s prognosis was associated to hospital mortality. There were 593 (34.4%), 215 (66.4%) and 51 (94.4%) deaths in the groups ascribed a prognosis of survival without disabilities, survival with severe disabilities or no survival, respectively (p < 0.001). Sensitivity was 31%, specificity was 91% and the area under the ROC curve was 0.61 for prediction of mortality. After multivariable analysis, severity of illness, performance status and ICU admission were associated to an increased likelihood of incorrect classification, while worse predicted prognosis was associated to a lower chance of incorrect classification. Physician\'s level of expertise had no effect on predictive ability. Discussion/Conclusion: In this study, a ICU admission triage algorithm demonstrated good reliability and validity. Moreover, the implementation of a decision-aid tool for ICU triage was associated with a reduction of potentially inappropriate ICU admissions. It was also found that physician\'s prediction was associated to hospital mortality, but overall accuracy was poor, mainly due to low sensitivity to detect mortality risk