Factors associated to vascular pedicle width in ARDS

Introduction: In previous studies, vascular pedicle width (VPW) was the best radiographic sign of intravascular volume status in critically ill patients and may enhance implementation and acceptance of the conservative fluid strategy into routine clinical practice. Objective: Our aim was to find the relationship among VPW and parameters of mechanical ventilation (MV) and baseline data. The hypothesis was that pressures, tidal volume and baseline data, as age, could be related to VPW in acute respiratory distress syndrome (ARDS). Methodology: It was a retrospective cohort study enrolled in the Open Lung Approach trial performed in moderate-severe acute respiratory distress syndrome recruited in São Paulo, Brazil. VPW was measured by two investigators in chestradiographs taken at diagnosis and after 24 hours of mechanical ventilation adjustments. The relationship between VPW, age, predicted body weight (PBW), positive end-expiratory pressure (PEEP), plateau pressure and tidal volume adjusted by PBW were evaluated. Results: 26 patients were included in analysis, with a total of 52 chest radiography analyzed. There was a significant change in VPW between diagnosis and after 24hours from MV adjustments (r = 0.64, p < 0.01).  Age was related to VPW before and after adjustments in MV (r= 0.57, p < 0.01). No correlation was found between MV parameters (PEEP, plateau pressure and tidal volume) with VPW. Conclusions: There was no correlation among pressures and tidal volume applied during MV and PDW, reinforcing thismethod as an easy, wide available and noninvasive way to estimate intravascular volume status in ARDS patients. Age was related to VPW, suggesting that the measure of VPW could be improved after correction based in this parameter

Prevalência de infecção em unidades de terapia intensiva de um hospital escola terciário

OBJECTIVE: To determine the prevalence rates of infections among intensive care unit patients, the predominant infecting organisms, and their resistance patterns. To identify the related factors for intensive care unit-acquired infection and mortality rates. DESIGN: A 1-day point-prevalence study. SETTING:A total of 19 intensive care units at the Hospital das Clínicas - University of São Paulo, School of Medicine (HC-FMUSP), a teaching and tertiary hospital, were eligible to participate in the study. PATIENTS: All patients over 16 years old occupying an intensive care unit bed over a 24-hour period. The 19 intensive care unit s provided 126 patient case reports. MAIN OUTCOME MEASURES: Rates of infection, antimicrobial use, microbiological isolates resistance patterns, potential related factors for intensive care unit-acquired infection, and death rates. RESULTS: A total of 126 patients were studied. Eighty-seven patients (69%) received antimicrobials on the day of study, 72 (57%) for treatment, and 15 (12%) for prophylaxis. Community-acquired infection occurred in 15 patients (20.8%), non- intensive care unit nosocomial infection in 24 (33.3%), and intensive care unit-acquired infection in 22 patients (30.6%). Eleven patients (15.3%) had no defined type. The most frequently reported infections were respiratory (58.5%). The most frequently isolated bacteria were Enterobacteriaceae (33.8%), Pseudomonas aeruginosa (26.4%), and Staphylococcus aureus (16.9%; [100% resistant to methicillin]). Multivariate regression analysis revealed 3 risk factors for intensive care unit-acquired infection: age >; 60 years (p = 0.007), use of a nasogastric tube (p = 0.017), and postoperative status (p = 0.017). At the end of 4 weeks, overall mortality was 28.8%. Patients with infection had a mortality rate of 34.7%. There was no difference between mortality rates for infected and noninfected patients (p=0.088). CONCLUSION: The rate of nosocomial infection is high in intensive care unit patients, especially for respiratory infections. The predominant bacteria were Enterobacteriaceae, Pseudomonas aeruginosa, and Staphylococcus aureus (resistant organisms). Factors such as nasogastric intubation, postoperative status, and age ³60 years were significantly associated with infection. This study documents the clinical impression that prevalence rates of intensive care unit-acquired infections are high and suggests that preventive measures are important for reducing the occurrence of infection in critically ill patients.OBJETIVO: Determinar a prevalência de infecções em pacientes de Terapia Intensiva, os agentes infecciosos mais comuns e seus padrões de resistência. Identificar os fatores relacionados a infecção adquirida na Unidade de Terapia Intensiva e as taxas de mortalidade. DESENHO: Estudo de prevalência de um dia. LOCAL:Um total de 19 Unidades de Terapia Intensiva do Hospital das Clínicas da FMUSP (HC-FMUSP) participaram do estudo. PACIENTES: Todos os pacientes com idade superior a 16 anos internados em leitos de terapia intensiva por mais de 24 horas foram incluídos. As 19 Unidades de Terapia Intensiva forneceram 126 casos. VARIÁVEIS:Taxas de infecção, uso de antibióticos, padrões de resistência microbiológica, fatores relacionados à infecção adquirida na Unidade de Terapia Intensiva, taxas de mortalidade. RESULTADOS: Um total de 126 pacientes foi estudado. Oitenta e sete (69%) receberam antibióticos no dia do estudo, sendo 72 (57%) para tratamento e 15 (12%) para profilaxia. Baseado no tipo, observou-se que a infecção adquirida na comunidade ocorreu em 15 pacientes (20,8%), infecção hospitalar fora da Unidade de Terapia Intensiva em 24 (33,3%), e infecção adquirida na Unidade de Terapia Intensiva em 22 pacientes (30,6%). Para 11 pacientes (15,3%) não se definiu o tipo de infecção. Quanto ao sítio de infecção, as respiratórias foram as infecções mais comuns (58,5%). Os agentes mais freqüentemente isolados foram: Enterobacteriaceae (33,8%), Pseudomonas aeruginosa (26,4%) e Staphylococcus aureus (16,9%; 100% meticilina-resistentes). Análise multivariada identificou 3 fatores associados à infecção adquirida na Unidade de Terapia Intensiva: idade maior ou igual a 60 anos (p=0,007), uso de sonda nasogástrica (p=0,017) e pós-operatório (p=0,017). Ao final de quatro semanas, a taxa de mortalidade foi de 28,8%. Entre os infectados, a mortalidade foi de 34,7%. Não houve diferença entre as taxas de mortalidade para pacientes infectados e não-infectados (p=0,088). CONCLUSÃO: A taxa de infecção é alta entre os pacientes de terapia intensiva, especialmente as infecções respiratórias. As bactérias predominantes foram: Enterobacteriaceae. Pseudomonas aeruginosa e Staphylococcus aureus (agentes resistentes). Fatores como uso de sonda nasogástrica, pós-operatório e idade maior ou igual a 60 anos mostraram associação com infecção. Este estudo documenta a impressão clínica de que a prevalência de infecção adquirida na Unidade de Terapia Intensiva é alta e sugere que medidas preventivas são importantes para reduzir a ocorrência de infecção em pacientes críticos

Infection as an independent risk factor for mortality in the surgical intensive care unit

OBJECTIVES: Medical and surgical intensive care unit patients represent two different populations and require different treatment approaches. The aim of this study was to investigate the parameters associated with mortality in medical and surgical intensive care units. METHODS: This was a prospective cohort study of adult patients admitted to a medical and surgical intensive care unit teaching hospital over an 11-month period. Factors associated with mortality were explored using logistic regression analysis. RESULTS: In total, 827 admissions were observed, and 525 patients >;18 years old and with a length of stay >;24 h were analyzed. Of these patients, 227 were in the medical and 298 were in the surgical intensive care unit. The surgical patients were older (

Ambulation capacity, age, immunosuppression, and mechanical ventilation are risk factors of in-hospital death in severe COVID-19: a cohort study

Importance: Despite ambulation capacity being associated with a decreased level of physical activity and survival may be influenced by the functional capacity, studies have not addressed the association between ambulation capacity and death in patients hospitalized by COVID-19. Objective: To verify the functional, clinical, and sociodemographic risk factors associated with in-hospital death in individuals with severe COVID-19. Methods: It is a cohort retrospective study performed at a large tertiary hospital. Patients 18 years of age or more, of both sexes, hospitalized due to severe COVID-19 were included. Cases with dubious medical records and/or missing essential data were excluded. Patients were classified according to their ambulation capacity before the COVID-19 infection. Information regarding sociodemographic characteristics, in-hospital death, total hospital stays, Intensive Care Unit (ICU) stays, and the necessity of Mechanical Ventilation (MV) were collected from medical records and registered in a RedCap database. Multiple logistic regression analysis was used to identify possible factors associated with the in-hospital death rate. Results: Data from 1110 participants were included in the statistical analysis. The median age of the patients was 57 (46‒66) years, 58.42% (n = 590) were male, and 61.73% (n = 602) were brown or black. The case fatality rate during hospitalization was 36.0% (n = 363). In-hospital death was associated with ambulation capacity; dependent ambulators (OR = 2.3; CI 95% = 1.2–4.4) and non-functional ambulation (OR = 1.9; CI 95% = 1.1–3.3), age [older adults (OR = 3.0; CI 95% = 1.9‒4.), ICU stays (OR = 1.4; CI 95% = 1.2‒1.4), immunosuppression (OR = 5.5 CI 95% = 2.3‒13.5) and mechanical ventilation (OR = 27.5; CI 95% = 12.0–62.9). Conclusion and relevance: Decreased ambulation capacity, age, length of ICU stay, immunosuppression, and mechanical ventilation was associated with a high risk of in-hospital death due to COVID-19

Long-term outcomes in moderate/severe acute respiratory distress syndrome survivors included in a randomized clinical trial (ARDSnet protocol vs. Open Lung Approach)

Apesar da utilização da ventilação mecânica protetora como estratégia para o tratamento da síndrome do desconforto respiratório agudo, ao menos um quarto dos pacientes com essa síndrome ainda apresentam redução na função pulmonar após 6 meses de seguimento. Não se sabe se esta redução está relacionada com a gravidade da síndrome ou associada com a forma de ventilar o paciente. Nosso objetivo neste trabalho foi avaliar a associação entre alterações funcionais e estruturais do pulmão com parâmetros de gravidade clínica e de ventilação mecânica. Foi realizada uma análise secundária dos dados obtidos em estudo randomizado e controlado que incluiu pacientes com síndrome do desconforto respiratório agudo moderada/grave, internados em seis unidades de terapia intensiva em um hospital terciário da cidade de São Paulo. Foram analisados dados de pacientes que tinham ao menos um teste de função pulmonar no seguimento. O teste funcional incluiu a medida da capacidade vital forçada, volumes pulmonares e a capacidade de difusão do monóxido de carbono após 1, 2 e 6 meses de seguimento. Foram considerados variáveis independentes o volume corrente, a pressão de distensão e a pressão positiva ao final da expiração (todos medidos após 24 horas da randomização) e um sistema de classificação de prognóstico (APACHE II), a relação PaO2/FIO2 e a complacência respiratória estática (todos medidos antes da randomização). Também foi realizada tomografia de alta resolução do tórax juntamente com os testes de função pulmonar, e posterior análise quantitativa das imagens. Na avaliação de 6 meses também foi realizado teste de caminhada de 6 minutos e um questionário de qualidade de vida (SF-36). Um total de 21 pacientes realizaram o teste de função pulmonar após 1 mês e 15 pacientes realizaram após 2 e 6 meses de seguimento. A capacidade vital forçada foi relacionada inversamente com a pressão de distensão na avaliação de 1, 2 e 6 meses (p < 0,01). A capacidade de difusão do monóxido de carbono relacionou-se inversamente com a pressão de distensão e com o APACHE II (ambos p < 0,01) na avaliação de 1 e 2 meses. Após 6 meses de seguimento, houve correlação inversa entre a pressão de distensão e a capacidade vital forçada independente do volume corrente, da pressão de platô e da complacência estática respiratória após ajustes (R2 = 0,51, p = 0,02). A pressão de distensão também se relacionou com o volume pulmonar total, a densidade pulmonar media e a porcentagem de volume pulmonar não aerado ou pobremente aerado medidos através da análise quantitativa da tomografia computadorizada de tórax realizada na avaliação de 6 meses. Também foi observada relação entre a qualidade de vida após 6 meses de seguimento e a pressão de distensão considerando o domínio estado geral de saúde. Nós concluímos que mesmo em pacientes ventilados com reduzido volume corrente e pressão de platô limitada, maiores valores de pressão de distensão relacionaram-se com menores valores de função pulmonar no seguimento de longo prazoEven after lung-protective ventilation had become the standard of care for acute respiratory distress syndrome, about 25% of moderate/severe acute respiratory distress syndrome patients present reduction in lung function at 6 months of follow-up. It is not known whether this reduction is related to the severity of acute respiratory distress syndrome or associated with mechanical ventilation strategy. Our aim was to evaluate the association between the functional impairment and mechanical ventilation. We performed a secondary analysis of data from a randomized controlled trial in acute respiratory distress syndrome that included patients with moderate/severe acute respiratory distress syndrome in six intensive care units at an academic tertiary hospital. Were analyzed data from patients who had at least one pulmonary function test at the follow-up. A pulmonary function test that included forced vital capacity, lung volumes and carbon monoxide diffusion capacity was performed at one, two and six months of follow-up. We considered as independent risk factors tidal volume, driving pressure and positive end expiratory pressure (all measured 24 hours after randomization), and a severity of disease classification system (APACHE II), the PaO2/FIO2 ratio and static respiratory compliance (all measured before randomization). We performed also a high-resolution computed tomography of the lungs in the same time of the pulmonary function test if it was possible with a quantitative analysis. At 6 months after acute respiratory distress syndrome, a six minute walk test and a quality of life questionnaire (short form-36 questionnaire) were performed. A total of 21 patients performed the test after one month and 15 patients performed after 2 and 6 months follow-up. At one, two and six months, forced vital capacity was related to driving pressure (p < 0.01). Carbon monoxide diffusion capacity was related to driving pressure (p < 0.01) and to APACHE II (p < 0.01) at one and two months. At six months of follow-up driving pressure was associated with lower FVC independently of tidal volume, plateau pressure and baseline static respiratory compliance after adjustments (r2 = 0.51, p = 0.02). Driving pressure was related with total lung volume, mean lung density and percentage of non or poorly aerated compartments in total lung volume measured by quantitative analysis of computed tomography at 6 months. Driving pressure was also related to quality of life at 6 months of follow-up. Despite using a lung-protective ventilation strategy, after 6 months we still observed lung function impairment and driving pressure was the only ventilation parameter correlated with pulmonary function changes. We concluded that even in patients ventilated with low tidal volume, greater driving pressure was associated with worse long-term pulmonary functio

Pneumonia aspirativa associada a alterações da deglutição: relato de caso Aspirative pneumonia associated to swallowing dysfunction: case report

JUSTIFICATIVA E OBJETIVOS: Os pacientes criticamente enfermos representam uma população com múltiplos fatores de risco para aspiração. Associa-se a essa complicação a redução do estado de consciência, ventilação mecânica e comorbidades como o acidente vascular encefálico (AVE), freqüentemente presente nos pacientes internados em unidade de terapia intensiva (UTI). A identificação das alterações da deglutição pode auxiliar na detecção de pacientes com alto risco de aspiração, prevenindo complicações pulmonares como a pneumonia aspirativa. O objetivo deste relato foi mostrar um caso de broncopneumonia aspirativa recorrente grave, após acidente vascular encefálico agudo e intubação traqueal, alertando para a necessidade do diagnóstico e do tratamento adequados nestes pacientes. RELATO DO CASO: Paciente do sexo masculino, 57 anos internado no hospital por AVE, evoluiu após 10 dias de internação com quadr o de pneumonia aspirativa, necessitando de intubação traqueal e transferência para a UTI. Permaneceu intubado por quatro dias, e logo após a extubação evoluiu com progressivo infiltrado pulmonar relacionado a novos episódios de aspiração. A avaliação fonoaudiológica na UTI classificou o paciente como portador de disfagia orofaríngea grave, com risco para penetração e aspiração laringotraqueal. Recebeu alta da UTI após 13 dias, porém na enfermaria evoluiu com novo quadro aspirativo após oito dias, necessitando de re-internação na UTI e prolongada internação hospitalar. CONCLUSÕES: Os pacientes internados em UTI devem ter seu risco para alterações de deglutição e de aspiração identificado para que medidas preventivas possam ser instituídas, evitando-se a morbidade e a mortalidade associada à aspiração.<br>BACKGROUND AND OBJECTIVES: Critically ill patients represent a population with multiple risk factors for aspiration. Features such as decreased level of consciousness, mechanical ventilation, and comorbities as stroke, correlate with this increased threat in intensive care unit (ICU) patients. Recognition of deglutition dysfunction may identify patients at high risk of aspiration, and thereby help to avoid pulmonary complications such as recurrent pneumonia. The goal of our report is show a severe case of recurrent aspirative pneumonia after acute stroke and intubation, alerting to appropriate diagnosis and treatment of this condition. CASE REPORT: A male patient, 57 year old, was admitted to the hospital because of acute stroke. Ten days later, the patient began to have fever and severe shortness of breath. He was admitted to the ICU necessitating of intratracheal intubation. Four days after intubation he was extubated, however, he had a new aspirative pneumonia in ICU, newly treated. An evaluation of swallowing demonstrated a severe deglutition dysfunction with a high risk of aspiration. The patient was transferred, but aspirative pneumonia was diagnosed eight days after his ICU discharge and he was readmitted, stayed for a long time in ICU and presenting severe morbidity. CONCLUSIONS: ICU patients who are at risk for swallowing dysfunction and aspiration should be identified to prevent their associated morbidity and mortality