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1.
Anaesthesiol Intensive Ther ; 49(2): 100-105, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28643321

RESUMO

BACKGROUND: Central venous pressure often fails to identify the true value of cardiac preload. Our purpose is to investigate whether Global End-Diastolic Volume (GEDV) values can control hemodynamic parameters for the measurement of fluid volume, cardiac preload and blood loss during liver transection. METHODS: This was a prospective clinical study that included patients undergoing liver resection. All patients were monitored by means of PiCCO technology and 222 hemodynamic measurements were performed in 74 patients. Fluid restriction was used. Transpulmonary thermodilutions were performed at different times of surgery, namely: 1. at the beginning of surgery; 2. before hepatectomy and after selective vascular exclusion (Time 1); 3. approximately half way through the liver transection (Time 2); and 4. after liver resection (Time 3). RESULTS: One hundred and twenty-nine of the 222 GEDV values were decreased (prevalence of hypovolemia of 58.1%). However, twenty two of the 222 CVP values were decreased (prevalence of 10.8%). Sensitivity of CVP with regard to volume depletion (GEDV > 650 mL m-2) on the times (1, 2 and 3) were 16.28 (4.08-28.48, 95% CI), 18.18 (5.65-30.75, 95% CI) and 21.43 (7.83-35.03, 95% CI), respectively. There was no correlation between CVP and GEDV. CONCLUSIONS: GEDV values may be more appropriate for monitoring cardiac preload during liver transection.


Assuntos
Perda Sanguínea Cirúrgica/prevenção & controle , Pressão Venosa Central/fisiologia , Hepatectomia/métodos , Termodiluição/métodos , Adulto , Idoso , Volume Sanguíneo , Feminino , Humanos , Hipovolemia/epidemiologia , Neoplasias Hepáticas/cirurgia , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Sensibilidade e Especificidade , Fatores de Tempo
2.
Respir Care ; 57(5): 743-52, 2012 May.
Artigo em Inglês | MEDLINE | ID: mdl-22152725

RESUMO

BACKGROUND: The physiological and clinical effects of noninvasive ventilation (NIV) on acute postoperative respiratory failure are relatively unknown. The aim of this study was to determine the prediction factors for failure in the use of NIV with a helmet in this context. METHODS: This was a prospective observational study. The use of NIV was assessed for a period of 2 years in a postoperative ICU. Demographic data were collected, as well as acute respiratory failure (ARF) and arterial gas readings. Hemodynamic changes were assessed using pulse contour cardiac output technology, and the clinical development of subjects was recorded. All subjects who developed ARF were treated using NIV as their primary care, depending on whether the technique was successful or the subject required intubation. The risk factors that determined failure in the application of NIV were subsequently determined. RESULTS: Of the 99 subjects presenting with postoperative ARF treated with NIV using a helmet, 74 did not require intubation (74.7%). Following a multivariate analysis using logistic regression, we determined that there are 3 independent risk factors for the failure of NIV. Three factors were associated with respiratory failure: ARDS, pneumonia, and lack of improvement with NIV in 1 hour (increase in the P(aO(2))/F(IO(2))). CONCLUSIONS: NIV using a helmet could provide an effective alternative to conventional ventilation in selected patients with postoperative ARF.


Assuntos
Dispositivos de Proteção da Cabeça , Complicações Pós-Operatórias , Respiração Artificial/instrumentação , Insuficiência Respiratória/terapia , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Hipóxia/etiologia , Hipóxia/fisiopatologia , Hipóxia/terapia , Masculino , Pessoa de Meia-Idade , Cloreto de Polivinila , Estudos Prospectivos , Insuficiência Respiratória/etiologia , Insuficiência Respiratória/fisiopatologia , Fatores de Risco , Falha de Tratamento
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