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Objective Despite the controversy regarding its clinical utility, the arterial oxygen partial pressure (PaO) to the fraction of inspired oxygen (FIO) ratio has been used to define the severity of acute respiratory distress syndrome (ARDS). This systematic review and meta-analysis (SRMA) details summary estimates of the predictive performance of PaO/FIO ratio in predicting mortality in patients with ARDS. Methods To clarify the integrated diagnostic accuracy, we included studies in which the study population comprised patients with ARDS in any clinical setting, included adult patients (≥18 years old), and evaluated mortality. The MEDLINE and Cochrane Central Registry of Controlled Trials databases were searched for articles in English. We performed SRMA on the accuracy of the diagnostic prognostic tests using the Quality Assessment of Diagnostic Accuracy Studies-2 tool to evaluate the risk of bias. We obtained summary point estimates of sensitivity and specificity and calculated the area under the receiver operating characteristic (AUROC) curve of the summary receiver operating characteristic curve with 95% confidence intervals (CIs). Results Twenty-eight trials with 38,270 patients were included in the quality assessment. Most of the studies were conducted in intensive-care units. Overall, the risk of bias is high. For PaO/FIO of 100 and 200 the pooled sensitivity, specificity, and AUROC were 44.8% (95% CI, 38.1-51.7%), 70.6% (95% CI, 65.9-74.9%), 0.60 (0.58-0.64) and 83.9% (95% CI, 78.9-87.8%), 26.1% (95% CI, 20.8-32.1%), 0.64 (0.60-0.69), respectively. Conclusion The PaO/FIO ratio alone did not have impressive prediction accuracy for mortality in patients with ARDS and might not be able to be used solely as a clinical prognostic tool.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12287575 | PMC |
http://dx.doi.org/10.2169/internalmedicine.4292-24 | DOI Listing |
Objective: The aim of the study was compare the prognostic value, efficacy and safety ofpositive end-expiratory pressure (PEEP) adjustment in conformity with lower inflection point of static "pressure-volume" loop (LIP) or end-expiratory esophageal pressure (EEEP) in parenchymal respiratory failure.
Methods: We included in the study 56 patients (39 males) at age 47 +/- 17.8 years with parenchymal respiratory failure (PaO2/FiO2 < 250 mmHg, bilateral infiltrates on chest X-ray or lung CT scan, no signs of left ventricular failure), who were mecAanically ventilated for less than 48 hours.
N Engl J Med
February 2013
John Radcliffe Hospital and the University of Oxford, Oxford, United Kingdom.
Background: Patients with the acute respiratory distress syndrome (ARDS) require mechanical ventilation to maintain arterial oxygenation, but this treatment may produce secondary lung injury. High-frequency oscillatory ventilation (HFOV) may reduce this secondary damage.
Methods: In a multicenter study, we randomly assigned adults requiring mechanical ventilation for ARDS to undergo either HFOV with a Novalung R100 ventilator (Metran) or usual ventilatory care.
Acta Anaesthesiol Scand
July 2004
Department of Anaesthesia and Intensive Care, Faculty of General Medicine, University of Pécs, Hungary.
Background: The aim of our trial was to evaluate the ability of microalbuminuria as an indicator of outcome and to investigate its relationship with the postoperative respiratory dysfunction in the initial postoperative period in a high-risk patient group.
Methods: In our prospective, observational study patients were consecutively recruited following elective oesophagectomy, total gastrectomy, Whipple-resection of the pancreas and liver resection due to tumour removal. Microalbuminuria (expressed as urine albumin:creatinine ratio, M:Cr) was measured before (tp), and after surgery (t0, t6, t24, t48, t72).
Crit Care Med
March 2003
Anesthesiology Department, Istanbul Medical Faculty, Turkey.
Objective: To investigate whether the response to sustained inflation and postinflation positive end-expiratory pressure varies between acute respiratory distress syndrome with pulmonary (ARDS(exp)) and extrapulmonary origin (ARDS(exp)).
Design: Prospective clinical study.
Setting: Multidisciplinary intensive care unit in a university hospital.