2017
DOI: 10.1155/2017/7894631
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Effect of High-Flow Nasal Cannula versus Conventional Oxygen Therapy for Patients with Thoracoscopic Lobectomy after Extubation

Abstract: Objective. To investigate whether high-flow nasal cannula (HFNC) oxygen therapy is superior to conventional oxygen therapy for reducing hypoxemia and postoperative pulmonary complications (PPC) in patients with thoracoscopic lobectomy after extubation. Methods. Patients with intermediate to high risk for PPC were enrolled in this study. Subjects were randomly assigned to HFNC group (HFNCG) or conventional oxygen group (COG) following extubation. Arterial blood samples were collected after extubation at 1, 2, 6… Show more

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Cited by 65 publications
(93 citation statements)
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References 24 publications
(26 reference statements)
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“…Four of the studies included only thoracic surgical patients,37424345 with two studying patients undergoing thoracoabdominal vascular repairs via a midline laparotomy,3841 and two RCTs including elective upper abdominal surgical patients 3940. Both trials of high flow nasal cannulas included patients with an intermediate to high predictive risk of PPCs (assessed as an ARISCAT score ≥26846), with one study recruiting a mixed population of emergency and elective abdominal and thoracic procedures,28 and one study recruiting only thoracic thoracoscopic lobectomy patients 45…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Four of the studies included only thoracic surgical patients,37424345 with two studying patients undergoing thoracoabdominal vascular repairs via a midline laparotomy,3841 and two RCTs including elective upper abdominal surgical patients 3940. Both trials of high flow nasal cannulas included patients with an intermediate to high predictive risk of PPCs (assessed as an ARISCAT score ≥26846), with one study recruiting a mixed population of emergency and elective abdominal and thoracic procedures,28 and one study recruiting only thoracic thoracoscopic lobectomy patients 45…”
Section: Resultsmentioning
confidence: 99%
“…Duration of ventilatory support ranged from two 120 minute cycles of helmet continuous positive airway pressure on the first postoperative day only to bi-level positive airway pressure provided preoperatively for seven days and then daily during the postoperative inpatient stay 43. Five of the nine trials involved provision of the intervention for less than 24 hours,2836373841 and one trial for three days,40 whereas the remainder continued to provide ventilator support while patients were in hospital 39424345. Full details of included trials and individual meta-analysis of prophylactic non-invasive ventilation are provided in appendix 2, section 6.…”
Section: Resultsmentioning
confidence: 99%
“…The RCTs included were all assessed to be at low risk of bias with respect to randomization and allocation concealment except for 3 trials [ 25 , 31 , 32 ] for which selection bias was deemed unclear. The same 3 trials also were assessed to be at unclear risk of bias with regard to blinded outcome assessment, completeness of outcomes data, selective outcomes reporting, and other potential sources of bias [ 25 , 31 , 32 ]. All trials were deemed to be at high risk of performance bias as blinding of patients, physicians, and research personnel to treatment allocation was not feasible (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…A total of 3 studies reported the rate of escalation of respiratory support. [ 32 , 34 , 35 ] The escalation of respiratory support in COT group is regarded as use of HFNC, NIV, or reintubation. The escalation of respiratory support in HFNC group is regarded as use of NIV or reintubation.…”
Section: Resultsmentioning
confidence: 99%