The effect of low versus high tidal volume ventilation on inflammatory markers in healthy individuals undergoing posterior spine fusion in the prone position: a randomized controlled trial
Abstract Study Objective To evaluate the effect of ventilation strategy on markers of inflammation in patients undergoing spine surgery in the prone position. Design Randomized controlled trial. Setting University-affiliated teaching hospital. Patients 26 ASA physical status 1 and 2 patients schedul...
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Veröffentlicht in: | Journal of clinical anesthesia 2012-06, Vol.24 (4), p.263-269 |
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Sprache: | eng |
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Zusammenfassung: | Abstract Study Objective To evaluate the effect of ventilation strategy on markers of inflammation in patients undergoing spine surgery in the prone position. Design Randomized controlled trial. Setting University-affiliated teaching hospital. Patients 26 ASA physical status 1 and 2 patients scheduled for elective primary lumbar decompression and fusion in the prone position. Interventions Patients were randomized to receive mechanical ventilation with either a tidal volume (VT ) of 12 mL/kg ideal body weight with zero positive end-expiratory pressure (PEEP) or VT of 6 mL/kg ideal body weight with PEEP of 8 cm H2 O. Measurements Plasma levels of interleukin (IL)-6 and IL-8 were determined at the beginning of ventilation and at 6 and 12 hours later. Urinary levels of desmosine were determined at the beginning of ventilation and on postoperative days 1 and 3. Main Results A significant increase in IL-6, IL-8, and urine desmosine levels was noted over time compared with baseline ( P < 0.01). However, no significant difference in the levels of markers was seen between the groups at any time point when controlling for demographics, ASA physical status, body mass index, duration of ventilation, or estimated blood loss. Conclusions Although markers of inflammation are increased after posterior spine fusion surgery, ventilation strategy has minimal impact on markers of systemic inflammation. |
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ISSN: | 0952-8180 1873-4529 |
DOI: | 10.1016/j.jclinane.2011.08.003 |