Why the study?
Assessing fluid responsiveness is problematic in critically ill patients with spontaneous breathing activity during pressure support ventilation because spontaneous breathing physiologically affects heart-lung interplay.
Does the SIGH35 test predict fluid responsiveness better than the end-expiratory occlusion test in critically ill patients undergoing pressure support ventilation?
Does the SIGH35 test predict fluid responsiveness better than the end-expiratory occlusion test in critically ill patients undergoing pressure support ventilation?
In critically ill patients undergoing pressure support ventilation, the SIGH35 test reliably predicts fluid responsiveness and performs better than the end-expiratory occlusion test.
SIGH35 may aid fluid assessment in pressure support ventilation; leaves open need for randomized validation before practice change.
Assessing fluid responsiveness is problematic for critically ill patients with spontaneous breathing activity, such as during Pressure Support Ventilation (PSV), since spontaneous breathing activity physiologically affects heart–lung interplay. We compared the reliability of two hemodynamic tests in predicting fluid responsiveness in this clinical setting: SIGH 35 , based on a ventilator-generated sigh applied at 35 cmH 2 O for 4 s and the end-expiratory occlusion test (EEOT). Prospective study conducted in a general intensive care unit (ICU) and enrolling patients in PSV showing different inspiratory effort [assessed by airway occlusion pressure (P0.1)] and requiring volume expansion (VE). Hemodynamic variables were recorded by means of the MOSTCARE ® system, patient received a VE using 4 ml/kg of crystalloids over 10 min and were considered responders if a cardiac output (CO) ≥ 10% was observed. The reliability of SIGH 35 and EEOT in discriminating fluid responsiveness was assessed using receiver operating characteristic (ROC) curve approach and the area (AUC) under ROC curves was compared. For the EEOT, we considered the percent changes of CO between baseline the end of the test, while for the SIGH 35 , the percent changes of pulse pressure (PP) between baseline and the lowest value recorded after SIGH 35 application. Sixty ICU patients were enrolled, and 56 patients analysed. The AUC of PP changes after SIGH 35 was 0.93 (0.84–0.99) [sensitivity of 93.1% (78.0–98.7%); specificity of 91.6 (73.0–98.9%)]; best threshold − 25% PP from baseline (grey zone − 15%/35%)]; and greater than the AUC of CO changes after EEOT [0.67 (0.52–0.81); sensitivity of 72.4% (54.3–85.3%) specificity of 70.3% (73.0–98.9%)]; best threshold 4% of CO increase from baseline (grey zone − 1%/10%)]. In the subgroup having a P0.1 < 1.5 cmH 2 O, the AUC of SIGH 35 [0.98 (0.94–0.99)] and of EEOT [0.89 (0.72–0.99] were comparable ( p = 0.26). In a selected ICU population undergoing PSV, SGH 35 reliably predicted fluid responsiveness and performed better than the EEOT, which is, however, still reliable in the subgroup of ICU patients having a small extent of inspiratory efforts.
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Messina et al. (2025) studied this question.
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