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Abstract
Background
Several studies have validated capillary refill time (CRT) as a marker of tissue hypoperfusion, and recent guidelines recommend CRT monitoring during septic shock resuscitation. Therefore, it is relevant to further explore its kinetics of response to short-term hemodynamic interventions with fluids or vasopressors. A couple of previous studies explored the impact of a fluid bolus on CRT, but little is known about the impact of norepinephrine on CRT when aiming at a higher mean arterial pressure (MAP) target in septic shock. We designed this observational study to further evaluate the effect of a fluid challenge (FC) and a vasopressor test (VPT) on CRT in septic shock patients with abnormal CRT after initial resuscitation. Our purpose was to determine the effects of a FC in fluid-responsive patients, and of a VPT aimed at a higher MAP target in chronically hypertensive fluid-unresponsive patients on the direction and magnitude of CRT response.
Methods
Thirty-four septic shock patients were included. Fluid responsiveness was assessed at baseline, and a FC (500 ml/30 mins) was administered in 9 fluid-responsive patients. A VPT was performed in 25 patients by increasing norepinephrine dose to reach a MAP to 80–85 mmHg for 30 min. Patients shared a multimodal perfusion and hemodynamic monitoring protocol with assessments at at least two time-points (baseline, and at the end of interventions).
Results
CRT decreased significantly with both tests (from 5 [3.5–7.6] to 4 [2.4–5.1] sec, p = 0.008 after the FC; and from 4.0 [3.3–5.6] to 3 [2.6 -5] sec, p = 0.03 after the VPT. A CRT-response was observed in 7/9 patients after the FC, and in 14/25 pts after the VPT, but CRT deteriorated in 4 patients on this latter group, all of them receiving a concomitant low-dose vasopressin.
Conclusions
Our findings support that fluid boluses may improve CRT or produce neutral effects in fluid-responsive septic shock patients with persistent hypoperfusion. Conversely, raising NE doses to target a higher MAP in previously hypertensive patients elicits a more heterogeneous response, improving CRT in the majority, but deteriorating skin perfusion in some patients, a fact that deserves further research.
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Details

1 Pontificia Universidad Católica de Chile, Departamento de Medicina Intensiva, Facultad de Medicina, Santiago, Chile (GRID:grid.7870.8) (ISNI:0000 0001 2157 0406)
2 Pontificia Universidad Católica de Chile, Departamento de Hematología Oncología, Facultad de Medicina, Santiago, Chile (GRID:grid.7870.8) (ISNI:0000 0001 2157 0406)
3 Hôpital Saint-Antoine, Assistance Publique-Hôpitaux de Paris, Sorbonne Université, Medical Intensive Care Unit, Paris, France (GRID:grid.412370.3) (ISNI:0000 0004 1937 1100)
4 INSERM U970, Université de Paris, Cardiovascular Research Center, Paris, France (GRID:grid.462416.3) (ISNI:0000 0004 0495 1460); Fundación Valle del Lili, Department of Intensive Care Medicine, Cali, Colombia (GRID:grid.477264.4); Universidad Icesi, Translational Research Laboratory in Critical Care Medicine (TransLab-CCM), Cali, Colombia (GRID:grid.440787.8) (ISNI:0000 0000 9702 069X)
5 Pontificia Universidad Católica de Chile, Departamento de Medicina Intensiva, Facultad de Medicina, Santiago, Chile (GRID:grid.7870.8) (ISNI:0000 0001 2157 0406); Erasmus MC University Medical Center, Department of Intensive Care Adults, Rotterdam, Netherlands (GRID:grid.5645.2) (ISNI:0000 0004 0459 992X)