- Open Access
Bedside prediction of intradialytic hemodynamic instability in critically ill patients: the SOCRATE study
Annals of Intensive Care volume 10, Article number: 47 (2020)
Despite improvements in intermittent hemodialysis management, intradialytic hemodynamic instability (IHI) remains a common issue that could account for increased mortality and delayed renal recovery. However, predictive factors of IHI remain poorly explored. The objective of this study was to evaluate the relationship between baseline macrohemodynamic, tissue hypoperfusion parameters and IHI occurrence.
Prospective observational study conducted in a 18-bed medical ICU of a tertiary teaching hospital. Cardiovascular SOFA score, index capillary refill time (CRT) and lactate level were measured just before (T0) consecutive intermittent hemodialysis sessions performed for AKI. The occurrence of IHI requiring a therapeutic intervention was recorded.
Two hundred eleven sessions, corresponding to 72 (34%) first sessions and 139 (66%) later sessions, were included. As IHI mostly occurred during first sessions (43% vs 12%, P < 0.0001), following analyses were performed on the 72 first sessions. At T0, cardiovascular SOFA score ≥1 (87% vs 51%, P = 0.0021) was more frequent before IHI sessions, as well as index CRT ≥ 3 s (55% vs 15%, P = 0.0004), and hyperlactatemia > 2 mmol/L (68% vs 29%, P = 0.0018). Moreover, the occurrence of IHI increased with the number of macrohemodynamic and tissue perfusion impaired parameters, named SOCRATE score (cardiovascular SOFA, index CRT and lactATE): 10% (95% CI [3%, 30%]), 33% (95% CI [15%, 58%]), 55% (95% CI [35%, 73%]) and 80% (95% CI [55%, 93%]) for 0, 1, 2 and 3 parameters, respectively (AUC = 0.79 [0.69–0.89], P < 0.0001). These results were confirmed by analyzing the 139 later sessions included in the study.
The SOCRATE score based on 3 easy-to-use bedside parameters correlates with the risk of IHI. By improving risk stratification of IHI, this score could help clinicians to manage intermittent hemodialysis initiation in critically ill AKI patients.
According to international consensus definitions, acute kidney injury (AKI) concerns 30 to 40% of patients admitted to intensive care unit (ICU) [1,2,3]. Renal replacement therapy (RRT) is required in 5 to 20% of patients [1, 2] and is associated with high mortality [2, 4]. Despite the improvement of intermittent hemodialysis management [5, 6], intradialytic hemodynamic instability (IHI) remains a common issue [5, 7,8,9,10,11,12] that could account for increased mortality and delayed renal recovery. Optimal timing to initiate RRT in critically ill patients is still uncertain [4, 13, 14]. Apart from life-threatening complications, an international survey reported that indications for initiating RRT varied widely among intensivists . Recent interventional trials demonstrated that delaying RRT in the absence of life-threatening complications of AKI does not impair survival and allows some patients to avoid RRT [4, 13]. Determination of risk factors for IHI could help clinicians to identify patients in whom initiation of RRT should be reconsidered in the absence of emergent criteria. However, factors associated with IHI remain poorly explored [8,9,10,11,12]. The pathophysiology of IHI is complex with a reduction of venous return and also an alteration of endothelial function that limits vascular tone adaptation to intermittent hemodialysis-induced hypovolemia [12, 16,17,18]. Pre-existing endothelial dysfunction, commonly observed in ICU patients [19,20,21,22,23], might worsen the negative hemodynamic impact of intermittent hemodialysis.
The evaluation of endothelial dysfunction at the bedside is very challenging, but its consequences on tissue hypoperfusion could be assessed more easily [24,25,26]. The prognosis value of lactate level and lactate clearance has been largely demonstrated [27, 28] and a therapeutic strategy targeting lactate normalization is recommended during sepsis and septic shock . Capillary refill time (CRT) is an easy-to-use bedside  marker of peripheral perfusion. Its relevance has been demonstrated in triage of patients in pre-hospital setting  and in the emergency department [32, 33]. CRT correlates with severity of organ failure and is strongly associated with prognosis during septic shock . Moreover, a recent multicenter study underlined the interest of a resuscitation strategy based on CRT monitoring in septic shock patients .
We hypothesized that critically ill patients with altered hemodynamics and/or impaired tissue perfusion might be more prone to develop IHI. In this prospective study, we tested whether cardiovascular SOFA score, index CRT and lactate level could be predictive of IHI requiring therapeutic intervention. The analyses led to the construction of a bedside score predictive of IHI.
We conducted a prospective observational study in the 18-bed medical ICU of a tertiary teaching hospital. During a 2-year period, all consecutive sessions of intermittent hemodialysis for AKI were recorded. Exclusion criteria were the following: dark skin because assessment of CRT was difficult, chronic intermittent hemodialysis and life-threatening complications such as hyperkalemia, and pulmonary edema in anuric patients indicating extreme emergency RRT.
Intermittent hemodialysis management
In the absence of strong evidence supporting the use of one modality of renal replacement therapy over the other, and in accordance with European  and French guidelines [5, 6], intermittent hemodialysis is the only technique used in our ICU. Intermittent hemodialysis was prescribed according to national [5, 6] and international guidelines  in order to optimize hemodynamic tolerance. Both lines of the circuit filled with 0.9% saline were connected simultaneously to the catheter. Bicarbonate buffered dialysis solution with a calcium concentration of 1.75 mmol/L was used. Dialysate flow rate was set at 500 mL/min. Blood flow rate was progressively increased from 100 mL/min to 200–250 mL/min. For patients with pre-existing hemodynamic instability, dialysate temperature was set 2 degrees under patient’s body temperature and dialysate sodium concentration was set at ≥ 145 mmol/L. Fluid removal, if required, was started 60 min after starting intermittent hemodialysis. Intermittent hemodialysis was performed on the GAMBRO® AK 200™ ULTRA S machine using NIPRO® ELISIO™-13M dialyzer.
Hemodynamic and tissue perfusion parameters collection
For each intermittent hemodialysis session, cardiovascular SOFA score, lactate level and index CRT were recorded just before starting the session (T0). Cut-off values defining tissue hypoperfusion were based on previously published studies: index CRT ≥ 3 s [26, 34, 35] and lactate level > 2 mmol/L [26, 29, 35]. Index CRT was measured in a standardized fashion as described before .
Intradialytic hemodynamic instability
As no consensual definition of IHI exists in the literature , we chose to use a pragmatic definition, as previous authors . IHI was defined as a blood pressure drop requiring therapeutic intervention, i.e., fluid resuscitation, introduction or increase in vasopressors, decrease or cessation of ultrafiltration. The occurrence of an IHI was recorded 60 minutes (just before starting ultrafiltration if needed), 120 minutes and 240 minutes after starting intermittent hemodialysis.
Continuous variables were described as medians [interquartile ranges] and categorical variables as proportions. Comparisons of proportions between groups were made using Fisher’s exact test. Comparisons of continuous variables between groups were made using Mann–Whitney test. Log-binomial models were used to estimate the relative risk of IHI according to hemodynamics and tissue perfusion variables at T0. Based on the relative risk estimates in the multivariable model, we proposed a simple scoring system by rounding log-coefficients and computed the area under the receiver operating characteristics (AUROC) value. As the same data were used to devise the score and compute its AUROC, we corrected for optimism using the bootstrap ; the corrected values were very close to the raw estimates and did not suggest overfitting. We computed the Net Reclassification Index (NRI) to quantify improvement in risk prediction with risk categories defined by above and below the average incidence.
Statistical significance was set at P < 0.05. Analyses were made using Prism and R statistical platform, version 3.0.2 (https://cran.r-project.org/).
This observational study was approved by the ethics committee of the French Intensive Care Society (Société de Réanimation de Langue Française). All patients and families were informed through a letter that anonymous data would be used for this research and gave their consent.
Characteristics of intermittent hemodialysis sessions
Two hundred eleven sessions performed in 88 patients were included in the study, after exclusion of 16 first intermittent hemodialysis sessions performed in extreme emergency. We therefore analyzed 72 first sessions (34% of all sessions) in 72 patients and 139 (66%) later sessions in 88 patients. Characteristics of the included patients are summarized in Table 1. Sessions were performed 8 [3–12] days after ICU admission. One hundred thirty (62%) sessions were performed in patients undergoing mechanical ventilation and 90 (43%) in patients receiving vasopressors. Median length of intermittent hemodialysis sessions was 4 [4-4] hours. Ultrafiltration was performed in 135 (64%) sessions, with a median volume of 2.5 [2.0–3.0] liters (Table 2).
Intradialytic hemodynamic instability mostly occurred during the first hour of the first intermittent hemodialysis session
IHI occurred in 48 (23%) sessions, mainly within the first hour of intermittent hemodialysis—35 (73%) before ultrafiltration was started if needed. Increase in vasopressors represented the main therapeutic intervention (73%), followed by fluid administration (31%) initiation of vasopressors (15%) and decrease (6%) or cessation of ultrafiltration (6%). IHI was more frequently observed during the first session than in later sessions (43% vs 12%, P < 0.0001). Compared to later sessions, first sessions were characterized by higher SOFA score at T0 (8 [4–13] vs 4 [1–9], P = 0.0001). Cardiovascular SOFA score ≥1 (67% vs 40%, P = 0.0003) and tissue perfusion alterations—index CRT ≥ 3 s (32% vs 11%, P = 0.0003) and lactate > 2 mmol/L (46% vs 12%, P < 0.0001)—were also more frequently observed at T0 for first sessions (Table 2).
Cardiovascular SOFA score, index capillary refill time and lactate level at T0 are associated with intradialytic hemodynamic instability
As IHI occurred more frequently during the first intermittent hemodialysis session, we tested whether bedside hemodynamic and tissue perfusion parameters were associated with IHI among the 72 non-emergency first sessions. AUROCs for the cardiovascular SOFA score was 0.67 (95% CI [0.56, 0.78]), it was 0.71 (95% CI [0.59, 0.84]) for index CRT and 0.76 (95% CI [0.66, 0.88]) for lactate. In a log-binomial regression, we found that the following characteristics were more frequent at T0 when intradialytic hemodynamic instability occurred: cardiovascular SOFA score ≥1 (87% vs 51%, P = 0.0021, RR = 2.5 95% CI [1.4, 4.5]), index CRT ≥ 3 s (55% vs 15%, P = 0.0004, RR = 2.6 95% CI [1.6, 4.3]) and lactate > 2 mmol/L (68% vs 29%, P = 0.0018, RR = 3.4 95% CI [1.3, 8.5]) (Table 3).
Bedside SOCRATE (cardiovascular SOFA, index Capillary Refill time and lactATE level) score correlates with the risk of intradialytic hemodynamic instability
The three relative risks reported above being of the same magnitude, we proposed the SOCRATE score, a simple scoring system derived from the linear predictor of the log-binomial model for IHI occurrence cumulating 1 point for each of cardiovascular SOFA ≥ 1, index Capillary Refill time ≥ 3 s and lactATE level > 2 mmol/L at T0. This score took values between 0 and 3 and split the first sessions in almost 4 equal groups: 28% (n = 20), 21% (n = 15), 30% (n = 22) and 21% (n = 15) for SOCRATE scores 0 to 3. IHI incidence was 10% (95% CI [3%, 30%]), 33% (95% CI [15%, 58%]), 55% (95% CI [35%, 73%]) and 80% (95% CI [55%, 93%]) for SOCRATE score of 0, 1, 2 and 3, respectively (Fig. 1), with a relative risk RR = 1.7 (95% CI [1.3, 2.2]) for each additional point in the SOCRATE score. The optimism-corrected AUROC was 0.79 [0.69–0.89] (P < 0.0001). NRIs between this model and that including only 2 out of the 3 variables suggested improved risk stratification for the SOCRATE score (Additional file 1: Table S1).
In sessions after the first, a low SOCRATE score was more common (0:55% (n = 76) and 1:36% (n = 50)) with fewer high scores (2:5% (n = 7) and 3:4% (n = 6)). The incidence of IHI still increased with the SOCRATE score: 3% (95% CI [0.7%, 9.1%]), 16% (95% CI [8%, 29%]), 29% (95% CI [8%, 64%]), 83% (95% CI [43%, 99%]) for a SOCRATE score of 0, 1, 2 and 3, respectively (P < 0.0001) (Fig. 1), with a relative risk of RR = 3.6 [2.4, 4.8] per additional score point. IHI occurrence during a previous session was also associated with an increased risk of IHI (RR = 2.6, 95% CI [1.1, 6.3]). However, adding an extra point to the score in case of previous instability did not improve the NRI with respect to the SOCRATE score alone.
In a prospective study including 211 hemodialysis sessions performed in a mixed ICU population, we found that IHI mostly occurred at the initiation of intermittent hemodialysis—during the first hour of the first session—despite the absence of fluid removal. A cardiovascular SOFA score ≥1, and two tissue hypoperfusion markers, index CRT ≥ 3 s and lactate level > 2 mmol/L, were associated with the occurrence of IHI. In addition, the risk of IHI increased with the number of abnormal parameters. A bedside score combining these three parameters, named SOCRATE score (cardiovascular SOFA score ≥ 1, index CRT ≥ 3 s and lactATE > 2 mmol/L), improved risk stratification with a good accuracy.
Intermittent hemodialysis is a key support therapy in ICU. Despite protocol-based optimization , IHI remains a frequent issue in critically ill patients. IHI incidence varies from one study to another because of discrepancies in IHI definition and in preventive protocols [5,6,7,8,9,10,11, 38, 39]. In our cohort, using a pragmatic definition of IHI, blood pressure drop requiring a medical intervention, we found an incidence of 23%. Using the same definition, Monnet et al.  found higher incidence (33%), but all patients underwent fluid removal.
IHI mainly occurred during the first hour of treatment in the absence of ultrafiltration. During intermittent hemodialysis, due to partial redistribution of blood volume from the intravascular compartment to the extracorporeal circuit, mild hypovolemia is constantly induced even in the absence of ultrafiltration. However, blood pressure does not systematically decrease because of counter-regulatory mechanisms such as tachycardia, increased cardiac contractility, plasma refilling and peripheral vasoconstriction [16, 40]. One could speculate that pre-existing alterations of macro- and microcirculation could interfere with these cardiovascular adaptation mechanisms and could promote IHI. Pre-existing microvascular endothelial dysfunction, commonly observed in ICU patients [19,20,21,22,23], might alter such adaptive vasoconstriction , promoting IHI. Hemodialysis, by itself, could also alter endothelial function. Meyer et al.  showed an increase in “vasculotoxic” cell-free hemoglobin in the plasma of chronically dialyzed patients during intermittent hemodialysis. In addition, microbubbles generated in the circuit could damage endothelium glycocalyx, triggering activation of coagulation, platelets, neutrophils and promoting oxygen reactive species release [41,42,43].
The evaluation of endothelial dysfunction at the bedside is very challenging [24, 25], but its consequences in term of tissue hypoperfusion, could be assessed more easily. We speculated that tissue hypoperfusion parameters reflect microvascular endothelial dysfunction and we investigated two easy-to-use parameters, rapidly available at the bedside, the lactate level and the index CRT. Lactate level, widely used in ICU, is inversely correlated with sublingual microvascular perfusion [44, 45] and is predictive of ICU mortality in septic shock patients . CRT measurement correlates with the pulsatility index, a surrogate ultrasound-derived parameter that reflects vascular tone of visceral organs  and with objective parameters of tissue perfusion, such as tissue oxygen saturation in patients with septic shock . CRT is associated with hyperlactatemia and severity of critical illness addressed by SOFA score  and predicts 14-day mortality in patients with septic shock independently of SOFA score .
Here, we found for the first time that increased index CRT and hyperlactatemia were associated with IHI occurrence, as well as impaired global hemodynamics defined by a cardiovascular SOFA score ≥1. More interestingly, we found a cumulative predictive effect of these parameters similar to that we observed in the setting of severe pulmonary embolism . Combining them in a score which can be quickly and easily calculated at the bedside could be helpful to improve risk stratification. IHI was rare in the absence of macro- and micro-circulatory disorders (10% in first sessions, 3% in all the sessions) and increased progressively with the number of abnormal parameters reaching 80% when all three markers were present. In the absence of emergency criteria, intermittent hemodialysis initiation might be reconsidered in patients with higher SOCRATE score, indicating a high risk of IHI. Such a hypothesis is supported by the fact that optimal timing to initiate RRT in critically ill patients is still uncertain [4, 13, 14]. Recent trials demonstrated that delaying RRT in the absence of life-threatening complications of AKI does not impair survival and allows some patients to avoid RRT [4, 13]. These results plead in favor of a reasoned strategy balancing risks and benefits for initiating RRT in ICU patients.
Moreover, if intermittent hemodialysis indication is retained, SOCRATE score might be helpful for clinicians to identify patients who may benefit from a therapeutic intervention aiming at optimizing hemodynamic status before intermittent hemodialysis initiation in order to decrease the occurrence of IHI.
Our study has several limitations. It is a monocentric study, and the results need to be confirmed in a multicenter study including a larger population. Nevertheless, we analyzed a large number of intermittent hemodialysis sessions in a mixed non-selected medical ICU population. We did not include patients with dark skin because CRT was difficult measure. It would be interesting to test the prognosis value of a score combining lactate and cardiovascular SOFA alone, or in association with other validated clinical parameters of peripheral hypoperfusion such as central-to-toe temperature difference . As we could not include sessions performed in extreme emergency because data could not be recorded before the beginning of intermittent hemodialysis, IHI incidence was probably underestimated. Finally, our study focused on patients receiving intermittent hemodialysis. Future studies also including patients receiving continuous RRT are needed to test whether SOCRATE score could help to identify patients at risk of hemodynamic instability whatever the modality of RRT.
The risk of intradialytic hemodynamic instability is maximal at intermittent hemodialysis initiation, during the first hour of the first sessions, even in the absence of ultrafiltration. Cardiovascular SOFA ≥ 1, hyperlactatemia and increased index capillary refill time are associated with an increasing risk of IHI and combining these parameters (SOCRATE score) improves risk stratification. A multicenter study would be useful to confirm these results, paving the way for a future trial evaluating whether a therapeutic strategy based on SOCRATE score before hemodialysis initiation may limit IHI.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Acute kidney injury
Capillary refill time
Intensive care unit
Intradialytic hemodynamic instability
Renal replacement therapy
Sequential Organ Failure Assessment
Clec’h C, Gonzalez F, Lautrette A, Nguile-Makao M, Garrouste-Orgeas M, Jamali S, et al. Multiple-center evaluation of mortality associated with acute kidney injury in critically ill patients: a competing risks analysis. Crit Care. 2011;15:R128.
Nisula S, Kaukonen K-M, Vaara ST, Korhonen A-M, Poukkanen M, Karlsson S, et al. Incidence, risk factors and 90-day mortality of patients with acute kidney injury in Finnish intensive care units: the FINNAKI study. Intensive Care Med. 2013;39:420–8.
Hoste EAJ, Bagshaw SM, Bellomo R, Cely CM, Colman R, Cruz DN, et al. Epidemiology of acute kidney injury in critically ill patients: the multinational AKI-EPI study. Intensive Care Med. 2015;41:1411–23.
Gaudry S, Hajage D, Schortgen F, Martin-Lefevre L, Pons B, Boulet E, et al. Initiation strategies for renal-replacement therapy in the intensive care unit. N Engl J Med. 2016;375:122–33.
Schortgen F, Soubrier N, Delclaux C, Thuong M, Girou E, Brun-Buisson C, et al. Hemodynamic tolerance of intermittent hemodialysis in critically ill patients: usefulness of practice guidelines. Am J Respir Crit Care Med. 2000;162:197–202.
Vinsonneau C, Allain-Launay E, Blayau C, Darmon M, Ducheyron D, Gaillot T, et al. Renal replacement therapy in adult and pediatric intensive care: recommendations by an expert panel from the French Intensive Care Society (SRLF) with the French Society of Anesthesia Intensive Care (SFAR) French Group for Pediatric Intensive Care Emergencies (GFRUP) the French Dialysis Society (SFD). Ann Intensive Care. 2015;5:58.
du Cheyron D, Terzi N, Seguin A, Valette X, Prevost F, Ramakers M, et al. Use of online blood volume and blood temperature monitoring during haemodialysis in critically ill patients with acute kidney injury: a single-centre randomized controlled trial. Nephrol Dial Transplant. 2013;28:430–7.
Chimot L, Gacouin A, Nardi N, Gros A, Mascle S, Marqué S, et al. Can we predict poor hemodynamic tolerance of intermittent hemodialysis with echocardiography in intensive care patients? J Ultrasound Med. 2014;33:2145–50.
Monnet X, Cipriani F, Camous L, Sentenac P, Dres M, Krastinova E, et al. The passive leg raising test to guide fluid removal in critically ill patients. Ann Intensive Care. 2016;6:46.
Bitker L, Bayle F, Yonis H, Gobert F, Leray V, Taponnier R, et al. Prevalence and risk factors of hypotension associated with preload-dependence during intermittent hemodialysis in critically ill patients. Crit Care. 2016;20:44.
Douvris A, Malhi G, Hiremath S, McIntyre L, Silver SA, Bagshaw SM, et al. Interventions to prevent hemodynamic instability during renal replacement therapy in critically ill patients: a systematic review. Crit Care. 2018;22:41.
Douvris A, Zeid K, Hiremath S, Bagshaw SM, Wald R, Beaubien-Souligny W, et al. Mechanisms for hemodynamic instability related to renal replacement therapy: a narrative review. Intensive Care Med. 2019;45:1333–46.
Barbar SD, Clere-Jehl R, Bourredjem A, Hernu R, Montini F, Bruyère R, et al. Timing of renal-replacement therapy in patients with acute kidney injury and sepsis. N Engl J Med. 2018;379:1431–42.
Zarbock A, Kellum JA, Schmidt C, Van Aken H, Wempe C, Pavenstädt H, et al. Effect of early vs delayed initiation of renal replacement therapy on mortality in critically ill patients with acute kidney injury: the ELAIN randomized clinical trial. JAMA. 2016;315:2190–9.
Legrand M, Darmon M, Joannidis M, Payen D. Management of renal replacement therapy in ICU patients: an international survey. Intensive Care Med. 2013;39:101–8.
Daugirdas JT. Pathophysiology of dialysis hypotension: an update. Am J Kidney Dis. 2001;38:S11–7.
Meyer C, Heiss C, Drexhage C, Kehmeier ES, Balzer J, Mühlfeld A, et al. Hemodialysis-induced release of hemoglobin limits nitric oxide bioavailability and impairs vascular function. J Am Coll Cardiol. 2010;55:454–9.
Bemelmans RHH, Boerma EC, Barendregt J, Ince C, Rommes JH, Spronk PE. Changes in the volume status of haemodialysis patients are reflected in sublingual microvascular perfusion. Nephrol Dial Transplant. 2009;24:3487–92.
Duffy MJ, Mullan BA, Craig TR, Shyamsundar M, MacSweeney RE, Thompson G, et al. Impaired endothelium-dependent vasodilatation is a novel predictor of mortality in intensive care. Crit Care Med. 2011;39:629–35.
Ait-Oufella H, Maury E, Lehoux S, Guidet B, Offenstadt G. The endothelium: physiological functions and role in microcirculatory failure during severe sepsis. Intensive Care Med. 2010;36:1286–98.
Vallet B. Endothelial cell dysfunction and abnormal tissue perfusion. Crit Care Med. 2002;30:S229–34.
Kirschenbaum LA, Astiz ME, Rackow EC, Saha DC, Lin R. Microvascular response in patients with cardiogenic shock. Crit Care Med. 2000;28:1290–4.
Trzeciak S, McCoy JV, Phillip Dellinger R, Arnold RC, Rizzuto M, Abate NL, et al. Early increases in microcirculatory perfusion during protocol-directed resuscitation are associated with reduced multi-organ failure at 24 h in patients with sepsis. Intensive Care Med. 2008;34:2210–7.
De Backer D, Ospina-Tascon G, Salgado D, Favory R, Creteur J, Vincent J-L. Monitoring the microcirculation in the critically ill patient: current methods and future approaches. Intensive Care Med. 2010;36:1813–25.
Ekbal NJ, Dyson A, Black C, Singer M. Monitoring tissue perfusion, oxygenation, and metabolism in critically ill patients. Chest. 2013;143:1799–808.
Hariri G, Joffre J, Leblanc G, Bonsey M, Lavillegrand J-R, Urbina T, et al. Narrative review: clinical assessment of peripheral tissue perfusion in septic shock. Ann Intensive Care. 2019;9(1):37.
Vincent J-L, Silva QEA, Couto L, Taccone FS. The value of blood lactate kinetics in critically ill patients: a systematic review. Crit Care. 2016;20:257.
Bakker J, Coffernils M, Leon M, Gris P, Vincent JL. Blood lactate levels are superior to oxygen-derived variables in predicting outcome in human septic shock. Chest. 1991;99:956–62.
Rhodes A, Evans LE, Alhazzani W, Levy MM, Antonelli M, Ferrer R, et al. Surviving sepsis campaign: international guidelines for management of sepsis and septic shock: 2016. Crit Care Med. 2017;45:486–552.
Alsma J, van Saase JLCM, Nanayakkara PWB, Schouten WEMI, Baten A, Bauer MP, et al. The Power of flash mob research: conducting a nationwide observational clinical study on capillary refill time in a single day. Chest. 2017;151:1106–13.
Jouffroy R, Saade A, Tourtier JP, Gueye P, Bloch-Laine E, Ecollan P, et al. Skin mottling score and capillary refill time to assess mortality of septic shock since pre-hospital setting. Am J Emerg Med. 2019;37:664–71.
Sansone CM, Prendin F, Giordano G, Casati P, Destrebecq A, Terzoni S. Relationship between capillary refill time at triage and abnormal clinical condition: a Prospective Study. Open Nurs J. 2017;11:84–90.
Coslovsky M, Takala J, Exadaktylos AK, Martinolli L, Merz TM. A clinical prediction model to identify patients at high risk of death in the emergency department. Intensive Care Med. 2015;41:1029–36.
Ait-Oufella H, Bige N, Boelle PY, Pichereau C, Alves M, Bertinchamp R, et al. Capillary refill time exploration during septic shock. Intensive Care Med. 40(7):958–64.
Hernández G, Ospina-Tascón GA, Damiani LP, Estenssoro E, Dubin A, Hurtado J, et al. Effect of a resuscitation strategy targeting peripheral perfusion status vs serum lactate levels on 28-day mortality among patients with septic shock: the ANDROMEDA-SHOCK randomized clinical trial. JAMA. 2019;321:654–64.
Jörres A, John S, Lewington A, ter Wee PM, Vanholder R, Van Biesen W, et al. A European Renal Best Practice (ERBP) position statement on the Kidney Disease Improving Global Outcomes (KDIGO) Clinical Practice Guidelines on Acute Kidney Injury: part 2: renal replacement therapy. Nephrol Dial Transplant. 2013;28:2940–5.
Miller ME, Hui SL, Tierney WM. Validation techniques for logistic regression models. Stat Med. 1991;10:1213–26.
VA/NIH Acute Renal Failure Trial Network, Palevsky PM, Zhang JH, O’Connor TZ, Chertow GM, Crowley ST, et al. Intensity of renal support in critically ill patients with acute kidney injury. N Engl J Med. 2008;359:7–20.
Rabindranath K, Adams J, Macleod AM, Muirhead N. Intermittent versus continuous renal replacement therapy for acute renal failure in adults. Cochrane Database Syst Rev. 2007;3:3773.
Gutierrez G, Reines HD, Wulf-Gutierrez ME. Clinical review: hemorrhagic shock. Crit Care. 2004;8:373–81.
Sato M, Morita H, Ema H, Yamaguchi S, Amano I. Effect of different dialyzer membranes on cutaneous microcirculation during hemodialysis. Clin Nephrol. 2006;66:426–32.
Cianciolo G, Stefoni S, Donati G, De Pascalis A, Iannelli S, Manna C, et al. Intra- and post-dialytic platelet activation and PDGF-AB release: cellulose diacetate vs polysulfone membranes. Nephrol Dial Transplant. 2001;16:1222–9.
Barak M, Nakhoul F, Katz Y. Pathophysiology and clinical implications of microbubbles during hemodialysis. Semin Dial. 2008;21:232–8.
Ospina-Tascon G, Neves AP, Occhipinti G, Donadello K, Büchele G, Simion D, et al. Effects of fluids on microvascular perfusion in patients with severe sepsis. Intensive Care Med. 2010;36:949–55.
De Backer D, Creteur J, Dubois M-J, Sakr Y, Koch M, Verdant C, et al. The effects of dobutamine on microcirculatory alterations in patients with septic shock are independent of its systemic effects. Crit Care Med. 2006;34:403–8.
Brunauer A, Koköfer A, Bataar O, Gradwohl-Matis I, Dankl D, Bakker J, et al. Changes in peripheral perfusion relate to visceral organ perfusion in early septic shock: a pilot study. J Crit Care. 2016;35:105–9.
Lima A, van Genderen ME, van Bommel J, Klijn E, Jansem T, Bakker J. Nitroglycerin reverts clinical manifestations of poor peripheral perfusion in patients with circulatory shock. Crit Care. 2014;18:R126.
Lima A, Jansen TC, van Bommel J, Ince C, Bakker J. The prognostic value of the subjective assessment of peripheral perfusion in critically ill patients. Crit Care Med. 2009;37:934–8.
Urbina T, Bigé N, Nguyen Y, Boelle P-Y, Dubée V, Joffre J, et al. Tissue perfusion alterations correlate with mortality in patients admitted to the intensive care unit for acute pulmonary embolism: an observational study. Medicine. 2018;97:e11993.
Bourcier S, Pichereau C, Boelle P-Y, Nemlaghi S, Dubée V, Lejour G, et al. Toe-to-room temperature gradient correlates with tissue perfusion and predicts outcome in selected critically ill patients with severe infections. Ann Intensive Care. 2016;6:63.
This research received no specific funding.
Ethics approval and consent to participate
This observational study was approved by the ethics committee of the French Intensive Care Society (Société de Réanimation de Langue Française). All patients and families were informed through a letter that anonymous data would be used for this research and gave their consent.
Consent for publication
The authors declare that they have no conflict of interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Bigé, N., Lavillegrand, J., Dang, J. et al. Bedside prediction of intradialytic hemodynamic instability in critically ill patients: the SOCRATE study. Ann. Intensive Care 10, 47 (2020). https://doi.org/10.1186/s13613-020-00663-x
- Acute kidney injury
- Hemodynamic instability
- Tissue perfusion
- Capillary refill time
- SOFA score