Microvascular reactivity is altered early in patients with acute respiratory distress syndrome
- Diego Orbegozo Cortés†1,
- Lokmane Rahmania†1,
- Marian Irazabal1,
- Carlos Santacruz1,
- Vito Fontana1,
- Daniel De Backer1,
- Jacques Creteur1 and
- Jean-Louis Vincent1Email author
© Orbegozo Cortés et al. 2016
Received: 30 December 2015
Accepted: 5 May 2016
Published: 17 May 2016
Acute respiratory distress syndrome (ARDS) is associated with vascular endothelial dysfunction. The resultant microvascular reactivity can be assessed non-invasively using near-infrared spectroscopy (NIRS) and a vascular occlusion test (VOT) and changes have been correlated with severity of organ dysfunction and mortality in other critically ill populations. We used NIRS to study the presence of microcirculatory alterations in patients with ARDS.
We studied 27 healthy volunteers and 32 ARDS patients admitted to our intensive care department. NIRS measurements were performed within 24 h after diagnosis (Berlin definition). VOTs were performed by inflating an arm-cuff to a pressure greater than the systolic pressure for 3 min, followed by rapid deflation. The descending (Desc) and ascending (Asc) thenar muscle oxygen saturation (StO2) slopes were calculated. We compared data from volunteers with those from ARDS patients, from ARDS survivors and non-survivors, and from ARDS survivors who required <7 days ventilatory support (good evolution) with those who required >7 days support or died (poor evolution).
ARDS patients had lower StO2 values [75(67–80) vs 79(76–81) %, p = 0.04] and Asc slopes [185(115–233) vs 258(216–306) %/min, p < 0.01] than healthy volunteers, but Desc slopes were similar. The Asc slope was lower in the patients with a poor evolution than in the other patients [121(90–209) vs 222(170–293) %/min, p < 0.01], and in the non-survivors than in the survivors [95(73–120) vs 212(165–252) %/min, p < 0.01].
In ARDS patients, microvascular reactivity is altered early, and the changes are directly related to the severity of the disease. The ascending slope is the best determinant of outcome.
Acute respiratory distress syndrome (ARDS), defined using the Berlin criteria , is diagnosed in 25 to 30 % of patients admitted to the intensive care unit (ICU) who need mechanical ventilation for more than 24 h [2, 3], and is associated with high mortality rates [2–4] and long term sequelae [5, 6]. The complex pathophysiological alterations include functional and morphological alterations in the pulmonary endothelium , which may be correlated with the severity of the disease and outcomes [8–10].
Different options are available to study this endothelial dysfunction and the microcirculatory alterations that take place during ARDS. Invasive studies can be performed in animals to directly visualize the microcirculation using intra-vital video-microscopy ; levels of specific molecules (biomarkers) can be dosed in the plasma or in the bronchoalveolar fluid ; biopsies can be performed in selected cases ; or anatomo-pathological studies can be performed in the lungs of patients who die . All these approaches have advantages and limitations. In clinical studies, the most invasive techniques can often not be applied and measurement of concentrations of single biomarkers does not reflect the complex underlying pathophysiology [14, 15].
Assessment of complex microvascular responses can now be performed non-invasively at the patient’s bedside using provocative tests of the microcirculation . For example, using near-infrared spectroscopy (NIRS) it is possible to characterize the local muscle oxygen saturation (StO2) by applying the properties of oxy- and deoxy-hemoglobin to infrared light . If the arterial supply to a region is transiently obstructed by a vascular occlusion test (VOT), the rate of decrease in the StO2 (desaturation) is a reflection of local oxygen consumption , and the rate of increase (re-saturation) after the VOT is related to the post-occlusive microcirculatory vascular hyperemia . This dynamic test has been used to demonstrate that microvascular reactivity is altered in patients with sepsis , multiple organ dysfunction , trauma , acute heart failure , cardiac surgery  or after cardiac arrest resuscitation  and that the changes are not entirely explained by global hemodynamic variables. However, there are no data currently available in patients with ARDS. We, therefore, used NIRS to evaluate the presence, severity and prognostic implications of early microcirculatory alterations in patients with ARDS.
This prospective, observational, non-invasive, physiological study was conducted in the 35-bed Department of Intensive Care of Erasme University Hospital (Brussels, Belgium). Institutional Ethical Committee approval was obtained, and all volunteers and patients (or their next of kin) provided written informed consent.
Patients and volunteers
Healthy adult volunteers were recruited from the hospital staff. Adult ICU patients with ARDS were enrolled between October 2013 and June 2015 when they fulfilled the Berlin diagnostic criteria , including a PaO2/FiO2 ratio ≤ 300 on mechanical ventilation with a positive end-expiratory pressure (PEEP) of at least 5 cmH2O, and the presence of bilateral infiltrates on chest radiography, not explained by cardiogenic edema and in the presence of a risk factor for ARDS. Patients were stratified for severity using the PaO2/FiO2 ratio as recommended . Patients were only included if a researcher was available to perform the NIRS measurements. All patients were managed according to current guidelines by a team of intensivists different from the researchers who performed the NIRS measurements.
The healthy volunteers were placed in a quiet, temperature controlled room within the department of intensive care, where they rested, comfortably seated for at least 15 min before the experiment. Heart rate (HR), respiratory rate (RR) and hemoglobin saturation by pulse oximetry (SpO2) were evaluated non-invasively with a Siemens SC 9000 monitor (Siemens, Erlangen, Germany). Non-invasive measurements of mean arterial pressure (MAP) were obtained on the opposite arm to that used for the NIRS measurements.
All patients were studied within 24 h after the diagnosis of ARDS was made. At the time when the NIRS VOT was performed, we recorded all measured hemodynamic and respiratory parameters from the monitoring systems. Biochemical and laboratory data closest to the time of the VOT were also recorded as was the presence or absence of any sedation. An APACHE II score  was calculated using the worst data during the first 24 h in the ICU, and a sequential organ failure assessment (SOFA) score  from the data present at the time of the NIRS measurements. We also recorded the duration of mechanical ventilation until definitive weaning from ventilatory support and calculated the ventilator-free days (VFD) at 28-days, giving a value of zero to non-survivors.
Survivors who required less than 7 days (arbitrarily selected) of respiratory support were classified as having a good evolution and those who required more than 7 days of mechanical ventilation or who died as having a poor evolution.
Statistical analysis was performed using SPSS 22.0 (IBM, New York, NY) software. Dependent variables were assessed for normality of distribution using Skewness and Kurtosis tests and Q-Q plots. All values are presented as median values with percentiles (25–75 %), unless otherwise specified. Categorical data are presented as numbers of events and percentages. Comparisons between different cohorts were performed using a t-test, Mann–Whitney U test or Kruskal-Wallis H test as appropriate. Proportions were compared with a Chi square test or Fisher’s exact test as appropriate. A binary logistic regression was performed to identify the role of different variables to predict poor evolution, calculating the odds ratio (OR) and its respective 95 % confidence interval (CI). All variables that presented a p value < 0.1 during the univariate analysis were introduced into a multivariate analysis. We plotted the sensitivities and specificities in receiving operating characteristic (ROC) graphs and the area under the curve (AUC) was calculated for the different variables. A 2-sided p value less than 0.05 was considered as significant for all analyses.
Main characteristics of the healthy volunteers and the ARDS patients at the time of the VOT
Volunteers (n = 27)
Total (n = 32)
Good evolution (n = 16)
Poor evolution (n = 16)
Body mass index (Kg/m2)
Mean arterial pressure (mmHg)
Heart rate (bpm)
Respiratory rate (bpm)
Hemoglobin O2 saturation (%)
Primary ARDS n(%)
Chronic lung disease n(%)
Inspired O2 fraction (%)
Positive end-expiratory pressure (cmH20)
Renal replacement therapy n(%)
Total bilirubin (mg/dL)
Leukocytes (cells x103/μL)
APACHE II score
ICU length of stay (days)
Ventilator free days at 28 days (days)
NIRS variables in healthy volunteers and ARDS patients
VOLUNTEERS (n = 27)
Total (n = 32)
Good evolution (n = 16)
Poor evolution (n = 16)
Survivors (n = 24)
Non-survivors (n = 8)
StO2 base (%)
THI base (au)
StO2 max (%)
Desc slope (%/min)
Asc slope (%/min)
The main finding of our study is that ARDS patients have altered peripheral microvascular reactivity as assessed using NIRS. This alteration is directly related to the severity of the disease characterized as death and/or prolonged need for mechanical ventilation.
The only published data on microcirculatory alterations in humans with acute respiratory failure assessed using non-invasive techniques were reported by our group in a small series of patients with acute lung injury due to Influenza AH1N1 . These patients had diminished capillary density in the sublingual area, with a low proportion of perfused vessels and a reduced microvascular flow index. In the thenar muscle, post-occlusive reactive hyperemia was impaired, as manifest by low values of the Asc slope, similar to those found in septic patients in other studies [29–31]. Our current study extends these data to a larger and more heterogeneous population of patients with ARDS.
Half of the patients in our study had sepsis, but microcirculatory alterations detected by NIRS are not pathognomonic of septic conditions. Numerous studies have shown alterations of the Asc slope in septic populations, especially in the presence of shock [20, 29, 30], but low values of the Asc slope have also been observed in other acute conditions (normal values of 288 and 323 %/min have been reported [20, 22]): Gomez et al. reported values of 172 ± 103 %/min in trauma patients ; Petroni et al. reported values of 77 ± 42 %/min in patients with severe acute heart failure requiring veno-arterial extracorporeal membrane oxygenation (ECMO) support ; Morel et al. reported values of 144 (126–228) %/min 6 h after cardiopulmonary bypass in patients who had undergone cardiac surgery ; Donadello et al. reported values of 68 ± 32 %/min in resuscitated cardiac arrest patients after cessation of therapeutic hypothermia ; and we previously reported values of 186 ± 89 %/min in patients with circulatory shock of different etiologies . In the present study, patients with septic shock had similar Asc slope values to patients with ARDS of non-septic causes. Although the mechanisms involved in the control of post-occlusive reactive hyperemia (NIRS Asc slope) have not been completely identified and are sometimes controversial [32, 33], it is well known that multiple vasodilator pathways (e.g., nitric oxide and prostaglandins) are necessary to obtain the transient increase in local blood flow  and complex inflammatory alterations will have been present in all the populations studied above [20, 22–25, 31]. Thus, the NIRS VOT is a functional test of the microcirculation, which measures its reserve (recruitability) under controlled ischemia, and involves multiple pathways.
Our findings suggest that microvascular endothelial dysfunction is present in the earliest stages of ARDS and is correlated with its severity. This concept fits well with the elevated concentrations of various pro-inflammatory molecules seen in patients with ARDS [8, 12, 34] and with autopsy findings revealing an initial pro-inflammatory and exudative phase [7, 35]. Dolinay and colleagues performed a series of experiments in mice and various cohorts of ARDS patients and showed that several inflammasome-regulated cytokines, including interleukin-18, play a major role in the development of ARDS . Orfanos and colleagues demonstrated that severe ARDS was associated with decreased pulmonary capillary endothelium-bound angiotensin converting enzyme (ACE) function in vivo (an indirect marker of endothelial injury) . More recently, Moussa et al. demonstrated that patients with ARDS in the context of sepsis had elevated numbers of circulating endothelial cells (a direct marker of endothelial injury), which were correlated with severity .
Early prognostication of outcome in ARDS is challenging. In large databases, the mortality rate is directly related to the severity of the alterations in gas exchange as expressed by the PaO2/FiO2 ratio, but the relationship is not very strong [38, 39], with an AUC of only 0.58 in a recent multicenter study . We used a main combined outcome of death or need for prolonged mechanical ventilation which is essentially the opposite of ventilator-free days , but we also observed positive results when mortality was considered alone. Previous investigators have tried to predict similar combined outcomes, but they needed to use clinical data obtained during the first three days of hospitalization , rather than just on the first day as in the present study. Other groups have developed scores mixing various clinical and demographic data at admission, but these were not superior to the APACHE II score for predicting mortality . We also observed that those patients who recovered rapidly had a similar Asc slope when compared with volunteers, despite the severe hypoxemia. Additionally, the NIRS Asc slope was the best predictor for death or more than 7 days on mechanical ventilation. Together these observations suggest that performing a NIRS VOT test on the first day of ARDS enables identification of patients at high-risk of poor outcome, potentially creating a target population for the testing of early interventions.
Our study has some limitations. First, it was a monocenter study and patient enrolment depended on researcher availability, although we included a heterogeneous sample of patients with different severities of ARDS. Second, we performed a single measurement and the time course of the Asc slope during subsequent days of treatment may provide additional information, as has been shown in septic patients . Third, our control group was comprised of healthy younger individuals who may have different vascular reactivity to that of ARDS patients. However, we have previously reported that NIRS values are quite similar in control cohorts of patients and in healthy younger volunteers [20, 31]. Our comparison enables the whole spectrum from the normal values of health to those in severe ARDS patients to be considered. Finally, the sample size of our population was small, potentially explaining the non-significant differences in some variables, for example, the norepinephrine doses between patients with good and poor evolution (Table 1) or the NIRS Asc slope in the different groups of PaO2/FiO2 ratios, despite trends in the data. Nevertheless, the clinical relevance of the NIRS Asc slope was higher than that of other studied variables and this variable needs to be investigated further.
In ARDS patients, there is an early, marked alteration in microvascular reactivity, which is directly related to the severity of the disease as reflected by the duration of mechanical ventilation and mortality.
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