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. 2020 Jul 9;24:412. doi: 10.1186/s13054-020-03133-9

Impact of initial respiratory compliance in ventilated patients with acute respiratory distress syndrome related to COVID-19

Florent Laverdure 1,, Amélie Delaporte 1, Astrid Bouteau 1, Thibaut Genty 1, François Decailliot 2, François Stéphan 1
PMCID: PMC7347264  PMID: 32646470

Dear Editor,

Coronavirus disease 2019 (COVID-19) is associated with a high fatality rate in patients requiring invasive mechanical ventilation (IMV) [1]. COVID-19-related acute respiratory distress syndrome (COVID-ARDS) might exhibit vascular insults, resulting in loss of hypoxic pulmonary vasoconstriction, and subsequent dissociation between profound hypoxemia and preserved static compliance of the respiratory system (Cst-rs) [2]. Experts recently distinguished two phenotypes of COVID-ARDS according to their Cst-rs [2]: patients were classified as groups L (low elastance (or high Cst-rs) and low recruitability) and H (high elastance and high recruitability). They recommended different ventilatory approaches [3], contrary to Sepsis Surviving Campaign guidelines [4]. We describe characteristics and outcomes in patients with different initial Cst-rs, but all receiving IMV following ARDS guidelines.

We report the courses of respiratory parameters and outcomes in an observational cohort of 36 patients who developed COVID-ARDS requiring IMV from March 17 to April 18, 2020. Patients were divided into two groups (low and high Cst-rs) according to their initial Cst-rs was above or below the median value. We applied institutional ARDS procedures to all patients. Our management was based on the systematic use of neuromuscular blockers for at least 48 h, positive end-expiratory pressures (PEEP) titrated on oxygenation, and prone positioning sessions if PaO2/FiO2 ratio dropped below 150. Patients’ data were analyzed until patients were discharged from the intensive care unit or died. Courses of Cst-rs, PEEP, and tidal volumes were analyzed using a linear mixed model.

The median baseline Cst-rs was 36 mL/cmH2O [interquartile range (IQR) 29–44]. Characteristics of the patients at baseline, therapeutic interventions, and outcome measures are provided in Table 1. Twenty-nine patients (80.6%) in whom PaO2/FiO2 ratio dropped below 150 were placed in prone position. Courses of Cst-rs, PEEP levels, and tidal volumes are provided in Fig. 1. Cst-rs did not vary over time in both groups and remained higher in the high Cst-rs group (mean difference 17.7 mL/cmH2O [95% CI 11.3–24.0] compared to the low Cst-rs group, P < 0.001). Tidal volumes were higher in the high Cst-rs group (mean difference 0.90 mL/kg [95% CI 0.31–1.50] compared to the low Cst-rs group, P = 0.005). PEEP levels were not different between groups and decreased over time.

Table 1.

Baseline characteristics, therapeutic interventions, and outcomes of patients, according to respiratory compliance

Overall (N = 36), no. (%) of patientsa High respiratory compliance (N = 17), no. (%) of patientsa Low respiratory compliance (N = 19), no. (%) of patientsa P value between groups
Baseline characteristics
 Age, mean ± SD, years 53.4 ± 10.2 56.1 ± 7.1 50.9 ± 12.1 0.12
 Male sex 30 (83.3) 16 (94.1) 14 (73.7) 0.18
 Obesityb 14 (38.9) 3 (17.7) 11 (57.9) 0.02
 Diabetes mellitus 11 (30.6) 5 (29.4) 6 (31.6) 1.0
 Arterial hypertension 16 (44.4) 11 (64.7) 5 (26.3) 0.19
 SAPS 2 score, median [IQR] 31 [27–36] 31 [29–36] 29 [22–39] 0.51
 SOFA score, median [IQR] 5 [4–7] 6 [4–7] 4 [3–6] 0.04
 Tidal volume, mean ± SD, mL/kg 6.1 ± 0.6 6.2 ± 0.3 6.0 ± 0.7 0.02
 Respiratory frequency, median [IQR], breaths/min 25 [24–27] 25 [24–26] 26 [24–28] 0.64
 FiO2, median [IQR], % 65 [50–100] 60 [40–80] 70 [60–100] 0.07
 PaO2/FiO2 ratio, median [IQR] 152 [112–240] 209 [150–256] 117 [83–201] 0.02
 PEEP, mean ± SD, cmH2O 13.4 ± 3.2 13.4 ± 3.6 13.4 ± 3.1 0.92
 Respiratory compliance, mean ± SD, mL/cmH2Oc 39.4 ± 16.9 51.8 ± 16.4 28.3 ± 6.1
Therapeutic interventions
 Prone positioning 29 (80.6) 12 (70.6) 17 (89.5) 0.22
 Number of sessions, median [IQR] 4.0 [2.0–6.0] 4.0 [2.5–5.0] 5.0 [1.7–6.0] 0.91
 Inhaled nitric oxide 9 (25.0) 2 (11.8) 7 (36.8) 0.13
 Venovenous ECMO 7 (19.4) 0 (0.0) 7 (36.8) 0.008
 Vasopressors 31 (86.1) 17 (100.0) 14 (73.7) 0.048
 Renal replacement therapy 7 (19.4) 3 (17.7) 4 (21.1) 1.0
 Hydroxychloroquine 32 (88.9) 16 (94.1) 16 (84.2) 0.6
 Steroïds 11 (30.6) 5 (29.4) 6 (31.6) 1.0
Outcomes
 Ventilator-free days, median [IQR] 3.0 [0.0–14.5] 10.0 [0.0–17.2] 0.0 [0.0–8.0] 0.04
 Mortality at day 28 4 (11.1) 1 (5.9) 3 (15.8) 0.61

Abbreviations: ECMO extracorporeal membrane oxygenation, FiO2 fraction of inspired oxygen, PEEP positive end-expiratory pressure

aUnless otherwise indicated

bObesity is defined by a body mass index above 30 kg/m2. The formula for body mass index is weight in kilograms divided by height in meters squared

cNo statistical comparison performed

Fig. 1.

Fig. 1

Course of the respiratory system static compliances (Cst-rs), positive end-expiratory pressures (PEEP), and tidal volumes (Vt). The means and 95% confidence intervals are represented respectively by solid lines and colored areas. Results are expressed in mean differences [95% CI]. a Cst-rs remained higher in the high initial Cst-rs group. There was no significant effect of time on Cst-rs (slope = − 0.03 mL/cmH2O/day of ventilation [95% CI − 0.17 to 0.12], P = 0.70). b PEEP levels did not differ between groups (high vs. low Cst-rs group − 0.69 cmH2O [95% CI − 2.05 to 0.66], P = 0.33). There was a statistically significant effect of time on PEEP (slope = − 0.10 cmH2O/day of ventilation [95% CI − 0.13 to − 0.06], P < 0.001). Vt were higher in the high Cst-rs group. There was no significant effect of time on Vt (slope = − 0.006 [− 0.02 to 0.007], P = 0.375)

On day 28, 32 patients (88.9%) survived and 25 (69.4%) were discharged from the intensive care unit. As of May 30, 2020, weaning from mechanical ventilation was effective in 16 high Cst-rs patients (94.1%) and 13 low Cst-rs patients (68.4%) (P = 0.09).

As previously suggested [3], some COVID-ARDS patients exhibit high initial Cst-rs. However, the median baseline Cst-rs was not different from Cst-rs observed in “typical” non-COVID-ARDS, as demonstrated in another study [5]. The high Cst-rs did not drop and remained different from the initial low Cst-rs during the first 28 days, suggesting a lack of transition from a high to a low Cst-rs phenotype in patients receiving neuromuscular blockers. We therefore hypothesize that if this transition exists, self-inflicted lung injury during spontaneous ventilation or asynchronies is one of its main determinants.

Although therapeutic management of low Cst-rs patients is not disputed [2, 6], a low-PEEP, high-FiO2, liberal tidal volume approach has been suggested for high Cst-rs patients. Using established ARDS therapies [3] with either low or high Cst-rs, the survival rate is better than initially reported [1], following a recent publication using the same strategy [5]. A low initial Cst-rs could be a marker of severity, as suggested by more extracorporeal membrane oxygenation requirement and less ventilator-free days at day 28.

Limitations include the small number of patients and the retrospective design. While further study is needed, our findings provide arguments to treat all COVID-ARDS with established ARDS therapies, whatever the initial value of Cst-rs.

Acknowledgements

We thank all clinical and nursing staff of Marie Lannelongue Hospital for their flawless commitment during this outbreak. We also thank Sebastien Morisset, MSc, for performing the statistical analysis, and Vincent Roth, MD (Easy CRF SAS®), for providing us the database.

Abbreviations

ARDS

Acute respiratory distress syndrome

COVID-19

Coronavirus disease 2019

Cst-rs

Static compliance of the respiratory system

IMV

Invasive mechanical ventilation

PEEP

Positive end-expiratory pressure

Authors’ contributions

FL and FS have designed the work. All authors have drafted the work. All authors have made the acquisition, analysis, and interpretation of the data. All contributors read and approved the manuscript.

Funding

The present study was supported solely by institutional sources.

Availability of data and materials

The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.

Ethics approval and consent to participate

The entire project was approved by the Groupe Hospitalier Paris Saint Joseph Ethics Board (IRB 00012157. Project number: 20-37816004), which waived informed consent.

Consent for publication

Not applicable

Competing interests

The authors declare that they have no competing interests.

Footnotes

Publisher’s Note

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References

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.


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