Abstract
Description of all consecutive critically ill COVID 19 patients hospitalized in ICU in University Hospital of Guadeloupe and outcome according to delay between steroid therapy initiation and mechanical ventilation onset. Very late mechanical ventilation defined as intubation after day 7 of dexamethasone therapy was associated with grim prognosis and a high mortality rate of 87%.
Keywords: Acute respiratory distress syndrome, Mechanical ventilation, COVID 19, Steroid, High flow nasal oxygen therapy
Dear Editor,
After large therapeutic trials, steroid and tocilizumab are now the cornerstones of COVID 19 pneumonia treatment [1, 2]. Outcome in case of respiratory radiological and clinical worsening under immunosuppressive treatment has to our knowledge not been evaluated. For COVID 19 pneumonia, timing and indications of mechanical ventilation are still heavily debated [3]. In these patients, it has been observed that high flow nasal oxygen (HFNO) could reduce the need for mechanical ventilation and associated morbidity [3, 4]. However, delayed intubation could also be harmful due to Patient-Self Induced Lung Injury (P-SILI) [5]. Here, we aimed to describe the characteristics and outcome of COVID-19 patients who were intubated very late after the onset of a severe form of the disease.
We retrospectively analyzed the characteristics and outcome of the 574 consecutive patients with severe acute respiratory failure and laboratory-confirmed SARS-CoV-2 infection admitted to the ICU of the Guadeloupe University hospital, Pointe-à-Pitre, France, between June 2020 and September 2021. Severe acute respiratory failure was defined as respiratory rate ≥ 25 min−1, bilateral pulmonary infiltrates on chest X-ray or CT scan and need for standard oxygen ≥ 10 L min−1 to maintain SpO2 ≥ 92%. Dexamethasone (DXM) was started for each COVID 19 pneumonia with oxygen requirement. Very late intubation (VLI) was defined as an intubation occurring more than seven days after DXM initiation.
Flowchart is shown in Fig. 1A. Patients were classified based on the time between steroid initiation and intubation. Briefly, sub-groups were similar in term of age, sex-ratio and comorbidities (Table 1). Possibly due to a longer time between DXM start and intubation, VLI patients received more adjunctive therapies (awake prone positioning and Tocilizumab) (Table 1). Noninvasive ventilation (NIV) use was similar between groups. Of the 398 patients intubated in the ICU, 30 (8%) met the criteria for VLI. They were mainly male (n = 17, 59%) with a median age of 63 years (interquartile range 56–66). VLI patients were intubated 9 days (7–13) after DXM start and 5 days (2–7) after HFNO initiation. All patients had pulmonary samples for microbiological analysis at intubation and only 3 (10%) had nosocomial pneumonia at intubation. Within 24 h following intubation, VLI patients had severe hypoxemia (median PaO2/FiO2 86 [70–110] mmHg) with very low respiratory system compliance (median 14 [12–20] ml cmH2O−1) and severe respiratory acidosis (pH < 7.30 mmHg) (55% of them, n = 17). ICU mortality was 87% in VLI patients, 49% in those intubated between two and seven day after DXM initiation and 54% in those intubated on the day of DXM initiation (p < 0.001) (Fig. 1B).
Fig. 1.
A Chart flow of pulmonary COVID 19 patients admitted in ICU in University Hospital of Guadeloupe. B ICU survival of very late intubated COVID-19 (after 7 days) patients compare to early intubated patients. Footnotes: All patients were SARS cov-2 PCR confirmed, p-value was calculated using fisher test, p < 0.001
Table 1.
Characteristics and outcome of COVID 19 patients hospitalized in ICU with delayed intubation 7 days after dexamethasone treatment (≥ 7 days) versus other patients admitted in the same ICU
| All patients (n = 556) | HNFO only (n = 152) | Intubation ≤ 1 day after DXM initiation (n = 196) | Intubation 2 to 7 days after DXM initiation (n = 178) | Intubation > 7 days after DXM initiation (n = 30) | p | |
|---|---|---|---|---|---|---|
| Patient’s characteristics | ||||||
| Age, years | 59 (50–66) | 58 (46–66) | 60 (50–66) | 59 (52–65) | 63 (57–66) | 0.56 |
| Gender male, n (%) | 336 (60) | 97 (64) | 110 (56) | 112 (63) | 17 (57) | 0.55 |
| SOFA | 4 (3–7) | 3 (2–4) | 7 (4–9) | 5 (3–7) | 5 (3–7) | < 0.01 |
| ROX score on day of HFNO onset, min−1 | 4.2 (3.0–6.0) | 6.7 (4.8–8.6) | 3.0 (2.2–4.0) | 4.2 (3.3–5.2) | 6.0 (4.0–7.5) | < 0.01 |
| ROX score at intubation, min−1 | 2.2 (2.0–2.7) | NA | 2.2 (2.0–2.8) | 2.3 (2.0–2.8) | 2.0 (2.0–2.1) | 0.45 |
| Comorbidities | ||||||
| Arterial hypertension, n (%) | 293 (53) | 67 (44) | 107 (55) | 99 (56) | 20 (67) | 0.38 |
| Diabetes, n (%) | 209 (38) | 49 (32) | 78 (40) | 72 (40) | 10 (33) | 0.18 |
| IMC > 30 kg m−2, n (%) | 291 (52) | 71 (47) | 116 (59) | 89 (50) | 15 (50) | 0.08 |
| Biology | ||||||
| White blood cells, G L−1 | 8.6 (6.3–11.3) | 8.4 (6.4–10.5) | 9.1 (6.8–11.2) | 8.7 (1.0–11.5) | 8.7 (6.0–11.8) | 0.757 |
| D-dimers, ng mL−1 | 1.4 (1.0–2.5) | 1.5 (0.9–2.8) | 1.2 (0.8–2.6) | 1.6 (0.9–2.4) | 1.4 (1.0–2.1) | 0.93 |
| Adjunctive therapies | ||||||
| Noninvasive ventilation, n (%) | 120 (22) | 24 (16) | 45 (23) | 43 (24) | 8 (27) | 0.66 |
| Awake prone positioning, n (%) | 154 (27) | 71 (50) | 18 (9) | 53 (30) | 12 (40) | < 0.01 |
| Tocilizumab, n (%) | 66 (12) | 33 (22) | 5 (3) | 19 (11) | 9 (30) | < 0.01 |
| Outcome | ||||||
| ICU mortality, n (%) | 219 (39) | 0 (0) | 105 (54) | 88 (49) | 26 (87) | < 0.01 |
Results are number n (percentage) of for categorical variables and median (q1–q3) for continuous variables. P values were obtained using Kruskal–Wallis for continuous variables, and Chi2 or fisher test when appropriate for categorical variables
HFNO—high flow nasal oxygen, DXM—dexamethasone, ICU—intensive care unit, SOFA—Sepsis-related Organ Failure Assessment
This is seemingly the first report of COVID-19 patients intubated very late after DXM initiation. Although VLI was uncommon (8% of the intubated patients in our study), it was associated with high mortality. In most studies on timing of intubation in COVID, patients with delayed intubation were actually intubated only 2 days after ICU admission [3, 4] without report on time between DXM start and intubation. The extreme respiratory severity of VLI patients suggests that severe lung damage unrelated to nosocomial bacterial pneumonia occurs prior to intubation. P-SILI [5] and/or a rapid pulmonary fibrotic evolution despite DXM treatment could explain this rapid and severe worsening. Deleterious effect of NIV before intubation on the prognosis of COVID-19 patients has been raised recently [6]. In our study, by definition, VLI patients were exposed to NIV and/or HFNO during a longer period of time, which could have contributed to the generation of P-SILI.
The retrospective and monocentric design without control group of the present study are its main limitations and results should be thus confirmed by other large cohorts.
Based on the grim prognosis of VLI in COVID 19 patients, our study highlights the need for criteria predicting steroid and NIV/HFNO failures in order to avoid delayed intubation.
Acknowledgments
None.
Abbreviations
- HFNO
High flow nasal oxygen
- NIV
Noninvasive ventilation
- ICU
Intensive care unit),
- DXM
Dexamethasone
- VLI
Very late intubation
Author contributions
LC, JDP, FM and MV designed the study. JDP, LC, AD and BT conducted the analyses. All authors significantly contributed to the research, discussed the results of the analyses, edited the draft manuscript, and approved the submitted version. All authors read and approved the final manuscript.
Funding
None.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Declarations
Ethics approval and consent to participate
This retrospective study was approved by the ethics committee of the Guadeloupe University Hospital under the number LJ-1002, which waived the need for informed consent from individual patients due to the retrospective nature of the study.
Consent for publication
Not applicable.
Competing interests
None.
Footnotes
Publisher's Note
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Data Availability Statement
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.