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Erschienen in: Critical Care 1/2021

Open Access 01.12.2021 | Research Letter

Can prone positioning be a safe procedure in patients with acute brain injury and moderate-to-severe acute respiratory distress syndrome?

verfasst von: Pauline Bernon, Ségolène Mrozek, Guillaume Dupont, Frédéric Dailler, Anne-Claire Lukaszewicz, Baptiste Balança

Erschienen in: Critical Care | Ausgabe 1/2021

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A comment to this article is available online at https://​doi.​org/​10.​1186/​s13054-021-03506-8.

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Dear Editor,
One third of patients with severe brain injury develop lung complication that affect their prognosis. Prone positioning (PP) improves the outcome of patients with an acute respiratory distress syndrome (ARDS) [1], but its effect on patients with acute brain injury is still debated. While it improves oxygenation, the impact of PP on intracranial pressure (ICP) remains controversial: PP has been reported not to affect ICP [2] and conversely to increase ICP, thereby worsening brain injuries [3]. There is currently no consensus on criteria to identify patients who will safely benefit from PP [4]. Therefore, the aim of the present study was to evaluate the safety and efficacy of PP in patients with acute brain injury and moderate-to-severe ARDS.
A retrospective analysis in three French intensive care units was conducted. A query on digital medical records identified 27 patients with an ICP, moderate-to-severe ARDS (according to the Berlin criteria) and PP. Data were collected before and during the first PP. Patients who had at least one ICP measurement > 25 mmHg were considered as having intracranial hypertension (IH) as it is associated with a poor prognosis and used to consider a decompressive craniectomy [5].
A total of 10 (37.0%) patients had traumatic brain injuries, 11 (40.7%) subarachnoid haemorrhage, and 7 (25.9%) haemorrhagic stroke (Table1). During PP, the median [IQR] PaO2/FiO2 increased significantly from 100 [89–126] before to 216 [171–257] after PP (Wilcoxon test, p < 0.001) and remained significantly higher back to supine position (146 [122–186], Wilcoxon test, p = 0.002). IH occurred in 14 (51.8%) patients. They had a significantly higher median [IQR] ICP before PP onset (20 [13–26] mmHg) compared to patients without IH (11 [7–12] mmHg, Mann–Whitney test, p = 0.005) and a greater ICP increase during PP (+ 19 mmHg [13–20] vs + 6 mmHg [3–8], Mann–Whitney test, p = 0.025), suggestive of a poorer brain compliance. PP was discontinued due to a sustain ICP increase in 5 patients (Fig. 1a).
Table 1
Population characteristics
 
Total population (n = 27)
IH (n = 14)
No-IH (n = 13)
p*
Age, median [IQR]
46 [36–55]
46 [36–50]
46 [37–56]
0.981
Female, n (%)
5 (18.5%)
2 (14.3%)
3 (23.1%)
0.648
BMI, median [IQR]
26 [23–31]
26 [22–30]
26 [23–33]
0.601
Traumatic brain injury, n (%)
10 (37.0%)
6 (42.9%)
4 (30.8%)
0.694
Subarachnoid haemorrhage, n (%)
11 (40.7%)
5 (35.7%)
6 (46.1%)
0.703
Haemorrhagic stroke, n (%)
7 (25.9%)
4 (28.6%)
3 (23.1%)
1.000
Ischemic stroke, n (%)
1 (3.7%)
0 (0%)
1 (7.7%)
0.481
Aspiration pneumonia, n (%)
13 (48.1%)
7 (50.0%)
6 (46.1%)
1.000
Ventilator-associated pneumonia, n (%)
14 (51.8%)
7 (50.0%)
7 (53.8%)
1.000
Severity
    
 SAPSII, median [IQR]
42 [34–53]
47 [41–55]
39 [30–46]
0.076
 Glasgow Coma Scale at intubation, median [IQR]
6 [4–8]
6 [4–8]
6 [4–7]
0.769
 First ICP measure, median [IQR]
22 [12–29]
24 [19–37]
16 [8–26]
0.274
IH treatment
    
 Craniectomy, n (%)
3 (11.1%)
1 (7.1%)
2 (15.4%)
0.595
 Hypothermia, n (%)
5 (18.5%)
3 (21.4%)
2 (15.4%)
1.000
 Osmotherapy, n (%)
11 (40.7%)
7 (50,0%)
4 (30.8%)
0.440
 Thiopental administration, n (%)
10 (37.0%)
6 (42.9%)
4 (30.8%)
0.694
 At least one of IH treatment, n (%)
14 (51.8%)
8 (57.1%)
6 (46.1%)
0.706
 EVD, n (%)
14 (51.8%)
7 (50.0%)
7 (53.9%)
1.000
ARDS treatment
    
 Neuromuscular blockade, n (%)
27 (100%)
14 (100%)
13 (100%)
 
 PP number, median [IQR]
1 [1–2]
1 [1–2]
1 [1–3]
0.295
 Duration of PP (hours), median [IQR]
14 [9–19]
13 [8–17]
16 [11–20]
0.305
 First PP delay, median days [IQR]
5 [4–7]
6 [5–7]
5 [4–6]
0.279
 Tidal volume mL/kg, median [IQR]
6.8 [6.4–7.5]
6.7 [6.4–7.5]
6.9 [6.4–7.5]
0.843
Parameters before PP
    
 Initial ICP (mmHg), median [IQR]
13 [8–20]
20 [13–26]
11 [7–12]
0.005
 Initial CPP (mmHg), median [IQR]
75 [66–82]
67 [64–75]
79 [77–87]
0.041
 Initial PEEP (cmH20), median [IQR]
10 [9–12]
10 [9–11]
10 [9–12]
0.657
 Initial FiO2, median (%) [IQR]
80 [60–89]
80 [71–100]
67 [60–81]
0.231
 Initial plateau pressure (cmH20), median [IQR]
23 [21–27]
23 [21–29]
23 [21–26]
0.689
 Initial PaO2/FiO2, median [IQR]
100 [89–126]
99 [88–113]
109 [93–142]
0.481
 Initial PaO2 (mmHg), median [IQR]
78 [74–95]
78 [74–90]
77 [74–99]
0.903
 Initial PaCO2 (mmHg), median [IQR]
43 [37–47]
43 [38–46]
44 [36–48]
0.884
Outcome
    
 Mechanical ventilation duration (days), median [IQR]
23 [11–36]
22 [7–35]
23 [16–37]
0.395
 Modified Rankin Scale at ICU discharge, median [IQR]
4 [4–5]
4 [4–6]
4 [4–5]
0.853
 Mortality, n (%)
7 (25.9%)
4 (28.6%)
3 (23.1%)
1.000
BMI Body mass index, CPP cerebral perfusion pressure, EVD external ventricular drainage, FiO2 inspiratory fraction of oxygen, ICP intracranial pressure, ICU intensive care unit, IH intracranial hypertension, PEEP positive end-expiratory pressure, PP prone positioning, SAPSII Simplified Acute Physiology Score 2
*p value IH group versus no-IH group (using the Mann–Whitney or the Fisher’s test)
All patients with an ICP > 17.5 mmHg prior to PP had an IH. Among patients with an ICP < 17.5 mmHg before PP onset, 13/18 (72%) had a safe PP session without IH. Rather than a single threshold of ICP changes, a grey zone approach was used to predict (i.e. sensitivity, Se > 90%) or exclude (i.e. specificity, Sp > 90%) a safe PP. The absence of ICP increase 1 h after the PP onset is suggestive of a preserved brain compliance and predicted a safe procedure (Sp = 93%), while an ICP elevation > 10 mmHg predicted the occurrence of IH (Sp = 93%). When the initial ICP was < 17.5 mmHg and did not increase 1 h after PP onset the manoeuvre took place without IH (Fig. 1b). Brain oxygen partial pressure was available for 4 patients and rose from 20.5 [18.8–23.5] mmHg to 28 [22–31] mmHg during PP.
The main limitations of this study are due to its retrospective design. The modalities for performing manually PP were not available although it can influence its tolerance [6]. In addition, the data collected during PP from the ICU software were sampled hourly at a specific time and may not reflect the average of the hour. Only 4 patients had an intracranial oxygenation probe improved during PP and suggested a preserved cerebral blood flow despite the ICP increase. Finally, the management of IH was not subject to protocol.
To conclude, we would argue for assessing the brain compliance before PP (e.g. transcranial Doppler), ICP, and the tolerance to an obstacle to venous return. Moreover, ICP changes within 1 h after PP onset could be useful to choose to pursue PP or not, as well as cerebral multimodal monitoring to evaluate PP tolerance. This strategy needs to be evaluated in a prospective clinical trial.

Acknowledgements

Not applicable.
The study was approved by the Ethics Committee of the French Intensive Care Society (no IRB 00010254–2018–064).
Not applicable.

Competing interests

The authors declare that they have no competing interests.
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Metadaten
Titel
Can prone positioning be a safe procedure in patients with acute brain injury and moderate-to-severe acute respiratory distress syndrome?
verfasst von
Pauline Bernon
Ségolène Mrozek
Guillaume Dupont
Frédéric Dailler
Anne-Claire Lukaszewicz
Baptiste Balança
Publikationsdatum
01.12.2021
Verlag
BioMed Central
Erschienen in
Critical Care / Ausgabe 1/2021
Elektronische ISSN: 1364-8535
DOI
https://doi.org/10.1186/s13054-020-03454-9

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