Acute chest syndrome (ACS) is the leading cause of admission to intensive care and the leading cause of death in patients with sickle cell disease. Irrespective of the cause of ACS, there is an heterogeneity in pulmonary ventilation/perfusion ratios, leading to worsening of the disease. Efficiency of awake prone positioning (APP) in acute respiratory failure (ARF) was particularly highlighted during the COVID-19 pandemic. Several physiological factors contribute to this benefit including an improvement in ventilatory drive and gas exchange. The investigator hypothesize that APP could lead to clinical improvement in ACS in terms of oxygenation and ventilatory drive, by improving the heterogeneity of ventilation
* Several physiological mechanisms contribute to the benefit of APP during ARF. In addition to hypoxemia improvement, there is also an effect on ventilatory drive, notably in terms of polypnea, ROX index and inspiratory effort. * Considering that hypoxemia in ACS contributes to the physiopathological process: deoxygenation of haemoglobin S - red blood cells falciformisation - vaso-occlusive event, APP could be an additional therapy in severe ACS. In addition, improving ventilation-perfusion ratios, mainly by recruiting dorsal zones, could be particularly useful in ACS, where pulmonary damage predominates in gravito-dependent zones.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
15
* APP are realized following the diagnosis of ACS * Prone positioning or supine positioning are performed under supervision of a physician or a nurse * Maximum session duration: 16 hours per day * Sessions of prone positioning can be shortened, if necessary (30 minutes minimum), for better tolerance * Tolerance of prone positioning is assessed by the physician in charge and sessions and may be stopped in case of poor tolerance
Service de Médecine Intensive Réanimation TENON
Paris, France
The total duration of APP during the stay in intensive care unit
Time frame: 28 days
Changes in respiratory parameters
Assessment of respiratory parameters changes
Time frame: Up to 28 days
GI measured by EIT
Time frame: Up to 28 days
ΔEELI measured by EIT
Time frame: Up to 28 days
Pain measurement assessed by visual analog scale,
Time frame: Up to 28 days
Pain measurement assessed by morphine consumption
Time frame: Up to 28 days
Pain measurement assessed by analgesic therapeutic escalation
Time frame: Up to 28 days
Occurrence of skin lesions during the intensive care unit stay
Time frame: 28 Days
Occurrence of displacement of devices during the intensive care unit stay
Time frame: 28 Days
Occurrence of use of vital support therapy during the intensive care unit stay
Time frame: 28 Days
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