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| ID | Type | Description | Link |
|---|---|---|---|
| 2026-A00423-48 | Other Identifier | Ministère chargé de la Santé, France |
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Sickle cell disease (SCD) is a severe hemoglobinopathy, considered the first monogenic disease in the world. Acute chest syndrome (ACS), one of the most frequent and serious complications of SCD, is defined by the association of fever and/or acute respiratory symptoms with a new pulmonary infiltrate on chest imaging. ACS is characterized by lung consolidation, severe pulmonary vascular dysfunction, with potential role for regional alveolar hypoxia. Therefore, improving alveolar oxygenation and limiting lung consolidation are key objectives of the treatment of ACS, in addition to ensuring pain relief and giving blood transfusions and antibiotics. Bilevel non-invasive ventilation failed in improving outcomes during ACS (Fartoukh 2010). These results are in accordance with those reported in other forms of acute lung injury (Frat 2015), with conflicting results. Among other explanations, NIV may favour high tidal volume ventilation leading to patient self-inflicted lung injury (P-SILI) (Carteaux 2016). Continuous positive airway pressure (CPAP) is a simple to use and affordable technique for non-invasive ventilatory support, that theoretically exposes to a lower risk of P-SILI (Carteaux 2021). In patients with acute hypoxemic respiratory failure (AHRF), applying a positive pressure to the airway opening has been shown to mitigate the reduction in functional residual capacity and to improve respiratory mechanics and gas exchange. In a randomized controlled trial (RCT) conducted in patients with AHRF, CPAP achieved early physiologic improvement (Delclaux 2000). Recent results also suggest that CPAP reduces the composite outcome of intubation or death in adults with AHRF due to COVID-19 in a large multicentre study (RECOVERY-R) (Perkins 2022). In addition, CPAP can be safely used at early stages in the wards, with a frugal approach, using virtual valves (Carteaux 2021). In patients with SCD, CPAP has shown benefits when used at night in children with sleep apnea (Marshall 2009), or for the peri-operative management (Leff 2007). CPAP is also used in clinical practice for hypoxemic ACS (Heilbronner 2021), but it has not been formally assessed in this setting.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| O2+CPAP group | Experimental | ACS episodes assigned to this group will receive supplemental O2 in addition to periods of CPAP. |
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| O2 group | No Intervention | ACS episodes assigned to the O2 group will receive supplemental O2 delivered through nasal cannula or high flow nasal cannula (for needs ≤6, and >6L/min, respectively) until endotracheal intubation, death, or fulfilment of O2 delivery cessation criteria (SpO2 ≥95% without supplemental O2). SpO2 will be measured on room air, at least every 12 hours. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| O2+CPAP group | Other | ACS episodes assigned to this group will receive supplemental O2 in addition to periods of CPAP. CPAP will target a positive pressure between 5 and 10 cmH2O. CPAP will be given discontinuously (≥6 hours/day) based on patient tolerance . CPAP sessions will be stopped when the patient achieves the criteria for cessation of supplemental O2. These criteria will be the same as in the O2 group. No sedation will be used for CPAP tolerance. |
| Measure | Description | Time Frame |
|---|---|---|
| Time to résolution of acute chest syndrome (ACS) | time to resolution of ACS, defined as the time from randomization to the joint resolution of fever (body temperature < 38°C), chest pain (visual analog scale, VAS ≤ 3 cm, morphine ≤ 40mg/24h), dyspnea (VAS ≤ 3 cm, respiratory rate < 25/min, no ventilatory support), and hypoxemia (SpO2 > 92% on room air) (Mekontso Dessap, Habibi, et al., 2025). If a VAS is unavailable, a verbal rating scale will be used. Resolution of ACS will be assessed every 8 to 12 hours and will be considered achieved if sustained across 2 to 3 consecutive evaluations (i.e., over a 24-hour period). | Up to randomization |
| Measure | Description | Time Frame |
|---|---|---|
| Mortality | All-cause mortality | up to hospital discharge or day-28 after randomisation (whichever occurs first), and at 3 months after randomisation. |
| Length of hospital stay | up to hospital discharge or day-28 after randomisation (whichever occurs first), and at 3 months after randomisation. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Samia BALOUL | Contact | 01 49 81 33 85 | samia.baloul@aphp.fr | |
| Armand MEKONTSO-DESSAP | Contact | armand.dessap@aphp.fr |
| Name | Affiliation | Role |
|---|---|---|
| Armand MEKONTSO-DESSAP, MD, PhD | Assistance public Hôpitaux de Paris | Study Chair |
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| ID | Term |
|---|---|
| D000755 | Anemia, Sickle Cell |
| D056586 | Acute Chest Syndrome |
| ID | Term |
|---|---|
| D000745 | Anemia, Hemolytic, Congenital |
| D000743 | Anemia, Hemolytic |
| D000740 | Anemia |
| D006402 | Hematologic Diseases |
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|
| Length of ICU stay | up to hospital discharge or day-28 after randomisation (whichever occurs first), and at 3 months after randomisation. |
| Need for catecholamine infusion | dobutamine, dopamine, adrenaline or noradrenaline | From randomisation to discharge or Day-28 |
| Number of red blood cell units transfused | From randomisation to discharge or Day-28 |
| Volume of blood exsanguination | From randomisation to discharge or Day-28 |
| Need for invasive ventilation | From randomisation to discharge or Day-28 |
| Number of days free from any respiratory support | From randomisation to discharge or Day-28 |
| Need for antibiotics therapy | From randomisation to discharge or Day-28 |
| Change in arterial blood gases (PaO2/FiO2 ratio), routine laboratory markers (lacticodeshydrogenase), and chest imaging (X-ray or lung ultrasound score) | within 3 days post-randomisation |
| Readmissions for VOC | up to 3 months |
| Readmissions for ACS | up to 3 months |
| Quality of life questionary | European Quality of life five-dimensions five-level questionnaire (EQ-5D-5L) | At inclusion, Day-28, and 3 months |
| D006425 |
| Hemic and Lymphatic Diseases |
| D006453 | Hemoglobinopathies |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D012120 | Respiration Disorders |