Evidence map›Paper›PMID 40967654›Full record

ArticleBMJ open2025

High flow oxygen for vaso-occlusive crisis: a multicentre, prospective, randomised, multi-arm, multi-stage clinical trial (OSONE).

Armand Mekontso Dessap, Anoosha Habibi, Constance Guillaud, Christian Kassasseya, Charlotte Larrat, Maïté Agbakou, Tona Tchoubou, Clara Candille, Benjamin Carpentier, Mickael Landais and 28 more

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03976180 (A Multicentre, Prospective, Randomized, Multi-arm, Multi-stage Clinical Trial of High-flow Oxygen for Vaso-occlusive Pain Crisis in Adult Patients With Sickle Cell Disease;), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03976180 narecruitingnot on this map

A Multicentre, Prospective, Randomized, Multi-arm, Multi-stage Clinical Trial of High-flow Oxygen for Vaso-occlusive Pain Crisis in Adult Patients With Sickle Cell Disease;

TypeinterventionalSponsorAssistance Publique - Hôpitaux de ParisRan2020 to 2025Enrolled350ConditionsSickle Cell DiseaseArmsStadard low-flow oxygen, HFNO with low FiO2 (21%-30%), HFNO with intermediate FiO2 (50%), HFNO with high FiO2 (100%)
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

38 authors.

Armand Mekontso DessapService de Médecine Intensive Réanimation, Hôpitaux Universitaires Henri-Mondor, AP-HP, Créteil, France armand.dessap@aphp.fr.ORCID http://orcid.org/0000-0001-5961-5577
Anoosha HabibiUnité des Maladies Génétiques du Globule Rouge, Hôpitaux Universitaires Henri Mondor, AP-HP, Créteil, France.
Constance GuillaudDépartement d'Aval des Urgences, Hôpitaux Universitaires Henri Mondor, AP-HP, Créteil, France.
Christian KassasseyaService d'Acceuil des Urgences, AP-HP, Hôpitaux Universitaires Henri Mondor, Créteil, France.
Charlotte LarratService de Médecine Intensive Réanimation, Hôpital Bretonneau, Tours, France.
Maïté AgbakouService de Médecine Intensive Réanimation, CHU de Nantes, Nantes, France.ORCID http://orcid.org/0000-0002-3768-3496
Tona TchoubouService de Médecine Intensive Réanimation, Hôpital Delafontaine, Saint-Denis, France.
Clara CandilleService de Médecine Intensive Réanimation, CHU Grenoble Alpes, Grenoble, Auvergne-Rhône-Alpes, France.
Benjamin CarpentierService d'Hématologie Clinique, Hôpital Saint Vincent de Paul, Groupe Hospitalier de l'Institut Catholique de Lille, Lille, France.
Mickael LandaisService de Réanimation médico-chirurgicale et unité de soins continus, Centre Hospitalier Le Mans, Le Mans, France.ORCID http://orcid.org/0000-0001-5320-4013
Jean-Benoît ArletFrench National reference center for sickle cell disease, Department of Internal Medicine, European Georges Pompidou Hospital, AP-HP, Paris-Cité University, Paris, France.
Muriel FartoukhGroupe de Recherche Clinique CARMAS, Université Paris Est Créteil (UPEC), Institut Mondor de Recherche Biomédicale (IMRB), INSERM U955, Créteil, France.
Arnaud DesclauxService des Maladies infectieuses et tropicales, CHU de Bordeaux, Bordeaux, France.
Agathe MasseauService de Médecine Interne, CHU de Nantes, Nantes, France.
Johanna OzielService de réanimation médico-chirurgicale, Hôpital Avicenne, APHP, Université Sorbonne Paris Nord, Bobigny, Île-de-France, France.
Sihem BouharaouaIntensive Care Unit, Institut Universitaire du Cancer de Toulouse (IUCT) Oncopole, Toulouse, France.
Comlan AffoService de Médecine Interne, Hôpital Louis-Mourier, AP-HP, Colombes, Île-de-France, France.
Damien ViglinoService des Urgences adultes Nord, CHU Grenoble Alpes, Grenoble, France.
Latifatou BoukariService de Médecine Interne, Hôpital Saint-Antoine, Paris, Île-de-France, France.
Luis Ensenyat MartinService de Médecine intensive Réanimation, CH Sud Francilien, Corbeil-Essonnes, France.
Stéphanie NgoService de Médecine Interne, CH Saint-Denis, Saint-Denis, Île-de-France, France.
Nadia AnguelService de Médecine Intensive Réanimation, Hôpital Bicêtre, AP-HP, Le Kremlin-Bicêtre, France.
Christelle ChantalatService de Médecine Interne - Immunologie, Hôpital Bicêtre, AP-HP, Le Kremlin-Bicêtre, France.
Anne Bourgarit-DurandService de Médecine Interne, Hôpital Jean-Verdier, AP-HP, Bondy, France.
Isabelle GentyService de Médecine Interne, Centre Hospitalier Intercommunal de Créteil, Créteil, Île-de-France, France.
Caroline MakowskiService de Médecine Interne, CHU Grenoble Alpes, Grenoble, France.
Stéphanie GuilletService de Médecine Interne, Hôpitaux Universitaires Henri Mondor, AP-HP, Créteil, Île-de-France, France.
Giovanna MelicaService d'Immunologie Clinique et Maladies Infectieuses, Hôpitaux Universitaires Henri Mondor, AP-HP, Créteil, France.
François LionnetService de Médecine Interne, Hôpital Tenon, AP-HP, Sorbonne Université, Paris, France.
Sylvain Le JeuneService de Médecine Interne, Hôpital Avicenne, AP-HP, Bobigny, France.
Laure JosephDépartement de biothérapie, Hôpital Necker-Enfants Malades, AP-HP, Paris, Île-de-France, France.
Fanny LanternierService des Maladies infectieuses et tropicales adultes, Hôpital Necker-Enfants Malades, AP-HP, Paris, France.
Pierre CougoulService de Médecine Interne, CHU de Toulouse, Institut Universitaire du Cancer de Toulouse (IUCT) Oncopole, Toulouse, France.
Ivan BertchanskyReference Centre for Rare Red Blood Cell Disorders, CHU de Montpellier, Montpellier, France.
Yvonnick BoueService de Médecine Intensive Réanimation, CH Mayotte, Mayotte, France.
Pablo BartolucciINSERM U955, Université Paris Est Créteil, Créteil, France.
Ségolène GendreauService de Médecine Intensive Réanimation, Hôpitaux Universitaires Henri-Mondor, AP-HP, Créteil, France.
Etienne AudureauService de Santé Publique, Unité de Recherche Clinique, Hôpitaux Universitaires Henri Mondor, AP-HP, Créteil, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSickle cell disease (SCD) is due to the mutation of haemoglobin (Hb), from HbA to HbS and characterised by recurrent vaso-occlusive crises (VOC), which can progress to acute chest syndrome (ACS), a leading cause of death in adults with SCD. Hypoxia is a key modifiable factor in the polymerisation of HbS and the pathogenesis of VOC. High-flow nasal oxygen (HFNO) delivers humidified gas at high oxygen concentrations and flow rates: the former may reverse sickling (metabolic effect) to accelerate VOC resolution and prevent ACS, while the latter may reduce the risk of ACS by mitigating hypercapnia and generating positive airway pressure that limits hypoventilation and atelectasis (pulmonary effect). The study hypothesises that HFNO is a safe and effective strategy for treating VOC and preventing secondary ACS, and will assess this using a multi-arm multi-stage (MAMS) trial design. METHODS AND ANALYSIS: This is a prospective, multicentre, randomised, open-label controlled trial following an MAMS design with three phases and four arms: one control (low-flow oxygen) and three HFNO intervention arms with varying fraction of inspired oxygen levels (low, intermediate, high). The pilot stage will assess safety and feasibility, using the rate of cardiac and neurological events as the primary endpoint. In the activity stage, arms demonstrating acceptable safety will be compared for efficacy based on the rate of VOC resolution without complications by day 5, allowing selection of the most promising arm. The final efficacy stage will compare the selected HFNO strategy to control, with prevention of secondary ACS by day 14 as the primary endpoint. The study aims to enrol up to 350 VOC episodes in total. ETHICS AND DISSEMINATION: The study has been granted ethical approval (CPP SUD MEDITERRANEE IV). Following the provision of informed consent, patients will be included in the study. The results will be submitted for publication in peer-reviewed journals. TRIAL REGISTRATION NUMBER: NCT03976180.

Indexed as

Acute Chest SyndromeAnemia, Sickle CellOxygenOxygen Inhalation TherapyAdultHumansMaleMulticenter Studies as TopicProspective StudiesRandomized Controlled Trials as TopicOxygenAnaemiaHyperoxiaRandomized Controlled Trial

Identifiers

PMID40967654
PMCPMC12458843

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.