Evidence map›Paper›PMID 26431718›Full record

Trial reportIntensive care medicine2015

Inhaled nitric oxide for acute chest syndrome in adult sickle cell patients: a randomized controlled study.

B Maitre, M Djibre, S Katsahian, A Habibi, K Stankovic Stojanovic, M Khellaf, I Bourgeon, F Lionnet, A Charles-Nelson, L Brochard and 5 more

Registry-linked trialAbstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Intensive care medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00748423 (Bicentric Study of the Effect of Inhaled Nitric Oxide Compared to Placebo in Acute Chest Syndrome of Adult Sickle Cell Patients), which is not on this map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
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.

NCT00748423 phase2 / phase3completednot on this map

Bicentric Study of the Effect of Inhaled Nitric Oxide Compared to Placebo in Acute Chest Syndrome of Adult Sickle Cell Patients

TypeinterventionalSponsorAssistance Publique - Hôpitaux de ParisRan2008 to 2012Enrolled100ConditionsSickle Cell Disease, Acute Chest SyndromeArmsNitric Oxide, Placebo
3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 47 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Using disease-modifying therapies in sickle cell disease.Hematology. American Society of Hematology. Education Program · 2023
    Article
  6. Evidence-based obstetric management of women with sickle cell disease in low-income countries.Hematology. American Society of Hematology. Education Program · 2022
    Article
  7. Increasing nitric oxide bioavailability fails to improve collateral vessel formation in humanized sickle cell mice.Laboratory investigation; a journal of technical methods and pathology · 2022
    Article
  8. Nitric oxide: Clinical applications in critically ill patients.Nitric oxide : biology and chemistry · 2022
    Review
  9. Inhaled pulmonary vasodilators: a narrative review.Annals of translational medicine · 2021
    Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. cGMP modulation therapeutics for sickle cell disease.Experimental biology and medicine (Maywood, N.J.) · 2019
    Review
  15. Review
  16. Article
  17. Article
  18. Inhaled nitric oxide.British journal of pharmacology · 2019
    Review
  19. Article
  20. Article
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

15 authors at 7 institutions in 1 country.

B MaitreAP-HP, Hôpitaux Universitaires Henri Mondor, DHU A-TVB, Service de Réanimation Médicale, Créteil, 94010, France. antenne.pneumo@hmn.aphp.fr.
M DjibreAP-HP, Hôpitaux Universitaires de l'Est Parisien, Hôpital Tenon, Pôle Thorax Voies aériennes, Unité de Réanimation Médico-chirurgicale, Paris, France.
S KatsahianUPEC, Faculté de Médecine, Créteil, 94010, France.
A HabibiUPEC, Faculté de Médecine, Créteil, 94010, France.
K Stankovic StojanovicAP-HP, Hôpitaux Universitaires de l'Est Parisien, Hôpital Tenon, Service de Médecine interne, Centre de Référence de la Drépanocytose Adulte, Paris, 75020, France.
M KhellafUPEC, Faculté de Médecine, Créteil, 94010, France.
I BourgeonAP-HP, Hôpitaux Universitaires Henri Mondor, DHU A-TVB, Service de Réanimation Médicale, Créteil, 94010, France.
F LionnetSorbonne Universités UPMC, Paris 06, France.
A Charles-NelsonUPEC, Faculté de Médecine, Créteil, 94010, France.
L BrochardAP-HP, Hôpitaux Universitaires Henri Mondor, DHU A-TVB, Service de Réanimation Médicale, Créteil, 94010, France.
F LemaireAP-HP, Hôpitaux Universitaires Henri Mondor, DHU A-TVB, Service de Réanimation Médicale, Créteil, 94010, France.
F GalacterosUPEC, Faculté de Médecine, Créteil, 94010, France.
C Brun-BuissonAP-HP, Hôpitaux Universitaires Henri Mondor, DHU A-TVB, Service de Réanimation Médicale, Créteil, 94010, France.
M FartoukhUPEC, Faculté de Médecine, GRC CARMAS, Créteil, 94010, France.
A Mekontso DessapAP-HP, Hôpitaux Universitaires Henri Mondor, DHU A-TVB, Service de Réanimation Médicale, Créteil, 94010, France.
Hôpitaux Universitaires Henri-Mondor · FRAssistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Universitaire Henri-Mondor · FRUniversité Paris-Est Créteil · FRHôpital Tenon · FRHôpitaux Universitaires Paris-Ouest · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePrevious clinical trials suggested that inhaled nitric oxide (iNO) could have beneficial effects in sickle cell disease (SCD) patients with acute chest syndrome (ACS).

methodsTo determine whether iNO reduces treatment failure rate in adult patients with ACS, we conducted a prospective, double-blind, randomized, placebo-controlled clinical trial. iNO (80 ppm, N = 50) gas or inhaled nitrogen placebo (N = 50) was delivered for 3 days. The primary end point was the number of patients with treatment failure at day 3, defined as any one of the following: (1) death from any cause, (2) need for endotracheal intubation, (3) decrease of PaO2/FiO2 ≥ 15 mmHg between days 1 and 3, (4) augmented therapy defined as new transfusion or phlebotomy.

resultsThe two groups did not differ in age, gender, genotype, or baseline characteristics and biological parameters. iNO was well tolerated, although a transient decrease in nitric oxide concentration was mandated in one patient. There was no significant difference in the primary end point between the iNO and placebo groups [23 (46 %) and 29 (58 %); odds ratio (OR), 0.8; 95 % CI, 0.54-1.16; p = 0.23]. A post hoc analysis of the 45 patients with hypoxemia showed that those in the iNO group were less likely to experience treatment failure at day 3 [7 (33.3 %) vs 18 (72 %); OR = 0.19; 95 % CI, 0.06-0.68; p = 0.009].

conclusionsiNO did not reduce the rate of treatment failure in adult SCD patients with mild to moderate ACS. Future trials should target more severely ill ACS patients with hypoxemia. CLINICAL

trial registrationNCT00748423.

Indexed as

Acute Chest SyndromeAdministration, InhalationAdultAnemia, Sickle CellDouble-Blind MethodEndothelium-Dependent Relaxing FactorsFemaleHumansMaleNitric OxideProspective StudiesYoung AdultEndothelium-Dependent Relaxing FactorsNitric OxideAcute chest syndromeAcute lung injuryAnemiaHemoglobinopathiesNitric oxideSickle cell

Identifiers

PMID26431718
OpenAlexW2187604395

What OpenQuestion holds

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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.