Evidence map›Paper›PMID 32893313›Full record

Trial reportIntensive care medicine2020

Neurally adjusted ventilatory assist in acute respiratory failure: a randomized controlled trial.

Robert M Kacmarek, Jesús Villar, Dácil Parrilla, Francisco Alba, Rosario Solano, Songqiao Liu, Raquel Montiel, Jesús Rico-Feijoo, Anxela Vidal, Carlos Ferrando and 14 more

Open access · bronzeAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Intensive care medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 4 pooled it
4.3field-weighted citation impact, top 4% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 4 syntheses or guidelines pooled it, 52 citations in OpenAlex.

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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

24 authors at 15 institutions in 3 countries.

Robert M KacmarekDepartment of Respiratory Care, Massachusetts General Hospital, 55 Fruit St, Warren 1225, Boston, MA, 01460, USA. rkacmarek@partners.org.
Jesús VillarCIBER de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain. jesus.villar54@gmail.com.ORCID 0000-0001-5687-3562
Dácil ParrillaIntensive Care Unit, Hospital Universitario N.S. de Candelaria, Santa Cruz de Tenerife, Spain.
Francisco AlbaIntensive Care Unit, Hospital N.S. del Prado, Talavera de La Reina, Toledo, Spain.
Rosario SolanoIntensive Care Unit, Hospital Virgen de La Luz, Cuenca, Spain.
Songqiao LiuIntensive Care Unit, Zhongda Hospital, Southeast University, Nanjing, China.
Raquel MontielIntensive Care Unit, Hospital Universitario N.S. de Candelaria, Santa Cruz de Tenerife, Spain.
Jesús Rico-FeijooDepartment of Anesthesia, Hospital Universitario Río Hortega, Valladolid, Spain.
Anxela VidalIntensive Care Unit, Hospital Universitario Fundación Jiménez Díaz, Madrid, Spain.
Carlos FerrandoCIBER de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain.
Isabel MurciaIntensive Care Unit, Complejo Universitario de Albacete, Albacete, Spain.
Ruth CorpasIntensive Care Unit, Hospital N.S. del Prado, Talavera de La Reina, Toledo, Spain.
Elena González-HiguerasIntensive Care Unit, Hospital Virgen de La Luz, Cuenca, Spain.
Qin SunIntensive Care Unit, Zhongda Hospital, Southeast University, Nanjing, China.
César E PinedoIntensive Care Unit, Hospital Universitario N.S. de Candelaria, Santa Cruz de Tenerife, Spain.
David PestañaDepartment of Anesthesia, Hospital Universitario Ramón Y Cajal, IRYCIS, Madrid, Spain.
Domingo MartínezIntensive Care Unit, Hospital Universitario Virgen de Arrixaca, Murcia, Spain.
César AldecoaDepartment of Anesthesia, Hospital Universitario Río Hortega, Valladolid, Spain.
José M AñónCIBER de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain.
Marina SoroDepartment of Anesthesia, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Jesús M González-MartínBiostatistics Division, Research Unit, Universitario Dr. Negrín, Las Palmas, Spain.
Cristina FernándezResearch Unit, Hospital Universitario Dr. Negrín, Barranco de la Ballena s/n, 4th Floor South Wing, 35019, Las Palmas de Gran Canaria, Spain.
Rosa L FernándezCIBER de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain.
NAVa In Acute respiraTORy failure (NAVIATOR) Network
Hospital Universitario La Paz · ESHospital Universitario Nuestra Señora de Candelaria · ESInstituto de Salud Carlos III · ESHospital Universitario Río Hortega · ESHospital Universitario de Gran Canaria Doctor Negrín · ESHospital Virgen de la Luz · ESZhongda Hospital Southeast University · CNBoston University · USComplejo Hospitalario Universitario de Albacete · ESHospital General Nuestra Señora del Prado · ESHospital Universitario Fundación Jiménez Díaz · ESHospital Universitario Virgen de la Arrixaca · ESInstituto Ramón y Cajal de Investigación Sanitaria · ESHospital Clínico Universitario de Valencia · ESMass General Brigham · US

Funding

Instituto de Salud Carlos III CB06/06/1088Instituto de Salud Carlos III PI13/0119Instituto de Salud Carlos III PI16/0049
6 · The paper itself

Abstract

purposeWe hypothesized that neurally adjusted ventilatory assist (NAVA) compared to conventional lung-protective mechanical ventilation (MV) decreases duration of MV and mortality in patients with acute respiratory failure (ARF).

methodsWe carried out a multicenter, randomized, controlled trial in patients with ARF from several etiologies. Intubated patients ventilated for ≤ 5 days expected to require MV for ≥ 72 h and able to breathe spontaneously were eligible for enrollment. Eligible patients were randomly assigned based on balanced treatment assignments with a computerized randomization allocation sequence to two ventilatory strategies: (1) lung-protective MV (control group), and (2) lung-protective MV with NAVA (NAVA group). Allocation concealment was maintained at all sites during the trial. Primary outcome was the number of ventilator-free days (VFDs) at 28 days. Secondary outcome was all-cause hospital mortality. All analyses were done according to the intention-to-treat principle.

resultsBetween March 2014 and October 2019, we enrolled 306 patients and randomly assigned 153 patients to the NAVA group and 153 to the control group. Median VFDs were higher in the NAVA than in the control group (22 vs. 18 days; between-group difference 4 days; 95% confidence interval [CI] 0 to 8 days; p = 0.016). At hospital discharge, 39 (25.5%) patients in the NAVA group and 47 (30.7%) patients in the control group had died (between-group difference - 5.2%, 95% CI - 15.2 to 4.8, p = 0.31). Other clinical, physiological or safety outcomes did not differ significantly between the trial groups.

conclusionNAVA decreased duration of MV although it did not improve survival in ventilated patients with ARF.

Indexed as

Interactive Ventilatory SupportRespiratory Distress SyndromeRespiratory InsufficiencyHumansRespiration, ArtificialVentilators, MechanicalAcute respiratory failureIntensive care unitLung-protective ventilationMortalityNeurally adjusted ventilatory assistVentilator-free days

Identifiers

PMID32893313
PMCPMC7474954
OpenAlexW3083155939

What OpenQuestion holds

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Registered trials

None linked

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.