Evidence map›Paper›PMID 24103805›Full record

ArticleCritical care (London, England)2013

Biphasic positive airway pressure minimizes biological impact on lung tissue in mild acute lung injury independent of etiology.

Felipe Saddy, Lillian Moraes, Cintia Lourenço Santos, Gisele Pena Oliveira, Fernanda Ferreira Cruz, Marcelo Marcos Morales, Vera Luiza Capelozzi, Marcelo Gama de Abreu, Cristiane Souza Nascimento Baez Garcia, Paolo Pelosi and 1 more

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Critical care (London, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.4field-weighted citation impact, top 11% 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.

NCT06755320 nanot yet recruitingnot on this mapstarted 2024, after this paper: background citation

Comparative Study Between Airway Pressure Release Ventilation and Bi-level Positive Airway Pressure Ventilation in Acute Respiratory Distress Syndrome

TypeinterventionalSponsorAin Shams UniversityRan2024 to 2025Enrolled50ConditionsARDS: Acute Respiratory Distress Syndrome, ARDSArmsmechanical ventilation (MV)
NCT06912906 nanot yet recruitingnot on this mapstarted 2025, after this paper: background citation

Comparison of Two Strategies to Allow Mechanical Ventilation Separation Using Biphasic Airway Pressure Ventilation Without Any Synchronization (BIPAP) or Pressure Support Ventilation (PSV): a Randomized Feasibility Trial

TypeinterventionalSponsorUniversity of Lausanne HospitalsRan2025 to 2027Enrolled84ConditionsMechanical Ventilation WeaningArmsBIPAPasynchro: byphaisc positive pressure modality without any synchronisation
3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Comparison of Local and Systemic Inflammation During Invasive Versus Noninvasive Ventilation in Rats.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2022
    Article
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  7. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 3 countries.

Felipe Saddy
Lillian Moraes
Cintia Lourenço Santos
Gisele Pena Oliveira
Fernanda Ferreira Cruz
Marcelo Marcos Morales
Vera Luiza Capelozzi
Marcelo Gama de Abreu
Cristiane Souza Nascimento Baez Garcia
Paolo Pelosi
Patricia Rieken Macêdo Rocco
Universidade Federal do Rio de Janeiro · BRFundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro · BRUniversidade de São Paulo · BROspedale Policlinico San Martino · ITRio de Janeiro Federal Institute of Education, Science and Technology · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionBiphasic positive airway pressure (BIVENT) is a partial support mode that employs pressure-controlled, time-cycled ventilation set at two levels of continuous positive airway pressure with unrestricted spontaneous breathing. BIVENT can modulate inspiratory effort by modifying the frequency of controlled breaths. Nevertheless, the optimal amount of inspiratory effort to improve respiratory function while minimizing ventilator-associated lung injury during partial ventilatory assistance has not been determined. Furthermore, it is unclear whether the effects of partial ventilatory support depend on acute lung injury (ALI) etiology. This study aimed to investigate the impact of spontaneous and time-cycled control breaths during BIVENT on the lung and diaphragm in experimental pulmonary (p) and extrapulmonary (exp) ALI.

methodsThis was a prospective, randomized, controlled experimental study of 60 adult male Wistar rats. Mild ALI was induced by Escherichia coli lipopolysaccharide either intratracheally (ALI(p)) or intraperitoneally (ALI(exp)). After 24 hours, animals were anesthetized and further randomized as follows: (1) pressure-controlled ventilation (PCV) with tidal volume (V(t)) = 6 ml/kg, respiratory rate = 100 breaths/min, PEEP = 5 cmH2O, and inspiratory-to-expiratory ratio (I:E) = 1:2; or (2) BIVENT with three spontaneous and time-cycled control breath modes (100, 75, and 50 breaths/min). BIVENT was set with two levels of CPAP (P(high) = 10 cmH2O and P(low) = 5 cmH2O). Inspiratory time was kept constant (T(high) = 0.3 s).

resultsBIVENT was associated with reduced markers of inflammation, apoptosis, fibrogenesis, and epithelial and endothelial cell damage in lung tissue in both ALI models when compared to PCV. The inspiratory effort during spontaneous breaths increased during BIVENT-50 in both ALI models. In ALI(p), alveolar collapse was higher in BIVENT-100 than PCV, but decreased during BIVENT-50, and diaphragmatic injury was lower during BIVENT-50 compared to PCV and BIVENT-100. In ALI(exp), alveolar collapse during BIVENT-100 and BIVENT-75 was comparable to PCV, while decreasing with BIVENT-50, and diaphragmatic injury increased during BIVENT-50.

conclusionsIn mild ALI, BIVENT had a lower biological impact on lung tissue compared to PCV. In contrast, the response of atelectasis and diaphragmatic injury to BIVENT differed according to the rate of spontaneous/controlled breaths and ALI etiology.

Indexed as

Acute Lung InjuryAnimalsApoptosisBiomarkersBrazilDisease Models, AnimalEndotheliumEpitheliumFibrosisInhalationIntermittent Positive-Pressure VentilationLungMaleProspective StudiesRatsRats, WistarBiomarkers

Identifiers

PMID24103805
PMCPMC4057608
OpenAlexW2107447236

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.