Evidence map›Paper›PMID 40214890›Full record

Trial reportNeurocritical care2025

Safety and Efficacy of a Novel Automated Intelligent Suction Device (VapCare) Among Mechanically Ventilated Neurocritical Care Patients: A Prospective Randomized Trial.

M S Varnitha, P Murlidhara, Archana Sharma, V Sudhir, Shwetha S Naik, Dhritiman Chakrabarti

Abstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Neurocritical care, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

M S VarnithaDepartment of Neuroanesthesia and Neurocritical Care, Apollo Hospitals, Bengaluru, India.
P MurlidharaDepartment of Oncoanesthesia, All India Institute of Medical Sciences, New Delhi, India.
Archana SharmaDepartment of Neuroanesthesia and Neurocritical Care, National Institute of Mental Health and Neurosciences, III Floor, Faculty Building, Bengaluru, 560029, India. drarchana7anesthesia@gmail.com.ORCID 0009-0007-3105-0640
V SudhirDepartment of Neuroanesthesia and Neurocritical Care, National Institute of Mental Health and Neurosciences, III Floor, Faculty Building, Bengaluru, 560029, India.
Shwetha S NaikDepartment of Neuroanesthesia and Neurocritical Care, National Institute of Mental Health and Neurosciences, III Floor, Faculty Building, Bengaluru, 560029, India.
Dhritiman ChakrabartiDepartment of Neuroanesthesia and Neurocritical Care, National Institute of Mental Health and Neurosciences, III Floor, Faculty Building, Bengaluru, 560029, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVentilator-associated pneumonia (VAP) is a significant concern in intensive care units (ICUs), affecting 7-32% of mechanically ventilated patients, which mounts to higher morbidity and mortality and extended hospital stays. Preventing VAP involves meticulous secretion management and oral hygiene, but in low-resource settings, VAP remains common owing to the absence of standardized oral care protocols. This randomized study assessed the efficacy and safety of the VapCare automated secretion management device in reducing microaspirations and improving clinical outcomes in ventilated patients.

methodsA single-center, open-label randomized trial was conducted involving adult neurocritical care patients requiring mechanical ventilation for 48 h or more, excluding tracheostomized patients and patients with bleeding disorders, difficult airways, or preexisting pneumonia. Participants were randomly assigned to a control group, receiving standard ICU care with manual oropharyngeal suctioning, or a study group, receiving VapCare management. We compared lung ultrasound scores (LUS), clinical pulmonary infection scores (CPIS), secretion volumes, tracheal cultures, and chest X-ray results from day 1 to day 5.

resultsThe VapCare group demonstrated a slower rise in LUS and CPIS compared to the control group. The median CPIS rose from 1 (interquartile range [IQR] 1-2) on the first day to 5 (IQR 2.75-6) on the fifth day in the control group versus 1 (IQR 0-2) on the first day to 3 (IQR 2-3) on the fifth day in the VapCare group (p < 0.001). The median LUS increased from 0 (IQR 0-2) on the first day to 6 (IQR 2-10) on the fifth in the control group, whereas the change was more muted in the VapCare group (0 [IQR 1-2] on the first day to 4 [IQR 2-6] on the fifth day [p < 0.001]). Additionally, chest X-ray scores were lower in the VapCare group (p = 0.028). Tracheal culture microbial growth and mortality were similar in both groups, but the length of ICU stay was significantly shorter in the VapCare group (p = 0.004). One patient in the VapCare group sustained mucosal erosions on the lip due to the VapCare mouthpiece.

conclusionsThe VapCare device effectively reduces microaspiration and mitigates lung changes, demonstrating its potential to reduce the burden of microaspiration and suctioning in ventilated patients.

Indexed as

Critical CarePneumonia, Ventilator-AssociatedRespiration, ArtificialAdultAgedFemaleHumansIntensive Care UnitsMaleMiddle AgedProspective StudiesSuctionClinical pulmonary infection scoreLung ultrasound scoreNeurocritical careSubglottic secretion drainageVapCare suction deviceVentilator-associated pneumonia

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Registered trials

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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.