# The epidemiology and clinical outcomes of ventilator-associated events among 20,769 mechanically ventilated patients at intensive care units: an observational study

**Authors:** Qiao He, Wen Wang, Shichao Zhu, Mingqi Wang, Yan Kang, Rui Zhang, Kang Zou, Zhiyong Zong, Xin Sun

PMC · DOI: 10.1186/s13054-021-03484-x · Critical Care · 2021-02-02

## TL;DR

This study examines ventilator-associated events in ICU patients in China, finding they are common and linked to longer hospital stays and higher mortality.

## Contribution

The study provides the first detailed epidemiology and clinical outcomes of ventilator-associated events in China using a large ICU registry.

## Key findings

- Ventilator-associated events occurred in 16.7 per 1000 ventilator-days, with the highest rate in surgical ICUs.
- Patients with ventilator-associated events had significantly longer hospital stays and over three times higher mortality.
- Infection-related ventilator-associated complications and possible ventilator-associated pneumonia were also strongly associated with poor outcomes.

## Abstract

Ventilator-associated pneumonia (VAP) is the most common hospital-acquired infection (HAI) in intensive care units (ICUs). Ventilator-associated event (VAE), a more objective definition, has replaced traditional VAP surveillance and is now widely used in the USA. However, the adoption outside the USA is limited. This study aims to describe the epidemiology and clinical outcomes of VAEs in China, based on a prospectively maintained registry.

An observational study was conducted using an ICU-HAI registry in west China. Patients that were admitted to ICUs and underwent mechanical ventilation (MV) between April 1, 2015, and December 31, 2018, were included. The characteristics and outcomes were compared between patients with and without VAEs. The rates of all VAEs dependent on different ICUs were calculated, and the pathogen distribution of patients with possible VAP (PVAP) was described.

A total of 20,769 ICU patients received MV, accounting for 21,723 episodes of mechanical ventilators and 112,697 ventilator-days. In all, we identified 1882 episodes of ventilator-associated condition (VAC) events (16.7 per 1000 ventilator-days), 721 episodes of infection-related ventilator-associated complications (IVAC) events (6.4 per 1000 ventilator-days), and 185 episodes of PVAP events (1.64 per 1000 ventilator-days). The rates of VAC varied across ICUs with the highest incidence in surgical ICUs (23.72 per 1000 ventilator-days). The median time from the start of ventilation to the onset of the first VAC, IVAC, and PVAP was 5 (3–8), 5 (3–9), and 6 (4–13) days, respectively. The median length of hospital stays was 28.00 (17.00–43.00), 30.00 (19.00–44.00), and 30.00 (21.00–46.00) days for the three VAE tiers, which were all longer than that of patients without VAEs (16.00 [12.00–23.00]). The hospital mortality among patients with VAEs was more than three times of those with non-VAEs.

VAE was common in ICU patients with ≥ 4 ventilator days. All tiers of VAEs were highly correlated with poor clinical outcomes, including longer ICU and hospital stays and increased risk of mortality. These findings highlight the importance of VAE surveillance and the development of new strategies to prevent VAEs.

## Full-text entities

- **Diseases:** -associated complication (MESH:D008107), malignant tumor (MESH:D009369), IVAC (MESH:D053717), heart diseases (MESH:D006331), Gastrointestinal bleeding (MESH:D006471), Pneumonia (MESH:D011014), Thromboembolism (MESH:D013923), critically ill (MESH:D016638), Hypertension (MESH:D006973), deaths (MESH:D003643), cardiovascular disease (MESH:D002318), ARDS (MESH:D012128), HAI (MESH:D003428), vasculature diseases (MESH:C565633), diabetes (MESH:D003920), II (MESH:C537730), Stress ulcer (MESH:D000079225), Kidney failure (MESH:D051437), lung disease (MESH:D008171), Shock (MESH:D012769), diseases (MESH:D004194), heart failure (MESH:D006333), liver failure (MESH:D017093), respiratory deterioration (MESH:D012131), Infection (MESH:D007239),  (MESH:D055397)
- **Chemicals:** EMV (-), oxygen (MESH:D010100), PVAPs (MESH:C036125)
- **Species:** Homo sapiens (human, species) [taxon 9606], Klebsiella pneumoniae (species) [taxon 573], Pseudomonas aeruginosa (species) [taxon 287], Acinetobacter baumannii (species) [taxon 470]

## Full text

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## Figures

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## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC7851639/full.md

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Source: https://tomesphere.com/paper/PMC7851639