# Tracheal Complications Following Prolonged Invasive Ventilation in Tracheostomized Pediatric Patients with Complex Chronic Conditions

**Authors:** Dejan Vlajnic, Deborah Wiesmann, Jens Ortmann, Mandira Reuther, Boris Zernikow

PMC · DOI: 10.3390/children12060769 · Children · 2025-06-13

## TL;DR

This paper reports on four pediatric patients who developed serious tracheal issues after long-term mechanical ventilation, stressing the need for regular monitoring and specialized care.

## Contribution

The study contributes four detailed case reports highlighting tracheal complications in chronically ventilated pediatric patients.

## Key findings

- Prolonged mechanical ventilation in pediatric patients can lead to severe tracheal complications such as obstruction and fistulas.
- Regular endoscopic surveillance is crucial for early detection and management of these complications.
- Specialized care is necessary to prevent life-threatening issues in this vulnerable patient group.

## Abstract

This case series presents four pediatric patients who developed tracheal complications after prolonged invasive mechanical ventilation. The first case involved an 11-year-old girl with severe hypoxic encephalopathy who developed extensive ulcerative granulation tissue obstructing 60% of the tracheal lumen. The second case was that of a 6-year-old boy with ACTA1-related nemaline myopathy who experienced recurrent tracheal obstruction due to granulomatous tissue formation. The third case involved a 9-year-old boy with hydroxyglutaric aciduria and a large plug obstructing his trachea. The last case involved a 19-year-old female with lissencephaly who developed a tracheoesophageal fistula. These cases highlight the importance of regular surveillance and early intervention in managing tracheal complications in pediatric patients with complex chronic conditions requiring long-term mechanical ventilation. The authors emphasize the need for specialized care and routine endoscopic examinations in order to prevent and address potentially life-threatening complications in this vulnerable patient population.

## Linked entities

- **Diseases:** lissencephaly (MONDO:0018838)

## Full-text entities

- **Genes:** ACTA1 (actin alpha 1, skeletal muscle) [NCBI Gene 58] {aka ACTA, ASMA, CFTD, CFTD1, CFTDM, CMYO2A}
- **Diseases:** granulomatous (MESH:D013968), hypoxic encephalopathy (MESH:D002534), lissencephaly (MESH:D054082), tracheal obstruction (MESH:D008476), Tracheal Complications (MESH:D014133), Chronic Conditions (MESH:D002908), nemaline myopathy (MESH:D017696), hydroxyglutaric aciduria (MESH:C535306), tracheoesophageal fistula (MESH:D014138)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12191466/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12191466/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12191466/full.md

---
Source: https://tomesphere.com/paper/PMC12191466