# Platypnea-Orthodeoxia Syndrome and COVID-19 Successfully Treated With Percutaneous Patent Foramen Ovale Closure: A Report of Two Cases and Literature Review

**Authors:** Fernando Jiménez-Segovia, Sara Luis-García, Candela González-San Narciso, Pablo Demelo-Rodríguez, Rita García-Martínez, Francisco Galeano-Valle

PMC · DOI: 10.7759/cureus.56655 · Cureus · 2024-03-21

## TL;DR

Two patients with severe COVID-19 and a rare breathing condition were successfully treated by closing a heart defect called patent foramen ovale.

## Contribution

This is the first report of successful PFO closure during acute COVID-19 in patients with platypnea-orthodeoxia syndrome.

## Key findings

- PFO closure resolved platypnea-orthodeoxia syndrome in two patients with severe COVID-19.
- Bubble echocardiography confirmed PFO with significant shunting in both cases.
- PFO closure during acute COVID-19 was safe and effective in these patients.

## Abstract

Platypnea-orthodeoxia syndrome (POS) is a rare clinical condition characterized by positional dyspnea and/or hypoxia. We report two cases of patients with COVID-19 bronchopneumonia with a torpid evolution. Due to clinical suspicion of POS, a diagnostic workup was performed, including a bubble echocardiography, which revealed a patent foramen ovale (PFO) with early and massive passage of bubbles to the left cavities. Both patients underwent percutaneous PFO closure with a resolution of POS. Here, we present the second and third cases of POS associated with PFO successfully closed during the acute phase of COVID-19. This suggests that PFO closure could be a potential treatment option for this condition.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096), bronchopneumonia (MONDO:0005682)

## Full-text entities

- **Diseases:** hypoxia (MESH:D000860), PFO (MESH:D054092), dyspnea (MESH:D004417), COVID-19 (MESH:D000086382), POS (MESH:D000092129)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11032186/full.md

## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC11032186/full.md

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Source: https://tomesphere.com/paper/PMC11032186