# Platypnea-Orthodeoxia Syndrome in Relation to Severe SARS-CoV-2 Infection

**Authors:** Teresa Valido, Ana Carolina Chumbo, Filipa Figueiredo, Teresa Cruz

PMC · DOI: 10.7759/cureus.79682 · Cureus · 2025-02-26

## TL;DR

A 90-year-old man with severe SARS-CoV-2 infection developed platypnea-orthodeoxia syndrome, likely due to lung fibrosis causing a physiological shunt.

## Contribution

This case highlights a potential underdiagnosed complication of SARS-CoV-2 infection: secondary POS due to fibrotic lung changes.

## Key findings

- A 90-year-old man with SARS-CoV-2 infection developed persistent dyspnea and orthodeoxia during convalescence.
- CT scans showed fibrotic lung changes, and secondary POS was presumed after ruling out intracardiac and intrapulmonary shunts.
- The condition resolved after a month of rehabilitation, suggesting a link between SARS-CoV-2 fibrotic sequelae and physiological shunts.

## Abstract

Platypnea-orthodeoxia syndrome (POS) is characterized by dyspnea and oxygen desaturation in the upright position, caused by arteriovenous shunts (intracardiac, intrapulmonary, or physiological). In recent years, POS has been described in patients with SARS-CoV-2 infection, in both acute and rehabilitation phases. This case describes a 90-year-old man who presented to the emergency department with a dry cough and dyspnea and was diagnosed with severe SARS-CoV-2 infection. He underwent non-invasive ventilation for refractory hypoxemia. During convalescence, CT scans revealed fibrotic changes predominantly in the lung bases. He experienced persistent dyspnea and oxygen desaturation upon standing. Blood gas analysis confirmed orthodeoxia. After ruling out intracardiac and intrapulmonary shunts, secondary POS due to SARS-CoV-2 infection was presumed. He continued rehabilitation with progressive improvement, resolving the condition a month after discharge. This phenomenon, likely induced by fibrotic sequelae of SARS-CoV-2 in the lung bases causing a physiological shunt, highlights a potentially underdiagnosed complication of interstitial lung diseases.

## Full-text entities

- **Diseases:** POS (MESH:D000092129), interstitial lung diseases (MESH:D017563), SARS-CoV-2 Infection (MESH:D000086382), dyspnea (MESH:D004417), dry cough (MESH:D003371), hypoxemia (MESH:D000860)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## Figures

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## References

9 references — full list in the complete paper: https://tomesphere.com/paper/PMC11954430/full.md

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Source: https://tomesphere.com/paper/PMC11954430