Evidence map›Paper›PMID 40977939›Full record

ArticleEuropean heart journal. Case reports2025

Platypnoea-orthodeoxia syndrome following transcatheter aortic valve implantation complicated by aortic annular rupture: a case report.

Stuart K Gibson, Arpudh Anandaraj, Christine F McDonald, Anoop N Koshy, Elizabeth Jones

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In one paragraph

Article in European heart journal. Case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

5 authors.

Stuart K GibsonDepartment of Cardiology, Austin Health, 145 Studley Road, Heidelberg, Victoria 3084, Australia.ORCID https://orcid.org/0000-0002-2117-0215
Arpudh AnandarajDepartment of Cardiology, Austin Health, 145 Studley Road, Heidelberg, Victoria 3084, Australia.ORCID https://orcid.org/0000-0003-2853-1105
Christine F McDonaldDepartment of Respiratory and Sleep Medicine, Austin Health, 145 Studley Road, Heidelberg, Victoria 3084, Australia.ORCID https://orcid.org/0000-0001-6481-3391
Anoop N KoshyDepartment of Cardiology, Austin Health, 145 Studley Road, Heidelberg, Victoria 3084, Australia.ORCID https://orcid.org/0000-0002-8741-8631
Elizabeth JonesDepartment of Cardiology, Austin Health, 145 Studley Road, Heidelberg, Victoria 3084, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Platypnoea-orthodeoxia syndrome (POS) is a rare disorder characterized by dyspnoea and hypoxaemia occurring while upright and improving while recumbent, most often caused by inter-atrial shunting. Diagnosis is challenging, and the syndrome carries considerable morbidity if left untreated. In patients with inter-atrial communications such as a patent foramen ovale (PFO), haemodynamic and structural changes occurring after transcatheter aortic valve implantation (TAVI) can lead to platypnoea-orthodeoxia. Case summary: A 77-year-old patient with severe aortic stenosis was referred for TAVI at our institution. On transthoracic echocardiography, dilatation of the ascending aorta (40 mm) and a mobile atrial septal aneurysm (ASA) were noted. Transcatheter aortic valve implantation was complicated by annular rupture and aortic intramural haematoma (IMH), managed conservatively. Three weeks after discharge, the patient re-presented with cholecystitis and underwent cholecystectomy. Post-operatively, marked hypoxaemia was noted during orthostasis. Transthoracic echocardiography showed the ASA bulging into the left atrium, with a strongly positive saline contrast study while upright. A PFO was identified on transoesophageal echocardiography and successfully percutaneously closed, with hypoxaemia resolving. Discussion: Platypnoea-orthodeoxia syndrome is a rare complication of TAVI, not previously reported after annular rupture. Aortic dilatation is often implicated in platypnoea-orthodeoxia, likely by compressing the interatrial septum and potentiating right-to-left shunting. In our patient, with a mildly dilated aorta prior to intervention, annular rupture and IMH may have further distorted atrial anatomy. Furthermore, rapid improvements in left ventricular compliance and left-sided filling pressures after TAVI may have facilitated the new onset of right-to-left shunting. Platypnoea-orthodeoxia syndrome should be considered in patients with unexplained hypoxaemia after TAVI.

Indexed as

Aortic stenosisCase reportPlatypnoea-orthodeoxiaStructural interventionTranscatheter aortic valve implantation

Identifiers

PMID40977939
PMCPMC12448197

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