Chronisch-thromboembolische pulmonale Hypertonie: pulmonale Ballonangioplastie

Jan B. Hinrichs; Karen M. Olsson; Frank K. Wacker; Bernhard C. Meyer

doi:10.1055/a-1269-3761

Gefäßmedizin Scan - Zeitschrift für Angiologie, Gefäßchirurgie, diagnostische und interventionelle Radiologie, Inhaltsverzeichnis

Gefäßmedizin Scan - Zeitschrift für Angiologie, Gefäßchirurgie, diagnostische und interventionelle Radiologie 2021; 8(01): 41-51
DOI: 10.1055/a-1269-3761

CME-Fortbildung

Chronisch-thromboembolische pulmonale Hypertonie: pulmonale Ballonangioplastie

Jan B. Hinrichs

,

Karen M. Olsson

,

Frank K. Wacker

,

Bernhard C. Meyer

Abstract

Als Ursache der CTEPH (chronisch-thromboembolische pulmonale Hypertonie) wird die inkomplette Auflösung thromboembolischen Materials nach Lungenarterienembolien mit konsekutiver Umwandlung in fibröse Gewebsstränge angesehen. Für inoperable CTEPH-Patienten wurde in den letzten Jahren die BPA (perkutane pulmonale Ballonangioplastie) weiterentwickelt. Der Beitrag gibt einen Überblick über Indikationsstellung, Technik und mögliche Komplikationen.

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