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A case of destination therapy for post-fulminant myocarditis with myelodysplastic syndrome.
Nakamura, Makiko; Imamura, Teruhiko; Hida, Yuki; Izumida, Toshihide; Nakagaito, Masaki; Nagura, Saori; Doi, Toshio; Fukahara, Kazuaki; Kinugawa, Koichiro.
Affiliation
  • Nakamura M; The Second Department of Internal Medicine, University of Toyama, 2630 Sugitani, Toyama, Toyama, 930-0194, Japan.
  • Imamura T; The Second Department of Internal Medicine, University of Toyama, 2630 Sugitani, Toyama, Toyama, 930-0194, Japan. teimamu@med.u-toyama.ac.jp.
  • Hida Y; The Second Department of Internal Medicine, University of Toyama, 2630 Sugitani, Toyama, Toyama, 930-0194, Japan.
  • Izumida T; The Second Department of Internal Medicine, University of Toyama, 2630 Sugitani, Toyama, Toyama, 930-0194, Japan.
  • Nakagaito M; The Second Department of Internal Medicine, University of Toyama, 2630 Sugitani, Toyama, Toyama, 930-0194, Japan.
  • Nagura S; Department of Cardiovascular Surgery, University of Toyama, Toyama, Toyama, Japan.
  • Doi T; Department of Cardiovascular Surgery, University of Toyama, Toyama, Toyama, Japan.
  • Fukahara K; Department of Cardiovascular Surgery, University of Toyama, Toyama, Toyama, Japan.
  • Kinugawa K; The Second Department of Internal Medicine, University of Toyama, 2630 Sugitani, Toyama, Toyama, 930-0194, Japan.
J Artif Organs ; 2024 Jun 11.
Article in En | MEDLINE | ID: mdl-38862744
ABSTRACT
We encountered a 64-year-old woman who experienced fulminant myocarditis and underwent treatment with veno-arterial extracorporeal membrane oxygenation and Impella CP support. Subsequently, she underwent a device upgrade to Impella 5.5 and received continuous hemodiafiltration for 3 months. During mechanical circulatory support, she developed refractory anemia and thrombocytopenia, leading to a diagnosis of myelodysplastic syndrome. Following the removal of the devices, she no longer required blood transfusions. She received HeartMate 3 left ventricular assist device implantation as a destination therapy indication despite the presence of myelodysplastic syndrome. She was successfully managed by aspirin-free antithrombotic therapy without any hemocompatibility-related adverse events for 4 months after index discharge on foot. We present a patient with a unique and rare presentation, wherein HeartMate 3 was implanted and successfully managed without aspirin to prevent bleeding complications associated with myelodysplastic syndrome.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Artif Organs Journal subject: ENGENHARIA BIOMEDICA Year: 2024 Document type: Article Affiliation country: Japan Country of publication: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Artif Organs Journal subject: ENGENHARIA BIOMEDICA Year: 2024 Document type: Article Affiliation country: Japan Country of publication: Japan