Initial experience with telemonitoring in left ventricular assist device patients.

Left ventricular assist device (LVAD) device thrombosis heart failure hypovolemia telemonitoring

Journal

Journal of thoracic disease
ISSN: 2072-1439
Titre abrégé: J Thorac Dis
Pays: China
ID NLM: 101533916

Informations de publication

Date de publication:
Apr 2019
Historique:
entrez: 12 6 2019
pubmed: 12 6 2019
medline: 12 6 2019
Statut: ppublish

Résumé

Left ventricular assist devices (LVAD) are increasingly used in patients with end stage heart failure. The HeartAssist 5 and aVAD LVADs offer telemetric monitoring capabilities. Here we report our initial single centre experience with the largest telemonitoring cohort of LVAD patients. Eleven patients (9 males) received a telemonitoring-capable LVAD and were included in our telemonitoring cohort. Waveforms and alarm data were obtained from the telemonitoring system and hospital records were reviewed for clinical data. Mean age at LVAD implantation was 59±5.1 years (mean ± standard deviation). Seven patients had non-ischemic cardiomyopathy and 4 patients had ischemic cardiomyopathy. Median LVEF at implant was 16% (IQR, 15-20%). The total follow-up time was 2,438 patient-days. A total of 6,216 alarm messages were generated in 11 patients. Most common were low flow alarms due to hypovolemia, followed by low flow alarms because of suspected pump thrombosis. One patient died during follow-up, one received a cardiac transplant and one had the LVAD explanted because of pump thrombosis. Pump thrombosis was suspected in 5 patients with 8 episodes of sudden flow decreases and laboratory signs of haemolysis. Real-time telemonitoring of LVAD pump flow, motor speed and power consumption is a promising tool in the follow-up of LVAD recipients. Trending pump flow over hours or days can assist in the early detection of complications, especially flow reductions due to hypovolemia and LVAD thrombosis. Further studies are warranted to delineate the impact of remote monitoring on patients' prognosis.

Sections du résumé

BACKGROUND BACKGROUND
Left ventricular assist devices (LVAD) are increasingly used in patients with end stage heart failure. The HeartAssist 5 and aVAD LVADs offer telemetric monitoring capabilities. Here we report our initial single centre experience with the largest telemonitoring cohort of LVAD patients.
METHODS METHODS
Eleven patients (9 males) received a telemonitoring-capable LVAD and were included in our telemonitoring cohort. Waveforms and alarm data were obtained from the telemonitoring system and hospital records were reviewed for clinical data.
RESULTS RESULTS
Mean age at LVAD implantation was 59±5.1 years (mean ± standard deviation). Seven patients had non-ischemic cardiomyopathy and 4 patients had ischemic cardiomyopathy. Median LVEF at implant was 16% (IQR, 15-20%). The total follow-up time was 2,438 patient-days. A total of 6,216 alarm messages were generated in 11 patients. Most common were low flow alarms due to hypovolemia, followed by low flow alarms because of suspected pump thrombosis. One patient died during follow-up, one received a cardiac transplant and one had the LVAD explanted because of pump thrombosis. Pump thrombosis was suspected in 5 patients with 8 episodes of sudden flow decreases and laboratory signs of haemolysis.
CONCLUSIONS CONCLUSIONS
Real-time telemonitoring of LVAD pump flow, motor speed and power consumption is a promising tool in the follow-up of LVAD recipients. Trending pump flow over hours or days can assist in the early detection of complications, especially flow reductions due to hypovolemia and LVAD thrombosis. Further studies are warranted to delineate the impact of remote monitoring on patients' prognosis.

Identifiants

pubmed: 31183165
doi: 10.21037/jtd.2018.10.37
pii: jtd-11-S6-S853
pmc: PMC6535490
doi:

Types de publication

Journal Article

Langues

eng

Pagination

S853-S863

Déclaration de conflit d'intérêts

Conflicts of Interest: B Lynch is an employee of Reliant Heart Inc., Houston, Texas. The other authors have no conflicts of interest to declare.

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Auteurs

Stephan Hohmann (S)

Department of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.

Christian Veltmann (C)

Department of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.

David Duncker (D)

Department of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.

Thorben König (T)

Department of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.

Dominik Berliner (D)

Department of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.

Jasmin Hanke (J)

Department of Cardiothoracic, Transplantation and Vascular Surgery, Hannover Medical School, Hannover, Germany.

Günes Dogan (G)

Department of Cardiothoracic, Transplantation and Vascular Surgery, Hannover Medical School, Hannover, Germany.

Anamika Chatterjee (A)

Department of Cardiothoracic, Transplantation and Vascular Surgery, Hannover Medical School, Hannover, Germany.

Christina Feldmann (C)

Department of Cardiothoracic, Transplantation and Vascular Surgery, Hannover Medical School, Hannover, Germany.

Bryan Lynch (B)

Reliant Heart Inc., Houston, TX, USA.

Daniel Burkhoff (D)

Presbyterian Hospital, Columbia University, New York City, NY, USA.

Axel Haverich (A)

Department of Cardiothoracic, Transplantation and Vascular Surgery, Hannover Medical School, Hannover, Germany.

Johann Bauersachs (J)

Department of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.

Jan D Schmitto (JD)

Department of Cardiothoracic, Transplantation and Vascular Surgery, Hannover Medical School, Hannover, Germany.

Classifications MeSH