Evidence map›Paper›PMID 42734655›Full record

ArticleMedizinische Klinik, Intensivmedizin und Notfallmedizin2026

[Left ventricular assist devices in emergency medicine : Case-based analysis for emergency medical services and emergency departments].

Mark-Alexander Solf, R Tomasi, C-E Kamla, J Kreuzer, M Feuerecker, P Scheiermann, D-J Höchter, T Schumann, C Müller

Abstract readEnglish Abstract
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In one paragraph

Article in Medizinische Klinik, Intensivmedizin und Notfallmedizin, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

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

9 authors.

Mark-Alexander SolfKlinik für Anaesthesiologie, LMU Klinikum, Ludwig-Maximilians-Universität München, Marchioninistraße 15, 81377, München, Deutschland. markalexander.solf@med.uni-muenchen.de.ORCID http://orcid.org/0009-0002-7246-3357
R TomasiKlinik für Anaesthesiologie, LMU Klinikum, Ludwig-Maximilians-Universität München, Marchioninistraße 15, 81377, München, Deutschland.
C-E KamlaKlinik und Poliklinik für Herzchirurgie, LMU Klinikum, Ludwig-Maximilians-Universität München, München, Deutschland.
J KreuzerKlinik für Anästhesiologie und operative Intensivmedizin, Klinikum Amberg, Amberg, Deutschland.
M FeuereckerKlinik für Anaesthesiologie, LMU Klinikum, Ludwig-Maximilians-Universität München, Marchioninistraße 15, 81377, München, Deutschland.
P ScheiermannKlinik für Anaesthesiologie, LMU Klinikum, Ludwig-Maximilians-Universität München, Marchioninistraße 15, 81377, München, Deutschland.
D-J HöchterKlinik für Anaesthesiologie, LMU Klinikum, Ludwig-Maximilians-Universität München, Marchioninistraße 15, 81377, München, Deutschland.
T SchumannDRF Stiftung Luftrettung gemeinnützige GmbH, Station München, München, Deutschland.
C MüllerKlinik und Poliklinik für Herzchirurgie, LMU Klinikum, Ludwig-Maximilians-Universität München, München, Deutschland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLeft ventricular assist devices (LVAD) are an established treatment for advanced heart failure. Due to the continuous flow, pulse palpation, noninvasive blood pressure measurement and pulse oximetry are often unreliable in acute care.

objectiveCase-based analysis of the acute care of patients with left ventricular assist devices in emergency medical services and emergency departments, exemplified by a patient supported with HeartMate 3® and derivation of practical recommendations for action. MATERIAL AND

methodsAnonymized prehospital and clinical documentation of a 67-year-old female patient was evaluated. Monitoring, clinical assessment, device and power supply checks, pump parameters, diagnostics and triage were analyzed using consensus documents, reviews, registry data and manufacturer's data.

resultsIn this study three key problem areas emerged: unreliable standard monitoring, initial misclassification as technical device failure and necessary contextual interpretation of pump parameters. Prehospital findings included dyspnea, cyanosis, impaired consciousness and inability to obtain blood pressure or oxygen saturation values. The later device readout showed stable parameters without acute pump malfunction. The underlying cause was severe Staphylococcus aureus bacteremia with renal replacement therapy-dependent renal failure.

conclusionSevere clinical deterioration in LVAD patients is not necessarily pump-related. Key elements are perfusion assessment, device and power supply checks, interpretation of pump parameters, extended diagnostics and early consultation with an LVAD center.

Indexed as

Emergency departmentEmergency medical servicesHeart failureShockVentricular assist devices

Identifiers

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.