# Early temporary ventricular assist device intervention improves survival in fulminant myocarditis with cardiogenic shock: experience from a single centre and national cohort

**Authors:** Jiun-Yu Lin, Yi-Ting Tsai, Chih-Yuan Lin, Hung-Yen Ke, Jia-Lin Chen, Hsiang-Yu Yang, Wu-Chien Chien, Tsu-Hsuan Weng, Chien-Sung Tsai, Yi-Chang Lin, Po-Shun Hsu

PMC · DOI: 10.3389/fcvm.2026.1727101 · Frontiers in Cardiovascular Medicine · 2026-02-23

## TL;DR

Early use of ventricular assist devices improves survival in patients with severe heart inflammation and heart failure.

## Contribution

Demonstrates that transitioning from ECMO to VAD improves survival in fulminant myocarditis with cardiogenic shock.

## Key findings

- 12 out of 16 patients (75%) survived after VAD implantation following ECPR.
- VAD group had higher 30-day survival (88%) compared to ECMO (52%) in a national cohort.
- High pulmonary artery pressure and inability to wean from epinephrine predicted mortality.

## Abstract

Acute fulminant myocarditis (AFM) complicated by cardiogenic shock (CS) often leads to rapid multi-organ failure. While extracorporeal life support (ECLS) is commonly used as an initial stabilizing measure, mortality remains high, particularly in patients requiring extracorporeal cardiopulmonary resuscitation (ECPR). Temporary ventricular assist devices (VADs) offer superior organ perfusion and more physiological hemodynamics compared to ECLS.

This retrospective study analyzed 16 AFM patients with CS who underwent VAD implantation following ECPR between December 2015 and February 2024. Clinical data, including laboratory profiles, vasopressor use, echocardiographic findings, and neurological status, were assessed. In parallel, survival outcomes from the Taiwan National Health Insurance Research Database (NHIRD) were compared among AFM patients treated with ECMO, VAD, or no mechanical circulatory support (MCS).

Of the 16 patients, 12 survived (75%) and 10 achieved cardiac recovery. Pre-VAD pulmonary artery pressure >40 mmHg and failure to wean from epinephrine by postoperative day 1 were associated with mortality. NHIRD analysis of 1,731 myocarditis patients showed the highest 30-day survival in the VAD group (88%) compared to ECMO (52%) or no MCS (71%; p = 0.003).

AFM with CS often rapidly progresses to multi-organ failure. While ECMO provides initial circulatory support, survival remains poor once initiated. Early transition from ECMO to VAD is critical in improving survival for AFM patients with CS, particularly those receiving ECPR.

## Linked entities

- **Diseases:** cardiogenic shock (MONDO:0800175)

## Full-text entities

- **Genes:** SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** Crash and burn (MESH:C536029), aortic valve injury (MESH:D000082862), hypotension (MESH:D007022), metabolic derangement (MESH:D008659), myocardial injury (MESH:D009202), myocarditis (MESH:D009205), strain (MESH:D013180), LV dysfunction (MESH:D018487), End-organ dysfunction (MESH:D009102), ventricular arrhythmias (MESH:D001145), cardiac arrest (MESH:D006323), pulmonary edema (MESH:D011654), biventricular failure (MESH:D051437), CS (MESH:D012770), diabetes mellitus (MESH:D003920), valvular regurgitation (MESH:D006349), ischemic (MESH:D002545), INTERMACS (MESH:D012769), hepatic or renal impairment (MESH:D008107), LV dilatation (MESH:C565277), inflammatory (MESH:D007249), hyperlipidemia (MESH:D006949), critically ill (MESH:D016638), pulmonary hypertension (MESH:D006976), immune dysregulation (OMIM:614878), AFM (MESH:D009103), VAD (MESH:D009471), cardiac perforation (MESH:D057112), vasoplegia (MESH:D056987), coronary artery disease (MESH:D003324), cardiac deterioration (MESH:D006331), Liver injury (MESH:D017093), acute cardiac failure (MESH:D006333), Renal dysfunction (MESH:D007674), acidosis (MESH:D000138), dilated cardiomyopathy (MESH:D002311), low cardiac output (MESH:D002303), ischemic injury (MESH:D017202), end-organ hypoperfusion (MESH:C564816), brain, liver, and renal dysfunction (MESH:D001927), hypertension (MESH:D006973), Mortality (MESH:D003643), CL (MESH:D002971), pulmonary congestion (MESH:D001261), thrombotic (MESH:D013927)
- **Chemicals:** norepinephrine (MESH:D009638), epinephrine (MESH:D004837), lactate (MESH:D019344), bilirubin (MESH:D001663), oxygen (MESH:D010100), creatinine (MESH:D003404), dopamine (MESH:D004298), Prolene (MESH:D011126), catecholamine (MESH:D002395), dobutamine (MESH:D004280), BiVAD (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12968178/full.md

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Source: https://tomesphere.com/paper/PMC12968178