# Mortality in children with fulminant myocarditis: a six-year multicenter retrospective study

**Authors:** Lijun Yang, Wenting Zhao, Xuming Mo, Yucai Zhang, Jie Wang, Yanqin Cui, Zhenhua Liang, Yuxiong Guo, Wei Wang, Zhigang Liu, Daqing Ma, Ru Lin, Qiang Shu

PMC · DOI: 10.1016/j.aicoj.2026.100030 · Annals of Intensive Care · 2026-01-23

## TL;DR

This study identifies early warning signs of death in children with severe heart inflammation, helping doctors decide on urgent treatments.

## Contribution

The study introduces a combined model using lactate, CK-MB, and ventricular tachycardia to predict mortality in pediatric fulminant myocarditis.

## Key findings

- Peak lactate and CK-MB are independent predictors of in-hospital mortality in pediatric FM.
- A composite model of CK-MB, peak lactate, and ventricular tachycardia achieved the best predictive performance (AUC 0.815).
- Elevated lactate 12 hours after advanced support increases mortality risk (OR 1.219).

## Abstract

Fulminant myocarditis (FM) in children can progress rapidly to cardiogenic shock, with high risk of mortality. Early recognition of prognostic markers is critical to guide timely escalation of circulatory support. This multicenter study sought to characterize clinical features and identify early predictors of in-hospital mortality in pediatric FM.

We conducted a retrospective cohort study of patients <18 years with FM admitted to eight ECMO-capable pediatric intensive care units between January 2018 and August 2023. Clinical, biochemical, electrocardiographic, and echocardiographic variables were analyzed. Logistic regression was used to identify predictors of mortality, and receiver operating characteristic (ROC) curves were generated to assess discriminatory performance.

A total of 187 children were included; 157 (84.0%) required ECMO. In-hospital mortality was 16.6% (31/187). Univariate analysis identified elevated CK-MB, higher peak lactate, and ventricular tachycardia as associated with mortality. In multivariate analysis, peak lactate (AUC 0.791) and CK-MB (AUC 0.774) remained independent predictors. A combined model of peak lactate and ventricular tachycardia demonstrated moderate discrimination (AUC 0.772), whereas a composite model incorporating CK-MB, peak lactate, and ventricular tachycardia achieved the best predictive performance (AUC 0.815). Elevated lactate measured 12 h after initiation of extracorporeal membrane oxygenation or intensive conventional therapy further increased mortality risk (OR 1.219, 95% CI 1.004–1.481).

Peak lactate, CK-MB, and ventricular tachycardia are early independent predictors of in-hospital mortality in pediatric FM. Persistent hyperlactatemia within 12 h of advanced support provides additional prognostic value and may assist clinicians in early risk stratification.

## Linked entities

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

## Full-text entities

- **Genes:** TNNT2 (troponin T2, cardiac type) [NCBI Gene 7139] {aka CMD1D, CMH2, CMPD2, LVNC6, RCM3, TnTC}, NPPB (natriuretic peptide B) [NCBI Gene 4879] {aka BNP, Iso-ANP}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, TNNI3 (troponin I3, cardiac type) [NCBI Gene 7137] {aka CMD1FF, CMD2A, CMH7, RCM1, TNNC1, cTnI}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, TNNT1 (troponin T1, slow skeletal type) [NCBI Gene 7138] {aka ANM, NEM5, STNT, TNT, TNTS}
- **Diseases:** electrocardiographic (MESH:C566733), extremity injuries (MESH:D014947), circulatory collapse (MESH:D012769), inflammatory (MESH:D007249), cerebral complications (MESH:D008107), critical illness (MESH:D016638), Pulmonary edema (MESH:D011654), cardiac arrest (MESH:D006323), abdominal pain (MESH:D015746), anuria (MESH:D001002), myocardial edema (MESH:D004487), neurological complications (MESH:D002493), Renal failure (MESH:D051437), cardiogenic shock (MESH:D012770), dyspnea (MESH:D004417), oliguria (MESH:D009846), Pulmonary Diseases (MESH:D008171), myocardial damage (MESH:D009202), chest pain (MESH:D002637), fatigue (MESH:D005221), stroke (MESH:D020521), acute kidney injury (MESH:D058186), FM (MESH:D009205), pneumonia (MESH:D011014), sudden cardiac death (MESH:D016757), left ventricular dysfunction (MESH:D018487), intracranial hemorrhage (MESH:D020300), brain death (MESH:D001926), arrhythmia (MESH:D001145), end-organ failure (MESH:D009102), autoimmune (MESH:D001327), pulmonary infiltrates (MESH:D017254), pericardial effusion (MESH:D010490), vomiting (MESH:D014839), neurological (MESH:D009461), ischemia (MESH:D007511), convulsions (MESH:D012640), fever (MESH:D005334), altered consciousness (MESH:D003244), neurological injury (MESH:D020196), encephalopathy (MESH:D001927), Mortality (MESH:D003643), CRRT (MESH:D014202), hypokinesia (MESH:D018476), respiratory symptoms (MESH:D012818), acute liver failure7 (MESH:D017114), cardiac rhythm disturbances (MESH:D020178), congenital heart disease (MESH:D006330), AV block (MESH:D054537), metabolic acidosis (MESH:D000138), dizziness (MESH:D004244), sudden death (MESH:D003645), myocardial infarction (MESH:D009203), uremic complications (MESH:D006463), cardiovascular (MESH:D002318), infection (MESH:D007239), gastrointestinal (MESH:D005767), low cardiac output (MESH:D002303), cerebral infarction (MESH:D002544), hyperammonemia (MESH:D022124)
- **Chemicals:** oxygen (MESH:D010100), Epinephrine (MESH:D004837), Lactate (MESH:D019344), bilirubin (MESH:D001663), noradrenaline (MESH:D009638), dobutamine (MESH:D004280), DM (-), creatinine (MESH:D003404), Dopamine (MESH:D004298), milrinone (MESH:D020105)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12934420/full.md

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Source: https://tomesphere.com/paper/PMC12934420