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March 16, 2026Current Cardiology Reviews0 citations

Real-World Pharmacovigilance Analysis of Drug-Induced DecreasedCardiac Ejection Function: Evidence from the FAERS Database(2004–2024)

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ZWZ. M. WangSCS. R. Wayne ChenGHGuilian He

Key Result

Patients receiving high-risk antineoplastic agents like doxorubicin require periodic echocardiographic monitoring due to the risk of decreased cardiac ejection function.

Key Points

  • To identify risk signals associated with drug-induced decreased cardiac ejection function (DCEF) using the FAERS database.
  • Analysis of data from the FAERS database covering 2004-2024
  • Identification of established and novel DCEF risk signals
  • Examination of onset timing and heterogeneity of risk among various drugs
  • Antineoplastic agents were primarily associated with DCEF risk
  • Highlighted the importance of monitoring left ventricular ejection fraction in high-risk drug users
  • Indicated a need for personalized follow-up strategies depending on the drug's toxicity profile

Structured PICO

Which drugs are associated with risk signals and varying onset timings for decreased cardiac ejection function in the FAERS database?

P
Population
Patients in the FAERS Database (2004–2024) evaluated for drug-induced decreased cardiac ejection function (DCEF)
I
Intervention
Antineoplastic agents and other high-risk drugs (e.g., mitoxantrone, trastuzumab, doxorubicin, pertuzumab)
O
Outcome
Drug-induced decreased cardiac ejection function (DCEF) risk signals and onset timingsafety

Antineoplastic agents are strongly associated with decreased cardiac ejection function, necessitating tailored periodic echocardiographic monitoring based on the specific drug's onset timing.

Abstract

This large-scale real-world analysis identifies both established and novel DCEF risk signals, highlights heterogeneity in onset timing, and emphasizes the predominance of antineoplastic agents. Clinically, these findings suggest the need for periodic echocardiographic monitoring of left ventricular ejection fraction, particularly in patients receiving high-risk drugs such as mitoxantrone, trastuzumab, doxorubicin, and pertuzumab. Early-phase monitoring is crucial for "early-failure" agents, while extended follow-up is warranted for drugs with delayed toxicity, such as doxorubicin. These results provide actionable evidence to support individualized risk management and regulatory label updates. .

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Cite This Study

Wang et al. (2026) studied this question. Patients receiving high-risk antineoplastic agents like doxorubicin require periodic echocardiographic monitoring due to the risk of decreased cardiac ejection function.

synapsesocial.com/papers/69b79e398166e15b153ab435https://doi.org/10.2174/011573403x416240251125055245
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