# Dilated Cardiomyopathy, De Novo Heart Failure, and Cardiogenic Shock With End-Organ Failure in a Patient With No Cardiac History Following a Trial of Amitriptyline

**Authors:** Zachary S Kauffman, Melaku Demede

PMC · DOI: 10.7759/cureus.67374 · Cureus · 2024-08-21

## TL;DR

A 69-year-old woman developed severe heart failure and organ damage after taking amitriptyline, despite having no prior heart issues.

## Contribution

Highlights a rare case linking amitriptyline use to acute cardiomyopathy and multi-organ failure.

## Key findings

- Patient developed dilated cardiomyopathy and heart failure after amitriptyline use.
- End-organ dysfunction included severely elevated liver enzymes and reduced kidney function.
- Cardiac MRI confirmed an ejection fraction of 14% with non-obstructive coronary disease.

## Abstract

A 69-year-old female with no cardiac history presented with dilated cardiomyopathy and de novo congestive heart failure, with an ejection fraction of less than 20%. This patient had struggled over the prior six weeks with exacerbation of chronic obstructive pulmonary disease complicated by pneumonia and as such had taken several trials of antibiotics. Four days prior to her presentation, she was prescribed amitriptyline by her primary care physician to help with sleep. Two days after the presentation, she developed cardiogenic shock secondary to acutely decompensated heart failure. End-organ dysfunction presented as aspartate aminotransferase (AST) and alanine aminotransferase (ALT) of greater than 1000 U/L and a glomerular filtration rate (GFR) as low as 23 mL/min. Cardiac catheterization showed non-obstructive coronary artery disease, and cardiac MRI showed an ejection fraction of 14%. She was discharged 14 days after her initial presentation with a diagnosis of NYHA Class 3 Stage C acute systolic heart failure with dilated cardiomyopathy.

## Linked entities

- **Chemicals:** amitriptyline (PubChem CID 2160)
- **Diseases:** dilated cardiomyopathy (MONDO:0005021), congestive heart failure (MONDO:0005009), chronic obstructive pulmonary disease (MONDO:0005002), pneumonia (MONDO:0005249)

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** coronary artery disease (MESH:D003324), Dilated Cardiomyopathy (MESH:D002311), De Novo Heart Failure (MESH:D006333), End-Organ Failure (MESH:D009102), systolic (MESH:D000092244), Cardiogenic Shock (MESH:D012770), chronic obstructive pulmonary disease (MESH:D029424), pneumonia (MESH:D011014)
- **Chemicals:** Amitriptyline (MESH:D000639)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11413831/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11413831/full.md

## References

7 references — full list in the complete paper: https://tomesphere.com/paper/PMC11413831/full.md

---
Source: https://tomesphere.com/paper/PMC11413831