Postpartum cardiomyopathy

Case contributed by Karen Machang'a
Diagnosis certain

Presentation

Underlying hypertension. 5 months postpartum presented with chest pain, cough, dyspnea, orthopnea, headaches, and nausea.

Patient Data

Age: 35 years
Gender: Female
x-ray

The heart is enlarged. Normal pulmonary vasculature. Costophrenic angles are clear. No pulmonary lesion noted.

ultrasound

Dilated left ventricle (6 cm) with severely impaired systolic function. Left ventricular ejection fraction (LVEF) of 18%.

Moderate mitral regurgitation. Mild tricuspid regurgitation (not shown) with a tricuspid regurgitation peak gradient (TRPG) of 33 mmHg.

Bi-atrial dilatation. Normal right ventricular size with normal systolic function. Trace pericardial effusion. No thrombus seen.

Tricuspid annular plane systolic excursion (TAPSE): 1.8cm.
Right ventricular systolic velocity: 10 cm/s.

Case Discussion

Postpartum cardiomyopathy is a type of dilated cardiomyopathy that occurs within the first 6 months after delivery (postpartum). The mechanism that leads to postpartum cardiomyopathy remains ill-defined. It is a diagnosis of exclusion that is typically considered in younger patients with no history of cardiac disease or causes of heart failure 1.

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