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Published on: February 10, 2013
[Is intermittent dobutamine treatment beneficial in patients with dilated cardiomyopathy?]
Namik Kemal Eryol1, Muhammed Güven, Ramazan Topsakal
1Department of Cardiology, Medical Faculty, Erciyes University, Kayseri. nkeryol@erciyes.edu.tr
Insights
Intermittent dobutamine infusions improved cardiac function and quality of life in dilated cardiomyopathy (DCM) patients short-term. However, these benefits diminished by month three, with increased adverse events like ventricular arrhythmias.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Dilated cardiomyopathy (DCM) is a significant cause of heart failure.
- Dobutamine, a sympathomimetic agent, is used to manage heart failure symptoms.
Purpose of the Study:
- To evaluate the effects of intermittent dobutamine administration on cardiac function and quality of life in DCM patients.
- To assess the short-term and medium-term outcomes of this therapeutic approach.
Main Methods:
- A study involving twelve DCM patients refractory to standard therapy.
- Intermittent dobutamine infusions (3-day cycles) administered over three months.
- Comprehensive assessments including echocardiography, exercise stress testing, ECG, cardiac catheterization, biomarkers, and quality of life questionnaires.
Main Results:
- Significant improvements in left ventricular ejection fraction (LVEF), cardiac output, cardiac index (CI), and quality of life were observed immediately after the first dobutamine treatment course.
- These improvements largely reverted to baseline levels by the third month.
- Increased incidence of ventricular premature beats and troponin-T positivity noted after three months of treatment.
Conclusions:
- Intermittent dobutamine offers transient benefits in systolic parameters and quality of life for DCM patients.
- Prolonged intermittent use may lead to diminished efficacy and increased adverse cardiac events.
Objective:
Dobutamine is a sympathomimetic drug, which can be used in patients with dilated cardiomyopathy (DCM). We investigated the effects of intermittent dobutamine use on cardiac parameters and quality of life in patients with DCM.
Methods:
Twelve patients with ischemic and idiopathic DCM, refractory to conventional therapy, have been included in the study. In addition to traditional treatment, dobutamine (1-2 micro g/kg/min infusion increasing up to 10 micro g/kg/min for 3 days) was administered, and repeated at the 1st, 2nd and 3rd months. The patients were evaluated 3 times, before and immediately after the first treatment and after the treatment on the third month, using echocardiography, exercise stress testing, ambulatory ECG, right ventricular catheterization, cardiac enzymes (creatine kinase MB isoenzyme - CK-MB, troponin-T) and the Minnesota Living with Heart Failure Questionnaire for quality of life.
Results:
After the first treatment, left ventricular ejection fraction (LVEF), cardiac output, cardiac index (CI), pulmonary wedge pressure and life quality improved significantly (p<0.05); but, after the treatment on the third month, these parameters except PCWP returned to nearly baseline values. Additionally, a significant increase in the number of patients with ventricular premature beats and with troponin-T positivity was detected after the third month of treatment.
Conclusion:
The use of dobutamine in addition to conventional therapy in patients with DCM provided improvements in some systolic parameters and quality of life particularly after the first treatment. In the late period of the treatment, however, it was determined that these beneficial effects tended to disappear and harmful effects became more evident.
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