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Published on: July 18, 2014
The temporary drop of serum octreotide concentration deteriorated ventricular tachycardia in an acromegalic patient
Tetsuhiro Kitamura1, Michio Otsuki, Masaya Yamaoka
1Department of Metabolic Medicine, Osaka University Graduate school of Medicine, Suita 565-0871, Japan.
Insights
Acromegaly patients with dilated hypertrophic cardiomyopathy and ventricular tachycardia may experience VT control issues when switching octreotide formulations. Maintaining serum octreotide levels during transitions is crucial for managing severe arrhythmias.
Area of Science:
- Cardiology
- Endocrinology
- Pharmacology
Background:
- Acromegaly commonly causes left ventricular hypertrophy (LVH), leading to ventricular dysfunction and potentially ventricular arrhythmias.
- Hypertrophic cardiomyopathy (HCM) can progress to a dilated phase, increasing the risk of ventricular tachycardia (VT).
- The combination of dilated HCM and VT in acromegaly patients is rarely reported.
Observation:
- A 56-year-old male with acromegaly presented with dilated HCM and sustained VT.
- Subcutaneous octreotide injections initially improved VT frequency and severity.
- Switching to octreotide long-acting release (LAR) led to VT deterioration, linked to a temporary drop in serum octreotide concentration.
Findings:
- This case highlights the first reported instance where changes in serum octreotide concentration influenced VT control in a patient with dilated HCM secondary to acromegaly.
- The transition from subcutaneous to octreotide LAR injections caused a temporary decrease in serum octreotide levels, correlating with worsened VT.
- Consistent serum octreotide levels appear critical for managing severe arrhythmias in this patient population.
Implications:
- Subcutaneous octreotide injections for two weeks may be necessary to maintain therapeutic serum octreotide concentrations during the transition to octreotide LAR.
- This finding provides crucial information for managing acromegalic patients with severe cardiac complications like dilated HCM and VT.
- Optimizing octreotide administration strategies can improve arrhythmia control and patient outcomes in acromegaly.
Abstract:
Acromegaly is frequently accompanied by left ventricular hypertrophy (LVH) which causes ventricular dysfunction. Ventricular arrhythmia is one of the important complications in acromegalic patients. Hypertrophic cardiomyopathy (HCM) is characterized by LVH with a nondilated chamber. About 10 % of HCM evolve into dilated phase of HCM, which is associated with an increased incidence of ventricular tachycardia (VT). However there is no report about a combination of dilated phase of HCM and VT in acromegalic patients. Octreotide is a somatostatin analog that has been used for medical therapy for acromegaly. We herein report that the first case of the change of serum octreotide concentration affected the control of VT, which was induced by dilated phase of HCM. A 56-year-old Japanese man was referred to our hospital for treatment of acromegaly. The patient was diagnosed the dilated phase of HCM with sustained VT. The frequency and severity of VT were gradually ameliorated by subcutaneous octreotide injection. However VT was deteriorated when its injection was changed to octreotide long-acting release (LAR) injection. The temporary drop in serum octreotide concentration was known at the transition from subcutaneous injection to LAR injection. This clinical course gives us the important information that subcutaneous octreotide injection for two weeks should be necessary to keep serum octreotide concentration when switing to octreotide LAR administration in acromegalic patients with severe arrhythmia.
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