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Published on: January 21, 2018
Perflutren lipid microspheres for echocardiogram contrast: a clinical case of anaphylaxis not caused by PEG
Chloe Wang1,2, Jackie Campbell2, Harriet Lea-Banks3,4
1Faculty of Science and Schulich School of Medicine & Dentistry, Western University, London, ON, Canada.
Background:
Perflutren lipid microsphere suspension, sold under the brand name Definity®, is a microbubble ultrasound contrast agent. The microspheres contain octafluoropropane (C3F8) gas encapsulated by an outer lipid shell of phospholipids and a polyethylene glycol (PEG)ylated phospholipid. Anaphylaxis to perflutren lipid microsphere is very rare, with only one case report clearly attributing the reaction to the PEG excipient. We report a novel case of anaphylaxis likely caused by a non-PEGylated component of Definity®.
Case Presentation:
Our patient is a healthy 54-year-old female, who underwent an exercise stress transthoracic echocardiogram using Definity® as an enhancing agent. She experienced anaphylaxis within 15 min of injection. Symptoms resolved after she was treated with diphenhydramine and epinephrine, followed by a systemic corticosteroid and ondansetron in the Emergency Department. The patient underwent allergy testing at our clinic for Definity® and various PEG-containing substances. While all PEG products tested negative, she had positive intradermal tests to Definity®. She also had negative skin prick testing to PEG 8000 and passed an oral challenge to PEG 3350, thus ruling out PEG as the causative agent of anaphylaxis.
Conclusions:
Our case report highlights a previously undocumented instance of anaphylaxis to Definity® not caused by PEG. We suspect the reaction to be an IgE-mediated response to a non-PEGylated component of Definity®. An alternative explanation for the reaction could be a complement activation-related pseudoallergy. This report provides critical information to physicians on the potential risks of using Definity® and contributes to growing research surrounding the profile of Definity®.
Insights
Anaphylaxis to Definity®, an ultrasound contrast agent, can occur due to non-polyethylene glycol (PEG) components. Allergy testing confirmed Definity® as the cause, not PEG, suggesting a novel hypersensitivity reaction.
Area of Science:
- Allergy and Immunology
- Radiology
- Pharmacology
Background:
- Perflutren lipid microsphere suspension (Definity®) is an ultrasound contrast agent composed of octafluoropropane gas, phospholipids, and PEGylated phospholipids.
- Anaphylaxis to Definity® is rare, with previous reports suggesting polyethylene glycol (PEG) as a potential allergen.
- This report details a case where anaphylaxis was likely caused by a non-PEGylated component of Definity®.
Purpose of the Study:
- To report a novel case of anaphylaxis to Definity®.
- To investigate the causative agent of anaphylaxis in a patient who received Definity®.
- To differentiate between PEG-mediated and non-PEG-mediated hypersensitivity to Definity®.
Main Methods:
- A 54-year-old female experienced anaphylaxis post-Definity® injection during an echocardiogram.
- Allergy testing included intradermal tests for Definity® and various PEG-containing substances, as well as skin prick testing and oral challenge for PEG.
- Treatment involved standard anaphylaxis management, including diphenhydramine, epinephrine, corticosteroids, and ondansetron.
Main Results:
- The patient developed anaphylaxis within 15 minutes of Definity® injection.
- Allergy testing was negative for PEG-containing substances but positive for Definity® via intradermal testing.
- Symptoms resolved with appropriate medical treatment.
Conclusions:
- This case highlights a previously undocumented cause of anaphylaxis to Definity®, unrelated to PEG.
- The reaction is suspected to be an IgE-mediated response or complement activation-related pseudoallergy to a non-PEGylated component.
- Physicians should be aware of potential non-PEG-related hypersensitivity reactions to Definity®.
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