Establishing low-density lipoprotein apheresis tolerability in patients with prior anaphylactoid reactions to lipoprotein apheresis using magnesium sulfate.


Journal

Journal of clinical apheresis
ISSN: 1098-1101
Titre abrégé: J Clin Apher
Pays: United States
ID NLM: 8216305

Informations de publication

Date de publication:
Jun 2021
Historique:
revised: 02 01 2021
received: 11 06 2020
accepted: 24 01 2021
pubmed: 19 2 2021
medline: 15 12 2021
entrez: 18 2 2021
Statut: ppublish

Résumé

Lipoprotein apheresis (LA) tolerability is a key factor for the utilization of this therapy. Common reactions to LA are hypotension and nausea. Serious reactions include severe hypotension and anaphylactoid reactions (0.13%-1.3% and 0.2%-0.4%, respectively). The bradykinin response drives these reactions and can worsen with the use of angiotensin-converting-enzyme inhibitors. Efforts to mitigate these reactions are necessary for the tolerability of LA with a dextran sulfate-adsorption (DSA) system. In an effort to increase apheresis tolerability, seven patients at The University of Kansas, Department of Clinical Pharmacology, who had prior anaphylactoid reactions (defined as general cutaneous flushing, nausea/vomiting, tongue swelling, lightheadedness, and hypotension) to the DSA despite pharmacologic intervention, were treated with pre-LA intravenous magnesium adapted from a protocol developed by co-author Eliaz. This protocol consists of 1.5 g of magnesium sulfate administered over 45 minutes. All seven patients were treated with intravenous magnesium sulfate immediately before LA. No episodes of anaphylactoid reactions during LA have been reported to date. Magnesium infusion before DSA can be utilized to establish tolerability in patients with prior anaphylactoid reactions to LA. Proposed mechanisms include temporary stabilization of the negative-positive interactions of the dextran sulfate filter leading to a reduction of circulating bradykinin, reduction of nitric oxide, and reduction of the sympathetic response to LA.

Sections du résumé

BACKGROUND BACKGROUND
Lipoprotein apheresis (LA) tolerability is a key factor for the utilization of this therapy. Common reactions to LA are hypotension and nausea. Serious reactions include severe hypotension and anaphylactoid reactions (0.13%-1.3% and 0.2%-0.4%, respectively). The bradykinin response drives these reactions and can worsen with the use of angiotensin-converting-enzyme inhibitors. Efforts to mitigate these reactions are necessary for the tolerability of LA with a dextran sulfate-adsorption (DSA) system.
MATERIALS AND METHODS METHODS
In an effort to increase apheresis tolerability, seven patients at The University of Kansas, Department of Clinical Pharmacology, who had prior anaphylactoid reactions (defined as general cutaneous flushing, nausea/vomiting, tongue swelling, lightheadedness, and hypotension) to the DSA despite pharmacologic intervention, were treated with pre-LA intravenous magnesium adapted from a protocol developed by co-author Eliaz. This protocol consists of 1.5 g of magnesium sulfate administered over 45 minutes. All seven patients were treated with intravenous magnesium sulfate immediately before LA.
RESULTS RESULTS
No episodes of anaphylactoid reactions during LA have been reported to date.
CONCLUSIONS CONCLUSIONS
Magnesium infusion before DSA can be utilized to establish tolerability in patients with prior anaphylactoid reactions to LA. Proposed mechanisms include temporary stabilization of the negative-positive interactions of the dextran sulfate filter leading to a reduction of circulating bradykinin, reduction of nitric oxide, and reduction of the sympathetic response to LA.

Identifiants

pubmed: 33599029
doi: 10.1002/jca.21884
doi:

Substances chimiques

Cholesterol, LDL 0
Magnesium Sulfate 7487-88-9
Dextran Sulfate 9042-14-2
Bradykinin S8TIM42R2W

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

437-442

Informations de copyright

© 2021 Wiley Periodicals LLC.

Références

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Auteurs

Ethan Alexander (E)

Division of Clinical Pharmacology, University of Kansas School of Medicine, Kansas City, Kansas, USA.

Patrick M Moriarty (PM)

Division of Clinical Pharmacology, University of Kansas School of Medicine, Kansas City, Kansas, USA.

Barry Wilk (B)

Eliaz Therapeutics, Santa Rosa, California, USA.

Isaac Eliaz (I)

Eliaz Therapeutics, Santa Rosa, California, USA.
Amitabha Medical Center, Santa Rosa, California, USA.

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