Modified Oral Metronidazole Desensitization Protocol

The Center for Disease Control guidelines recommend desensitization to metronidazole in patients with trichomoniasis and hypersensitivity to metronidazole. There is only one published oral metronidazole desensitization protocol. The purpose of this study was to design a new, more gradual oral desens...

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Main Authors: Samantha R. Gendelman M.D., Lily C. Pien M.D., Ravi C. Gutta M.D., Susan R. Abouhassan M.D.
Format: Article
Language:English
Published: SAGE Publishing 2014-06-01
Series:Allergy & Rhinology
Online Access:https://doi.org/10.2500/ar.2014.5.0080
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author Samantha R. Gendelman M.D.
Lily C. Pien M.D.
Ravi C. Gutta M.D.
Susan R. Abouhassan M.D.
author_facet Samantha R. Gendelman M.D.
Lily C. Pien M.D.
Ravi C. Gutta M.D.
Susan R. Abouhassan M.D.
author_sort Samantha R. Gendelman M.D.
collection DOAJ
description The Center for Disease Control guidelines recommend desensitization to metronidazole in patients with trichomoniasis and hypersensitivity to metronidazole. There is only one published oral metronidazole desensitization protocol. The purpose of this study was to design a new, more gradual oral desensitization protocol to decrease systemic reactions that may occur when using the previously published protocol. We present two patients with presumed IgE-mediated allergy to metronidazole who underwent oral desensitization using our modified protocol. Case 1 was a 65-year-old woman with trichomoniasis who presented for metronidazole desensitization with a history of intraoperative anaphylaxis and positive skin tests to metronidazole. The patient tolerated six doses of the modified desensitization but developed systemic symptoms of nasal congestion and diffuse pruritus after the 25- and 100-mg doses. Both reactions were treated with intravenous (i.v.) antihistamines. Because of gastrointestinal irritation, the desensitization was completed at a dose of 250 mg orally every 6 hours. Case 2 was a 42-year-old woman with trichomoniasis and a history of hives immediately after administration of i.v. metronidazole who presented for desensitization. The patient had negative skin-prick and intradermal testing to metronidazole. She developed lip tingling and pruritus on her arms 15 minutes after the 10-mg dose. Fexofenadine at 180 mg was given orally and symptoms resolved. She tolerated the rest of the protocol without reaction and received a total dose of 2 g of metronidazole. Our oral metronidazole desensitization for presumed IgE-mediated reactions offers a second option for physicians wishing to use a more gradual escalation in dose.
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spelling doaj.art-43c6a1b440cc41e187a35ce47f4f44a42022-12-22T00:15:25ZengSAGE PublishingAllergy & Rhinology2152-65672014-06-01510.2500/ar.2014.5.0080Modified Oral Metronidazole Desensitization ProtocolSamantha R. Gendelman M.D.0Lily C. Pien M.D.1Ravi C. Gutta M.D.2Susan R. Abouhassan M.D.3Department of Allergy and Immunology, Cleveland Clinic Foundation, Respiratory Institute, Cleveland, OhioDepartment of Allergy and Immunology, Cleveland Clinic Foundation, Respiratory Institute, Cleveland, OhioDepartment of Allergy and Immunology, Cleveland Clinic Foundation, Respiratory Institute, Cleveland, OhioDepartment of Allergy and Immunology, Cleveland Clinic Foundation, Respiratory Institute, Cleveland, OhioThe Center for Disease Control guidelines recommend desensitization to metronidazole in patients with trichomoniasis and hypersensitivity to metronidazole. There is only one published oral metronidazole desensitization protocol. The purpose of this study was to design a new, more gradual oral desensitization protocol to decrease systemic reactions that may occur when using the previously published protocol. We present two patients with presumed IgE-mediated allergy to metronidazole who underwent oral desensitization using our modified protocol. Case 1 was a 65-year-old woman with trichomoniasis who presented for metronidazole desensitization with a history of intraoperative anaphylaxis and positive skin tests to metronidazole. The patient tolerated six doses of the modified desensitization but developed systemic symptoms of nasal congestion and diffuse pruritus after the 25- and 100-mg doses. Both reactions were treated with intravenous (i.v.) antihistamines. Because of gastrointestinal irritation, the desensitization was completed at a dose of 250 mg orally every 6 hours. Case 2 was a 42-year-old woman with trichomoniasis and a history of hives immediately after administration of i.v. metronidazole who presented for desensitization. The patient had negative skin-prick and intradermal testing to metronidazole. She developed lip tingling and pruritus on her arms 15 minutes after the 10-mg dose. Fexofenadine at 180 mg was given orally and symptoms resolved. She tolerated the rest of the protocol without reaction and received a total dose of 2 g of metronidazole. Our oral metronidazole desensitization for presumed IgE-mediated reactions offers a second option for physicians wishing to use a more gradual escalation in dose.https://doi.org/10.2500/ar.2014.5.0080
spellingShingle Samantha R. Gendelman M.D.
Lily C. Pien M.D.
Ravi C. Gutta M.D.
Susan R. Abouhassan M.D.
Modified Oral Metronidazole Desensitization Protocol
Allergy & Rhinology
title Modified Oral Metronidazole Desensitization Protocol
title_full Modified Oral Metronidazole Desensitization Protocol
title_fullStr Modified Oral Metronidazole Desensitization Protocol
title_full_unstemmed Modified Oral Metronidazole Desensitization Protocol
title_short Modified Oral Metronidazole Desensitization Protocol
title_sort modified oral metronidazole desensitization protocol
url https://doi.org/10.2500/ar.2014.5.0080
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