Perioperative Anaphylaxis: A Systematic Approach to Evaluate High‐Risk Drug Allergy

Determining the etiology of perioperative anaphylaxis is a challenging task, as multiple medications are often administered simultaneously during anesthesia. This is compounded by the paucity of validated skin testing. While drug challenges are the definitive means of assessing for IgE-mediated drug allergy, they must be weighed with the risk of severe reaction. As such, multidisciplinary collaboration is warranted to ensure drug provocation testing is performed thoughtfully and safely. Here, we present a case of an 18-year-old male with juvenile kyphosis who underwent anesthesia prior to spinal fusion surgery. He was given intravenous fentanyl, propofol, dexamethasone, remifentanil, tranexamic acid, methadone, and cefazolin. Additionally, iodine, chlorhexidine, and tincture of benzoin were applied topically. Shortly after the start of anesthesia and prior to incision, he developed bronchospasm, hypoxia, hypotension, and pulseless electrical activity with a return of spontaneous circulation following cardiopulmonary resuscitation. A tryptase level drawn during the event was elevated at 23.7 <i>μ</i>g/L (reference range: 0-11.4 <i>μ</i>g/L). Months later, the patient underwent skin prick and intradermal testing in an allergy clinic, which was largely unrevealing for a culprit. Given the absence of validated predictive values for skin testing, drug provocation testing was performed with the patient admitted to the intensive care unit due to the high-risk nature of testing. Medications were selected for a challenge after multidisciplinary discussions with specialists in anesthesia and surgery based on the availability of alternative medications. Following negative drug provocation testing to intravenous dexamethasone, intravenous fentanyl, oral midazolam, intravenous methadone, and intravenous tranexamic acid, as well as topical challenges to chlorhexidine, iodine, and tincture of benzoin, the patient was instructed to continue to avoid cefazolin, propofol, and remifentanil and was able to subsequently undergo spinal fusion surgery safely. This case demonstrates a systematic approach for high-risk drug allergy testing that was facilitated by collaboration with allergy, intensive care, anesthesia, and surgery.

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Publication Details

Journal
Case Reports in Critical Care
Published
2025-01-01
DOI
https://doi.org/10.1155/crcc/8845963
Citations
1
Primary Topic
Drug-Induced Adverse Reactions
Type
article
Field-Weighted Citation Impact
1.39

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article

Perioperative Anaphylaxis: A Systematic Approach to Evaluate High‐Risk Drug Allergy

Stanislaw J. Gabryszewski, E Robbins, Alexandra Navard-Keck, J. Lee et al.
1 citations
Case Reports in Critical Care
Drug-Induced Adverse Reactions
1.39
article

Perioperative Anaphylaxis: A Systematic Approach to Evaluate High‐Risk Drug Allergy

Stanislaw J. Gabryszewski, E Robbins, Alexandra Navard-Keck, J. Lee, Joseph Cafone
article en
1 citations

Abstract

Determining the etiology of perioperative anaphylaxis is a challenging task, as multiple medications are often administered simultaneously during anesthesia. This is compounded by the paucity of validated skin testing. While drug challenges are the definitive means of assessing for IgE-mediated drug allergy, they must be weighed with the risk of severe reaction. As such, multidisciplinary collaboration is warranted to ensure drug provocation testing is performed thoughtfully and safely. Here, we present a case of an 18-year-old male with juvenile kyphosis who underwent anesthesia prior to spinal fusion surgery. He was given intravenous fentanyl, propofol, dexamethasone, remifentanil, tranexamic acid, methadone, and cefazolin. Additionally, iodine, chlorhexidine, and tincture of benzoin were applied topically. Shortly after the start of anesthesia and prior to incision, he developed bronchospasm, hypoxia, hypotension, and pulseless electrical activity with a return of spontaneous circulation following cardiopulmonary resuscitation. A tryptase level drawn during the event was elevated at 23.7 <i>μ</i>g/L (reference range: 0-11.4 <i>μ</i>g/L). Months later, the patient underwent skin prick and intradermal testing in an allergy clinic, which was largely unrevealing for a culprit. Given the absence of validated predictive values for skin testing, drug provocation testing was performed with the patient admitted to the intensive care unit due to the high-risk nature of testing. Medications were selected for a challenge after multidisciplinary discussions with specialists in anesthesia and surgery based on the availability of alternative medications. Following negative drug provocation testing to intravenous dexamethasone, intravenous fentanyl, oral midazolam, intravenous methadone, and intravenous tranexamic acid, as well as topical challenges to chlorhexidine, iodine, and tincture of benzoin, the patient was instructed to continue to avoid cefazolin, propofol, and remifentanil and was able to subsequently undergo spinal fusion surgery safely. This case demonstrates a systematic approach for high-risk drug allergy testing that was facilitated by collaboration with allergy, intensive care, anesthesia, and surgery.

Case Reports in Critical CareVol. 2025(1)
National Institutes of Health (US), Children's Hospital of Philadelphia (US), National Institute of Allergy and Infectious Diseases (US)
National Institutes of Health
Openalex Percentile: Top 22%
Drug-Induced Adverse Reactions
1.39
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