Multicenter Australian Study to Determine Criteria for Low- and High-Risk Penicillin Testing in Outpatients.


Journal

The journal of allergy and clinical immunology. In practice
ISSN: 2213-2201
Titre abrégé: J Allergy Clin Immunol Pract
Pays: United States
ID NLM: 101597220

Informations de publication

Date de publication:
02 2020
Historique:
received: 27 03 2019
revised: 24 08 2019
accepted: 22 09 2019
pubmed: 12 10 2019
medline: 15 5 2021
entrez: 12 10 2019
Statut: ppublish

Résumé

Recent single-center studies promote oral penicillin challenges, without skin testing, in patients with low risk/likelihood of true allergy. However, how best to define a low-risk penicillin allergy history is uncertain. To statistically determine an optimal low-risk definition, to select patients for safe outpatient penicillin challenges, without skin testing. In a multicenter Australian study (February 2016 to May 2018), testing strategy (skin test and/or oral penicillin challenge) and outcomes were retrospectively collected for all penicillin-allergic patients. Statistical modeling was performed with 8 low-risk definitions, to determine an optimal low-risk definition. A total of 447 subjects (mean age, 45.3 years; 63.8% females) were analyzed. A history of benign, immediate, or delayed rash, more than 1 year before review, was the optimal low-risk definition. A total of 244 of 447 (54.6%) patients met this definition, of which 97.1% tolerated a 1- or 2-dose penicillin challenge, with no anaphylaxis in those who reacted. Of 203 patients designated higher risk, 54 (26.6%) had their allergy confirmed by skin test (n = 45) or challenge (n = 9). History of penicillin-associated rash (without angioedema, mucosal ulceration, or systemic involvement), more than 1 year ago, is sufficient to select a patient for a direct oral penicillin challenge. This large multicenter study demonstrates that this approach appears safe, and risk is comparable to that in other procedures being performed in primary care in Australia. The higher risk patients are more likely to benefit from skin testing. This simple risk-based delabeling strategy could potentially be used by nonallergists, leading to more efficient penicillin allergy delabeling service provision.

Sections du résumé

BACKGROUND
Recent single-center studies promote oral penicillin challenges, without skin testing, in patients with low risk/likelihood of true allergy. However, how best to define a low-risk penicillin allergy history is uncertain.
OBJECTIVE
To statistically determine an optimal low-risk definition, to select patients for safe outpatient penicillin challenges, without skin testing.
METHODS
In a multicenter Australian study (February 2016 to May 2018), testing strategy (skin test and/or oral penicillin challenge) and outcomes were retrospectively collected for all penicillin-allergic patients. Statistical modeling was performed with 8 low-risk definitions, to determine an optimal low-risk definition.
RESULTS
A total of 447 subjects (mean age, 45.3 years; 63.8% females) were analyzed. A history of benign, immediate, or delayed rash, more than 1 year before review, was the optimal low-risk definition. A total of 244 of 447 (54.6%) patients met this definition, of which 97.1% tolerated a 1- or 2-dose penicillin challenge, with no anaphylaxis in those who reacted. Of 203 patients designated higher risk, 54 (26.6%) had their allergy confirmed by skin test (n = 45) or challenge (n = 9).
CONCLUSIONS
History of penicillin-associated rash (without angioedema, mucosal ulceration, or systemic involvement), more than 1 year ago, is sufficient to select a patient for a direct oral penicillin challenge. This large multicenter study demonstrates that this approach appears safe, and risk is comparable to that in other procedures being performed in primary care in Australia. The higher risk patients are more likely to benefit from skin testing. This simple risk-based delabeling strategy could potentially be used by nonallergists, leading to more efficient penicillin allergy delabeling service provision.

Identifiants

pubmed: 31604129
pii: S2213-2198(19)30851-7
doi: 10.1016/j.jaip.2019.09.025
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Penicillins 0

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

681-689.e3

Informations de copyright

Copyright © 2019 American Academy of Allergy, Asthma & Immunology. All rights reserved.

Auteurs

Brittany Stevenson (B)

Department of Immunology, Sir Charles Gairdner Hospital, Perth, WA, Australia; Department of Immunology, Fiona Stanley Hospital, Perth, WA, Australia; Department of Immunology, PathWest Laboratory Medicine, Perth, WA, Australia.

Michelle Trevenen (M)

Centre for Applied Statistics, The University of Western Australia, Perth, WA, Australia.

Elizabeth Klinken (E)

Department of Immunology, Sir Charles Gairdner Hospital, Perth, WA, Australia; Department of Immunology, Fiona Stanley Hospital, Perth, WA, Australia; Department of Immunology, PathWest Laboratory Medicine, Perth, WA, Australia.

William Smith (W)

AllergySA, Beulah Park, Adelaide, SA, Australia; Clinical Immunology and Allergy, Royal Adelaide Hospital, Adelaide, SA, Australia.

Carlo Yuson (C)

AllergySA, Beulah Park, Adelaide, SA, Australia; Clinical Immunology and Allergy, Royal Adelaide Hospital, Adelaide, SA, Australia.

Constance Katelaris (C)

Immunology/Allergy Unit, Campbelltown Hospital, Campbelltown, NSW, Australia.

Fiona Perram (F)

Immunology/Allergy Unit, Campbelltown Hospital, Campbelltown, NSW, Australia.

Pamela Burton (P)

Immunology/Allergy Unit, Campbelltown Hospital, Campbelltown, NSW, Australia.

James Yun (J)

Immunology and Rheumatology, Nepean Hospital, Sydney, NSW, Australia.

Fenfen Cai (F)

St Vincent's Hospital, Sydney, NSW, Australia.

Sara Barnes (S)

Department of Allergy/Immunology, Monash Health, Melbourne, VIC, Australia.

Kymble Spriggs (K)

Department of Allergy/Immunology, Monash Health, Melbourne, VIC, Australia; Melbourne Medical School, The University of Melbourne, Melbourne, VIC, Australia.

Samar Ojaimi (S)

Department of Allergy/Immunology, Monash Health, Melbourne, VIC, Australia; Centre of Inflammatory Diseases, Monash University, Melbourne, VIC, Australia.

Raymond Mullins (R)

John James Medical Centre, Canberra, ACT, Australia.

Sam Salman (S)

Department of Immunology, Sir Charles Gairdner Hospital, Perth, WA, Australia; Department of Immunology, Fiona Stanley Hospital, Perth, WA, Australia; Department of Immunology, PathWest Laboratory Medicine, Perth, WA, Australia; School of Medicine, The University of Western Australia, Perth, WA, Australia.

Patricia Martinez (P)

Department of Immunology, Fiona Stanley Hospital, Perth, WA, Australia; Department of Immunology, PathWest Laboratory Medicine, Perth, WA, Australia; School of Medicine, The University of Western Australia, Perth, WA, Australia.

Kevin Murray (K)

School of Population and Global Health, University of Western Australia, Perth, WA, Australia.

Michaela Lucas (M)

Department of Immunology, Sir Charles Gairdner Hospital, Perth, WA, Australia; Department of Immunology, PathWest Laboratory Medicine, Perth, WA, Australia; School of Medicine, The University of Western Australia, Perth, WA, Australia. Electronic address: michaela.lucas@health.wa.gov.au.

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Classifications MeSH