Evidence map›Paper›PMID 32176248›Full record

ArticleJAMA internal medicine2020

Development and Validation of a Penicillin Allergy Clinical Decision Rule.

Jason A Trubiano, Sara Vogrin, Kyra Y L Chua, Jack Bourke, James Yun, Abby Douglas, Cosby A Stone, Roger Yu, Lauren Groenendijk, Natasha E Holmes and 1 more

5 registry-linked trialsOpen access · bronzeAbstract readValidation Study
In one paragraph

Article in JAMA internal medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 5 registered trials, which are not on this map. Cited by 165 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
165citing papers in PubMed, 8 pooled it
20.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04454229 nacompletednot on this mapstarted 2021, after this paper: background citation

The Use of Penicillin Allergy Clinical Decision Rule to Enable Direct Oral Penicillin Challenge - An International Multicenter Randomized Control Trial - The PALACE Study

TypeinterventionalSponsorAustin HealthRan2021 to 2022Enrolled382ConditionsHypersensitivity, Immediate, Hypersensitivity, Delayed, Hypersensitivity ResponseArmsDirect oral penicillin challenge, Standard of care
NCT05464615 early_phase1terminatednot on this mapstarted 2024, after this paper: background citation

Geisinger Antibiotic Allergy Pilot Program: Assess and Address (GAAP) Penicillin Allergy De-labeling in Inpatient Setting by Performing Direct Oral Amoxicillin Challenge in Low-risk Patients

TypeinterventionalSponsorGeisinger ClinicRan2024 to 2026Enrolled20ConditionsPenicillin AllergyArmsAmoxicillin
NCT06303128 phase3recruitingnot on this mapstarted 2024, after this paper: background citation

Penicillin Allergy Delabeling After a One-Dose Versus Two-Dose Graded Direct Oral Challenge

TypeinterventionalSponsorJames Tarbox, MDRan2024 to 2026Enrolled380ConditionsPenicillin AllergyArmsAmoxicillin 250 MG, Placebo, Amoxicillin 62.5mg, Amoxicillin 187.5mg
NCT06755281 narecruitingnot on this mapstarted 2025, after this paper: background citation

Risk-stratified Testing for Safe Removal of Penicillin Allergy Labels

TypeinterventionalSponsorDeniz GöcebeRan2025 to 2027Enrolled100ConditionsPenicillin Allergy, Hypersensitivity, Immediate, Hypersensitivity, Delayed, Hypersensitivity ResponseArmsDirect Oral challenge, standard of care
NCT07604597 completednot on this mapstarted 2025, after this paper: background citation

Optimization of Antibiotic Treatment in Patients With a Reported Penicillin Allergy Using a Digital Clinical Decision Support Tool.

TypeobservationalSponsorAlthaia Xarxa Assistencial Universitària de ManresaRan2025 to 2026Enrolled182ConditionsPenicillin Allergy, In-hospital Process Optimization
3 · Its place in the literature

Who cites it

165 citing papers in PubMed, 8 syntheses or guidelines pooled it, 338 citations in OpenAlex.

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105 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 2 countries.

Jason A TrubianoCentre for Antibiotic Allergy and Research, Department of Infectious Diseases, Austin Health, Heidelberg, Australia.
Sara VogrinDepartment of Medicine, St Vincent's Hospital, University of Melbourne, Fitzroy, Australia.
Kyra Y L ChuaCentre for Antibiotic Allergy and Research, Department of Infectious Diseases, Austin Health, Heidelberg, Australia.
Jack BourkeDepartment of Allergy and Immunology, Fiona Stanley Hospital, Murdoch, Australia.
James YunFaculty of Medicine and Health, University of Sydney, Sydney, Australia.
Abby DouglasPeter MacCallum Cancer Centre, Department of Infectious Diseases and The National Centre for Infections in Cancer, Parkville, Australia.
Cosby A StoneDepartment of Infectious Diseases, Vanderbilt University Medical Centre, Nashville, Tennessee.
Roger YuDepartment of Infectious Diseases, Vanderbilt University Medical Centre, Nashville, Tennessee.
Lauren GroenendijkFaculty of Medicine and Health, University of Sydney, Sydney, Australia.
Natasha E HolmesCentre for Antibiotic Allergy and Research, Department of Infectious Diseases, Austin Health, Heidelberg, Australia.
Elizabeth J PhillipsDepartment of Infectious Diseases, Vanderbilt University Medical Centre, Nashville, Tennessee.
Austin Health · AUVanderbilt University Medical Center · USUniversity of Sydney · AUFiona Stanley Hospital · AUPeter MacCallum Cancer Centre · AUUniversity of Melbourne · AU

Funding

Understanding and preventing HLA-associated drug reactionsP50GM115305 · NIGMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RODEN, DAN M · 2015 to 2019
$13.0M
Learning Health System Scholar Program at VanderbiltK12HS026395 · AHRQ · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ROTHMAN, RUSSELL L., ROUMIE, CHRISTIANNE L. · 2018 to 2022
$2.7M
Single Cell definition of pathogenic T cells in Drug-induced Stevens-Johnson-Syndrome/Toxic epidermal necrolysisR21AI139021 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PHILLIPS, ELIZABETH · 2018 to 2019
$435k
NATIENS: A Phase III Randomized Study to Determine the Mechanisms and Optimal Management of Stevens-Johnson Syndrome and Toxic Epidermal NecrolysisR34AI136815 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PHILLIPS, ELIZABETH · 2018 to 2018
$205k
AHRQ HHS K12 HS026395NIAID NIH HHS R34 AI136815NIGMS NIH HHS P50 GM115305
6 · The paper itself

Abstract

Importance: Penicillin allergy is a significant public health issue for patients, antimicrobial stewardship programs, and health services. Validated clinical decision rules are urgently needed to identify low-risk penicillin allergies that potentially do not require penicillin skin testing by a specialist. Objective: To develop and validate a penicillin allergy clinical decision rule that enables point-of-care risk assessment of patient-reported penicillin allergies. Design, Setting, and Participants: In this diagnostic study, a multicenter prospective antibiotic allergy-tested cohort of 622 patients from 2 tertiary care sites in Melbourne, Australia (Austin Health and Peter MacCallum Cancer Centre) was used for derivation and internal validation of a penicillin allergy decision rule. Backward stepwise logistic regression was used to derive the model, including clinical variables predictive of a positive penicillin allergy test result. Internal validation of the final model used bootstrapped samples and the model scoring derived from the coefficients. External validation was performed in retrospective penicillin allergy-tested cohorts consisting of 945 patients from Sydney and Perth, Australia, and Nashville, Tennessee. Patients who reported a penicillin allergy underwent penicillin allergy testing using skin prick, intradermal, or patch testing and/or oral challenge (direct or after skin testing). Data were collected from June 26, 2008, to June 3, 2019, and analyzed from January 9 to 12, 2019. Main Outcomes and Measures: The primary outcome for the model was any positive result of penicillin allergy testing performed during outpatient or inpatient assessment. Results: From an internal derivation and validation cohort of 622 patients (367 female [59.0%]; median age, 60 [interquartile range{IQR}, 48-71] years) and an external validation cohort of 945 patients (662 female [70.1%]; median age, 55 [IQR, 38-68] years), the 4 features associated with a positive penicillin allergy test result on multivariable analysis were summarized in the mnemonic PEN-FAST: penicillin allergy, five or fewer years ago, anaphylaxis/angioedema, severe cutaneous adverse reaction (SCAR), and treatment required for allergy episode. The major criteria included an allergy event occurring 5 or fewer years ago (2 points) and anaphylaxis/angioedema or SCAR (2 points); the minor criterion (1 point), treatment required for an allergy episode. Internal validation showed minimal mean optimism of 0.003 with internally validated area under the curve of 0.805. A cutoff of less than 3 points for PEN-FAST was chosen to classify a low risk of penicillin allergy, for which only 17 of 460 patients (3.7%) had positive results of allergy testing, with a negative predictive value of 96.3% (95% CI, 94.1%-97.8%). External validation resulted in similar findings. Conclusions and Relevance: In this study, PEN-FAST was found to be a simple rule that accurately identified low-risk penicillin allergies that do not require formal allergy testing. The results suggest that a PEN-FAST score of less than 3, associated with a high negative predictive value, could be used by clinicians and antimicrobial stewardship programs to identify low-risk penicillin allergies at the point of care.

Indexed as

AgedAnti-Bacterial AgentsClinical Decision RulesDrug HypersensitivityFemaleHumansMaleMiddle AgedPenicillinsProspective StudiesRisk AssessmentAnti-Bacterial AgentsPenicillins

Identifiers

PMID32176248
PMCPMC7076536
OpenAlexW3012112115

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.