Randomized Multicenter Trial for the Validation of an Easy-to-Administer Algorithm to Define Penicillin Allergy Status in Sexually Transmitted Infection Clinic Outpatients

Author:

Lillis Rebecca A1,Barbee Lindley A2,McNeil Candice J3,Newman Lori4,Fortenberry J Dennis5,Alvarez-Arango Santiago67,Zenilman Jonathan M8ORCID

Affiliation:

1. Section of Infectious Diseases, Louisiana State University School of Medicine , New Orleans, Louisiana , USA

2. Division of Infectious Diseases, University of Washington , Seattle, Washington , USA

3. Section of Infectious Diseases, Wake Forest University School of Medicine , Winston-Salem, North Carolina , USA

4. National Institute of Allergy and Infectious Diseases , Rockville, Maryland , USA

5. Division of Adolescent Medicine, Indiana University School of Medicine , Indianapolis, Indiana , USA

6. Division of Clinical Pharmacology, Johns Hopkins University School of Medicine , Baltimore, Maryland , USA

7. Division of Allergy and Clinical Immunology, Johns Hopkins University School of Medicine , Baltimore, Maryland , USA

8. Division of Infectious Diseases, Johns Hopkins University School of Medicine , Baltimore, Maryland , USA

Abstract

Abstract Background Approximately 15% of patients in sexually transmitted infection (STI) clinics report penicillin allergies, complicating treatment for syphilis and gonorrhea. Nonetheless, >90% do not have a penicillin allergy when evaluated. We developed and validated an algorithm to define which patients reporting penicillin allergy can be safely treated at STI clinics with these drugs. Methods Randomized controlled trial to assess feasibility and safety of penicillin allergy evaluations in STI clinics. Participants with reported penicillin allergy answered an expert-developed questionnaire to stratify risk. Low-risk participants underwent penicillin skin testing (PST) followed by amoxicillin 250 mg challenge or a graded oral challenge (GOC)—amoxicillin 25 mg followed by 250 mg. Reactions were recorded, and participant/provider surveys were conducted. Results Of 284 participants, 72 (25.3%) were deemed high risk and were excluded. Of 206 low-risk participants, 102 (49.5%) underwent PST without reactions and 3 (3%) had mild reactions during the oral challenge. Of 104 (50.5%) participants in the GOC, 95 (91.3%) completed challenges without reaction, 4 (4.2%) had mild symptoms after 25 mg, and 4 (4.2%) after 250-mg doses. Overall, 195 participants (94.7%) successfully completed the study and 11 (5.3%) experienced mild symptoms. Of 14 providers, 12 (85.7%) completed surveys and 11 (93%) agreed on the safety/effectiveness of penicillin allergy assessment in STI clinics. Conclusions An easy-to-administer risk-assessment questionnaire can safely identify patients for penicillin allergy evaluation in STI clinics by PST or GOC, with GOC showing operational feasibility. Using this approach, 67% of participants with reported penicillin allergy could safely receive first-line treatments for gonorrhea or syphilis. Clinical Trials Registration. Clinicaltrials.gov (NCT04620746).

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

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