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Safety and Efficacy of an Oral Penicillin Challenge in Low Risk Hospitalized Patients

Safety and Efficacy of an Oral Penicillin Challenge in Low Risk Hospitalized Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04408508
Enrollment
50
Registered
2020-05-29
Start date
2023-12-31
Completion date
2024-06-30
Last updated
2023-04-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Penicillin Allergy

Keywords

beta-lactam, penicillin, hypersensitivity, drug allergy

Brief summary

Penicillin allergy is the most common drug allergy reported by patients. Approximately 10% of the population and 20% of inpatients carry a label of penicillin allergy. However, less than 5%-10% of them have a confirmed allergy following comprehensive investigations. Reported penicillin allergy leads to higher medical costs and excess complications and presents a major challenge to antimicrobial stewardship. There is a high demand for allergy services however penicillin allergy testing (including skin testing and oral drug challenge) is not routinely available for inpatients even in major centres. Direct oral amoxicillin challenges are safe and effective in delabeling low risk patients who report penicillin allergy in large paediatric and adult studies and does not necessitate specialist referral. The study team seeks to determine the safety and efficacy of a single-dose oral penicillin challenge pilot program in adult in-patients with self-reported penicillin allergy admitted to hospital under the internal medicine Clinical Teaching Unit (CTU). The study investigators will determine the number of patients successfully delabelled of their penicillin allergy prior to discharge from hospital over a 12 month period. The study doctors will also assess the economic impact of the investigator's model and ease of implementation in the busy inpatient setting. In the future this model could be implemented generally as an inpatient or outpatient penicillin allergy program where low risk patients, who do not require referral to an allergist, are expeditiously delabelled.

Detailed description

Penicillin allergy is the most common drug allergy reported by patients. Approximately 10% of the population and 20% of inpatients carry a label of penicillin allergy. However, only \<5%-10% of them have a confirmed allergy following comprehensive investigations. Reported penicillin allergy leads to higher medical costs and excess complications and presents a major challenge to antimicrobial stewardship. There is a high demand for allergy services however penicillin allergy testing (including skin testing and oral drug challenge) is not routinely available for inpatients even in major centres. Consequently, patients with a penicillin allergy label receive alternative antibiotics such as carbapenems, fluoroquinolones, and vancomycin for the treatment of common and serious infections and for pre-surgical prophylaxis. Patients with penicillin allergy label have longer hospital stays and higher rates of infections with Clostridioides (Clostridium) difficile, VRE and MRSA in comparison with patients without a documented allergy. Direct oral amoxicillin challenges are safe and effective in delabeling patients stratified as low risk for penicillin allergy in large pediatric and adult studies. Low-risk penicillin allergy histories include patients who have had isolated nonallergic symptoms (eg, gastrointestinal symptoms) or patients solely with a family history of a penicillin allergy, pruritus without rash, or remote (\>10 years) unknown reactions without features suggestive of an IgE-mediated reaction. The study investigators seek to determine the safety and efficacy of a single-dose oral penicillin challenge pilot program in adult in-patients with self-reported penicillin allergy admitted to hospital under the internal medicine Clinical Teaching Unit (CTU). Identified patients that fulfill the exclusion and inclusion criteria will be reviewed at the time of discharge for suitability, as per the algorithm, modelled after a previous study of similar design. Based on patient's reported allergy, and upon obtaining informed consent, participants will receive a supervised challenge of amoxicillin 250 mg once orally and subsequently observed for 1 hour before discharge home. After antibiotic challenge, patient outcome will be defined as (1) tolerated oral challenge with no adverse drug reaction or (2) adverse drug reaction. By challenging carefully selected low risk patient that are unlikely to be truly allergic while in hospital, the study doctors can delabel patients of their penicillin allergy and as a result cut health care expenditures and promote good antimicrobial stewardship. In the future this model could be implemented generally as an inpatient or outpatient penicillin allergy program where low risk patients, who do not require referral to an allergist, are expeditiously delabeled.

Interventions

Low dose oral amoxicillin will be administered to patients enrolled in the study meeting the inclusion and exclusion criteria.

Sponsors

Saskatchewan Health Authority - Regina Area
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

Patients reporting penicillin allergy will be enrolled based on eligibility criteria for direct oral amoxicillin challenge. There will be one treatment group of patients assigned low risk for penicillin allergy.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Assessed to be low risk of having a penicillin allergy as per the risk stratification questionnaire 2. One of the following: i) An unknown reaction \>10 years before, ii) A type A adverse drug reaction (pharmacologically predictable drug side effect or intolerance), or iii) A history of a benign childhood rash, nonurticarial rash, or maculopapular exanthem more than 10 years ago 3. Age 18 years or older 4. Hemodynamically stable and suitable for discharge home

Exclusion criteria

1. Declines participation in the study 2. Cognitive impairment and where a collateral history could not be obtained 3. History of anaphylaxis or angioedema attributed to a penicillin-based antibiotic 4. History of severe cutaneous adverse reactions attributed to a penicillin-based antibiotic 5. History of acute kidney injury or severe liver impairment attributed to a penicillin-based antibiotic 6. Currently taking an angiotensin-converting enzyme inhibitor, angiotensin-receptor blocker or a beta blocker 7. Hemodynamically unstable 8. History of idiopathic urticaria or idiopathic anaphylaxis 9. Currently taking an antibiotic(s) for treatment of an active infection

Design outcomes

Primary

MeasureTime frameDescription
Number of patients tolerating oral amoxicillin challenge12 monthsThe number of patients tolerating a single dose oral amoxicillin (250 mg) challenge without adverse reaction(s) up to one hour of administration

Secondary

MeasureTime frameDescription
Number of patients reporting a delayed reaction to amoxicillin12 monthsNumber of patients reporting a delayed reaction to amoxicillin (between 1 hour - 12 weeks) following observation and discharge from hospital
Average delay in discharge attributable to amoxicillin challenge12 monthsAverage delay in discharge (minutes) attributable to penicillin challenge, recorded by the resident or staff physician performing the questionnaire
The number of patients excluded from the study due to staff time constraints12 monthsNumber of patients excluded from the study due to resident/staff time constraints
Type of immediate reaction attributed to the oral amoxicillin: maculopapular rash, urticaria, angioedema, airway compromise, diarrhea, vomiting or other (including subjective symptoms)12 monthsNature of immediate adverse reaction if challenge unsuccessful

Contacts

Primary ContactSarah Lohrenz, MD
skl621@usask.ca13067156011
Backup ContactAndrea Fong, MD, FRCPC
andrea.fong@usask.ca13062061291

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026