2021
DOI: 10.1007/s11882-021-01009-8
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How to Incorporate Oral Immunotherapy into Your Clinical Practice

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Cited by 15 publications
(6 citation statements)
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“…This case series did not warrant formal ethics review, since the University of British Columbia ethics committee categorized it as quality improvement. Parents were advised to introduce peanut starting from 10 mg peanut protein on a daily basis with a gradual dose increased to 320 mg ~2 weeks apart according to the previously published peanut OIT protocols that showed a low risk of anaphylaxis ( 2 , 13 ). Patients could start the OIT at a lower dose if the cumulative threshold was ≤10 mg based on OFC.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…This case series did not warrant formal ethics review, since the University of British Columbia ethics committee categorized it as quality improvement. Parents were advised to introduce peanut starting from 10 mg peanut protein on a daily basis with a gradual dose increased to 320 mg ~2 weeks apart according to the previously published peanut OIT protocols that showed a low risk of anaphylaxis ( 2 , 13 ). Patients could start the OIT at a lower dose if the cumulative threshold was ≤10 mg based on OFC.…”
Section: Methodsmentioning
confidence: 99%
“… * World Allergy Organization Subcutaneous Immunotherapy Systemic Reaction Grading System ( 13 ) . # Suggest introduce peanut at home or arrange observed ingestion/oral food challenge .…”
Section: Methodsmentioning
confidence: 99%
“…As a result, several guidelines, published for OIT in recent years, indicated that OIT is efficient in children, but referred to OIT in adults only as "may be indicated," due to insufficient data. [9][10][11][12] Unfortunately, alternative forms of immunotherapy for this population, such as epicutaneous immunotherapy, are currently unavailable 13 .…”
Section: Backg Rou N Dmentioning
confidence: 99%
“…Before initiating OIT, patients should have a personalized action plan to guide them in the management of adverse effects. Families should be equipped with an algorithm providing guidance for situations such as missed doses or illness (49). They should also be able to contact a professional to whom they can address questions and concerns during treatment.…”
Section: Patient Safetymentioning
confidence: 99%
“…In the build-up phase, patients are generally monitored for 1 h after up-dosings (49), but the timeframe can vary depending on the clinical practice and increased surveillance could be necessary in higher-risk patients (e.g. patient with previous delayed reaction to up-dosing).…”
Section: Patient Safetymentioning
confidence: 99%