Objectives: Few machine learning (ML) models are successfully deployed in clinical practice. One of the common pitfalls across the field is inappropriate problem formulation: designing ML to fit the data rather than to address a real-world clinical pain point.
Methods: We introduce a practical toolkit for user-centred design consisting of four questions covering: (1) solvable pain points, (2) the unique value of ML (eg, automation and augmentation), (3) the actionability pathway and (4) the model's reward function.
Background: Acquired cold-induced urticaria (ACU) has not been well evaluated in pediatrics.
Objective: To further evaluate the presentation of ACU in children and associated risk of anaphylaxis.
Methods: A retrospective chart review was performed in children 18 years or younger diagnosed with ACU at Boston Children's Hospital (US, Northeast) from 1996 to 2017.
J Allergy Clin Immunol Pract
February 2019
Background: We successfully used omalizumab to facilitate peanut oral immunotherapy (OIT) in children with reactivity to ≤50mg peanut protein and with high peanut IgE (median, 229 kU/L).
Objective: We report on long-term OIT outcomes in these patients, including dosing changes, adverse events, peanut immunoglobulin changes, and quality of life (QoL).
Methods: Patients were followed for up to 72 months (67 months of maintenance).
Background: The rate of systemic reactions (SRs) to venom immunotherapy (VIT) in children has not been well evaluated.
Objective: To evaluate the rate of SRs to VIT in pediatric patients age 5 to 18 years who were treated with a standard protocol.
Methods: A retrospective chart review was conducted to identify patients who received VIT at Boston Children's Hospital from 1996 through 2018.
Background: The 2003 Joint Task Force on Practice Parameters recommended standardizing allergen subcutaneous immunotherapy (SCIT). Data from longitudinal surveillance survey in North America reported a systemic reaction (SR) rate of 0.1% to 0.
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