An algorithm for diagnosing IgE-mediated food allergy in study participants who do not undergo food challenge.

BACKGROUND: Food allergy diagnosis in clinical studies can be challenging. Oral food challenges (OFC) are time-consuming, carry some risk and may, therefore, not be acceptable to all study participants. OBJECTIVE: To design and evaluate an algorithm for detecting IgE-mediated food allergy in clinical study participants who do not undergo OFC. METHODS: An algorithm for trial participants in the Barrier Enhancement for Eczema Prevention (BEEP) study who were unwilling or unable to attend OFC was developed. BEEP is a pragmatic, multi-centre, randomized-controlled trial of daily emollient for the first year of life for primary prevention of eczema and food allergy in high-risk infants (ISRCTN21528841). We built on the European iFAAM consensus guidance to develop a novel food allergy diagnosis algorithm using available information on previous allergenic food ingestion, food reaction(s) and sensitization status. This was implemented by a panel of food allergy experts blind to treatment allocation and OFC outcome. We then evaluated the algorithm's performance in both BEEP and Enquiring About Tolerance (EAT) study participants who did undergo OFC. RESULTS: In 31/69 (45%) BEEP and 44/55 (80%) EAT study control group participants who had an OFC the panel felt confident enough to categorize children as "probable food allergy" or "probable no food allergy". Algorithm-derived panel decisions showed high sensitivity 94% (95%CI 68, 100) BEEP; 90% (95%CI 72, 97) EAT and moderate specificity 67% (95%CI 39, 87) BEEP; 67% (95%CI 39, 87) EAT. Sensitivity and specificity were similar when all BEEP and EAT participants with OFC outcome were included. CONCLUSION: We describe a new algorithm with high sensitivity for IgE-mediated food allergy in clinical study participants who do not undergo OFC. CLINICAL RELEVANCE: This may be a useful tool for excluding food allergy in future clinical studies where OFC is not conducted

Scientific Methods Must Be Public, and Descriptive Experience Sampling Qualifies

Hurlburt and Schwitzgebel’s groundbreaking book, Describing Inner Experience: Proponent Meets Skeptic, examines a research method called Descriptive Experience Sampling (DES). DES, which was developed by Hurlburt and collaborators, works roughly as follows. An investigator gives a subject a random beeper. During the day, as the subject hears a beep, she writes a description of her conscious experience just before the beep. The next day, the investigator interviews the subject, asks for more details, corrects any apparent mistakes made by the subject, and draws conclusions about the subject’s mind. Throughout the book, Schwitzgebel challenges some of Hurlburt’s specific conclusions. Yet both agree – and so do I – that DES is a worthy method

Biofeedback - October 1984

Archived record for the USA Biomedical Library newsletter for October 1984. Content includes: Welcome from Robert Donnell, Head of the Biomedical Library Who to Contact at the Biomedical Library New Circulation Policy Faculty News Public Services Comments From the Online Services Coordinator Library Orientation Bibliographic Instruction Medical Center Library Inventory Beep, Beep, Beep Selected Recent Acquisition