Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/44463
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dc.contributor.authorLloyd M.-
dc.contributor.authorAshley S.-
dc.contributor.authorHsiao K.-
dc.contributor.authorPitkin S.-
dc.contributor.authorDunn Galvin A.-
dc.contributor.authorJayawardana K.-
dc.contributor.authorLozinsky A.C.-
dc.contributor.authorLoke P.-
dc.contributor.authorTang M.L.-
dc.date.accessioned2022-02-09T05:29:11Z-
dc.date.available2022-02-09T05:29:11Z-
dc.date.copyright2021-
dc.date.issued2021-12-09en
dc.identifier.citationAllergy: European Journal of Allergy and Clinical Immunology. Conference: European Academy of Allergy and Clinical Immunology Hybrid Congress, EAACI 2021. Krakow Poland. 76(SUPPL 110) (pp 545-546), 2021. Date of Publication: November 2021.-
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/44463-
dc.description.abstractBackground: Previously, we have reported that probiotic and peanut oral immunotherapy (PPOIT) improved health-related quality eof life (HRQL), and improvement was specifically linked to acquisition of sustained unresponsiveness (SU). PPOIT-002 is a single arm open-label study which aimed to investigate long-term outcomes at 3-years post-treatment after 18-months of PPOIT treatment. Method(s): Participants (aged 1-12 years) with challenge-proven peanut allergy received PPOIT for 18-months. HRQL was evaluated at screening (T0), end-of- treatment (T2), and 12-months (T4) and 3-years (T5) post-treatment, using the Food Allergy Quality of Life Questionnaire -Parent Form (FAQLQ-PF) and Food Allergy Impact Measure (FAIM). FAQLQ-PF total score and sub-scores (emotional impact, food anxiety, and social and dietary limitations) were assessed. Difference in scores between timepoints was evaluated using paired t-tests. Result(s): Of 20 enrolled participants, 16 remained in the study at end-of- treatment (T2), and 12 achieved 8-week SU. Twenty participated in outcome assessments at T0, 16 at T2, 14 at T4, and 12 at T5. Both the FAQLQ-PF and FAIM total scores improved significantly in the 12-months following treatment completion (change in score T2 to T4: 0.44, 95% CI 0.17-0.70, p = 0.004; and 0.37, 95% CI 0.10-0.65, p = 0.01; respectively). Improvements in FAQLQ and FAIM scores were maintained at 3-years post-treatment (see Table 1). Improvement was also seen in each of the FAQLQ-PF sub-scores for emotional impact, food anxiety, and social and dietary limitations. Conclusion(s): PPOIT treatment for 18 months leads to significant and long-lasting improvement in quality of life and food allergy impact burden, as perceived by caregivers. (Table Presented).-
dc.publisherBlackwell Publishing Ltd-
dc.relation.ispartofAllergy: European Journal of Allergy and Clinical Immunology-
dc.subject.meshanxiety-
dc.subject.meshcaregiver-
dc.subject.meshdiet-
dc.subject.meshinfant-
dc.subject.meshoral immunotherapy-
dc.subject.meshpeanut allergy-
dc.subject.meshphase 2-
dc.subject.meshquality of life-
dc.subject.meshprobiotic agent-
dc.titleLong-term longitudinal quality of life outcomes following a phase 2a open-label study of probiotic and peanut oral immunotherapy (PPOIT).-
dc.typeConference Abstract-
dc.identifier.affiliationPaediatric - Allergy and Immunology-
dc.description.conferencenameEuropean Academy of Allergy and Clinical Immunology Hybrid Congress, EAACI 2021-
dc.description.conferencelocationKrakow, Poland-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1111/all.15096-
local.date.conferencestart2021-07-10-
dc.identifier.institution(Loke) Monash Children's Hospital, Clayton, Australiaen
dc.identifier.institution(Lloyd, Ashley, Hsiao, Pitkin, Jayawardana, Lozinsky, Loke, Tang) Murdoch Children's Research Institute, Melbourne, Australiaen
dc.identifier.institution(Lloyd, Loke, Tang) University of Melbourne, Melbourne, Australiaen
dc.identifier.institution(Lloyd, Ashley, Lozinsky, Loke, Tang) Royal Children's Hospital, Melbourne, Australiaen
dc.identifier.institution(Hsiao) Starship Children's Hospital, Auckland, New Zealanden
dc.identifier.institution(Hsiao) University of Auckland, Auckland, New Zealanden
dc.identifier.institution(Dunn Galvin) University College Cork, Cork, Irelanden
local.date.conferenceend2021-07-12-
dc.subect.keywordsclinical article-
dc.subect.keywordsconference abstract-
dc.subect.keywordscontrolled study-
dc.subect.keywordsfemale-
dc.subect.keywordshuman-
dc.subect.keywordsmale-
dc.subect.keywordsquestionnaire-
dc.identifier.affiliationext(Lloyd, Ashley, Hsiao, Pitkin, Jayawardana, Lozinsky, Loke, Tang) Murdoch Children's Research Institute, Melbourne, Australia-
dc.identifier.affiliationext(Lloyd, Loke, Tang) University of Melbourne, Melbourne, Australia-
dc.identifier.affiliationext(Lloyd, Ashley, Lozinsky, Loke, Tang) Royal Children's Hospital, Melbourne, Australia-
dc.identifier.affiliationext(Hsiao) Starship Children's Hospital, Auckland, New Zealand-
dc.identifier.affiliationext(Hsiao) University of Auckland, Auckland, New Zealand-
dc.identifier.affiliationext(Dunn Galvin) University College Cork, Cork, Ireland-
dc.identifier.affiliationmh(Loke) Monash Children's Hospital, Clayton, Australia-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairetypeConference Abstract-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
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