Evidence map›Paper›PMID 31917366›Full record

ArticleThe journal of allergy and clinical immunology. In practice2020

Prospective Assessment of Pediatrician-Diagnosed Food Protein-Induced Allergic Proctocolitis by Gross or Occult Blood.

Victoria M Martin, Yamini V Virkud, Hannah Seay, Alanna Hickey, Renata Ndahayo, Rachael Rosow, Caroline Southwick, Michael Elkort, Brinda Gupta, Eileen Kramer and 6 more

Open access · greenAbstract read
In one paragraph

Article in The journal of allergy and clinical immunology. In practice, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
8.1field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

59 citing papers in PubMed, 101 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 2 countries.

Victoria M MartinFood Allergy Center, Massachusetts General Hospital, Boston, Mass; Division of Pediatric Gastroenterology, Hepatology and Nutrition, Massachusetts General Hospital, Boston, Mass; Department of Pediatrics, Harvard Medical School, Boston, Mass; Food Allergy Science Initiative of the Broad Institute, Cambridge, Mass.
Yamini V VirkudFood Allergy Center, Massachusetts General Hospital, Boston, Mass; Department of Pediatrics, Harvard Medical School, Boston, Mass; Food Allergy Science Initiative of the Broad Institute, Cambridge, Mass; Division of Pediatric Allergy and Immunology, Massachusetts General Hospital, Boston, Mass.
Hannah SeayDivision of Pediatric Allergy and Immunology, Massachusetts General Hospital, Boston, Mass.
Alanna HickeyDivision of Pediatric Allergy and Immunology, Massachusetts General Hospital, Boston, Mass.
Renata NdahayoDivision of Pediatric Allergy and Immunology, Massachusetts General Hospital, Boston, Mass.
Rachael RosowDivision of Pediatric Allergy and Immunology, Massachusetts General Hospital, Boston, Mass.
Caroline SouthwickDivision of Pediatric Allergy and Immunology, Massachusetts General Hospital, Boston, Mass.
Michael ElkortDepartment of Pediatrics, Harvard Medical School, Boston, Mass; Pediatrics at Newton Wellesley, P.C., Newton, Mass.
Brinda GuptaPediatrics at Newton Wellesley, P.C., Newton, Mass.
Eileen KramerPediatrics at Newton Wellesley, P.C., Newton, Mass.
Tetiana PronchickPediatrics at Newton Wellesley, P.C., Newton, Mass.
Susan ReuterPediatrics at Newton Wellesley, P.C., Newton, Mass.
Corinne KeetDivision of Pediatric Allergy and Immunology, John's Hopkins Hospital, Baltimore, Md; Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Md.
Kuan-Wen SuFood Allergy Center, Massachusetts General Hospital, Boston, Mass; Department of Pediatrics, Keelung Chang Gung Memorial Hospital, Keelung, Taiwan; Graduate Institute of Clinical Medical Sciences, Chang Gung University, Taoyuan, Taiwan.
Wayne G ShrefflerFood Allergy Center, Massachusetts General Hospital, Boston, Mass; Department of Pediatrics, Harvard Medical School, Boston, Mass; Food Allergy Science Initiative of the Broad Institute, Cambridge, Mass; Division of Pediatric Allergy and Immunology, Massachusetts General Hospital, Boston, Mass.
Qian YuanFood Allergy Center, Massachusetts General Hospital, Boston, Mass; Division of Pediatric Gastroenterology, Hepatology and Nutrition, Massachusetts General Hospital, Boston, Mass; Department of Pediatrics, Harvard Medical School, Boston, Mass; Food Allergy Science Initiative of the Broad Institute, Cambridge, Mass; Pediatrics at Newton Wellesley, P.C., Newton, Mass. Electronic address: qyuan@mgh.harvard.edu.
Massachusetts General Hospital · USNewton Wellesley Hospital · USHarvard University · USJohns Hopkins Medicine · US

Funding

The Harvard Clinical and Translational Science CenterUL1TR002541 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2018 to 2022
$93.0M
Early Peanut Introduction: Translation to Clinical PracticeU01AI125290 · NIAID · JOHNS HOPKINS UNIVERSITY · PI KEET, CORINNE, WOOD, ROBERT A · 2016 to 2020
$4.3M
MGHfC Digestive Disease Summer Research ProgramR25DK103579 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI BRYAN P HURLEY · 2015 to 2026
$1.2M
Endophenotypes of food allergy in response to oral immunotherapyK23AI130408 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI VIRKUD, YAMINI V · 2018 to 2022
$1.0M
NCATS NIH HHS UL1 TR002541NIAID NIH HHS K23 AI130408NIAID NIH HHS U01 AI125290NIDDK NIH HHS R25 DK103579
6 · The paper itself

Abstract

backgroundFood protein-induced allergic proctocolitis (FPIAP) is an early and common manifestation of food allergy, yet its epidemiology and relationship to other allergic diseases remain unclear.

objectiveTo prospectively define the incidence of FPIAP as it is being diagnosed clinically in the community and to identify factors associated with its development.

methodsA total of 1003 of 1162 eligible serial healthy newborn infants recruited from a single suburban pediatrics practice were followed prospectively for the diagnosis of FPIAP. Investigators reviewed each case to confirm prespecified inclusion criteria, including documented gross or occult blood in the stool.

resultsA total of 903 infants were analyzed (46% females, 89% term, 32% caesarian-section, 9% neonatal antibiotics); 153 cases met inclusion criteria, a cumulative incidence of 17%, while 63 (7%) had gross blood. Infants initially fed both breast milk and formula were 61% less likely to develop FPIAP compared with those exclusively formula-fed (hazard ratio, 0.39; P = .005). Breast milk and formula at any point during the first 4 months were also associated with lower risk compared with exclusive formula or exclusive breast milk (hazard ratio, 0.44; P = .005; hazard ratio, 0.62; P = .0497). Eczema (odds ratio, 1.5; 95% confidence interval, 1.1- 2.2; P = .02) or a first-degree relative with food allergies (odds ratio, 1.9; 95% confidence interval, 1.2-2.8; P = .005) were among risk factors for FPIAP development.

conclusionsThe prospectively defined incidence of FPIAP when diagnosed clinically by community pediatricians without challenge is markedly higher than published estimates. Combination feeding of formula and breast milk is associated with the lowest rate of FPIAP in this population.

Indexed as

Food HypersensitivityMilk HypersensitivityProctocolitisAnimalsChildFemaleHumansInfantInfant, NewbornMaleOccult BloodPediatriciansPregnancyProspective StudiesCow's milk protein allergyFood protein–induced allergic proctocolitisNon–IgE-mediated milk allergy

Identifiers

PMID31917366
PMCPMC8403015
OpenAlexW3000711280

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.