Cow's Milk-Related Symptom Score (CoMiSS): From Bristol to Brussels Stool Scale
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
37668589
PubMed Central
PMC10583930
DOI
10.1097/mpg.0000000000003932
PII: 00005176-990000000-00478
Knihovny.cz E-zdroje
- MeSH
- alergeny MeSH
- alergie na mléko * komplikace diagnóza MeSH
- feces MeSH
- kojenec MeSH
- lidé MeSH
- mléko * MeSH
- skot MeSH
- zvířata MeSH
- Check Tag
- kojenec MeSH
- lidé MeSH
- skot MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- alergeny MeSH
OBJECTIVES: The Cow's Milk-related Symptom Score (CoMISS) is an awareness tool for evaluating cow's milk-related symptoms in otherwise healthy infants <1 year of age. This study assessed whether replacing the Bristol Stool Form Scale (BSFS) with the Brussels Infants and Toddlers Stool Scale (BITSS) in non-toilet-trained infants would modify the overall CoMiSS and change the clinical approach regarding potential cow's milk allergy. METHODS: Non-toilet-trained infants aged <13 months were assessed by CoMiSS using the 7 images from the BSFS (CoMiSS-BSFS) compared to the 4 images of stools from BITSS (CoMiSS-BITSS). The Wilcoxon signed-rank test and Pearson correlation coefficient were calculated. A post hoc analysis using identical tests was performed in subsets of CoMiSS-BSFS scores ≥10, ≥12, ≤5, and ≥6. RESULTS: Eight hundred forty-four pairwise scores were collected. Applying the Wilcoxon test over the complete dataset, the difference between CoMiSS-BSFS and CoMiSS-BITSS was statistically significant ( P < 0.001). However, there was no significant difference in the subsets with CoMiSS-BSFS ≥10, ≥12, and ≥6 ( P = 0.84, P = 0.48, and P = 0.81, respectively). The significant difference remained restricted to the group with CoMiSS-BSFS ≤5, considered at low risk for CM-related symptoms ( P < 0.001). CONCLUSION: Replacing BSFS with BITSS does not change the cutoff for awareness of possible CM-related symptoms and will not impact the use of CoMiSS in clinical practice. Changes in CoMiSS remained limited to the subgroup with a low risk for CM-related symptoms.
Children's Hospital University of Helsinki and Helsinki University Hospital Helsinki Finland
Paris Descartes University France et Clinique Marcel Sembat Boulogne Billancourt Ramsay Group France
Pediatric Gastroenterology La Fe University Hospital and La Fe Research Institute Valencia Spain
the Department of Dietetics Winchester University Winchester UK
the Department of Medicine KU Leuven Leuven Belgium
the Department of Paediatrics Imperial College London London UK
the Department of Paediatrics The Medical University of Warsaw Warsaw Poland
the Department of Paediatrics University of Insubria Varese Italy
the Department of Translational Medical Sciences University of Naples Federico 2 Napoli Italy
Vrije Universiteit Brussel UZ Brussel KidZ Health Castle Brussels Belgium
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