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Cow's Milk-Related Symptom Score (CoMiSS): From Bristol to Brussels Stool Scale
K. Bajerova, S. Salvatore, C. Dupont, M. Kuitunen, R. Meyer, C. Ribes-Koninckx, R. Shamir, H. Szajewska, A. Staiano, Y. Vandenplas
Language English Country United States
Document type Journal Article
- MeSH
- Allergens MeSH
- Milk Hypersensitivity * complications diagnosis MeSH
- Feces MeSH
- Infant MeSH
- Humans MeSH
- Milk * MeSH
- Cattle MeSH
- Animals MeSH
- Check Tag
- Infant MeSH
- Humans MeSH
- Cattle MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article 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
References provided by Crossref.org
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- $a Bajerova, Katerina $u From the Department of Pediatrics, University Hospital Brno and Masaryk's University, Brno, Czech Republic $u the Department of Internal Medicine, Geriatrics and Practical Medicine, University Hospital Brno and Masaryk's University, Brno, Czech Republic
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- $a 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.
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