Faculty Opinions recommendation of Diagnostic approach and management of cow's-milk protein allergy in infants and children: ESPGHAN GI Committee practical guidelines.

Author(s):  
Neil Shah
2017 ◽  
Vol 14 (2) ◽  
pp. 55-65
Author(s):  
L S Namazova-Baranova ◽  
S G Makarova ◽  
G A Novik ◽  
E A Vishneva

Professional medical communities create clinical recommendations based on principles of «evidencebased medicine» to optimize the provision of medical care to patients with various pathologies. Following these recommendations allows doctors to avoid mistakes in the management of patients and to achieve a positive result of treatment in most of the patients. Early started and properly administered treatment of children with cow’s milk protein allergy (CMPA) significantly improves the prognosis of the disease and can interrupt the socalled «allergic march». The purpose of the publication is to introduce the current national clinical guidelines for the provision of medical care to children with CMPA to wide range of pediatricians and physicians of other specialties.


2019 ◽  
Vol 36 (1-2) ◽  
pp. 67-76
Author(s):  
Yosra M. Mohsen ◽  
Mostafa A. El-Hodhod ◽  
Mohammed H. Soliman ◽  
Safaa A. M. Hashem

2016 ◽  
Vol 58 (1) ◽  
pp. 1 ◽  
Author(s):  
Aydan Kansu ◽  
Aysel Yüce ◽  
Buket Dalgıç ◽  
Bülent Enis Şekerel ◽  
Fügen Çullu-Çokuğraş ◽  
...  

2021 ◽  
Author(s):  
Kornilia Nikaki ◽  
Tracey Johnson ◽  
Haidee Norton ◽  
Gabis Chana ◽  
Amrita Garcha ◽  
...  

2021 ◽  
Vol 10 (8) ◽  
pp. 1595
Author(s):  
María Roca ◽  
Ester Donat ◽  
Ana Rodriguez Varela ◽  
Eva Carvajal ◽  
Francisco Cano ◽  
...  

Our aim is to assess the efficacy of fecal calprotectin (fCP) and fecal eosinophil-derived neurotoxin (fEDN) as diagnostic markers of cow’s milk protein allergy (CMPA) and for monitoring the infants’ response to a non-IgE mediated cow’s milk protein (CMP)-free diet. We prospectively recruited infants aged 0 to 9 months. Stool samples were taken from 30 infants with CMPA, 19 with mild functional gastrointestinal disorders, 28 healthy infants, and 28 children who presented mild infections. Despite the fact that levels of fCP and fEDN in CMPA infants were higher than in healthy infants at month 0, differences for both parameters did not reach statistical significance (p-value 0.119 and 0.506). After 1 month of an elimination diet, no statistically significant differences in fCP with basal levels were found (p-values 0.184) in the CMPA group. We found a high variability in the fCP and fEDN levels of young infants, and discrepancies in individual behavior of these markers after a CMP-free diet was started. It seems that neither fCP nor fEDN levels are helpful to discriminate between healthy infants and those with signs or symptoms related to non-IgE-mediated CMPA. Additionally, it is debatable if on an individual basis, fCP or fEDN levels could be used for clinical follow-up and dietary compliance monitoring. However, prospective studies with larger populations are needed to draw robust conclusions.


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