Open Access

Cow's milk protein allergy in children: a practical guide

  • Carlo Caffarelli1Email author,
  • Francesco Baldi2,
  • Barbara Bendandi3,
  • Luigi Calzone4,
  • Miris Marani5 and
  • Pamela Pasquinelli6
Italian Journal of Pediatrics201036:5

DOI: 10.1186/1824-7288-36-5

Received: 11 December 2009

Accepted: 15 January 2010

Published: 15 January 2010

Abstract

A joint study group on cow's milk allergy was convened by the Emilia-Romagna Working Group for Paediatric Allergy and by the Emilia-Romagna Working Group for Paediatric Gastroenterology to focus best practice for diagnosis, management and follow-up of cow's milk allergy in children and to offer a common approach for allergologists, gastroenterologists, general paediatricians and primary care physicians.

The report prepared by the study group was discussed by members of Working Groups who met three times in Italy. This guide is the result of a consensus reached in the following areas. Cow's milk allergy should be suspected in children who have immediate symptoms such as acute urticaria/angioedema, wheezing, rhinitis, dry cough, vomiting, laryngeal edema, acute asthma with severe respiratory distress, anaphylaxis. Late reactions due to cow's milk allergy are atopic dermatitis, chronic diarrhoea, blood in the stools, iron deficiency anaemia, gastroesophageal reflux disease, constipation, chronic vomiting, colic, poor growth (food refusal), enterocolitis syndrome, protein-losing enteropathy with hypoalbuminemia, eosinophilic oesophagogastroenteropathy. An overview of acceptable means for diagnosis is included. According to symptoms and infant diet, three different algorithms for diagnosis and follow-up have been suggested.

Introduction

Cow's milk protein allergy (CMPA) affects from 2 to 6% of children, with the highest prevalence during the first year of age [1]. About 50% of children have been shown to resolve CMPA within the first year of age, 80-90% within their fifth year [2, 3]. The rate of parent-reported CMPA is about 4 times higher than the real one in children [4]. So, many children are referred for suspected CMPA based on parent perception, symptoms such as cutaneous eruption, insomnia, persistent nasal obstruction, sebhorreic dermatitis or positive results to unorthodox investigations. Moreover, parents often put their children on unnecessary diet without an adequate medical and dietary supervision. These inappropriate dietary restrictions may provoke nutritional unbalances, especially in the first year of age. Therefore, an accurate diagnosis of CMPA is important in order to avoid not only the risk of rickets, decreased bone mineralization [5], anaemia, poor growth and hypoalbuminemia, but also that of immediate clinical reactions or severe chronic gastroenteropathy leading to malabsorption.

Recently, three guidelines [68] reporting different approaches to the infant with CMPA have been published.

In view of these considerations, a study group with expert representatives of Emilia-Romagna Working Group for Paediatric Allergy and of that for Paediatric Gastroenterology (EWGPGA), was constituted. As mmembers of the expert panel, the authors were assigned to review practice with regard to diagnosis, management and follow-up of CMPA for both community and hospital paediatrician in order to share the same approach towards the child. The document prepared by the study group was based on existing recommendations, clinical experience and evidence from the literature. The report was discussed and received input by the members (see participant list in acknowledgments) of EWGPGA which included clinicians experienced in paediatric allergy, paediatric gastroenterology and general paediatricians, in three meetings held in November 2008, February 2009 and March 2009 and a consensus was reached. According to the symptoms and the type of infant diet, three different algorithms for diagnosis and follow-up have been suggested. These approaches refer to the child in the first year of age. Recommendations for older children have been briefly reported.

Cow's milk protein allergy: when should we doubt?

A positive atopic familiar history is common in children with suspected CMPA [9]. The diagnosis of CMPA is based on a detailed history of symptoms (Fig. 1), skin prick test and serum specific IgE to cow's milk protein, elimination diet and oral food challenge. Clinical manifestations due to CMPA [614] can be divided into IgE-mediated immediate clinical reactions (onset of the symptoms within the 30 minutes after the ingestion of cow's milk) and non IgE-mediated delayed reactions (hours-days after food ingestion), most affecting the skin and the gastrointestinal system. However, immediate and delayed reactions can be associated in atopic eczema and in eosinophilic oesophageal gastroenteritis (Fig. 1).
https://static-content.springer.com/image/art%3A10.1186%2F1824-7288-36-5/MediaObjects/13052_2009_Article_53_Fig1_HTML.jpg
Figure 1

Immediate and late onset reactions in children with cow's milk protein allergy.

The negative predictive value of skin prick test/specific IgE for immediate reaction is excellent (>95%) [15], however a small number of these patients can have clinical reaction. Therefore, despite negative IgE tests if there is a strong suspicion of CMPA, an oral food challenge is necessary to confirm the absence of clinical allergy. On the other hand, about 60% of children with positive IgE tests have CMPA [15, 16]. Prick by prick test with cow's milk substitutes may be considered.

Oral food challenge, open or blind, remains the 'gold standard" to definitely ascertain children with food allergy when the diagnosis is unclear [17]. OFC should be performed under medical supervision in a setting with emergency facilities, especially in case of positive skin prick test or serum specific IgE to cow's milk and in infants at risk of an immediate reaction.

Cow's milk substitutes

About 10% of children with CMPA react to extensively hydrolyzed formula (eHF) [7]. In comparison with eHF, soy formula (SF) provokes more frequently reactions in children with CMPA aged less than 6 months [18] but not in older children. SF mainly induces gastrointestinal symptoms.

Amino acid formula (AAF) is non allergenic [19]. Its use is limited by the high cost and bad taste.

Rice is allergenic and is often involved in the onset of enterocolitis syndrome in Australian infants [20]. Contrasting data have been reported on the effect of protein content on growth [21]. In Italian children, rice formula has been shown to be tolerated by children with CMPA [22]. Larger long-term studies are warranted to clarify the use of rice formula in infants with CMPA. Rice formula may be a choice in selected cases taking into consideration the taste and the cost.

Home-made meals may be a dietary option after 4 months of age.

Mammalian milks are not nutritionally adequate. Goat's milk commonly provokes clinical reactions in more than 90% of children with CMPA [23], donkey's milk in about 15% [24, 25] and has a high cost.

A child fed with cow's milk formula with mild- moderate symptoms (Fig. 2)

https://static-content.springer.com/image/art%3A10.1186%2F1824-7288-36-5/MediaObjects/13052_2009_Article_53_Fig2_HTML.jpg
Figure 2

Algorithm for children < 1 year fed with cow's milk formula and mild-moderate symptoms.

In infants with immediate symptoms (vomiting, acute hives, angioedema, wheezing, rhinitis, dry cough) or late symptoms (moderate/severe atopic dermatitis, diarrhoea, blood in the stools, iron deficiency anaemia, gastroesophageal reflux disease (GORD), constipation) a CMPA can be suspected [68, 1014]. Other causes are to be considered for patients unresponsive to treatment. Infant colic (more than 3 hours of crying a day, 3 days for more than 3 weeks) is not unanimously considered as a consequence of CMPA. The paediatrician has to consider the opportunity of a cow's milk free diet in the most troublesome cases [26, 27]. Mild immediate reactions may be of difficult interpretation because they can be the result of causes different from CMPA. However, if these symptoms are strongly related to cow's milk ingestion, we recommend to eliminate cow's milk and follow the algorithm for severe reactions (Fig. 2).

Regarding delayed onset gastrointestinal symptoms, other pathologies (i.e. infections) should be excluded before investigating allergic sensitization.

In mild atopic dermatitis, investigations for CMPA are not necessary in the absence of a clear relation between cow's milk intake and onset of symptoms.

When a CMPA is suspected, infants should go on a 2-4 week diet without cow's milk protein. Four weeks should be considered for chronic gastrointestinal symptoms. Infants should be fed with eHF or SF in children aged more than 6 months and without gastrointestinal symptoms.

If the symptoms improve on a restrict diet, an OFC to cow's milk is necessary to definitely ascertain the diagnosis. If the oral food challenge is positive, the child must follow the elimination diet and can be re-challenged after 6 months (a shorter period for GORD) and in any case, after 9-12 months of age. If the oral food challenge is negative, a free-diet can be followed.

When there is strong suspicion of IgE-mediated reactions, in infants who do not respond to a diet with eHF or SF an attempt may be made with a 14-days diet with AAF.

Cow's milk substitutes are used in children aged less than 12 months. In older children with CMPA, eHF or AAF are not usually necessary because an adequate diet is easily accessible.

A child fed with cow's milk formula with severe symptoms (Fig. 3)

https://static-content.springer.com/image/art%3A10.1186%2F1824-7288-36-5/MediaObjects/13052_2009_Article_53_Fig3_HTML.jpg
Figure 3

Algorithm for children <1 year fed with cow's milk formula and severe symptoms. In child less than1 year of age, infant formula is not compulsory.

Immediate severe symptoms are considered laryngeal edema, acute asthma with severe respiratory difficulty, anaphylaxis. The following are delayed onset severe symptoms: chronic diarrhoea or chronic vomiting with poor growth, intestinal bleeding with iron deficiency anaemia, protein losing enteropathy with hypoalbuminemia, eosinophilic gastroenteropathy confirmed by biopsy [7, 8, 1014].

If any of these immediate symptoms are observed as a consequence of suspected CMPA, infants should follow a cow's milk free diet. As substitutes, SF (if older than 6 months of age) or eHF or AAF can be used. eHF and SF should be started under medical supervision because of possible clinical reactions. If an AAF is adopted, it may be administered for 2 weeks and then the infant may be switched to SF or eHF.

In children with late severe gastrointestinal symptoms with poor growth, anaemia or hypoalbuminemia or eosinophilic oesophagogastroenteropathy, it is recommended to start an elimination diet with AAF and then switched with eHF. The effect of the diet should check out within 10 days for enterocolitis syndrome, 1-3 weeks for enteropathy and 6 weeks for eosinophilic oesophagogastroenteropathy.

In children with anaphylaxis and concordant positive IgE tests or severe gastrointestinal reactions, oral food challenge is not necessary for diagnosis. The oral food challenge for tolerance acquisition should be performed not before 6-12 months after the last reaction. Children have to eliminate cow's milk until 12 months of age, but in those with enterocolitis syndrome until 2-3 years of age [28].

Children with any severe symptoms should be referred to a specialized centre.

eHF or AAF is used in children aged less than 12 months and in older children with severe gastrointestinal symptoms. In children > 12 months with anaphylaxis, cow's milk substitutes are not always nutritionally required.

A breast-fed infant with a suspected CMPA (Fig. 4)

https://static-content.springer.com/image/art%3A10.1186%2F1824-7288-36-5/MediaObjects/13052_2009_Article_53_Fig4_HTML.jpg
Figure 4

Algorithm for breast-fed infants with suspected non-IgE mediated reactions to cow's milk protein.

In exclusively breast-fed infants, suspected symptoms to the cow's milk proteins are almost always non IgE-mediated as atopic dermatitis, vomiting, diarrhoea, blood in the stools, GORD, colic [29].

A maternal diet without cow's milk is not recommended for mild symptoms.

There is no evidence that a maternal diet without egg and cow's milk in infants with bloody stools (proctocolitis) is of value [30, 31].

In infants with moderate-severe symptoms, cow's milk protein, eggs and other foods should be eliminated by the mother's diet only if history suggests an unequivocal reaction. Moreover, the infant should be referred to a specialized centre. The maternal elimination diet has to be followed for 4 weeks. If there is no improvement the diet should be stopped. If symptoms improved, it's recommended that the mother ingested large amounts of cow's milk for one week. If symptoms occurred, the mother will continue the diet with supplemental intake of calcium. The infant can be weaned as recommended for healthy children, but cow's milk should be avoided until 9-12 months of age and for at least 6 months from the beginning of the diet. If the volume of breast milk is insufficient, eHF or SF formula (if > 6 months) should be administered.

If after the reintroduction of cow's milk in mother's diet symptoms do not occur, the excluded foods can be introduced one by one in the diet.

Conclusions

The diagnosis of CMPA is based on oral food challenge that follows a 2-4 week elimination diet.

A diagnostic oral food challenge is unnecessary in immediate reactions or late gastrointestinal reactions with anaemia, poor growth or hypoalbuminemia if the causative role of cow's milk is clear. Children can be challenged after 6-12 months from the reaction and not before 12-24 months of age according to the symptoms.

Diets must be nutritionally balanced. In children with CMPA, a supplementation with calcium must be evaluated.

Diet is not requested in children with mild atopic dermatitis and negative history for cow's milk reactions.

SF should not be used in infants < 6 months of age with allergic symptoms and in those with late gastrointestinal symptoms.

Children with gastrointestinal reactions and anaemia, poor growth or hypoalbuminemia should be given AAF and then switched to eHF.

eHF or AAF is used in children aged less than 12 months and in older children with severe gastrointestinal symptoms. In children > 12 months with anaphylaxis, cow's milk substitutes are not always nutritionally required.

List of abbreviations

CMPA: 

cow's milk protein allergy

EWGPAG: 

Emilia-Romagna Working Group for Paediatric Allergy and of that for Paediatric Gastroenterology

eHF: 

extensively hydrolyzed formula

SF: 

soy

AAF: 

amino acid formula

GORD: 

gastroesophageal reflux disease.

Declarations

Acknowledgements

Physicians and specialists of Emilia-Romagna Emilia-Romagna Working Group for Paediatric Allergy and for Paediatric Gastroenterology (EWGPGA) who contributed to this guide.

Paediatric gastroenterology: Patrizia Alvisi (U.O. di Pediatria Ospedale Maggiore, Bologna, Italy), Sergio Amarri (U.O. di Pediatria, Reggio Emilia, Italy), Paolo Baldassarri (U.O. di Pediatria, Forlì,), Sandra Brusa (U.O. di Pediatria, Imola, Italy), Marisa Calacoci (Pediatra Libero Professionista, Ferrara, Italy), Iliana Cecchini (U.O. di Pediatria, Cesena, Italy), Sara Denti (U.O. di Pediatria, Carpi, Italy), Annarita Di Biase (U.O. di Pediatria, Modena, Italy), Cristina Host (U.O. di Pediatria, Ferrara, Italy), Andrea Lambertini (U.O. di Pediatria Ospedale Maggiore, Bologna, Italy), Angelo Miano (Pediatra Libero Professionista, Cesena, Italy), Annamaria Metri (U.O. di Pediatria, Faenza, Italy), Marco Occari (U.O. di Pediatria, Mantova, Italy), Renzo Pini (U.O. di Pediatria, Rimini, Italy), Marina Rossidoria (Pediatra Libero Professionista, Bologna, Italy).

Paediatric allergy: Andrea Valenti (U.O. di Pediatria, Lugo, Italy), Monica Vallini (Pediatra Libera scelta, Bologna, Italy, Italy), Iole Venturi (U.O. di Pediatria, Ravenna, Italy), Laura Viola (U.O. di Pediatria, Rimini, Italy). Ermanno Baldo (U.O.di Pediatria, Rovereto, Italy), Mauro Bandini (U.O. di Pediatria, Ravenna, Italy), Filippo Bernardi (Clinica Pediatrica Ospedale S. Orsola, Bologna, Italy), Adriana Borghi (U.O. Pediatria, Carpi, Italy), Paolo Bottau (U.O. di Pediatria, Imola, Italy), Lucetta Capra (U.O. di Pediatria Azienda Ospedaliera-Universitaria S. Anna, Ferrara, Italy), Giovanni Cavagni (Ospedale Pediatrico Bambin Gesù, Roma, Italy), Matteo Corchia (Clinica Pediatrica, Parma, Italy), Danilo Dalpozzo (U.O.di Pediatria, Imola, Italy), Leonardo Loroni (U.O. di Pediatria, Ravenna, Italy), Laura Giovannini (Pediatra Libero Professionista, Lugo, Italy), Massimo Masi (Dipartimento "Salute della donna, del bambino e dell'adolescente, Policlinico S. Orsola-Malpighi, Bologna, Italy), Giuseppe Menna (ISS Istituto Sicurezza Sociale, U.O.C.Pediatria-Ospedale della Repubblica di San Marino, Italy), Patrizia Preti (U.O. di Pediatria Ospedale Maggiore, Bologna, Italy), Giampaolo Ricci (Dipartimento "Salute della donna, del bambino e dell'adolescente, Policlinico S. Orsola-Malpighi, Bologna, Italy), Giuseppe Timoncini (U.O. di Pediatria, Forlì, Italy), Loretta Biserna (U.O. di Pediatria, Ravenna, Italy), Elena Zamuner (U.O. di Pediatria, Ravenna, Italy).

Authors’ Affiliations

(1)
Dipartimento dell'Età Evolutiva, Clinica Pediatrica Università di Parma
(2)
UO di Pediatria, AUSL Imola
(3)
Dipartimento "Salute della donna, del bambino e dell'adolescente" Policlinico S Orsola-Malpighi, Clinica Pediatrica
(4)
Dipartimento Emergenza ed Accettazione diagnostica, UO di Pediatria
(5)
Pediatria, AUSL di Ravenna
(6)
UO Pediatria, AUSL di Cesena
(7)
EWGPAG

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This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.