2022
DOI: 10.1016/j.waojou.2022.100682
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World Allergy Organization (WAO) Diagnosis and Rationale for Action against Cow's Milk Allergy (DRACMA) guideline update – XIII – Oral immunotherapy for CMA – Systematic review

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Cited by 11 publications
(9 citation statements)
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“…anaphylaxis) or eosinophilic oesophagitis, an AAF might be indicated. 13,14 In addition to proven efficacy, these formulas need to be nutritionally complete and support normal growth and development. 15 Whilst soya formula (SF) is not an FSMP, this formula can be used in infants >6 months as long as they are not soya allergic.…”
Section: Bms and Prevention Of Allergic Diseasesmentioning
confidence: 99%
See 1 more Smart Citation
“…anaphylaxis) or eosinophilic oesophagitis, an AAF might be indicated. 13,14 In addition to proven efficacy, these formulas need to be nutritionally complete and support normal growth and development. 15 Whilst soya formula (SF) is not an FSMP, this formula can be used in infants >6 months as long as they are not soya allergic.…”
Section: Bms and Prevention Of Allergic Diseasesmentioning
confidence: 99%
“…Moreover, in severe CMA (i.e. anaphylaxis) or eosinophilic oesophagitis, an AAF might be indicated 13,14 . In addition to proven efficacy, these formulas need to be nutritionally complete and support normal growth and development 15 .…”
Section: Introductionmentioning
confidence: 99%
“…Several systematic reviews have addressed OIT as a treatment for peanut, egg, and/or milk allergy 12,18–22 . Nurmatov et al's 18 systematic review included 25 RCTs and 6 non‐randomized studies published up to March 2016.…”
Section: Introductionmentioning
confidence: 99%
“…16,17 Several systematic reviews have addressed OIT as a treatment for peanut, egg, and/or milk allergy. 12,[18][19][20][21][22] Nurmatov et al's 18 systematic review included 25 RCTs and 6 non-randomized studies published up to March 2016. A limitation of this systematic review was the pooling of heterogeneous studies and methods.…”
mentioning
confidence: 99%
“…These are just some of the questions that spontaneously arise when faced with the new approval of the Omalizumab indication. Others concern the opportunity to select patients based on their severity [17], the cost–benefit ratio of the drug [18], its use in patients with pretreatment IgE exceeding 1850 kUI/l [19], and the need for predictive indices of its effectiveness [20]. Beyond them, what is certain is the FDA approval is an epochal event as also recorded by the mainstream press (https://www.nytimes.com/2024/02/25/health/children-food-allergies-xolair.html, accessed on 15 March 2024).…”
mentioning
confidence: 99%