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. 2024 Apr 8;11(4):450.
doi: 10.3390/children11040450.

Study on Nocturnal Infant Crying Evaluation (NICE) and Reflux Disease (RED)

Affiliations

Study on Nocturnal Infant Crying Evaluation (NICE) and Reflux Disease (RED)

Greta Carabelli et al. Children (Basel). .

Abstract

Background: Nocturnal infant crying is often empirically treated with acid suppressants. The aim of this study was to evaluate the prevalence and characteristics of gastroesophageal reflux (GER) in infants with unexplained persistent crying.

Methods: We enrolled all infants (0-12 months) referred for suspected GER disease who underwent esophageal impedance-pH monitoring (MII-pH) for unexplained persistent crying not improved by parental reassurance, dietary modification or alginate. Gastrointestinal malformation/surgery, neurological impairment and infections were exclusion criteria. Demographic and anthropometric parameters, GER symptoms and questionnaires (I-GERQ-R) and MII-pH data were recorded and analyzed. Normal MII-pH was defined when acid exposure was <3%, symptom index was <50% and symptom association probability was <95%. Acid exposure >5% and >10% was also considered. Statistical analysis was performed using Chi-Square and univariate and multivariable regression analysis.

Results: We included 50 infants (median age 3.5 months) who fulfilled the study criteria: 30 (60%) had normal MII-pH. I-GERQ-R score was abnormal in 33 (66%) infants, and 21/33 (64%) had normal MII-pH (p = 0.47). In the 26 (52%) infants with nocturnal crying, MII-pH was normal in 16 (54%) (p = 0.82). Associated regurgitation (>3 or >10 episodes/die) did not predict abnormal MII-pH (p = 0.74, p = 0.82, respectively). Univariate and multivariable regression analysis did not identify any clinical variable significantly associated with abnormal MII-pH.

Conclusions: Infants with persistent unexplained and nocturnal crying should not be empirically treated with acid inhibitors.

Keywords: MII-pH; acid suppressant; crying; distress; esophageal impedance–pH monitoring; gastroesophageal reflux; infant; proton pump inhibitors; regurgitation; sleep.

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Conflict of interest statement

S. Salvatore has participated as a consultant and/or speaker and/or been a part of an advisory board for Aurora Biofarma, Bioprojet, Danone-Mellin, D.M.G. Italia, Humana Italia, Nestlé, Noos. All the above had no role in the design of the study; in the collection, analysis, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results. The other authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Variables analyzed in the NICE RED study.

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