Disagreement between symptom-reflux association analysis parameters in pediatric gastroesophageal reflux disease investigation.

World J Gastroenterol

Division of Gastroenterology, Departement of Pediatrics, Hospital of Fribourg, CH-1708 Fribourg, Switzerland.

Published: May 2010

Aim: To assess the agreement within 3 commonly used symptom-reflux association analysis (SAA) parameters investigating gastroesophageal reflux disease (GERD) in infants.

Methods: Twenty three infants with suspected GERD were included in this study. Symptom index (SI), Symptom sensitivity index (SSI) and symptom association probability (SAP) related to cough and irritability were calculated after 24 h combined pH/multiple intraluminal impedance (MII) monitoring. Through defined cut-off values, SI, SSI and SAP values are differentiated in normal and abnormal, whereas abnormal values point towards gastroesophageal reflux (GER) as the origin of symptoms. We analyzed the correlation and the concordance of the diagnostic classification of these 3 SAA parameters.

Results: Evaluating the GER-irritability association, SI, SSI and SAP showed non-identical classification of normal and abnormal cases in 39.2% of the infants. When irritability was taken as a symptom, there was only a poor inter-parameter association between SI and SSI, and between SI and SAP (Kendall's tau b = 0.37, P < 0.05; Kendall's tau b = 0.36, P < 0.05, respectively). Evaluating the GER-cough association, SI, SSI and SAP showed non-identical classification of normal and abnormal cases in 52.2% of the patients. When cough was taken as a symptom, only SI and SSI showed a poor inter-parameter association (Kendall's tau b = 0.33, P < 0.05).

Conclusion: In infants investigated for suspected GERD with pH/MII-monitoring, SI, SSI and SAP showed a poor inter-parameter association and important disagreements in diagnostic classification. These limitations must be taken into consideration when interpreting the results of SAA in infants.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2874145PMC
http://dx.doi.org/10.3748/wjg.v16.i19.2401DOI Listing

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