Skip to main content
. Author manuscript; available in PMC: 2019 Sep 1.
Published in final edited form as: Expert Rev Clin Immunol. 2018 Aug 24;14(9):771–780. doi: 10.1080/1744666X.2018.1512405

Table 3.

Prenatal exposure to acid suppressant medications and the development of asthma: meta-analysis results

Author
(year)
# of
Studies
Included
Author (year) of studied included Publication bias (P
value for Egger test)
Asthma*
Prenatal Exposure Result Heterogeneity
Devine (2017) [35] 8 Dehlink (2009), Kallen (2013), Hak (2013), Mulder (2013), Mulder (2014), Andersen (2012), Cea Soriano (2016), Yitshak-Sade (2016) Unlikely (P=0.415) Any ASM
H2RA
PPI
RR 1.36 (1.16 −1.61)
RR 1.46 (1.29-1.65)
RR 1.30 (1.07-1.56)
I2 = 87.6%
I2= 15.3%
I2= 42.5%
Lai (2018) [36] 8 Dehlink (2009), Kallen (2013), Hak (2013), Mulder (2013), Mulder (2014, Andersen (2012), Cea Soriano (2016), Yitshak-Sade (2016) Unlikely (P>0.05) Any ASM
H2RA
PPI
RR 1.31 (1.15-1.49)
RR 1.57 (1.46-1.69)
RR 1.34 (1.18-1.52)
I2 = 84%
I2= 0%
I2= 46%
5 Dehlink (2009), Kallen (2013), Mulder (2013), Mulder (2014), Andersen (2012), Cea Soriano (2016) Unlikely (P>0.05) Any ASM** RR 1.45 (1.35-1.56) I2 = 0%

Abbreviations: ASM: acid suppressant medications, BMI: body mass index, GRADE: Grading of Recommendations, Assessment, Development and Evaluation, H2RA: histamine-2 receptor antagonist, PPI: proton pump inhibitor, NOS: Newcastle-Ottowa Sclae.

*

Other allergic diseases included atopic dermatitis, food allergy, allergic rhinitis, eosinophilic esophagitis, drug hypersensitivity reaction or other allergic reactions. However, there was insufficient data for analysis of these outcomes.

**

Results of sensitivity analysis.