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Inequalities in uptake of prenatal screening according to ethnicity and socio‐economic status in the four largest cities of the Netherlands (2011–2013)
Author(s) -
Posthumus Anke G.,
Peters Ingrid A.,
Borsboom Gerard J.,
Knapen Maarten F. C. M.,
Bonsel Gouke J.
Publication year - 2017
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/pd.5089
Subject(s) - ethnic group , inequality , demography , prenatal diagnosis , medicine , geography , environmental health , pregnancy , sociology , fetus , biology , genetics , mathematics , anthropology , mathematical analysis
Objectives In the Netherlands, all women are claimed to have equal access to prenatal screening (PS). Prior research demonstrated substantial inequalities in PS uptake associated with socioeconomic status (SES) and ethnic background. The suggested pathway was a lack of intention to participate in PS among these subgroups. We studied the background of inequalities in PS participation, challenging intention heterogeneity as the single explanation. Methods Multivariable logistic regression analyses of the national PS registry, focusing on the four largest cities in the Netherlands ( n  = 4578, years 2011–2013), stratified by SES. Outcome measures: (1) any uptake of PS (yes/no) and (2) uptake (one/two tests) for women who intended to participate in two tests. Determinants included intention, ethnicity, practice, and age. Results Of non‐Western women, 85.7% were screened versus 89.7% of Western women. Intention was an important explanatory factor in all models. However, after correction for intention, ethnicity remained a significant determinant for differences in uptake. Ethnicity and SES also interacted, indicating that non‐Western women in low SES areas had the lowest uptake (corrected for intention). Conclusions for Practice Socioeconomic status and ethnicity related inequalities in PS uptake are only partially explained by intention heterogeneity; other pathways, in particular provider‐related determinants, may play a role. © 2017 John Wiley & Sons, Ltd.

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