Various experiences and preferences of Dutch parents in prenatal counseling in extreme prematurity.

Geurtzen, Rosa; Draaisma, Jos; Hermens, Rosella; Scheepers, Hubertina; Woiski, Mallory; van Heijst, Arno; Hogeveen, Marije · Patient Educ Couns · 2018

cross_sectional · Level IV

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Abstract

To investigate experienced and preferred prenatal counseling among parents of extremely premature babies. A Dutch nationwide, multicenter, cross-sectional study using an online survey. Surveys were sent to all parents of extremely premature babies born between 2010 and 2013 at 24<sup>+0/7</sup>-24<sup>+6/7</sup> weeks of gestation. Sixty-one out of 229 surveys were returned. A minority (14%) had no counseling conversation. Conversations were done more often by neonatologists (90%) than by obstetricians (39%) and in 37% by both these experts. Supportive material was rarely used (19%). Mortality (92%) and short-term morbidity (88%) were discussed the most, and more frequently than long-term morbidity (65%), practical items (63%) and delivery mode (52%). Most decisions on active care or palliative comfort care were perceived as decisions by doctor and parents together (61%). 80% felt they were involved in decision-making. The preferred way of involvement in decision-making varied among parents. The vast majority of parents were counseled: mostly by neonatologists, and mainly about mortality and short-term morbidity. Parents wanted to be involved in the decision-making process but differed on the preferred extent of involvement. Practice implications Understanding of shared decision-making may contribute to meet the various preferences of parents.

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