Fetal MRI, lower acceptance by women in research vs. clinical setting

Author:

van der Knoop Bloeme J.12,Vermeulen Roland J.3,Verbeke Jonathan I.M.L.4,Pistorius Lourens R.5,de Vries Johanna I.P.67

Affiliation:

1. Department of Obstetrics and Gynaecology , VU University Medical Center , P.O. Box 7057 , 1007 MB Amsterdam , The Netherlands , Tel.: +31 (0) 20 4443239 or +31 (0) 20 4444444, pager 6112, Fax: +31 (0) 20 4443333

2. Neuroscience Campus , VU University , Amsterdam , The Netherlands

3. Department of Child Neurology , VU University Medical Center , P.O. Box 7057, 1007 MB Amsterdam , The Netherlands

4. Department of Pediatric Radiology , VU University Medical Center , P.O. Box 7057, 1007 MB Amsterdam , The Netherlands

5. Department of Obstetrics and Gynaecology , University Medical Center Utrecht , Utrecht , The Netherlands

6. Department of Obstetrics and Gynaecology , VU University Medical Center , P.O. Box 7057, 1007 MB Amsterdam , The Netherlands

7. Research Institute MOVE , VU University , Amsterdam , The Netherlands

Abstract

Abstract Aim: To determine acceptance of pregnant women to undergo fetal magnetic resonance imaging (MRI) examination in research and clinical setting. Methods: A prospective study included a research group [part of a study comparing brain ultrasound (US) to MRI in fetuses at risk for acquired brain damage] and a clinical group [fetuses with suspected (brain) anomalies after structural US examination] from 2011 to 2014. All women were advised to use sedatives. MRI declinations, use of sedation, MRI duration and imaging quality were compared between both groups. Results: Study participation was accepted in 57/104 (55%) research cases. Fetal MRI was performed in 34/104 (33%) research and 43/44 (98%) clinical cases. Reasons to decline study participation were MRI related in 41%, and participation was too burdensome in 46%. Acceptance was highest for indication infection and lowest in alloimmune thrombocytopenia and monochorionic twin pregnancy. Sedatives were used in 14/34 research and 43/43 clinical cases. Scan duration and quality were comparable (21 and 20 min in research and clinical cases, respectively, moderate/good quality in both groups). Conclusions: Pregnant women consider MRI more burdensome than professionals realize. Two-third of women at risk for fetal brain damage decline MRI examination. Future studies should evaluate which information about fetal MRI is supportive.

Publisher

Walter de Gruyter GmbH

Subject

Obstetrics and Gynecology,Pediatrics, Perinatology and Child Health

Reference43 articles.

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3. Guideline. ACR-SPR Practice Guideline for the safe and optimal performance of fetal magnetic resonance imaging (MRI). Available from: https://www.acr.org/Quality-Safety/Standards-Guidelines/Practice-Guidelines-by-Modality/MRI. 2010.

4. Simon EM, Goldstein RB, Coakley FV, Filly RA, Broderick KC, Musci TJ, et al. Fast MR imaging of fetal CNS anomalies in utero. AJNR Am J Neuroradiol. 2000;21:1688–98.

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1. Perceptions of Magnetic Resonance Imaging During Pregnancy: A Newfoundland and Labrador Perspective;Journal of Obstetrics and Gynaecology Canada;2023-11

2. Prevalence of and risk factors for failure of fetal magnetic resonance imaging due to maternal claustrophobia or malaise;Ultrasound in Obstetrics & Gynecology;2023-02-11

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