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27<br />

ABSTRACT #O2<br />

WHAT WOMEN WANT: PATIENTS’ PREFERENCES ABOUT REPORTING OF<br />

ULTRASOUND SOFT MARKERS<br />

Rebecca Cash [R](1), Myuri Manogaran (2), Hana Sroka (3), Nan Okun (4)<br />

(1) <strong>Department</strong> <strong>of</strong> <strong>Obstetrics</strong> <strong>and</strong> Gynaecology, <strong>University</strong> <strong>of</strong> <strong>Toronto</strong>, (2) <strong>University</strong> <strong>of</strong> <strong>Toronto</strong>,<br />

(3) <strong>Department</strong> <strong>of</strong> Genetics, Mount Sinai Hospital (4) Maternal Fetal Medicine Division,<br />

<strong>Department</strong> <strong>of</strong> <strong>Obstetrics</strong> <strong>and</strong> Gynaecology, Mount Sinai Hospital<br />

Objective: The Society <strong>of</strong> Obstetricians <strong>and</strong> Gynecologists <strong>of</strong> Canada (SOGC) recommends<br />

routine use <strong>of</strong> a single ultrasound at 18-20 weeks in all pregnancies. New guidelines from the<br />

SOGC , the American College <strong>of</strong> <strong>Obstetrics</strong> <strong>and</strong> Gynecology (ACOG) <strong>and</strong> the American College<br />

<strong>of</strong> Medical Genetics recommend that all pregnant women, regardless <strong>of</strong> their age, be <strong>of</strong>fered<br />

screening for Down syndrome. S<strong>of</strong>t marker screening at the time <strong>of</strong> anatomical ultrasound has<br />

been incorporated into the multitude <strong>of</strong> genetic screens available to pregnant women. The process<br />

<strong>of</strong> informed consent for ultrasound screening has been shown to be grossly inadequate. To date,<br />

there are no studies that examine women’s views on the examination for, <strong>and</strong> reporting <strong>of</strong><br />

ultrasound s<strong>of</strong>t markers. We conducted a survey <strong>of</strong> women’s prior knowledge <strong>and</strong> opinions on<br />

ultrasound s<strong>of</strong>t markers.<br />

Methods: A prospective survey <strong>of</strong> 263 women undergoing18-20 week anatomy ultrasound at<br />

Mount Sinai Hospital, a level three perinatal referral center for a multiethnic population <strong>of</strong><br />

approximately 2.5 million, after ethics approval.<br />

Results: Prior to reading an information pamphlet provided in the context <strong>of</strong> this survey, 30 %<br />

(79/263) <strong>of</strong> women reported having heard <strong>of</strong> the term s<strong>of</strong>t marker <strong>and</strong> 59% (47/79) <strong>of</strong> these women<br />

had discussed s<strong>of</strong>t markers with their caregiver. 85% <strong>of</strong> women attending a midwife who had heard<br />

<strong>of</strong> the term s<strong>of</strong>t marker reported having discussed this with that caregiver compared to 54% <strong>of</strong><br />

comparable women attending an obstetrician. The latter group more commonly reported their<br />

source <strong>of</strong> information to be from a genetic counselor or from the internet. Of women who were<br />

familiar with the term s<strong>of</strong>t marker 25% attended an obstetrician, 35% attended a family doctor <strong>and</strong><br />

68% attended a midwife for prenatal care. Of all respondents, 53% preferred that s<strong>of</strong>t marker<br />

findings should be reported routinely, 20% said they should be reported if the caregiver thought it<br />

was required <strong>and</strong> 23% preferred they be reported only after discussion prior to the ultrasound<br />

exam. A minority <strong>of</strong> respondents (8%) had not participated in prenatal screening for aneuploidy.<br />

Of these women, all preferred that s<strong>of</strong>t markers should only be reported after prior discussion.<br />

Conclusions: The study demonstrates that a majority <strong>of</strong> women have received little to no<br />

counseling regarding routine examination for s<strong>of</strong>t markers at second trimester ultrasound. Only 8%<br />

<strong>of</strong> our study population had not participated in genetic screening in the first trimester <strong>of</strong> her<br />

pregnancy. Of these women, all stated that they believed s<strong>of</strong>t markers should only be reported after<br />

prior discussion. These findings validate <strong>and</strong> emphasize the importance <strong>of</strong> counseling our patients<br />

appropriately <strong>and</strong> attaining adequate informed consent for genetic screening not only conducted in<br />

the first trimester but also at the time <strong>of</strong> second trimester ultrasound scan.

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