Can Increased Body Mass Index Prevent Adequate Ultrasound Examination for Trisomy 21 Risk Assessment?

January 16, 2016 updated by: ahmed abdulmoneim altraigey, Benha University
Determine Cutoff BMI at which transabdominal sonography (TAS) is not satisfactory for aneuploidy risk assessment.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Obesity is a common public health problem which is increasing worldwide at an alarming rate. According to National nutrition survey statistics of 2007, the prevalence of obesity in the kingdom of Saudi Arabia was 23.6% in women and 14% in men. Also the prevalence of overweight in the Saudi community was determined to be 30.7% for men as compared to 28.4% for the women.

First trimester screening between 11-14 weeks gestation is known to be an effective and reliable screening test for Down syndrome and trisomy 18.First trimester screening allows earlier identification of the pregnancy at risk for fetal aneuploidy and anatomic defects, particularly, cardiac anomalies, therefore, providing an option of earlier diagnosis by chorionic villus sampling and analysis of amniocytes.

The well-known association of obesity during pregnancy with a variety of maternal and fetal complications increases the importance of early aneuploidy screening.

Fetal aneuploidy risk assessment is based on a combination of maternal age, prior affected pregnancy or family history, maternal serum biochemical tests and fetal ultrasound markers.

The impact of obesity on the quality of prenatal ultrasound examination is well established with a greater risk for suboptimal visualization, in particular, the fetal cardiac structures and the craniospinal structures only when body mass index above the 90th percentile.

The quality of prenatal screening for aneuploidy via nuchal translucency thickness measurement is significantly limited among obese pregnant women, thus, increased risk of fetal anomalies.

Gandhiet al, have noted that increased BMI is not associated with suboptimal visualization of nuchal translucency, but it is associated with a longer time to perform the first-trimester ultrasound examination for aneuploidy risk assessment, increased need for transvaginal ultrasound examination for optimum nuchal translucency visualization.

There is evidence suggesting that fetal anatomic evaluation in the low-risk gravida can be better accomplished in the first trimester using the transvaginal route, providing a valuable option for obese patients.

Study Type

Observational

Enrollment (Actual)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Asir,
      • Khamis Mushait,, Asir,, Saudi Arabia, 101
        • antenatal clinic of Armed Forces Hospital, Southern Region

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 35 years (ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

Inclusion criteria will consist of women who have a live, intrauterine, singleton pregnancy between 11- 14 weeks gestation.

Description

Inclusion Criteria:

  • women who have a live, intrauterine, singleton pregnancy between 11- 14 weeks gestation.

Exclusion Criteria:

  • multiple gestation.
  • fetal size outside of nuchal translucency screening age (crown-rump length (CRL) outside of 46-71 mm).
  • presence of a cystic hygroma.
  • fetal demise.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
obese pregnant women

With the use of trans-abdominal ultrasound, the following measurements will be recorded:

  • Fetal nuchal translucency thickness.
  • Nasal bone.
  • Fetal facio-maxillary angle.
  • The flow across the tricuspid valve as normal or regurgitated.
  • A-wave in the ductus venosus as normal or reversed.
trans abdominal or trans vaginal ultrasound to detect some of the soft markers of trisomy screening
lean pregnant women

With the use of trans-abdominal ultrasound, the following measurements will be recorded:

  • Fetal nuchal translucency thickness.
  • Nasal bone.
  • Fetal facio-maxillary angle.
  • The flow across the tricuspid valve as normal or regurgitated.
  • A-wave in the ductus venosus as normal or reversed.
trans abdominal or trans vaginal ultrasound to detect some of the soft markers of trisomy screening

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Cutoff body mass index for the use of transvaginal ultrasound for aneuploidy risk assessment.
Time Frame: 30 minutes
30 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The time of the study. (time needed for satisfactory ultrasound risk assessment in minutes)
Time Frame: 30 minutes
time needed for satisfactory ultrasound risk assessment in minutes
30 minutes
The tolerance of the woman for trans-vaginal ultrasound.
Time Frame: 30 minutes
preference of the patients towards transabdominal and transvaginal ultrasound
30 minutes
The harmful effect to the patient
Time Frame: 12 hours
Infection, Bleeding, Injury to vagina or cervix and uterine irritability.
12 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: magdy eldumairy, Armed Forces Hospitals, Southern Region, Saudi Arabia

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2015

Primary Completion (ACTUAL)

December 1, 2015

Study Completion (ACTUAL)

January 1, 2016

Study Registration Dates

First Submitted

May 2, 2015

First Submitted That Met QC Criteria

May 13, 2015

First Posted (ESTIMATE)

May 14, 2015

Study Record Updates

Last Update Posted (ESTIMATE)

January 20, 2016

Last Update Submitted That Met QC Criteria

January 16, 2016

Last Verified

January 1, 2016

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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