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The New Prenatal Screening Tests

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Obstetrics and Gynecology, Burnaby Hospital. Pacific Centre for Reproductive Medicine ... I have no financial relationship with pharmaceutical or medical ultrasound ... – PowerPoint PPT presentation

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Title: The New Prenatal Screening Tests


1
The New Prenatal Screening Tests
  • Langley Memorial Hospital
  • Grand Rounds
  • November 8, 2007
  • Ken Seethram, MD, FRCSC, FACOG
  • Obstetrics and Gynecology, Burnaby Hospital
  • Pacific Centre for Reproductive Medicine

2
Disclosure statement
I have no financial relationship with
pharmaceutical or medical ultrasound corporations
associated with prenatal screening and/or
diagnosis.
I will provide a website link from
pacificfertility.ca for relevant literature and a
copy of this talk.
3
  • ..wow, things have changed

4
Objectives
  • To make you current with 2007/08 information and
    guidelines from ACOG and SOCG with regards to
    Prenatal screening options
  • Help fully understand all options in order to
    better counsel
  • Help understand how and when to get your patients
    screened once their options are known

5
Quick Definitions
  • DR Detection rate
  • the rate at which a test will pick up the
    problem. This is accuracy, not reliability
  • FPR False positive rate
  • the chance that the screening tool will be
    positive when the condition is absent
  • Note the use of screen positive
  • Screen positive
  • the literature term to describe the number of
    times the test will be positive (either truly or
    falsely)

6
Background
  • What are we screening for?
  • Aneuploidy majority of which is Trisomy 21,
    with T18, T13, and monosomy X (45X) being less
    likely
  • Secondary screening benefits?
  • Dating the pregnancy
  • Anatomy evaluation, placental evaluation, twins,
    early anomalies

7
Evolution of screening
  • 1930s first association made with maternal age
    and risk of major malformations
  • due to egg age, declining quality of spindle
    mechanism nondisjunction at meiosis I prior to
    fertilization - triples chromosomes
  • late 1970s - first put to use to triage women
    for amniocentesis

8
Evolution of screening
  • Age 35 became the high risk age
  • at which the rate of aneuploidy was equal to the
    rate of amniocentesis/CVS related miscarriage.
    Therefore, maternal age was the first screening
    tool.
  • Bad news its the worst screening tool, with
    only 30 detection rate
  • Today erosion of the age 35 as a cut-off

9
1980s 2nd Trimester serum
  • AFP
  • Total hCG
  • Unconjugated estriol uE3
  • Inhibin A

10
TMS and Quad Screening
  • Nothing really has changed with multiple marker
    screening tools
  • Uses 2-4 biochemical markers to adjust the age
    related risks
  • Problem - specificity drops as disease prevalence
    increases
  • i.e. Many false positives

11
What has evolved in the first trimester?
  • Nuchal Translucency (NT)
  • Serum biochemistry
  • Nasal Bone (NB)
  • Tricuspid regurgitation (TR)
  • Frontomaxillary facial angle (FMF Angle)

12
The First Trimester - NT
  • US measurement, 11-14w spine to skin
  • Fetal Medicine Foundation
  • Aneuploidy - a change in extracellular matrix and
    potential for cardiac/lymphatic changes causing
    increased NT

13
What has evolved in the first trimester?
  • Nuchal Translucency (NT)
  • Serum biochemistry
  • Nasal Bone (NB)
  • Tricuspid regurgitation (TR)
  • Frontomaxillary facial angle (FMF Angle)

14
PAPP-A free beta hCG
  • Serum biochemistry
  • Free beta hCG (different than TMS/Quad)
  • PAPP-A (Preg Assoc. plasma protein-A)
  • relative levels are used to predict T21, T13, T18
  • Low PAPP-A
  • may be associated with a poorly developing
    placenta
  • Evolving method of screening for placental
    disease (IUGR, PIH)

15
What has evolved in the first trimester?
  • Nuchal Translucency (NT)
  • Serum biochemistry
  • Nasal Bone (NB)
  • Tricuspid regurgitation (TR)
  • Frontomaxillary facial angle (FMF Angle)

16
Nasal Bone (NB)
  • 60-70 of T21 absent Nasal bone
  • 99 of euploid fetuses have Nasal bone
  • tremendous increase in detection rates of FTS.
    High learning curve

17
The First Trimester TR and FMF
  • Tricuspid Regurge and FMF angle are somewhat
    experimental and not wide clinically used outside
    of research settings
  • On the horizon

18
Frontomaxillary Facial Angle
19
First Trimester Screening (FTS)
20
Screening Strategies
  • First Trimester Screen
  • Second Trimester Screen
  • Combined screening
  • Serum integrated
  • Integrated
  • Sequential
  • Contingency
  • FTS only

21
Models of Screening with high detection rates
  • FTS with NT NB serum alone
  • Serum Integrated Pregnancy Screening (SIPS)
  • 1st TM PAPP-A Quad (SURUSS trial)
  • Results disclosed at 17/18w
  • Integrated Pregnancy Screening (IPS)
  • 1st TM PAPP-A NT alone TMS/Quad
  • Results disclosed at 17/18w

22
Models of Screening
  • Sequential screening model
  • IPS but disclosed after 1st, and then 2nd TM
  • Contingency Screening model
  • FTS done - lt11000, no further testing
  • If risks gt150, CVS offered
  • If risks 150-1999, quad offered
  • Nasal bone contingency offer NB to intermediate
    group

23
Which test is best?
  • The recent data would suggest that Contingency
    screening with the nasal bone model will turn out
    to be the highest detection rates, with least
    amount of resources, and lowest FPR
  • -gives 90 DR for 2.5 FPR
  • How does each model perform

24
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25
Best performance
  • For a first trimester result
  • FTS with NT NB serum
  • Contingency screening programs
  • For a combined result
  • Contingency screening programs

26
What do the guidelines say?
  • ACOG released similar guidelines in January 2007,
    and SOGC in February
  • Basics
  • TMS is no longer good enough
  • Dont use age as a screening tool
  • Aim for highest DRs and lowest FPRs in any
    method
  • Consent and review all options
  • Quality assurance important in FTS programs

27
ACOG
  • Regardless of which screening tests you decide to
    offer your patients, information about the
    detection and false-positive rates, advantages,
    disadvantages, and limitations, as well as the
    risks and benefits of diagnostic procedures,
    should be available to patients so that they can
    make informed decisions

28
SOGC
  • All women regardless of age, should be offered
    consented screening for the most significant
    aneuploidies, and a second trimester sonogram for
    dating, growth and anomalies
  • age screening is a poor minimum standard and
    should be removed
  • Amnio/CVS can be offered to women over age 40,
    without screening, but screening should still be
    offered.

29
Whats the best test?
  • One size does not fit all
  • As long as the definitive diagnosis involves an
    invasive procedure which can cause miscarriage of
    a normal pregnancy, there is simply no substitute
    to explaining all the options, their benefits,
    and downsides to all our patients
  • best screen is the one which will service
    patients needs for time of results, and action
    depending on the results

30
Current Western Canada options
  • Alberta
  • Edmonton/Calgary FTS programs, provincially
    insured
  • British Columbia
  • TMS program (does not yet comply with SOGC)
  • SIPS for women over age 38 (does not comply)
  • IPS for women over age 40 (complies)
  • Private centre's for FTS with or without NB
    (complies)
  • MOH investigating new options

31
Accredited FTS Centres, BC
  • Pacific Centre for Reproductive Medicine
  • NT NB serum
  • Genesis Fertility Centre
  • NT serum
  • Follow with TMS in second trimester

32
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33
Resources
  • www.fetalmedicine.com
  • www.earlyriskassessment.com
  • www.pacificfertility.ca
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