Title: The New Prenatal Screening Tests
1The 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
2Disclosure 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
4Objectives
- 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
5Quick 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)
6Background
- 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
7Evolution 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
8Evolution 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
91980s 2nd Trimester serum
- AFP
- Total hCG
- Unconjugated estriol uE3
- Inhibin A
10TMS 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
11What has evolved in the first trimester?
- Nuchal Translucency (NT)
- Serum biochemistry
- Nasal Bone (NB)
- Tricuspid regurgitation (TR)
- Frontomaxillary facial angle (FMF Angle)
12The 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
13What has evolved in the first trimester?
- Nuchal Translucency (NT)
- Serum biochemistry
- Nasal Bone (NB)
- Tricuspid regurgitation (TR)
- Frontomaxillary facial angle (FMF Angle)
14PAPP-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)
15What has evolved in the first trimester?
- Nuchal Translucency (NT)
- Serum biochemistry
- Nasal Bone (NB)
- Tricuspid regurgitation (TR)
- Frontomaxillary facial angle (FMF Angle)
16Nasal 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
17The 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
18Frontomaxillary Facial Angle
19First Trimester Screening (FTS)
20Screening Strategies
- First Trimester Screen
- Second Trimester Screen
- Combined screening
- Serum integrated
- Integrated
- Sequential
- Contingency
- FTS only
21Models 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
22Models 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
23Which 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
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25Best performance
- For a first trimester result
- FTS with NT NB serum
- Contingency screening programs
- For a combined result
- Contingency screening programs
26What 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
27ACOG
- 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
28SOGC
- 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.
29Whats 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
30Current 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
31Accredited FTS Centres, BC
- Pacific Centre for Reproductive Medicine
- NT NB serum
- Genesis Fertility Centre
- NT serum
- Follow with TMS in second trimester
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33Resources
- www.fetalmedicine.com
- www.earlyriskassessment.com
- www.pacificfertility.ca