NHS Fetal Anomaly Screening Programme Marie Coughlin Screening

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NHS Fetal Anomaly Screening Programme Marie Coughlin Screening Lead January 25 th 2010

NHS Fetal Anomaly Screening Programme Marie Coughlin Screening Lead January 25 th 2010

Today’s Session l First of 6 Antenatal & Newborn sessions throughout 2010 l Same

Today’s Session l First of 6 Antenatal & Newborn sessions throughout 2010 l Same format will be used – feedback on this would be useful

Reasons for Today’s Session l As a result of Cha. MPs commissioned review of

Reasons for Today’s Session l As a result of Cha. MPs commissioned review of screening l A need to further engage public health in Antenatal & Newborn Screening Programmes l At the request of public health screening leads l Part of C&M Screening Action Plan l Thought it useful to invite commissioners also

Aim of the Session l To increase knowledge base within public health

Aim of the Session l To increase knowledge base within public health

Session Format l Overview of UK NSC/NWSHA structure l Overview of Fetal Anomaly Screening

Session Format l Overview of UK NSC/NWSHA structure l Overview of Fetal Anomaly Screening l Review of patient pathway l Data and QA l Future developments l Questions/comments

Overarching Structure l UK NSC oversees 6 Antenatal & Newborn Screening Programmes l SHA

Overarching Structure l UK NSC oversees 6 Antenatal & Newborn Screening Programmes l SHA coordinators with regional and national role l NWSHA coordinator jobs out to advert l UK NSC has defined accountability & governance structure for SHA, PCT and provider

Purpose of Fetal Anomaly Screening l Aim to offer women 2 ultrasound tests at

Purpose of Fetal Anomaly Screening l Aim to offer women 2 ultrasound tests at 10 -12 weeks and 18 -20 weeks of pregnancy l First scan for dating and pregnancy viability l Second scan screens for major structural anomalies l Down’s Syndrome Screening Programme now part of Fetal Anomaly Screening Programme l Screens for down’s syndrome between 10 -18 weeks depending on local screening strategies

Cont… l Aspires to give women an informed choice l Does not screen for

Cont… l Aspires to give women an informed choice l Does not screen for all conditions l For down’s syndrome only gives an indication of risk, does not confirm l Unlike other screening programmes, emphasis not on high uptake rates

Cont. . . l Conditions screened for: — Alobar Holoprosencepathy (HPE) — Anencephaly —

Cont. . . l Conditions screened for: — Alobar Holoprosencepathy (HPE) — Anencephaly — Bilateral Renal Agenesis — Cleft Lip/Palate — Congenital Diaphragmatic Hernia (CDH) — Congenital Heart Disease — Down’s Syndrome

Cont… l Conditions screened for: — Edward’s Syndrome (Trisomy 18) — Exomphalos (Omphalocele) —

Cont… l Conditions screened for: — Edward’s Syndrome (Trisomy 18) — Exomphalos (Omphalocele) — Gastroschisis — Lethal Skeletal Dysplasia — Spina Bifida — Trisomy 13 (Patau’s Syndrome)

Patient Pathway…

Patient Pathway…

NHS Fetal Anomaly Screening Programme (FASP) Rebecca Till Screening Midwife Macclesfield District General Hospital

NHS Fetal Anomaly Screening Programme (FASP) Rebecca Till Screening Midwife Macclesfield District General Hospital 26 th January 2010

Aim l Programme breakdown l Strategies & Tests l Pathways

Aim l Programme breakdown l Strategies & Tests l Pathways

Fetal Anomaly Screening Programme UK National Screening Programme Chromosomal (Down’s Syndrome Screening) Equality of

Fetal Anomaly Screening Programme UK National Screening Programme Chromosomal (Down’s Syndrome Screening) Equality of access Structural (18 -20+6 Week anomaly scan) Equitable Service

Down’s Syndrome Screening Recommendations l 75% detection rate (DR) for 3% false positive (FP)

Down’s Syndrome Screening Recommendations l 75% detection rate (DR) for 3% false positive (FP) l 90% detection rate (DR) for 3% false positive Benchmark timeframe - April 2010

Screening Strategies l 1 st Trimester Combined l Quadruple Test

Screening Strategies l 1 st Trimester Combined l Quadruple Test

1 st Trimester Combined Biochemical markers in maternal serum (10 -14 weeks) l Bh.

1 st Trimester Combined Biochemical markers in maternal serum (10 -14 weeks) l Bh. CG l PAPPA-A 87%DR - 3%FPR (1: 150) Nuchal Translucency Scan (11 -13+6 weeks)

The Quadruple Test (2 nd Trimester) l 15 -21+6 weeks l Gestation l Maternal

The Quadruple Test (2 nd Trimester) l 15 -21+6 weeks l Gestation l Maternal Age l Ethnicity l Smoking l Weight 84% DR - 5% FPR PAPP-A Alphafeta Alpha-feta Protein Bh. CG Unconjugated Oestriol

Fetal Anomaly Ultrasound Aims & Objectives Two Ultrasound Scans PAPP-A Structural Dating & Anomalies

Fetal Anomaly Ultrasound Aims & Objectives Two Ultrasound Scans PAPP-A Structural Dating & Anomalies Viability (8+ (18 -20+6 weeks) Screening Choices Management and Termination Options Verbal Consent

Fetal Anomaly Ultrasound l Abnormalities l Development l Show fetus/heartbeat l Listed anatomy l

Fetal Anomaly Ultrasound l Abnormalities l Development l Show fetus/heartbeat l Listed anatomy l Measurements l Discuss results l Printed handout

Patient Pathway and Timelines l Screening Timeline l Pathway for Trisomy 21 Screening l

Patient Pathway and Timelines l Screening Timeline l Pathway for Trisomy 21 Screening l Pathway for raised NT > 3. 5 mm l Pathway for Fetal Anomaly Screening

Conclusions l Robust l Implications on Implementation l Resources

Conclusions l Robust l Implications on Implementation l Resources

Data, Performance & QA l Very difficult to obtain data – not held centrally

Data, Performance & QA l Very difficult to obtain data – not held centrally l Trusts required to produce annual report l QA for laboratories l Developing QA for the rest of the service – NW coordinator roles will aid this

Future Developments l 1 st trimester screening for Down’s Syndrome to be implemented by

Future Developments l 1 st trimester screening for Down’s Syndrome to be implemented by April 2010 — C&M PCTs not on target for this l QA function to be developed further l I. T. system to improve data collection to be developed

Questions/Comments l How/who monitors annual reports within PCT organisations? l How can we achieve

Questions/Comments l How/who monitors annual reports within PCT organisations? l How can we achieve 1 st trimester screening by April 2010? l With regard to QA, how do we assure our Boards that local programmes run satisfactorily?

My Questions l Did you find this session useful? l What will you do

My Questions l Did you find this session useful? l What will you do differently as a result of this session?

Thank You

Thank You