Introduction to Fetal Medicine Lloyd R. Feit M.D. Associate - - PowerPoint PPT Presentation

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Introduction to Fetal Medicine Lloyd R. Feit M.D. Associate - - PowerPoint PPT Presentation

Introduction to Fetal Medicine Lloyd R. Feit M.D. Associate Professor of Pediatrics Warren Alpert Medical School Brown University Introduction to Fetal Medicine Fetal Cardiology Important in evaluation of high risk pregnancies. Information


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Introduction to Fetal Medicine

Lloyd R. Feit M.D. Associate Professor of Pediatrics Warren Alpert Medical School Brown University

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Introduction to Fetal Medicine Lloyd R. Feit M.D.

Fetal Cardiology

Important in evaluation of high risk pregnancies. Information obtainable in > 95% of patients attempted. Allows for assessment of developmental cardiovascular physiology. Appropriate management depends on strong collaboration between subspecialists: perinatology ultrasonography genetics pediatric cardiology

  • bstetrics internal medicine

neonatology cardiac surgery

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Introduction to Fetal Medicine Lloyd R. Feit M.D.

Fetal Circulation

Placenta: low resistance circuit, organ of gas exchange, nutrient supply. Lungs: high resistance, non-functional, breathing important. Brain development is primary! Shunt pathways: Foramen ovale Ductus arteriosus Ductus venosus

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Introduction to Fetal Medicine Lloyd R. Feit M.D.

Fetal Circulation

Shunt Pathways:

Ductus venosus: bypasses fetal liver Foramen ovale: R-L shunt across atrial septum Ductus arteriosus: bypasses high resistance (non- aerated) lungs

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Introduction to Fetal Medicine Lloyd R. Feit M.D.

Transitional circulation

 Separation from low resistance placenta

– >> increased SVR – low flow constricts ductus venosus

 First breath expands lungs

– >> decreased PVR – increased pulmonary blood flow – increased LA pressure closes PFO – increased PaO2 >> constricts PDA

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Introduction to Fetal Medicine Lloyd R. Feit M.D.

Fetal Echocardiography

First observations of normal cardiac anatomy utilizing M- mode by Winsberg in 1972. Prenatal diagnosis of congenital heart disease by Kleinman, et al (and others) in 1980. High resolution cross-sectional scanners allow real-time directed utilization of: Two-dimensional imaging Pulsed & color flow Doppler M-mode

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Introduction to Fetal Medicine Lloyd R. Feit M.D.

Diagnostic capabilities

 Cardiac ultrastructure

2 - dimensional, M - mode

 Vascular & intracardiac flow patterns

Color, pulsed & continuous wave Doppler

 Cardiac rate and rhythm

M – mode & Doppler evaluation of electromechanical events.

 Myocardial function

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Introduction to Fetal Medicine Lloyd R. Feit M.D.

Indications

Fetal factors: IUGR Arrhythmia Hydrops fetalis Abnormal genetic screen Extracardiac anomalies – nuchal translucency Diminished fetal movement Abnormal 4 - chamber screen

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Introduction to Fetal Medicine Lloyd R. Feit M.D.

Indications

Maternal factors: CHD Poly/oligo - hydramnios Diabetes Collagen vascular disease Teratogen exposure Pre - eclampsia Advanced parental age

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Introduction to Fetal Medicine Lloyd R. Feit M.D.

Indications

Familial factors: CHD Genetic syndromes; Marfan Noonan Ellis van Crevald Hypertrophic cardiomyopathy Tuberous sclerosis

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Introduction to Fetal Medicine Lloyd R. Feit M.D.

Fetal echocardiography

 No known adverse fetal effects  Optimal timing – 16 -22 wks

– Diagnosis possible at 12-14 wks

 No uniformly accepted approach

– 4-chamber screen – Addition of great vessels/outflow tracts – Association with increased nuchal translucency

(>99%ile >>> 3-5x risk of CHD)

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Introduction to Fetal Medicine Lloyd R. Feit M.D.

Technique

Establish fetal lie, complete level II. Cardiac & abdominal situs. Fetal heart rate and rhythm. Four chamber view. (92% sensitivity, 99% specificity) Segmental approach for venous and arterial connections and Doppler flow patterns: Systemic, pulmonary veins AV valves LV, RV outflow tracts Aortic, ductal arch

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Four Chamber view

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Introduction to Fetal Medicine Lloyd R. Feit M.D.

LV outflow tract

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Introduction to Fetal Medicine Lloyd R. Feit M.D.

RV outflow tract

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Systemic venous confluence

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Aortic and Ductal arch

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Aortic arch

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Introduction to Fetal Medicine Lloyd R. Feit M.D.

Doppler flow patterns

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Sinus rhythm – Doppler

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AV Canal Defect

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Tricuspid valve dysplasia

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Intracardiac rhabdomyoma

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Introduction to Fetal Medicine Lloyd R. Feit M.D.

Arrhythmias

Isolated extrasystoles Sustained arrhythmia: Any irregular rhythm, or any regular rhythm outside the normal fetal range of 100 - 160 bpm, and not associated with uterine contraction.

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Introduction to Fetal Medicine Lloyd R. Feit M.D.

Arrhythmias

Indications for Fetal Arrhythmia Evaluation

Suspected arrhythmia Non-immune hydrops fetalis (esp heterotaxy syndromes, corrected transposition) Fetal cardiac tumors Maternal collagen vascular disease Maternal medications/toxins that may predispose fetus to arrhythmia

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Arrhythmias

Isolated extrasystoles (benign) Tachycardia: SVT: > 90 % reentry (AVRT) Atrial flutter / fibrillation Ventricular tachycardia (rare) Bradycardia: High degree AV block associated with collagen vascular disease or complex CHD. Hydrops indicates poor prognosis.

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Arrhythmias: M-mode

SVT Atrial Flutter

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Arrhythmias

Progression of fetal CHF: atrial dilation (AV valve regurgitation) liver engorgement peripheral edema &/or ascites polyhydramnios fetal demise

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Therapeutics

Consideration for intervention must incorporate: in utero and postnatal natural history of lesion. risk / benefit for both mother and fetus. Arrhythmias: sustained vs intermittent transplacental (oral, IV) vs direct (PUBS) knowledge of electrophysiologic mechanism.

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Therapeutics

Tachycardias: SVT – digoxin, type IA (procainamide, quinidine) type IC (flecainide) Atrial fib / flutter - digoxin, type IA, type III (amiodarone) VT - type IB (lidocaine, mexilitene, amiodarone) Bradycardia: ? steroids, plasmapheresis, pacemaker ??? Early delivery?!?

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Does antenatal diagnosis make a difference?

 Obstetric decisions:

– parental reassurance (~95% for ‘follow-up’ patients) – amniocentesis, genetic counseling (20 - 38 % aneuploid) – search for other anomalies – frequency of follow – up – ? termination – time, mode, place of delivery

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Does antenatal diagnosis make a difference?

 Neonatal decisions:

– appropriate facility, staff – need for prostaglandin infusion – avoid circulatory collapse in duct dependant lesions – very difficult to prove/quantitate survival or

  • utcomes benefit except for:

 HLHS  Coarctation  TGA

– Counseling !!!

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Prenatal counseling

 Know local nursery results  Know local surgical results

– Inter-stage morbidity and mortality

 Long term outcomes

– Physical – Neurologic – Family dynamics

 Allows families to prepare for challenges of

‘altered normality’

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Fetal intervention

Fetal interventional catheterization: 1991-Maxwell, et al in utero balloon aortic

  • valvuloplasty. 4 patients, 5 attempts; 1 survivor.

2004-Marshall, et al. 20 attempts for patients with fetal aortic stenosis, 14 technically successful 3 HLHS prevented ?? 12 HLHS 5 demise: 3 in utero, 1 previable, 1 termination

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Fetal Intervention

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Fetal Intervention

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Fetal intervention

 Critical aortic stenosis / HLHS

– 85 attempts (~15% fetal demise) – ~ 80% technically successful – ~ 33% get to 2 ventricle repair!

 Intact atrial septum

– 25 attempts (~10% fetal demise) – ~90% technical success – ~33% avoid emergent cath at birth

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Future Directions

 Results are likely to improve

– Better patient selection, timing – Improved instrumentation – Experience - - learning curve

 Ethical issues

– Can a pregnant woman really give informed consent?? – What about dad??

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Two ventricles are better than one!

“Human subtlety will never devise an invention more beautiful, more simple or more direct than does Nature, because in her inventions, nothing is lacking and nothing is superfluous.” Leonardo da Vinci