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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 - Alpert Medical Schoolmed.brown.edu/pedisurg/Fetal/Seminar/Slides/Cardiology.pdf · Introduction to Fetal Medicine Lloyd R. Feit M.D. ... peripheral

Mar 29, 2018

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Page 1: Introduction to Fetal Medicine - Alpert Medical Schoolmed.brown.edu/pedisurg/Fetal/Seminar/Slides/Cardiology.pdf · Introduction to Fetal Medicine Lloyd R. Feit M.D. ... peripheral

Introduction to Fetal Medicine

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

Brown University

Page 2: Introduction to Fetal Medicine - Alpert Medical Schoolmed.brown.edu/pedisurg/Fetal/Seminar/Slides/Cardiology.pdf · Introduction to Fetal Medicine Lloyd R. Feit M.D. ... peripheral

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. Best clinical management depends on strong

collaboration between subspecialists: perinatology ultrasonography

genetics pediatric cardiology obstetrics 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 (risk increases from ~1% to 4-5%)

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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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

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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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

Systemic venous confluence

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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

Aortic and Ductal arch

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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

Aortic arch

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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

Doppler flow patterns

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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

Sinus rhythm – Doppler

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Introduction to Fetal Medicine

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AV Canal Defect

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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

AV Canal

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Complex single ventricle (Dbl inlet/dbl outlet LV)

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Complex single ventricle

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TV dysplasia

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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

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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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

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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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

Arrhythmias: M-mode

SVT Atrial Flutter

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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

Arrhythmias

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

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Introduction to Fetal Medicine

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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

& typical postnatal response.

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Introduction to Fetal Medicine

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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 / Heart Block: Steroids – no clear benefit, may limit progression Plasmapheresis, pacemaker ???

Early delivery?!?

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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

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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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

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

outcomes benefit except for: HLHS Coarctation TGA

– Counseling !!!

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Introduction to Fetal Medicine

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Does antenatal diagnosis make a difference?

Parental counseling Know local surgical results

– Inter-stage morbidity and mortality Long term outcomes

– Physical – Neurologic – Family dynamics

Potential termination Allows families to prepare for challenges of ‘altered

normality’

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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

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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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

Fetal Intervention

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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

Fetal Intervention

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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

Fetal intervention

Critical aortic stenosis / HLHS – >120 attempts (~10% fetal demise) – ~ 80% technically successful – ~ 33% get to 2 ventricle repair! - high rate of EFE

(endocardial fibro-elastosis) ALL need postnatal cardiac interventions

HLHS w/intact atrial septum – 25 attempts (~10% fetal demise) – ~95% technical success – ~50% avoid emergent cath at birth

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Introduction to Fetal Medicine

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Future Directions

Results are likely to improve – Better patient selection, timing

Pretty clear results for predicting AS > HLHS – Improved instrumentation

Robotics? – Experience - - learning curve

Ethical issues – Can a pregnant woman really give informed consent?? – What about dad?? – Natural history of any disease process MUST be well

understood before undertaking any fetal intervention!!

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Introduction to Fetal Medicine

Lloyd R. Feit M.D.

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