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PA IVS
ManagementDr. Sweta Mohanty
Consultant Pediatric Cardiologist
RxDx Healthcare, Rainbow Hospital,
Bangalore
Image: Plasticsurgerykey.org
Severely hypoplastic RV Good sized RV
Single-
ventricle
repair
Two-
ventricle
repair
Image: J Pediatr Cardiol Surg, Thoracickey
Factors that influence
management strategy
Tricuspid valve
Stenotic, hypoplastic
annulus
Dysplastic / Ebstein-
like, with TR
Image: doctorlib
Right ventricle
Image: JACC
Hypoplastic, unipartite RV
TV Z-score correlates with RV size
Large, thin-walled RV
Seen with profound TR
Nature of pulmonary atresia
Muscular atresia: Narrow
infundibulum, primitive PV
Membranous atresia: Well-formed
infundibulum, commissural fusion
High pressure
retrograde flow through
epicardial coronaries
Endothelial
damage
Coronary
stenoses
Intrinsic
coronary
abnormality
Lack of blood-
egress from RV
Elevated RV
pressure
Blood forced
retrograde through
thebesian veins
Coronary
sinusoids
Coronary
cameral Fistulae
Ventriculocoronary connections
Image: doctorlib
Dilated LAD with retrograde filling Dilated RCA with retrograde filling
PSAX view
Image: Giglia et al, Circulation
Potential of adverse outcome after
RV decompression:
RV to coronary
Fistula without
coronary stenosis
Potential RV steal
phenomenon
RV to coronary Fistula
with proximal ± distal
coronary stenosis
Potential RV steal/
ischemia
RV to coronary Fistula
with Coronary
occlusion/ atresia
Potential Isolation
and MI
Ventriculocoronary connections
 With coronary
obstructive lesions,
normal aortic
diastolic pressure
insufficient to drive
coronary blood flow
 Palliative measures
like BT shunt further
lower aortic diastolic
pressure  coronary
ischemia
 In RVDCC,
myocardial perfusion
sustained by
retrograde coronary
flow from
hypertensive RV,
during systole
 Any decrease in
RVSP by RV
decompressive
procedures 
coronary ischemia
RV dependent coronary
circulation (RVDCC)
Coronary artery abnormalities requiring RV
systolic events:
 Absent aorto-coronary connections
 Coronary artery interruption or stenosis
 Profound coronary cameral steal or fistula
Atrial septum
 PFO or OS ASD with
obligatory R- L shunt
 Oxygenated pulmonary
venous blood shunts L-
to-R across TV 
perfuses the
myocardium
 Nonrestrictive flow is
essential
Subcostal view: IAS with
aneurysmal flap, R-L shunt
Image: pedcards.com
Associated abnormalities
 LPA coarctation at site of PDA insertion
 Bilateral PDAs or MAPCAs when PAs non-confluent
 Endocardial fibroelastosis, ventricular dysfunction
 LV outflow tract obstruction
 Aneurysm of septum primum
Procedures in
newborn period
Being a condition with PDA-
dependent pulmonary
circulation, intervention is almost
always required in neonatal
period
Goal: To increase
pulmonary blood flow
Well-developed RV, mild/
no TR, no RVDCC

Surgical or transcatheter
pulmonary valvotomy, or
RVOT reconstruction
Goal: To enable RV to provide
pulmonary circulation
Severe RV hypoplasia,
RVDCC

PGE1, PDA stent or
systemic- PA shunt
Is RV size adequate to support 2-
ventricle repair?
 (i) Presence of three portions of the RV i.e.
tripartite, bipartite vs. unipartite
 (ii) TV annulus diameter and its z-score
 (iii) TV/MV diameter ratio >0.5 & TV z-score >
-2.5  possibility of 2-ventricle repair
Is there an infundibulum? Is MPA
in continuity with the imperforate
pulmonary valve?
 Transcatheter RF valvotomy or RVOT
transannular patch Growth of the
hypoplastic RV is stimulated
 Simultaneous PDA stenting or modified BT
shunt allows for adequate pulmonary blood
flow while RV is allowed to grow
Pulmonary valvotomy
 Well-developed tripartite RV
 Mild or no TR
 No significant RV-CACs
 BPV/ transcatheter wire perforation,
laser or radiofrequency assisted
OR
 Surgical valvotomy
Ductal patency may be maintained by
PGE before the procedure
Image: Thoracickey
Dilated – normal sized - mildly
hypoplastic RV
 RV size ≥ 2/3rd of normal
 TV Z score 0 to -2
 Consider surgical valvotomy with RVOT
reconstruction (RVOTR)
 If additional source of PBF felt necessary,
systemic-to-PA shunt may be simultaneously
placed
RVOT Reconstruction Surgery
For fixed obstruction at subvalvar or annulus level:
 1] Initially, RV-CACs are ligated reversibly, off CPB.
If ligation is not tolerated only shunt surgery
If no WMA or s/o injury ligation is completed
 2] Relief of RVOTO performed:
Infundibular resection + TAP or surgical valvotomy
 3] ASD is snared to achieve mild restriction - To encourage TV
flow
*If mostly RVDCC Single ventricle pathway
Role of Post-op. PGE1
 Post- procedure, cyanosis may persist
 Cause: Low RV compliance from myocardial
hypertrophy or fibrosis Elevated RV diastolic
pressure elevated RA pressure R-L shunt
through the foramen ovale
 Adequate PBF may not be achieved for days to
weeks
 May continue PGE1 in a low dose to maintain
ductus patency
RVOT Patch + arterial shunt
RVOTR + BT
Shunt
ASD and
Shunt can be
closed: 2VR
TV & RV
growth
failure:
BDGS
RV moderate
sized:
1 ½ VR
Low cardiac output syndrome
Following RVOTR & modified BT shunt:
 1) Due to low diastolic pressure or
unrecognized RVDCC with myocardial
ischemia
 2) Preferential pulmonary blood flow
as PVR very low and SVR high
 3) Due to “Circular shunt”: when
trans-annular patch (resulting in
pulmonary regurgitation) is combined
with BT shunt.
Image: Ultrasound Obgyn
Blood flow: LA -> LV -> Aorta -> BT
shunt -> PA -> Retrograde into RV,
across RVOT -> Retrograde into RA,
across TV -> LA, across the ASD
Severely Hyoplastic RV
 Pulmonary blood supply depends
entirely on systemic- pulmonary
connections
 Systemic venous return reaches RA->
PFO -> LA
 Q.1. Adequacy of PDA to sustain
pulmonary blood flow?
 Q. 2. Adequacy of ASD for
decompression of systemic venous
return to LA?
 Management option is to perform
systemic-PA shunt or PDA stent
Systemic-PA shunt or PDA stent
Indications:
 Severe RV hypoplasia (TV Z score < -
4.5)
 RVDCC (these patients are candidates
for eventual SVR)
Implantation of a stent in the PDA can
achieve the same end
Image rch.org.edu
Balloon atrial septostomy
 If systemic-to-pulmonary artery shunt
contemplated, with presumed single-ventricle
pathway
 Unrestrictive atrial communication necessary
 If restrictive PFO, BAS to be done
Transcatheter procedural
considerations
Pulmonary valve perforation
Image: Pediat Therapeut 2012
4F JR2- JR4- Tip placed close
to PV- AP & Lat views
Atretic PV perforated with stiff
end of regular guide wire/
CTO guide wire/ Laser/ RF
perforation wire
5 mm Gooseneck snare placed
retrograde (FA PDA MPA)
Balloon catheter advanced
across perforated PV, over wire
(± veno-arterial loop)
Serial balloon valvuloplasty (3
mm PTCA balloon to 6-8 mm
balloons)
• Femoral v. & a. access
preferred over
umbilical (easier
catheter
manipulation)
• Heparin 50-100 U/kg
(target ACT> 200 s)
Hybrid approach
 Sternotomy followed by placement of a purse
string suture in RV free wall, at a suitable location
aiming at the RVOT/ PV
 Advance needle via the purse-string suture,
towards PV
 Using TEE, perforate the PV
 Advance guidewire and remove needle
 Guide wire position confirmed by fluoroscopy
 4 French sheath placed over guidewire and
secured by the surgeon
 Serial balloon dilatations performed
Post-procedure role of PGE1
 Dynamic obstruction of RVOT secondary to strong
contraction of the hypertrophic RV infundibulum
noted immediately after successful BPV 
Continue PGE1 ±βblocker dynamic sub-PS may
resolve in a few days as RV hypertrophy resolves
 RV volume decreases compared to pre-
intervention volume by approx. 40-50%
Continue PGE1RV volume increases back to
pre-intervention volume by approx. 3 weeks
PDA Stenting
Types of PDA in PA IVS
Usual: normal origin from
proximal descending aorta and a
short straight course with
constriction at insertion onto
MPA
Less common: More proximal
origin from aortic arch, opposite
origin of LSCA, at acute angle
Image: Alwi, Ann Pediatr Cardiol. 2008
4F long sheath tip
positioned near the
ampulla
Using 4F JR catheter,
0.014” guidewire
passed, Ao PDA
MPA RV RA IVC
3.5 mm-4.5mm
diameter pre-mounted
stent positioned
balloon inflated and
stent expanded
balloon deflated
Post-expansion
angiogram: Entire
length of ductus is
covered by stent; no
encroachment of origin
of branch PA
PGE1 turned off before procedure
Femoral artery cannulated with 4F sheath
Heparin 50 units/kg, repeated every 1-1 ½ hour
Image: Alwi, Ann Pediatr Cardiol. 2008
Definitive
Repair
Goal: Complete separation of
pulmonary and systemic
circulations
Severely
hypoplastic
RV, RVDCC,
failed attempt
to induce TV
growth
Good sized,
tripartite RV,
successful
attempt to
induce TV
growth
Fontan
pathway
2VR-
Valvotomy/
RVOTR-
infundibular
resection &
patch
Image: J Pediatr Cardiol Surg, Thoracickey
 
Image: EJCTS 2011
Group A:
TV Z-score >-2.5
Good infundibulum,
Membranous atresia
Tripartite RV
No major sinusoids
Variable TR
Valvotomy & dilation

Dilation of restenosis,
RVOTR or TV repair
Group B
TV Z-score -2.5 to -4.5
Patent Infundibulum,
Subvalvular PS
Bipartite RV
Major sinusoids ±
Variable TR
Valvotomy & dilation, PDA
stenting ± BAS
TAP + modified BT shunt

RVOTR Or
BDGS (1 ½ VR) if RV fails
to develop*
Group C
TV Z-score < -4.5
Absent infundibulum,
Muscular atresia
Unipartite RV
Major sinusoids
Usually competent TV
PDA stenting or modified
BT shunt
± BAS

BDGS
 Fontan/ Cardiac
transplantation*
*If extreme TR
Starnes approach
Intermediate RV size
If no fixed RVOTO (e.g. small PV annulus):
Reasonable to wait 3–4 years (with interim
valvotomy & PDA stenting) in anticipation of
RV growth.
If failure of RV growth: bidirectional Glenn
shunt and closure of ASD (1½ ventricle
repair) may be performed.
Aim: to retain the RV in the circulation if it is
capable of maintaining even part of
Pulmonary Blood Flow
One-and-half ventricle repair
The heart is
surgically septated (may
include ASD closure, RV-
PA conduit).
Additionally, a superior
cavopulmonary shunt is
created.
BDGS provides preload
reduction for the limited
right heart, thereby
avoiding right heart
failure.
Advantages of one-and-half
repair over BDGS:
 No increase in LV volume load (as
no ASD)
 Systemic saturation is complete
 No risk of paradoxical emboli
Additional
procedures
TV repair for TS or TR
 Valvar stenosis can be improved by BPV or
open valvoplasty. By open valvoplasty,
division of fused commissures/ fused papillary
muscles can be performed
 If TV insufficiency significant-> valvar repair
Dysplastic TV with Marked TR / Ebstein
malformation
 Difficult to manage, high mortality
 Systemic to PA shunt may relieve cyanosis, but
combination of increased LVVO ( from shunt), and RVVO
(from TR) often induces cardiac failure
 If patient requires placement of RVOT patch when 2VR
is considered-> PR results; 2 regurgitant valves (TV and
PV) in series make adequate C.O unlikely -> repair/
replacement of TV required
Dysplastic TV with Marked TR /
Ebstein malformation
 Contemporary approach:
Convert to tricuspid
atresia, (Starnes)+
construct systemic-PA
shunt
 Later cavopulmonary
palliation
Image: Sakurai, JTCVS, 2018
Closing the ASD
If right heart structures
fail to grow, or patient
remains too cyanotic
If ASD too large, size of
ASD should be
reduced
Device closure may be
performed if trial of
balloon occlusion is
tolerated
Heart failure from PR
 In infants who have had surgical
opening of the RV infundibulum
and the annulus of the valve
 If PR significant  Large RV
volume overload  marked RV
enlargement & progressive right
heart failure
 With progressive RV enlargement
-> pulmonary valve replacement
necessary
Image: JUM
Contemporary Approaches
 Fetal treatment: in utero
valvotomies- reported at
about 28 weeks (23-32
weeks). Providing forward
flow encourages RV and TV
growth.
 Transplantation: subset of
patients where there are
significant RV-CACs and no
continuation between aorta
and coronary a.
Intrauterine BPV
Image: Ultrasound Obstet Gynecol
Take Home Message
Image: EJCTS 2011
Group A:
TV Z-score >-2.5
Good infundibulum,
Membranous atresia
Tripartite RV
No major sinusoids
Variable TR
Valvotomy & dilation

Dilation of restenosis,
RVOTR or TV repair
Group B
TV Z-score -2.5 to -4.5
Patent Infundibulum,
Subvalvular PS
Bipartite RV
Major sinusoids ±
Variable TR
Valvotomy & dilation, PDA
stenting ± BAS
TAP + modified BT shunt

RVOTR Or
BDGS (1 ½ VR) if RV fails
to develop*
Group C
TV Z-score < -4.5
Absent infundibulum,
Muscular atresia
Unipartite RV
Major sinusoids
Usually competent TV
PDA stenting or modified
BT shunt
± BAS

BDGS
 Fontan/ Cardiac
transplantation*
*If extreme TR
Starnes approach
References
 Nykanen DG. Pulmonary atresia and intact ventricular septum. In Ed.
Allen HD, Driscoll DJ, Shaddy RE, Feltes TF. Moss and Adam’s Heart
Disease in infants, children and adolescents. Seventh ed. Philadelphia,
Lippincott Williams and Wilkins
 Burkholder H, Balaguru D. Pulmonary Atresia with Intact Ventricular
Septum: Management Options and Decision-making. Pediat Therapeut
2012, S5
 Alwi M. Management Algorithm in Pulmonary Atresia With IVS.
Catheterization & Cardio-vascular Interventions 2006; 67:679–686
 Alwi M. Stenting the ductus arteriosus. Case selection, technique and
possible complications. Ann Pediatr Cardiol. 2008;1: 38–45.
 Chikkabyrappa SM, Loomba RS, Tretter JT. Pulmonary Atresia With an
Intact Ventricular Septum: Preoperative Physiology, Imaging, and
Management. Seminars in Cardiothoracic and Vascular Anesthesia ·
February 2018
 Foker JE et al. Treatment algorithm for PA with IVS. Progress in Pediatric
Cardiology 2010;29:61–63
 Pulmonary atresia with IVS: Long-term results of 1&1/2 ventricle repair.
Kagami et al. AnnThoracic Surgery 1995;60:1762-1764
Pulmonary atresia with intact interventricular septum management

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Pulmonary atresia with intact interventricular septum management

  • 1. PA IVS ManagementDr. Sweta Mohanty Consultant Pediatric Cardiologist RxDx Healthcare, Rainbow Hospital, Bangalore Image: Plasticsurgerykey.org
  • 2. Severely hypoplastic RV Good sized RV Single- ventricle repair Two- ventricle repair Image: J Pediatr Cardiol Surg, Thoracickey
  • 3.
  • 5. Tricuspid valve Stenotic, hypoplastic annulus Dysplastic / Ebstein- like, with TR Image: doctorlib
  • 6. Right ventricle Image: JACC Hypoplastic, unipartite RV TV Z-score correlates with RV size Large, thin-walled RV Seen with profound TR
  • 7. Nature of pulmonary atresia Muscular atresia: Narrow infundibulum, primitive PV Membranous atresia: Well-formed infundibulum, commissural fusion
  • 8. High pressure retrograde flow through epicardial coronaries Endothelial damage Coronary stenoses Intrinsic coronary abnormality Lack of blood- egress from RV Elevated RV pressure Blood forced retrograde through thebesian veins Coronary sinusoids Coronary cameral Fistulae Ventriculocoronary connections
  • 9. Image: doctorlib Dilated LAD with retrograde filling Dilated RCA with retrograde filling PSAX view
  • 10. Image: Giglia et al, Circulation Potential of adverse outcome after RV decompression: RV to coronary Fistula without coronary stenosis Potential RV steal phenomenon RV to coronary Fistula with proximal ± distal coronary stenosis Potential RV steal/ ischemia RV to coronary Fistula with Coronary occlusion/ atresia Potential Isolation and MI
  • 11. Ventriculocoronary connections  With coronary obstructive lesions, normal aortic diastolic pressure insufficient to drive coronary blood flow  Palliative measures like BT shunt further lower aortic diastolic pressure  coronary ischemia  In RVDCC, myocardial perfusion sustained by retrograde coronary flow from hypertensive RV, during systole  Any decrease in RVSP by RV decompressive procedures  coronary ischemia
  • 12. RV dependent coronary circulation (RVDCC) Coronary artery abnormalities requiring RV systolic events:  Absent aorto-coronary connections  Coronary artery interruption or stenosis  Profound coronary cameral steal or fistula
  • 13. Atrial septum  PFO or OS ASD with obligatory R- L shunt  Oxygenated pulmonary venous blood shunts L- to-R across TV  perfuses the myocardium  Nonrestrictive flow is essential Subcostal view: IAS with aneurysmal flap, R-L shunt Image: pedcards.com
  • 14. Associated abnormalities  LPA coarctation at site of PDA insertion  Bilateral PDAs or MAPCAs when PAs non-confluent  Endocardial fibroelastosis, ventricular dysfunction  LV outflow tract obstruction  Aneurysm of septum primum
  • 15. Procedures in newborn period Being a condition with PDA- dependent pulmonary circulation, intervention is almost always required in neonatal period
  • 16. Goal: To increase pulmonary blood flow Well-developed RV, mild/ no TR, no RVDCC  Surgical or transcatheter pulmonary valvotomy, or RVOT reconstruction Goal: To enable RV to provide pulmonary circulation Severe RV hypoplasia, RVDCC  PGE1, PDA stent or systemic- PA shunt
  • 17. Is RV size adequate to support 2- ventricle repair?  (i) Presence of three portions of the RV i.e. tripartite, bipartite vs. unipartite  (ii) TV annulus diameter and its z-score  (iii) TV/MV diameter ratio >0.5 & TV z-score > -2.5  possibility of 2-ventricle repair
  • 18. Is there an infundibulum? Is MPA in continuity with the imperforate pulmonary valve?  Transcatheter RF valvotomy or RVOT transannular patch Growth of the hypoplastic RV is stimulated  Simultaneous PDA stenting or modified BT shunt allows for adequate pulmonary blood flow while RV is allowed to grow
  • 19. Pulmonary valvotomy  Well-developed tripartite RV  Mild or no TR  No significant RV-CACs  BPV/ transcatheter wire perforation, laser or radiofrequency assisted OR  Surgical valvotomy Ductal patency may be maintained by PGE before the procedure Image: Thoracickey
  • 20. Dilated – normal sized - mildly hypoplastic RV  RV size ≥ 2/3rd of normal  TV Z score 0 to -2  Consider surgical valvotomy with RVOT reconstruction (RVOTR)  If additional source of PBF felt necessary, systemic-to-PA shunt may be simultaneously placed
  • 21. RVOT Reconstruction Surgery For fixed obstruction at subvalvar or annulus level:  1] Initially, RV-CACs are ligated reversibly, off CPB. If ligation is not tolerated only shunt surgery If no WMA or s/o injury ligation is completed  2] Relief of RVOTO performed: Infundibular resection + TAP or surgical valvotomy  3] ASD is snared to achieve mild restriction - To encourage TV flow *If mostly RVDCC Single ventricle pathway
  • 22. Role of Post-op. PGE1  Post- procedure, cyanosis may persist  Cause: Low RV compliance from myocardial hypertrophy or fibrosis Elevated RV diastolic pressure elevated RA pressure R-L shunt through the foramen ovale  Adequate PBF may not be achieved for days to weeks  May continue PGE1 in a low dose to maintain ductus patency
  • 23. RVOT Patch + arterial shunt RVOTR + BT Shunt ASD and Shunt can be closed: 2VR TV & RV growth failure: BDGS RV moderate sized: 1 ½ VR
  • 24. Low cardiac output syndrome Following RVOTR & modified BT shunt:  1) Due to low diastolic pressure or unrecognized RVDCC with myocardial ischemia  2) Preferential pulmonary blood flow as PVR very low and SVR high  3) Due to “Circular shunt”: when trans-annular patch (resulting in pulmonary regurgitation) is combined with BT shunt. Image: Ultrasound Obgyn Blood flow: LA -> LV -> Aorta -> BT shunt -> PA -> Retrograde into RV, across RVOT -> Retrograde into RA, across TV -> LA, across the ASD
  • 25. Severely Hyoplastic RV  Pulmonary blood supply depends entirely on systemic- pulmonary connections  Systemic venous return reaches RA-> PFO -> LA  Q.1. Adequacy of PDA to sustain pulmonary blood flow?  Q. 2. Adequacy of ASD for decompression of systemic venous return to LA?  Management option is to perform systemic-PA shunt or PDA stent
  • 26. Systemic-PA shunt or PDA stent Indications:  Severe RV hypoplasia (TV Z score < - 4.5)  RVDCC (these patients are candidates for eventual SVR) Implantation of a stent in the PDA can achieve the same end Image rch.org.edu
  • 27. Balloon atrial septostomy  If systemic-to-pulmonary artery shunt contemplated, with presumed single-ventricle pathway  Unrestrictive atrial communication necessary  If restrictive PFO, BAS to be done
  • 30. Image: Pediat Therapeut 2012 4F JR2- JR4- Tip placed close to PV- AP & Lat views Atretic PV perforated with stiff end of regular guide wire/ CTO guide wire/ Laser/ RF perforation wire 5 mm Gooseneck snare placed retrograde (FA PDA MPA) Balloon catheter advanced across perforated PV, over wire (± veno-arterial loop) Serial balloon valvuloplasty (3 mm PTCA balloon to 6-8 mm balloons) • Femoral v. & a. access preferred over umbilical (easier catheter manipulation) • Heparin 50-100 U/kg (target ACT> 200 s)
  • 31. Hybrid approach  Sternotomy followed by placement of a purse string suture in RV free wall, at a suitable location aiming at the RVOT/ PV  Advance needle via the purse-string suture, towards PV  Using TEE, perforate the PV  Advance guidewire and remove needle  Guide wire position confirmed by fluoroscopy  4 French sheath placed over guidewire and secured by the surgeon  Serial balloon dilatations performed
  • 32. Post-procedure role of PGE1  Dynamic obstruction of RVOT secondary to strong contraction of the hypertrophic RV infundibulum noted immediately after successful BPV  Continue PGE1 ±βblocker dynamic sub-PS may resolve in a few days as RV hypertrophy resolves  RV volume decreases compared to pre- intervention volume by approx. 40-50% Continue PGE1RV volume increases back to pre-intervention volume by approx. 3 weeks
  • 34. Types of PDA in PA IVS Usual: normal origin from proximal descending aorta and a short straight course with constriction at insertion onto MPA Less common: More proximal origin from aortic arch, opposite origin of LSCA, at acute angle Image: Alwi, Ann Pediatr Cardiol. 2008
  • 35. 4F long sheath tip positioned near the ampulla Using 4F JR catheter, 0.014” guidewire passed, Ao PDA MPA RV RA IVC 3.5 mm-4.5mm diameter pre-mounted stent positioned balloon inflated and stent expanded balloon deflated Post-expansion angiogram: Entire length of ductus is covered by stent; no encroachment of origin of branch PA PGE1 turned off before procedure Femoral artery cannulated with 4F sheath Heparin 50 units/kg, repeated every 1-1 ½ hour Image: Alwi, Ann Pediatr Cardiol. 2008
  • 36. Definitive Repair Goal: Complete separation of pulmonary and systemic circulations
  • 37. Severely hypoplastic RV, RVDCC, failed attempt to induce TV growth Good sized, tripartite RV, successful attempt to induce TV growth Fontan pathway 2VR- Valvotomy/ RVOTR- infundibular resection & patch Image: J Pediatr Cardiol Surg, Thoracickey  
  • 38. Image: EJCTS 2011 Group A: TV Z-score >-2.5 Good infundibulum, Membranous atresia Tripartite RV No major sinusoids Variable TR Valvotomy & dilation  Dilation of restenosis, RVOTR or TV repair Group B TV Z-score -2.5 to -4.5 Patent Infundibulum, Subvalvular PS Bipartite RV Major sinusoids ± Variable TR Valvotomy & dilation, PDA stenting ± BAS TAP + modified BT shunt  RVOTR Or BDGS (1 ½ VR) if RV fails to develop* Group C TV Z-score < -4.5 Absent infundibulum, Muscular atresia Unipartite RV Major sinusoids Usually competent TV PDA stenting or modified BT shunt ± BAS  BDGS  Fontan/ Cardiac transplantation* *If extreme TR Starnes approach
  • 39. Intermediate RV size If no fixed RVOTO (e.g. small PV annulus): Reasonable to wait 3–4 years (with interim valvotomy & PDA stenting) in anticipation of RV growth. If failure of RV growth: bidirectional Glenn shunt and closure of ASD (1½ ventricle repair) may be performed. Aim: to retain the RV in the circulation if it is capable of maintaining even part of Pulmonary Blood Flow
  • 40. One-and-half ventricle repair The heart is surgically septated (may include ASD closure, RV- PA conduit). Additionally, a superior cavopulmonary shunt is created. BDGS provides preload reduction for the limited right heart, thereby avoiding right heart failure.
  • 41. Advantages of one-and-half repair over BDGS:  No increase in LV volume load (as no ASD)  Systemic saturation is complete  No risk of paradoxical emboli
  • 43. TV repair for TS or TR  Valvar stenosis can be improved by BPV or open valvoplasty. By open valvoplasty, division of fused commissures/ fused papillary muscles can be performed  If TV insufficiency significant-> valvar repair
  • 44. Dysplastic TV with Marked TR / Ebstein malformation  Difficult to manage, high mortality  Systemic to PA shunt may relieve cyanosis, but combination of increased LVVO ( from shunt), and RVVO (from TR) often induces cardiac failure  If patient requires placement of RVOT patch when 2VR is considered-> PR results; 2 regurgitant valves (TV and PV) in series make adequate C.O unlikely -> repair/ replacement of TV required
  • 45. Dysplastic TV with Marked TR / Ebstein malformation  Contemporary approach: Convert to tricuspid atresia, (Starnes)+ construct systemic-PA shunt  Later cavopulmonary palliation Image: Sakurai, JTCVS, 2018
  • 46. Closing the ASD If right heart structures fail to grow, or patient remains too cyanotic If ASD too large, size of ASD should be reduced Device closure may be performed if trial of balloon occlusion is tolerated
  • 47. Heart failure from PR  In infants who have had surgical opening of the RV infundibulum and the annulus of the valve  If PR significant  Large RV volume overload  marked RV enlargement & progressive right heart failure  With progressive RV enlargement -> pulmonary valve replacement necessary Image: JUM
  • 48. Contemporary Approaches  Fetal treatment: in utero valvotomies- reported at about 28 weeks (23-32 weeks). Providing forward flow encourages RV and TV growth.  Transplantation: subset of patients where there are significant RV-CACs and no continuation between aorta and coronary a. Intrauterine BPV Image: Ultrasound Obstet Gynecol
  • 50. Image: EJCTS 2011 Group A: TV Z-score >-2.5 Good infundibulum, Membranous atresia Tripartite RV No major sinusoids Variable TR Valvotomy & dilation  Dilation of restenosis, RVOTR or TV repair Group B TV Z-score -2.5 to -4.5 Patent Infundibulum, Subvalvular PS Bipartite RV Major sinusoids ± Variable TR Valvotomy & dilation, PDA stenting ± BAS TAP + modified BT shunt  RVOTR Or BDGS (1 ½ VR) if RV fails to develop* Group C TV Z-score < -4.5 Absent infundibulum, Muscular atresia Unipartite RV Major sinusoids Usually competent TV PDA stenting or modified BT shunt ± BAS  BDGS  Fontan/ Cardiac transplantation* *If extreme TR Starnes approach
  • 51. References  Nykanen DG. Pulmonary atresia and intact ventricular septum. In Ed. Allen HD, Driscoll DJ, Shaddy RE, Feltes TF. Moss and Adam’s Heart Disease in infants, children and adolescents. Seventh ed. Philadelphia, Lippincott Williams and Wilkins  Burkholder H, Balaguru D. Pulmonary Atresia with Intact Ventricular Septum: Management Options and Decision-making. Pediat Therapeut 2012, S5  Alwi M. Management Algorithm in Pulmonary Atresia With IVS. Catheterization & Cardio-vascular Interventions 2006; 67:679–686  Alwi M. Stenting the ductus arteriosus. Case selection, technique and possible complications. Ann Pediatr Cardiol. 2008;1: 38–45.  Chikkabyrappa SM, Loomba RS, Tretter JT. Pulmonary Atresia With an Intact Ventricular Septum: Preoperative Physiology, Imaging, and Management. Seminars in Cardiothoracic and Vascular Anesthesia · February 2018  Foker JE et al. Treatment algorithm for PA with IVS. Progress in Pediatric Cardiology 2010;29:61–63  Pulmonary atresia with IVS: Long-term results of 1&1/2 ventricle repair. Kagami et al. AnnThoracic Surgery 1995;60:1762-1764