50
Congenital diaphragmatic hernia: prediction of pulmonary hypoplasia JM Martínez, B Puerto, E Gratacós

Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Embed Size (px)

Citation preview

Page 1: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Congenital diaphragmatic hernia:

prediction of pulmonary hypoplasia

JM Martínez, B Puerto, E Gratacós

Page 2: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

1/2400-4000 neonates

– isolated: 1/5.000 (100/ year)

Localization

– 90% postero-lateral (Bochdaleck)

– 95% unilateral

• 80% left

• 20% right

Congenital diaphragmatic hernia (CDH)

Page 3: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

1. Defect pleuroperitoneal membrane 8-12 wk

– Secondary pulmonary hypoplasia

2. Primary pulmonary hypoplasia

– Secondary CDH

CDH: etiopathogenesis

Page 4: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

1. Defect pleuroperitoneal membrane 8-12 wk

– Secondary pulmonary hypoplasia

2. Primary pulmonary hypoplasia

– Secondary CDH

CDH: etiopathogenesis

PULMONARY HYPOPLASIA

+/-

PULMONARY HYPERTENSION

Page 5: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Canalicular 28 17

Pseudoglandular 18 7

Saccular 40 25

Alveolar 30 2 yrs

Embryonic 8 4

vascular

development

end of conduct

generation

IMPAIRMENT OF GROWTH

Normal lung development

Page 6: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Canalicular 28 17

Pseudoglandular 18 7

Saccular 40

25

Alveolar 30 2 yrs

Embryonic 8 4

vascular

development

end of conduct

generation

immaturity vascular damage Impaired airway number

IMPAIRMENT OF GROWTH

Lung hypoplasia

Page 7: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Ultrasound diagnosis of CDH

Page 8: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Normal thorax

Page 9: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

─ Heterogeneous mass

─ Mediastinum shift

─ Abdominal viscera

─ PolyH, hydrothorax

Left CDH

Page 10: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

─ Homogeneous mass

─ Mediastinum shift

─ Liver

─ PolyH, hydrothorax

Right CDH

Page 11: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

30-40% associated anomalies

1. ultrasound

2. echocardio: 10-15%

3. Karyotype: 25%

t21,t18,iso12p

4. ¿MRI?

Page 12: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

30-40% associated anomalies

1. ultrasound

2. echocardio: 10-15%

3. Karyotype: 25%

t21,t18,iso12p

4. ¿MRI?

Page 13: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Prognosis of CDH:

prediction of pulmonary hypoplasia

Page 14: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Isolated CDH: 60-70%

conflict obstetrical vs. pediatrical data

good prognosis poor prognosis

intrauterine prognostic factors

Euro-CDH group LHR and liver to predict outcome in left CDH:

a multicenter study. AJOG 2006

J. Jani1, A. Benachi2, R. Favre4, R. Keller3,

H. Vandecruys6, J. Becker5, M. Harrison7, J. Matis4,

E. Gratacos5, K. Nicolaides6, J. Deprest1

Leuven - Barcelona - London - Paris - Strasbourg - San Francisco

global perinatal mortality: 30-40%

Page 15: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Global mortality 30-40%

– LETHAL PULMONARY HYPOPLASIA

1. Respiratory insufficiency

2. Pulmonary hypertension

Isolated CDH: 1/5.000 (100/ year)

Page 16: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Pulmonary hypoplasia

• Pulmonary hypoplasia degree:

1. Size of the defect

2. Visceral herniation

• It is bilateral!!!

Page 17: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Ultrasound

– 3D-ultrasound

Doppler

– Pulsed

– Angio-power

MRI

– 3D-MRI

Prediction of pulmonary hypoplasia

Page 18: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

30-40% perinatal mortality ‘qualified’:

o/e LHR + liver

Pulmonary hypoplasia

• Pulmonary hypoplasia degree:

1. Size of the defect

2. Visceral herniation

• It is bilateral!!!

Page 19: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

‘Lung-to-head ratio’ (Metkus 1996)

1. 4 chamber view

2. 1 rib

3. Perpendicular max

diameters

Metkus 1996

Page 20: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

‘Lung-to-head ratio’

1. 4 chamber view

2. 1 rib

3. Perpendicular max

diameters

Page 21: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

LHR: 17.0x9.9/218= 0.78

‘Lung-to-head ratio’

Page 22: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

o/e LHR (customization)

Jani et al UOG 2007

Page 23: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Poor prognosis: o/e LHR < 40-45%

Jani et al UOG 2007

Page 24: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

LHR o/e LHR

>1.4 > 40%

1.0-1.4 25-40%

0.8-1.0 15-25%

< 0.8 < 15%

Correlation

Page 25: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

o/e LHR and liver

bad prognosis ‘good’ prognosis

Page 26: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Prediction of survival according to o/e LHR and liver position

Left Right

CDH expectant management (n=100)

Page 27: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Prediction of morbidity

CDH expectant management (n=100)

Jani et al 2007

≤ 25 26-45 >45

Patch rate (%)

0

10

20

30

40

50

60

70

80

90

100

O/E LHR (%)

0

10

20

30

40

50

60

Conventional ventilation

days

≤ 25 26-45 >45

O/E LHR (%)

0

10

20

30

40

50

60

Enteral feeding

days

<25 26-45 >45

O/E LHR (%)

0

10

20

30

40

50

60

NICU

days

<25 26-45 >45

O/E LHR (%)

0

10

20

30

40

50

60

70

80

90

≤ 25 26-45 >45

O/E LHR (%)

Oxygen O2 at 28d (%)

100

Page 28: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

sagital coronal transversal

3D ultrasound / MRI … not yet

Page 29: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Risk prediction by LHR

LHR predicts

lethal hypoplasia

LHR predicts

nothing

Arkovitz MS, JPS 07

Heiling KS, UOG 05

Bashat, UOG 07

review & meta-analysis most published studies excluded

Metkus, JPS 96

Lipshutz GS, JPS 97

Laudy JA, Pren Diag 03

Keller RL, UOG 03

Jani J, UOG 2006

Jani J, AJOG 06

Yang SH, AJOG 07

Hedrick,AJOG 07(worse than liver)

Datin-D,AJOG07(better than liver)

It is not perfect but it is the

BEST AVAILABLE PARAMETER

Page 30: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Options for isolated CDH

1. TOP

2. ‘Standard’ postnatal treatment

3. Postnatal treatment + FETAL THERAPY

• if survival ≤ 60%

Page 31: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Prenatal therapy for CDH

Page 32: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Fetal therapy: fetoscopic tracheal occlusion

• Mecanism: Induces accelerated lung growth

1. Direct mechanical stimuli: prevents exit of normal

tracheobronchial fluid

2. Secretion of growth factors

• Timing

– 27-29 wk if LHR O/E < 25%

– 30-32 wk if LHR O/E > 25-40%

Page 33: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

FETO: Leuven-BCN-London (n> 350)

Page 34: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Post-fetoscopy

Page 35: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Post-fetoscopy

Page 36: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

elegible: FETO: ‘update’ results: 210 cases (october 2008)

Page 37: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

FETO: removal of balloon

Page 38: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Fetal therapy for CDH: survival

Left CDH: 24.1% to 49.1%

Right CDH: 0% to 35.3%

Page 39: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Aive and well 73%

Respiratory 4%

Feeding 7%

Neurodevelopmental 2%

Scoliosis 2%

Fetal therapy for CDH: morbidity (6-60 months)

Page 40: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Fetal therapy for CDH : complications

Rotura de tràquea: 4 (1.9%)

– 3 fetoscopia 8-14 días

Polihidramnios severo: 18 (8.5%)

Hemorragia intramaniótica (transfusión): 1 (0.5%)

Corioamnionitis: 5 (2.3%)

Page 41: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Future challenges in CDH

Page 42: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

FETO survival + 30% S

urv

ival ra

te (

%)

≤15% 16%-25% 25%- 40% ≥41%

0

10

20

30

40

50

60

70

80

90

100

1. 50-60%: good response

high survival

2. 25%: lung growth BUT severe PHT

high mortality

3. 15-20%: no response

extreme mortality

¿How can we identify those cases with good or

poor lung response to FETO?

Page 43: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Conduct randomized studies

Improved thecnological issues

Refine pathophysiological understanding

– Define subgrups at risk

• Survival

• Morbidity

Fetal therapy for CDH: future challenges

Page 44: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Eurofetus vs randomized USA

Page 45: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

US diagnosis

•US (LHR)

•MRI (liver-up)

•detailed US scan

•karyotype

O/E < 15%

(LHR< 0.6)

pilot study TO 22-24w

+

eventually RCT

O/E 15-25%

(LHR 0.7-0.99)

TO vs expectant

SURVIVAL

O/E 25-40%

(LHR 1.0-1.4)

TO 30-32 w vs expectant

MORBIDITY

EURO-CDH - RCT STUDIES ON CDH IN UTERO TREATMENT EURO-CDH: Barcelona-Leuven-London

RCT studies on CDH in utero treatment

Page 46: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

CDH: Doppler evalaution

PSV

PERDF

Page 47: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

CDH: Doppler evalaution

PSV

PERDF

Page 48: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Doppler prediction of response after FETO

+

Page 49: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

Doppler evaluation of perfusion

Page 50: Congenital diaphragmatic hernia: prediction of · PDF fileCongenital diaphragmatic hernia (CDH) 1. Defect pleuroperitoneal membrane 8-12 wk – Secondary pulmonary hypoplasia 2. Primary

1. Isolated: only 50%

2. Global mortality 30-40%

3. Variable and predictable outcome (o/e LHR)

4. Fetal therapy: 30-35 % survival

5. If survives: good quality of life

CDH: conclusions