Diaphragmatic Hernia
Diaphragmatic Hernia
Clinical Anatomy
Clinical Anatomy
 musculotendinous membrane
musculotendinous membrane
 central:
central: tendinous
tendinous
 peripheral:
peripheral: muscular
muscular
HIATUS
HIATUS
 Aorta: T12 azygos vein, thoracic duct
Aorta: T12 azygos vein, thoracic duct
 Esophagus:T10 vagus nerves
Esophagus:T10 vagus nerves
 IVC:T8
IVC:T8
BLOOD SUPPLY
BLOOD SUPPLY
 abdominal aorta: RPA, LPA
abdominal aorta: RPA, LPA
 thoracic aorta: SPA
thoracic aorta: SPA
 internal mammary artery
internal mammary artery
VENOUS DRAINAGE
VENOUS DRAINAGE
 left phrenic vein
left phrenic vein
 right phrenic vein
right phrenic vein
Both drain into IVC
Both drain into IVC
INNERVATION
INNERVATION
 Right phrenic nerve: motor innervation
Right phrenic nerve: motor innervation
 Left phrenic nerve: motor innervation
Left phrenic nerve: motor innervation
 Intercostal nerve: sensory innervation
Intercostal nerve: sensory innervation
Diaphragm develops
Diaphragm develops
Transverse septum
Transverse septum
Pleuroperitoneal membrane
Pleuroperitoneal membrane
Dorsal and lateral body wall
Dorsal and lateral body wall
Mesentery of esophagus
Mesentery of esophagus
Diaphragm develops between the 4
Diaphragm develops between the 4th
th
and
and
8
8th
th
weeks of gestation
weeks of gestation
separates thoracic cavity from abdomen
separates thoracic cavity from abdomen
The crura develop from the mesentery of
The crura develop from the mesentery of
esophagus
esophagus
CONGENITAL DIAPHRAGMATIC
CONGENITAL DIAPHRAGMATIC
HERNIA
HERNIA
 BOCHDALEK HERNIA
BOCHDALEK HERNIA
 MORGAGNI HERNIA
MORGAGNI HERNIA
 ESOPHAGEAL HIATAL HERNIA
ESOPHAGEAL HIATAL HERNIA
BOCHDALEK HERNIA
BOCHDALEK HERNIA
 Failure of closure of the
Failure of closure of the
pericardio- peritoneal canal cause CDH
pericardio- peritoneal canal cause CDH
(bochdalek hernia)
(bochdalek hernia)
 Most common type (Bochdalek hernia
Most common type (Bochdalek hernia
occurs in 1:4000-5000 live birth)
occurs in 1:4000-5000 live birth)
 Posterolateral defect
Posterolateral defect
 Male:female 2/1
Male:female 2/1
 Left sided 90%/ Right sided 10%
Left sided 90%/ Right sided 10%
BOCHDALEK HERNIA
BOCHDALEK HERNIA
-
-Genetic mutations have been
Genetic mutations have been
implicated, Amniocentesis with
implicated, Amniocentesis with
karyotyping may identify
karyotyping may identify
chromosomal defects especially
chromosomal defects especially
trisomy 18 and 21
trisomy 18 and 21
-surfactant deficiency
-surfactant deficiency
-Associated anomalies are Heart
-Associated anomalies are Heart
anomalies and abdominal wall defects
anomalies and abdominal wall defects
BOCHDALEK HERNIA
BOCHDALEK HERNIA
 Diaphragmatic defect allows abdominal
Diaphragmatic defect allows abdominal
viscera to fill thoracic cavity
viscera to fill thoracic cavity
 Abdomen remains small and scaphoid
Abdomen remains small and scaphoid
 Lungs are hypoplastic with decreased
Lungs are hypoplastic with decreased
bronchial and vascular branching
bronchial and vascular branching
CDH may be discovered prenataly on
CDH may be discovered prenataly on
routine ultrasoundas early as 15
routine ultrasoundas early as 15th
th
week of
week of
gestation
gestation
-herniation of abdominal viscera into
-herniation of abdominal viscera into
chest
chest
-change in liver position
-change in liver position
-mediastinal shift
-mediastinal shift
-Lung to heart ratio may be used to
-Lung to heart ratio may be used to
predict hiatus hernia
predict hiatus hernia
Clinical Finding in neonates/
Clinical Finding in neonates/
infants
infants
 Respiratory distress (caused by
Respiratory distress (caused by
hypoplastic ipsilateral lung, pulmonary
hypoplastic ipsilateral lung, pulmonary
hypertension and mediastinal shift
hypertension and mediastinal shift
compromising air exchange in opposite
compromising air exchange in opposite
lung)
lung)
 Absence of breath sounds
Absence of breath sounds
 Bowel sound in chest
Bowel sound in chest
 Scaphoid abdomen
Scaphoid abdomen
After birth
After birth
 CXR
CXR
 BARIUM SWALLOW
BARIUM SWALLOW
TREATMENT
TREATMENT
 Earlier the treatment of Diaphragmatic
Earlier the treatment of Diaphragmatic
Hernia was considered a surgical
Hernia was considered a surgical
emergency
emergency
 It is now accepted that Pulmonary
It is now accepted that Pulmonary
Hypertension with right to left shunt and
Hypertension with right to left shunt and
degree of Pulmonary hypoplasia are leading
degree of Pulmonary hypoplasia are leading
causes of cardiopulmonary insufficiency
causes of cardiopulmonary insufficiency
 The emphasis is on controlled ventilation
The emphasis is on controlled ventilation
and avoiding over-inflation of un-involved
and avoiding over-inflation of un-involved
Lung
Lung
 Avoiding pulmonary hypertension via
Avoiding pulmonary hypertension via
Hypoxia, Nitric oxide may be helpful
Hypoxia, Nitric oxide may be helpful
 Correction of acidosis
Correction of acidosis
 Excess administration of IV fluids
Excess administration of IV fluids
should be avoided lest it compounds
should be avoided lest it compounds
cardiac failure
cardiac failure
 Infants who remain severely hypoxic
Infants who remain severely hypoxic
may need ECMO. Gradually the lung
may need ECMO. Gradually the lung
function improves over 7-10 days
function improves over 7-10 days
TREATMENT
TREATMENT
treatment
treatment
 Nasogastric tube
Nasogastric tube
 Fluid and electrolyte
Fluid and electrolyte
 PEEP or ECMO
PEEP or ECMO
 surgery
surgery
OPERATION
OPERATION
 Infants who are not on ECMO should be
Infants who are not on ECMO should be
operated as soon as hemodynamic
operated as soon as hemodynamic
status has been optimized
status has been optimized
 Others have to wait till pulmonary
Others have to wait till pulmonary
function has improved
function has improved
 Abdominal or thoracic approach may be
Abdominal or thoracic approach may be
used (Right side:thoracotomy
used (Right side:thoracotomy
Left side:laparotomy)
Left side:laparotomy)
COMPLICATIONS
COMPLICATIONS
 Bleeding from liver/spleen while
Bleeding from liver/spleen while
reducing into abdomen
reducing into abdomen
 Hemothorax
Hemothorax
 Problems due to Hypoplastic lung or
Problems due to Hypoplastic lung or
pulmonary hypertension
pulmonary hypertension
Mortality 30-50% in 24
Mortality 30-50% in 24
hours
hours
Long term problems in CDH
Long term problems in CDH
 Gastroesophageal reflux
Gastroesophageal reflux
 Chronic lung disease
Chronic lung disease
 Hearing loss
Hearing loss
 Pectus excavatum
Pectus excavatum
 seizure
seizure
MORGAGNI HERNIA
MORGAGNI HERNIA
 Larrey hernia or retrosternal
Larrey hernia or retrosternal
 Much less common
Much less common
 2% of all diaphragmatic hernia
2% of all diaphragmatic hernia
 Contained sac may contain Omentum,
Contained sac may contain Omentum,
Colon, Stomach, Liver or Small intestine
Colon, Stomach, Liver or Small intestine
 Rarely symptomatic
Rarely symptomatic
 May be symptomatic after 40 years
May be symptomatic after 40 years
HIATAL HERNIA
HIATAL HERNIA
 Sliding
Sliding
 Paraesophageal
Paraesophageal
 Mixed
Mixed
 Usually associated with GER
Usually associated with GER
 Treatment Medical/Surgical
Treatment Medical/Surgical
Eventration of diaphragm
Eventration of diaphragm
 Congenital(non paralysed)
Congenital(non paralysed)
 Acquired(paralysed)
Acquired(paralysed)
Trauma to diaphragm
Trauma to diaphragm
(Acquired Diaphragmatic
(Acquired Diaphragmatic
Hernia)
Hernia)
 90% left sided
90% left sided
 Early diagnosis:laparotomy
Early diagnosis:laparotomy
 Late diagnosis:thoracotomy
Late diagnosis:thoracotomy
DIAPHRAGMATIC HERNIA etiopathogenesis.ppt

DIAPHRAGMATIC HERNIA etiopathogenesis.ppt

  • 1.
  • 2.
    Clinical Anatomy Clinical Anatomy musculotendinous membrane musculotendinous membrane  central: central: tendinous tendinous  peripheral: peripheral: muscular muscular
  • 3.
    HIATUS HIATUS  Aorta: T12azygos vein, thoracic duct Aorta: T12 azygos vein, thoracic duct  Esophagus:T10 vagus nerves Esophagus:T10 vagus nerves  IVC:T8 IVC:T8
  • 4.
    BLOOD SUPPLY BLOOD SUPPLY abdominal aorta: RPA, LPA abdominal aorta: RPA, LPA  thoracic aorta: SPA thoracic aorta: SPA  internal mammary artery internal mammary artery
  • 5.
    VENOUS DRAINAGE VENOUS DRAINAGE left phrenic vein left phrenic vein  right phrenic vein right phrenic vein Both drain into IVC Both drain into IVC
  • 6.
    INNERVATION INNERVATION  Right phrenicnerve: motor innervation Right phrenic nerve: motor innervation  Left phrenic nerve: motor innervation Left phrenic nerve: motor innervation  Intercostal nerve: sensory innervation Intercostal nerve: sensory innervation
  • 7.
    Diaphragm develops Diaphragm develops Transverseseptum Transverse septum Pleuroperitoneal membrane Pleuroperitoneal membrane Dorsal and lateral body wall Dorsal and lateral body wall Mesentery of esophagus Mesentery of esophagus
  • 8.
    Diaphragm develops betweenthe 4 Diaphragm develops between the 4th th and and 8 8th th weeks of gestation weeks of gestation separates thoracic cavity from abdomen separates thoracic cavity from abdomen The crura develop from the mesentery of The crura develop from the mesentery of esophagus esophagus
  • 10.
    CONGENITAL DIAPHRAGMATIC CONGENITAL DIAPHRAGMATIC HERNIA HERNIA BOCHDALEK HERNIA BOCHDALEK HERNIA  MORGAGNI HERNIA MORGAGNI HERNIA  ESOPHAGEAL HIATAL HERNIA ESOPHAGEAL HIATAL HERNIA
  • 12.
    BOCHDALEK HERNIA BOCHDALEK HERNIA Failure of closure of the Failure of closure of the pericardio- peritoneal canal cause CDH pericardio- peritoneal canal cause CDH (bochdalek hernia) (bochdalek hernia)  Most common type (Bochdalek hernia Most common type (Bochdalek hernia occurs in 1:4000-5000 live birth) occurs in 1:4000-5000 live birth)  Posterolateral defect Posterolateral defect  Male:female 2/1 Male:female 2/1  Left sided 90%/ Right sided 10% Left sided 90%/ Right sided 10%
  • 13.
    BOCHDALEK HERNIA BOCHDALEK HERNIA - -Geneticmutations have been Genetic mutations have been implicated, Amniocentesis with implicated, Amniocentesis with karyotyping may identify karyotyping may identify chromosomal defects especially chromosomal defects especially trisomy 18 and 21 trisomy 18 and 21 -surfactant deficiency -surfactant deficiency -Associated anomalies are Heart -Associated anomalies are Heart anomalies and abdominal wall defects anomalies and abdominal wall defects
  • 14.
    BOCHDALEK HERNIA BOCHDALEK HERNIA Diaphragmatic defect allows abdominal Diaphragmatic defect allows abdominal viscera to fill thoracic cavity viscera to fill thoracic cavity  Abdomen remains small and scaphoid Abdomen remains small and scaphoid  Lungs are hypoplastic with decreased Lungs are hypoplastic with decreased bronchial and vascular branching bronchial and vascular branching
  • 15.
    CDH may bediscovered prenataly on CDH may be discovered prenataly on routine ultrasoundas early as 15 routine ultrasoundas early as 15th th week of week of gestation gestation -herniation of abdominal viscera into -herniation of abdominal viscera into chest chest -change in liver position -change in liver position -mediastinal shift -mediastinal shift -Lung to heart ratio may be used to -Lung to heart ratio may be used to predict hiatus hernia predict hiatus hernia
  • 16.
    Clinical Finding inneonates/ Clinical Finding in neonates/ infants infants  Respiratory distress (caused by Respiratory distress (caused by hypoplastic ipsilateral lung, pulmonary hypoplastic ipsilateral lung, pulmonary hypertension and mediastinal shift hypertension and mediastinal shift compromising air exchange in opposite compromising air exchange in opposite lung) lung)  Absence of breath sounds Absence of breath sounds  Bowel sound in chest Bowel sound in chest  Scaphoid abdomen Scaphoid abdomen
  • 17.
    After birth After birth CXR CXR  BARIUM SWALLOW BARIUM SWALLOW
  • 20.
    TREATMENT TREATMENT  Earlier thetreatment of Diaphragmatic Earlier the treatment of Diaphragmatic Hernia was considered a surgical Hernia was considered a surgical emergency emergency  It is now accepted that Pulmonary It is now accepted that Pulmonary Hypertension with right to left shunt and Hypertension with right to left shunt and degree of Pulmonary hypoplasia are leading degree of Pulmonary hypoplasia are leading causes of cardiopulmonary insufficiency causes of cardiopulmonary insufficiency  The emphasis is on controlled ventilation The emphasis is on controlled ventilation and avoiding over-inflation of un-involved and avoiding over-inflation of un-involved Lung Lung
  • 21.
     Avoiding pulmonaryhypertension via Avoiding pulmonary hypertension via Hypoxia, Nitric oxide may be helpful Hypoxia, Nitric oxide may be helpful  Correction of acidosis Correction of acidosis  Excess administration of IV fluids Excess administration of IV fluids should be avoided lest it compounds should be avoided lest it compounds cardiac failure cardiac failure  Infants who remain severely hypoxic Infants who remain severely hypoxic may need ECMO. Gradually the lung may need ECMO. Gradually the lung function improves over 7-10 days function improves over 7-10 days TREATMENT TREATMENT
  • 22.
    treatment treatment  Nasogastric tube Nasogastrictube  Fluid and electrolyte Fluid and electrolyte  PEEP or ECMO PEEP or ECMO  surgery surgery
  • 23.
    OPERATION OPERATION  Infants whoare not on ECMO should be Infants who are not on ECMO should be operated as soon as hemodynamic operated as soon as hemodynamic status has been optimized status has been optimized  Others have to wait till pulmonary Others have to wait till pulmonary function has improved function has improved  Abdominal or thoracic approach may be Abdominal or thoracic approach may be used (Right side:thoracotomy used (Right side:thoracotomy Left side:laparotomy) Left side:laparotomy)
  • 24.
    COMPLICATIONS COMPLICATIONS  Bleeding fromliver/spleen while Bleeding from liver/spleen while reducing into abdomen reducing into abdomen  Hemothorax Hemothorax  Problems due to Hypoplastic lung or Problems due to Hypoplastic lung or pulmonary hypertension pulmonary hypertension
  • 25.
    Mortality 30-50% in24 Mortality 30-50% in 24 hours hours
  • 26.
    Long term problemsin CDH Long term problems in CDH  Gastroesophageal reflux Gastroesophageal reflux  Chronic lung disease Chronic lung disease  Hearing loss Hearing loss  Pectus excavatum Pectus excavatum  seizure seizure
  • 27.
    MORGAGNI HERNIA MORGAGNI HERNIA Larrey hernia or retrosternal Larrey hernia or retrosternal  Much less common Much less common  2% of all diaphragmatic hernia 2% of all diaphragmatic hernia  Contained sac may contain Omentum, Contained sac may contain Omentum, Colon, Stomach, Liver or Small intestine Colon, Stomach, Liver or Small intestine  Rarely symptomatic Rarely symptomatic  May be symptomatic after 40 years May be symptomatic after 40 years
  • 28.
    HIATAL HERNIA HIATAL HERNIA Sliding Sliding  Paraesophageal Paraesophageal  Mixed Mixed  Usually associated with GER Usually associated with GER  Treatment Medical/Surgical Treatment Medical/Surgical
  • 29.
    Eventration of diaphragm Eventrationof diaphragm  Congenital(non paralysed) Congenital(non paralysed)  Acquired(paralysed) Acquired(paralysed)
  • 30.
    Trauma to diaphragm Traumato diaphragm (Acquired Diaphragmatic (Acquired Diaphragmatic Hernia) Hernia)  90% left sided 90% left sided  Early diagnosis:laparotomy Early diagnosis:laparotomy  Late diagnosis:thoracotomy Late diagnosis:thoracotomy