PATHOPHYSIOLOGY OF CYANOTIC CHD - PowerPoint PPT Presentation

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PATHOPHYSIOLOGY OF CYANOTIC CHD

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pathophysiology of cyanotic chd by j. a. al-ata cosultant & assistant professor of pediatric cardiology – PowerPoint PPT presentation

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Title: PATHOPHYSIOLOGY OF CYANOTIC CHD


1
PATHOPHYSIOLOGY OFCYANOTIC CHD
  • BY
  • J. A. AL-ATA
  • COSULTANT ASSISTANT PROFESSOR OF PEDIATRIC
    CARDIOLOGY

2
CYANOSIS
  • BLUISH discoloration of SKIN MM due to
    doxyhemoglobin.
  • Desaturated arterial blood Central cyanosis.
  • Peripheral cyanosis Normal Art. Sat.
  • Detected clinically ( sat below 85 ), pulse
    oximetry, or ABG.

3
CAUSES OF CYANOSIS
  • Central cyanosis
  • Respiratory
  • CNS
  • Muscular
  • Cardiac
  • Peripheral cyanosis
  • CHF
  • Shock
  • Acrocyanosis
  • Abnormal hemoglobin

4
Types of Cyanotic CHD
  • With pulmonary blood flow
  • D-TGA
  • Truncus arteriosus
  • TAPVD
  • DORV
  • Single ventricle no ps.
  • With pulmonary blood flow
  • TOF
  • Critical pulmonary stenosis
  • Pulmonary Atresia

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D-TGA
  • Parallel circulation not in series
  • Body----RA----RV----AO----Body
  • Lungs---LA----LV----PA----Lungs
  • Poor mixing
  • Hypoxia Acidemia
  • Hyperventilation
  • Increased pulmonary flow
  • CHF
  • Myocardial depression

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TRUNCUS ARTERIOSUS
  • Complete mixing so cyanosis is minimal
  • VSD always present
  • Identical pressures in both ventricles
  • Systemic saturation is proportional to pulmonary
    blood flow ( PBF )
  • PVR PA.s caliber determine PBF
  • CHF is a usual presentation
  • Eisenmenger syndrome may develop
  • AS AI are complicating factors

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TAPVR
  • NON-Obstructed TAPVR
  • Similar hemodynamics to a large ASD
  • Lt to Rt shunt magnitude is determined by RV
    compliance ASD size
  • Rt heart pulmonary volume overload
  • Complete mixing at RA level
  • Minimal cyanosis due to large PBF
  • Slight PA pressure elevation

16
TAPVR, CONT
  • Obstructed TAPVR
  • Pulmonary venous hypertension secondary PA RV
    hypertension
  • Less RV PA volume overload
  • Pulmonary venous oedema
  • More cyanosis respiratory distress
  • Complete mixing

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TRICUSPID ATRESIA
  • Increased RA pressure size
  • Dependant on the ASD or PFO
  • Dilated LA LV
  • Complete mixing in LV
  • With TGA PBF SAT.
  • Variable degree of cyanosis

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EBSTEIN ANOMALY
  • Variable degrees of cyanosis depending on amount
    of Rt to Lt shunt across ASD or PFO
  • Hugely dilated RA
  • Incompetent TV
  • Atrialized small poorly functional RV
  • RVOTO PS can be associations
  • SVT ( WPW ) can be associated

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TETRALOGY OF FALLOT
  • Decreased PBF Amount of RT to LT shunt
    determine degree of cyanosis
  • PBF is mainly determined by RVOTO PS
  • Pink TOF mod RVOTO balanced shunting across
    the VSD
  • Increased PBF can result from PDA or MAPCAS
  • Equal ventricular pressures

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HYPERCYANOTIC SPELL
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PULMONARY ATRESIA
  • With VSD
  • An extreme form of TOF
  • Early cyanosis when PDA closes
  • Ductal dependant
  • CHF with MAPCAS / PDA
  • Balanced form

30
PULMONARY ATRESIA CONT
  • Without VSD
  • Early marked cyanosis ( extremely decreased PBF )
  • Ductal dependant
  • RV sinusoids
  • RV decompression by TR
  • ASD or PFO mandatory

31
SUMMARY
  • Central cyanosis is the hallmark of cyanotic CHD
  • Cyanosis is a serious symptom or sign
  • Variable degrees of cyanosis occur due to
    variability in PBF, PVR, RVOTO, presence size
    of shunting site e.g. ASD and hemoglobin
    concentration
  • CHF can occur in cyanotic CHD due to increased
    PBF
  • Pulmonary AVMs Methemoglobinemia are
    non-cardiac causes of central cyanosis.

32
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