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Respiratory distress in a
newborn baby
CASE 1
•B/O A
•1st issue
•Antenatal history -uneventful
•Term, Born by LSCS , meconium stained
liquor, CIAB ,shifted mother side
•12 hrs later developed tachypnea, so
shifted to NICU ,Required ventilation
•Spo2 rt upper limb 96, rt lower limb 89
ABG- Ph 7.12, PCO2-12, HCO3- 11
CXR-
CASE 2
Primi, Full term, 2.9 kg, Male child,
delivered by vaginal route
Cried immediately
Had respiratory distress & grunt
since birth
registered pregnancy
H/O poly-hydroamnios
No any drug history or any other
illness
On admission:
HR 168/min,RR 58/min,SPO2 92%
on room air,CRT 4sec
R/S:
shape:asymmetrical,
hyperinflsted
Air entry diminshed on Lt side,
Mediastinum shifted on Rt side
P/A: scaphoid
X-ray chest
CASE 3
33 wks,2.2 kg, male child deliverd by
LSCS(ivo dimished fetal activity and
fetal bradycardia)
Cried immediately
Had respiratory distress and grunt
On examination……
HR 165/min
RR 60/min
CRT 3sec
spo2 85% with NPO2 2 ltr/min
PP well felt
R/S: b/L air entry diminished
Grunting +nt, subcostal
retraction +nt
CVS :normal
CNS: normal
Rx:
non invasive ventilation given but
grunt & tachypnoea persist,so x ray
chest done
Inubated, required high pressure
surfactant given
Post surfactant FiO2 & pressure
requirement decreases
6 hours Post surfactant x ray
CASE 4
Primi,Full term, 2.3 kg, Male
child,delivered by vaginal route in
Govt. hospital
Cried immediately
Had respiratory distress & grunt after
30 minutes of life
Unregistered pregnancy
H/O polyhydroamnios on 3rd trimester
scan 1 month back
No any drug history or any other
illness
On Examination…….
HR 175/min
RR 60/min
CRT 3sec
spo2 90% with NPO2 2 ltr/min
PP low volume,+nt on all 4 limbs
Fine white froathy bubbles of mucus
present(+nt) in mouth
R/S:
B/L air entry diminshed
B/L crepitation +nt,grunting +nt
subcostal retraction +nt
CVS:
S1 S2 heard,no murmer
P/A:
soft,but no gastric sounds on
auscultation
X-ray
CASE 5
•antenatal history uneventful
•Born by lscs
•Did not cry after birth
•Required suction stimulation, bag and
mask ventilation for 1.30 min, then
improved.
•Shifted to nicu
•o/e : HR- 100/min, RR-80/min, grunting
present, air entry normal
•Inv – ph-7.12, pco2- 20, Pa02-130,
hco3- 10
Respiratory distress
• Cause of significant morbidity and
mortality
• Incidence 4 to 6% of live births
• Many are preventable
• Early recognition, timely referral,
appropriate treatment essential
• RR > 60/ min*
• Retractions
• Grunt
• + Cyanosis
Respiratory distress
Pathophysiology considerations
unique to the newborn
Prolonged and unattended distress
leads to hypoxemia, hypercarbia and
acidosis. This leads to pulmonary
vasoconstriction and persistence of
fetal circulation with right to left
shunting through the ductus and
foramen ovale , thereby aggravating
hypoxemia.
Causes of respiratory distress -
Medical
• Respiratory distress syndrome (RDS)
• Meconium aspiration syndrome (MAS)
• Transient tachypnoea of newborn (TTNB)
• Asphyxial lung disease
• Pneumonia- Congenital, aspiration, nosocomial
• Persistent pulmonary hypertension (PPHN)
• Cardiac: Congenital heart disease, Ductus dependant
lesions, PDA of prematurity,
• Metabolic: Acidosis, hypoglycemia, polycythemia, anemia
• Shock due to any cause
Surgical causes of respiratory
distress
• Tracheo-esophageal fistula
• Diaphragmatic hernia
• Lobar emphysema
• Pierre -Robin syndrome
• Choanal atresia
Approach to respiratory distress
History
• Onset of distress
• Gestation
• Predisposing factors- PROM, fever
• Meconium stained amniotic fluid
• Asphyxia
Approach to respiratory distress
Examination
• Severity of respiratory
distress
• Neurological status
• Blood pressure, CFT
• Hepatomegaly
• Cyanosis
• Features of sepsis
• Look for malformations
Approach to respiratory distress
Chest examination
• Air entry
• Mediastinal shift
• Adventitious sounds
• Hyperinflation
• Heart sounds
Suspect surgical cause
• Obvious malformation
• Scaphoid abdomen
• Frothing
• History of aspiration
Were there any risk factors in the antepartum
period or evidence of foetal distress prior to
delivery? (Birth asphyxia or PPHN)
Did the mother receive antenatal steroids if it
was a preterm delivery? (Antenatal steroids
decrease the incidence of HMD by 50%)
Was there a history of premature rupture of
membranes and fever? (congenital pneumonia
or sepsis)
Was there meconium stained amniotic fluid?
(MAS is a possibility)
A look at the antenatal ultrasonography (USG) for
the amount of amniotic fluid would tell us the status
of the foetal lung. (congenital anomalies of lung)
Was resuscitation required at birth? (resuscitation
trauma/PPHN/ acidosis)
Did the distress appear immediately or a few hours
after birth? (HMD appears earlier than pneumonia)
Was it related to feeding or frothing at the mouth?
(tracheo-esophageal fistula or aspiration)
Does the distress decrease with crying? (choanal
atresia).
For babies presenting later with distress we
have to ask a few other questions :-
Is the distress associated with feed refusal
and lethargy? (sepsis, pneumonia)
Did the distress appear slowly after starting
feeds? (IEM).
Is there a family history of early neonatal
deaths? (CHD, IEM).
Clinical Examination
A preterm baby weighing <1500 gms with retractions and
grunt is likely to have HMD.
A term baby born through meconium stained amniotic fluid
with an increase in the anterior- posterior diameter of the
chest (full chest) is likely to be suffering from MAS.
A depressed baby with poor circulation is likely to have
neonatal sepsis with or without congenital pneumonia.
A near term baby with no risk factors and mild distress may
have TTNB
An asphyxiated baby may have PPHN.
A growth retarded baby with a plethoric look may have
polycythaemia.
A baby with respiratory distress should be checked for
an air leak by placing a cold light source over the chest
wall in a darkened room.
A baby presenting with tachypnoea and a cardiac
murmur - congenital heart disease.
Inability to pass an 5F catheter through the nostril --
choanal atresia.
Congenital Pneumonia
Assessment of respiratory
distress
Score
*
0 1 2
1. Resp. rate
2. Central
<60
None
60-80
None with
>80
Needs
cyanosis 40% FiO2 >40% FiO2
3. Retractions None Mild Severe
4. Grunting None Minimal Obvious
5. Air entry Good Decreased Very poor
* Score > 6 indicates severe
distress
Silverman Andersons scoring
Score > 6 indicates severe distress
Investigations
• Gastric aspirate
• Polymorph count
• Sepsis screen
• Chest X-ray
• Blood gas analysis
Pulse oximetry
• Effective non invasive monitoring of
oxygen therapy
• Ideally must for all sick neonates and
those requiring oxygen therapy
• Maintain SaO2 between 90 – 95 %
Shake test
• Take a test tube
• Mix 0.5 ml gastric aspirate +
0.5 ml absolute alcohol
• Shake for 15 seconds
• Allow to stand 15 minutes for
interpretation of result
Arterial blood gas (ABG) analysis:
Blood gas is essential because with clinical
assessment and pulse oximetry alone, one
would not be able to assess PaO2, PCO2
and pH.
Normal & abnormal values:
PaO2: Pre-ductal PaO2 50–70 mmHg with an
O2 saturation of 87-93%. A PaO2 up to 80
mmHg is acceptable in term infants
PaO2:
Hypoxemia: PaO2<50 mmHg
Low normal oxygenation: PaO2 - 50-
60mmHg
Hyperoxemia: >80 mmHg in preterm
and >90 in term.
Hyperoxia is associated with adverse
effects like ROP and BPD due to
increase in the reactive oxygen
species (ROS).
PaCO2:
Normal PaCO2 is 35-45 mmHg
Acceptable upper limit: 45-50mmHg,
There is increasing evidence that the strategy of
permissive hypercapnia reduces the duration of
ventilation and decreases the severity of
bronchopulmonary dysplasia (BPD) .
Hypocarbia: <35 mmHg.
Hypocarbia with PaCO2<30 mmHg increases the
risk of periventricular leucomalacia (PVL) in
preterm neonates
Assessment of gas exchange
1)Alveolar-arterial Oxygen
gradient (A-aDO2)
2)a/A ratio
3)Oxygenation Index (OI)
A-aDO2 (alveolar arterial oxygen diffusion
gradient):
This is to be calculated as shown below.
A-a DO2 =PAO2 – PaO2
= [(PB-PW) × FiO2 – PaCO2/RQ] – PaO2
= [(760-47) × FiO2 – PaCO2/.8] – PaO2
Normally it ranges between 5-15, if breathing room
air.
A-aDO2 is considered to be abnormal if more than
40.
2) a /A ratio:
Ratio of PaO2 to PAO2.
It is considered to be a better indicator of gas
exchange as the ratio is usually not affected by
changes in FiO2
Interpretation:
a) Greater than 0.8: Normal
b) Less than 0.6: indicates need for O2 therapy
c) Less than 0.15: severe hypoxemia
3)Oxygenation Index (OI):
Recommended in babies
who are mechanically ventilated as this index
includes mean airway pressure (MAP).
OI = (MAP × FiO2 ×100) / PaO2
Interpretation:
a) OI 25 – 40: severe respiratory failure;
mortality risk is 50 – 60%
b) OI > 40: Mortality risk is >80%
A comparison of indices of respiratory failure in ventilated
preterm infants
N V Subhedar, A T Tan, E M Sweeney, N J Shaw
There was no evidence of a Significant
difference between the performance of the a/A
ratio, A-aDO2, and OI in predicting adverse
respiratory outcomes.
use of the OI is recommended because of its
ease of calculation.
Respiratory distress -
Management
• Monitoring
• Supportive
- IV fluid
- Maintain vital signs
- Oxygen therapy
- Respiratory support
• Specific
Oxygen therapy*
Indications
• All babies with distress
• Cyanosis
• Pulse oximetry SaO2 <90%
Method
• Flow rate 2-5 L/ min
• Humidified oxygen by hood or nasal prongs
* Cautious administration in pre-term
[*Failure of CPAP (): Even on a CPAP of
7cmH2O and 70% FiO2if the neonate has
excessive work of breathing (or)
PCO2>60mmHg with pH <7.2 (or)
recurrent apnea or hypoxemia (PaO2 <50
mmHg), this should be considered as
failure of CPAP].
Respiratory distress syndrome
(RDS)
• Pre-term baby
• Early onset within 6 hours
• Supportive evidence: Negative shake test
• Radiological evidence
X-ray - RDS
Pathogenesis of RDS
• Decreased or abnormal surfactant
• Alveolar collapse
• Impaired gas exchange
• Respiratory failure
RDS - Predisposing factors
• Prematurity
• Cesarean born
• Asphyxia
• Maternal diabetes
RDS - Protective factors
• PROM
• IUGR
• Steroids
Antenatal corticosteroid
- Simple therapy that saves neonatal lives
• Preterm labor 24-34 weeks of gestation
irrespective of PROM, hypertension and
diabetes
• Dose:
Inj Betamethasone 12mg IM every 24 hrs X
2 doses; or Inj Dexamethasone 6 mg IM
every 12 hrs X 4 doses
• Multiple doses not beneficial
Surfactant therapy - Issues
• Should be used only if facilities for
ventilation available
• Cost
• Prophylactic Vs rescue
Surfactant therapy - Issues
Prophylactic therapy
Extremely preterm <28 wks
<1000 gm
Not routine in India
Rescue therapy
Any neonate diagnosed to have RDS
Dose 100mg/kg phospholipid Intra tracheal
Meconium aspiration syndrome
(MAS)
• Meconium staining
- Antepartum, intrapartum
• Thin
- Chemical pneumonitis
• Thick
- Atelectasis, airway blockage,
air leak syndrome
Meconium aspiration syndrome
• Post term/SFD
• Meconium staining – cord, nails, skin
• Onset within 4 to 6 hours
• Hyperinflated chest
X-ray - MAS
MAS - Prevention
• Oropharyngeal suction before delivery of
shoulder for all neonates born through
MSAF
• Endotracheal suction for non vigorous*
neonates born through MSAF
*Avoid bag & mask ventilation till trachea
is cleared
Transient tachypnoea of newborn
(TTNB)
• Cesarean born, term baby
• Delayed clearance of lung fluid
• Diagnosis by exclusion
• Management: supportive
• Prognosis - good
X-ray- TTNB
Congenital pneumonia
Predisposing factors
PROM >24 hours, foul smelling liquor,
Peripartal fever, unclean or multiple
per vaginal
Treatment
Thermoneutral environment, NPO, IV
fluids, Oxygen, antibiotics-
(Amp+Gentamicin)
X-ray – Congenital pneumonia
Nosocomial pneumonia
Risk
Factor
: Ventilated neonates
: Preterm neonates
Prevention : Handwash
: Use of disposables
: Infection control measures
Antibiotic
s
: Usually require
higher antibiotics
Respiratory distress in a neonate with
asphyxia
• Myocardial dysfunction
• Cerebral edema
• Asphyxial lung injury
• Metabolic acidosis
• Persistent pulmonary hypertension
Pneumothorax
Etiology
Spontaneous, MAS, Positive pressure
ventilation (PPV)
Clinical features
Sudden distress, indistinct heart sounds
Management
Needle aspiration, chest tube
X-ray - Pneumothorax
Persistent pulmonary
hypertension (PPHN)
Causes
• Primary
• Secondary: MAS, asphyxia, sepsis
Management
• Severe respiratory distress needing
ventilatory support, pulmonary
vasodilators
• Poor prognosis

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Approach to Respiratory distress in neonates ppt

  • 1. Respiratory distress in a newborn baby
  • 2. CASE 1 •B/O A •1st issue •Antenatal history -uneventful •Term, Born by LSCS , meconium stained liquor, CIAB ,shifted mother side •12 hrs later developed tachypnea, so shifted to NICU ,Required ventilation •Spo2 rt upper limb 96, rt lower limb 89
  • 3. ABG- Ph 7.12, PCO2-12, HCO3- 11 CXR-
  • 4.
  • 5. CASE 2 Primi, Full term, 2.9 kg, Male child, delivered by vaginal route Cried immediately Had respiratory distress & grunt since birth registered pregnancy H/O poly-hydroamnios No any drug history or any other illness
  • 6. On admission: HR 168/min,RR 58/min,SPO2 92% on room air,CRT 4sec R/S: shape:asymmetrical, hyperinflsted Air entry diminshed on Lt side, Mediastinum shifted on Rt side P/A: scaphoid
  • 8. CASE 3 33 wks,2.2 kg, male child deliverd by LSCS(ivo dimished fetal activity and fetal bradycardia) Cried immediately Had respiratory distress and grunt
  • 9. On examination…… HR 165/min RR 60/min CRT 3sec spo2 85% with NPO2 2 ltr/min PP well felt R/S: b/L air entry diminished Grunting +nt, subcostal retraction +nt CVS :normal CNS: normal
  • 10. Rx: non invasive ventilation given but grunt & tachypnoea persist,so x ray chest done
  • 11.
  • 12. Inubated, required high pressure surfactant given Post surfactant FiO2 & pressure requirement decreases
  • 13. 6 hours Post surfactant x ray
  • 14. CASE 4 Primi,Full term, 2.3 kg, Male child,delivered by vaginal route in Govt. hospital Cried immediately Had respiratory distress & grunt after 30 minutes of life
  • 15. Unregistered pregnancy H/O polyhydroamnios on 3rd trimester scan 1 month back No any drug history or any other illness
  • 16. On Examination……. HR 175/min RR 60/min CRT 3sec spo2 90% with NPO2 2 ltr/min PP low volume,+nt on all 4 limbs Fine white froathy bubbles of mucus present(+nt) in mouth
  • 17. R/S: B/L air entry diminshed B/L crepitation +nt,grunting +nt subcostal retraction +nt CVS: S1 S2 heard,no murmer P/A: soft,but no gastric sounds on auscultation
  • 18. X-ray
  • 19. CASE 5 •antenatal history uneventful •Born by lscs •Did not cry after birth •Required suction stimulation, bag and mask ventilation for 1.30 min, then improved. •Shifted to nicu •o/e : HR- 100/min, RR-80/min, grunting present, air entry normal •Inv – ph-7.12, pco2- 20, Pa02-130, hco3- 10
  • 20. Respiratory distress • Cause of significant morbidity and mortality • Incidence 4 to 6% of live births • Many are preventable • Early recognition, timely referral, appropriate treatment essential
  • 21. • RR > 60/ min* • Retractions • Grunt • + Cyanosis Respiratory distress
  • 22. Pathophysiology considerations unique to the newborn Prolonged and unattended distress leads to hypoxemia, hypercarbia and acidosis. This leads to pulmonary vasoconstriction and persistence of fetal circulation with right to left shunting through the ductus and foramen ovale , thereby aggravating hypoxemia.
  • 23. Causes of respiratory distress - Medical • Respiratory distress syndrome (RDS) • Meconium aspiration syndrome (MAS) • Transient tachypnoea of newborn (TTNB) • Asphyxial lung disease • Pneumonia- Congenital, aspiration, nosocomial • Persistent pulmonary hypertension (PPHN) • Cardiac: Congenital heart disease, Ductus dependant lesions, PDA of prematurity, • Metabolic: Acidosis, hypoglycemia, polycythemia, anemia • Shock due to any cause
  • 24. Surgical causes of respiratory distress • Tracheo-esophageal fistula • Diaphragmatic hernia • Lobar emphysema • Pierre -Robin syndrome • Choanal atresia
  • 25. Approach to respiratory distress History • Onset of distress • Gestation • Predisposing factors- PROM, fever • Meconium stained amniotic fluid • Asphyxia
  • 26. Approach to respiratory distress Examination • Severity of respiratory distress • Neurological status • Blood pressure, CFT • Hepatomegaly • Cyanosis • Features of sepsis • Look for malformations
  • 27. Approach to respiratory distress Chest examination • Air entry • Mediastinal shift • Adventitious sounds • Hyperinflation • Heart sounds
  • 28. Suspect surgical cause • Obvious malformation • Scaphoid abdomen • Frothing • History of aspiration
  • 29. Were there any risk factors in the antepartum period or evidence of foetal distress prior to delivery? (Birth asphyxia or PPHN) Did the mother receive antenatal steroids if it was a preterm delivery? (Antenatal steroids decrease the incidence of HMD by 50%) Was there a history of premature rupture of membranes and fever? (congenital pneumonia or sepsis) Was there meconium stained amniotic fluid? (MAS is a possibility)
  • 30. A look at the antenatal ultrasonography (USG) for the amount of amniotic fluid would tell us the status of the foetal lung. (congenital anomalies of lung) Was resuscitation required at birth? (resuscitation trauma/PPHN/ acidosis) Did the distress appear immediately or a few hours after birth? (HMD appears earlier than pneumonia) Was it related to feeding or frothing at the mouth? (tracheo-esophageal fistula or aspiration) Does the distress decrease with crying? (choanal atresia).
  • 31. For babies presenting later with distress we have to ask a few other questions :- Is the distress associated with feed refusal and lethargy? (sepsis, pneumonia) Did the distress appear slowly after starting feeds? (IEM). Is there a family history of early neonatal deaths? (CHD, IEM).
  • 32. Clinical Examination A preterm baby weighing <1500 gms with retractions and grunt is likely to have HMD. A term baby born through meconium stained amniotic fluid with an increase in the anterior- posterior diameter of the chest (full chest) is likely to be suffering from MAS. A depressed baby with poor circulation is likely to have neonatal sepsis with or without congenital pneumonia. A near term baby with no risk factors and mild distress may have TTNB
  • 33. An asphyxiated baby may have PPHN. A growth retarded baby with a plethoric look may have polycythaemia. A baby with respiratory distress should be checked for an air leak by placing a cold light source over the chest wall in a darkened room. A baby presenting with tachypnoea and a cardiac murmur - congenital heart disease. Inability to pass an 5F catheter through the nostril -- choanal atresia.
  • 35.
  • 36. Assessment of respiratory distress Score * 0 1 2 1. Resp. rate 2. Central <60 None 60-80 None with >80 Needs cyanosis 40% FiO2 >40% FiO2 3. Retractions None Mild Severe 4. Grunting None Minimal Obvious 5. Air entry Good Decreased Very poor * Score > 6 indicates severe distress
  • 37. Silverman Andersons scoring Score > 6 indicates severe distress
  • 38. Investigations • Gastric aspirate • Polymorph count • Sepsis screen • Chest X-ray • Blood gas analysis
  • 39. Pulse oximetry • Effective non invasive monitoring of oxygen therapy • Ideally must for all sick neonates and those requiring oxygen therapy • Maintain SaO2 between 90 – 95 %
  • 40. Shake test • Take a test tube • Mix 0.5 ml gastric aspirate + 0.5 ml absolute alcohol • Shake for 15 seconds • Allow to stand 15 minutes for interpretation of result
  • 41. Arterial blood gas (ABG) analysis: Blood gas is essential because with clinical assessment and pulse oximetry alone, one would not be able to assess PaO2, PCO2 and pH. Normal & abnormal values: PaO2: Pre-ductal PaO2 50–70 mmHg with an O2 saturation of 87-93%. A PaO2 up to 80 mmHg is acceptable in term infants
  • 42. PaO2: Hypoxemia: PaO2<50 mmHg Low normal oxygenation: PaO2 - 50- 60mmHg Hyperoxemia: >80 mmHg in preterm and >90 in term. Hyperoxia is associated with adverse effects like ROP and BPD due to increase in the reactive oxygen species (ROS).
  • 43. PaCO2: Normal PaCO2 is 35-45 mmHg Acceptable upper limit: 45-50mmHg, There is increasing evidence that the strategy of permissive hypercapnia reduces the duration of ventilation and decreases the severity of bronchopulmonary dysplasia (BPD) . Hypocarbia: <35 mmHg. Hypocarbia with PaCO2<30 mmHg increases the risk of periventricular leucomalacia (PVL) in preterm neonates
  • 44. Assessment of gas exchange 1)Alveolar-arterial Oxygen gradient (A-aDO2) 2)a/A ratio 3)Oxygenation Index (OI)
  • 45. A-aDO2 (alveolar arterial oxygen diffusion gradient): This is to be calculated as shown below. A-a DO2 =PAO2 – PaO2 = [(PB-PW) × FiO2 – PaCO2/RQ] – PaO2 = [(760-47) × FiO2 – PaCO2/.8] – PaO2 Normally it ranges between 5-15, if breathing room air. A-aDO2 is considered to be abnormal if more than 40.
  • 46. 2) a /A ratio: Ratio of PaO2 to PAO2. It is considered to be a better indicator of gas exchange as the ratio is usually not affected by changes in FiO2 Interpretation: a) Greater than 0.8: Normal b) Less than 0.6: indicates need for O2 therapy c) Less than 0.15: severe hypoxemia
  • 47. 3)Oxygenation Index (OI): Recommended in babies who are mechanically ventilated as this index includes mean airway pressure (MAP). OI = (MAP × FiO2 ×100) / PaO2 Interpretation: a) OI 25 – 40: severe respiratory failure; mortality risk is 50 – 60% b) OI > 40: Mortality risk is >80%
  • 48. A comparison of indices of respiratory failure in ventilated preterm infants N V Subhedar, A T Tan, E M Sweeney, N J Shaw There was no evidence of a Significant difference between the performance of the a/A ratio, A-aDO2, and OI in predicting adverse respiratory outcomes. use of the OI is recommended because of its ease of calculation.
  • 49. Respiratory distress - Management • Monitoring • Supportive - IV fluid - Maintain vital signs - Oxygen therapy - Respiratory support • Specific
  • 50. Oxygen therapy* Indications • All babies with distress • Cyanosis • Pulse oximetry SaO2 <90% Method • Flow rate 2-5 L/ min • Humidified oxygen by hood or nasal prongs * Cautious administration in pre-term
  • 51.
  • 52.
  • 53. [*Failure of CPAP (): Even on a CPAP of 7cmH2O and 70% FiO2if the neonate has excessive work of breathing (or) PCO2>60mmHg with pH <7.2 (or) recurrent apnea or hypoxemia (PaO2 <50 mmHg), this should be considered as failure of CPAP].
  • 54. Respiratory distress syndrome (RDS) • Pre-term baby • Early onset within 6 hours • Supportive evidence: Negative shake test • Radiological evidence
  • 56. Pathogenesis of RDS • Decreased or abnormal surfactant • Alveolar collapse • Impaired gas exchange • Respiratory failure
  • 57. RDS - Predisposing factors • Prematurity • Cesarean born • Asphyxia • Maternal diabetes RDS - Protective factors • PROM • IUGR • Steroids
  • 58. Antenatal corticosteroid - Simple therapy that saves neonatal lives • Preterm labor 24-34 weeks of gestation irrespective of PROM, hypertension and diabetes • Dose: Inj Betamethasone 12mg IM every 24 hrs X 2 doses; or Inj Dexamethasone 6 mg IM every 12 hrs X 4 doses • Multiple doses not beneficial
  • 59. Surfactant therapy - Issues • Should be used only if facilities for ventilation available • Cost • Prophylactic Vs rescue
  • 60. Surfactant therapy - Issues Prophylactic therapy Extremely preterm <28 wks <1000 gm Not routine in India Rescue therapy Any neonate diagnosed to have RDS Dose 100mg/kg phospholipid Intra tracheal
  • 61. Meconium aspiration syndrome (MAS) • Meconium staining - Antepartum, intrapartum • Thin - Chemical pneumonitis • Thick - Atelectasis, airway blockage, air leak syndrome
  • 62. Meconium aspiration syndrome • Post term/SFD • Meconium staining – cord, nails, skin • Onset within 4 to 6 hours • Hyperinflated chest
  • 64. MAS - Prevention • Oropharyngeal suction before delivery of shoulder for all neonates born through MSAF • Endotracheal suction for non vigorous* neonates born through MSAF *Avoid bag & mask ventilation till trachea is cleared
  • 65. Transient tachypnoea of newborn (TTNB) • Cesarean born, term baby • Delayed clearance of lung fluid • Diagnosis by exclusion • Management: supportive • Prognosis - good
  • 67. Congenital pneumonia Predisposing factors PROM >24 hours, foul smelling liquor, Peripartal fever, unclean or multiple per vaginal Treatment Thermoneutral environment, NPO, IV fluids, Oxygen, antibiotics- (Amp+Gentamicin)
  • 68. X-ray – Congenital pneumonia
  • 69. Nosocomial pneumonia Risk Factor : Ventilated neonates : Preterm neonates Prevention : Handwash : Use of disposables : Infection control measures Antibiotic s : Usually require higher antibiotics
  • 70. Respiratory distress in a neonate with asphyxia • Myocardial dysfunction • Cerebral edema • Asphyxial lung injury • Metabolic acidosis • Persistent pulmonary hypertension
  • 71. Pneumothorax Etiology Spontaneous, MAS, Positive pressure ventilation (PPV) Clinical features Sudden distress, indistinct heart sounds Management Needle aspiration, chest tube
  • 73. Persistent pulmonary hypertension (PPHN) Causes • Primary • Secondary: MAS, asphyxia, sepsis Management • Severe respiratory distress needing ventilatory support, pulmonary vasodilators • Poor prognosis

Editor's Notes

  1. Assessment of gas exchange Though the blood gas parameters indicate oxygenation and ventilation at a single point of time, these parameters alone would not be sufficient to evaluate gas exchange. Interpretation of PaO2 without FiO2 is misleading. Hence the gas exchange should be assessed using various parameters like
  2. It is measure of oxigenation. Normal -2.5+.21*age in year
  3. Determines severity of hypoxia and guide to timing of intervention