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Perinatal asphyxia.lecture.pptx
1. Neonatal sepsis
1
Introduction
â Sepsis neonatorum describes any systemic
bacterial infection documented by blood culture
in the first month of life.
â Remain an important cause of neonatal mortality
and morbidity despite the advent of antibiotics
â It was almost always fatal in preterms with VLBW
before the antibiotic era and advancement in
neonatal care
2. IntroductionâŚcont
2
â Why neonates, especially preterms are susceptible
to infections?
ďąImmature and ineffective neonatal immune
system
oAntibodies
oComplement
oNeutrophils
oSkin/mucosal barriers
oLymphocytes
ďąSocioeconomic and health care problems
exacerbates the incidence as well as the outcome
3. EPIDEMIOLOGY
3
â Incidence (during antibiotic era)
⢠Mortality
â13-63% world wide
â13-15% of neonatal deaths(USA)
âIn Ethiopia⌠33%, WHO/2006
⢠Meningitis
â0.4-2.8/1000 livebirths world wide
âMortality 13-59% worldwide
⢠Sepsis
â1-21/1000 livebirths world wide
âHigher in preterms
5. Epidemiology âŚcont
5
â Disease pattern based on postnatal age
⢠Early onsetâŚwithin 7days of life
âTime of onset: 85% within 24hrs
⢠Late onsetâŚâŚwithin 7 to 30 days of life
⢠Late late onsetâŚâŚ.30-90 days
âPreterms and VLBW who stayed in NICU
7. Etiopathogenesis
7
Pathogenesis
⢠Early onset âŚvertical transmission
âAscending intra-amniotic infection aspirated
by fetus
âTransplacental: syphilis and L.monocytogene
âColonization of birth canal and poor nursery:
GBS, E.coli
âInvasive procedures
âProlonged labor or ROM increases infection
⢠Late onset
âFrom maternal birth canal or postnatal
11. Differential Diagnosis
11
Non-specific symptomatology
â Non-bacterial infections
⢠HSV and other viruses
⢠Fungal infections
⢠TORCH infections
â Non-infectious etiologies
⢠RDS: HMD, TTN, MAS
⢠Hypothermia, Hypoglycemia, Asphyxia
⢠ICH
⢠Drug withdrawal
⢠Errors in metabolism
⢠Many other disorders
12. Laboratory Investigations
12
A) Microbiologic tests
1) Culture (Blood, Urine, CSF)
I. Blood Culture (more than one sample)
ÂťGrowth within 24-48 hrs is possible
ÂťAvoids contaminant pathogens
II. Urine Culture
ÂťCan be positive in the absence of UTI
ÂťYield is low, especially in EONS
ÂťMay be positive in the absence of
sepsis in older newborns with UTI
13. Lab investigation
⢠Low total white count and absolute
neutropenia (< 1000/mL), all suggest neonatal
bacterial infection.
⢠â˘Thrombocytopenia (low platelet count in bd)
is also a common feature
⢠Definitive diagnosis is made by positive
cultures from blood, CSF, or other body fluids.
14. Neonatal Meningitis
⢠Any newborn with bacterial sepsis is at risk for
meningitis.
⢠The presence of seizure increases the suspicion
for meningitis.
⢠The most common organisms are GBS and gram-
negative enteric bacteria.
⢠Early diagnosis and therapy is mandatory
improve short and long term outcomes
15. Clinical manifestation
⢠Suspect neonatal meningitis if a neonate with
septicaemia have s/s of:
⢠fever
⢠seizures (convulsion or twitching)
⢠Staring look
⢠Bulging anterior fontanel
⢠Abnormal high pitched cry or excessive crying
16. Lab investigations:
Dx is suggested by:
⢠a CSF protein level higher than 150 mg/dL,
⢠glucose less than 30 mg/dL,
⢠leukocytes of more than 25/micro L, and a
positive Gram stain.
⢠The diagnosis is confirmed by culture.
17. Treatment
⢠â˘Sepsis can be treated IV for 10â14 days, but
meningitis often requires 21 days.
⢠â˘i.e Gram-negative infections, in particular, are
difficult to eradicate, and may relapse.
⢠â˘The mortality rate of neonatal meningitis is
approximately 10%, with significant neurologic
morbidity present in one-third of the survivors
21. Perinatal Asphyxia (PNA)
Insult to the fetus/neonate due to hypoxia
and/or ischemia to various organs
Defined 'Perinatal asphyxia' as "a condition in the
neonate where there is the following combination:
o Severely reduce oxygen delivery and lead to
acidosis; and
o A failure of function of at least two organs
(may include lung, heart, liver, brain, kidneys
and hematological) consistent with the effects of
acute asphyxia.
23. Consider PNA in our set up if:
⢠Low 1st minute APGAR (0-6)
⢠Hypotonia and
⢠Seizure
⢠Exceptional cases
â Preterm babies
â Babies who had birth trauma
â Babies with congenital neurological anomalies
24. PNA
⢠Incidence is 1-2% in developed countries
⢠Indirectly related with GA & birth weight
⢠Responsible for around 23% of perinatal deaths
⢠Causes:
ďPlacental insufficiency (90%)- inability of the
placenta to provide O2 & remove CO2 & H from
the fetus
ď10% is due to CardioVascular, Pulmonary and
neurologic diseases
25. Risk factors:
ďśThe incidence of antenatal and intrapartal asphyxia is
higher in complicated pregnancies, particularly those
associated with diminished placental reserve:
Hypertensive disease of pregnancy or pre-
eclampsia,
Intrauterine growth restriction,
Placental abruption,
Maternal anemia,
Placental aging,
Malpresentation including vasa praevia.
28. ďśAs asphyxia progresses with severe hypoxia:
o Acidosis
o Decreased HR & BP
o Anaerobic metabolism with accumulation
of lactic acidosis
o Finally (hypotension, acidosis &
progressive hypoxia) leads to multiple
organ damage
29. Perinatal asphyxia may result in
âFetal demise,
âNeonatal death, or
âA period of recovery during which
there is organ dysfunction with
possible long-term effects,
particularly in neurological function
31. Clinical manifestations:
⢠Depression of the neonate at
birth with a low APGAR score and
acidosis,
⢠Multiple organ involvement:
⢠Hypoxic ischemic encephalopathy
(HIE),
32. Multiple organ system dysfunction:
ď§ Renal: ATN (Oligouria and elevated
creatinine)
ď§ CVS: MI,CMP, poor contractility,
hypotension (25%),
ď§ Pulmonary: respiratory distress and
persistent pulmonary hypertension of the
neonate, pul.hemorrhage (25%),
ď§ Hematologic: DIC
34. Sarnat H. & Sarnat M. staging of HIE
signs stage 1 stage 2 stage 3
Consciousness hyperalert lethargic stuporous/coma
Tone normal hypotonic flaccid
Posture normal flexion decerebration
Tendon reflexes hyperactive hyperactive absent
Moro strong weak absent
Pupils mydriasis meiosis unequal
Seizures none common decerebration
EEG normal seizure activity burst suppresion
Duration <24hrs 24hrs-14days days-weeks
Outcome good variable death, severe sequelae
35. Management of PNA
Principles
⢠Supportive care, correct metabolic
abnormalities
⢠Directed at the organ system manifestation
⢠Ventilatory support
⢠Hemodynamic stabilization
⢠Rx of seizure- aggressive
36. Prognosis of PNA
⢠Outcome ranges from complete recovery to death
⢠Depends on:
Whether metabolic & cardiopulmonary
complications (hypoxia, hypoglycemia, shock)
can be treated
Gestational Age (inverse relation) and birth
weight
Severity of HIE
37. ⢠Poor prognostic features includes:
ď§ Stage 3 HIE
ď§ Refractory seizure
⢠Death, severe cognitive & motor deficit are also
predicted from:
ďLow APGAR at 20 minutes
ďAbsence of spontaneous respiration at
20minutes
ďPersistence of abnormal neurologic signs at
2wks of age
ďSeizure occurring on the first day
ďLow voltage or suppression pattern on EEG
38. ⢠Late sequalae of PNA:
o Cerebral palsy
o Mental retardation
o Microcephally
o Motor deficit
o Hearing loss