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Reproductive System
Perinatology Division, Child Heath Department,
Medical Faculty of Hasanuddin University
Infection in neonate
 According to timing of transmission:
 Congenital Infection
 Neonatal infection
 According to severity:
 Mild infection
 Severe infection  Neonatal Sepsis
Timing of
transmission
NEONATAL INFECTIONCONGENITAL INFECTION
Route of
infection
Time of
presentation Month or years
later
First few weeks of
life:
-Early onset : <72 h
-Late onset : > 72 h
At birth or
month/year later
Transplacental / birth canal /
breastmilk
Transplacental
Shortly before or at delivery or
post natally
In- utero
Viral Others
CMV
Rubella
Parvovirus
VZV
Toxoplasmosis
Syphilis
Malaria
TB
Bacterial Viral Fungal
- Grouo B
streptococcus
- Gram (-) organism
- Listeria
monocytogenes
- Coagulase negative
Staph. Aureus
- Chlamidia
- Gonococcus
HSV
VZV
Enterovir
us
HIV
Hepatitis B
Hepatitis C
HPV
HTLV-1
Congenital
Infection
 May precipitate abortion, stillbirth or preterm delivery
 Head :
 Intracerebral calcification
 Hydrocephalus
 Microcephalus
 Eye:
 Cataracts
 Microphthalmia
 Retinitis
 Ear : Deafness
 Heart defect: Cardiomegaly, PDA
 Pneumonitis
 Splenomegaly
 Hepatomegaly
 Jaundice
 Anemia, Neutropenia,
Thrombocytopenia
 Bone abnormalities
 Rash
 IUGR
Clinical Features
ANTENATAL POSTNATAL
Maternal
-History (rash, contact)
-Screening serology-seroconversion (IgG, IgM, IgA)
-Culture/PCR of lession e.g.cervical herpes, blood, urine
Fetal
-Ultrasound scanning for anomalies
-Amniocentesis for
serology/culture/PCR
Placenta
-Histologi/microscopic
-Culture/PCR
Infant
- Culture/PCR: blood, urine, CSF, stool,
nasopharyngeal aspirate, skin lesion
Diagnosis
Neonatal Infection
Classification:
Severe Infection  Sepsis
 Early onset Sepsis (<72 hours)
 Late Onset Sepsis (>72 hours)
Mild infection: Skin, eye, umbilical, mouth, etc
Timing of
transmission
NEONATAL INFECTION
Route of
infection
Time of
presentation
Month or years
later
Nosocomial
Birth canal
Transplacental
Chorioamnionitis
Birth canal
Birth canal
Nosocomial
Breastmilk
Early onset sepsis
(<72 hours)
Shortly before or at delivery or post natally
HIV
Hepatitis B
Hepatitis C
HPV
HTLV-1
Late onset sepsis
(>72 hours)
Bacterial
- Grouo B streptococcus
- Gram (-) organism
-Listeria monocytogenes
-Staphylococcus Aureus
TERM PRETERM
- Grouo B
streptococcus
-Gram (-) organisms
-Coagulase negative
Staphylococcus
(CONS)
-Gram (-) organisms
-Group B
streptococcus
-Staphylococcus
Aureus
-Enterococcus
-Fungal
 Infections 32%
 Asphyxia 29%
 Complications of prematurity 24%
 Congenital anomalies 10%
 Other 5%
Case fatality due to neonatal sepsis is 12 to 68% in
developing countries
Neonatal Mortality
Neonatal sepsis- morbidity
 Brain damage due to
meningitis, septic shock, or
hypoxemia
 Other organ damage - lung,
liver, limbs, joints
Early Onset Sepsis - risk factors
 Maternal chorioamnionitis
 Prolonged rupture of membranes >18 h
 Foul smelling amniotic fluid
 Handling by untrained midwife
 Maternal urinary tract infection
 Premature labor
Chorioamnionitis
Maternal fever during labor  38ºC
± uterine tenderness
± leucocytosis
± fetal tachycardia
High risk of neonatal sepsis
Late Onset Sepsis -
risk factors
 Prematurity/ LBW
 In hospital
 Invasive procedures- ventilator, IV lines, central
lines, urine catheter, chest tube
 Contact with infectious disease - doctors, nurses,
babies with infections,
 Not fed maternal breast milk
 POOR HYGIENE in NICU
Bacterial Pathogens Responsible for Sepsis in
Developing Countries
 Early onset sepsis
 Gram negative bacilli
 E.coli
 Klebsiella
 Enterococcus
 Group B streptococcus
 Late onset sepsis
 Gram negative bacilli
 Pseudomonas
 Klebsiella
 Staph aureus
 Coagulase negative
staphylococci
Diagnosis of Neonatal Sepsis
 Clinical signs and symptoms
 Laboratory tests
 culture of bacterial pathogen
 other laboratory indicators
 Radiologic
Clinical signs and symptoms
Clinical Signs: early signs non- specific, may be subtle
 Respiratory distress- 90%
 Apnea
 Temperature instability-  temp more common
 Decreased activity
 Irritability
 Poor feeding
 Abdominal distension
 Hypotension, shock, purpura, seizures- late signs
Laboratory Tests
 Cultures to identify bacterial pathogen
 blood, CSF, urine, other
 Hematological tests
 WBC count (normal 5.000 – 25.000/uL)
 Platelet count (Trombocytopenia  < 100.000/mm3)
 Erythrocyte Sedimentation Rate (ESR)
 Other tests
 C- reactive protein
Lumbar Puncture
 Possibility of meningitis 1-10%
 Babies with meningitis may not have specific symptoms
 15% of babies with meningitis will have negative blood
cultures
First line therapy
 Ampicillin 50 mg/ kg
 every 12 hours in 1st week of life
 every 8 hours from 2- 4 weeks
PLUS
 Gentamicin once daily.
 > 35 weeks gestation: 4 mg / kg every 24 hours
 30 - 34 weeks gestation:
 0 - 7 days: 4.5 mg/kg every 36 hours
 > 8 days: 4 mg/kg every 24 hours
Supportive Care
 Temperature support
 GI support - vomiting, ileus
 Cardiorespiratory support
 hypoxia, apnea, ARDS, shock
 Hematological support: anemia, thrombocytopenia, DIC
 Neurological support- seizures
Prevention of Hospitalized acquired Infection
(Nosocomial Infection)
 Hand washing
 Early feeding
 Maternal breast milk
 Decrease use of broad spectrum antibiotics
 Decreased use of invasive procedures
 Proper sterilization procedures
21
22
 At first  vesicle
 Purulent encounter hyperemic area
 Multiple  severe systemic infection
R/ :
Isolation + aseptic treatment
A.B : Cloxacillin 50 mg/kgBW
Incise the bulla
A.B zalp
R/ topical
23
 Infection with Neisseria gonorrheae ( a gram-negative
diplococcus)  a reproductive tract infection
 transmission to the fetus/ neonate in pregnancy
Clinical presentation :
 Hyperemic
 Palpebra Edema
 Purulent secret
 Unilateral/ bilateral
  cornea  Blind
24
D/ : Gram’s stain of exudate  diplococcus  gram (-)
R/ :
Isolation
Eye  Topical A.B.
Systemic A.B.
25
E/ : Staphylococcus aureus
Hyperemic, edema, exudate
Severe  lig. falciforme  multiple abscess
Chronic  granulom
R/ :
 Topical : A.B
 Granuloma : nitras argenti 3%
UMBILICAL INFECTION
26
Thrush patches in the baby’s mouth, lips, tongue
DD/ remain milk  easy to remove
E/ fungus : Candida albicans
If : - immunocompromize
- Using A.B. for long periode
- Using corticosteroid for long periode
diarrhea +
Parenteral infection/ sepsis
Overgrowth

Moniliasis
Oral Thrush
27
D/ : sediaan hapus  mycellium + spora
R/ :
 Gentian violet 0 – 5 – 1 %
 Borax glicerin
 Nistatin solution 3 x 100.000 U/day
 Severe : amphotericin B/ Fluconazol
THANK YOU

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Infection in neonate

  • 1. Reproductive System Perinatology Division, Child Heath Department, Medical Faculty of Hasanuddin University
  • 2. Infection in neonate  According to timing of transmission:  Congenital Infection  Neonatal infection  According to severity:  Mild infection  Severe infection  Neonatal Sepsis
  • 3. Timing of transmission NEONATAL INFECTIONCONGENITAL INFECTION Route of infection Time of presentation Month or years later First few weeks of life: -Early onset : <72 h -Late onset : > 72 h At birth or month/year later Transplacental / birth canal / breastmilk Transplacental Shortly before or at delivery or post natally In- utero Viral Others CMV Rubella Parvovirus VZV Toxoplasmosis Syphilis Malaria TB Bacterial Viral Fungal - Grouo B streptococcus - Gram (-) organism - Listeria monocytogenes - Coagulase negative Staph. Aureus - Chlamidia - Gonococcus HSV VZV Enterovir us HIV Hepatitis B Hepatitis C HPV HTLV-1
  • 4. Congenital Infection  May precipitate abortion, stillbirth or preterm delivery  Head :  Intracerebral calcification  Hydrocephalus  Microcephalus  Eye:  Cataracts  Microphthalmia  Retinitis  Ear : Deafness  Heart defect: Cardiomegaly, PDA  Pneumonitis  Splenomegaly  Hepatomegaly  Jaundice  Anemia, Neutropenia, Thrombocytopenia  Bone abnormalities  Rash  IUGR Clinical Features
  • 5. ANTENATAL POSTNATAL Maternal -History (rash, contact) -Screening serology-seroconversion (IgG, IgM, IgA) -Culture/PCR of lession e.g.cervical herpes, blood, urine Fetal -Ultrasound scanning for anomalies -Amniocentesis for serology/culture/PCR Placenta -Histologi/microscopic -Culture/PCR Infant - Culture/PCR: blood, urine, CSF, stool, nasopharyngeal aspirate, skin lesion Diagnosis
  • 6. Neonatal Infection Classification: Severe Infection  Sepsis  Early onset Sepsis (<72 hours)  Late Onset Sepsis (>72 hours) Mild infection: Skin, eye, umbilical, mouth, etc
  • 7. Timing of transmission NEONATAL INFECTION Route of infection Time of presentation Month or years later Nosocomial Birth canal Transplacental Chorioamnionitis Birth canal Birth canal Nosocomial Breastmilk Early onset sepsis (<72 hours) Shortly before or at delivery or post natally HIV Hepatitis B Hepatitis C HPV HTLV-1 Late onset sepsis (>72 hours) Bacterial - Grouo B streptococcus - Gram (-) organism -Listeria monocytogenes -Staphylococcus Aureus TERM PRETERM - Grouo B streptococcus -Gram (-) organisms -Coagulase negative Staphylococcus (CONS) -Gram (-) organisms -Group B streptococcus -Staphylococcus Aureus -Enterococcus -Fungal
  • 8.  Infections 32%  Asphyxia 29%  Complications of prematurity 24%  Congenital anomalies 10%  Other 5% Case fatality due to neonatal sepsis is 12 to 68% in developing countries Neonatal Mortality
  • 9. Neonatal sepsis- morbidity  Brain damage due to meningitis, septic shock, or hypoxemia  Other organ damage - lung, liver, limbs, joints
  • 10. Early Onset Sepsis - risk factors  Maternal chorioamnionitis  Prolonged rupture of membranes >18 h  Foul smelling amniotic fluid  Handling by untrained midwife  Maternal urinary tract infection  Premature labor
  • 11. Chorioamnionitis Maternal fever during labor  38ºC ± uterine tenderness ± leucocytosis ± fetal tachycardia High risk of neonatal sepsis
  • 12. Late Onset Sepsis - risk factors  Prematurity/ LBW  In hospital  Invasive procedures- ventilator, IV lines, central lines, urine catheter, chest tube  Contact with infectious disease - doctors, nurses, babies with infections,  Not fed maternal breast milk  POOR HYGIENE in NICU
  • 13. Bacterial Pathogens Responsible for Sepsis in Developing Countries  Early onset sepsis  Gram negative bacilli  E.coli  Klebsiella  Enterococcus  Group B streptococcus  Late onset sepsis  Gram negative bacilli  Pseudomonas  Klebsiella  Staph aureus  Coagulase negative staphylococci
  • 14. Diagnosis of Neonatal Sepsis  Clinical signs and symptoms  Laboratory tests  culture of bacterial pathogen  other laboratory indicators  Radiologic
  • 15. Clinical signs and symptoms Clinical Signs: early signs non- specific, may be subtle  Respiratory distress- 90%  Apnea  Temperature instability-  temp more common  Decreased activity  Irritability  Poor feeding  Abdominal distension  Hypotension, shock, purpura, seizures- late signs
  • 16. Laboratory Tests  Cultures to identify bacterial pathogen  blood, CSF, urine, other  Hematological tests  WBC count (normal 5.000 – 25.000/uL)  Platelet count (Trombocytopenia  < 100.000/mm3)  Erythrocyte Sedimentation Rate (ESR)  Other tests  C- reactive protein
  • 17. Lumbar Puncture  Possibility of meningitis 1-10%  Babies with meningitis may not have specific symptoms  15% of babies with meningitis will have negative blood cultures
  • 18. First line therapy  Ampicillin 50 mg/ kg  every 12 hours in 1st week of life  every 8 hours from 2- 4 weeks PLUS  Gentamicin once daily.  > 35 weeks gestation: 4 mg / kg every 24 hours  30 - 34 weeks gestation:  0 - 7 days: 4.5 mg/kg every 36 hours  > 8 days: 4 mg/kg every 24 hours
  • 19. Supportive Care  Temperature support  GI support - vomiting, ileus  Cardiorespiratory support  hypoxia, apnea, ARDS, shock  Hematological support: anemia, thrombocytopenia, DIC  Neurological support- seizures
  • 20. Prevention of Hospitalized acquired Infection (Nosocomial Infection)  Hand washing  Early feeding  Maternal breast milk  Decrease use of broad spectrum antibiotics  Decreased use of invasive procedures  Proper sterilization procedures
  • 21. 21
  • 22. 22  At first  vesicle  Purulent encounter hyperemic area  Multiple  severe systemic infection R/ : Isolation + aseptic treatment A.B : Cloxacillin 50 mg/kgBW Incise the bulla A.B zalp R/ topical
  • 23. 23  Infection with Neisseria gonorrheae ( a gram-negative diplococcus)  a reproductive tract infection  transmission to the fetus/ neonate in pregnancy Clinical presentation :  Hyperemic  Palpebra Edema  Purulent secret  Unilateral/ bilateral   cornea  Blind
  • 24. 24 D/ : Gram’s stain of exudate  diplococcus  gram (-) R/ : Isolation Eye  Topical A.B. Systemic A.B.
  • 25. 25 E/ : Staphylococcus aureus Hyperemic, edema, exudate Severe  lig. falciforme  multiple abscess Chronic  granulom R/ :  Topical : A.B  Granuloma : nitras argenti 3% UMBILICAL INFECTION
  • 26. 26 Thrush patches in the baby’s mouth, lips, tongue DD/ remain milk  easy to remove E/ fungus : Candida albicans If : - immunocompromize - Using A.B. for long periode - Using corticosteroid for long periode diarrhea + Parenteral infection/ sepsis Overgrowth  Moniliasis Oral Thrush
  • 27. 27 D/ : sediaan hapus  mycellium + spora R/ :  Gentian violet 0 – 5 – 1 %  Borax glicerin  Nistatin solution 3 x 100.000 U/day  Severe : amphotericin B/ Fluconazol

Editor's Notes

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