Académique Documents
Professionnel Documents
Culture Documents
It is the most common cause of neonatal mortality even though they are preventable and treatable.
Infection can occur in, intra-uterine life, or during delivery, or neonatal period.
When pathogenic bacteria gains access into the blood stream, they may cause an overwhelming
infection like septicemia, localized infections, pneumonia or meningitis.
Sepsis is a serious illness and can quickly cause death (a clinical syndrome of bacteremia with
systemic signs and symptoms of infection).
Incidence:
According to The World Bank (2015), the neonatal mortality rate of Nepal is 22 per thousand live births.
It was 38.6 per 1000 live birth in 2001 AD.
About 30-50 % of the total neonatal death in developing countries occurs due to neonatal sepsis. Among
which about 64% are male and 36% female.
Etiology:
The most common bacteria leading to neonatal sepsis are E. coli, Staphylococcus aureus, Group
B Streptococcus and klebsiella species. Other various types of bacteria, virus and fungi may also cause
neonatal sepsis.
1. Abdomen
Peritonitis
Gastro-enteritis
Omphalitis
Hepatitis
2. Brain
Meningitis
3. Cardio-vascular
Pericarditis
Endocarditis
Myocarditis
4. Ocular
Ophthalmic neonatrum
Conjunctivitis
5. Skeletal
Arthritis
Osteomyelitis
6. Respiratory tract
1
Pneumonia
Empyema
7. Skin
Pemphigus neonatrum
Fasciitis
Impetigo
8. Others
UTI
Neonatal tetanus
Risk factors:
i. Maternal history of uterine infection or fever anytime from the onset of labour to 3 days after
birth or rupture of membranes for more than 18 hours before birth
ii. Prolonged labour
iii. Unclean delivery
iv. Complicated or different labor
v. New onset illness:
Human contact
Cross infection
Contaminated article
Invasive procedure
Infected environment
Type:
Early Sepsis
Usually seen within 72 hours
Early onset sepsis manifests frequently as pneumonia and less commonly as septicemia or
meningitis
The predisposing factors are low birth weight, prolonged rupture of membrane, foul smelling liquor,
multiple per vaginal examination, maternal fever, difficult or prolonged labor, meconium aspiration
2
Late Sepsis
Seen after 72 hours
Caused by organism thriving in the external environment
Infection is often transmitted through caregiver
The predisposing factors are low birth weight, lack of breastfeeding, poor cord care, superficial
infection, disruption of skin integrity with needle prick or cannula, etc.
Clinical Manifestation:
1. In eyes:
Redness and swelling
Discharge may be watery, purulent or mucopurulent
Eyelids may be sticky or markedly swollen
2. Irritable and always crying
3. Alteration in feeding pattern- unable to suck or sucks poorly
4. Rigid muscles- locked jaw, rigid abdomen, neck and trunk
5. Vomiting all feeding
6. Diarrhoea with or without mucus and blood
7. Breathing too slow or apnea
8. Lethargy, difficult to arouse
9. Hypothermia or hyperthermia
10. Respiratory rate >60 breath/ min, lower chest indrawing, nasal flaring, grunting
11. Abdominal distention
12. Bulging or sunken fontanelle
13. Drowsiness
14. Convulsion
15. Jaundice
16. Bleeding from any site
17. Umbilical redness and swelling extending to surrounding skin
18. Discharge from the umbilical site
19. Superficial blisters may be present on any part of the skin.
Diagnostic investigations:
1. History taking
2. Physical examination
3. Culture- blood, urine, discharge from ear, nose
4. Total Leucocyte Count <5000/mm
5. Differential Count
6. Lumbar Puncture and CSF assessment
7. C-reactive protein positive
8. Chest X-ray
9. Maternal or neonatal serology
3
Treatment and Management:
2. Management in hospital:
Institute prompt treatment
Antibiotic therapy:
S.N. Clinical situation Septicemia and Meningitis
Pneumonia
1. First line Ampicillin or Penicillin Cefotaxime
Community acquired, resistant strains and Gentamycin
unlikely
2. Second line Ampicillin or Cloxacillin Add Cefotaxime
Hospital acquired or when there is low to and Amikacin
moderate probability of resistant strains
3. Third line Cefotaxime and
Hospital acquired sepsis or when there is Amikacin
high probability of resistant strains
If the baby’s condition is improving after 3 days of treatment with antibiotic, and if the culture is
negative then discontinue antibiotics after 5 days of treatment with antibiotic; if the culture is
positive then continue antibiotic upto 10 days of treatment.
If the baby’s condition is not improving after 3 days of treatment with antibiotic, and if the
culture is positive then change the antibiotic according to the result of culture and sensitivity, and
give antibiotics for 7 days after signs of improvement are first noted
If culture is not possible or organism cannot be identified, discontinue ampicillin. Give cefotaxime
IV according to the baby age, in addition to gentamycin, for 7 days after signs of improvement
are first noted.
4
After 12 hours of treatment with antibiotic or when the baby’s condition begins to improve,
allow the baby to breastfeed. If the baby cannot breastfeed, give expressed breast milk using an
alternative feeding method.
3. Supportive Care:
Ensure adequate warmth:
Provide warmth, ensure consistent normal temperature.
Kangaroo Mother Care is a useful modality especially in case of low birth weight babies.
Adequate nutrition:
Exclusive breastfeeding is to be initiated and continued, or spoon feeding/ cup feeding of
expressed breast milk is to be done.
Ensure optimal nutrition.
Parenteral nutrition or NG feeding is to be given if the newborn is very sick (inactive).
If hypoglycemia, then infuse 10% glucose 2ml/kg. Do not use glucose bolus.
Adequate hydration:
Start IV infusion as per requirement to maintain fluid and electrolyte balance and tissue
perfusion.
Monitor intake and output of the newborn.
Diagnosis:
Identify the disease condition and treat as per that disease’s treatment protocol.
5
Family Support:
Counsel and educate mother and family- gently explain findings, diagnosis and plan of care using
good communication and counseling skills
Preventive Measures:
REFERENCES
Essential Newborn Care (Training Package for PCL Nursing Program) Participant’s Manual- (Revised
2014).CTEVT and Save The Children
Ghai,O.P.(2009).Ghai Essential Paediatrics,(7thed.).CBS publishers and distributors
Nelson(2008).Text Book of Paediatrics Volume1 part1-XVI,(18thed.).Elsevier Publication
Prasai,D.S., and Bhattarai,S.G.(2012).Midwifery Nursing Part-III,(1sted.).Medhavi Publication
Shrestha,T.(2012).Essential Child Health Nursing,(1sted.).Medhavi Publication
Tuitui,R.(2009).Manual of Midwifery Nursing III,(6thed.). VidyarthiPustakBhandar