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HIGH RISK NEWBORN
High risk newborn is defined as a
newborn, regardless of gestational age
or birth weight , who has a greater
than average chance of mortality or
morbidity because of conditions or
circumstances associated with birth
and the adjustment to existance
Classification according to size
Low birth weight infant
Very low weight infant
Extremely low birth weight infant
Classification according to age
Low birth weight
Low birth weight is less than 2500gm
irrespective of the gestational age
Etiology
Causes is unknown
Uterine anomalies
Previous obstetric history
Multiple Pregnancy
Maternal disease in Pregnancy
Infection
Chronic diseases
Fetal causes
Classsification
Pre term
The growth potential is normal and is appropriate for
the gestational period
Small for gestational age
The term is to designate the newborns with birth
weight less than 10 percentile
A fetus of small for gestational may be constitutionally
small or due to pathologic process there may be fetal
growthrestriction
Birth weight is the single most important marker o
f
adverse perinatal and neonatal outcome.
Babies with a birth weight of less than 2,500g,
irrespective of their gestation are classified as low
birth weight babies.
These include both preterm and small-for-dates
babies.
Preterm infants (also called premature infants) are
those born before the beginning of 38th week of
gestation.
Moderately preterm infants are those born between 32
and 36 completed weeks of gestation.
Late preterm infants fall in the moderately preterm
group.
Very preterm infants are those born before 32
completed weeks of gestation. (Mehrban Singh,2010)
About 10 to 12 percent of Indian babies are born
preterm ( less than 37 completed weeks) as
compared to 5 to 7 percent incidence in the west.
These infants are anatomically and functionally
immature and therefore their neonatal mortality is
high.
The mechanisms initiating normal labour are not
clearly understood and much less is known about
the triggers that initiate labour before term.
Spontaneous
Induced
Poor socio-economic status
Low maternal weight
Chronic and acute systemic maternal
illness
Antepartumhemorrhage
Cervicalincompetence
Maternal genital colonization and
infections
Cigarette smoking during pregnancy
Threatened abortion
Acute emotional stress
Physicalexertion
Sexualactivity
Trauma
Bi-cornuateuterus
Multiplepregnancy
Congenitalmalformations
The labour is often induced before term when there is
impending danger to mother or foetal life in-utero.
Maternal diabetes mellitus
Placental dysfunction as indicated by unsatisfactory
foetal growth
Eclampsia
Foetal hypoxia
Antepartum haemorrhage and
Severe rhesus iso-immunization.
Their size is smallwith
relatively large head.
Crown-heel length i
s
less than 47cm
Head circumference is
less than 33cm but
exceeds the chest
circumference by more
than 3cm.
The general activityi
s
poor
Their automatic reflex
responses such as moro
response, sucking and
swallowing are sluggishor
incomplete.
The baby assumes an
extended posture dueto
poor tone.
Disproportionately
large head size
Sutures are widely
separated and the
fontanels are large
Small chin,
protruding eyes due
to shallow orbits and
absent buccal pad
of fat.
Optic nerve isoften un-
myelinated but presenceof
papillary membrane makes
its visualization difficult.
Ear cartilage isdeficiento
r
absent with poor recoil.
Hair appear woolly and
fuzzy and individual hair
fibres can be seen
separately.
skin is thin,gelatinous,
shiny and excessively
pink with abundant
lanugo andvery little
vernix caseosa.
Edema may be
present.
Subcutaneous fat is
deficient and breast
nodule is small or
absent.
Deep sole creases a
r
e
often not present.
Inmale testes are
undescended and
scrotum is poorly
developed.
Infemaleinfants, labia
majora are widely
separated exposing
labia minora and
hypertrophied clitoris.
Immaturity of central
nervous system is
expressed as inactivity
and lethargy, poor
cough reflexand
in-coordinated sucking
and swallowing
Resuscitation difficulties at
birth and recurrent apneic
attacks.
Retinopathy ofprematurity .
Vulnerable for intra-
ventricular –periventricular
hemorrhage and leuco-
malacia
Inefficient blood brain
barrier
Cuboidal alveolar lining-
poor alveolar diffusion of
gases
Hyaline
membrane
disease
Breathing ismostly
diaphragmatic, periodic
and associated with
intercostal recessions
Pulmonary
aspiration and
atelectasis
They are vulnerable t
o
develop chronic
pulmonary
insufficiency
The closure ofductus
arteriosus isdelayed.
Ingrossly immature
infants( less than 32
weeks) EKG showsleft
ventricular
preponderance.
Risk to develop thrombo-
embolic complications
and hypertension.
Due to poor and
incoordinated suckingand
swallowing.
Animal fat is not tolerated a
s
well as the vegetablefat.
Regurgitation and aspiration
are common.
Hypoglycaemia
Abdominal distention and
functional intestinal
obstruction
Entero-colitis
Immaturity of theglucuronyl
transferase system in theliver
leads to hyper-bilirubinemia.
Development ofkernicterus
at lower serum bilirubin
levels.
Hypothermiais invariable.
Excessive heat loss due to
relatively large surfacearea
due to paucity of brown fat
in the baby who is
equipped with an
inefficient thermostat.
Infections are theimportant
cause of neonatal mortality.
The low levels of IgG
antibodies and inefficient
cellular immunity
Excessive handling, humid
and warm atmosphere,
contaminated incubators
and resuscitators expose
them to infectingorganisms.
The blood urea nitrogen is
high due to low glomerular
filtrate rate.
The renal tubular ammonia
mechanism is poorly
developed thus acidosis
occurs early.
They vulnerable to
develop late metabolic
acidosis especially when
fed with a high protein milk
formula.
Concentration of urine i
s
poor.
Preterm has to pass
4 to 5 ml of urine excrete
one milliosmole of solute
Baby gets dehydrated.
The solute retention and
low serum proteinsexplain
occurrence of edema in
preterm infants.
Poor hepatic
detoxification and
reduced renal
clearance make a
preterm baby
vulnerable to toxic
effects of drugs
Develop anemia around 6
to 8 weeks of age.
Deficiencies of folic acid
and vitaminE.
Develop haemolytic
anemia, thrombocytopenia
and edema 6 to 10 weeks
of age.
Osteopenia and rickets
These babies are
prone to develop :
Hypoglycaemia
Hypocalcemia
Hypoprotenemia
Acidosis and
Hypoxia.
Bed rest and sedation.
Tocolytic agents
Sympathomimetic agents-beta-2-adrenergic
receptors.
Isoxsuprine (duvadilan)-beta-1 and beta-2receptors.
Ritodrine
Salbutamol andterbutaline -beta-2 receptor
Magnesium sulphate
Indomethacin
Maturity of fetus should be ascertained by
examination of amniotic fluid for phosphatidyl
glycerol or L/Sratio.
Corticosteroids should be administered to t
h
e
mother to enhance fetal lung maturity.
Inj.betamethasone12mg IM
every 24 hours --2doses or
dexamethasone 6mg IM
every 12 hours for 4doses.
The optimal effect is seen if
delivery occurs after 24
hours of the initiation of
therapy and its therapeutic
effect lasts for 7days.
Delayed clamping of cord.
Elective intubation of extremely LBW babies (<1000g).
Should be promptly dried, kept effectively covered and
warm.
Vitamin K 1mg ( 0.5mg in babies <1500g) should be
given intra-muscularly.
Transferred by the doctor or nurse to the NICU as soon a
s
breathing isestablished.
Vital signs.
Activity and behaviour.
Colour.
Tissueperfusion.
Fluids, electrolytes and ABG’s.
Tolerance of feeds .
Watched for developmento
f
RDS, apneic attacks, sepsis,
PDA, NEC, IVH,etc.
Weight gain velocity.
The vital signs should be stable.
The healthy baby is alert and active, looks
pink and healthy, trunk is warm to touch and
extremities are reasonably warm and pink.
The baby is able to tolerate enteral feeds and
there is no respiratory distress or apneic attacks
and baby is having a steady weight gain of 1-1.5 %
of his body weight every day.
Create a soft, comfortable,
“nestled” andcushioned bed.
Avoid excessive stimuli.
Effective analgesia and
sedation.
Provide warmth.
Ensure asepsis.
Prevent evaporative skinlosses.
Provide effective and safe
oxygenation.
Partial parenteral nutrition
and give trophic feeds
with expressed breastmilk
(EBM).
Provide rhythmic
gentle tactile and
kinaesthetic
stimulation.
Thermo-neutral
environment.
Application of oil or liquid
paraffin on theskin.
Should be covered with a
cellophane or thin
transparent or thin
transparent plastic sheet.
Provide partial
kangaroo0mother-care.
Oxygen should be administered
with a head box when SpO2 falls
below 85%and it should be
gradually withdrawn whenSpO2
goes above 90%.
The lowest ambient concentration
and flow rates should be used to
maintain SpO2 between 85-95%
and PaO2 between 60-80 mmHg.
Early phototherapyis
adviced to keep the serum
bilirubin level within safe
limits in order to obviate the
need for exchange blood
transfusion.
The handling should be b
a
r
e
minimum.
Vigilance should be
maintained on all
procedures.
Early diagnosis and prompt
treatment of infections.
Intra-venous dextrose solution (
10% dextrose in babies >1000g
and 5%dextrose in babies
<1000g).
Trophic feeds with EBM through
NG tube.
Condition is stabilized -e
n
t
e
r
a
l
feeds.
Fluid requirements are higher in LBW infants due
to:
Greater insensible water losses
Faster breathing rates
Decreased ability to concentrate urine
Greater use of radiant warmers
Greater use of phototherapy units
Birth weight Fluid rate
(ml/kg/day)
(g)
500 - 600
601 - 800
801 - 1000
1000 - 1500
>1500
140 - 200
120 - 130
90 - 110
80 - 100
60 - 80
*on first 2 days of life
Fluid rate can be increased by 10-20 ml/kg/dto
gradually reach 150 ml/kg/d
Fluid requirements need to be
individualized for each baby
Enteral nutrition has to be considered once
the baby is stable
Infants with BW ≤ 1000 g
Infants with BW ≤ 1500 g, done in
conjunction with slowly advancing enteral
nutrition
Infants with BW 1501-1800 g for whom
enteral intake is not expected for > 3 days
Glucose : 6 - 8 mg/kg/min
Amino acids : 1.5 - 2 g/kg/d
Lipid
Sodium
Potassium
Chloride
: 0.5 - 1 g/kg/d
: 2 - 4 mEq/kg/d
: 2 - 3 mEq/kg/d
: 2 - 4 mEq/kg/d
Trophic feeding/ Gut priming
Practice of feeding very small amounts of enteral nourishment
to stimulate development of the immature GIT
Advantages:
Improves GI motility
Enhances enzyme maturation
Improves mineral absorption
Lowers incidence of cholestasis
Shortens time to regain birth weight
Breast milk or ½ or full strength preterm formula at
10ml/kg/d by intermittent gavage/ continuous
nasogastric drip
Increase by 10-15 ml/kg/d to reach 150ml/kg/d
Increments not >20 ml/kg/d
IV fluids can be stopped once 120ml/kg/d is reached
On reaching 150ml/kg/d,calorie density can be
increased
PRETERMS
<1200 g/ <32 wks: IV fluids for first 2-3 days, once
stable start gavage feeding
1200-1800 g/ 32-34 wks: Start gavage feeding, o
n
c
e
vigorous start spoon/ breast feeding
>1800 g/ >34 wks: Start breast feeding directly; if
trial feed takes>20 mins or intake is less than
required, switch to gavage feeding
Advantages:
Higher concentrations of amino acids
Higher concentrations of essential fatty acids
Lower renal solute load
Specific bio-active factors provide immunity
Promotes intestinal maturation
Disadvantages:
Low concentrations of
Vitamin D, Ca, P
Inadequate iron
Energy : 130 - 175 Kcal/kg/d
Protein :3.4 - 4.2g/kg/d
Fat :6 - 8 g/kg/d
Na :3 - 7 mEq/kg/d
Cl :3 - 7 mEq/kg/d
K :2 - 3 mEq/kg/d
Ca :100 – 220 mg/kg/d
Multivitamindrops.
Ironsupplementation.
VitaminE supplementation.
Supplements of calcium
(220mg/day) and
phosphorus (100mg/day).
Gentle touch, massage,
cuddling, stroking and flexing.
Rocking bed or placing a
preterm baby on inflated
gloves.
Soothing auditory stimuli.
Visualinputs.
Kangaroo care is placing a
premature baby in an upright position on a
mother’s bare chest allowing tummy to
tummy contact and placing the premature
baby in between the mother’s breasts.
The baby’s head is turned so that the ear i
s
above the parent’sheart.
Bodyt
e
m
p
e
r
a
t
u
r
e
 Mothers have thermal synchrony with their baby.
 The study also concluded that when the baby was
cold, the mother’s body temperature would increase
to warm the baby up and vice versa.
Breastfeeding:
Kangaroo care allows easy access to the breast and
skin-to-skin contact increasesmilk let-down.
Increase weightgain
Kangaroo care allows the baby to fall into a deep
sleep which allows the baby to conserve energy for
more important things. Increased weight gain
means shorter hospital stay.
Increased intimacy anda
t
t
a
c
h
m
e
n
t
A single dose of
dexamethasone 0.2mg/kg IVat
4 hours of age.
Inhaledsteroids.
Nosocomialinfections
Hypothermia
Respiratorydistress syndrome
Aspiration
Patent ductus arteriosus
Chronic lung disease
NEC & IVH
ROP & Late metabolic acidosis
Nutritionaldisorders
Drugtoxicity
Loss is upto a maximum of 1
0
to 15percent.
Regain their birth weight b
y
the end of second week of
life.
Excessive weight loss, delay in
regaining the birth weight or
slow weight gain- suggest
baby isnot being fed
adequately or unwell and
needs immediate attention.
Routine oxygenation without
monitoring.
Intravenousimmuno-globulins.
Prophylacticantibiotics.
Prophylactic administration of
indomethacin or high doses of
vitamin E.
Unnecessary blood
transfusions.
Formulafeeds.
Rough handling, excessive
light and loud sound.
Itisdesirable to administer0
-
day vaccines(BCG, OPV,
HBV) on the day of
discharge from thehospital.
Ifmother isHBV carrier and i
s
e-antigen positive- hepatitis
Bvaccine and hepatitis B
specific immunoglobulins
within 72 hours of age.
Live vaccines should be
avoided in symptomatic HIV-
positive mothers.
WHO recommends that BCG
and oral polio vaccine can be
given to asymptomatic HIV-
positive infants.
The family dynamics a
r
e
greatly disturbed.
The problems and issues
should be handled with
equanimity, compassion,
concern and caring attitude
of the healthteam.
Encouraged to touch and
talk with herbaby.
Providekangaroo-mother-
care.
Emotional support and
guidance.
A baby who is feeding from the
bottle or cup and is reasonably
active with a stable body
temperature, irrespective of his
weight, qualifies for transfer to the
open cot.
The mother should be
mentally prepared and
provided with essential
training and skills.
The mother- baby dy
ad
should be kept in step-
down nursery.
The baby should be
stable, maintaining his
body temperature and
should not have any
evidences of cold stress.
At the time of discharge,
the baby should be having
daily steady weight gain
velocity of at least 10g/kg.
The homeconditions
should be satisfactory
before the baby is
discharged.
The public health nurse
should assess the home
conditions and visit the
family at home every week
for a month or so.
Common infective illnesses,
reactive airway disease,
hypertension, renal dysfunction,
gastro-oesophageal reflux.
Feeding and nutrition.
Immunizations.
Physical growth, nutritional
status, anemia, osteopenia/
rickets.
Neuro-motor development,
cognition and seizures.
Eyes: Retinopathy of
prematurity, vision,strabismus.
Hearing.
Behavioural problems,
language disordersand
learning disabilities.
She must be explained
aboutthe importance of
asepsis.
Keeping the baby warm
and ensuring satisfactory
feeding routine.
The services of
postpartum programme
public health nurse and
social worker can be
utilized.
The infant should be effectively covered taking care to
avoid smothering.
Woollen cap, socks and mittens should be worn.
The infant should preferably lie next to the mother.
Inwinter, the room can be warmed with a
radiant heater or angeethi.
A table lamp having 100 watt bulb can be used to
provide direct radiantheat.
Hot water bottle should never come in contact with
the baby.
The cot of the mother and infant should be located
away from thewalls .
The mother and health worker should be trained to
assess the temperature of the newborn baby by touch.
The visitors and handling of the infant should be
restricted to the bare minimum.
The hands must be washed before touching or
feeding the baby.
The emotional urge for kissing the baby should be
curbed.
The linen should be clean and sun-dried.
Whenever feasible, breast feeding is ideal and
must be encouraged.
When infant is unable to suck from the breast, E
B
M
should be given with a bottle or dropper or spoon
or paladay depending upon his maturity.
Formula for premature babies is recommended.
If cow’s or buffalo’s milk is unavoidable it should be
given after 3:1dilution.
Mother must be given detailed instructions and
practical demonstration for maintenance of bottle
hygiene to prevent contamination of feeds.
The riskof neurodevelopmental
handicaps isincreased3-fold for LBW
babies and 10-fold for very LBW
babies(<1500g).
The prognosis isgood if nobirth
asphyxia, apneic attacks,RDS,
hypoglycaemia and
hyperbilirubinemia.
Preterm AFD babies catch up in
their physical growth with term
counterparts by the age of 1 to 2
years.
15 to 20 %
incidence of
neurological handicaps in the
form of CP, seizures, ROP,
hydrocephalus, deafness and
MR.
There ishigh incidence of
minor neurologic disabilities.
Neurological prognosis is
adversely affected bydegree
of immaturity.
Obtain detailed antenatal, intra-
natal history.
Assess the gestational age and
birth weight of the baby.
Assess the features ofclinical
immaturity.
Assess the behaviour of preterm
neonate.
Assessment of c
o
m
m
o
n
problems.
1. Impaired gas exchange related to immaturity of
lungs and deficiency of surfactant
Assess the respiratory pattern and colour of t
h
e
baby
Observe for any apneic episode.
Oxygen hood is often used for able to
breathe alone but need extra oxygen.
Oxygen also may be given by nasal cannula to t
h
e
infant who breathesalone.
Humidify the oxygen
CPAP may be necessary to keep the alveoli open
and improve expansion of lungs
2.Impaired breathing pattern :distress related to
immaturity and surfactantdeficiency
Assess the respiratory rate, heart rate and c
h
e
s
t
retractions
Position the child for maximal ventilatory efficiency
and airway patency
Provide humidified oxygen
Spo2monitoring
Providesuctioning
Provide chest physiotherapy
Administerbronchodilators
Administer anti inflammatory medications
Administerantibiotics
3. Activity intolerance related to increased work of
breathing secondary todistress
Arrange to provide routine care
Schedule periods of uninterrupted rest
Determine infant’s stress level
Reduce nonessential lighting
Use positioningdevices
4. Ineffective airway clearance related to excessive
trachea-bronchial secretions
Assess the child’s breathing pattern
Checkthe vital signs
Provide suctioning
Provide humidifiedoxygen
Assess the ABG analysis
Provide C-PAP using mask /hood/nasal prongs
Observe for risksof C-PAP
Assist in CMV with PEEP if needed
5. Hypothermia related toimmature thermoregulation
system
Monitor vitalsigns frequently
Wrap the baby well and keep warm
Provide small and frequent breast feeding as tolerated
Look forhypoglycemia
Administer IV fluids if not tolerating the feed
Monitor the vital signs and blood pressure
Assess the skin tone, pallor and signs of dehydration
Administer IVfluids
6. Imbalanced nutrition less than bodyrequirement
related to feeding difficulty, respiratory distress, or
NPO status
Assess the sucking and swallowing ability of t
h
e
newborn
Assess the tolerance of the child
Monitor the blood glucose level frequently
Administer IV fluids if not tolerating oral fluids
Administer human milk fortifier if the child is preterm
7. Fatigue related to increased demand for nutrients
and deterioration of the general condition of the
baby
Assess the general condition of the baby
Assess the level of activity
Monitor the blood glucose level
Breast fed the baby
Check for from any part of the body
Provide top up feed
8. Risk for complications hypotension, shock, cerebral
hypoxia related to progression of the disease condition
Assess the vital signs, respiratory rate, pulse rate,
temperature and bloodpressure
Check blood culture and sensitivity and sepsis screening
Monitor for any signs of dehydration
Administer IV fluids or blood as necessary
Assess the serum electrolyte values and ABG values
Closely monitor for the early signs and symptoms o
f
complications
9. Anxiety of parents related to the outcome of the
newborn condition
Assess the mental status, anxiety and knowledge of
family members
Assess the supporting system for the family
Assess the coping strategies of the family members
Explain the disease process to the family members
Explain each and every procedure to the care giver
Provide psychological support to the family
members
10. Interrupted mother-child bonding relatedto
infectious process
Assess the breast feeding ability including
sucking and swallowing ability
Keep the child with the mother if possible
Provide frequent breast feed 2 hourly
If breast feeding is not tolerated give EBM
Allow the mother to visit the child
Provide kangaroo mother care in case of pre term if
tolerated
11. Interrupted family process relatedto
hospitalization of thenewborn
Assess the mental status, anxiety and knowledge
of familymembers
Encourage mother-child bonding if possible
Assess the coping strategies of the family members
Explain the disease process to the family members
Explain each and every procedure to the
care giver
Allow the family members to visit the child
12. Knowledge deficit regarding care of the baby
and treatmentmodalities
Assess the knowledge level of the care giver
Explain disease condition and it’s progress to t
h
e
family members
Educate regarding treatment and its prevention
Educate about the monitoring of the baby
Provide adequate explanation regarding
nutritional need of thebaby
Clarify their doubts and promote understanding
Definition and incidence
Causes of prematurity
Clinical features
Physiological handicaps
Management
Careof preterm babies
Prognosis
Nursing assessment
Nursing diagnosis and
interventions
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pretermbabies-130723101340-phpapp01-converted.pptx

  • 1.
  • 2. HIGH RISK NEWBORN High risk newborn is defined as a newborn, regardless of gestational age or birth weight , who has a greater than average chance of mortality or morbidity because of conditions or circumstances associated with birth and the adjustment to existance
  • 3. Classification according to size Low birth weight infant Very low weight infant Extremely low birth weight infant
  • 5. Low birth weight Low birth weight is less than 2500gm irrespective of the gestational age
  • 6. Etiology Causes is unknown Uterine anomalies Previous obstetric history Multiple Pregnancy Maternal disease in Pregnancy Infection Chronic diseases Fetal causes
  • 7. Classsification Pre term The growth potential is normal and is appropriate for the gestational period Small for gestational age The term is to designate the newborns with birth weight less than 10 percentile A fetus of small for gestational may be constitutionally small or due to pathologic process there may be fetal growthrestriction
  • 8. Birth weight is the single most important marker o f adverse perinatal and neonatal outcome. Babies with a birth weight of less than 2,500g, irrespective of their gestation are classified as low birth weight babies. These include both preterm and small-for-dates babies.
  • 9. Preterm infants (also called premature infants) are those born before the beginning of 38th week of gestation. Moderately preterm infants are those born between 32 and 36 completed weeks of gestation. Late preterm infants fall in the moderately preterm group. Very preterm infants are those born before 32 completed weeks of gestation. (Mehrban Singh,2010)
  • 10. About 10 to 12 percent of Indian babies are born preterm ( less than 37 completed weeks) as compared to 5 to 7 percent incidence in the west. These infants are anatomically and functionally immature and therefore their neonatal mortality is high.
  • 11. The mechanisms initiating normal labour are not clearly understood and much less is known about the triggers that initiate labour before term. Spontaneous Induced
  • 12. Poor socio-economic status Low maternal weight Chronic and acute systemic maternal illness Antepartumhemorrhage Cervicalincompetence Maternal genital colonization and infections
  • 13. Cigarette smoking during pregnancy Threatened abortion Acute emotional stress Physicalexertion Sexualactivity Trauma Bi-cornuateuterus Multiplepregnancy Congenitalmalformations
  • 14. The labour is often induced before term when there is impending danger to mother or foetal life in-utero. Maternal diabetes mellitus Placental dysfunction as indicated by unsatisfactory foetal growth Eclampsia Foetal hypoxia Antepartum haemorrhage and Severe rhesus iso-immunization.
  • 15.
  • 16. Their size is smallwith relatively large head. Crown-heel length i s less than 47cm Head circumference is less than 33cm but exceeds the chest circumference by more than 3cm.
  • 17. The general activityi s poor Their automatic reflex responses such as moro response, sucking and swallowing are sluggishor incomplete. The baby assumes an extended posture dueto poor tone.
  • 18. Disproportionately large head size Sutures are widely separated and the fontanels are large Small chin, protruding eyes due to shallow orbits and absent buccal pad of fat.
  • 19. Optic nerve isoften un- myelinated but presenceof papillary membrane makes its visualization difficult. Ear cartilage isdeficiento r absent with poor recoil. Hair appear woolly and fuzzy and individual hair fibres can be seen separately.
  • 20. skin is thin,gelatinous, shiny and excessively pink with abundant lanugo andvery little vernix caseosa. Edema may be present.
  • 21. Subcutaneous fat is deficient and breast nodule is small or absent. Deep sole creases a r e often not present.
  • 22. Inmale testes are undescended and scrotum is poorly developed.
  • 23. Infemaleinfants, labia majora are widely separated exposing labia minora and hypertrophied clitoris.
  • 24.
  • 25. Immaturity of central nervous system is expressed as inactivity and lethargy, poor cough reflexand in-coordinated sucking and swallowing
  • 26. Resuscitation difficulties at birth and recurrent apneic attacks. Retinopathy ofprematurity . Vulnerable for intra- ventricular –periventricular hemorrhage and leuco- malacia Inefficient blood brain barrier
  • 27. Cuboidal alveolar lining- poor alveolar diffusion of gases Hyaline membrane disease Breathing ismostly diaphragmatic, periodic and associated with intercostal recessions
  • 28. Pulmonary aspiration and atelectasis They are vulnerable t o develop chronic pulmonary insufficiency
  • 29. The closure ofductus arteriosus isdelayed. Ingrossly immature infants( less than 32 weeks) EKG showsleft ventricular preponderance. Risk to develop thrombo- embolic complications and hypertension.
  • 30. Due to poor and incoordinated suckingand swallowing. Animal fat is not tolerated a s well as the vegetablefat. Regurgitation and aspiration are common. Hypoglycaemia
  • 31. Abdominal distention and functional intestinal obstruction Entero-colitis Immaturity of theglucuronyl transferase system in theliver leads to hyper-bilirubinemia. Development ofkernicterus at lower serum bilirubin levels.
  • 32. Hypothermiais invariable. Excessive heat loss due to relatively large surfacearea due to paucity of brown fat in the baby who is equipped with an inefficient thermostat.
  • 33. Infections are theimportant cause of neonatal mortality. The low levels of IgG antibodies and inefficient cellular immunity Excessive handling, humid and warm atmosphere, contaminated incubators and resuscitators expose them to infectingorganisms.
  • 34. The blood urea nitrogen is high due to low glomerular filtrate rate. The renal tubular ammonia mechanism is poorly developed thus acidosis occurs early. They vulnerable to develop late metabolic acidosis especially when fed with a high protein milk formula. Concentration of urine i s poor.
  • 35. Preterm has to pass 4 to 5 ml of urine excrete one milliosmole of solute Baby gets dehydrated. The solute retention and low serum proteinsexplain occurrence of edema in preterm infants.
  • 36. Poor hepatic detoxification and reduced renal clearance make a preterm baby vulnerable to toxic effects of drugs
  • 37. Develop anemia around 6 to 8 weeks of age. Deficiencies of folic acid and vitaminE. Develop haemolytic anemia, thrombocytopenia and edema 6 to 10 weeks of age. Osteopenia and rickets
  • 38. These babies are prone to develop : Hypoglycaemia Hypocalcemia Hypoprotenemia Acidosis and Hypoxia.
  • 39.
  • 40. Bed rest and sedation. Tocolytic agents Sympathomimetic agents-beta-2-adrenergic receptors. Isoxsuprine (duvadilan)-beta-1 and beta-2receptors. Ritodrine Salbutamol andterbutaline -beta-2 receptor Magnesium sulphate Indomethacin
  • 41. Maturity of fetus should be ascertained by examination of amniotic fluid for phosphatidyl glycerol or L/Sratio. Corticosteroids should be administered to t h e mother to enhance fetal lung maturity.
  • 42. Inj.betamethasone12mg IM every 24 hours --2doses or dexamethasone 6mg IM every 12 hours for 4doses. The optimal effect is seen if delivery occurs after 24 hours of the initiation of therapy and its therapeutic effect lasts for 7days.
  • 43.
  • 44. Delayed clamping of cord. Elective intubation of extremely LBW babies (<1000g). Should be promptly dried, kept effectively covered and warm. Vitamin K 1mg ( 0.5mg in babies <1500g) should be given intra-muscularly. Transferred by the doctor or nurse to the NICU as soon a s breathing isestablished.
  • 45. Vital signs. Activity and behaviour. Colour. Tissueperfusion. Fluids, electrolytes and ABG’s. Tolerance of feeds . Watched for developmento f RDS, apneic attacks, sepsis, PDA, NEC, IVH,etc. Weight gain velocity.
  • 46. The vital signs should be stable. The healthy baby is alert and active, looks pink and healthy, trunk is warm to touch and extremities are reasonably warm and pink. The baby is able to tolerate enteral feeds and there is no respiratory distress or apneic attacks and baby is having a steady weight gain of 1-1.5 % of his body weight every day.
  • 47. Create a soft, comfortable, “nestled” andcushioned bed. Avoid excessive stimuli. Effective analgesia and sedation. Provide warmth. Ensure asepsis. Prevent evaporative skinlosses.
  • 48. Provide effective and safe oxygenation. Partial parenteral nutrition and give trophic feeds with expressed breastmilk (EBM). Provide rhythmic gentle tactile and kinaesthetic stimulation.
  • 49. Thermo-neutral environment. Application of oil or liquid paraffin on theskin. Should be covered with a cellophane or thin transparent or thin transparent plastic sheet. Provide partial kangaroo0mother-care.
  • 50. Oxygen should be administered with a head box when SpO2 falls below 85%and it should be gradually withdrawn whenSpO2 goes above 90%. The lowest ambient concentration and flow rates should be used to maintain SpO2 between 85-95% and PaO2 between 60-80 mmHg.
  • 51. Early phototherapyis adviced to keep the serum bilirubin level within safe limits in order to obviate the need for exchange blood transfusion.
  • 52. The handling should be b a r e minimum. Vigilance should be maintained on all procedures. Early diagnosis and prompt treatment of infections.
  • 53.
  • 54. Intra-venous dextrose solution ( 10% dextrose in babies >1000g and 5%dextrose in babies <1000g). Trophic feeds with EBM through NG tube. Condition is stabilized -e n t e r a l feeds.
  • 55. Fluid requirements are higher in LBW infants due to: Greater insensible water losses Faster breathing rates Decreased ability to concentrate urine Greater use of radiant warmers Greater use of phototherapy units
  • 56. Birth weight Fluid rate (ml/kg/day) (g) 500 - 600 601 - 800 801 - 1000 1000 - 1500 >1500 140 - 200 120 - 130 90 - 110 80 - 100 60 - 80 *on first 2 days of life
  • 57. Fluid rate can be increased by 10-20 ml/kg/dto gradually reach 150 ml/kg/d Fluid requirements need to be individualized for each baby Enteral nutrition has to be considered once the baby is stable
  • 58. Infants with BW ≤ 1000 g Infants with BW ≤ 1500 g, done in conjunction with slowly advancing enteral nutrition Infants with BW 1501-1800 g for whom enteral intake is not expected for > 3 days
  • 59. Glucose : 6 - 8 mg/kg/min Amino acids : 1.5 - 2 g/kg/d Lipid Sodium Potassium Chloride : 0.5 - 1 g/kg/d : 2 - 4 mEq/kg/d : 2 - 3 mEq/kg/d : 2 - 4 mEq/kg/d
  • 60. Trophic feeding/ Gut priming Practice of feeding very small amounts of enteral nourishment to stimulate development of the immature GIT Advantages: Improves GI motility Enhances enzyme maturation Improves mineral absorption Lowers incidence of cholestasis Shortens time to regain birth weight
  • 61. Breast milk or ½ or full strength preterm formula at 10ml/kg/d by intermittent gavage/ continuous nasogastric drip Increase by 10-15 ml/kg/d to reach 150ml/kg/d Increments not >20 ml/kg/d IV fluids can be stopped once 120ml/kg/d is reached On reaching 150ml/kg/d,calorie density can be increased
  • 62. PRETERMS <1200 g/ <32 wks: IV fluids for first 2-3 days, once stable start gavage feeding 1200-1800 g/ 32-34 wks: Start gavage feeding, o n c e vigorous start spoon/ breast feeding >1800 g/ >34 wks: Start breast feeding directly; if trial feed takes>20 mins or intake is less than required, switch to gavage feeding
  • 63. Advantages: Higher concentrations of amino acids Higher concentrations of essential fatty acids Lower renal solute load Specific bio-active factors provide immunity Promotes intestinal maturation
  • 65. Energy : 130 - 175 Kcal/kg/d Protein :3.4 - 4.2g/kg/d Fat :6 - 8 g/kg/d Na :3 - 7 mEq/kg/d Cl :3 - 7 mEq/kg/d K :2 - 3 mEq/kg/d Ca :100 – 220 mg/kg/d
  • 67. Gentle touch, massage, cuddling, stroking and flexing. Rocking bed or placing a preterm baby on inflated gloves. Soothing auditory stimuli. Visualinputs.
  • 68. Kangaroo care is placing a premature baby in an upright position on a mother’s bare chest allowing tummy to tummy contact and placing the premature baby in between the mother’s breasts. The baby’s head is turned so that the ear i s above the parent’sheart.
  • 69. Bodyt e m p e r a t u r e  Mothers have thermal synchrony with their baby.  The study also concluded that when the baby was cold, the mother’s body temperature would increase to warm the baby up and vice versa.
  • 70. Breastfeeding: Kangaroo care allows easy access to the breast and skin-to-skin contact increasesmilk let-down.
  • 71. Increase weightgain Kangaroo care allows the baby to fall into a deep sleep which allows the baby to conserve energy for more important things. Increased weight gain means shorter hospital stay.
  • 73. A single dose of dexamethasone 0.2mg/kg IVat 4 hours of age. Inhaledsteroids.
  • 74. Nosocomialinfections Hypothermia Respiratorydistress syndrome Aspiration Patent ductus arteriosus Chronic lung disease NEC & IVH ROP & Late metabolic acidosis Nutritionaldisorders Drugtoxicity
  • 75. Loss is upto a maximum of 1 0 to 15percent. Regain their birth weight b y the end of second week of life. Excessive weight loss, delay in regaining the birth weight or slow weight gain- suggest baby isnot being fed adequately or unwell and needs immediate attention.
  • 76. Routine oxygenation without monitoring. Intravenousimmuno-globulins. Prophylacticantibiotics. Prophylactic administration of indomethacin or high doses of vitamin E. Unnecessary blood transfusions. Formulafeeds. Rough handling, excessive light and loud sound.
  • 77. Itisdesirable to administer0 - day vaccines(BCG, OPV, HBV) on the day of discharge from thehospital. Ifmother isHBV carrier and i s e-antigen positive- hepatitis Bvaccine and hepatitis B specific immunoglobulins within 72 hours of age.
  • 78. Live vaccines should be avoided in symptomatic HIV- positive mothers. WHO recommends that BCG and oral polio vaccine can be given to asymptomatic HIV- positive infants.
  • 79. The family dynamics a r e greatly disturbed. The problems and issues should be handled with equanimity, compassion, concern and caring attitude of the healthteam. Encouraged to touch and talk with herbaby. Providekangaroo-mother- care. Emotional support and guidance.
  • 80. A baby who is feeding from the bottle or cup and is reasonably active with a stable body temperature, irrespective of his weight, qualifies for transfer to the open cot.
  • 81. The mother should be mentally prepared and provided with essential training and skills. The mother- baby dy ad should be kept in step- down nursery. The baby should be stable, maintaining his body temperature and should not have any evidences of cold stress.
  • 82. At the time of discharge, the baby should be having daily steady weight gain velocity of at least 10g/kg. The homeconditions should be satisfactory before the baby is discharged. The public health nurse should assess the home conditions and visit the family at home every week for a month or so.
  • 83. Common infective illnesses, reactive airway disease, hypertension, renal dysfunction, gastro-oesophageal reflux. Feeding and nutrition. Immunizations. Physical growth, nutritional status, anemia, osteopenia/ rickets.
  • 84. Neuro-motor development, cognition and seizures. Eyes: Retinopathy of prematurity, vision,strabismus. Hearing. Behavioural problems, language disordersand learning disabilities.
  • 85. She must be explained aboutthe importance of asepsis. Keeping the baby warm and ensuring satisfactory feeding routine. The services of postpartum programme public health nurse and social worker can be utilized.
  • 86. The infant should be effectively covered taking care to avoid smothering. Woollen cap, socks and mittens should be worn. The infant should preferably lie next to the mother. Inwinter, the room can be warmed with a radiant heater or angeethi. A table lamp having 100 watt bulb can be used to provide direct radiantheat. Hot water bottle should never come in contact with the baby.
  • 87. The cot of the mother and infant should be located away from thewalls . The mother and health worker should be trained to assess the temperature of the newborn baby by touch. The visitors and handling of the infant should be restricted to the bare minimum. The hands must be washed before touching or feeding the baby. The emotional urge for kissing the baby should be curbed. The linen should be clean and sun-dried.
  • 88. Whenever feasible, breast feeding is ideal and must be encouraged. When infant is unable to suck from the breast, E B M should be given with a bottle or dropper or spoon or paladay depending upon his maturity. Formula for premature babies is recommended. If cow’s or buffalo’s milk is unavoidable it should be given after 3:1dilution. Mother must be given detailed instructions and practical demonstration for maintenance of bottle hygiene to prevent contamination of feeds.
  • 89. The riskof neurodevelopmental handicaps isincreased3-fold for LBW babies and 10-fold for very LBW babies(<1500g). The prognosis isgood if nobirth asphyxia, apneic attacks,RDS, hypoglycaemia and hyperbilirubinemia. Preterm AFD babies catch up in their physical growth with term counterparts by the age of 1 to 2 years.
  • 90. 15 to 20 % incidence of neurological handicaps in the form of CP, seizures, ROP, hydrocephalus, deafness and MR. There ishigh incidence of minor neurologic disabilities. Neurological prognosis is adversely affected bydegree of immaturity.
  • 91. Obtain detailed antenatal, intra- natal history. Assess the gestational age and birth weight of the baby. Assess the features ofclinical immaturity. Assess the behaviour of preterm neonate. Assessment of c o m m o n problems.
  • 92.
  • 93. 1. Impaired gas exchange related to immaturity of lungs and deficiency of surfactant Assess the respiratory pattern and colour of t h e baby Observe for any apneic episode. Oxygen hood is often used for able to breathe alone but need extra oxygen. Oxygen also may be given by nasal cannula to t h e infant who breathesalone. Humidify the oxygen CPAP may be necessary to keep the alveoli open and improve expansion of lungs
  • 94. 2.Impaired breathing pattern :distress related to immaturity and surfactantdeficiency Assess the respiratory rate, heart rate and c h e s t retractions Position the child for maximal ventilatory efficiency and airway patency Provide humidified oxygen Spo2monitoring Providesuctioning Provide chest physiotherapy Administerbronchodilators Administer anti inflammatory medications Administerantibiotics
  • 95. 3. Activity intolerance related to increased work of breathing secondary todistress Arrange to provide routine care Schedule periods of uninterrupted rest Determine infant’s stress level Reduce nonessential lighting Use positioningdevices
  • 96. 4. Ineffective airway clearance related to excessive trachea-bronchial secretions Assess the child’s breathing pattern Checkthe vital signs Provide suctioning Provide humidifiedoxygen Assess the ABG analysis Provide C-PAP using mask /hood/nasal prongs Observe for risksof C-PAP Assist in CMV with PEEP if needed
  • 97. 5. Hypothermia related toimmature thermoregulation system Monitor vitalsigns frequently Wrap the baby well and keep warm Provide small and frequent breast feeding as tolerated Look forhypoglycemia Administer IV fluids if not tolerating the feed Monitor the vital signs and blood pressure Assess the skin tone, pallor and signs of dehydration Administer IVfluids
  • 98. 6. Imbalanced nutrition less than bodyrequirement related to feeding difficulty, respiratory distress, or NPO status Assess the sucking and swallowing ability of t h e newborn Assess the tolerance of the child Monitor the blood glucose level frequently Administer IV fluids if not tolerating oral fluids Administer human milk fortifier if the child is preterm
  • 99. 7. Fatigue related to increased demand for nutrients and deterioration of the general condition of the baby Assess the general condition of the baby Assess the level of activity Monitor the blood glucose level Breast fed the baby Check for from any part of the body Provide top up feed
  • 100. 8. Risk for complications hypotension, shock, cerebral hypoxia related to progression of the disease condition Assess the vital signs, respiratory rate, pulse rate, temperature and bloodpressure Check blood culture and sensitivity and sepsis screening Monitor for any signs of dehydration Administer IV fluids or blood as necessary Assess the serum electrolyte values and ABG values Closely monitor for the early signs and symptoms o f complications
  • 101. 9. Anxiety of parents related to the outcome of the newborn condition Assess the mental status, anxiety and knowledge of family members Assess the supporting system for the family Assess the coping strategies of the family members Explain the disease process to the family members Explain each and every procedure to the care giver Provide psychological support to the family members
  • 102. 10. Interrupted mother-child bonding relatedto infectious process Assess the breast feeding ability including sucking and swallowing ability Keep the child with the mother if possible Provide frequent breast feed 2 hourly If breast feeding is not tolerated give EBM Allow the mother to visit the child Provide kangaroo mother care in case of pre term if tolerated
  • 103. 11. Interrupted family process relatedto hospitalization of thenewborn Assess the mental status, anxiety and knowledge of familymembers Encourage mother-child bonding if possible Assess the coping strategies of the family members Explain the disease process to the family members Explain each and every procedure to the care giver Allow the family members to visit the child
  • 104. 12. Knowledge deficit regarding care of the baby and treatmentmodalities Assess the knowledge level of the care giver Explain disease condition and it’s progress to t h e family members Educate regarding treatment and its prevention Educate about the monitoring of the baby Provide adequate explanation regarding nutritional need of thebaby Clarify their doubts and promote understanding
  • 105. Definition and incidence Causes of prematurity Clinical features Physiological handicaps Management Careof preterm babies Prognosis Nursing assessment Nursing diagnosis and interventions