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Premature
infant
Gestation <
38
weeks
Lanugo
covers entire back and face
Thin
,
pinkish
skin with few creases on soles and scrotum
Relaxed
posture
Postmature
infant
Gestation >
42
weeks
Abundant
hair
on scalp,
absence
of lanugo
Visible creases on
soles
Minimal fat
deposits
IUGR (Intrauterine Growth Retardation)
SGA: birth weight
below
10th percentile
LGA: birth weight
above
90th percentile, >
4000g
Causes of IUGR
Poor
nutrition
during pregnancy
Placental
defects
Age:
-18
or +
35
Maternal condition:
hypertension
, anemia,
DM
Nursing interventions for IUGR
1.
Initiation
and
maintenance
of respiration
2. Maintenance of
hydration
and normal
glucose
3.
Thermoregulation
4.
Breastfeeding
q 3-4h
5. Monitor VS, keep hydrated, assess skin
integrity
for newborns under radiant
warmers
LGA (Large for Gestational Age)
Body size is
proportionate
Poor
motor
skills
Difficulty
regulating
behavioral state
Complications of LGA
Fetal:
stillbirth
, shoulder
dystocia
Neonatal: low APGAR,
hypoglycemia
, hypocalcemia,
polycythemia
, jaundice, feeding difficulties
Long term:
obesity
,
T2
DM, neurologic/behavioral problems
Respiratory Distress Syndrome
Condition of
surfactant
deficiency and physiologic immaturity of the
thorax
, common in preterm infants
Diagnostic exams for RDS
X-ray
Blood glucose
Arterial Blood Gas Analysis
Fetal Lung Maturity Assay
Findings in
RDS
Broken glass
appearance on chest x-ray
Hypoxemia
Increased
CO2
Respiratory
acidosis
Medications for RDS
Artificial surfactant
Nitric oxide
Clinical manifestations of RDS
Tachypnea
Flaring
nares
Grunting
Dyspnea
Chest
retractions
Seesaw
respirations
Meconium Aspiration Syndrome
Aspiration
of amniotic fluid containing
meconium
, occurs primarily in full-term and post-term infants
Assessment findings in Meconium Aspiration Syndrome
Barrel-chest
Green
stains on skin, umbilical cord, and
nails
Nursing interventions for Meconium Aspiration Syndrome
1. Assist in
tracheal suctioning
2.
O2 support
,
extracorporeal membrane oxygenation
if severe
3.
Exogenous surfactant
administration
4.
IVF
administration
5. Antibiotics: Ampicillin,
Gentamicin
,
Amikacin
Sudden Infant Death Syndrome
Unexpected death of any infant
younger
than 1 year, usually during
sleep
Nursing management for SIDS
Teach parents to
avoid
smoking during/after pregnancy
Encourage
supine
or side-lying position during sleep
Avoid co-sleeping,
soft
beddings, pillows, and
blankets
in crib
Hyperbilirubinemia
Excessive bilirubin in the blood, characterized by
jaundice
Types of
hyperbilirubinemia
Pathologic Jaundice:
first 24hrs
of
life
Physiologic Jaundice: after
24hrs
of
life
Nursing interventions for hyperbilirubinemia
Phototherapy
: cover eyes and genitalia, check skin turgor, turn infants q2hrs, breastfeed
q2-4hrs
Sepsis
Infection in the
bloodstream
, can be early onset (maternal) or
late
onset (nosocomial)
Clinical manifestations of sepsis
Pallor
,
cyanosis
, mottling
Hypotension
Tachycardia
Irregular respiration
Jaundice
Dehydration
Temperature instability
Laboratory and diagnostic tests for sepsis
Blood
culture
UA
and
CSF
CBC
Erythrocyte
Sedimentation Rate and
C-reactive
Protein
Necrotizing Enterocolitis
Acute inflammatory
disease of the bowel, common in
preterm
infants
Signs and symptoms of NEC
Poor
feeding
Distended
abdomen
Blood
in
stool
Vomiting
Apnea
Nursing interventions for NEC
1. Assess for
abdominal
distention
2. Report any episode of
gastric
residuals
3. NPO as
ordered
if symptoms are observed
Newborn screening
is a procedure to determine if the newborn has heritable
congenital metabolic
disorders
G6PD
Deficiency
Lack of
enzyme
leading to
premature destruction
of RBCs and hemolytic anemia
Symptoms of
G6PD Deficiency
Jaundice
Dark colored urine
Back pain
Anemia
Complications of G6PD Deficiency
Severe
anemia
Hyperbilirubinemia
Management of
G6PD
Deficiency
Avoid
food
, drugs, and
chemicals
that cause oxidative stress
Congenital Hypothyroidism
Absence or lack of development of the
thyroid
gland, causing absence of
thyroxine
needed for metabolism and growth
Signs and symptoms of
Congenital Hypothyroidism
Short
stature
Macroglossia
Delayed closure of
fontanelles
Hypotonia
Nursing interventions for Congenital Hypothyroidism
1.
Medication
throughout child's
lifetime
2. Administration of
thyroid hormone
3.
Early
management to prevent
mental retardation
Phenylketonuria
Deficiency or absence of enzymes needed to metabolize essential amino acids like
phenylalanine
Early management of
Phenylketonuria
will prevent mental retardation or
cognitive
impairment
Goal of treatment for
Phenylketonuria
Meeting child's
nutritional
needs for
optimal growth
If left untreated,
Phenylketonuria
will result in failure to thrive, absence of
melanin
pigmentation, and unpredictable/erratic behavior
Galactosemia
Build up of
galactose
in the infant's system due to inability to fully break down the substance, which may
damage organs
Atrial Septal Defect
Hole in the wall (
septum
) that divides the upper chambers (
atria
) of the heart, causing left to right shunting
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