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Disorder Description Causes Signs and Symptoms Management: Preterm
Disorder Description Causes Signs and Symptoms Management: Preterm
overproduction of
nutrients and
Macrosomia
growth hormone in
BW above the Assess infant’s HR
LARGE FOR the utero
90th percentile on Assess for
GESTATIONAL AGE obese women
the intrauterine hypoglycemia in the
multiparty
growth chart early hours of life
beckwith-
Wiederman
Syndrome
sonogram
born after 41st
POST TERM INFANT CS Birth
week of
pregnancy Follow up care
Non-stress test
RESPIRATORY hyaline premature Subtle signs: surfactant
DISTRESS SYNDROME membrane newborns decrease body replacement
disease newborn with temp. oxygen
MAS Nasal flaring administration
sepsis cyanotic mucous Ventilation
pneumonia membrane Nitric Oxide- potent
newborn who is sternal and vascular dilator
slow to transition subcostal Extracorpureal
to extrauterine life retractions membrane
heart failure (dec. oxygenation
I/O and edema) Supportive care
Pale gray skin
Periods of apnea
Bradycardia
Pneumothorax
the respiratory
rate doesn’t slow mild retractions close observation
as a result of a and some nasal mild glucosteroid to
TACHYPNEA delayed
CS birth flaring reduce respiratory
absorption of
alveolar fluid in difficulty feeding tract inflammation
the lungs
SUDDEN INFANT sudden unexplained Occur at high rates Autopsy reveals parents counseling
DEATH SYNDROME death in infancy adolescents mother petechiae in the
infants of closely lungs and mild
spaced pregnancies inflammation and
congestion in the
underweight and respi tract
preterm infants
Possible contributing
factors:
sleeping prone
rather than supine
viral respi or
botulism infx
exposure to
secondary smoke
Pulmonary edema
Home apnea
monitoring used for
characterized by a
noticeable color this high-risk infant
APPARENT LIFE change, some during sleep to alert
apnea
THREATENING EVENT degree of apnea the parents of any
and decreased apnea episodes
tone cardiopulmonary
resuscitation
the term
hemolytic is latin
for destruction Exchange
(lysis) of RBC Transfusion
Rh Incompatibility Rising anti-Rh
present when initiation of early
ABO tiler in woman
HYPERBILIRUBINEMIA there is occlusive feeding (bowel
Incompatibility during pregnancy
destruvtion of peristalsis)
RBC, which leads Phototherapy
to elevated
bilirubin levels
caused by
immature retinal
vasoconstriction
BV constrict when
of immature
exposed to high Cryosurgery/ Laser
retinal BV
RETINOPATHY O2 concentration therapy
PREMATURITY (ROP) acquired ocular
Blood PO2 levels Secure oxygen
disease that leads
rise to higher than saturation levels
to partial or total
100 mmHg
blindness
Ophthalmia is an eye infection The most The conjunctivae If gonococci are identified, intravenous
Neonatorum that occurs at birth common become fiery red, with ceftriaxone (Rocephin) and penicillin are
or during the first causative thick pus. effective drugs.
month organisms are The eyelids are If chlamydia is identified, an ophthalmic
(MacDonald, Neisseria edematous solution of erythromycin is used.
Mailman, & Desai, gonorrhoeae In addition to systemic antibiotic therapy,
2008). and Chlamydia the eyes are irrigated with sterile saline
trachomatis. solution to clear the copious discharge.
The mother of the infected infant needs
treatment for gonorrhea or chlamydia,
before fallopian tube sterility or pelvic
inflammatory disease results
Sexual contacts of the mother should be
treated also
Prevention
The prophylactic instillation of
erythromycin ointment into the eyes of
newborns prevents both gonococcal and
chlamydial conjunctivitis.
Hepatitis B virus contact with infected Liver cancer Routinely vaccinated at birth
(HBV) can be vaginal blood at birth Administered immune serum globulin
transmitted to the when the mother is (HBIG) within 12 hours of birth to
newborn through positive for the virus decrease the possibility of infection.
Hepatitis B Virus
contact with (HBsAg%). The infant should be bathed as soon as
Infection
infected vaginal possible after birth to remove HBV-
blood at birth when infected blood and secretions.
the mother is
positive for the
virus (HBsAg%).
A herpes simplex Contracted Infants has vesicles An antiviral drug such as Acyclovir
virus type 2 (HSV- from the covering the skin. (Zovirax), a drug that inhibits viral
2) infection, most vaginal Neurologic Damage deoxyribonucleic acid synthesis, is effective
prevalent among secretions of a Loss of appetite, low- in combating this overwhelming infection.
women with mother who grade fever, and Cesarean Birth
multiple sexual has active lethargy. Stomatitis Infants with an infection should be
Generalized partners, can be herpetic (ulcers of the mouth) or separated from other infants.
Herpes virus contracted by a vulvovaginitis
Infection
a few vesicles on the Health care personnel who have herpes
fetus across the at the time of skin appear. (Day 4-7) simplex infections should not care for
placenta if the birth. Dyspnea newborns until the lesions are crusted.
mother has a Jaundice Urge a woman who is separated from her
primary infection Purpura newborn at birth to view her infant from the
during pregnancy nursery window and participate in planning
Convulsions
Shock care to aid bonding.
Human Caused by
Immunodeficienc placental
y Virus Infection transfer or
direct contact
with maternal
blood during
birth.
Alcohol Intake Alcohol crosses the Possible problems at birth All pregnant women are advised to avoid
placenta in the same Prenatal and postnatal alcohol intake to prevent any teratogenic
concentration as is growth restriction; effects on their newborn
present in the maternal central nervous system
bloodstream. This involvement such as
results in fetal alcohol cognitive challenge,
exposure and fetal microcephaly, and
alcohol syndrome cerebral palsy; and a
distinctive facial
feature of a short
An Infant With palpebral fissure and
Fetal Alcohol thin upper lip.
Exposure Neonatal Period
Tremulous, fidgety, and
irritable and may
demonstrate a weak
sucking reflex.
Sleep disturbances
Long term effect:
Cognitive challenge
Hyperactivity
Growth Deficiencies
Disorders of the Skeletal System
Disorder Description Causes Signs and Symptoms Management
1. Absent or Absence or Congenital skeletal disorders may Absent or malformed upper Fitted with a prosthesis early in life
result from reasons such as: Children will have better function if malformed
maternal drug ingestion portion is amputated before prosthesis is fitted
malformity of the
virus invasion during pregnancy Lower extremity: prostheses are fitted as early as 6
Malformed upper and/or lower and/or lower extremities or
amniotic band formation in months; gait training
Extremities extremities or fingers fingers or toes
utero Upper extremity: prostheses are fitted at 6 mos
or toes.
In most instances, the cause of Encourage positive outlook in life
anomaly cannot be established. Rehabilitation
Passive stretching exercises
Infant holds the head tilted
Lying the infant on a flat surface & rotating the
to the side of the muscle
head through a full ROM
Occurs as a congenital anomaly involved; the chin rotates to
Encourage infant to look in the direction of the
when sternocleidomastoid the opposite side.
affected muscle by:
Torticollis is a term muscle is injured & bleeds Becomes evident only as the
Feeding
2. Torticollis (Wry derived from tortus during birth original hemorrhage recedes
Placing a mobile on child’s crib
Neck) (twisted) and collum Tends to occur in NBs w/ wide and fibrous contraction
Speaking to and handing objects to the child
(neck). shoulders when pressure is occurs at 1 to 2 months of
If it still exists at 1 y/o: surgical correction followed
exerted on the head to deliver age.
by a neck immobilizer
the shoulder A thick mass over the muscle
Adults w/ spastic torticollis: botulism (Botox)
can usually be palpated at
injections (not recommended or necessary for
this time.
most infants)
Surgical Procedures:
Ravitch: Surgeon removes abnormal cartilage &
ribs, fractures sternum, and places a support
Indentation of the
system in the chest to hold it in the proper
lower portion of the
3. Pectus Children usually are born with this position. Typically used for 14 to 21 y/o.
sternum. As a result, Depression in the chest (in
Excavatum condition, but they may also Nuss: More recent, less invasive. Using small
lung volume the sternum area)
(Funnel or develop it after chronic obstructive incisions, surgeon inserts a curved metal bar to
decreases and heart Lower ribs might flare out
Sunken Chest) lung disease or rickets. push out the sternum & ribs, helping reshape
is displaced to the
them. A stabilizer bar is added to keep it in
left.
place. The chest is permanently reshaped in 3
years and both bars are surgically removed.
Procedure can be used with age 8 and older.
4. Craniosynostosis Premature closure of May occur in utero or early in Sagittal suture line closes Continuous measurement of head circumference
the sutures of the infancy because of rickets or prematurely: child’s head on children age 2 years or younger
skull. The posterior irregularities of calcium or tends to grow anteriorly and If sagittal suture line: Careful observation
posteriorly.
phosphate metabolism Coronal suture line fuses
fontanelle normally Also occurs as a dominantly early: orbits of eyes become
closes at 2 months of inherited trait misshapen, and the
If coronal suture line: Surgically open to prevent
age, the anterior Occurs ore often in boys increased ICP may lead to
brain compression & an abnormally shaped head
fontanelle at 12 to Premature close of coronal exophthalmos, nystagmus,
18 months. suture line is associated with papilledema, strabismus, and
syndactyly atrophy of optic nerve w/
consequent loss of vision.
Stunted arms and legs
Failure of bone Head appears abnormally
growth inherited as a large (because this grows
dominant trait. It normally); prominent
Children may be prescribed growth hormone to
5. Achondroplasia causes a disorder in forehead & flattened bridge
Epiphyseal bones can’t produce increase their ultimate height or, although
or cartilage prod. in of nose
adequate cartilage for longitudinal controversial, leg lengthening may be possible.
Chondrodystro- utero. Women will Thoracic kyphosis (outward
bone growth. Encourage positive outlook in life
phia have difficulty w/ curve) and lumbar lordosis
Continued guidance or counseling
childbearing because (inward curve) of the spine
of a small pelvis, may develop
necessitating a CS. Rarely reach a height of
more than 4 ft 6 in (140 cm)
6. Talipes Disorders Latin words talus Occurs more often in boys Shoe size may vary as much Make a habit of straightening all NB feet to the
(ankle) & pes (foot). Probably inherited as a as two shoe sizes midline as part of initial assessment
These are ankle–foot polygenic pattern child may have asymmetry of Cast is applied while the foot is placed in an
disorders, aka Usually a unilateral problem leg length overcorrected position; cast extends above knee to
clubfoot. 4 types: Some have a pseudo-talipes Pseudo-talipes: foot looks ensure firm correction; casts must be changed
a) plantarflexion disorder d/t intrauterine turned in but can be brought almost every 1 or 2 wks; after approx. 6 wks (time
(an equinus or position into a straight position by varies depending on extent of problem), final cast
“horsefoot” manipulation is removed
position; True talipes: foot cannot be Change diapers freq. to prevent a wet diaper from
forefoot lower properly aligned without touching the cast and causing it to become soaked
than heel) further intervention w/ urine or meconium
b) dorsiflexion (heel Review w/ parents how to check infant’s toes for
is lower than coldness/blueness & how to blanch a toenail bed
forefoot or and watch it turn pink to assess for good circulation
anterior foot is
flexed toward
anterior leg)
c) varus deviation
Since NB cannot report pain except by crying,
(foot turns in)
crying episodes must be evaluated carefully
d) valgus deviation
After removal of cast: perform passive foot
(foot turns out)
exercises; infant may have to sleep in Denis Brown
Most children have a
splints (shoes attached to a metal bar to maintain
combination or an
position) or a high-top shoes at night for a few mos
equinovarus or a
Surgery can also be done
calcaneovalgus
disorder (child walks
on the heel w/ foot
everted)
Subluxated hip: femur “rides
Idiopathic up” d/t flat acetabulum
May be from a polygenic Dislocated hip: femur rides
inheritance pattern so far up that it actually
May also occur from a uterine leaves the acetabulum
Positioning the hip into a flexed, abducted
position that causes less-than- Sometimes affected leg may
(externally rotated) position to press the femur
usual pressure of the femur appear slightly shorter than
7. Developmental head against the acetabulum and cause it to
Improper formation head on the acetabulum the other bec. femur head
Hip Dysplasia / deepen its contour by the pressure
& function of the hip Occurs most often in children rides so high in the socket.
Congenital Hip Splints, halters, or casts may be used
socket of Mediterranean ancestry This is most noticeable when
Dysplasia Those who do not achieve correction by these
Found 6x more in girls, possibly child is supine and thighs are
methods will have surgery and a pin inserted to
because hips are more flaring flexed to a 90° angle toward
stabilize the hip
in females & possibly because abd. One knee will appear to
maternal hormone relaxin be lower than the other.
causes pelvic ligaments to be Subluxated or dislocated hips
more relaxed are best assessed by noting
whether the hips abduct