Download - Immediate Newborn Care
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IMMEDIATE NEWBORN CARE
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Goals: • To establish, maintain and support
respirations.
• To provide warmth and prevent hypothermia.
• To ensure safety, prevent injury and infection.
• To identify actual or potential problems that may require immediate attention.
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• Establish respiration and maintain clear airway - The most important need for the newborn immediately after
birth is a clear airway to enable the newborn to breathe effectively
• To establish and maintain respirations
1. Wipe mouth and nose of secretions after delivery of the head2. Suction secretions from mouth and nose3. A crying infant is a breathing infant. Stimulate the baby to cry if
baby does not cry spontaneously, or if the cry is weak.
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4. Oral mucous may cause the newborn, to choke, cough or gag during the first 12 to 18 hours of life. Place the infant in a position that would promote drainage of secretions
5. Keep the nares patent. Remove mucus and other particles that may be cause obstruction
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Care of the Eyes
Neisseria gonorrhea- the causative agent for gonorrhea conjunctivitis or opthalmia neonatorum, may be passed on the fetus from the vaginal canal during delivery.
Drug of choice:
- Erythromycin or tetracycline Opthalmic Ointment
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Care of the cord
•Report any unusual signs and symptoms which indicates infection.
- Foul odor in the cord- Presence of discharges- Redness around the cord- The cord remains wet and does not fall off within 7 to 10 days- Newborn fever
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It may be treated with:1. Bactericidal substance
2. Antibiotic substance
3. Alcohol (70%)
4. Cleansed with mild soap solution
5. Air dry
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ASSESS 0 1
2
HEART RATE Absent Below 100 Above 100
RESPIRATION Absent Slow Good crying
MUCLE TONE Flaccid Some flexion Active motion
REFLEX IRRITABILITY No response Grimace Vigorous cry
COLOR Blue all over Body pinkExtremities blue
Pink all over
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ASSESSING THE AVERAGE NEWBORN
Head Circumference 34 – 35 cm
Temperature 97.6 – 98.6 F axillary
Chest Circumference 32 – 33 cm
Heart Rate 120 – 140 bpm
Respirations 30 – 60 bpm
Weight 2.5 to 3.4 kg
Length 46 to 54 cm
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REMEMBER:
1. Crowning – ready for suction
2. Expulsion of head – wipe face and nose
3. Expulsion of newborn – provide warmth, take note of time and sex of baby
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4 Mechanisms of Heat Lose
1. Convection
2. Conduction
3. Radiation
4. Evaporation
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Other Means of Heat Loss:1. Insulation
2. Constriction of blood vessels and moving blood away from skin
3. Brown fat
4. Drying and wrapping newborns
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WEIGHT
Varies depending on:
1.Race2.Nutritional status3.Intrauterine factor4.Genetic factor
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REASONS for Wt.Loss1. 1st few days after birth
2. Diuresis
3. Voiding and passage of stool
4. Breastfed newborns
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Bathing
- Remove blood, amniotic fluid, and excessive vernix caseosa as soon after birth as the temperature is stable
- It decreases exposure to maternal blood and possible bloodborne organism on th infants skin
e.g. Hep.B and HIV
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Administer Vitamin KSite: Right Vastus LateralisClassification: - fat soluble vitamin - antihemorrhagic agentAction: -promotes the formation of factors II,VII,IX,X by the liver
for clottingfactor,thus prevent bleeding- Provides Vit.k which is not synthesized in the intestine
for the first 5 to 8 days after birth because the newborn lacks intestinal flora necessary for Vit.K production
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DOCUMENT birth record1. Proper identification of the newborn and footprints must be
taken and kept in the chart.2. Attach ID bracelet with a number that corresponds to the
mother’s hospital number, mother’s full name, sex, date and time of birth.
3. Inspect for the presence of 2 arteries and 1 vein.
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ASSESSMENT OF CARDIORESPIRATORY STATUS
AIRWAY
1.Respiratory rate – assess respirations at least once every 30 mins. until stable for 2 hours after birth.
Observe for:1.Periodic breathing2.Apnea
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2. Breath sounds – auscultate anterior and posterior lung fields for equal sounds
- Sounds of moisture in the lungs during the 1st hour or two after birth is NOT UNUSUAL because fetal lung fluid has not been completely absorbed.
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SIGNS OF RESPIRATORY DISTRESS1.Tachypnea – respiratory rate above 60
bpm2.Retractions – due to infant’s weak chest
wall muscles that are used to help draw air into the lungs
3. Flaring of Nares – a reflexive widening of nostrils
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4.Central cyanosis – a purplish blue discoloration due to insufficient oxygen supply ( lips,tongue,mucous membrane and trunks )
• Peripheral cyanosis (acrocyanosis) – due to poor perfusion of blood to the periphery of the body
• Bruising of face – due to tight nuchal cord or pressure during birth and may look like central cyanosis
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How to check for Cyanosis?
1. apply pressure to the area
2. use of pulse oximeter
3. Color of mucous membrane
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5. Grunting – a noise made on expiration when air crosses partially closed vocal cords
6. Seesaw respirations – when the chest falls the abdomen rises and vice versa
7. Asymmetry – decreased on one side of the lung may indicate a collapse of the lung ( atelectasis )
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Choanal atresia - Blockage of one or both nasal passages by
a narrowed bone or membrane that protrudes into the area
How to asses ?1.By closing the infant’s mouth and occluding
one nostrils at a time and observe for breathing while each nostril is occluded
2.Placing a cold metal object under the nostrils and observe for fogging
3.Passing a catheter (fr.5 or 8) thru each nostril tto check for patency
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Color 1.Pallor – indicates slight hypoxia or
anemia2.Ruddy color ( plethora) – an excessive
number of RBC ( >65%)
Heart sounds- Auscultate for rate, rhythm and
presence of murmurs or abnormal sounds
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Rhythm – should be regular , the 1st and 2nd sounds should be heard clearly, abnormalities should be noted.
Murmurs – abnormal sounds caused by abnormal blood flow through the heart and may indicate openings in the septum of the heart
- results from an incomplete transition from fetal to neonatal circulation
- is common until the ductus arteriosus functionally closed
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Brachial and Femoral Pulses- Should be present equally and bilaterally
Blood pressure- Taken on all extremities if the infant has unequal
pulses or other signs of cardiac complications
Method:1.Doppler UTZ
Average BP:Systolic – 65 – 95 mmHgDiastolic – 30 – 60 mmHg
Capillary Refill
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• Capillary Refill - assessed to help determine if
perfusion is adequate
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B. Assessment of Thermoregulation
- Temperature should be assessed at least once every 30 minutes until the infant has been stable for 2 hours after birth
Method:1.Axillary 2.Rectal
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Types of Thermometer
1.Mercurial 2.Digital 3.Disposable Plastic Strips4.Tympanic
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C. PHYSICAL ASSESSMENT
A. HEAD & NECK
Head – makes up one fourth of the length of the body and is much larger in proportion to the rest of the body
- should be palpated to assess the shape and identify abnormalities
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Note for:1.Molding – caused by overriding of the
cranial bones at the suture and is common especially a long second stage of labor
- parietal bones often override the occipital and frontal bones and a ridge can be felt at the areas
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Craniosynostosis - a hard ridged area that is not a result
of molding due to premature closure of the cranial sutures before or shortly after birth which may impair brain growth and shape
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Types:a. Single Suture Synostosis Sagittal (SAJ-
ut-ul)/ Scaphocephaly
- The sagittal suture is located on the midline, on top of the head and extends from the soft spot towards the back of the head. When the head is palpated, a ridge can be felt along the suture.
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Preoperations at age 5 months
7 months Post operation
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2. Coronal (co-RO-nul) Suture Synostosis / Plagiocephaly
- The coronal suture is located on the side of the head and extends from the soft spot to an area just in front of the ear. It allows the forehead and the frontal lobe to grow and expand forward.
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3. Metopic (mih-TOP-ick) SutureSynostosis/ Trigonocephaly- This midline suture is located in the
middle of the forehead and extends from the soft spot to the root of the nose. It allows both frontal lobes to expand forward and sideways as well as the eye socket to move to either side.
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4. Lambdoidal (lam-DOID-ul) Suture Synostosis
- Closure leads to posterior plagiocephalus (PLAY-gee-o-SEF-a-lee) with flattening of the back of the head on the affected side, protrusion of the mastoid bone and lowering of the affected ear. It may also cause the skull to tilt sideways.
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2. Fontanels – are areas of the head where sutures between the bones meet
2.1 Anterior - is a diamond shape area where the frontal and parietal bones met - Measures 2 to 4 cm - Closes between 12 to 18 months of age
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2.2 Posterior- Is a triangular area where the occipital
and parietal bones meet - Measures 0.5 to 1cm- Closes by the time the infant is 2 to 3
months
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3. Caput succedaneum- Due to the pressure against the
mother’s cervix and it interferes the blood flow in the area causing localized edema which crosses suture lines
4. Cephalhematoma- Bleeding between the periosteum and
the skull
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Face assessed for:-Symmetry -Positioning of facial features-Movement-Expression
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• Mouth assessed for:
- cleft lip/palate- Precocious teeth- Epstein’s pearl
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B. Neck and ClaviclesNeck – assess visually and note the ease with
which the head turns from side to sidee.g. Turner’s syndrome
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Turner syndrome or Ullrich-Turner syndrome (also known as "Gonadal dysgenesis") encompasses several conditions, of which monosomy X (absence of an entire sex chromosome, the Barr body) is most common. It is a chromosomal abnormality in which all or part of one of the sex chromosomes is absent (unaffected humans have 46 chromosomes, of which two are sex chromosomes). Typical females have two X chromosomes, but in Turner syndrome, one of those sex chromosomes is missing or has other abnormalities. In some cases, the chromosome is missing in some cells but not others, a condition referred to as mosaicism[2] or 'Turner mosaicism'.
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The syndrome manifests itself in a number of ways. Characteristic :1. physical abnormalities - short stature, swelling, - broad chest - low hairline - low set ears - webbed necks.[5] Girls with Turner syndrome typically
experience gonadal dysfunction (non-working ovaries), which results inamenorrhea (absence of menstrual cycle) and sterility.
2. Concurrent health concerns are also frequently present, - congenital heart - hypothyroidism (reduced hormone secretion by the thyroid) - diabetes - vision problems - hearing concerns
Turner's syndrome is named after Henry H. Turner.
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Clavicle – fracture are more likely to occur in large infants
e.g. shoulder dystocia Shoulder dystocia is a specific case of dystocia
whereby after the delivery of the head, the anterior shoulder of the infant cannot pass below the pubic symphysis, or requires significant manipulation to pass below the pubic symphysis. It is diagnosed when the shoulders fail to deliver shortly after the fetal head. In shoulder dystocia, it is the chin that presses against the walls of the perineum. Shoulder dystocia is an obstetrical emergency, and fetal demise can occur if the infant is not delivered, due to compression of the umbilical cord within the birth canal.
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Fracture – a lump or tenderness over the area
Method of Detecting:Moro Reflex – a difference in the movement of
the arm
Treatment :- Immobilization of the affected part for a short
time
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C. Cord – should contain three (3) vessels arteries – (2) - are small and may stand up at the end cut vein - (1) - is larger than the arteries and resembles a slit
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Thin cord – the infant may have been poorly nourished in uteroYellow Brown or Green tinge cord - indicates that meconium was released sometime before birthPatent urachus – abnormal connection between the umbilucus and bladderUmbilical cord hernia - "Paraumbilical Hernias" develop in and
around the area of the umbilicus (belly button or navel). - A congenital weakness (meaning present since birth)
exists in the naval area in the region where vessels of the fetal and infant umbilical cord exited through the muscle of the abdominal wall. After birth, although the umbilical cord disappears (leaving just the dimpled belly-button scar), the weakness or gap in the muscle may persist.
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D. Extremities - normally a term infant should remain sharply
flexed & resist extension during examination
Poor muscle tone – results in a limp or “floppy” infant
Continued poor muscle tone – may result from prematurity or neurologic changes
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All extremities are examines for signs of fracture:
1.Crepitus2.Redness3. Lumps or swelling4. Lack of use /immobility
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Erb-Duchenne paralysis - paralysis of the arm resulting from injury to the brachial plexus (usually during childbirth)
- Instead of the usual flexed position, the affected arm is extended at the infant’s side with the forearm prone
Treatment: - exercise - splinting or both
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A. Hands and Feet- Are examined for extra digits which are often
small and may not have bones
Nails : - in term infants it should extend to the end of
the fingers or slightly beyond
Creases :- normally, two long transverse creases extend
most of the way across the palm
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Polydactyly - is a condition in which a person has more than five fingers per hand or five toes per foot.
Syndactyly - is a condition where two or more digits are fused together. It occurs normally in some mammals, such as the siamang and kangaroo, but is an unusual condition in humans.
Syndactyly can be complete or incomplete. In complete syndactyly, the skin is joined all the way
to the tip of the finger In incomplete syndactyly, the skin is only joined part
of the distance to the fingertip.Syndactyly can be simple or complex. In simple syndactyly, adjacent fingers or toes are
joined by soft tissue. In complex syndactyly, the bones of adjacent digits
are fused. The kangaroo exhibits complex syndactyly.
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Feet – are assessed for club foot
Talipes equinovarus: The common ("classic") form of clubfoot. Talipes is made up of the Latin talus (ankle) + pes (foot). Equino- indicates the heel is elevated (like a horse's) and -varus indicates it is turned inward. With this type of clubfoot, the foot is turned in sharply and the person seems to be walking on their ankle.
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A club foot, or congenital talipes equinovarus (CTEV) is a congenital deformity involving one foot or both.The affected foot appears rotated internally at the ankle.
TEV is classified into 2 groups: 1. Postural TEV 2. Structural TEV
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2. Hips - Are examined for signs of developmental
dysplasia which occurs more often on breech presentation
- Normally both legs should abduct equally in normal infants with “click” sound while in dysplasia is a “ clunk” sound
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Dysplasia – instability of the hip joint which occurs at the head of the femur which can be moved in and out of the acetabulum
Methods of Assessing:
1. The Barlow maneuver is a physical examination performed on infants to screen for developmental dysplasia of the hip.
- It is named for T.G. Barlow, 1962 at Hope Hospital Salford,
Manchester
- The maneuver is easily performed by adducting the hip (bringing the thigh towards the midline) while applying light pressure on the knee, directing the force posteriorly. If the hip is dislocatable - that is, if the hip can be popped out of socket with this maneuver - the test is considered positive. The Ortolani maneuver is then used, to confirm the positive finding (i.e., that the hip actually dislocated).
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2. The Ortolani test or Ortolani maneuver is a physical examination for developmental dysplasia of the hip.
It is performed by an examiner first flexing the hips and knees of a supine infant to 90 degrees, then with the examiner's index fingers placing anterior pressure on the greater trochanters, gently and smoothly abducting the infant's legs using the examiner's thumbs.
A positive sign is a distinctive 'clunk' which can be heard and felt as the femoral head relocates anteriorly into the acetabulum:
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This is part of the standard infant exam performed preferably in early infancy; it usually becomes negative after 2 months of age.
It is named for Marino Ortolani, who developed it in 1937.[3
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3. Vertebral Column
- palpate the entire length of the newborn’s vertebral column to discover any defects in the vertebrae.
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Check for:
Spina bifida - (Latin: "split spine") is a developmental congenital disorder caused by the incomplete closing of the embryonic neural tube. Some vertebrae overlying the spinal cord are not fully formed and remain unfused and open. If the opening is large enough, this allows a portion of the spinal cord to protrude through the opening in the bones. There may or may not be a fluid-filled sac surrounding the spinal cord.
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Other neural tube defects:
1. anencephaly, a condition in which the portion of the neural tube which will become the cerebrum does not close,
2. encephalocele, which results when other parts of the brain remain unfused.
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Classification:
1. Spina bifida occulta
Occulta is Latin for "hidden". This is the mildest forms of spina bifida.
In occulta, the outer part of some of the vertebrae are not completely closed. The split in the vertebrae is so small that the spinal cord does not protrude. The skin at the site of the lesion may be normal, or it may have some hair growing from it; there may be a dimple in the skin, or a birthmark.
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2. Spina bifida cystica In spina bifida cystica, a cyst protrudes through
the defect in the vertebral arch. These conditions can be diagnosed in utero on the basis of elevated levels of alpha-fetoprotein, after amniocentesis, and by ultrasound imaging. Spina bifida cystica may result in hydrocephalus and neurological deficits.
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3. Meningocele- The least common form of spina bifida is a
posterior meningocele (or meningeal cyst).
- In a posterior meningocele, the vertebrae develop normally, however the meninges are forced into the gaps between the vertebrae. As the nervous system remains undamaged, individuals with meningocele are unlikely to suffer long-term health problems
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- A meningocele may also form through dehiscences in the base of skull. These may be classified by their localisation to occipital, frontoethmoidal, or nasal. Endonasal meningoceles lie at the roof of the nasal cavity and may be mistaken for a nasal polyp. They are treated surgically.
- Encephalomeningoceles are classified in the same way and also contain brain tissue.
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4. Myelomeningocele- In this, a serious and common form, the unfused
portion of the spinal column allows the spinal cord to protrude through an opening. The meningeal membranes that cover the spinal cord form a sac enclosing the spinal elements.
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Nsg. Responsibility1.The protruding tissue should be covered with moist sterile saline
dressing immediately after birth
2. Intravenous antibiotics are started to prevent meningitis.
3. An adhesive plastic surgical field drape taped over the buttocks deflects feces away from the back--"mud flap.“
4. The most important words to say at the baby's birth are: "Congratulations on the birth of your child!" These words extend joy, optimism, reverence, respect, acceptance, and nonabandonment. This simple step facilitates parental interest, learning, and care provision.
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D. Assessment of Body Systems
I. Neurologic system
a. Reflexes - assessment of the presence and strength of the
reflexes is important to determine the health of the newborns central nervous system
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Moro reflex – is the most dramatic reflex - startle reflex or infantile reflex - It may be observed in incomplete form in premature birth after the 28th week of gestation, and is usually present in complete form by week 34 (3rd trimester) - It is normally present in all infants/newborns up to 4 or 5 months of age, and its absence indicates a profound disorder of the motor system
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An absent or inadequate Moro response on one side is found in infants with :
- hemiplegia,- brachial plexus palsy- fractured clavicle.
Persistence of the Moro response beyond 4 or 5 months of age is noted only in infants with severe neurological defects.
* It was discovered and first described by Austrian pediatrician Ernst Moro (1874-1951).
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• The primary significance of this reflex is evaluating integration of the central nervous system (CNS), and it involves 3 distinct components:
• spreading out the arms(abduction) - the reflex is initiated by pulling the infant up
from the floor and then releasing him; • unspreading the arms (adduction) - spreads arms and pulls arms in• crying (usually)
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Palmar Grasp reflex - a flexion of the fingers caused by stimulation of the palm of the hand. The reflex is present at birth and usually disappears by 6 months of age.
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Plantar Grasp reflex - a reflex characterized by the flexion of the toes when the sole of the foot is stroked gently. It is present in babies at birth but should disappear after 6 weeks.
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Babinski reflex - is obtained by stimulating the external portion (the outside) of the sole. The examiner begins the stimulation back at the heel and goes forward to the base of the toes.
- Most newborn babies are not neurologically mature and therefore show a Babinski response - A Babinski response in an older child or adult is abnormal. It is a sign of a problem in the (CNS), most likely in a part called the pyramidal tract.
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Rooting reflex - A reflex in infants in which rubbing or scratching about the mouth causes the infant to turn its head toward the stimulus.
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Sucking reflex - sucking movements of the lips of an infant elicited by touching the lips or the skin near the mouth.
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Stepping reflex - movements of progression elicited when the infant is held upright and inclined forward with the soles of the feet touching a
flat surface.
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Tonic Neck reflex - extensions of the arm and sometimes of the leg on the side to which the head is forcibly turned, with flexion of the contralateral limbs;
seen normally in the newborn.
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II. Sensory Assessment
A. Ears
assessed for :1. Placement 2. Appearance3. Maturity
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Expected findings:* Loud noise elicits Startle Reflex
* Flexible pinna with cartilage present* Pinna top on horizontal line with outer
canthus of eye
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Common variations:
* Skin tags on or around ears
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Signs of potential distress or deviations from expected findings:
• Ear placement low• Clefts present• Malformations• Cartilage absent• Preauricular sinus
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b. Eyes
Expected findings:• Slate gray or blue eye color• No tears• Fixation at times - with ability to follow objects to
midline• Red reflex• Blink reflex• Distinct eyebrows• Cornea bright and shiny• Pupils equal and reactive to light
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Common variations:* Edematous Eyelids
* May focus for a few seconds* Uncoordinated movements
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Signs of potential distress or deviations from expected findings:
• Discharges• Opaque lenses• Absence of Red Reflex• Epicanthal folds in newborns not of Oriental descent• Reflexes absent• "Doll's Eyes" Reflex (beyond 10 days of age):
When the head is moved slowly to the right or left, the eyes do not follow nor adjust immediately to the position of the head. This reflex should not be elicited once fixation is present. The persistence of the Doll's Eyes Reflex suggests neurologic damage.
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Chemical conjunctivitis
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* Subconjunctival hemorrhage
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Causative Agent:
1.Staphylococcus2.Chlamydia gram (-) bacteria3.Neisseria gonorrhoea
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Assessment on hepatic system
A.Newborns with hypoglycemia- a medical condition referred to as
neonatal hypoglycemia- have low levels of blood sugar in the
first days following birth. - Sugar levels in newborns may drop for a
number of reasons, including elevated insulin levels, decreased glycogen levels, low glucose production or overuse of glucose stores.
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Signs:1. Irritability – high pitched cry2. Lethargy3. Seizure / jitteriness4. Sweating 5. Poor sucking6. Respiratory distress : - Tachypnea- Dyspnea- Apnea7. Discoloration / Cyanosis8. Poor appetite9. Excessive drowsiness
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Causes of Hypoglycemia:1.Maternal diabetes2.Prematurity3.Infection / Illness4.Intrauterine growth retardation (IUGR)
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Blood Sugar Level in Newborns- should remain above 40 milligrams per
deciliter, or mg/dL. • Levels below 35 mg/dL indicate severe
hypoglycemia• levels under 50 mg/dL warrant close
observation. • A level between 54 and 72 mg/dL indicates
a more normal newborn blood glucose• At-risk infants need blood glucose
monitoring within the first two hours after birth.
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Treatment• If the baby can eat and the blood glucose
level is not too low, giving formula, sugar water or breast milk will raise blood glucose levels in most cases.
• Babies who can't eat or those with very low blood glucose levels need intravenous infusion of dextrose, a type of sugar, to raise their blood sugar.
• Infants receiving glucose infusions may develop temporary hyperglycemia, or blood glucose levels over 125 mg/dL, which usually requires no treatment,
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Prevention
- At-risk infants require blood glucose screening via heel stick or from blood drawn from a central umbilical line.
- The baby may need frequent blood tests in the first 12 hours after birth to ensure that levels don't drop.
- Hypoglycemia most often develops within the first 24 hours after birth,
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B. Newborn Jaundice• Jaundice is a yellow discoloration of the skin
and the white part (the sclera) of the eyes. It results from having too much of a substance called bilirubin in the blood.
• Bilirubin is formed when the body breaks down old red blood cells. The liver usually processes and removes the bilirubin from the blood.
• Jaundice in babies usually occurs because their immature livers are not efficient at removing bilirubin from the bloodstream.
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Causes:
• Jaundice in newborns most commonly occurs because their livers are not mature enough to remove bilirubin from the blood. Jaundice may also be caused by a number of other medical conditions.
1. Physiologic jaundice is the most common form of newborn jaundice
2. Neonatal jaundice will be seen in cases of maternal-fetal blood type incompatibility
3. hemolysis
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4. Polycythemia
5. Cephalohematoma
6. Sometimes a baby swallows blood during birth
7. A mother who has diabetes
8. Crigler-Najjar syndrome
9. Lucey-Driscoll syndrome
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• Carotenemia - A condition that causes a yellowish discoloration of the skin and tends to be a darker orange than seen with jaundice.
• Eating a lot of yellow vegetables causes this condition.
• Children with carotenemia have normal bilirubin levels.
• Unlike jaundice, carotenemia does not cause a discoloration of the white part of the eyes.
• This condition causes no harm and requires no treatment.
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Symptoms:• As a baby's bilirubin levels rise: jaundice moves from the head to include the arms, trunk,
and finally the legs. • bilirubin levels are very high : a baby will appear jaundiced below the knees and on the
palms of his or her hands.
How to Assess?- One easy way to check for jaundice is to press a finger
against your baby's skin, temporarily pushing the blood out of it. Normal skin will turn white when you do this, but jaundiced skin will stay yellow.
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• Exams and Tests Before a baby can be treated, the exact
cause of an infant's jaundice must be determined. In some cases, a careful examination by a pediatrician is all that is needed. In other cases, blood tests may be required.
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• Laboratory Tests:1. First, the total serum bilirubin level will be
checked. Based on this test, the doctor may request that more tests be done.
2. A Coombs test checks for antibodies that destroy an infant's red blood cells.
3. A complete blood count may be done. 4. A reticulocyte count checks to be sure your
baby is making enough new red blood cells.
5. Certain red blood cell diseases are found in people of Mediterranean descent. In such cases, it may be necessary to check blood samples for a condition known as G6PD deficiency.
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Treatment• Self-Care at Home
* Sunlight helps to break down bilirubin so that a baby's liver can process it more easily.
– Placing a child in a well-lit window for 10 minutes twice a day is often all that is needed to help cure mild jaundice. Never place an infant in direct sunlight.
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• If the bilirubin level is too high, the child may need to be placed under a special type of light.
This treatment is called phototherapy - These lights are able to penetrate a baby's skin
and affect the bilirubin within the child. The light changes bilirubin into lumirubin, which is easily handled by the baby's body.
• If an infant's bilirubin levels are very high or if the child appears ill, the baby will most likely be admitted to the hospital for treatment.
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Assessment in gastrointestinal system
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Assessment on endocrine system
• The endocrine glands are considered better organized than other systems. Disturbances are most often related to maternally provided hormones (estrogen, luteal, and prolactin) that may cause the following conditions:
a. Vaginal discharge and/or bleeding may occur in female infants.
b. Enlargement of the mammary glands may occur in both sexes
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Physical Assessment—Genitourinary System
• Important to note that infant is voiding• Keep record of number of voiding
A. Male infants• Assess for descended testicles.• Care following circumcision• Care of the uncircumcised infant
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B. Female infants• Labia may be swollen.• May have blood-tinged discharge.• Teach per-care.
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Integumentary systemSKIN – is fragile and shows marked easily
especially for infants with fair color
Nsg. Responsibility:1.Must examine every inch of the skin
surface carefully during the initial assessment and at the beginning of the shift.
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ASSESS for:1.Harlequin coloration- a clear color division over the body from the
head to the abdomen with one half deep pink or red and the other half pale or of normal color
- indicate shunting of blood with cardiac problems or sepsis. Redness may occur on the lower side when the infant lies on the side
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2. Mottling (cutis marmorata)- Is a lacy pattern from dilated blood vessels
under the skin
May be a sign of:- Cold stress- Overstimulation- Sepsis
- - if persistent, may indicate chromosomal abnormality
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3. Vernix caseosa- A thick ,white substance that resembles
cream cheese- Provides a protective covering for the fetal
skin in utero
4. Lanugo - Fine hair that covers the fetus during
intrauterine life
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5. Milia- Are white cysts, 1-2 mm in size resulting
from distention of sebaceous glands that are not yet functioning properly
6. Erythema toxicum- A red, blotchy areas that may have white
or yellow papules or vesicles in the center- Commonly called as fleabite or newborn
rash
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7. Birthmarks- Assess the size and location and should be
carefully documented
7.1 Mongolian spots – are bluish-black marks that resembles bruises
- Usually found in sacral area but may appear in arm andshoulder
7.2 Nevus simplex – also called salmon patch, stork bite or
telangiectatic nevus - a flat, pink or reddish discoloration from capillaries that
occur over the eyelids, just above the bridge of the nose or at the nape of the neck.
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7.3 Nevus flammeus (port-wine stain) - is a permanent, flat dark, reddish-purple mark
and varies in size, location and blanches minimally or not at all with pressure.
- located over the forehead and eyelid and may be associated with Sturge-Weber syndrome
7.4 Nevus Vasculosus (strawberry hemangioma) - consists of enlarged capillaries in the outer layer
of the skin - is a dark red and raised with a rough surface
giving a strawberry like appearance
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7.5 Café-au-lait spots - are permanent,light brown areas that may occur
anywhere on the body. Although harmless, the number and size are important.
8. Markings from Delivery
8.1 Petechiae – pinpoint bruises that resembles a rash, may appear over areas such as the back, face and groin
- due to increase intravascular pressure during the birth process such as in nuchal cord
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8.2 Bruises – may occur on any part of the body where pressure occurred during delivery especially when second-stage labor was difficult
8.3 Small puncture mark – is present on the newborn’s head if a fetal monitor scalp electrode was attached
8.4 Forceps mark – occurs over the checks and ears where the instrument applied
- size and location are carefully documented, lack of movement or asymmetry of the face may indicate injury of the facial nerve
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Breasts – note the placement of the nipple and look for extra nipples which may appear on the chest or axilla
Hair and Nails – hair should be silky and soft - nails come to the end of finger or beyond
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ASSESSMENT OF GESTATIONAL AGE- Is an examination of the newborn’s physical and
neurological characteristics to determine the number of weeks from conception to birth
TOOLS:1.DUBOWITZ SCORING- is an in-depth, detailed
assessment tool that includes examination of physical, neurological and behavioral; characteristics
1.NEW BALLARD SCORE- focuses on physical and neuromuscular characteristics, eliminating the behavioral
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I. Neuromuscular Characteristicsa. Posture – posture and degree of flexion of the
extremities are scoredb. Square Window- is elicited by bending the hand at the
wrist until the palm is as flat against the forearm as possible with gentle pressure
c. Arm recoil – nurse hold the neonates arms fully flexed at the elbows for 5 seconds, then extends the am by pulling the hands straight down to the sides and released quickly and the degree of flexion is measured
d. Popliteal Angle – newborns lower leg is folded against the thigh, with the thigh on the abdomen the lower leg is straightened just until resistance is met
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e. Scarf Sign – the nurse grasps the infant’s head and brings the arm across the body to the opposite side, keeping the shoulder flat on the bed and the head in the middle of the body
f. Heel to Ear – the nurse gasps the infants foot and pulls it straight up alongside the body toward the ears while the hips remain flat on the bed surface
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II. Physical Characteristicsa. SkinAssessed for:- Color- Visibility of veins- Peeling and cracking
b. Lanugo – appears at 20 wks of gestation and increases in amount until 28 wks and begins to disappear until little is left
c. Plantar Surface- begins to appear at 32 wks of gestation although the creases are only red lines near to toes at first, they gradually spread down toward the heal and become deeper
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d. Breasts Assess:- Nipple- Areola- Size of breast bud
e. Eyes and EarsEyes- are fused until 26 to 28 weeks of gestationEars – the incurvation and thickness of pinna rated
f. GenitalsAssess:(Female)- Size of clitoris- -labia majora and minoraMale: location of testes and rugae of scrotum
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THANK YOU!!!!!!!!!!!
and
GOD BLESS U