HIGH RISK NEWBORN & FAMILY
ASSESSMENT NURSING
HISTORY PHYSICAL ASSESSMENT DIAGNOSTIC
ASSESSMENT Obvious
congenital anomalies Gestational age
IMMEDIATE NEEDS OF THE NEWBORN
AIRWAY 2. BREATHING 3. CIRCULATION 4. WARMTH 1.
Immediate Assessment of the Newborn
The newborn infant should undergo a complete P.E within 24 hours of birth. NOTE
:
It
is easier to listen to the heart and lungs first when the infant is quiet
Warmth
the stethoscope before using to decrease the likehood of making the infant cry
Newborn Priorities in first day of life 1. 2. 3. 4. 5. 6. 7. 8.
Initiation and maintenance of respiration Establishment of extrauterine circulation Control of body temperature Intake of adequate nourishment Establishment of waste elimination Prevention of infection Establishment of an infant-parent relationship Developmental care or care that balances physiologic needs and stimulation for best development
DIAGNOSIS Ineffective
airway clearance Ineffective cardiovascular tissue perfusion Ineffective thermoregulation Risk for imbalance of nutrition Risk for parenting Deficit diversional activity (lack of stimulation)
Planning/Implementation
ALTERED GESTATIONAL AGE OR BIRTHWEIGHT Infant
is evaluated as soon as possible after birth to determine : Weight Gestational
Birthweight Colorado
age
is plotted on a Growth Chart
intrauterine Growth Chart ( LUBCHENCO CHART)
Pre
term – born before the 38th week
Full
term – born at 38 to 42 weeks
Post
term – born after 42 weeks
BIRTHWEIGHT
Appropriate Gestational Age (AGA) – BW within 10-90th percentile Small Gestational Age (SGA) – BW is < 10th percentile Large Gestational Age (LGA) – BW > 90th percentile
LBW – BW < 2,500 grams VLBW – BW 1000-1,500 grams Extremely-VLBW – 500-1000g
GESTATIONAL AGE It
is determine in the first 4 hours after birth so that age related problems can be identified and appropriate care can be initiated. Second assessment is done within 24 hours. New ballard Score is the most commonly used tool
It has 2 element External physical characteristics Neuromuscular maturity
GESTATIONAL ASSESSMENT (DUBOWITZ) FINDING
0 – 36
37 – 38
39 & OVER
SOLE CREASES ANTERIOR
OCCASIONAL CREASES IN ANTERIOR 2/3
SOLE COVERED W/ CREASES
BREAST NODULE 2 DIAMETER (MM)
4
7
SCALP HAIR
FINE & FUZZY
FINE & FUZZY
COARSE & SILKY
EAR LOBE
PLIABLE, NO CARTILAGE
SOME CARTILAGE
STIFFENED BY THICK CARTILAGE
TESTES & SCROTUM
TESTES IN LOWER CANAL, SCROTUM SMALL, RUGAE
SOME CARTILAGETESTES PENDULOUS, INTERMEDIATE
TRANSVERSE CREASE ONLY
SCROTUM FALL, EXTENSIVE RUGAE
posture
Square window
Popliteal angle
Scarf sign
Heel to ear
creases
Breast
Causes of Small –for-Gestational-Age Infant ( SGA)
SGA infant experienced intrauterine growth restriction (IUGR) Most common cause of IUGR is PLACENTAL ANOMALY Mother’s nutrition during pregnancy play a major rule in fetal growth. severe DM mother PIH Mother who smokes heavily Use of narcotics Baby with Rubella & chromosomal abnormality
SGA PRENATAL
ASSESSMENT:
Fundic
height ultrasound Biophysical profile NST Placental
grading Amniotic fluid amount
What do they look like??? SGA
appearance
Infant
suffer nutritional deprivation
EARLY in pregnancy
Increase in number of body cells Below average Weight, length & head circumference
Late
in Pregnancy
Increase in cell size Below average weight
Most SGA APPEAR LIKE?? Wasted
appearance Small liver Poor skin turgor Large head Skull suture widely separated – lack of normal bone growth Dull hair Sunken abdomen Cord dry & stained yellow
Common problem of SGA Birth
asphyxia – common problem
Underdeveloped
chest muscles
Risk
of meconium aspiration syndrome due to anoxia during labor.
Lack
of subcutaneous fat
Less
able to control body temperature
DIAGNOSTICS CBC High
hematocrit Increase RBC ( polycythemia) Blood
glucose
Hypoglycemia
<40mg/dl
Outcome Evaluation: Gain
weight & height – end of first year Discuss ways to parents to promote infant development. Needs adequate stimulation to reach normal growth & developmental milestone Encourage
parents to provide suitable toys as per chronological age not physical size.
LARGE-for-Gestational-Age Infant (LGA)
LGA Macrosomia
– above 90th percentile on an intrauterine growth chart for that gestational age CAUSES: Overproduction
of growth hormone in utero Infant with DM mother Obese mother Multiparous women
LGA Assessment: Uterus
unusually large for the date of pregnancy UTZ , NST amniocentesis for lung maturity
LGA appearance Immature
reflexes Skin color ecchymosis, jaundice & erythema Low score on Gestational age examination Extensive bruising & birth injury Broken clavicle Erb-Duchenne paralysis – cervical nerve injury
Prominent
caput succedaneum, cephalhematoma or molding
LGA - DIAGNOSTICS Increase
serum bilirubin hypoglycemia
LGA – outcome evaluation Infant
need careful watching Encourage parents to nurture infant
PRETERM INFANT
Preterm infant Live-born
infant born before the end of 37 weeks of gestation Weight less than 2,500 ( 5lbs 8 oz ) Immature and small but well proportioned for age
PRETERM High
Risk for :
Respiratory distress syndrome (RDS) Hypoglycemia Intracranial hemorrhage
Mortality
: 80-90% CAUSES: Exact cause : rarely known Low socioeconomic- inadequate nutrition Lack of prenatal care Age of mother – younger than age 20 PROM
PRETERM POTENTIAL Anemia
COMPLICATION:
of prematurity Kernicterus PDA Intraventricular/Periventricular Hemorrhage RDS – HMD Apnea Necrotizing enterocolitis Retinopathy of prematurity
Management 1. 2. 3. 4. 5. 6.
Maintain patent airway Incubator care VS monitoring O2 therapy Feeding Infection precautions
Preterm
infant
Nutrition Feeding
schedule Gavage feeding Formula Breast milk
ILLNESS IN THE NEWBORN
ILLNESS IN THE NEWBORN 1. 2. 3. 4. 5. 6. 7.
RDS TRANSIENT TACHYPNEA OF THE NB MECONIUM ASPIRATION SYNDROME APNEA SUDDEN INFANT DEATH SYNDROME HEMOLYTIC DISEASE OF THE NB HEMORRHAGIC DISEASE OF THE NB
Respiratory distress syndrome
2 types 1. 2.
Hyaline membrane disease(HMD) Transient tacypnea of the NB (TTN)
Respiratory distress syndrome >HMD( hyaline membrane disease)
Common:1. preterm infant 2.infant of diabetic mother 3.meconium aspiration
Pathologic feature :
hyaline-like membrane formed fr an exudate of infant blood line the terminal bronchioles, alveolar.duct,and alveoli this membrane prevent exchange of O2 and CO2 at alveolar-capillary membrane
RDS Causes: Low
level or absence of surfactant
Surfactant
–
phospholipid lines the alveoli that reduces surface tension on expiration keep the alveoli from collapsing on expiration Form @ 34 wks AOG
Assessment S/Sx:
initial 1.low body temperature 2.nasal flaring 3.sternal and subcostal retraction 4.tachypnea 5. cyanotic mucus membrane
Assessment S/Sx:
late 1. seesaw respiration 2. heart failure 3. pale gray skin 4. period of apnea 5. bradycardia 6. pneumothorax
Diagnosis: Clinical sign : grunting, cyanosis in room air, nasal flaring, retraction and shock Chest X-ray: reveal diffuse pattern of radio opaque areas
MANAGEMENT 1. surfactant replacement 2. oxygen administration 3.Ventilation 4. Additional therapy: - Indomethacin or Ibuprofen – to close PDA - muscle relaxant increase pulmonary blood flow
PILLITTERI pp 778 Vol 1
Prevention:
Steroid quicken the formation of lecithins given 12 and 24 hours prior to delivery most effective when given between weeks 24- 34 of pregnancy
Transient Tachypnea of the Newborn
Transient Tachypnea of the Newborn RR
@ birth – up to 80/min when crying Normal RR – 30-60/ min S/sx: Rapid
RR – 80-120/min Mild retraction No marked cyanosis Mild hypoxia & hypercapnia
Causes: Transient tachypnea of the newborn result from slow absorption of lungs fluid reflect slight decrease in production of mature surfactant limit the amount of alveolar surface area available to an infant for oxygenation exchange infant tend to increase RR and depth
TTN - Peak in intensity at approx. 36hrs in life @ 72hrs of life spontaneously fade as lung fluid is absorbed common: 1.infant born via CS 2.infants whose mother received extensive fluid administration during labor 3. preterm infants
TTN Management:
1. Close observation 2.O2 administration
MECONIUM ASPIRATION SYNDROME
MECONIUM ASPIRATION SYNDROME - Meconium present in fetal bowel as early as 10 wks gestation
Meconium aspiration - Infant
may aspirate meconium either in utero or in first breath after birth.
Cause severe respiratory distress in 3 ways: 1.causes inflammation of bronchioles because a foreign substance 2.block small bronchioles by mechanical
it’s
plugging
3. cause a decrease in surfactant production through lung cell trauma
Meconium aspiration sign and symptoms: 1. tachypnea 2. Retraction 3. Cyanosis 4. Barrel chest – due to air trapping DIAGNOSTICS: CXR: bilateral coarse infiltrates ( honey comb effect) ABG: dec. 02 & inc. Pc02
Meconium aspiration Syndrome Management: 1.suctioning with bulb syringe or catheter while at the perineum 2.severe aspiration infant might intubate 3. don’t administer O2 under pressure 4. antibiotic therapy 5. chest physiotherapy and chest clapping
APNEA
Apnea : >pause
in respiration longer than 20 secs. With accompanying bradycardia commonly seen in: 1.preterm infant 2.infection 3.hyperbilirubinemia 4.hypoglycemia
APNEA MANAGEMENT: 1. gently shaking an infant or flicking the sole of the feet 2. Closely observe all NB esp. Preterm 3. always suction the secretion gently to minimize nasopharyngeal irritation 4. Use gently handling to avoid excessive fatigue 5. never take rectal temperature in infant prone to apnea cause vagal stimulation w/c result to Apnea
APNEA Drug
use to stimulate respiration
Theophylline Caffeine
They
sodium benzoate
help increase infant sensitivity to carbon dioxide ensuring better respiratory function.
Sudden Infant Death Syndrome SID is a sudden unexplained death in infancy Cause is unknown who are at risk: 1. infant of adolescent mother 2.infant of closely spaced pregnancies 3.underweight infant 4. preterm infant
SIDS Contributory factors: 1. viral respiratory infection 2.botulism infection 3. brain stem abnormalities 4.neurotransmitter deficiency 5. heart rate abnormality 6.decrease arousal responses 7. possible lack of surfactant in alveoli 8. sleeping prone
Nsg Care Support
parents – view second child as an individual child not as a replacement for the one who died New baby born to a family in which a SIDS infant died is screened – sleep study as precaution within the first 2 wks of life. New baby placed on continuous apnea monitoring
Hemolytic disease of the newborn ABO
incompatibility: set up is mother’s type is O baby’s type is A, B, AB Sign and symptom- primarily jaundice Mgt: 1.phototherapy 2.if with severe jaundice can do exchange transfusion 3.initiation of early feeding
RH incompatibility:
mother is RH(-)( has D antigen) baby is RH (+) Sign and symptoms: kernicterus hydrops fetalis (edema) ( lethal state)
Therapeutic
management
Initiation
of early feeding Phototherapy Continuously
exposed to specialized light – cool white day light or blue fluorescent light Light placed 12-30 inches above the NB bassinet or incubator at 25-28 hours of age Bilirubin level : term 15 mg/dl
Preterm – 10-12 mg/dl Exchange
transfusion-
Nursing Stool
care phototherapy
of infant – bright green & loose Urine darked colored Assess skin turgor Assess I & O – to ensure hydration Monitor temp When infant is feeding removed from phototherapy – for interaction
Hemorrhagic disease of newborn
Hemorrhagic disease of newborn due to deficiency of vitamin K bleeding occurs on 2nd to 5th day of life complication: subdural hemorrhage - fatal Sign and symptoms: 1. petechiae 2.vomit fresh blood or pass black tarry stool
Hemorrhagic disease of newborn Management:1. 2.
IM /IV administration of vitamin K if with severe bleeding transfusion of fresh whole blood can be done
NEWBORN AT RISK DUE TO MATERNAL INFECTION/ILLNESS 1. 2. 3. 4. 5. 6. 7.
Beta-hemolytic, Group B Streptococcal Infection Hepatitis B Virus Infection Herpes Virus Infection HIV Mother Infant Of Diabetic Mother Infant Of Drug Dependent Mother Infant With Fetal Alcohol Syndrome
Beta-hemolytic, Group B Streptococcal Infection GBS
– major cause of infection of NB Natural habitant – female genital tract MOT : spread from baby to baby by contact Risk : prolonged rupture of membrane
Beta-hemolytic, Group B Streptococcal Infection S/sx Early
onset
First
day of life – Pneumonia
Tachypnea Apnea Shock – dec urine output, extreme paleness or hypotonia Can die within 24 hours of life
Beta-hemolytic, Group B Streptococcal Infection S/sx late
onset Occurs at 2-4 weeks of age- meningitis Lethargy, fever , loss of appetite Bulging fontanelles – increased ICP Mortality 15%
Beta-hemolytic, Group B Streptococcal Infection Diagnostics
mother’s vaginal culture Blood culture of NB
Therapeutic Ampicillin
management
IV @ 28 wks AOG & during labor ( reduce NB exposure) Bld test positive : gentamicin, ampicillin & penicillin
Hepatitis B Virus Infection Transmitted
to the NB through contact with infected vaginal blood at birth – mother is HBsAg+ Destructive illness 70-90% of infected infant can become chronic carrier Complication : liver cancer later in life
Hepatitis B Virus Infection Vaccinate
the NB
Hepatitis
B vaccine + immune serum globulin (HBIG)within 12H – decrease possibility of infection.
Bathed
infant as soon as possible after birth – removed blood Gentle suctioning- avoid trauma Breastfed infant – if HBIG is given
Herpes Virus Infection HSV-2 Common
Multiple sexual partner
MOT: Contracted
through the placenta – if mother has primary infection during pregnancy . Vaginal secretion of mother.
Herpes Virus Infection S/sx: Herpes
vesicles clustered with reddened base – covering the skin Severe neurologic damage If acquired at birth: ( D4 & D7 of life) Loss
of appetite Low grade fever & lethargy Dyspnea , jaundice, purpura , convulsion & shock Death occur within hours or days
Herpes Virus Infection Diagnosis: Culture
from vesicles Blood serum analyzed for IgM antibodies Therapeutic Acyclovir
Mgt:
( zovirax) Advised CS- minimize newborn exposure Isolate infant
Infant Of Diabetic Mother Macrosomia-
LGA Chance to have Congenital anomaly – cardiac Limp / lethargic first day of life – hypoglycemia Greater chance of birth injury hyperbilirubinemia Pp 791 pillitteri
Infant Of Diabetic Mother Diagnostics Serum
glucose <40 mg/dl NB
Therapeutic
Mgt
Fed
early with formula or administered a continuous infusion of glucose
Pp 791 pillitteri
Infant Of Drug Dependent Mother
SGA infant Infant show withdrawal syndrome
Irritability , disturbed sleep pattern Constant movement Tremors Frequent sneezing Shrill high pitched cry , hyperreflexia Convulsion Tachypnea , vomiting , diarrhea
Infant Of Drug Dependent Mother
withdrawal period Opiate – signs usually begin 24- 48 HOL max: 10 days , last 2 weeks Heroin – begin first 2 wks of life
ave.onset 72 HOL last 8-16 wks or longer
Methadone –begin 24-28 HOL reappear : 2-4 wks of age no sign : 2-3 wks old Cocaine : no predictable sequence
Infant Of Drug Dependent Mother
CARE Swaddled
infant Small isolation nursery – avoid excessive stimulation Darkened room Infant Heroin addicted mother – quiet if given pacifier Maintain fluid & electrolyte IV infusion if with diarrhea & vomiting
Infant Of Drug Dependent Mother
DRUG USED TO COUNTERACT WITHDRAWAL SYMPTOMS Phenobarbital Chlorpromazine
( thorazine) Diazepam ( valium)
avoid breastfeeding – to avoid passing narcotics Mother need treatment for withdrawal symptoms & follow care.
Infant With Fetal Alcohol Syndrome Alcohol
crosses the placenta , same concentration as present in the maternal bloodstream. s/sx : Growth retardation Microcephaly Cerebral palsy Thin upper lip Tremor Irritable, sleep disturbance Weak sucking reflex Behavioral problem
Infant With Fetal Alcohol Syndrome Follow
infant for any future problem Mother needs follow up- reduce alcohol intake
END