NCMA219 - Midterms

Subdecks (1)

Cards (209)

  • Pointers to Review
    • High risk newborn
    • IUGR/ SGA/ LGA/ Preterm
    • RDS
    • MAS
    • SIDS
    • Hyperbilirubinemia
    • Neonatal Sepsis
    • Necrotizing enterocolitis
    • G6PD/Congenital Hypothyroidism
    • Phenylketonuria
    • Galactosemia
    • Tetralogy of Fallot
    • Rheumatic fever/ RHD
    • ASD/ VSD/ PDA
    • Kawasaki Disease
    • Streptococcal pharyngitis
    • Tonsillitis
    • Sickle Cell Anemia/IDA
    • CROUP syndrome /LTB/ Epiglottitis
  • Premature Infant
    Infant born < 38 weeks gestation
  • Premature Infant
    • Birth that takes place more than three weeks before the baby's estimated due date
    • Occurs before the start of the 37th week of pregnancy
    • Lanugo covers the entire back and face, soles a few creases, scrotum little rugae
    • Thin and pinkish skin, plenty of lanugo and relaxed posture
  • Full Term Infant
    Infant born between the beginning of 38 weeks and the completion of 42 weeks of gestation regardless of birth weight
  • Postmature Infant
    Baby delivered after 42 weeks of gestation
  • Postmature Infant
    • Abundant scalp hair
    • Visible creases on palms and soles of feet
    • Minimal fat deposits
    • Absence of lanugo
  • IUGR
    Small for Gestational Age Infants
  • Infants whose rate of intrauterine growth was slowed and whose birth weight falls below the 10th percentile on the intrauterine growth chart
  • Causes of IUGR
    • Poor nutrition during pregnancy
    • Placental defects and complications
    • Teenage pregnancies
    • Hypertensive mother
  • Nursing Management for IUGR/SGA Newborn
    • Priority nursing care in the first few days of life
    • Initiation and maintenance of respirations
    • Maintenance of hydration and normal glucose – glucose IVF, thermoregulation, correct IVF rate, breastfeeding every 3-4 hours
    • Monitor glucose level every 4 hours
    • Control of body temperature
    • For newborns under radiant warmers – monitor vital signs, keep the newborn hydrated, assess integrity of the skin
    • Maintaining a neutral thermal environment permits the neonate to maintain a normal core temperature with minimal oxygen consumption
  • Large for Gestational Age Infants
    Infant whose birth weight falls ABOVE 90th percentile on intrauterine growth charts
  • Respiratory Distress Syndrome (Hyaline Membrane Disease)

    Refers to a condition of surfactant deficiency and physiologic immaturity of the thorax
  • Diagnostic exams for RDS
    • X-ray blood glucose
    • ABG
    • Fetal Lung Maturity Assay (the fastest)
  • Diagnostic Findings for RDS
    • Radiographic findings – diffuse granular pattern like broken glass appearance on chest x-ray
    • Hypoxemia
    • Increased carbon dioxide and respiratory acidosis on ABG
  • Medications for RDS
    • Artificial surfactant
    • Nitric Oxide (It will dilate pulmonary bronchus)
  • Major Signs of RDS
    • Tachypnea 60>
    • Flaring nares
    • Expiratory grunting, Dyspnea
    • Chest Retractions – sternal and subcostal
    • Seesaw respirations
  • Meconium Aspiration Syndrome
    Is the aspiration of amniotic fluid containing meconium into fetal or newborn trachea in utero or at first breath
  • Occurs primarily in full-term and post-term infants during relaxation of the anal sphincter and passage of meconium in amniotic fluid due to intrauterine stress
  • Assessment of MAS

    • Widened anteroposterior diameter of the chest (barrel-chest)
    • Greenish stains on the skin, umbilical cord and nails
  • Nursing Management for MAS
    • Suctioning - oropharyngeal and tracheal
    • O2 support (Severe: Extracorporeal Membrane Oxygenation)
    • Exogenous surfactant administration
    • IV fluid administration
    • Administer systemic antibiotics as prescribed (Ampicillin, Gentamicin, Amikacin)
  • Sepsis
    • Early onset – occurs less than 3 days after birth, caused by maternal infection
    • Late onset - occurs on the 4th up to 7th days after birth, nosocomial infection
  • Clinical Manifestations of Sepsis
    • Pallor, Cyanosis, or Mottling
    • Hypotension
    • Tachycardia
    • Irregular respirations
    • Jaundice
    • Dehydration
    • Temperature instability
  • Laboratory and Diagnostic Studies for Sepsis
    • Blood culture
    • Urine, blood culture and CSF (Cerebrospinal Fluid) analysis
    • CBC – WBC increased
    • ESR and C–reactive protein - increased
  • Hyperbilirubinemia
    Refers to an excessive level of accumulated bilirubin the blood and characterized by jaundice
  • Types of Hyperbilirubinemia
    • Pathologic Jaundice - appears in the first 24 hours of life
    • Physiologic Jaundice - appears after 24 hours of life
  • Complication of Hyperbilirubinemia is Kernicterus
  • Nursing Management for Hyperbilirubinemia
    • Cover the eyes (opaque eye covers) and genitalia
    • Check skin turgor for hydration
    • Turn the infant every 2 hours
    • Instruct the mother to continue breastfeeding every 2-4 hours
  • Sudden Infant Death Syndrome (SIDS)

    Sudden unexpected death of any infant younger than 1 year old age
  • Death usually occurs during sleep–"CRIB Death"
  • Most common cause of death in children ages 1 month to 1 year
  • Peak: 2-4 months, 90% before 6th months
  • Nursing Management for SIDS
    • Teach parents how to minimize the risk of SIDS
    • Avoid smoking during and after pregnancy
    • Encourage supine position or side-lying position
    • Avoid co-sleeping
    • Avoid soft beddings, use of pillows, blankets on the crib
    • Avoid maternal smoking
  • Necrotizing Enterocolitis
    An acute inflammatory disease of the bowel
  • Signs of Necrotizing Enterocolitis
    • Poor feeding
    • Distended abdomen
    • Blood in the stool
    • Vomiting
    • Apnea
  • Nursing Management for Necrotizing Enterocolitis
    • Assessing patient for presence of abdominal distention
    • Reporting to the doctor any episodes of gastric residuals
    • Placing the patient on NPO as per doctor's order if symptoms of NEC are observed
  • Newborn Screening
    Procedure to determine if the newborn infant has a heritable congenital metabolic disorder
  • Congenital Hypothyroidism
    Results from the absence or lack of development of thyroid gland causing absence or lack of thyroxine needed for metabolism and growth of the body and the brain
  • Signs & Symptoms of Congenital Hypothyroidism
    • Short stature
    • Macroglossia
    • Delayed closure of the fontanelles
    • Hypotonia
  • Management of Congenital Hypothyroidism
    • Medication will be needed throughout the child's lifetime
    • Administration of thyroid hormone will prevent problems, if managed early it will not cause mental retardation
    • Synthroid – taken in the morning (report signs of tremors, toxicity)
  • Phenylketonuria
    Deficiency or absence of enzyme needed to metabolize essential amino acid like phenylalanine