NCC NNP-BC flashcards
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32 cards. Read the term and the definition here. The deck at the top of this page is optional.
- Category I FHR tracing
- Baseline 110-160 bpm with moderate variability and no late or variable decelerations. Accelerations and early decelerations may be present. It indicates a normal fetal status and requires no intervention.
- Uterine tachysystole
- More than five contractions in ten minutes averaged over thirty minutes. It may reduce placental perfusion. Management includes repositioning, intravenous fluids, and reducing or stopping oxytocin.
- Late deceleration
- A gradual decrease in fetal heart rate beginning after the contraction peak and returning after it ends. It reflects uteroplacental insufficiency and warrants intrauterine resuscitation.
- Group B streptococcus prophylaxis
- Penicillin G is first-line for colonized mothers in labor. Cefazolin is used for non-anaphylactic penicillin allergy. Clindamycin requires documented susceptibility testing before use.
- Neonatal resuscitation compression ratio
- When heart rate remains below 60 bpm despite effective ventilation, provide three compressions to one breath. This equals 90 compressions and 30 breaths per minute.
- Neonatal epinephrine dose
- Intravenous or intraosseous epinephrine is 0.01-0.03 mg/kg of the 0.1 mg/mL concentration. The endotracheal dose is 0.05-0.1 mg/kg of the 1 mg/mL concentration.
- Apgar score components
- Five components scored zero to two each: heart rate, respiratory effort, muscle tone, reflex irritability, and color. Scores are assigned at one and five minutes and do not guide resuscitation.
- Delayed cord clamping
- Clamping the cord at least 30-60 seconds after birth in infants not requiring immediate resuscitation. It improves iron stores and reduces transfusion needs, especially in preterm infants.
- Respiratory distress syndrome
- Caused by surfactant deficiency, leading to decreased compliance and atelectasis. Chest radiograph shows ground-glass opacities with air bronchograms. Treatment includes surfactant and respiratory support.
- Transient tachypnea of newborn
- Respiratory distress appearing within hours of birth from delayed clearance of fetal lung fluid. Chest radiograph shows perihilar streaking. It typically resolves within 24-72 hours.
- Apnea of prematurity
- A pause in breathing lasting 20 seconds or longer, or shorter if accompanied by bradycardia or desaturation. Caffeine citrate is the standard treatment.
- Bronchopulmonary dysplasia definition
- In infants born before 32 weeks, it is an oxygen requirement for at least 28 days, graded by respiratory support needed at 36 weeks postmenstrual age.
- Prostaglandin E1 infusion
- Given at 0.01-0.1 mcg/kg/min to maintain ductal patency in ductal-dependent congenital heart lesions. Side effects include apnea, fever, and hypotension.
- Hyperoxia test
- An arterial oxygen tension above 150 mmHg after 100% oxygen suggests pulmonary disease rather than a cyanotic cardiac lesion. Lower values raise concern for cyanotic heart disease.
- Hypoplastic left heart syndrome
- A ductal-dependent lesion with inadequate systemic blood flow. Initial management includes prostaglandin E1 and avoiding excessive pulmonary blood flow by limiting supplemental oxygen.
- Patent ductus arteriosus closure
- Indomethacin or ibuprofen may close a hemodynamically significant patent ductus arteriosus. Contraindications include renal failure, thrombocytopenia, and necrotizing enterocolitis.
- Therapeutic hypothermia
- Cooling to 33.5-34.5 degrees Celsius for 72 hours, started within 6 hours of birth, for moderate to severe hypoxic-ischemic encephalopathy. Slow rewarming and monitoring are required.
- Intraventricular hemorrhage grading
- Papile grades I-IV: grade I is germinal matrix only, grade II is intraventricular without dilation, grade III adds ventricular dilation, and grade IV includes parenchymal hemorrhage.
- Kernicterus
- Bilirubin deposition in basal ganglia and brainstem causing lethargy, poor feeding, hypertonia, and retrocollis acutely. It can result in permanent neurologic damage.
- Necrotizing enterocolitis
- Presents with feeding intolerance, abdominal distension, and bloody stools. Radiograph may show pneumatosis intestinalis. Management includes bowel rest, antibiotics, and parenteral nutrition.
- Physiologic jaundice timing
- Jaundice appearing after 24 hours of life is physiologic. Jaundice within the first 24 hours is pathologic and requires urgent bilirubin measurement and evaluation.
- Pyloric stenosis presentation
- Projectile nonbilious vomiting at 3-6 weeks of age with visible peristalsis. Laboratory findings include hypochloremic hypokalemic metabolic alkalosis. Treatment is surgical pyloromyotomy.
- Newborn urine output
- Normal output is 1-3 mL/kg/hour. Oliguria is defined as less than 1 mL/kg/hour. Potassium should not be given until urine output is established.
- Physiologic weight loss
- Term infants may lose up to 7-10% of birth weight in the first week. Preterm infants may lose up to 15%. Greater loss requires feeding and hydration assessment.
- Physiologic anemia of infancy
- Hemoglobin nadir occurs at 8-12 weeks in term infants and 4-8 weeks in preterm infants. It results from low erythropoietin and shortened red cell lifespan.
- Vitamin K prophylaxis
- A single intramuscular dose of 0.5-1 mg at birth prevents hemorrhagic disease of the newborn. It is recommended for all newborns unless parents decline after informed discussion.
- Early-onset neonatal sepsis
- Sepsis presenting within 72 hours of birth. Risk factors include maternal group B streptococcus colonization, prolonged rupture of membranes, chorioamnionitis, and prematurity.
- Congenital cytomegalovirus
- The leading nongenetic cause of sensorineural hearing loss. Diagnosis uses urine or saliva polymerase chain reaction. Hearing screening and developmental follow-up are required.
- Congenital hypothyroidism
- Detected by newborn screening. Levothyroxine should begin within 2 weeks of life to prevent intellectual disability. Repeat testing and dose adjustment follow.
- Congenital adrenal hyperplasia
- 21-hydroxylase deficiency causes salt-wasting crisis with hyponatremia, hyperkalemia, and hypotension in the second week of life. Newborn screening measures 17-hydroxyprogesterone.
- Trisomy 21 features
- Features include hypotonia, upslanting palpebral fissures, and a single palmar crease. Associated risks include congenital heart disease, duodenal atresia, and thyroid disease.
- Turner syndrome
- A 45,X chromosomal disorder in females presenting with webbed neck, lymphedema, short stature, and coarctation of the aorta. Pubertal hormone replacement is often needed.