pediatrics Flashcards
A parent brings her 7-year-old child into the clinic with the chief concern of a fever that lasted for 3 days and, upon resolution, was followed by flushed and red cheeks. Upon exam, the nurse practitioner notes a lacy, maculopapular rash along the arms and trunk. Which of the following is the most likely diagnosis for this patient?
Erythema infectiosum
Erythema infectiosum (A), also known as fifth disease, is caused by parvovirus B19. Classically, patients present with prodromal symptoms like fever, headache, myalgia, nausea, or diarrhea. After approximately 2–5 days, patients develop an erythematous facial rash often described as having a slapped-cheek appearance. A couple of days later, a reticulated or lacy rash develops on the patient’s trunk and extremities. Erythema infectiosum is a self-limited disease and only requires supportive care and symptom management. In certain populations, like pregnant individuals and children with hematologic disorders where red blood cell destruction is increased (e.g., sickle cell disease), parvovirus B19 can cause significant illness, and these patients should be closely monitored.
Which of the following children would require asymptomatic screening for celiac disease?
Patient with Down Syndrome
While screening asymptomatic adults for celiac disease is often not recommended, there are certain pediatric patients who have a high risk for the condition who should undergo asymptomatic screening. Risk factors include first-degree relatives with celiac disease, type 1 diabetes, IgA deficiency, and certain genetic syndromes, including trisomy 21 (Down syndrome). Therefore, the appropriate patient to screen in this situation would be the 7-year-old girl with Down syndrome (B).
The most common pathogenic organism that causes external otitis is
Pseudomonas aeruginosa
Genu varum, or “bow legs,” occurs when the knees stay apart despite the child standing with their feet together. It is a common and normal finding in children that typically resolves spontaneously by
2 years old
what is the preferred treatment for bullous impetigo in small children
amoxicillin
The nurse practitioner has just diagnosed an adolescent patient with mononucleosis. This diagnosis is associated with an increased risk for which of the following latent onset cancers?
burkittt lymphoma
genu recurvatum
This is a rare congenital anomaly that involves the dislocation or hyperextension of one or both knees. The most common precipitating factor is breech positioning in utero followed by oligohydramnios. Girls are more commonly affected. Nurse practitioners should recognize that this anomaly requires an immediate referral to a pediatric orthopedic surgeon because as the child grows, the ability to relocate the joints becomes increasingly difficult. When hyperextension is identified, physical therapy and serial splinting are often performed. Dislocation will require surgery.
An 11-year-old patient reports a severe sore throat, fever, nausea, and headache. Upon exam, the nurse practitioner sees a strawberry red pharynx with petechiae on the hard palate. The remainder of the exam is benign. What would be the best initial test to order for this patient?
rapid antigen detection test
A 3-year-old girl presents to the clinic after 48 hours of fever and irritability. Her fever responds well to acetaminophen and ibuprofen. Her parent states she has been pulling at her left ear, her appetite is decreased, and she has been irritable. Upon exam, you note marked erythema and bulging of the left tympanic membrane with effusion, a heart rate of 132 bpm, temperature of 102.3°F, and a cleft palate repair. Which of the following would be the appropriate diagnosis and management of this patient?
Antibiotics are proven to decrease the length of illness and pain associated with acute otitis media (AOM). The risk of tympanic membrane perforation is higher if AOM is left untreated. Antibiotic therapy should include coverage against Streptococcus pneumoniae. The first-line antibiotic preference is amoxicillin at a dose of 90 mg/kg by mouth per day (B).
A newborn infant presents with hypotonia, poor moro reflex, hyperextensible joints, low-set ears, and slanted palpebral fissures. The prenatal history is signficant for low alpha fetoprotein level and increased nuchal translucency at 18 weeks gestation. Which of the following is the best plan of care for the infant at this time?
refer to neonatology for comphehensive exam and testing
he most appropriate next step is to refer to neonatology for a comprehensive examination and testing (D). A low alpha-fetoprotein (AFP) level in the first trimester can be indicative of trisomy 21 or Down syndrome. The exam findings of hypotonia, poor moro reflex, hyperextensible joints, low-set ears, redundant skin at the nape of the neck, and slanted palpebral fissures are indicative of trisomy 21. Newborns with trisomy 21 are at risk for poor cardiovascular function, metabolic disorders, and hematologic abnormalities and thus require close monitoring immediately after birth. A comprehensive exam and evaluation is required to rule out congenital heart defects, hypoglycemia, thyroid dysfunction, and abnormalities in red blood cells.
A 10-year-old girl presents for a wellness exam today. Upon examination, breast budding is noted as well as a few fine pubic hairs. She and her parent mention that her breasts just began to grow and ask when they should expect her menses to start. What anticipatory guidance should be provided during this visit?
Menarche should start in the next 3 years (C) once a girl begins puberty or enters Tanner stage 2. Tanner stage 2 peaks in girls aged 12-13 years. In this stage, breast buds become palpable, areola enlarge, and minimal coarse pubic hair is visible on the labia.
Newborns should pass meconium within the first 48 hours after birth. When this does not occur, the differential diagnosis will include conditions such as meconium ileus. Which of the following diseases is commonly associated with meconium ileus?
cystic fibrosis
Meconium ileus is considered a bowel obstruction and is most often diagnosed in the immediate newborn period. Meconium should form during fetal development and is expected to evacuate the large bowel within 48 hours of birth. Cystic fibrosis (A), the most common autosomal recessive inherited disorder diagnosed in newborns and is associated with a defect at the CFTR gene, resulting in deficient chloride channel function and the formation of thick, sticky mucus and stool.
At what age is it most common to see iron deficiency anemia in children?
6-24 months
A 4-year-old girl with a medical history of frequent UTIs presents to the office with her parent for abdominal pain with urination. This is her third visit over the past month for similar concerns, and her symptoms are worsening despite UTI prophylaxis and normal urinalysis and urine culture results. Her parent states the girl started wetting her pants despite being fully potty trained and is urinating frequently. On exam, the nurse practitioner is able to palpate hardened stool in the abdomen. Review of the results of a recent voiding cystourethrogram is significant for retrograde flow of urine without dilation of the ureters. What diagnosis is most likely?
vesicoureteral reflux
Vesicoureteral reflux (VUR) (D) is the most likely diagnosis. VUR can be primary or secondary. Primary VUR is congenital and caused by inadequate closure of the ureterovesical junction inside the bladder. Patients with VUR have a sphincter that is incompetent, causing urine to reflux from the bladder back into the ureters or kidneys. Secondary VUR happens as a result of separate bladder dysfunction. The most common symptoms of VUR are urinary frequency, urinary leakage, abdominal pain, constipation, and frequent UTIs. VUR is a common cause of hydronephrosis, in which the kidney and ureter dilate and swell due to backup of urine. This condition is most common in female individuals.
A child was recently diagnosed with transfusion-dependent beta-thalassemia. When providing education to the parents about this condition, the nurse practitioner explains that treatment of this condition can potentially lead to which of the following complications?
hemochromatosis
Beta-thalassemia is treated with blood transfusions. However, this can lead to transfusional iron overload, or hemochromatosis (A), as the body does not have a way to excrete excess iron. Iron overload can lead to heart failure, cardiac dysrhythmias, and cirrhosis.
Thalassemia is a hereditary condition. Beta-thalassemia begins to manifest within the first year of life, and an individual’s lifespan may be dramatically shortened without aggressive treatment.
Which of the following manifestations is not associated with Duchenne muscular dystrophy?
dipolopia
Duchenne muscular dystrophy (DMD) is an inherited condition in which the muscles become progressively weaker over time. Onset of weakness typically occurs at around 2 to 3 years of age. Additionally, those with this condition may also have delayed physical milestones in their early years. Beyond muscle weakness, DMD can impact many aspects of life, including cognitive function. Large calf muscles are normal in these children due to scar tissue buildup from muscle brea down. Due to proximal weakness, they also progress to eventually having a waddling gait. Diplopia (A) is unlikely to be seen with DMD and instead would be more likely to be seen with oculopharyngeal muscular dystrophy. A multidisciplinary approach is best to help improve quality of life for these patients, as DMD affects multiple body systems. Support in the form of physical therapy, occupational therapy, speech therapy, and language therapy is also important. Most patients will lose the ability to ambulate and will use a wheelchair by the age of 12. Life expectancy is shortened, but with medical advancements, patients may now live into adulthood.
Asthma controlled with daily low- or medium-dose inhaled corticosteroids (ICS) (C) is defined
moderate asthma
first line tx for scarlet fever is
amoxicillin for 10 days
An 8-year-old boy presents to the clinic accompanied by his parents for his annual well-child visit. Physical exam reveals a small amount of axillary hair. They report no abnormal body odor. Which of the following describes the most appropriate plan of care?
refer to endocrinologist due to precocious puberty
The nurse practitioner should recommend a referral to an endocrinologist due to precocious puberty (A). Development of secondary sexual characteristics before the age of 9 years in male patients and 8 years in female patients is considered precocious puberty. This warrants a referral to endocrinology for further investigation. Specialist evaluation may include imaging to assess bone age and brain imaging and a comprehensive hormone laboratory evaluation.
Which of the following symptoms is the least likely manifestation of epiglottitis in children?
preauricular adenopathy
Epiglottitis is a serious medical condition in which the upper airways begin to swell. It is caused by the organism Haemophilus influenzae type B. Children < 5 years old typically present with respiratory distress and an acute onset of sore throat and fever. The patient rapidly deteriorates with labored breathing and difficulty swallowing. The patient may have drooling and be seated in a tripod position in which the neck is hyperextended in an attempt to maintain the airway. Preauricular adenopathy (C) is not a typical symptom of epiglottis in children.
The dx tool for both asthma and COPD is
spirometry
Slipped capital fermoral epiphysis is
is a displacement of the proximal femoral epiphysis through the growth plate. Involvement of the growth plate categorizes this a Salter-Harris fracture, and it is further associated with a Salter-Harris type 1 fracture (B).
SCFE commonly occurs in adolescents. Stress on the femoral growth plate causes a shearing force to occur that will eventually result in proximal femoral displacement. Obesity causes increased stress on the femoral growth plate and is the most common risk factor for SCFE. SCFE can be classified as either stable or unstable based on the ability of the patient to bear weight on the extremity. It can occur acutely after a traumatic injury or can be associated with chronic leg pain. Patients may have a positive Trendelenburg test, which is a sagging of the pelvis when they stand on the affected leg. However, this test is not specific for SCFE alone. X-rays of the hip and pelvis can be used to confirm the diagnosis. Patients should be offered immediate orthopedic referral upon diagnosis as they are at risk for avascular necrosis of the hip.
Which of the following primitive reflexes should begin to disappear at about 2-3 months of age in a normal infant?
rooting
A newborn infant will turn its head toward anything that strokes its cheek or mouth, searching for the object by moving its head in steadily decreasing arcs until the object is found. The rooting reflex starts to disappear at about 2-3 months of age.
Turner syndrome is caused by a
deletion in the X chromosome
There are three entities to the female athlete triad, which include
infrequent menstrual cycles (C) or amenorrhea, low availability of energy with or without an eating disorder, and low bone mineral density associated with osteopenia or osteoporosis. T
Aphthous stomatitis ulcers are the most common mucosal lesions and are commonly referred to as canker sores. These typically present as a
shallow, tender, yellowish ulceration (B) on the inside of the mouth on the oral mucosa.