In which subtype of juvenile idiopathic arthritis (JIA) is there a highest prevalence of AA amyloidosis?

Questions 230

ATI RN

ATI RN Test Bank

Pediatric NCLEX Practice Quiz Questions

Question 1 of 5

In which subtype of juvenile idiopathic arthritis (JIA) is there a highest prevalence of AA amyloidosis?

Correct Answer: A

Rationale: In juvenile idiopathic arthritis (JIA), AA amyloidosis is a serious complication that can arise due to chronic inflammation. The subtype of JIA with the highest prevalence of AA amyloidosis is systemic JIA. This is because systemic JIA is characterized by systemic inflammation involving multiple organs, especially the liver and spleen. The chronic systemic inflammation in systemic JIA can lead to the production of amyloid A protein, which can accumulate in various tissues, causing AA amyloidosis. Oligoarticular JIA is characterized by arthritis affecting fewer than five joints, and it typically has a milder course compared to systemic JIA. Polyarticular JIA involves arthritis affecting five or more joints, but it is less likely to lead to systemic inflammation and AA amyloidosis compared to systemic JIA. Psoriatic arthritis is a form of arthritis associated with psoriasis and is not typically associated with the development of AA amyloidosis. Understanding the different subtypes of JIA and their associated complications is crucial for healthcare providers caring for pediatric patients with arthritis. Recognizing the increased risk of AA amyloidosis in systemic JIA highlights the importance of early detection, monitoring, and appropriate management to prevent this serious complication. This knowledge is essential for nurses, nurse practitioners, and other healthcare professionals working with pediatric patients to provide comprehensive and effective care for children with JIA.

Question 2 of 5

A 3-month-old baby girl admitted to pediatric intensive care unit with severe head injury (evident by CT scan), the history given by parents was trivial and not informative. You suspected child abuse. Of the following, the MOST helpful study to support your suspicion is

Correct Answer: D

Rationale: In this scenario, the most helpful study to support the suspicion of child abuse in a 3-month-old baby with a severe head injury is a radionuclide bone scan (Option D). This is because a radionuclide bone scan can help identify occult fractures that may not be evident on plain X-rays. Option A, infantogram, is not the most appropriate choice as it provides a general overview of the entire body but may miss subtle fractures. Option B, X-rays of the spine, is not the most helpful study in this context as the primary concern is the head injury. Option C, X-rays of the skull, may show obvious fractures but can miss subtle or occult injuries that a radionuclide bone scan can reveal. Educationally, understanding the importance of selecting the most appropriate diagnostic study in cases of suspected child abuse is crucial for healthcare providers working with pediatric patients. Recognizing the limitations of certain imaging modalities and knowing when to utilize more sensitive tests like a radionuclide bone scan can aid in the accurate diagnosis and appropriate management of cases involving child abuse.

Question 3 of 5

An infant has the following findings at 5 minutes of life: pulse per minute, cyanotic hands and feet, good muscle tone, and a strong cry and grimace This infant's Apgar score is

Correct Answer: A

Rationale: In this scenario, the correct Apgar score for the infant is 7. The Apgar score is a quick assessment tool used to evaluate a newborn's physical condition at 1 and 5 minutes after birth. The components assessed are: heart rate, respiratory effort, muscle tone, reflex irritability, and color. In this case, the infant has a heart rate below 100 bpm (1 point), cyanotic hands and feet indicating some degree of central cyanosis (1 point), good muscle tone (1 point), a strong cry indicating good respiratory effort (1 point), and a grimace in response to stimulation (1 point). This totals to an Apgar score of 7. Option B (8) would be incorrect because the infant is showing signs of central cyanosis (1 point) which would lower the Apgar score to 7, not 8. Option C (9) would also be incorrect as the presence of cyanosis would prevent a score of 9. Option D is incomplete and not a valid option. Educationally, understanding the Apgar scoring system is crucial for healthcare providers working with newborns to quickly assess their well-being and determine if any immediate interventions are needed. It helps in prompt decision-making and appropriate care for newborns in the critical moments after birth.

Question 4 of 5

A newborn female has a ventricular septal defect, cleft lip and palate, and imperforate anus All of the following laboratory tests would be appropriate EXCEPT

Correct Answer: C

Rationale: In this case, the correct answer is C) Renal ultrasonography. The presence of a ventricular septal defect, cleft lip and palate, and imperforate anus suggests a genetic syndrome or chromosomal abnormality, which is why option A) A karyotype analysis is appropriate. The TORCH titer (option B) is important to rule out infections that could have contributed to the multiple congenital anomalies. Ultrasonography of the brain (option D) can help detect any brain abnormalities that may be present. Renal ultrasonography (option C) is not directly indicated based on the given conditions. It would be more relevant to focus on imaging studies that assess the specific anomalies observed in the newborn in this scenario. Understanding the reasoning behind each test is crucial in pediatric nursing as it helps in making informed clinical decisions and providing appropriate care for patients with complex medical conditions.

Question 5 of 5

A patient with Apgar scores of and at and 5 minutes, respectively, appears hyperalert and has hyperactive deep tendon reflexes and mydriasis The most likely diagnosis is

Correct Answer: A

Rationale: In this scenario, the correct answer is A) Stage I hypoxic ischemic encephalopathy. A newborn with Apgar scores of 7 and 9 at 1 and 5 minutes, respectively, exhibiting hyperalertness, hyperactive deep tendon reflexes, and mydriasis is showing signs of central nervous system irritability, which are characteristic of Stage I HIE. This stage is marked by transient neurological signs due to cerebral irritability without structural damage. Option B) Stage II HIE involves more severe symptoms like seizures, coma, and abnormal neuroimaging findings, which are not present in this case. Option C) Stage III HIE includes severe symptoms such as stupor, coma, and significant brain injury, which are not evident here. Option D) Kernicterus is a condition caused by severe jaundice leading to bilirubin deposition in the brain, presenting with specific symptoms like choreoathetoid cerebral palsy and hearing loss, which are not described in the case. Educationally, understanding the progression and manifestations of hypoxic ischemic encephalopathy in neonates is crucial for pediatric nurses and healthcare providers to provide appropriate care and interventions. Recognizing the different stages of HIE helps in early identification, management, and prevention of long-term neurological sequelae in newborns.

Access More Questions!

ATI RN Basic


$89/ 30 days

ATI RN Premium


$150/ 90 days

Similar Questions