Chapter 6: Problem 3
The nurse is assessing an infant with polycystic kidney disease. Which structural anomaly is typical in the infant with polycystic kidney disease? A. Webbed neck B. High arched palate C. Scaphoid abdomen D. Low-set ears
Short Answer
Expert verified
Answer: None of the given options (A, B, C, and D) are typical structural anomalies associated with polycystic kidney disease in infants.
Step by step solution
01
Understand Polycystic Kidney Disease
Polycystic kidney disease is a genetic disorder that causes numerous cysts to grow in the kidneys. These cysts are filled with fluid, and over time, they can lead to kidney damage and, eventually, kidney failure. This disease has various physical symptoms and signs associated with it.
02
Analyze the Options
Now that we have a basic understanding of polycystic kidney disease, let's analyze each option:
A. Webbed neck - A webbed neck is not a characteristic of polycystic kidney disease.
B. High arched palate - A high arched palate is not a characteristic of polycystic kidney disease.
C. Scaphoid abdomen - A scaphoid abdomen can be associated with certain medical conditions, but it is not a typical structural anomaly in a patient with polycystic kidney disease.
D. Low-set ears - Low-set ears are not a characteristic of polycystic kidney disease.
After analyzing all the options, we can see that none of the given choices are typical structural anomalies in an infant with polycystic kidney disease.
03
Additional Information
Since none of the given options is a typical structural anomaly of an infant with polycystic kidney disease, it is useful to know some common signs and symptoms of the disease to provide a more accurate answer. Some possible signs and symptoms include high blood pressure, urinary tract infections, kidney stones, and enlarged kidneys due to the growth of cysts in the kidney.
04
Conclusion
None of the given options (A, B, C, and D) are typical structural anomalies associated with polycystic kidney disease in infants. The question's choices may be misleading, and it is essential to have prior knowledge about the disease to answer this question correctly.
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Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Structural Anomalies
In the context of polycystic kidney disease, structural anomalies refer to physical irregularities in the body related to faulty development during the early stages of life. While the condition leads to the formation of numerous fluid-filled cysts in the kidneys, it does not necessarily manifest as external structural anomalies. Instead, it might cause changes within the kidneys that eventually lead to their enlargement. These internal changes can sometimes result in symptoms such as pain or discomfort, but are not typically visible or detectable from external structures early in life. Understanding that polycystic kidney disease presents more internally than externally can help in distinguishing it from conditions that display more obvious anatomical changes.
Kidney Disorders in Infants
When infants suffer from kidney disorders like polycystic kidney disease, it signifies that the normal filtering function of their kidneys is compromised. In infants, such disorders are critical because kidneys play a vital role in maintaining the balance of water and salts in the body, removing waste, and producing essential hormones. Kidney problems in infants could manifest through symptoms such as:
- Swelling in the body due to fluid retention.
- Vomiting due to electrolyte imbalance.
- Poor appetite or feeding issues.
- More significant urine output or infections.
Genetic Disorders
Polycystic kidney disease is a prime example of a genetic disorder. This means that the condition is inherited and is caused by mutations in specific genes. These mutations affect the normal development and functioning of the kidneys. In families with a history of genetic disorders, there are considerations and strategies for understanding the potential genetic risks and implications. For prospective parents, genetic counseling can provide insights into the likelihood of passing such conditions on to their offspring. Moreover, understanding the genetic basis can guide both diagnosis and treatment, helping caregivers and medical professionals adopt a more personalized approach to patient care.
Nursing Assessment
Nursing assessment plays a pivotal role when caring for infants with polycystic kidney disease. Nurses conduct thorough evaluations to identify symptoms and assess the patient's overall health status. During an assessment, nurses may:
- Monitor vital signs to detect abnormalities.
- Evaluate growth parameters like weight and length.
- Check for signs of fluid retention or dehydration.
- Assess the infant's feeding patterns and nutritional intake.
Pediatric Nursing
Pediatric nursing involves the specialized care of children from infancy through adolescence, including those with conditions like polycystic kidney disease. Nurses in this field need to be skilled in pediatric assessment techniques, patient and family education, and the management of chronic conditions. They play a vital role in:
- Providing compassionate care that's tailored to the developmental stage of the infant or child.
- Supportive counseling for families, helping them understand and cope with the child's condition.
- Collaborating with a multidisciplinary team to ensure that all health aspects of the child are addressed.
- Implementing healthcare plans focused on improving quality of life and promoting healthy development.