pediatric immunity Flashcards

1
Q

A nurse practitioner is educating a group of students on phagocytic disorders. Establish why further education is needed.

The most common sites of infection are the respiratory tract and skin.

Phagocytic disorders result from abnormalities in monocytes or neutrophils.

Infants may experience poor wound healing.

The musculoskeletal system is most frequently impacted.

A

The musculoskeletal system is most frequently impacted.

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2
Q

When educating a parent on primary immune disorders (PIDs), what statement is accurate?

Maternal autoimmune neutropenia can result in neonatal neutropenia resulting in PID.

Neonatal hypogammaglobulinemia caused by immunoglobulin loss into the gastrointestinal tract is an indication of PID.

Primary immune disorders are categorized by the compartment(s) of the immune system that is affected.

In utero exposure to immunosuppressive medications given to the mother can result in PID.

A

Primary immune disorders are categorized by the compartment(s) of the immune system that is affected.

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3
Q

A nurse practitioner is evaluating a patient for complement disorders. Propose an indication for patient screening.

Failure to thrive and thrombocytopenia

Recurrent unexplained infections of the respiratory tract and skin

Infants presenting with severely impaired neutrophil function

Multiple family members with Neisseria infections

A

Multiple family members with Neisseria infections

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4
Q

A nurse practitioner is educating a group of students on secondary immunodeficiency in children. Determine an accurate statement regarding secondary immunodeficiency.

Secondary immunodeficiencies are far more common than primary immunodeficiencies.

Hypogammaglobulinemia contributes to the state of secondary immunodeficiency and susceptibility to infections.

High-dose corticosteroids can be used prophylactically to prevent secondary immune disorders.

Neonates have decreased susceptibility to secondary immune disorders.

A

Secondary immunodeficiencies are far more common than primary immunodeficiencies.

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5
Q

A nurse practitioner is concerned about a patient presenting with an antibody disorder. Establish an accurate statement regarding antibody disorders.

Antibody disorders are characterized by the absence or presence of B cells.

Severe combined immunodeficiency (SCID) is the most severe form of antibody disorders.

Antibody disorders involve infections with encapsulated organisms and are often characterized by Neisseria infections.

Antibody disorders manifest as an unusual sensitivity to viruses.

A

Antibody disorders are characterized by the absence or presence of B cells.

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6
Q

A nurse practitioner is evaluating a child presenting for failure to thrive. Determine the patient who should be evaluated for a primary immune deficiency.

A newborn recently delivered after the mother experienced placenta previa

A 3-month-old with a family history of primary immune disorders

A newborn exposed to cytomegalovirus in utero

A premature infant with anemia

A

A 3-month-old with a family history of primary immune disorders

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7
Q

A nurse practitioner is concerned about a patient presenting with an antibody disorder. Recommend the laboratory screening for a patient presenting with an antibody disorder.

IgE

Factor VIII

T cells

Neutropenia

A

IgE

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8
Q

A nurse practitioner is evaluating an infant for severe combined immunodeficiency (SCID). Propose an accurate statement.

Treatment is not indicated in infants presenting with SCID.

Chronic granulomatous disease is common in patients with SCID.

It is the most severe form of T cell disorders.

Treatment typically involves high-dose antibiotics and radiation therapy.

A

It is the most severe form of T cell disorders.

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9
Q

A nurse practitioner is concerned about a patient presenting with an antibody disorder. Establish an accurate statement regarding antibody disorders.

Antibody disorders usually present once maternal immunoglobulins from placental transfer are no longer present.

Infants with antibody immunodeficiency have deficiencies of both T cell and B cell immunity.

Severe combined immunodeficiency (SCID) is the most severe form of antibody disorders.

Antibody disorders involve infections with encapsulated organisms and are often characterized by Neisseria infections.

A

Antibody disorders usually present once maternal immunoglobulins from placental transfer are no longer present.

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10
Q

A nurse practitioner is reviewing T cell disorders in children. Propose an accurate statement regarding T cell disorders.

Congenital neutropenia is a common T cell disorder.

DiGeorge syndrome is a T cell disorder.

Celiac disease is commonly seen in infants with T cell disorders.

Most T cell deficiencies present early in life.

A

Most T cell deficiencies present early in life.

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11
Q

A nurse practitioner is educating a group of students on secondary immunodeficiency in children. Predict what is consistent with a patient presenting with secondary immune deficiency.

A 6-month-old with a family history of chronic granulomatous disease

A patient presenting with Type 2 diabetes

A newborn presenting with low or deficient levels of any of the immunoglobulins

A newborn with a history of recurrent life-threatening infections

A

A patient presenting with Type 2 diabetes

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12
Q

When providing education on primary immune deficiencies, the nurse practitioner notes that these can be identified as what?

Acquired disorders resulting from a compromised immune system

Diseases of the immune system itself

A weak immune system as a result of another condition

Most often diagnosed in children and adolescents

A

Diseases of the immune system itself

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13
Q

A nurse practitioner is evaluating a patient for complement disorders. Propose an indication for patient screening.

Female patients presenting without lymph nodes

Recurrent Neisseria infections at any age

Failure to thrive and thrombocytopenia

Infants presenting with severely impaired neutrophil function

A

Recurrent Neisseria infections at any age

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14
Q

A nurse practitioner is educating a group of students on secondary immunodeficiency in children. Determine an accurate statement regarding secondary immunodeficiency.

Hypogammaglobulinemia contributes to the state of secondary immunodeficiency and susceptibility to infections.

The immune defects observed in secondary immunodeficiency are usually heterogeneous in their clinical presentation.

High-dose corticosteroids can be used prophylactically to prevent secondary immune disorders.

Antibody disorders are the most common secondary immune disorders.

A

The immune defects observed in secondary immunodeficiency are usually heterogeneous in their clinical presentation.

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15
Q

Determine an accurate statement regarding disorders of the complement system.

A complete blood count with differential is the gold standard of care.

The complement system is unable to kill catalase-positive organisms, including Staphylococcus aureus.

Neutropenia suggests a complementary disorder.

A CH50 assay is used to test the classic pathway that involves C1–C9.

A

A CH50 assay is used to test the classic pathway that involves C1–C9.

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16
Q

A nurse practitioner is educating a group of students on primary immunological disorders. Determine an example of a primary immune disorder.

Malignancy

AIDS resulting from HIV infection

Congenital neutropenia

Severe malnutrition

A

Congenital neutropenia

17
Q

Question 12
Establish the characteristic of a child presenting with agammaglobulinemia.

Agammaglobulinemia is typically detected when the child is 8–10 years old.

On physical examination, the child is without lymph nodes.

The infant has an abnormal immunoglobulin response to vaccinations.

The infant presents with low levels of any of immunoglobulins.

A

On physical examination, the child is without lymph nodes.

18
Q

Propose a goal of therapy for children presenting with systemic lupus erythematosus.

Improve quality of life and achieve the lowest possible disease activity

Discourage exercise because it leads to stressful living conditions

Maximize duration of treatment for improved efficacy

Minimize patient education because it will typically will confuse patients and their families.

A

Improve quality of life and achieve the lowest possible disease activity

19
Q

Propose a risk factor associated with the recurrence of acute rheumatic fever.

Previous exposure to varicella

Greater number of previous attacks

Longer time intervals since the last attack

Older age at onset

A

Greater number of previous attacks

20
Q

A nurse practitioner is evaluating a patient in the clinic for juvenile idiopathic arthritis (JIA). Predict an accurate statement about JIA.

Patients with JIA experience a high risk for pertussis and varicella.

It typically occurs 2–4 weeks following group A Streptococcus (GAS) infection.

It is the most common type of arthritis in children under the age of 16.

It is an acute autoimmune disease that can have an acute insidious onset.

A

It is the most common type of arthritis in children under the age of 16.

21
Q

When evaluating and diagnosing a patient with juvenile idiopathic arthritis (JIA), the nurse practitioner identifies classifications and subtypes. What is one of the primary subtypes of JIA?

Osteoarthritis

Systemic arthritis

Systemic lupus

Rheumatoid arthritis

A

Systemic arthritis

22
Q

Decide on an appropriate treatment for the management of a patient presenting with juvenile idiopathic arthritis (JIA).

In severe cases of JIA, hip and knee replacements may be necessary.

Opioid therapy is recommended for patients with severe pain.

Primary recommendations include glucocorticoids with the methotrexate.

Biologic DMARDs, such as interleukin (IL) 1 or IL-6 inhibitors, are not recommended for patients with treatment failure.

A

In severe cases of JIA, hip and knee replacements may be necessary.

23
Q

Predict a common characteristic of polyarticular juvenile idiopathic arthritis.

Asymmetric involvement

High, intermittent spiking fevers

Further divided into RF positive and RF negative disease

Confinement to the lower extremities

A

Further divided into RF positive and RF negative disease

24
Q

A nurse practitioner is evaluating a patient who presents with musculoskeletal discomfort. Propose a form of management for patients presenting with juvenile fibromyalgia.

Therapy starts with confirmation of the diagnosis.

Nonsteroidal anti-inflammatory drugs (NSAIDs) are the mainstay of treatment.

Gabapentin is not recommended in pediatric patients.

High-impact exercises are recommended to help improve strength.

A

Therapy starts with confirmation of the diagnosis.

25
Q

Establish an accurate statement regarding the management of systemic lupus erythematosus (SLE).

Treatment with prednisone has significantly lowered the mortality rate in patients presenting with SLE.

The treatment for most manifestations of SLE differ among adults and children.

Extended immunosuppressive therapy is not recommended in pediatric patients.

Antibiotic therapy is essential to disease management in patients with SLE.

A

Treatment with prednisone has significantly lowered the mortality rate in patients presenting with SLE.

26
Q

A nurse practitioner is diagnosing a patient with systemic lupus erythematosus (SLE). Predict the basis of a diagnosis.

Laboratory studies are not indicated when diagnosing SLE.

Lupus has a usual, typical presentation, making diagnosis predictable.

Children who fulfill the American College of Rheumatology (ACR) criteria are considered to have definite SLE.

For accurate diagnosis, all of the manifestations required by the American College of Rheumatology must be present when the child is first seen.

A

Children who fulfill the American College of Rheumatology (ACR) criteria are considered to have definite SLE.

27
Q

Determine a sign or symptom of systemic lupus erythematosus (SLE).

Classic malar rash.

Joint instability

Gradual development of limp

Hyperthyroidism

A

Classic malar rash.

28
Q

A nurse practitioner is educating a group of students on juvenile idiopathic arthritis (JIA). Determine the accurate statement regarding oligoarticular arthritis.

It typically involves five or more joints.

It is the most common form of JIA.

It is always accompanied by osteonecrosis.

It commonly occurs in patients with scoliosis.

A

It is the most common form of JIA.

29
Q

Decide on an appropriate treatment for the management of a patient presenting with juvenile idiopathic arthritis (JIA).

Primary recommendations include glucocorticoids with the methotrexate.

Nonsteroidal anti-inflammatory drugs are the first line of medications used for patients with JIA.

Biologic DMARDs, such as interleukin (IL) 1 or IL-6 inhibitors, are not recommended for patients with treatment failure.

Proven treatments for JIA include observation followed by bracing and surgery.

A

Nonsteroidal anti-inflammatory drugs are the first line of medications used for patients with JIA.

30
Q

The diagnosis of fibromyalgia is made clinically and is based upon the presence of the typical clinical features. Propose a major criterion when determining a diagnosis of fibromyalgia.

Chronic anxiety or tension

Irritable bowel syndrome

Generalized musculoskeletal aching at three or more sites for at least 3 months

Fatigue

A

Generalized musculoskeletal aching at three or more sites for at least 3 months

31
Q

Recommended a pharmacological intervention for patients presenting with juvenile fibromyalgia.

Vancomycin

Cephalexin

Carbapenem

Pregabalin

A

Pregabalin

32
Q

Predict a major manifestation of acute rheumatic fever.

Fever

Erythema marginatum

Arthralgia

Prolonged PR interval on the electrocardiogram

A

Erythema marginatum

33
Q

Recommend a treatment regimen for children presenting with acute rheumatic fever.

Orapred 2mg/kg/day

Amoxicillin, 800 mg daily

Bactrim, 400 mg orally twice daily

Penicillin V, 250 mg orally twice daily

A

Penicillin V, 250 mg orally twice daily

34
Q

Determine the symptom of patients presenting with post-streptococcal reactive arthritis (PSRA).

Tenosynovitis and renal abnormalities are less common in patients with PSRA.

There is a poor response of arthritis to aspirin.

Erythrocyte sedimentation rate tends to be lower than in the setting of acute rheumatic fever.

Evidence of carditis is not seen in these patients.

A

Evidence of carditis is not seen in these patients.

35
Q

Propose a goal of therapy for children presenting with systemic lupus erythematosus.

Prevent organ damage

Discourage exercise because it leads to stressful living conditions

Maximize duration of treatment for improved efficacy

Minimize patient education because it will typically will confuse patients and their families.

A

Prevent organ damage

36
Q

Determine the proceeding symptom necessary when evaluating a patient for acute rheumatic fever.

Occurs 1–2 weeks following a tick bite.

Occurs 2–4 weeks following group A Streptococcus pharyngitis.

Exposure to mites

Exposure to varicella

A

Occurs 2–4 weeks following group A Streptococcus pharyngitis.