PEDS PULM AND CA Flashcards

1
Q

When is Cancer seen mostly in children (of any age)?

A

Infancy to 4 years old and 15 to 19 years old (times of growth)

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2
Q

What is Cancer etiology?

A

Genetic alteration results in unregulated proliferation of cells including Apoptosis (programmed cell death); Oncogenes (genes that activate tumor growth) and Tumor suppressor genes (genes that keep tumor growth in “check”)

Can result from mutiple genetic events but doesn’t mean hereditary

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3
Q

What are some Risk factors associated with Cancer (CA)?

What is a major concern with Childhood CA?

A

Lifestyle related factors have little to no effect on cancer in children: (UNLIKE IN ADULTS)!!!

There are a few, well-established risk factors including:
Exposure to radiation; Carcinogenic drugs; Immunosuppression therapy
;Certain viral infections (EBV, HPV); Race/ethnicity; Genetic conditions

Of major concern is the risk of developing secondary malignant neoplasms because of curative treatment for childhood cancer

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4
Q

What has changed with Surivial Rates?

What group is behind on survival rates?

What is the Criteria for a “Cure”?

A

Increased dramatically over the last 50 years since chemotherapy was first given to children

Survival improvements among adolescents has lagged compared to other age groups

Cure = completion of all therapy, no clinical and radiological evidence of diseases, and 5 years since diagnosis

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5
Q

What is the Major concern with the long-term effects of Childhood CA?

A

Factors that affects the patient into adulthood (relationships, coping skills, emotional well-being)

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6
Q

What are the CARDINAL SIGNS of CA in Children? What is the overall takeaway with these signs?

A

An unsual lump or swelling
Unexplained paleness and loss of energy

Easy bruising or bleeding

Ongoing pain in one area of the body

Limping. unexplained fever or illness that does not resolve

Frequent H/A (often w/ vomiting)

Sudden eye changes or vision changes

Sudden unexplained weight loss

Overall takeaway: Anything that NOT normal and DOESN’T GO AWAY

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7
Q

How should the S/E of treatment be handled?

S/S include (Infection – destruction of WBC; Hemorrhage –loss of platelets; Anemia – loss of RBCs; Nausea and Vomiting; Altered Nutrition; Mucosal Ulceration – mouth, pharynx, esophagus, rectal; Neurologic Problems neurotoxicity; Hemorrhagic cystitis chemotherapy injures bladder lining; Alopecia)

A

Inf- S&S of infection and sepsis, IV therapy treatment, prophylaxis common, biologics, prevent infection is important!

Hem- Used to be leading cause of death in cancer pts, avoid skin puncture when possible!, avoid additional trauma, platelet transfusions during bleeding episodes

Anemia- RNC transfusions, let child regulate activity

N/V- meds (pheng, Compazine, Tigan),

Altered Nutrition- assess weight, intake, height, etc. High calorie foods, d/t mucosal ulcers

Mucosal Ulceration –bland food, soft toothbrush or tooth sponge, antiseptic mouth washes, warm sitz bath, ointments

Neuro- jaw pain, foot drop, numbness, weakness, constipation

Hemorrhagic- Lots of fluid before, during, after chemo.

Alopecia- set expectations

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8
Q

What is Leukemia(s)?

What is the most common form of Childhood Cancer?

A

Umbrella term for cancers of the blood, bone marrow, and lymphatic system

In health children, bone marrow makes blood stem cells which mature into lymphoid or myeloid stem cells
Myeloid stem cells–> Red blood cells, Platelets, WBCs and Lymphoid stem cells–> Lymphoblasts (become B and T lymphocytes) and natural killer cells

Acute Lymphoblastic Leukemia (ALL) is the most common form of childhood cancer (80% of leukemias)

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9
Q

Where does the most common solid tumor in children arise from?

A

Tumors of the CNS are the most common solid tumor in children

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10
Q

What are some Manifestations/Behaviors of Brain Tumors?

A

Signs and symptoms are directly related to their location and size

Headache and vomiting upon waking (increased ICP)

Behavioral changes, visual disturbances, motor skill disruption, seizures, hemiparesis (half of the body is paralyzed)

Diagnosis based on:
Clinical signs and symptoms
Imaging
Biopsy (usually done during surgery)

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11
Q

Treatment for Brain tumors includes?

A

Surgery: Survival increases with complete tumor removal

Chemotherapy

Radiation
Shrinks tumor before attempting
surgical removal
Kill remaining tumor cells after
surgery

Treatment depends on the type of tumor involved

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12
Q

What are s/s of bone tumors?

A

Pain in affected site

Limping, stops physical activity, unable to hold heavy objects

Palpable mass

Cord compression & Respiratory distress (Ewing’s sarcoma)

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13
Q

What are examples of Bone tumors?

A

Osteosarcoma: Most common bone tumor in adolescents and young adults; Thought to originate during rapid bone growth; Tumor sites often in long bones near growth plate (40% in femur)

Ewing’s sarcoma
Less common – approx. 200 cases per year; Predominantly in Caucasians; More than half are adolescents

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14
Q

What is a neuroblastoma?

What are S/S?

A

Most common extracranial childhood solid tumor

S/S include:
Depend on location and extent of the disease progress

Most common site: abdomen
Other sites: head and neck, chest, pelvis

Firm, non-tender, irregular mass that crosses the midline (TEST Q)
Excrete catecholamines if tumor on adrenal glands or sympathetic chain. Urinary excretion can be measured to determine

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15
Q

What is a Wilm’s Tumor? (AKA)?

A

Also called nephroblastoma

Most common kidney tumor of childhood

Approximately 10% of children with Wilms have congenital anomalies

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16
Q

What are manifestations of a Wilm’s Tumor?

A

Swelling or mass in abdomen that does not cross midline

Mass is firm, non-tender, one sided, deep in flank

Pain

Hematuria (less than 25% of children)

17
Q

What is the treatment for Wilm’s tumor?

What is a important nursing consideration?

A

Surgery
Nephrectomy for unilateral disease (keep capsulated tumor intact)
Renal transplant for bilateral disease (Stage V)

Chemotherapy (Vincristine can cause peripheral IV necrosis)

Do NOT palpate abdomen – risk of disseminating cancer cells into abdominal cavity (TEST Q)

18
Q

What is a Rhabdomyosarcoma?
What are the most common sites?

A

Cancer that arises from striated (rhabdo) tissue

Originate from muscles, tendons, bursae, and fascia

Most common primary sites are in head and neck (especially the orbit)

19
Q

What is a Retinoblastoma?
What’s a common sign?

A

Cancer that arises from the retina

Most common intraocular malignancy of childhood

Whitish “glow” in the pupil – cat’s eye reflex

20
Q

What is Cystic Fibrosis?

What is the genetic inheritance?

A

A respiratory disorder that’s characterized by mucus glands that sectrete an increase in the quality of thick, tenacious mucus leading to mechanical obstruction of organs

Most common lethal genetic illness among Caucasian children, adolescent, and young adults

Autosomal recessive trait (meaning both parents have a trait for the disease)

21
Q

What labs are increased that helps indicated CF?

What is the goal of treatment?

A

Sodium, chloride, and increased in sweat glands. Sweat chloride test (>60mEqs/L)

Goal (to prevent or minimize pulmonary complications. ensure adequate nutrition, and Quality of life)