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Pediatric Cancers
Cause is mostly unknown
Difficult to diagnose
Leukemia & brain tumors are the top 2 cancers
Cardinal S/S
Overt Signs
Directly observable
More noticeable
Covert signs
Hidden
Harder to notice
Children often present w/ advanced disease
Presenting w/ metastasis much more frequently than adults
Cardinal S/S (Overt Signs)
Pallor
Weight loss
Persistent fever
A mass
Purpura
Whitish reflection in the eye
Early morning vomiting
Cardinal S/S (Covert Signs)
Headache
Bone pain
Persistent lymphadenopathy
Change in balance, gait, &/or personality
Fatigue
Malaise
Diagnostic Tests
Bone Marrow Aspiration
Iliac crest, sternum
Diagnosis & monitoring of effectiveness of therapy
Biopsy
Identifies, classifies, & stages
Lab
CBC
Special tests
Alpha-fetoprotein, VMA or HVA, elevated Catecholamines
PET scan
Cancer Tx
Chemotherapy
Radiation
Other
Hematopoietic Stem Cell Transplantation (HSCT)
Steroid Therapy
Biologic Agents
Chemotherapy
Non-selectively kills rapidly dividing cells
Other areas impacted
Bone marrow
Gi
Skin
Unique protocols
Type of cancer
Stage & cellular characteristics
Central line:
CVL
Port (Under the skin, Bent needle)
PICC line
Adverse Effects of Chemotherapy (General)
Most common Sx
Pain
Nausea
Fatigue
Bone marrow suppression peaks 7-14 days after chemo
Greatest concern is infection
BM suppression causes:
Neutropenia
Anemia
Thrombocytopenia
Care of the Neutropenic Child
Screen visitors
Wear masks
No live plants in the room
IV care
Maintain sterility of central lines
Prevent line infections
Freq. temp.
Often the only sign of infection
Timely administration of antibiotics if signs of infection
Meticulous mouth care
NO live vaccines
Care of the Thrombocytopenic Child (Assess)
Increased bruising
Signs of bleeding
Urine
Stool
Gums
Care of the Thrombocytopenic Child (Avoid)
Activities that could cause injury
NO rectal medications or temps.
AVOID Aspirin/ NSAIDS
Care of the Thrombocytopenic Child (Use)
A soft bristle brush
Care during shaving
Caution during lab draws
Hold pressure for prolonged time
Adverse Effects of Chemotherapy (GI Tract)
N/V
Assess fluid/ electrolytes
Prophylactic, scheduled individualized antiemetics
Ondansetron (Zofran)
Aprepitant (Emend)
Anorexia
Associated w/ nausea & change in taste
High protein, high calorie foods
May needs NG or G-tube feedings
Stomatitis
Mouth care before/ after meals
NS or plain water mouth rinse
Rectal Ulcers
Warm, sitz bath
Meticulous cleaning of area
Constipation
Adverse Effects of Chemotherapy (Others)
Hemorrhagic Cystitis
Bladder inflammation leading to blood in the urine
Increase fluid > 1.5 times normal maintenance rate
Encourage frequent voiding
Alopecia
Very challenging for older school-age & teens
Ice cap during chemo
Alternative hair accessories
Hair will grow back after Tx
Fatigue
Educate patient & family
Radiation Therapy (Frightening)
Big, loud machine
Alone in the room
Have to be still
May need skin marking on the radiation area
Radiation Therapy (Interventions/ Prep,)
Tour of the department
Child-friendly facility
Pictures/ Talk to other children
Work w/ child life therapist
Sedation may be needed
Less radiation used than w/ adults
Adverse Effects of Radiation Therapy
Used more cautiously in children due to tissues, bones, & organs being more vulnerable to adverse effects
Radiation is NOT a Tx of choice in children < 3 years of age
Can be cognitively devastating
Side effects usually appear 7-10 days after initiation of therapy
Fatigue
Burns to the skin at the site
Redness, darkening, peeling, increased sensitivity
Hair loss
N/V, anorexia
Radiation Therapy (Nursing Care)
Assess the child’s skin daily at the Tx site
Aloe vera lotion or aqueous creams only
AVOID perfumed lotions & soap
Meticulous mouth & skin care
Adequate nutrition & fluid intake
Antiemetics
Diphenhydramine or hydrocortisone 1% cream for itching
Sunscreen
Skin is photosensitive
Other Cancer Therapeutics
Hematopoietic Stem Cell Transplantation (HSCT)
Steroid Therapy
Biologic Agents
Other Cancer Therapeutics (HSCT)
Hematopoietic Stem Cell Transplantation
Stem cells can differentiate into any type of hematologic cell
Healthy bone marrow cells are transfused into the patient’s blood & migrate to bone marrow
Other Cancer Therapeutics (Steroid Therapy)
Leukemia Tx & to control N/V
Have many side effects
Immunosuppression
Other Cancer Therapeutics (Biologic Agents0
Used to enhance cell recovery
Colony-stimulating factors (CSFs), Filgrastim (Neupogen)
Stimulate WBC recovery
Epogen (Epoetin alfa)
Stimulates RBC recovery
Reduced need for blood products
Leukemia
Most common cancer
1/3 of all cases
Disorder of the bone marrow
Overproduction of abnormal WBCs
Lymphoblasts
Suppresses normal cell formation in bone marrow
Leading to decreased RBC, WBC, & platelets
Acute leukemias are more common in children
Cause is generally unknown
May be a genetic factor
Types of Leukemia
Acute Lymphoblastic Leukemia (ALL)
Acute Myelogenous Leukemia (AML)
Types of Leukemia (ALL)
77%
Immature Lymphocytes
More common in boys
90% survival rate at 5 years
Types of Leukemia (AML)
25%
Immature Myelocytes
50% long-term survival rate
Leukemia (S/S)
Bone/ joint pain
Hallmark classic sign
Hepatosplenomegaly
Bone marrow suppression
Anemia
Leukopenia or leukocytosis
Thrombocytopenia
Leukemia (Diagnosis)
Initial CBC
The higher the WBC at initial diagnosis = The worse the disorder will be
Confirmatory bone marrow aspiration & biopsy
LP
Checks for CNS involvement
Therapeutic mngmnt.
Chemotherapy
Leukemia (Tx)
Involves 3 phases
Painful procedure over time
Induction
Consolidation
Maintenance
Leukemia (Tx Induction Phase)
To induce remission
< 5% blast cells in the bone marrow
98% of cases achieve remission by 1 month
Frequent bone marrow aspirations & LP
To track effectiveness of chemo
Leukemia (Tx Consolidation Phase)
Therapy to maintain remission
Leukemia (Tx Maintenance Phase)
Maintenance chemo given over 2-3 years
Brain Tumors
Most common solid tumor & second most prevalent malignancy in children
Mortality rate is close to 30%
70% will be long-term survivors but many will have functional neurologic deficits
Brain Tumors (S/S)
Based on location, size of the tumor, & child’s age
Headache upon arising (Waking up in the morning)
Vomiting unrelated to feeding
Brain Tumors (Nursing Care)
Attention to:
Neuro exam
VS
Preventing increased ICP
Pre- & post-op care & education
Brain Tumors (Diagnosis)
MRI
CT
PET Scan
LP
Presence of Alpha-fetoprotein or HCG
Brain Tumors (Tx)
Surgical Removal
If possible
Based on location
Radiation
> 3 years of age
Chemotherapy
In children < 3 years
Neuroblastoma
Mainly occurs in the adrenal gland
Tumor on the adrenal gland
Above the kidney
Abdominal mass crosses the midline
90% diagnosed before 5 years of age
The younger the kid, the better the outcomes tend to be
Neuroblastoma (S/S)
Pain
Abdominal mass crosses the midline
Elevated urine, HVA, VMA
24 hr urine culture
Neuroblastoma (Tx)
Surgical removal w/ radiation & chemo
Osteosarcoma & Ewing’s Sarcoma
Highly malignant bone cancers
Found mostly in teens
Osteosarcoma & Ewing’s Sarcoma (S/S)
Intermittent pain that progressively worsens
Mass at the tumor site
Limp or pathologic fracture at tumor site
Osteosarcoma & Ewing’s Sarcoma (Labs/ Diagnostics)
CT
MRI
Biopsy
Elevated serum alkaline phosphate (ALP)
Elevated lactate dehydrogenase (LDH)
Osteosarcoma & Ewing’s Sarcoma (Tx)
Osteosarcoma Tx
Chemo
Surgical excision
Chemo for additional year
Ewing’s Sarcoma Tx
Chemo
Surgical excision
Radiation
Rhabdomyosarcoma
Soft tissue tumor
Originates in tissues that become bones/ muscles
Rhabdomyosarcoma (S/S)
Often an asymptomatic mass
Locations
Head/ neck
Urinary tract
Extremities
Rhabdomyosarcoma (Tx)
Chemo
Surgical removal of tumor depending on location
Further chemo
Radiation if there is residual disease
Nephroblastoma “Wilm’s Tumor”
Kidney cancer
Tumor
90% survival rate
Nephroblastoma “Wilm’s Tumor” (S/S)
Fast growing abdominal mass
Firm, Non-tender, UNILATERAL
Hematuria
HTN
Nephroblastoma “Wilm’s Tumor” (Diagnosis)
Renal or abdominal US, CT, MRI
Negative HVA & VMA
Nephroblastoma “Wilm’s Tumor” (Nursing Mngmnt.)
Do NOT palpate tumor
Surgical removal
Removal of the tumor & the affected kidney
Radiation
Chemo
Retinoblastoma
Rare, malignant tumor of embryonic retinal cells
Hereditary component in some cases
90% of cases in children < 5 years
Goal
Save the child’s life & preserve the eye w/ useful vision
May have to remove the eye to save the child’s life
95% cure if detected early
Retinoblastoma (S/S)
Leukocoria “Cat’s eye”
Abnormal white or yellow reflection in the retina
Strabismus
Cross-eyed
Pain, redness, inflammation of the eye
Retinoblastoma (Diagnosis)
CT/MRI to visualize the tumor