Oncological and Hematological Problems Flashcards

1
Q

Cancer

A
  • a malignant neoplastic disorder that can involve all body organs with manifestations that vary according to the body system affected and type of tumor cells.
  • cells lose their normal growth-controlling mechanism, and the growth of cells is uncontrolled.
  • cancer produces serious health problems such as impaired immune and hematopoietic (blood-producing) function, altered GI tract structure and function, motor and sensory deficits, and decreased respiratory function.
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2
Q

Metastasis

A
  • cancer cells move from their original location to other sites.
  • routes:
    = local seeding: distribution of shed cancer cells occurs in the local area of the primary tumor.
    = bloodborne metastasis: tumor cells enter the blood, which is the most common cause of cancer spread.
    = lymphatic spread: primary sites rich in lymphatics are more susceptible to early metastatic spread.
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3
Q

Cancer classification

A
  • solid tumors: associated with the organs from which they develop, such as breast or lung cancer.
  • hematological cancers: originate from the blood cell-forming tissues, such as leukemias, lymphomas, and multiple myeloma.
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4
Q

Cancer grading and staging

A
  • grading and staging are methods used to describe the tumor.
  • these methods describe the extent of the tumor, the extent to which malignancy has increased in size, the involvement of regional nodes, and metastatic development.
  • grading a tumor classifies the cellular aspects of the cancer and is an indicator of tumor growth rate and spread.
  • staging classifies the severity and clinical aspects of the cancer and degree of metastasis at diagnosis.
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5
Q

Grading

A
  • Grade I: cells differ slightly from normal cells and are well differentiated (mild dysplasia).
  • Grade II: cells are more abnormal and are moderately differentiated (moderate dysplasia).
  • Grade III: cells are very abnormal and are poorly differentiated (severe dysplasia).
  • Grade IV: cells are immature (anaplasia) and undifferentiated; cell of origin is difficult to determine.
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6
Q

Staging

A
  • Stage 0: carcinoma in situ.
  • Stage I: tumor limited to the tissue of origin; localized tumor growth.
  • Stage II: limited local spread.
  • Stage III: extensive local and regional spread.
  • Stage IV: distant metastasis.
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7
Q

Factors that influence cancer development

A

Environmental factors:

  • chemical carcinogen include industrial chemicals, meds, and tobacco.
  • physical carcinogen include ionizing radiation, UV radiation, chronic irritation, and tissue trauma.
  • viral carcinogen (also known as oncoviruses) include Epistein-Barr virus, Hep B virus, and human papillomavirus.
  • Helicobacter pylori infection is associated with an increased risk of gastric cancer.
  • obesity and dietary factors, including preservatives, contaminants, additives, alcohol, and nitrates.
  • genetic predisposition, age, and immune function.
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8
Q

Early detection

A
  • mammography
  • papanicolau test
  • rectal exams and stools for occult blood
  • sigmoidoscopy, colonoscopy
  • breast self-examination and clinical beast examination
  • testicular self-examination
  • skin inspection
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9
Q

Warning signs of cancer - CAUTION

A
Change in bowel or bladder habits
Any sore that does not heal
Unusual bleeding or discharge
Thickening or lump in breast or elsewhere
Indigestion
Obvious change in wart or mole
Nagging cough or hoarseness
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10
Q

Diagnostic tests

A
  • Biopsy (needle, incisional, excisional, staging)
  • bone marrow examination
  • chest radiograph
  • complete blood count
  • CT; PET
  • cytological studies (papanicolaou)
  • evaluation of serum tumor markers (carcinoembryonic antigen and alpha-fetoprotein)
  • liver function studies
  • MRI
  • proctoscopic examination
  • radiographic studies (mammography)
  • radioisotope scanning (liver, brain, bone, lung)
  • tumor markers
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11
Q

Pain control

A
  • Causes: bone destruction, obstruction of an organ, compression of peripheral nerves, infiltration, distension of tissue, inflammation, necrosis, psychological factors (such as fear or anxiety).
  • Interventions: adm pain meds (severe pain is treated with opioids), monitor VS and effectiveness of meds, provide nonpharmacological techniques of pain control.
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12
Q

Surgery

A
  • indicated to diagnose, stage, and treat certain types of cancer.
  • Prophylactic: performed in clients with an existing premalignant condition or a known family history or genetic mutation that strongly predisposes to the development of cancer.
  • Curative: all gross and microscopic tumor is removed or destroyed.
  • Control (cytoreductive or debulking): consists of removing a large portion of a locally invasive tumor; decreases the number of cancer cells (therefore increases the chance that other therapies will be successful.
  • Palliative: performed to improve quality of life; to reduce pain, relieve airway obstruction, relieve obstructions in the GI or urinary tract, relieve pressure on the brain or spinal cord, prevent hemorrhage, remove infected or ulcerated tumors, or drain abscesses.
  • Reconstructive or rehabilitative: performed to improve quality of life by restoring maximal function and appearance (such as breast reconstruction).
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13
Q

Adverse effects of surgery

A
  • loss of function of a specific body part
  • reduced function as a result of organ loss
  • scarring or disfigurement
  • grieving about altered body image or imposed change in lifestyle.
  • pain, infection, bleeding, thromboembolism.
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14
Q

Chemotherapy

A
  • kills or inhibits the reproduction of neoplastic cells and kills normal cells; effects are systemic.
  • normal cells mos profoundly affected include those of the skin, hair, and lining of the GI tract; spermatocytes; and hematopoietic cells.
  • usually used a combination therapy to increase the therapeutic response and is planned by the PHCP so that meds with overlapping toxicities and nardis are not adm at or near the same time.
  • may be combined with other treatments, such as surgery and radiation.
  • common side effects: fatigue, alopecia, nausea, vomiting, mucositis, skin changes, and myelosuppression (neutropenia, anemia, and thrombocytopenia).
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15
Q

Radiation Therapy

A
  • destroys cancer cells, with minimal exposure of normal cells; the damaged cells die or become unable to divide.
  • is effective on tissues directly within the path of the radiation beam.
  • side effects include local skin changes and irritation, alopecia, fatigue, and altered taste sensation (vary according to site).
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16
Q

Radiation Therapy: External beam radiation

A
  • also called teletherapy.
  • radiation source is external to the client.
  • instruct the client regarding self-care of the skin.
  • client does not emit radiation and does not pose a hazard to anyone.
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17
Q

Radiation Therapy: Brachytherapy

A
  • radiation source comes into direct, continuous contact with tumor tissues for a specific time.
  • source is within the client for a period of time, therefore emits radiation and can pose a hazard to others.
  • includes an unsealed source or a sealed source of radiation.
  • unsealed: adm is via the oral or IV route or by instillation into body cavities; source is not confined completely and eventually is eliminated via various excreta (which are radioactive and harmful); most of the source is eliminated within 48h.
  • sealed: temporary or permanent radiation source (solid implant) is implanted within the tumor target tissues; client emits radiation while the implant is in place, but the excreta are not radio active.
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18
Q

Hematopoietic Stem Cell Transplantation: description

A
  • bone marrow transplantation (BMT) and peripheral blood stem cell transplantation (PBSCT) are procedures that replace stem cells that have been destroyed by high doses of chemotherapy and/or radiation therapy.
  • BMT and PBSCT are most commonly used in the treatment of leukemia and lymphoma but are also used to treat other cancers, such as neuroblastoma and multiple myeloma.
  • goal of treatment is to rid the client of all leukemic or other malignant cells through treatment with high doses of chemotherapy and whole-body irradiation.
  • because these treatments are damaging to bone marrow cells, without the replacement of blood-forming stem cell function through transplantation, the client would die of infection or hemorrhage.
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19
Q

Hematopoietic Stem Cell Transplantation:

Types of Donor Stem Cells

A
  • Allogenic: stem cell donor is usually a sibling, a parent with a similar tissue type, or a person who is not related.
  • Syngeneic: stem cells are from an identical twin.
  • Autologous: most common type; client receives their own stem cells, which are harvested during disease remission and are stored frozen to be reinfused later.
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20
Q

Hematopoietic Stem Cell Transplantation: Procedure

A
  • Harvest: stem cells used in PBSCT come from the bloodstream in a 4-6h process called apheresis or leukapheresis (blood is removed through a CVC and an apheresis machine removes the stem cells and returns the remainder of the blood to the donor); in BMT, marrow is harvested through multiple aspirations from the iliac crest to retrieve sufficient bone marrow; marrow from the client is filtered for residual cancer cells; allogenic marrow is transfused immediately; autologous is frozen for later use; harvesting is done before the initiation of the conditioning regimen.
  • Conditioning: refers to immunosuppression therapy regimen used to eradicate all malignant cells, provide a state, and create space in the bone marrow for the engraftment of the new marrow.
  • Transplatation: stem cells are adm through the client’s CVC similar to a blood transfusion (ma be adm by IV infusion or by push).
  • Engraftment: transfused stem cells move to the marrow-forming sites of the recipient’s bones; engraftment occurs when the WBC, erythrocyte, and platelet counts begin to rise; when successful, the engraftment process takes 2-5 weeks.
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21
Q

Hematopoietic Stem Cell Transplantation: Complications

A
  • infection, bleeding, or neutropenia and thrombocytopenia are major concerns until engraftment occurs.
  • failure to engraft: client will die unless another transplantation is attempted and successful.
  • graft x host disease in allogeneic transplants: the immune-competent cells of the donor recognize the recipient’s cells as foreign and mount an immune offense against them; managed with immunosuppressive agents.
  • hepatic veno-occlusive disease: involves occlusion of the hepatic venules by thrombosis or phlebitis; treated with fluids and supportive therapy (early detection is critical because there is no known way to open the vessels); sings include abd pain, jaundice, ascites, weight gain, and hepatomegaly.
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22
Q

Leukemia: description

A
  • are a group of hematological malignancies involving abnormal overproduction of leukocytes (usually at a immature stage, in the bone marrow).
  • 2 major types are lymphocytic and myelocytic or myelogenous.
  • may be acute, with a sudden onset, or chronic, with a slow onset and persistent symptoms over a period of years.
  • affects the bone marrow causing anemia, leukopenia, the production of immature cells, thrombocytopenia, and a decline in immunity.
  • cause is unknown and appears to involve genetically damaged cells.
  • risk factors: genetic, viral, immunological, and environmental factors and exposure to radiation, chemicals, and medications, such as previous chemotherapy.
  • infection is a major cause of death and bleeding a major concern.
  • chemotherapy: induction, consolidation, and maintenance.
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23
Q

Leukemia: assessment

A
  • anorexia, fatigue, weakness, weight loss, anemia, overt bleeding, occult bleeding, ecchymoses, petechiae, prolonged bleeding after minor trauma, elevated temp, enlarged lymph nodes, spleen, and liver, palpitations, tachycardia, orthostatic hypotension, pallor and dyspnea on exertion, headache, bone pain and joint swelling, normal, elevated or reduced WBC count, decreased Hb and Ht levels, decreased platelet count, positive bone marrow biopsy.
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24
Q

Classification of Leukemia

A
  • Acute Lymphocytic: mostly lymphoblasts present in bone marrow; age of onset is younger than 15y.
  • Acute Myelogenous: mostly myeloblasts present in bone marrow; age of onset is between 15-39y.
  • Chronic Myelogenous: mostly granulocytes present in bone marrow; age of onset is in the fourth decade.
  • Chronic Lymphocytic: mostly lymphocytes present in bone marrow; age of onset is after 50y.
25
Q

Lymphoma: Hodgkin’s Disease

A
  • classified as Hodgkin’s and non-Hodgkin’s depending on the cell type, are characterized by abnormal proliferation of lymphocytes.
  • is a malignancy of the lymph nodes that originates in a single lymph node or a chain of nodes.
  • metastasis occur to other, adjacent lymph structures and eventually invades nonlymphoid tissue.
  • the disease usually involves lymph nodes, tonsils, spleen, and bone marrow and is characterized by the presence of Reed-Sternberg cells inn the nodes.
  • possible causes include viral infections; clients treated with combination chemotherapy for Hodgkin’s disease have a greater risk of developing acute leukemia and non-Hodgkin’s lymphoma, among other secondary malignancies.
  • prognosis depend on the stage of the disease.
26
Q

Lymphoma: Hodgkin’s Disease

Assessment and Interventions

A
  • Assessment: fever, malaise, fatigue, weakness, night sweats, loss of appetite and significant weight loss, anemia and thrombocytopenia, enlarged lymph nodes, spleen, and liver, positive biopsy of lymph nodes (cervical most often affected first), presence of Reed-Sternberg cells in nodes, positive CT scan of the liver and spleen.
  • Interventions: for early stages (I and II), without mediastinal node involvement, the treatment of choice is extensive external radiation; with more extensive disease, radiation and multi-agent chemotherapy are used. Monitor for side effects, signs of infection and bleeding (maintain precautions); discuss the possibility of sterility.
27
Q

Multiple Myeloma

A
  • a malignant proliferation of plasma cells within the bone that invade the bone marrow and destroy; invasion of lymph nodes, spleen, and liver occurs.
  • abnormal plasma cells produce abnormal antibody (myeloma protein or the Bence Jones protein) found in the blood and urine.
  • causes decreased production of immunoglobulin and antibodies and increased levels of uric acid and calcium, which can lead to kidney failure.
  • typically develops slowly and the cause is unknown.
  • assessment: bone pain, weakness, fatigue, recurrent infections, anemia, urinalysis shows Bence jones proteinuria and elevated total serum protein level, osteoporosis, thrombocytopenia and leukopenia, elevated calcium and uric acid levels, kidney failure, spinal cord compression and paraplegia, bone marrow aspiration shows and abnormal number of immature plasma cells.
  • interventions: chemotherapy, radiation, IV fluids, diuretics, blood transfusions, ATB, analgesics, bisphosphonate meds (slow bone damage and reduce pain and risk of fractures).
28
Q

Testicular Cancer

A
  • arises from germinal epithelium from the sperm-producing germ cells or from nongerminal epithelium from other structures in the testicles.
  • most often occurs between ages 15-40y and cause is unknown (but a history of undescended testicle and genetic predisposition have been associated).
  • metastasis occur to the lung, liver, bone, and adrenal glands via the blood and the retroperitoneal lymph nodes.
  • early detection: perform monthly self-examination.
  • assessment: painless testicular swelling, “dragging” or “pulling” sensation, palpable lymphadenopathy, abd masses, and gynecomastia (may indicate metastasis); late signs include back or bone pain and respiratory symptoms.
  • interventions: chemo and radiation therapy; unilateral orchiectomy (or radical); retroperitoneal lymph node dissection; discuss reproduction, sexuality, and fertility.
29
Q

Cervical Cancer

A
  • preinvasive cancer is limited to the cervix; invasive cancer is in the cervix and other pelvic structures.
  • metastasis usually is confined to the pelvis, but distant metastasis occurs through lymphatic spread.
  • stages: I mild dysplasia; II moderate dysplasia; III severe dysplasia to carcinoma in situ.
  • risk factors: HPV, cigarette smoking, reproductive behavior, multiple partners.
  • assessment: painless vaginal postmenstrual and postcoital bleeding; foul-smelling or serosanguineous vaginal discharge; pelvic lower back, leg, or groin pain; anorexia and weight loss; leakage of urine and feces from the vagina; dysuria, hematuria; cytological changes on Pap test.
  • nonsurgical interventions: chemotherapy, cryosurgery, external radiation, internal radiation implants, laser therapy.
  • surgical interventions: conization, hysterectomy, pelvic exenteration.
30
Q

Ovarian Cancer

A
  • grows rapidly, spreads fast, and is often bilateral.
  • metastasis occurs by direct spread to the organs in the pelvis, by distal spread through lymphatic drainage, or by peritoneal seeding.
  • in early stages is often asymptomatic; because most women are diagnosed in advanced stages, has a higher mortality rate than any other cancer of the female reproductive system.
  • an exploratory laparotomy is performed to diagnose and stage the tumor.
  • assessment: abd discomfort or swelling, GI disturbances, dysfunctional vaginal bleeding, abd mass, elevated tumor marker (CA-125).
  • interventions: radiation, chemotherapy (postop), intraperitoneal chemotherapy, total abd hysterectomy and bilateral salpingo-oophrectomy with tumor debulking may be necessary.
31
Q

Endometrial (uterine) Cancer

A
  • a slow-growing tumor arising from the endometrial mucosa of the uterus, associated with the menopausal years.
  • metastasis occurs through the lymphatic system to the ovaries and pelvis; via the blood to the lungs, liver, and bone; or intra-abdominally to the peritoneal cavity.
  • risk factors: use of estrogen replacement therapy, nulliparity, polycystic ovary disease, increased age, late menopause, family history, obesity, hypertension, DM.
  • assessment: abnormal bleeding, vaginal discharge, low back, pelvic, or abd pain, enlarged uterus (advanced stages).
  • interventions: radiation alone or in combination with surgery (depending on stage); chemotherapy (advanced or recurrent); progesterone therapy may be prescribed for estrogen-dependent tumors; antiestrogen may also be prescribed.
  • surgical interventions: total abd hysterectomy and bilateral salpingo-oophrectomy.
32
Q

Breast Cancer: description and risk factors

A
  • classified as invasive when it penetrates the tissue surrounding the mammary duct and grows in an irregular pattern.
  • metastasis occurs via lymph nodes; common sites are the bone and lungs, may also affect the brain and liver.
  • diagnosis is made by breast biopsy (needle aspiration or by surgical removal).
  • risk factors: age, family history; early menarche and late menopause; previous cancer of the breast, uterus, or ovaries; nulliparity, late first birth; obesity; high-dose radiation exposure to chest.
33
Q

Breast Cancer: assessment and BSE

A
  • assessment: mass felt during BSE; presence of the lesion on mammography, a fixed, irregular non-encapsulated mass (usually painless); asymmetry; bloody or clear nipple discharge; nipple retraction or elevation; skin dimpling, retraction, or ulceration; skin edema or peau d’orange skin; axillary lymphadenopathy; lymphedema of the affected arm; symptoms of bone or lung metastasis in late stage.
  • early detection: perform BSE regularly 7-10 days after menses; postmenopausal clients or who have had a hysterectomy should perform regularly as well.
34
Q

Breast Cancer: Interventions

A
  • nonsurgical: chemotherapy, radiation, hormonal manipulation, monoclonal antibodies (such as trastuzumab).
  • surgical: breast procedures with possible breast reconstruction.
  • postop: monitor VS, maintain semi-fowler’s, affected arm elevated above the level of the heart to promote drainage; coughing and deep breathing; if a drain is present, maintain suction and record amount and characteristics; assess operative site and monitor incision; provide pressure sleeve if edema is severe; provide diuretics and low-salt diet for severe lymphedema.
  • no IV, no injections, no BP measurements, and no venipunctures should be done in the arm on the side of the mastectomy.
35
Q

Esophageal cancer

A
  • a malignancy found in the esophageal mucosa, formed by squamous cell carcinoma (SCC) or adenocarcinoma.
  • cause is unknown but major risk factors include cigarette smoking, alcohol, chronic reflux, Barrett’s esophagus, and vitamin deficiencies.
  • complications include dysphagia, painful swallowing, loss of appetite, and malaise.
  • goal of treatment is to inhibit tumor growth and maintain nutrition.
  • assessment: dysphagia, odynophagia, epigastric pain or sternal pain.
  • interventions: monitor daily weight, intake and output, calories consumed; prepare for chemotherapy and radiation; prepare for surgical resection of the tumor.
36
Q

Gastric Cancer: description

A
  • malignant growth of the mucosal cells in the inner lining of the stomach, with invasion to the muscle and beyond in advanced disease.
  • no single causative agent but it is believed that H. Pyloru infection and a diet of smoked, highly salted, processed, or spiced foods have carcinogenic effects; other risks include smoking, alcohol and nitrate ingestion, and a history of gastric ulcers.
  • complications: hemorrhage, obstruction, metastasis, and dumping syndrome.
  • goal of treatment is to remove the tumor and provide a nutritional program.
37
Q

Gastric Cancer: assessment and interventions

A
  • early: indigestion, abd discomfort, full feeling, epigastric, back, or retrosternal pain.
  • late: weakness and fatigue; anorexia and weight loss; nausea and vomiting; a sensation of pressure in the stomach; dysphagia and obstructive symptoms; iron deficiency anemia; ascites; palpable epigastric mass.
  • interventions: monitor VS, Hb, Ht, weight, intake and output; assess nutritional status; place in fowler’s position; prepare for chemo or radiation or surgical resection; adm analgesics, antiemetics, fluids. In postop maintain NPO for 1-3 days and monitor nasogastric suction (bloody for 24hs, then turns brown and then yellow or clear); do not irrigate or remove nasogastric tube; monitor for complications: hemorrhage, dumping syndrome, diarrhea, hypoglycemia, and vit B12 deficiency.
38
Q

Surgical Interventions for Gastric Cancer

A

Subtotal Gastrectomy
- Billroth I: also called gastroduodenostomy; partial gastrectomy, with remaining segment anastomosed to the duodenum.
- Billroth II: also called gastrojejunostomy; partial gastrectomy, with remaining segment anastomosed to the jejunum.
Total Gastrectomy
- also called esophagojejunostomy; removal of the stomach, with attachment of the esophagus to the jejunum or duodenum.

39
Q

Pancreatic Cancer

A
  • most are highly malignant, rapidly growing adenocarcinomas originating from the epithelium of the ductal system.
  • associated with increased age, DM, alcohol use, history of previous pancreatitis, smoking, high-fat diet, and exposure to environmental chemicals.
  • symptoms usually do not occur until the tumor is large (therefore, poor prognosis).
  • assessment: nausea, vomiting, jaundice, unexplained weight loss, clay-colored stools, glucose intolerance, abd pain.
  • interventions: radiation, chemo, whipple procedure (pancreaticoduodenectomy with removal of the distal third of the stomach, pancreaticojejunostomy, grastrojejunostomy, and choledochojejunostomy).
40
Q

Intestinal Tumors: description and risk factors

A
  • are malignant lesions that develop in the cells lining the wall or develop as adenomatous polyps in the colon or rectum.
  • tumor spread is by direct invasion and through the lymphatic and circulatory systems.
  • complications include bowel perforation with peritonitis, abscess and fistula formation, hemorrhage, and complete intestinal obstruction.
  • risk factors: >50y, familial polyposis, family history, previous colorectal polyps, history of colorectal cancer, chronic inflammatory bowel disease, ovarian or breast, endometrial, and stomach cancers.
41
Q

Intestinal Tumors: assessment and interventions

A
  • blood in stool, anorexia, vomiting, weight loss, anemia.
  • abnormal stools: diarrhea (ascending colon tumor); constipation or some diarrhea, or flat, ribbon-like stool caused by a partial obstruction; alternating constipation and diarrhea (rectal tumor).
  • guarding or abd distension, abd mass (late sign); cachexia (late sign).
  • masses noted on barium enema, colonoscopy, CT scan, sigmoidoscopy.
    Interventions
  • monitor for signs of complications, prepare for preop radiation and postop chemo. Instruct preop diet and bowel preparation. Postop monitor for complications, care for stoma, assess function, and provide prescribed diet, analgesics and ATB.
    Surgical interventions:
  • bowel resection, local lymph node resection, and creation of a colostomy or ileostomy.
42
Q

Lung Cancer: description, causes, assessment

A
  • malignant tumor of the bronchi and peripheral lung tissue (common target for metastasis).
  • bronchogenic cancer: tumor originate in the epithelium of the bronchus and spreads through direct extension and lymphatic dissemination.
  • classified according to histological cell type: small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC); epidermal (squamous cell), adenocarcinoma, and large cell anaplastic carcinoma are classified as NSCLC because of their similar responses to treatment.
  • diagnosis: chest x-ray, CT and PET scan, or MRI; bronchoscopy and sputum studies.
  • causes: smoking, exposure to environmental and occupational pollutants.
  • assessment: cough, wheezing, dyspnea, hoarseness, hemoptysis, blood-tinged or purulent sputum, chest pain, anorexia, weight loss, weakness, diminished or absent breath sounds, respiratory changes.
43
Q

Lung Cancer: Interventions

A

General:
- monitor, fowler’s position, adm analgesics, bronchodilators and corticosteroids.
- provide a diet high in calorie, protein, and vitamin.
- chemotherapy and radiation
Surgical interventions:
- laser therapy; thoracentesis and pleurodesis (remove fluid); thoracotomy with pneumonectomy (removal of 1 lung); with lobectomy (removal of 1 lobe); with segmental resection (removal of a lobe segment).
Postop:
- monitor, maintain chest tube drainage system, assess for complications, avoid complete lateral turning, adm oxygen, encourage range-of-motion exercises.

44
Q

Laryngeal Cancer

A
  • malignant tumor presented as ulcerations with underlying infiltration and is spread by local extension and by lymphatic system.
  • diagnosis made by laryngoscopy and biopsy; chest x-ray, CT, and MRI are used for staging.
  • risk factors: smoking, heavy alcohol use, exposure to environmental pollutants or radiation.
  • assessment: persistent hoarseness or sore throat and ear pain; painless neck mass; feeling of a lump or burning sensation in the throat; dysphagia; change in voice quality; dyspnea; weakness and weight loss; hemoptysis; foul breath odor.
  • non-surgical interventions: radiation and chemo.
  • surgical interventions: goal is to remove the tumor while preserving as much normal function as possible. Types of resection include cordal stripping, cordectomy, partial laryngectomy, and total laryngectomy (tracheostomy is needed and permanent)
45
Q

Prostate Cancer: description, assessment, risk factors, diagnosis

A
  • slow-growing malignancy; most are adenocarcinomas arising from androgen-dependent epithelial cells.
  • can spread via direct invasion or by metastasis through the bloodstream and lymphatics, to the bony pelvis and spine.
  • cause is unclear, but >50y, heavy metal exposure, smoking, history of STDs.
  • assessment: asymptomatic in early stages; hard, pea-size nodule or irregularities palpated on rectal examination; gross, painless hematuria; weight loss, urinary obstruction, and bone pain (late signs).
  • prostate-specific antigen level is elevated (used to monitor response to therapy not diagnosis)
  • diagnosis is made through biopsy.
46
Q

Prostate Cancer: interventions

A
  • hormone manipulation therapy (androgen suppression) or active surveillance with PSA and digital rectal examination.
  • luteinizing hormone may be prescribed to slow the rate of growth of the tumor.
  • adverse effects: reduced libido, hot flashes, breast tenderness, osteoporosis, loss of muscle mass, and weight gain.
  • pain med, radiation, corticosteroid, and bisphosphonates may be prescribed for palliation of advanced cancer.
  • prepare for external beam radiation or brachytherapy (may be prescribed alone or with surgery, preop or postop, to reduce the lesion and limit metastasis.
    chemotherapy in cases of hormone treatment resistant tumors.
  • orchiectomy (palliative) will limit the production of testosterone.
  • radical prostatectomy can be performed via a retropubic, perineal, or suprapubic approach.
  • cryosurgical ablation is a minimally invasive procedure that may be an alternative to radical prostatectomy.
  • transurethral resection of the prostate (TURP) may be performed for palliation (monitor for resection syndrome or severe hyponatremia postop).
47
Q

Bladder Cancer

A
  • a papillomatous growth in the bladder urothelium that undergoes malignant changes and may infiltrate the bladder wall.
  • risk factors: smoking, exposure to industrial chemicals, and exposure to radiation.
  • common sites for metastasis: liver, bones, and lungs.
  • as the tumor progresses, it can extend into the rectum, vagina, other pelvic soft tissues, and retroperitoneal structures.
  • assessment: gross or microscopic, painless hematuria; frequency, urgency, dysuria; clot-induced obstruction; bladder wash specimens and biopsy confirm diagnosis.
  • interventions: radiation (advanced disease that can be eradicated with surgery); chemotherapy; transurethral resection of bladder tumor (early tumors or palliation in inoperable tumors); partial cystectomy (early stage); cystectomy and urinary diversion; ileal conduit; kock pouch; indiana pouch; creation of a neobladder; percutaneous nephrostomy or pyelostomy (prevent or treat obstruction); ureterostomy (palliative if obstruction by tumor).
48
Q

Oncological Emergencies: sepsis and disseminated intravascular coagulation (DIC)

A
  • due to increased risk of infection and DIC is frequently associated.
  • maintain strict aseptic technique.
  • adm ATB, anticoagulants (early phase DIC), cryoprecipitated clotting factors (when DIC progresses and hemorrhage is the primary problem).
49
Q

Oncological Emergencies: syndrome of inappropriate antidiuretic hormone (SIADH)

A
  • tumors can produce, secrete, or stimulate substances that mimic antidiuretic hormone.
  • initiate fluid restriction and increased sodium intake.
  • adm an antagonist to antidiuretic hormone.
  • monitor sodium levels and treat underlying cause with chemo or radiation to achieve tumor regression.
50
Q

Oncological Emergencies: spinal cord compression

A
  • tumor directly enters the spinal cord.
  • causes back pain and neurological deficits occur with progression.
  • adm high-dose corticosteroids to reduce swelling.
  • radiation and chemo to reduce size of tumor.
  • surgery may be necessary.
  • use of neck or back braces.
51
Q

Oncological Emergencies: hypercalcemia

A
  • late manifestation of extensive malignancy that occurs most often with bone metastasis, when the bone releases calcium into the bloodstream.
  • monitor calcium level, adm fluids and meds that lower the calcium level and control nausea and vomiting.
  • prepare for dialysis if the condition becomes life threatening.
  • encourage walking to prevent breakdown of bone.
52
Q

Oncological Emergencies: superior vena cava syndrome

A
  • occurs when the SVC is compressed or obstructed by tumor growth (commonly associated with lung cancer and lymphoma).
  • signs and symptoms result from blockage of blood flow in the venous system. Starts with edema of face and neck, then progresses to arms and hands, dyspnea, erythema of the upper body, swelling of veins in the chest and epistaxis.
  • place in semi-fowler’s position, adm corticosteroids and diuretics as prescribed.
  • high-dose radiation to the mediastinal area and possible surgery to insert a metal stent in the vena cava.
53
Q

Oncological Emergencies: tumor lysis syndrome

A
  • occurs when large quantities of tumor cells are destroyed rapidly and intracellular components such as potassium and uric acid are released into the blood stream faster than the body can eliminate them.
  • if left untreated, it can cause severe tissue damage and death.
  • hyperkalemia, hyperphosphatemia with resultant hypocalcemia, and hyperuricemia occur.
  • encourage hydration, monitor renal function, intake and output, and ensure a diet low in potassium and phosphorus.
  • adm IV fluids, diuretics, meds to increase the excretion of purines (such as allopurinol).
  • IV infusion of glucose ans insulin to treat hyperkalemia.
  • dialysis if hyperkalemia and hyperuricemia persist.
54
Q

Anemia

A
  • condition in which the blood lacks adequate healthy red blood cells or hemoglobin.
  • treatment is focused on the cause.
  • assessment: fatigue, weakness, pallor or slight jaundice, shortness of breath, dysrhythmias, chest pain, tachycardia, cool extremities.
  • interventions: adm blood products and hematopoietic meds; encourage diet rich in the deficient nutrient if the anemia is caused by malnutrition (iron, folate, vit B12); control and adress the source of bleeding.
55
Q

Iron Deficiency Anemia

A
  • iron stores are depleted, resulting in a decreased iron supply for the manufacture of hemoglobin in red blood cells.
  • commonly results from blood loss, increased metabolic demands, syndromes of GI malabsorption, and dietary inadequacy.
  • assessment: pallor, weakness, fatigue; low hemoglobin, hematocrit, and mean cellular volume (MCV) levels; red blood cells are microcytic and hypochromic.
  • interventions: increase oral intake of iron, adm iron supplements (take between meals, with a multivitamin or fruit juice because vit C increases absorption; don’t take with milk or antacids), IM injections if iron (using Z-track) or IV may be prescribed in severe cases.
  • side effects of supplements: black stools, constipation, and foul aftertaste. Liquid iron stains the teeth and should be taken through a straw and teeth should be brushed after.
56
Q

Vitamin B12 Deficiency Anemia

A
  • a macrocytic anemia that results from an inadequate intake of vit B12 or lack of absorption of ingested vit B12 from the intestinal tract (intrinsec factor secreted by the gastric mucosa necessary for absorption).
  • assessment: severe pallor, fatigue, weight loss, smooth, beefy red tongue, slight jaundice, paresthesias of the hands and feet, disturbances with gait and balance.
  • interventions: increased intake of foods rish in vit B12; adm vit B12 injections, weekly initially and monthly for maintenance (lifelong) if is a result of deficiency of intrinsec factor or disease or surgery of the ileum.
57
Q

Folate Deficiency Anemia

A
  • a macrocytic anemia in which red blood cells are larger than normal and are oval-shapped dua to the lack of inadequate intake of folate (vit B9).
  • folic acid is required for DNA synthesis required for red blood cell formation and maturation.
  • common causes: dietary deficiency, malabsorption syndromes (celiac disease, chron’s disease, or small bowel resection), meds that decrease absorption (antiseizure), a condition (pregnancy, which increases requirements), chronic alcoholism, and chronic hemodialysis.
  • assessment: dyspepsia, smooth beefy red tongue, pallor, fatigue, weaknes, tinnitus, tachycardia.
  • intervention: encourage foods high in folic acid and supplement.
58
Q

Aplastic Anemia

A
  • deficiency of circulating erythrocyte and all other formed elements of blood, resulting from the arrested development of cells within the bone marrow.
  • can be primary (birth) or secondary (acquired).
  • causes: chronic exposure to myelotoxic agents, viruses and infections such as hepatitis, Epistein-Barr virus, autoimmune disorders (such as HIV), and allergic states.
  • diagnosis is determined by bone marrow aspiration.
  • management focuses on restoring function to the bone marrow and involves immunosuppressive therapy and bone marrow transplantation.
  • assessment: pancytopenia, petechiae, purpura, bleeding, pallor, weakness, tachycardia, and fatigue.
  • interventions: prepare for bone marrow transplantation; adm immunosuppressive meds; colony-stimulating factors may be prescribed to enhance bone marrow production; corticosteroids and cyclosporine maybe prescribed; blood transfusions.