section name header

Information

[Section Outline]

The most common problems are superior vena cava syndrome; pericardial effusion/tamponade; spinal cord compression; seizures (Chap. 184 Seizures and Epilepsy) and/or increased intracranial pressure; and intestinal, urinary, or biliary obstruction. The last three conditions are discussed in Chap. 71 in HPIM-20.

Superior Vena Cava Syndrome !!navigator!!

Obstruction of the superior vena cava reduces venous return from the head, neck, and upper extremities (Fig. 27-1. Superior Vena Cava Syndrome (SVCS)). About 85% of cases are due to lung cancer; lymphoma and thrombosis of central venous catheters are other causes. Pts often present with facial swelling, dyspnea, and cough. In severe cases, the mediastinal mass lesion may cause tracheal obstruction. Dilated neck veins and increased collateral veins on anterior chest wall are noted on physical examination. Chest x-ray (CXR) documents widening of the superior mediastinum; 25% of pts have a right-sided pleural effusion.

TREATMENT

Superior Vena Cava Syndrome

Radiation therapy is the treatment of choice for non-small-cell lung cancer and other solid tumors; chemotherapy is effective in small-cell lung cancer, lymphoma, and germ cell tumors. Symptoms recur in 10-30% of pts and can be palliated by venous stenting. Clotted central catheters producing this syndrome should be removed and anticoagulation therapy initiated.

Pericardial Effusion/Tamponade !!navigator!!

Accumulation of fluid in the pericardium impairs filling of the heart and decreases cardiac output. Most commonly seen in pts with lung or breast cancers, leukemias, or lymphomas, pericardial tamponade may also develop as a late complication of mediastinal radiation therapy (constrictive pericarditis). Common symptoms are dyspnea, cough, chest pain, orthopnea, and weakness. Pleural effusion, sinus tachycardia, jugular venous distention, hepatomegaly, and cyanosis are frequent physical findings. Paradoxical pulse, decreased heart sounds, pulsus alternans, and friction rub are less common with malignant than nonmalignant pericardial disease. Echocardiography is diagnostic; pericardiocentesis may show serous or bloody exudate, and cytology usually shows malignant cells.

TREATMENT

Pericardial Effusion/Tamponade

Drainage of fluid from the pericardial sac may be lifesaving until a definitive surgical procedure (pericardial stripping or window) can be performed.

Spinal Cord Compression !!navigator!!

Primary spinal cord tumors occur rarely, and cord compression is most commonly due to epidural metastases from vertebral bodies involved with tumor, especially from prostate, lung, breast, lymphoma, and myeloma primaries. Pts present with back pain, worse when recumbent, with local tenderness. Loss of bowel and bladder control may occur. On physical examination, pts have a loss of sensation below a horizontal line on the trunk, called a sensory level, which usually corresponds to one or two vertebrae below the site of compression. Weakness and spasticity of the legs and hyperactive reflexes with upgoing toes on Babinski testing are often noted. Spine radiographs may reveal erosion of the pedicles (winking owl sign), lytic or sclerotic vertebral body lesions, and vertebral collapse. Collapse alone is not a reliable indicator of tumor; it is a common manifestation of a more common disease, osteoporosis. MRI can visualize the cord throughout its length and define the extent of tumor involvement.

TREATMENT

Spinal Cord Compression (See Chap. 22 Spinal Cord Compression)

Emergent Paraneoplastic Syndromes !!navigator!!

Most paraneoplastic syndromes have an insidious onset (Chap. 78 Paraneoplastic Endocrine Syndromes). Hypercalcemia, syndrome of inappropriate antidiuretic hormone secretion (SIADH), and adrenal insufficiency may present as emergencies.

Hypercalcemia !!navigator!!

The most common paraneoplastic syndrome, hypercalcemia occurs in about 10% of cancer pts, particularly those with lung, breast, head and neck, and kidney cancer and myeloma. Bone resorption mediated by parathyroid hormone-related protein is the most common mechanism; interleukin 1 (IL-1), IL-6, tumor necrosis factor, and transforming growth factor β may act locally in tumor-involved bone. Pts usually present with nonspecific symptoms: fatigue, anorexia, constipation, weakness. Hypoalbuminemia associated with malignancy may make symptoms worse for any given serum calcium level because more calcium will be free rather than protein bound.

TREATMENT

Hypercalcemia

Saline hydration, antiresorptive agents (e.g., pamidronate, 60-90 mg IV over 4 h, or zoledronate, 4-8 mg IV), and glucocorticoids usually lower calcium levels significantly within 1-3 days. Treatment effects usually last several weeks. Treatment of the underlying malignancy is also important.

SIADH !!navigator!!

Induced by the action of arginine vasopressin produced by certain tumors (especially small cell cancer of the lung), SIADH is characterized by hyponatremia, inappropriately concentrated urine, and high urine sodium excretion in the absence of volume depletion. Most pts with SIADH are asymptomatic. When serum sodium falls to <115 meq/L, pts may experience anorexia, depression, lethargy, irritability, confusion, weakness, and personality changes.

TREATMENT

SIADH

Water restriction controls mild forms. Demeclocycline (150-300 mg PO tid or qid) inhibits the effects of vasopressin on the renal tubule but has a slow onset of action (1 week). Conivaptan can be given PO (20-120 mg bid) or IV (10-40 mg); tolvaptan (15 mg PO daily) is a vasopressin agonist that can be used. Treatment of the underlying malignancy is also important. If the pt has mental status changes with sodium levels <115 meq/L, normal saline infusion plus furosemide to increase free water clearance may provide more rapid improvement. Rate of correction should not exceed 0.5-1 meq/L per hour. More rapid change can produce fluid shifts that lead to brain damage.

Adrenal Insufficiency !!navigator!!

The infiltration of the adrenals by tumor and their destruction by hemorrhage are the two most common causes. In addition, the immunologic checkpoint inhibiting antibodies, ipilimumab, nivolumab, and pembrolizumab can produce an autoimmune hypophysitis that leads to adrenal insufficiency. Symptoms such as nausea, vomiting, anorexia, and orthostatic hypotension may be attributed to progressive cancer or to treatment side effects. Certain treatments (e.g., ketoconazole, aminoglutethimide) may directly interfere with steroid synthesis in the adrenal.

TREATMENT

Adrenal Insufficiency

In emergencies, a bolus of 100-mg IV hydrocortisone is followed by a continuous infusion of 10 mg/h. In nonemergent but stressful circumstances, 100-200 mg/d oral hydrocortisone is the beginning dose, tapered to maintenance of 15-37.5 mg/d. Fludrocortisone (0.1 mg/d) may be required in the presence of hyperkalemia.

Outline

Section 2. Medical Emergencies