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Seminar in Palliative Care September 26 – October 02, 2010 Salzburg, Austria in Collaboration with The EPEC-O TM Education in Palliative and End-of-life Care - Oncology Project The EPEC-O Curriculum is produced by the EPECTM Project with major funding provided by NCI, with supplemental funding provided by the Lance Armstrong Foundation. Fluid Metabolism, Edema, Effusions Jamie H. Von Roenn, MD Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA Ascites Malignant ascites . . . • Definition: accumulation of fluid in the abdomen . . . Malignant ascites Epidemiology • 10 % caused by malignancy • 80 % of malignant ascites is epithelial: Ovaries Endometrium Breast Colon GI tract Pancreas Runyon, et al. Hepatology, 1998. . . . Malignant ascites • Impact: dyspnea, early satiety, fatigue, abdominal pain • Prognosis: poor Mean survival with malignant ascites < 4 months If chemo-responsive cancer, eg, newly Dx ovarian ca, mean survival = 6 months – 1 year Key points 1. Pathophysiology 2. Assessment 3. Management Pathophysiology . . . • Normal physiology: Intravascular pressure = extravascular pressure No extravascular fluid accumulation • Ascites: Fluid influx increases Fluid outflow decreases Fluid accumulates . . . Pathophysiology • Elevated hydrostatic pressure e.g., congestive heart failure, cirrhosis • Decreased osmotic pressure e.g., nephrotic syndrome, malnutrition • Fluid production > fluid resorption ( infections, malignancy ) Assessment . . . History & symptoms • • • • • • • Ankle swelling Weight gain Girth Fullness Bloating Discomfort Heaviness • • • • • • Indigestion Nausea Vomiting Reflux Umbilical changes Hemorrhoids . . . Assessment Physical examination • • • • Bulging flanks Flank dullness Shifting dullness Fluid wave Extra-abdominal signs of ascites • • • • • • Enlarged liver Hernias Scrotal edema Lower extremity edema Abdominal venous engorgement Flattened, protuberant umbilicus Diagnostic imaging • If physical exam is equivocal • Detects small amounts of fluid, loculation • ‘Ground Glass’ X-ray • CT scan Diagnostic paracentesis • • • • • Color Cytology Cell count Total protein concentration Serum-ascites albumin gradient Hoefs J. Lab Clin Med, 1983. Diagnosing ascites - Summary • Malignant etiology likely when ascitic fluid has: Blood Positive cytology Absolute neutrophil count < 250 cells / ml Total protein concentration > 25 gm / L Serum-ascites albumin gradient < 11 gm / L Management • Goal: to relieve the symptoms • With little or no discomfort – don’t treat • Before intervening, discuss prognosis, benefits, risks When to treat ? • With these symptoms: Dyspnea Abdominal pain Fatigue Anorexia Early satiety Reduced exercise tolerance Therapeutic options • • • • • Dietary restriction Chemotherapy Diuretics Therapeutic paracentesis Surgery Dietary management • Sodium and severe fluid restriction Difficult for patients Discuss benefits, burdens & other treatment options first Diuretics • Effective • Well-tolerated • Treatment goals: Remove only enough fluid to manage the symptoms Slow & gradual diuresis Pockros J, et al. Gastroenterology, 1992. Selecting a diuretic • Spironolactone 25 mg – 50 mg / day • Amiloride 5 mg / day • Furosemide 20 mg / day Precautions with diuretics • Avoid salt substitutes • Evaluate benefits & burdens • Not appropriate in patients with: Limited mobility UT flow problems Poor appetite, poor oral intake Polypharmacy problems Diuretic adverse effects • Problems with Sleep deprivation Self-esteem Skin Safety Fatigue Hypotension Therapeutic paracentesis • Indications: Respiratory distress Diuretic failure Rapid symptomatic relief • Safe • In clinic or home Therapeutic paracentesis technique • Patient supine or • semirecumbent • • Select site • Cleanse, • disinfect skin Insert Attach 3-way connector Evacuate • Reposition Surgery • Peritoneovenous shunts Drains ascitic fluid into internal jugular vein Rarely done • Tenckhoff, other catheters Local anesthesia Large volume ascites Outpatient use Barnett TD, Rubins J. J Vasc Intery Radio, 2002. Burger JA, et al. Ann Oncol, 1997. Summary . . . • Ascites causes distress in patients with advanced cancer • Rule out nonmalignant causes • Treatment is palliative • Dietary, pharmacological, and interventional options are available Malignant Pleural Effusions Malignant pleural effusions . . . • Definition: fluid accumulation in the potential space between the visceral (inner) layer covering the lungs and the parietal (outer) layer covering the chest wall . . . Malignant pleural effusions Impact: • • • • Dyspnea Cough Chest pain Decreased mobility and fear Overview • • • • • • • Scope of the problem Causes Pathophysiology Diagnosis Prognosis Management options Treatment strategies Impact • > 25 % of newly diagnosed pleural effusions are due to malignancy • 50 % of cancer patients will develop a pleural effusion • In US, approx. 100,000 malignant effusions / year • Life expectancy 4 – 12 months Causes • Breast and lung cancer • Lymphoma, GU, GI • Unknown primary 50 – 65 % 25 % 7 – 15 % Prognosis • Mortality 54 % at 1 month, 84 % at 6 months • Survival ~ 10 months where pleural effusion is first evidence of cancer • Known CA, exudate, negative cytology poor prognosis compared to positive cytology • Role of pH, Karnofsky Performance Scale ? Key points 1. Pathophysiology 2. Assessment 3. Management Pathophysiology • Fluid production = fluid resorption • Causes Tumor cells blocking lymphatic drainage Changes in colloid osmotic pressure due to hypoalbuminemia Assessment • History of dyspnea, chest pain, cough • Physical examination of decreased breath sounds, dullness to percussion . . . Assessment • Symptoms: dyspnea, dry cough, pleuritic pain, chest discomfort, limited exercise tolerance • Exam: decreased breath sounds, dullness to auscultation and percussion • CXR PA, lateral and decubitus films • Chest CT or U / S if loculated Differential diagnosis • • • • Parapneumonic effusion Empyema Chylothorax Transudate Benign vs. malignant effusions . . . • Light’s criteria Pleural fluid LDH > 0.6 Serum LDH Pleural fluid protein > 0.5 Serum protein Pleural fluid LDH > 2 / 3 ULN serum LDH . . . Benign vs. malignant effusions . . . • Heffner meta-analysis: Pleural LDH > 0.45 ULN Pleural cholesterol > 45 mg / dl Pleural protein > 2.9 gm / dl Heffner 1997. . . . Benign vs. malignant effusions • Cytology Positive in approximately 55 – 65 % initially Yield up to 77 % on 3 pleural fluid samples Management Intrapleural catheter Doxycycline pleurodesis Initial drainage 97 % 68 % Pleurodesis 46 % 54 % Late recurrence 13 % 21 % 13 % outpt 14 % inpt Complications Putnam 1999. Management options • • • • • • • • Thoracentesis Tube thoracostomy Small-bore chest tubes Pleurodesis Thoracoscopy Intrapleural catheters Pleuroperitoneal shunting Subcutaneous access ports Thoracentesis • • • • Diagnostic, therapeutic Temporary relief Many contraindications Risks: Pneumothorax Reexpansion pulmonary edema ( especially if > 1,500 ml removed ) Treatment recommendations… • Thoracentesis: diagnosis, palliation until more definitive procedure, medically ill, short-life expectancy • Tube thoracostomy: free-flowing effusions, unable to tolerate general anesthesia …Treatment recommendations • Thoracoscopy: life expectancy > 3 months, loculated effusions, biopsies • Intrapleural catheters: outpatient pleurodesis Thoracoscopy benefits… • Direct visualization of lung re-expansion • Identify loculated areas and drain • Administration of dry talc, chest tube placement • Confirm equal distribution of talc …Thoracoscopy benefits • Shorter hospital stay than tube thoracostomy • Diagnostic yield 90 %, pleurodesis success rate 90% Tube thoracostomy and pleurodesis . . . • More definitive than repeated thoracentesis for recurrent effusions • Chest tube 12 – 24 hr or until drainage < 250 ml / 24 hr . . . Tube thoracostomy and pleurodesis • Sclerosing agent when dry Talc, bleomycin, doxycycline Tube clamping controversial Rotation vs. nonrotation • Failure rate 10 – 40 % • Most widely used and cost effective method Summary Use comprehensive assessment and pathophysiology-based therapy to treat the cause and improve the cancer experience