Polycythemia vera - Study guides, Class notes & Summaries

Polycythemia vera Treatment ~ •Hydroxyurea drug of choice to decrease the number of blood cells in bone marrow (less chance for leukemia) •Phlebotomy, 300-500mL, to reduce the blood volume and iron levels •Low dose Aspirin to prevent clotting Hemolytic disease of fetus and newborn ~ Alloimmune disease in which maternal antibodies are directed against fetal antigens S/S: •Pallor •Hepatosplenomegaly •Anemia •Hyperbilirubinemia especially after birth •Erythroblastosi...

1. A patient is admitted to the same day surgery unit for liver biopsy. Which of the following laboratory tests assesses coagulation? Select all that apply. 1. Partial thromboplastin time. 2. Prothrombin time. 3. Platelet count. 4. Hemoglobin 5. Complete Blood Count 6. White Blood Cell Count Answer: 1, 2, and 3 Prothrombin time, partial thromboplastin time, and platelet count are all included in coagulation studies. The hemoglobin level, though important information prior to an invasiv...

Dunphy Primary Care Hematological Disorders Test Questions and Answers 100% Solved Is polycythemia vera primary or secondary? Primary -- it is neoplastic proliferation of mature myeloid cells, mainly RBCs What do labs look like with polycythemia vera? Elevated RBC, HGB, HCT What gene mutation confirms diagnosis in 95% of cases of Polycythemia Vera? JAK2 V617 Secondary causes of polycythemia vera? Smoking, hypoxia, erythropoietin secreting cyst of tumor Does secondary polycythemia ve...

What do you do if a patient comes in and has chest pain 10/10, midsternal, L arm, what do you do first What does the EKG REVEAL? If we have a STEMI where do they go Someone with PAD what will you see Someone with PVD what will you see What do you educate about PVD What is thrombolytic therapy What do you do for sickle cell anemia? Polycythemia Vera is what What do we educate those patients What is leukemia What do you see in leukemia Wh...

Absolute polycythemia - excessive red blood cell production; a physiologic response resulting from increased erythropoietin secretion in response to chronic hypoxia or as a symptom of polycythemia vera. Absorption atelectasis - see Atelectasis. Acid maltase deficiency (glycogen storage disease type II or Pompe disease) - an autosomal recessive metabolic disorder that damages muscle and nerve cells throughout the body by an accumulation of glycogen in the lysosome attributable to defici...

Phlebotomy Training Specialists Questions with complete solution Quiz 1: What is Polycythemia Vera characterized by? - correct answer A high red blood cell count Quiz 1: What are the most common practices of Phlebotomy? - correct answer Extraction of blood donation and testing substances contained within it Quiz 1: What is therapeutic phlebotomy? - correct answer Extracting large volumes of blood to bring certain values in the blood in line Quiz 1: What is the concept behind blood...

MMSC 433 Exam 3| 53 Questions & Answers, Rated A+| a "dry tap" bone marrow aspiration may be seen with what chronic myeloid proliferative disease? A: essential thrombocythemia B: polycythemia vera C: primary myelofibrosis D: Chronic myeloid leukemia - Primary myelofibrosis what clinical feature is more often associated with essential thrombocythemia than with the other chronic myeloproliferative disorders? A: bleeding and thrombosis B: infections C: splenomegaly D: fatigue - blee...

1. A patient is admitted to the same day surgery unit for liver biopsy. Which of the following laboratory tests assesses coagulation? Select all that apply. 1. Partial thromboplastin time. 2. Prothrombin time. 3. Platelet count. 4. Hemoglobin 5. Complete Blood Count 6. White Blood Cell Count Answer Answers and Rationale 1. Answer: 1, 2, and 3 Prothrombin time, partial thromboplastin time, and platelet count are all included in coagulation studies. The hemoglobin level, though important i...

ASCP Haematology Exam-MLT| Actual Questions Solved 100% Correct | Score Guide The characteristic peripheral blood morphologic feature in multiple myeloma is: A. cytotoxic T cells B. rouleax formation C. spherocytes D. macrocytosis (Answer: - B. rouleax formation In polycythemia vera, the homeoglobin, hematocrit, red blood cell count, and red cell mass are: A. elevated B. normal C. decreased (Answer: - A. elevated The M:E ratio in polycythemia vera is usually: A. normal B. ...

Absolute polycythemiaexcessive red blood cell production; a physiologic response resulting from increased erythropoietin secretion in response to chronic hypoxia or as a symptom of polycythemia vera. Absorption atelectasissee Atelectasis. Acid maltase deficiency (glycogen storage disease type II or Pompe disease)an autosomal recessive metabolic disorder that damages muscle and nerve cells throughout the body by an accumulation of glycogen in the lysosome attributable to deficiency of t...