Medicine by Praveen Aggarwal PDF Free Download

Medicine by Praveen Aggarwal PDF

Download Medicine by Praveen Aggarwal PDF: Hello guys in this article we will provide you the latest book of George K Mathew and Praveen Aggarwal’s Medicine: Prep Manual for Undergraduates PDF in English. The book is published by Elsevier Health Science. You can easily download this book from the end of the article.

Medicine by Praveen Aggarwal PDF Summary

Best book for exam preparation ONLY. Very easy to understand the concepts, lifesaver for proofs only. Would surely recommend it. It will be easy for you to revise medicine in a short span or within a month of the exam Flow charts, boxes, and pointwise will be very useful in a theory exam.

With ever-expanding knowledge and advances in medicine, the sixth edition of this book is significantly revised and presented in a new full-color format. Structured in question-answer format, this book is a must-have for all undergraduate medical students as it prepares them for both theory and viva-voce examinations. It is also useful for dentistry and nursing students.

Updates on Zika, Ebola, Nipah, sepsis, monoclonal antibodies, adult immunisation, paracetamol poisoning, acute radiation syndrome, myelodysplastic syndrome, lymphoid malignancies, influenza, tuberculosis, human immunodeficiency virus infection, hepatitis B and C, heart failure, rheumatic fever, pulmonary hypertension and hyperlipidaemia.

Contents of Medicine by Praveen Aggarwal PDF

Diseases of the blood:

  • Give a brief account of erythropoietin (EPO), recombinant human erythropoietin (rHuEP0), and darbepoetin alpha.
  • What are the ectopic sources of EPO?
  • Discuss briefly hematopoietic growth factors (HGFs)
  • Define eosinophilia. What are the common causes of eosinophilia?
  • Discuss the abnormalities of red cells that can be seen
  • Describe various blood indices used in patients with anemia.
  • Discuss the etiology, classification, clinical features, and general management of anemia.
  • Give a brief description of the anemias due to blood loss
  • Discuss the etiology, clinical manifestations, diagnosis, and management of iron-deficiency anemia.
  • Write a short note on Plummer-Vinson syndrome (sideropenic dysphagia; Patterson-Kelly syndrome)
  • How will you differentiate various causes of hypochromic microcytic anemias?
  • Give a brief account of sideroblastic anemias
  • Enumerate the causes of macrocytosis.
  • Discuss the etiology, pathogenesis, clinical features, diagnosis, and management of Addisonian pernicious anemia.
  • Write a short note on vitamin B12
  • Discuss briefly the causes, manifestations, and management of vitamin Bi2 deficiency.
  • Give a brief account of folic acid.
  • Discuss briefly the causes, manifestations, diagnosis, and management of folate deficiency.
  • Enumerate the causes and management of normocytic anemia.
  • Discuss briefly the anemia of chronic disease.
  • Discuss briefly anemia of critical illness.
  • What are the causes of pancytopenia?
  • Define aplastic anemia. Discuss the etiology, clinical features, investigations, and management of aplastic anemia.
  • Discuss the etiology, classification, clinical features, diagnosis, and management of hemolytic anemias
  • Briefly outline hereditary spherocytosis.
  • Discuss the etiology, precipitating causes, clinical features, investigations, and management of glucose-6 phosphate dehydrogenase (G6PD) deficiency.
  • Describe the structure of normal hemoglobin.
  • Discuss the pathogenesis, clinical features, investigations, and management of sickle cell anemia.
  • Give a brief account of methemoglobinemia.
  • What are thalassaemias? What are the common forms and genetics of thalassaemias?
  • Discuss the clinical features, salient investigations, and management of B-thalassaemia major (cooley’s anemia).
  • Discuss briefly thalassemia minor (trait) and thalassemia intermedia.
  • Give a brief account of paroxysmal nocturnal hemoglobinuria (PNH).
  • Give a brief account of autoimmune hemolytic anemias.
  • What is the significance of coombs’ test?
  • Discuss cold haemagglutinin disease (CHAD) in brief.
  • Write briefly on paroxysmal cold hemoglobinuria (PCH).
  • Write a short note on drug-induced immune hemolytic anemia.
  • What are myeloproliferative diseases or myeloproliferative neoplasms (MPN)?
  • What are myelodysplastic syndromes (MDS)?
  • Classify myeloid neoplasms.
  • What is polycythemia? How do you classify polycythemia?
  • What are the clinical manifestations of polycythemia?
  • Discuss the clinical features, diagnosis, and management of polycythemia vera.
  • How will you differentiate primary polycythemia (polycythemia vera) from secondary polycythemia with hypoxia (e.g. chronic obstructive pulmonary disease [COPDJ)?
  • Discuss the causes, clinical features, and management of agranulocytosis.
  • How do you classify leukemias?
  • Discuss the etiology of leukemias.
  • Define acute leukemia. Discuss the clinical features, investigations, and management of acute leukemias.
  • How do you differentiate acute lymphoblastic leukemia from acute myeloblastic leukemia?
  • Describe sub-leukemic leukemia.
  • Define aleukaemic leukemia.
  • Discuss briefly leukemoid reaction.
  • Define and classify stem cells. Discuss their clinical applications.
  • Give a brief account of hematopoietic stem cells (HSC).
  • Write a short note on peripheral blood stem cell transplantation.
  • Briefly outline borne marrow transplantation.
  • Discuss the natural course, clinical features, and investigations of chronic myeloid leukemia. Give a brief account of the treatment.
  • Write a brief note on the Philadelphia chromosome (Ph).
  • Discuss the clinical features, investigations, and management of primary myelofibrosis (agnogenic myeloid metaplasia, myelofibrosis with myeloid metaplasia).
  • Define myelophthisis and discuss its causes
  • How do you differentiate chronic myeloid leukemia from
  • Describe the etiology, classification, clinical features, diagnosis, and treatment of myelodysplastic syndrome (MDS).
  • Discuss the types, clinical features, investigations, clinical staging, and management of chronic lymphocytic leukemia (CLL).
  • Discuss the clinical features, investigations, and management of hairy cell leukemia.
  • How do you classify splenomegaly? Enumerate the common causes of splenomegaly.
  • Enumerate the common causes of massive splenomegaly. Discuss the differential diagnosis.
  • Enumerate the causes, clinical features, and treatment of hypersplenism.
  • What are lymphomas? What are the common types of lymphomas?
  • Discuss the pathological classification, clinical features, clinical staging, investigations, and treatment of Hodgkin’s lymphoma.
  • Give a brief account of the read-Sternberg (RS) cell.
  • Discuss the pathological classification, clinical staging, clinical features, investigations, and management of non-Hodgkin’s lymphoma.
  • How do you differentiate Hodgkin’s lymphoma from non- Hodgkin’s lymphoma?
  • Describe burkitÅ¥’s lymphoma/leukemia.
  • Briefly discuss adult T-cell lymphoma/leukemia.
  • Explain what is mucosa-associated lymphoid tissue (MALT) Lymphoma or primary gastric lymphoma.
  • What are plasma cell disorders?
  • Discuss the immunopathology, pathology, clinical features, investigations, and treatment of multiple myeloma
  • Write a short note on POEMS syndrome
  • What are the causes of the M-component on electrophoresis?
  • What are the causes of renal failure in multiple myeloma?
  • What are the indicators of poor prognosis in multiple myeloma?
  • Discuss the role of radiographic examination in the diagnosis of multiple myeloma.
  • What is monoclonal gammopathy of undetermined significance (MGUS)?
  • How do you differentiate between multiple myeloma and monoclonal gammopathy of undetermined significance (MGUS)?
  • Describe solitary plasmacytoma of bone.
  • What is solitary extramedullary plasmacytoma?
  • Give a brief account of Waldenstrom’s macroglobulinemia.
  • Briefly outline the side effects, precautions, and dosage of thalidomide.
  • Discuss the mechanism of hemostasis.
  • Write in brief about platelets and their functions.
  • Briefly outline the natural inhibitors of coagulation.
  • Describe the fibrinolytic system.
  • Discuss the evaluation of a patient with a bleeding disorder.
  • Define thrombocytopenia. Enumerate the common causes, clinical manifestations, investigations, and management of thrombocytopenia.
  • Describe tourniquet test (capillary resistance test of Hess, Hess test).
  • Enumerate the common conditions inhibiting platelet function or qualitative platelet disorders.
  • Discuss the pathogenesis, clinical features, investigations, and management of immune (idiopathic) thrombocytopenic purpura (ITP)
  • Discuss thrombotic thrombocytopenic purpura.
  • Discuss the clinical features, investigations, and treatment of hemolytic-uraemic syndrome (HUS).
  • What are the common causes of thrombocytosis?
  • Discuss the etiology, classification, clinical features, diagnosis, and management of hemophilia A.
  • Write a short note on acquired hemophilia A.
  • Briefly discuss hemophilia B (Christmas disease) and its management.
  • Discuss the etiology, clinical features, investigations, and treatment of von Willebrand’s disease (WD).
  • Write briefly on recombinant factor Vl activated.
  • Discuss the causes, pathogenesis, clinical features, lab features, and management of disseminated intravascular coagulation (DIC; defibrination syndrome; consumption coagulopathy).
  • Give a brief account of vitamin K.
  • Give a brief account of anti-platelet drugs
  • Classify anti-coagulants. Give a brief account of the commonly used anti-coagulants.
  • Briefly describe thrombolytics.
  • Discuss blood transfusion and blood component transfusion.
  • What are the complications of blood transfusion?
  • Discuss the differential diagnosis of generalized lymphadenopathy in an adult.

Diseases of the respiratory system:

  • Define a bronchopulmonary segment. Name the bronchopulmonary segments.
  • Give the normal arterial blood gas (ABG) levels.
  • Discuss the causes, mechanisms, clinical features, investigations, and management of hypercapnia philopatry (carbon dioxide [CO2| narcosis)
  • Discuss the causes, clinical features, and management of hypoxemia.
  • Define clubbing. Enumerate the causes and give the mechanism of clubbing.
  • Describe abnormalities in nails due to systemic diseases.
  • Enumerate the pulmonary function tests and give their clinical significance.
  • Define respiratory failure. Describe in detail the causes and management of various types of respiratory failures
  • Discuss the role of oxygen therapy in chronic type II respiratory failure complicating the chronic obstructive pulmonary disease.
  • What are sleep apnoea syndromes?
  • What are the common therapeutic indications of oxygen therapy in clinical practice? Add a note on the hazards of oxygen therapy
  • Describe acute respiratory distress syndrome (ARDS).
  • What Is non-cardiogenic pulmonary edema?
  • Discuss non-invasive ventilation.
  • Discuss the etiology, clinical features, investigations, complications, and management of seasonal influenza.
  • Discuss briefly swine flu (H1N1 influenza) and prevention of human influenza pandemic.
  • Briefly discuss avian influenza.
  • Write a short note on severe acute respiratory syndrome (SARS).
  • Write a short note on middle east respiratory syndrome (MERS
  • Discuss the etiology, classification, investigations, complications, indications for hospitalization, and treatment of pneumonia.
  • Describe suppurative pneumonia and necrotizing pneumonia.
  • Discuss the etiology, clinical features, diagnosis, complications, and management of pneumococcal pneumonia (lobar pneumonia).
  • Give a brief account of staphylococcal pneumonia.
  • Give a brief account of Klebsiella pneumonia (Friedlander’s pneumonia).
  • Discuss the etiology, clinical features, investigations, and treatment of atypical pneumonia.
  • Give a brief account of legionella pneumonia (Legionnaire’s disease).
  • Give a brief account of actinomycosis.
  • Give a brief description of pneumonia caused by viruses (viral pneumonia).
  • Give a brief account of acute bronchopneumonia.
  • Describe eosinophilic pneumonia.
  • Discuss in brief pulmonary infiltrates with eosinophilia.
  • Briefly discuss chronic eosinophilic pneumonia (Carrington’s disease).
  • What is tropical pulmonary eosinophilia? Explain.
  • Give a brief account of aspiration pneumonia.
  • What is meant by hospital-acquired pneumonia? How will you manage it?
  • Write a short note on ventilator-associated pneumonia.
  • What is nosocomial pneumonia?
  • How do you classify mycobacteria? Give an account of diseases produced by them.
  • Describe mycobacteria other than tuberculosis (MOTT).
  • Write a brief note on non-tuberculous mycobacteria (NTM).
  • Discuss the pathogenesis, pathology, clinical manifestations, and diagnosis of primary pulmonary tuberculosis.
  • Write in brief about the primary complex of Ranke and Ghon’s complex.
  • Discuss the pathogenesis, pathology, clinical manifestations, complications, and diagnoSIs of post-primary pulmonary tuberculosis.
  • Enumerate the causes of hemoptysis in pulmonary tuberculosis.
  • Give a brief account of sputum smear examination for mycobacteria.
  • List down the radiological features of pulmonary tuberculosis.
  • Write a short note on tuberculin testing.
  • What is the Mantoux test?
  • How do you make an assessment of the activity of tuberculosis?
  • Describe latent tuberculosis infection.
  • What do you understand by the terms “bactericidal action and “sterilizing action in relation to antituberculous drugs?
  • What are antituberculous drugs and what are their dosages in adults?
  • Discuss modes of action of first-line drugs.
  • Describe rifampicin-related anti-tubercular agents.
  • What are the side effects of the commonly used antituberculous drugs?
  • Discuss regimen of antituberculous chemotherapy.
  • What is short-course chemotherapy? What are the advantages of short-course chemotherapy?
  • What is the “fall and rise” phenomenon?
  • How can the progress of anti-tubercular treatment be monitored and the treatment result assessed?
  • Discuss the directly observed treatment, short-course (DOTS).
  • What is the stop TB strategy?
  • What is the end TB strategy?
  • What is the DOTS-plus strategy?
  • What are the forms of drug resistances encountered during antituberculous chemotherapy?

Details of Medicine by Praveen Aggarwal PDF

Book Name:Medicine: Prep Manual for Undergraduates
Author:Praveen Aggarwal & George K Mathew
Publisher:Elsevier Health Science
Pages:1080
Release date:28 June 2019
Format:PDF
Language:English

About the Author

K George Mathew, MD: He is an Associate Specialist in Orthogeriatrics, Torbay Hospital, Torquay, Devon, United Kingdom. He is an Associate Professor (Formerly), Department of Medicine, Kasturba Medical College, Manipal, Karnataka, India.

Praveen Aggarwal, MD, DNB: He is a Professor and Head, Department of Emergency Medicine, All India Institute of Medical Sciences, New Delhi, India.

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