This document discusses cardiovascular system and heart failure. It describes the structure of the heart including the four chambers and major blood vessels. It explains that heart failure occurs when the heart can no longer compensate for increased workload. There are two types of heart failure - acute and chronic (congestive). Chronic heart failure results from sustained pressure or volume overload on the heart or loss of contractility. It causes peripheral and cardiac compensations to maintain circulation. Left heart failure affects the lungs, while right heart failure causes generalized venous congestion.
1) Blood components like packed red cells, platelet concentrates and fresh frozen plasma can be prepared by separating whole blood into its components using centrifugation and expressors.
2) Optimal storage conditions and times allow individual components to be stored and transfused separately as needed rather than transfusing whole blood.
3) The document outlines the equipment, procedures and quality indicators for preparing the main blood components from a single donor to benefit multiple recipients.
This document discusses tissue fixation, which involves using chemicals to preserve tissue samples for examination. It defines fixation as preventing post-mortem changes while maintaining tissue characteristics. The goals of fixation are to prevent autolysis and putrefaction, penetrate tissues rapidly and evenly, harden tissues, and not interfere with staining. Common fixatives discussed include formalin, glutaraldehyde, Bouin's solution, and Zenker's solution. Factors that influence fixation such as temperature, specimen size, fixation time, and choice of fixative are also reviewed.
There are three main types of cell counting: manual, semi-automated, and automated. Fully automated cell counters use either impedance or optical methods like light scattering to count and classify cells. Automated counting has advantages over manual counting like being objective, eliminating errors, and providing additional parameters. Automated counters can provide a 3, 5, or 7-part differential count based on cell volume, staining properties, and light scattering characteristics. Newer technologies like flow cytometry provide more detailed analysis of cellular features.
This document discusses various anticoagulants used in hematology. It describes the characteristics anticoagulants should have and provides details on commonly used anticoagulants including EDTA, oxalates, heparin, sodium citrate, and sodium fluoride/potassium oxalate mixtures. The anticoagulants are classified as calcium chelators or non-calcium chelators and the mechanisms of action, concentrations, advantages, and disadvantages of each type are outlined.
The document discusses various components of a basic blood test. It provides details on the normal composition and functions of blood, as well as procedures for blood specimen collection. It also explains the clinical implications and reference ranges for various components analyzed in a complete blood count test, including red blood cells, white blood cells, platelets, hematocrit, hemoglobin, and sedimentation rate.
This document provides information on methods for performing a complete blood count (CBC), including white blood cell (WBC) count, corrected WBC count, and differential leukocyte count (DLC). The WBC count involves using a counting chamber, pipettes, and diluting fluids to count WBCs under a microscope. The DLC involves making a blood smear, staining it, counting different types of WBCs, and reporting results as relative or absolute counts. Normal ranges are provided for WBC subtype percentages and counts.
This document discusses laboratory safety and accidents. It identifies several types of laboratory hazards including chemical, physical, infectious and fire hazards. Common laboratory accidents such as cuts, burns, infections and chemical exposures are described. First aid measures for various types of laboratory accidents are provided. The importance of safe chemical handling and storage is emphasized to prevent injuries. Laboratory safety can be improved by proper training, careful work practices, and maintaining well-stocked first aid kits.
1) Blood components like packed red cells, platelet concentrates and fresh frozen plasma can be prepared by separating whole blood into its components using centrifugation and expressors.
2) Optimal storage conditions and times allow individual components to be stored and transfused separately as needed rather than transfusing whole blood.
3) The document outlines the equipment, procedures and quality indicators for preparing the main blood components from a single donor to benefit multiple recipients.
This document discusses tissue fixation, which involves using chemicals to preserve tissue samples for examination. It defines fixation as preventing post-mortem changes while maintaining tissue characteristics. The goals of fixation are to prevent autolysis and putrefaction, penetrate tissues rapidly and evenly, harden tissues, and not interfere with staining. Common fixatives discussed include formalin, glutaraldehyde, Bouin's solution, and Zenker's solution. Factors that influence fixation such as temperature, specimen size, fixation time, and choice of fixative are also reviewed.
There are three main types of cell counting: manual, semi-automated, and automated. Fully automated cell counters use either impedance or optical methods like light scattering to count and classify cells. Automated counting has advantages over manual counting like being objective, eliminating errors, and providing additional parameters. Automated counters can provide a 3, 5, or 7-part differential count based on cell volume, staining properties, and light scattering characteristics. Newer technologies like flow cytometry provide more detailed analysis of cellular features.
This document discusses various anticoagulants used in hematology. It describes the characteristics anticoagulants should have and provides details on commonly used anticoagulants including EDTA, oxalates, heparin, sodium citrate, and sodium fluoride/potassium oxalate mixtures. The anticoagulants are classified as calcium chelators or non-calcium chelators and the mechanisms of action, concentrations, advantages, and disadvantages of each type are outlined.
The document discusses various components of a basic blood test. It provides details on the normal composition and functions of blood, as well as procedures for blood specimen collection. It also explains the clinical implications and reference ranges for various components analyzed in a complete blood count test, including red blood cells, white blood cells, platelets, hematocrit, hemoglobin, and sedimentation rate.
This document provides information on methods for performing a complete blood count (CBC), including white blood cell (WBC) count, corrected WBC count, and differential leukocyte count (DLC). The WBC count involves using a counting chamber, pipettes, and diluting fluids to count WBCs under a microscope. The DLC involves making a blood smear, staining it, counting different types of WBCs, and reporting results as relative or absolute counts. Normal ranges are provided for WBC subtype percentages and counts.
This document discusses laboratory safety and accidents. It identifies several types of laboratory hazards including chemical, physical, infectious and fire hazards. Common laboratory accidents such as cuts, burns, infections and chemical exposures are described. First aid measures for various types of laboratory accidents are provided. The importance of safe chemical handling and storage is emphasized to prevent injuries. Laboratory safety can be improved by proper training, careful work practices, and maintaining well-stocked first aid kits.
This document provides instructions for performing hemocytometry, which is the manual or automated counting of red blood cells, white blood cells, and platelets from a blood sample. It describes how to count WBCs using a Neubauer chamber, including dilution of the sample, loading the chamber, and calculating cell counts per microliter based on the number observed. Procedures for counting RBCs and platelets are also outlined. Potential sources of error in cell counts are discussed, and clinical significance of the test results is explained.
Hemolysis, or the rupturing of red blood cells, can occur in vivo or in vitro and is caused by hemolysins damaging the cell membrane. It accounts for about 60% of rejected blood specimens and can be caused by improper collection or handling techniques. Hemolysis causes problems in chemistry, hematology, and blood bank testing due to interference from the released cell contents. Careful venipuncture and avoidance of techniques that can damage cells, such as using too small a needle or leaving a tourniquet on too long, can prevent hemolysis.
This document discusses hematology and hematopoiesis. It summarizes that hematology is the study of blood and its components, which provide nutrients, remove waste, and protect the body. Hematopoiesis, or blood cell formation, occurs exclusively in the bone marrow and involves pluripotent stem cells differentiating into various blood cell types through cytokine influences. In particular, it focuses on erythropoiesis, the formation of red blood cells, which involves erythropoietin signaling proliferation and differentiation of red blood cell precursors over 5-7 days from pronormoblast to reticulocyte to mature red blood cell.
Automated blood cell counter by yasin arafatYasin Arafat
Automated blood cell counters provide several advantages over manual counting methods. They ensure high precision and accuracy through automation that eliminates manual errors. Modern counters can measure numerous blood parameters from a single sample, including white blood cell, red blood cell, platelet, and differential counts. This level of automation saves time and reduces costs compared to manual methods that require making blood slides and examining them under a microscope. While automated counts are precise, microscopic review of abnormal samples remains important for diagnosis. Understanding an analyzer's limitations is also key to correctly interpreting test results.
Laboratory tests of hemostasis and coagulation system (dr ellinor peerschke ...derosaMSKCC
This document provides an introduction to coagulation testing, including preanalytical and analytical variables. It discusses specimen collection and processing, common coagulation assays, and how to interpret their results. Prolonged screening tests can indicate factor deficiencies or circulating anticoagulants like lupus anticoagulant, requiring additional studies. New direct oral anticoagulants affect clot-based assays in a concentration-dependent manner. D-dimer assays are used to evaluate for fibrinolysis or thrombosis. HIT testing involves screening ELISA to detect heparin-PF4 antibodies followed by confirmatory assays if needed.
This document outlines guidelines for blood transfusion services including donor selection, blood collection, component preparation, storage, transportation, and quality control of equipment and reagents. It describes the necessary steps and safety procedures that must be followed at each stage of the blood transfusion process to ensure the quality and safety of blood products. Key aspects covered include donor screening and eligibility criteria, proper labelling and storage of blood components, maintenance and calibration of equipment, and frequency of quality control testing for reagents.
This document discusses the classification, rules, ethics, codes of conduct, and policies of medical laboratories. It begins by classifying laboratories into four levels based on biosafety: basic level I and II laboratories work with low-risk organisms, containment level III laboratories work with more hazardous organisms, and maximum containment level IV laboratories work with the most dangerous pathogens. The document then outlines rules for laboratory request forms, record keeping, and delivering results. It also lists codes of conduct including maintaining professional standards, treating results confidentially, and following safety procedures. Finally, it states that laboratory policies cover hours, tests performed, specimen collection, and workload capacity.
PRINCIPLES OF OPERATIONOF THE AUTOMATED COAGULATION ANALZER.pptxEmmanuelAdoku
The document discusses the principles of operation of an automated coagulation analyzer. It begins by introducing the importance of blood clotting and how coagulation tests are used to analyze clotting abnormalities. It then describes how an automated coagulation analyzer generates reliable data quickly to test coagulation efficiency. The main body explains the various techniques automated analyzers use to detect the coagulation endpoint, including electromechanical methods using impedance and photo-optical analysis using scattered or transmitted light detection. It provides details on specific techniques like rotating cuvettes and steel balls. In conclusion, the document emphasizes that automated analyzers provide precise testing, though tilt tube remains the gold standard.
This document discusses quality assurance in haematology. It defines quality and introduces the concepts of quality control and quality assurance. Quality control aims to minimize errors through statistical sampling and verification of consistent performance. Quality assurance ensures reliable test results through adherence to standards within and outside the laboratory. This includes internal quality control, external quality assessment, and standardization using reference materials and methods. Several examples are provided of potential pre-analytical errors in sample collection, transport, and handling that can affect test results. Adherence to proper procedures is emphasized to avoid issues like hemolysis, clotting, and dilution.
This document discusses automation in hematology. It begins by outlining the necessity for automation in cell counting, diagnosing various blood conditions, and performing multiple tests on a single platform. The document then covers the advantages and disadvantages of automation, including increased speed and accuracy versus high costs. It describes the various principles used in automated hematology analyzers, such as electrical impedance, optical light scattering, and flow cytometry. Finally, it provides details on specific analyzers like the Pentra ES 60 and Pentra DF Nexus.
The document discusses blood film examination and abnormalities seen in red blood cells. Key points include:
Blood films are prepared manually or automatically and stained using Romanowsky stains like Giemsa or Leishman's. Films are examined under low then high power microscopy to assess cell morphology and identify abnormalities.
Abnormal red blood cell morphology seen in various anemias includes microcytosis in iron deficiency, macrocytosis in megaloblastic anemia, poikilocytosis in thalassemia, and hypochromia in iron deficiency. Specific abnormalities include target cells, sickle cells, spherocytes, and nucleated red blood cells. The differential diagnosis is considered based on the
PHLEBOTOMY
The process of collecting a blood sample is called
phlebotomy
This procedure is also known as Venipuncture
A person who performs phlebotomy is called a
phlebotomist, although doctors nurses, and medical
laboratory scientists.
BLOOD SPECIMEN COLLECTION AND PROCESSING
The first step in acquiring a quality lab. Test result for any
patient is the specimen collection procedure.
Blood specimen are obtained through capillary skin puncture
(finger, toe, heel), arterial , venous sampling.
VENIPUNCTURE
Venipuncture is the process of obtaining blood samples from veins
for lab testing
VENIPUNCTURE PROCEDURE STEPS
STEP 1:- Preparation of specimen collection material:
Following material should be readily available in the specimen
collection section-
Disposable syringes and needles or vacutainer systems.
Disposable lancets
Gauze pads or cotton
Tourniquet
70% (V/V) ethanol
Clean and dry wide mouth bottles
Leak- proof transportation bags and containers
A puncture-resistant sharp container
Blood collection tubes
VENIPUNCTURE PROCEDURE STEPS
STEP 1: Preparation of specimen collection material:
Sterile glass or plastic tubes with rubber caps
Vacuum-extraction blood tubes
Glass tubes with screw caps
Sterile glass or bleeding pack (collapsible) if large
quantities of blood are to be collected
well-fitting, non-sterile gloves
Laboratory specimen labels
Writing equipment
Laboratory forms
ORDER OF DRAW
To avoid cross-contamination, blood must be drawn and collected in
tubes in a specific order. This is known as the Order of Draw.
Blood culture
Blue tube for coagulation (Sodium Citrate)
Red No Gel
Gold SST (Plain tube w/gel and clot activator additive)
Green and Dark Green (Heparin, with and without gel)
Lavender (EDTA)
Pink - Blood Bank (EDTA)
Gray (Oxalate/Fluoride)
Black ( ESR)
VENIPUNCTURE PROCEDURE STEPS
Step 2:- Patient preparation:
Following instruction is given to the patient
patient should be on balanced diet at least for 2 to 3 days prior
to the test.
The day before sample collection, the patient should not drink
intoxicating substance, esp. alcoholic drinks and eat tobacco.
Patient should report to the lab. After fasting for 8-12 hrs.
Patient should not drink tea, or coffee or any other drinks
except one glassful of water.
VENIPUNCTURE PROCEDURE STEPS
Step 2 – Identify and prepare the patient
Where the patient is adult and conscious, follow the steps
outlined below.
Introduce yourself to the patient, and ask the patient to state their
full name.
Check that the laboratory form matches the patient’s identity (i.e.
match the patient’s details with the laboratory form, to ensure
accurate identification).
Ask whether the patent has allergies, phobias or has ever fainted
during previous injections or blood draws.
If the patient is anxious or afraid, reassure the person and ask what
would make them more comfortable.
capillary method
aretial method
The document defines hematocrit as the volume of red blood cells (RBCs) relative to the total volume of whole blood, expressed as a percentage. It notes there are two methods for measuring hematocrit: the macrohematocrit and microhematocrit methods. Normal hematocrit ranges are provided for men, women, infants/children, and newborns. Factors that can increase or decrease hematocrit levels are outlined, and indications for estimating hematocrit are given as screening for anemia and calculating red blood cell indices.
This document discusses laboratory hazards and precautions for working in a biochemical lab. It identifies three main types of laboratory hazards: physical, chemical, and biological. Specific physical hazards mentioned include fire, sharp objects, electricity, and poor housekeeping. Chemical hazards include corrosive, flammable, toxic, and carcinogenic substances. Biological hazards can arise from pathogens, animals, and body fluids. The document provides many safety precautions for each type of hazard, such as always wearing protective equipment like gloves and goggles, properly disposing of sharps and biological waste, and following general lab safety rules.
Hematology is the branch of medicine, that is concerned with the study of blood, blood forming organs and blood diseases. It includes study of etiology, diagnosis, treatment, prognosis and prevention of blood diseases .
After the completion of this presentation we will know about:
What is hematology and its purpose.
hematology laboratory.
Blood and its compositions and collections
Hematology lab equipment's
Some hematological tests , disease and hazards too.
EDTA is commonly used as an anticoagulant in hematology because it preserves cell morphology well. The document provides a procedure for preparing EDTA anticoagulant tubes and vials. EDTA powder is weighed and dissolved in distilled water to make a 10% w/v solution. 40μl of this solution is pipetted into each vial to provide 4mg of EDTA, enough to prevent coagulation in 2.5ml of blood. The vials are then dried in a hot air oven. Too little or too much EDTA can affect blood cells and indices.
Rh typing and its technique , BLOOD TYPING , Rhesus (Rh) typing , procedures of rh typing, process of Rh typing, Test limitations, Sources of Error in Rh Antigen Typing, False positive reactions' reason, False negative reactions' reasons
The document lists various instruments and equipment used in a blood bank laboratory, including personal protective equipment to protect workers, instruments for measuring and transferring liquids, equipment for separating blood components like centrifuges, refrigerators and freezers for storing blood and its components, microscopes, and waste segregation materials. It describes the uses of common lab equipment like test tubes, pipettes, balances, and autoclaves. Protective equipment and carefully measuring and storing blood are essential aspects of working in a blood bank laboratory.
This document discusses congestive heart failure (CHF), including its causes, pathophysiology, and effects on the left and right sides of the heart. CHF is caused by conditions that weaken the heart muscle, such as heart attacks, high blood pressure, and heart valve diseases. When the left ventricle fails to pump properly, blood backs up in the lungs leading to pulmonary edema and congestion. When the right ventricle fails, blood backs up in the liver, abdomen, and legs causing swelling. Common symptoms include shortness of breath, fatigue, swelling, and coughing. Treatment involves medications, lifestyle changes, and sometimes surgery.
This document provides instructions for performing hemocytometry, which is the manual or automated counting of red blood cells, white blood cells, and platelets from a blood sample. It describes how to count WBCs using a Neubauer chamber, including dilution of the sample, loading the chamber, and calculating cell counts per microliter based on the number observed. Procedures for counting RBCs and platelets are also outlined. Potential sources of error in cell counts are discussed, and clinical significance of the test results is explained.
Hemolysis, or the rupturing of red blood cells, can occur in vivo or in vitro and is caused by hemolysins damaging the cell membrane. It accounts for about 60% of rejected blood specimens and can be caused by improper collection or handling techniques. Hemolysis causes problems in chemistry, hematology, and blood bank testing due to interference from the released cell contents. Careful venipuncture and avoidance of techniques that can damage cells, such as using too small a needle or leaving a tourniquet on too long, can prevent hemolysis.
This document discusses hematology and hematopoiesis. It summarizes that hematology is the study of blood and its components, which provide nutrients, remove waste, and protect the body. Hematopoiesis, or blood cell formation, occurs exclusively in the bone marrow and involves pluripotent stem cells differentiating into various blood cell types through cytokine influences. In particular, it focuses on erythropoiesis, the formation of red blood cells, which involves erythropoietin signaling proliferation and differentiation of red blood cell precursors over 5-7 days from pronormoblast to reticulocyte to mature red blood cell.
Automated blood cell counter by yasin arafatYasin Arafat
Automated blood cell counters provide several advantages over manual counting methods. They ensure high precision and accuracy through automation that eliminates manual errors. Modern counters can measure numerous blood parameters from a single sample, including white blood cell, red blood cell, platelet, and differential counts. This level of automation saves time and reduces costs compared to manual methods that require making blood slides and examining them under a microscope. While automated counts are precise, microscopic review of abnormal samples remains important for diagnosis. Understanding an analyzer's limitations is also key to correctly interpreting test results.
Laboratory tests of hemostasis and coagulation system (dr ellinor peerschke ...derosaMSKCC
This document provides an introduction to coagulation testing, including preanalytical and analytical variables. It discusses specimen collection and processing, common coagulation assays, and how to interpret their results. Prolonged screening tests can indicate factor deficiencies or circulating anticoagulants like lupus anticoagulant, requiring additional studies. New direct oral anticoagulants affect clot-based assays in a concentration-dependent manner. D-dimer assays are used to evaluate for fibrinolysis or thrombosis. HIT testing involves screening ELISA to detect heparin-PF4 antibodies followed by confirmatory assays if needed.
This document outlines guidelines for blood transfusion services including donor selection, blood collection, component preparation, storage, transportation, and quality control of equipment and reagents. It describes the necessary steps and safety procedures that must be followed at each stage of the blood transfusion process to ensure the quality and safety of blood products. Key aspects covered include donor screening and eligibility criteria, proper labelling and storage of blood components, maintenance and calibration of equipment, and frequency of quality control testing for reagents.
This document discusses the classification, rules, ethics, codes of conduct, and policies of medical laboratories. It begins by classifying laboratories into four levels based on biosafety: basic level I and II laboratories work with low-risk organisms, containment level III laboratories work with more hazardous organisms, and maximum containment level IV laboratories work with the most dangerous pathogens. The document then outlines rules for laboratory request forms, record keeping, and delivering results. It also lists codes of conduct including maintaining professional standards, treating results confidentially, and following safety procedures. Finally, it states that laboratory policies cover hours, tests performed, specimen collection, and workload capacity.
PRINCIPLES OF OPERATIONOF THE AUTOMATED COAGULATION ANALZER.pptxEmmanuelAdoku
The document discusses the principles of operation of an automated coagulation analyzer. It begins by introducing the importance of blood clotting and how coagulation tests are used to analyze clotting abnormalities. It then describes how an automated coagulation analyzer generates reliable data quickly to test coagulation efficiency. The main body explains the various techniques automated analyzers use to detect the coagulation endpoint, including electromechanical methods using impedance and photo-optical analysis using scattered or transmitted light detection. It provides details on specific techniques like rotating cuvettes and steel balls. In conclusion, the document emphasizes that automated analyzers provide precise testing, though tilt tube remains the gold standard.
This document discusses quality assurance in haematology. It defines quality and introduces the concepts of quality control and quality assurance. Quality control aims to minimize errors through statistical sampling and verification of consistent performance. Quality assurance ensures reliable test results through adherence to standards within and outside the laboratory. This includes internal quality control, external quality assessment, and standardization using reference materials and methods. Several examples are provided of potential pre-analytical errors in sample collection, transport, and handling that can affect test results. Adherence to proper procedures is emphasized to avoid issues like hemolysis, clotting, and dilution.
This document discusses automation in hematology. It begins by outlining the necessity for automation in cell counting, diagnosing various blood conditions, and performing multiple tests on a single platform. The document then covers the advantages and disadvantages of automation, including increased speed and accuracy versus high costs. It describes the various principles used in automated hematology analyzers, such as electrical impedance, optical light scattering, and flow cytometry. Finally, it provides details on specific analyzers like the Pentra ES 60 and Pentra DF Nexus.
The document discusses blood film examination and abnormalities seen in red blood cells. Key points include:
Blood films are prepared manually or automatically and stained using Romanowsky stains like Giemsa or Leishman's. Films are examined under low then high power microscopy to assess cell morphology and identify abnormalities.
Abnormal red blood cell morphology seen in various anemias includes microcytosis in iron deficiency, macrocytosis in megaloblastic anemia, poikilocytosis in thalassemia, and hypochromia in iron deficiency. Specific abnormalities include target cells, sickle cells, spherocytes, and nucleated red blood cells. The differential diagnosis is considered based on the
PHLEBOTOMY
The process of collecting a blood sample is called
phlebotomy
This procedure is also known as Venipuncture
A person who performs phlebotomy is called a
phlebotomist, although doctors nurses, and medical
laboratory scientists.
BLOOD SPECIMEN COLLECTION AND PROCESSING
The first step in acquiring a quality lab. Test result for any
patient is the specimen collection procedure.
Blood specimen are obtained through capillary skin puncture
(finger, toe, heel), arterial , venous sampling.
VENIPUNCTURE
Venipuncture is the process of obtaining blood samples from veins
for lab testing
VENIPUNCTURE PROCEDURE STEPS
STEP 1:- Preparation of specimen collection material:
Following material should be readily available in the specimen
collection section-
Disposable syringes and needles or vacutainer systems.
Disposable lancets
Gauze pads or cotton
Tourniquet
70% (V/V) ethanol
Clean and dry wide mouth bottles
Leak- proof transportation bags and containers
A puncture-resistant sharp container
Blood collection tubes
VENIPUNCTURE PROCEDURE STEPS
STEP 1: Preparation of specimen collection material:
Sterile glass or plastic tubes with rubber caps
Vacuum-extraction blood tubes
Glass tubes with screw caps
Sterile glass or bleeding pack (collapsible) if large
quantities of blood are to be collected
well-fitting, non-sterile gloves
Laboratory specimen labels
Writing equipment
Laboratory forms
ORDER OF DRAW
To avoid cross-contamination, blood must be drawn and collected in
tubes in a specific order. This is known as the Order of Draw.
Blood culture
Blue tube for coagulation (Sodium Citrate)
Red No Gel
Gold SST (Plain tube w/gel and clot activator additive)
Green and Dark Green (Heparin, with and without gel)
Lavender (EDTA)
Pink - Blood Bank (EDTA)
Gray (Oxalate/Fluoride)
Black ( ESR)
VENIPUNCTURE PROCEDURE STEPS
Step 2:- Patient preparation:
Following instruction is given to the patient
patient should be on balanced diet at least for 2 to 3 days prior
to the test.
The day before sample collection, the patient should not drink
intoxicating substance, esp. alcoholic drinks and eat tobacco.
Patient should report to the lab. After fasting for 8-12 hrs.
Patient should not drink tea, or coffee or any other drinks
except one glassful of water.
VENIPUNCTURE PROCEDURE STEPS
Step 2 – Identify and prepare the patient
Where the patient is adult and conscious, follow the steps
outlined below.
Introduce yourself to the patient, and ask the patient to state their
full name.
Check that the laboratory form matches the patient’s identity (i.e.
match the patient’s details with the laboratory form, to ensure
accurate identification).
Ask whether the patent has allergies, phobias or has ever fainted
during previous injections or blood draws.
If the patient is anxious or afraid, reassure the person and ask what
would make them more comfortable.
capillary method
aretial method
The document defines hematocrit as the volume of red blood cells (RBCs) relative to the total volume of whole blood, expressed as a percentage. It notes there are two methods for measuring hematocrit: the macrohematocrit and microhematocrit methods. Normal hematocrit ranges are provided for men, women, infants/children, and newborns. Factors that can increase or decrease hematocrit levels are outlined, and indications for estimating hematocrit are given as screening for anemia and calculating red blood cell indices.
This document discusses laboratory hazards and precautions for working in a biochemical lab. It identifies three main types of laboratory hazards: physical, chemical, and biological. Specific physical hazards mentioned include fire, sharp objects, electricity, and poor housekeeping. Chemical hazards include corrosive, flammable, toxic, and carcinogenic substances. Biological hazards can arise from pathogens, animals, and body fluids. The document provides many safety precautions for each type of hazard, such as always wearing protective equipment like gloves and goggles, properly disposing of sharps and biological waste, and following general lab safety rules.
Hematology is the branch of medicine, that is concerned with the study of blood, blood forming organs and blood diseases. It includes study of etiology, diagnosis, treatment, prognosis and prevention of blood diseases .
After the completion of this presentation we will know about:
What is hematology and its purpose.
hematology laboratory.
Blood and its compositions and collections
Hematology lab equipment's
Some hematological tests , disease and hazards too.
EDTA is commonly used as an anticoagulant in hematology because it preserves cell morphology well. The document provides a procedure for preparing EDTA anticoagulant tubes and vials. EDTA powder is weighed and dissolved in distilled water to make a 10% w/v solution. 40μl of this solution is pipetted into each vial to provide 4mg of EDTA, enough to prevent coagulation in 2.5ml of blood. The vials are then dried in a hot air oven. Too little or too much EDTA can affect blood cells and indices.
Rh typing and its technique , BLOOD TYPING , Rhesus (Rh) typing , procedures of rh typing, process of Rh typing, Test limitations, Sources of Error in Rh Antigen Typing, False positive reactions' reason, False negative reactions' reasons
The document lists various instruments and equipment used in a blood bank laboratory, including personal protective equipment to protect workers, instruments for measuring and transferring liquids, equipment for separating blood components like centrifuges, refrigerators and freezers for storing blood and its components, microscopes, and waste segregation materials. It describes the uses of common lab equipment like test tubes, pipettes, balances, and autoclaves. Protective equipment and carefully measuring and storing blood are essential aspects of working in a blood bank laboratory.
This document discusses congestive heart failure (CHF), including its causes, pathophysiology, and effects on the left and right sides of the heart. CHF is caused by conditions that weaken the heart muscle, such as heart attacks, high blood pressure, and heart valve diseases. When the left ventricle fails to pump properly, blood backs up in the lungs leading to pulmonary edema and congestion. When the right ventricle fails, blood backs up in the liver, abdomen, and legs causing swelling. Common symptoms include shortness of breath, fatigue, swelling, and coughing. Treatment involves medications, lifestyle changes, and sometimes surgery.
18. heart part 1 basic & congestive heart failuresulochan_lohani
This document provides information on the structure and function of the normal and diseased heart. It discusses the components of the myocardium, blood supply, effects of aging, types of heart disease, cardiac hypertrophy, and left and right sided heart failure. Congestive heart failure is characterized by diminished cardiac output and backflow of blood, with morphological changes in the lungs, kidneys, liver, and brain.
This document discusses heart failure, including its definition, causes, types, and compensatory mechanisms. Heart failure occurs when the heart is unable to pump enough blood to meet the body's needs. It can be caused by intrinsic pump failure, an increased workload on the heart, or impaired filling of the cardiac chambers. The types of heart failure include acute or chronic, right-sided or left-sided, and forward or backward failure. When the heart begins to fail, compensatory mechanisms such as cardiac hypertrophy, dilation, and increased heart rate attempt to maintain adequate blood circulation.
This document discusses heart failure, including its classification, pathophysiology, clinical manifestations, investigations, and clinical syndromes. It describes how heart failure occurs when the heart is overloaded or the heart muscle is disordered. It discusses the neuroendocrine and cellular changes that occur in heart failure and how this impacts fluid retention, circulatory pressures, and organ function. Specifically, it outlines the features of left heart failure including common causes, symptoms of pulmonary congestion, physical exam findings, investigations such as echocardiography and natriuretic peptide levels, and how to differentiate it from other conditions like pulmonary disease.
This document defines and describes heart failure, its causes, forms, and pathophysiology. Heart failure is defined as the inability of the heart to pump enough blood to meet the body's needs. It is most often caused by impaired contractility from conditions like ischemic heart disease or cardiomyopathy. Heart failure can present as systolic or diastolic dysfunction and can affect the left or right ventricle. The body undergoes adaptive and maladaptive changes like neurohormonal activation to try to maintain cardiac output as heart function declines.
The document provides a lesson plan on congestive heart failure (CHF). It defines CHF and lists its causes such as coronary artery disease and hypertension. It discusses the pathophysiology of CHF including how the heart initially tries to compensate through hypertrophy, dilation, and stimulation of the sympathetic nervous system. However, these compensatory mechanisms can ultimately cause further damage. The document also covers the types of CHF (systolic and diastolic), diagnostic procedures, and management of the condition.
This document summarizes heart failure, including its classification, pathophysiology, clinical manifestations, investigations, and management. Heart failure means the heart cannot pump sufficient blood for the body's needs. It can affect the left side, right side, or both sides of the heart. Management involves correcting underlying causes, reducing demands on the heart through diet and exercise, and pharmacological therapy including diuretics, ACE inhibitors, and other drugs to modify neuroendocrine and renal responses. The goals of treatment are to alleviate symptoms and improve prognosis.
The document discusses the anatomy and function of the heart. It describes the four chambers of the heart, including the left and right ventricles that pump blood to the lungs and body. It also discusses the causes and features of heart failure, which can occur when the heart is unable to pump sufficiently due to conditions that weaken it over time. Common causes include hypertension, heart attacks, and cardiac diseases. Features involve congestion in the lungs and other organs from blood backing up.
Left-sided heart failure occurs when the left side of the heart, which pumps oxygenated blood to the body, cannot pump sufficiently. This causes a back-up of blood in the lungs, resulting in respiratory symptoms like shortness of breath and cough. It is usually due to conditions that damage or weaken the heart muscle over time such as heart attacks or high blood pressure. Treatment involves lifestyle changes and medications to help the heart function more efficiently and reduce symptoms.
Heart failure, also known as cardiac decompensation or cardiac insufficiency, occurs when the heart is unable to pump enough blood to meet the body's needs. It can be caused by conditions that impair the heart muscle's ability to contract effectively or limit ventricular filling. Symptoms vary depending on whether the left or right ventricle is primarily affected and include dyspnea, fatigue, edema and others. Diagnostic tests may include echocardiography, ECG, chest x-ray and BNP level. Treatment focuses on managing symptoms, slowing disease progression, and preventing hospitalizations through lifestyle changes and medication.
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Systemic pathology cardiovascular system
1. Page 1
Systemic Pathology PATH-202 3(2-1)
Dr. Mansoor Tariq Samo
Assistant Professor, Veterinary Pathology,SAU, Tandojam.
CARDIOVASCULAR SYSTEM
The cardiovascular system consists of a heart and blood vessels.
1. HEART
Heart is a muscular pumping organ which consists of four chambers; The two smaller one are right atrium and left atrium
while the bigger one are right ventricle and left ventricle.
1.2. RIGHT ATRIUM
The deoxygenated blood from the
entire body is received by this
chamber by means of two major
blood vessels; superiorvena cava
(coming from upside), inferior vena
cava (coming from lowerside)
1.3. PERICARDIUM
It may be referred asthe glistening
and protecting covering of the heart.
Pericardial Sac: The space between
the pericardium and heart.
Pericardial Fluid: The fluid present
inside the pericardial sac.
Epicardium: Thin layer
Myocardium: Muscular layer
Endocardium: very much glistening membrane.
1.4. STRUCTURE PERTAINING TO HEART
Tricuspid valve: is present between the Right atrium and Right ventricle.Bicuspid or Mitral Valve: is present between the
Left atrium and Left ventricle. The Wall of Right ventricle is thinner ascompared to that of Left ventricle.
Papillary Muscles: are the muscular projections of the myocardium which are attached to each
Coradae tendinae : other by means of thread like processes known as Cordae tendinae. The upper broader part of the
heart is known as Base while the lowernarrowing part is Apex.The artery carries blood to the heart muscles
(myocardium) named as Coronary Artery.
The fat lies on the coronary artery at the base part known as “Coronary Fat”.
From the left ventricle,a big blood vessel originates which is named as “Aorta”.
2. Page 2
The small blood vessels coming to the left atrium are known as “Pulmonary Veins” while the vessel arising from the
right ventricle is called “Pulmonary Artery”.
THE HEART
1.4.1.1 GENERAL:
The heart has an enormous capacity to deal with transient increases in workload, as long as adequate in tervals are
provided for the recovery of nutritive and electrolyte levels. However, if the heart is forced to work against a sustained
overload, it eventually becomes unable to deliver a normal output of blood. This leads to cardiac enlargement (dilatation
and hypertrophy) which is the cardinal sign of heart disease. The onset of myocardial fatigue is characterized by slight
acute dilatation of the heart which is due primarily to stretching of individual myocardial fibers subsequent to overfilling
with blood during diastole. Eventually, the myocardium respondsto sustained overload by undergoing hypertrophy and
chronic dilatation. Cardiac hypertrophy and dilatation are compensatory in nature and they usually occur together.
However,in order for cardiac hypertrophy to develop,a healthy myocardium and adequate nutrition (blood supply) are
required. If these factorsare lacking, dilatation in the absence of hypertrophy occurs.
1.4.1.2 HEART FAILURE
Heart failure occurs when the myocardium is no longer able to compensate for increases in workload.
"Congestive Heart Failure" is the clinical syndrome resulting from the inability of cardiac output to keep pace with
venous return. It is characterized by pulmonary and/or generalized venous congestion and low cardiac output. Congestive
heart failure is the final pathway of several important types of heart diseases. Subsequent to a failing heart, there is
retention of sodium and water by the body (apparently from decreased renal blood flow and adrenal cortical
mechanisms). This further distendsthe venous bed so that the heart cannot keep up with the amount of blood delivered.
The clinical signs of congestive heart failure are the secondary effects of a failing circulation. Lesionsare most prominent
and extensive in the lungs and liver.
The componentsof the cardiac reserve are increased of rate of contraction and increased stroke volume; however,
there are limits to the effectiveness of each. Increased stroke volume is the most effective of the two components.
Lesions responsible for heat block are hemorrhages, infarction,and deposition of Ca, tumors, abscesses necrotic
foci and fibrosis. There causes of heart block and the lesions must be close to and impinges the main parts of the condition
system (The ventricular bundle or its right and left branches).The most crucial location of such lesionstherefore is in the
dorsal aspects of the ventricular septum,where the ventricular bundle has its origin
In cardiac failure (decompensation), many circulatory reflexes become active. The net effect is that of a
coordinated sympathetic nervous system stimulation with reciprocal parasympathetic inhibition.The strong sympathetic
stimulation increasesthe force of myocardial contractions and increases the tone in most of the blood vessels of the body.
The normal cardiac output can be broadly defined as the output necessary to meet the needsof the organism at rest. The
ability of the heart to respond to circulatory demandsover and above those of the animal at rest is referred to as the
cardiac reserve.Any cardiac lesion which impairsthe efficiency of the heart reduces the cardiac reserve. Therefore,
when the cardiac reserve is exhausted and the circulatory requirements of the animal at rest can no longer be
met,"congestive heart failure" follows. Heart failure occurs in animals aswell, but the incidence is much lower. Heart
failure can be broken down into two broad categories, acute heart failure and chronic (or congestive) heart failure.
Congestive heart failure,also known as chronic heart failure,is the result of failure of the heart to maintain adequate
circulation overa period of time. General causes of chronic heart failure include:
3. Page 3
• sustained systolic pressure overload,
• sustained volume overload
• loss of myocardial contractile capacity
• interference with ventricular filling during diastole,
The body makes many adjustments,or compensations, when faced with chronic heart failure. These adjustments to
chronic heart failure can be divided into two main categories – peripheral and cardiac. Peripheral adjustments for
insufficient cardiac output would include trying to maintain blood flow to vital organs, increasing the amount of red blood
cells to help with oxygenation, and controlling the blood volume to decrease the load on the heart.
Cardiac adjustments to heart failure are those compensations that allow the heart to respond to circulatory demands over
and above those of the normal animal at rest.
Congestive heart failure is often further divided into right-sided or left-sided heart failure. Failure on one side usually
leads to failure on the other, so it doesn’t matter all that much.
When one side of the heart fails.The ensuing sequence of events usually makes the opposite side fail as well. However, it
is convenient to discuss the manifestations of left and right-sided heart failure separately.
Remember, the manifestations of left and right heart failure apply to many of the diseases and conditions to be discussed
later in this section.
1.4.1.3 LEFT-SIDED HEART FAILURE:
The clinical signs of left heart failure are primarily pulmonary (lungs),and include dyspnea on exertion, cough, and
orthopnea.Common causes of left heart failure include:
• (1) myocarditis,
• (2) degeneration of the myocardium,
• (3) stenosis and insufficiency of the mitral and semilunar valves, and
• (4) congenital heart diseases.
Regardless of the cause, there is progressive dilatation of the left ventricle and atrium which may be followed by
left ventricular and atrial hypertrophy. If the heart is unable to maintain a state of compensation, blood
accumulates in the pulmonary veins and lung capillaries. Pulmonary (lung) congestion,edema, and induration
ensue. The reduction in pulmonary vital capacity and impaired gaseous exchange result in hypoxic stimulation of
the carotid sinus. Eventually, right heart failure develops subsequent to increased pulmonary resistance and
increased pressure in the pulmonary artery (refer to the manifestations of right heart failure).
It should be noted that coughing is usually the most distinctive and alarming feature of left heart failure in the
dog. The productive cough is explained by the increased production of mucous, stimulated by severe lung
congestion.
1.4.1.4 RIGHT-SIDED HEART FAILURE:
Clinical signs of right heart failure are the manifestations of generalized venouscongestion,and include distention of the
jugular and other superficial veins, liver and spleen enlargement, and an accumulation of fluid in serous cavities and in
tissues (generalized edema).Common causes of right-heart failure include:
4. Page 4
• (1) left-sided heart failure,
• (2) myocardial degeneration,
• (3) myocarditis,
• (4) factors that cause increased pulmonary resistance,
• (5) hydropericardium,
• (6) exudative pericarditis,and
• (7) endocarditisand defective tricuspid and semilunar valves.
Regardless of the causes, there is progressive dilatation of the right ventricle and atrium which may be followed by right
ventricular and atrial hypertrophy.As the heart fails,blood accumulates in the vena cava leading to generalized venous
congestion. Centrilobular congestion, degeneration, necrosis, and fibrosis of the liver ensue. The splenic red pulp
becomes engorged, and there is generalized edema (ascites, etc.). Eventually, the effects of right heart failure are
reflected in the left heart and lungs (if the animal lives long enough).
Generalized edema is a prominent feature of right heart failure and there are some species differences in the location of
the edematousfluid.In the horse and cow, a dependent subcutaneous edema is expected (subcutaneous edema is scant
or absent in other species). In the dog, the predominant accumulation of fluid is in the peritoneal cavity (ascites);
whereas in the cat, fluid is most commonly encountered in the thorax (hydrothorax).
Remember, Cor pulmonale is the clinical term applied to right ventricular strain produced by diffuse pulmonary diseases
(chronic emphysema, etc.).
1.4.1.5 HYPERTROPHYAND DILATATION OF THE HEART
Remember, cardiac enlargement is the "cardinal sign" of heart disease. Myocardial hypertrophy is an increase in bulk
of cardiac muscle due to an increase in size of component fibers. There are three descriptive types ofhypertrophy:
SIMPLE HYPERTROPHY
Is the term used when hypertrophy occurs in the absence of dilatation.
ECCENTRIC HYPERTROPHY
Is the term used when there is both hypertrophy and dilatation of the heart. Eccentric hypertrophy (volume overload
hypertrophy). occursin response to chronic pressure-overloading caused by, systemic or pulmonary hypertension.
Eccentric hypertrophy is characterized by increased ventricular chamber volume with normal ordecreased ventricular
wall thickness. However, the total cardiac weight is increased due to a greater muscle mass surrounding the dilated
chamber.
CONCENTRICHYPERTROPHY
Is the term used when hypertrophy results in a decrease in size of the heart chambers. Concentric hypertrophy (pressure
overload hypertrophy). Occurs in response to chronic pressure-overloading caused by systemic or pulmonary
hypertension. Concentric myocardial hypertrophy is characterized by increased ventricular wall thicknessand decreased
ventricular chamber volume. Concentric hypertrophy must be accompanied by a compensatory increase in heart rate in
order to maintain cardiac output.
Hypertrophy affects the left heart more frequently than the right and the ventricles more frequently than the atria.
Hypertrophy of the right heart makes the heart broader at the base; whereashypertrophy of the left heart increases the
5. Page 5
organ length. Bilateral hypertrophy results in a more rounded shape than normal. Grossly, increased thickness and a
rubbery firmness are the best indices of cardiac hypertrophy.
Cardiac dilatation may involve one or both chambers of the heart. Grossly, the dilated heart is globose shaped, the walls
are soft, pliable, and thin. The endocardium is usually diffusely thickened and opaque.
1.6 PERICARDIUM OF THEHEART
The pericardium is the fibro-serous sac which enclosesthe heart. The fibrousor outer layer is rather thin b ut strong and
inelastic. The serous layer is an enclosed sac surrounded by the fibrouslayerand invaginated by the heart. It is smooth
and glistening and normally contains a small amount of clear serousfluid.The parietal part of the serous layer lines t he
fibrous layer,to which it is closely attached; whereas the visceral part of the serous layer covers the heart and partsof t he
great vessels. This portion is referred to as the epicardium.
Most diseases of the pericardium are secondary to disease processes in the heart, lungs, pleura,and other sites in the body.
Usually, pericardial diseasesare detected clinically only when they cause an accumulation of fluid within the pericardial
sac.
1.6.1 HYDROPERICARDIUM
Hydropericardium refersto the accumulation of fluid (transudate) within the pericardial sac (remember, a small
amount of clear fluid is found normally in the sac). Hydropericardium is caused by those factors responsible for
generalized and/or local edema.
Hydropericardium indicates the accumulation of serous fluid of non-inflammatory origin within the pericardial sac
Hydropericardium is associated.
1. With conditions which increase the blood pressure of the coronary circulation.
2. In conditions in which there is decrease in the colloid osmotic pressure of the blood plasma.
3. With increased capillary permeability.
Two good examples of condition which may raise the venous coronary pressure are stenosis and insufficiency of the
right atrio-ventricular valve. The extra cardial lesions which may result in some venous disturbance are chronic
pulmonary-emphysema and diffuses interstitial fibrosisof lung. As a result of any of these conditionsthe capillaries of the
coronary circulation become dilated and the capillary blood pressure is raised.These conditions render the capillary wall
more permeable to plasma protein and therefore the way foroedema to occur.
Stomach worm infestation causes a decrease in the colloid osmotic pressure of the blood plasma which may result in
hypropericardium.
Remember, a small increase in pericardial fluid occursby transudation after death which is soon reddened by the
products of postmortem hemolysis.
1.6.2 HEMOPERICARDIUM
Hemopericardium refers to an accumulation of pure blood in the pericardial sac. The condition is uncommon in animals
except in the following instances;
• Following cardiac punctures.
• Spontaneous rupture of the intrapericardial aorta of horses.
• In uremic dogs with ulcerative atrial endocarditis.
6. Page 6
• Following rupture of the coronary artery.
Remember, the term cardiac tamponade refersto compression of the heart subsequent to the accumulation of any fluid
within the pericardial sac. The chief causes are trauma, spontaneous rupture (Degeneration)and dilatation (Aneurysm)
and rupture of the coronary artery.
1.6.3 PNEUMOPERICARDIUM.
Denotes air or gas in the pericardial sac.It may be result of a compound fracture and the penetration of a
broken rib into the sac. It may also be due to gas forming organism in traumatic pericarditis.
1.6.4 PYOPERICARDIUM.
Indicates the pus in the pericardial sac. It is the result of supportive or purulent inflammatory condition of
the pericardium. It is commonly caused by micrococci and streptococci.
1.6.5 INFLAMMATIONOF THE PERICARDIUM(Pericarditis)
Pericarditis refers to inflammation of both the parietal and visceral surfacesof the pericardium. A true pericarditis is
nearly always infectious with an accumulation of exudate within the sac. Infectious agents usually reach the pericardium
by extension from surrounding structures and/or by way of the blood stream (hematogenous route). The hematogenous
route of infection is most common and the exudate tends to-be of the fibrinous or sero-fibrinous type.It should be noted
that infection involving the pericardial (epicardial) surface seldom showsan appreciable spread into the underlying
myocardium.
1.6.5.1 FIBRINOUS PERICARDITIS
is a characterized by an accumulation of fibrin within the pericardial sac. In many cases the exudate coagulates, forming a
thin fibrinouscovering over the pericardial surfaces. Such a form is known as fibrinous pericarditis. Where the exudation
is profuse and much fibrin is formed, the rubbing together of the fibrin-covered surfaces causes the heart to assume
shaggy or so called bread and butter appearance. Grossly,the fluid is grayish to yellow, and flecks of blood may be
present. In cattle, it is commonly a part of blackleg, pasteurellosis, contagious bovine pleuropneumonia,sporatic bovine
encephalomyelitis, and some forms of neonatal coliform infections. In swine, fibrinous pericarditis is frequently
associated with Glasser's disease, pasteurellosis, and salmonellosis. In the horse, streptococci are usually present.
1.6.5.2 PURULENT PERICARDITIS
is characterized by the accumulation of pusin the pericardial sac (due to pyogenic bacteria) and may be associated with
septicaemia or pyaemia. It occurs most commonly as a result of traumatic perforation by a foreign body originating from
the reticulum (traumatic pericarditis). Also, in traumatic pericarditis the exudate may be fibrinous or fibrino-purulent in
nature.
Pus within the pericardial sac may appearas a thin cloudy exudate, as frank creamy exudate, or as a mixture of purulent
exudate and masses of pus.The accumulation of pusin the sac places tension on the pericardium which may be reflected
in pooling of venous blood (congestive heart failure).
In both fibrinous and purulent pericarditis,healing is usually by organization.
7. Page 7
Ultimately, the organizing fibrous connective tissue joins the two surfaces of the serous pericardium resulting in an
adhesive pericarditis. Thus, considerable pressure is exerted, and the heart muscles become more or less rigid
(constrictive pericarditis). This pressure on the myocardium and large vesselscausescompensatory ventricular dilatation
and hypertrophy.Subsequently, generalized venous congestion occursand death may ensue from "congestive heart
failure."
1.6.5.3 TRAUMATICPERICARDITIS
This condition occurs in cattle as a result of traumatic perforation of the pericardium by a foreign body originating in the
reticulum (traumatic reticulitis). In cattle,this form arises from the swallowing of a foreign body such as nail, needle or
a piece of wire.This become lodged in the reticulum and on account of the muscular contractions, is some times driven in
to the mucous membrane. The foreign body may then be forced through the reticulum wall into and through the
diaphragm.The entrance of bacteria along with the foreign body gives rise to inflammation and ulceration, producing a
supportive tract.Adhesions are formed between the reticulum and diaphragm. The latter is usually pierced opposite the
apex of the heart, and the continued forward movement of the foreign body some -times leads top perforation of the
pericardium and occasionally the heart. (as well as the myocardium and endocardium) resulting in an exudative
pericarditis). At the end it may cause, lesions in the pleura and lungs and even in the liver,spleen and peritoneum.
The penetration of the pericardium by foreign body sets up pericarditis but the type of inflammation which results
depends on the nature of the organism which accompanies the foreign body. It is generally purulent but it may be
fibrinous, sero-fibrinous or hemorrhagic. The heart itself is commonly hypertrophied due to the hampering of its action by
exudatesand adhesions.
1.6.5.4 SEROUS ATROPHY OF PERICARDIAL FAT
In any cachexia and/or debilitating condition,there is progressive mobilization of depot fat, including that beneath the
epicardium. As normal lipid vacuolesare reduced in size,they are replaced by a proteinaceous fluid; subsequently,normal
fat is converted to grayish-brown gelatinous masses.
1.7 ENDOCARDIUM OF THE HEART
The endocardium linesthe cavities of the heart, and is continuous with the intima of vessels which enter and leave the
organ. Its free surface is smooth and glistening and is formed by a layer of endothelial cells. This endothelial layer rest o n
a thin layer of fibroelastic tissue which is connected to the myocardium by subendothelial elastic tissue containing nerves
and vessels.
1.7.1 INFLAMMATIONOF THE ENDOCARDIUM
Endocarditis refersto inflammation of the endocardium which may be valvular ormural. In domestic animals, valvular
endocarditis occurs more frequently than mural.
Endocarditis is usually caused by bacterial agents, but occasionally parasites and mycotic agents may serve as causative
factors. A large number of bacteria are capable of causing endocarditis; however, the manner by which these bacter ia
localize on a valve is not clear.Apparently, endocarditis occurs subsequent to a substained or recurrent bacteremia. In the
dog and horse, streptococci and staphylococci are most commonly isolated from valvular lesions: whereas
Corynebacterium pyogenes is most frequently recovered in cattle.
The location of endocarditis varies with the animal species involved. In cattle,lesions are most common in the right heart;
whereas in the horse. dog, and pig, endocarditis occurs most frequently in the left heart. In cattle, the tricuspid valve is
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most commonly affected followed by the mitral, pulmonary, and aortic valve. In the horse, the aortic valve is most
frequently involved, followed by the mitral and finally the pulmonary valve. In the pig and dog, lesions are most
commonly observed in the mitral valve, followed by the aortic,tricuspid, and the pulmonary valve.
Acute ulcerative mural endocarditis is commonly encountered in dogs suffering from acute renal insufficiency (uremia).
The lesions (ulcers and thrombi) occur primarily in the left atrium, but may be found in the left ventricle and large
elastic arteries. Experimentally, lesionsoccurmore commonly in dogs fed diets high in fat prior to the onset of renal
failure. Also, ulcerative mural endocarditis occurs frequently in the left atrium of calves with blackleg.
Regardless of the cause, thrombi are formed in those areas where the endothelium is damaged (valvular or mural). The
terms "vegetative" or "cauliflower" are commonly used to describe the gross appearance of these thrombi. The surfaces
of the thrombi are friable and embolism may occur. Organization proceeds from the base by the usual process of
granulation.
Remember, valvular thrombi are almost always serious since they tend to obstruct the normal flow of blood, prevent
perfect closure of the valves, and/or result in embolism.
1.7.2 CALCIFICATION OF THEENDOCARDIUM
Calcification of the elastic fibers of the endocardium is encountered in dogs, cattle, sheep, and horses. In dogs,
endocardial calcification occurs most commonly in those which have recovered from acute ulcerative endocarditis of renal
insufficiency.It occurs in calvesand lambs with vitamin E and selenium deficiency (white muscle disease), and in older
cattle with hypomagnesemia. Also, endocardial calcification may be associated with any debilitating disease.
1.8 MYOCARDIUMOF THE HEART
1.8.1 INFLAMMATIONOF THE MYOCARDIUM
Myocarditis refers to inflammation of the myocardium, which is usually secondary to a wide variety of systemic diseases.
The causative agents may reach the myocardium by extension or by the hematogenous route. The lesions are usually focal
and may be overlooked on causal gross inspection.
1.8.1.1 SUPPURATIVEMYOCARDITIS
Is associated with the presence of pyogenic organisms, and abscessformation is common. The inflammation is usually
localized and is characterized by the formation of abscesses. The bacteria reach the myocardium by way of the blood
stream or extension from adjacent organs. As a result, local suppurative myocarditis is associated with septicemia or
bacteremia when the organismsare carried to the heart from suppurative processesin other organs. Septic emboli may
lodge in a coronary artery and produce an abscess.The myocardium may also be involved in suppurative inflammation by
extension of process from a near by inflamed organ or part e.g. from the pericardium, endocardium, plura lungs,bronchial
or mediastional lymph glands.
1.8.1.2 NON-SUPPURATIVE MYOCARDITIS
Is associated with various toxemias. The irritant may be mineral, poison or toxin from bacterial or parasitic infections or
necrotic tissue as occurs in coagulative necrosis.
1.8.2 DEGENERATIVE AND RELATEDCHANGES OF THE MYOCARDIUM
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Cardiac muscle is subject to the same type of degenerative changes as skeletal muscle. However, there is a greater
tendency for heart muscle to undergo degenerative changesas a response to non-specific causes.
HYALINE CHANGES (and necrosis) of the myocardium occursas a part of "white muscle disease syndrome" and
gossypol poisoning. Calcification of the myocardium is usually dystrophic in type, and it occurs whenever there are dead
or dying myocytes. In organomercurial poisoning of cattle, calcium salts are selectively deposited in the purkinje network.
1.8.3 NECROSIS ANDISCHEMIA OF THE MYOCARDIUM
Myocardial infarction precipitated by arteriosclerosis of the coronary artery is a burden of aging humans, but is rare in
domesticated animals.In animals however,acute obstruction of the coronary arteries due to emboli occurs with some
frequency,with the development of infarction.If the coronary obstruction is chronic, the end result is diffuse scarring of
the myocardium and markedly altered function. Coagulative necrosis of the myocardium is a lesion commonly associated
with vitamin E and selenium deficiency (white muscle disease) in lambs,calves, and pigs.
1.8.4 HEMORRHAGES OF THE HEART AND ITS MEMBRANES
Petechial, ecchymotic,and larger hemorrhages occur beneath the epicardium and endocardium asagonal changes. Agonal
hemorrhages are due to anoxia and rupture of small vessels that occurduring the process of dying. Also,subendocardial
and subepicardial hemorrhages are commonly associated with septicemias, bacteremias, toxemias, and hypoxic
conditions.
VASCULITIS is defined as an inflammation of vessels characterized by presence of inflammatory cells within and around
vessel walls. Lesionscan be more specifically designated asarteritis (arteries), phlebitis (veins),or omphalophlebitis
(umbilical veins). Vasculitis is commonly associated with septicemic, viremic, and toxemic diseases. Endothelial cell
damage is a primary factor in the pathogenesisof many diseasesincluding: canine herpes, infectious canine hepatitis,
swine fever, heartwater, African horse sickness,epizootic hemorrhagic disease, bluetongue and endotoxemia.
1.10 ARTERIES
1.10.1 Inflammation of Arteries (Arteritis)
Arteritis is characterized by the presence of inflammatory exudate (neutrophils, etc.) within the layersof the vessel wall.
A non-specific type of arteritis is a component of all acute inflammatory lesions. The inflammatory reaction occurs in
arteries which pass through inflamed areas,or which contain infected thrombi oremboli. It is usually the smaller arteries
that are involved and the arteritis is, therefore, of little consequence except in cases of thrombolic infarction or embolism.
In general, non-specific arteritis is secondary to and correlates directly with the inciting cause. Specific types of arteritis
occur in a wide variety of systemic infectious diseases.Damage may be due to direct effect of a microbial agent or its
toxin on any component of the vascular wall. In the horse arteritis commonly occurs subsequent to invasion of the anterior
mesenteric artery by immature Strongylus vulgaris. Also, arteritis is an important lesion in Newcastle disease of birds,
equine viral arteritis, malignant catarrhal fever, renal insufficiency in dogs, dirofilariasis, etc.
Arteritis subsequent to immunologici injury occurs when munecomplexes (antigen/antibody/complement) attach to
vascular endothelium. Initially, antigens localize in vascular walls and subsequently complex with circulating
precipitating antibodies. The antigen/antibody complexes attract complement. The arteritis is caused by neutrophils for
which the complement containing complexes are chemotactic (neutrophils are attacked by terminal complement
fragments). Immunologic arteritis occursin the Arthus reaction,acute serum sickness. Aleutian disease,and in cases of
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glomurulo-nephritis. The Arthus reaction is the classical experimental model of immune complex disease and the basic
lesion is an intense arteritis.
1.11 SOME SPECIFIC DISEASES AND CONDITIONS CHARACTERIZEDBY ARTERITIS
1.11.1 EQUINE VIRAL ARTERITIS
1.11.2 ARTERITIS OF RENAL INSUFFICIENCYOF DOGS
1.11.3 DIROFILARIASIS
1.12 Non inflammatory Lesionsof Arteries
1.12.1 CALCIFICATION: Arterial calcification occursfrequently in animals as a dystrophic or metastatic process.
Calcium salts may be deposited in the intima or media. Calcification of the media is commonly associated with chronic
renal insufficiency in dogs, vitamin D toxicosis, and a variety of debilitating diseases of cattle.
1.12.2 ANEURYSM OF ARTERIES
An aneurysm is a pathological, more-or-less circumscribed, dilatation of an artery (or chamber of the heart). The arterial
wall is composed of stretched intima and adventitia with only remnants of media. There is a tendency for aneurysms to
enlarge progressively and to ultimately rupture. A false aneurysm is a blood-containing cavity that communicateswith the
arterial lumen. The wall is formed from surrounding tissues. A dissecting aneurysm is characterized by the presence of
blood between the layersof the arterial wall (usually in the media). The blood current gains access to a defect in the
media and the resulting blood pressure forcesthe blood for some distance between the layers.
ANEURYSM: It is a local dilatation of an artery Aneurysm of an artery,when of recent formation,has a wall consisting
of the three arterial layers.In older lesions,the normal structure of the wall disappears and being replaced by granulation
tissue of which may contain cerium the deposits. An aneurysm is a localized dilatation of an artery. Dilatations of the
veins are called varicosities (singular varicose) rather than aneurysms.
A true aneurysm results from formation of a sac by the arterial all three walls layer. It is most often associated with
atherosclerosis.
A false aneurysm usually is caused by trauma. In this case, the wall of the blood vessel is ruptured and blood escapes into
surrounding tissues and formsa clot (hematoma).
CLASSIFICATION.
1. A fusiform aneurysm; is spindle shaped.Entire circumstance dilates and the aneurysm is spindle shaped.
2. A saccular aneurysm; is one-sided dilatation where only part of the circumference is involved.
3. A dissecting aneurysm; as the name suggests occurswhen the blood accumulated in between the coat of the
artery wall following a damaged intima.
4. Millary aneurysm; are very small aneurysm which are found in the cerebral arteries.
5. A cricoid aneurysm; which is sometimesfound in subcutaneous tissues, consists of a mass of dilated and
tortuous arteries which formsa pulsating swelling. It is congenital.
6. A traumatic aneurysm is a false aneurysm which follows rupture of an artery wall, the blood accumulating
in the connective tissue.
CAUSES.
An aneurysm results from the pressure of blood on the wall of an artery, which has been weakened through one
cause or another. Often there are no symptoms,but a ruptured aneurysm can lead to death. Rarely but can been seen in
older animals. The following are the chief causesin animals.
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1. Parasites, e.g. strangles vulgaris larvae in the anterior mesenteric artery of the horse. The aneurysm may
become as much as six inches in diameter when involving the truck of the anterior mesenteric artery.
2. Trauma, Disease of the artery wall, e.g. atheroma,Embolism.
SEQUALAE.
1. Aneurysm may rupture and cause death.
2. They may cause pressure atrophy of the surrounding tissue and, if important structures are involved death
may follow.
3. The contentsof the aneurysm may give rise to embolism.
4. Thrombosis and complete stoppage of the circulation through the vessel may occur.
5. Parasitic aneurysms of the mesenteric artery of the horse may cause colic.
1.12.3 HYPERTROPHYOF ARTERIES
Hypertrophy of arteries may affect one orall componentsof the vascularwall. It occurs in response to the need to carry an
extra load. Medial hypertrophy of the pulmonary arteries occurs commonly in the lungs of cats. The condition is
characterized by marked hypertrophy of the muscular media so that the lumen is reduced to rather small slits. There are no
apparent clinical signs and the cause is unclear.
1.12.4 ARTERIOSCLEROSIS : is an umbrella term for several types of changes that cause hardening of arteries.
Arteriosclerosis without lipid deposition can occur due to increased connective tissue, vascular mineralization (Johne’s
disease), or hyaline degeneration (Coronary arteries of old dogs).
Ateriosclerosis with lipid deposition, also known as atherosclerosis,is common in humansbut infrequent in animals.
Arteriosclerosis literally means hardening of the arteries. It includes those degenerative changes characterized by
induration (fibrous thickening), lossof elasticity, and narrowing of the lumen. Usually arteriosclerotic lesionsdevelop as
multiple or focal sclerotic changes superimposed upon a generalized,age-related increase in connective tissue elements of
the vessel wall.
The "hallmark" of arteriosclerosis is the fibrous plaque which appears as a white, firm, glistening elevation on the
luminal surface of arteries. The well-developed fibrous plaque consists largely of "modified" smooth muscle cells
(myocytes) surrounded by increased amounts of extracellular matrix.
Subclassifications within the broad category of arteriosclerosisare atherosclerosis,medial sclerosis, and arteriolosclerosis.
Atherosclerosis is characterized by the accumulation of lipid in larger arteries in the form of elevated,lipid-filled plaques
called atheromas. The atheroma beginsas an intimal lesion which progressively extends into and affects the media.
In animals, atherosclerosis occurs primarily in the aorta and small muscular arteries. In the dog, severe systemic
atherosclerosis is associated with advanced age, obesity, and hyperlipoproteinemia . The majority of these dogs have
hyperthyroidism which leadsto hypercholesterolemia and, indirectly,to atherosclerosis.
In aged humans, atherosclerosisis an extremely common lesion and disease. The aorta, coronary, iliac, and cerebral
arteries are most often affected.Because atherosclerotic lesionscan occlude blood vessels, serious consequences such as
myocardial infarction and stroke may occur.
ATHEROMA
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It is a localized or patchy condition of in timed thickening of arterial wall (due to deposition of lipids and
formation of fibrous tissue) which is more often found affecting the aorta, particularly at the arch or the point of exit of
other blood vessels. The lesions may also involve the coronary and cerebral arteries and sometimesthe endocardium.
CAUSES: Little is known regarding the causation of the condition and have a toxic origin orit may followdietetic errors.
NAKED EYE APPEARANCES.
In the larger vessels, such as the aorta,the lesion is in the form of hard,well-defined, whitish or yellowish
spots which project in to the lumen of the vessel. The colour is due to the presence of fatty changes in the deeper layers of
the intima, and the hardnessfollows the deposition of lime salts.The smaller vessels are characterically tortuous.
MICROSCOPIC APPEARANCES.
The changes in atheroma are confined to the intima,and the features of thiscondition,both proliferative
and degenerative changes are present. The superficial layer of the intima presents an increased amount of connective
tissue, and the deeper layer, fatty degeneration is prominent.
SEQUALAE.
1. Weakening of the arterial wall may lead to dilatation and the formation of the aneurysm.
2. The occurrence of thrombosis or the narrowing of the lumen may lead to nutritional changes,e.g. disease of
the coronary arteries causes atrophy and fibrosis of the heart.
3. The disease may extend to the endocardium.
4. Ulceration may occur and embolism and infarction result.
1.12 VEINS
1.12.1 Inflammation of Veins (Phlebitis)
Phlebitis is the inflammation of veins characterized by presence of inflammatory exudate, thickening of the wall and
dilation of the lumen. The condition is less common than arteritis. Some time occurs with thrombophelibitis and
Omphalophlebitis. Omphalophlebitis in which the umbilical veins, particularly in farm animals, become infected and
inflamed after birth. Acute phlebitis occurs in "navel infection" (omphalophlebitis) of calves, lambs and foals.
Some parasitessuch as Schistosoma sp (blood fluke trematode) cause parasitic phlebitis.
ACUTE PHLEBITIS: Is invariable result of bacterial infection and is always associated with thrombosis.
CAUSES.
1. Blood infection. The organisms present in the blood, setup inflammation of the endothelial lining and
thrombosis results.
2. Extension from neighboring inflamed tissue as in the utrines veins from septic metritis.
3. A phlebitis of the jugular vein (vine section)may arise as the result of improper intravenous injection or
faulty techniques.
4. Omphalophlebitis-phlebitis occurs in young animalsbefore the umbilicus has healed.
MACROSCOPICALLY.
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The wall of the umbilical vein is thickened, the lumen dilated and contains thick necrotic material, after
removal of which the inner surface of the vessel appears rough and redden.
MICROSCOPICALLY.
There is pronounced leococytic infiltration of the wall but gradually becomes less in number from within
out. Other pathological conditions which may involve veins are asfollows.
1. Spontaneous rupture, most frequently in the posteriorvena cava.
2. Thrombi formation, seen in the mammary, portal and uterin veins.
3. Parasitic obstruction.
SEQUELAE.
1. Resolution may occur.
2. The thrombus may become organized and obliteratesthe lumen of the vein.
3. In suppurative affection, septic emboli may cause pyaemia.
4. The thrombus may classify and form a phelebolith.
5. Embolism of the pulmonary artery.
THE LYMPHATIC SYSTEM is a network of organs (i.e tonsils, spleen and thymus), cells (lymphocytes), ducts
(lymph vessels), and glands (lymph nodes) can be found throughout the body. Lymph travelsthrough the body along
lymphatic vessels and collects fats, bacteria, and other waste products from cells and tissues. The lymph nodes then filter
these harmful materials out of the fluid and produce more white blood cells to fight off the infection.
PATHOLOGICALCONDITION OF LYMPHATIC SYSTEM
Lymphangitis is an inflammation of the lymphatic system, which is a major component of the immune system.
Lymphadenitis Inflammation of lymph glands. Lymphatic system problems can include infections, blockage,and cancer.
Lymphoid leukaemias and lymphomas are nowconsidered to be tumours,
“Leukaemia" when tumour in the blood or marrowand
“Lymphoma" when tumour in lymphatic tissue. And togetherthey called “Lymphoid malignancy"
LYMPHADENITIS.
Inflammation of lymphatic gland. Acute lymphadenitis is found in many cases of the acute septicaemic
diseases especially in the early stages and in the nodes draining an organ or part of the body undergoing acute
inflammation. Bronchial lymph glandsare unchanged and inflamed in pneumonia, supra mammary glands depends
simply to mastitis, pharange at swell in rhinitis or infected with. It is frequent in acute septicaemia such as anthrax,
pasteurellosis. In the mesenteric nodes it is one of the lesions of suckling calves,lambs and kids.
MACROSCOPICALLY.
The lymph nodes are enlarged and soft, the cut surface is moist,bulgesand is reddened.
MICROSCOPICALLY.
There are hyperaema,oedema and haemorrhage (erythrocytes in the lymph sinuses),In the parenchyma of
the gland the lymphoid hyperplasia may produce atrophy of the germinal centers.
CHRONIC LYMPHADENITIS.
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Chronic lymphadenitis occurs in the mesenteric lymph nodes of cattle with paratuberculosis. Bovine tuberculosis
is a chronic inflammation usually characterized by caseous necrosis and calcification.The enlarged, firm, grey nodes
contain cheesy yellowarea which are often gritty when cut. In glanders, actinobacillosis and actinomycosis a chronic
suppurative lymphadenitis occurs. In any of these diseases the nodes are enlarged usually and contain thick walled abscess
cavities.
LYMPHANGITIS INFLAMMATIONOF THE LYMPHATIC VESSELS.
Acute sero fibrinous lymphangitis occurs in the lungs in the course of inflammatory diseases (catarrhal
pneumonia of dogs and horses)characterized by peribronchitis and peribronchiolitis. Acute suppurative lympangitis arises
in connection with suppurative processes in the area drained by the affected lymph vessels. Chronic suppurative
lymphangitis is an important lesion in glanders,epizootic and ulcerative lymphangitis of horses.
Lymphangitis occurswhen viruses and bacteria invade the vessels of the lymphatic system, typically through
an infected cut or wound. Lymphangitis occurs when bacteria or virusesenter the lymphatic channels. They may enter
through a cut or wound, orby an existing infection. Bronchial lymph glands are involved and inflamed in pneumonia
cases. In mastitis, enlarged supramammary, iliac and lumbar lymph nodes. Also Mycobacterium paratuberculosis &
Brucella abortus infection. Pharynges are involved due to tonsils swelling in rhinitis or in infection.
LYMPHEDEMA: If lymphatic system not working properly, fluid builds in body tissues and causes swelling,
called Lymphedema. Lymph edema classified into primary and secondary
• Primary lymph edema is usually congenital and hereditary due to anomalous development of the lymphatic
system.
• Secondary lymph edema occurs because of obstruction of previous normal lymphatic duct due to infection,
inflammation, tumour,or injury.
Lymph edema is because of the predispose affected area,usually limb, to secondary bacterial infection and poor wound
healing.
LYMPHATIC FILARIASIS is caused by the worms Wuchereria bancrofti, Brugia malayi,and Brugia timori. These
worms occupy the lymphatic system, including the lymph nodes; in chronic cases, these worms lead to the syndrome
of ELEPHANTIASIS.These are transmitted by mosquitoes and their life cycles are start.Infective larvae enter peripheral
lymphatics, migrate to nearest lymph nodes and develop 2 weeksbefore migrating to nearest lymph nodes and mature
their and produce gramalomatous lymphangitis and lymphadenitis and cause lymphoedema and elephantiasis.
CHYLOTHORAX: characterized by the accumulation of chyle within the thoracic cavity due to leakage orrupture of the
thoracic duct. Infrequently seen in dogs and cats.Chyle hasa characteristic milky color contains small molecules of fat
after digestion. the fatty component of the meal is further broken down into small molecules termed chylomicrons. The
intestinal lymphatic system that travels to a structure called the cisterna chyli (CC), which is locate in the front portion of
the abdomen, near the kidneys, absorbs these small molecules. The CC is a lymphatic reservoir that receives chyle from
the intestine but also receives lymphatic fluid from the rest of the abdomen and pelvic limbs.
The thoracic duct (TD) is the extension of the CC into the chest, which carries chyle into the thoracic cavity and
eventually emptiesits contents into the cranial vena cava (CrVC) close to the heart. In pets affected with chylothorax
there is an abnormality in the TD that causesit to leak chyle into the thoracic cavity. These pets have difficulty breathing
as the chyle that buildsup in the chest prevents their lungs from fully inflating with air. The lymphatic fluid that is also a
main component of chyle contains protein, white blood cells, and vitamins.The lossof large amounts of chyle into the
thorax can weaken your pet’s immune system and create severe metabolic disorders.Chyle is also an irritant and chronic
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exposure to the lining of the lungs (pleura) and heart (pericardium) can lead to inflammation of those surfaces with further
deleteriousconsequences.
PATHOLOGICALVARIATION OF REDCORPUSCLES.
A. VARIATION IN NUMBER.
1. Polycythemia. Increase in number as seen in diarrhea and excessive perspiration.
2 Olygocythaemia. Decrease in number. The condition is present in anaemia or piroplosmosis.
B. ANISOCYTOSIS.
Variation in the size of erythrocytes seen in anaemia. Cells smaller than average red cell are called
microcytesand those larger than average are called as megalocytes.Still larger are called as gigantocytes.
C. POIKILOCYTOSIS.
Variation in shape is seen in anaemia.
D. NUCLEATED FORMS ORERYTHROBLASTS.
Erythroblasts are seen in severe forms of anaemia . They are seen in bone-tumour and myeloid leukaemia.
If the cell are larger than normal they are called megaloblast and if smaller microblasts. Mucleated SRBCS of normal size
are called normoblasts.
E. VARIATION IN STAINING REACTION.
1. Plychromasia or Basaphilia: Cells having bluish tint.
2. Punctate basophilia.Where the cells are studied with purple stained granules. Seen in chronic lead poisoning
and anaemia of toxic origin.
3. Reticulated cells. These are young cells which have recently lost theirnuclei and in which a definite reticulum
is apparent.
PATHOLOGICALVARIATION OF LEUCOCYTES.
A. Variation in numbers.
Leucocytosis: Increase in number of leucocytesgenerally neutrophils seen in suppurative conditions and in malignant
growing conditions.
Lymphocytosis: Increase in number of lymphocytes, this is seen in chronic wasting diseases, rickets and following the
injection of tuberculin.
Eosinophilia: Increased number of eosinophils. It occursin chronic skin disease, some formsof sensitizations.
Leucopenia: Decreased number of leucocytes. Seen in certain virus infections, anemia, starvation and malnutrition.
B. VARIATION IN TYPE.
1. Myeloblast: This is the precursor of all granular leucocytes. Presence in circulation indicates some
interference with the function of formative bone-marrow.
2. Myelocytes: seen in myloid leukaemia and rarely in acute cases of “Anaemia”.
3. Lymphoblast: Seen as precursorof lymphocyte and is seen in circulation in lymphatic leukaemia.
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ANAEMIA: Is a deficiency of erythrocytes or of haemoglobin or of both.While the most frequent forms of anaemia are
characterized by the deficiency of erythrocytes but there can be an anaemia characterized by too little haemoglobin in
each cell, the numberof cells being normal.
Since in anaemia, the erythrocytes may have the normal size or may be enlarged or diminished in size. In case the
size is normal it is temed as normocytic and when the red cells are smaller in size it is designated as microcytic anaemia.
The anaemia is called ashypochromic if the quantity of haemoglobin in each cell is lese than normal and colour is
pale, the oxygen capacity is reduced even of the red cell count is normal.A normochrome cell contains a saturated
solution of haemoglobin from the stand point of causation,the anaemia may be classified as follows.
TYPES OF ANAEMIA.
1. Haemorrhagic anaemia.
2. Haemolytic anaemia.
3. Aplastic anaemia.
4. Deficiency anaemia.
1. HAEMORRHAGIC ANAEMIA.
Results from severe haemorrhage.Chronic haemorrhagic anaemia arisesfrom continued loss of blood or
a series of small haemorrhages e.g. Parasites Haemonchus contortus of sheep and Stranglesof the horse Poikylocytosts
distinet in this form of anaemia.
2. HAEMOLYTIC ANAEMIA.
Results from excessive distruction of the circulating erythrocytes,occurring within the blood stream. The
blood picture shows nucleated red cells, and reticulocytes. The causesare as under.
1. Piroplasmosis.
2. Anaplasmosis.
3. Virus of equine infections anaemia.
4. Trypanosomiasis, acute bacterial infectionsincluding those due to Cl. Haemolyticum and Cl. Velchii.Certain
Aemicals, poisions have a similar effectsincluding. Pot and sod chlorides,lead usually is a chronic poioning.
3. DIFICIENCY ANAEMIA.
(a) Due to defective absorption and assimilation of factors necessary for haemoglobin formation chiefly iron
and other substancessuch as Cu, Co, manganes etc.
(b) Due to defective production or assimilation of anti-anaemic factor.
The formation of red corpusclesin the bone marrowdepends on several specific and nonspecific factors. The
specific factorsare iron and erythrocyte maturing or antianaemic factorpresent in liver and stomach.It is said that most
animals secrete in normal gastric juice an intrinsic enzyme factorsand this interacts with extrinsic substances present in
certain food and formsas haemopoietic or antianaemic factor which is stored in the liver from here this factor conveyed
when required, to the bone-marrow, where it is necessary for the maturation of the red blood-corpuseles before they are
released into the blood stream.
Aplastic anaemia, in this form of anaemia the haemopoitic tissue of the bone marrow are infected in such a away
that their ability to produce erythrocytes is impaired or destroyed.The causes of this type of anaemia are either toxic
radiation or toxic substance brought to the marrow cells in the circulating blood.Irradiation whether rays, X. Rays,radium
or radio active isotopes,is highly destructive of the hemopoietic tissue and this action is the chief reason that any butvery
small dosage are lethal.
SIGNIFICIANCES AND EFFECTS OF ANAEMIA.
Anoxia of the tissuesis the most important product of anaemia that lead to fatty degeneration of the myocardium
and other susceptible organs and even Necrosis supervene.
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In haemolytic anaemia the spleen contains Phagocytised haemosidrium. When oedema accompanies anaemia it is
due to increased permeability.
CHANGES IN ANAEMIA.
The red carpusels which may be reduced in number are pale in colour due to deficiency of haemoglobin,
Anisocytosis like Leucocytosis,polychromia and nucleated from are sometimes seen. The mucus membranes r eveal
haemorrhagesand tissues are often oedematous.
The organs are pale but the lymphatic glands and lymoid tissues show no changes. When there is great cell
destruction haemosiderous becomes evident in some organs.
PERNICIOUS ANAEMIA.
This anaemia in man appears to result from the absence of the anti-anaemic factor. Neither thiscondition has been
recognized in animal nor it has been produced experimentally but it is possible that absence of this factor may play a part
in some anaemia in animals.
LEUKAEMIA.
Leukaemia is a disease of the leucocyte forming tissue in which hyperplastic changes occur, these being
associated with an increased in the number of leucocytes, many of them immature in the circulation. The causes of the
condition is unknown but it is regarded by some as form of neoplasia. There are two forms of leukaemia.
a. Myeloid leukaemia; or mylogenous leukaemia.
b. Lymphatic leukaemia; or lymphogenousleukaemia.
MYELOID LEUKAEMIA.
In myeloid leukaemia the myeloid tissues are principally involved and cell of the myeloid series predominate in
the blood picture. A fairly large number of neutrophils and neutrophil myelocytesare seen in the marked blood film taken
from such a case, although there may be increased in the number of other forms of leucocytes also.
The fatty bone marrow is replaced by hyperplasia of myeloid cells,giving it a pinkish gray colour. The spleen is
enlarged but there is no change in the lymphtic glands. The internal organs often show fatty changes and small
haemorrhages are frequently present.
LYMPHATIC LEUKAEMIA.
It occurs in lymphoid tissue of lymphocytic and their precursorin blood film in which lymphocytes may number
more than 95 percent of the cells present. Lymphoblasts may become more numerousin very acute con dition, the red
corpuscles sometimes show evidence of anaemia. In lymphatic leukaemia the most preominant changes are in the
lymphatic glands,these being invariably enlarged.The spleen is also enlarged. Changes are also present in the bone -
marrow, the normal cells being replaced by lymphocytes. Lymphocytic infiltration is often in the liver,kidney and other
organs. The organs may be uniformally enlarged and palerthan normal or well defined tumour like swellings may be
present. Internal organs may show degenerative changesof fatty nature and petechial haemorrhagesmay be present on the
serious membranes.
SPLENITIS.
Inflammatory swelling of the spleen is seen in anthrax,anaplasmosis of cattle and acute infectious anaemia of
horses.
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Macroscopically the spleen is enlarged and soft and its cut surface is dark red black,and the parenchyma is so soft
that it may flow.
MICROSCOPICALLY.
There is marked hyperaemia, with collection of neutraphils, lympocytes, plasma cells and swelling is
finally disintegration of the reticulum.
CHRONIC SPLENITIS.
May be characterized, either by induration (increase in the reticulum)or by cellular hyperplasia (increase in the
parenchyma). The interstitial form of chronic splenitis is rarely seen in animals. Chronic splenitis in which pulp is
increased is also uncommon. Specific infectious diseases,which supply good example of it are piroplasmosis of dogs
infections anaemia of horses. In both diseases spleen is enlarged. In equine infectious anaemia the splenomegaly is due to
increase in the size of the splenic nodules. The hyperplasia of the nodules is interpreted to be an attempt to increase
antibody production.
SUPPURATIVE SPLENITIS MAYARISE DUE TO.
1. As a result of septic emboli originating from mitral endocarditis or a result of metastatic lesion of pyogenic
bacteria from more distant localized suppurative processes. In horses it occursin connection with strangles.
2. By penetration of infected sharp foreign bodies from the reticulum in cattle.