The document discusses pleural effusion, which is an excess collection of fluid in the pleural space. It classifies pleural effusions as transudates or exudates and describes differences in their physical appearance, microscopy, and biochemical characteristics. It also discusses different types of pleural effusions including dry/plastic pleurisy, serofibrinous pleurisy, and purulent pleurisy/empyema. For each type, it describes their causes, clinical features, pathology, treatment and stages in the case of empyema.
The document discusses pleural effusions, including:
1. The anatomy and mechanisms of pleural fluid turnover, with fluid entering and leaving the pleural space through membranes.
2. The etiology and pathogenesis of pleural effusions, which can result from elevated pressures, inflammation, or decreased oncotic pressure.
3. Approaches to evaluating patients with pleural effusions, including diagnostic thoracentesis to classify effusions and determine the disease cause.
This document discusses the approach to nephrotic syndrome. It describes the case of a 15-year old male patient presenting with swelling of the face and limbs and decreased urine output. Examinations and investigations revealed nephrotic syndrome. A renal biopsy showed membranoproliferative glomerulonephritis. The document then discusses nephrotic syndrome including definitions, classifications of primary and secondary causes, diagnostic workup including renal biopsy, complications of renal biopsy, and treatment approach.
The apex beat is the point of maximum impulse of the heart, normally felt on the left side of the chest. It is caused by the contraction of the left ventricle. Abnormalities can occur in the character, position, or presence of the apex beat. A hyperdynamic apex beat indicates volume overload of the left ventricle from conditions like mitral regurgitation. A heaving apex beat suggests pressure overload from aortic stenosis or hypertension. Other abnormalities include a tapping apex in mitral stenosis, or a double or absent apex beat from various cardiac and pulmonary conditions.
This document outlines an approach to evaluating and diagnosing dyspnea. It begins by defining dyspnea and noting its high prevalence. Types of dyspnea like orthopnea and paroxysmal nocturnal dyspnea are described. The diagnostic approach involves obtaining a detailed history regarding onset, duration, patterns and associated symptoms. A physical exam assesses respiratory effort, oxygenation, and signs of heart failure. Initial tests may include EKG, chest x-ray, and bloodwork. Further tests are guided by initial findings and may include echocardiogram, pulmonary function tests, CT, or arterial blood gas. Treatment focuses on the underlying cause identified through diagnosis.
This document describes a case of a 25-year-old male smoker who presented with coughing up blood for 3 days. On examination, his vitals were normal and physical exam was unremarkable aside from some bloody sputum. Differential diagnoses included infections like tuberculosis or pneumonia, autoimmune diseases, pulmonary vascular issues or cancer. Key evaluations included bloodwork, chest x-ray, CT scan and bronchoscopy. The document also provides overview information on hemoptysis causes, classifications, evaluations and treatments.
Chronic leukemias have an insidious onset and are usually less aggressive than acute leukemias. The two main types are chronic myeloid leukemia, characterized by the Philadelphia chromosome, and chronic lymphocytic leukemia, which mainly affects B cells. These diseases involve increased numbers of mature but dysfunctional white blood cells and are diagnosed based on blood counts, bone marrow examination, and identification of genetic abnormalities.
Leukaemia is a progressive neoplastic disease characterized by unregulated proliferation of immature blood cells. The main types are acute and chronic leukaemia. Acute leukaemia has a rapid onset and is more aggressive, while chronic leukaemia has a gradual onset and is less aggressive. Leukaemia is further classified as lymphoid or myeloid depending on the origin of the leukemic stem cell clone. Acute myeloid leukaemia is composed of immature myeloid cells and causes bone marrow failure, while acute lymphoid leukaemia is composed of immature lymphoid cells and most commonly affects children.
This case involves a 12-year-old female presenting with weakness, lethargy, and inability to work for 2 months. She had her first menstrual period last month that lasted 20 days and is currently having heavy bleeding on her 15th day of this period. On examination, she has pallor and a heart murmur. Laboratory tests show microcytic anemia. The presentation is suggestive of iron deficiency anemia likely due to heavy menstrual bleeding given her family history of menorrhagia. Further workup is needed to confirm the etiology and guide treatment.
The document discusses pleural effusions, including:
1. The anatomy and mechanisms of pleural fluid turnover, with fluid entering and leaving the pleural space through membranes.
2. The etiology and pathogenesis of pleural effusions, which can result from elevated pressures, inflammation, or decreased oncotic pressure.
3. Approaches to evaluating patients with pleural effusions, including diagnostic thoracentesis to classify effusions and determine the disease cause.
This document discusses the approach to nephrotic syndrome. It describes the case of a 15-year old male patient presenting with swelling of the face and limbs and decreased urine output. Examinations and investigations revealed nephrotic syndrome. A renal biopsy showed membranoproliferative glomerulonephritis. The document then discusses nephrotic syndrome including definitions, classifications of primary and secondary causes, diagnostic workup including renal biopsy, complications of renal biopsy, and treatment approach.
The apex beat is the point of maximum impulse of the heart, normally felt on the left side of the chest. It is caused by the contraction of the left ventricle. Abnormalities can occur in the character, position, or presence of the apex beat. A hyperdynamic apex beat indicates volume overload of the left ventricle from conditions like mitral regurgitation. A heaving apex beat suggests pressure overload from aortic stenosis or hypertension. Other abnormalities include a tapping apex in mitral stenosis, or a double or absent apex beat from various cardiac and pulmonary conditions.
This document outlines an approach to evaluating and diagnosing dyspnea. It begins by defining dyspnea and noting its high prevalence. Types of dyspnea like orthopnea and paroxysmal nocturnal dyspnea are described. The diagnostic approach involves obtaining a detailed history regarding onset, duration, patterns and associated symptoms. A physical exam assesses respiratory effort, oxygenation, and signs of heart failure. Initial tests may include EKG, chest x-ray, and bloodwork. Further tests are guided by initial findings and may include echocardiogram, pulmonary function tests, CT, or arterial blood gas. Treatment focuses on the underlying cause identified through diagnosis.
This document describes a case of a 25-year-old male smoker who presented with coughing up blood for 3 days. On examination, his vitals were normal and physical exam was unremarkable aside from some bloody sputum. Differential diagnoses included infections like tuberculosis or pneumonia, autoimmune diseases, pulmonary vascular issues or cancer. Key evaluations included bloodwork, chest x-ray, CT scan and bronchoscopy. The document also provides overview information on hemoptysis causes, classifications, evaluations and treatments.
Chronic leukemias have an insidious onset and are usually less aggressive than acute leukemias. The two main types are chronic myeloid leukemia, characterized by the Philadelphia chromosome, and chronic lymphocytic leukemia, which mainly affects B cells. These diseases involve increased numbers of mature but dysfunctional white blood cells and are diagnosed based on blood counts, bone marrow examination, and identification of genetic abnormalities.
Leukaemia is a progressive neoplastic disease characterized by unregulated proliferation of immature blood cells. The main types are acute and chronic leukaemia. Acute leukaemia has a rapid onset and is more aggressive, while chronic leukaemia has a gradual onset and is less aggressive. Leukaemia is further classified as lymphoid or myeloid depending on the origin of the leukemic stem cell clone. Acute myeloid leukaemia is composed of immature myeloid cells and causes bone marrow failure, while acute lymphoid leukaemia is composed of immature lymphoid cells and most commonly affects children.
This case involves a 12-year-old female presenting with weakness, lethargy, and inability to work for 2 months. She had her first menstrual period last month that lasted 20 days and is currently having heavy bleeding on her 15th day of this period. On examination, she has pallor and a heart murmur. Laboratory tests show microcytic anemia. The presentation is suggestive of iron deficiency anemia likely due to heavy menstrual bleeding given her family history of menorrhagia. Further workup is needed to confirm the etiology and guide treatment.
1. The document discusses the differentiation between myeloid leukemoid reaction, chronic myeloid leukemia (CML), and chronic neutrophilic leukemia (CNL).
2. Key differences include peripheral smear findings, bone marrow aspirate/biopsy pictures, LAP scores, cytogenetics, and immunophenotyping results.
3. A leukemoid reaction is secondary to an underlying cause and shows features of that cause, while CML and CNL are myeloproliferative neoplasms with distinct clinical features, lab findings, and disease progression.
1. Diseases of the pleura include accumulation of excess fluid in the pleural space (pleural effusion) due to inflammatory processes or defects in lymphatic absorption. Pleural effusions can be transudative or exudative depending on their protein content and other characteristics.
2. Pleural effusions are classified as dry, plastic, serofibrinous, or purulent depending on the associated symptoms and fluid characteristics. Purulent pleurisy or empyema involves infection and pus in the pleural space which can lead to complications if not properly treated.
3. Key signs of pleural effusion include dullness on percussion of the chest, decreased or absent breath sounds, and
Hereditary spherocytosis is an inherited condition related to RBC destruction. its diagnosis is require to differentiate immune hemolytic anemia and G-6-P-D deficiency anemia
Café-au-lait spots, neurofibromas, Lisch nodules, and axillary freckling are characteristic of neurofibromatosis type 1. Plexiform neurofibromas appear as subcutaneous elastic tumors over the face, scalp, neck and chest. Adenoma sebaceum presents as numerous discrete smooth papules over the butterfly area of the face and nasolabial folds. Shagreen patches are irregular cobblestone-like plaques in the lumbosacral area, a characteristic of tuberous sclerosis. Ocular and cutaneous telangiectasias occur in Ataxia telangiectasia, appearing as dilated blood vessels over
Parapneumonic effusion and PneumothoraxPratap Tiwari
This document discusses parapneumonic effusion and pneumothorax. It defines parapneumonic effusion as a pleural effusion caused by pneumonia or lung abscess. It describes the three stages of parapneumonic effusion: exudative, fibropurulent, and fibrotic. Pneumothorax is defined as air in the pleural space. Primary spontaneous pneumothorax occurs without lung disease, while secondary pneumothorax is associated with lung conditions like COPD. Risk factors, signs and symptoms, and management strategies are outlined for both conditions.
- Places fingers over the lower ribs on the left side
- Asks patient to take a deep breath
You:
- Percuss over the assistant's fingers
- Dullness indicates splenic enlargement crossing
the midline
Positive Nixon's sign suggests splenomegaly.
This document discusses chronic leukemias and myeloproliferative disorders including chronic myeloid leukemia (CML) and myelofibrosis. CML is distinguished from other myeloproliferative disorders by the presence of the Philadelphia chromosome and BCR-ABL fusion gene. CML is characterized by leukocytosis, thrombocytosis, and anemia. It progresses through chronic, accelerated, and blast phases defined by increasing blast counts and symptoms. The massive spleen seen in CML is indicative of the underlying myeloproliferative process.
Causes of Splenomegaly By Dr Bashir Ahmed Dar Chinkipora Sopore Kashmir Assoc...Prof Dr Bashir Ahmed Dar
Dr.Bashir Ahmed Dar Chinkipora Sopore Kashmir India,Associate Prof of medicine presently working in malaysia is a keen teacher, educator and takes pride in his clinical and research accomplishments. His interests include publishing articles related to health issues.Email drbashir123@gmail.com
This document provides an overview of hemolytic anemia in children. It defines hemolytic anemia as anemia resulting from increased red blood cell destruction. The document describes the different types of hemolytic anemia including hereditary, immune, and non-immune causes. It outlines the pathophysiology, clinical features, diagnostic approach and management of common forms of hemolytic anemia in children such as hereditary spherocytosis, thalassemia, sickle cell anemia, and G6PD deficiency. Investigations for diagnosis include blood counts, peripheral smear, reticulocyte count, hemoglobin electrophoresis and enzyme or genetic testing depending on etiology.
This document discusses spherocytes, which are red blood cells that have lost their biconcavity and appear as densely stained spheres. Spherocytes can be caused by membrane defects or immune-mediated lysis of the membrane. The most common membrane defect is hereditary spherocytosis, which is caused by a genetic defect in membrane proteins. Immune-mediated hemolytic anemias that can cause spherocytosis include warm autoimmune hemolytic anemia and cold agglutinin disease. Laboratory tests shown to identify spherocytes include a peripheral smear, osmotic fragility testing, and Coombs testing to distinguish immune from non-immune causes.
Pleural effusion is an abnormal accumulation of fluid in the pleural space between the lungs and chest wall. It can be caused by conditions that alter fluid pressure or permeability of the pleura. A pleural effusion is classified based on its location, mechanism, and fluid characteristics. Evaluation involves physical exam, chest x-ray, ultrasound, and thoracentesis to analyze the fluid. Management depends on treating the underlying cause, with antibiotics for infections, diuretics for heart failure, or drainage procedures for large or infected effusions.
This document discusses fever and rash, including definitions, diagnostic approaches, and specific conditions that can present with fever and rash. It defines fever and discusses methods of taking temperature. It describes patterns of fever such as continuous, remittent, and intermittent fever. It then discusses specific conditions that can present with fever and a rash, categorizing them based on the type of rash: centrally distributed maculopapular eruptions (such as measles, rubella, epidemic typhus), nodular eruptions (such as erythema nodosum), and purpuric eruptions (such as meningococcal disease). It emphasizes taking a thorough history, physical exam, and conducting appropriate laboratory
Dr. Renesha Islam and Dr. Farzana AlamMou presented two cases of pediatric patients with bleeding and low platelet counts. The first case was a 5-year-old boy, Yasin, with petechiae and bleeding who had a platelet count of 35,000/cmm. The second case was a 13-year-old girl, Asma, with ecchymosis and menorrhagia who had a platelet count of 20,000/cmm. The doctors then discussed immune thrombocytopenia, including its history, pathophysiology involving autoantibodies and impaired platelet production, classification as acute or chronic, and clinical manifestations ranging from no symptoms to severe bleeding.
This document discusses shortness of breath (dyspnoea), including its definition, grading scales, common causes, history taking, physical examination findings, differential diagnosis, initial investigations, and basic management. It defines dyspnoea as an uncomfortable sensation of breathing that feels inappropriate or disproportionate. Grading scales like the MRC and NYHA are described. Common causes involve the cardiovascular, respiratory, and other body systems. A thorough history and physical exam are important for determining the underlying etiology. Initial tests may include pulse oximetry, peak flow measurement, chest x-ray, ECG, and lung biopsy. Treatment is aimed at addressing the specific cause, and may involve pharmacological therapies, oxygen supplementation, or non-
This document discusses the World Health Organization (WHO) classification of lupus nephritis based on histopathological findings. It describes the six WHO classes of lupus nephritis, including minimal mesangial lupus nephritis (Class I), mesangial proliferative lupus nephritis (Class II), focal proliferative lupus nephritis (Class III), diffuse proliferative lupus nephritis (Class IV), membranous lupus nephritis (Class V), and advanced sclerosing lupus nephritis (Class VI). Each class is defined by its characteristic immunopathological staining patterns, light microscopy appearance, and percentage of glomer
The document discusses an integrated approach to diagnosing splenomegaly. It begins by defining splenomegaly and examining the spleen. A step-wise approach is then outlined involving taking a thorough history, conducting a physical exam, ordering lab and imaging tests, and performing specialized testing to investigate for possible etiologies of splenomegaly such as infection, infiltration, congestion, and hyperplasia. The goal is to determine the underlying cause and provide appropriate treatment.
Approach to child with generalized edemaAhmed Bahamid
- A 19-month-old boy presented with generalized body swelling that began 3 months prior and gradually progressed. On examination, he had generalized edema, hepatomegaly, ascites, pallor, and mild jaundice.
- Differential diagnoses included cardiac causes like congestive heart failure, restrictive cardiomyopathy, and constrictive pericarditis as well as hepatic causes such as viral hepatitis, metabolic diseases, or malignancy.
- Imaging showed markedly enlarged liver with dilated hepatic veins and IVC, ascites, pleural effusion, and pericardial effusion. This was consistent with restrictive cardiomyopathy and congestive heart failure.
Lecture 28. common repratory pathological condirtion part 3ayeayetun08
Simple coal worker's pneumoconiosis is caused by inhalation of carbon particles and presents as small black macules near respiratory bronchioles. Progressive massive fibrosis develops from coalescence of coal nodules and scarring, forming large intensely blackened lesions over years. Bronchiectasis is characterized by permanent dilation of bronchi and bronchioles caused by repeated cycles of obstruction and infection, clinically presenting as chronic cough and copious purulent sputum. Pneumoconiosis describes occupational lung diseases from mineral dust inhalation like silicosis, with pathogenesis involving particle-induced macrophage activation and pulmonary fibrosis.
This document provides guidance on taking a chest history from patients. It discusses the importance of history taking in making an accurate diagnosis. The general approach to history taking is described, including introducing oneself, treating the patient with respect, listening, and asking clear questions. Specific aspects of the chest history are then covered in detail, including personal history, chief complaint, history of present illness, past history, and family history. Cardinal and minor chest symptoms are defined. Case examples are presented to demonstrate applying the history to form a provisional diagnosis and plan appropriate investigations.
BODY FLUIDS EXAMINATION.pptx FOR MBBS AND PGNehaBanseria1
Eleven body fluids we couldn't live without
Bile. Bile is a brown to dark green fluid that is produced by the liver, stored in the gallbladder (a synonym for bile is gall), and released into the intestines when we eat. ...
Blood. Give a little. ...
Menstrual fluid. ...
Mucus. ...
Pus. ...
Semen. ...
Saliva. ...
Sweat.
More items...•3 Nov 2015
Search Anything...
Browse
Create
Presentation Creator
Pro
Upload
analysis of body cavity fluids
1 / 34
Analysis of Body Cavity Fluids
Sep 08, 2014
• 1.12k likes • 3.37k Views
Analysis of Body Cavity Fluids. Lab 8. Indications and Sampling. Indications: - Identifies the type of fluid present: transudate, exudate, neoplastic or other effusion and may identify the cause of fluid accumulation Sampling: - Sterile preparation of site
cells
cell type
nucleated cells
mesothelial cells
cute septic inflammation
small mixed nucleated cells
teige
teige
+ Follow
Download Presentation
Analysis of Body Cavity Fluids
An Image/Link below is provided (as is) to download presentation
Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author.
Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server.
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Presentation Transcript
Analysis of Body Cavity Fluids Lab 8
Indications and Sampling Indications: - Identifies the type of fluid present: transudate, exudate, neoplastic or other effusion and may identify the cause of fluid accumulation Sampling: - Sterile preparation of site - Use a fine needle (21- 23 G) - Avoid movement or causing pain during sampling - Split sample into EDTA & plain sterile tubes - Process as soon as possible - Monitor the animal
Tests Applied Four basic tests are applied: • Appearance of fluid • Protein content • Nucleated cell count (NCC) • Examination of a direct and/or sediment smear to identify cell type Additional tests such as biochemistry may be used in certain clinical situations, e.g. urea or creatinine, if uroabdomen (from bladder rupture) is suspected.
Specimen Management for Smears - Mix sample well - Make a direct smear - Centrifuge & smear the deposit (sediment smears) - Air-dry rapidly & stain Special centrifuges (cytocentrifuges) yield better smears A standard centrifuge may be used at a slow speed for a short period (<1000 rpm)
Procedure to get a smear “Wedge” method Flat-slide method A drop of the fluid is placed on a cleaned glass slide A smear can be made by the “wedge” method used for making blood smears Alternatively, a 2nd slide may be superimposed on the first, and the two are drawn smoothly apart to make two thin smears.
Examination of sediment smears • Blood stains e.g. Diff-Quik or Giemsa usually used • The smear is scanned at low power, to locate cells and cell clusters • NORMAL FINDINGS: N
This document provides normal ranges for many common medical lab tests in both the Indonesian and English systems of measurement. It includes normal values for blood counts like hemoglobin, white blood cell count, and platelet count. It also lists normal ranges for blood chemistries including glucose, BUN, creatinine, liver enzymes, lipids, and more. Normal ranges are provided for urine analysis tests and immunoserology tests for pregnancy. Microbiology tests like sputum, malaria, and gram stain analyses are also listed.
1. The document discusses the differentiation between myeloid leukemoid reaction, chronic myeloid leukemia (CML), and chronic neutrophilic leukemia (CNL).
2. Key differences include peripheral smear findings, bone marrow aspirate/biopsy pictures, LAP scores, cytogenetics, and immunophenotyping results.
3. A leukemoid reaction is secondary to an underlying cause and shows features of that cause, while CML and CNL are myeloproliferative neoplasms with distinct clinical features, lab findings, and disease progression.
1. Diseases of the pleura include accumulation of excess fluid in the pleural space (pleural effusion) due to inflammatory processes or defects in lymphatic absorption. Pleural effusions can be transudative or exudative depending on their protein content and other characteristics.
2. Pleural effusions are classified as dry, plastic, serofibrinous, or purulent depending on the associated symptoms and fluid characteristics. Purulent pleurisy or empyema involves infection and pus in the pleural space which can lead to complications if not properly treated.
3. Key signs of pleural effusion include dullness on percussion of the chest, decreased or absent breath sounds, and
Hereditary spherocytosis is an inherited condition related to RBC destruction. its diagnosis is require to differentiate immune hemolytic anemia and G-6-P-D deficiency anemia
Café-au-lait spots, neurofibromas, Lisch nodules, and axillary freckling are characteristic of neurofibromatosis type 1. Plexiform neurofibromas appear as subcutaneous elastic tumors over the face, scalp, neck and chest. Adenoma sebaceum presents as numerous discrete smooth papules over the butterfly area of the face and nasolabial folds. Shagreen patches are irregular cobblestone-like plaques in the lumbosacral area, a characteristic of tuberous sclerosis. Ocular and cutaneous telangiectasias occur in Ataxia telangiectasia, appearing as dilated blood vessels over
Parapneumonic effusion and PneumothoraxPratap Tiwari
This document discusses parapneumonic effusion and pneumothorax. It defines parapneumonic effusion as a pleural effusion caused by pneumonia or lung abscess. It describes the three stages of parapneumonic effusion: exudative, fibropurulent, and fibrotic. Pneumothorax is defined as air in the pleural space. Primary spontaneous pneumothorax occurs without lung disease, while secondary pneumothorax is associated with lung conditions like COPD. Risk factors, signs and symptoms, and management strategies are outlined for both conditions.
- Places fingers over the lower ribs on the left side
- Asks patient to take a deep breath
You:
- Percuss over the assistant's fingers
- Dullness indicates splenic enlargement crossing
the midline
Positive Nixon's sign suggests splenomegaly.
This document discusses chronic leukemias and myeloproliferative disorders including chronic myeloid leukemia (CML) and myelofibrosis. CML is distinguished from other myeloproliferative disorders by the presence of the Philadelphia chromosome and BCR-ABL fusion gene. CML is characterized by leukocytosis, thrombocytosis, and anemia. It progresses through chronic, accelerated, and blast phases defined by increasing blast counts and symptoms. The massive spleen seen in CML is indicative of the underlying myeloproliferative process.
Causes of Splenomegaly By Dr Bashir Ahmed Dar Chinkipora Sopore Kashmir Assoc...Prof Dr Bashir Ahmed Dar
Dr.Bashir Ahmed Dar Chinkipora Sopore Kashmir India,Associate Prof of medicine presently working in malaysia is a keen teacher, educator and takes pride in his clinical and research accomplishments. His interests include publishing articles related to health issues.Email drbashir123@gmail.com
This document provides an overview of hemolytic anemia in children. It defines hemolytic anemia as anemia resulting from increased red blood cell destruction. The document describes the different types of hemolytic anemia including hereditary, immune, and non-immune causes. It outlines the pathophysiology, clinical features, diagnostic approach and management of common forms of hemolytic anemia in children such as hereditary spherocytosis, thalassemia, sickle cell anemia, and G6PD deficiency. Investigations for diagnosis include blood counts, peripheral smear, reticulocyte count, hemoglobin electrophoresis and enzyme or genetic testing depending on etiology.
This document discusses spherocytes, which are red blood cells that have lost their biconcavity and appear as densely stained spheres. Spherocytes can be caused by membrane defects or immune-mediated lysis of the membrane. The most common membrane defect is hereditary spherocytosis, which is caused by a genetic defect in membrane proteins. Immune-mediated hemolytic anemias that can cause spherocytosis include warm autoimmune hemolytic anemia and cold agglutinin disease. Laboratory tests shown to identify spherocytes include a peripheral smear, osmotic fragility testing, and Coombs testing to distinguish immune from non-immune causes.
Pleural effusion is an abnormal accumulation of fluid in the pleural space between the lungs and chest wall. It can be caused by conditions that alter fluid pressure or permeability of the pleura. A pleural effusion is classified based on its location, mechanism, and fluid characteristics. Evaluation involves physical exam, chest x-ray, ultrasound, and thoracentesis to analyze the fluid. Management depends on treating the underlying cause, with antibiotics for infections, diuretics for heart failure, or drainage procedures for large or infected effusions.
This document discusses fever and rash, including definitions, diagnostic approaches, and specific conditions that can present with fever and rash. It defines fever and discusses methods of taking temperature. It describes patterns of fever such as continuous, remittent, and intermittent fever. It then discusses specific conditions that can present with fever and a rash, categorizing them based on the type of rash: centrally distributed maculopapular eruptions (such as measles, rubella, epidemic typhus), nodular eruptions (such as erythema nodosum), and purpuric eruptions (such as meningococcal disease). It emphasizes taking a thorough history, physical exam, and conducting appropriate laboratory
Dr. Renesha Islam and Dr. Farzana AlamMou presented two cases of pediatric patients with bleeding and low platelet counts. The first case was a 5-year-old boy, Yasin, with petechiae and bleeding who had a platelet count of 35,000/cmm. The second case was a 13-year-old girl, Asma, with ecchymosis and menorrhagia who had a platelet count of 20,000/cmm. The doctors then discussed immune thrombocytopenia, including its history, pathophysiology involving autoantibodies and impaired platelet production, classification as acute or chronic, and clinical manifestations ranging from no symptoms to severe bleeding.
This document discusses shortness of breath (dyspnoea), including its definition, grading scales, common causes, history taking, physical examination findings, differential diagnosis, initial investigations, and basic management. It defines dyspnoea as an uncomfortable sensation of breathing that feels inappropriate or disproportionate. Grading scales like the MRC and NYHA are described. Common causes involve the cardiovascular, respiratory, and other body systems. A thorough history and physical exam are important for determining the underlying etiology. Initial tests may include pulse oximetry, peak flow measurement, chest x-ray, ECG, and lung biopsy. Treatment is aimed at addressing the specific cause, and may involve pharmacological therapies, oxygen supplementation, or non-
This document discusses the World Health Organization (WHO) classification of lupus nephritis based on histopathological findings. It describes the six WHO classes of lupus nephritis, including minimal mesangial lupus nephritis (Class I), mesangial proliferative lupus nephritis (Class II), focal proliferative lupus nephritis (Class III), diffuse proliferative lupus nephritis (Class IV), membranous lupus nephritis (Class V), and advanced sclerosing lupus nephritis (Class VI). Each class is defined by its characteristic immunopathological staining patterns, light microscopy appearance, and percentage of glomer
The document discusses an integrated approach to diagnosing splenomegaly. It begins by defining splenomegaly and examining the spleen. A step-wise approach is then outlined involving taking a thorough history, conducting a physical exam, ordering lab and imaging tests, and performing specialized testing to investigate for possible etiologies of splenomegaly such as infection, infiltration, congestion, and hyperplasia. The goal is to determine the underlying cause and provide appropriate treatment.
Approach to child with generalized edemaAhmed Bahamid
- A 19-month-old boy presented with generalized body swelling that began 3 months prior and gradually progressed. On examination, he had generalized edema, hepatomegaly, ascites, pallor, and mild jaundice.
- Differential diagnoses included cardiac causes like congestive heart failure, restrictive cardiomyopathy, and constrictive pericarditis as well as hepatic causes such as viral hepatitis, metabolic diseases, or malignancy.
- Imaging showed markedly enlarged liver with dilated hepatic veins and IVC, ascites, pleural effusion, and pericardial effusion. This was consistent with restrictive cardiomyopathy and congestive heart failure.
Lecture 28. common repratory pathological condirtion part 3ayeayetun08
Simple coal worker's pneumoconiosis is caused by inhalation of carbon particles and presents as small black macules near respiratory bronchioles. Progressive massive fibrosis develops from coalescence of coal nodules and scarring, forming large intensely blackened lesions over years. Bronchiectasis is characterized by permanent dilation of bronchi and bronchioles caused by repeated cycles of obstruction and infection, clinically presenting as chronic cough and copious purulent sputum. Pneumoconiosis describes occupational lung diseases from mineral dust inhalation like silicosis, with pathogenesis involving particle-induced macrophage activation and pulmonary fibrosis.
This document provides guidance on taking a chest history from patients. It discusses the importance of history taking in making an accurate diagnosis. The general approach to history taking is described, including introducing oneself, treating the patient with respect, listening, and asking clear questions. Specific aspects of the chest history are then covered in detail, including personal history, chief complaint, history of present illness, past history, and family history. Cardinal and minor chest symptoms are defined. Case examples are presented to demonstrate applying the history to form a provisional diagnosis and plan appropriate investigations.
BODY FLUIDS EXAMINATION.pptx FOR MBBS AND PGNehaBanseria1
Eleven body fluids we couldn't live without
Bile. Bile is a brown to dark green fluid that is produced by the liver, stored in the gallbladder (a synonym for bile is gall), and released into the intestines when we eat. ...
Blood. Give a little. ...
Menstrual fluid. ...
Mucus. ...
Pus. ...
Semen. ...
Saliva. ...
Sweat.
More items...•3 Nov 2015
Search Anything...
Browse
Create
Presentation Creator
Pro
Upload
analysis of body cavity fluids
1 / 34
Analysis of Body Cavity Fluids
Sep 08, 2014
• 1.12k likes • 3.37k Views
Analysis of Body Cavity Fluids. Lab 8. Indications and Sampling. Indications: - Identifies the type of fluid present: transudate, exudate, neoplastic or other effusion and may identify the cause of fluid accumulation Sampling: - Sterile preparation of site
cells
cell type
nucleated cells
mesothelial cells
cute septic inflammation
small mixed nucleated cells
teige
teige
+ Follow
Download Presentation
Analysis of Body Cavity Fluids
An Image/Link below is provided (as is) to download presentation
Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author.
Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server.
E N D
Presentation Transcript
Analysis of Body Cavity Fluids Lab 8
Indications and Sampling Indications: - Identifies the type of fluid present: transudate, exudate, neoplastic or other effusion and may identify the cause of fluid accumulation Sampling: - Sterile preparation of site - Use a fine needle (21- 23 G) - Avoid movement or causing pain during sampling - Split sample into EDTA & plain sterile tubes - Process as soon as possible - Monitor the animal
Tests Applied Four basic tests are applied: • Appearance of fluid • Protein content • Nucleated cell count (NCC) • Examination of a direct and/or sediment smear to identify cell type Additional tests such as biochemistry may be used in certain clinical situations, e.g. urea or creatinine, if uroabdomen (from bladder rupture) is suspected.
Specimen Management for Smears - Mix sample well - Make a direct smear - Centrifuge & smear the deposit (sediment smears) - Air-dry rapidly & stain Special centrifuges (cytocentrifuges) yield better smears A standard centrifuge may be used at a slow speed for a short period (<1000 rpm)
Procedure to get a smear “Wedge” method Flat-slide method A drop of the fluid is placed on a cleaned glass slide A smear can be made by the “wedge” method used for making blood smears Alternatively, a 2nd slide may be superimposed on the first, and the two are drawn smoothly apart to make two thin smears.
Examination of sediment smears • Blood stains e.g. Diff-Quik or Giemsa usually used • The smear is scanned at low power, to locate cells and cell clusters • NORMAL FINDINGS: N
This document provides normal ranges for many common medical lab tests in both the Indonesian and English systems of measurement. It includes normal values for blood counts like hemoglobin, white blood cell count, and platelet count. It also lists normal ranges for blood chemistries including glucose, BUN, creatinine, liver enzymes, lipids, and more. Normal ranges are provided for urine analysis tests and immunoserology tests for pregnancy. Microbiology tests like sputum, malaria, and gram stain analyses are also listed.
This document lists the reference ranges for over 60 common medical lab tests. It provides the normal range of values considered healthy for tests such as pH, alcohol, bilirubin, calcium, cholesterol, glucose, hemoglobin, platelets, sodium, and thyroid and liver enzymes. Each test entry indicates the standard measurement unit and range that would not require medical attention. This reference guide serves as a tool for medical professionals to interpret patient test results.
This document provides reference values for normal lab results in hematology, chemistry, liver/pancreas functions, lipids, other tests, blood gases, urine analysis, cerebrospinal fluid analysis, ascitic/pleural fluid analysis, gram stains of organisms, and differential diagnoses of microcytic anemia. It includes parameters such as hemoglobin, white blood cell count, platelet count, electrolytes, kidney and liver enzymes, lipid panels, protein levels, and other biochemical measures. Reference ranges are provided for males and females where applicable.
This document provides reference values for normal lab results in hematology, chemistry, endocrinology, blood gases, urine analysis, cerebrospinal fluid analysis, ascitic/pleural fluid analysis, and microbiology. It includes normal ranges for components like hemoglobin, white blood cell count, electrolytes, liver enzymes, thyroid hormones, microorganisms, and more. Differentials are also provided for conditions like anemia subtypes and body fluid analyses.
The document discusses body fluids, cerebrospinal fluid (CSF), and distinguishing between transudates and exudates. Key points include:
- CSF is produced by the choroid plexus at a rate of 500 ml per day and acts as a cushion and lubricant for the brain. Analysis of CSF provides information about infections and CNS disorders.
- Transudates have a low protein content and occur due to decreased plasma proteins or increased venous pressure. Exudates have a high protein content and occur due to inflammation or tissue damage.
- CSF analysis involves examination of appearance, chemical properties like glucose and protein levels, cell counts, and microbiological tests to identify infections. Abnormal results can indicate conditions
The Blood: Lifeline of the Body - Exploring the Vital Fluid that Sustains LifeNursing Mastery
Blood: Lifeline of the Body - Exploring the Vital Fluid that Sustains Life
Dive into the pulsating world of blood with our immersive SlideShare presentation. From its crimson hues to its life-sustaining properties, journey through the veins and arteries to uncover the secrets of this vital fluid that courses through our bodies.
In this captivating presentation, we unravel the complexities of blood, exploring its composition, functions, and crucial role in maintaining homeostasis. Delve into the cellular components of blood – red blood cells, white blood cells, and platelets – and learn how they work in harmony to fulfill essential tasks such as oxygen transport, immune defense, and clotting.
Through stunning visuals, insightful diagrams, and engaging narratives, we shed light on the fascinating world of blood types, transfusion medicine, and the physiology of circulation. Understand how disruptions in the blood's equilibrium can lead to diseases such as anemia, leukemia, and hemophilia, and discover the innovative therapies revolutionizing the field of hematology.
Whether you're a healthcare professional, biology enthusiast, or simply curious about the fluid that sustains life, our presentation offers a comprehensive overview of blood's multifaceted nature. Join us as we navigate through the arteries and capillaries, unraveling the mysteries of this remarkable substance that serves as the lifeline of the body.
Don't miss this opportunity to deepen your understanding of blood and its profound impact on human health and well-being. Embark on a journey into the heart of this vital fluid and gain a newfound appreciation for its indispensable role in sustaining life.
This document provides information about microscopic examination of urine sediments. It describes how to prepare and examine urine samples under a microscope. Key points include:
- Centrifuging a urine sample to concentrate the sediment, then examining a drop under the microscope using both low and high power fields.
- Common elements found in urine sediments include red and white blood cells, epithelial cells, casts, crystals, bacteria, yeast, parasites, mucus, fat and other elements.
- Additional staining techniques can aid in identification, such as using Sternheimer-Malbin to identify white blood cells and epithelial cells.
- Findings should be reported semi-quantitatively as rare, few, moderate or many.
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Blood is a connective tissue composed of plasma and cellular elements. Plasma is 55% of blood and contains water, proteins, nutrients, gases, and electrolytes. It transports these throughout the body. The cellular elements are red blood cells, white blood cells, and platelets. Red blood cells contain hemoglobin and transport oxygen and carbon dioxide. White blood cells help fight infection in different ways. Platelets help the blood clot and prevent bleeding. The study of blood is called hematology.
This document discusses the importance of urine testing in clinical laboratories. It describes how urine is produced in the kidneys and excreted from the body. Urine formation occurs through nephrons, which filter blood in the glomerulus and remove waste through tubules. Urine composition and properties can indicate various medical conditions like urinary tract infections or metabolic disorders. Clinical labs use reagent strips and confirmation tests to detect proteins, blood, glucose, and other substances in urine samples in order to diagnose illnesses.
This document provides information and instructions for collecting urine samples and performing a urinalysis. It discusses obtaining first morning voids, clean-catch samples, and timed urine collections. The types of urinalysis covered are macroscopic examination, chemical analysis using urine dipsticks, microscopic examination, and culture. Specific tests on the dipstick like glucose, bilirubin, ketones, specific gravity, blood, pH, protein, urobilinogen, nitrite, and leukocyte esterase are explained.
men analysis, also known as a sperm count test, analyzes the health and viability of a man’s sperm. Semen is the fluid containing sperm (plus other sugar and protein substances) that’s released during ejaculation. A semen analysis measures three major factors of sperm health:
the number of sperm
the shape of the sperm
the movement of the sperm, also known as “sperm motility”
Doctors will often conduct two or three separate sperm analyses to get a good idea of sperm’s health. According to the American Association for Clinical Chemistry (AACC), the tests should be conducted at least seven days apart and over the course of two to three months. Sperm counts can vary on a daily basis. Taking an average of the sperm samples can give the most conclusive result.
Why undergo semen analysis?
Test for male infertility
A semen analysis is often recommended when couples are having problems getting pregnant. The test will help a doctor determine if a man is infertile. The analysis will also help determine if low sperm count or sperm dysfunction is the reason behind infertility.
Test for vasectomy success
Men who have had a vasectomy undergo semen analysis to make sure no sperm are in their semen. In a vasectomy, the tubes that send sperm from the testicles to the penis are cut and sealed as a permanent form of birth control. After a vasectomy, doctors often recommend that men take a sperm analysis once a month for three months to ensure that sperm is no longer present in their semen.
How to prepare for semen analysis
Your doctor will let you know what you should do in preparation for the semen analysis. It’s very important to follow these instructions for accurate results.
To get the best sample:
Avoid ejaculation for 24 to 72 hours before the test.
Avoid alcohol, caffeine, and drugs such as cocaine and marijuana two to five days before the test.
Stop taking any herbal medications, such as St. John’s wort and echinacea, as instructed by your healthcare provider.
Avoid any hormone medications as instructed by your healthcare provider.
Discuss any medications you’re taking with your doctor.
How is semen analysis conducted?
You’ll need to provide your doctor with a semen sample for a semen analysis. There are four main ways to collect a semen sample:
masturbation
sex with a condom
sex with withdrawal before ejaculation
ejaculation stimulated by electricity
Masturbation is considered the preferred way to get a clean sample.
Getting a good sample
Two main factors are crucial to having a good testing sample. First, the semen must be kept at body temperature. If it gets too warm or too cold, the results will be inaccurate. Second, the semen must be delivered to the testing facility within 30 to 60 minutes of leaving the body.
Test interference
Some factors can negatively affect the test, including:
semen coming into contact with spermicide
taking the test when you’re ill or stressed
lab technician error
contamination of the sample
There are no known risk
1) The document discusses blood physiology, describing the components and functions of blood including plasma, red blood cells, white blood cells, and platelets.
2) Plasma contains water, proteins, blood sugar, lipids, inorganic salts, hormones, enzymes, and gases which help maintain homeostasis, transport nutrients, remove waste, and fight infections.
3) Red blood cells contain hemoglobin and transport oxygen and carbon dioxide throughout the body. White blood cells help fight infections and disease. Platelets help the blood clot and repair damaged tissues.
This document provides information about performing and interpreting a urinalysis. It discusses specimen collection methods, types of analyses including macroscopic examination, chemical dipstick testing, and microscopy. For each dipstick parameter (glucose, bilirubin, ketones, specific gravity, blood, pH, protein) the chemical principles, significance, limitations, and alternative tests are outlined. Causes of proteinuria including functional, renal, pre-renal, and post-renal are also listed.
This document discusses standardization of urinalysis, including specimen collection, preservation, and analysis techniques. It covers macroscopic examination of urine volume, appearance, odor, and color. Chemical analysis includes dipstick testing for glucose, bilirubin, ketones, specific gravity, blood, pH, protein, urobilinogen, nitrite, and leukocyte esterase. Microscopic examination standards are provided for cells, casts, crystals, bacteria, and yeast seen in urine sediment. Automated urine analyzers are also discussed. Standardization is important for uniformity and accurate interpretation of urinalysis results.
This document provides information on renal function tests. It discusses the functions of the kidney including regulation of water, electrolytes and acid-base balance, and excretion of metabolic waste. Various indications for renal function testing are mentioned, including diagnosis and assessment of renal disease. Common tests discussed include urine analysis, blood tests of creatinine, electrolytes, and glomerular and tubular function tests such as creatinine clearance. Methods for urine collection and important parameters in urine and blood tests are outlined. Abnormal findings and their causes are described for several urine dipstick and microscopic tests.
Blood test normal values and it's importanceGOPAL KHODVE
Laboratory tests check a sample of your blood, urine, or body tissues. A technician or your doctor analyzes the test samples to see if your results fall within the normal range. The tests use a range because what is normal differs from person to person. Many factors affect test results. These include
Your sex, age and race
What you eat and drink
Medicines you take
How well you followed pre-test instructions
Your doctor may also compare your results to results from previous tests. Laboratory tests are often part of a routine checkup to look for changes in your health. They also help doctors diagnose medical conditions, plan or evaluate treatments, and monitor diseases.
Urine examination how to approach final.ppt1Sachin Verma
This document provides information on urine examination, including the composition, collection, physical characteristics, and chemical analysis of urine. It discusses normal ranges and clinical significance of various urine components like pH, specific gravity, proteins, glucose, ketones, bile pigments, and more. Detection methods for different analytes include dipstick tests, precipitation, electrophoresis, and quantitative assays. Causes of abnormalities in urine components related to kidney and metabolic diseases are also outlined.
This document provides information about urine analysis (urinalysis). It discusses the purpose of urine analysis in diagnosing kidney, urinary tract, and other systemic diseases. It covers proper urine collection and storage. The key components of a urinalysis that are examined are described in detail, including physical characteristics, chemical constituents, and microscopic examination of urine sediment. Urine culture is also discussed as a way to confirm bacterial infection and determine appropriate treatment. The document provides guidance on interpreting urinalysis results and what they may indicate about a patient's health conditions.
3. Pleural effusion: Introduction
• Collection of excess quantity of fluid in pleural space
• Inflammatory or non inflammatory causes
4. Pleural effusion: Classification
• Transudates: due to diseases that affect the
filtration of pleural fluid- CHF & hypoproteinemia
• Exudates: inflammation or injury increases pleural
membrane permeability to proteins and various
types of cells
21. Dry pleurisy: Pathology
• Involvement of visceral pleura with small amount of
yellow serous fluid
• Adhesion between pleural surfaces
• Pleural thickening
• Fibrothorax due to fibrin deposition and severe
adhesions
22. Dry pleurisy: Clinical manifestations
• Signs & symptoms of primary disease
• Dull pleural pain, exaggerated by deep
inspiration,cough, straining, referred to shoulder and
back
• Increased dullness on percussion and decreased breath
sounds
• Leathery, rough inspiratory and expiratory friction rub
early in the disease
• X-ray- haziness at the pleural surface or a dense, sharply
demarcated shadow
23. Dry pleurisy: Treatment
• Treat underlying condition
• If pneumonia is not present- strapping of chest to
restrict expansion and analgesics
• Strapping and cough suppressants not given if
pneumonia is present
24. 2. Serofibrinous pleurisy
• Infections of lungs
• Inflammatory conditions of mediastinum
• Less commonly with- SLE, RF, neoplasms
25. Serofibrinous pleurisy: Clinical features
• Initially signs and symptoms of dry pleurisy
• Asymptomatic if effusion is small
• Large effusion: cough, dyspnoea, retractions,
orthopnoea, cyanosis
• Shift of mediastinum away from affected side,
fullness of intercostal space, diminished tactile vocal
fremitus
• Dullness to flatness on percussion
• Decreased or absent breath sounds
26. Serofibrinous pleurisy: Clinical features...
• In infants- bronchial breath sounds instead of absent
breath sounds
• Friction rub in the early stages
• X-ray: homogenous opacity obliterating the normal
pulmonary marking, obliteration of costophrenic
angles and widening of interlobar fissure
28. Serofibrinous pleurisy: Treatment
• Treat underlying cause
• Thoracocentesis, up to 1 Liter of fluid
• Tube thoracostomy in older child with
parapneumonic effusion if pleural fluid pH<7.2 or
glucose <50mg/dl
29. 3. Purulent pleurisy / Empyema
• Pus or microorganism in pleural fluid
• Microorganism- by smear or culture
In the absence of these:
• pH of pleural fluid < 7.2
• Lactic dehydrogenase (LDH) >1000IU/L
• Glucose <than 40mg/dl
• Lactate > 45mg/ml
30. Empyema: Predisposing factors
• Pneumonia in ½ of cases
• Preceding H/O of pustules
• Blunt trauma to chest/surgery/thoracocentesis
• Viral infections (chickenpox, measles)
• Severe malnutrition
• Neglected foreign body
• Extension from subphrenic, amoebic liver abscess
• CHD
• Peridontal disease, steroid, immunodeficiency
32. Stages of Empyema
• Exudative (1 to 3 days):
parapneumonic effusion
• Fibrino purulent (4 to 14 days):
polymorpho nuclear & fibrin accumulation
• Organizing stage (after 14 days):
fibroblasts grow and producing an inelastic membrane
33. Empyema: Exudative stage
• Fluid is thin
• Cellular content is low
• Lungs are expandable
• Pleural fluid- pH >7.3, glucose >60mg/dl, pleural fluid
/serum glucose ratio >0.5, LDH < 1000 IU/L, Gram
stain and culture negative
34. Empyema: Fibrino purulent stage
• pH and glucose level fall, LDH rises
• Purulent and vicious, accumulation of neutrophils
and fibrin
• Tendency for loculations and limiting membranes
• purulent fluid, PH <7.10, glucose <40mg/dl LDH
>1000IU/L, Gram stain & culture +ve
35. Empyema: Organizing stage
• Thick pleura prevent entry of anti microbial drugs in
the pleural space- drug resistance
• Restrict lung movement
36. Empyema: Clinical features
• Common in poor socioeconomic group
• Peak incidence 0-3 years
• Chills, fever, dyspnoea, chest pain, referred pain,
night sweat, malaise, cough, ↑sputum production
• Pain abdomen & ileus
• Tachypnoeic, anxious, pleural rub (disappear after
fluid accumulates)
37. Empyema: Clinical features...
• Large fluid- fullness of intercostal spaces, diminished
chest excursions
• Shift of mediastinum
• Dullness to percussion, decreased air entry,
decreased tactile & vocal fremitus
38. Empyema: Investigation & Diagnosis
• History and examination findings
• Confirm the presence of empyema, etiological agent
& complications
• Polymorph predominance, rarely leukopenia
• X-ray chest- blunting of costophrenic angle,
opacification of hemithorax with mediastinal shift to
opposite side , lateral decubitus for small volume
41. Empyema: Treatment
Aims
• Control infection
• Drainage of pus
• Expansion of lungs
42. Empyema drainage
• Inter costal drainage (ICD), under water seal, large
catheter inserted in the site of pus accumulation
• Loculated fluid/pus- drainage continued for 1 week
• Chest tube kept till drainage is nil or < 30 ml/day
46. Empyema: Treatment...
• Based on culture and sensitivity
• Monotherapy not recommended
• In anerobic infection- Clindamycin: 6-12wk
• MRSA- Vancomycin
• Antibiotics till afebrile, WBC normal, thoracostomy
yield <50ml/day, X-ray clearing
• H influenzae & S pneumoniae: 7-14 days
• S aureus: 3-4 wk, anerobic: (variable) 6-12wk
47. Empyema: Thrombolytic therapy
• Multiloculated empyema by thoracostomy tube
• Streptokinase 2,50,000 unit or urokinase 1,00.000
unit in 100ml normal saline instilled through tube &
clamped for 3 hrs
48. Empyema: Surgical therapy
• Remains febrile and dyspnoeic after IV antibiotics
and thorcostomy drain
• Pleural thickening- decortication
• Non expansion of lung
• Bronchopleural fistula
• Video assisted thoracoscopic surgery in multi
loculated effusion
• Thorocoscopic debridement and irrigation in
multiloculated effusion
55. Pneumothorax: Causes
• Rupture of pleural blebs • Transthoracic aspiration
• Penetrating or non needle
penetrating injuries • Thoracentesis
• Pneumonia • Central intravenous
• Asthma catheters
• Cystic fibrosis • Mechanical Ventilation
• COPD/ Bronchitis
• Resuscitative efforts
• Inhalation of some toxic
substances, most
notably crack cocaine
56. Clinical Signs & Symptoms
• Severity depends on the extent of the lung collapse.
• Simple pneumothorax - asymptomatic or chest
pain, dyspnea.
• Extensive pneumothorax often produces pleuritic
chest pain, dyspnea, tachypnea, cyanosis,
Hyperresonance to percussion on the affected side.
• Decreased breath sounds on the involved side.
• If pneumothorax due to trauma - look for contusions
or abrasions on the chest wall or a small puncture
wound that does not allow free movement of air
between the outside and the pleural cavity.
57. Tension Pneumothorax: Signs/Symptoms
• Clinical Presentation - Chest pain (90%), Dyspnea
(80%), Anxiety, Fatigue
• Physical examination - Respiratory distress and/or
arrest, Cyanosis, Tracheal deviation, Pulsus paradoxus,
Tachypnea, Tachycardia, Hypotension, Jugular venous
distension
• Hyperresonance of the chest wall on percussion
• Unilaterally decreased or absent lung sounds
• Increasing resistance to providing adequate ventilation
assistance
• Mental status changes, including decreased alertness
and/or consciousness
• Abdominal distension
58. Tension Pneumothorax
Lung parenchymal or
bronchial injury
one-way valve
air trapping
mediastinal structures
- pushed to the
contralateral side.
mediastinum impinges on
and compresses the
contralateral lung
61. Pneumothorax: Treatment
Without continued air leak, asymptomatic and mildly
symptomatic small pneumothorax
• 100% oxygen
• Sedation
62. Tension Pneumothorax: Treatment
• Severe respiratory and circulatory embarrassment
• Emergency Needle aspiration
• Either immediately or after needle aspiration a chest
tube (ICD) should be inserted and attached to
underwater seal drainage
63. Decompression by Needle / ICD
• 2nd intercostal space on the mid clavicular line
• Upper border of the lower rib
• Needle / ICD have to be connected to the
underwater sealed drainage