This document discusses various body fluids, including cerebrospinal fluid (CSF), pleural fluid, and peritoneal fluid. It provides details on the production, composition, and evaluation of these fluids. Key points include that CSF is produced in the brain ventricles and circulates around the brain and spinal cord, transporting nutrients and removing waste. Pleural and peritoneal fluids accumulate as exudates or transudates depending on fluid balance mechanisms. Biochemical analysis of these fluids can help diagnose conditions like meningitis, tuberculosis, and liver disease.
Pathological analysis of body fluids with lab investigations,
Including Amniotic fluid, Semen analysis, Synovial fluid, Gastric fluid
Other body fluids: Sweat,saliva,tear
It is fluid which is present
in the pericardial cavity of
heart b/w parietal pericardium n visceral pericardium.
The pericardial cavity is a
potential space lined by
mesothelium of the visceral n parietal pericardium.
An immature red blood cell without a nucleus, having a granular or reticulated appearance when suitably stained.
Reticulocytes are the immature RBC that contain nucleus.
They are originally seen at the site of their formation i.e. bone marrow. They take 2-3 (lays for maturation only about 1-2% of circulating RBCs are Reticulocytes.
Pathological analysis of body fluids with lab investigations,
Including Amniotic fluid, Semen analysis, Synovial fluid, Gastric fluid
Other body fluids: Sweat,saliva,tear
It is fluid which is present
in the pericardial cavity of
heart b/w parietal pericardium n visceral pericardium.
The pericardial cavity is a
potential space lined by
mesothelium of the visceral n parietal pericardium.
An immature red blood cell without a nucleus, having a granular or reticulated appearance when suitably stained.
Reticulocytes are the immature RBC that contain nucleus.
They are originally seen at the site of their formation i.e. bone marrow. They take 2-3 (lays for maturation only about 1-2% of circulating RBCs are Reticulocytes.
I have listed out the LE cells structure and Microscopical examinaton of LE CELLS, Difference between tart cells and le cells, clinical symptoms and diagnostic procedure.
I have listed out the LE cells structure and Microscopical examinaton of LE CELLS, Difference between tart cells and le cells, clinical symptoms and diagnostic procedure.
Body fluid & electrolytes........Dr.Muhammad Anwarul Kabir,FCPS(Medicine)kabirshiplu
Body fluid & electrolyte disturbances are one of the critical but commonest problems in our day to day practices.This presentation helps to make a basic ideas dealing with dyselectrolytaemia
Here i made a presentation on the topic GLYCOLYSIS. I Demonstrated the ten steps of Glycolysis in a few word and flow chart so that you can easily learn about it.
synovial fluid is the fluid which is present within the joint for lubrication, provide of nutrition, to prevent from shock. fluid analysis is very important in medical field for the diagnosis of many diseases, on the basis of which a patient may be properly treated.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
These lecture slides, by Dr Sidra Arshad, offer a quick overview of physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
HOT NEW PRODUCT! BIG SALES FAST SHIPPING NOW FROM CHINA!! EU KU DB BK substit...GL Anaacs
Contact us if you are interested:
Email / Skype : kefaya1771@gmail.com
Threema: PXHY5PDH
New BATCH Ku !!! MUCH IN DEMAND FAST SALE EVERY BATCH HAPPY GOOD EFFECT BIG BATCH !
Contact me on Threema or skype to start big business!!
Hot-sale products:
NEW HOT EUTYLONE WHITE CRYSTAL!!
5cl-adba precursor (semi finished )
5cl-adba raw materials
ADBB precursor (semi finished )
ADBB raw materials
APVP powder
5fadb/4f-adb
Jwh018 / Jwh210
Eutylone crystal
Protonitazene (hydrochloride) CAS: 119276-01-6
Flubrotizolam CAS: 57801-95-3
Metonitazene CAS: 14680-51-4
Payment terms: Western Union,MoneyGram,Bitcoin or USDT.
Deliver Time: Usually 7-15days
Shipping method: FedEx, TNT, DHL,UPS etc.Our deliveries are 100% safe, fast, reliable and discreet.
Samples will be sent for your evaluation!If you are interested in, please contact me, let's talk details.
We specializes in exporting high quality Research chemical, medical intermediate, Pharmaceutical chemicals and so on. Products are exported to USA, Canada, France, Korea, Japan,Russia, Southeast Asia and other countries.
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
Follow us on: Pinterest
Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
2. Body Fluids
Extracellular fluid (ECF) Intracellular fluid (ICF)
• plasma, 1/4th • Interstitial fluid, 3/4th
liquid found between
the cells or tissue fluid
Eg. lymph
• Transcellular fluid
A body fluid that is not inside cells
but is separated from plasma and
interstitial fluid by cellular barriers.
• CSF
• pleural fluid
• synovial fluid
• Peritoneal fluid, etc
4. Cerebrospinal Fluid (CSF)
• Produced at the Choroid plexus of the 4 ventricles by
modified Ependymal cells
• At rate @20 ml / hr (adults)
• CSF flows through the Subarachnoid
space
• Where a volume of 90 – 150 ml is
maintained (adults)
• Neonate volume 10-60 mL
• Reabsorbed at the Arachnoid villus /
granulation
• to be eventually reabsorbed into the
blood
5. FUNCTIONS OF CSF
▪As shock absorber
▪ As mechanical buffer
▪ Act as cushion between the brain and cranium
▪ Act as a reservoir and regulates the contents of the cranium
▪ Serves as a medium for nutritional exchange in CNS
▪ Transport hormones and hormone releasing factors
▪ Removes the metabolic waste products through absorption
6.
7. CSF Evaluation
• Tube 1- for cell count and differential
• Tube 2- for glucose, protein & enzymes
• Tube 3- for culture, Gram stain, AFB stain,
India ink etc
• Tube 4- for cytology
12. Cerebrospinal fluid (CSF)
Mechanism of increased CSF protein:
– increased permeability of the blood brain barrier d/t damage
– Decreased reabsorption at the arachnoid villi
– Mechanical obstruction of CSF flow due to spinal block above
the puncture site
– Increased in inthrathecal immunoglobulin synthesis
• inflammatory meningitis - ↑ to about 125mg-1gm/dl
• Neurosyphilis, encephalitis, abscess, tumor - ↑ to 20-300mg/dl
• Spinal cord tumor – 100 – 2000mg/dl
13. Cerebrospinal fluid (CSF)
Low CSF protein:
• May normally occur in young children between 6 months to
12 years
• Patient with increased CSF turnover
– removal of large volume of CSF
– CSF leak induced by trauma or lumbar puncture
– increased intracranial pressure, probably due to an
increased rate of protein reabsorption by the arachnoid
vili
14. Cerebrospinal fluid (CSF)
CSF protein estimation:
1) Turbidimetric method:
– Uses trichloroacetic acid (TCA) or sulfosalicylic acid (SSA) and
sodium sulphate for protein precipitation
– Benzethonium chloride or benzalkonium chloride
2) Colorimetric method:
– Uses Lowry method (Folin phenol reagent) or
– Dye binding method using Coomassie brilliant blue (CBB) or
Ponceau S and
– Biuret method
15. Cerebrospinal fluid (CSF)
Pyrogallol red technique:
• Protein present in CSF will quantitatively bind with pyrogallol
red molybdate reagent dye at pH 2.5 violet colored
complex
• intensity of this colored complex is measured at 600 nm in a
spectrophotometer
• higher the concentration of protein, more intense or darker
will be the color of the CSF solution
16. Cerebrospinal fluid (CSF)
Serum and CSF Albumin &IgG ratio:
• assess permeability of blood brain barrier
CSF/Se. albumin index = CSF albumin (mg/dl)
Se. albumin (g/dl)
• Normal ratio: 1: 230
17. Cerebrospinal fluid (CSF)
CSF IgG:
• 3-5%
• MS - ↑ to about 15-18%
• Increased intrathecal IgG assessed by
CSF/Se. IgG ratio = CSF IgG (mg/dl)
Se. IgG (g/dl)
• Normal ratio: 1:390
19. Cerebrospinal fluid (CSF)
Electrophoresis of CSF:
• Using cellulose acetate or agarose
• Pre-albumin, albumin, alpha1, alpha2, beta1, beta2 and
gammaglobulins
• CSF always contain pre-albumin and plasma does not
• Pre-albumin or Transthyretin is thyroxine (T4) and retinol-
binding protein
20. Cerebrospinal fluid (CSF)
• Pattern is abnormal when IgG synthesis increases
• MS – gammaglobulin fraction↑(ologoclonal bands seen)
• Multiple sclerosis(MS): is an inflammatory disease in
which the insulating covers of nerve cells in
the brain and spinal cord are damaged
• CSF total protein/Gammaglobulin fraction exceeds 0.12 in
about 65% of cases of MS
21. Cerebrospinal fluid (CSF)
High resolution agarose gel
electrophoresis:
• Shows discrete patterns of
IgG, oligoclonal bands
• Two or more bands necessary
for diagnosis
• A highly sensitive stain like
silver stain or Coomassie
Brilliant Blue is required to
identify the proteins in the gel
22. Cerebrospinal fluid (CSF)
• detection of oligoclonal bands is performed if there is suspicion
of an inflammatory or demyelinating condition
• Concomitant serum sample for elecrophoresis and protein
estimation is mandatory
• presence of oligoclonal bands in CSF combined with their
absence in blood serum often indicates that immunoglobulins
are produced in CNS
• Oligoclonal bands are detected in upto 90% of MS
24. Cerebrospinal fluid (CSF)
Glucose:
– 50-85mg/dl (2.8-4.4mmol/L), about 2/3rd of plasma value
– normal CSF/plasma glucose ratio = 0.3-0.9
– Hypoglycorrhachia = < 35mg/dl (characteristic of
bacterial, tuberculous and fungal meningitis)
– Some viral meningoencephalitis have low CSF glucose but
not to that extent as in bacterial meningoencephalitis
26. Cerebrospinal fluid (CSF)
• Decreased CSF glucose results from increased anaerobic
glycolysis in brain tissue and leucocytes and impaired
transport to CSF
• CSF glucose normalize before protein levels and cells count
during recovery of meningitis, making it a useful parameter
in assessing response to treatment
27. Cerebrospinal fluid (CSF)
Lactate:
• 9.0-26mg/dl (1.0-2.9mmol/L)
• Elevated CSF lactate reflects CNS anaerobic metabolism due
to tissue hypoxia
• Persistently increased – poor prognosis in patient with head
injury
• Usually done to differentiate viral from bacterial,
mycoplasma, fungal and tuberculous meningitis where
routine parameters yield equivocal results
• Viral meningitis - always <35mg/dl
• Bacterial meningitis - >35mg/dl
28. Cerebrospinal fluid (CSF)
F2 isoprostanes:
• Increased in Alzheimer’s disease
Urea:
• Level is slightly lower than in blood
• In uremia, urea conc. in CSF rises in parallel with that in
blood
30. Reference range
ADA ( pleural
fluid)
Normal: <40 mg/dl
Suspect: 40—50
Strong suspect: >50-60
Positive: > 60
ADA(CSF) <10 mg/dl
ADA(Serum)
<15 mg/dl
ADA
∙ADA involved in purine metabolism
∙It converts Adenosine to inosine
∙found mostly in lymphocytes and macrophages
31. 1. Tuberculosis (cut off value > 60 U/L for pleural fluid)
2. ADA is also increased in various infectious disease
like
• infectious mononucleosis
• Typhoid
• Viral hepatitis
• Initial stage of HIV
• Incase of malignant tumors
• SLE
32. Cerebrospinal fluid (CSF)
Creatine kinase (CK):
• Increased CSF CK activity are seen in numerous CSF disorders:
– Hydrocephalus, cerebral infraction, primary brain tumors and
subarachnoid hemorrhage
• In patient with head trauma, CSF CK levels correlate directly with
the severity of the Concussion
• CK-BB isoenzyme – better than CK-total
33. Cerebrospinal fluid (CSF)
• CK-BB isoenzyme increases about 6 hour following an
ischemic or anoxic insult
CK-BB:
< 5U/L - minimum neurological damage
5-20U/L - mild to moderate neurological
damage
21-50U/L - commonly correlated with death
34. Cerebrospinal fluid (CSF)
LDH:
• < 40 U/L
• used as the marker in estimating the potential outcome during the
early stages of ischemic brain injury
• Also elevated in bacterial meningitis but not in aseptic or viral
meningitis
Ammonia:
• Increased levels are generally proportional to the degree of
existing hepatic encephalopathy
• Generally correlates with blood value
• Also increases in Reye’s syndrome, inherited hyperammonemias
35. Cerebrospinal fluid (CSF)
Catecholamines:
• Homovanillic acid (HVA), the major catabolite of dopamine
and 5-hydroxyindoleacetic acid (5-HIAA), the major
catabolite of serotonin, are normally present in CSF
• The levels of both catabolites are reduced in patients with
idiopathic or drug induced parkinsonism
36. Cerebrospinal fluid (CSF)
Tumor marker
• Various tumor markers have been seen increased in CSF
of patients with both primary and metastatic tumors
• eg. CEA, HCG, ALP
41. Pleural Fluid
• pleural cavity normally contains small amount of fluid that
facilitates movement of two membranes against each other
• Plasma filtrate derived from capillaries of the parietal pleura
• Produced continuously at the rate dependent on capillary
hydrostatic pressure, plasma oncotic pressure and capillary
permeability
• Reabsorbed – lymphatics and venules of visceral pleura
• Volume – about 10ml each
42. Pleural Fluid
• Accumulation of fluid – an effusion, results from imbalance
between the fluid production and reabsorption
• Fluid accumulation in pleural, pericardial and peritoneal
cavities serous effusion
43. Transudate
• Clear, pale yellow, watery substance
• Influenced by systemic factors that alter the
formation or absorption of fluid
• Increase in hydrostatic pressure
• Decrease in plasma oncotic pressure
• Contains few protein cells
• Common causes: CHF and liver or kidney disease
44. Exudate
• Pale yellow and cloudy substance
• Influenced by local factors where fluid absorption is altered
(inflammation, infection, cancer)
• Rich in protein (serum protein greater than 0.5)
• Ratio of pleural fluid LDH and serum LDH is >0.6
• Pleural fluid LDH is more the two-thirds normal upper limit
for serum
• Rich in white blood cells and immune cells
• Always has a low pH
• Common causes: pneumonia, cancer, and trauma
45. Pleural Fluid
According to Light’s criteria exudate meets one or more of
following criteria:
1. Pleural fluid protein/serum protein > 0.5
2. Pleural fluid LDH/serum LDH > 0.6
3. Pleural fluid LDH more than two-thirds normal upper
limit for serum
46. Pleural Fluid
Biochemical constituents:
Protein:
– contain < 50% of serum protein level
– Estimation helps in differentiating transudate or exudate
– Protein electrophoresis shows pattern similar to serum except
for higher proportion of albumin
Glucose:
– Similar to serum glucose level
– Low pleural fluid glucose – malignancy, TB, rheumatoid
pleuritis, non purulent bacterial infections, lupus pleuritis, etc
47. Pleural Fluid
Lactate:
– Useful adjunct - rapid diagnosis of infectious pleuritis
(>90mg/dl)
– Levels are significantly high in bacterial and tuberculous
pleural infections
Enzymes:
Adenosine Deaminase:
– Normal – about 36U/L
– Significantly increased in tuberculous pleuritis
48. Pleural Fluid
Amylase:
– Elevations above the serum level (usually 1.5-2 or more
times greater) – pancreatitis, esophageal rupture or
malignant effusion
LDH:
– Levels rise in proportion to degree of inflammation
– Declining LDH level in course of an effusion – resolving of
inflammatory process
49. Pleural Fluid
Interferon – gamma (INF-gamma):
– Useful diagnostic modality for TB pleural effusion
– Levels increases significantly in pleural fluid of patient
with tuberculous pleuritis (>136pg/ml)
Lipids:
– Pleural fluid Tg level > 110mg/dl – a chylous effusion
– Pleural fluid/Se. cholesterol ≥ 0.32 – exudate
50. Pleural Fluid
Tuberculostearic acid (TSA):
– Structural component of Mycobacteriun tuberculosis, not
present normally in human tissue
– Using gas chromatography or mass spectroscopy TSA is
measured in sputum, bronchial aspirates, washings or pleural
fluid
Tumor markers:
– Not recommended routinely
– May be useful in diagnosing cases with negative cytology or
unexplained effusions
52. Peritoneal fluid
• Ascites – pathologic accumulation of excess fluid in the
peritoneal cavity
• Normal volume – 50ml
• Produced as an ultrafiltrate of plasma dependent on vascular
permeability, hydrostatic and oncotic pressure
53. Peritoneal fluid
Biochemical constituents:
Protein:
• serum-ascites albumin gradient or gap (SAAG)
SAAG = albumin conc. of serum - albumin conc. of ascitic fluid
• high gradient:
– > 1.1 g/dL – due to portal hypertension
• Important causes of high SAAG (> 1.1 g/dL) include:
– high protein : heart failure, Budd Chiari syndrome
– low protein : cirrhosis of the liver
54. Peritoneal fluid
• Low gradient:
– < 1.1 g/dL - causes of ascites not associated with
increased portal pressure such
as tuberculosis, pancreatitis, nephrotic syndrome and
various types of peritoneal cancer
Glucose:
– Decreased level in tuberculous ascites (< 50mg/dl)
– Ascites glucose estimation are of little value
55. Peritoneal fluid
Enzymes:
Amylase:
– Amylase activity in normal peritoneal fluid is similar to
plasma level
– Level greater than three times the plasma value is
good evidence of pancreas related ascites
– Also increases in gastroduodenal perforation, acute
mesenteric vein thrombosis, intestinal strangulation
or necrosis
57. Peritoneal fluid
ADA:
– Increases in tuberculous peritonitis
Lactate:
– Increased in malignant and tuberculous ascites
Creatinine and urea:
– Essential in differentiating peritoneal fluid from urine
– Increased peritoneal fluid urea and creatinine along with
increased serum urea but normal serum creatinine
urinary bladder rupture
58. Peritoneal fluid
Bilirubin:
– Ascitic fluid bilirubin > 6mg/dl and ascitic fluid/serum
bilirubin > 1.0 choleperitoneum
Tuberculostearic acid: helpful
Tumor markers:
– little value, however, CEA, PSA, α – fetoprotein found to
be very specific for serous fluid malignancies
60. Pericardial fluid
• Normal volume: 10-50ml
• Pericardial effusion – excess accumulation
• Often caused by viral infection, most common by enterovirus
61. Pericardial fluid
• It may be:
– transudative (congestive heart failure, myxoedema, nephrotic
syndrome),
– exudative (tuberculosis, spread from empyema)
– haemorrhagic (trauma, rupture of aneurysms, malignant
effusion).
– malignant (due to fluid accumulation caused by metastasis)
• Light’s criteria - reliable diagnostic tool for identifying pericardial
exudates and transudates
62. • Other indicators suggestive of exudate -
Specific gravity >1.015, total protein >3.0
mg/dL, LDH >300 U/dL, glucose fluid-to-serum
ratio < 1
63. Pericardial fluid
Biochemical constituents:
• Biochemical parameters for the diagnosis of pericardial
effusions have not been studied to the same extent as in
other body fluids
Glucose:
– Value < 40mg/dl (2.22mmol/L) – bacterial, tuberculous,
rheumatic or malignant effusion
64. Pericardial fluid
Enzymes:
LDH:
– Level > 200U/L suggests pericardial exudate
• Significantly increased pericardial fluid levels of CK-MB,
myoglobin and Troponin I in postmortem pericardial fluid –
myocardial injury
ADA :
– Useful adjunctive test for tuberculous pericardits
65. Pericardial fluid
Interferon-gamma:
– Increased in tuberculous pericarditis
– Cutoff value – 200pg/L
PCR:
– More specific than ADA in diagnosing tuberculous
pericarditis but
– Negative test does not rule out tuberculous pericarditis
since some pericardial fluids from patients with large
tuberculous effusions may not contain M. tuberculosis
67. SYNOVIAL FLUID
• Ultrafiltrate of blood plasma combined with hyaluronic acid
produced in the joints space by the synovial cells lining
synovial tendon sheaths, joints, etc
• Composition similar to plasma as small ions and molecules
readily pass into the joint space
• Reabsorption – lymphatics
• Acts as a lubricant and adhesive, and provides nutrients for
the avascular articular cartilage
68. SYNOVIAL FLUID
• Examination of synovial fluid is essential to differentiate infectious
from non-infectious arthritis
Biochemical parameters:
• Adds only supportive information
to the routine test
Mucin clot test:
• Add acetic acid to SF precipitates hyaluronate into a mucin clot
which may be graded as good, fair or poor
• Fair to poor mucin clot reflects dilution and depolymerization
of hyaluronic acid, a non-specific finding of several inflammatory
arthrites
69. SYNOVIAL FLUID
Glucose:
• Proper interpretation of SF glucose values requires comparison
with serum levels, ideally preceded by eight hours fast to allow
glucose to equilibrate across the synovial membrane
• Normally, Serum – synovial = < 10mg/dl, also in many non-
inflammatory conditions
• In septic arthritis, this difference increases from 20-60mg/dl
70. SYNOVIAL FLUID
Protein:
• Mean normal – 1.0-3.0 g/dl
• Total protein estimation is not generally useful
• With increasing inflammation, larger proteins enter the synovial
space
Enzymes:
LDH:
• Increased in RA, gout, failed arthroplasties and infectious arthritis
reflecting neutrophilic infiltration
71. SYNOVIAL FLUID
Acid phosphatase:
• Elevated acid phosphatase may have negative prognostic
value in RA but is non-specific
Organic acids:
Lactic acid:
• increased in septic arthritis
• Increased > 30mg/dl septic arthritis due to gram +ve
cocci and gram –ve bacilli
72. SYNOVIAL FLUID
• Using gas-liquid chromatography, presence of other organic acids
not normally present in SF (eg. n-valeric, n-hexanoic and succinic
acids) may be helpful in differentiating septic from non-septic
arthritis
Uric acid:
• Increased SF uric acid level supports a diagnosis of gout
Lipids:
• Contains extremely low conc. of lipids than in plasma
• Helps when cholesterol crystals of SF resemble MSU or CPPD
75. AMNIOTIC FLUID
• fluid surrounds, protects, and nourishes a growing fetus
during pregnancy
• allows the baby to move relatively freely and helps maintain a
stable temperature
• increases in volume as fetus grows
• Highest – 34wks
• At first, it is mainly water with electrolytes, by about 12-14th week
- proteins, carbohydrates, lipids and phospholipids and urea(all of
which aid in the growth of the fetus)
76. AMNIOTIC FLUID
• detect and diagnose some birth defects, genetic diseases, and
chromosome abnormalities in a fetus, especially if pregnancy
screening tests are abnormal
• to evaluate fetal lung maturity
• obtained through a procedure
- amniocentesis
77. AMNIOTIC FLUID
• 15 and 20 weeks - for genetic diseases, chromosome
abnormalities and open neural tube defects
• after 32 weeks - to evaluate fetal lung maturity, when
there is an increased risk of premature delivery
78. AMNIOTIC FLUID
• For genetic testing and chromosome analysis, fetal cells in the
amniotic fluid are cultured and grown for several days in the
laboratory, then are analyzed
• Biochemical tests, such as bilirubin and alpha-fetoprotein, and
sometimes genetic tests can be performed directly on the
amniotic fluid
79. AMNIOTIC FLUID
• Chromosome analysis, a cytogenetics test that may also be called
karyotyping - detect chromosome abnormalities associated with a
variety of disorders. (It evaluates the 22 paired chromosomes and
the sex chromosomes (XY) in the nucleus of cells cultured from
those collected in the sample of amniotic fluid and can be used to
diagnose a variety of chromosomal disorders)(down’s, klinefelter,
edward, patau’s, turner)
• Genetic testing, also called molecular testing.( It looks at
fetal DNA to identify specific gene mutations and diagnose a
variety of inherited diseases)(cystic fibrosis, tay sach’s disease,
sickle cell anemia, thalessemia)
80. AMNIOTIC FLUID
• AFP (alpha-fetoprotein)—increased with neural tube defects
• Acetylcholinesterase—increased with neural tube defects and
also other anatomic abnormalities
• Testing to evaluate fetal lung maturity- (tests are based upon
the presence of adequate protective liquid substances called
surfactants in the lungs, which are necessary for proper lung
function)
• Tests for bilirubin may be performed on a regular basis, starting
at about 25 weeks of pregnancy, to detect, evaluate and
monitor the severity of the hemolytic anemia in the fetus
82. SEMINAL FLUID
• Semi-gelatinous or liquid suspension containing spermatozoa and
secretions from male accessory organ
• Net fluid formed by mixing of the testicular fluid, prostatic fluid
and secretion from the seminal vesicles
• Composition is most suitable for the maintenance and survival of
spermatozoa
83. SEMINAL FLUID
• Has same pH as blood plasma
• Conc. of lactate, phosphate and citrate is higher than in
blood
• Chloride and cholesterol are lower
• Sugar content is high –fructose
• If fructose is low – infertility (spermatozoa can’t survive)
84. SEMINAL FLUID
• semen analysis is used to determine whether a man might
be infertile