This document provides information on various tests and procedures used to evaluate pulmonary function and diagnose respiratory conditions. It discusses examinations of sputum, chest radiology, CT, MRI, bronchoscopy, and biopsies. It also covers pulmonary function testing in detail, including indications, contraindications, instructions for patients, classifications of lung defects, normal and abnormal spirometry findings, and how to evaluate test results. A table lists various respiratory investigations and their indications.
Pulmonary Oedema is accumulation of fluid in lungs. It can be due to cardiogenic or non-cardiogenic causes. This presentation was a class presentation and discussed its management alongwith diagnosis.
Pulmonary Oedema is accumulation of fluid in lungs. It can be due to cardiogenic or non-cardiogenic causes. This presentation was a class presentation and discussed its management alongwith diagnosis.
PULMONARY FUNCTION TESTS - LAB DATA INTERPRETATIONLincyAsha
PULMONARY FUNCTION TESTS
LAB DATA INTERPRETATION
CLINICAL PHARMACY PRACTICE
M.PHARMACY
PHARMACY PRACTICE
1ST YEAR
Pulmonary function tests are a series of tests performed to examine a patient’s respiratory system and identify the severity of pulmonary impairment.
These tests are performed to measure a patient’s lung volume, capacity, flow rate and gas exchange.
This allows medical professionals to obtain an accurate diagnosis and determine the best course of medical intervention for the patient.
In general there are two types of lung disorders that these tests can be used to assess
Obstructive lung diseases
Restrictive lung diseases
1.OBSTRUCTIVE LUNG DISEASES
It include conditions that make it difficult to exhale air out of the lungs
This results in shortness of breath that occurs from narrowing and constriction of the airways and causes the patient to have decreased flow rates. Eg. COPD, Asthma
2.RESTRICTIVE LUNG DISEASES
It include conditions that make it difficult to fully fill the lungs with air during inhalation.
When the lungs aren’t fully able to expand it causes the patient to have decreased lung volumes. Eg. Pulmonary fibrosis, interstitial lung disease
Pulmonary function tests would be indicated for the following:
On healthy patients as part of a routine physical exam
Evaluate signs and symptoms of lung disease
Diagnosis of certain medical conditions
Measure current stage of disease and evaluate its progress
Assess how a patient is responding to different treatments
Determine patient’s condition before surgery to assess the risk of respiratory complications
Screen people who are at risk of pulmonary disease
Determine how much a patient’s airways have narrowed due to disorders
In certain types of work environments to assess the health of employees.
Additionally PFTs may be indicated for the following
Chronic lung conditions
Restrictive airway problems
Asthma
COPD
Shortness of breath
Impairment or disability
Early morning wheezing
Chest muscle weakness
Lung cancer
Respiratory infections
STATIC LUNG VOLUMES
Lung volume is the amount of air breathed by an individual under a specific condition.
1.Tidal Volume (TV)
It is the volume of air inspired or expired during normal breathing at rest.
2.Inspiratory Reserve Volume (IRV)
It is the volume of air inspired with maximum effort over and above the normal tidal volume.
3.Expiratory Reserve Volume (ERV)
It is the volume of air expired forcefully after a normal respiration.
4.Residual Volume (RV)
It is the volume of air remaining in the lungs after a forceful expiration
STATIC LUNG CAPACITIES
1.Inspiratory capacity (IC)
It is the amount of air a person can inspire forcefully after a normal respiration.
IC = TV+IRV
2.Functional Residual Capacity (FRC)
It is the amount of air that remains in the lungs at the end of normal respiration.
FRC = ERV+RV
3.Vital Capacity (VC)
It is the maximum volume of air exhaled forcefully from the lungs after a maximum inspiration.
4.Total Lung Capacity
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
Title: Sense of Smell
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 primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
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.
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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
7. Three layer test
In conditions like bronchiectasis and
lung abscess the sputum forms three
distinct layers
Thick Nummular purulent sputum
below
Serous fluid in middle
Froth above
25. PULMONARY FUNCTION TESTING
• Process of having the patient perform specific inspiratory and
expiratory maneuvers
• Important to be familiar with these tests and values even if
you do not work in a PFT lab
• Used for the following:
• Medical diagnosis
• Surgery related evaluation
• Disability evaluation
• Public Health/Research
• Studying the effects of exercise on the lungs
26. CONTRAINDICATIONS
•Recent abdominal, thoracic, or eye surgery
•Hemodynamic instability
•Symptoms of acute severe illness
•Chest pain, nausea, vomiting, high fever, dyspnea
•Recent hemoptysis
•Pneumothorax
•Recent history of abdominal, thoracic, or cerebral
aneurysm
27. PATIENT INSTRUCTIONS PRIOR TO
TESTING
• Should not drink alcohol for four hours prior to test
• Should not smoke at least one hour before test
• Do not eat a large meal two hours prior to test
• No vigorous exercise 30 minutes before test
• Do not wear tight fitting clothes
• May need to remove loose dentures for test
• Should wait at least one month post MI, consider impact of
problems that may affect results (chest/abdominal pain, oral
or facial pain, stress incontinence, dementia, physical
deformities or medical conditions)
• Bring a list of all medications – potentially withhold
bronchodilators, corticosteroids
28. CLASSIFICATION OF LUNG DEFECTS
OBSTRUCTIVE
• Expiratory flow is below
normal
• Anatomic site can be
identified
• Diseases:
• Cystic fibrosis
• Bronchitis
• Asthma
• Bronchiectasis
RESTRICTIVE
• Lung volumes are
reduced
• Diseases:
• Neuromuscular
• Cardiovascular
• Pulmonary
• Trauma/chest wall
dysfunction
• Obesity
33. TOTAL LUNG CAPACITY
• Increased with obstructive disease
• Decreased with restrictive disorders
• Sum of the vital capacity and residual volume
• Obtain RV by:
• Body plethysmography
• Nitrogen washout
• Helium dilution
34. BODY PLETHYSMOGRAPHY
• Uses the “body box”
• Boyles Law
Unknown lung gas vol = Gas pressure of the box
Known box gas vol Gas pressure of the lungs
35. In body plethysmography, the patient sits inside
an airtight box, inhales or exhales to a particular
volume (usually FRC), and then a shutter drops
acroSs their breathing valve. The subject makes
respiratory efforts against the closed shutter
causing their chest volume to expand and
decompressing the air in their lungs. The increase
in their chest volume slightly reduces the box
volume and thus increases the pressure in the
box. This method of measuring FRC actually
measures all the conducting pathways including
abdominal gas; the actual measurement made is
VTG (Volume of Thoracic gas).
36. NITROGEN WASHOUT
• Open circuit method
• Patient breathes
100% oxygen while the nitrogen
washed out of the lungs
• Assumes 79% of lung volume is
nitrogen
• Several “problems” with this test
37. HELIUM DILUTION
• Closed system
• Known volume and
concentration of He
added and it will be
diluted in proportion to
the size of the lung
volume
38. FEV1
• Maximal volume exhaled during the first second of
expiration
• Best indicator of obstructive lung disease
• Flow characteristics of the larger airways
• Best expressed as a percentage of the FVC (FEV1/FVC)
• Should be able to exhale 70% of the vital capacity in the
first second
• Decreased in obstructive disorders
39. FORCED EXPIRATORY FLOW
• Examines the middle 50% of
the exhaled curve
• Reflects degree of airway
patency/condition of the
medium to small airways
• Early indicator of obstructive
dysfunction
• Normal value is 4-5 L/sec
FEF 25-75%
40. FORCED EXPIRATORY FLOW
FEF 200-1200
• Average flow after the first
200ml is exhaled
• Good indicator of the integrity
of large airway funtioning
• Decreased in obstructive
disorders
• Normal value is 6-7L/se
41. PEAK EXPIRATORY FLOW RATE
• Maximum flow rate achieved during an FVC
• Used in asthmatics to identify the severity of airway
obstruction and guide therapy
• Dependent on patient effort
• Normal value is 10L/sec (600L/min), decreases with
age and obstruction
42. MAXIMUM VOLUNTARY VENTILATION
• MVV – patient breathes as
fast and deep as possible for
12-15 seconds
• Tests for overall lung
function, ventilatory reserve
capacity and air trapping
• Normal = 170L/min
• Decreased in obstructive
disorders
45. DIFFUSION CAPACITY (DL)
• Represents the gas
exchange capabilities of
the lungs
• Measures the ability of
gas to diffuse across the
alveolar-capillary
membrane using carbon
monoxide: DLCO
46. DLCO
• Diseases that reduce surface
area – DL
• emphysema
• Interstitial altering of the
membrane integrity - DL
• Pulmonary fibrosis,
Asbestosis, Sarcoidosis
47. EVALUATION OF RESULTS
Evaluation of the Vital Capacity
• can be reduced in obstructive and restrictive disease
• if VC is reduced, evaluate the TLC
• if the TLC is increased = obstruction
• if the TLC is decreased = restriction
• if VC is normal, evaluate the TLC
• if the FVC is greater than 90% of the SVC = normal
• if the FVC is less than 90% of the SVC = obstruction
48. EVALUATION OF RESULTS
• Evaluation of FEF 25-75%
• if normal then normal lungs or
possible restriction
• if reduced = peripheral
obstruction
• Evaluation of the FEV1/FVC
• if the FEV1/FVC is normal
then the lungs are normal or
restrictive
• if the FEV1/FVC is reduced =
obstruction
• Evaluation of the Total Lung Capacity:
% pred.
• increased =hyperinflation present
evaluate the FEV1
Normal = normal lungs
Decreased = obstruction
• Decreased
evaluate the FEV1
Normal = restrictive
Decreased = obstructive and
restrictive
52. Investigations Indication/comment
Blood tests
White cell count High in lower respiratory tract
infection
Haematocrit Elevated in polycythaemia
Eosinophil count High in:
Allergic asthma
Pulmonary eosinophilia
Allergic bronchopulmonary
aspergillosis
Churg–Strauss syndrome
53. Investigations Indication/comment
C REACTIVE PROTEIN High in:
Pneumonia
Empyema
Serum sodium Reduced in:
Small cell lung cancer
(inappropriate antidiuretic
hormone
(ADH) secretion)
Legionnaire’s disease and any
severe pneumonia
54. Blood and urine osmolality Inappropriate ADH secretion
Serum calcium Elevated in bony metastases,
sarcoidosis and squamous cell lung
cancer
Liver function tests Metastatic liver disease
Immunoglobulins Deficiencies in bronchiectasis
Angiotensin-converting enzyme
activity
Elevated in sarcoidosis
55. Alpha-1-antitrypsin
Deficiency in hereditary panacinar
emphysema
Total and specific (radioallergosorbent test) IgE Atopic status (asthma)
Antinuclear factor Idiopathic pulmonary fibrosis (fibrosing
alveolitis)
Antineutrophil cytoplasmic antibody (ANCA)
Proteinase 3 (cANCA)
Myeloperoxidase (pANCA)
Granulomatosis with polyangiitis (Wegener’s
granulomatosis)
Microscopic polyangiitis
Churg–Strauss syndrome
Farmer’s lung and avian precipitins Hypersensitivity pneumonitis (extrinsic allergic
alveolitis)
Cold agglutinins (IgM) Mycoplasma infection
56. Serology (IgG antibodies) Viral respiratory tract infection, e.g. influenza,
respiratory syncytial
virus
Small bacterial infection, e.g. Mycoplasma,
Legionella, Chlamydia
D-dimer Venous thromboembolism
Immunoreactive trypsin Screening for cystic fibrosis
Complement fixation transmembrane regulator
(CFTR) genotyping
Cystic fibrosis
Gamma-interferon release assay Latent infection with Mycobacterium
tuberculosis
57. Respiratory function
Arterial blood gas tensions
Respiratory failure
acid–base balance
Spirometry Diagnosis/monitoring of COPD and
asthma
Carbon monoxide gas transfer Reduced in:
Interstitial lung disease
Emphysema/COPD
Flow–volume curves Detection of extra- and intrathoracic
large airway obstruction
Maximal mouth pressures Respiratory neuromuscular disorders
58. Exercise test
6-minute run
Diagnosis of asthma in children and young adults
6-minute walk test Assessment of disability, e.g. in COPD
Cardiopulmonary exercise test Peak oxygen consumption (VO2)
Differentiates breathlessness due to lung
disease from that due to
heart disease
Bronchial challenge test Exclusion of asthma
Bronchial provocation studies Asthma, especially occupational asthma
Exhaled nitric oxide Inhaled steroid dosage in asthma
Overnight sleep study Sleep apnoea/hypopnoea syndrome
59. Radiology
CT thorax
Pulmonary or mediastinal mass
Staging of lung cancer
Pleural disease
High-resolution CT Interstitial lung disease
Bronchiectasis
Isotope VQ lung scan Pulmonary thromboembolism
CT pulmonary angiogram Pulmonary thromboembolism
Pulmonary hypertension
Echocardiogram Right heart dilatation (cor pulmonale)
Ultrasound of chest wall Localisation of pleural effusion
Positron emission tomography/CT Staging of lung cancer
60. Invasive Lymph node aspiration Cervical lymphadenopathy
Bronchoscopy Suspected lung cancer
Suspected foreign-body inhalation
Obtaining specimens for microbiology
Transbronchial lung biopsy Suspected pulmonary sarcoidosis
Suspected diffuse malignancy
Pleural aspiration and biopsy Undiagnosed pleural effusion
Percutaneous fine-needle lung aspiration Peripheral lesion/suspected lung cancer
Mediastinoscopy Staging of lung cancer
Mediastinal mass
Thoracoscopy Undiagnosed pleural disease
Lung biopsy (open or video-assisted thoracoscopic
surgery)
Interstitial lung disease