Occupational asthma is a form of asthma caused or aggravated by substances in the workplace. Common triggers include isocyanates, animal antigens, anhydrides, and various dusts and metals. It is characterized by narrowing of the airways and breathing difficulties. While not all workers exposed will develop it, risk factors include a history of asthma/allergies, family history, smoking, and low fitness. Early diagnosis is important as occupational asthma can be prevented or potentially cured by avoiding exposure.
A description of Work related asthma, Occupational Asthma and Work exacerbated asthma
References: Murray and Nadel's Textbook of Respiratory Medicine
American College of Chest Physicians 2008 Consensus Statement
Hope you find it useful.
A description of Work related asthma, Occupational Asthma and Work exacerbated asthma
References: Murray and Nadel's Textbook of Respiratory Medicine
American College of Chest Physicians 2008 Consensus Statement
Hope you find it useful.
This is a powerpoint presentation on Emphysema topic taken from Robin's and Cotran textbook of pathology
contans :
1) definition
2) types and pathogenesis of emphysema
3) morphology of early and advanced stage of emphysema
Byssinosis is a lung disease caused by occupational exposure to dust from cotton, hemp or flax.
Other names for byssinosis include Monday fever, brown lung disease, mill fever or cotton workers' lung.
New Latin, from Latin byssinus of fine linen.
This is a powerpoint presentation on Emphysema topic taken from Robin's and Cotran textbook of pathology
contans :
1) definition
2) types and pathogenesis of emphysema
3) morphology of early and advanced stage of emphysema
Byssinosis is a lung disease caused by occupational exposure to dust from cotton, hemp or flax.
Other names for byssinosis include Monday fever, brown lung disease, mill fever or cotton workers' lung.
New Latin, from Latin byssinus of fine linen.
Montelukast is a selective and orally active leukotriene receptor antagonist that inhibits the Cysteinyl leukotriene CysLT1 receptor. Each 10 mg film-coated Loctril tablet contains 10.4 mg Montelukast sodium, which is equivalent to 10 mg of Montelukast.
Asthma is a lung condition that makes the primary airways—known as the bronchi—in the lungs swollen and inflamed all of the time. People who have asthma are more sensitive than other people to things inhaled from the environment, known as triggers.
Asthma is a chronic disease involving the airways in the lungs.
Asthma is a condition in which your airways narrow and swell and may produce extra mucus.
This can make breathing difficult and trigger coughing, a whistling sound (wheezing) when you breathe out, and shortness of breath.
Asthma is a condition in which your airways narrow and swell and produce extra mucus. This can make breathing difficult and trigger coughing, wheezing and shortness of breath. For some people, asthma is a minor nuisance.
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
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.
- 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
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
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.
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
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.
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.
2. WHAT IS ASTHMA?WHAT IS ASTHMA?
• Asthma is described as a diseaseAsthma is described as a disease
that causes narrowing of thethat causes narrowing of the
airways and constricted breathing.airways and constricted breathing.
• The usual symptoms of asthmaThe usual symptoms of asthma
include wheezing, shortness ofinclude wheezing, shortness of
breath, tightness in the chest etc.,breath, tightness in the chest etc.,
ranging in severity to a liferanging in severity to a life
threatening condition.threatening condition.
3. 08.07.1708.07.17
SaAICSaAIC
FSM-PVFSM-PV
Definition of
asthma
Asthma is a chronic inflammatory disorder of the airways
in which many cells play a role.
The chronic inflammation causes an associated increase in
airway hyperresponsiveness that leads to recurrent episodes
of wheezing, breathlessness, chest tightness and coughing
particularly at night or early morning.
These episodes are usually associated with widespread but
variable airflow obstruction that is often reversible either
spontaneously or with treatment.
4. WHATWHAT ISIS OCCUPATIONOCCUPATION ALASTHMA?ALASTHMA?
Occupational asthma is a form ofOccupational asthma is a form of
asthma in which the symptoms areasthma in which the symptoms are
caused or aggravated by the workplacecaused or aggravated by the workplace
environment. Unlike other forms ofenvironment. Unlike other forms of
asthma, occupational asthma isasthma, occupational asthma is
preventable and possibly curable ifpreventable and possibly curable if
diagnosed early.diagnosed early.
6. What is OccupationalWhat is Occupational
Asthma?Asthma?
Some substances canSome substances can
cause allergies if youcause allergies if you
breathe them in. Theybreathe them in. They
are called sensitisers.are called sensitisers.
They can causeThey can cause
permanent damage topermanent damage to
your nose, throat andyour nose, throat and
lungs.lungs.
9. WHO MAY DEVELOPWHO MAY DEVELOP
WORKPLACE INDUCEDWORKPLACE INDUCED
ASTHMA?ASTHMA?• Certainly not all workers exposed to irritant chemicals, fumes,Certainly not all workers exposed to irritant chemicals, fumes,
dusts, allergens etc at their workplace will develop occupationaldusts, allergens etc at their workplace will develop occupational
asthma. A number of factors are known to increase the risk andasthma. A number of factors are known to increase the risk and
these include:these include:
– past history of asthma and/or allergy;past history of asthma and/or allergy;
– family history of asthma;family history of asthma;
– smoking; andsmoking; and
– low physical fitness.low physical fitness.
• Other factors such as respiratory infections and seasonalOther factors such as respiratory infections and seasonal
reactions to environmental allergens (pollens, mould spores) canreactions to environmental allergens (pollens, mould spores) can
make a worker more susceptible to the danger of air pollutants inmake a worker more susceptible to the danger of air pollutants in
the workplacethe workplace
10. PathophysiologyPathophysiology
• Hallmark is narrowing of bronchial airwayHallmark is narrowing of bronchial airway
diameter secondary to:diameter secondary to:
a. Smooth muscle contractiona. Smooth muscle contraction
b. Airway edemab. Airway edema
c. Respiratory vascular congestionc. Respiratory vascular congestion
d. Increase in airway secretionsd. Increase in airway secretions
e. Hypertrophy of basement membranee. Hypertrophy of basement membrane
• Other respiratory changes include:Other respiratory changes include:
a. Decrease in expiratory flow ratesa. Decrease in expiratory flow rates
b. Increased respiratory workload and muscleb. Increased respiratory workload and muscle
fatiguefatigue
c. Ventilation-perfusion mismatchc. Ventilation-perfusion mismatch
d. Arterial blood gas abnormalitiesd. Arterial blood gas abnormalities
e. Pulmonary hypertensione. Pulmonary hypertension
11. What is the Pathophysiology?What is the Pathophysiology?
• Trigger FactorTrigger Factor
• Mast cellMast cell
• Mediators :Mediators :
histamine,prostaglandin,leukotrienes,as well ashistamine,prostaglandin,leukotrienes,as well as
cytokines.cytokines.
• Inflammatory cellsInflammatory cells
• Sustained Inflammatory responseSustained Inflammatory response
• Contraction of airway smooth musclesContraction of airway smooth muscles
(Bronchoconstriction)(Bronchoconstriction)
12. Pathophysiology (Cont.)Pathophysiology (Cont.)
• Airway wall swelling (mucosal edema)Airway wall swelling (mucosal edema)
• Airway hyper responsivenessAirway hyper responsiveness
• Chronic changesChronic changes
• Hypertrophy of the smooth muscles, thickening ofHypertrophy of the smooth muscles, thickening of
the basement membranethe basement membrane
• Airway remodelingAirway remodeling
• There is good evidence that asthma occurs inThere is good evidence that asthma occurs in
families.families.
13. What are the Triggering Factors?What are the Triggering Factors?
• Domestic dust mitesDomestic dust mites
• Air pollutionAir pollution
• Tobacco smokeTobacco smoke
• Occupational irritantsOccupational irritants
• CockroachCockroach
• Animal with furAnimal with fur
• PollenPollen
20. 08.07.1708.07.17
SaAICSaAIC
FSM-PVFSM-PV
bronchial asthma
many parameters. any correlations
inflammation
bronchial obstruction
symptoms
signs
hyperresponsiveness
compliance
allergy
quality of life
reliever drugs
environment
work
remodeling
exacerbation
drug adverse reactions
?
?
?
controller drugs
21. 08.07.1708.07.17
patient report
SaAICSaAIC
FSM-PVFSM-PV
symptoms
3. Nat ura dei sintomi
3.1. Respiratori :
Tosse Si No ND
Espettorazione Si No ND
Oppressione toracica Si No ND
Sibili/fischi Si No ND
Difficolta’ respiratoria a riposo Si No ND
Difficolta’ respiratoria da sforzo Si No ND
Disfonia Si No ND
3.2. Generali :
Febbre Si No ND
Brividi Si No ND
Dolori muscolari o articolari Si No ND
Altri : …………………………………………………………………………………………………………………..
3.3. Rinite :
Ostruzione nasale Si No ND
Rinorrea Si No ND
Starnutazione Si No ND
Prurito nasale/ faringeo Si No ND
3.4. Congiuntivite :
Prurito oculare Si No ND Lacrimazione
Si No ND
Eritema congiuntivale Si No ND
3.5. Cutanei :
Orticaria / eritema cutaneo Si No ND
Eczema (delle mani) Si No ND
1. Cronologia dei sintomi respiratori
-Intervallo tra l’inizio dell’esposizione professionale e l’inizio dei sintomi : ……… mesi
- Intervallo tra l’inizio dei sintomi e il presente questionario : ……… mesi
- Intervallo tra l’ultima esposizione professionale e il presente questionario : ……… mesi
5. Relazione “lavoro-sintomi respiratori” :
- « Come sta dal punto di vista respiratorio nei giorni in cui lavora rispetto ai giorni in cui non lavora ?»:
Meglio Nello stesso modo Peggio
Se Peggio o Meglio, precisi (sono possibili piu’ risposte):
questionnaire
wheezing
breathlessness
chest tightness
coughing
...............
25. ClassificationClassification
• Mild intermittent asthmaMild intermittent asthma
a. Mild asthma symptoms once or twicea. Mild asthma symptoms once or twice
weeklyweekly
b. Nighttime asthma two or fewer timesb. Nighttime asthma two or fewer times
per monthper month
c. Pulmonary function tests are 80% orc. Pulmonary function tests are 80% or
more of predicted normalmore of predicted normal
d. PEF variability less than 20%d. PEF variability less than 20%
26. ClassificationClassification
• Mild persistent asthmaMild persistent asthma
a. Symptoms more than two times pera. Symptoms more than two times per
week but less than once per dayweek but less than once per day
b. Nighttime asthma more than two timesb. Nighttime asthma more than two times
per monthper month
c. Pulmonary function tests 80% or morec. Pulmonary function tests 80% or more
of predicted normalof predicted normal
d. PEF variability 20 to 30%d. PEF variability 20 to 30%
27. ClassificationClassification
• Moderate persistent asthmaModerate persistent asthma
a. Daily asthma symptoms with two ora. Daily asthma symptoms with two or
more exacerbations per weekmore exacerbations per week
b. Nighttime asthma more than once perb. Nighttime asthma more than once per
weekweek
c. Pulmonary function tests more 60 andc. Pulmonary function tests more 60 and
less than 80% predicted normalless than 80% predicted normal
d. PEF variability more than 30%d. PEF variability more than 30%
28. ClassificationClassification
• Severe persistent asthmaSevere persistent asthma
a. Continual symptoms with frequenta. Continual symptoms with frequent
exacerbationsexacerbations
b. Frequent nighttime asthmab. Frequent nighttime asthma
c. Pulmonary function tests 60% or lessc. Pulmonary function tests 60% or less
predicted normalpredicted normal
d. PEF variability more than 30%d. PEF variability more than 30%
29. Confirming the
diagnosis of
occupational asthma
• Specific challenge testsSpecific challenge tests
= international golden standard for diagnosis= international golden standard for diagnosis
of occupational asthmaof occupational asthma
• to prove the cause-effect relationshipto prove the cause-effect relationship
between the agent from the workplacebetween the agent from the workplace
and the asthmatic reaction in individualand the asthmatic reaction in individual
levellevel
30. TestsTests
• Pulmonary function tests; increase in FEVPulmonary function tests; increase in FEV11 afterafter
aa ββ--agonist or PEFagonist or PEF
• CBC: detect eosinophilia in atopic patientsCBC: detect eosinophilia in atopic patients
• IgEIgE
• Sputum exam: May show eosinophilia orSputum exam: May show eosinophilia or
Curschmann’s spiralsCurschmann’s spirals
• Wright peak flow measurementWright peak flow measurement
• Pulse oximetryPulse oximetry
• Chest filmChest film
• Arterial blood gas measurementArterial blood gas measurement
31. Occupational asthma,Occupational asthma,
diagnosticsdiagnostics
• Work related asthmatic symptomsWork related asthmatic symptoms
• Exposure to a sensitizing agent atExposure to a sensitizing agent at
workwork
• Cause-effect relationship between theCause-effect relationship between the
exposure material and asthmaexposure material and asthma
– Sensitization (skin prick tests/specific IgESensitization (skin prick tests/specific IgE
antibodies)antibodies)
– Positive provocation testPositive provocation test
32. Diagnostics ofDiagnostics of
occupational asthmaoccupational asthma
• PEF-surveillance at home andPEF-surveillance at home and
at the workplace always, ifat the workplace always, if
possiblepossible
– Positive finding supports the diagnosisPositive finding supports the diagnosis
– Negative finding does not exclude theNegative finding does not exclude the
diagnosisdiagnosis
33. Prerequirements forPrerequirements for
challenge testschallenge tests
1. Clinical picture fits with occupational1. Clinical picture fits with occupational
asthma, but the diagnosis has not yetasthma, but the diagnosis has not yet
been verifiedbeen verified
2. Asthma is stable. Inhaled steroid may be2. Asthma is stable. Inhaled steroid may be
used, stable dose every evening.used, stable dose every evening.
3. Differential diagnostics done.3. Differential diagnostics done.
4. No contraindications to challenge tests.4. No contraindications to challenge tests.
34. Prerequirements forPrerequirements for
challenge testschallenge tests
1. Clinical picture fits with occupational1. Clinical picture fits with occupational
asthma, but the diagnosis has not yetasthma, but the diagnosis has not yet
been verifiedbeen verified
2. Asthma is stable. Inhaled steroid may be2. Asthma is stable. Inhaled steroid may be
used, stable dose every evening.used, stable dose every evening.
3. Differential diagnostics done.3. Differential diagnostics done.
4. No contraindications to challenge tests.4. No contraindications to challenge tests.
35. Contraindications toContraindications to
challenge testschallenge tests
• Acute infectionsAcute infections
• Unstable asthma or some other diseaseUnstable asthma or some other disease
• Poor lung functionPoor lung function
• Facts, that prevent proper interpretation of theFacts, that prevent proper interpretation of the
challenge tests (e.g. non co-operating patient)challenge tests (e.g. non co-operating patient)
• Highly toxic or irritative substancesHighly toxic or irritative substances
• Anaphylactic or otherwise very strong reactionAnaphylactic or otherwise very strong reaction
to the challenge material in historyto the challenge material in history
36. Requirements, whenRequirements, when
performing challengeperforming challenge
teststests
• 24-hour follow up and facilities to treat24-hour follow up and facilities to treat
acute and late asthmatic ( and other)acute and late asthmatic ( and other)
reactionsreactions
• Aduquate challenge chamber and wellAduquate challenge chamber and well
trained stafftrained staff
37. Challenge chamberChallenge chamber
• Adequate ventilationAdequate ventilation
• Safety of the patientSafety of the patient
• Safety of the personnelSafety of the personnel
– exhaust ventilationexhaust ventilation
– easy to cleaneasy to clean
• Facilities for generation of dusts, vaporsFacilities for generation of dusts, vapors
and aerosols in controlled concentrationsand aerosols in controlled concentrations
38. Challenge test withChallenge test with
active agentactive agent
• Commercial allergen extractsCommercial allergen extracts
• Tests simulating work tasksTests simulating work tasks
(patient handles the material from(patient handles the material from
workplace)workplace)
– Individual planning: challenge materia,Individual planning: challenge materia,
concentration, duration of test e.g.concentration, duration of test e.g.
– Occupational hygienist/chemistOccupational hygienist/chemist
consultations when neededconsultations when needed
– Controlled concentrationsControlled concentrations
39. Criteria for aCriteria for a
positive provocationpositive provocation
test reactiontest reaction
• minimum 20% FEVminimum 20% FEV11 /PEF decrease/PEF decrease
compared to baseline before exposurecompared to baseline before exposure
and to control testand to control test
• tests with allergen extractstests with allergen extracts
– minimum 15% decrease in immediateminimum 15% decrease in immediate
reactionreaction
(during one hour after challenge)(during one hour after challenge)
40. Criteria for aCriteria for a
positive provocationpositive provocation
test reactiontest reaction
• Findings supporting positive challenge test:Findings supporting positive challenge test:
– symptomssymptoms
– wheezing raleswheezing rales
– dose-responsedose-response
– increase in hyperreactivityincrease in hyperreactivity
– recovery of the reaction on the following dayrecovery of the reaction on the following day
– increase in exhaled nitric oxide?increase in exhaled nitric oxide?
– increase in peripheral resistance (impulseincrease in peripheral resistance (impulse
oscillometry)oscillometry)
41. Diagnostics ofDiagnostics of
occupational asthmaoccupational asthma
• Provocation tests not necessaryProvocation tests not necessary
– typical work related asthmatic symptomstypical work related asthmatic symptoms
– exposure to a known sensitizerexposure to a known sensitizer
– sensitization confirmedsensitization confirmed
– asthma and work related bronchoconstrictionasthma and work related bronchoconstriction
confirmed (asthma diagnosis done, PEF-confirmed (asthma diagnosis done, PEF-
surveillance at home and at the workplacesurveillance at home and at the workplace
typical for occupational asthma)typical for occupational asthma)
42. Procedures afterProcedures after
diagnosing occupationaldiagnosing occupational
asthmaasthma
• Statements neededStatements needed (medical certificates,(medical certificates,
Announcement of a new occupational disease to theAnnouncement of a new occupational disease to the
Register of Occupational Diseases as well to localRegister of Occupational Diseases as well to local
officials in Finland e.g.)officials in Finland e.g.)
• Stopping/minimizing exposure at theStopping/minimizing exposure at the
workplaceworkplace
• Treatment and follow up of asthmaTreatment and follow up of asthma
Aim:Aim: To discontinue exposure in order toTo discontinue exposure in order to
prevent the disease from worsening/gettingprevent the disease from worsening/getting
chronic or make it possible for the disease tochronic or make it possible for the disease to
heal totallyheal totally
43. Procedures after diagnosingProcedures after diagnosing
occupational asthmaoccupational asthma
How to discontinue/minimizeHow to discontinue/minimize
exposure?exposure?
• Changing agents used in the workplaceChanging agents used in the workplace
• Changing work tasks/working area/environmentChanging work tasks/working area/environment
(replacement in another kind of work task or working(replacement in another kind of work task or working
environment)environment)
• Changing the work tasksChanging the work tasks
• Restrictions to the workerRestrictions to the worker
• Use of respiratory protective deviceUse of respiratory protective device
• Re-education to another occupation ( in FinlandRe-education to another occupation ( in Finland
legally set that the insurance company of thelegally set that the insurance company of the
employer is responsible for re-education)employer is responsible for re-education)
• RetirementRetirement
45. TreatmentTreatment
Mild intermittent asthmaMild intermittent asthma
a. No daily medication for long-terma. No daily medication for long-term
controlcontrol
b. Short-acting: bronchodilatorb. Short-acting: bronchodilator
(inhaled(inhaled ββ2-agonist) as needed for2-agonist) as needed for
symptomssymptoms
46. TreatmentTreatment
Mild persistent asthmaMild persistent asthma
a. One of the following as a daily medicationa. One of the following as a daily medication
for long-term control:for long-term control:
1. Anti-inflammation medication (inhaled1. Anti-inflammation medication (inhaled
Corticosteroid 200-500Corticosteroid 200-500μμgg
2. Sustained-release Theophylline2. Sustained-release Theophylline
3. Disodium cromoglycate3. Disodium cromoglycate
4. Nedocromil sodium4. Nedocromil sodium
b. Short-acting: inhaledb. Short-acting: inhaled ββ2-agonist2-agonist
47. TreatmentTreatment
Moderate persistent asthmaModerate persistent asthma
a. Daily medication for long-term contrala. Daily medication for long-term contral
1. Inhaled Corticosteroid 500-8001. Inhaled Corticosteroid 500-800μμgandgand
long-acting bronchodilator (long-actinglong-acting bronchodilator (long-acting
inhaledinhaled ββ2-agonist, sustained-release2-agonist, sustained-release
Theophylline, orTheophylline, or long-actinglong-acting ββ2-agonist2-agonist
tablettablet
b. Short-acting: inhaledb. Short-acting: inhaled ββ2-agonist as2-agonist as
needed for symptomsneeded for symptoms
48. TreatmentTreatment
Severe persistent asthmaSevere persistent asthma
a. Daily medications for long-term controla. Daily medications for long-term control
1. Inhaled Corticosteroid 800-20001. Inhaled Corticosteroid 800-2000 μμgg
2. Long-acting2. Long-acting ββ2-agonist, sustained-2-agonist, sustained-
release Theophylline, or long-actingrelease Theophylline, or long-acting
ββ2-agonist tablets2-agonist tablets
3. Corticosteroid tablets or syrup3. Corticosteroid tablets or syrup
b. Short-acting: inhaledb. Short-acting: inhaled ββ2-agonist as2-agonist as
needed for symptomsneeded for symptoms
49. How to Control ExposureHow to Control Exposure
EmployerEmployer
• Minimise ExposureMinimise Exposure
• Provide informationProvide information
• Provide trainingProvide training
• Supply PPESupply PPE
• Supply ventilationSupply ventilation
• Comply with the lawComply with the law
EmployeeEmployee
• Be aware of asthmaBe aware of asthma
• Take care withTake care with
substancessubstances
• Use PPEUse PPE
• Maintain PPEMaintain PPE
• Report symptomsReport symptoms
50. OccupatiOnal asthmaOccupatiOnal asthma
checklistchecklist
• Remember, if you have trouble withRemember, if you have trouble with
wheezing, coughing or shortness of breath atwheezing, coughing or shortness of breath at
work, you could have occupational asthma:work, you could have occupational asthma:
• Consult your physician. He or she may suggest aConsult your physician. He or she may suggest a
pulmonary function test.pulmonary function test.
• See your work supervisor for details about potentialSee your work supervisor for details about potential
hazards in your work environment.hazards in your work environment.
• Have the tests and evaluation required to prove theHave the tests and evaluation required to prove the
suspected occupational asthma and its cause.suspected occupational asthma and its cause.
• Seek your physician's advice about therapy forSeek your physician's advice about therapy for
occupational asthma.occupational asthma.
51. Emergency boxEmergency box
Treatment of severe asthmaTreatment of severe asthma
At homeAt home
• The patient is assessed. Tachycardia, a highThe patient is assessed. Tachycardia, a high
respiratory rate and inability to speak in sentencesrespiratory rate and inability to speak in sentences
indicate a severe attack.indicate a severe attack.
• If the PEF is less than 150L/min (in adult), anIf the PEF is less than 150L/min (in adult), an
ambulance should be called. (All doctors should carryambulance should be called. (All doctors should carry
peak flow meters.)peak flow meters.)
• Nebulized salbutamol 5 mg or terbutaline 10 mg isNebulized salbutamol 5 mg or terbutaline 10 mg is
administered.administered.
• Hydrocortisone sodium succinate 200 mg i.v. is given.Hydrocortisone sodium succinate 200 mg i.v. is given.
• Oxygen 40-60% is given if available.Oxygen 40-60% is given if available.
• Prednisolone 60 mg is given orally.Prednisolone 60 mg is given orally.
52. Emergency boxEmergency box
At hospitalAt hospital
• The patient is reassessed.The patient is reassessed.
• Oxygen 40-60%is given.Oxygen 40-60%is given.
• The PEF is measured using a low-reading peak flow meter, as an ordinaryThe PEF is measured using a low-reading peak flow meter, as an ordinary
meter measures only from 60L/min upwards. Measure Ometer measures only from 60L/min upwards. Measure O22 saturation with asaturation with a
pulse oximeter.pulse oximeter.
• Nebulized salbutamol 5 mg or terbutaline 10 mg is repeated andNebulized salbutamol 5 mg or terbutaline 10 mg is repeated and
administered 4-hourly.administered 4-hourly.
• Add nebulized ipratropiun bromide 0.5 mg to nebulizedAdd nebulized ipratropiun bromide 0.5 mg to nebulized
salbutamol/terbutaline.salbutamol/terbutaline.
• Hydorcortisone 200 mg i.v. is given 4-hourly for 24 hours.Hydorcortisone 200 mg i.v. is given 4-hourly for 24 hours.
• Predisolone is continued at 60 mg orally daily for 2 wks.Predisolone is continued at 60 mg orally daily for 2 wks.
• Arterial blood gases are measured; if the PaCOArterial blood gases are measured; if the PaCO22 is greater than 7 kpa,is greater than 7 kpa,
ventilation should be considered.ventilation should be considered.
• A chest x-ray is performed to exclude pneumothorax.A chest x-ray is performed to exclude pneumothorax.
• One of the following intravenous infusions is given if no improvement isOne of the following intravenous infusions is given if no improvement is
seen:seen: salbutamol 3-20salbutamol 3-20 μμg/min, or terbutaline 1.5-5.0g/min, or terbutaline 1.5-5.0 μμg/min.g/min.