Asthma or COPD?
More features favor COPD:
- Age >40 years
- Smoking history
- Chronic symptoms not fully relieved by SABA
- Previous LRTI requiring hospitalization
Diagnosis: COPD
This document discusses asthma-COPD overlap (ACO), where patients exhibit features of both asthma and chronic obstructive pulmonary disease (COPD). It defines the conditions and notes that distinguishing them can be difficult, especially in smokers and older adults. Patients with ACO features experience more exacerbations and poorer outcomes than those with asthma or COPD alone. The document provides guidance on diagnosing and initially treating ACO based on GINA and GOLD guidelines, emphasizing inhaled corticosteroids to reduce exacerbation risk in all patients with chronic airflow limitation. Further research is still needed to better classify and treat ACO phenotypes.
An update on the management of Idiopathic Pulmonary Fibrosis (IPF)Sarfraz Saleemi
This document provides a historical overview and update on the management of idiopathic pulmonary fibrosis (IPF). It discusses the evolution of IPF diagnosis and classification over time based on clinical and pathological criteria. Key risk factors for IPF like older age, family history, smoking and genetics are summarized. The document also reviews prognostic indicators, comorbidities, current pharmacological therapies including pirfenidone and nintedanib, and the multidisciplinary approach to diagnosis and management of IPF.
Hypersensitivity pneumonitis is a lung disease caused by an allergic reaction to inhaled organic dusts or chemicals. It can present acutely with fever and respiratory symptoms or chronically with fibrosis. The diagnosis is based on exposure history, symptoms improving away from exposure, and radiologic/pathologic findings. Treatment involves identifying and removing the causative agent along with corticosteroids in more severe cases. Prognosis depends on the severity and duration of exposure, with chronic forms at higher risk of permanent lung damage.
Practical approach to Idiopathic Pulmonary Fibrosis.Hiba Ashibany
This document provides information on idiopathic pulmonary fibrosis (IPF), including its causes, diagnosis, clinical features, prognosis, and treatment approaches. It summarizes that IPF is a progressive lung disease of unknown cause where scarring develops in the lungs. Diagnosis involves ruling out other conditions, imaging, and sometimes biopsies. Prognosis is generally poor with median survival of 3 years. Treatment includes drugs like pirfenidone and nintedanib that can slow disease progression in mild to moderate IPF.
1. The document discusses DLCO (diffusing capacity of the lungs for carbon monoxide), which measures the efficiency of the lungs in transporting oxygen across the alveolar capillary membrane.
2. It describes the single breath hold method for measuring DLCO, which involves inhaling a gas mixture containing carbon monoxide and exhaling into a collection device to measure gas concentrations.
3. DLCO can be lowered in conditions that decrease the surface area for diffusion like emphysema, or increase the thickness of the alveolar capillary membrane like interstitial lung diseases.
2 types (a) cellular NSIP
(b) Fibrotic NSIP (more common)
Fibrosis may involve alveolar septa, peribronchivascular interstitium, interlobular septa and visceral pleura.
Prognosis of fibrotic NSIP is worse , cellular NSIP has good prognosis.
HRCT finding may show both, airspace and interstitial patterns
This document provides an overview of asthma-COPD overlap syndrome (ACOS). It discusses how asthma and COPD were traditionally viewed as distinct conditions but some patients exhibit features of both. Patients with ACOS have worse health outcomes than those with asthma or COPD alone. The document reviews clinical features of ACOS and provides guidance on diagnosing patients based on their symptoms, lung function tests, and other features. It also discusses treatment approaches for ACOS.
This document provides information on the pulmonary manifestations of aspergillosis. It discusses the various types of aspergillosis including allergic, colonization, and invasive forms. Key points include:
- Aspergillus fumigatus is the most common pathogenic species. It produces gliotoxin which inhibits the immune response.
- Allergic forms include allergic bronchopulmonary aspergillosis (ABPA), bronchocentric granulomatosis, and extrinsic allergic alveolitis. Invasive forms include chronic necrotizing pulmonary aspergillosis.
- Diagnosis involves radiology, culture, serology and biopsy. Treatment depends on the specific
This document discusses various asthma phenotypes and endotypes. It begins by defining asthma and noting that it is a heterogeneous syndrome rather than a single disease. It then discusses several clinically observed phenotypes categorized by factors like age of onset, severity, triggers, and treatment response. Molecular mechanisms like T-helper type 2 inflammation are discussed and used to define endotypes. Specific phenotypes discussed in more depth include early onset allergic asthma, late onset eosinophilic asthma, aspirin exacerbated respiratory disease, exercise induced asthma, obesity related asthma, and neutrophilic asthma. Biomarkers, genetics, and treatment approaches are covered for each phenotype.
This document defines non-resolving pneumonia and discusses its causes and diagnostic evaluation. Non-resolving pneumonia is defined as persistence of clinical symptoms and radiographic abnormalities for longer than expected despite adequate antibiotic therapy. Common causes include inappropriate antibiotic therapy, complications of the initial infection, host factors, and presence of resistant or unusual pathogens. A thorough diagnostic evaluation includes assessing treatment response, looking for complications or superinfections, evaluating for unusual organisms, and examining host immune function. Radiological imaging, bronchoscopy with protected specimen brushing or biopsy, and CT-guided biopsies can help identify causative organisms or underlying conditions.
This document provides information on chronic obstructive pulmonary disease (COPD). It discusses the epidemiology, definition, risk factors, pathogenesis, pathology, classification, management, and exacerbations of COPD. Key points include: cigarette smoking is the primary cause of COPD worldwide; the disease involves inflammation in the lungs from noxious particles leading to airflow limitation; emphysema and chronic bronchitis are the major pathological changes; severity is classified based on lung function tests; and management involves reducing risk factors, treating stable COPD, and managing exacerbations.
This document discusses the approach to bullous lung disease. It defines a bulla as a large air-containing space within the lung larger than 1 cm in diameter. Bullae can occur with emphysema, pulmonary fibrosis, or in otherwise normal lungs. HRCT is useful for evaluating the size, number and relationships of bullae. Pulmonary function testing may show obstructive lung disease, hyperinflation and reduced diffusion capacity. For surgical candidates, bullectomy or lung volume reduction surgery may be considered to treat symptoms or complications like spontaneous pneumothorax.
This document discusses asthma and COPD, including key differences and updates. It provides an overview of asthma, describing it as a chronic inflammatory airway disorder characterized by recurrent wheezing, breathlessness, and coughing. It also provides an overview of COPD, describing it as a common lung disease associated with exposure to noxious particles or gases. The document reviews epidemiology, pathophysiology, diagnosis, management, and updates from the GINA and GOLD guidelines for both conditions.
Interstitial Lung Diseases [ILD] Approach to ManagementArun Vasireddy
Diffuse (interstitial) lung disease includes a wide variety of relatively uncommon conditions presenting with characteristic clusters of clinical features and marked by an immune response. There are over 200 specific diffuse lung diseases, many of unknown etiology. The combined incidence is 50 per 100,000, or 1 in 2000 people. Because these conditions cause aberrant lung function, morbidity and mortality due to lung injury and fibrosis are not uncommon. Both environmental and genetic factors are believed to contribute to the development of diffuse lung disease. Antigen processing and presentation are important in the development of the immune response seen in the disease, and it is thought that the likely candidate genes predisposing patients to this category of disease are those of the major histocompatibility complex. Genes that affect the immune, inflammatory, and fibrotic processes may also influence who develops the disease. If we can identify the genes that cause diseases characterized by lung injury and fibrosis, we can eventually develop genetic interventional approaches to treatment.
New technology called Electromagnetic Navigation Bronchoscopy® (ENB) that uses virtual bronchoscopy and real time 3-dimensional CT images that enable me to localize these peripheral lung nodules for diagnosis and treatment. This outpatient procedure is minimally invasive and therefore has a small risk of pneumothorax (2-3%) and its published diagnostic yield rates range from 67% - 86%
Bronchiectasis is defined as an irreversible dilation of the airways called bronchi or bronchioles. It can be classified based on the shape and extent of involvement. The dilation is caused by destruction of the muscle and elastic tissue in the bronchial wall. Common causes include cystic fibrosis, tuberculosis, and pneumonia. Symptoms include productive cough, sputum, and hemoptysis. Diagnosis involves imaging like chest X-ray or CT scan showing tram track sign. Treatment focuses on improving secretion clearance with chest physiotherapy and antibiotics to eradicate bacteria. Surgery may be considered for localized lesions that do not respond to medical treatment or for recurrent hemoptysis.
This document provides guidance on diagnosing and treating patients with asthma, COPD, or asthma-COPD overlap syndrome (ACOS). It outlines a step-wise approach including 1) determining if a patient has chronic airways disease, 2) making a syndromic diagnosis of asthma, COPD, or ACOS, 3) confirming with spirometry, 4) initiating initial treatment, and 5) referring for further testing if needed. Key points include distinguishing features of asthma and COPD, the overlapping characteristics of ACOS, and ensuring appropriate controller therapy is used depending on the diagnosis. The goal is to accurately diagnose this common problem to optimize treatment outcomes.
Interpretation of Pulmonary Function TestDrSuman Roy
This document provides an overview of pulmonary function tests (PFTs) including:
- PFTs are used to diagnose symptomatic diseases, screen for early asymptomatic diseases, prognosticate known diseases, and monitor response to treatment.
- Spirometry specifically measures airflow and lung volumes through tests like FEV1 and FVC to classify obstructive, restrictive, or pulmonary vascular lung diseases.
- COPD severity is staged based on post-bronchodilator FEV1 levels according to GOLD criteria, with lower FEV1 indicating more severe COPD.
Asthma management phenotype based approachGamal Agmy
Phenotypes and endotypes are approaches to classifying asthma subtypes based on clinical characteristics and underlying biological mechanisms. The document discusses several potential asthma endotypes including:
1) TH2-high endotypes like early-onset allergic asthma characterized by genetics predisposing to TH2 cytokines, biomarkers like elevated IgE and eosinophils, and response to anti-IgE therapy.
2) Late-onset eosinophilic asthma characterized by persistent sputum eosinophilia despite steroids and potential response to anti-IL5 therapy.
3) Aspirin-exacerbated respiratory disease which may be a similar endotype to intrinsic or allergic asthma due to acquired NSA
This document discusses expanding understanding of asthma phenotypes. It defines 9 asthma phenotypes in 3 categories: trigger-induced (allergic, non-allergic, aspirin-exacerbated respiratory disease, infection, exercise-induced), clinical presentation (pre-asthma wheezing in infants, exacerbation-prone), and inflammatory markers (eosinophilic and neutrophilic). Recognizing phenotypes is important for interpreting studies, comparisons between studies, and genetics research correlating phenotype to genotype.
The document discusses the role of capnography in the emergency room. It begins by defining capnography as the noninvasive measurement of carbon dioxide levels in exhaled breath. It then covers the basic science behind capnography, different equipment used, how to interpret the waveform, and various clinical uses in pre-hospital and emergency room settings. Specific topics include assessing ventilation, optimizing ventilation rates, evaluating shock, pulmonary embolism, asthma, mechanical obstructions, and emphysema. The document emphasizes that capnography can provide valuable information about a patient's ventilation, perfusion, and metabolism.
Allergic BronchoPulmonary Aspergillosis (ABPA) is an inflammatory lung disease caused by an allergic response to the fungus Aspergillus fumigatus. It mostly affects people with asthma or cystic fibrosis. ABPA is characterized by elevated IgE levels, eosinophilia, fleeting pulmonary opacities on imaging, and bronchial wall thickening or bronchiectasis. Diagnosis requires specific criteria involving immunological markers and radiological findings. Management involves use of oral steroids and antifungal azole drugs.
COPD systemic effects and comorbiditiesAshique Ali
This document discusses systemic inflammation and comorbidities in COPD. It states that COPD is associated with various important comorbidities that contribute to its overall severity. Markers of systemic inflammation are consistently increased in COPD patients, including CRP, fibrinogen, and cytokines. This systemic inflammation is thought to be caused by spillover from the lungs and an independent pro-inflammatory phenotype. The systemic inflammation is linked to several comorbidities like cardiovascular disease, diabetes, osteoporosis, and cancer. Cardiovascular disease is a major cause of death in COPD patients. Endothelial dysfunction and a pro-coagulant state brought on by systemic inflammation may also contribute to comorbidities.
The document provides information on the Global Initiative for Chronic Obstructive Lung Disease (GOLD) including its objectives to increase awareness of COPD, improve diagnosis and management, and stimulate research. It defines COPD as a preventable disease characterized by airflow limitation caused by an abnormal inflammatory response to noxious particles. The document also outlines the classification of COPD severity based on lung function tests, risk factors, pathogenesis, management approaches, and goals of reducing symptoms and disease progression.
Pulmonary arterial hypertension (PAH) is high blood pressure in the arteries connecting the heart and lungs. The document defines PAH and related types, and discusses risk factors, symptoms, diagnosis, classification, complications and treatments. PAH has no known cause in many cases, but can result from other conditions. Common symptoms include shortness of breath, chest pain and fatigue. Diagnosis involves medical tests and right heart catheterization. Treatment aims to improve symptoms and outcomes through medications, supplemental oxygen, diet changes and exercise.
Poncet's disease is a rare condition where a patient presents with symmetrical polyarthritis involving large joints like the knees, which can precede, follow, or occur simultaneously with active extrapulmonary tuberculosis. The diagnosis is largely clinical, made by excluding other potential causes and supported by a strongly positive tuberculin test result. The arthritis resolves completely within days of starting anti-tuberculosis treatment, confirming the diagnosis. It is considered a para-infective arthritis triggered by a tuberculosis infection elsewhere in the body.
This document discusses various inhalation delivery systems used for asthma and COPD treatment. It describes pressurized metered dose inhalers, dry powder inhalers, nebulizers, and the drugs commonly used with each. The advantages and disadvantages of each delivery system are provided. For asthma, inhaled glucocorticoids, long-acting beta-agonists, cromolyn, and short-acting beta-agonists are discussed. For COPD, long-acting beta-agonists, anticholinergics like tiotropium, and inhaled corticosteroids alone or in combination are covered. Proper inhaler technique is emphasized for optimal treatment.
This document discusses asthma-COPD overlap syndrome (ACOS). It defines asthma and COPD, noting their differences and similarities. Both are chronic inflammatory airway diseases but COPD is characterized by persistent airflow limitation and progressive lung function decline while asthma is often reversible. The document then discusses clinical features that can help distinguish asthma from COPD. It notes that some patients have features of both diseases, termed ACOS. Spirometry, biomarkers, imaging and response to treatment are discussed to help identify ACOS. The inflammatory patterns in asthma and COPD are compared, showing that eosinophilic inflammation is more prominent in asthma while neutrophilic inflammation dominates in COPD.
This document discusses various asthma phenotypes and endotypes. It begins by defining asthma and noting that it is a heterogeneous syndrome rather than a single disease. It then discusses several clinically observed phenotypes categorized by factors like age of onset, severity, triggers, and treatment response. Molecular mechanisms like T-helper type 2 inflammation are discussed and used to define endotypes. Specific phenotypes discussed in more depth include early onset allergic asthma, late onset eosinophilic asthma, aspirin exacerbated respiratory disease, exercise induced asthma, obesity related asthma, and neutrophilic asthma. Biomarkers, genetics, and treatment approaches are covered for each phenotype.
This document defines non-resolving pneumonia and discusses its causes and diagnostic evaluation. Non-resolving pneumonia is defined as persistence of clinical symptoms and radiographic abnormalities for longer than expected despite adequate antibiotic therapy. Common causes include inappropriate antibiotic therapy, complications of the initial infection, host factors, and presence of resistant or unusual pathogens. A thorough diagnostic evaluation includes assessing treatment response, looking for complications or superinfections, evaluating for unusual organisms, and examining host immune function. Radiological imaging, bronchoscopy with protected specimen brushing or biopsy, and CT-guided biopsies can help identify causative organisms or underlying conditions.
This document provides information on chronic obstructive pulmonary disease (COPD). It discusses the epidemiology, definition, risk factors, pathogenesis, pathology, classification, management, and exacerbations of COPD. Key points include: cigarette smoking is the primary cause of COPD worldwide; the disease involves inflammation in the lungs from noxious particles leading to airflow limitation; emphysema and chronic bronchitis are the major pathological changes; severity is classified based on lung function tests; and management involves reducing risk factors, treating stable COPD, and managing exacerbations.
This document discusses the approach to bullous lung disease. It defines a bulla as a large air-containing space within the lung larger than 1 cm in diameter. Bullae can occur with emphysema, pulmonary fibrosis, or in otherwise normal lungs. HRCT is useful for evaluating the size, number and relationships of bullae. Pulmonary function testing may show obstructive lung disease, hyperinflation and reduced diffusion capacity. For surgical candidates, bullectomy or lung volume reduction surgery may be considered to treat symptoms or complications like spontaneous pneumothorax.
This document discusses asthma and COPD, including key differences and updates. It provides an overview of asthma, describing it as a chronic inflammatory airway disorder characterized by recurrent wheezing, breathlessness, and coughing. It also provides an overview of COPD, describing it as a common lung disease associated with exposure to noxious particles or gases. The document reviews epidemiology, pathophysiology, diagnosis, management, and updates from the GINA and GOLD guidelines for both conditions.
Interstitial Lung Diseases [ILD] Approach to ManagementArun Vasireddy
Diffuse (interstitial) lung disease includes a wide variety of relatively uncommon conditions presenting with characteristic clusters of clinical features and marked by an immune response. There are over 200 specific diffuse lung diseases, many of unknown etiology. The combined incidence is 50 per 100,000, or 1 in 2000 people. Because these conditions cause aberrant lung function, morbidity and mortality due to lung injury and fibrosis are not uncommon. Both environmental and genetic factors are believed to contribute to the development of diffuse lung disease. Antigen processing and presentation are important in the development of the immune response seen in the disease, and it is thought that the likely candidate genes predisposing patients to this category of disease are those of the major histocompatibility complex. Genes that affect the immune, inflammatory, and fibrotic processes may also influence who develops the disease. If we can identify the genes that cause diseases characterized by lung injury and fibrosis, we can eventually develop genetic interventional approaches to treatment.
New technology called Electromagnetic Navigation Bronchoscopy® (ENB) that uses virtual bronchoscopy and real time 3-dimensional CT images that enable me to localize these peripheral lung nodules for diagnosis and treatment. This outpatient procedure is minimally invasive and therefore has a small risk of pneumothorax (2-3%) and its published diagnostic yield rates range from 67% - 86%
Bronchiectasis is defined as an irreversible dilation of the airways called bronchi or bronchioles. It can be classified based on the shape and extent of involvement. The dilation is caused by destruction of the muscle and elastic tissue in the bronchial wall. Common causes include cystic fibrosis, tuberculosis, and pneumonia. Symptoms include productive cough, sputum, and hemoptysis. Diagnosis involves imaging like chest X-ray or CT scan showing tram track sign. Treatment focuses on improving secretion clearance with chest physiotherapy and antibiotics to eradicate bacteria. Surgery may be considered for localized lesions that do not respond to medical treatment or for recurrent hemoptysis.
This document provides guidance on diagnosing and treating patients with asthma, COPD, or asthma-COPD overlap syndrome (ACOS). It outlines a step-wise approach including 1) determining if a patient has chronic airways disease, 2) making a syndromic diagnosis of asthma, COPD, or ACOS, 3) confirming with spirometry, 4) initiating initial treatment, and 5) referring for further testing if needed. Key points include distinguishing features of asthma and COPD, the overlapping characteristics of ACOS, and ensuring appropriate controller therapy is used depending on the diagnosis. The goal is to accurately diagnose this common problem to optimize treatment outcomes.
Interpretation of Pulmonary Function TestDrSuman Roy
This document provides an overview of pulmonary function tests (PFTs) including:
- PFTs are used to diagnose symptomatic diseases, screen for early asymptomatic diseases, prognosticate known diseases, and monitor response to treatment.
- Spirometry specifically measures airflow and lung volumes through tests like FEV1 and FVC to classify obstructive, restrictive, or pulmonary vascular lung diseases.
- COPD severity is staged based on post-bronchodilator FEV1 levels according to GOLD criteria, with lower FEV1 indicating more severe COPD.
Asthma management phenotype based approachGamal Agmy
Phenotypes and endotypes are approaches to classifying asthma subtypes based on clinical characteristics and underlying biological mechanisms. The document discusses several potential asthma endotypes including:
1) TH2-high endotypes like early-onset allergic asthma characterized by genetics predisposing to TH2 cytokines, biomarkers like elevated IgE and eosinophils, and response to anti-IgE therapy.
2) Late-onset eosinophilic asthma characterized by persistent sputum eosinophilia despite steroids and potential response to anti-IL5 therapy.
3) Aspirin-exacerbated respiratory disease which may be a similar endotype to intrinsic or allergic asthma due to acquired NSA
This document discusses expanding understanding of asthma phenotypes. It defines 9 asthma phenotypes in 3 categories: trigger-induced (allergic, non-allergic, aspirin-exacerbated respiratory disease, infection, exercise-induced), clinical presentation (pre-asthma wheezing in infants, exacerbation-prone), and inflammatory markers (eosinophilic and neutrophilic). Recognizing phenotypes is important for interpreting studies, comparisons between studies, and genetics research correlating phenotype to genotype.
The document discusses the role of capnography in the emergency room. It begins by defining capnography as the noninvasive measurement of carbon dioxide levels in exhaled breath. It then covers the basic science behind capnography, different equipment used, how to interpret the waveform, and various clinical uses in pre-hospital and emergency room settings. Specific topics include assessing ventilation, optimizing ventilation rates, evaluating shock, pulmonary embolism, asthma, mechanical obstructions, and emphysema. The document emphasizes that capnography can provide valuable information about a patient's ventilation, perfusion, and metabolism.
Allergic BronchoPulmonary Aspergillosis (ABPA) is an inflammatory lung disease caused by an allergic response to the fungus Aspergillus fumigatus. It mostly affects people with asthma or cystic fibrosis. ABPA is characterized by elevated IgE levels, eosinophilia, fleeting pulmonary opacities on imaging, and bronchial wall thickening or bronchiectasis. Diagnosis requires specific criteria involving immunological markers and radiological findings. Management involves use of oral steroids and antifungal azole drugs.
COPD systemic effects and comorbiditiesAshique Ali
This document discusses systemic inflammation and comorbidities in COPD. It states that COPD is associated with various important comorbidities that contribute to its overall severity. Markers of systemic inflammation are consistently increased in COPD patients, including CRP, fibrinogen, and cytokines. This systemic inflammation is thought to be caused by spillover from the lungs and an independent pro-inflammatory phenotype. The systemic inflammation is linked to several comorbidities like cardiovascular disease, diabetes, osteoporosis, and cancer. Cardiovascular disease is a major cause of death in COPD patients. Endothelial dysfunction and a pro-coagulant state brought on by systemic inflammation may also contribute to comorbidities.
The document provides information on the Global Initiative for Chronic Obstructive Lung Disease (GOLD) including its objectives to increase awareness of COPD, improve diagnosis and management, and stimulate research. It defines COPD as a preventable disease characterized by airflow limitation caused by an abnormal inflammatory response to noxious particles. The document also outlines the classification of COPD severity based on lung function tests, risk factors, pathogenesis, management approaches, and goals of reducing symptoms and disease progression.
Pulmonary arterial hypertension (PAH) is high blood pressure in the arteries connecting the heart and lungs. The document defines PAH and related types, and discusses risk factors, symptoms, diagnosis, classification, complications and treatments. PAH has no known cause in many cases, but can result from other conditions. Common symptoms include shortness of breath, chest pain and fatigue. Diagnosis involves medical tests and right heart catheterization. Treatment aims to improve symptoms and outcomes through medications, supplemental oxygen, diet changes and exercise.
Poncet's disease is a rare condition where a patient presents with symmetrical polyarthritis involving large joints like the knees, which can precede, follow, or occur simultaneously with active extrapulmonary tuberculosis. The diagnosis is largely clinical, made by excluding other potential causes and supported by a strongly positive tuberculin test result. The arthritis resolves completely within days of starting anti-tuberculosis treatment, confirming the diagnosis. It is considered a para-infective arthritis triggered by a tuberculosis infection elsewhere in the body.
This document discusses various inhalation delivery systems used for asthma and COPD treatment. It describes pressurized metered dose inhalers, dry powder inhalers, nebulizers, and the drugs commonly used with each. The advantages and disadvantages of each delivery system are provided. For asthma, inhaled glucocorticoids, long-acting beta-agonists, cromolyn, and short-acting beta-agonists are discussed. For COPD, long-acting beta-agonists, anticholinergics like tiotropium, and inhaled corticosteroids alone or in combination are covered. Proper inhaler technique is emphasized for optimal treatment.
This document discusses asthma-COPD overlap syndrome (ACOS). It defines asthma and COPD, noting their differences and similarities. Both are chronic inflammatory airway diseases but COPD is characterized by persistent airflow limitation and progressive lung function decline while asthma is often reversible. The document then discusses clinical features that can help distinguish asthma from COPD. It notes that some patients have features of both diseases, termed ACOS. Spirometry, biomarkers, imaging and response to treatment are discussed to help identify ACOS. The inflammatory patterns in asthma and COPD are compared, showing that eosinophilic inflammation is more prominent in asthma while neutrophilic inflammation dominates in COPD.
This document summarizes CT findings that are useful for diagnosing chronic pulmonary thromboembolism (CPTE). It describes risk factors, clinical manifestations, and CT features of CPTE including vascular signs like pulmonary artery obstruction and dilation, parenchymal signs like scarring and mosaic perfusion patterns, and signs of pulmonary hypertension. Differential diagnoses including idiopathic pulmonary hypertension and acute PE are also discussed. CT is important for identifying treatable CPTE in patients with unexplained pulmonary hypertension.
Turmeric consists of the dried rhizome of Curcuma longa and contains curcumin, which is responsible for turmeric's bright yellow color and pharmacological effects. Curcumin has anti-bacterial, anti-fungal, anti-protozoal, and anti-viral effects. It may help treat digestion issues, circulation problems, cough, menstrual problems, and skin disorders. Turmeric is also used for diabetes, arthritis, anemia, wounds, and more when applied locally or taken internally.
This document discusses pulmonary thromboembolism (PE), which refers to blood clots (thrombi) traveling from deep veins to the lungs. Most clots originate in the lower extremities. Risk factors include inherited conditions, surgery, trauma, immobilization, cancer and pregnancy. PE can cause hypoxemia and pulmonary hypertension. Diagnosis involves clinical assessment, D-dimer testing, chest imaging like CT pulmonary angiogram (gold standard), ventilation-perfusion scanning and echocardiogram. Treatment aims to relieve symptoms and prevent complications like right heart strain.
(1) Retroviruses like HIV contain RNA as their genetic material instead of DNA. The reverse transcriptase enzyme produces a DNA copy of the viral RNA that integrates into the host cell DNA.
(2) The structure of HIV includes an outer envelope containing glycoproteins like gp120 and gp41, as well as internal core proteins. The glycoproteins help HIV bind to and fuse with target CD4+ cells.
(3) The HIV lifecycle involves binding to and entering target cells, reverse transcription of its RNA into DNA, integration of the DNA into the host genome, production of new viral components, assembly, and budding of new virus particles to infect other cells.
Air, water, and land pollution were discussed. Air pollution comes from natural sources like volcanoes and human sources such as factories and cars. Major air pollutants include carbon monoxide, sulfur dioxide, and particulate matter which can cause health issues. Water pollution comes from point sources like factories and non-point sources like agricultural runoff. Land pollution is caused by construction, agriculture, and domestic and industrial waste. Pollution has consequences like acid rain, smog, and damage to plants and wildlife. Reducing pollution requires efforts from individuals, industries, and governments.
This document discusses bronchopleural fistula (BPF), which is an abnormal communication between the bronchial tree and pleural space that can occur after lung surgery or due to other non-operative causes. It presents classifications of air leaks, risk factors, clinical presentation, diagnosis, and treatment approaches for BPF. Treatment may involve drainage, antibiotics, ventilation strategies, bronchoscopic techniques, or surgical procedures depending on the size and location of the fistula. Anesthesia management for surgery aims to isolate the healthy lung and prevent complications from air loss through the fistula.
This document discusses ground-glass opacities seen on CT scans. It defines ground-glass opacities as a hazy increase in lung opacity while preserving bronchial and vascular markings. Various pathologies can cause ground-glass opacities by partially filling the airspaces. The document then describes different patterns of ground-glass opacities including diffuse, patchy, focal, halo, and peripheral distributions. For each pattern, common diseases that may present with that appearance are listed and briefly characterized.
The document discusses various types of environmental pollutants and their effects. It defines occupational, environmental and ecotoxicology. It describes different types of pollution like air, land and water pollution and their sources. It explains concepts like bioaccumulation and biomagnification. Key air pollutants like sulfur dioxide, nitrogen dioxide, carbon monoxide and their health impacts are summarized. Specific pollutants like solvents and insecticides and their mechanisms of action are also outlined.
MIDDLE EAST RESPIRATORY SYNDROME CORONA VIRUS (MERS CoV)Dhruvendra Pandey
Middle East Respiratory Syndrome, countries affected by MERS virus, preventive and control strategies for MERS infection, recommendation for healthcare professionals and hospitals in case of MERS corona virus infection, time trend of different events in corona virus infection, MERS Cov is associated with camels, Saudi Arabia guideline for travellers to haj and umrah, MERS CoV Vaccine
This document discusses pulmonary thromboembolism (PE), which occurs when a blood clot blocks the pulmonary artery or its branches in the lungs. PE is usually caused by deep vein thrombosis, where a clot breaks off and travels to the lungs. Symptoms include dyspnea, chest pain, and coughing. Risk factors include prolonged immobilization, recent surgery or trauma, oral contraceptive use, pregnancy, and inherited or acquired hypercoagulable states. Diagnosis involves chest x-ray, ventilation-perfusion scanning, and pulmonary angiography to detect clots in the pulmonary arteries.
This document summarizes evidence from medical studies linking air pollution to various negative health impacts. It finds that air pollution causes thousands of premature deaths annually in the US from heart and lung diseases. Common pollutants like ozone and particulate matter are associated with increased asthma attacks, heart attacks, strokes, and lung cancer as well as decreased lung function and development, especially in children. Reducing air pollution could significantly improve health outcomes and lower healthcare costs.
Asthma vs COPD - A quick summary of the differences between themLGM Pharma
Asthma is a lung disease that affects almost 20 million Americans. COPD, or chronic obstructive pulmonary disease is a chronic lung disease that afflicts 24 million patients in the U.S. COPD is mainly caused by smoking or secondhand smoke, while asthma can by caused by exposure to allergens, dust and air pollutants. Innovative treatments are needed to combat both asthma and COPD, and LGM Pharma provides quality API's for the R&D needs of clients seeking treatments for these lung diseases.
This patient presents with an acute exacerbation of asthma/COPD. The document reviews guidelines on asthma and COPD, including epidemiology, pathophysiology, diagnosis and treatment approaches. It also presents two case studies, one involving a 19-year old female student with asthma symptoms and another involving a 72-year old female with multiple inhalers for COPD. Treatment strategies and inhaler techniques are discussed.
2 Global Strategy for Asthma ManagementYaser Ammar
The document provides guidelines for the global strategy of asthma management according to the 2016 GINA update. It outlines the 5 major domains of asthma management which are diagnosis and assessment, symptom control and risk reduction, patient education and self-management, management of exacerbations, and managing comorbidities and special situations. Key points include diagnosing asthma through documentation of variable respiratory symptoms and airflow limitation via spirometry or peak flow meters. Assessment involves evaluating symptom control, future risk of exacerbations, severity, treatment adherence, and comorbidities. The goals of treatment are achieving symptom control and reducing future risks through the stepwise use of reliever and controller medications such as SABA, ICS, LABA, and others depending on severity
This document discusses various antiviral drugs used to treat viral eye infections caused by DNA and RNA viruses such as herpes simplex virus and cytomegalovirus. It describes first and second generation antiviral drugs such as trifluorothymidine, acyclovir, ganciclovir and foscarnet. It provides details on the mechanisms of action, indications, dosages and side effects of these drugs for treating ocular conditions.
This presentation focuses on a short history of bioterrorism, description, its advantages and disadvantages and organisms incorporated into weapons are also shown here.
The document discusses the asthma-COPD overlap (ACO) phenotype. It notes that ACO is not a single disease, but rather represents different clinical phenotypes that likely have different underlying mechanisms. The terminology has changed from "Asthma COPD Overlap Syndrome" to "ACO" to avoid implying it is a single disease. Diagnosing ACO helps identify COPD patients who may benefit from treatment with inhaled corticosteroids. Experts recommend inhaled corticosteroid/long-acting beta agonist combination as first-line therapy for ACO.
Asthma-COPD Overlap Translating Guidelines into Clinical Pracice - CasesAshraf ElAdawy
This document discusses the diagnosis of a 50-year-old female patient presenting with increased shortness of breath, cough, and wheezing. Spirometry results show obstructive lung disease with partially reversible airflow obstruction. The document examines features that favor a diagnosis of asthma, COPD, or asthma-COPD overlap syndrome (ACOS). It outlines definitions and diagnostic criteria for ACOS proposed by various medical organizations. ACOS is defined as having characteristics of both asthma and COPD, with persistent airflow limitation and a history of smoking. The document concludes the patient's diagnosis requires consideration of ACOS.
Chronic obstructive pulmonary disease (COPD) refers to progressive lung diseases such as emphysema and chronic bronchitis. It is characterized by increasing breathlessness over many years that is caused by an abnormal inflammatory response of the lungs to noxious particles, primarily from cigarette smoking. While COPD affects the lungs, it also produces systemic effects. The main symptoms include worsening shortness of breath, chronic cough, and excess mucus production. Diagnosis involves assessing symptoms, medical history, and lung function tests. Treatment focuses on smoking cessation and medications to relieve symptoms.
Chronic Obstructive Pulmonary Disease (COPD) is a chronic lung disorder characterized by airflow obstruction that does not change markedly over time. The obstruction is caused by emphysema, chronic bronchitis, or both. Emphysema involves destruction of lung tissue, while chronic bronchitis involves inflammation of the airways accompanied by mucus hypersecretion. Symptoms include cough, sputum production, wheezing and shortness of breath. Diagnosis is based on patient history, symptoms, and lung function tests showing airflow obstruction. Management involves reducing risk factors, treating stable disease and exacerbations, and rehabilitation.
This document summarizes the key differences between asthma and COPD. Both conditions involve airflow obstruction, but asthma is characterized by reversible obstruction while COPD involves obstruction that is not fully reversible. Symptoms are similar but COPD generally involves more sputum production. Asthma is often episodic and triggered by factors like allergens, while COPD severity does not vary as much throughout the year. Diagnosis involves pulmonary function tests showing reversibility for asthma but not COPD. Treatment also differs, with asthma management focusing on suppressing inflammation and COPD treatment aiming to reduce symptoms.
This document provides information on Chronic Obstructive Pulmonary Disease (COPD). It defines COPD as a disease characterized by persistent airflow limitation that is usually progressive. The primary cause of COPD is tobacco smoking. It discusses the characteristics and components of COPD including chronic bronchitis and emphysema. The document also covers the diagnosis, assessment of severity, management including medications, oxygen therapy, pulmonary rehabilitation, and end of life care considerations for COPD patients.
Chronic obstructive pulmonary disease (COPD) is characterized by persistent airflow limitation that is usually progressive. It includes chronic bronchitis and emphysema. COPD is diagnosed based on spirometry showing airflow limitation. Symptoms include breathlessness, cough, and wheezing. Management involves reducing risk factors, managing stable COPD with bronchodilators and rehabilitation, and treating exacerbations with bronchodilators and glucocorticoids. The severity of COPD is classified based on lung function, and treatment is escalated based on severity from short-acting bronchodilators to long-term oxygen for very severe COPD.
This document provides an overview of Chronic Obstructive Pulmonary Disease (COPD). It begins with an introduction to COPD, describing it as a common lung disease that makes breathing difficult. It then covers the anatomy and physiology of COPD, defining it as a progressive lung disease involving chronic inflammation and airflow obstruction. The document discusses the incidence of COPD globally and risk factors. It provides details on the pathophysiology, stages and symptoms of the disease. Diagnostic tests like spirometry and chest x-rays are described. The document outlines complications of COPD and approaches to medical management including pharmacology, surgery, and nursing care. It provides details on specific drugs like bronchodilators and corticosteroids used to
This document provides information on diagnosing and differentially diagnosing COPD, including:
- Key indicators that should prompt consideration of a COPD diagnosis including dyspnea, chronic cough, sputum production, and risk factor exposure. Spirometry is required to confirm COPD.
- Spirometry is the basic investigation needed to diagnose COPD. It assesses airflow limitation through FEV1/FVC ratio and severity through FEV1 levels. Reversibility testing can help differentiate COPD from asthma.
- Additional optional investigations that may be used include imaging like chest X-rays and CT scans to identify emphysema and airway abnormalities, lung volume measurements, diffusing capacity tests, and
This document provides an overview of content to be covered in a 1.5 hour session on respiratory medicine. It includes objectives to familiarize learners with potential OSCE scenarios and key respiratory conditions, signs, symptoms, investigations, and management. It also provides sample OSCE scenarios and outlines content on topics like asthma, COPD, pneumonia, and tuberculosis that will be discussed, followed by some sample SBA questions for practice.
Chronic obstructive pulmonary disease (COPD) is a chronic lung disease characterized by airflow limitation caused by damage to the lungs, usually from smoking. It involves emphysema and small airway fibrosis leading to trapped air in the lungs. Symptoms include shortness of breath and cough. Diagnosis involves assessing risk factors, symptoms, and lung function tests showing airflow limitation that is often only partially reversible with bronchodilators. Treatment focuses on stopping smoking and using bronchodilators and inhaled corticosteroids to relieve symptoms and reduce exacerbations.
Chronic obstructive pulmonary disease (COPD) refers to chronic conditions such as chronic bronchitis and emphysema that obstruct airflow from the lungs. The main causes are cigarette smoking and exposure to air pollutants. Symptoms include shortness of breath, cough, and excess mucus production. Treatment focuses on reducing symptoms through medications like bronchodilators and steroids. For severe cases, surgery or lung transplantation may be options. Managing COPD involves smoking cessation and lifestyle changes to improve lung health.
The document summarizes chronic obstructive pulmonary disease (COPD). It covers the general considerations, epidemiology, risk factors, pathogenesis, clinical findings, differential diagnosis, diagnostic testing including spirometry and imaging, and treatment including smoking cessation, oxygen therapy, bronchodilators, corticosteroids, and antibiotics. COPD is characterized by airflow obstruction due to chronic bronchitis or emphysema and is generally progressive. Cigarette smoking is the most important risk factor.
The document discusses COPD (chronic obstructive pulmonary disease), its causes, symptoms, differences from asthma, classifications, treatments, and management. It provides information from Dr. Mohammad Zannatul Rayhan on COPD, including that it is a lung disease caused by chronic interference with lung airflow and impairs breathing. The major cause of COPD is smoking. Treatments discussed include bronchodilators, anti-inflammatory drugs, oxygen therapy, pulmonary rehabilitation, and smoking cessation.
Chronic obstructive pulmonary disease (COPD)- Preeti sharmaEducate with smile
COPD is a type of obstructive lung disease and related conditions. it is very helpful presentation to you about information of COPD.
It includes all things that is definition, causes, symptoms, pathophysiology, diagnostic evaluation, types, treatment and role of nurses for COPD patient.
Chronic obstructive pulmonary disease (COPD) refers to chronic conditions like chronic bronchitis and emphysema that obstruct airflow from the lungs. Cigarette smoking is the leading cause of COPD. The document defines COPD and describes its symptoms, risk factors, diagnosis, treatment through medications and surgery, complications, and approaches to managing the disease.
COPD is a common lung disease characterized by persistent airflow limitation caused by damage to the lungs, usually from smoking. It is the fourth leading cause of death. Symptoms include shortness of breath, chronic cough, and sputum production. Diagnosis is confirmed by pulmonary function tests showing airflow limitation that is not fully reversible. Treatment focuses on reducing symptoms and exacerbations through bronchodilators, inhaled corticosteroids, pulmonary rehabilitation, oxygen therapy, and managing comorbidities.
COPD is a progressive lung disease characterized by airflow obstruction caused by chronic bronchitis or emphysema. It is the fourth leading cause of death in the US. Symptoms include cough, sputum production, and shortness of breath. Management involves smoking cessation, bronchodilators, corticosteroids, oxygen therapy, and lifestyle changes. Nurses play a key role in assessing patients, educating on self-management, and providing interventions to improve breathing and nutrition.
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Adulterants screening in Herbal products using Modern Analytical Techniques28SamruddhiKadam
Basic introduction to adulteration in Herbal products, M Pharm Pharmaceutical Analysis Semester 2
Basic types of Adulterations in herbal products.
Modern hyphenated techniques used in determination of adulteration of herbal drugs which includes TLC, HPTLC, HPLC, LC-MS, LC-NMR, SFC, LC-IR,etc.
Various modern analytical techniques used in Quantification of Adulterants present in herbal product.
Examples of various drugs causing adulteration in Herbal products.
Huntington's disease is a rare, inherited, progressive brain disorder caused by a defect in a single gene (HTT) leading to the breakdown of nerve cells, resulting in uncontrolled movements, cognitive decline, and emotional problems.
Chair, Nitin Jain, MD, discusses chronic lymphocytic leukemia in this CME/AAPA activity titled “Time-Limited Innovation for CLL Control: Changing the Treatment Story With Evidence and Emerging Consensus on 1L BTKi -BCL2i Combinations.” For the full presentation, downloadable Practice Aid, and complete CME/AAPA information, and to apply for credit, please visit us at https://bit.ly/4gi5jVw. CME/AAPA credit will be available until April 3, 2026.
Lipid Autocoids: A Comprehensive Overview
Introduction
Lipid autocoids, also known as eicosanoids and related lipid mediators, are bioactive molecules derived from polyunsaturated fatty acids (PUFAs). These molecules play crucial roles in inflammation, immunity, hemostasis, cardiovascular function, and various physiological and pathological processes. Unlike classical hormones, lipid autocoids act locally, exerting their effects at or near their site of synthesis.
This document provides an in-depth analysis of lipid autocoids, covering their biosynthesis, classification, physiological roles, and clinical significance.
Classification of Lipid Autocoids
Lipid autocoids are broadly classified into the following categories:
1. Eicosanoids (Derived from Arachidonic Acid)
Prostaglandins (PGs)
Thromboxanes (TXs)
Leukotrienes (LTs)
Lipoxins (LXs)
2. Specialized Pro-resolving Mediators (SPMs)
Resolvins
Protectins
Maresins
3. Endocannabinoids
Anandamide (AEA)
2-Arachidonoylglycerol (2-AG)
4. Platelet-Activating Factor (PAF)
5. Sphingolipid-Derived Mediators
Sphingosine-1-Phosphate (S1P)
Ceramides
Biosynthesis of Lipid Autocoids
Lipid autocoids are derived from membrane phospholipids through enzymatic pathways:
1. Phospholipase A2 (PLA2) Activation:
PLA2 catalyzes the release of arachidonic acid (AA) from membrane phospholipids.
2. Cyclooxygenase (COX) Pathway:
Converts AA into prostaglandins and thromboxanes.
COX-1: Constitutive enzyme (housekeeping functions).
COX-2: Inducible enzyme (inflammation and pain response).
3. Lipoxygenase (LOX) Pathway:
Converts AA into leukotrienes and lipoxins.
5-LOX: Leads to leukotrienes (inflammation, bronchoconstriction).
12-LOX & 15-LOX: Lead to lipoxins (anti-inflammatory action).
4. Cytochrome P450 (CYP) Pathway:
Converts AA into epoxyeicosatrienoic acids (EETs), which regulate vascular tone.
5. Endocannabinoid Biosynthesis:
Derived from membrane phospholipids via enzymatic reactions.
Degraded by fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL).
Physiological Roles of Lipid Autocoids
1. Inflammation and Immune Response
Prostaglandins (e.g., PGE2) modulate fever and pain.
Leukotrienes mediate allergic responses and asthma.
Lipoxins and resolvins promote resolution of inflammation.
2. Cardiovascular System
Thromboxanes (TXA2) induce platelet aggregation and vasoconstriction.
Prostacyclin (PGI2) inhibits platelet aggregation and promotes vasodilation.
EETs regulate blood pressure and vascular homeostasis.
3. Pulmonary Function
Leukotrienes (LTC4, LTD4, LTE4) are potent bronchoconstrictors.
PGE2 has bronchodilatory effects.
4. Renal Function
Prostaglandins regulate glomerular filtration rate and sodium excretion.
EETs contribute to natriuresis.
5. Neurotransmission and Pain
Endocannabinoids modulate pain perception and neuroprotection.
Prostaglandins contribute to central pain sensitization.
6. Reproductive System
P
Psychopharmacological Agents or Antipsychotic drugs are the drugs which are used in treatment of psychiatric disorders like schizophrenia, mania, anxiety and depression.
ANAESTHESIA MACHINE.pptx.pdf different partsSneha103657
An anesthesia machine is a medical device used to deliver anesthetic gases and oxygen to a patient undergoing surgery or other medical procedures. It ensures that the patient remains unconscious, pain-free, and properly ventilated.
Main Components of an Anesthesia Machine:
Gas Supply:
Oxygen (O₂), nitrous oxide (N₂O), and medical air are commonly used.
Can come from cylinders or a hospital’s central gas supply.
Flow Meters:
Control the flow rate of gases going to the patient.
Measured in liters per minute (L/min).
Vaporizers:
Convert liquid anesthetic agents (like isoflurane, sevoflurane) into gas form.
Allows precise control of anesthetic concentration.
Breathing Circuit:
Connects the machine to the patient via a face mask or endotracheal tube.
Includes inspiratory and expiratory pathways.
Ventilator:
Provides controlled or assisted breathing to the patient.
Works in different modes like volume-controlled or pressure-controlled ventilation.
Scavenging System:
Removes excess anesthetic gases to prevent leakage into the operating room.
Ensures safety for healthcare providers.
Carbon Dioxide Absorber:
Uses soda lime or another absorbent to remove CO₂ from exhaled air in a closed circuit.
Safety Features:
Alarms for oxygen failure, low pressure, or high airway pressure.
Oxygen flush system for emergencies.
Hypoxic guard to prevent delivery of pure nitrous oxide (ensuring oxygen is always mixed i
PROFESSIONAL Integrity, Honesty and Responsibility ppt (1).pdfBhumikaSingh805349
Professional integrity, honesty, and responsibility are fundamental pillars of ethical conduct in the workplace.
Integrity involves consistently upholding ethical standards and maintaining a strong moral compass, ensuring that actions align with core values and principles.
Honesty emphasizes transparency and truthfulness in communication and actions, fostering trust among colleagues, clients, and stakeholders.
Responsibility focuses on taking ownership of one’s actions and their consequences, fulfilling commitments, and being accountable for decisions made in a professional context.
Together, these qualities promote a positive work environment, enhance relationships, and contribute to long-term success and respect in any profession.
This PPT includes - two topics - Liver abscess & Liver timours which is very much essential for MBBS - Students. The students should know the causes, clinical features & management aspects of the above liver diseases. Also it includes the latest staging system of liver tumours.
This comprehensive seminar presentation on Emerging and Re-emerging Diseases explores one of the most critical challenges in global public health today. The content delves into the definitions, differences, and classifications of emerging and re-emerging infectious diseases, shedding light on the dynamic nature of disease epidemiology in the 21st century.
The presentation highlights factors contributing to the emergence and resurgence of diseases, including globalization, increased human-animal interaction, urbanization, climate change, deforestation, antimicrobial resistance (AMR), and gaps in immunization. Through relevant case studies and recent outbreaks such as COVID-19, Nipah virus, Zika, Ebola, Monkeypox, Dengue, Tuberculosis, and others, the seminar underscores the importance of disease surveillance, rapid response systems, and the “One Health” approach.
It also discusses the role of national and international health agencies like WHO, CDC, and India’s IDSP in disease monitoring and control. The presentation is enriched with visuals, stats, and key strategies for prevention and control, making it a valuable educational tool for medical students, community medicine postgraduates, public health professionals, and policy makers.
By the end of this seminar, viewers will gain a deeper understanding of how emerging and re-emerging diseases pose evolving threats and how a proactive, multidisciplinary public health response is essential to safeguard communities globally.
Chair, Andrea Necchi, MD, Sia Daneshmand, MD, and Shilpa Gupta, MD, discuss bladder cancer in this CME/MOC/AAPA/IPCE activity titled “Maximizing Therapeutic Innovations in Bladder Cancer: Expert Strategies for Comprehensive Care Across Disease Stages.” For the full presentation, downloadable Practice Aids, and complete CME/MOC/AAPA/IPCE information, and to apply for credit, please visit us at https://bit.ly/422z9Kf. CME/MOC/AAPA/IPCE credit will be available until March 14, 2026.
A BRIEF STUDY OF REGIONAL REPERTORY (3).pdfsadanandarya1
Regional repertories in homeopathy are specialized reference works that focus on specific parts or systems of the body, such as the eyes, skin, respiratory system, or digestive organs. Unlike general repertories, which cover a wide range of symptoms and modalities across the entire body, regional repertories offer a more in-depth and concentrated analysis of particular areas, allowing practitioners to narrow down remedies with greater precision.
This study aims to understand the role and relevance of regional repertories in clinical practice. It explores various examples such as "Repertory of the Eyes" by William Jefferson Guernsey, and "Repertory of the Head" by J.B. Garth Wilkinson, among others. These repertories serve as valuable tools in cases where the pathology is strongly localized, and where a detailed repertorial analysis of that specific region is needed.
The study also highlights the advantages and limitations of regional repertories. While they provide focused insight and can enhance remedy selection in specific cases, they may lack the broader context required in complex or multi-systemic conditions. Thus, they are most effective when used in conjunction with general repertories and thorough case-taking.
regional repertories play a significant role in enhancing the accuracy of homeopathic prescriptions, especially in localized diseases. Their study is essential for practitioners seeking to deepen their understanding and refine their skills in remedy selection.
Medicinal and Toilet Preparations Act, 1955 – Excise Duty Regulations on Alco...Dr.Navaneethakrishnan S
This presentation provides a comprehensive overview of the Medicinal and Toilet Preparations Act, 1955, which regulates the excise duty on medicinal and cosmetic products containing alcohol, opium, or narcotics in India. It covers key definitions, the distinction between bonded and non-bonded manufactories, licensing requirements, excise duty regulations, manufacturing guidelines, and penalties for violations. Special provisions related to Ayurvedic preparations, government hospital exemptions, and testing procedures are also highlighted. The presentation is valuable for pharmacy students, regulatory professionals, manufacturers, and excise officers involved in the pharmaceutical and cosmetic industries.
Emergency Studies in Nuclear Medicine .pdfMiadAlsulami
This lecture can serve as a bullet-point review of the emergency studies in nuclear medicine. The outline is as follows:
- Pulmonary Embolism.
- GI Bleeding.
- ATN.
- Shunt Patency.
- Brain Death.
Emergency Studies in Nuclear Medicine .pdfMiadAlsulami
Acos
1. DEFINITIONS
Asthma
*A heterogeneous disease, usually characterized by chronic airway
inflammation.
*It is defined by the history of respiratory symptoms such as wheeze,
shortness of breath, chest tightness and cough that vary over time
and in intensity, together with variable expiratory airflow limitation.
COPD
*A common preventable and treatable disease.
*Characterized by persistent airflow limitation that is usually
progressive and associated with enhanced chronic inflammatory
responses in the airways and the lungs to noxious particles or gases.
2. *Exacerbations and comorbidities contribute to the overall
severity in individual patients.
ACOS
*Characterized by persistent airflow limitation.
With
*Several features usually associated with asthma.
And
* Several features usually associated with COPD.
*ACOS is therefore identified by the features that it shares with
both asthma and COPD
4. Step 1
DIAGNOSE
CHRONIC
AIRWAY
DISEASE
Do symptoms suggest chronic airways disease?
NoYes Consider other diseases first
Step 2
SYNDROMIC
DIAGNOSIS OF
AIRWAYS
DISEASE
1- Assemble the features for asthma and for COPD
that best describe the pt.
2- Compare the number of features in favor of each
diagnosis and select diagnosis .
Step 3
SPIROMETRY
ASTHMA : Marked reversible airflow limitation
(pre – post BD)
ACOS & COPD : FEV1/FVC <0.7 post BD
5. Step 4
INITIAL
TREATMENT
Asthma drugs
but No LABA
monotherapy
( possible or
Asthma )
ICS and
LABA +/or
LAMA
( ACOS)
COPD drugs
but No ICS
monotherapy
(Possible or COPD)
Step 5
SPECIALIZED
INVESTIGATIO
NS OR REFER
IF:
*Persistent symptoms and / or exacerbation despite treatment.
* Diagnostic uncertainty eg suspected PAH , CVD , and other
causes of respiratory symptoms.
*Suspected Asthma or COPD with atypical or additional s&s eg
haem0ptysis, w. loss , n. sweats , fever, signs of bronchiectasis
other structural lung disease.
* Fews features of either asthma or COPD .
* Co morbidities present.
6. Step 1: Does the patient have chronic airways disease?
Clinical history
*History of chronic or recurrent cough, sputum production, dyspnea,
or wheezing; or repeated acute LRTI.
*Report of a previous doctor diagnosis of asthma or COPD.
*History of prior treatment with inhaled medications .
*History of smoking tobacco and/or other substances.
*Exposure to air pollution e.g. occupational or domestic.
7. Step 1: Does the patient have chronic airways disease? (cont)
Physical examination
*May be normal .
*hyperinflation and other features of chronic lung disease or R.failure .
*Abnormal auscultation (wheeze and/or crackles).
Radiology (CXR or CT)
*May be normal, particularly in early stages .
*May be abnormal (hyperinflation, airway wall thickening, air
trapping, hyperlucency, bullae or other features of emphysema).
Or
*Alternative diagnosis, including bronchiectasis ,lung infections such
as tuberculosis, ILD or CHF.
8. STEP 2: Syndromic diagnosis of airways disease ? (cont)
*Brief review of Usual features of asthma , COPD and ACOS.
*From the following boxes:-
1- Count the number of check boxes in each column.
2- If three or more boxes are checked for either asthma or COPD, that
diagnosis is suggested.
3- If there are similar numbers of checked boxes in each column, the
diagnosis of ACOS should be considered.
*If the syndromic assessment suggests asthma or ACOS, or there is
significant uncertainty about the diagnosis of COPD, it is prudent to
start treatment as for asthma until further investigation has been
performed to confirm or refute this initial position.
9. 1- Usual features of asthma , COPD and ACOS
Feature Asthma COPD ACOS
Age of
onset
Usually childhood
onset but can
commence at any age.
Usually > 40 years
of age
Usually age ≥40
years, but may have
had symptoms in
childhood or early
adulthood
Pattern of
respiratory
symptoms
Symptoms may vary
over time (day to day,
or over longer
periods), often limiting
activity. Often
triggered by exercise,
emotions including
laughter, dust or
exposure to allergens
Chronic usually
continuous
symptoms,
particularly during
exercise, with
‘better’ and
‘worse’ days
Respiratory
symptoms including
exertional dyspnea
are persistent but
variability may be
prominent
10. 2- Usual features of asthma , COPD and ACOS
Feature Asthma COPD ACOS
Lung
function
Current and/or historical
variable airflow
limitation, e.g. BD
reversibility, AHR
FEV1 may be
improved by
therapy, but post-
BD FEV1/FVC < 0.7
persists
Airflow limitation not
fully reversible, but often
with current or historical
variability
Lung
function
between
symptoms
May be normal between
symptoms
Persistent airflow
limitation
Persistent airflow
limitation
Past history
or family
history
Many patients have
allergies and a personal
history of asthma in
childhood, and/or family
history of asthma
History of exposure
to noxious particles
and gases (mainly
tobacco smoking
and biomass fuels)
Frequently a history of
doctor- diagnosed asthma
(current or previous),
allergies and a family
history of asthma, and/or
a history of noxious
exposures
11. 3- Usual features of asthma , COPD and ACOS
Feature Asthma COPD ACOS
Time
course
Often improves
spontaneously or
with treatment,
but may result in
fixed airflow
limitation
Generally,
slowly
progressive over
years despite
treatment
Symptoms are partly but
significantly reduced by
treatment. Progression is
usual and treatment needs
are high
Chest X-ray Usually normal
Severe
hyperinflation &
other changes of
COPD
Similar to COPD
12. 4- Usual features of asthma , COPD and ACOS
Feature Asthma COPD ACOS
Exacerbation
Exacerbations
occur, but the risk
of exacerbations
can be
considerably
reduced by
treatment
Exacerbations can
be reduced by
treatment.
If present,
comorbidities
contribute to
impairment
Exacerbations may
be more common
than in COPD but
are reduced by
treatment.
Comorbidities can
contribute to
impairment
Typical airway
inflammation
Eosinophils and/or
neutrophils
Neutrophils in
sputum,
lymphocytes in
airways, may have
systemic
inflammation
Eosinophils and/or
neutrophils in
sputum.
13. 1- Asthma or COPD
Feature Favors asthma Favors COPD
Age of onset Before age 20 years After age 40 years
Pattern of
respiratory
symptoms
Variation in symptoms over
minutes, hours or days
Symptoms worse during the
night or early morning
Symptoms triggered by exercise,
emotions including laughter, dust or
exposure to allergens
Persistence of symptoms
despite treatment
Good and bad days but
always daily symptoms and
exertional dyspnea
Chronic cough and
sputum preceded onset of
dyspnea, unrelated to
triggers
14. 2- Asthma or COPD
Feature Favors asthma Favors COPD
Lung
function
Variable airflow limitation
(spirometry, peak flow)
Persistent airflow limitation
(post-bronchodilator FEV1/FVC <
0.7 )
Lung
function
between
symptoms
Normal Abnormal
Past
history or
family
history
Previous doctor diagnosis of
asthma
Family history of asthma,
and other allergic conditions
(allergic rhinitis or eczema)
Previous doctor diagnosis of
COPD, chronic bronchitis or
emphysema
Heavy exposure to a risk factor:
tobacco smoke, biomass fuels
15. 3- Asthma or COPD
Feature Favors asthma Favors COPD
Time course
No worsening of symptoms over
time. Symptoms vary either seasonally,
or from year to year.
May improve spontaneously or
have an immediate response to BD or
to ICS over weeks
Symptoms slowly
worsening over time
(progressive course over
years)
Rapid-acting
bronchodilator treatment
provides only limited
relief.
Chest X-ray Normal Severe hyperinflation
DIAGNOSIS
BA
Some features
OF BA
Features OF
both
Some features
OF COPD COPD
CONFIDENCE IN
DIAGNOSIS BA Possible BA ACOS Possible COPD COPD
NOTE: *These features best distinguish between athma and COPD.
* postive features (3 or more) for either asthma or COPD sugest that diagnosis.
*If there are a similar number for both asthma and COPD consider ACOS.
16. STEP 3: Spirometry
*Spirometry is essential for the assessment of patients with suspected
chronic disease of the airways.
*It must be performed at either the initial or a subsequent visit, if
possible before and after a trial of treatment.
*Early confirmation or exclusion of the diagnosis may avoid needless
trials of therapy, or delays in initiating other investigations.
*Spirometry confirms chronic airflow limitation but is of more limited
value in distinguishing between asthma with fixed airflow obstruction,
COPD and ACOS .
*PEF, although not an alternative to spirometry, if performed
repeatedly on the same meter over a period of 1–2 weeks may help to
confirm the diagnosis of asthma by demonstrating excessive
variability, but a normal PEF does not rule out either asthma or COPD.
17. STEP 3: Spirometry (cont)
*A high level of variability in lung function may also be found in ACOS.
*Spirometry at a single visit is not always confirmatory of a diagnosis.
*Further tests might therefore be necessary either to confirm the
diagnosis or to assess the response to initial and subsequent ttt.
*Spirometric measures in asthma, COPD and ACOS
18. Spirometric measures in asthma, COPD and ACOS
Spiro metric
variable
Asthma COPD ACOS
normal
FEV1/FVC pre-
or post BD
Compatible with
diagnosis
Not compatible
with
diagnosis
Not compatible
unless other
evidence of
chronic
airflow limitation
Post-BD
FEV1/FVC
<0.7
Indicates airflow
limitation but may
improvespontaneously
or on treatment
Required for
diagnosis
Usually present
19. Spirometric measures in asthma, COPD and ACOS
Spiro metric
variable
Asthma COPD ACOS
FEV1
≥80%
predicted
Compatible with
diagnosis
(good asthma
control
or interval
between
symptoms)
Compatible with
GOLD classification
of mild airflow
limitation(categories
A or B) if post- BD
FEV1/FVC <0.7
Compatible with
diagnosis
of mild ACOS
FEV1
<80%
predicted
Compatible with
diagnosis.
Risk factor for
asthma
exacerbations
An indicator of
severity of
airflow limitation
and risk of future
events (e.g.
mortality and COPD
exacerbations)
An indicator of
severity of
airflow limitation and
risk of future events
(e.g. mortality and
exacerbations)
20. Spirometric measures in asthma, COPD and ACOS
Spirometric variable Asthma COPD ACOS
Post-BD increase in
FEV1>12% and 200 ml
from baseline
(reversible airflow
limitation)
Usual at some
time in course
of asthma, but
may not be
present when
well-controlled
or on
controllers
Common and
more likely when
FEV1
is low, but ACOS
should also be
considered
Common and
more likely when
FEV1
is low, but COPD
should also be
considered
Post-BD increase in
FEV1>12% and 400ml
from baseline
(marked reversibility)
High
probability of
asthma
Unusual in COPD.
Consider ACOS
Compatible with
diagnosis of ACOS
21. STEP 4: Commence initial therapy
*ACOS start treatment with ICS because of the pivotal role of ICS in
preventing morbidity and even death in pt with uncontrolled asthma
symptoms, for whom even seemingly ‘mild’ symptoms (compared to
those of moderate or severe COPD) might indicate significant risk of a
life-threatening attack.
*If the syndromic assessment suggests asthma or ACOS, or there is
significant uncertainty about the diagnosis of COPD, it is prudent to
start treatment as for asthma until further investigation has been
performed to confirm or refute this initial position. ( Treatments will
include an ICS and LABA should also be continued -if already
prescribed-, or added.
* No LABA mono therapy if there are features of asthma.
22. STEP 4: Commence initial therapy (cont)
*COPD, appropriate symptomatic treatment with bronchodilators or
combination therapy should be commenced, but not ICS mono
therapy.
*Treatment of ACOS should also include advice about other
therapeutic strategies including:-
1- Smoking cessation.
2- Pulmonary rehabilitation.
3- Vaccinations.
4-Treatment of co morbidities .
*In a majority of patients, the initial management of asthma and
COPD can be satisfactorily carried out at primary care level.
23. Drugs for Asthma & COPD & ACOS
Inhaler
Short Acting BD SABA as Salbutamol, Terbutaline & SAMA as
Ipratropium
Long Acting BD LABA as Salmeterol, Formoterol & LAMA as
Tioptropium
ICS As Fluticasone, Budesonide, beclomethasone
Combination
SABA + SAMA as Salbutamol + Ipratropium
LABA + ICS as Salmeterol + Fluticasone and
Formoterol + Budesonide
Non inhaler
LTRAs montelukast
Anti- IgE Ab Omalizumab
SCS Prednisolone , methylprednisolone ,
hydrocortisone
24. Specialized investigations sometimes used in distinguishing asthma and COPD
Asthma COPD
DLCO Normal (or slightly elevated). Often reduced
ABG
Normal between
exacerbations
May be chronically abnormal
between exacerbations in more
severe forms of COPD
AHR
Not useful on its own in distinguishing asthma from COPD, but
high levels of AHR favor asthma
High
resolution CT
Scan
Usually normal but air
trapping and increased
bronchial wall thickness
may be observed.
Low attenuation areas denoting
either air trapping or
emphysematous change can be
quantitated ; bronchial wall
thickening and features of
pulmonary hypertension may be
seen.
25. Inflammatory
biomarkers
Asthma COPD
Test for atopy (specific
IgE
and/or skin prick tests)
Modestly increases
probability of asthma;
not essential for
diagnosis
Conforms to background
prevalence; does not rule
out COPD
FENO
A high level (>50 ppb) in
nonsmokers supports a
diagnosis of eosinophilic
airway inflammation
Usually normal.
Low in current smokers
Blood eosinophilia
Supports asthma
diagnosis
May be present during
exacerbations
Sputum inflammatory
cell analysis
Role in differential diagnosis is not established in
large populations
27. CASE 1
* 19 year old female student.
* C/O: 3 days cough, wheezing, SOB.
- Precipitated by exercise .
- Relieved by salbutamol nebulization (past 3 nights)
- Self medicated with prednisone 10mg 1 dose
* (+ve) history of asthma attacks during childhood
* (+ve) family Hx of asthma (mother).
* (+ve) Hx of atopy.
* EX: talks in sentences & wheeze.
Diagnosis
Athma
28. Case 2
* 72 year old housewife
* C/O: on and off cough, wheezing, shortness of breath
- Relieved by SABA nebulization
- lately is more bothersome after hosting a birthday party
- with grayish sputum, difficulty sleeping
- Has consulted several doctors; has 4 inhaler devices
* Smoker
* Previously hospitalized due to LRTI 3 months ago
* EX: talks in phrases & wheezing both lung fields
Diagnosis
COPD
29. Case 3
* 55 year old, male, teacher
* C/O: cough, wheezing, shortness of breath 7 days
- Precipitated by exposure to dust.
- Sneezing, itchy throat
- Unable to sleep due to SOB, partially relieved by SABA neb
* (+ve) history of childhood asthma
* (+ve) 20 pack year (current) smoker
* (+ve) history of antibiotic (Co-amox) intake 4 weeks ago after
diagnosed with pneumonia as outpatient.
*EX: talks in sentences & wheezing both lung fields
Diagnosis
ACOS
30. What is the single most effective intervention
to slow the progression of COPD?
1
Home
Oxygen
2
Pulmonary
Rehab.
3
Smoking
Cessation
4
Flu
Vaccination
Smoking Cessation
Evidence A
32. 1- Distinguishing asthma from COPD can be problematic, particularly
in smokers and older adults.
2- ACOS is identified by the features that it shares with both asthma
and COPD.
3- A stepwise approach to diagnosis is advised, comprising
recognition of the presence of a chronic airways disease, syndromic
categorization as asthma, COPD or ACOS, confirmation by spirometry
and, if necessary, referral for specialized investigations.
4- Although initial recognition and treatment of ACOS may be made
in primary care, referral for confirmatory investigations is
encouraged.
5- Outcomes for ACOS are often worse than for asthma or COPD
alone.
33. 6- The single most effective intervention to slow the progression
of COPD is Smoking Cessation.
7- Initial treatment of Pt with features of asthma is adequate
controller therapy including ICS, but not LABA mono therapy.
8- Patients with COPD receive appropriate symptomatic
treatment with bronchodilators or combination therapy , but not
ICS mono therapy.
9- ACOS need further study of the character and treatments for
this common clinical problem.
34. 10- Inhaler use is a skill - must be learned and maintained
*Up to 70–80% are unable to use their inhaler correctly.
*Unfortunately, many health care providers are unable to
correctly demonstrate how to use the inhalers they prescribe.
*Most people with incorrect technique are unaware that they
have a problem.
*There is no ‘perfect’ inhaler - patients can have problems
using any inhaler device.