'+pages+''); $('.stream > div:odd').addClass('bgr_color'); updateHeight('#history'); }); window.activateTabArea = ensure(function(tab, areas){ var parsed = false; var parts = (areas || '').split('/'); window.fsonload = $.inArray('fs', parts) >= 0; if(fsonload){ parts.splice(parts.indexOf('fs'), 1); } var replayMode = false; if($.inArray('replay', parts)>=0){ replayMode = 'replay'; } var noSoundMode = false; if($.inArray('nosound', parts)>=0){ noSoundMode = 'nosound'; } if($.inArray('ns', parts)>=0){ noSoundMode = 'ns'; } var previewMode = null; if($.inArray('p', parts)>=0){ previewMode = 'p'; } if($.inArray('preview', parts)>=0){ previewMode = 'preview'; } if($.inArray('repeat', parts)>=0){ replayMode = 'repeat'; } if($.inArray('r', parts)>=0 || $.inArray('ro', parts)>=0){ replayMode = 'r'; } if(replayMode){ parts.splice(parts.indexOf(replayMode), 1); } if(noSoundMode){ parts.splice(parts.indexOf(noSoundMode), 1); } if(previewMode){ parts.splice(parts.indexOf(previewMode), 1); } if(previewMode){ if(!parts.length){ parts = ['1-14', '999:59']; } } var area = parts[0]; if(tab == 'history' && false){ var page = parseInt(area || '1') || 1; $.ajax({ url: 'https://login.wn.com/recent/json/?pp='+history_pp+'&skip='+history_pp*(page-1), dataType: 'jsonp', success: function(response){ $ensure(function(){ renderHistory(response, page); }); } }); return true; } if(tab == 'global_history' && false){ var page = parseInt(area || '1') || 1; globalHistory.fetchStream(page, '', function(){ updateHeight('#global_history'); }); return true; } if(tab == 'my_playlists' && false){ var page = parseInt(area || '1') || 1; myPlaylists.fetchStream(page, '', function(){ updateHeight('#my_playlists'); }); return true; } if(tab == 'my_videos' && false){ var page = parseInt(area || '1') || 1; myVideos.fetchStream(page, '', function(){ updateHeight('#my_videos'); }); return true; } if(tab == 'related_sites' && areas && matchPosition(areas)){ var seconds = parsePosition(areas); scrollRelated(seconds); return false; } if(matchPosition(area) || matchAction(area)){ parts.unshift('1'); area = parts[0]; } if(tab == 'expand' && area && area.match(/\d+/)) { var num = parseInt(area); if(num < 100){ //FIX ME. 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vp.playFromPlaylist(pls[pls.length-1]); vp.playVideo(); scrollToPlaylistPosition(vp); }); return true; } } if(playQueue){ playQueueUpdate(); vp.playVideo(); parsed = true; playShouldStart = 0; } } if(previewMode){ var vids = []; var dur = 0; var pl = vp.getActualPlaylist(); area = parts[0]; if(parts.length == 1 && matchPosition(parts[0])){ vids = parseDash('1-'+pl.length); dur = parsePosition(parts[0]); parts = []; }else if(parts.length == 1 && matchDash(parts[0])){ vids = parseDash(parts[0]); dur = parsePosition("999:59"); parts = []; } if(parts.length == 2 && matchDash(parts[0]) && matchPosition(parts[1])){ vids = parseDash(parts[0]); dur = parsePosition(parts[1]); parts = []; } for(var i = 0; i < vids.length; i++){ playQueue.push({ 'video': pl[vids[i]-1], 'start': 0, 'stop': dur }) } if(playQueue){ playQueueUpdate(); vp.playVideo(); parsed = true; } } if(parts.length>1){ for(var i = 0; i < parts.length; i++){ var sel = findMatchingVideo(vp, parts[i]); if(sel){ playQueue.push({ 'video': sel, 'start': 0, 'stop': null }) } } if(playQueue){ playQueueUpdate(); 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  Interstitial Lung Disease

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  Interstitial Lung Disease

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Usual interstitial pneumonia

Usual interstitial pneumonia (UIP) is a form of lung disease characterized by progressive scarring of both lungs. The scarring (fibrosis) involves the supporting framework (interstitium) of the lung. UIP is thus classified as a form of interstitial lung disease. The term "usual" refers to the fact that UIP is the most common form of interstitial fibrosis. "Pneumonia" indicates "lung abnormality", which includes fibrosis and inflammation. A term previously used for UIP in the British literature is cryptogenic fibrosing alveolitis, a term that has fallen out of favor since the basic underlying pathology is now thought to be fibrosis, not inflammation.

Causes

The cause of the scarring in UIP may be known (less commonly) or unknown (more commonly). Since the medical term for conditions of unknown cause is "idiopathic", the clinical term for UIP of unknown cause is idiopathic pulmonary fibrosis (IPF). Examples of known causes of UIP include systemic sclerosis/scleroderma, rheumatoid arthritis, asbestosis, and chronic nitrofurantoin toxicity.

Read more

This page contains text from Wikipedia, the Free Encyclopedia - https://wn.com/Usual_interstitial_pneumonia

Interstitial lung disease

Interstitial lung disease (ILD), also known as diffuse parenchymal lung disease (DPLD), is a group of lung diseases affecting the interstitium (the tissue and space around the air sacs of the lungs). It concerns alveolar epithelium, pulmonary capillary endothelium, basement membrane, perivascular and perilymphatic tissues.

The term ILD is used to distinguish these diseases from obstructive airways diseases.

Prolonged ILD may result in pulmonary fibrosis, but this is not always the case. Idiopathic pulmonary fibrosis is interstitial lung disease for which no obvious cause can be identified (idiopathic), and is associated with typical radiographic (basal and pleural based fibrosis with honeycombing) and pathologic (temporally and spatially heterogeneous fibrosis, histopathologic honeycombing and fibroblastic foci) findings.

Causes

ILD may be classified according to the cause. One method of classification is as follows:

Inhaled substances

• Inorganic
  • Silicosis
  • Asbestosis
  • Berylliosis
• Organic
  • Hypersensitivity pneumonitis

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This page contains text from Wikipedia, the Free Encyclopedia - https://wn.com/Interstitial_lung_disease

Podcasts:

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Email this Page Play all in Full Screen Show More Related Videos

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  Interstitial Lung Disease (ILD) - Classification, pathophysiology, signs and symptoms

  Where do I get my information from: http://armandoh.org/resource "Interstitial lung disease also known as diffuse parenchymal lung diseases (DPLDs) are a group of disorders based on similar clinical, radiographic, physiologic, and pathologic changes. Present primarily with shortness of breath and a non productive cough usually chronic over weeks to months without response to initial treatment of puffers. If there is clinical suspicion of ILD a full pulmonary function test should be done. Characteristic changes of ILD include: reduced total lung capacity (TLC) and DLCO. The diffuse parenchymal lung diseases are divided into those that are associated with known causes or unknown causes and other weird and wonderful rare causes." 🎥 DON'T JUST WATCH, LEARN ACTIVELY! TRY THE QUIZ! 🤓 https...

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  This video “Interstitial Lung Disease (ILD): Overview” is part of the Lecturio course “Interstitial Lung Disease” ► WATCH the complete course on http://lectur.io/ildyoutube ► LEARN ABOUT: - classification of interstital lung disease ► THE PROF: Professor Jeremy Brown is a clinician scientist with an interest in respiratory infection. He studied medicine in London, graduating with honors, and continued his postgraduate medical training in a variety of London hospitals. He completed his PhD in molecular microbiology in 1999 and obtained a prestigious Welcome Advanced Research Fellowship for further scientific training at the University of Adelaide. His research is mainly focused on respiratory complications of haematological disease and stem cell transplantation. His educational and scien...

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  Please read and agree to the disclaimer before watching this video. . Subscribe to the drbeen Channel HERE: http://bit.ly/2GBhiS0 For more content from drbeen, click HERE: http://bit.ly/2GB41bU Watch drbeen videos HERE: http://bit.ly/2GB41bU Like drbeen on Facebook HERE: http://bit.ly/2GSSTGS Follow drbeen on Twitter HERE: http://bit.ly/2XeSVhV Follow drbeen on Instagram HERE: http://bit.ly/2ST2Zih Get new medical lectures across your devices. Stream anywhere, anytime. Try it for free! http://bit.ly/2QsIwQ5 This video presents the introduction to restrictive lung diseases. We will discuss:  Definition Types  Extrapulmonary restrictive lung diseases * Obesity * Scoliosis Pulmonary parenchymal restrictive lung diseases * Idiopathic * Autoimmune * Granulomatous (Wagner's granulomatosis, Sar...

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11:40

Interstitial Lung Disease (ILD) - Classification, pathophysiology, signs and symptoms

• Order: Reorder
• Duration: 11:40
• Uploaded Date: 17 Jan 2021
• views: 208004

Where do I get my information from: http://armandoh.org/resource "Interstitial lung disease also known as diffuse parenchymal lung diseases (DPLDs) are a group...

Where do I get my information from: http://armandoh.org/resource "Interstitial lung disease also known as diffuse parenchymal lung diseases (DPLDs) are a group of disorders based on similar clinical, radiographic, physiologic, and pathologic changes. Present primarily with shortness of breath and a non productive cough usually chronic over weeks to months without response to initial treatment of puffers. If there is clinical suspicion of ILD a full pulmonary function test should be done. Characteristic changes of ILD include: reduced total lung capacity (TLC) and DLCO. The diffuse parenchymal lung diseases are divided into those that are associated with known causes or unknown causes and other weird and wonderful rare causes." 🎥 DON'T JUST WATCH, LEARN ACTIVELY! TRY THE QUIZ! 🤓 https://youmakr.ai/test-playground/questionnaire/673d32a1859b9c170836ea51 👆Hit this quiz and show of your main character aura! Support me: 🖼️ Buy PDFs: http://armandoh.org/shop 💵 Patreon: http://www.patreon.com/armando 👕 Buy shirts: https://teespring.com/stores/ah-7 Social media: 📷 Instagram: http://instagram.com/armandohasudungan 🐦 Twitter: https://twitter.com/armandohasudung 📔 Facebook: https://www.facebook.com/ArmandoHasudungan Resources: 📕 Books: http://armandoh.org/resource 🎞️ Equipment: armandoh.org/armando-faigl You can send me mail: 📫 PO BOX 166, Randwick NSW 2031, Australia

https://wn.com/Interstitial_Lung_Disease_(Ild)_Classification,_Pathophysiology,_Signs_And_Symptoms

Where do I get my information from: http://armandoh.org/resource "Interstitial lung disease also known as diffuse parenchymal lung diseases (DPLDs) are a group of disorders based on similar clinical, radiographic, physiologic, and pathologic changes. Present primarily with shortness of breath and a non productive cough usually chronic over weeks to months without response to initial treatment of puffers. If there is clinical suspicion of ILD a full pulmonary function test should be done. Characteristic changes of ILD include: reduced total lung capacity (TLC) and DLCO. The diffuse parenchymal lung diseases are divided into those that are associated with known causes or unknown causes and other weird and wonderful rare causes." 🎥 DON'T JUST WATCH, LEARN ACTIVELY! TRY THE QUIZ! 🤓 https://youmakr.ai/test-playground/questionnaire/673d32a1859b9c170836ea51 👆Hit this quiz and show of your main character aura! Support me: 🖼️ Buy PDFs: http://armandoh.org/shop 💵 Patreon: http://www.patreon.com/armando 👕 Buy shirts: https://teespring.com/stores/ah-7 Social media: 📷 Instagram: http://instagram.com/armandohasudungan 🐦 Twitter: https://twitter.com/armandohasudung 📔 Facebook: https://www.facebook.com/ArmandoHasudungan Resources: 📕 Books: http://armandoh.org/resource 🎞️ Equipment: armandoh.org/armando-faigl You can send me mail: 📫 PO BOX 166, Randwick NSW 2031, Australia

• published: 17 Jan 2021
• views: 208004

16:50

Interstitial Lung Disease (ILD) in a Nutshell

• Order: Reorder
• Duration: 16:50
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• views: 164407

An overview of ILD (also known as diffuse parenchymal lung diseases), including definition, classification, etiologies, and diagnostic evaluation (e.g. CT and P...

An overview of ILD (also known as diffuse parenchymal lung diseases), including definition, classification, etiologies, and diagnostic evaluation (e.g. CT and PFT findings).

https://wn.com/Interstitial_Lung_Disease_(Ild)_In_A_Nutshell

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• published: 07 May 2019
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Interstitial Lung Disease (ILD): Overview– Interstitial Lung Disease | Lecturio

• Order: Reorder
• Duration: 4:25
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This video “Interstitial Lung Disease (ILD): Overview” is part of the Lecturio course “Interstitial Lung Disease” ► WATCH the complete course on http://lectur.i...

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https://wn.com/Interstitial_Lung_Disease_(Ild)_Overview–_Interstitial_Lung_Disease_|_Lecturio

This video “Interstitial Lung Disease (ILD): Overview” is part of the Lecturio course “Interstitial Lung Disease” ► WATCH the complete course on http://lectur.io/ildyoutube ► LEARN ABOUT: - classification of interstital lung disease ► THE PROF: Professor Jeremy Brown is a clinician scientist with an interest in respiratory infection. He studied medicine in London, graduating with honors, and continued his postgraduate medical training in a variety of London hospitals. He completed his PhD in molecular microbiology in 1999 and obtained a prestigious Welcome Advanced Research Fellowship for further scientific training at the University of Adelaide. His research is mainly focused on respiratory complications of haematological disease and stem cell transplantation. His educational and scientific experience enables him to teach students and professionals about respiratory medicine. ►LECTURIO is your single-point resource for medical school: Study for your classes, USMLE Step 1, USMLE Step 2, MCAT or MBBS with video lectures by world-class professors, recall & USMLE-style questions and textbook articles. Create your free account here: http://lectur.io/ildyoutube ► INSTALL our free Lecturio app iTunes Store: https://app.adjust.com/z21zrf Play Store: https://app.adjust.com/b01fak ► READ TEXTBOOK ARTICLES related to this video: Interstitial Lung Disease (ILD) — Types and Symptoms http://lectur.io/ildarticle ► SUBSCRIBE to our YouTube channel: http://lectur.io/subscribe ► WATCH MORE ON YOUTUBE: http://lectur.io/playlists ► LET’S CONNECT: • Facebook: https://www.facebook.com/lecturio.medical.education.videos • Instagram: https://www.instagram.com/lecturio_medical_videos

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Restrictive Lung Diseases - Interstitial Pulmonary Fibrosis. Pathology, Clinical, Tests, Treatment

• Order: Reorder
• Duration: 24:26
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• views: 116395

Please read and agree to the disclaimer before watching this video. . Subscribe to the drbeen Channel HERE: http://bit.ly/2GBhiS0 For more content from drbeen, ...

Please read and agree to the disclaimer before watching this video. . Subscribe to the drbeen Channel HERE: http://bit.ly/2GBhiS0 For more content from drbeen, click HERE: http://bit.ly/2GB41bU Watch drbeen videos HERE: http://bit.ly/2GB41bU Like drbeen on Facebook HERE: http://bit.ly/2GSSTGS Follow drbeen on Twitter HERE: http://bit.ly/2XeSVhV Follow drbeen on Instagram HERE: http://bit.ly/2ST2Zih Get new medical lectures across your devices. Stream anywhere, anytime. Try it for free! http://bit.ly/2QsIwQ5 This video presents the introduction to restrictive lung diseases. We will discuss:  Definition Types  Extrapulmonary restrictive lung diseases * Obesity * Scoliosis Pulmonary parenchymal restrictive lung diseases * Idiopathic * Autoimmune * Granulomatous (Wagner's granulomatosis, Sarcoidosis) * Occupational (pneumoconiosis, silicosis, asbestosis, coal, etc.) * Other irritants * Chronic infections (Tuberculosis) Neuromuscular restrictive lung diseases * Myasthenia gravis * Diaphragm issues * Polio Cellular events/pathogenesis * Damaged Type I Pneumocytes * Hypertrophy of Type II Pneumocytes * Irritated epithelium * Irritated macrophages * Apoptosis of epithelium * Tissue damage leading to local inflammation and lung destruction/scaring. * Neutrophils releasing cytokines, proteases, tumor growth factors (TGF) * Macrophages releasing transforming growth factor beta, tumor necrosis factor (TNF), platelet activation factor. * Fibroblasts overactivity resulting in more extracellular matrix and hardening. * Epithelial-mesenchymal transformation. * Smooth muscle proliferation. * Respiratory interface thickening. Disrupted gaseous exchange. Clinical: Dry hacking cough * Dyspnea * Hypoxia * Respiratory alkalosis * Late inspiratory crackles Abnormal chest X-Ray * Reduced volume in chest X-Ray * Lower lobes show more involvement and the reason why. * Right heart failure/cor pulmonale  Lung Function Changes * FEV1/FVC ratio increases above 80% (normal or above normal) Treatment * Anti-inflammatory (may not be very effective) * TGF Beta-blockers * Oxygen * Lung transplant ... Disclaimer: This video is not intended to provide assessment, diagnosis, treatment, or medical advice; it also does not constitute provision of healthcare services. The content provided in this video is for informational and educational purposes only. Please consult with a physician or healthcare professional regarding any medical or mental health related diagnosis or treatment. No information in this video should ever be considered as a substitute for advice from a healthcare professional. ... Disclaimer: This video is not intended to provide assessment, diagnosis, treatment, or medical advice; it also does not constitute provision of healthcare services. The content provided in this video is for informational and educational purposes only. Please consult with a physician or healthcare professional regarding any medical or mental health related diagnosis or treatment. No information in this video should ever be considered as a substitute for advice from a healthcare professional.

https://wn.com/Restrictive_Lung_Diseases_Interstitial_Pulmonary_Fibrosis._Pathology,_Clinical,_Tests,_Treatment

Please read and agree to the disclaimer before watching this video. . Subscribe to the drbeen Channel HERE: http://bit.ly/2GBhiS0 For more content from drbeen, click HERE: http://bit.ly/2GB41bU Watch drbeen videos HERE: http://bit.ly/2GB41bU Like drbeen on Facebook HERE: http://bit.ly/2GSSTGS Follow drbeen on Twitter HERE: http://bit.ly/2XeSVhV Follow drbeen on Instagram HERE: http://bit.ly/2ST2Zih Get new medical lectures across your devices. Stream anywhere, anytime. Try it for free! http://bit.ly/2QsIwQ5 This video presents the introduction to restrictive lung diseases. We will discuss:  Definition Types  Extrapulmonary restrictive lung diseases * Obesity * Scoliosis Pulmonary parenchymal restrictive lung diseases * Idiopathic * Autoimmune * Granulomatous (Wagner's granulomatosis, Sarcoidosis) * Occupational (pneumoconiosis, silicosis, asbestosis, coal, etc.) * Other irritants * Chronic infections (Tuberculosis) Neuromuscular restrictive lung diseases * Myasthenia gravis * Diaphragm issues * Polio Cellular events/pathogenesis * Damaged Type I Pneumocytes * Hypertrophy of Type II Pneumocytes * Irritated epithelium * Irritated macrophages * Apoptosis of epithelium * Tissue damage leading to local inflammation and lung destruction/scaring. * Neutrophils releasing cytokines, proteases, tumor growth factors (TGF) * Macrophages releasing transforming growth factor beta, tumor necrosis factor (TNF), platelet activation factor. * Fibroblasts overactivity resulting in more extracellular matrix and hardening. * Epithelial-mesenchymal transformation. * Smooth muscle proliferation. * Respiratory interface thickening. Disrupted gaseous exchange. Clinical: Dry hacking cough * Dyspnea * Hypoxia * Respiratory alkalosis * Late inspiratory crackles Abnormal chest X-Ray * Reduced volume in chest X-Ray * Lower lobes show more involvement and the reason why. * Right heart failure/cor pulmonale  Lung Function Changes * FEV1/FVC ratio increases above 80% (normal or above normal) Treatment * Anti-inflammatory (may not be very effective) * TGF Beta-blockers * Oxygen * Lung transplant ... Disclaimer: This video is not intended to provide assessment, diagnosis, treatment, or medical advice; it also does not constitute provision of healthcare services. The content provided in this video is for informational and educational purposes only. Please consult with a physician or healthcare professional regarding any medical or mental health related diagnosis or treatment. No information in this video should ever be considered as a substitute for advice from a healthcare professional. ... Disclaimer: This video is not intended to provide assessment, diagnosis, treatment, or medical advice; it also does not constitute provision of healthcare services. The content provided in this video is for informational and educational purposes only. Please consult with a physician or healthcare professional regarding any medical or mental health related diagnosis or treatment. No information in this video should ever be considered as a substitute for advice from a healthcare professional.

• published: 03 Dec 2017
• views: 116395

4:56

Interstitial lung disease, Causes, Signs and Symptoms, Diagnosis and Treatment

• Order: Reorder
• Duration: 4:56
• Uploaded Date: 31 Jan 2021
• views: 41426

. Chapters 0:00 Introduction 1:18 Causes of Interstitial lung disease 3:13 Symptoms and Diagnosis of Interstitial lung disease 3:53 Treatment of Interstitial ...

. Chapters 0:00 Introduction 1:18 Causes of Interstitial lung disease 3:13 Symptoms and Diagnosis of Interstitial lung disease 3:53 Treatment of Interstitial lung disease. Interstitial lung disease (ILD), or diffuse parenchymal lung disease (DPLD),[3] is a group of respiratory diseases affecting the interstitium (the tissue and space around the alveoli (air sacs) of the lungs.[4] It concerns alveolar epithelium, pulmonary capillary endothelium, basement membrane, and perivascular and perilymphatic tissues. It may occur when an injury to the lungs triggers an abnormal healing response. Ordinarily, the body generates just the right amount of tissue to repair damage, but in interstitial lung disease, the repair process is disrupted, and the tissue around the air sacs (alveoli) becomes scarred and thickened. This makes it more difficult for oxygen to pass into the bloodstream. The disease presents itself with the following symptoms: shortness of breath, nonproductive coughing, fatigue, and weight loss, which tend to develop slowly, over several months. The average rate of survival for someone with this disease is between three and five years.[5] The term ILD is used to distinguish these diseases from obstructive airways diseases. There are specific types in children, known as children's interstitial lung diseases. The acronym ChILD is sometimes used for this group of diseases.[6] Prolonged ILD may result in pulmonary fibrosis, but this is not always the case. Idiopathic pulmonary fibrosis is interstitial lung disease for which no obvious cause can be identified (idiopathic) and is associated with typical findings both radiographic (basal and pleural-based fibrosis with honeycombing) and pathologic (temporally and spatially heterogeneous fibrosis, histopathologic honeycombing, and fibroblastic foci).

https://wn.com/Interstitial_Lung_Disease,_Causes,_Signs_And_Symptoms,_Diagnosis_And_Treatment

. Chapters 0:00 Introduction 1:18 Causes of Interstitial lung disease 3:13 Symptoms and Diagnosis of Interstitial lung disease 3:53 Treatment of Interstitial lung disease. Interstitial lung disease (ILD), or diffuse parenchymal lung disease (DPLD),[3] is a group of respiratory diseases affecting the interstitium (the tissue and space around the alveoli (air sacs) of the lungs.[4] It concerns alveolar epithelium, pulmonary capillary endothelium, basement membrane, and perivascular and perilymphatic tissues. It may occur when an injury to the lungs triggers an abnormal healing response. Ordinarily, the body generates just the right amount of tissue to repair damage, but in interstitial lung disease, the repair process is disrupted, and the tissue around the air sacs (alveoli) becomes scarred and thickened. This makes it more difficult for oxygen to pass into the bloodstream. The disease presents itself with the following symptoms: shortness of breath, nonproductive coughing, fatigue, and weight loss, which tend to develop slowly, over several months. The average rate of survival for someone with this disease is between three and five years.[5] The term ILD is used to distinguish these diseases from obstructive airways diseases. There are specific types in children, known as children's interstitial lung diseases. The acronym ChILD is sometimes used for this group of diseases.[6] Prolonged ILD may result in pulmonary fibrosis, but this is not always the case. Idiopathic pulmonary fibrosis is interstitial lung disease for which no obvious cause can be identified (idiopathic) and is associated with typical findings both radiographic (basal and pleural-based fibrosis with honeycombing) and pathologic (temporally and spatially heterogeneous fibrosis, histopathologic honeycombing, and fibroblastic foci).

• published: 31 Jan 2021
• views: 41426

8:35

Interstitial Lung Disease

• Order: Reorder
• Duration: 8:35
• Uploaded Date: 30 Jul 2018
• views: 18035

Interstitial lung disease or ILD is an autoimmune condition of the lung. In some people, the body will attack itself and when it happens in the lung, it is a p...

Interstitial lung disease or ILD is an autoimmune condition of the lung. In some people, the body will attack itself and when it happens in the lung, it is a problem. Once the body begins to attack the lung, you become more short of breath. This video will tell you why.

https://wn.com/Interstitial_Lung_Disease

Interstitial lung disease or ILD is an autoimmune condition of the lung. In some people, the body will attack itself and when it happens in the lung, it is a problem. Once the body begins to attack the lung, you become more short of breath. This video will tell you why.

• published: 30 Jul 2018
• views: 18035

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  11:40

  Interstitial Lung Disease (ILD) - Classification, pathophysiology, signs and symptomsremove from playlistshare this video

  Interstitial Lung Disease (ILD) - Classification, pathophysiology, signs and symptoms

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  • published: 17 Jan 2021
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  Where do I get my information from: http://armandoh.org/resource "Interstitial lung disease also known as diffuse parenchymal lung diseases (DPLDs) are a group of disorders based on similar clinical, radiographic, physiologic, and pathologic changes. Present primarily with shortness of breath and a non productive cough usually chronic over weeks to months without response to initial treatment of puffers. If there is clinical suspicion of ILD a full pulmonary function test should be done. Characteristic changes of ILD include: reduced total lung capacity (TLC) and DLCO. The diffuse parenchymal lung diseases are divided into those that are associated with known causes or unknown causes and other weird and wonderful rare causes." 🎥 DON'T JUST WATCH, LEARN ACTIVELY! TRY THE QUIZ! 🤓 https://youmakr.ai/test-playground/questionnaire/673d32a1859b9c170836ea51 👆Hit this quiz and show of your main character aura! Support me: 🖼️ Buy PDFs: http://armandoh.org/shop 💵 Patreon: http://www.patreon.com/armando 👕 Buy shirts: https://teespring.com/stores/ah-7 Social media: 📷 Instagram: http://instagram.com/armandohasudungan 🐦 Twitter: https://twitter.com/armandohasudung 📔 Facebook: https://www.facebook.com/ArmandoHasudungan Resources: 📕 Books: http://armandoh.org/resource 🎞️ Equipment: armandoh.org/armando-faigl You can send me mail: 📫 PO BOX 166, Randwick NSW 2031, Australia

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  16:50

  Interstitial Lung Disease (ILD) in a Nutshellremove from playlistshare this video

  Interstitial Lung Disease (ILD) in a Nutshell

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  • published: 07 May 2019
  • views: 164407

  An overview of ILD (also known as diffuse parenchymal lung diseases), including definition, classification, etiologies, and diagnostic evaluation (e.g. CT and PFT findings).

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  4:25

  Interstitial Lung Disease (ILD): Overview– Interstitial Lung Disease | Lecturioremove from playlistshare this video

  Interstitial Lung Disease (ILD): Overview– Interstitial Lung Disease | Lecturio

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  • published: 18 Feb 2020
  • views: 31595

  This video “Interstitial Lung Disease (ILD): Overview” is part of the Lecturio course “Interstitial Lung Disease” ► WATCH the complete course on http://lectur.io/ildyoutube ► LEARN ABOUT: - classification of interstital lung disease ► THE PROF: Professor Jeremy Brown is a clinician scientist with an interest in respiratory infection. He studied medicine in London, graduating with honors, and continued his postgraduate medical training in a variety of London hospitals. He completed his PhD in molecular microbiology in 1999 and obtained a prestigious Welcome Advanced Research Fellowship for further scientific training at the University of Adelaide. His research is mainly focused on respiratory complications of haematological disease and stem cell transplantation. His educational and scientific experience enables him to teach students and professionals about respiratory medicine. ►LECTURIO is your single-point resource for medical school: Study for your classes, USMLE Step 1, USMLE Step 2, MCAT or MBBS with video lectures by world-class professors, recall & USMLE-style questions and textbook articles. Create your free account here: http://lectur.io/ildyoutube ► INSTALL our free Lecturio app iTunes Store: https://app.adjust.com/z21zrf Play Store: https://app.adjust.com/b01fak ► READ TEXTBOOK ARTICLES related to this video: Interstitial Lung Disease (ILD) — Types and Symptoms http://lectur.io/ildarticle ► SUBSCRIBE to our YouTube channel: http://lectur.io/subscribe ► WATCH MORE ON YOUTUBE: http://lectur.io/playlists ► LET’S CONNECT: • Facebook: https://www.facebook.com/lecturio.medical.education.videos • Instagram: https://www.instagram.com/lecturio_medical_videos

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  24:26

  Restrictive Lung Diseases - Interstitial Pulmonary Fibrosis. Pathology, Clinical, Tests, Treatmentremove from playlistshare this video

  Restrictive Lung Diseases - Interstitial Pulmonary Fibrosis. Pathology, Clinical, Tests, Treatment

  • Report rights infringement
  • published: 03 Dec 2017
  • views: 116395

  Please read and agree to the disclaimer before watching this video. . Subscribe to the drbeen Channel HERE: http://bit.ly/2GBhiS0 For more content from drbeen, click HERE: http://bit.ly/2GB41bU Watch drbeen videos HERE: http://bit.ly/2GB41bU Like drbeen on Facebook HERE: http://bit.ly/2GSSTGS Follow drbeen on Twitter HERE: http://bit.ly/2XeSVhV Follow drbeen on Instagram HERE: http://bit.ly/2ST2Zih Get new medical lectures across your devices. Stream anywhere, anytime. Try it for free! http://bit.ly/2QsIwQ5 This video presents the introduction to restrictive lung diseases. We will discuss:  Definition Types  Extrapulmonary restrictive lung diseases * Obesity * Scoliosis Pulmonary parenchymal restrictive lung diseases * Idiopathic * Autoimmune * Granulomatous (Wagner's granulomatosis, Sarcoidosis) * Occupational (pneumoconiosis, silicosis, asbestosis, coal, etc.) * Other irritants * Chronic infections (Tuberculosis) Neuromuscular restrictive lung diseases * Myasthenia gravis * Diaphragm issues * Polio Cellular events/pathogenesis * Damaged Type I Pneumocytes * Hypertrophy of Type II Pneumocytes * Irritated epithelium * Irritated macrophages * Apoptosis of epithelium * Tissue damage leading to local inflammation and lung destruction/scaring. * Neutrophils releasing cytokines, proteases, tumor growth factors (TGF) * Macrophages releasing transforming growth factor beta, tumor necrosis factor (TNF), platelet activation factor. * Fibroblasts overactivity resulting in more extracellular matrix and hardening. * Epithelial-mesenchymal transformation. * Smooth muscle proliferation. * Respiratory interface thickening. Disrupted gaseous exchange. Clinical: Dry hacking cough * Dyspnea * Hypoxia * Respiratory alkalosis * Late inspiratory crackles Abnormal chest X-Ray * Reduced volume in chest X-Ray * Lower lobes show more involvement and the reason why. * Right heart failure/cor pulmonale  Lung Function Changes * FEV1/FVC ratio increases above 80% (normal or above normal) Treatment * Anti-inflammatory (may not be very effective) * TGF Beta-blockers * Oxygen * Lung transplant ... Disclaimer: This video is not intended to provide assessment, diagnosis, treatment, or medical advice; it also does not constitute provision of healthcare services. The content provided in this video is for informational and educational purposes only. Please consult with a physician or healthcare professional regarding any medical or mental health related diagnosis or treatment. No information in this video should ever be considered as a substitute for advice from a healthcare professional. ... Disclaimer: This video is not intended to provide assessment, diagnosis, treatment, or medical advice; it also does not constitute provision of healthcare services. The content provided in this video is for informational and educational purposes only. Please consult with a physician or healthcare professional regarding any medical or mental health related diagnosis or treatment. No information in this video should ever be considered as a substitute for advice from a healthcare professional.

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  4:56

  Interstitial lung disease, Causes, Signs and Symptoms, Diagnosis and Treatmentremove from playlistshare this video

  Interstitial lung disease, Causes, Signs and Symptoms, Diagnosis and Treatment

  • Report rights infringement
  • published: 31 Jan 2021
  • views: 41426

  . Chapters 0:00 Introduction 1:18 Causes of Interstitial lung disease 3:13 Symptoms and Diagnosis of Interstitial lung disease 3:53 Treatment of Interstitial lung disease. Interstitial lung disease (ILD), or diffuse parenchymal lung disease (DPLD),[3] is a group of respiratory diseases affecting the interstitium (the tissue and space around the alveoli (air sacs) of the lungs.[4] It concerns alveolar epithelium, pulmonary capillary endothelium, basement membrane, and perivascular and perilymphatic tissues. It may occur when an injury to the lungs triggers an abnormal healing response. Ordinarily, the body generates just the right amount of tissue to repair damage, but in interstitial lung disease, the repair process is disrupted, and the tissue around the air sacs (alveoli) becomes scarred and thickened. This makes it more difficult for oxygen to pass into the bloodstream. The disease presents itself with the following symptoms: shortness of breath, nonproductive coughing, fatigue, and weight loss, which tend to develop slowly, over several months. The average rate of survival for someone with this disease is between three and five years.[5] The term ILD is used to distinguish these diseases from obstructive airways diseases. There are specific types in children, known as children's interstitial lung diseases. The acronym ChILD is sometimes used for this group of diseases.[6] Prolonged ILD may result in pulmonary fibrosis, but this is not always the case. Idiopathic pulmonary fibrosis is interstitial lung disease for which no obvious cause can be identified (idiopathic) and is associated with typical findings both radiographic (basal and pleural-based fibrosis with honeycombing) and pathologic (temporally and spatially heterogeneous fibrosis, histopathologic honeycombing, and fibroblastic foci).

  • Show More
• Reorder
  

  8:35

  Interstitial Lung Diseaseremove from playlistshare this video

  Interstitial Lung Disease

  • Report rights infringement
  • published: 30 Jul 2018
  • views: 18035

  Interstitial lung disease or ILD is an autoimmune condition of the lung. In some people, the body will attack itself and when it happens in the lung, it is a problem. Once the body begins to attack the lung, you become more short of breath. This video will tell you why.

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Interstitial Lung Disease (ILD) - Classification, pathophysiology, signs and symptoms

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• published: 17 Jan 2021
• views: 208004

Where do I get my information from: http://armandoh.org/resource "Interstitial lung disease also known as diffuse parenchymal lung diseases (DPLDs) are a group of disorders based on similar clinical, radiographic, physiologic, and pathologic changes. Present primarily with shortness of breath and a non productive cough usually chronic over weeks to months without response to initial treatment of puffers. If there is clinical suspicion of ILD a full pulmonary function test should be done. Characteristic changes of ILD include: reduced total lung capacity (TLC) and DLCO. The diffuse parenchymal lung diseases are divided into those that are associated with known causes or unknown causes and other weird and wonderful rare causes." 🎥 DON'T JUST WATCH, LEARN ACTIVELY! TRY THE QUIZ! 🤓 https://youmakr.ai/test-playground/questionnaire/673d32a1859b9c170836ea51 👆Hit this quiz and show of your main character aura! Support me: 🖼️ Buy PDFs: http://armandoh.org/shop 💵 Patreon: http://www.patreon.com/armando 👕 Buy shirts: https://teespring.com/stores/ah-7 Social media: 📷 Instagram: http://instagram.com/armandohasudungan 🐦 Twitter: https://twitter.com/armandohasudung 📔 Facebook: https://www.facebook.com/ArmandoHasudungan Resources: 📕 Books: http://armandoh.org/resource 🎞️ Equipment: armandoh.org/armando-faigl You can send me mail: 📫 PO BOX 166, Randwick NSW 2031, Australia

• Show More

11:40

Interstitial Lung Disease (ILD) - Classification, pathophysiology, signs and symptoms

Where do I get my information from: http://armandoh.org/resource "Interstitial lung disea...

published: 17 Jan 2021

Play in Full Screen

Interstitial Lung Disease (ILD) - Classification, pathophysiology, signs and symptoms

Interstitial Lung Disease (ILD) - Classification, pathophysiology, signs and symptoms

• Report rights infringement
• published: 17 Jan 2021
• views: 208004

Where do I get my information from: http://armandoh.org/resource "Interstitial lung disease also known as diffuse parenchymal lung diseases (DPLDs) are a group of disorders based on similar clinical, radiographic, physiologic, and pathologic changes. Present primarily with shortness of breath and a non productive cough usually chronic over weeks to months without response to initial treatment of puffers. If there is clinical suspicion of ILD a full pulmonary function test should be done. Characteristic changes of ILD include: reduced total lung capacity (TLC) and DLCO. The diffuse parenchymal lung diseases are divided into those that are associated with known causes or unknown causes and other weird and wonderful rare causes." 🎥 DON'T JUST WATCH, LEARN ACTIVELY! TRY THE QUIZ! 🤓 https://youmakr.ai/test-playground/questionnaire/673d32a1859b9c170836ea51 👆Hit this quiz and show of your main character aura! Support me: 🖼️ Buy PDFs: http://armandoh.org/shop 💵 Patreon: http://www.patreon.com/armando 👕 Buy shirts: https://teespring.com/stores/ah-7 Social media: 📷 Instagram: http://instagram.com/armandohasudungan 🐦 Twitter: https://twitter.com/armandohasudung 📔 Facebook: https://www.facebook.com/ArmandoHasudungan Resources: 📕 Books: http://armandoh.org/resource 🎞️ Equipment: armandoh.org/armando-faigl You can send me mail: 📫 PO BOX 166, Randwick NSW 2031, Australia

• Show More

16:50

Interstitial Lung Disease (ILD) in a Nutshell

An overview of ILD (also known as diffuse parenchymal lung diseases), including definition...

published: 07 May 2019

Play in Full Screen

Interstitial Lung Disease (ILD) in a Nutshell

Interstitial Lung Disease (ILD) in a Nutshell

• Report rights infringement
• published: 07 May 2019
• views: 164407

An overview of ILD (also known as diffuse parenchymal lung diseases), including definition, classification, etiologies, and diagnostic evaluation (e.g. CT and PFT findings).

• Show More

4:25

Interstitial Lung Disease (ILD): Overview– Interstitial Lung Disease | Lecturio

This video “Interstitial Lung Disease (ILD): Overview” is part of the Lecturio course “Int...

published: 18 Feb 2020

Play in Full Screen

Interstitial Lung Disease (ILD): Overview– Interstitial Lung Disease | Lecturio

Interstitial Lung Disease (ILD): Overview– Interstitial Lung Disease | Lecturio

• Report rights infringement
• published: 18 Feb 2020
• views: 31595

This video “Interstitial Lung Disease (ILD): Overview” is part of the Lecturio course “Interstitial Lung Disease” ► WATCH the complete course on http://lectur.io/ildyoutube ► LEARN ABOUT: - classification of interstital lung disease ► THE PROF: Professor Jeremy Brown is a clinician scientist with an interest in respiratory infection. He studied medicine in London, graduating with honors, and continued his postgraduate medical training in a variety of London hospitals. He completed his PhD in molecular microbiology in 1999 and obtained a prestigious Welcome Advanced Research Fellowship for further scientific training at the University of Adelaide. His research is mainly focused on respiratory complications of haematological disease and stem cell transplantation. His educational and scientific experience enables him to teach students and professionals about respiratory medicine. ►LECTURIO is your single-point resource for medical school: Study for your classes, USMLE Step 1, USMLE Step 2, MCAT or MBBS with video lectures by world-class professors, recall & USMLE-style questions and textbook articles. Create your free account here: http://lectur.io/ildyoutube ► INSTALL our free Lecturio app iTunes Store: https://app.adjust.com/z21zrf Play Store: https://app.adjust.com/b01fak ► READ TEXTBOOK ARTICLES related to this video: Interstitial Lung Disease (ILD) — Types and Symptoms http://lectur.io/ildarticle ► SUBSCRIBE to our YouTube channel: http://lectur.io/subscribe ► WATCH MORE ON YOUTUBE: http://lectur.io/playlists ► LET’S CONNECT: • Facebook: https://www.facebook.com/lecturio.medical.education.videos • Instagram: https://www.instagram.com/lecturio_medical_videos

• Show More

24:26

Restrictive Lung Diseases - Interstitial Pulmonary Fibrosis. Pathology, Clinical, Tests, Treatment

Please read and agree to the disclaimer before watching this video. . Subscribe to the drb...

published: 03 Dec 2017

Play in Full Screen

Restrictive Lung Diseases - Interstitial Pulmonary Fibrosis. Pathology, Clinical, Tests, Treatment

Restrictive Lung Diseases - Interstitial Pulmonary Fibrosis. Pathology, Clinical, Tests, Treatment

• Report rights infringement
• published: 03 Dec 2017
• views: 116395

Please read and agree to the disclaimer before watching this video. . Subscribe to the drbeen Channel HERE: http://bit.ly/2GBhiS0 For more content from drbeen, click HERE: http://bit.ly/2GB41bU Watch drbeen videos HERE: http://bit.ly/2GB41bU Like drbeen on Facebook HERE: http://bit.ly/2GSSTGS Follow drbeen on Twitter HERE: http://bit.ly/2XeSVhV Follow drbeen on Instagram HERE: http://bit.ly/2ST2Zih Get new medical lectures across your devices. Stream anywhere, anytime. Try it for free! http://bit.ly/2QsIwQ5 This video presents the introduction to restrictive lung diseases. We will discuss:  Definition Types  Extrapulmonary restrictive lung diseases * Obesity * Scoliosis Pulmonary parenchymal restrictive lung diseases * Idiopathic * Autoimmune * Granulomatous (Wagner's granulomatosis, Sarcoidosis) * Occupational (pneumoconiosis, silicosis, asbestosis, coal, etc.) * Other irritants * Chronic infections (Tuberculosis) Neuromuscular restrictive lung diseases * Myasthenia gravis * Diaphragm issues * Polio Cellular events/pathogenesis * Damaged Type I Pneumocytes * Hypertrophy of Type II Pneumocytes * Irritated epithelium * Irritated macrophages * Apoptosis of epithelium * Tissue damage leading to local inflammation and lung destruction/scaring. * Neutrophils releasing cytokines, proteases, tumor growth factors (TGF) * Macrophages releasing transforming growth factor beta, tumor necrosis factor (TNF), platelet activation factor. * Fibroblasts overactivity resulting in more extracellular matrix and hardening. * Epithelial-mesenchymal transformation. * Smooth muscle proliferation. * Respiratory interface thickening. Disrupted gaseous exchange. Clinical: Dry hacking cough * Dyspnea * Hypoxia * Respiratory alkalosis * Late inspiratory crackles Abnormal chest X-Ray * Reduced volume in chest X-Ray * Lower lobes show more involvement and the reason why. * Right heart failure/cor pulmonale  Lung Function Changes * FEV1/FVC ratio increases above 80% (normal or above normal) Treatment * Anti-inflammatory (may not be very effective) * TGF Beta-blockers * Oxygen * Lung transplant ... Disclaimer: This video is not intended to provide assessment, diagnosis, treatment, or medical advice; it also does not constitute provision of healthcare services. The content provided in this video is for informational and educational purposes only. Please consult with a physician or healthcare professional regarding any medical or mental health related diagnosis or treatment. No information in this video should ever be considered as a substitute for advice from a healthcare professional. ... Disclaimer: This video is not intended to provide assessment, diagnosis, treatment, or medical advice; it also does not constitute provision of healthcare services. The content provided in this video is for informational and educational purposes only. Please consult with a physician or healthcare professional regarding any medical or mental health related diagnosis or treatment. No information in this video should ever be considered as a substitute for advice from a healthcare professional.

• Show More

4:56

Interstitial lung disease, Causes, Signs and Symptoms, Diagnosis and Treatment

. Chapters 0:00 Introduction 1:18 Causes of Interstitial lung disease 3:13 Symptoms and ...

published: 31 Jan 2021

Play in Full Screen

Interstitial lung disease, Causes, Signs and Symptoms, Diagnosis and Treatment

Interstitial lung disease, Causes, Signs and Symptoms, Diagnosis and Treatment

• Report rights infringement
• published: 31 Jan 2021
• views: 41426

. Chapters 0:00 Introduction 1:18 Causes of Interstitial lung disease 3:13 Symptoms and Diagnosis of Interstitial lung disease 3:53 Treatment of Interstitial lung disease. Interstitial lung disease (ILD), or diffuse parenchymal lung disease (DPLD),[3] is a group of respiratory diseases affecting the interstitium (the tissue and space around the alveoli (air sacs) of the lungs.[4] It concerns alveolar epithelium, pulmonary capillary endothelium, basement membrane, and perivascular and perilymphatic tissues. It may occur when an injury to the lungs triggers an abnormal healing response. Ordinarily, the body generates just the right amount of tissue to repair damage, but in interstitial lung disease, the repair process is disrupted, and the tissue around the air sacs (alveoli) becomes scarred and thickened. This makes it more difficult for oxygen to pass into the bloodstream. The disease presents itself with the following symptoms: shortness of breath, nonproductive coughing, fatigue, and weight loss, which tend to develop slowly, over several months. The average rate of survival for someone with this disease is between three and five years.[5] The term ILD is used to distinguish these diseases from obstructive airways diseases. There are specific types in children, known as children's interstitial lung diseases. The acronym ChILD is sometimes used for this group of diseases.[6] Prolonged ILD may result in pulmonary fibrosis, but this is not always the case. Idiopathic pulmonary fibrosis is interstitial lung disease for which no obvious cause can be identified (idiopathic) and is associated with typical findings both radiographic (basal and pleural-based fibrosis with honeycombing) and pathologic (temporally and spatially heterogeneous fibrosis, histopathologic honeycombing, and fibroblastic foci).

• Show More

8:35

Interstitial Lung Disease

Interstitial lung disease or ILD is an autoimmune condition of the lung. In some people, ...

published: 30 Jul 2018

Play in Full Screen

Interstitial Lung Disease

Interstitial Lung Disease

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• published: 30 Jul 2018
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Interstitial lung disease or ILD is an autoimmune condition of the lung. In some people, the body will attack itself and when it happens in the lung, it is a problem. Once the body begins to attack the lung, you become more short of breath. This video will tell you why.

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Usual interstitial pneumonia

Usual interstitial pneumonia (UIP) is a form of lung disease characterized by progressive scarring of both lungs. The scarring (fibrosis) involves the supporting framework (interstitium) of the lung. UIP is thus classified as a form of interstitial lung disease. The term "usual" refers to the fact that UIP is the most common form of interstitial fibrosis. "Pneumonia" indicates "lung abnormality", which includes fibrosis and inflammation. A term previously used for UIP in the British literature is cryptogenic fibrosing alveolitis, a term that has fallen out of favor since the basic underlying pathology is now thought to be fibrosis, not inflammation.

Causes

The cause of the scarring in UIP may be known (less commonly) or unknown (more commonly). Since the medical term for conditions of unknown cause is "idiopathic", the clinical term for UIP of unknown cause is idiopathic pulmonary fibrosis (IPF). Examples of known causes of UIP include systemic sclerosis/scleroderma, rheumatoid arthritis, asbestosis, and chronic nitrofurantoin toxicity.

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This page contains text from Wikipedia, the Free Encyclopedia - https://wn.com/Usual_interstitial_pneumonia

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