'+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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playShouldStart = null; } }; function loadMoreVideos(playerId, vp, start, finish, callback){ var playlistInfo = playlists[playerId-1]; if(playlistInfo.loading >= finish) return; playlistInfo.loading = finish; $.ajax({ url: '/api/upge/cheetah-photo-search/query_videos2', dataType: 'json', data: { query: playlistInfo.query, orderby: playlistInfo.orderby, start: start, count: finish-start }, success: function(response){ var pl = vp.getPlaylist().slice(0); pl.push.apply(pl, response); vp.setPlaylist(pl); callback(); } }); } if(parts.length == 1 && matchDash(parts[0])){ var pl = vp.getActualPlaylist(); var vids = parseDash(parts[0]); parts = []; for(var i = 0; i < vids.length; i++){ playQueue.push({ 'video': pl[vids[i]-1], 'start': 0, 'stop': null }) } if(vids.length){ if(vids[vids.length-1]-1>=pl.length){ loadMoreVideos(playerId, vp, pl.length, vids[vids.length-1], function(){ if(fsonload){ activateTabArea(tab, parts[0]+'/fs'); }else{ activateTabArea(tab, parts[0]); } var pls = vp.getPlaylist(); 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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if(window.history && history.replaceState && document.location.hostname.match(/^(youtube\.)?(\w{2,3}\.)?wn\.com$/)){ if(path == main_tab || path == main_tab+'/' || path == '' || path == '/') { path = basepath; } else if( path.match('^'+main_tab+'/') ){ path = basepath + '/' + path.replace(main_tab+'/', '').replace('--','/'); } else { path = basepath + '/' + path.replace('--','/'); } if(document.location.search){ path += document.location.search; } if(window.lastHistory) { history.pushState(null, null, path); } else if(window.lastHistory != path){ history.replaceState(null, null, path); window.lastHistory = path; } } else{ path = path.replace('--','/'); if(path == main_tab || path == main_tab+'/' || path == '' || path == '/') { path = ''; } if(window.lastHistory != '/'+path){ window.location.hash = path? '/'+path : ''; window.lastHistory = '/'+path; } } }); $('.tabtrigger li a').live('click', ensure(function() { var tab = $(this).attr('id'); if(tab.substring(0,1) == '#'){ var name = tab.substring(1); if(name in menu_names){ name = menu_names[name][0]; } realTab = rev_names[name]; $('#'+realTab).show(); if(window.console && console.log) console.log("Triggering tab: "+name+(window.activeArea?" activeArea="+window.activeArea:'')); var path = name; if(window.activeArea){ path = path + '/' + window.activeArea; } if(tab.match(/#playlist\d+/) || tab.match(/#details\d+/)){ $('.multiple-playlists').show(); $('.related_playlist').show(); $('.longest_videos_playlist').show(); }else { $('.multiple-playlists').hide(); $('.related_playlist').hide(); $('.longest_videos_playlist').hide(); } // start the related script only when the tab is on screen showing if (tab.match(/related_sites/)) { if (mc) { mc.startCredits(); } } window.activeTab = realTab; addHistory(path); setTimeout(ensure(function(){ if(tab.match(/language--/)){ $('.tabtrigger').offscreentabs('activateTab', 'language'); } if(tab.match(/weather/)) { $('.tabtrigger').offscreentabs('activateTab', 'weather'); loadContinent(); } updateMenus(tab); updateHeight(); }), 10); } return false; })); }); -->

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  Pulmonary Fibrosis

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  Pulmonary Fibrosis

• Pulmonary fibrosis

Pulmonary fibrosis

Pulmonary fibrosis (literally "scarring of the lungs") is a respiratory disease in which scars are formed in the lung tissues, leading to serious breathing problems. Scar formation, the accumulation of excess fibrous connective tissue (the process called fibrosis), leads to thickening of the walls, and causes reduced oxygen supply in the blood. As a consequence patients suffer from perpetual shortness of breath.

In some patients the specific cause of the disease can be diagnosed, but in others the probable cause cannot be determined, a condition called idiopathic pulmonary fibrosis. There is no known cure for the scars and damage in the lung due to pulmonary fibrosis.

Signs and symptoms

Symptoms of pulmonary fibrosis are mainly:

Shortness of breath, particularly with exertion

Chronic dry, hacking coughing

Fatigue and weakness

Chest discomfort including chest pain

Loss of appetite and rapid weight loss

Pulmonary fibrosis is suggested by a history of progressive shortness of breath (dyspnea) with exertion. Sometimes fine inspiratory crackles can be heard at the lung bases on auscultation. A chest x-ray may or may not be abnormal, but high-resolution CT will frequently demonstrate abnormalities.

Read more

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

Podcasts:

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

• 

  Understanding Pulmonary Fibrosis

  Randy was diagnosed with idiopathic pulmonary fibrosis (IPF) on Christmas Eve 2008 – a day he will never forget. If you, or someone you love, has been diagnosed with pulmonary fibrosis, there are steps you can take to make living with this disease easier. Dr. Jane Dematte and Randy share more information about living and managing this rare lung disease. Learn more about pulmonary fibrosis, and access American Lung Association resources, at Lung.org/pf. Produced with support from Three Lakes Partners.

  published: 20 Feb 2018
• 

  Life With Pulmonary Fibrosis | What is Pulmonary Fibrosis?

  Dr. David J. Lederer, Senior Medical Advisor for Education and Awareness for the Pulmonary Fibrosis Foundation, Explains Pulmonary Fibrosis. Dr. David Lederer explains that the big picture of lung disease is vast and includes a family of diseases called interstitial lung diseases (ILD), which consist of more than 100 different diseases. These diseases are grouped together because they share two common features - inflammation and scar tissue, which occur in the walls of the tiny air sacs of the lungs. The difference between interstitial lung disease and pulmonary fibrosis is that interstitial lung diseases include all of the diseases in which there is inflammation or scar tissue in the walls of the air sacs. Pulmonary fibrosis is not a specific disease but is a general term that refers ...

  published: 02 May 2018
• 

  Idiopathic Pulmonary Fibrosis - pathophysiology, signs and symptoms, investigation and treatment

  "Idiopathic pulmonary fibrosis is a chronic progressive fibrotic interstitial lung disease of unknown cause that primarily occurs in older adults. Doctors suspect interstitial lung disease when an adult presents with unexplained exertional dyspnoea, chronic dry cough or inspiratory velcro-like crackles on examination. Fibrosis is typically in the lower lobes of the lung. Clubbing , low oxygen saturation and dyspnoea is the hallmark of idiopathic pulmonary fibrosis. High resolution CT chest is cold standard for diagnosis. Here you see the pathological pattern of usual interstitial pneumonia: low base predominance, traction bronchiectasis, honeycombing and reticular changes without significance ground glass changes" Support me: 🖼️ Buy PDFs: http://armandoh.org/shop 💵 Patreon: http://www.p...

  published: 21 Aug 2021
• 

  Pulmonary Fibrosis: Everything You Need To Know

  . Chapters 0:00 Introduction 0:50 Causes of Pulmonary Fibrosis 1:08 Factors include 2:35 Symptoms of Pulmonary Fibrosis 2:52 Diagnosis and treatment of Pulmonary Fibrosis 3:15 Treatment for Pulmonary Fibrosis Pulmonary fibrosis is a condition in which the lungs become scarred over time.[1] Symptoms include shortness of breath, a dry cough, feeling tired, weight loss, and nail clubbing.[1] Complications may include pulmonary hypertension, respiratory failure, pneumothorax, and lung cancer.[2] Causes include environmental pollution, certain medications, connective tissue diseases, infections, and interstitial lung diseases.[1][3][6] Idiopathic pulmonary fibrosis (IPF), an interstitial lung disease of unknown cause, is most common.[1][3] Diagnosis may be based on symptoms, medical imag...

  published: 27 Sep 2022
• 

  Idiopathic pulmonary fibrosis - an Osmosis preview

  What is idiopathic pulmonary fibrosis (IPF)? Idiopathic pulmonary fibrosis is where the lungs undergo scarring and fibrosis for some unknown reason. Find our complete video library only on Osmosis Prime: http://osms.it/more. Hundreds of thousands of current & future clinicians learn by Osmosis. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. Subscribe to our Youtube channel at http://osms.it/subscribe. Get early access to our upcoming video releases, practice questions, giveaways, and more when you follow us on social media: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram: http://osms.it/instagram Our Vision: Everyone who cares for so...

  published: 11 Dec 2018
• 

  Behind Each Breath: Shedding Light on Idiopathic Pulmonary Fibrosis

  Learn more about Idiopathic Pulmonary Fibrosis (IPF) here: https://www.gene.com/stories/behind-each-breath-shedding-light-on-idiopathic-pulmonary-fibrosis

  published: 08 Sep 2020
• 

  Is Pulmonary Fibrosis the same as Idiopathic Pulmonary Fibrosis?

  In this video we attempt to answer a number of questions relevant for patients diagnosed with Pulmonary Fibrosis and Idiopathic Pulmonary Fibrosis IPF. These questions cover a wide variety of topics including oxygen content, treatments and symptoms. Please let us know if you have any comments or better answers to some of these common and difficult questions. Subscribe to the McMaster Demystifying Medicine YouTube channel: https://www.youtube.com/c/DemystifyingMedicine This video is provided for general and educational information only. Please consult your health care provider for Information about your health. This video was made by Tristan Richardson & Anuj Patel in collaboration with the McMaster Demystifying Medicine Program Copyright McMaster University 2016 #DemystifyingMedi...

  published: 06 May 2016
• 

  Idiopathic Pulmonary Fibrosis | Restrictive Lung Disease | Pulmonology

  😍🖼Animated Mnemonics (Picmonic): https://www.picmonic.com/viphookup/medicosis/ - With Picmonic, get your life back by studying less and remembering more. Medical and Nursing students say that Picmonic is the most comprehensive and effective way to bridge learning and test prep... Disclaimer: I use affiliate links.... ►👨‍🏫💊Antibiotics Lectures: https://www.medicosisperfectionalis.com/products/courses/antibiotics/ ... Check out my brand new "Electrolytes" course at https://www.medicosisperfectionalis.com/products/course/electrolytes/ and use the PROMO code: ELECTROLYTES50 to get a 50% discount. If you like my videos, please consider leaving a tip at https://www.paypal.me/perfectionalis/ ► Visit my website: https://www.medicosisperfectionalis.com/ My Favorite Productivity App: https://...

  published: 26 Sep 2019
• 

  Hamish Osborne - Beating pulmonary fibrosis, thanks to the University of Maryland

  Hamish S. Osborne and Christine C. Osborne are among the founding supporters of the Program in Lung Healing at the University of Maryland School of Medicine. Mr. Osborne’s diagnosis of idiopathic pulmonary fibrosis resulted in a life-saving double-lung transplant at the University of Maryland Medical Center. He is the only reported patient to survive retransplantation after contracting a rare fungal disease called pulmonary mucormycosis after his first single lung transplant. In this video, Hamish Osborne talks about his illness, and what led him to support the Program in Lung Healing. To learn more and make gift, visit: http://medschool.umaryland.edu/development/ The University of Maryland School of Medicine serves as the anchor for a large academic health center which aims to provid...

  published: 01 Dec 2015

3:29

Understanding Pulmonary Fibrosis

• Order: Reorder
• Duration: 3:29
• Uploaded Date: 20 Feb 2018
• views: 58766

Randy was diagnosed with idiopathic pulmonary fibrosis (IPF) on Christmas Eve 2008 – a day he will never forget. If you, or someone you love, has been diagnose...

Randy was diagnosed with idiopathic pulmonary fibrosis (IPF) on Christmas Eve 2008 – a day he will never forget. If you, or someone you love, has been diagnosed with pulmonary fibrosis, there are steps you can take to make living with this disease easier. Dr. Jane Dematte and Randy share more information about living and managing this rare lung disease. Learn more about pulmonary fibrosis, and access American Lung Association resources, at Lung.org/pf. Produced with support from Three Lakes Partners.

https://wn.com/Understanding_Pulmonary_Fibrosis

Randy was diagnosed with idiopathic pulmonary fibrosis (IPF) on Christmas Eve 2008 – a day he will never forget. If you, or someone you love, has been diagnosed with pulmonary fibrosis, there are steps you can take to make living with this disease easier. Dr. Jane Dematte and Randy share more information about living and managing this rare lung disease. Learn more about pulmonary fibrosis, and access American Lung Association resources, at Lung.org/pf. Produced with support from Three Lakes Partners.

• published: 20 Feb 2018
• views: 58766

5:17

Life With Pulmonary Fibrosis | What is Pulmonary Fibrosis?

• Order: Reorder
• Duration: 5:17
• Uploaded Date: 02 May 2018
• views: 176496

Dr. David J. Lederer, Senior Medical Advisor for Education and Awareness for the Pulmonary Fibrosis Foundation, Explains Pulmonary Fibrosis. Dr. David Lederer...

Dr. David J. Lederer, Senior Medical Advisor for Education and Awareness for the Pulmonary Fibrosis Foundation, Explains Pulmonary Fibrosis. Dr. David Lederer explains that the big picture of lung disease is vast and includes a family of diseases called interstitial lung diseases (ILD), which consist of more than 100 different diseases. These diseases are grouped together because they share two common features - inflammation and scar tissue, which occur in the walls of the tiny air sacs of the lungs. The difference between interstitial lung disease and pulmonary fibrosis is that interstitial lung diseases include all of the diseases in which there is inflammation or scar tissue in the walls of the air sacs. Pulmonary fibrosis is not a specific disease but is a general term that refers to any kind of ILD in which scar tissue is present in the walls of the air sacs. The Pulmonary Fibrosis Foundation (PFF) offers essential programs and resources for people with pulmonary fibrosis. The mission of the PFF is to mobilize people and resources to provide access to high quality care and to lead research for a cure so that people with PF will lead longer, healthier lives. For more information, visit pulmonaryfibrosis.org. Social media platforms - Twitter - @PFFORG Facebook - @PFFORG Instagram - @PFFORG LinkedIn- Pulmonary Fibrosis Foundation Please note that any information contained in this presentation is for informational and/or educational purposes only. It is not intended to be a substitute for professional medical advice. Always consult your personal physician or health care provider with any questions you may have regarding your specific medical condition. This presentation is protected by U.S. and International copyright laws. Reproductions and distribution of this presentation without written permission from the Pulmonary Fibrosis Foundation is prohibited. © 2018 Pulmonary Fibrosis Foundation

https://wn.com/Life_With_Pulmonary_Fibrosis_|_What_Is_Pulmonary_Fibrosis

Dr. David J. Lederer, Senior Medical Advisor for Education and Awareness for the Pulmonary Fibrosis Foundation, Explains Pulmonary Fibrosis. Dr. David Lederer explains that the big picture of lung disease is vast and includes a family of diseases called interstitial lung diseases (ILD), which consist of more than 100 different diseases. These diseases are grouped together because they share two common features - inflammation and scar tissue, which occur in the walls of the tiny air sacs of the lungs. The difference between interstitial lung disease and pulmonary fibrosis is that interstitial lung diseases include all of the diseases in which there is inflammation or scar tissue in the walls of the air sacs. Pulmonary fibrosis is not a specific disease but is a general term that refers to any kind of ILD in which scar tissue is present in the walls of the air sacs. The Pulmonary Fibrosis Foundation (PFF) offers essential programs and resources for people with pulmonary fibrosis. The mission of the PFF is to mobilize people and resources to provide access to high quality care and to lead research for a cure so that people with PF will lead longer, healthier lives. For more information, visit pulmonaryfibrosis.org. Social media platforms - Twitter - @PFFORG Facebook - @PFFORG Instagram - @PFFORG LinkedIn- Pulmonary Fibrosis Foundation Please note that any information contained in this presentation is for informational and/or educational purposes only. It is not intended to be a substitute for professional medical advice. Always consult your personal physician or health care provider with any questions you may have regarding your specific medical condition. This presentation is protected by U.S. and International copyright laws. Reproductions and distribution of this presentation without written permission from the Pulmonary Fibrosis Foundation is prohibited. © 2018 Pulmonary Fibrosis Foundation

• published: 02 May 2018
• views: 176496

11:06

Idiopathic Pulmonary Fibrosis - pathophysiology, signs and symptoms, investigation and treatment

• Order: Reorder
• Duration: 11:06
• Uploaded Date: 21 Aug 2021
• views: 123017

"Idiopathic pulmonary fibrosis is a chronic progressive fibrotic interstitial lung disease of unknown cause that primarily occurs in older adults. Doctors suspe...

"Idiopathic pulmonary fibrosis is a chronic progressive fibrotic interstitial lung disease of unknown cause that primarily occurs in older adults. Doctors suspect interstitial lung disease when an adult presents with unexplained exertional dyspnoea, chronic dry cough or inspiratory velcro-like crackles on examination. Fibrosis is typically in the lower lobes of the lung. Clubbing , low oxygen saturation and dyspnoea is the hallmark of idiopathic pulmonary fibrosis. High resolution CT chest is cold standard for diagnosis. Here you see the pathological pattern of usual interstitial pneumonia: low base predominance, traction bronchiectasis, honeycombing and reticular changes without significance ground glass changes" 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/Idiopathic_Pulmonary_Fibrosis_Pathophysiology,_Signs_And_Symptoms,_Investigation_And_Treatment

"Idiopathic pulmonary fibrosis is a chronic progressive fibrotic interstitial lung disease of unknown cause that primarily occurs in older adults. Doctors suspect interstitial lung disease when an adult presents with unexplained exertional dyspnoea, chronic dry cough or inspiratory velcro-like crackles on examination. Fibrosis is typically in the lower lobes of the lung. Clubbing , low oxygen saturation and dyspnoea is the hallmark of idiopathic pulmonary fibrosis. High resolution CT chest is cold standard for diagnosis. Here you see the pathological pattern of usual interstitial pneumonia: low base predominance, traction bronchiectasis, honeycombing and reticular changes without significance ground glass changes" 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: 21 Aug 2021
• views: 123017

4:19

Pulmonary Fibrosis: Everything You Need To Know

• Order: Reorder
• Duration: 4:19
• Uploaded Date: 27 Sep 2022
• views: 129349

. Chapters 0:00 Introduction 0:50 Causes of Pulmonary Fibrosis 1:08 Factors include 2:35 Symptoms of Pulmonary Fibrosis 2:52 Diagnosis and treatment of Pulmon...

. Chapters 0:00 Introduction 0:50 Causes of Pulmonary Fibrosis 1:08 Factors include 2:35 Symptoms of Pulmonary Fibrosis 2:52 Diagnosis and treatment of Pulmonary Fibrosis 3:15 Treatment for Pulmonary Fibrosis Pulmonary fibrosis is a condition in which the lungs become scarred over time.[1] Symptoms include shortness of breath, a dry cough, feeling tired, weight loss, and nail clubbing.[1] Complications may include pulmonary hypertension, respiratory failure, pneumothorax, and lung cancer.[2] Causes include environmental pollution, certain medications, connective tissue diseases, infections, and interstitial lung diseases.[1][3][6] Idiopathic pulmonary fibrosis (IPF), an interstitial lung disease of unknown cause, is most common.[1][3] Diagnosis may be based on symptoms, medical imaging, lung biopsy, and lung function tests.[1] There is no cure and there are limited treatment options available.[1] Treatment is directed towards efforts to improve symptoms and may include oxygen therapy and pulmonary rehabilitation.[1][4] Certain medications may be used to try to slow the worsening of scarring.[4] Lung transplantation may occasionally be an option.[3] At least 5 million people are affected globally.[5] Life expectancy is generally less than five years.[3] Symptoms of pulmonary fibrosis are mainly:[7] Shortness of breath, particularly with exertion Chronic dry, hacking coughing Fatigue and weakness Chest discomfort including chest pain Loss of appetite and rapid weight loss Pulmonary fibrosis is suggested by a history of progressive shortness of breath (dyspnea) with exertion. Sometimes fine inspiratory crackles can be heard at the lung bases on auscultation. A chest X-ray may or may not be abnormal, but high-resolution CT will frequently demonstrate abnormalities.[3] Cause Further information: Interstitial lung disease Pulmonary fibrosis may be a secondary effect of other diseases. Most of these are classified as interstitial lung diseases. Examples include autoimmune disorders, viral infections and bacterial infection like tuberculosis which may cause fibrotic changes in both lung's upper or lower lobes and other microscopic injuries to the lung. However, pulmonary fibrosis can also appear without any known cause. In this case, it is termed "idiopathic".[8] Most idiopathic cases are diagnosed as idiopathic pulmonary fibrosis. This is a diagnosis of exclusion of a characteristic set of histologic/pathologic features known as usual interstitial pneumonia (UIP). In either case, there is a growing body of evidence which points to a genetic predisposition in a subset of patients. For example, a mutation in surfactant protein C (SP-C) has been found to exist in some families with a history of pulmonary fibrosis.[9] Autosomal dominant mutations in the TERC or TERT genes, which encode telomerase, have been identified in about 15 percent of pulmonary fibrosis patients.[10] Diseases and conditions that may cause pulmonary fibrosis as a secondary effect include:[3][9] Inhalation of environmental and occupational pollutants, such as metals[11] in asbestosis, silicosis and exposure to certain gases. Coal miners, ship workers and sand blasters among others are at higher risk.[8] Hypersensitivity pneumonitis, most often resulting from inhaling dust contaminated with bacterial, fungal, or animal products Cigarette smoking can increase the risk or make the illness worse[8] Some typical connective tissue diseases[8] such as rheumatoid arthritis, ankylosing spondylitis, SLE and scleroderma Other diseases that involve connective tissue, such as sarcoidosis and granulomatosis with polyangiitis Infections, including COVID-19 Certain medications, e.g. amiodarone, bleomycin (pingyangmycin), busulfan, methotrexate,[8] apomorphine,[12] and nitrofurantoin[13] Radiation therapy to the chest Chapters 0:00 Introduction 0:50 Causes of Pulmonary Fibrosis 1:08 Factors of Pulmonary Fibrosis 2:35 Symptoms of Pulmonary Fibrosis 2:52 Diagnosis for Pulmonary Fibrosis 3:16 Treatment for Pulmonary Fibrosis

https://wn.com/Pulmonary_Fibrosis_Everything_You_Need_To_Know

. Chapters 0:00 Introduction 0:50 Causes of Pulmonary Fibrosis 1:08 Factors include 2:35 Symptoms of Pulmonary Fibrosis 2:52 Diagnosis and treatment of Pulmonary Fibrosis 3:15 Treatment for Pulmonary Fibrosis Pulmonary fibrosis is a condition in which the lungs become scarred over time.[1] Symptoms include shortness of breath, a dry cough, feeling tired, weight loss, and nail clubbing.[1] Complications may include pulmonary hypertension, respiratory failure, pneumothorax, and lung cancer.[2] Causes include environmental pollution, certain medications, connective tissue diseases, infections, and interstitial lung diseases.[1][3][6] Idiopathic pulmonary fibrosis (IPF), an interstitial lung disease of unknown cause, is most common.[1][3] Diagnosis may be based on symptoms, medical imaging, lung biopsy, and lung function tests.[1] There is no cure and there are limited treatment options available.[1] Treatment is directed towards efforts to improve symptoms and may include oxygen therapy and pulmonary rehabilitation.[1][4] Certain medications may be used to try to slow the worsening of scarring.[4] Lung transplantation may occasionally be an option.[3] At least 5 million people are affected globally.[5] Life expectancy is generally less than five years.[3] Symptoms of pulmonary fibrosis are mainly:[7] Shortness of breath, particularly with exertion Chronic dry, hacking coughing Fatigue and weakness Chest discomfort including chest pain Loss of appetite and rapid weight loss Pulmonary fibrosis is suggested by a history of progressive shortness of breath (dyspnea) with exertion. Sometimes fine inspiratory crackles can be heard at the lung bases on auscultation. A chest X-ray may or may not be abnormal, but high-resolution CT will frequently demonstrate abnormalities.[3] Cause Further information: Interstitial lung disease Pulmonary fibrosis may be a secondary effect of other diseases. Most of these are classified as interstitial lung diseases. Examples include autoimmune disorders, viral infections and bacterial infection like tuberculosis which may cause fibrotic changes in both lung's upper or lower lobes and other microscopic injuries to the lung. However, pulmonary fibrosis can also appear without any known cause. In this case, it is termed "idiopathic".[8] Most idiopathic cases are diagnosed as idiopathic pulmonary fibrosis. This is a diagnosis of exclusion of a characteristic set of histologic/pathologic features known as usual interstitial pneumonia (UIP). In either case, there is a growing body of evidence which points to a genetic predisposition in a subset of patients. For example, a mutation in surfactant protein C (SP-C) has been found to exist in some families with a history of pulmonary fibrosis.[9] Autosomal dominant mutations in the TERC or TERT genes, which encode telomerase, have been identified in about 15 percent of pulmonary fibrosis patients.[10] Diseases and conditions that may cause pulmonary fibrosis as a secondary effect include:[3][9] Inhalation of environmental and occupational pollutants, such as metals[11] in asbestosis, silicosis and exposure to certain gases. Coal miners, ship workers and sand blasters among others are at higher risk.[8] Hypersensitivity pneumonitis, most often resulting from inhaling dust contaminated with bacterial, fungal, or animal products Cigarette smoking can increase the risk or make the illness worse[8] Some typical connective tissue diseases[8] such as rheumatoid arthritis, ankylosing spondylitis, SLE and scleroderma Other diseases that involve connective tissue, such as sarcoidosis and granulomatosis with polyangiitis Infections, including COVID-19 Certain medications, e.g. amiodarone, bleomycin (pingyangmycin), busulfan, methotrexate,[8] apomorphine,[12] and nitrofurantoin[13] Radiation therapy to the chest Chapters 0:00 Introduction 0:50 Causes of Pulmonary Fibrosis 1:08 Factors of Pulmonary Fibrosis 2:35 Symptoms of Pulmonary Fibrosis 2:52 Diagnosis for Pulmonary Fibrosis 3:16 Treatment for Pulmonary Fibrosis

• published: 27 Sep 2022
• views: 129349

1:04

Idiopathic pulmonary fibrosis - an Osmosis preview

• Order: Reorder
• Duration: 1:04
• Uploaded Date: 11 Dec 2018
• views: 51957

What is idiopathic pulmonary fibrosis (IPF)? Idiopathic pulmonary fibrosis is where the lungs undergo scarring and fibrosis for some unknown reason. Find our ...

What is idiopathic pulmonary fibrosis (IPF)? Idiopathic pulmonary fibrosis is where the lungs undergo scarring and fibrosis for some unknown reason. Find our complete video library only on Osmosis Prime: http://osms.it/more. Hundreds of thousands of current & future clinicians learn by Osmosis. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. Subscribe to our Youtube channel at http://osms.it/subscribe. Get early access to our upcoming video releases, practice questions, giveaways, and more when you follow us on social media: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram: http://osms.it/instagram Our Vision: Everyone who cares for someone will learn by Osmosis. Our Mission: To empower the world’s clinicians and caregivers with the best learning experience possible. Learn more here: http://osms.it/mission Medical disclaimer: Knowledge Diffusion Inc (DBA Osmosis) does not provide medical advice. Osmosis and the content available on Osmosis's properties (Osmosis.org, YouTube, and other channels) do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcare professional in diagnosis and treatment of any person or animal. The determination of the need for medical services and the types of healthcare to be provided to a patient are decisions that should be made only by a physician or other licensed health care provider. Always seek the advice of a physician or other qualified healthcare provider with any questions you have regarding a medical condition.

https://wn.com/Idiopathic_Pulmonary_Fibrosis_An_Osmosis_Preview

What is idiopathic pulmonary fibrosis (IPF)? Idiopathic pulmonary fibrosis is where the lungs undergo scarring and fibrosis for some unknown reason. Find our complete video library only on Osmosis Prime: http://osms.it/more. Hundreds of thousands of current & future clinicians learn by Osmosis. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. Subscribe to our Youtube channel at http://osms.it/subscribe. Get early access to our upcoming video releases, practice questions, giveaways, and more when you follow us on social media: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram: http://osms.it/instagram Our Vision: Everyone who cares for someone will learn by Osmosis. Our Mission: To empower the world’s clinicians and caregivers with the best learning experience possible. Learn more here: http://osms.it/mission Medical disclaimer: Knowledge Diffusion Inc (DBA Osmosis) does not provide medical advice. Osmosis and the content available on Osmosis's properties (Osmosis.org, YouTube, and other channels) do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcare professional in diagnosis and treatment of any person or animal. The determination of the need for medical services and the types of healthcare to be provided to a patient are decisions that should be made only by a physician or other licensed health care provider. Always seek the advice of a physician or other qualified healthcare provider with any questions you have regarding a medical condition.

• published: 11 Dec 2018
• views: 51957

2:17

Behind Each Breath: Shedding Light on Idiopathic Pulmonary Fibrosis

• Order: Reorder
• Duration: 2:17
• Uploaded Date: 08 Sep 2020
• views: 16160

Learn more about Idiopathic Pulmonary Fibrosis (IPF) here: https://www.gene.com/stories/behind-each-breath-shedding-light-on-idiopathic-pulmonary-fibrosis

Learn more about Idiopathic Pulmonary Fibrosis (IPF) here: https://www.gene.com/stories/behind-each-breath-shedding-light-on-idiopathic-pulmonary-fibrosis

https://wn.com/Behind_Each_Breath_Shedding_Light_On_Idiopathic_Pulmonary_Fibrosis

Learn more about Idiopathic Pulmonary Fibrosis (IPF) here: https://www.gene.com/stories/behind-each-breath-shedding-light-on-idiopathic-pulmonary-fibrosis

• published: 08 Sep 2020
• views: 16160

4:35

Is Pulmonary Fibrosis the same as Idiopathic Pulmonary Fibrosis?

• Order: Reorder
• Duration: 4:35
• Uploaded Date: 06 May 2016
• views: 83385

In this video we attempt to answer a number of questions relevant for patients diagnosed with Pulmonary Fibrosis and Idiopathic Pulmonary Fibrosis IPF. These qu...

In this video we attempt to answer a number of questions relevant for patients diagnosed with Pulmonary Fibrosis and Idiopathic Pulmonary Fibrosis IPF. These questions cover a wide variety of topics including oxygen content, treatments and symptoms. Please let us know if you have any comments or better answers to some of these common and difficult questions. Subscribe to the McMaster Demystifying Medicine YouTube channel: https://www.youtube.com/c/DemystifyingMedicine This video is provided for general and educational information only. Please consult your health care provider for Information about your health. This video was made by Tristan Richardson & Anuj Patel in collaboration with the McMaster Demystifying Medicine Program Copyright McMaster University 2016 #DemystifyingMedicine, #IPF Works Cited 1. Learn About Pulmonary Fibrosis [Internet]. American Lung Association. 2016 [cited 16 March 2016]. Available from: http://www.lung.org/lung-health-and-diseases/lung-disease-lookup/pulmonary-fibrosis/learn-about-pulmonary.html?referrer=https://www.google.ca/ 2. Nalysnyk L, Cid-Ruzafa J, Rotella P, Esser D. Incidence and prevalence of idiopathic pulmonary fibrosis: review of the literature. European Respiratory Review. 2012;21(126):355-361. 3. Kuranishi L, Leslie K, Ferreira R, Coletta E, Storrer K, Soares M et al. Airway-centered interstitial fibrosis: etiology, clinical findings and prognosis. Respiratory Research. 2015;16(1). 4. Bronchus / Bronchi / Bronchioles [Internet]. Cts.usc.edu. 2016 [cited 16 March 2016]. Available from: http://www.cts.usc.edu/zglossary-bronchus.html 5. Kerkhoff A. Normal Range of Blood Oxygen Level | LIVESTRONG.COM [Internet]. LIVESTRONG.COM. 2014 [cited 16 March 2016]. Available from: http://www.livestrong.com/article/124374-normal-range-blood-oxygen-level/ 6. Participation Program for Pulmonary FIbrosis [Internet]. National Jewish Health. 2016 [cited 16 March 2016]. Available from: https://www.nationaljewish.org/Participation-Program-for-Pulmonary-Fibrosis/Community/Blog/Participation-Program-for-Pulmonary-Fibrosis/October-2013/How-can-I-be-short-of-breath-when-my-saturation-is-93 7. Jones R, Hilldrup S, Hope-Gill B, Eccles R, Harrison N. Mechanical induction of cough in Idiopathic Pulmonary Fibrosis. Cough. 2011;7(1):2. 8. Scholand M, Wolff R, Crossno P, Sundar K, Winegar M, Whipple S et al. Severity of cough in idiopathic pulmonary fibrosis is associated with MUC5 B genotype. Cough. 2014;10(1):3. 9. Chamberlain S, Garrod R, Birring S. Cough suppression therapy: Does it work?. Pulmonary Pharmacology & Therapeutics. 2013;26(5):524-527. 10. How Is Idiopathic Pulmonary Fibrosis Diagnosed? - NHLBI, NIH [Internet]. Nhlbi.nih.gov. 2016 [cited 16 March 2016]. Available from: https://www.nhlbi.nih.gov/health/health-topics/topics/ipf/diagnosis 11. Gotway M, Freemer M, King T. Challenges in pulmonary fibrosis {middle dot} 1: Use of high resolution CT scanning of the lung for the evaluation of patients with idiopathic interstitial pneumonias. Thorax. 2007;62(6):546-553.

https://wn.com/Is_Pulmonary_Fibrosis_The_Same_As_Idiopathic_Pulmonary_Fibrosis

In this video we attempt to answer a number of questions relevant for patients diagnosed with Pulmonary Fibrosis and Idiopathic Pulmonary Fibrosis IPF. These questions cover a wide variety of topics including oxygen content, treatments and symptoms. Please let us know if you have any comments or better answers to some of these common and difficult questions. Subscribe to the McMaster Demystifying Medicine YouTube channel: https://www.youtube.com/c/DemystifyingMedicine This video is provided for general and educational information only. Please consult your health care provider for Information about your health. This video was made by Tristan Richardson & Anuj Patel in collaboration with the McMaster Demystifying Medicine Program Copyright McMaster University 2016 #DemystifyingMedicine, #IPF Works Cited 1. Learn About Pulmonary Fibrosis [Internet]. American Lung Association. 2016 [cited 16 March 2016]. Available from: http://www.lung.org/lung-health-and-diseases/lung-disease-lookup/pulmonary-fibrosis/learn-about-pulmonary.html?referrer=https://www.google.ca/ 2. Nalysnyk L, Cid-Ruzafa J, Rotella P, Esser D. Incidence and prevalence of idiopathic pulmonary fibrosis: review of the literature. European Respiratory Review. 2012;21(126):355-361. 3. Kuranishi L, Leslie K, Ferreira R, Coletta E, Storrer K, Soares M et al. Airway-centered interstitial fibrosis: etiology, clinical findings and prognosis. Respiratory Research. 2015;16(1). 4. Bronchus / Bronchi / Bronchioles [Internet]. Cts.usc.edu. 2016 [cited 16 March 2016]. Available from: http://www.cts.usc.edu/zglossary-bronchus.html 5. Kerkhoff A. Normal Range of Blood Oxygen Level | LIVESTRONG.COM [Internet]. LIVESTRONG.COM. 2014 [cited 16 March 2016]. Available from: http://www.livestrong.com/article/124374-normal-range-blood-oxygen-level/ 6. Participation Program for Pulmonary FIbrosis [Internet]. National Jewish Health. 2016 [cited 16 March 2016]. Available from: https://www.nationaljewish.org/Participation-Program-for-Pulmonary-Fibrosis/Community/Blog/Participation-Program-for-Pulmonary-Fibrosis/October-2013/How-can-I-be-short-of-breath-when-my-saturation-is-93 7. Jones R, Hilldrup S, Hope-Gill B, Eccles R, Harrison N. Mechanical induction of cough in Idiopathic Pulmonary Fibrosis. Cough. 2011;7(1):2. 8. Scholand M, Wolff R, Crossno P, Sundar K, Winegar M, Whipple S et al. Severity of cough in idiopathic pulmonary fibrosis is associated with MUC5 B genotype. Cough. 2014;10(1):3. 9. Chamberlain S, Garrod R, Birring S. Cough suppression therapy: Does it work?. Pulmonary Pharmacology & Therapeutics. 2013;26(5):524-527. 10. How Is Idiopathic Pulmonary Fibrosis Diagnosed? - NHLBI, NIH [Internet]. Nhlbi.nih.gov. 2016 [cited 16 March 2016]. Available from: https://www.nhlbi.nih.gov/health/health-topics/topics/ipf/diagnosis 11. Gotway M, Freemer M, King T. Challenges in pulmonary fibrosis {middle dot} 1: Use of high resolution CT scanning of the lung for the evaluation of patients with idiopathic interstitial pneumonias. Thorax. 2007;62(6):546-553.

• published: 06 May 2016
• views: 83385

11:01

Idiopathic Pulmonary Fibrosis | Restrictive Lung Disease | Pulmonology

• Order: Reorder
• Duration: 11:01
• Uploaded Date: 26 Sep 2019
• views: 92238

😍🖼Animated Mnemonics (Picmonic): https://www.picmonic.com/viphookup/medicosis/ - With Picmonic, get your life back by studying less and remembering more. Medi...

😍🖼Animated Mnemonics (Picmonic): https://www.picmonic.com/viphookup/medicosis/ - With Picmonic, get your life back by studying less and remembering more. Medical and Nursing students say that Picmonic is the most comprehensive and effective way to bridge learning and test prep... Disclaimer: I use affiliate links.... ►👨‍🏫💊Antibiotics Lectures: https://www.medicosisperfectionalis.com/products/courses/antibiotics/ ... Check out my brand new "Electrolytes" course at https://www.medicosisperfectionalis.com/products/course/electrolytes/ and use the PROMO code: ELECTROLYTES50 to get a 50% discount. If you like my videos, please consider leaving a tip at https://www.paypal.me/perfectionalis/ ► Visit my website: https://www.medicosisperfectionalis.com/ My Favorite Productivity App: https://airtable.com/invite/r/2zH40fus/ 📱Save on your mobile phone bill: http://fbuy.me/q6bMj 🏦 Qbank (TrueLearn): https://truelearn.referralrock.com/l/MEDICOSIS/

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😍🖼Animated Mnemonics (Picmonic): https://www.picmonic.com/viphookup/medicosis/ - With Picmonic, get your life back by studying less and remembering more. Medical and Nursing students say that Picmonic is the most comprehensive and effective way to bridge learning and test prep... Disclaimer: I use affiliate links.... ►👨‍🏫💊Antibiotics Lectures: https://www.medicosisperfectionalis.com/products/courses/antibiotics/ ... Check out my brand new "Electrolytes" course at https://www.medicosisperfectionalis.com/products/course/electrolytes/ and use the PROMO code: ELECTROLYTES50 to get a 50% discount. If you like my videos, please consider leaving a tip at https://www.paypal.me/perfectionalis/ ► Visit my website: https://www.medicosisperfectionalis.com/ My Favorite Productivity App: https://airtable.com/invite/r/2zH40fus/ 📱Save on your mobile phone bill: http://fbuy.me/q6bMj 🏦 Qbank (TrueLearn): https://truelearn.referralrock.com/l/MEDICOSIS/

• published: 26 Sep 2019
• views: 92238

3:25

Hamish Osborne - Beating pulmonary fibrosis, thanks to the University of Maryland

• Order: Reorder
• Duration: 3:25
• Uploaded Date: 01 Dec 2015
• views: 7498

Hamish S. Osborne and Christine C. Osborne are among the founding supporters of the Program in Lung Healing at the University of Maryland School of Medicine. Mr...

Hamish S. Osborne and Christine C. Osborne are among the founding supporters of the Program in Lung Healing at the University of Maryland School of Medicine. Mr. Osborne’s diagnosis of idiopathic pulmonary fibrosis resulted in a life-saving double-lung transplant at the University of Maryland Medical Center. He is the only reported patient to survive retransplantation after contracting a rare fungal disease called pulmonary mucormycosis after his first single lung transplant. In this video, Hamish Osborne talks about his illness, and what led him to support the Program in Lung Healing. To learn more and make gift, visit: http://medschool.umaryland.edu/development/ The University of Maryland School of Medicine serves as the anchor for a large academic health center which aims to provide the best medical education, conduct the most innovative biomedical research and provide the best patient care and community service to Maryland and beyond.

https://wn.com/Hamish_Osborne_Beating_Pulmonary_Fibrosis,_Thanks_To_The_University_Of_Maryland

Hamish S. Osborne and Christine C. Osborne are among the founding supporters of the Program in Lung Healing at the University of Maryland School of Medicine. Mr. Osborne’s diagnosis of idiopathic pulmonary fibrosis resulted in a life-saving double-lung transplant at the University of Maryland Medical Center. He is the only reported patient to survive retransplantation after contracting a rare fungal disease called pulmonary mucormycosis after his first single lung transplant. In this video, Hamish Osborne talks about his illness, and what led him to support the Program in Lung Healing. To learn more and make gift, visit: http://medschool.umaryland.edu/development/ The University of Maryland School of Medicine serves as the anchor for a large academic health center which aims to provide the best medical education, conduct the most innovative biomedical research and provide the best patient care and community service to Maryland and beyond.

• published: 01 Dec 2015
• views: 7498

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  3:29

  Understanding Pulmonary Fibrosisremove from playlistshare this video

  Understanding Pulmonary Fibrosis

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  • published: 20 Feb 2018
  • views: 58766

  Randy was diagnosed with idiopathic pulmonary fibrosis (IPF) on Christmas Eve 2008 – a day he will never forget. If you, or someone you love, has been diagnosed with pulmonary fibrosis, there are steps you can take to make living with this disease easier. Dr. Jane Dematte and Randy share more information about living and managing this rare lung disease. Learn more about pulmonary fibrosis, and access American Lung Association resources, at Lung.org/pf. Produced with support from Three Lakes Partners.

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  5:17

  Life With Pulmonary Fibrosis | What is Pulmonary Fibrosis?remove from playlistshare this video

  Life With Pulmonary Fibrosis | What is Pulmonary Fibrosis?

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  • published: 02 May 2018
  • views: 176496

  Dr. David J. Lederer, Senior Medical Advisor for Education and Awareness for the Pulmonary Fibrosis Foundation, Explains Pulmonary Fibrosis. Dr. David Lederer explains that the big picture of lung disease is vast and includes a family of diseases called interstitial lung diseases (ILD), which consist of more than 100 different diseases. These diseases are grouped together because they share two common features - inflammation and scar tissue, which occur in the walls of the tiny air sacs of the lungs. The difference between interstitial lung disease and pulmonary fibrosis is that interstitial lung diseases include all of the diseases in which there is inflammation or scar tissue in the walls of the air sacs. Pulmonary fibrosis is not a specific disease but is a general term that refers to any kind of ILD in which scar tissue is present in the walls of the air sacs. The Pulmonary Fibrosis Foundation (PFF) offers essential programs and resources for people with pulmonary fibrosis. The mission of the PFF is to mobilize people and resources to provide access to high quality care and to lead research for a cure so that people with PF will lead longer, healthier lives. For more information, visit pulmonaryfibrosis.org. Social media platforms - Twitter - @PFFORG Facebook - @PFFORG Instagram - @PFFORG LinkedIn- Pulmonary Fibrosis Foundation Please note that any information contained in this presentation is for informational and/or educational purposes only. It is not intended to be a substitute for professional medical advice. Always consult your personal physician or health care provider with any questions you may have regarding your specific medical condition. This presentation is protected by U.S. and International copyright laws. Reproductions and distribution of this presentation without written permission from the Pulmonary Fibrosis Foundation is prohibited. © 2018 Pulmonary Fibrosis Foundation

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  11:06

  Idiopathic Pulmonary Fibrosis - pathophysiology, signs and symptoms, investigation and treatmentremove from playlistshare this video

  Idiopathic Pulmonary Fibrosis - pathophysiology, signs and symptoms, investigation and treatment

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  • published: 21 Aug 2021
  • views: 123017

  "Idiopathic pulmonary fibrosis is a chronic progressive fibrotic interstitial lung disease of unknown cause that primarily occurs in older adults. Doctors suspect interstitial lung disease when an adult presents with unexplained exertional dyspnoea, chronic dry cough or inspiratory velcro-like crackles on examination. Fibrosis is typically in the lower lobes of the lung. Clubbing , low oxygen saturation and dyspnoea is the hallmark of idiopathic pulmonary fibrosis. High resolution CT chest is cold standard for diagnosis. Here you see the pathological pattern of usual interstitial pneumonia: low base predominance, traction bronchiectasis, honeycombing and reticular changes without significance ground glass changes" 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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  4:19

  Pulmonary Fibrosis: Everything You Need To Knowremove from playlistshare this video

  Pulmonary Fibrosis: Everything You Need To Know

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  • published: 27 Sep 2022
  • views: 129349

  . Chapters 0:00 Introduction 0:50 Causes of Pulmonary Fibrosis 1:08 Factors include 2:35 Symptoms of Pulmonary Fibrosis 2:52 Diagnosis and treatment of Pulmonary Fibrosis 3:15 Treatment for Pulmonary Fibrosis Pulmonary fibrosis is a condition in which the lungs become scarred over time.[1] Symptoms include shortness of breath, a dry cough, feeling tired, weight loss, and nail clubbing.[1] Complications may include pulmonary hypertension, respiratory failure, pneumothorax, and lung cancer.[2] Causes include environmental pollution, certain medications, connective tissue diseases, infections, and interstitial lung diseases.[1][3][6] Idiopathic pulmonary fibrosis (IPF), an interstitial lung disease of unknown cause, is most common.[1][3] Diagnosis may be based on symptoms, medical imaging, lung biopsy, and lung function tests.[1] There is no cure and there are limited treatment options available.[1] Treatment is directed towards efforts to improve symptoms and may include oxygen therapy and pulmonary rehabilitation.[1][4] Certain medications may be used to try to slow the worsening of scarring.[4] Lung transplantation may occasionally be an option.[3] At least 5 million people are affected globally.[5] Life expectancy is generally less than five years.[3] Symptoms of pulmonary fibrosis are mainly:[7] Shortness of breath, particularly with exertion Chronic dry, hacking coughing Fatigue and weakness Chest discomfort including chest pain Loss of appetite and rapid weight loss Pulmonary fibrosis is suggested by a history of progressive shortness of breath (dyspnea) with exertion. Sometimes fine inspiratory crackles can be heard at the lung bases on auscultation. A chest X-ray may or may not be abnormal, but high-resolution CT will frequently demonstrate abnormalities.[3] Cause Further information: Interstitial lung disease Pulmonary fibrosis may be a secondary effect of other diseases. Most of these are classified as interstitial lung diseases. Examples include autoimmune disorders, viral infections and bacterial infection like tuberculosis which may cause fibrotic changes in both lung's upper or lower lobes and other microscopic injuries to the lung. However, pulmonary fibrosis can also appear without any known cause. In this case, it is termed "idiopathic".[8] Most idiopathic cases are diagnosed as idiopathic pulmonary fibrosis. This is a diagnosis of exclusion of a characteristic set of histologic/pathologic features known as usual interstitial pneumonia (UIP). In either case, there is a growing body of evidence which points to a genetic predisposition in a subset of patients. For example, a mutation in surfactant protein C (SP-C) has been found to exist in some families with a history of pulmonary fibrosis.[9] Autosomal dominant mutations in the TERC or TERT genes, which encode telomerase, have been identified in about 15 percent of pulmonary fibrosis patients.[10] Diseases and conditions that may cause pulmonary fibrosis as a secondary effect include:[3][9] Inhalation of environmental and occupational pollutants, such as metals[11] in asbestosis, silicosis and exposure to certain gases. Coal miners, ship workers and sand blasters among others are at higher risk.[8] Hypersensitivity pneumonitis, most often resulting from inhaling dust contaminated with bacterial, fungal, or animal products Cigarette smoking can increase the risk or make the illness worse[8] Some typical connective tissue diseases[8] such as rheumatoid arthritis, ankylosing spondylitis, SLE and scleroderma Other diseases that involve connective tissue, such as sarcoidosis and granulomatosis with polyangiitis Infections, including COVID-19 Certain medications, e.g. amiodarone, bleomycin (pingyangmycin), busulfan, methotrexate,[8] apomorphine,[12] and nitrofurantoin[13] Radiation therapy to the chest Chapters 0:00 Introduction 0:50 Causes of Pulmonary Fibrosis 1:08 Factors of Pulmonary Fibrosis 2:35 Symptoms of Pulmonary Fibrosis 2:52 Diagnosis for Pulmonary Fibrosis 3:16 Treatment for Pulmonary Fibrosis

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  1:04

  Idiopathic pulmonary fibrosis - an Osmosis previewremove from playlistshare this video

  Idiopathic pulmonary fibrosis - an Osmosis preview

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  • published: 11 Dec 2018
  • views: 51957

  What is idiopathic pulmonary fibrosis (IPF)? Idiopathic pulmonary fibrosis is where the lungs undergo scarring and fibrosis for some unknown reason. Find our complete video library only on Osmosis Prime: http://osms.it/more. Hundreds of thousands of current & future clinicians learn by Osmosis. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. Subscribe to our Youtube channel at http://osms.it/subscribe. Get early access to our upcoming video releases, practice questions, giveaways, and more when you follow us on social media: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram: http://osms.it/instagram Our Vision: Everyone who cares for someone will learn by Osmosis. Our Mission: To empower the world’s clinicians and caregivers with the best learning experience possible. Learn more here: http://osms.it/mission Medical disclaimer: Knowledge Diffusion Inc (DBA Osmosis) does not provide medical advice. Osmosis and the content available on Osmosis's properties (Osmosis.org, YouTube, and other channels) do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcare professional in diagnosis and treatment of any person or animal. The determination of the need for medical services and the types of healthcare to be provided to a patient are decisions that should be made only by a physician or other licensed health care provider. Always seek the advice of a physician or other qualified healthcare provider with any questions you have regarding a medical condition.

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  Behind Each Breath: Shedding Light on Idiopathic Pulmonary Fibrosisremove from playlistshare this video

  Behind Each Breath: Shedding Light on Idiopathic Pulmonary Fibrosis

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  Learn more about Idiopathic Pulmonary Fibrosis (IPF) here: https://www.gene.com/stories/behind-each-breath-shedding-light-on-idiopathic-pulmonary-fibrosis

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  4:35

  Is Pulmonary Fibrosis the same as Idiopathic Pulmonary Fibrosis?remove from playlistshare this video

  Is Pulmonary Fibrosis the same as Idiopathic Pulmonary Fibrosis?

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  • published: 06 May 2016
  • views: 83385

  In this video we attempt to answer a number of questions relevant for patients diagnosed with Pulmonary Fibrosis and Idiopathic Pulmonary Fibrosis IPF. These questions cover a wide variety of topics including oxygen content, treatments and symptoms. Please let us know if you have any comments or better answers to some of these common and difficult questions. Subscribe to the McMaster Demystifying Medicine YouTube channel: https://www.youtube.com/c/DemystifyingMedicine This video is provided for general and educational information only. Please consult your health care provider for Information about your health. This video was made by Tristan Richardson & Anuj Patel in collaboration with the McMaster Demystifying Medicine Program Copyright McMaster University 2016 #DemystifyingMedicine, #IPF Works Cited 1. Learn About Pulmonary Fibrosis [Internet]. American Lung Association. 2016 [cited 16 March 2016]. Available from: http://www.lung.org/lung-health-and-diseases/lung-disease-lookup/pulmonary-fibrosis/learn-about-pulmonary.html?referrer=https://www.google.ca/ 2. Nalysnyk L, Cid-Ruzafa J, Rotella P, Esser D. Incidence and prevalence of idiopathic pulmonary fibrosis: review of the literature. European Respiratory Review. 2012;21(126):355-361. 3. Kuranishi L, Leslie K, Ferreira R, Coletta E, Storrer K, Soares M et al. Airway-centered interstitial fibrosis: etiology, clinical findings and prognosis. Respiratory Research. 2015;16(1). 4. Bronchus / Bronchi / Bronchioles [Internet]. Cts.usc.edu. 2016 [cited 16 March 2016]. Available from: http://www.cts.usc.edu/zglossary-bronchus.html 5. Kerkhoff A. Normal Range of Blood Oxygen Level | LIVESTRONG.COM [Internet]. LIVESTRONG.COM. 2014 [cited 16 March 2016]. Available from: http://www.livestrong.com/article/124374-normal-range-blood-oxygen-level/ 6. Participation Program for Pulmonary FIbrosis [Internet]. National Jewish Health. 2016 [cited 16 March 2016]. Available from: https://www.nationaljewish.org/Participation-Program-for-Pulmonary-Fibrosis/Community/Blog/Participation-Program-for-Pulmonary-Fibrosis/October-2013/How-can-I-be-short-of-breath-when-my-saturation-is-93 7. Jones R, Hilldrup S, Hope-Gill B, Eccles R, Harrison N. Mechanical induction of cough in Idiopathic Pulmonary Fibrosis. Cough. 2011;7(1):2. 8. Scholand M, Wolff R, Crossno P, Sundar K, Winegar M, Whipple S et al. Severity of cough in idiopathic pulmonary fibrosis is associated with MUC5 B genotype. Cough. 2014;10(1):3. 9. Chamberlain S, Garrod R, Birring S. Cough suppression therapy: Does it work?. Pulmonary Pharmacology & Therapeutics. 2013;26(5):524-527. 10. How Is Idiopathic Pulmonary Fibrosis Diagnosed? - NHLBI, NIH [Internet]. Nhlbi.nih.gov. 2016 [cited 16 March 2016]. Available from: https://www.nhlbi.nih.gov/health/health-topics/topics/ipf/diagnosis 11. Gotway M, Freemer M, King T. Challenges in pulmonary fibrosis {middle dot} 1: Use of high resolution CT scanning of the lung for the evaluation of patients with idiopathic interstitial pneumonias. Thorax. 2007;62(6):546-553.

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  Idiopathic Pulmonary Fibrosis | Restrictive Lung Disease | Pulmonologyremove from playlistshare this video

  Idiopathic Pulmonary Fibrosis | Restrictive Lung Disease | Pulmonology

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  • published: 26 Sep 2019
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  😍🖼Animated Mnemonics (Picmonic): https://www.picmonic.com/viphookup/medicosis/ - With Picmonic, get your life back by studying less and remembering more. Medical and Nursing students say that Picmonic is the most comprehensive and effective way to bridge learning and test prep... Disclaimer: I use affiliate links.... ►👨‍🏫💊Antibiotics Lectures: https://www.medicosisperfectionalis.com/products/courses/antibiotics/ ... Check out my brand new "Electrolytes" course at https://www.medicosisperfectionalis.com/products/course/electrolytes/ and use the PROMO code: ELECTROLYTES50 to get a 50% discount. If you like my videos, please consider leaving a tip at https://www.paypal.me/perfectionalis/ ► Visit my website: https://www.medicosisperfectionalis.com/ My Favorite Productivity App: https://airtable.com/invite/r/2zH40fus/ 📱Save on your mobile phone bill: http://fbuy.me/q6bMj 🏦 Qbank (TrueLearn): https://truelearn.referralrock.com/l/MEDICOSIS/

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  Hamish Osborne - Beating pulmonary fibrosis, thanks to the University of Marylandremove from playlistshare this video

  Hamish Osborne - Beating pulmonary fibrosis, thanks to the University of Maryland

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  • published: 01 Dec 2015
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  Hamish S. Osborne and Christine C. Osborne are among the founding supporters of the Program in Lung Healing at the University of Maryland School of Medicine. Mr. Osborne’s diagnosis of idiopathic pulmonary fibrosis resulted in a life-saving double-lung transplant at the University of Maryland Medical Center. He is the only reported patient to survive retransplantation after contracting a rare fungal disease called pulmonary mucormycosis after his first single lung transplant. In this video, Hamish Osborne talks about his illness, and what led him to support the Program in Lung Healing. To learn more and make gift, visit: http://medschool.umaryland.edu/development/ The University of Maryland School of Medicine serves as the anchor for a large academic health center which aims to provide the best medical education, conduct the most innovative biomedical research and provide the best patient care and community service to Maryland and beyond.

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Understanding Pulmonary Fibrosis

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Randy was diagnosed with idiopathic pulmonary fibrosis (IPF) on Christmas Eve 2008 – a day he will never forget. If you, or someone you love, has been diagnosed with pulmonary fibrosis, there are steps you can take to make living with this disease easier. Dr. Jane Dematte and Randy share more information about living and managing this rare lung disease. Learn more about pulmonary fibrosis, and access American Lung Association resources, at Lung.org/pf. Produced with support from Three Lakes Partners.

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3:29

Understanding Pulmonary Fibrosis

Randy was diagnosed with idiopathic pulmonary fibrosis (IPF) on Christmas Eve 2008 – a day...

published: 20 Feb 2018

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Understanding Pulmonary Fibrosis

Understanding Pulmonary Fibrosis

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Randy was diagnosed with idiopathic pulmonary fibrosis (IPF) on Christmas Eve 2008 – a day he will never forget. If you, or someone you love, has been diagnosed with pulmonary fibrosis, there are steps you can take to make living with this disease easier. Dr. Jane Dematte and Randy share more information about living and managing this rare lung disease. Learn more about pulmonary fibrosis, and access American Lung Association resources, at Lung.org/pf. Produced with support from Three Lakes Partners.

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5:17

Life With Pulmonary Fibrosis | What is Pulmonary Fibrosis?

Dr. David J. Lederer, Senior Medical Advisor for Education and Awareness for the Pulmonary...

published: 02 May 2018

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Life With Pulmonary Fibrosis | What is Pulmonary Fibrosis?

Life With Pulmonary Fibrosis | What is Pulmonary Fibrosis?

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Dr. David J. Lederer, Senior Medical Advisor for Education and Awareness for the Pulmonary Fibrosis Foundation, Explains Pulmonary Fibrosis. Dr. David Lederer explains that the big picture of lung disease is vast and includes a family of diseases called interstitial lung diseases (ILD), which consist of more than 100 different diseases. These diseases are grouped together because they share two common features - inflammation and scar tissue, which occur in the walls of the tiny air sacs of the lungs. The difference between interstitial lung disease and pulmonary fibrosis is that interstitial lung diseases include all of the diseases in which there is inflammation or scar tissue in the walls of the air sacs. Pulmonary fibrosis is not a specific disease but is a general term that refers to any kind of ILD in which scar tissue is present in the walls of the air sacs. The Pulmonary Fibrosis Foundation (PFF) offers essential programs and resources for people with pulmonary fibrosis. The mission of the PFF is to mobilize people and resources to provide access to high quality care and to lead research for a cure so that people with PF will lead longer, healthier lives. For more information, visit pulmonaryfibrosis.org. Social media platforms - Twitter - @PFFORG Facebook - @PFFORG Instagram - @PFFORG LinkedIn- Pulmonary Fibrosis Foundation Please note that any information contained in this presentation is for informational and/or educational purposes only. It is not intended to be a substitute for professional medical advice. Always consult your personal physician or health care provider with any questions you may have regarding your specific medical condition. This presentation is protected by U.S. and International copyright laws. Reproductions and distribution of this presentation without written permission from the Pulmonary Fibrosis Foundation is prohibited. © 2018 Pulmonary Fibrosis Foundation

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11:06

Idiopathic Pulmonary Fibrosis - pathophysiology, signs and symptoms, investigation and treatment

"Idiopathic pulmonary fibrosis is a chronic progressive fibrotic interstitial lung disease...

published: 21 Aug 2021

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Idiopathic Pulmonary Fibrosis - pathophysiology, signs and symptoms, investigation and treatment

Idiopathic Pulmonary Fibrosis - pathophysiology, signs and symptoms, investigation and treatment

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"Idiopathic pulmonary fibrosis is a chronic progressive fibrotic interstitial lung disease of unknown cause that primarily occurs in older adults. Doctors suspect interstitial lung disease when an adult presents with unexplained exertional dyspnoea, chronic dry cough or inspiratory velcro-like crackles on examination. Fibrosis is typically in the lower lobes of the lung. Clubbing , low oxygen saturation and dyspnoea is the hallmark of idiopathic pulmonary fibrosis. High resolution CT chest is cold standard for diagnosis. Here you see the pathological pattern of usual interstitial pneumonia: low base predominance, traction bronchiectasis, honeycombing and reticular changes without significance ground glass changes" 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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4:19

Pulmonary Fibrosis: Everything You Need To Know

. Chapters 0:00 Introduction 0:50 Causes of Pulmonary Fibrosis 1:08 Factors include 2:35...

published: 27 Sep 2022

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Pulmonary Fibrosis: Everything You Need To Know

Pulmonary Fibrosis: Everything You Need To Know

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. Chapters 0:00 Introduction 0:50 Causes of Pulmonary Fibrosis 1:08 Factors include 2:35 Symptoms of Pulmonary Fibrosis 2:52 Diagnosis and treatment of Pulmonary Fibrosis 3:15 Treatment for Pulmonary Fibrosis Pulmonary fibrosis is a condition in which the lungs become scarred over time.[1] Symptoms include shortness of breath, a dry cough, feeling tired, weight loss, and nail clubbing.[1] Complications may include pulmonary hypertension, respiratory failure, pneumothorax, and lung cancer.[2] Causes include environmental pollution, certain medications, connective tissue diseases, infections, and interstitial lung diseases.[1][3][6] Idiopathic pulmonary fibrosis (IPF), an interstitial lung disease of unknown cause, is most common.[1][3] Diagnosis may be based on symptoms, medical imaging, lung biopsy, and lung function tests.[1] There is no cure and there are limited treatment options available.[1] Treatment is directed towards efforts to improve symptoms and may include oxygen therapy and pulmonary rehabilitation.[1][4] Certain medications may be used to try to slow the worsening of scarring.[4] Lung transplantation may occasionally be an option.[3] At least 5 million people are affected globally.[5] Life expectancy is generally less than five years.[3] Symptoms of pulmonary fibrosis are mainly:[7] Shortness of breath, particularly with exertion Chronic dry, hacking coughing Fatigue and weakness Chest discomfort including chest pain Loss of appetite and rapid weight loss Pulmonary fibrosis is suggested by a history of progressive shortness of breath (dyspnea) with exertion. Sometimes fine inspiratory crackles can be heard at the lung bases on auscultation. A chest X-ray may or may not be abnormal, but high-resolution CT will frequently demonstrate abnormalities.[3] Cause Further information: Interstitial lung disease Pulmonary fibrosis may be a secondary effect of other diseases. Most of these are classified as interstitial lung diseases. Examples include autoimmune disorders, viral infections and bacterial infection like tuberculosis which may cause fibrotic changes in both lung's upper or lower lobes and other microscopic injuries to the lung. However, pulmonary fibrosis can also appear without any known cause. In this case, it is termed "idiopathic".[8] Most idiopathic cases are diagnosed as idiopathic pulmonary fibrosis. This is a diagnosis of exclusion of a characteristic set of histologic/pathologic features known as usual interstitial pneumonia (UIP). In either case, there is a growing body of evidence which points to a genetic predisposition in a subset of patients. For example, a mutation in surfactant protein C (SP-C) has been found to exist in some families with a history of pulmonary fibrosis.[9] Autosomal dominant mutations in the TERC or TERT genes, which encode telomerase, have been identified in about 15 percent of pulmonary fibrosis patients.[10] Diseases and conditions that may cause pulmonary fibrosis as a secondary effect include:[3][9] Inhalation of environmental and occupational pollutants, such as metals[11] in asbestosis, silicosis and exposure to certain gases. Coal miners, ship workers and sand blasters among others are at higher risk.[8] Hypersensitivity pneumonitis, most often resulting from inhaling dust contaminated with bacterial, fungal, or animal products Cigarette smoking can increase the risk or make the illness worse[8] Some typical connective tissue diseases[8] such as rheumatoid arthritis, ankylosing spondylitis, SLE and scleroderma Other diseases that involve connective tissue, such as sarcoidosis and granulomatosis with polyangiitis Infections, including COVID-19 Certain medications, e.g. amiodarone, bleomycin (pingyangmycin), busulfan, methotrexate,[8] apomorphine,[12] and nitrofurantoin[13] Radiation therapy to the chest Chapters 0:00 Introduction 0:50 Causes of Pulmonary Fibrosis 1:08 Factors of Pulmonary Fibrosis 2:35 Symptoms of Pulmonary Fibrosis 2:52 Diagnosis for Pulmonary Fibrosis 3:16 Treatment for Pulmonary Fibrosis

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1:04

Idiopathic pulmonary fibrosis - an Osmosis preview

What is idiopathic pulmonary fibrosis (IPF)? Idiopathic pulmonary fibrosis is where the lu...

published: 11 Dec 2018

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Idiopathic pulmonary fibrosis - an Osmosis preview

Idiopathic pulmonary fibrosis - an Osmosis preview

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What is idiopathic pulmonary fibrosis (IPF)? Idiopathic pulmonary fibrosis is where the lungs undergo scarring and fibrosis for some unknown reason. Find our complete video library only on Osmosis Prime: http://osms.it/more. Hundreds of thousands of current & future clinicians learn by Osmosis. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. Subscribe to our Youtube channel at http://osms.it/subscribe. Get early access to our upcoming video releases, practice questions, giveaways, and more when you follow us on social media: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram: http://osms.it/instagram Our Vision: Everyone who cares for someone will learn by Osmosis. Our Mission: To empower the world’s clinicians and caregivers with the best learning experience possible. Learn more here: http://osms.it/mission Medical disclaimer: Knowledge Diffusion Inc (DBA Osmosis) does not provide medical advice. Osmosis and the content available on Osmosis's properties (Osmosis.org, YouTube, and other channels) do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcare professional in diagnosis and treatment of any person or animal. The determination of the need for medical services and the types of healthcare to be provided to a patient are decisions that should be made only by a physician or other licensed health care provider. Always seek the advice of a physician or other qualified healthcare provider with any questions you have regarding a medical condition.

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2:17

Behind Each Breath: Shedding Light on Idiopathic Pulmonary Fibrosis

Learn more about Idiopathic Pulmonary Fibrosis (IPF) here: https://www.gene.com/stories/be...

published: 08 Sep 2020

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Behind Each Breath: Shedding Light on Idiopathic Pulmonary Fibrosis

Behind Each Breath: Shedding Light on Idiopathic Pulmonary Fibrosis

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• published: 08 Sep 2020
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Learn more about Idiopathic Pulmonary Fibrosis (IPF) here: https://www.gene.com/stories/behind-each-breath-shedding-light-on-idiopathic-pulmonary-fibrosis

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4:35

Is Pulmonary Fibrosis the same as Idiopathic Pulmonary Fibrosis?

In this video we attempt to answer a number of questions relevant for patients diagnosed w...

published: 06 May 2016

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Is Pulmonary Fibrosis the same as Idiopathic Pulmonary Fibrosis?

Is Pulmonary Fibrosis the same as Idiopathic Pulmonary Fibrosis?

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• published: 06 May 2016
• views: 83385

In this video we attempt to answer a number of questions relevant for patients diagnosed with Pulmonary Fibrosis and Idiopathic Pulmonary Fibrosis IPF. These questions cover a wide variety of topics including oxygen content, treatments and symptoms. Please let us know if you have any comments or better answers to some of these common and difficult questions. Subscribe to the McMaster Demystifying Medicine YouTube channel: https://www.youtube.com/c/DemystifyingMedicine This video is provided for general and educational information only. Please consult your health care provider for Information about your health. This video was made by Tristan Richardson & Anuj Patel in collaboration with the McMaster Demystifying Medicine Program Copyright McMaster University 2016 #DemystifyingMedicine, #IPF Works Cited 1. Learn About Pulmonary Fibrosis [Internet]. American Lung Association. 2016 [cited 16 March 2016]. Available from: http://www.lung.org/lung-health-and-diseases/lung-disease-lookup/pulmonary-fibrosis/learn-about-pulmonary.html?referrer=https://www.google.ca/ 2. Nalysnyk L, Cid-Ruzafa J, Rotella P, Esser D. Incidence and prevalence of idiopathic pulmonary fibrosis: review of the literature. European Respiratory Review. 2012;21(126):355-361. 3. Kuranishi L, Leslie K, Ferreira R, Coletta E, Storrer K, Soares M et al. Airway-centered interstitial fibrosis: etiology, clinical findings and prognosis. Respiratory Research. 2015;16(1). 4. Bronchus / Bronchi / Bronchioles [Internet]. Cts.usc.edu. 2016 [cited 16 March 2016]. Available from: http://www.cts.usc.edu/zglossary-bronchus.html 5. Kerkhoff A. Normal Range of Blood Oxygen Level | LIVESTRONG.COM [Internet]. LIVESTRONG.COM. 2014 [cited 16 March 2016]. Available from: http://www.livestrong.com/article/124374-normal-range-blood-oxygen-level/ 6. Participation Program for Pulmonary FIbrosis [Internet]. National Jewish Health. 2016 [cited 16 March 2016]. Available from: https://www.nationaljewish.org/Participation-Program-for-Pulmonary-Fibrosis/Community/Blog/Participation-Program-for-Pulmonary-Fibrosis/October-2013/How-can-I-be-short-of-breath-when-my-saturation-is-93 7. Jones R, Hilldrup S, Hope-Gill B, Eccles R, Harrison N. Mechanical induction of cough in Idiopathic Pulmonary Fibrosis. Cough. 2011;7(1):2. 8. Scholand M, Wolff R, Crossno P, Sundar K, Winegar M, Whipple S et al. Severity of cough in idiopathic pulmonary fibrosis is associated with MUC5 B genotype. Cough. 2014;10(1):3. 9. Chamberlain S, Garrod R, Birring S. Cough suppression therapy: Does it work?. Pulmonary Pharmacology & Therapeutics. 2013;26(5):524-527. 10. How Is Idiopathic Pulmonary Fibrosis Diagnosed? - NHLBI, NIH [Internet]. Nhlbi.nih.gov. 2016 [cited 16 March 2016]. Available from: https://www.nhlbi.nih.gov/health/health-topics/topics/ipf/diagnosis 11. Gotway M, Freemer M, King T. Challenges in pulmonary fibrosis {middle dot} 1: Use of high resolution CT scanning of the lung for the evaluation of patients with idiopathic interstitial pneumonias. Thorax. 2007;62(6):546-553.

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11:01

Idiopathic Pulmonary Fibrosis | Restrictive Lung Disease | Pulmonology

😍🖼Animated Mnemonics (Picmonic): https://www.picmonic.com/viphookup/medicosis/ - With Pi...

published: 26 Sep 2019

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Idiopathic Pulmonary Fibrosis | Restrictive Lung Disease | Pulmonology

Idiopathic Pulmonary Fibrosis | Restrictive Lung Disease | Pulmonology

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😍🖼Animated Mnemonics (Picmonic): https://www.picmonic.com/viphookup/medicosis/ - With Picmonic, get your life back by studying less and remembering more. Medical and Nursing students say that Picmonic is the most comprehensive and effective way to bridge learning and test prep... Disclaimer: I use affiliate links.... ►👨‍🏫💊Antibiotics Lectures: https://www.medicosisperfectionalis.com/products/courses/antibiotics/ ... Check out my brand new "Electrolytes" course at https://www.medicosisperfectionalis.com/products/course/electrolytes/ and use the PROMO code: ELECTROLYTES50 to get a 50% discount. If you like my videos, please consider leaving a tip at https://www.paypal.me/perfectionalis/ ► Visit my website: https://www.medicosisperfectionalis.com/ My Favorite Productivity App: https://airtable.com/invite/r/2zH40fus/ 📱Save on your mobile phone bill: http://fbuy.me/q6bMj 🏦 Qbank (TrueLearn): https://truelearn.referralrock.com/l/MEDICOSIS/

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Hamish Osborne - Beating pulmonary fibrosis, thanks to the University of Maryland

Hamish S. Osborne and Christine C. Osborne are among the founding supporters of the Progra...

published: 01 Dec 2015

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Hamish Osborne - Beating pulmonary fibrosis, thanks to the University of Maryland

Hamish Osborne - Beating pulmonary fibrosis, thanks to the University of Maryland

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Hamish S. Osborne and Christine C. Osborne are among the founding supporters of the Program in Lung Healing at the University of Maryland School of Medicine. Mr. Osborne’s diagnosis of idiopathic pulmonary fibrosis resulted in a life-saving double-lung transplant at the University of Maryland Medical Center. He is the only reported patient to survive retransplantation after contracting a rare fungal disease called pulmonary mucormycosis after his first single lung transplant. In this video, Hamish Osborne talks about his illness, and what led him to support the Program in Lung Healing. To learn more and make gift, visit: http://medschool.umaryland.edu/development/ The University of Maryland School of Medicine serves as the anchor for a large academic health center which aims to provide the best medical education, conduct the most innovative biomedical research and provide the best patient care and community service to Maryland and beyond.

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Pulmonary fibrosis

Pulmonary fibrosis (literally "scarring of the lungs") is a respiratory disease in which scars are formed in the lung tissues, leading to serious breathing problems. Scar formation, the accumulation of excess fibrous connective tissue (the process called fibrosis), leads to thickening of the walls, and causes reduced oxygen supply in the blood. As a consequence patients suffer from perpetual shortness of breath.

In some patients the specific cause of the disease can be diagnosed, but in others the probable cause cannot be determined, a condition called idiopathic pulmonary fibrosis. There is no known cure for the scars and damage in the lung due to pulmonary fibrosis.

Signs and symptoms

Symptoms of pulmonary fibrosis are mainly:

Shortness of breath, particularly with exertion

Chronic dry, hacking coughing

Fatigue and weakness

Chest discomfort including chest pain

Loss of appetite and rapid weight loss

Pulmonary fibrosis is suggested by a history of progressive shortness of breath (dyspnea) with exertion. Sometimes fine inspiratory crackles can be heard at the lung bases on auscultation. A chest x-ray may or may not be abnormal, but high-resolution CT will frequently demonstrate abnormalities.

Read more

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

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Understanding Pulmonary Fibrosis...

Life With Pulmonary Fibrosis | What is Pulmonary F...

Idiopathic Pulmonary Fibrosis - pathophysiology, s...

Pulmonary Fibrosis: Everything You Need To Know...

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Latest News for: pulmonary fibrosis

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Pliant Therapeutics Provides Update on BEACON-IPF, a Phase 2b/3 Trial in Patients with Idiopathic Pulmonary Fibrosis

Nasdaq Globe Newswire 03 Mar 2025

... panel, Pliant has discontinued the BEACON-IPF Phase 2b trial evaluating bexotegrast in patients with idiopathic pulmonary fibrosis (IPF).

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Twitchell, Patricia Ann Faulter

Times of Wayne County 03 Mar 2025

June 27, 1941 - February 25, 2025. Predeceased by her loving husband of 59 years Lowell T. Twitchell, siblings ... Survived by children ... In lieu of flowers, donations may be made in her name to URMC Pulmonary Fibrosis Research & Education Fund. .

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Bernie Williams Exclusive: Yankees Legend Talks Juan Soto Departure, Cody Bellinger Addition, Ending Title Drought

Sportslens 03 Mar 2025

Bernie Williams Exclusive ... 28. He has worked to raise awareness of interstitial lung diseases since 2001, when Williams’ father, Bernabe Sr., died of idiopathic pulmonary fibrosis ... To learn more about Tune In to Lung Health, click here. Q ... Q ... Q ... Q ... Q ... Q ... Q ... Q.

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Additional Talent Announced for 15th Annual Broadway Belts for PFF! Benefit Performance

Hill Country Community Journal 28 Feb 2025

27, 2025 /PRNewswire/ -- The Pulmonary Fibrosis ...

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Pigeons, the messengers of old times, can be passengers of deadly lung diseases. How?

The Times of India 27 Feb 2025

Chronic exposure can cause fibrosisLong-term inhalation of pigeon allergens does not only provoke allergic reactions but also results in pulmonary fibrosis-a case where lung tissue becomes stiffened ...

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Trevi Therapeutics to Participate in Upcoming March Investor Conferences

Longview News-Journal 27 Feb 2025

... with idiopathic pulmonary fibrosis (IPF) and refractory ....

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‘He never stopped loving boxing’: Petrolia resident, pro boxer Mark Weinman dies at 62

Times Standard 27 Feb 2025

“He loved to work with people. He loved to pass on his knowledge ... “He was a good guy ... (Contributed/Brian Christensen) ... “Yeah ... 8 from complications related to idiopathic pulmonary fibrosis, a respiratory ailment he had been diagnosed with 12 years prior ... .

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Every Wrestler Who Has Jumped From WWE To AEW (& Vice Versa)

What Culture 27 Feb 2025

Spoiler alert. A lot of wrestlers have jumped from WWE to AEW and from All Elite back to the E since Tony Khan launched his own would-be competitor in early-2019 ... 2.0 ... AQA ... Brodie sadly passed away from idiopathic pulmonary fibrosis on 26 December 2020.

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Obituary - Dorothy G. 'Dottie' Rice

Havre Daily News 26 Feb 2025

“Dottie” Rice, 77, passed away after an extended battle with pulmonary fibrosis ...

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Trevi Therapeutics Completes Enrollment for Phase 2b CORAL Trial of Haduvio in Idiopathic Pulmonary Fibrosis ...

Victoria Advocate 25 Feb 2025

Topline results continue to be expected in the first half of 2025 ....

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Obituary -�Dorothy G. 'Dottie' Rice

Havre Daily News 25 Feb 2025

"Dottie" Rice, 77, passed away after an extended battle with pulmonary ...

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Trevi Therapeutics Completes Enrollment for Phase 2b CORAL Trial of Haduvio in Idiopathic Pulmonary Fibrosis Patients with Chronic Cough

PR Newswire 25 Feb 2025

About Idiopathic Pulmonary Fibrosis Chronic CoughChronic cough is highly prevalent in IPF patients, impacting up to 85% of the IPF population ... fibrosis (IPF) and refractory chronic cough (RCC).

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SSc-ILD Treatment Market 2034: EMA, PDMA, FDA Approvals, Clinical Trials, Epidemiology, Medication, NDA Approvals, Pipeline, ...

GetNews 22 Feb 2025

Systemic sclerosis-associated interstitial lung disease (SSc-ILD) is a severe pulmonary complication of systemic sclerosis (SSc), an autoimmune connective tissue disorder ... Pulmonary function tests ...

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Interstitial Lung Disease Market Set to Grow Substantially Through 2032, DelveInsight Projects | J2H Biotech, ...

GetNews 21 Feb 2025

Topline results from the Phase III FIBRONEER-ILD study (NCT05321082) indicate that nerandomilast enhanced lung function in patients with progressive fibrosing interstitial lung diseases (PF-ILDs), excluding idiopathic pulmonary fibrosis (IPF).

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Why drying clothes indoors could put your health at risk

RTE 21 Feb 2025

Analysis ... Moulds like aspergillus cause infections in patients with limited immune function, or who have lung damage from diseases like asthma, cystic fibrosis and chronic obstructive pulmonary disease (COPD) associated with heavy smoking ... READ ... .

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