-
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/
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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
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?
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
"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
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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
.
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
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
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?
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
😍🖼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/
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https://wn.com/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://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
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
-
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
-
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
-
Signs & Symptoms of Idiopathic Pulmonary Fibrosis (IPF)
published: 07 Sep 2017
-
Introduction into idiopathic pulmonary fibrosis (IPF)
Idiopathic pulmonary fibrosis (or IPF) is a life-threatening lung disease. The pathophysiology of this condition is not fully understood, though it is believed to arise through successive injury to the alveolar epithelial cell compartment.
published: 29 Nov 2016
-
Idiopathic Pulmonary Fibrosis: Bills Story
Bill Van Nierop, who lives with Idiopathic Pulmonary Fibrosis (IPF), defines himself as an IPF patient not an IPF sufferer. Bill talks about the stigma surrounding lung disease, the impact this has on research and his goal to to help others living with a lung disease through raising awareness and changing community perspectives.
published: 10 Apr 2019
-
Idiopathic Pulmonary Fibrosis: The Simple Facts
This simple video presents a basic understanding of idiopathic pulmonary fibrosis (IPF). This fatal condition does not have a known cause, and research investigating its pathology is ongoing.
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 McMaster students Adrienne Lee, Kim Rod, Patrick Rudak, Ria Oommen and Shylendra Mahendran, in an effort to increase awareness and understanding about IPF, in collaboration with the McMaster Demystifying Medicine Program
© 2015. McMaster University.
#DemystifyingMedicine, #IPF
published: 16 May 2015
-
Breath of Awareness: Exploring Interstitial Lung Disease (ILD) | Interstitial Lung Disease podcast
Interstitial Lung Disease (ILD) consists of various lung disorders that cause progressive scarring and inflammation of the lung tissue. This scarring of lung tissue can result in difficulty breathing and impair oxygen supply to the bloodstream, making it critical for daily activities. With over 200 different types of ILD, including idiopathic pulmonary fibrosis and sarcoidosis, understanding this condition can be distressing. In this episode of the Interstitial Lung Disease (ILD) podcast, we will explore this complex and most often misunderstood condition, which has symptoms similar to those of other lung disorders, such as breathlessness and chest tightness.
Join the PACE Hospitals Podcast with Dr. Pradeep Kiran Panchadi, Consultant Interventional Pulmonologist and specialist in Broncho...
published: 04 Jul 2024
-
Managing idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis is a slowly progressive disease that causes the lungs to fill with scar tissue. Dr. Andrew Limper, a pulmonary and critical care medicine physician, talks about the advantages of coming to Mayo Clinic for treatment.
published: 07 Dec 2012
-
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
-
Idiopathic Pulmonary Fibrosis (an Update) and Progressive Pulmonary Fibrosis in Adults
This American Thoracic Society, European Respiratory Society, Japanese Respiratory Society, and Asociación Latinoamericana de Tórax guideline updates prior idiopathic pulmonary fibrosis (IPF) guidelines and addresses the progression of pulmonary fibrosis in patients with interstitial lung diseases (ILDs) other than IPF.
Read the guidelines here: https://www.atsjournals.org/doi/full/10.1164/rccm.202202-0399ST
published: 12 Sep 2022
11:06
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 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:
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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
11:01
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. 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/
https://wn.com/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://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
1:13
Introduction into idiopathic pulmonary fibrosis (IPF)
Idiopathic pulmonary fibrosis (or IPF) is a life-threatening lung disease. The pathophysiology of this condition is not fully understood, though it is believed ...
Idiopathic pulmonary fibrosis (or IPF) is a life-threatening lung disease. The pathophysiology of this condition is not fully understood, though it is believed to arise through successive injury to the alveolar epithelial cell compartment.
https://wn.com/Introduction_Into_Idiopathic_Pulmonary_Fibrosis_(Ipf)
Idiopathic pulmonary fibrosis (or IPF) is a life-threatening lung disease. The pathophysiology of this condition is not fully understood, though it is believed to arise through successive injury to the alveolar epithelial cell compartment.
- published: 29 Nov 2016
- views: 41660
3:53
Idiopathic Pulmonary Fibrosis: Bills Story
Bill Van Nierop, who lives with Idiopathic Pulmonary Fibrosis (IPF), defines himself as an IPF patient not an IPF sufferer. Bill talks about the stigma surround...
Bill Van Nierop, who lives with Idiopathic Pulmonary Fibrosis (IPF), defines himself as an IPF patient not an IPF sufferer. Bill talks about the stigma surrounding lung disease, the impact this has on research and his goal to to help others living with a lung disease through raising awareness and changing community perspectives.
https://wn.com/Idiopathic_Pulmonary_Fibrosis_Bills_Story
Bill Van Nierop, who lives with Idiopathic Pulmonary Fibrosis (IPF), defines himself as an IPF patient not an IPF sufferer. Bill talks about the stigma surrounding lung disease, the impact this has on research and his goal to to help others living with a lung disease through raising awareness and changing community perspectives.
- published: 10 Apr 2019
- views: 9845
4:43
Idiopathic Pulmonary Fibrosis: The Simple Facts
This simple video presents a basic understanding of idiopathic pulmonary fibrosis (IPF). This fatal condition does not have a known cause, and research investig...
This simple video presents a basic understanding of idiopathic pulmonary fibrosis (IPF). This fatal condition does not have a known cause, and research investigating its pathology is ongoing.
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 McMaster students Adrienne Lee, Kim Rod, Patrick Rudak, Ria Oommen and Shylendra Mahendran, in an effort to increase awareness and understanding about IPF, in collaboration with the McMaster Demystifying Medicine Program
© 2015. McMaster University.
#DemystifyingMedicine, #IPF
https://wn.com/Idiopathic_Pulmonary_Fibrosis_The_Simple_Facts
This simple video presents a basic understanding of idiopathic pulmonary fibrosis (IPF). This fatal condition does not have a known cause, and research investigating its pathology is ongoing.
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 McMaster students Adrienne Lee, Kim Rod, Patrick Rudak, Ria Oommen and Shylendra Mahendran, in an effort to increase awareness and understanding about IPF, in collaboration with the McMaster Demystifying Medicine Program
© 2015. McMaster University.
#DemystifyingMedicine, #IPF
- published: 16 May 2015
- views: 80071
17:45
Breath of Awareness: Exploring Interstitial Lung Disease (ILD) | Interstitial Lung Disease podcast
Interstitial Lung Disease (ILD) consists of various lung disorders that cause progressive scarring and inflammation of the lung tissue. This scarring of lung ti...
Interstitial Lung Disease (ILD) consists of various lung disorders that cause progressive scarring and inflammation of the lung tissue. This scarring of lung tissue can result in difficulty breathing and impair oxygen supply to the bloodstream, making it critical for daily activities. With over 200 different types of ILD, including idiopathic pulmonary fibrosis and sarcoidosis, understanding this condition can be distressing. In this episode of the Interstitial Lung Disease (ILD) podcast, we will explore this complex and most often misunderstood condition, which has symptoms similar to those of other lung disorders, such as breathlessness and chest tightness.
Join the PACE Hospitals Podcast with Dr. Pradeep Kiran Panchadi, Consultant Interventional Pulmonologist and specialist in Bronchoscopy and EBUS at PACE Hospitals, Hitech City, Hyderabad, India, to learn about Interstitial Lung Disease (ILD).
👇 Chapters of Interstitial Lung Disease (ILD) podcast
00:40 What is Interstitial lung disease?
04:36 What exactly causes of Interstitial lung disease?
07:01 How do we classify Interstitial lung disease?
08:04 How is ILD diagnosed? What are the various diagnostic methods?
13:00 How is Interstitial lung disease treated?
15:28 What are the complication of Interstitial lung disease?
Dr. Pradeep Kiran Panchadi - Interventional Pulmonologist, Specialist in Bronchoscopy and EBUS https://www.pacehospital.com/dr-pradeep-kiran-panchadi
PACE Hospitals Podcast - Health and Wellness Podcasts:
https://www.pacehospital.com/podcast
Breath of Awareness: Exploring Interstitial Lung Disease (ILD):
https://www.pacehospital.com/com/podcast/interstitial-lung-disease-podcast
Interstitial Lung Disease - Causes, Symptoms and Treatment:
https://www.pacehospital.com/interstitial-lung-disease-causes-symptoms-and-treatment
#Interstitiallungdisease #Interstitiallungdiseasepodcast #ILDpodcast #lungdisease #pulmonologypodcast #lungdisorderpodcast #lungs #lunghealth #healthpodcast #Pulmonologist #pulmonology #Pacehospitalspodcast #pacehospitals #hyderabad #india
PACE Hospitals
Hitech City and Madinaguda,
Hyderabad, Telangana, India
T: 04048486868
https://www.pacehospital.com/
Follow us:
Facebook - https://www.facebook.com/PaceHospitals
Instagram - https://www.instagram.com/pacehospitals/
Google - https://g.page/pacehospitals
LinkedIn - https://www.linkedin.com/in/pace-hospitals-11716956/
Twitter - https://twitter.com/PACEHospitals
Reddit - https://www.reddit.com/u/Pacehospital
Quora - https://www.quora.com/profile/Pace-Hospitals-2
Related: Interstitial Lung Disease, ILD, lung disorder, lung disease, Interstitial Lung Disease awareness, ILD awareness, Interstitial Lung Disease podcast, ILD podcast, pulmonology podcast, lung disease podcast, disease podcast, health podcast, digital health, digital healthcare, digital health solutions, digital health solutions, Health and Wellness podcast, wellness podcasts, Patient Care podcast, medical podcast, digital health podcasts, healthcare podcast, pulmonology, pulmonologist, PACE Hospitals podcast
https://wn.com/Breath_Of_Awareness_Exploring_Interstitial_Lung_Disease_(Ild)_|_Interstitial_Lung_Disease_Podcast
Interstitial Lung Disease (ILD) consists of various lung disorders that cause progressive scarring and inflammation of the lung tissue. This scarring of lung tissue can result in difficulty breathing and impair oxygen supply to the bloodstream, making it critical for daily activities. With over 200 different types of ILD, including idiopathic pulmonary fibrosis and sarcoidosis, understanding this condition can be distressing. In this episode of the Interstitial Lung Disease (ILD) podcast, we will explore this complex and most often misunderstood condition, which has symptoms similar to those of other lung disorders, such as breathlessness and chest tightness.
Join the PACE Hospitals Podcast with Dr. Pradeep Kiran Panchadi, Consultant Interventional Pulmonologist and specialist in Bronchoscopy and EBUS at PACE Hospitals, Hitech City, Hyderabad, India, to learn about Interstitial Lung Disease (ILD).
👇 Chapters of Interstitial Lung Disease (ILD) podcast
00:40 What is Interstitial lung disease?
04:36 What exactly causes of Interstitial lung disease?
07:01 How do we classify Interstitial lung disease?
08:04 How is ILD diagnosed? What are the various diagnostic methods?
13:00 How is Interstitial lung disease treated?
15:28 What are the complication of Interstitial lung disease?
Dr. Pradeep Kiran Panchadi - Interventional Pulmonologist, Specialist in Bronchoscopy and EBUS https://www.pacehospital.com/dr-pradeep-kiran-panchadi
PACE Hospitals Podcast - Health and Wellness Podcasts:
https://www.pacehospital.com/podcast
Breath of Awareness: Exploring Interstitial Lung Disease (ILD):
https://www.pacehospital.com/com/podcast/interstitial-lung-disease-podcast
Interstitial Lung Disease - Causes, Symptoms and Treatment:
https://www.pacehospital.com/interstitial-lung-disease-causes-symptoms-and-treatment
#Interstitiallungdisease #Interstitiallungdiseasepodcast #ILDpodcast #lungdisease #pulmonologypodcast #lungdisorderpodcast #lungs #lunghealth #healthpodcast #Pulmonologist #pulmonology #Pacehospitalspodcast #pacehospitals #hyderabad #india
PACE Hospitals
Hitech City and Madinaguda,
Hyderabad, Telangana, India
T: 04048486868
https://www.pacehospital.com/
Follow us:
Facebook - https://www.facebook.com/PaceHospitals
Instagram - https://www.instagram.com/pacehospitals/
Google - https://g.page/pacehospitals
LinkedIn - https://www.linkedin.com/in/pace-hospitals-11716956/
Twitter - https://twitter.com/PACEHospitals
Reddit - https://www.reddit.com/u/Pacehospital
Quora - https://www.quora.com/profile/Pace-Hospitals-2
Related: Interstitial Lung Disease, ILD, lung disorder, lung disease, Interstitial Lung Disease awareness, ILD awareness, Interstitial Lung Disease podcast, ILD podcast, pulmonology podcast, lung disease podcast, disease podcast, health podcast, digital health, digital healthcare, digital health solutions, digital health solutions, Health and Wellness podcast, wellness podcasts, Patient Care podcast, medical podcast, digital health podcasts, healthcare podcast, pulmonology, pulmonologist, PACE Hospitals podcast
- published: 04 Jul 2024
- views: 65
4:28
Managing idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis is a slowly progressive disease that causes the lungs to fill with scar tissue. Dr. Andrew Limper, a pulmonary and critical care m...
Idiopathic pulmonary fibrosis is a slowly progressive disease that causes the lungs to fill with scar tissue. Dr. Andrew Limper, a pulmonary and critical care medicine physician, talks about the advantages of coming to Mayo Clinic for treatment.
https://wn.com/Managing_Idiopathic_Pulmonary_Fibrosis
Idiopathic pulmonary fibrosis is a slowly progressive disease that causes the lungs to fill with scar tissue. Dr. Andrew Limper, a pulmonary and critical care medicine physician, talks about the advantages of coming to Mayo Clinic for treatment.
- published: 07 Dec 2012
- views: 28955
2:17
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
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
3:16
Idiopathic Pulmonary Fibrosis (an Update) and Progressive Pulmonary Fibrosis in Adults
This American Thoracic Society, European Respiratory Society, Japanese Respiratory Society, and Asociación Latinoamericana de Tórax guideline updates prior idio...
This American Thoracic Society, European Respiratory Society, Japanese Respiratory Society, and Asociación Latinoamericana de Tórax guideline updates prior idiopathic pulmonary fibrosis (IPF) guidelines and addresses the progression of pulmonary fibrosis in patients with interstitial lung diseases (ILDs) other than IPF.
Read the guidelines here: https://www.atsjournals.org/doi/full/10.1164/rccm.202202-0399ST
https://wn.com/Idiopathic_Pulmonary_Fibrosis_(An_Update)_And_Progressive_Pulmonary_Fibrosis_In_Adults
This American Thoracic Society, European Respiratory Society, Japanese Respiratory Society, and Asociación Latinoamericana de Tórax guideline updates prior idiopathic pulmonary fibrosis (IPF) guidelines and addresses the progression of pulmonary fibrosis in patients with interstitial lung diseases (ILDs) other than IPF.
Read the guidelines here: https://www.atsjournals.org/doi/full/10.1164/rccm.202202-0399ST
- published: 12 Sep 2022
- views: 4751