- published: 25 Nov 2016
- views: 231414
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This video presents information about cystic fibrosis (CF), which is an autosomal recessive disorder. The video outlines the basic biological principles behind CF, along with an overview of the disease and available treatment options. The video begins by mentioning the genetic mutation to the cystic fibrosis transmembrane conductance regulatory (CFTR) gene on chromosome 7 which is the main cause of CF. Subsequently, the video entails the symptoms of the disease, including increased perspiration, pancreatic insufficiencies and lung infections. The epidemiology of this disease is also mentioned as the video states that 1 in 3600 children born in Canada is affected by CF. Furthermore, a significant portion of the video explains the organs affected by the disease and any treatment options that patients have. It is thoroughly explained that CF affects multiple organs including the lungs, pancreas and intestines. Many of these complications are due to blockages caused by the buildup of mucus. For instance, blockages caused in the intestines due to mucus buildup creates inefficiencies in digestion, specifically for fats and proteins. Considering there are multiple body parts affected by CF, there is a wide range of treatment options available to alleviate the condition of the disease. A majority of the treatment options serve the function of removing buildups of mucus and the blockages that occur. A patient with CF will most likely experience lung infections which are often treated with different types of antibiotics based on the severity of the disease and type of bacteria that is present. Other medications, most notably, bronchodilators, are also considered as treatment options for this disease. Lastly, there are also physical treatments such as Chest Physical Therapy (CPT) which also attempt to clear mucus using physical techniques. Overall, our video attempts to explain the basic processes that cause CF, subsequently followed by its overall impact on the patient’s body and the treatments that are available.
This video was made by 4DM3 students Zubair Banoor, Jaskeerat Kaur, Sina Nastarani, Monica Persaud and Kritika Seth
Copyright McMaster University 2016
Please let us know how we can improve our videos and additional topics should be addressed below.
What is cystic fibrosis? Cystic fibrosis, or CF, is an autosomal recessive disorder where there’s a mutation in the CFTR gene, and it is considered to be the most common lethal genetic disease in the Caucasian population.
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.
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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: 03 May 2021
- views: 24523
See how the lungs work normally and how cystic fibrosis can affect the lungs over time.
https://www.cff.org/Life-With-CF/Treatments-and-Therapies/Airway-Clearance/Basics-of-Lung-Care/
- published: 19 May 2017
- views: 131106
Cystic fibrosis NCLEX nursing review: Cystic fibrosis is a genetic disorder that causes the exocrine glands to work incorrectly.
This can lead to major complications that affect the respiratory, digestive (pancreas, liver, intestines), integumentary, and reproductive systems along with the sinuses.
What are exocrine glands? These are glands that produce and transfer it’s secretions (ex: mucous, tears, sweat, digestive enzymes) via DUCTS to it’s intended area of the body rather than directly into the bloodstream like the endocrine glands.
In cystic fibrosis, there is a gene that is mutated that prevents the exocrine gland from working properly. It is called the CFTR gene!
The CFTR gene, which stands for cystic fibrosis transmembrane regulator, is a protein that controls the channels of sodium and chloride. Hence the sodium and water transport in and out of the cell, and these channels are within the membrane of the cells that makes our sweat, mucous, tears, and digestive enzymes.
However, in CF these channels don’t work properly. Therefore, normally these channels would properly regulated sodium and water transport in and out of the cells, which helps control the flow of water within these structures among other things. But this is not what happens in a person with cystic fibrosis.
The mucous is thick and sticky rather than thin and slippery. This mucous will block the airways in the lower respiratory system and block the pancreatic duct from delivering pancreatic enzymes. In addition, the sweat glands produce excessive amounts of salt.
CF tends to affect Caucasians and males more. The current median life expectancy of a person with cystic fibrosis is 37 years of age (source: NIH.gov). It is currently diagnosed with a sweat test where pilocaprine and electric current is delivered to the skin to make it sweat. The amount of salt in the sweat is measured. Results 60 mmol/L or more is considered positive for CF.
Nursing interventions to cystic fibrosis include: chest physiotherapy (chest PT), monitor for complications, educating about PEP devices, preventing infection, administering medications and more (see the video for a detailed review of the nursing interventions)
Quiz: http://www.registerednursern.com/cystic-fibrosis-nclex-questions/
Notes: http://www.registerednursern.com/cystic-fibrosis-nclex-review/
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- published: 03 Jul 2018
- views: 519318
Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas, liver, kidneys, and intestine.
CF is inherited in an autosomal recessive manner.It is caused by the presence of mutations in both copies of the gene for the cystic fibrosis transmembrane conductance regulator (CFTR) protein.
Source : Wikipedia
- published: 17 Jan 2018
- views: 48894
Molly Pam, a senior at Stanford University, on living with cystic fibrosis as a child and making a smooth transition from seeing a pediatric physician at Packard Children’s Hospital, to getting regular care from a CF specialist at the Adult Cystic Fibrosis Center at Stanford Health Care.
Visit: http://stanfordhealthcare.org
- published: 22 Jun 2012
- views: 90278
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- published: 16 Sep 2019
- views: 38213
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This video presents Cystic Fibrosis, a type of obstructive lung disease.
Following topics are discussed:
Definition
Causes
CFTR gene mutation and the sweat glands
CFTR gene mutation and the pulmonary issues
- published: 25 Nov 2017
- views: 70512
http://on.chbos.org/cystic_fibrosis Watch as Boston Children's physician Debra Boyer explains cystic fibrosis -- and how it affects the body -- in our new series, Pediatric Playbooks.
Cystic fibrosis (CF) is a common hereditary (inherited) chronic disease that can affect multiple parts of your child's body --- most commonly her lungs and digestive system. The goals of treatment are to ease severity of your child's symptoms and slow the progression of the disease. At the present time, there is no cure for CF, but with medical and psychosocial support, many children and adolescents with CF can cope well and lead a productive life.
- published: 24 Feb 2011
- views: 72815
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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: 17 Sep 2019
- views: 17380
developed with YouTube
Cystic fibrosis
Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs but also the pancreas, liver, kidneys, and intestine. Long-term issues include difficulty breathing and coughing up mucus as a result of frequent lung infections. Other signs and symptoms include sinus infections, poor growth, fatty stool, clubbing of the fingers and toes, and infertility in males among others. Different people may have different degrees of symptoms.
CF is inherited in an autosomal recessive manner. It is caused by the presence of mutations in both copies of the gene for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. Those with a single working copy are carriers and otherwise mostly normal. CFTR is involved in production of sweat, digestive fluids, and mucus. When CFTR is not functional, secretions which are usually thin instead become thick. The condition is diagnosed by a sweat test and genetic testing. Screening of infants at birth takes place in some areas of the world.
This page contains text from Wikipedia, the Free Encyclopedia - https://wn.com/Cystic_fibrosis
-
What Is Cystic Fibrosis?
This video presents information about cystic fibrosis (CF), which is an autosomal recessive disorder. The video outlines the basic biological principles behind CF, along with an overview of the disease and available treatment options. The video begins by mentioning the genetic mutation to the cystic fibrosis transmembrane conductance regulatory (CFTR) gene on chromosome 7 which is the main cause of CF. Subsequently, the video entails the symptoms of the disease, including increased perspiration, pancreatic insufficiencies and lung infections. The epidemiology of this disease is also mentioned as the video states that 1 in 3600 children born in Canada is affected by CF. Furthermore, a significant portion of the video explains the organs affected by the disease and any treatment options that...
published: 25 Nov 2016 -
Cystic fibrosis: pathology review
What is cystic fibrosis? Cystic fibrosis, or CF, is an autosomal recessive disorder where there’s a mutation in the CFTR gene, and it is considered to be the most common lethal genetic disease in the Caucasian population. 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/...
published: 03 May 2021 -
How Cystic Fibrosis Affects the Lungs
See how the lungs work normally and how cystic fibrosis can affect the lungs over time. https://www.cff.org/Life-With-CF/Treatments-and-Therapies/Airway-Clearance/Basics-of-Lung-Care/
published: 19 May 2017 -
Cystic Fibrosis Nursing | Cystic Fibrosis Symptoms, Causes, Treatment, NCLEX Review
Cystic fibrosis NCLEX nursing review: Cystic fibrosis is a genetic disorder that causes the exocrine glands to work incorrectly. This can lead to major complications that affect the respiratory, digestive (pancreas, liver, intestines), integumentary, and reproductive systems along with the sinuses. What are exocrine glands? These are glands that produce and transfer it’s secretions (ex: mucous, tears, sweat, digestive enzymes) via DUCTS to it’s intended area of the body rather than directly into the bloodstream like the endocrine glands. In cystic fibrosis, there is a gene that is mutated that prevents the exocrine gland from working properly. It is called the CFTR gene! The CFTR gene, which stands for cystic fibrosis transmembrane regulator, is a protein that controls the channels...
published: 03 Jul 2018 -
Cystic Fibrosis | Molecular Mechanism & Genetics
Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas, liver, kidneys, and intestine. CF is inherited in an autosomal recessive manner.It is caused by the presence of mutations in both copies of the gene for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. Source : Wikipedia
published: 17 Jan 2018 -
Stanford Hospital's Adult Cystic Fibrosis Clinic - Molly Pam's Story
Molly Pam, a senior at Stanford University, on living with cystic fibrosis as a child and making a smooth transition from seeing a pediatric physician at Packard Children’s Hospital, to getting regular care from a CF specialist at the Adult Cystic Fibrosis Center at Stanford Health Care. Visit: http://stanfordhealthcare.org
published: 22 Jun 2012 -
Cystic Fibrosis | Definition, Pathogenesis, Symptoms and Complications
😍🖼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/ *** As a small gift for my viewers, here are 2 FREE audiobooks from Audible https://amzn.to/2FQurW...
published: 16 Sep 2019 -
Cystic Fibrosis - Pathophysiology, Genetics, Causes, Signs and Symptoms
Subscribe to the drbeen Channel HERE: http://bit.ly/2GBhiS0 For more content from drbeen, click HERE: http://bit.ly/2GB41bU Watch drbeen videos HERE: http://bit.ly/2GB41bU Like drbeen on Facebook HERE: http://bit.ly/2GSSTGS Follow drbeen on Twitter HERE: http://bit.ly/2XeSVhV Follow drbeen on Instagram HERE: http://bit.ly/2ST2Zih Get new medical lectures across your devices. Stream anywhere, anytime. Try it for free! http://bit.ly/2QsIwQ5 This video presents Cystic Fibrosis, a type of obstructive lung disease. Following topics are discussed: Definition Causes CFTR gene mutation and the sweat glands CFTR gene mutation and the pulmonary issues
published: 25 Nov 2017 -
Pediatric Playbook - Cystic Fibrosis
http://on.chbos.org/cystic_fibrosis Watch as Boston Children's physician Debra Boyer explains cystic fibrosis -- and how it affects the body -- in our new series, Pediatric Playbooks. Cystic fibrosis (CF) is a common hereditary (inherited) chronic disease that can affect multiple parts of your child's body --- most commonly her lungs and digestive system. The goals of treatment are to ease severity of your child's symptoms and slow the progression of the disease. At the present time, there is no cure for CF, but with medical and psychosocial support, many children and adolescents with CF can cope well and lead a productive life.
published: 24 Feb 2011 -
Cystic Fibrosis Diagnosis And Management
😍🖼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/ *** As a small gift for my viewers, here are 2 FREE audiobooks from Audible https://amzn.to/2FQurW...
published: 17 Sep 2019
developed with YouTube
5:46
What Is Cystic Fibrosis?
- Order: Reorder
- Duration: 5:46
- Uploaded Date: 25 Nov 2016
- views: 231414
This video presents information about cystic fibrosis (CF), which is an autosomal recessive disorder. The video outlines the basic biological principles behind ...
This video presents information about cystic fibrosis (CF), which is an autosomal recessive disorder. The video outlines the basic biological principles behind CF, along with an overview of the disease and available treatment options. The video begins by mentioning the genetic mutation to the cystic fibrosis transmembrane conductance regulatory (CFTR) gene on chromosome 7 which is the main cause of CF. Subsequently, the video entails the symptoms of the disease, including increased perspiration, pancreatic insufficiencies and lung infections. The epidemiology of this disease is also mentioned as the video states that 1 in 3600 children born in Canada is affected by CF. Furthermore, a significant portion of the video explains the organs affected by the disease and any treatment options that patients have. It is thoroughly explained that CF affects multiple organs including the lungs, pancreas and intestines. Many of these complications are due to blockages caused by the buildup of mucus. For instance, blockages caused in the intestines due to mucus buildup creates inefficiencies in digestion, specifically for fats and proteins. Considering there are multiple body parts affected by CF, there is a wide range of treatment options available to alleviate the condition of the disease. A majority of the treatment options serve the function of removing buildups of mucus and the blockages that occur. A patient with CF will most likely experience lung infections which are often treated with different types of antibiotics based on the severity of the disease and type of bacteria that is present. Other medications, most notably, bronchodilators, are also considered as treatment options for this disease. Lastly, there are also physical treatments such as Chest Physical Therapy (CPT) which also attempt to clear mucus using physical techniques. Overall, our video attempts to explain the basic processes that cause CF, subsequently followed by its overall impact on the patient’s body and the treatments that are available.
This video was made by 4DM3 students Zubair Banoor, Jaskeerat Kaur, Sina Nastarani, Monica Persaud and Kritika Seth
Copyright McMaster University 2016
Please let us know how we can improve our videos and additional topics should be addressed below.
https://wn.com/What_Is_Cystic_Fibrosis
This video presents information about cystic fibrosis (CF), which is an autosomal recessive disorder. The video outlines the basic biological principles behind CF, along with an overview of the disease and available treatment options. The video begins by mentioning the genetic mutation to the cystic fibrosis transmembrane conductance regulatory (CFTR) gene on chromosome 7 which is the main cause of CF. Subsequently, the video entails the symptoms of the disease, including increased perspiration, pancreatic insufficiencies and lung infections. The epidemiology of this disease is also mentioned as the video states that 1 in 3600 children born in Canada is affected by CF. Furthermore, a significant portion of the video explains the organs affected by the disease and any treatment options that patients have. It is thoroughly explained that CF affects multiple organs including the lungs, pancreas and intestines. Many of these complications are due to blockages caused by the buildup of mucus. For instance, blockages caused in the intestines due to mucus buildup creates inefficiencies in digestion, specifically for fats and proteins. Considering there are multiple body parts affected by CF, there is a wide range of treatment options available to alleviate the condition of the disease. A majority of the treatment options serve the function of removing buildups of mucus and the blockages that occur. A patient with CF will most likely experience lung infections which are often treated with different types of antibiotics based on the severity of the disease and type of bacteria that is present. Other medications, most notably, bronchodilators, are also considered as treatment options for this disease. Lastly, there are also physical treatments such as Chest Physical Therapy (CPT) which also attempt to clear mucus using physical techniques. Overall, our video attempts to explain the basic processes that cause CF, subsequently followed by its overall impact on the patient’s body and the treatments that are available.
This video was made by 4DM3 students Zubair Banoor, Jaskeerat Kaur, Sina Nastarani, Monica Persaud and Kritika Seth
Copyright McMaster University 2016
Please let us know how we can improve our videos and additional topics should be addressed below.
- published: 25 Nov 2016
- views: 231414
16:33
Cystic fibrosis: pathology review
- Order: Reorder
- Duration: 16:33
- Uploaded Date: 03 May 2021
- views: 24523
What is cystic fibrosis? Cystic fibrosis, or CF, is an autosomal recessive disorder where there’s a mutation in the CFTR gene, and it is considered to be the mo...
What is cystic fibrosis? Cystic fibrosis, or CF, is an autosomal recessive disorder where there’s a mutation in the CFTR gene, and it is considered to be the most common lethal genetic disease in the Caucasian population.
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:
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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/Cystic_Fibrosis_Pathology_Review
What is cystic fibrosis? Cystic fibrosis, or CF, is an autosomal recessive disorder where there’s a mutation in the CFTR gene, and it is considered to be the most common lethal genetic disease in the Caucasian population.
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: 03 May 2021
- views: 24523
2:03
How Cystic Fibrosis Affects the Lungs
- Order: Reorder
- Duration: 2:03
- Uploaded Date: 19 May 2017
- views: 131106
See how the lungs work normally and how cystic fibrosis can affect the lungs over time.
https://www.cff.org/Life-With-CF/Treatments-and-Therapies/Airway-Clear...
See how the lungs work normally and how cystic fibrosis can affect the lungs over time.
https://www.cff.org/Life-With-CF/Treatments-and-Therapies/Airway-Clearance/Basics-of-Lung-Care/
https://wn.com/How_Cystic_Fibrosis_Affects_The_Lungs
See how the lungs work normally and how cystic fibrosis can affect the lungs over time.
https://www.cff.org/Life-With-CF/Treatments-and-Therapies/Airway-Clearance/Basics-of-Lung-Care/
- published: 19 May 2017
- views: 131106
26:13
Cystic Fibrosis Nursing | Cystic Fibrosis Symptoms, Causes, Treatment, NCLEX Review
- Order: Reorder
- Duration: 26:13
- Uploaded Date: 03 Jul 2018
- views: 519318
Cystic fibrosis NCLEX nursing review: Cystic fibrosis is a genetic disorder that causes the exocrine glands to work incorrectly.
This can lead to major compli...
Cystic fibrosis NCLEX nursing review: Cystic fibrosis is a genetic disorder that causes the exocrine glands to work incorrectly.
This can lead to major complications that affect the respiratory, digestive (pancreas, liver, intestines), integumentary, and reproductive systems along with the sinuses.
What are exocrine glands? These are glands that produce and transfer it’s secretions (ex: mucous, tears, sweat, digestive enzymes) via DUCTS to it’s intended area of the body rather than directly into the bloodstream like the endocrine glands.
In cystic fibrosis, there is a gene that is mutated that prevents the exocrine gland from working properly. It is called the CFTR gene!
The CFTR gene, which stands for cystic fibrosis transmembrane regulator, is a protein that controls the channels of sodium and chloride. Hence the sodium and water transport in and out of the cell, and these channels are within the membrane of the cells that makes our sweat, mucous, tears, and digestive enzymes.
However, in CF these channels don’t work properly. Therefore, normally these channels would properly regulated sodium and water transport in and out of the cells, which helps control the flow of water within these structures among other things. But this is not what happens in a person with cystic fibrosis.
The mucous is thick and sticky rather than thin and slippery. This mucous will block the airways in the lower respiratory system and block the pancreatic duct from delivering pancreatic enzymes. In addition, the sweat glands produce excessive amounts of salt.
CF tends to affect Caucasians and males more. The current median life expectancy of a person with cystic fibrosis is 37 years of age (source: NIH.gov). It is currently diagnosed with a sweat test where pilocaprine and electric current is delivered to the skin to make it sweat. The amount of salt in the sweat is measured. Results 60 mmol/L or more is considered positive for CF.
Nursing interventions to cystic fibrosis include: chest physiotherapy (chest PT), monitor for complications, educating about PEP devices, preventing infection, administering medications and more (see the video for a detailed review of the nursing interventions)
Quiz: http://www.registerednursern.com/cystic-fibrosis-nclex-questions/
Notes: http://www.registerednursern.com/cystic-fibrosis-nclex-review/
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https://wn.com/Cystic_Fibrosis_Nursing_|_Cystic_Fibrosis_Symptoms,_Causes,_Treatment,_Nclex_Review
Cystic fibrosis NCLEX nursing review: Cystic fibrosis is a genetic disorder that causes the exocrine glands to work incorrectly.
This can lead to major complications that affect the respiratory, digestive (pancreas, liver, intestines), integumentary, and reproductive systems along with the sinuses.
What are exocrine glands? These are glands that produce and transfer it’s secretions (ex: mucous, tears, sweat, digestive enzymes) via DUCTS to it’s intended area of the body rather than directly into the bloodstream like the endocrine glands.
In cystic fibrosis, there is a gene that is mutated that prevents the exocrine gland from working properly. It is called the CFTR gene!
The CFTR gene, which stands for cystic fibrosis transmembrane regulator, is a protein that controls the channels of sodium and chloride. Hence the sodium and water transport in and out of the cell, and these channels are within the membrane of the cells that makes our sweat, mucous, tears, and digestive enzymes.
However, in CF these channels don’t work properly. Therefore, normally these channels would properly regulated sodium and water transport in and out of the cells, which helps control the flow of water within these structures among other things. But this is not what happens in a person with cystic fibrosis.
The mucous is thick and sticky rather than thin and slippery. This mucous will block the airways in the lower respiratory system and block the pancreatic duct from delivering pancreatic enzymes. In addition, the sweat glands produce excessive amounts of salt.
CF tends to affect Caucasians and males more. The current median life expectancy of a person with cystic fibrosis is 37 years of age (source: NIH.gov). It is currently diagnosed with a sweat test where pilocaprine and electric current is delivered to the skin to make it sweat. The amount of salt in the sweat is measured. Results 60 mmol/L or more is considered positive for CF.
Nursing interventions to cystic fibrosis include: chest physiotherapy (chest PT), monitor for complications, educating about PEP devices, preventing infection, administering medications and more (see the video for a detailed review of the nursing interventions)
Quiz: http://www.registerednursern.com/cystic-fibrosis-nclex-questions/
Notes: http://www.registerednursern.com/cystic-fibrosis-nclex-review/
More Pediatric Reviews: https://www.youtube.com/watch?v=QCgcUtWkWqE&list;=PLQrdx7rRsKfXmfA3CoozS5N767bLpnrbm
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Diabetes Health Managment: https://www.youtube.com/playlist?list=PLQrdx7rRsKfXtEx17D7zC1efmWIX-iIs9
- published: 03 Jul 2018
- views: 519318
4:04
Cystic Fibrosis | Molecular Mechanism & Genetics
- Order: Reorder
- Duration: 4:04
- Uploaded Date: 17 Jan 2018
- views: 48894
Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas, liver, kidneys, and intestine.
CF is inherited in an autosomal ...
Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas, liver, kidneys, and intestine.
CF is inherited in an autosomal recessive manner.It is caused by the presence of mutations in both copies of the gene for the cystic fibrosis transmembrane conductance regulator (CFTR) protein.
Source : Wikipedia
https://wn.com/Cystic_Fibrosis_|_Molecular_Mechanism_Genetics
Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas, liver, kidneys, and intestine.
CF is inherited in an autosomal recessive manner.It is caused by the presence of mutations in both copies of the gene for the cystic fibrosis transmembrane conductance regulator (CFTR) protein.
Source : Wikipedia
- published: 17 Jan 2018
- views: 48894
5:13
Stanford Hospital's Adult Cystic Fibrosis Clinic - Molly Pam's Story
- Order: Reorder
- Duration: 5:13
- Uploaded Date: 22 Jun 2012
- views: 90278
Molly Pam, a senior at Stanford University, on living with cystic fibrosis as a child and making a smooth transition from seeing a pediatric physician at Packar...
Molly Pam, a senior at Stanford University, on living with cystic fibrosis as a child and making a smooth transition from seeing a pediatric physician at Packard Children’s Hospital, to getting regular care from a CF specialist at the Adult Cystic Fibrosis Center at Stanford Health Care.
Visit: http://stanfordhealthcare.org
https://wn.com/Stanford_Hospital's_Adult_Cystic_Fibrosis_Clinic_Molly_Pam's_Story
Molly Pam, a senior at Stanford University, on living with cystic fibrosis as a child and making a smooth transition from seeing a pediatric physician at Packard Children’s Hospital, to getting regular care from a CF specialist at the Adult Cystic Fibrosis Center at Stanford Health Care.
Visit: http://stanfordhealthcare.org
- published: 22 Jun 2012
- views: 90278
17:19
Cystic Fibrosis | Definition, Pathogenesis, Symptoms and Complications
- Order: Reorder
- Duration: 17:19
- Uploaded Date: 16 Sep 2019
- views: 38213
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https://wn.com/Cystic_Fibrosis_|_Definition,_Pathogenesis,_Symptoms_And_Complications
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- published: 16 Sep 2019
- views: 38213
16:09
Cystic Fibrosis - Pathophysiology, Genetics, Causes, Signs and Symptoms
- Order: Reorder
- Duration: 16:09
- Uploaded Date: 25 Nov 2017
- views: 70512
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This video presents Cystic Fibrosis, a type of obstructive lung disease.
Following topics are discussed:
Definition
Causes
CFTR gene mutation and the sweat glands
CFTR gene mutation and the pulmonary issues
https://wn.com/Cystic_Fibrosis_Pathophysiology,_Genetics,_Causes,_Signs_And_Symptoms
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This video presents Cystic Fibrosis, a type of obstructive lung disease.
Following topics are discussed:
Definition
Causes
CFTR gene mutation and the sweat glands
CFTR gene mutation and the pulmonary issues
- published: 25 Nov 2017
- views: 70512
3:03
Pediatric Playbook - Cystic Fibrosis
- Order: Reorder
- Duration: 3:03
- Uploaded Date: 24 Feb 2011
- views: 72815
http://on.chbos.org/cystic_fibrosis Watch as Boston Children's physician Debra Boyer explains cystic fibrosis -- and how it affects the body -- in our new seri...
http://on.chbos.org/cystic_fibrosis Watch as Boston Children's physician Debra Boyer explains cystic fibrosis -- and how it affects the body -- in our new series, Pediatric Playbooks.
Cystic fibrosis (CF) is a common hereditary (inherited) chronic disease that can affect multiple parts of your child's body --- most commonly her lungs and digestive system. The goals of treatment are to ease severity of your child's symptoms and slow the progression of the disease. At the present time, there is no cure for CF, but with medical and psychosocial support, many children and adolescents with CF can cope well and lead a productive life.
https://wn.com/Pediatric_Playbook_Cystic_Fibrosis
http://on.chbos.org/cystic_fibrosis Watch as Boston Children's physician Debra Boyer explains cystic fibrosis -- and how it affects the body -- in our new series, Pediatric Playbooks.
Cystic fibrosis (CF) is a common hereditary (inherited) chronic disease that can affect multiple parts of your child's body --- most commonly her lungs and digestive system. The goals of treatment are to ease severity of your child's symptoms and slow the progression of the disease. At the present time, there is no cure for CF, but with medical and psychosocial support, many children and adolescents with CF can cope well and lead a productive life.
- published: 24 Feb 2011
- views: 72815
8:36
Cystic Fibrosis Diagnosis And Management
- Order: Reorder
- Duration: 8:36
- Uploaded Date: 17 Sep 2019
- views: 17380
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https://wn.com/Cystic_Fibrosis_Diagnosis_And_Management
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*** As a small gift for my viewers, here are 2 FREE audiobooks from Audible https://amzn.to/2FQurW0 Learning has never been easier..
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🥰 Picture-Mnemonics https://www.picmonic.com/referrals/JK55NQXQQB9JLC119 ...You can thank me later 😉.
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- published: 17 Sep 2019
- views: 17380
5:46
What Is Cystic Fibrosis?
This video presents information about cystic fibrosis (CF), which is an autosomal recessiv...
published: 25 Nov 2016
What Is Cystic Fibrosis?
What Is Cystic Fibrosis?
- Report rights infringement
- published: 25 Nov 2016
- views: 231414
This video presents information about cystic fibrosis (CF), which is an autosomal recessive disorder. The video outlines the basic biological principles behind CF, along with an overview of the disease and available treatment options. The video begins by mentioning the genetic mutation to the cystic fibrosis transmembrane conductance regulatory (CFTR) gene on chromosome 7 which is the main cause of CF. Subsequently, the video entails the symptoms of the disease, including increased perspiration, pancreatic insufficiencies and lung infections. The epidemiology of this disease is also mentioned as the video states that 1 in 3600 children born in Canada is affected by CF. Furthermore, a significant portion of the video explains the organs affected by the disease and any treatment options that patients have. It is thoroughly explained that CF affects multiple organs including the lungs, pancreas and intestines. Many of these complications are due to blockages caused by the buildup of mucus. For instance, blockages caused in the intestines due to mucus buildup creates inefficiencies in digestion, specifically for fats and proteins. Considering there are multiple body parts affected by CF, there is a wide range of treatment options available to alleviate the condition of the disease. A majority of the treatment options serve the function of removing buildups of mucus and the blockages that occur. A patient with CF will most likely experience lung infections which are often treated with different types of antibiotics based on the severity of the disease and type of bacteria that is present. Other medications, most notably, bronchodilators, are also considered as treatment options for this disease. Lastly, there are also physical treatments such as Chest Physical Therapy (CPT) which also attempt to clear mucus using physical techniques. Overall, our video attempts to explain the basic processes that cause CF, subsequently followed by its overall impact on the patient’s body and the treatments that are available.
This video was made by 4DM3 students Zubair Banoor, Jaskeerat Kaur, Sina Nastarani, Monica Persaud and Kritika Seth
Copyright McMaster University 2016
Please let us know how we can improve our videos and additional topics should be addressed below.
16:33
Cystic fibrosis: pathology review
What is cystic fibrosis? Cystic fibrosis, or CF, is an autosomal recessive disorder where ...
published: 03 May 2021
Cystic fibrosis: pathology review
Cystic fibrosis: pathology review
- Report rights infringement
- published: 03 May 2021
- views: 24523
What is cystic fibrosis? Cystic fibrosis, or CF, is an autosomal recessive disorder where there’s a mutation in the CFTR gene, and it is considered to be the most common lethal genetic disease in the Caucasian population.
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2:03
How Cystic Fibrosis Affects the Lungs
See how the lungs work normally and how cystic fibrosis can affect the lungs over time.
...
published: 19 May 2017
How Cystic Fibrosis Affects the Lungs
How Cystic Fibrosis Affects the Lungs
- Report rights infringement
- published: 19 May 2017
- views: 131106
See how the lungs work normally and how cystic fibrosis can affect the lungs over time.
https://www.cff.org/Life-With-CF/Treatments-and-Therapies/Airway-Clearance/Basics-of-Lung-Care/
26:13
Cystic Fibrosis Nursing | Cystic Fibrosis Symptoms, Causes, Treatment, NCLEX Review
Cystic fibrosis NCLEX nursing review: Cystic fibrosis is a genetic disorder that causes th...
published: 03 Jul 2018
Cystic Fibrosis Nursing | Cystic Fibrosis Symptoms, Causes, Treatment, NCLEX Review
Cystic Fibrosis Nursing | Cystic Fibrosis Symptoms, Causes, Treatment, NCLEX Review
- Report rights infringement
- published: 03 Jul 2018
- views: 519318
Cystic fibrosis NCLEX nursing review: Cystic fibrosis is a genetic disorder that causes the exocrine glands to work incorrectly.
This can lead to major complications that affect the respiratory, digestive (pancreas, liver, intestines), integumentary, and reproductive systems along with the sinuses.
What are exocrine glands? These are glands that produce and transfer it’s secretions (ex: mucous, tears, sweat, digestive enzymes) via DUCTS to it’s intended area of the body rather than directly into the bloodstream like the endocrine glands.
In cystic fibrosis, there is a gene that is mutated that prevents the exocrine gland from working properly. It is called the CFTR gene!
The CFTR gene, which stands for cystic fibrosis transmembrane regulator, is a protein that controls the channels of sodium and chloride. Hence the sodium and water transport in and out of the cell, and these channels are within the membrane of the cells that makes our sweat, mucous, tears, and digestive enzymes.
However, in CF these channels don’t work properly. Therefore, normally these channels would properly regulated sodium and water transport in and out of the cells, which helps control the flow of water within these structures among other things. But this is not what happens in a person with cystic fibrosis.
The mucous is thick and sticky rather than thin and slippery. This mucous will block the airways in the lower respiratory system and block the pancreatic duct from delivering pancreatic enzymes. In addition, the sweat glands produce excessive amounts of salt.
CF tends to affect Caucasians and males more. The current median life expectancy of a person with cystic fibrosis is 37 years of age (source: NIH.gov). It is currently diagnosed with a sweat test where pilocaprine and electric current is delivered to the skin to make it sweat. The amount of salt in the sweat is measured. Results 60 mmol/L or more is considered positive for CF.
Nursing interventions to cystic fibrosis include: chest physiotherapy (chest PT), monitor for complications, educating about PEP devices, preventing infection, administering medications and more (see the video for a detailed review of the nursing interventions)
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4:04
Cystic Fibrosis | Molecular Mechanism & Genetics
Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pan...
published: 17 Jan 2018
Cystic Fibrosis | Molecular Mechanism & Genetics
Cystic Fibrosis | Molecular Mechanism & Genetics
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Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas, liver, kidneys, and intestine.
CF is inherited in an autosomal recessive manner.It is caused by the presence of mutations in both copies of the gene for the cystic fibrosis transmembrane conductance regulator (CFTR) protein.
Source : Wikipedia
5:13
Stanford Hospital's Adult Cystic Fibrosis Clinic - Molly Pam's Story
Molly Pam, a senior at Stanford University, on living with cystic fibrosis as a child and ...
published: 22 Jun 2012
Stanford Hospital's Adult Cystic Fibrosis Clinic - Molly Pam's Story
Stanford Hospital's Adult Cystic Fibrosis Clinic - Molly Pam's Story
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Molly Pam, a senior at Stanford University, on living with cystic fibrosis as a child and making a smooth transition from seeing a pediatric physician at Packard Children’s Hospital, to getting regular care from a CF specialist at the Adult Cystic Fibrosis Center at Stanford Health Care.
Visit: http://stanfordhealthcare.org
17:19
Cystic Fibrosis | Definition, Pathogenesis, Symptoms and Complications
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Cystic Fibrosis | Definition, Pathogenesis, Symptoms and Complications
Cystic Fibrosis | Definition, Pathogenesis, Symptoms and Complications
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Cystic Fibrosis - Pathophysiology, Genetics, Causes, Signs and Symptoms
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published: 25 Nov 2017
Cystic Fibrosis - Pathophysiology, Genetics, Causes, Signs and Symptoms
Cystic Fibrosis - Pathophysiology, Genetics, Causes, Signs and Symptoms
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This video presents Cystic Fibrosis, a type of obstructive lung disease.
Following topics are discussed:
Definition
Causes
CFTR gene mutation and the sweat glands
CFTR gene mutation and the pulmonary issues
3:03
Pediatric Playbook - Cystic Fibrosis
http://on.chbos.org/cystic_fibrosis Watch as Boston Children's physician Debra Boyer expl...
published: 24 Feb 2011
Pediatric Playbook - Cystic Fibrosis
Pediatric Playbook - Cystic Fibrosis
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http://on.chbos.org/cystic_fibrosis Watch as Boston Children's physician Debra Boyer explains cystic fibrosis -- and how it affects the body -- in our new series, Pediatric Playbooks.
Cystic fibrosis (CF) is a common hereditary (inherited) chronic disease that can affect multiple parts of your child's body --- most commonly her lungs and digestive system. The goals of treatment are to ease severity of your child's symptoms and slow the progression of the disease. At the present time, there is no cure for CF, but with medical and psychosocial support, many children and adolescents with CF can cope well and lead a productive life.
8:36
Cystic Fibrosis Diagnosis And Management
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Cystic Fibrosis Diagnosis And Management
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Cystic fibrosis
Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs but also the pancreas, liver, kidneys, and intestine. Long-term issues include difficulty breathing and coughing up mucus as a result of frequent lung infections. Other signs and symptoms include sinus infections, poor growth, fatty stool, clubbing of the fingers and toes, and infertility in males among others. Different people may have different degrees of symptoms.
CF is inherited in an autosomal recessive manner. It is caused by the presence of mutations in both copies of the gene for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. Those with a single working copy are carriers and otherwise mostly normal. CFTR is involved in production of sweat, digestive fluids, and mucus. When CFTR is not functional, secretions which are usually thin instead become thick. The condition is diagnosed by a sweat test and genetic testing. Screening of infants at birth takes place in some areas of the world.
This page contains text from Wikipedia, the Free Encyclopedia - https://wn.com/Cystic_fibrosis
What Is Cystic Fibrosis?...
Cystic fibrosis: pathology review...
How Cystic Fibrosis Affects the Lungs...
Cystic Fibrosis Nursing | Cystic Fibrosis Symptoms...
Cystic Fibrosis | Molecular Mechanism & Genetics...
Stanford Hospital's Adult Cystic Fibrosis Clinic -...
Cystic Fibrosis | Definition, Pathogenesis, Sympto...
Cystic Fibrosis - Pathophysiology, Genetics, Cause...
Pediatric Playbook - Cystic Fibrosis...
Cystic Fibrosis Diagnosis And Management...
Cystic Fibrosis
Inherited disorder manifests with no cure
Defective genes carry this abnormality
Cell clusters fail to create necessary juices
Deficient pancreatic enzymes prohibit the digestive process
Weakling newborn not capable of fending for itself
Clogged passages instill upper lung infection
Obstruction of intestinal glands
Foul smelling stool blocks the bowel
Gradual liver atrophy impairs insulin production
Infant ravaged with diabetes
Medicine administered to stabilize blood sugar
Thick mucus blocks the exocrine glands
Respiratory contamination spreads within
Debilitating illness cuts chance of survival
Latest News for: cystic fibrosis
Edit
The Bradford Era
04 Nov 2021
Spirovant Presents Preclinical Data Showing SP-101 Restores CF Transmembrane Conductance Regulator Function at the 2021 ...
The Bradford Era
04 Nov 2021
... respiratory diseases including cystic fibrosis (CF), today presented SP-101, an investigational novel recombinant adeno-associated virus (AAV) gene therapy selected for its tropism to human airway epithelia, at the 2021 North American Cystic Fibrosis Conference (NACFC 2021).
Edit
EffRx Obtains Swiss Marketing Authorization for Bronchitol® in Cystic Fibrosis
... of cystic fibrosis (CF) in adults and in children aged 6 years and above as add‐on to other medicines.
Edit
'You've got to pinch yourself': Coffey's 'awesome' Melbourne Cup debut
Harry Coffey says he's never had so much support for finishing third last in a horse race. The jockey, who rode in this week's Melbourne Cup, hopes his ride inspires others with cystic fibrosis to chase their dreams ... .
Edit
The Macon County News
04 Nov 2021
Classifieds for November 4, 2021
The Macon County News
04 Nov 2021
Rentals. RV/CAMPER LOT Short distance to town. $325/month. 6-month minimum. Includes water, sewer, and trash. Text your email address to (828)346-1200 for all the details ... Services ... OUR FINAL CYSTIC FIBROSIS Extravaganza November 5 & 6 and November 11, 12 &13, 8am-4pm ... OUR FINAL CYSTIC FIBROSIS Extravaganza November 5 & 6 and November 11, 12 &13, 8am-4am ... .
Edit
Spirovant Presents Preclinical Data Showing SP-101 Restores CF Transmembrane Conductance Regulator Function at the 2021 North American Cystic Fibrosis Conference
... respiratory diseases including cystic fibrosis (CF), today presented SP-101, an investigational novel recombinant adeno-associated virus (AAV) gene therapy selected for its tropism to human airway epithelia, at the 2021 North American Cystic Fibrosis Conference (NACFC 2021).
Edit
Nine lung transplants performed in B.C. as a result of COVID infections
Nine British Columbians “on the precipice of death” have received double-lung transplants since April after they suffered severe internal damage from COVID-19, according the director of the lung transplant program at Vancouver General Hospital ... are performed on patients with cystic fibrosis, emphysema and pulmonary fibrosis, according to the B.C ... 3 ... .
Edit
Murfreesboro Post
04 Nov 2021
Susan Steen: Keep up the compassion for other people’s chronic illness
Murfreesboro Post
04 Nov 2021
Jackson Brown Jr. It’s true ... I hope mine will think well of me ... Alzheimer’s, arthritis, asthma, cancer, celiac, chronic migraines, COPD, Crohn disease, cystic fibrosis, dementia, diabetes, epilepsy, fibromyalgia, heart disease, HIV/AIDS, mood disorders (bipolar, cyclothymic, and depression), multiple sclerosis, and Parkinson’s disease, to name a few.
Edit
The Marshall News Messenger
04 Nov 2021
Moderna Reports Third Quarter Fiscal Year 2021 Financial Results and Provides Business Updates
The Marshall News Messenger
04 Nov 2021
Edit
The Maryville Daily Times
03 Nov 2021
ReCode Therapeutics Presents Preclinical Data from mRNA-based Cystic Fibrosis Program at 2021 North American Cystic ...
The Maryville Daily Times
03 Nov 2021
... genetic medicines using its proprietary LNP delivery platform, presented new preclinical data today from the Company’s inhaled mRNA-based therapeutic program for cystic fibrosis (CF) during an oral poster session at the 2021 North American Cystic Fibrosis Conference (NACFC).
Edit
The Marshall News Messenger
03 Nov 2021
Cystic Fibrosis Foundation Strikes First-of-Its-Kind Deal With Pioneering Medicines, a Flagship Pioneering Initiative
The Marshall News Messenger
03 Nov 2021
Today, the Cystic Fibrosis Foundation announced a first-of-its-kind collaboration with Pioneering Medicines, an initiative of Flagship Pioneering, to spur the development of genetic-based therapies for cystic fibrosis ... The Cystic Fibrosis Foundation is the world's leader in the search for a cure for cystic fibrosis ... Cystic Fibrosis Foundation.
Edit
MSU, Spectrum partnership strengthens cystic fibrosis research
A team of Michigan State University College of Human Medicine physicians partnered with a group from Spectrum Health to advance studies into a potential cystic fibrosis treatment ... Three pulmonologists from Spectrum Health and Helen DeVos Children’s Hospital Cystic Fibrosis Center, Dr.
Edit
Daily Times Chronicle
03 Nov 2021
Pioneering Medicines, An Initiative Of Flagship Pioneering, Establishes First-Of-Its-Kind Partnership With The Cystic Fibrosis Foundation ...
Daily Times Chronicle
03 Nov 2021
3, 2021 /PRNewswire/ -- Flagship Pioneering today announced a first-of-its-kind strategic partnership with the Cystic Fibrosis Foundation and Flagship's Pioneering Medicines to develop therapeutics that address the unmet needs of people living with cystic fibrosis by leveraging the innovations and teams of multiple Flagship-founded companies.
Edit
The Marshall News Messenger
03 Nov 2021
Tessera Therapeutics Announces R&D; Collaboration with Cystic Fibrosis Foundation as Part of a Portfolio of ...
The Marshall News Messenger
03 Nov 2021
... to rewrite the genetic codes that cause cystic fibrosis ... “The Cystic Fibrosis Foundation’s extensive network of scientists, companies, and clinicians knowledgeable about cystic fibrosis will help accelerate screening and development of our cystic fibrosis-targeting Gene Writers.
Edit
Chance of organ transplant linked to Covid-19 vaccination status
However, Philip Watt, chairman of the Irish Donor Network and chief executive of Cystic Fibrosis Ireland, said he didn’t agree with the “dogmatic” perspective of a US expert who said unvaccinated people should not be eligible. There is no directive in Ireland saying that if you are not vaccinated you will not get an organ donation, Mr Watt said ... .
Edit
Colorado fertility doctor sued again for allegedly using own sperm to inseminate patient
Paul B. Jones ... Jones, reached by phone Tuesday, declined to comment. The family also claimed that Jones carried cystic fibrosis, and that several of the half-siblings connected to Jones also have the genetic disease, which can cause persistent lung infections and limit an individual’s ability to breathe ... .
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