Pass 5: Describe possible ways of monitoring a long-term physical condition This is an essay which links to case studies and has supporting research which is Harvard referenced. It is important to remember monitoring can be used to diagnose a condition but also to assess how well the condition is being managed, if the treatment works or when the treatment needs to be adjusted or changed. Case A: Jackie and Tom have a four year old claughter, Lucy. Lucy has been diagnosed with cystic fibrosis and will need long-term treatment and monitoring In the UK, all newborn babies are screened for cystic fibrosis as part of the newborn blood spot test (heelprick test) carried out shortly aftler they're born. If the screening test suggests a child may have cystic fibrosis, they'llneed these additionaltests to confirm they have the condition: https://www.nhs.uk/conditions/baby/newborn-screening/blood-spot-test/ diagnosis https://www.nhs.uk/conditions/cystic-fibrosis/ a sweat test- to measure the amount of salt in sweat, which will be abnormally high in someone with cystic fibrosis a genetic test - where a sample of blood or saliva is checked for the faulty gene that causes cystic fibrosis. clinical observation-tell me all about the monitoring of the disease, any checks they may have for the digestive and respiratory problems, ising nhs site and cystic fibrosis site.or https://www.cff.org/What-is-CF/About-Cystic-Fibrosis/ nclude monitoring by GP, Family history, medical history, lifestyle, bp, pulse, temp, weight, height, BMI, blood, uring, sputum, dody fluid tests xrays scans etc
Pass 5: Describe possible ways of monitoring a long-term physical condition This is an essay which links to case studies and has supporting research which is Harvard referenced. It is important to remember monitoring can be used to diagnose a condition but also to assess how well the condition is being managed, if the treatment works or when the treatment needs to be adjusted or changed. Case A: Jackie and Tom have a four year old claughter, Lucy. Lucy has been diagnosed with cystic fibrosis and will need long-term treatment and monitoring In the UK, all newborn babies are screened for cystic fibrosis as part of the newborn blood spot test (heelprick test) carried out shortly aftler they're born. If the screening test suggests a child may have cystic fibrosis, they'llneed these additionaltests to confirm they have the condition: https://www.nhs.uk/conditions/baby/newborn-screening/blood-spot-test/ diagnosis https://www.nhs.uk/conditions/cystic-fibrosis/ a sweat test- to measure the amount of salt in sweat, which will be abnormally high in someone with cystic fibrosis a genetic test - where a sample of blood or saliva is checked for the faulty gene that causes cystic fibrosis. clinical observation-tell me all about the monitoring of the disease, any checks they may have for the digestive and respiratory problems, ising nhs site and cystic fibrosis site.or https://www.cff.org/What-is-CF/About-Cystic-Fibrosis/ nclude monitoring by GP, Family history, medical history, lifestyle, bp, pulse, temp, weight, height, BMI, blood, uring, sputum, dody fluid tests xrays scans etc
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Pass 5: Describe possible ways of monitoring a long-term physical condition
This is an essay which links to case studies and has supporting research which is Harvard
referenced. It is important to remember monitoring can be used to diagnose a condition but also to
assess how well the condition is being managed, if the treatment works or when the treatment
needs to be adjusted or changed.
Case A: Jackie and Tom have a four vear old daughter, Lucy. Lucy has been diagnosed
with cystic fibrosis and will need long-ternm treatment and monitoring.
In the UK, all newborn babies are screened for cystic fibrosis as part of the newborn blood spot test
(heelprick test) carried out shortly aftler they're born. If the screening test suggests a child may have
cystic fibrosis, they'll need these additionaltests to confirm they have the condition:
https://www.nhs.uk/conditions/baby/newborn-5creening/blaod-spot-test/
diagnosis
https://www.nhs.uk/conditions/cystic-fibrosis/
a sweat test- to measure the amount of salt in sweat, which will be abnormally high in someone
with cystic fibrosis
a genetic test -where a sample of blood or saliva is checked for the faulty gene that causes cystic
fibrosis.
clinical observation-tell me all about the monitoring of the disease,
any checks they may have for the digestive and respiratory problems,
using nhs site and cystic fibrosis site.or https://www.cff.org/What-is-CF/About-Cystic-Fibrosis/
Include monitoring by GP,
Family history, medical history, lifestyle, bp, pulse, temp, weight, height, BMI, blood, uring, sputum,
body fluid tests
xrays scans etc
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