༜ A sweat test measures the amount of salt chemicals (sodium and chloride) in sweat. ༜ Sodium and chloride are part of your body’s electrolyte balance,

Slides:



Advertisements
Similar presentations
What causes cystic fibrosis?
Advertisements

By: Ryan M. and Anthony L..
Cystic Fibrosis By: Brendon McGehee.
30,000 American’s; 3,000 Canadian’s; and over 20,000 European’s have this disease. 1 in every 20 Americans carry the abnormal CF gene approximately 2,500.
WHAT IS COMMON COLD? It is an illness caused by a virus infection inside the nose. It also involves the ears, sinus and bronchial tubes COMMON SYMPTOMS.
The Urinary System The organs, tubes, muscles, and nerves that work together to create, store, and carry urine are the urinary system. The urinary system.
By: Marki Wong and Rebecca den Hollander What is Cystic Fibrosis? It affects the mucus glands, causing problems in the lungs and pancreas, leading to.
Megan Forziati Troy Antonucci CYSTIC FIBROSIS. Definition A life-threatening disorder that causes severe lung damage and nutritional deficiencies. Affects.
Cystic Fibrosis Gina Brandl, RN BSN Nursing Instructor, Pediatrics.
Cystic fibrosis. Cystic fibrosis (CF) is an autosomal recessive genetic disorder that affects most critically the lungs, and also the pancreas, liver,
What is Genetics When organisms reproduce the offspring tend to resemble their parents. They are not, however, identical to either parent, and they are.
Tiffany Rimmer.  CF is the most common lethal autosomal recessive genetic disease in Caucasians.  It affects over 30,000 individuals in the United States.
CYSTIC FIBROSIS FANOURAKI MARIA CHARALAMPIDOU ALEXANDRA
Three main types of lung disease Airway diseases -- These diseases affect the tubes (airways) that carry oxygen and other gases into and out of the lungs.
Sputum Sputum is a mucousy substance (consisting of cells and other matter) that is secreted into the airways of the respiratory tract(lungs,bronchi, trachea)
Cystic Fibrosis- is an inherited disease of the mucus glands that affects many body systems. It causes the mucus glands to create a thick and sticky mucus.
Berkeley Fial Michaela McNiff.  Someone gets Cystic Fibrosis when they inherit two mutated genes – one from each parent.  The CF gene is on chromosome.
 The first known definition of Cystic Fibrosis was written in 1938 by Dr. Dorothy Anderson, a pathologist in the New York Babies Hospital.  In the 17.
Cystic Fibrosis Bronte Short. What Cause Cystic Fibrosis? Cystic fibrosis, is an autosomal recessive hereditary disease that mostly affects the lungs,
Information found on:
By: Jennifer Novatt  Cystic Fibrosis is sometimes called “65 roses”.  The nickname came from a little boy who overheard his mom talking about the condition.
By Taliyah and Selina. Cystic Fibrosis CF Mucoviscidosis.
IIt is a genetic disease that is passed down through families that causes a thick, sticky mucus to build up in the lungs, digestive tract, and other.
Symptoms In newborns: – Delayed growth – Failure to gain weight normally during childhood – No bowel movements in first 24 to 48 hours of life – Salty-tasting.
Respiratory system. The primary function of the respiratory system is the supply of oxygen to the blood and the removal of carbon dioxide.
Patient: Lily Johnson Case study by Alexa Angelo
Recall.... Why is diffusion important? - Gas exchange b/w a living cell & the environment always takes place by diffusion across a moist surface. - The.
Chromosomal Mutations and Karyotypes Genetic Variation- differences in genetic material Caused by: segregation crossing over (during meiosis) recombination.
HOW THE LUNGS WORK AND WHAT THEY SOUND LIKE!. INSPIRATION: During inhalation (Inspiration), the chest expands up and outward The diaphragm contracts and.
Bronchiectasis Sami ur Rahman Roll No: Overview Definition Etiology Pathology Clinical Presentation Diagnosis Treatment.
Cystic Fibrosis Kayla Barber. What is it? Cystic Fibrosis is a hereditary disease that a person gets when BOTH parents are carriers. It causes abnormally.
The following disorders all prevent adequate ventilation of the lungs and lead to insufficient supply of oxygen and the retention of carbon dioxide in.
CAUSES OF CYSTIC FIBROSIS CF is caused by a mutation in the gene for the protein cystic fibrosis transmembrane conductance regulator (CFTR). This protein.
Respiratory Disorders. Asthma Condition where smooth muscle that lines the airways contracts, making it difficult to breathe. –Allergy-induced Asthma.
Sweat Test. A sweat test measures the amount of salt chemicals (sodium and chloride) in sweat. Sodium and chloride are part of your body’s electrolyte.
Respiratory System The process of exchanging gases between the atmosphere and body cells is called respiration.
Cystic Fibrosis By: Morgan. Definition Cystic fibrosis is a thick mucus that clogs the air ways and tends to cause lung diseases. A diseases common among.
Things That Can Go Wrong With the Lungs and Respiratory System
7.3 – Respiratory Health Respiratory health problems can be identified as conditions that affect either the upper respiratory tract, or the lower respiratory.
Cystic fibrosis is an inherited disease that causes thick, sticky mucus to build up in the lungs and digestive tract.
Lung Disease. Pulmonary Tuberculosis Symptoms Persistent cough Tiredness Loss of appetite – weight loss Fever Coughing of blood.
Cystic Fibrosis Hereditary recessive trait disease
Objectives Review the causes of cystic fibrosis (CF) Describe the symptoms and laboratory findings in CF Review current and emerging CF treatments Review.
Jacob Baughan, Mike Marshall, Deronta Darden  Cystic fibrosis (SIS-tik fi-BRO-sis), or CF, is an inherited disease of the secretary (see-KREH- tor-ee)
(A disease that hurts) Regular Mucus Mucus with a person that has Cystic Fibrosis Normal mucus in the lungs is wet and slippery. But when a person has.
Respiratory Problems. HICCUPS Diaphragm, the muscle below your chest cavity, sudden jerks and you find yourself sucking in air quickly. The air flow causes.
A GENETIC, CHRONIC, AND LIFE-THREATENING DISEASE THAT CAUSES THICK, STICKY MUCUS TO BUILD UP IN THE LUNGS, DIGESTIVE TRACT, AND OTHER AREAS OF THE BODY.
Cellular Biochemistry and metabolism 1 CLS 331
Cystic Fibrosis.
Cystic Fibrosis A defect in a gene called the cystic fibrosis trans-membrane conductance regulator gene.
Chapter 4: Respiration and Excretion
Cystic Fibrosis BD 2011.
Cystic Fibrosis.
CCystic Fibrosis is an inherited chronic disease IIt affects the lungs and digestive system SSymptoms IIt clogs the lungs with phlegm and causes.
How cystic fibrosis affects the lungs Symptoms: Severe coughing - to remove excess mucus. Breathlessness - shortage of oxygen increases tiredness and.
Other names for cystic fibrosis are CF, Pancreas fibrocystic disease, and Pancreatic cystic fibrosis. The name was chosen because cystic means biliary.
BY: TERESA KRASZEWSKI CYSTIC FIBROSIS. BACKGROUND AND HISTORY Late 16th century babies who had “salty skin” when kissed were likely to die 1938 Dr. Dorothy.
What we know Halogen (Grp 7) Yellow-green gas Elec. Config: [Ne] 3s 2 3p 5 3 rd most Electronegative Strong Oxidizer Commonly: NaCl salt.
Cystic Fibrosis By:YaYPhineas(Edward). What is Cystic Fibrosis? A genetic disorder that affects your digestive and respiratory system You inherit a defective.
Fluid and Electrolyte Balance
Cystic fibrosis.
Conditions of the Respiratory System
By: Tilda, Dina and Jenny
Objectives Compare mechanical digestion with chemical digestion.
Cystic fibrosis BY: NATALIE ALZAGA STEPHANY GODINEZ STEPHANY TORO
Cystic Fibrosis Learning Objective
Sweat Test.
Lab 13 Sweat Test.
Dr. Pratima Ghimire June, 2009
Presentation transcript:

༜ A sweat test measures the amount of salt chemicals (sodium and chloride) in sweat. ༜ Sodium and chloride are part of your body’s electrolyte balance, and combine to form the salt found in sweat. ༜ They help regulate the fluid balance in your tissues. ༜ It is done to help diagnose cystic fibrosis. ༜ Normally, sweat on the skin surface contains very little sodium and chloride. People with cystic fibrosis (CF) have 2 to 5 times the normal amount of sodium and chloride in their sweat.

༜ Cystic fibrosis (CF), mucoviscoidosis, or mucoviscidosis, is a life-threatening hereditary disease inherited as autosomal recessive and is characterized by: 1.Increased viscosity of mucous secretions, including pancreas, intestinal glands, tracheal, peritracheal, bronchial. ༜ Thick mucus production, as well as a less competent immune system, cause mucus to build up and clog some of the organs in the body, particularly in the lungs and pancreas. ༜ When mucus clogs the lungs, it makes breathing very difficult.

༜ It also causes bacteria (or germs) to stuck in the airways causing inflammation (or swelling) and infections which ultimately leads to lung damage. ༜ Mucus also can block the digestive tract and pancreas causing stop of digestive enzymes from getting to the intestines. 2. Increased concentration of electrolytes especially Na and CL, in secretion of other gland notably (sweat glands, Parotid salivary glands, lachrymal glands).

1.Thick, viscous mucus secretions in the lungs 2.Repeated infections. 3.Pale or clay colored Stools, foul smelling, or stools that float meconium ileus is a typical finding in newborn babies with CF 4.Recurrent pneumonia 5.Chronic cough, possibly with blood streaking 6.Wheezing 7.Bronchitis

8.Chronic sinusitis 9.Asthma 10.Weight loss, failure to thrive in infants, abdominal swelling 11.Excessive salt in sweat, dehydration 12.Failure of newborn to pass stool 13.Abdominal pain, flatulence 14.Fatigue 15.Changes in color and amount of sputum (material coughed up from the lungs)

༜ Two methods of sweat analysis are most frequently used: 1. Chloride concentration The sweat chloride analysis is recommended as the diagnostic test for CF. 2. Conductivity measurement. Sweat conductivity may be used to screen for CF.

1. A tiny amount of a sweat-stimulating liquid is applied to a small patch of skin on the arm or leg. 2. An electrode is then placed over the site & a weak electrical current stimulates the area. This is a painless procedure that may create a tingling or warm sensation. 3. After several minutes, the area is cleaned and sweat is collected for about thirty minutes, either into a plastic coil of tubing or onto a piece of gauze or filter paper. 4. The sweat obtained is then analyzed.

 Done on a baby's right arm or thigh.  With older child or adult, the test is usually done on the inside of the right forearm.  Sweat may be collected and analyzed from two different sites.

1. Skin is washed and dried & then, 2 small gauze pads are placed the skin. - One pad is soaked with a medicine (called pilocarpine) makes skin sweat. - The other pad is soaked with salt water such as NaNO3. 2. The other pads called electrodes are placed over the gauze pads.

The sweat test usually takes 45 minutes to 1 hour.

3. After 5 to 10 minutes, the gauze pads and electrodes are removed, then the skin is cleaned with water and then dried. The skin will look red in the area under the medicine- containing pad 4. A dry gauze pad, paper collection pad, or special tubing is taped to the red patch of skin. This pad is covered with plastic or wax to prevent fluid loss (evaporation).

5. The new pad will soak up the sweat for up to 30 minutes, then it is removed and placed in a sealed bottle. It is then weighed to measure how much sweat the skin produced, and it is checked to find out how much salt chemical (sodium and/or chloride) the sweat contains. 6. After the collection pad is removed, the skin is washed and dried again. 7. Then we measure CL by automated or manual titration method and Na by flame photometry or ion exchange electrode.

༜ A sweat test measures the amount of salt chemicals (sodium and chloride) in sweat. Generally, chloride (sweat chloride) is measured. ༜ Sweat chloride –Normal Less than 40 mill moles per liter (mmol/L) –Borderline 40–60 mmol/L. –Abnormal More than 60 mmol/L. –Abnormal (high) values: Usually mean a person has cystic fibrosis. Some people with cystic fibrosis have borderline or even normal sweat chloride levels