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Understanding Your Lipid Panel (Cholesterol Test) – What You Need to Know

Published: July 31, 2026Updated: August 16, 2026

The sweat chloride test measures the amount of chloride in sweat to help diagnose cystic fibrosis.

Quick summary

{"A sweat chloride test checks for cystic fibrosis by measuring chloride levels in sweat","The test is painless and involves collecting a small sample of sweat from the skin","Higher than normal chloride levels (above 60 mmol/L) may indicate cystic fibrosis","Results are typically available within a few days","This test is safe for patients of all ages, including newborns"}

Medically reviewed by WellAlly Editorial TeamLast reviewed August 16, 2026Editorial policy

Key facts at a glance

LOINC
2077-6
Short code
Sweat Cl
Synonyms
Chloride Sweat-sCnc
Category
electrolyte
Sample
serum
Container
Schalbe or Macroduct sweat collection system with coiled capillary tubing
Units
not specified
Ref low
0
Ref high
29
Critical range
— – 60 not specified
Fasting
false
Population
adult
Sex
all
Age range
≥ 0 years
Method
Pilocarpine iontophoresis with quantitative ion-selective electrode or coulometric titration
CPT
89230
SNOMED
313295005
Specimen volume
Minimum 75 mg sweat weight (ideally >100 mg)
Stability
Analyze within 4 hours of collection; if delay up to 24 hours, store at 2-8°C
Hemolysis max
500
Lipemia max
1000
Icterus max
500
TAT
24–72 hours
Order
routine

This test measures the levels of different types of cholesterol and fats in your blood. It helps assess your risk for heart disease and stroke by checking your total cholesterol, LDL (bad) cholesterol, HDL (good) cholesterol, and triglycerides. Your doctor may order this test as part of a routine checkup or if you have risk factors like obesity, diabetes, or family history of heart disease. Knowing these numbers can guide lifestyle changes or medications to keep your heart healthy.

The sweat chloride test is a diagnostic test that measures the concentration of chloride in your sweat. Chloride is a component of salt (sodium chloride) that is normally found in sweat. This test is primarily used to diagnose cystic fibrosis (CF), a genetic condition that affects the lungs and digestive system.

The test is a simple blood draw. A healthcare professional will clean a small area on your arm, usually the inside of the elbow, and tie an elastic band around your upper arm to make the vein more visible. They will insert a thin needle into the vein and collect a small amount of blood into a vial or tube. After removing the needle, they will apply pressure and a bandage. The procedure takes only a few minutes and is generally well tolerated. Some people may feel a quick sting or minor discomfort.

During the test, a small area of skin (usually on the forearm or thigh) is stimulated to produce sweat using a mild electrical current or a special sweat-inducing medication. The sweat is collected on a filter paper or in a coil and sent to a laboratory for analysis. The procedure is painless and typically takes 30 to 60 minutes. Two samples are usually collected to ensure accurate results.

For accurate results, you usually need to fast for 9 to 12 hours before the blood draw. This means no eating or drinking anything except water during that time. It is best to schedule the test in the morning before breakfast. Avoid alcohol for 24 hours prior, and tell your doctor about any medications or supplements you take, as some can affect cholesterol levels. If you are unsure, follow your doctor's specific instructions. Fasting helps ensure your triglyceride levels are measured correctly.

No special preparation is needed for this test. You should keep your skin clean and avoid applying creams, lotions, or oils on the day of the test. Inform your healthcare provider about any medications you are taking, as some medications may affect sweat composition. The test can be performed on patients of all ages, including newborns.

Your results will show your cholesterol and triglyceride numbers, measured in milligrams per deciliter (mg/dL). The target ranges depend on your overall risk profile, but generally, a total cholesterol below 200 is desirable, LDL below 100 is optimal, HDL above 60 is protective, and triglycerides below 150 are normal. Your doctor will interpret these values along with your age, blood pressure, and other risk factors. If your levels are off, you may need to adopt a heart-healthy diet or take medications like statins. Always discuss your results with your doctor to understand what they mean for you.

Normal sweat chloride levels are typically below 30 mmol/L. Levels between 30 and 60 mmol/L are considered borderline and may require additional testing. Results above 60 mmol/L on two separate occasions strongly suggest cystic fibrosis. Your healthcare provider will interpret your results in the context of your symptoms and other test findings.

Reference range

≤29 mmol/Lnot specified

Specimen: serum

No fasting required. Ensure patient is well hydrated; avoid applying creams, lotions, or ointments to the collection site prior to testing.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

The sweat chloride test is the gold standard for diagnosing cystic fibrosis. In people with CF, the defective gene causes sweat glands to produce sweat with abnormally high levels of chloride. Elevated chloride levels can lead to excessive salt loss through sweat, which may cause dehydration, especially in hot weather. Early diagnosis through newborn screening or this test allows for timely treatment and better long-term outcomes.

This test may also be used to monitor treatment effectiveness in patients already diagnosed with cystic fibrosis. Additionally, it can help distinguish between cystic fibrosis and other lung or digestive conditions that may have similar symptoms.

Frequently asked questions

Is the sweat chloride test painful?
The test is generally not painful. You may feel a mild tingling or warming sensation during the sweat collection process due to the stimulation method used. The procedure is well-tolerated by most patients, including children and infants.
How long does it take to get results?
Results are typically available within 2 to 3 days after sample collection. Your healthcare provider will discuss the results with you during a follow-up appointment.
Can this test be done on newborns?
Yes, the sweat chloride test can be performed on newborns. In fact, it is part of newborn screening programs in many countries. The test is safe and can be done within the first few days of life if needed.
What happens if my results are borderline?
Borderline results (30-60 mmol/L) do not provide a clear diagnosis. Your healthcare provider may recommend repeating the test, conducting genetic testing, or performing additional clinical assessments to determine if cystic fibrosis is present.
Are there any risks or side effects?
The sweat chloride test is very safe. Possible minor side effects include skin irritation, redness, or slight discomfort at the collection site. These effects are usually temporary and resolve quickly.
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy