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Understanding the Lipid Panel: A Complete Patient Guide to the Cholesterol Blood Test, Including What It Measures, How It Is Done, and How to Prepare for Accurate Results and Heart Health Assessment.

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

A diagnostic test that measures chloride levels in sweat to help diagnose cystic fibrosis.

Quick summary

{"Collects a small sweat sample, usually from the forearm","Elevated chloride levels may indicate cystic fibrosis","The test is painless and takes about 30-60 minutes","Results are typically available within a few days","Often repeated if initial results are abnormal"}

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

Key facts at a glance

LOINC
108639-6
Short code
CL-SWEAT
Synonyms
Chloride Msmt Sweat
Category
electrolyte
Sample
serum
Container
Specific sweat collection device (Macroduct or Wescor collection system) with polyethylene 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
89261
SNOMED
313295004
Specimen volume
Minimum 75 mg sweat weight (approximately 75-150 μL)
Stability
Analyze within 24 hours; if delay >24 hours, store at 2-8°C for up to 72 hours. Do not freeze.
Hemolysis max
500
Lipemia max
1000
Icterus max
500
TAT
24–72 hours
Order
routine

The lipid panel is a blood test that measures the levels of cholesterol and triglycerides in your bloodstream. It helps your doctor evaluate your risk for heart disease and stroke by checking your total cholesterol, LDL (the "bad" cholesterol), HDL (the "good" cholesterol), and triglycerides. This test is often used as a routine screening for adults, to monitor how well cholesterol-lowering treatments are working, or to assess cardiovascular risk in people with diabetes, high blood pressure, or a family history of heart problems. Understanding your results empowers you to make healthier lifestyle choices.

The sweat chloride test measures the amount of chloride (a component of salt) in your sweat. It is primarily used to diagnose cystic fibrosis (CF), a genetic condition that affects the lungs and digestive system. People with CF have higher levels of chloride in their sweat because their bodies do not properly regulate salt.

A healthcare professional will draw a small sample of blood from a vein in your arm. First, they clean the area with an antiseptic wipe to prevent infection. Then they place a tight band (tourniquet) around your upper arm to make the vein more visible and easier to access. After that, they insert a thin needle into the vein and collect blood into a small vial. You might feel a brief pinch or stinging sensation when the needle goes in, but most people find it tolerable. Once enough blood is collected, the needle is removed, pressure is applied to the site to stop any bleeding, and a bandage is placed. The entire process takes just a few minutes, and the sample is sent to a laboratory for analysis.

A small area of skin, usually on the forearm, is cleaned and stimulated to produce sweat using a mild electrical current or a special medication. Sweat is then collected on a filter paper or in a small coil for about 30-60 minutes. The sample is sent to a laboratory to measure its chloride concentration. The test is painless, though you may feel a slight tingling sensation during stimulation.

For accurate results, you need to fast—meaning no food or drinks except water—for 9 to 12 hours before the test. Schedule your appointment early in the morning so fasting is easier. You can usually take your regular medications with water, but inform your doctor about all prescriptions, over-the-counter drugs, and supplements you use, as some may affect results. Avoid alcohol for at least 24 hours before the test. Tell your healthcare provider if you have any bleeding disorders, are taking blood thinners, or have had recent illness or stress, as these can influence your numbers. Wear a short-sleeved or loose-fitting shirt to make the blood draw simple and comfortable.

No special preparation is needed. You should continue your normal activities and medications unless your doctor instructs otherwise. Avoid applying creams, lotions, or oils to the test area on the day of the test. Bring a list of your current medications to your appointment.

Reference range

0-29 mmol/Lnot specified

Specimen: serum

No fasting required. Avoid lotions, creams, oils or powders on skin for 24 hours prior. Ensure adequate hydration.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

Normal sweat chloride levels are less than 30 mmol/L. Levels between 30-59 mmol/L are considered borderline and may require repeat testing. Levels of 60 mmol/L or higher are strongly indicative of cystic fibrosis. This test is an important tool for diagnosing CF, especially in newborns and children with symptoms such as chronic cough, recurrent lung infections, poor growth, or salty-tasting skin.

Abnormal results may also be seen in other conditions, so your doctor may order additional tests to confirm a diagnosis. Early diagnosis of CF is important for starting treatment that can improve quality of life and long-term outcomes.

Frequently asked questions

Is the sweat chloride test painful?
The test is generally not painful. You may feel a mild tingling or warming sensation when the sweat is stimulated. The procedure is well-tolerated by most patients, including infants and young children.
How long does it take to get results?
Results are typically available within 1-3 days after the sample is collected. Your healthcare provider will contact you with the results and discuss what they mean.
Do I need to fast before the test?
No fasting is required for the sweat chloride test. You can eat and drink normally before the procedure.
What happens if my results are abnormal?
If your sweat chloride level is elevated, your doctor will likely recommend repeat testing to confirm the results. Additional genetic testing or clinical evaluations may also be needed to confirm a diagnosis of cystic fibrosis.
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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