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The purpose of testing may be to:

  • Screen those at risk for malabsorption because of an underlying condition such as cystic fibrosis
  • Detect malabsorption, identify its underlying cause(s), and evaluate the types and severity of nutrient deficiencies present
  • Detect complications such as anemia
  • Monitor the effectiveness of treatment in people with malabsorption

There is no single test that can identify malabsorption or the underlying cause. Typically, a healthcare practitioner will take into account many factors when ordering tests, including results from a physical examination, family history, medical history, and signs and symptoms. Testing will often be performed in steps with results leading toward a diagnosis while ruling out other possible causes. Testing typically involves ordering:

  • An initial set of general tests that evaluate body organs, cells, and digestion and that look for a cause for a person's persistent diarrhea, one of the most common symptoms of malabsorption
  • Specific follow-up tests that are used to detect or exclude diseases associated with malabsorption and to identify specific deficiencies and/or complications

Laboratory Tests

Initial testing may include:

Based upon initial testing results, the person's symptoms, and the healthcare practitioner's suspicions, follow-up testing may include one or more of the following:

Tests sometimes ordered include:

Non-Laboratory Tests

Testing to examine the digestive tract, liver, and/or pancreas is sometimes necessary and may include:

  • Abdominal ultrasound
  • CT scan
  • Endoscopy
  • Endoscopic retrograde pancreatography (ERCP)

Learn more about these imaging procedures at

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