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Volume 35Issue 4Article 35342023Urinebased detection of intestinal mucosal cell damage in neonates with suspected necrotizing enterocolitis Fady M. Elgendy Menoufia UniversityHanan M. ElSayed Menoufia
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01
Collect urine sample in a clean, dry container.
02
Ensure that the container is labeled with the patient's information.
03
If required, mix the urine sample gently to ensure homogeneity.
04
Using a pipette or dropper, place the recommended amount of urine on the test strip or in the detection reagent as per the manufacturer's instructions.
05
Wait for the specified amount of time for the results to develop, usually a few minutes.
06
Compare the results against the provided reference chart to interpret the findings.
07
Dispose of the urine sample and any used materials following appropriate safety guidelines.

Who needs urine-based detection of intestinal?

01
Individuals showing symptoms of gastrointestinal issues, such as unexplained abdominal pain, diarrhea, or changes in bowel habits.
02
Patients with a history of intestinal infections or diseases.
03
Individuals undergoing routine screenings for gastrointestinal health.
04
Those with risk factors for intestinal disorders, such as family history or chronic health conditions.
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Urine-based detection of intestinal refers to the use of urine samples to identify or diagnose intestinal conditions or infections, utilizing specific biomarkers present in the urine.
Typically, individuals who are undergoing medical evaluations for intestinal disorders, healthcare providers, or laboratories responsible for testing may be required to file urine-based detection forms.
To fill out urine-based detection forms, one should provide patient information, including demographics, medical history, and the reason for testing, along with a description of the sample collection process.
The purpose of urine-based detection of intestinal is to diagnose and monitor intestinal diseases, infections, or other gastrointestinal disorders through the analysis of urine samples.
Information that must be reported includes patient identification details, type of test conducted, date of sample collection, and results of the analysis along with any relevant clinical information.
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