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THISISNOTATESTREQUESTFORM. Pleasefilloutthisformandsubmititwiththetestrequestformorelectronicpackinglist.PATIENTHISTORYFORFETALFIBRONECTINTESTING PatientName PhysicianDateofBirthPracticeSpecialtyPhysicianPhone
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Start by entering the patient's demographic information, including name, date of birth, and contact details.
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Provide detailed information about the current pregnancy, including gestational age, symptoms, and any relevant test results.
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arup-form-1043 fetal fibronectin is typically needed by healthcare providers and obstetricians who suspect premature labor or want to assess the risk of preterm delivery. It is often used in pregnant women who exhibit signs and symptoms of preterm labor, such as regular contractions, cervical changes, or a history of preterm birth. The test helps determine the likelihood of spontaneous preterm birth within the next two weeks, allowing healthcare professionals to make informed decisions regarding management and intervention for the patient.
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ARUP Form 1043 fetal fibronectin is a laboratory test that measures the presence of fetal fibronectin in the cervico-vaginal fluid, which can help assess the risk of preterm labor.
Healthcare providers who suspect a patient may be at risk for preterm labor are typically required to file ARUP Form 1043 for fetal fibronectin testing.
To fill out ARUP Form 1043, the healthcare provider must provide patient demographic information, clinical history, and any relevant laboratory and imaging results before submitting the sample for testing.
The purpose of ARUP Form 1043 fetal fibronectin is to evaluate the risk of preterm birth by detecting the presence of fetal fibronectin in a pregnant patient's cervico-vaginal fluid.
Information to be reported on ARUP Form 1043 includes the patient's name, date of birth, clinical indication for test, and relevant medical history.
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