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Get the free Request for Cord/neonate Blood Testing

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This document is a requisition form used by the Perinatal Laboratory at Canadian Blood Services, Winnipeg Centre for requesting cord and neonate blood testing. It includes sections for patient details, mother\'s information, and sample collection requirements, ensuring accurate labeling and documentation.
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How to fill out request for cordneonate blood

01
Obtain the request form for cordneonate blood from the healthcare provider or hospital.
02
Fill in the patient's details, including their name, date of birth, and medical record number.
03
Provide the mother's information, including her name and contact details.
04
Specify the reason for the request, such as testing for specific conditions or compatibility.
05
Include any necessary clinical information that may support the request.
06
Sign and date the request form to validate it.
07
Submit the completed form to the appropriate department or lab as instructed.

Who needs request for cordneonate blood?

01
Parents expecting a newborn who may require cordneonate blood for medical purposes.
02
Healthcare providers and specialists involved in the care of infants needing blood tests or transfusions.
03
Patients with specific medical conditions that may benefit from the use of cordneonate blood.
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A request for cordneonate blood refers to the process of acquiring blood from the umbilical cord and placenta immediately after childbirth, which is collected for potential medical use, particularly for stem cell therapies.
Typically, the parents or guardians of the newborn are required to file the request for cordneonate blood, often facilitated by healthcare providers.
To fill out the request for cordneonate blood, the parents need to provide necessary details such as the mother’s and baby’s medical history, consent forms, and specific collection instructions as required by the facility.
The purpose of the request for cordneonate blood is to ensure the collection and preservation of potentially lifesaving stem cells which can be used for treating various diseases and medical conditions.
Information that must be reported includes the identities of the mother and newborn, the date and time of birth, any medical conditions, consent signatures, and details relevant to the collection process.
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