HL7 OMB_O27 Blood Product Order
OMB_O27 is the blood product order message. It exists because blood product orders need detail that ordinary order messages do not capture well: component type, processing requirements, amount, intended use, dispense timing, destination, indication, and consent.
This is a high-consequence workflow. A blood product order is not just another supply request. The receiving blood bank or transfusion service needs enough structured detail to assess appropriateness, prepare the right component, and route it safely.
A small OMB O27 example
What workflow it represents
The sender is usually an EHR, order entry system, transfusion module, or integration engine. The receiver is usually the blood bank, transfusion service, or lab system responsible for reviewing and fulfilling the product order. The response is commonly ORB_O28.
The receiver uses BPO to understand the product and requirements, DG1 and OBX for clinical context, and SPM when specimen context is relevant.
How to read the structure
The optional patient group is the usual PID/PV1/insurance/allergy context. The required ORDER group starts with ORC, can include timing, and then requires BPO. It can also include specimen, notes, diagnoses, observations, financial transactions, and billing.
BPO is the center of the message. Use it for blood product component, processing requirements, quantity, requested dispense time and destination, indication for use, and consent indicator. Keep that data structured; free text should support the order, not replace it.
Implementation traps
Do not map processing requirements as casual notes. Irradiated, leukoreduced, CMV-negative, washed, and similar requirements change what is prepared and issued. They need explicit codes both systems understand.
Also separate clinical indication from delivery logistics. The reason for transfusion and the location where the product should be dispensed are different decisions and belong in different fields.
Reference notes
The HL7 v2+ OMB_O27 page says blood product orders need additional detail beyond standard order messages, including component, special processing, amount, and relevant clinical information for prospective review.