Coding of an antibiogram.Coding of an antibiogram. This organizer MUST be placed as a component within a Pathogen Detection Laboratory Isolate Organizer.An ID for this item MAY be filled for traceability.MUST contain the OID of the system that issued the ID. OIDs of code systems, which are published in the public OID registry for the Swiss health care system (oid.refdata.ch) are REQUIRED. Others are NOT ALLOWED.Contains the ID itself. The ID MUST be unique within the system that issued the ID.The antibiogram MUST be declared using the LOINC code 29576-6 "Bacterial susceptibility panel".
The status 'completed' means that all expected results for this results group are present and in a final state.
The status 'aborted' means that the examinations had to be aborted. Some results MAY be available.
Timestamp or period of findings (physiologically relevant period) for all results in this result group.Timestamp. Accuracy of the value: Date and time with hour and minute. If it is not known, nullFavor='UNK' must be used.Start of the period. Accuracy of the value: Date and time with hour and minute. If it is not known, nullFavor='UNK' must be used.A precision of date and time of day with at least hour and minute is required.End of the period. Accuracy of the value: Date and time with hour and minute. If it is not known, nullFavor='UNK' must be used.A precision of date and time of day with at least hour and minute is required.Either the imestamp or the period of the findings MUST be declared. If it is not known, nullFavor='UNK' must be used.IF this result group is based on a specimen of a non-human material, the subject element MUST be declared.This CAN be used to indicate who has performed the test. This information supersedes any information recorded at higher level.This CAN be used to indicate who has documented the result. This information supersedes any information recorded at higher level. This CAN be used to identify other parties:
Who has verified the result (AUTHEN).
Which external laboratory has delivered the result (RESP).
Which device (analyzer) was used to determine the result (DEV).
Who has verified the result (AUTHEN). This information supersedes any information recorded at higher level.Which external laboratory has delivered the result (RESP). This information supersedes any information recorded at higher level.Which device (analyzer) was used to determine the result (DEV). This information supersedes any information recorded at higher level.For "Laboratory Observation" coding, use the filter 'property:susc class:abxbact' on search.loinc.org (see https://search.loinc.org/searchLOINC/search.zul?query=property%3Asusc+class%3Aabxbact).For observation coding, use the filter 'property:susc class:abxbact' on search.loinc.org (see https://search.loinc.org/searchLOINC/search.zul?query=property%3Asusc+class%3Aabxbact).This CAN be used to make reference to an external document.The antibiogram must be placed in a Pathogen Detection Laboratory Isolate Organizer.