ID

19581

Beschrijving

Sentinel: Overview and Description of the Common Data Model v6.0 "The primary goal of the Sentinel pilot is to build and operate a national public health surveillance system to monitor the safety of FDA-regulated medical products, including drugs, biologics, and devices. Sentinel is part of the Sentinel Initiative, the FDA’s response to a congressional mandate to create an active surveillance system using electronic health data. The Sentinel program will undertake three major types of activities: (1) prospective evaluation of accumulating experience about specific medical products and specific suspected safety problems; (2) evaluation of the impact of FDA actions (e.g., labeling changes) on medical practice and health outcomes; and (3) rapid assessment of past experience in response to FDA questions about specific exposures and outcomes." Sentinel Collaborating Institutions maintain data resources and provide technical, scientific, and methodological expertise as needed to meet the public health surveillance requirements of Sentinel. The Collaborating Institutions also participate as members of the Planning Board, the Safety Science Committee, the Sentinel Operations Center (SOC), and various Sentinel workgroups. Sentinel Common Data Model "The SOC Data Core coordinates the network of Sentinel Data Partners and leads development of the Sentinel Common Data Model (SCDM), a standard data structure that allows Data Partners to quickly execute distributed programs against local data. The SOC Scientific Systems Division manages creation of the Sentinel Distributed Database (SDD) using the SCDM, and maintains complete documentation of the implementation and characteristics of the SDD. The SDD refers to the data held and maintained by the Data Partners in the SCDM format. The SCDM was developed in accordance with the SCDM Guiding Principles and was modeled after the HMO Research Network Virtual Data Warehouse. The SCDM currently includes 13 tables that represent information for the data elements needed for Sentinel activities. Records are linked across tables by a unique person identifier, PatID. Details of the 13 tables are provided in this document. An additional 13 Summary Tables are created from the ""parent tables"" and are also described in this document. Revisions and enhancements to the SCDM are expected, including the addition of clinical information, incorporation of other data types and sources, and revisions based on lessons learned from use of the SDD. This may include adopting variables and formats developed by other programs." This data model is freely available to all. For more information about Sentinel visit the website at: www.sentinelsystem.org For comments and suggestions, please email: info@sentinelsystem.org

Link

www.sentinelsystem.org

Trefwoorden

Versies (4)
  1. 11-01-17 11-01-17 -
  2. 29-01-17 29-01-17 -
  3. 25-08-19 25-08-19 -
  4. 25-08-19 25-08-19 -
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11 januari 2017

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Sentinel Common Data Model Laboratory Results

Engels

Sentinel Common Data Model Laboratory Results

1 Formulieren  
Laboratory Results
Beschrijving

Laboratory Results

Alias
UMLS CUI-1
C1254595
Unique member identifier
Beschrijving

Arbitrary person-level identifier. Populated for all records. Used to link across tables. Note: PatID is a pseudoidentifier with a consistent crosswalk to the true identifier retained by the source Data Partner. For analytical data sets requiring patient-level data, only the pseudoidentifier is used to link across all information belonging to a patient.

Datatype

text

Alias
UMLS CUI [1]
C2348585
Test Name
Beschrijving

Abbreviated test name. Populated for all records. Several LOINC codes (LOINC) and/or local codes (LOCAL_CD) can point to one MS_Test_Name.

Datatype

text

Alias
UMLS CUI [1]
C0022885
Laboratory Result Type
Beschrijving

Indicates whether the laboratory test result is numeric (e.g., 100 ug/mL, <100 ug/mL, >100 ug/mL) and MS_Result_N will be populated, or character (e.g., for character results such as: +, POS, POSITIVE, and ranges, such as 50-100 mg/mL) and MS_Result_C will be populated, based on Data Partner’s source data.

Datatype

integer

Alias
UMLS CUI [1,1]
C2826772
UMLS CUI [1,2]
C0332307
Test Name Subcategory
Beschrijving

"Sub-category for MS_Test_Name. Sub-categories apply to only select laboratory tests. ‘DIRECT’ and ‘CALCULATED’ is only populated for MS_Test_Name = CHOL_LDL. ‘DDU’ and ‘FEU’ is only populated for MS_Test_Name = D_DIMER, Result_Type = N. ‘BHCG’ AND ‘HCG’ is only populated for MS_Test_Name = PG. "

Datatype

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C1515010
Fasting Indicator
Beschrijving

Fasting Indicator. Not all laboratory tests are differentiated by fasting status. For laboratory tests where fasting status is not considered to interpret results, Fast_Ind is marked “X” (not applicable). For laboratory test results where fasting status may be considered to interpreting results (e.g., glucose), Fast_Ind is marked “F” (fasting) only if the source data included with the laboratory test result indicates fasting test. All other laboratory test results where fasting status may be considered that is not explicitly marked as fasting, Fast_Ind is marked “R” (random).

Datatype

integer

Alias
UMLS CUI [1]
C2985769
Specimen source
Beschrijving

Specimen source. Populated for all records. Some laboratory tests have several possible valid values for Specimen_Source.

Datatype

text

Alias
UMLS CUI [1,1]
C0449416
UMLS CUI [1,2]
C0370003
LOINC code
Beschrijving

"Logical Observation Identifiers, Names, and Codes (LOINC) is a universal coding system for tests, measurements, and observations developed by the Regenstrief Institute. LOINC provides very granular information about the tests such as the long name of the test, test definition/description, component, system, property, timing, scale, method, and examples of units. All parts of the LOINC code, including the hyphen, are included. The last digit of the LOINC code is a check digit and is always preceded by a hyphen. If a record utilizes a local LOINC (e.g., LOINC candidate codes), the result of that record is included, however, the LOINC variable is set to null. Values in the LOINC variable do not contain leading zeros. LOINC is populated when available, thus not all records have LOINC. "

Datatype

text

Alias
UMLS CUI [1]
C1136323
Immediacy of test
Beschrijving

Immediacy of test. The intent of this variable is to determine whether the test was obtained as part of routine care or as an emergent/urgent diagnostic test (designated as Stat or Expedite).

Datatype

integer

Alias
UMLS CUI [1]
C2188402
Patient location
Beschrijving

Patient location where the lab specimen was obtained.

Datatype

text

Alias
UMLS CUI [1]
C0450429
Location of the test result
Beschrijving

Location of the test result. Point of Care locations may include anticoagulation clinic, newborn nursery, finger stick in provider office, or home. The default value is ‘L’ unless the result is Point of Care. There are not any null values.

Datatype

text

Alias
UMLS CUI [1]
C3898629
Unique to each Data Partner
Beschrijving

Local code (non-LOINC) related to an individual lab test. Values for LOCAL_CD are not required. LOCAL_CD is only populated if available in source data. This variable will not be used in queries, but may be used by local programmers to identify and extract the required CDM tests.

Datatype

text

Alias
UMLS CUI [1,1]
C2826912
UMLS CUI [1,2]
C0205276
Unique to each Data Partner
Beschrijving

Local code (non-LOINC) related to a battery or panel of lab tests. Values for BATTERY_CD are not required. BATTERY_CD is only populated if available in source data. This variable will not be used in queries, but may be used by local programmers to identify and extract the required CDM tests.

Datatype

text

Alias
UMLS CUI [1]
C0200378
Procedure code
Beschrijving

Procedure Code associated with the laboratory result record. Values for PX are not required. PX is only populated if available in source data. PX is populated if PX_CODETYPE is populated.

Datatype

text

Alias
UMLS CUI [1]
C1550373
Procedure code type.
Beschrijving

Procedure code type associated with the laboratory result record. Values for PX_CODETYPE are not required. PX_CODETYPE is only populated if available in source data. PX_CODETYPE is populated if PX is populated.

Datatype

integer

Alias
UMLS CUI [1,1]
C1550373
UMLS CUI [1,2]
C0332307
Date of Laboratory Order
Beschrijving

Date that the test was ordered, represented as a SAS date value. SAS format is MMDDYY10. This date could fall anywhere from the same day the specimen was collected to months before the specimen was collected. Please see footnote 3.

Datatype

date

Alias
UMLS CUI [1,1]
C0677076
UMLS CUI [1,2]
C0011008
Date of specimen collection
Beschrijving

Date that the specimen was collected, represented as a SAS date value. SAS format is MMDDYY10. For most Sentinel activities, this is the most relevant date. Please see footnote 3.

Datatype

date

Alias
UMLS CUI [1,1]
C0200345
UMLS CUI [1,2]
C0011008
Time of specimen collection
Beschrijving

Time of day that the specimen was collected, represented as a SAS time value. SAS format is HHMM. Valid values are between 00:00 to 23:59. Please note that LAB_TM is associated with LAB_DT.

Datatype

time

Alias
UMLS CUI [1,1]
C0200345
UMLS CUI [1,2]
C0040223
Date of Laboratory Result
Beschrijving

Date that the laboratory test was resulted, represented as a SAS date value. SAS format is MMDDYY10. Dependent on the time of the test, this date could be the same day the specimen was collected or any date up to weeks later. Please see footnote 3.

Datatype

date

Alias
UMLS CUI [1,1]
C1254595
UMLS CUI [1,2]
C0011008
Time of Laboratory Result
Beschrijving

Time that the laboratory test was resulted, represented as a SAS time value. SAS format is HHMM. Valid values are between 00:00 to 23:59.

Datatype

time

Alias
UMLS CUI [1,1]
C1254595
UMLS CUI [1,2]
C0040223
Original Result
Beschrijving

Orig_Result is populated for all records. If Result_Type equals “N”, then the Orig_Result value represents the numeric portion of the test result, stripped of any modifiers (e.g., >, LE, GT) and/or result units (e.g., ng/ml, cells/mm3, %). If Result_Type equals “C”, Orig_Result value reflects the test string based on source data. Additionally, for records where Result_Type = C, values may include a decimal point (‘.’), a sign (‘-‘, ‘+’) or text (e.g., ‘POSITIVE’, ‘NEGATIVE’, ‘DETECTED’). For records where Result_Type = N, the symbols >, <, >=, <= are removed from the value and stored in the Modifier variable and result units are removed and stored as Orig_Result_Unit variable.

Datatype

text

Alias
UMLS CUI [1]
C2826772
Result value
Beschrijving

This standardized result value is only populated for text or character results (Result_Type = C) and is null for numeric results (Result_Type = N). If Result_Type = “C” and the source result is a range (e.g., 50-100 mg/mL), then populate MS_Result_C using Orig_Result with the start and end values of the range delimited by a vertical bar (e.g., "50-100 mg/mL" becomes "50|100 mg/mL").

Datatype

text

Alias
UMLS CUI [1]
C2348527
Numeric digits with or without a decimal
Beschrijving

Standardized/converted numeric result for records where Result_Type=N. Acceptable values are numeric digits with or without a decimal (“.”). If the standardized result unit (STD_RESULT_UNIT) differs from an acceptable MS_RESULT_UNIT for a numeric test (RESULT_TYPE=N), then ORIG_RESULT is converted prior to populating the MS_RESULT_N value. Additionally, MS_RESULT_UNIT reflects this conversion. This variable is only populated for numeric results (RESULT_TYPE = N) and does not contain negative values. This variable is null for text/character results (RESULT_TYPE = C).

Datatype

float

Alias
UMLS CUI [1]
C2347373
Modifier
Beschrijving

Modifier for result values. Any relational operators in the original source data value (e.g., <, >, or =) are reflected in the Modifier variable. For example, if the original source data value is "<=200", then Orig_Result = 200 and Modifier = ‘LE’. If the original source data result value is text, then Modifier = TX. If the original source data result value is numeric (digits with or without decimal) and does not contain an operator, then Modifier = EQ.

Datatype

text

Alias
UMLS CUI [1]
C3542952
Original Result Unit
Beschrijving

Original units for the test result, as reported in source data. This variable is directly related to ORIG_RESULT and MODIFIER. This variable does not include the test name, or any special characters, unless that character is part of the unit value. For example, special characters are included in “10^9/L”. However, special characters are not included in “^U/L^”, as these carats are not part of the unit value. Some laboratory tests may not have a result unit.

Datatype

text

Alias
UMLS CUI [1]
C2826314
Standardized units
Beschrijving

Standardized units for the result. The purpose of STD_RESULT_UNIT is to modify ORIG_RESULT_UNIT from free text to a standardized unit, as an intermediary step in converting from ORIG_RESULT_UNIT to MS_RESULT_UNIT. This variable is only populated for records where Result_type = N. Common rules and guidelines for populating STD_RESULT_UNIT, include: converting all text values for ORIG_RESULT_UNIT to uppercase, and using standard abbreviations as provided by SOC. This variable does not include special characters, unless that character is part of the unit. For example, special characters are included in “10^9/L”. However, special characters are not included in “^U/L^”, as these carats are not part of the unit value. This value is not usually null, though there are exceptions, such as when the test result is a ratio (e.g., International Normalized Ratio [INR]). This value is null for character tests (Result_Type=C) until that test has been reviewed and characterized by the Clinical Data Elements Workgroup.

Datatype

text

Alias
UMLS CUI [1,1]
C1255664
UMLS CUI [1,2]
C1519795
Converted/standardized result units
Beschrijving

Converted/standardized result units for the value populated in MS_RESULT_N. This value is null for records where Result_Type = C, and null for Laboratory Tests that have not been characterized and reviewed by the Clinical Data Elements Workgroup. This value may be null for some numeric tests (e.g., as International Normalized Ratio [INR] is a ratio, it does not have a result unit). For tests that require a result unit, MS_RESULT_UNIT is set to “UNKNOWN” for all records where the original result unit is missing or blank, “NULL”, “N/A”, “NA”, or “UNK."" Guidance is provided for only Laboratory Tests that have been reviewed by the Clinical Data Elements Workgroup.

Datatype

text

Alias
UMLS CUI [1]
C1519795
Normal Range: Low
Beschrijving

Lower bound of the normal reference range, as assigned by the laboratory. The normal range associated with a test, as assigned by the laboratory is parsed out into the following variables: NORM_RANGE_LOW, MODIFIER_LOW, NORM_RANGE_HIGH, MODIFIER_HIGH, and reflects what is seen in source data. Value only contains the value of the lower bound of the normal reference range. This value is not converted and unit of measure is not included. It is assumed that the associated unit is the same as the original result unit from the source data. The symbols >, <, >=, <= are removed. For example, if the normal range for a test is >100 and <300, then ""100"" is entered. Additionally, this value is null for records where Result_Type = C.

Datatype

text

Alias
UMLS CUI [1]
C2700150
Modifier for Normal Range: Low
Beschrijving

Modifier for Norm_Range_low values. The normal range associated with a test, as assigned by the laboratory is parsed out into the following variables: NORM_RANGE_LOW, MODIFIER_LOW, NORM_RANGE_HIGH, MODIFIER_HIGH and reflects what is seen in source data. This value is null for records where Result_Type=C. For numeric results one of the following needs to be true: 1) Both Modifier_low and Modifier_high contain EQ (e.g., normal values fall in the range 3-10). 2) Modifier_low contains GT or GE and Modifier_high is null (e.g., normal values are >3 with no upper boundary). 3) Modifier_high contains LT or LE and Modifier_low is null (e.g., normal values are <=10 with no lower boundary).

Datatype

text

Alias
UMLS CUI [1,1]
C2700150
UMLS CUI [1,2]
C1514623
Normal Range: high
Beschrijving

Upper bound of the normal reference range, as assigned by the laboratory. The normal range associated with a test, as assigned by the laboratory is parsed out into the following variables: NORM_RANGE_LOW, MODIFIER_LOW, NORM_RANGE_HIGH, MODIFIER_HIGH and reflects what is seen in source data. Value only contains the value of the upper bound of the normal reference range. This value is not converted and unit of measure is not included. It is assumed that the associated unit is the same as the original result unit from source data. The symbols >, <, >=, <= are removed. For example, if the normal range for a test is >100 and <300, then ""100"" is entered. Additionally, this value is null for records where Result_Type = C.

Datatype

text

Alias
UMLS CUI [1]
C2700149
Modifier for Normal Range: High
Beschrijving

Modifier for Norm_Range_high values. The normal range associated with a test, as assigned by the laboratory is parsed out into the following variables: NORM_RANGE_LOW, MODIFIER_LOW, NORM_RANGE_HIGH, MODIFIER_HIGH and reflects what is seen in source data. The value is null for records where Result_Type=C. For numeric results one of the following needs to be true: 1) Both Modifier_low and Modifier_high contain EQ (e.g., normal values fall in the range 3-10). 2) Modifier_low contains GT or GE and Modifier_high is null (e.g., normal values are >3 with no upper boundary). 3) Modifier_high contains LT or LE and Modifier_low is null (e.g., normal values are <=10 with no lower boundary).

Datatype

text

Alias
UMLS CUI [1,1]
C2700149
UMLS CUI [1,2]
C1514623
Abnormal Result Indicator
Beschrijving

Abnormal result indicator. This value comes directly from the source data; this value is not created programmatically based on variables such as MS_Result_N, Norm_Range_high, or Norm_Range_low.

Datatype

text

Alias
UMLS CUI [1]
C0459424
Unique to each Data Partner
Beschrijving

Local code for ordering provider department. Values for ORDER_DEPT are not required. Populate only if ordering provider department is available in source data.

Datatype

text

Alias
UMLS CUI [1,1]
C0677076
UMLS CUI [1,2]
C0805701
Servicing provider identifier
Beschrijving

Local facility code that identifies the hospital or clinic. Taken from facility claims. Values for FACILITY_CODE are not required. Populate only if facility code is available in source data. This information is useful when locating medical charts for review.

Datatype

text

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0019994
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Similar models

Sentinel Common Data Model Laboratory Results

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Laboratory Results
C1254595 (UMLS CUI-1)
Patient ID
Item
Unique member identifier
text
C2348585 (UMLS CUI [1])
Item
Test Name
text
C0022885 (UMLS CUI [1])
Test Name
Code List
Test Name
CL Item
alkaline phosphatase  (ALP )
CL Item
alanine aminotransferase  (ALT )
CL Item
absolute neutrophil count (ANC )
CL Item
total bilirubin  (BILI_TOT )
CL Item
cholesterol high density lipoprotein (CHOL_HDL )
CL Item
cholesterol low density  ("CHOL_LDL )
CL Item
lipoprotein" (lipoprotein")
CL Item
cholesterol total (CHOL_TOT )
CL Item
creatine kinase total (CK )
CL Item
creatine kinase MB (CK_MB )
CL Item
creatine kinase MB/creatine kinase total  (CK_MBI )
CL Item
creatinine (CREATININE )
CL Item
d-dimer (D_DIMER )
CL Item
glucose (GLUCOSE )
CL Item
hemoglobin (HGB )
CL Item
glycosylated hemoglobin (HGBA1C )
CL Item
influenza virus A (INF_A )
CL Item
influenza virus A + B (INF_AB )
CL Item
influenza virus B (INF_B )
CL Item
influenza virus not specified (INF_NS )
CL Item
international normalized ratio (INR )
CL Item
lipase (LIPASE )
CL Item
pregnancy test (PG )
CL Item
platelet count (PLATELETS )
CL Item
sodium (SODIUM )
CL Item
triglycerides (TRIG )
CL Item
troponin I cardiac (TROP_I )
CL Item
troponin T cardiac (TROP_T )
CL Item
thyroid stimulating hormone (TSH )
Item
Laboratory Result Type
integer
C2826772 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Laboratory Result Type
Code List
Laboratory Result Type
CL Item
numeric (1 )
CL Item
character (2 )
Item
Test Name Subcategory
text
C0022885 (UMLS CUI [1,1])
C1515010 (UMLS CUI [1,2])
Test Name Subcategory
Code List
Test Name Subcategory
CL Item
beta human choriogonadotropin (BHCG )
CL Item
calculated (CLC )
CL Item
d-dimer units (DDU )
CL Item
direct (DIRECT)
CL Item
enzyme immunoassay (EIA )
CL Item
fibrinogen equivalent units (FEU )
CL Item
human choriogonadotropin (HCG )
CL Item
immunofluorescence (IF )
CL Item
not specified (NS )
CL Item
probe and target amplification (PCR )
CL Item
organism-specific culture (VTC )
Item
integer
C2985769 (UMLS CUI [1])
Fasting Indicator
Code List
Fasting Indicator
CL Item
fasting (1 )
CL Item
random (2 )
CL Item
not applicable (3 )
Item
Specimen source
text
C0449416 (UMLS CUI [1,1])
C0370003 (UMLS CUI [1,2])
Specimen source
Code List
Specimen source
CL Item
bronchoalveolar lavage ("BAL )
CL Item
" (")
CL Item
bronchoalveolar biopsy  (BALBX )
CL Item
blood (BLOOD )
CL Item
cerebrospinal fluid (CSF )
CL Item
nasopharyngeal swab (NPH )
CL Item
nasopharyngeal wash  (NPWASH )
CL Item
nasal swab or nose specimen (NSWAB )
CL Item
nasal wash  (NWASH )
CL Item
other (OTHER )
CL Item
plasma (PLASMA )
CL Item
platelet poor plasma (PPP )
CL Item
serum (SERUM )
CL Item
sputum  (SPUTUM )
CL Item
serum/plasma (SR_PLS )
CL Item
throat swab, oropharyngeal swab (THRT )
CL Item
unknown or null (UNK )
CL Item
urine (URINE )
LOINC
Item
LOINC code
text
C1136323 (UMLS CUI [1])
Item
Immediacy of test
integer
C2188402 (UMLS CUI [1])
Urgency of Test
Code List
Immediacy of test
CL Item
Expedite  (1 )
CL Item
Routine (2 )
CL Item
Stat (3 )
CL Item
Unknown or null (4 )
Item
Patient location
text
C0450429 (UMLS CUI [1])
Location
Code List
Patient location
CL Item
Emergency department (1 )
CL Item
Home (2 )
CL Item
Inpatient (3)
CL Item
Outpatient (4 )
CL Item
Unknown or null (5 )
Item
Location of the test result
text
C3898629 (UMLS CUI [1])
Laboratory Location
Code List
Location of the test result
CL Item
Lab (1 )
CL Item
Point of Care (2 )
Local Laboratory Code
Item
Unique to each Data Partner
text
C2826912 (UMLS CUI [1,1])
C0205276 (UMLS CUI [1,2])
Laboratory Test Panel
Item
Unique to each Data Partner
text
C0200378 (UMLS CUI [1])
Procedure Code
Item
Procedure code
text
C1550373 (UMLS CUI [1])
Item
Procedure code type.
integer
C1550373 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Procedure code type
Code List
Procedure code type.
CL Item
ICD-9-CM (09 )
CL Item
ICD-10-CM (10 )
CL Item
ICD-11-CM (11 )
CL Item
CPT Category II (C2 )
CL Item
CPT Category III (C3 )
CL Item
CPT-4 (i.e., HCPCS Level I) (C4 )
CL Item
HCPCS Level III (H3 )
CL Item
HCPCS (i.e., HCPCS Level II) (HC )
CL Item
LOINC (LC )
CL Item
Local homegrown (LO )
CL Item
NDC (ND )
CL Item
Other (OT )
CL Item
Revenue (RE )
Date of Laboratory Order
Item
Date of Laboratory Order
date
C0677076 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Date of specimen collection
Item
Date of specimen collection
date
C0200345 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Time of specimen collection
Item
Time of specimen collection
time
C0200345 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Date of Laboratory Result
Item
Date of Laboratory Result
date
C1254595 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Time of Laboratory Result
Item
Time of Laboratory Result
time
C1254595 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Original Result
Item
Original Result
text
C2826772 (UMLS CUI [1])
Item
Result value
text
C2348527 (UMLS CUI [1])
Result value
Code List
Result value
CL Item
BORDERLINE (BORDERLINE)
CL Item
NEGATIVE (NEGATIVE)
CL Item
POSITIVE (POSITIVE)
CL Item
UNDETERMINED (UNDETERMINED)
CL Item
RANGE: start|end unit (RANGE: start|end unit)
Numeric Result
Item
Numeric digits with or without a decimal
float
C2347373 (UMLS CUI [1])
Item
Modifier
text
C3542952 (UMLS CUI [1])
Modifier
Code List
Modifier
CL Item
equal (EQ )
CL Item
greater than or equal to (GE )
CL Item
greater than (GT )
CL Item
less than or equal to  (LE )
CL Item
less than (LT )
CL Item
text (TX )
Original Result Unit
Item
Original Result Unit
text
C2826314 (UMLS CUI [1])
Standardized units
Item
text
C1255664 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Unit
Item
Converted/standardized result units
text
C1519795 (UMLS CUI [1])
Normal Range: Low
Item
Normal Range: Low
text
C2700150 (UMLS CUI [1])
Item
Modifier for Normal Range: Low
text
C2700150 (UMLS CUI [1,1])
C1514623 (UMLS CUI [1,2])
Modifier for Normal Range
Code List
Modifier for Normal Range: Low
CL Item
equal (EQ )
CL Item
greater than or equal to (GE )
CL Item
greater than (GT )
Normal Range: high
Item
text
C2700149 (UMLS CUI [1])
Item
Modifier for Normal Range: High
text
C2700149 (UMLS CUI [1,1])
C1514623 (UMLS CUI [1,2])
Modifier for Normal Range: High
Code List
Modifier for Normal Range: High
CL Item
equal (EQ )
CL Item
less than or equal to  (LE )
CL Item
less than (LT )
Item
Abnormal Result Indicator
text
C0459424 (UMLS CUI [1])
Abnormal Result Indicator
Code List
Abnormal Result Indicator
CL Item
abnormal  (AB )
CL Item
abnormally  high (AH )
CL Item
abnormally low (AL )
CL Item
critically high (CH )
CL Item
critically low  (CL )
CL Item
critical (CR )
CL Item
inconclusive (IN )
CL Item
normal (NL )
CL Item
unknown (UN )
Order Code
Item
Unique to each Data Partner
text
C0677076 (UMLS CUI [1,1])
C0805701 (UMLS CUI [1,2])
Centre ID
Item
Servicing provider identifier
text
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
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