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DICOM PS3.16 2020a - Content Mapping Resource​

Page 451​

TID 10021

 

TID 10022

 

TID 1002

 

Radiopharmaceutical

 

 

Radiopharmaceutical

 

 

Observer Context

 

Radiation Dose

 

Administration Event

 

 

 

 

 

 

TID 10024

 

TID 10023

 

 

 

 

Imaging Agent

 

Organ Dose

 

 

 

 

Administration

 

 

 

 

 

 

 

 

 

 

 

Patient Characteristics

 

 

 

 

 

 

 

 

 

TID 1020

 

 

 

 

 

 

 

Person Participant

 

 

 

 

 

 

 

 

Figure A-17. Radiopharmaceutical Radiation Dose SR IOD Template Structure​

TID 10021 Radiopharmaceutical Radiation Dose​

This Template defines a container (the root) with subsidiary Content Items, each of which corresponds to a single Radiopharmaceut-​ ical Administration Dose event entry. There is a defined recording observer (the system and/or person responsible for recording the​ assay of the radiopharmaceutical, and the person administered the radiopharmaceutical). Multiple Radiopharmaceutical Radiation​ Dose objects may be created for one study. Radiopharmaceutical Start DateTime in TID 10022 “Radiopharmaceutical Administration​ Event Data” will convey the order of administrations.​

Type:​

Extensible​

Order:​

Significant​

Root:​

Yes​

Table TID 10021. Radiopharmaceutical Radiation Dose​

 

NL​

Rel with Parent​

VT​

Concept Name​

VM​

Req​ Condition​ Value Set​

 

 

 

 

 

 

 

Type​

Constraint​

1​

 

 

CONTAINER​EV (113500, DCM,​

1​

M​

Root node​

 

 

 

 

 

"Radiopharmaceutical Radiation​

 

 

 

 

 

 

 

 

Dose Report")​

 

 

 

1b​

>​

HAS CONCEPT​ INCLUDE​

DTID 1204 “Language of Content​

1​

U​

 

 

 

MOD​

 

 

Item and Descendants”​

 

 

 

2​

>​

HAS CONCEPT​ CODE​

EV(363589002,SCT,"Associated​

1​

M​

DCID 3108​

 

 

MOD​

 

 

Procedure")​

 

 

“NM/PET​

 

 

 

 

 

 

 

 

Procedures”​

3​

>>​

HAS CONCEPT​ CODE​

EV (363703001, SCT, "Has​

1​

M​

DCID 3629​

 

 

MOD​

 

 

Intent")​

 

 

“Procedure​

 

 

 

 

 

 

 

 

Intent”​

4​

>​

CONTAINS​

INCLUDE​

DTID10022“Radiopharmaceutical​

1​

M​

 

 

 

 

 

 

Administration Event Data”​

 

 

 

5​

>​

CONTAINS​

INCLUDE​

DTID 10024 “Imaging Agent​

1​

U​

 

 

 

 

 

 

Administration Patient​

 

 

 

 

 

 

 

 

Characteristics”​

 

 

 

6​

>​

CONTAINS​

TEXT​

EV (121106, DCM, "Comment")​

1​

U​

 

Content Item Descriptions​

Row 2​

The associated procedure is the procedure performed, or if no procedure was performed the procedure​

 

that was ordered.​

TID 10022 Radiopharmaceutical Administration Event Data​

The Radiopharmaceutical Administration Event conveys the dose and assay and time information of a single radiopharmaceutical​ event. A Radiopharmaceutical Administration event is one radioactive pharmaceutical administered to a patient.​

Type:​

Extensible​

Order:​

Significant​

- Standard -​

Page 452​

DICOM PS3.16 2020a - Content Mapping Resource​

Root:​

No​

 

 

 

Table TID 10022. Radiopharmaceutical Administration Event Data​

NL​ Rel with​

VT​

Concept Name​

VM​

Req​ Condition​ Value Set Constraint​

Parent​

 

 

 

Type​

1​

CONTAINER​EV (113502, DCM,​

1​

M​

 

 

"Radiopharmaceutical​

 

 

 

 

Administration")​

 

 

2​

>​

CONTAINS​

CODE​

EV (349358000, SCT,​

1​

M​

 

 

 

 

"Radiopharmaceutical​

 

 

 

 

 

 

agent")​

 

 

3​

>>​

HAS​

CODE​

EV (89457008, SCT,​

1​

M​

 

 

PROPERTIES​

"Radionuclide")​

 

 

4​

>>​

HAS​

NUM​

EV (304283002, SCT,​

1​

M​

 

 

PROPERTIES​

"Radionuclide Half Life")​

 

 

5​

>​

CONTAINS​

NUM​

EV (123007, DCM,​

1​

U​

 

 

 

 

"Radiopharmaceutical​

 

 

 

 

 

 

Specific Activity")​

 

 

6​

>​

CONTAINS​

UIDREF​

EV (113503, DCM,​

1​

M​

 

 

 

 

"Radiopharmaceutical​

 

 

 

 

 

 

Administration Event UID")​

 

 

7​

>​

CONTAINS​

CODE​

EV (113505, DCM,​

1-n​

U​

 

 

 

 

"Intravenous Extravasation​

 

 

 

 

 

 

Symptoms")​

 

 

8​

>​

CONTAINS​

NUM​

EV (113506, DCM,​

1​

U​

 

 

 

 

"Estimated Extravasation​

 

 

 

 

 

 

Activity")​

 

 

9​

>​

CONTAINS​

DATETIME​ EV (123003, DCM,​

1​

M​

 

 

 

 

"Radiopharmaceutical Start​

 

 

 

 

 

 

DateTime")​

 

 

10​

>​

CONTAINS​

DATETIME​ EV (123004, DCM,​

1​

U​

 

 

 

 

"Radiopharmaceutical Stop​

 

 

 

 

 

 

DateTime")​

 

 

11​

>​

CONTAINS​

NUM​

EV (113507, DCM,​

1​

M​

 

 

 

 

"Administered activity")​

 

 

12​

>​

CONTAINS​

NUM​

EV (123005, DCM,​

1​

U​

 

 

 

 

"Radiopharmaceutical​

 

 

 

 

 

 

Volume")​

 

 

13​

>​

CONTAINS​

NUM​

EV (113508, DCM,​

1​

U​

 

 

 

 

"Pre-Administration​

 

 

 

 

 

 

Measured Activity")​

 

 

14​

>>​

HAS OBS​

CODE​

EV (113540, DCM, "Activity​

1​

U​

 

 

CONTEXT​

 

Measurement Device")​

 

 

15​

>>​

HAS OBS​

INCLUDE​

DTID 1002 “Observer​

1-n​

U​

 

 

CONTEXT​

 

Context”​

 

 

DCID 25​ “Radiopharmaceuticals”​

DCID 4021 “PET​

Radiopharmaceutical”​

DCID 18 “Isotopes in​ Radiopharmaceuticals”​

DCID 4020 “PET​

Radionuclide”​

UNITS = EV (s, UCUM,​ "seconds")​

UNITS = EV (Bq/mmol,​

UCUM, "Bq/mmol")​

DCID 10043​ “Intravenous​ Extravasation​ Symptoms”​

UNITS = EV(%, UCUM,​ "percent")​

UNITS = EV (MBq,​

UCUM, "MBq")​

UNITS = EV (cm3,​

UCUM, "cm3")​

UNITS = EV (MBq,​

UCUM, "MBq")​

DCID 10041 “Source of​ Radioisotope Activity​ Information”​

- Standard -​

 

 

 

DICOM PS3.16 2020a - Content Mapping Resource​

Page 453​

 

NL​

Rel with​

VT​

Concept Name​

VM​

Req​ Condition​

Value Set Constraint​

 

 

Parent​

 

 

 

Type​

 

16​

>​

CONTAINS​

NUM​

EV (113509, DCM,​

1​

U​

UNITS = EV (MBq,​

 

 

 

 

"Post-Administration​

 

 

UCUM, "MBq")​

 

 

 

 

Measured Activity")​

 

 

 

17​

>>​

HAS OBS​

CODE​

EV (113540, DCM, "Activity​

1​

U​

DCID 10041 “Source of​

 

 

CONTEXT​

 

Measurement Device")​

 

 

Radioisotope Activity​

 

 

 

 

 

 

 

Information”​

18​

>>​

HAS OBS​

INCLUDE​

DTID 1002 “Observer​

1-n​

U​

 

 

 

CONTEXT​

 

Context”​

 

 

 

19​

>​

CONTAINS​

INCLUDE​

DTID 10023 “Organ Dose”​

1-n​

U​

 

20​

>​

CONTAINS​

CODE​

EV(410675002,SCT,"Route​ 1​

M​

BCID 11 “Route of​

 

 

 

 

of administration")​

 

 

Administration”​

21​

>>​

HAS​

CODE​

EV (272737002, SCT, "Site​

1​

MC​IF Row 20​

DCID 3746​

 

 

PROPERTIES​

of")​

 

equals​

“Percutaneous Entry​

 

 

 

 

 

 

(47625008,​

Site”​

 

 

 

 

 

 

SCT,​

 

 

 

 

 

 

 

"Intravenous​

 

 

 

 

 

 

 

route") or​

 

 

 

 

 

 

 

(78421000,​

 

 

 

 

 

 

 

SCT,​

 

 

 

 

 

 

 

"Intramuscular​

 

 

 

 

 

 

route")​

 

22​

>>>​ HAS​

CODE​

EV (272741003, SCT,​

1​

MC​IF Row 21 has​DCID 244 “Laterality”​

 

 

CONCEPT​

 

"Laterality")​

 

laterality​

 

 

 

MOD​

 

 

 

 

 

23​

>​

CONTAINS​

INCLUDE​

DTID 1020 “Person​

1-n​

M​

$PersonProcedureRole​

 

 

 

 

Participant”​

 

 

= EV (113851, DCM,​

 

 

 

 

 

 

 

"Irradiation​

 

 

 

 

 

 

 

Administering")​

24​

>​

CONTAINS​

CODE​

EV (121147, DCM, "Billing​

1-n​

U​

 

 

 

 

 

Code(s) ")​

 

 

 

25​

>​

CONTAINS​

CODE​

EV (113510, DCM, "Drug​

1-n​

U​

 

 

 

 

 

Product Identifier")​

 

 

 

26​

>​

CONTAINS​

TEXT​

EV (111529, DCM, "Brand​

1​

U​

 

 

 

 

 

Name")​

 

 

 

27​

>​

CONTAINS​

TEXT​

EV (113511, DCM,​

1​

U​

 

 

 

 

 

"Radiopharmaceutical​

 

 

 

 

 

 

 

Dispense Unit Identifier")​

 

 

 

28​

>>​

CONTAINS​

TEXT​

EV (113512, DCM,​

1-n​

U​

 

 

 

 

 

"Radiopharmaceutical Lot​

 

 

 

 

 

 

 

Identifier")​

 

 

 

29​

>>​

CONTAINS​

TEXT​

EV(113513,DCM,"Reagent​1-n​

U​

 

 

 

 

 

Vial Identifier")​

 

 

 

30​

>>​

CONTAINS​

TEXT​

EV (113514, DCM,​

1-n​

U​

 

 

 

 

 

"Radionuclide Identifier")​

 

 

 

31​

>​

CONTAINS​

TEXT​

EV (113516, DCM,​

1​

U​

 

 

 

 

 

"Prescription Identifier")​

 

 

 

32​

>​

CONTAINS​

TEXT​

EV (121106, DCM,​

1​

U​

 

 

 

 

 

"Comment")​

 

 

 

Content Item Descriptions​

- Standard -​

Page 454​

 

 

DICOM PS3.16 2020a - Content Mapping Resource​

 

Row 4​

The value of Half-life that was used for computing the decay of the administered radiopharmaceutical. It​

 

 

is not intended for use by the receiver for any further computation.​

 

Row 5​

Activity per unit mass of the radiopharmaceutical at Radiopharmaceutical Start Time​

Row 6​

Unique identification of a single radiopharmaceutical administration event.​

 

Row 8​

The estimated percentage of administered activity lost at the injection site. The estimation includes​

 

 

extravasation, paravenous administration and leakage at the injection site.​

 

Row 9​

The time the radiopharmaceutical was administered to the patient for imaging purposes.​

Row 11​

TotalamountofradioactivityadministeredtothepatientatRadiopharmaceuticalStartTime.Itisacomputed​

 

 

field from the TID 10022 Pre-Administration Measured Activity Row 13, TID 10022 Post-Administration​

 

 

Measured Activity Row 17, Radionuclide Half Life Row 4 and Radiopharmaceutical Start Time Row 9.​

 

 

Does not include estimated extravasation activity.​

 

 

 

Rows 13, 16​

Observation DateTime (0040,A032) shall be used to record when the measurement was taken.​

Row 23​

Identifies the person administering the product.​

 

 

 

Row 24​

The billing codes for the preparation and administration of the radiopharmaceutical. It does not include​

 

 

performance and interpretation of the imaging.​

 

 

 

Row 25​

Registered drug establishment code for the product. A coding scheme example is NDC, WHO-DDE or​

 

 

RxNorm. Multiple entries can be used for equivalent drug product codes.​

 

Row 27​

The human readable identification of the specific radiopharmaceutical quantity (dose) administered to the​

 

 

patient.​

 

 

 

 

 

Row 28​

Identifies the vial, batch or lot number from which the individual radiopharmaceutical quantity (dose) was​

 

 

produced. Row 27 the Radiopharmaceutical Identifier records the identification for each individual dose.​

Row 29​

Identifies the lot or unit serial number for the reagent component for the radiopharmaceutical identified in​

 

 

row 27.​

 

 

 

 

 

Row 30​

Identifiesthelotorunitserialnumberfortheradionuclidecomponentfortheradiopharmaceuticalidentified​

 

 

in row 27.​

 

 

 

 

 

TID 10023 Organ Dose​

 

 

 

 

 

This Template conveys the information about the dose to a single organ.​

 

 

 

Type:​

 

Extensible​

 

 

 

 

Order:​

 

Significant​

 

 

 

 

Root:​

 

No​

 

 

 

 

 

 

 

 

Table TID 10023. Organ Dose​

 

 

 

NL​

Rel with Parent​

VT​

Concept Name​

VM​

Req​ Condition​Value Set Constraint​

 

 

 

 

 

 

 

Type​

 

1​

 

 

CONTAINER​EV (113517, DCM, "Organ​

1​

M​

 

 

 

 

 

 

Dose Information")​

 

 

 

2​

>​

HAS CONCEPT​ CODE​

EV (363698007, SCT,​

1​

M​

DCID 10044​

 

 

MOD​

 

 

"Finding Site")​

 

 

“Radiosensitive​

 

 

 

 

 

 

 

 

Organs”​

3​

>​

HAS CONCEPT​ CODE​

EV (272741003, SCT,​

1​

MC​ IFF​

DCID 244 “Laterality”​

 

 

MOD​

 

 

"Laterality")​

 

anatomy​

 

 

 

 

 

 

 

 

has​

 

 

 

 

 

 

 

 

laterality​

 

4​

>​

CONTAINS​

NUM​

EV (118538004, SCT,​

1​

U​

UNITS = EV (g,​

 

 

 

 

 

"Mass")​

 

 

UCUM, "grams")​

5​

>>​

HAS CONCEPT​ TEXT​

EV (370129005, SCT,​

1​

M​

 

 

 

MOD​

 

 

"Measurement Method")​

 

 

 

- Standard -​

 

 

 

 

DICOM PS3.16 2020a - Content Mapping Resource​

Page 455​

 

NL​

Rel with Parent​

VT​

Concept Name​

VM​

Req​

Condition​Value Set Constraint​

 

 

 

 

 

 

 

Type​

 

6​

>​

CONTAINS​

NUM​

EV (113518, DCM, "Organ​

1​

M​

UNITS = EV (mGy,​

 

 

 

 

 

Dose")​

 

 

UCUM, "mGy")​

7​

>>​

HAS​

CODE​

EV (121406, DCM,​

1​

MC​ XORRow8​BCID 10040​

 

 

PROPERTIES​

 

 

"Reference Authority")​

 

 

“Radiopharmaceutical​

 

 

 

 

 

 

 

 

OrganDoseReference​

 

 

 

 

 

 

 

 

Authority”​

8​

>>​

HAS​

TEXT​

EV (121406, DCM,​

1​

MC​ XORRow7​

 

 

PROPERTIES​

 

 

"Reference Authority")​

 

 

 

Content Item Descriptions​

 

 

 

 

 

 

Row 3​

For paired organs, use (51440002, SCT, "Bilateral") to report the estimated absorbed dose for both​

 

 

organs.​

 

 

 

 

 

Row 4​

The estimated mass of organ in grams used when calculating the organ dose.​

Row 5​

Method used to obtain the estimate. This could include a method that does not involve performing a​

 

 

measurement (e.g., Standard Organ Mass Tables).​

 

 

Row 6​

Organ dose (in units of mGy). Organ is specified by row 2.​

 

TID 10024 Imaging Agent Administration Patient Characteristics​

This Template describes the characteristics of the patient that are specific to the current clinical presentation (visit). In the case of​ radiopharmaceuticals, the characteristics noted may affect the activity received, and how dose is calculated for the patient. Patient​ Characteristic concepts in this Template, which may replicate attributes in the Patient Study Module, are included here as possible​ targets of by-reference relationships from other Content Items in the SR tree.​

Type:​

Extensible​

Order:​

Significant​

Root:​

No​

Table TID 10024. Imaging Agent Administration Patient Characteristics​

 

NL​ Rel with Parent​ VT​

Concept Name​

VM​

Req​Condition​ Value Set Constraint​

 

 

 

 

 

 

Type​

 

1​

 

 

CONTAINER​EV (121118, DCM, "Patient​

 

 

 

 

 

 

 

Characteristics")​

 

 

 

2​

>​

CONTAINS​

CODE​

EV (109054, DCM, "Patient​ 1-n​

U​

DCID 10045​

 

 

 

 

state")​

 

 

“Radiopharmaceutical​

 

 

 

 

 

 

 

Patient State”​

 

 

 

 

 

 

 

DCID 64 “Imaging Agent​

 

 

 

 

 

 

 

Administration Patient​

 

 

 

 

 

 

 

State”​

3​

>​

CONTAINS​

NUM​

EV (121033, DCM, "Subject​ 1​

U​

UNITS = DCID 7456 “Units​

 

 

 

 

Age")​

 

 

of Measure for Age”​

4​

>​

CONTAINS​

CODE​

EV (121032, DCM, "Subject​ 1​

U​

DCID 7455 “Sex”​

 

 

 

 

Sex")​

 

 

 

5​

>​

CONTAINS​

NUM​

EV (8302-2, LN, "Patient​

1​

U​

UNITS = EV (cm, UCUM,​

 

 

 

 

Height")​

 

 

"cm")​

6​

>​

CONTAINS​

NUM​

EV (29463-7, LN, "Patient​

1​

U​

UNITS = EV (kg, UCUM,​

 

 

 

 

Weight")​

 

 

"kg").​

7​

>​

CONTAINS​

NUM​

EV (8277-6, LN, "Body​

1​

U​

UNITS = EV (m2, UCUM,​

 

 

 

 

Surface Area")​

 

 

"m^2")​

- Standard -​

Источник: https://studfile.net/preview/14585769/

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