Health and Social Care Information Centre
NHS Data Model and Dictionary Service
Type: | Patch |
Reference: | 1430 |
Version No: | 1.0 |
Subject: | Links and Update Patch |
Effective Date: | Immediate |
Reason for Change: | Patch |
Publication Date: | 23 January 2014 |
Background:
This patch updates the NHS Data Model and Dictionary and includes:
- Website links updated
- Items amended to adhere to the NHS Data Model and Dictionary Editorial Policy
- HTML format corrected.
To view a demonstration on "How to Read an NHS Data Model and Dictionary Change Request", visit the NHS Data Model and Dictionary help pages at: http://www.datadictionary.nhs.uk/Flash_Files/changerequest.htm.
Note: if the web page does not open, please copy the link and paste into the web browser.
Summary of changes:
Date: | 23 January 2014 |
Sponsor: | Richard Kavanagh, Head of Data Standards - Interoperability Specifications, Health and Social Care Information Centre |
Note: New text is shown with a blue background. Deleted text is crossed out. Retired text is shown in grey. Within the Diagrams deleted classes and relationships are red, changed items are blue and new items are green.
Click here for a printer friendly view of this page.
Change to Data Set: Changed Description
National Neonatal Data Set Overview
The National Neonatal Data Set has been incorporated early to allow users to see the changes, but please note that the implementation date is 1 June 2014.
The Mandatory, Required or Optional (M/R/O) column indicates the recommendation for the inclusion of data.
- M = Mandatory: this data element is mandatory and the technical process (e.g. submission of the data set, production of output etc) cannot be completed without this data element being present
- R = Required: NHS business processes cannot be delivered without this data element
- O = Optional: the inclusion of this data element is optional as required for local purposes
Note: items in the M/R/O column which are shown with notation P have not been approved by the Information Standards Board for Health and Social Care, and are included to facilitate piloting and testing of future Neonatal Data Analysis Unit data requirements, prior to formal inclusion in later versions of the data set. These items have been included in the data set layout in order to provide advance notice to data providers and system suppliers of the intention to require these items at a later date. Unless ORGANISATIONS are engaged in piloting activities relating to these items, they should NOT submit any data item marked P. Unless ORGANISATIONS are engaged in piloting activities relating to these items, they should NOT submit any data item marked P.
DEMOGRAPHICS AND BIRTH INFORMATION (BABY) |
---|
One of the following Baby Demographics Data Group Structures must be used:
Baby Demographics (Standard): To carry the Baby's demographic details where anonymisation of the record is NOT required. One occurrence of this group is required. | |
M/R/O | Data Set Data Elements |
R | NHS NUMBER (BABY) |
M | NHS NUMBER STATUS INDICATOR CODE (BABY) |
R | COMMUNITY HEALTH INDEX NUMBER (BABY) |
R | HEALTH AND CARE NUMBER (BABY) |
M | BABY LOCAL PATIENT IDENTIFIER (NATIONAL NEONATAL DATA SET) |
R | DATE TIME OF BIRTH (BABY) |
M | SITE CODE (OF ACTUAL PLACE OF DELIVERY) or ORGANISATION CODE (OF ACTUAL PLACE OF DELIVERY) |
R | BIRTH WEIGHT |
O | BIRTH LENGTH |
O | BIRTH HEAD CIRCUMFERENCE |
O | GESTATION LENGTH (AT DELIVERY) |
O | GESTATION LENGTH (REMAINING DAYS AT DELIVERY) |
R | PERSON PHENOTYPIC SEX |
P | PERSON GENOTYPIC SEX (NATIONAL NEONATAL DATA SET) |
O | BLOOD GROUP (BABY) |
O | RHESUS GROUP (BABY) |
R | BASE DEFICIT CONCENTRATION (WORST WITHIN 12 HOURS AFTER BIRTH) |
OR
Baby Demographics (Withheld): To carry the Baby's demographic details where anonymisation of the record IS required. One occurrence of this group is required. | |
M/R/O | Data Set Data Elements |
M | NHS NUMBER STATUS INDICATOR CODE (BABY) |
M | BABY LOCAL PATIENT IDENTIFIER (NATIONAL NEONATAL DATA SET) |
R | YEAR AND MONTH OF BIRTH (BABY) |
M | SITE CODE (OF ACTUAL PLACE OF DELIVERY) or ORGANISATION CODE (OF ACTUAL PLACE OF DELIVERY) |
R | BIRTH WEIGHT |
O | BIRTH LENGTH |
O | BIRTH HEAD CIRCUMFERENCE |
O | GESTATION LENGTH (AT DELIVERY) |
O | GESTATION LENGTH (REMAINING DAYS AT DELIVERY) |
R | PERSON PHENOTYPIC SEX |
P | PERSON GENOTYPIC SEX (NATIONAL NEONATAL DATA SET) |
O | BLOOD GROUP (BABY) |
O | RHESUS GROUP (BABY) |
R | BASE DEFICIT CONCENTRATION (WORST WITHIN 12 HOURS AFTER BIRTH) |
PARENTS |
---|
One of the following Parent's Demographics Data Group Structures should be used:
Parents Demographics (Standard): To carry the Parent's demographic details where anonymisation of the record is NOT required. One occurrence of this group is permitted. | |
R | NHS NUMBER (MOTHER) |
M | NHS NUMBER STATUS INDICATOR CODE (MOTHER) |
R | COMMUNITY HEALTH INDEX NUMBER (MOTHER) |
R | HEALTH AND CARE NUMBER (MOTHER) |
R | YEAR OF BIRTH (MOTHER) |
M | POSTCODE OF USUAL ADDRESS (MOTHER) |
P | QUALIFICATION ATTAINMENT LEVEL MOTHER (NATIONAL NEONATAL DATA SET) |
O | OCCUPATION MOTHER (SNOMED CT) |
R | ETHNIC CATEGORY (MOTHER) |
R | GENERAL MEDICAL PRACTICE CODE (PATIENT REGISTRATION (MOTHER)) |
R | YEAR OF BIRTH (FATHER) |
R | ETHNIC CATEGORY (FATHER) |
R | PARENTS CONSANGUINEOUS INDICATOR |
OR
Parents Demographics (Withheld): To carry the Parent's demographic details where anonymisation of the record IS required. One occurrence of this group is permitted. | |
M | NHS NUMBER STATUS INDICATOR CODE (MOTHER) |
R | YEAR OF BIRTH (MOTHER) |
P | QUALIFICATION ATTAINMENT LEVEL MOTHER (NATIONAL NEONATAL DATA SET) |
O | OCCUPATION MOTHER (SNOMED CT) |
R | ETHNIC CATEGORY (MOTHER) |
R | GENERAL MEDICAL PRACTICE CODE (PATIENT REGISTRATION (MOTHER)) |
R | YEAR OF BIRTH (FATHER) |
R | ETHNIC CATEGORY (FATHER) |
R | PARENTS CONSANGUINEOUS INDICATOR |
ANTENATAL |
---|
LABOUR AND DELIVERY |
---|
ADMISSION TO NEONATAL CRITICAL CARE |
---|
DISCHARGE FROM NEONATAL CRITICAL CARE UNIT |
---|
Procedures Recorded At Discharge: To carry details of procedures recorded at discharge. Multiple occurrences of this group are permitted. | |
M/R/O | Data Set Data Elements |
R | PROCEDURE (OPCS RECORDED ON DISCHARGE FROM NEONATAL CRITICAL CARE) and/or PROCEDURE (SNOMED CT RECORDED ON DISCHARGE FROM NEONATAL CRITICAL CARE) |
R | PROCEDURE DATE AND TIME (DURING NEONATAL CRITICAL CARE PERIOD) or PROCEDURE YEAR AND MONTH (DURING NEONATAL CRITICAL CARE PERIOD) and NUMBER OF MINUTES (BIRTH TO EVENT) |
CLINICAL TRIALS (EPISODIC) |
---|
Clinical Trials Details: To carry details of Clinical Trial enrolment at any time during the Neonatal Critical Care Period. Multiple occurrences of this group are permitted. | |
M/R/O | Data Set Data Elements |
O | CLINICAL TRIAL NAME |
O | CLINICAL TRIAL MEDICATION ADMINISTERED NAME Multiple occurrences of this item are permitted |
INFECTION CULTURES (EPISODIC) |
---|
Infection Culture Indicators: To carry indicators relating to Infection Cultures undertaken at any time during the Neonatal Critical Care Period. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
P | INFECTION CULTURE TEST INDICATOR (BLOOD) |
P | INFECTION CULTURE TEST INDICATOR (CEREBROSPINAL FLUID) |
P | INFECTION CULTURE TEST INDICATOR (URINE) |
Infection Cultures: To carry information relating to Infection Cultures at any time during the Neonatal Critical Care Period. Multiple occurrences of this group are permitted. | |
M/R/O | Data Set Data Elements |
R | SAMPLE COLLECTION DATE AND TIME or SAMPLE COLLECTION YEAR AND MONTH and NUMBER OF MINUTES (BIRTH TO EVENT) |
R | SAMPLE TYPE (NATIONAL NEONATAL DATA SET) |
R | CLINICAL SIGN OBSERVED AT SAMPLE COLLECTION Multiple occurrences of this item are permitted |
R | SAMPLE TEST RESULT ORGANISM TYPE (SNOMED CT) Multiple occurrences of this item are permitted |
O | SAMPLE ANTIBIOTIC SENSITIVITY RESULT (SNOMED CT DM+D) Multiple occurrences of this item are permitted |
ABDOMINAL X-RAYS (EPISODIC) |
---|
Abdominal X-Ray Indicator: To carry an indicator relating to Abdominal X-Rays undertaken at any time during the Neonatal Critical Care Period. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
P | ABDOMINAL X-RAY PERFORMED INDICATOR |
Abdominal X-Rays: To carry information relating to Abdominal X-Rays at any time during the Neonatal Critical Care Period. Multiple occurrences of this group are permitted. | |
M/R/O | Data Set Data Elements |
R | PROCEDURE DATE AND TIME (ABDOMINAL X-RAY) or PROCEDURE YEAR AND MONTH (ABDOMINAL X-RAY) and NUMBER OF MINUTES (BIRTH TO EVENT) |
R | ABDOMINAL X-RAY PERFORMED TO INVESTIGATE ABDOMINAL SIGNS INDICATOR |
R | CONDITION SEEN IN ABDOMEN DURING X-RAY Multiple occurrences of this item are permitted |
R | ABDOMINAL X-RAY PERFORMED REASON Multiple occurrences of this item are permitted |
R | TRANSFERRED FROM NEONATAL INTENSIVE CARE UNIT FOR NECROTISING ENTEROCOLITIS MANAGEMENT INDICATOR |
R | LAPAROTOMY FOR NECROTISING ENTEROCOLITIS INDICATION CODE |
R | VISUAL INSPECTION CONFIRMED NECROTISING ENTEROCOLITIS DURING LAPAROTOMY INDICATOR |
R | HISTOLOGY CONFIRMED NECROTISING ENTEROCOLITIS FOLLOWING LAPAROTOMY INDICATOR |
R | PERITONEAL DRAIN INSERTED FOLLOWING ABDOMINAL X-RAY INDICATOR |
RETINOPATHY OF PREMATURITY SCREENING (EPISODIC) |
---|
Retinopathy of Prematurity Screening Indicator: To carry an indicator relating to Retinopathy of Prematurity Screening undertaken at any time during the Neonatal Critical Care Period. One occurrence of this group is required. | |
M/R/O | Data Set Data Elements |
M | RETINOPATHY OF PREMATURITY SCREENING PERFORMED INDICATOR |
CRANIAL ULTRASOUND SCANS (EPISODIC) |
---|
Cranial Ultrasound Scan Indicator: To carry an indicator relating to Cranial Ultrasound Scans undertaken at any time during the Neonatal Critical Care Period. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
P | CRANIAL ULTRASOUND SCAN PERFORMED INDICATOR |
Cranial Ultrasound Scan: To carry information relating to Cranial Ultrasound Scans at any time during the Neonatal Critical Care Period. Multiple occurrences of this group are permitted. | |
M/R/O | Data Set Data Elements |
R | PROCEDURE DATE AND TIME (CRANIAL ULTRASOUND SCAN) or PROCEDURE YEAR AND MONTH (CRANIAL ULTRASOUND SCAN) and NUMBER OF MINUTES (BIRTH TO EVENT) |
O | INTRAVENTRICULAR HAEMORRHAGE GRADE (LEFT SIDE) |
O | PORENCEPHALIC CYST VISIBLE DURING CRANIAL ULTRASOUND SCAN INDICATOR (LEFT SIDE) |
O | VENTRICULAR DILATION DIAGNOSED DURING CRANIAL ULTRASOUND SCAN INDICATOR (LEFT SIDE) |
O | INTRAVENTRICULAR HAEMORRHAGE GRADE (RIGHT SIDE) |
O | PORENCEPHALIC CYST VISIBLE DURING CRANIAL ULTRASOUND SCAN INDICATOR (RIGHT SIDE) |
O | VENTRICULAR DILATION DIAGNOSED DURING CRANIAL ULTRASOUND SCAN INDICATOR (RIGHT SIDE) |
O | CYSTIC PERIVENTRICULAR LEUKOMALACIA OBSERVED DURING CRANIAL ULTRASOUND SCAN INDICATOR |
O | POST HAEMORRHAGIC HYDROCEPHALUS OBSERVED DURING CRANIAL ULTRASOUND SCAN INDICATOR |
NEWBORN BLOOD SPOT BIOCHEMICAL SCREENING (EPISODIC) |
---|
Newborn Blood Spot Test Indicator: To carry an indicator relating to Newborn Blood Spot Tests undertaken at any time during the Neonatal Critical Care Period. One occurrence of this group is required. | |
M/R/O | Data Set Data Elements |
M | NEWBORN BLOOD SPOT TEST PERFORMED INDICATOR |
Newborn Blood Spot Screening: To carry details of Newborn Blood Spot Biochemical Screening undertaken at any time in the Neonatal Critical Care Period. Multiple occurrences of this group are permitted. | |
M/R/O | Data Set Data Elements |
R | BLOOD SPOT CARD COMPLETION DATE or BLOOD SPOT CARD COMPLETION YEAR AND MONTH and NUMBER OF MINUTES (BIRTH TO EVENT) |
NEWBORN HEARING SCREENING (EPISODIC) |
---|
Newborn Hearing Screening Indicator: To carry an indicator relating to Newborn Hearing Screening undertaken at any time during the Neonatal Critical Care Period. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
P | NEWBORN HEARING SCREENING PERFORMED INDICATOR |
Newborn Hearing Screening: To carry information relating to Newborn Hearing Screening at any time during the Neonatal Critical Care Period. Multiple occurrences of this group are permitted. | |
M/R/O | Data Set Data Elements |
R | PROCEDURE DATE AND TIME (NEWBORN HEARING SCREENING) or PROCEDURE YEAR AND MONTH (NEWBORN HEARING SCREENING) and NUMBER OF MINUTES (BIRTH TO EVENT) |
O | NEWBORN HEARING SCREENING OUTCOME LEFT EAR (NATIONAL NEONATAL DATA SET) |
O | NEWBORN HEARING SCREENING OUTCOME RIGHT EAR (NATIONAL NEONATAL DATA SET) |
O | NEWBORN HEARING SCREENING TEST TYPE |
DAILY CARE INFORMATION |
---|
Daily Care Respiratory: To carry Respiratory information relating to Daily Care. One occurrence of this group is required. | |
M/R/O | Data Set Data Elements |
P | RESPIRATORY SUPPORT DEVICE TYPE (NATIONAL NEONATAL DATA SET) Multiple occurrences of this item are permitted |
P | RESPIRATORY SUPPORT MODE (NATIONAL NEONATAL DATA SET) Multiple occurrences of this item are permitted |
R | NITRIC OXIDE GIVEN INDICATOR |
R | CHEST DRAIN IN SITU INDICATOR |
R | TRACHEOSTOMY TUBE IN SITU INDICATOR |
R | REPLOGLE TUBE IN SITU INDICATOR |
R | SURFACTANT GIVEN INDICATOR (ON NEONATAL CRITICAL CARE DAILY CARE DATE) |
P | FRACTION OF INSPIRED OXYGEN PERCENTAGE |
Daily Care Cardiovascular: To carry Cardiovascular information relating to Daily Care. One occurrence of this group is required. | |
M/R/O | Data Set Data Elements |
R | CONTINUOUS INFUSION OF PULMONARY VASODILATOR RECEIVED INDICATOR |
R | INOTROPE INFUSION RECEIVED INDICATOR |
R | PROSTAGLANDIN INFUSION RECEIVED INDICATOR |
R | TREATMENT TYPE FOR PATENT DUCTUS ARTERIOSUS Multiple occurrences of this item are permitted |
Daily Care Gastrointestinal: To carry Gastrointestinal information relating to Daily Care. One occurrence of this group is required. | |
M/R/O | Data Set Data Elements |
R | PERITONEAL DIALYSIS RECEIVED INDICATOR |
R | HAEMOFILTRATION RECEIVED INDICATOR |
R | TREATMENT TYPE FOR NECROTISING ENTEROCOLITIS |
R | MORE THAN THREE RECTAL WASHOUTS RECEIVED INDICATOR |
R | STOMA PRESENT INDICATOR |
Daily Care Blood Transfusion: To carry Blood Transfusion information relating to Daily Care. Multiple occurrences of this group are permitted. | |
M/R/O | Data Set Data Elements |
R | BLOOD TRANSFUSION TYPE |
R | BLOOD TRANSFUSION PRODUCT TYPE Multiple occurrences of this item are permitted |
Daily Care Neurology: To carry Neurology information relating to Daily Care. One occurrence of this group is required. | |
M/R/O | Data Set Data Elements |
R | CENTRAL TONE STATUS |
R | NEONATAL CONSCIOUSNESS STATUS |
R | SEIZURE OCCURRED INDICATOR |
R | NEONATAL ABSTINENCE SYNDROME OBSERVED INDICATOR |
R | BRAIN ACTIVITY SCAN PERFORMED INDICATOR |
R | THERAPEUTIC HYPOTHERMIA INDUCED INDICATOR |
R | HYPOXIC ISCHEMIC ENCEPHALOPATHY GRADE (HIGHEST ON NEONATAL CRITICAL CARE DAILY CARE DATE) |
Daily Care Retinopathy of Prematurity Screening: To carry Retinopathy of Prematurity information relating to Daily Care. One occurrence of this group is required. | |
M/R/O | Data Set Data Elements |
R | RETINOPATHY OF PREMATURITY SCREENING PERFORMED INDICATOR |
Daily Care Fluids and Feeding: To carry Fluids and Feeding information relating to Daily Care. One occurrence of this group is required. | |
M/R/O | Data Set Data Elements |
R | VASCULAR LINE TYPE IN SITU Multiple occurrences of this item are permitted |
R | PARENTERAL NUTRITION RECEIVED INDICATOR |
R | INTRAVENOUS INFUSION OF GLUCOSE AND ELECTROLYTE SOLUTION RECEIVED INDICATOR |
R | ENTERAL FEED TYPE GIVEN Multiple occurrences of this item are permitted |
R | FORMULA MILK OR MILK FORTIFIER TYPE Multiple occurrences of this item are permitted or FORMULA MILK OR MILK FORTIFIER TYPE (SNOMED CT DM+D) Multiple occurrences of this item are permitted |
R | TOTAL VOLUME OF MILK RECEIVED |
O | ENTERAL FEEDING METHOD Multiple occurrences of this item are permitted |
Daily Care Infections: To carry Infection information relating to Daily Care. One occurrence of this group is required. | |
M/R/O | Data Set Data Elements |
R | SEPSIS SUSPECTED INDICATOR |
Daily Care Jaundice: To carry Jaundice information relating to Daily Care. One occurrence of this group is required. | |
M/R/O | Data Set Data Elements |
R | PHOTOTHERAPY RECEIVED INDICATOR |
Daily Care Medication: To carry Medication Administered information relating to Daily Care. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
R | MEDICATION GIVEN DURING NEONATAL CRITICAL CARE DAILY CARE DATE (SNOMED CT DM+D) Multiple occurrences of this item are permitted |
Change to Data Set: Changed Description
National Neonatal Data Set Overview
The National Neonatal Data Set has been incorporated early to allow users to see the changes, but please note that the implementation date is 1 June 2014.
The Mandatory, Required or Optional (M/R/O) column indicates the recommendation for the inclusion of data.
- M = Mandatory: this data element is mandatory and the technical process (e.g. submission of the data set, production of output etc) cannot be completed without this data element being present
- R = Required: NHS business processes cannot be delivered without this data element
- O = Optional: the inclusion of this data element is optional as required for local purposes.
Note: items in the M/R/O column which are shown with notation P have not been approved by the Information Standards Board for Health and Social Care, and are included to facilitate piloting and testing of future Neonatal Data Analysis Unit data requirements, prior to formal inclusion in later versions of the data set. These items have been included in the data set layout in order to provide advance notice to data providers and system suppliers of the intention to require these items at a later date. Unless ORGANISATIONS are engaged in piloting activities relating to these items, they should NOT submit any data item marked P. Unless ORGANISATIONS are engaged in piloting activities relating to these items, they should NOT submit any data item marked P.
TWO YEAR NEONATAL OUTCOMES ASSESSMENT |
---|
One of the following Child Demographics Data Group Structures must be used:
Child Demographics (Standard): To carry the Child's demographic details where anonymisation of the record is NOT required. One occurrence of this group is required. | |
M/R/O | Data Set Data Elements |
R | NHS NUMBER |
M | NHS NUMBER STATUS INDICATOR CODE |
R | COMMUNITY HEALTH INDEX NUMBER |
R | HEALTH AND CARE NUMBER |
M | BABY LOCAL PATIENT IDENTIFIER (NATIONAL NEONATAL DATA SET) |
R | DATE TIME OF BIRTH |
M | SITE CODE (OF ACTUAL PLACE OF DELIVERY) or ORGANISATION CODE (OF ACTUAL PLACE OF DELIVERY) |
O | GESTATION LENGTH (AT DELIVERY) |
O | GESTATION LENGTH (REMAINING DAYS AT DELIVERY) |
R | PERSON PHENOTYPIC SEX or PERSON GENOTYPIC SEX (NATIONAL NEONATAL DATA SET) |
OR
Child's Demographics (Withheld): To carry the Child's demographic details where anonymisation of the record IS required. One occurrence of this group is required. | |
M/R/O | Data Set Data Elements |
M | NHS NUMBER STATUS INDICATOR CODE |
M | BABY LOCAL PATIENT IDENTIFIER (NATIONAL NEONATAL DATA SET) |
R | YEAR AND MONTH OF BIRTH |
M | SITE CODE (OF ACTUAL PLACE OF DELIVERY) or ORGANISATION CODE (OF ACTUAL PLACE OF DELIVERY) |
O | GESTATION LENGTH (AT BIRTH) |
O | GESTATION LENGTH (REMAINING DAYS AT DELIVERY) |
R | PERSON PHENOTYPIC SEX or PERSON GENOTYPIC SEX (NATIONAL NEONATAL DATA SET) |
One of the following Two Year Assessment Administration Data Group Structures must be used:
Two Year Assessment Administration (Standard): To carry administrative information relating to the Two Year Neonatal Outcomes Assessment where anonymisation of the record is NOT required. One occurrence of this group is required. | |
M/R/O | Data Set Data Elements |
M | TWO YEAR NEONATAL OUTCOMES ASSESSMENT DATE |
O | CARE PROFESSIONAL JOB ROLE CODE (TWO YEAR NEONATAL OUTCOMES ASSESSMENT) |
R | POSTCODE OF USUAL ADDRESS (AT TWO YEAR NEONATAL OUTCOMES ASSESSMENT) |
M | SITE CODE (OF TWO YEAR NEONATAL OUTCOMES ASSESSMENT) or ORGANISATION CODE (OF TWO YEAR NEONATAL OUTCOMES ASSESSMENT) |
R | TWO YEAR NEONATAL OUTCOMES ASSESSMENT NOT CARRIED OUT REASON |
R | PERSON DEATH DATE (POST DISCHARGE FROM NEONATAL CRITICAL CARE) |
OR
Two Year Administration (Withheld): To carry administrative information relating to the Two Year Neonatal Outcomes Assessment where anonymisation of the record IS required. One occurrence of this group is required. | |
M/R/O | Data Set Data Elements |
R | TWO YEAR NEONATAL OUTCOMES ASSESSMENT YEAR AND MONTH and NUMBER OF MINUTES (BIRTH TO EVENT) |
O | CARE PROFESSIONAL JOB ROLE CODE (TWO YEAR NEONATAL OUTCOMES ASSESSMENT) |
R | SITE CODE (OF TWO YEAR NEONATAL OUTCOMES ASSESSMENT) or ORGANISATION CODE (OF TWO YEAR NEONATAL OUTCOMES ASSESSMENT) |
R | TWO YEAR NEONATAL OUTCOMES ASSESSMENT NOT CARRIED OUT REASON |
R | PERSON DEATH YEAR AND MONTH (POST DISCHARGE FROM NEONATAL CRITICAL CARE) and NUMBER OF MINUTES (BIRTH TO EVENT) |
Two Year TPRG-SEND - Neuromotor: To carry information relating to TPRG-SEND Neuromotor at the Two Year Neonatal Outcomes Assessment. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROMOTOR QUESTION A) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROMOTOR QUESTION B) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROMOTOR QUESTION C) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROMOTOR QUESTION D) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROMOTOR QUESTION E) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROMOTOR QUESTION F) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROMOTOR QUESTION G) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROMOTOR QUESTION H) |
Two Year TPRG-SEND - Malformations: To carry information relating to TPRG-SEND Malformations at the Two Year Neonatal Outcomes Assessment. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (MALFORMATIONS QUESTION A) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (MALFORMATIONS QUESTION B) |
Two Year TPRG-SEND - Respiratory and Cardiovascular: To carry information relating to TPRG-SEND Respiratory and Cardiovascular System at the Two Year Neonatal Outcomes Assessment. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (RESPIRATORY AND CARDIOVASCULAR SYSTEM QUESTION A) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (RESPIRATORY AND CARDIOVASCULAR SYSTEM QUESTION B) |
Two Year TPRG-SEND - Gastrointestinal Tract: To carry information relating to TPRG-SEND Gastrointestinal Tract at the Two Year Neonatal Outcomes Assessment. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (GASTRO-INTESTINAL TRACT QUESTION A) |
R | SPECIAL DIET DESCRIPTION |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (GASTRO-INTESTINAL TRACT QUESTION B) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (GASTRO-INTESTINAL TRACT QUESTION C) |
Two Year TPRG-SEND - Renal: To carry information relating to TPRG-SEND Renal at the Two Year Neonatal Outcomes Assessment. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (RENAL QUESTION A) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (RENAL QUESTION B) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (RENAL QUESTION C) |
Two Year TPRG-SEND - Neurology: To carry information relating to TPRG-SEND Neurology at the Two Year Neonatal Outcomes Assessment. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROLOGY QUESTION A) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROLOGY QUESTION B) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROLOGY QUESTION C) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROLOGY QUESTION D) |
Two Year TPRG-SEND - Growth: To carry information relating to TPRG-SEND Growth at the Two Year Neonatal Outcomes Assessment. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
R | PERSON WEIGHT (AT TWO YEAR NEONATAL OUTCOMES ASSESSMENT) |
P | OBSERVATION DATE (WEIGHT) or OBSERVATION YEAR AND MONTH (WEIGHT) and NUMBER OF MINUTES (BIRTH TO EVENT) |
R | PERSON HEIGHT IN CENTIMETRES (AT TWO YEAR NEONATAL OUTCOMES ASSESSMENT) |
P | OBSERVATION DATE (HEIGHT) or OBSERVATION YEAR AND MONTH (HEIGHT) and NUMBER OF MINUTES (BIRTH TO EVENT) |
R | HEAD CIRCUMFERENCE IN CENTIMETRES (AT TWO YEAR NEONATAL OUTCOMES ASSESSMENT) |
P | OBSERVATION DATE (HEAD CIRCUMFERENCE) or OBSERVATION YEAR AND MONTH (HEAD CIRCUMFERENCE) and NUMBER OF MINUTES (BIRTH TO EVENT) |
Two Year TPRG-SEND - Development: To carry information relating to TPRG-SEND Development at the Two Year Neonatal Outcomes Assessment. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (DEVELOPMENT ADDITIONAL QUESTION FOR NATIONAL NEONATAL DATA SET) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (DEVELOPMENT QUESTION A) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (DEVELOPMENT QUESTION B) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (DEVELOPMENT QUESTION C) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (DEVELOPMENT QUESTION D) |
R | NEURODEVELOPMENTAL ASSESSMENT ALREADY TAKEN INDICATOR |
R | NEURODEVELOPMENTAL ASSESSMENT TEST NAME |
Two Year TPRG-SEND - Neurosensory: To carry information relating to TPRG-SEND Neurosensory at the Two Year Neonatal Outcomes Assessment. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROSENSORY QUESTION A) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROSENSORY QUESTION B) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROSENSORY QUESTION C) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROSENSORY QUESTION D) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROSENSORY QUESTION E) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (NEUROSENSORY QUESTION F) |
Two Year TPRG-SEND - Communication: To carry information relating to TPRG-SEND Communication at the Two Year Neonatal Outcomes Assessment. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (COMMUNICATION QUESTION A) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (COMMUNICATION QUESTION B) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (COMMUNICATION QUESTION C) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (COMMUNICATION QUESTION D) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (COMMUNICATION QUESTION E) |
Two Year TPRG-SEND - Special Questions: To carry information relating to TPRG-SEND Special Questions at the Two Year Neonatal Outcomes Assessment. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (SPECIAL QUESTIONS QUESTION A) |
R | TPRG-SEND TWO YEAR CORRECTED AGE OUTCOME ASSESSMENT SCORE (SPECIAL QUESTIONS QUESTION B) |
R | CHILD DIFFICULT TO TEST REASON CODE Multiple occurrences of this item are permitted |
Two Year TPRG-SEND - Neurological Diagnosis: To carry information relating to TPRG-SEND Neurological Diagnosis at the Two Year Neonatal Outcomes Assessment. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
R | PATIENT DIAGNOSIS INDICATOR (CEREBRAL PALSY) |
R | CEREBRAL PALSY TYPE CODE (NATIONAL NEONATAL DATA SET) |
R | DIAGNOSIS (ICD NEUROLOGICAL) Multiple occurrences of this item are permitted |
Two Year Bayley III Assessment: To carry information relating to the Bayley III Assessment. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
P | ASSESSMENT TOOL COMPLETION DATE or ASSESSMENT TOOL COMPLETION YEAR AND MONTH and NUMBER OF MINUTES (BIRTH TO EVENT) |
Two Year Bayley III - Cognitive: To carry information relating to the Bayley III Cognitive sub-scale. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
R | BAYLEY III COGNITIVE TOTAL RAW SCORE |
R | BAYLEY III COGNITIVE SCALE SCORE |
R | BAYLEY III COGNITIVE DEVELOPMENTAL AGE EQUIVALENT SCORE |
R | BAYLEY III COGNITIVE COMPOSITE SCORE |
Two Year Bayley III - Neuromotor: To carry information relating to the Bayley III Neuromotor sub-scales. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
R | BAYLEY III NEUROMOTOR (FINE MOTOR) TOTAL RAW SCORE |
R | BAYLEY III NEUROMOTOR (FINE MOTOR) SCALE SCORE |
R | BAYLEY III NEUROMOTOR (FINE MOTOR) DEVELOPMENTAL AGE EQUIVALENT SCORE |
R | BAYLEY III NEUROMOTOR (FINE MOTOR) COMPOSITE SCORE |
R | BAYLEY III NEUROMOTOR (GROSS MOTOR) TOTAL RAW SCORE |
R | BAYLEY III NEUROMOTOR (GROSS MOTOR) SCALE SCORE |
R | BAYLEY III NEUROMOTOR (GROSS MOTOR) DEVELOPMENTAL AGE EQUIVALENT SCORE |
R | BAYLEY III NEUROMOTOR (GROSS MOTOR) COMPOSITE SCORE |
R | BAYLEY III NEUROMOTOR SUM TOTAL RAW SCORE |
R | BAYLEY III NEUROMOTOR SUM TOTAL SCALE SCORE |
R | BAYLEY III NEUROMOTOR SUM TOTAL DEVELOPMENTAL AGE EQUIVALENT SCORE |
R | BAYLEY III NEUROMOTOR SUM TOTAL COMPOSITE SCORE |
Two Year Bayley III - Social-Emotional: To carry information relating to the Bayley III Social-Emotional sub-scale. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
R | BAYLEY III SOCIAL-EMOTIONAL TOTAL RAW SCORE |
R | BAYLEY III SOCIAL-EMOTIONAL SCALE SCORE |
R | BAYLEY III SOCIAL-EMOTIONAL DEVELOPMENTAL AGE EQUIVALENT SCORE |
R | BAYLEY III SOCIAL-EMOTIONAL COMPOSITE SCORE |
Two Year Griffiths: To carry information relating to Griffiths Scale of Infant Development. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
P | ASSESSMENT TOOL COMPLETION DATE or ASSESSMENT TOOL COMPLETION YEAR AND MONTH and NUMBER OF MINUTES (BIRTH TO EVENT) |
R | GRIFFITHS LOCOMOTOR SCALE SCORE |
R | GRIFFITHS PERSONAL-SOCIAL SCALE SCORE |
R | GRIFFITHS LANGUAGE SCALE SCORE |
R | GRIFFITHS EYE AND HAND CO-ORDINATION SCALE SCORE |
R | GRIFFITHS PERFORMANCE SCALE SCORE |
R | GRIFFITHS PRACTICAL REASONING SCALE SCORE |
Two Year Schedule of Growing: To carry information relating to Schedule of Growing Skills. One occurrence of this group is permitted. | |
M/R/O | Data Set Data Elements |
P | ASSESSMENT TOOL COMPLETION DATE or ASSESSMENT TOOL COMPLETION YEAR AND MONTH and NUMBER OF MINUTES (BIRTH TO EVENT) |
R | SCHEDULE OF GROWING SKILLS (PASSIVE POSTURE) SCALE SCORE |
R | SCHEDULE OF GROWING SKILLS (ACTIVE POSTURE) SCALE SCORE |
R | SCHEDULE OF GROWING SKILLS (LOCOMOTOR) SCALE SCORE |
R | SCHEDULE OF GROWING SKILLS (MANIPULATIVE) SCALE SCORE |
R | SCHEDULE OF GROWING SKILLS (VISUAL) SCALE SCORE |
R | SCHEDULE OF GROWING SKILLS (HEARING AND LANGUAGE) SCALE SCORE |
R | SCHEDULE OF GROWING SKILLS (SPEECH AND LANGUAGE) SCALE SCORE |
R | SCHEDULE OF GROWING SKILLS (INTERACTIVE SOCIAL) SCALE SCORE |
R | SCHEDULE OF GROWING SKILLS (SELF-CARE SOCIAL) SCALE SCORE |
Change to Data Set: Changed Description
This return is out of date therefore the information should not be used.
For the latest version of the guidance, please see the Department of Health part of the gov.uk website at: Stop Smoking Service: monitoring and guidance update.
Stop Smoking Service Quarterly Data Set Overview
Change to Supporting Information: Changed Description
Accident and Emergency Attendance is a CARE CONTACT.An Accident and Emergency Attendance is a CARE CONTACT..
An individual visit by one PATIENT to an Accident and Emergency Department to receive treatment from the accident and emergency service.An Accident and Emergency Attendance is an individual visit by one PATIENT to an Accident and Emergency Department to receive treatment from the accident and emergency service.
Note that the accident and emergency service may be provided by staff from other MAIN SPECIALTY.
During an Accident and Emergency Attendance the PATIENT may temporarily leave the Accident and Emergency Department, e.g. for an X-ray, whilst still under the responsibility of the Accident and Emergency Department.
An Accident and Emergency Attendance may be as a result of a request from a GENERAL PRACTITIONER for help with a diagnosis or treatment.
Attendances at Out-Patient Clinic run in the Accident and Emergency Department should not be recorded as Accident and Emergency Attendance but should be recorded as Out-Patient Attendance Consultant or Clinic Attendance Non-Consultant depending upon the type of Out-Patient Clinic attended.
Any facility set up to receive and treat emergency cases is regarded as an Accident and Emergency Department for this purpose.
Accident and Emergency Attendance include both first and follow-up attendances.Accident and Emergency Attendances include both first and follow-up attendances. A follow-up attendance is any subsequent Accident and Emergency Attendance at the same Accident and Emergency Department for the same incident. All attendances for the same incident will constitute an Accident and Emergency Episode.
Each Accident and Emergency Attendance, which is a first attendance or an unplanned follow-up attendance, should be assigned an A AND E STREAM.
Any PATIENT diagnoses and interventions should be recorded using the A & E specific codes, see ACCIDENT AND EMERGENCY DIAGNOSIS, ACCIDENT AND EMERGENCY INVESTIGATION and ACCIDENT AND EMERGENCY TREATMENT.
For each Accident and Emergency Attendance the following times should be recorded: ARRIVAL TIME, A and E INITIAL ASSESSMENT TIME (first attendances and unplanned follow-up attendances), A and E TIME SEEN FOR TREATMENT, A and E ATTENDANCE CONCLUSION TIME and A and E DEPARTURE TIME.
For first attendances and unplanned follow-up attendances the A AND E INITIAL ASSESSMENT TRIAGE CATEGORY and A AND E STREAM need to be recorded.
Information recorded for an Accident and Emergency Attendance includes:
Change to Supporting Information: Changed Description
Accident and Emergency Attendance Conclusion Date is an ACTIVITY DATE TIME.An Accident and Emergency Attendance Conclusion Date is an ACTIVITY DATE TIME.
Accident and Emergency Attendance Conclusion Date is the date that a PATIENT's Accident and Emergency Attendance concludes or when treatment in the Accident and Emergency Department is completed (whichever is the later).An Accident and Emergency Attendance Conclusion Date is the date that a PATIENT's Accident and Emergency Attendance concludes or when treatment in the Accident and Emergency Department is completed (whichever is the later).
For those PATIENTS admitted into hospital, the ACCIDENT AND EMERGENCY ATTENDANCE CONCLUSION DATE is recorded as the date when the DECISION TO ADMIT was made.
Change to Supporting Information: Changed Description
Accident and Emergency Attendance Conclusion Time is an ACTIVITY DATE TIME.An Accident and Emergency Attendance Conclusion Time is an ACTIVITY DATE TIME.
Accident and Emergency Attendance Conclusion Time is the time, recorded using a 24 hour clock:An Accident and Emergency Attendance Conclusion Time is the time, recorded using a 24 hour clock:
- that a PATIENT's Accident and Emergency Attendance concludes or
- when treatment in an Accident and Emergency Department is completed (whichever is the later).
For those PATIENTS admitted into hospital, the A and E ATTENDANCE CONCLUSION TIME is recorded as the time when the DECISION TO ADMIT was made.
Change to Supporting Information: Changed Description
Accident and Emergency Date Seen For Treatment is an ACTIVITY DATE TIME.
Accident and Emergency Date Seen For Treatment is the date, that the PATIENT is seen by a clinical decision maker (someone who can define the management plan and discharge the PATIENT) to diagnose the problem and arrange or start definite treatment as necessary.
Notes: For guidance on the use of this data item in the Accident and Emergency Clinical Quality Indicators, further information is available on the Department of Health website.For guidance on the use of this data item in the Accident and Emergency Clinical Quality Indicators, further information is available on the Health and Social Care Information Centre website.
Change to Supporting Information: Changed Description
Accident and Emergency Department is a DEPARTMENT.An Accident and Emergency Department is a DEPARTMENT.
These may be either major units, providing a 24 hour service seven days a week to which the great majority of emergency ambulance cases are taken, or small units commonly called casualty departments, in which services are often only available for limited hours and which may not deal with emergency ambulance cases.Accident and Emergency Departments may be either major units, providing a 24 hour service seven days a week to which the great majority of emergency ambulance cases are taken, or small units commonly called casualty departments, in which services are often only available for limited hours and which may not deal with emergency ambulance cases.
A casualty department is not always part of a Hospital Site. Additional activities may also take place such as: elective surgical work of a minor nature, observation and treatment of PATIENTS in Hospital Beds and the holding of Out-Patient Clinics.
Hospital Beds either within or adjacent to a department will be counted as a WARD or part of a WARD. Work apart from the accident and emergency service should be recorded in the appropriate data system.
An accident and emergency service offers care to PATIENTS who arrive with urgent problems and who have not usually been seen previously by a GENERAL PRACTITIONER.
In the case of serious illness or accident, the treatment provided will be vital resuscitation only before the PATIENT is admitted to hospital.
Change to Supporting Information: Changed Description
Accident and Emergency Departure Date is an ACTIVITY DATE TIME.An Accident and Emergency Departure Date is an ACTIVITY DATE TIME.
Accident and Emergency Departure Date is the date that a PATIENT leaves an Accident and Emergency Department after an Accident and Emergency Attendance has concluded.An Accident and Emergency Departure Date is the date that a PATIENT leaves an Accident and Emergency Department after an Accident and Emergency Attendance has concluded.
Notes:
- This date may be different from the Accident and Emergency Attendance Conclusion Date for PATIENTS who wait for patient transport or who are LODGED PATIENTS prior to admission to a WARD.
ThePATIENTmay leave theAccident and Emergency Departmenttemporarily during anAccident and Emergency Attendance, e.g. for an X-ray but they remain under the care of an Accident and EmergencyCONSULTANT.For guidance on the use of this data item in the Accident and Emergency Clinical Quality Indicators, further information is available on theDepartment of Health website.- The PATIENT may leave the Accident and Emergency Department temporarily during an Accident and Emergency Attendance, for example, for an X-ray but they remain under the care of an Accident and Emergency CONSULTANT.
Change to Supporting Information: Changed Description
Accident and Emergency Departure Time is an ACTIVITY DATE TIME.An Accident and Emergency Departure Time is an ACTIVITY DATE TIME.
Accident and Emergency Departure Time is the time recorded using a 24 hour clock that a PATIENT leaves an Accident and Emergency Department after an Accident and Emergency Attendance has concluded.An Accident and Emergency Departure Time is the time recorded using a 24 hour clock that a PATIENT leaves an Accident and Emergency Department after an Accident and Emergency Attendance has concluded.
- This time will be different from the Accident and Emergency Attendance Conclusion Time for PATIENTS who wait for patient transport or who are LODGED PATIENTS prior to admission to a WARD.
ThePATIENTmay leave theAccident and Emergency Departmenttemporarily during anAccident and Emergency Attendance, e.g. for an X-ray but they remain under the care of an Accident and EmergencyCONSULTANT.For guidance on the use of this data item in the Accident and Emergency Clinical Quality Indicators, further information is available on theDepartment of Health website.- The PATIENT may leave the Accident and Emergency Department temporarily during an Accident and Emergency Attendance, for example, for an X-ray but they remain under the care of an Accident and Emergency CONSULTANT.
Change to Supporting Information: Changed Description
Accident and Emergency Episode is an ACTIVITY GROUP.An Accident and Emergency Episode is an ACTIVITY GROUP.
The visits to an Accident and Emergency Department of one PATIENT for a particular incident. The PATIENT may receive treatment during the episode from the accident and emergency service and from other MAIN SPECIALTIES.An Accident and Emergency Episode involves visits to an Accident and Emergency Department of one PATIENT for a particular incident. The PATIENT may receive treatment during the Accident and Emergency Episode from the accident and emergency service and from other MAIN SPECIALTIES.
Each Accident and Emergency Episode takes place at a single Accident and Emergency Department and consists of one or more Accident and Emergency Attendance.
The Accident and Emergency Episode may give rise to a DECISION TO ADMIT.
Information recorded for an Accident and Emergency Episode includes:
Change to Supporting Information: Changed Description
Accident and Emergency Initial Assessment Date is an ACTIVITY DATE TIME.An Accident and Emergency Initial Assessment Date is an ACTIVITY DATE TIME.
Accident and Emergency Initial Assessment Date is the date, that the PATIENT is first assessed in the Accident and Emergency Department.An Accident and Emergency Initial Assessment Date is the date that the PATIENT is first assessed in the Accident and Emergency Department.
Initial Assessment would include:An Initial Assessment would include:
- the taking of a brief PATIENT medical history
- pain assessment
- early warning scores (including vital signs)
The assessment should be conducted by medical or nursing staff who have received appropriate training.
Notes: For guidance on the use of this data item in the Accident and Emergency Clinical Quality Indicators, further information is available on the Department of Health website.For guidance on the use of this data item in the Accident and Emergency Clinical Quality Indicators, further information is available on the Health and Social Care Information Centre website.
Change to Supporting Information: Changed Description
Accident and Emergency Initial Assessment Time is an ACTIVITY DATE TIME.An Accident and Emergency Initial Assessment Time is an ACTIVITY DATE TIME.
Accident and Emergency Initial Assessment Time is the time, recorded using the 24 hour clock, that the PATIENT is first assessed in the Accident and Emergency Department.An Accident and Emergency Initial Assessment Time is the time, recorded using the 24 hour clock, that the PATIENT is first assessed in the Accident and Emergency Department for first attendances and unplanned follow-up attendances.
Initial Assessment would include:An Initial Assessment would include:
- the taking of a brief PATIENT medical history
- pain assessment
- early warning scores (including vital signs)
The assessment should be conducted by medical or nursing staff who have received appropriate training.
Notes: For guidance on the use of this data item in the Accident and Emergency Clinical Quality Indicators, further information is available on the Department of Health website.For guidance on the use of this data item in the Accident and Emergency Clinical Quality Indicators, further information is available on the Health and Social Care Information Centre website.
Change to Supporting Information: Changed Description
Accident and Emergency Time Seen For Treatment is an ACTIVITY DATE TIME.An Accident and Emergency Time Seen For Treatment is an ACTIVITY DATE TIME.
Accident and Emergency Time Seen For Treatment is the time, recorded using the 24 hour clock, that the PATIENT is seen by a clinical decision maker (someone who can define the management plan and discharge the PATIENT) to diagnose the problem and arrange or start definite treatment as necessary.An Accident and Emergency Time Seen For Treatment is the time, recorded using the 24 hour clock, that the PATIENT is seen by a clinical decision maker (someone who can define the management plan and discharge the PATIENT) to diagnose the problem and arrange or start definite treatment as necessary.
Notes: For guidance on the use of this data item in the Accident and Emergency Clinical Quality Indicators, further information is available on the Department of Health website.For guidance on the use of this data item in the Accident and Emergency Clinical Quality Indicators, further information is available on the Health and Social Care Information Centre website.
Change to Supporting Information: Changed Description
This item has been retired from the NHS Data Model and Dictionary.
The last live version of this item is available in the ?????? release of the NHS Data Model and Dictionary.The last live version of this item is available in the September 2013 release of the NHS Data Model and Dictionary.
Access to this version can be obtained by emailing information.standards@hscic.gov.uk with "NHS Data Model and Dictionary - Archive Request" in the email subject line.
Change to Supporting Information: Changed Description
Arrival Date At Accident and Emergency Department is an ACTIVITY DATE TIME.An Arrival Date At Accident and Emergency Department is an ACTIVITY DATE TIME.
Arrival Date At Accident and Emergency Department is the date the PATIENT:An Arrival Date At Accident and Emergency Department is the date the PATIENT:
- self presented at the Accident and Emergency Department or
- arrived in an Ambulance at the Accident and Emergency Department.
Notes: For the Accident and Emergency Clinical Quality Indicators, for PATIENTS arriving by Emergency Ambulance, the Arrival Time At Accident and Emergency Department is when handover occurs, or 15 minutes after the Emergency Ambulance arrives at the Accident and Emergency Department, whichever is the sooner. Further guidance is available on the Department of Health website.For the Accident and Emergency Clinical Quality Indicators, for PATIENTS arriving by Emergency Ambulance, the Arrival Time At Accident and Emergency Department is when handover occurs, or 15 minutes after the Emergency Ambulance arrives at the Accident and Emergency Department, whichever is the sooner.
Change to Supporting Information: Changed Description
Arrival Time At Accident and Emergency Department is an ACTIVITY DATE TIME.An Arrival Time At Accident and Emergency Department is an ACTIVITY DATE TIME.
Arrival Time At Accident and Emergency Department is the time the PATIENT:An Arrival Time At Accident and Emergency Department is the time the PATIENT:
- self presented at the Accident and Emergency Department or
- arrived in an Ambulance at the Accident and Emergency Department.
The time should be recorded using the 24 hour clock.
Notes: For the Accident and Emergency Clinical Quality Indicators, for PATIENTS arriving by Emergency Ambulance, the Arrival Time At Accident and Emergency Department is when handover occurs, or 15 minutes after the Emergency Ambulance arrives at the Accident and Emergency Department, whichever is the sooner. Further guidance is available on the Department of Health website.For the Accident and Emergency Clinical Quality Indicators, for PATIENTS arriving by Emergency Ambulance, the Arrival Time At Accident and Emergency Department is when handover occurs, or 15 minutes after the Emergency Ambulance arrives at the Accident and Emergency Department, whichever is the sooner.
Change to Supporting Information: Changed Description
Arrival Time For Transport Requests is an ACTIVITY DATE TIME.An Arrival Time For Transport Requests is an ACTIVITY DATE TIME.
Arrival Time For Transport Requests is the time (for TRANSPORT REQUESTS) that the vehicle arrives at the specified destination.An Arrival Time For Transport Requests is the time (for TRANSPORT REQUESTS) that the vehicle arrives at the specified destination.
The time should be recorded using the 24 hour clock.
Change to Supporting Information: Changed Description
The Department of Health (DH) is an ORGANISATION.
The Department of Health helps people to live better for longer. They lead, shape and fund health and care in England, making sure people have the support, care and treatment they need, with the compassion, respect and dignity they deserve.
For further information on the Department of Health, see the Department of Health website.For further information on the Department of Health, see the Department of Health part of the gov.uk website.
The new health and care system became fully operational from 1 April 2013 to deliver the ambitions set out in the Health and Social Care Act 2012.A new health and care system became fully operational from 1 April 2013 to deliver the ambitions set out in the Health and Social Care Act 2012.
To achieve this, the Department of Health is supported by a number of agencies and public bodies, including:
For further information on the role of the Department of Health in the new system, see the Department of Health website.For further information on the role of the Department of Health in the new system, see the Department of Health part of the gov.uk website.
Change to Supporting Information: Changed Description
Elective Admission List is a WAITING LIST.An Elective Admission List is a WAITING LIST.
A list of PATIENTS, for whom a DECISION TO ADMIT has been made, currently awaiting admission regardless of whether a date to admit has been given. This list may be maintained in several forms, including CONSULTANTS' diaries.An Elective Admission List is a list of PATIENTS, for whom a DECISION TO ADMIT has been made, currently awaiting admission regardless of whether a date to admit has been given.
It does not include PATIENTS waiting for a first Out-Patient Attendance Consultant.An Elective Admission List does not include PATIENTS waiting for a first Out-Patient Attendance Consultant.
Lists can be maintained in several forms, using either computer or manual systems, including CONSULTANTS' diaries. They may be kept by TREATMENT FUNCTION CODE or for an individual CARE PROFESSIONAL. A PATIENT can be on more than one Elective Admission List. This may be because the PATIENT needs treatment for more than one condition or because the PATIENT has been placed on the list of more than one provider for the same condition.Elective Admission Lists:
- can be maintained in several forms, using either computer or manual systems, including CONSULTANTS' diaries
A PATIENT can be on more than one Elective Admission List. This may be because the PATIENT needs treatment for more than one condition or because the PATIENT has been placed on the list of more than one Health Care Provider for the same condition.
It is also possible for a PATIENT to be entered on an Elective Admission List more than once, either for a different condition or for the same condition, where two or more admissions are required. For example, a PATIENT would have two ELECTIVE ADMISSION LIST ENTRIES on a list where the intention was to perform two or more operations requiring two or more admissions, such as repair of inguinal hernia and operation on varicose veins. Only one ELECTIVE ADMISSION LIST ENTRY should be made in the event of the intention to perform two or more procedures during one admission.
PATIENTS already in a Hospital Bed who are waiting for transfer in the same Health Care Provider unit or to another Health Care Provider unit cannot be included in an Elective Admission List. Elective Admission List is only for PATIENTS without a current Hospital Provider Spell, waiting for admission to hospital to start a Hospital Provider Spell.
Change to Supporting Information: Changed Description
A Health and Wellbeing Board is an ORGANISATION.
A Health and Wellbeing Board (HWB) is a forum where key leaders from the health and care system work together to improve the health and wellbeing of their local population and reduce health inequalities.
Each Local Authority in England has a fully operational Health and Wellbeing Board.
For further information on Health and Wellbeing Boards, see the Department of Health website.For further information on Health and Wellbeing Boards, see the Health and Social Care Act 2012: fact sheets.
Change to Supporting Information: Changed Description
This item has been retired from the NHS Data Model and Dictionary.
The last live version of this item is available in the ?????? release of the NHS Data Model and Dictionary.The last live version of this item is available in the September 2013 release of the NHS Data Model and Dictionary.
Access to this version can be obtained by emailing information.standards@hscic.gov.uk with "NHS Data Model and Dictionary - Archive Request" in the email subject line.
Change to Supporting Information: Changed Description
Introduction
The National Interim Clinical Imaging Procedure Code Set (NICIP Code Set) is a comprehensive national standard set of codes and descriptions for imaging procedures and is maintained by the UK Terminology Centre. It is intended for use in all Imaging Department information systems.
Background
The NICIP Code Set has been approved by the Information Standards Board for Health and Social Care (ISB) and is mandated for all in-scope use cases. Further detail about the initial information standard and subsequent amendments can be found on the Information Standards Board for Health and Social Care website at: ISB 0148 "Interim Clinical Imaging Procedure Codes".
Distribution
The NICIP Code Set is released biannually. The release dates are the 1st of April and the 1st of October each year.
All versions of the NICIP Code Set, both with and without SNOMED CT maps, are only available from the Technology Reference Data Update Distribution Service (TRUD).
Changes to the Code Set
Clinicians and system managers working with the Picture Archiving and Communication Systems (PACS) and Radiology Information Systems (RIS) can make requests for additions to the NICIP Code Set. All requests must first be checked for conformance to the Editorial Principles. All requests must first be checked for conformance to the Editorial Principles.
Requests for changes to the NICIP Code Set should be made via the Information Standards Service Desk and clearly marked “Diagnostic Imaging."
For further information on the National Interim Clinical Imaging Procedure Code Set, see the UK Terminology website.For further information on the National Interim Clinical Imaging Procedure Code Set, see the UK Terminology website.
Change to Supporting Information: Changed Description
Neonatal Level Of Care Period is an ACTIVITY GROUP.A Neonatal Level Of Care Period is an ACTIVITY GROUP.
A period of time during a Hospital Provider Spell that a neonate is identified as receiving a particular level of care classified by the list in NEONATAL LEVEL OF CARE. Note that it is agreed nationally that the level of care should be recorded daily, as a minimum, but locally it may be desirable that it is recorded more frequently showing the time as well as date. During the Neonatal Level Of Care Period a number of PATIENT DIAGNOSES may be recorded.A Neonatal Level Of Care Period is a period of time during a Hospital Provider Spell that a Neonate is identified as receiving a particular level of care classified by the NEONATAL LEVEL OF CARE.
Information recorded for a Neonatal Level Of Care Period includes:Note that it is agreed nationally that the level of care should be recorded daily, as a minimum, but locally it may be desirable that it is recorded more frequently showing the time as well as date.
Change to Supporting Information: Changed Description
Nurse or Midwife Contact is a CARE CONTACT.A Nurse or Midwife Contact is a CARE CONTACT.
A contact, attendance or visit as defined in each of the following:A Nurse or Midwife Contact is a contact, attendance or visit as defined in each of the following:
There must be only one Nurse or Midwife Contact recorded for an actual face to face contact, classified in the above list, whether it be at a clinic or any other location at one Health Care Provider.There must be only one Nurse or Midwife Contact recorded for a face to face contact, whether it is at a clinic or any other location at one Health Care Provider.
There must be only one responsible NURSE or MIDWIFE for each Nurse or Midwife Contact.
Nursing contacts may actually be made either by qualified NURSES or by community support workers (nursing).Nursing contacts may be made either by qualified NURSES or by community support workers (nursing).
A Nurse or Midwife Contact may be made by one of the NURSE types classified in CARE PROFESSIONAL GROUP TYPE.
Change to Supporting Information: Changed Description
Nutritional Assessment is a CARE CONTACT.A Nutritional Assessment is a CARE CONTACT.
Nutritional Assessment is a dietary and weight assessment.A Nutritional Assessment is a dietary and weight assessment. This may be a partial or full assessment.
Change to Supporting Information: Changed Description
Introduction
The OPCS Classification of Interventions and Procedures (OPCS-4) is a Fundamental Information Standard. The classification is used by Health Care Providers and Strategic Health Authorities.
OPCS-4 is used to support operational and strategic planning, resource utilisation, performance management, reimbursement, research and epidemiology. It is used by NHS suppliers to build/update software to support NHS business functions and interoperability.
The OPCS-4 is subject to annual review and potential update to ensure that modern clinical practice is represented appropriately. This will be continued until further notice as shown below:
Year | Version of OPCS-4* |
Up to 31 March 2006 | OPCS-4.2 |
01-Apr-2006 to 31-Mar-2007 | OPCS-4.3 |
01-Apr-2007 to 31-Mar-2008 01-Apr-2008 to 31-Mar-2009 | OPCS-4.4 |
01-Apr-2009 to 31-Mar-2011 | OPCS-4.5 |
01-Apr-2011 until further notification | OPCS-4.6 |
*Tables of Coding Equivalences are issued for mapping back to previous versions are available from the Technology Reference Data Update Distribution Service (TRUD).
The NHS Data Model and Dictionary contains a number of data collections that require OPCS-4 codes, such as Central Returns and Commissioning Data Sets. All data collections should use the latest version of the OPCS-4 classification as specified in the table above.
Background
The classification of Surgical Operations and Procedures was originally issued by the Office of Population Censuses and Surveys (OPCS). The 4th revision was first implemented in hospital information systems in 1987. This was subject to a significant number of amendments and a consolidated version was reproduced in 1990.
The OPCS Classification of Surgical Operations and Procedures (OPCS-4.2) was substantially enhanced to ensure that modern clinical practice was represented appropriately within the classification and a new version was implemented in 2006 titled OPCS Classification of Interventions and Procedures (OPCS-4.3) with a commitment to undertake annual review and potential update. The classification comprises a list of alphanumeric codes with mainly anatomically based chapters, most of which relate to the whole or part of a body system. Each chapter is designated alphabetically e.g. Chapter A covers the nervous system and Chapter K is assigned to the heart. The alphabetic character for each chapter forms the prefix of the 3 and 4 digit codes within it. The strict link between chapters and body systems with specific procedures being listed for individual organs was breached in OPCS-4.3 because of limited capacity.
There are instances where an existing category needs extension because all the available codes have been allocated. In such cases an extended category is created within the Tabular List chapter. These categories are referred to as principal category or extended category and identified by an accompanying note to ease navigation.
Chapters that have reached capacity are extended using alphanumeric categories which are assigned using the free alpha O. This has occurred within three chapters (Chapters L, W and Z). Codes created in this way still form part of an existing chapter even though they have a different alpha prefix to the rest of that chapter. Such new codes will, therefore, logically sit at the end of the body system chapter and are readily identified within the alphabetical index. There is an additional chapter (Chapter X) for operations on multiple systems using miscellaneous procedures.
The classification is published in two volumes. The Tabular List and Alphabetical Index are available from The Stationery Office at www. The Tabular List and Alphabetical Index are available from The Stationery Office at www.tsoshop.co.uk
OPCS-4 Requests Portal
The OPCS-4 Requests Portal allows stakeholders to submit change requests to the NHS Classification Service all year round. A cut-off date is necessary to support the annual review of requests and business case to proceed with an update to the classification.
For further information and access to the OPCS-4 Requests Portal, see Submissions for review of OPCS-4.
High Cost Drugs and Chemotherapy Regimens
The listings of High Cost Drugs and Chemotherapy Regimens which are mapped to OPCS-4 codes are provided as look-up tables downloadable either from:
Change to Supporting Information: Changed Name
- Changed Name from Data_Dictionary.NHS_Business_Definitions.P.Person_Nationality_Or_Residency_Status to Data_Dictionary.NHS_Business_Definitions.P.Person_Nationality_or_Residency_Status
Change to Supporting Information: Changed Description
The Read Coded Clinical Terms are a comprehensive computerised coded thesaurus for use by clinicians. They are available in two main formats, known as Version 2 and Clinical Terms Version 3 (CTV3). They are designed for use in the electronic health care record. Clinical Terms Version 3 (CTV3) of the Read Codes is a "Superset" of all the codes from the earlier versions.
Read Coded Clinical Terms may be used for coding within local systems but are not acceptable directly for coding Hospital Episode Statistics which are extracted from the Admitted Patient Care Commissioning Data Sets. Version 2 and Clinical Terms Version 3 (CTV3) of the Read Codes contain mapping tables which can be used to generate ICD-10 and OPCS-4 codes.
For further information on Read Coded Clinical Terms, see Read Codes.For further information on Read Coded Clinical Terms, see Read Codes.
Change to Supporting Information: Changed Description
This return is out of date therefore the information should not be used.
For the latest version of the guidance, please see the Department of Health part of the gov.uk website at: Stop Smoking Service: monitoring and guidance update.
- Smoking is one of the most significant contributing factors to life expectancy, health inequalities and ill health, particularly cancer and coronary heart disease.
The Department of Health requires information on services provided by NHS Health Care Providers.
- The Stop Smoking Services Quarterly Data Set provides essential information used to monitor the process of achieving the NHS targets to increase life expectancy at birth in England and to monitor the performance of Stop Smoking Services.
Collection and Submission
This return relates to ACTIVITY taking place over a 3 month period. The return is made quarterly and should be submitted by the thirty second working day after the end of the quarter to which it relates.
This data should be submitted for each Primary Care Trust.
The data should be collected on responsible Primary Care Trust basis. The Primary Care Trust's responsible population comprises:
- all PERSONS registered with a GP Practice that forms part of the Primary Care Trust, regardless of where the PERSON is resident, plus any PERSONS not registered with a GP Practice who are resident within the Primary Care Trust's statutory geographical boundary.
- Note that PERSONS resident within the Primary Care Trust's statutory geographical boundary, but registered with a GP Practice that forms part of another Primary Care Trust, are the responsibility of that other Primary Care Trust.
- The only exception to the above rules is where PERSONS receive a Stop Smoking Service at or near their workplace, which may be some distance from their home. For example, a Stop Smoking Service might be provided for commuters at their workplace in a large city. In such circumstances it is likely that people will be drawn from a range of places in the surrounding area e.g. commuters to London who live all around the south-east of England. Where a PERSON is judged to meet these criteria, the Primary Care Trust providing the Stop Smoking Service should include these people in their returns.
- all PERSONS registered with a GP Practice that forms part of the Primary Care Trust, regardless of where the PERSON is resident, plus any PERSONS not registered with a GP Practice who are resident within the Primary Care Trust's statutory geographical boundary.
The information in this Central Return Data Set is transmitted at aggregate level to the Health and Social Care Information Centre's web based data collection systems at https://stopsmokingservices.hscic.gov.uk/welcome.aspx. NHS providers enter their data directly.
Further information on the NHS Stop Smoking Services and the monitoring guidance can be found on the Department of Health part of the gov.uk website at Stop Smoking Service: monitoring and guidance update.
Synopsis of Data Set Content
The Stop Smoking Services Quarterly Data Set requires the REPORTING PERIOD START DATE and REPORTING PERIOD END DATE for the quarter to which it relates.
The collection is for:
- Part 1A - The number of PERSONS with a Person Stop Smoking Episode setting a SMOKING QUIT DATE and successfully quitting by ETHNIC CATEGORY and PERSON GENDER. Pregnant women should be included but not separately identified.
- Part 1B - The number of PERSONS setting a SMOKING QUIT DATE by AGE BAND AT SMOKING QUIT DATE and PERSON GENDER together with the outcome at 4 week follow-up. Pregnant women should be included but not separately identified.
- Part 1C - The number of PERSONS with a PREGNANCY STATUS of 'Yes' at the time of the SMOKING QUIT DATE and the outcome at 4 week follow-up.
- Part 1D - The number of PERSONS setting a SMOKING QUIT DATE and successful quitters with a FREE PRESCRIPTIONS INDICATOR of 'Entitled to free prescriptions'.
- Part 1E - The number of PERSONS setting a SMOKING QUIT DATE and successful quitters by SOCIO-ECONOMIC CLASSIFICATION
- Part 1F - The number of PERSONS setting a SMOKING QUIT DATE and successful quitters by PHARMACOTHERAPY STOP SMOKING AID RECEIVED
- Part 1G - The number of PERSONS setting a SMOKING QUIT DATE and successful quitters by INTERVENTION SESSION TYPE
- Part 1H - The number of PERSONS setting a SMOKING QUIT DATE and successful quitters by INTERVENTION SETTING
- Part 2A - Financial Allocations for the year by type of allocation. (See STOP SMOKING SERVICE PCT FINANCIAL ALLOCATION and
STOP SMOKING SERVICE OTHER FINANCIAL ALLOCATION.)
Figures should be to the nearest pound. - Part 2B - Cumulative total spend on Stop Smoking Services in the year up to the REPORTING PERIOD END DATE.
(See STOP SMOKING SERVICE CUMULATIVE TOTAL SPEND.)
Parts 2A and 2B should include all monies from whatever source which have been specifically allocated to, or spent on, Stop Smoking Services e.g. additional funding such as Neighbourhood Renewal Funding.
Figures should be to the nearest pound.
- Part 1A - The number of PERSONS with a Person Stop Smoking Episode setting a SMOKING QUIT DATE and successfully quitting by ETHNIC CATEGORY and PERSON GENDER. Pregnant women should be included but not separately identified.
Change to Class: Changed Relationships
Change to Class: Changed Supertype
- Changed Supertype from Data_Dictionary.Classes.P.PERSON_PROPERTY to null
Change to Class: Changed Attributes
Change to Class: Changed Attributes
APGAR SCORE 10 MINUTES | ||
APGAR SCORE 1 MINUTE | ||
APGAR SCORE 5 MINUTES | ||
BCG ADMINISTERED | ||
BIRTH ORDER | ||
DELIVERY METHOD | ||
DELIVERY PLACE TYPE | ||
DELIVERY TIME | ||
EXAMINATION OF HIPS | ||
FOLLOW UP CARE | ||
GESTATION LENGTH IN DAYS | ||
GESTATION LENGTH IN WEEKS | ||
LIVE OR STILL BIRTH | ||
METABOLIC SCREENING | ||
MODE OF DELIVERY | ||
NUMBER OF BABIES IDENTIFIER | ||
PARENTS CONSANGUINEOUS INDICATOR | ||
PRESENCE OF JAUNDICE | ||
PRESENTATION AT ONSET OF LABOUR | ||
PRESENTATION OF FETUS | ||
RESUSCITATION METHOD DRUGS | ||
RESUSCITATION METHOD POSITIVE PRESSURE | ||
STATUS OF PERSON CONDUCTING DELIVERY |
Change to Class: Changed Description
REFERRAL REQUESTDIAGNOSTIC TEST REQUESTPRESCRIPTIONA request for the provision of care services to a PATIENT.
A request for the provision of care services to a PATIENT.Subtypes of SERVICE REQUEST are:
Change to Attribute: Changed Description
The means by which a PATIENT arrived at an Accident and Emergency Department.The mode by which a PATIENT arrived at an Accident and Emergency Department.
National Codes:
1 | Brought in by Emergency Ambulance (including helicopter/'Air Ambulance') |
2 | Other |
Notes: For guidance on the use of this data item in the Accident and Emergency Clinical Quality Indicators, further information is available on the Department of Health website.For guidance on the use of this data item in the Accident and Emergency Clinical Quality Indicators, further information is available on the Health and Social Care Information Centre website.
Change to Attribute: Changed Description
A code to identify how an Accident and Emergency Attendance might end.
National Codes:
01 | Admitted to a Hospital Bed /became a LODGED PATIENT of the same Health Care Provider |
02 | Discharged - follow up treatment to be provided by GENERAL PRACTITIONER |
03 | Discharged - did not require any follow up treatment |
04 | Referred to A&E Clinic |
05 | Referred to Fracture Clinic |
06 | Referred to other Out-Patient Clinic |
07 | Transferred to other Health Care Provider |
10 | Died in DEPARTMENT |
11 | Referred to other health CARE PROFESSIONAL |
12 | Left DEPARTMENT before being seen for treatment |
13 | Left DEPARTMENT having refused treatment |
14 | Other |
Notes: For the Accident and Emergency Clinical Quality Indicators, further guidance on National Code 'Left DEPARTMENT before being seen for treatment' is available on the Department of Health website.For the Accident and Emergency Clinical Quality Indicators, further guidance on National Code 'Left DEPARTMENT before being seen for treatment' is available on the Health and Social Care Information Centre website.
Change to Attribute: Changed Description
A classification of Accident and Emergency Department according to the ACTIVITY performed.The type of Accident and Emergency Department according to the ACTIVITY performed.
National Codes:
01 | Emergency departments are a CONSULTANT led 24 hour service with full resuscitation facilities and designated accommodation for the reception of accident and emergency PATIENTS |
02 | Consultant led mono specialty accident and emergency service (e.g. ophthalmology, dental) with designated accommodation for the reception of PATIENTS |
03 | Other type of A&E/minor injury ACTIVITY with designated accommodation for the reception of accident and emergency PATIENTS. The department may be doctor led or NURSE led and treats at least minor injuries and illnesses and can be routinely accessed without APPOINTMENT. A SERVICE mainly or entirely APPOINTMENT based (for example a GP Practice or Out-Patient Clinic) is excluded even though it may treat a number of PATIENTS with minor illness or injury. Excludes NHS walk-in centres |
04 | NHS walk in centres |
Change to Attribute: Changed Name
- Changed Name from Data_Dictionary.Attributes.A.Ap.APGAR_SCORE_10_MINUTE to Data_Dictionary.Attributes.A.Ap.APGAR_SCORE_10_MINUTES
Change to Attribute: Changed Name
- Changed Name from Data_Dictionary.Attributes.A.Ap.APGAR_SCORE_5_MINUTE to Data_Dictionary.Attributes.A.Ap.APGAR_SCORE_5_MINUTES
Change to Attribute: Changed Description
This item has been retired from the NHS Data Model and Dictionary.
The last live version of this item is available in the ?????? release of the NHS Data Model and Dictionary.The last live version of this item is available in the September 2013 release of the NHS Data Model and Dictionary.
Access to this version can be obtained by emailing information.standards@hscic.gov.uk with "NHS Data Model and Dictionary - Archive Request" in the email subject line.
Change to Attribute: Changed Description
The date on which the decision was made to refer a PATIENT with suspected cancer to an appropriate cancer specialist.
An appropriate cancer specialist is the PERSON who is most able to progress the diagnosis of the primary Tumour.
This date will be one of the following:
Change to Attribute: Changed Description
The type of CARE CONTACT.
National Codes:
Note: The list is not in alphabetical order.
Change to Attribute: Changed Description
An indication of whether or not carer support is available to the PATIENT at their normal residence. This does not include any paid support or support from a voluntary organisation, unless the PATIENT is normally resident in a Care Home.An indication of whether carer support is available to the PATIENT at their normal residence.
This does not include any paid support or support from a voluntary organisation, unless the PATIENT is normally resident in a Care Home.
National Codes:
01 | Yes |
02 | No |
Change to Attribute: Changed Description
The date the decison was made to offer an APPOINTMENT to a PATIENT following the receipt of an Appointment Request. It is on this date it is considered that the PATIENT has been added to the APPOINTMENT WAITING LIST for the APPOINTMENT with the expectation that it will take place.
It is on this date it is considered that the PATIENT has been added to the APPOINTMENT WAITING LIST for the APPOINTMENT with the expectation that it will take place.
One or more APPOINTMENT OFFERS with different dates should then be offered to the PATIENT for the APPOINTMENT.
Change to Attribute: Changed Description
An indication of whether or not the Drug Misuser has ever injected.An indication of whether the Drug Misuser has ever injected.
Classification:
a. | Yes |
b. | No |
Change to Attribute: Changed Description
An indication of whether or not a shared injecting equipment has ever been used by a Drug Misuser.An indication of whether a shared injecting equipment has ever been used by a Drug Misuser.
Classification:
a. | Yes |
b. | No |
Change to Attribute: Changed Description
This indicates whether a PATIENT is making a first attendance or contact; or a follow-up attendance or contact.An indication of whether a PATIENT is making a first attendance or contact; or a follow-up attendance or contact and whether the CONSULTATION MEDIUM USED national code was 'Face to face communication' or 'Telephone' or 'Telemedicine web camera'.
A first attendance is the first in a series, or only attendance of an APPOINTMENT which took place regardless of how many previous APPOINTMENTS were made which did not take place for whatever reason. All subsequent attendances in the series which take place should be recorded as follow-up.
National Codes:
1 | First attendance face to face |
2 | Follow-up attendance face to face |
3 | First telephone or telemedicine consultation |
4 | Follow-up telephone or telemedicine consultation |
5 | Referral To Treatment Clock Stop Administrative Event* |
*Referral to Treatment Clock Stop Administrative Event allows the Secondary Uses Service to build accurate PATIENT PATHWAYS for the reporting of 18 weeks activity.Note: *Referral to Treatment Clock Stop Administrative Event allows the Secondary Uses Service to build accurate PATIENT PATHWAYS for the reporting of 18 weeks activity. It flows through the CDS V6-1 Type 020 - Outpatient Commissioning Data Set/CDS V6-2 Type 020 - Outpatient Commissioning Data Set structure. See Referral To Treatment Clock Stop Administrative Event.
Change to Attribute: Changed Description
Someone is entitled to get free prescriptions if they:Someone is entitled for free prescriptions if they:
- are under 16
- are under 19 and in full-time education
- are aged 60 or over
- get Income Support, Income-based Jobseeker's Allowance or Pension Credit Guarantee Credit
- have an NHS tax credit exemption certificate
- have a prescription exemption certificate (pregnant or have had a child in the past year or have a qualifying medical condition)
- are on a low income and have an HC2 certificate
- are a war pensioner if treatment is connected with the pensionable disability
National Codes:
01 | Eligible for free prescriptions |
02 | Not eligible |
Change to Attribute: Changed Description
A classifier of whether or not there was an intervention during an Imaging or Radiodiagnostic Event. This is regardless of whether or not the intervention was successful or it failed.An indication of whether there was an intervention during an Imaging or Radiodiagnostic Event.
This is regardless of whether or not the intervention was successful or it failed. An intervention is any invasive procedure during imaging which is performed for purposes other than primarily for introduction of a contrast medium.
Classification:
a. | Yes |
b. | No |
Change to Attribute: Changed Description
An indicator of whether or not an invasive breast cancer detected is a special type.An indication of whether an invasive breast cancer detected is a special type.
National Codes:
Y | Yes |
N | No |
Change to Attribute: Changed Description
The date on which an OFFERED FOR ADMISSION DATE of an OFFER OF ADMISSION is accepted by, or on behalf of a PATIENT.
ADMISSION OFFER OUTCOME records whether or not the admission took place on the OFFERED FOR ADMISSION DATE.ADMISSION OFFER OUTCOME records whether the admission took place on the OFFERED FOR ADMISSION DATE.
Change to Attribute: Changed Description
National Codes:
1 | Hospital provided |
2 | Privately arranged |
3 | Other |
Change to Attribute: Changed Description
An indication of whether a PATIENT TRANSPORT JOURNEY is a return journey.
National Codes:
Y | Yes |
N | No |
Change to Attribute: Changed Description
Change to Attribute: Changed Description
Change to Attribute: Changed Description
An indication of whether or not injecting equipment was shared with another Drug Misuser during the last four weeks.An indication of whether injecting equipment was shared with another Drug Misuser during the last four weeks.
Classification:
a. | Yes |
b. | No |
Change to Attribute: Changed Description
National Codes:
01 | An Emergency Ambulance |
02 | A Rapid Response Vehicle |
03 | An approved First Responder equipped with a defibrillator, who is accountable to the Ambulance Service |
Change to Attribute: Changed Description
Identifies the type of WAITING LIST.The type of WAITING LIST.
National Codes:
01 | Elective Admission List |
02 | Out-Patient Waiting List |
Change to Data Element: Changed Description
Format/Length: | an2 |
HES Item: | |
National Codes: | See ACCIDENT AND EMERGENCY DEPARTMENT TYPE |
Default Codes: |
Notes:
A and E DEPARTMENT TYPE is the same as attribute ACCIDENT AND EMERGENCY DEPARTMENT TYPE.
Change to Data Element: Changed Description
Format/Length: | max n7 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
ADMITTED ADULT PATIENTS IN MONTH TOTAL is the total number of adult PATIENTS (aged 18 and over) admitted to a Hospital Provider in the month, for all PATIENT CLASSIFICATIONS.
Change to Data Element: Changed Description
Format/Length: | max n7 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
ADMITTED ADULT PATIENTS RISK ASSESSED FOR VENOUS THROMBOEMBOLISM IN MONTH TOTAL is the total number of adult PATIENTS (aged 18 and over) admitted to a Hospital Provider in the month, for all PATIENT CLASSIFICATIONS, who are risk assessed using the Venous Thromboembolism Risk Assessment Tool.
Change to Data Element: Changed Description
Format/Length: | an1 |
HES Item: | |
National Codes: | See CALCULATED CREATININE CLEARANCE TYPE |
Default Codes: |
Notes:
CALCULATED CREATININE CLEARANCE TYPE is the same as attribute CALCULATED CREATININE CLEARANCE TYPE.
Change to Data Element: Changed Description
Format/Length: | an1 |
HES Item: | |
National Codes: | See CANCER SCREENING STATUS |
Default Codes: | 9 - Not Known (PATIENT cancer screening status unknown) |
Notes:
CANCER SCREENING STATUS is the same as attribute CANCER SCREENING STATUS.
Change to Data Element: Changed Description
Format/Length: | an1 |
HES Item: | |
National Codes: | See CANCER TREATMENT INTENT |
Default Codes: | 9 - Not known (Not Recorded) |
Notes:
CANCER TREATMENT INTENT is the same as attribute CANCER TREATMENT INTENT.
Change to Data Element: Changed Description
Format/Length: | an1 |
HES Item: | |
National Codes: | See CAPSULE STATUS |
Default Codes: |
Notes:
CAPSULE STATUS is the same as attribute CAPSULE STATUS.
Change to Data Element: Changed Description
Format/Length: | n2.n2 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes: The CARDIOVASCULAR DISEASE RISK SCORE is the PERSON SCORE calculated from the Cardiovascular Disease Risk Calculator.
Change to Data Element: Changed Description
Format/Length: | an10 CCYY-MM-DD |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
DATE is the day, month, year and century, or any combination of these elements, of an event.
DATE should be used for all new and developing systems and for XML messages.
Note:
This was e-GIF approved for use in NHS England.
e-GIF and the Government Data Standards Catalogue have been archived and are available for reference only.
Change to Data Element: Changed Description
Format/Length: | See DATE |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
DATE FIRST SEEN (RENAL PHYSICIAN) is the DATE the PATIENT is first seen by a renal specialist.
This may be following the first referral to a CONSULTANT working from a renal unit providing Renal Dialysis, leading to continuous follow up care.
Change to Data Element: Changed Description
Format/Length: | See DATE AND TIME |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
DATE TIME OF BIRTH (BABY) is the same as data element DATE AND TIME, from the End Date and End Time of the Fetus Episode.
The DATE corresponds to:
a | the PERSON BIRTH DATE of the baby, where a REGISTRABLE BIRTH was recorded | |
or | ||
b | the recorded End Date of the Fetus Episode, where the PATIENT miscarried a Fetus during the associated Maternity Episode i.e. where the pregnancy ends in or before the 24th week of gestation (which excludes it being recorded as a REGISTRABLE BIRTH). |
Note that for the National Neonatal Data Set - Episodic and Daily Care the baby is always a REGISTRABLE BIRTH so b) above does not apply.
Change to Data Element: Changed Description
Format/Length: | an1 |
HES Item: | |
National Codes: | See DEATH LOCATION TYPE |
Default Codes: |
Notes:
DEATH LOCATION TYPE (ACTUAL) is the same as attribute DEATH LOCATION TYPE.
The actual place where the PATIENT died.DEATH LOCATION TYPE (ACTUAL) is the actual place where the PATIENT died.
Change to Data Element: Changed Description
Format/Length: | an1 |
HES Item: | |
National Codes: | See DEATH LOCATION TYPE |
Default Codes: | 9 - The CARE PROFESSIONAL did not discuss the preferred place of death prior to the death of the PATIENT |
Notes:
DEATH LOCATION TYPE (PREFERRED) is the same as attribute DEATH LOCATION TYPE.
This is the preferred place of death as specified by the PATIENT.DEATH LOCATION TYPE (PREFERRED) is the preferred place of death as specified by the PATIENT.
Change to Data Element: Changed Description
Format/Length: | max an5 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
FINAL FIGO STAGE is the same as attribute CLINICAL CLASSIFICATION CODE.
FINAL FIGO STAGE is the final International Federation of Gynecology and Obstetrics (FIGO) stage as agreed by the Multidisciplinary Team at PATIENT DIAGNOSIS for a PATIENT during a Gynaecological Cancer Care Spell.
Change to Data Element: Changed Description
Format/Length: | max n4 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
FINAL OUTCOME OF ASSESSMENT CANCER DIAGNOSED TOTAL is the total number of women who attend a Breast Assessment and after further diagnostic tests have a BREAST ASSESSMENT OUTCOME recorded as National Code 'Cancer diagnosed'.
Change to Data Element: Changed Description
Format/Length: | max n4 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
FINAL OUTCOME OF ASSESSMENT FAILED TO ATTEND TOTAL is the total number of women who were sent an APPOINTMENT to attend a Breast Assessment and have a BREAST ASSESSMENT OUTCOME recorded as National Code 'Failed to attend for assessment'.
Change to Data Element: Changed Description
Format/Length: | max n4 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
FINAL OUTCOME OF ASSESSMENT NOT KNOWN TOTAL is the total number of women who attend a Breast Assessment and have a BREAST ASSESSMENT OUTCOME recorded as National Code 'Not known'.
Change to Data Element: Changed Description
Format/Length: | max n4 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
FINAL OUTCOME OF ASSESSMENT ROUTINE RECALL TOTAL is the total number of women who attend a Breast Assessment and after further diagnostic tests have a BREAST ASSESSMENT OUTCOME recorded as National Code 'Routine recall'.
Change to Data Element: Changed Description
Format/Length: | max n4 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
FINAL OUTCOME OF ASSESSMENT SHORT TERM RECALL TOTAL is the total number of women who attend a Breast Assessment and after further diagnostic tests have a BREAST ASSESSMENT OUTCOME recorded as National Code 'Short term recall'.
Change to Data Element: Changed Description
Format/Length: | an1 |
HES Item: | |
National Codes: | See FIRST ATTENDANCE |
Default Codes: |
Notes:
FIRST ATTENDANCE CODE is the same as attribute FIRST ATTENDANCE.
FIRST ATTENDANCE CODE indicates whether a PATIENT is making a FIRST ATTENDANCE or follow-up attendance or contact and whether the CONSULTATION MEDIUM USED national code was 'Face to face communication', 'Telephone' or 'Telemedicine web camera'.
A FIRST ATTENDANCE is the first in a series, or only attendance of an APPOINTMENT which took place regardless of how many previous APPOINTMENTS were made which did not take place for whatever reason. All subsequent attendances in the series which take place should be recorded as follow-up.
FIRST ATTENDANCE National Code 5 - "Referral to Treatment Clock Stop Administrative Event" allows the Secondary Uses Service to build accurate PATIENT PATHWAYS for the reporting of 18 weeks activity. It flows through the CDS V6-2 Type 020 - Outpatient CDS structure. See Referral To Treatment Clock Stop Administrative Event.
FIRST ATTENDANCE CODE replaces FIRST ATTENDANCE, and should be used for all new and developing data sets and for XML messages.
Change to Data Element: Changed Description
Format/Length: | an1 |
HES Item: | |
National Codes: | See GENDER IDENTITY CODE FOR HIV |
Default Codes: |
Notes:
GENDER IDENTITY CODE (HIV) is the same as attribute GENDER IDENTITY CODE FOR HIV.
Change to Data Element: Changed Description
Format/Length: | max n2 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
GENERALISED ANXIETY DISORDER PENN STATE WORRY SCORE is the PERSON SCORE for an APPOINTMENT where the ASSESSMENT TOOL TYPE is 'Generalised Anxiety Disorder Penn State Worry Questionnaire'.
The score will be between 16 and 80.
If one or two values are missing from the score, then they can be substituted with the average score of the non-missing items. Questionnaires with more than two missing values should be disregarded.
Change to Data Element: Changed Description
Format/Length: | max n2 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
GENERALISED ANXIETY DISORDER SCORE is the PERSON SCORE for an APPOINTMENT where the ASSESSMENT TOOL TYPE is 'Generalised Anxiety Disorder Questionnaire'.
The score will be between 0 and 21.
If one or two values are missing from the score, then they can be substituted with the average score of the non-missing items. Questionnaires with more than two missing values should be disregarded.
Change to Data Element: Changed Description
Format/Length: | an1 |
HES Item: | |
National Codes: | See GENETIC CONFIRMATION INDICATOR |
Default Codes: | X - Test not done |
Notes:
GENETIC CONFIRMATION INDICATOR is the same as attribute GENETIC CONFIRMATION INDICATOR.
Change to Data Element: Changed Description
Format/Length: | See HAEMOGLOBIN CONCENTRATION |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
HAEMOGLOBIN CONCENTRATION (PRE-DIALYSIS) is the same as data element HAEMOGLOBIN CONCENTRATION where this is recorded pre-dialysis.
Change to Data Element: Changed Description
Format/Length: | See HAEMOGLOBIN CONCENTRATION |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
HAEMOGLOBIN CONCENTRATION (PRIOR END STAGE RENAL FAILURE) is the same as data element HAEMOGLOBIN CONCENTRATION where this is recorded prior to the start of end stage renal failure.
Change to Data Element: Changed Description
Format/Length: | an1 |
HES Item: | |
National Codes: | See IMAGING OR RADIODIAGNOSTIC EVENT INDICATION CODE FOR RENAL CARE |
Default Codes: |
Notes:
IMAGING OR RADIODIAGNOSTIC X-RAY (CHEST) is the same as attribute IMAGING OR RADIODIAGNOSTIC EVENT INDICATION CODE FOR RENAL CARE.
Change to Data Element: Changed Description
Format/Length: | an1 |
HES Item: | |
National Codes: | See KEY WORKER SEEN INDICATOR |
Default Codes: | 9 - Not Known (Not Recorded) |
Notes:
KEY WORKER SEEN INDICATOR (CANCER RECURRENCE) is the same as attribute KEY WORKER SEEN INDICATOR for a recurrence of cancer.
Change to Data Element: Changed Description
Format/Length: | an2 |
HES Item: | |
National Codes: | See KIDNEY PERFUSION FLUID TYPE |
Default Codes: | 99 - Unknown |
Notes:
KIDNEY PERFUSION FLUID TYPE is the same as attribute KIDNEY PERFUSION FLUID TYPE.
Change to Data Element: Changed Description
Format/Length: | an1 |
HES Item: | |
National Codes: | See KIDNEY PERFUSION QUALITY CODE |
Default Codes: | 9 - Unknown |
Notes:
KIDNEY PERFUSION QUALITY CODE (RIGHT KIDNEY) is the same as attribute KIDNEY PERFUSION QUALITY CODE for the right kidney.
Change to Data Element: Changed Description
Format/Length: | an2 |
HES Item: | |
National Codes: | See KIDNEY RETRIEVED CODE |
Default Codes: |
Notes:
KIDNEY RETRIEVED CODE is the same as attribute KIDNEY RETRIEVED CODE.
Change to Data Element: Changed Description
Format/Length: | an2 |
HES Item: | |
National Codes: | See KIDNEY TRANSPLANTED CODE |
Default Codes: |
Notes:
KIDNEY TRANSPLANTED CODE is the same as attribute KIDNEY TRANSPLANTED CODE.
Change to Data Element: Changed Description
Format/Length: | an5 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
LABORATORY CODE is the same as attribute LABORATORY CODE.
Change to Data Element: Changed Description
Format/Length: | See DATE |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
LAST MENSTRUAL PERIOD DATE is the same as attribute LAST MENSTRUAL PERIOD DATE.
Change to Data Element: Changed Description
Format/Length: | an2 |
HES Item: | |
National Codes: | See MAIN SPECIALTY CATEGORY CODE FOR BED AVAILABILITY AND OCCUPANCY |
Default Codes: |
Notes:
MAIN SPECIALTY CATEGORY CODE FOR BED AVAILABILITY AND OCCUPANCY is the same as attribute MAIN SPECIALTY CATEGORY CODE FOR BED AVAILABILITY AND OCCUPANCY.
For the purposes of the Quarterly Bed Availability and Occupancy Data Set (KH03), the mapping of CARE PROFESSIONAL MAIN SPECIALTY CODES applicable to each MAIN SPECIALTY CATEGORY CODE FOR BED AVAILABILITY AND OCCUPANCY is available by emailing Unify@dh.gsi.gov.uk.
Change to Data Element: Changed Description
Format/Length: | an10 |
HES item: | |
National Codes: | |
Default Codes: |
Notes: MANTOUX TESTS PERFORMED TOTAL (TUBERCULOSIS) reports the total number Mantoux Tests performed for each IMMUNISATION AGE GROUP (TUBERCULOSIS), within a REPORTING PERIOD.
Change to Data Element: Changed Description
Format/Length: | an1 |
HES Item: | |
National Codes: | See PALLIATIVE TREATMENT REASON CODE FOR UPPER GASTROINTESTINAL |
Default Codes: |
Notes:
PALLIATIVE TREATMENT REASON CODE (UPPER GASTROINTESTINAL) is the same as attribute PALLIATIVE TREATMENT REASON CODE FOR UPPER GASTROINTESTINAL.
Change to Data Element: Changed Description
Format/Length: | max n2 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
PANIC DISORDER SEVERITY SCALE SCORE is the PERSON SCORE for an APPOINTMENT where the ASSESSMENT TOOL TYPE is 'Panic Disorder Severity Scale'.
The score will be between 0 and 28.
Change to Data Element: Changed Description
Format/Length: | an1 |
HES Item: | |
National Codes: | See PARACERVICAL OR PARAMETRIAL INVOLVEMENT INDICATOR |
Default Codes: |
Notes:
PARACERVICAL OR PARAMETRIAL INVOLVEMENT INDICATOR is the same as attribute PARACERVICAL OR PARAMETRIAL INVOLVEMENT INDICATOR.
Change to Data Element: Changed Description
Change to Data Element: Changed Description
Format/Length: | n6 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes: The number of completed REFERRAL TO TREATMENT PERIODS during the REPORTING PERIOD reported by
- the REFERRAL TO TREATMENT PERIOD TIME BAND of the REFERRAL TO TREATMENT PERIOD DURATION (ADJUSTED) in completed weeks
and
- TREATMENT FUNCTION CODE (REFERRAL TO TREATMENT PERIOD).
Change to Data Element: Changed Description
Format/Length: | n6 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes: The number of completed REFERRAL TO TREATMENT PERIODS during the REPORTING PERIOD reported by
Change to Data Element: Changed Description
Format/Length: | n6 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes: The number of completed REFERRAL TO TREATMENT PERIODS during the reporting month where the PATIENT was referred to a CONSULTANT and where there is no Hospital Provider Spell within the REFERRAL TO TREATMENT PERIOD reported by REFERRAL TO TREATMENT PERIOD TIME BAND and TREATMENT FUNCTION CODE (REFERRAL TO TREATMENT PERIOD).
- there is no Hospital Provider Spell within the REFERRAL TO TREATMENT PERIOD reported by REFERRAL TO TREATMENT PERIOD TIME BAND and TREATMENT FUNCTION CODE (REFERRAL TO TREATMENT PERIOD).
The number of completed weeks is the period from the REFERRAL TO TREATMENT PERIOD START DATE and the REFERRAL TO TREATMENT PERIOD END DATE.
That is the number of REFERRAL TO TREATMENT PERIODS where:
a. | the REFERRAL TO TREATMENT PERIOD has a REFERRAL TO TREATMENT PERIOD END DATE within the REPORTING PERIOD. | ||
and | |||
b. | the SERVICE REQUEST is made to a CONSULTANT ORGANISATION | ||
and | |||
c. | the ACTIVITY is a SERVICE PROVIDED UNDER AGREEMENT | ||
i.e. only commissioned care is included, private PATIENTS and PATIENTS who are Overseas Visitors are excluded. | |||
and | |||
d. | the ACTIVITY that ends the REFERRAL TO TREATMENT PERIOD is not a Hospital Provider Spell |
Change to Data Element: Changed Description
Format/Length: | n7 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
The total number of REFERRAL TO TREATMENT PERIODS with a REFERRAL TO TREATMENT PERIOD END DATE during the REPORTING PERIOD, excluding those REFERRAL TO TREATMENT PERIODS with an unknown REFERRAL TO TREATMENT PERIOD START DATE.
Change to Data Element: Changed Description
Format/Length: | n7 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
The total number of REFERRAL TO TREATMENT PERIODS with a REFERRAL TO TREATMENT PERIOD END DATE during the REPORTING PERIOD, including those REFERRAL TO TREATMENT PERIODS with an unknown REFERRAL TO TREATMENT PERIOD START DATE.
Change to Data Element: Changed Description
Format/Length: | n7 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
The number of REFERRAL TO TREATMENT PERIODS with a REFERRAL TO TREATMENT PERIOD END DATE during the REPORTING PERIOD, reported by REFERRAL TO TREATMENT PERIOD TIME BAND.
Change to Data Element: Changed Description
Format/Length: | n4 |
HES Item: | |
National Codes: | |
Default Codes: | 9997 - 9997 days or more |
9998 - Not applicable | |
9999 - Not known (i.e. no date known for REFERRAL TO TREATMENT PERIOD END DATE) |
The duration (or anticipated duration) of a REFERRAL TO TREATMENT PERIOD adjusted to take account of the duration of the time between the earliest of at least two Reasonable Offers and the date from which the PATIENT makes themselves available again for admission.
Notes:
REFERRAL TO TREATMENT PERIOD DURATION (ADJUSTED) is the duration (or anticipated duration) of a REFERRAL TO TREATMENT PERIOD adjusted to take account of the duration of the time between the earliest of at least two Reasonable Offers and the date from which the PATIENT makes themselves available again for admission.
- For a REFERRAL TO TREATMENT PERIOD which does not end with First Definitive Treatment during an Elective Admission it is the same as REFERRAL TO TREATMENT PERIOD DURATION (UNADJUSTED).
- For a REFERRAL TO TREATMENT PERIOD which ends with First Definitive Treatment during an Elective Admission and the PATIENT has declined at least two Reasonable Offers, it is REFERRAL TO TREATMENT PERIOD DURATION (UNADJUSTED) less the number of completed days between the EARLIEST REASONABLE OFFER DATE of the Elective Admission and the REFERRAL TO TREATMENT PERIOD END DATE.
- For a REFERRAL TO TREATMENT PERIOD which ends with First Definitive Treatment during an Elective Admission where the PATIENT has not declined at least two Reasonable Offers, it is the same as REFERRAL TO TREATMENT PERIOD DURATION (UNADJUSTED).
Example:
Where a REFERRAL TO TREATMENT PERIOD which ends with First Definitive Treatment during an Elective Admission has a REFERRAL TO TREATMENT PERIOD START DATE of 1 January, REFERRAL TO TREATMENT PERIOD END DATE of 30 January and EARLIEST REASONABLE OFFER DATE of 28 January the REFERRAL TO TREATMENT PERIOD DURATION (ADJUSTED) will be 0027 days (29 days REFERRAL TO TREATMENT PERIOD DURATION (UNADJUSTED) less 2 days for the adjustment).
Change to Data Element: Changed Description
Format/Length: | n4 |
HES Item: | |
National Codes: | |
Default Codes: | 9997 - 9997 days or more |
9998 - Not applicable | |
9999 - Not known (i.e. no date known or planned for REFERRAL TO TREATMENT PERIOD END DATE) |
Notes:
REFERRAL TO TREATMENT PERIOD DURATION (UNADJUSTED) is the duration (or anticipated duration) of a REFERRAL TO TREATMENT PERIOD.
The duration (or anticipated duration) of a REFERRAL TO TREATMENT PERIOD.REFERRAL TO TREATMENT PERIOD DURATION (UNADJUSTED) is the number of completed days between the REFERRAL TO TREATMENT PERIOD START DATE and REFERRAL TO TREATMENT PERIOD END DATE.
It is the number of completed days between the REFERRAL TO TREATMENT PERIOD START DATE and REFERRAL TO TREATMENT PERIOD END DATE.
Example:
Where a REFERRAL TO TREATMENT PERIOD has a REFERRAL TO TREATMENT PERIOD START DATE of 1 January and REFERRAL TO TREATMENT PERIOD END DATE of 28 January the REFERRAL TO TREATMENT PERIOD DURATION (UNADJUSTED) will be 0027 days.
Change to Data Element: Changed Description
Format/Length: | n7 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
The total number of REFERRAL TO TREATMENT PERIODS without a REFERRAL TO TREATMENT PERIOD END DATE during the REPORTING PERIOD, excluding those REFERRAL TO TREATMENT PERIODS with an unknown REFERRAL TO TREATMENT PERIOD START DATE.
Change to Data Element: Changed Description
Format/Length: | n6 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes: The number of REFERRAL TO TREATMENT PERIODS during the reporting month where the PATIENTS was referred to a CONSULTANT with no REFERRAL TO TREATMENT PERIOD END DATE reported by REFERRAL TO TREATMENT PERIOD TIME BAND and TREATMENT FUNCTION CODE (REFERRAL TO TREATMENT PERIOD).
The number of completed weeks is the period from the REFERRAL TO TREATMENT PERIOD START DATE to the reporting date.
That is the number of REFERRAL TO TREATMENT PERIODS where:
a. | the REFERRAL TO TREATMENT PERIOD does not have a REFERRAL TO TREATMENT PERIOD END DATE | ||
and | |||
b. | the SERVICE REQUEST is made to a CONSULTANT ORGANISATION | ||
and | |||
c. | the ACTIVITY is a SERVICE PROVIDED UNDER AGREEMENT | ||
i.e. only commissioned care is included, private PATIENTS and PATIENTS who are Overseas Visitors are excluded. |
Change to Data Element: Changed Description
Format/length: | n6 |
HES item: | |
National Codes: | |
Default Codes: |
Notes: For PATIENTS with no DECISION TO ADMIT for treatment, the number of REFERRAL TO TREATMENT PERIODS during the REPORTING PERIOD with no REFERRAL TO TREATMENT PERIOD END DATE, reported by REFERRAL TO TREATMENT PERIOD BREACH TIME BAND.
That is, for patients with no DECISION TO ADMIT for treatment, the number of REFERRAL TO TREATMENT PERIODS where there is either:That is, for PATIENTS with no DECISION TO ADMIT for treatment, the number of REFERRAL TO TREATMENT PERIODS where there is either:
a. | no future APPOINTMENT for a PLANNED ACTIVITY where the planned ACTIVITY has a REFERRAL TO TREATMENT PERIOD STATUS of 30 | ||
OR | |||
b. | a future APPOINTMENT for a PLANNED ACTIVITY where the planned ACTIVITY has a REFERRAL TO TREATMENT PERIOD STATUS of 30, but the APPOINTMENT DATE is not before the REFERRAL TO TREATMENT PERIOD BREACH DATE. |
Change to Data Element: Changed Description
Format/Length: | n2 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes:
For inter-provider transfers, a restricted list of REFERRAL TO TREATMENT PERIOD STATUSES are used.
Permitted National Codes:
For first and subsequent activity | |
12 | consultant referral - the first activity at the start of a new REFERRAL TO TREATMENT PERIOD following a decision to refer directly to the CONSULTANT for a separate condition |
20 | subsequent ACTIVITY during a REFERRAL TO TREATMENT PERIOD - further ACTIVITIES anticipated |
For activity not part of a Referral to Treatment Period | |
90 | after treatment - first treatment occurred previously (e.g. admitted as an emergency from A&E or the ACTIVITY is after the start of treatment) |
98 | not applicable - ACTIVITY not applicable to REFERRAL TO TREATMENT PERIODS |
Change to Data Element: Changed Description
Format/Length: | an7 |
HES Item: | |
National Codes: | |
Default Codes: |
Notes: The time band for the Referral To Treatment Data Set and National Direct Access Audiology Waiting Times Data Set in weeks. For example, the 17-18 week time band covers days 120 - 126.REFERRAL TO TREATMENT PERIOD TIME BAND is the time band for the Referral To Treatment Data Set and National Direct Access Audiology Waiting Times Data Set in weeks.
For example, the 17-18 week time band covers days 120 - 126.
This is expressed as below:
0-1 | less than or equal to 1 week |
>1-2 | greater than 1 week to 2 weeks |
>2-3 | greater than 2 weeks to 3 weeks |
>3-4 | greater than 3 weeks to 4 weeks |
>4-5 | greater than 4 weeks to 5 weeks |
>5-6 | greater than 5 weeks to 6 weeks |
>6-7 | greater than 6 weeks to 7 weeks |
>7-8 | greater than 7 weeks to 8 weeks |
>8-9 | greater than 8 weeks to 9 weeks |
>9-10 | greater than 9 weeks to 10 weeks |
>10-11 | greater than 10 weeks to 11 weeks |
>11-12 | greater than 11 weeks to 12 weeks |
>12-13 | greater than 12 weeks to 13 weeks |
>13-14 | greater than 13 weeks to 14 weeks |
>14-15 | greater than 14 weeks to 15 weeks |
>15-16 | greater than 15 weeks to 16 weeks |
>16-17 | greater than 16 weeks to 17 weeks |
>17-18 | greater than 17 weeks to 18 weeks |
>18-19 | greater than 18 weeks to 19 weeks |
>19-20 | greater than 19 weeks to 20 weeks |
>20-21 | greater than 20 weeks to 21 weeks |
>21-22 | greater than 21 weeks to 22 weeks |
>22-23 | greater than 22 weeks to 23 weeks |
>23-24 | greater than 23 weeks to 24 weeks |
>24-25 | greater than 24 weeks to 25 weeks |
>25-26 | greater than 25 weeks to 26 weeks |
>26-27 | greater than 26 weeks to 27 weeks |
>27-28 | greater than 27 weeks to 28 weeks |
>28-29 | greater than 28 weeks to 29 weeks |
>29-30 | greater than 29 weeks to 30 weeks |
>30-31 | greater than 30 weeks to 31 weeks |
>31-32 | greater than 31 weeks to 32 weeks |
>32-33 | greater than 32 weeks to 33 weeks |
>33-34 | greater than 33 weeks to 34 weeks |
>34-35 | greater than 34 weeks to 35 weeks |
>35-36 | greater than 35 weeks to 36 weeks |
>36-37 | greater than 36 weeks to 37 weeks |
>37-38 | greater than 37 weeks to 38 weeks |
>38-39 | greater than 38 weeks to 39 weeks |
>39-40 | greater than 39 weeks to 40 weeks |
>40-41 | greater than 40 weeks to 41 weeks |
>41-42 | greater than 41 weeks to 42 weeks |
>42-43 | greater than 42 weeks to 43 weeks |
>43-44 | greater than 43 weeks to 44 weeks |
>44-45 | greater than 44 weeks to 45 weeks |
>45-46 | greater than 45 weeks to 46 weeks |
>46-47 | greater than 46 weeks to 47 weeks |
>47-48 | greater than 47 weeks to 48 weeks |
>48-49 | greater than 48 weeks to 49 weeks |
>49-50 | greater than 49 weeks to 50 weeks |
>50-51 | greater than 50 weeks to 51 weeks |
>51-52 | greater than 51 weeks to 52 weeks |
52+ | more than 52 weeks |
unknown | PATIENTS with unknown REFERRAL TO TREATMENT PERIOD START DATE |
Change to Data Element: Changed Description
Format/Length: | an1 |
HES Item: | |
National Codes: | See VIABLE TUMOUR INDICATOR |
Default Codes: | U - Uncertain |
Notes:
VIABLE TUMOUR INDICATOR is the same as attribute VIABLE TUMOUR INDICATOR.
For enquiries about this Change Request, please email information.standards@hscic.gov.uk