Health and Social Care Information Centre

NHS Data Model and Dictionary Service

Type:Patch
Reference:1398
Version No:1.0
Subject:Units of Measure
Effective Date:Immediate
Reason for Change:Patch
Publication Date:12 September 2013

Background:

It has been identified that some of the units of measure in the NHS Data Model and Dictionary are incorrect, e.g. grammes should be grams.

This patch:

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Summary of changes:

Diagrams
MATERNITY SERVICES SECONDARY USES DIAGRAM   Changed Diagram
 
Supporting Information
BIRTH LENGTH renamed from BIRTH LENGTH   Changed Description, Name
BIRTH WEIGHT renamed from BIRTH WEIGHT   Changed Description, Name
BLOOD PRESSURE   Changed Description
BODY MASS INDEX   Changed Description
DIASTOLIC BLOOD PRESSURE   Changed Description
FORCED EXPIRATORY VOLUME IN 1 SECOND (ABSOLUTE AMOUNT)   Changed Description
FORCED EXPIRATORY VOLUME IN 1 SECOND (PERCENTAGE)   Changed Description
HAND GRIP STRENGTH   Changed Description
HBA1C   Changed Description
HEAD CIRCUMFERENCE   Changed Description
HEART RATE   Changed Description
HEIGHT   Changed Description
HIP MEASUREMENT   Changed Description
LUNG CAPACITY (RETIRED) renamed from LUNG CAPACITY   Changed Description, status to Retired, Name
MID ARM CIRCUMFERENCE   Changed Description
PERCENTAGE WEIGHT LOSS   Changed Description
SERUM CHOLESTEROL LEVEL   Changed Description
SERUM CREATININE LEVEL   Changed Description
SYSTOLIC BLOOD PRESSURE   Changed Description
TEMPERATURE   Changed Description
URINE OUTPUT   Changed Description
WAIST MEASUREMENT   Changed Description
WEIGHT   Changed Description
 
Class Definitions
REGISTRABLE BIRTH   Changed Attributes
 
Attribute Definitions
CHEMOTHERAPY ACTUAL DOSE   Changed Description
ESTIMATED ENERGY INTAKE   Changed Description
ESTIMATED POTASSIUM INTAKE   Changed Description
ESTIMATED PROTEIN INTAKE   Changed Description
FINAL EXCISION MARGIN AFTER WIDE LOCAL EXCISION   Changed Description
MEASUREMENT VALUE TYPE CODE   Changed Description
RADIOTHERAPY ACTUAL DOSE   Changed Description
RADIOTHERAPY PRESCRIBED DOSE   Changed Description
TUMOUR VOLUME AT DIAGNOSIS CODE   Changed Description
 
Data Elements
ALBUMIN LEVEL   Changed Description
ALPHA FETOPROTEIN   Changed Description
ANTENATAL OBSERVATION (MATERNAL HEIGHT)   Changed Description
ANTENATAL OBSERVATION (MATERNAL WEIGHT)   Changed Description
BASE EXCESS CONCENTRATION   Changed Description
BETA2 MICROGLOBULIN LEVEL   Changed Description
BETA HUMAN CHORIONIC GONADOTROPIN   Changed Description
BICARBONATE CONCENTRATION   Changed Description
BILIRUBIN CONCENTRATION   Changed Description
BIRTH WEIGHT   Changed Description
BLOOD FLOW RATE (DIALYSIS)   Changed Description
BLOOD LYMPHOCYTE COUNT   Changed Description
BLOOD PRESSURE AVERAGED   Changed Description
BLOOD PRESSURE HIGHEST   Changed Description
BLOOD PRESSURE LOWEST   Changed Description
BLOOD PRESSURE SITTING   Changed Description
BLOOD UREA CONCENTRATION   Changed Description
BLOOD UREA CONCENTRATION (DONOR ON ADMISSION)   Changed Description
BLOOD UREA CONCENTRATION (DONOR ON RETRIEVAL)   Changed Description
BODY MASS INDEX   Changed Description
BRESLOW THICKNESS   Changed Description
CALCULATED CREATININE CLEARANCE   Changed Description
CHEMOTHERAPY ACTUAL DOSE   Changed Description
CHOLESTEROL HIGH DENSITY LIPOPROTEIN CONCENTRATION   Changed Description
CHOLESTEROL LOW DENSITY LIPOPROTEIN CONCENTRATION   Changed Description
CHOLESTEROL TOTAL CONCENTRATION   Changed Description
DIALYSATE 24 HOUR CREATININE CONCENTRATION   Changed Description
DIALYSATE 24 HOUR PROTEIN LOSS   Changed Description
DIALYSATE 24 HOUR UREA CONCENTRATION   Changed Description
DIALYSATE 24 HOUR VOLUME   Changed Description
DIALYSATE EFFLUENT VOLUME (4 HOUR)   Changed Description
DIALYSATE GLUCOSE END OF DWELL (4 HOUR)   Changed Description
DIALYSATE GLUCOSE START OF DWELL (4 HOUR)   Changed Description
DIASTOLIC BLOOD PRESSURE   Changed Description
DISTANCE BEYOND MUSCULARIS PROPRIA   Changed Description
DISTANCE FROM DENTATE LINE   Changed Description
DISTANCE TO CIRCUMFERENTIAL EXCISION MARGIN   Changed Description
DISTANCE TO CLOSEST NON PERITONEALISED RESECTION MARGIN   Changed Description
DISTANCE TO DISTAL RESECTION MARGIN   Changed Description
DISTANCE TO MARGIN   Changed Description
DISTANCE TO SEROSA   Changed Description
ESTIMATED ENERGY INTAKE   Changed Description
ESTIMATED GLOMERULAR FILTRATION RATE   Changed Description
ESTIMATED POTASSIUM INTAKE   Changed Description
ESTIMATED PROTEIN INTAKE   Changed Description
FINAL EXCISION MARGIN AFTER WIDE LOCAL EXCISION   Changed Description
FORCED EXPIRATORY VOLUME IN 1 SECOND (ABSOLUTE AMOUNT)   Changed Description
FORCED EXPIRATORY VOLUME IN 1 SECOND (PERCENTAGE)   Changed Description
GLUCOSE CONCENTRATION (DONOR)   Changed Description
HAEMOGLOBIN CONCENTRATION   Changed Description
HAND GRIP STRENGTH   Changed Description
HBA1C CONCENTRATION (DCCT)   Changed Description
HBA1C CONCENTRATION (IFCC)   Changed Description
HEAD CIRCUMFERENCE (RENAL PAEDIATRIC)   Changed Description
HEART RATE   Changed Description
HIP MEASUREMENT   Changed Description
HUMAN CHORIONIC GONADOTROPIN   Changed Description
ISOTOPIC GLOMERULAR FILTRATION RATE (LIVING DONOR)   Changed Description
LESION SIZE (RADIOLOGICAL)   Changed Description
MEASURED 24HR CREATININE CLEARANCE   Changed Description
MEASURED CREATININE CLEARANCE   Changed Description
MEASURED GLOMERULAR FILTRATION RATE   Changed Description
MITOTIC RATE   Changed Description
MYCOPHENOLIC ACID TROUGH LEVEL (RECIPIENT)   Changed Description
NUMBER OF SENTINEL NODES POSITIVE   Changed Description
NUMBER OF SENTINEL NODES POSITIVE (POST SENTINEL NODE COMPLETION LYMPHADENECTOMY)   Changed Description
NUMBER OF SENTINEL NODES SAMPLED   Changed Description
NUMBER OF SENTINEL NODES SAMPLED (POST SENTINEL NODE COMPLETION LYMPHADENECTOMY)   Changed Description
OBSERVATION DATE (WAIST MEASUREMENT)   Changed Description
PERCENTAGE WEIGHT LOSS   Changed Description
PERITONEAL DIALYSIS TOTAL WEEKLY FLUID VOLUME   Changed Description
PERSON HEIGHT IN CENTIMETRES   Changed Description
PERSON HEIGHT IN METRES   Changed Description
PERSON OBSERVATION (BMI)   Changed Description
PERSON OBSERVATION (HBA1C LEVEL)   Changed Description
PERSON OBSERVATION (SERUM CHOLESTEROL LEVEL)   Changed Description
PERSON OBSERVATION (SERUM CREATININE LEVEL)   Changed Description
PERSON OBSERVATION (URINARY ALBUMIN LEVEL)   Changed Description
PERSON WEIGHT   Changed Description
PERSON WEIGHT (POST DIALYSIS)   Changed Description
PERSON WEIGHT (PRE-DIALYSIS)   Changed Description
PERSON WEIGHT (RENAL CARE)   Changed Description
PHOSPHATE CONCENTRATION   Changed Description
POSITIVE END-EXPIRATORY PRESSURE   Changed Description
POTASSIUM CONCENTRATION (DONOR ON ADMISSION)   Changed Description
POTASSIUM CONCENTRATION (DONOR ON RETRIEVAL)   Changed Description
PRESCRIBED DOSE   Changed Description
PRESCRIBED DOSE (ALEMTUZUMAB)   Changed Description
PRESCRIBED DOSE (ANTI-HUMAN T-LYMPHOCYTE GLOBULIN)   Changed Description
PRESCRIBED DOSE (ANTITHYMOCYTE GLOBULIN)   Changed Description
PRESCRIBED DOSE (AZATHIOPRINE)   Changed Description
PRESCRIBED DOSE (BASILIXIMAB)   Changed Description
PRESCRIBED DOSE (CICLOSPORIN)   Changed Description
PRESCRIBED DOSE (DACLIZUMAB)   Changed Description
PRESCRIBED DOSE (GROWTH HORMONE)   Changed Description
PRESCRIBED DOSE (MUROMONAB-CD3)   Changed Description
PRESCRIBED DOSE (MYCOPHENOLATE MOFETIL)   Changed Description
PRESCRIBED DOSE (MYCOPHENOLATE SODIUM)   Changed Description
PRESCRIBED DOSE (PREDNISOLONE OR PREDNISONE)   Changed Description
PRESCRIBED ITEM (VOLUME OF 136 GLUCOSE FLUID)   Changed Description
PRESCRIBED ITEM (VOLUME OF 227 GLUCOSE FLUID)   Changed Description
PRESCRIBED ITEM (VOLUME OF 386 GLUCOSE FLUID)   Changed Description
PRESCRIBED ITEM (VOLUME OF AMINO ACID DIALYSIS FLUID)   Changed Description
PRESCRIBED ITEM (VOLUME OF ICODEXTRIN DIALYSIS FLUID)   Changed Description
PRESCRIBED ITEM SIZE (PERITONEAL BAG)   Changed Description
PRESCRIBED ITEM VOLUME USAGE PER OVERNIGHT (PERITONEAL DIALYSIS FLUID ON AUTOMATED PERITONEAL DIALYSIS)   Changed Description
PRESCRIBED TOTAL DAILY DOSE (ALEMTUZUMAB)   Changed Description
PRESCRIBED TOTAL DAILY DOSE (AZATHIOPRINE)   Changed Description
PRESCRIBED TOTAL DAILY DOSE (BASILIXIMAB)   Changed Description
PRESCRIBED TOTAL DAILY DOSE (CICLOSPORIN)   Changed Description
PRESCRIBED TOTAL DAILY DOSE (DACLIZUMAB)   Changed Description
PRESCRIBED TOTAL DAILY DOSE (MYCOPHENOLATE MOFETIL)   Changed Description
PRESCRIBED TOTAL DAILY DOSE (MYCOPHENOLATE SODIUM)   Changed Description
PRESCRIBED TOTAL DAILY DOSE (PREDNISOLONE OR PREDNISONE)   Changed Description
PRESCRIBED TOTAL DAILY DOSE (SIROLIMUS)   Changed Description
PRESCRIBED TOTAL DAILY DOSE (TACROLIMUS)   Changed Description
PRIMARY TUMOUR SIZE (RADIOLOGICAL)   Changed Description
PROCEDURE (NET DAILY ULTRAFILTRATION)   Changed Description
PROSTATE SPECIFIC ANTIGEN (DIAGNOSIS)   Changed Description
PROSTATE SPECIFIC ANTIGEN (PRE-TREATMENT)   Changed Description
PROTEIN CREATININE RATIO   Changed Description
RADIOTHERAPY ACTUAL DOSE   Changed Description
RADIOTHERAPY PRESCRIBED DOSE   Changed Description
RADIOTHERAPY TOTAL DOSE   Changed Description
RED CELL FOLATE CONCENTRATION   Changed Description
S CATEGORY (LACTATE DEHYDROGENASE)   Changed Description
SERUM ALBUMIN CONCENTRATION   Changed Description
SERUM ALUMINIUM CONCENTRATION   Changed Description
SERUM B12 CONCENTRATION   Changed Description
SERUM BICARBONATE CONCENTRATION   Changed Description
SERUM CALCIUM CONCENTRATION   Changed Description
SERUM C-REACTIVE PROTEIN CONCENTRATION   Changed Description
SERUM CREATININE CONCENTRATION   Changed Description
SERUM FERRITIN CONCENTRATION   Changed Description
SERUM INTACT PARATHYROID HORMOME CONCENTRATION   Changed Description
SERUM MAGNESIUM CONCENTRATION   Changed Description
SERUM POTASSIUM CONCENTRATION   Changed Description
SERUM UREA CONCENTRATION (POST DIALYSIS)   Changed Description
SERUM UREA CONCENTRATION (PRE-DIALYSIS)   Changed Description
SIROLIMUS TROUGH LEVEL (RECIPIENT)   Changed Description
SODIUM CONCENTRATION   Changed Description
SYSTOLIC BLOOD PRESSURE   Changed Description
TACROLIMUS 12 HOUR TROUGH LEVEL (RECIPIENT)   Changed Description
TEMPERATURE   Changed Description
TOTAL CHOLESTEROL HIGH DENSITY LIPOPROTEIN RATIO   Changed Description
TOTAL CHOLESTEROL LEVEL   Changed Description
TRIGLYCERIDES CONCENTRATION   Changed Description
URIC ACID CONCENTRATION   Changed Description
URINE CREATININE CONCENTRATION   Changed Description
URINE OUTPUT LAST 24 HOURS   Changed Description
URINE OUTPUT LAST HOUR   Changed Description
URINE UREA CONCENTRATION   Changed Description
URINE VOLUME   Changed Description
VIRAL LOAD COUNT   Changed Description
VITAMIN D CONCENTRATION   Changed Description
WAIST MEASUREMENT   Changed Description
WHITE BLOOD CELL COUNT   Changed Description
 

Date:12 September 2013
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.

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MATERNITY SERVICES SECONDARY USES DIAGRAM

Change to Diagram: Changed Diagram

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BIRTH LENGTH  renamed from BIRTH LENGTH

Change to Supporting Information: Changed Description, Name

The length of a baby at birth. This should be recorded in cms and forms part of the neonatal clinical option.Birth Length is a MEASURED PERSON OBSERVATION.

 Birth Length is the length of a baby at birth.

 

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BIRTH LENGTH  renamed from BIRTH LENGTH

Change to Supporting Information: Changed Description, Name

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BIRTH WEIGHT  renamed from BIRTH WEIGHT

Change to Supporting Information: Changed Description, Name

The Weight of a baby at birth recorded in grammes.Birth Weight is a MEASURED PERSON OBSERVATION.

 Birth Weight is the Weight of a baby at birth.

 

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BIRTH WEIGHT  renamed from BIRTH WEIGHT

Change to Supporting Information: Changed Description, Name

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BLOOD PRESSURE

Change to Supporting Information: Changed Description

Blood Pressure is a PERSON PROPERTY.

Blood Pressure is comprised of Systolic Blood Pressure and Diastolic Blood Pressure.Blood Pressure is the the pressure of the blood within the arteries and is comprised of:

 
  • Systolic Blood Pressure and
  • Diastolic Blood Pressure.
  •  

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    BODY MASS INDEX

    Change to Supporting Information: Changed Description

    Body Mass Index is a PERSON PROPERTY.Body Mass Index (BMI) is a PERSON PROPERTY.

    Body Mass Index is derived from Weight and Height.Body Mass Index is a measure of body fat based on Height and Weight.

    For further information on Body Mass Index, see the NHS Choices website.

     

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    DIASTOLIC BLOOD PRESSURE

    Change to Supporting Information: Changed Description

    Diastolic Blood Pressure is a MEASURED PERSON OBSERVATION.

    Diastolic Blood Pressure is the reading of a PERSON's Blood Pressure relaxing between heart beats and is measured in 'mmHg'.Diastolic Blood Pressure is the reading of a PATIENT's Blood Pressure relaxing between heart beats.

     

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    FORCED EXPIRATORY VOLUME IN 1 SECOND (ABSOLUTE AMOUNT)

    Change to Supporting Information: Changed Description

    Forced Expiratory Volume in 1 second (Absolute Amount) is a MEASURED PERSON OBSERVATION.

    Forced Expiratory Volume in 1 second (Absolute Amount) is the forced expiratory volume (i.e. the volume of air that a PERSON can breathe out in one second) measured in 'Litres'.Forced Expiratory Volume in 1 second (Absolute Amount) is the volume of air that can forcibly be blown out in one second, after full inspiration.

     

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    FORCED EXPIRATORY VOLUME IN 1 SECOND (PERCENTAGE)

    Change to Supporting Information: Changed Description

    Forced Expiratory Volume in 1 second (Percentage) is a MEASURED PERSON OBSERVATION.

    Forced Expiratory Volume in 1 second (Percentage) is the forced expiratory volume (i.e. the volume of air that a PERSON can breathe out in one second) as a percentage of the predicted value.Forced Expiratory Volume in 1 second (Percentage) is the volume of air that can forcibly be blown out in one second, after full inspiration, as a percentage of the predicted value.

     

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    HAND GRIP STRENGTH

    Change to Supporting Information: Changed Description

    Hand Grip Strength is a MEASURED PERSON OBSERVATION.

    Hand Grip Strength is the PERSON's hand grip strength.Hand Grip Strength is the PATIENT's hand grip strength.

     

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    HBA1C

    Change to Supporting Information: Changed Description

    HbA1c (Hemoglobin A1c), also known as Glycated Hemoglobin is a MEASURED PERSON OBSERVATION.HbA1c (Hemoglobin A1c), also known as Glycated Hemoglobin, is a MEASURED PERSON OBSERVATION.

    The HbA1c test measures the amount of glucose that is being carried by the red blood cells in the body and is measured in 'mmol/L (millimoles per litre)'.The HbA1c test measures the amount of glucose that is being carried by the red blood cells in the body.

     

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    HEAD CIRCUMFERENCE

    Change to Supporting Information: Changed Description

    Head Circumference is a MEASURED PERSON OBSERVATION.

    Head Circumference is the PERSON's head circumference.Head Circumference is the circumference of the PATIENT's head.

     

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    HEART RATE

    Change to Supporting Information: Changed Description

    Heart Rate is a MEASURED PERSON OBSERVATION.

    Heart Rate is the number of heartbeats per unit of time, usually expressed as beats per minute (bpm).Heart Rate is the number of heart beats per unit of time. 

     

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    HEIGHT

    Change to Supporting Information: Changed Description

    Height is a MEASURED PERSON OBSERVATION.

    The Height of a PERSON on a given date, where the MEASUREMENT VALUE TYPE CODE is National Code 'Metres' or 'Centimetres'.Height is the height of a PATIENT on a given date, where the MEASUREMENT VALUE TYPE CODE is 'Metres (m)' or 'Centimetres (cm)'.

     

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    HIP MEASUREMENT

    Change to Supporting Information: Changed Description

    Hip Measurement is a MEASURED PERSON OBSERVATION

    Hip Measurement is the PERSON's hip measurement.Hip Measurement is the measurement of the PATIENT's hips.

     

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    LUNG CAPACITY (RETIRED)  renamed from LUNG CAPACITY

    Change to Supporting Information: Changed Description, status to Retired, Name

    Lung Capacity is a PERSON PROPERTY.This item has been retired from the NHS Data Model and Dictionary.

    The Lung Capacity of a PERSON.The last live version of this item is available in the July 2013 release of the NHS Data Model and Dictionary.

    Lung Capacity is made up of Forced Expiratory Volume in 1 second (Absolute Amount) and Forced Expiratory Volume in 1 second (Percentage).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.

     

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    LUNG CAPACITY (RETIRED)  renamed from LUNG CAPACITY

    Change to Supporting Information: Changed Description, status to Retired, Name

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    MID ARM CIRCUMFERENCE

    Change to Supporting Information: Changed Description

    Mid Arm Circumference is a MEASURED PERSON OBSERVATION.

    Mid Arm Circumference is the PERSON's mid arm circumference.Mid Arm Circumference is the circumference of the PATIENT's mid arm.

     

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    PERCENTAGE WEIGHT LOSS

    Change to Supporting Information: Changed Description

    Percentage Weight Loss is a MEASURED PERSON OBSERVATION.

    Percentage Weight Loss is the percentage of Weight lost by a PATIENT over a specified period.

    Percentage Weight Loss is used as an indicator of malnutrition.

     

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    SERUM CHOLESTEROL LEVEL

    Change to Supporting Information: Changed Description

    Serum Cholesterol Level is a MEASURED PERSON OBSERVATION.

    Serum Cholesterol Level is the cholesterol level in a PERSON's blood and is measured in 'mmol/L (millimoles per litre)'.Serum Cholesterol Level is the cholesterol level in a PATIENT's blood.

     

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    SERUM CREATININE LEVEL

    Change to Supporting Information: Changed Description

    Serum Creatinine Level is a MEASURED PERSON OBSERVATION.

    Serum Creatinine Level is the concentration of creatinine in serum, used as an indicator of renal function and is measured in 'micromoles/litre (µmol/L)'.Serum Creatinine Level is the concentration of creatinine in serum (used as an indicator of renal function).

     

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    SYSTOLIC BLOOD PRESSURE

    Change to Supporting Information: Changed Description

    Systolic Blood Pressure is a MEASURED PERSON OBSERVATION.

    Systolic Blood Pressure is the reading of a PERSON's Blood Pressure at each heart beat and is measured in 'mmHg'.Systolic Blood Pressure is the reading of a PATIENT's Blood Pressure at each heart beat.

     

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    TEMPERATURE

    Change to Supporting Information: Changed Description

    Temperature is a MEASURED PERSON OBSERVATION.

    The Temperature of a PERSON which is measured in Celsius.Temperature is the degree of internal heat of a PATIENT's body.

     

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    URINE OUTPUT

    Change to Supporting Information: Changed Description

    Urine Output is a MEASURED PERSON OBSERVATION

    Urine Output is a PERSON's Urine Output measured in millilitres (ml) over a specified period of time (i.e. last hour, last 24 hours).Urine Output is the output of urine of a PATIENT over a specified period of time (i.e. last hour, last 24 hours).

     

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    WAIST MEASUREMENT

    Change to Supporting Information: Changed Description

    Waist Measurement is a MEASURED PERSON OBSERVATION.

    The Waist Measurement of a PERSON measured in Centimetres.Waist Measurement is the measurement of a PATIENT's waist.

     

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    WEIGHT

    Change to Supporting Information: Changed Description

    Weight is a MEASURED PERSON OBSERVATION.

    Weight identifies the Weight of a PERSON on a given date. The type of measurement is Kilograms.Weight is the weight of a PATIENT on a given date, where the MEASUREMENT VALUE TYPE CODE is 'Kilograms (kg)' or 'Grams (g)'.

     

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    REGISTRABLE BIRTH

    Change to Class: Changed Attributes

    Attributes of this Class are:
    APGAR SCORE 1 MINUTE
    APGAR SCORE 5 MINUTE
    BCG ADMINISTERED
    BIRTH HEAD CIRCUMFERENCE
    BIRTH LENGTH
    BIRTH ORDER
    BIRTH WEIGHT
    DELIVERY METHOD
    DELIVERY PLACE TYPE
    DELIVERY TIME
    EXAMINATION OF HIPS
    FOLLOW UP CARE
    GESTATION LENGTH
    LIVE OR STILL BIRTH
    METABOLIC SCREENING
    NUMBER OF BABIES IDENTIFIER
    PRESENCE OF JAUNDICE
    PRESENTATION AT ONSET OF LABOUR
    RESUSCITATION METHOD DRUGS
    RESUSCITATION METHOD POSITIVE PRESSURE
    STATUS OF PERSON CONDUCTING DELIVERY

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    CHEMOTHERAPY ACTUAL DOSE

    Change to Attribute: Changed Description

    The actual Chemotherapy dose given in milligrams or other applicable unit for each administration in a Systemic Anti-Cancer Drug Cycle.The actual Chemotherapy dose given.

     For the Systemic Anti-Cancer Therapy Data Set, this is for each administration in a Systemic Anti-Cancer Drug Cycle.

     

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    ESTIMATED ENERGY INTAKE

    Change to Attribute: Changed Description

    The PATIENT's estimated energy intake in kcal recorded by a CARE PROFESSIONAL during a Nutritional Assessment.The PATIENT's estimated energy intake recorded by a CARE PROFESSIONAL during a Nutritional Assessment. 

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    ESTIMATED POTASSIUM INTAKE

    Change to Attribute: Changed Description

    The estimated potassium intake in a PATIENT's diet recorded in mmols by a CARE PROFESSIONAL during a Nutritional Assessment.The estimated potassium intake in a PATIENT's diet recorded by a CARE PROFESSIONAL during a Nutritional Assessment. 

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    ESTIMATED PROTEIN INTAKE

    Change to Attribute: Changed Description

    The PATIENT's estimated protein intake in grammes recorded by a CARE PROFESSIONAL during a Nutritional Assessment.The PATIENT's estimated protein intake recorded by a CARE PROFESSIONAL during a Nutritional Assessment.

     

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    FINAL EXCISION MARGIN AFTER WIDE LOCAL EXCISION

    Change to Attribute: Changed Description

    The final margin of excision, measured in 'Millimetres (mm)' during a Skin Cancer Care SpellThe final margin of excision, during a Skin Cancer Care Spell.

    FINAL EXCISION MARGIN AFTER WIDE LOCAL EXCISION is recorded after the wide local excision procedures and is an amalgamation of clinical and histopathological data.For the Cancer Outcomes and Services Data SetFINAL EXCISION MARGIN AFTER WIDE LOCAL EXCISION is recorded after the wide local excision procedures and is an amalgamation of clinical and histopathological data.

     

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    MEASUREMENT VALUE TYPE CODE

    Change to Attribute: Changed Description

    The type of measurement used for the MEASURED PERSON OBSERVATION being recorded.

    The unit of measurement is based on the MEASURED PERSON OBSERVATION TYPE CODE for that MEASURED PERSON OBSERVATION.

    National Codes:

    01Millimoles per litre (mmol/L)
    02Micromoles per litre (µmol/L)
    03Micrograms per litre (ug/L)
    04Micrograms per millimole (ug/mmol)
    05Microgram albumin per hour (ug/ml/hr)
    06Microgram albumin per minute (ug/min)
    07Microgram albumin per 24 hours (ug/24hr)
    08Number
    03Micrograms per litre (µg/Ll)
    04Micrograms per millimole (µg/mmol)
    05Microgram albumin per hour (µg/ml/hr)
    06Microgram albumin per minute (µg/min)
    07Microgram albumin per 24 hours (µg/24hr)
    08Number (Retired September 2013)
    09Percentage (%)
    10Kilograms (kg)
    11Metres (m)
    13Square Metres (m2)
    14Millilitres per Minute (ml/min)
    15Millimetre of mercury (mmHg)
    15Millimetres of mercury (mmHg)
    16Litres (l)
    17Beats per minute (bpm)
    18Centimetres (cm)
    19Milligrams (mg)
    20Millilitres (ml)
    21Minutes
    22Celsius
    22Celsius (ºC)
    23Millimetres (mm)
    24Grammes per decilitre (g/dl)
    25Grammes per litre (g/l)
    26Milligrammes per litre (mg/l)
    24Grams per decilitre (g/dl)
    25Grams per litre (g/l)
    26Milligrams per litre (mg/l)
    27Nanograms per millilitre (ng/ml)
    28International units per litre (IU/L)
    29Decilitre (d/l)
    28International Units per litre (IU/L)
    29Decilitres (d/l)
    30Square Millimetres (mm2)
    31Millilitres (ml)
    31Millilitres (ml) (Retired September 2013)
    32Grays (Gy)
    33International Units per kilogram (IU/kg)
    34Grams (g)
    35Kilocalories (kcal)
    36Millimoles (mmol)
    37Millimoles per mole (mmol/mol)
    38Picomoles per litre (pmol/L)
    39Milligrams per millimole (mg/mmol)
    40Nanograms per litre (ng/l)
    41Micrograms per millilitre (µg/ml)
    42Millimetres of water (mmH2O)
     

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    RADIOTHERAPY ACTUAL DOSE

    Change to Attribute: Changed Description

    The total actual absorbed radiation dose given in grays (Gy) as received during a course of treatment.The total actual absorbed radiation dose received during a course of Radiotherapy treatment.

     

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    RADIOTHERAPY PRESCRIBED DOSE

    Change to Attribute: Changed Description

    The total prescribed absorbed radiation dose in grays (Gy).The total prescribed absorbed radiation dose for Radiotherapy treatment.

     

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    TUMOUR VOLUME AT DIAGNOSIS CODE

    Change to Attribute: Changed Description

    The radiologically calculated estimate of the Tumour volume at PATIENT DIAGNOSIS in 'millilitres (ml)'.The radiologically calculated estimate of the Tumour volume at PATIENT DIAGNOSIS, in 'Millilitres (ml)'.

    National Codes:

    LLess than 200ml
    M200ml or greater
     

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    ALBUMIN LEVEL

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    Format/Length:n2
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    ALBUMIN LEVEL is the result of the Clinical Investigation which measures the PATIENT's concentration of albumin in serum, in 'Grammes per litre (g/l)'.ALBUMIN LEVEL is the result of the Clinical Investigation which measures the PATIENT's concentration of albumin in serum in 'Grams per litre (g/l)'. 

    The value is presented in the range 10-80.

    For the Cancer Outcomes and Services Data Set, ALBUMIN LEVEL is measured pre-treatment.

     

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    ALPHA FETOPROTEIN

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    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    ALPHA FETOPROTEIN is the outcome of the Clinical Investigation to determine the PATIENT's serum Tumour markers for alpha fetoprotein (AFP) (a protein found in abnormal amounts in the blood of PATIENTS with cancer), in 'Nanograms per millilitre (ng/ml)'.ALPHA FETOPROTEIN is the result of the Clinical Investigation to determine the PATIENT's serum Tumour markers for alpha fetoprotein (AFP) (a protein found in abnormal amounts in the blood of PATIENTS with cancer) in 'Nanograms per millilitre (ng/ml)'. 

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    ANTENATAL OBSERVATION (MATERNAL HEIGHT)

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    Format/Length:n1.max n2
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    ANTENATAL OBSERVATION (MATERNAL HEIGHT) is the same as data element PERSON HEIGHT IN METRES.ANTENATAL OBSERVATION (MATERNAL HEIGHT) is the same as data element PERSON HEIGHT IN METRES, where the MEASUREMENT VALUE TYPE CODE is 'Metres (m)' .

    ANTENATAL OBSERVATION (MATERNAL HEIGHT) is the Height of the PERSON measured during an Antenatal period.ANTENATAL OBSERVATION (MATERNAL HEIGHT) is the Height of the mother measured during an Antenatal period.

     

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    ANTENATAL OBSERVATION (MATERNAL WEIGHT)

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    HES Item: 
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    Default Codes: 

    Notes:
    ANTENATAL OBSERVATION (MATERNAL WEIGHT) is the same as data element PERSON WEIGHT.ANTENATAL OBSERVATION (MATERNAL WEIGHT) is the same as data element PERSON WEIGHT, where the MEASUREMENT VALUE TYPE CODE is 'Kilograms (kg)'.

    ANTENATAL OBSERVATION (MATERNAL WEIGHT) is the Weight of the PERSON measured during an Antenatal period.ANTENATAL OBSERVATION (MATERNAL WEIGHT) is the Weight of the mother measured during an Antenatal period.

     

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    BASE EXCESS CONCENTRATION

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    Default Codes: 

    Notes:
    BASE EXCESS CONCENTRATION is the result of the Clinical Investigation which measures the PERSON's base excess concentration in 'mmol/L'.BASE EXCESS CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's base excess concentration in 'Millimoles per litre (mmol/L)'.  

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    BETA2 MICROGLOBULIN LEVEL

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    Format/Length:max n2.n1
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    BETA2 MICROGLOBULIN LEVEL is the result of the Clinical Investigation which measures the PATIENT's beta2 microglobulin in serum (protein found on the surface of many CELLS), in 'Milligrammes per litre (mg/l)'.BETA2 MICROGLOBULIN LEVEL is the result of the Clinical Investigation which measures the PATIENT's beta2 microglobulin (protein found on the surface of many CELLS) in serum in 'Milligrams per litre (mg/l)'. 

    For the Cancer Outcomes and Services Data SetBETA2 MICROGLOBULIN LEVEL is measured pre-treatment.

     

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    BETA HUMAN CHORIONIC GONADOTROPIN

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    Format/Length:max n3
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    BETA HUMAN CHORIONIC GONADOTROPIN is the outcome of the Clinical Investigation to determine the PATIENT's serum Tumour markers for beta human chorionic gonadotropin (bHCG) (a hormone normally found in the blood and urine during pregnancy), in 'International units per litre (IU/L)'.BETA HUMAN CHORIONIC GONADOTROPIN is the result of the Clinical Investigation to determine the PATIENT's serum Tumour markers for beta human chorionic gonadotropin (bHCG) (a hormone normally found in the blood and urine during pregnancy), in 'International Units per Litre (IU/L)'.

    BETA HUMAN CHORIONIC GONADOTROPIN may also be produced by some Tumour CELLS. An increased level of beta-human chorionic gonadotropin may be a sign of cancer of the testis, uterus, ovary, liver, stomach, pancreas, or lungs.

     

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    BICARBONATE CONCENTRATION

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    Default Codes: 

    Notes:
    BICARBONATE CONCENTRATION is the result of the Clinical Investigation which measures the PERSON's bicarbonate concentration (HCO3) in 'mmol/L'.BICARBONATE CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's bicarbonate concentration (HCO3) in 'Millimoles per litre (mmol/L)'. 

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    BILIRUBIN CONCENTRATION

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    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    BILIRUBIN CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's bilirubin concentration in 'µmol/L'.BILIRUBIN CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's bilirubin concentration in 'Micromoles per litre (µmol/L)'. 

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    BIRTH WEIGHT

    Change to Data Element: Changed Description

    Format/Length:n4
    HES Item:BIRWEIT
    National Codes: 
    Default Codes:9999 - Not known

    Notes:
    BIRTH WEIGHT is the same as attribute BIRTH WEIGHT.BIRTH WEIGHT is the Birth Weight, where the MEASUREMENT VALUE TYPE CODE is 'Grams (g)'. 

    BIRTH WEIGHT is the baby's Weight in grammes between 0001 to 9998.The range is 0001 to 9998.

     

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    BLOOD FLOW RATE (DIALYSIS)

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    HES Item: 
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    Notes:
    BLOOD FLOW RATE (DIALYSIS) is the PATIENT's blood flow rate during a Haemodialysis measured in 'ml/min'.BLOOD FLOW RATE (DIALYSIS) is the result of the Clinical Investigation which measures the PATIENT's blood flow rate during Haemodialysis, in 'Millilitres per Minute (ml/min)'. 

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    BLOOD LYMPHOCYTE COUNT

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    Default Codes: 

    Notes:
    BLOOD LYMPHOCYTE COUNT is the outcome of the Clinical Investigation which measures the number of lymphocytes (white blood CELLS in the vertebrate immune system) in the PATIENT's blood.BLOOD LYMPHOCYTE COUNT is the result of the Clinical Investigation which measures the number of lymphocytes (white blood CELLS in the vertebrate immune system) in the PATIENT's blood.

    For the Cancer Outcomes and Services Data Set, BLOOD LYMPHOCYTE COUNT is measured pre-treatment.

     

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    BLOOD PRESSURE AVERAGED

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    Notes:
    BLOOD PRESSURE AVERAGED is the outcome of the Clinical Investigation which measures the average Blood Pressure of the PERSON in 'mmHg' BLOOD PRESSURE AVERAGED is the result of the Clinical Investigation which measures the average Blood Pressure of the PATIENT in 'Millilitres of mercury (mmHg)'. 

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    BLOOD PRESSURE HIGHEST

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    Default Codes: 

    Notes:
    BLOOD PRESSURE HIGHEST is the outcome of the Clinical Investigation which measures the highest Blood Pressure of the PERSON in 'mmHg' BLOOD PRESSURE HIGHEST is the result of the Clinical Investigation which measures the highest Blood Pressure of the PATIENT in 'Millilitres of mercury (mmHg)'. 

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    BLOOD PRESSURE LOWEST

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    Notes:
    BLOOD PRESSURE LOWEST is the outcome of the Clinical Investigation which measures the lowest Blood Pressure of the PERSON in 'mmHg' BLOOD PRESSURE LOWEST is the result of the Clinical Investigation which measures the lowest Blood Pressure of the PATIENT in 'Millilitres of mercury (mmHg)'. 

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    BLOOD PRESSURE SITTING

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    Default Codes: 

    Notes:
    BLOOD PRESSURE SITTING is the outcome of the Clinical Investigation which measures the Blood Pressure of the PERSON whilst sitting.BLOOD PRESSURE SITTING is the result of the Clinical Investigation which measures the Blood Pressure of the PATIENT whilst sitting, in 'Millilitres of mercury (mmHg)'. 

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    BLOOD UREA CONCENTRATION

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    Default Codes: 

    Notes:
    BLOOD UREA CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's blood urea concentration in 'mmol/L'.BLOOD UREA CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's blood urea concentration in 'Millimoles per litre (mmol/L)'. 

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    BLOOD UREA CONCENTRATION (DONOR ON ADMISSION)

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    Format/Length:max n2.max n1
    HES Item: 
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    Default Codes: 

    Notes:
    BLOOD UREA CONCENTRATION (DONOR ON ADMISSION) is the result of the Clinical Investigation which measures the ORGAN OR TISSUE DONOR's blood urea concentration on admission in 'mmol/L'.BLOOD UREA CONCENTRATION (DONOR ON ADMISSION) is the result of the Clinical Investigation which measures the ORGAN OR TISSUE DONOR's blood urea concentration on admission in 'Millimoles per litre (mmol/L)'. 

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    BLOOD UREA CONCENTRATION (DONOR ON RETRIEVAL)

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    Format/Length:max n2.max n1
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    BLOOD UREA CONCENTRATION (DONOR ON RETRIEVAL) is the result of the Clinical Investigation which measures the ORGAN OR TISSUE DONOR's blood urea concentration on retrieval in 'mmol/L'.BLOOD UREA CONCENTRATION (DONOR ON RETRIEVAL) is the result of the Clinical Investigation which measures the ORGAN OR TISSUE DONOR's blood urea concentration on retrieval in 'Millimoles per litre (mmol/L)'.  

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    BODY MASS INDEX

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    Format/Length:n2.n1
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    BODY MASS INDEX (BMI) is the Body Mass Index of the PERSON.BODY MASS INDEX (BMI) is the Body Mass Index of the PATIENT.

    For the Cancer Outcomes and Services Data Set, BODY MASS INDEX is the estimate of a PATIENT's Body Mass Index at PATIENT DIAGNOSIS.

    BODY MASS INDEX replaces PERSON OBSERVATION (BMI) and should be used for all new and developing data sets and for XML messages.

     

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    BRESLOW THICKNESS

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    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    BRESLOW THICKNESS is the outcome of the Clinical Investigation which measures the PERSON's Breslow Thickness, in 'Millimetres (mm)', to the nearest 0.BRESLOW THICKNESS is the result of the Clinical Investigation which measures the PERSON's Breslow Thickness, in 'Millimetres (mm)', to the nearest 0.01mm. 

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    CALCULATED CREATININE CLEARANCE

    Change to Data Element: Changed Description

    Format/Length:max n3.max n2
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    CALCULATED CREATININE CLEARANCE is the outcome of the Clinical Investigation which measures the patients calculated creatinine clearance in 'ml/min'. For the renal data set this is for PATIENTS under 18 years only.CALCULATED CREATININE CLEARANCE is the result of the Clinical Investigation which measures the PATIENT's calculated creatinine clearance, in 'Millilitres per Minute (ml/min)'. For the National Renal Data SetCALCULATED CREATININE CLEARANCE is for PATIENTS under 18 years only.

     

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    CHEMOTHERAPY ACTUAL DOSE

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    Format/Length:max n7
    HES Item: 
    National Codes: 
    Default Codes: 


    Notes:
    CHEMOTHERAPY ACTUAL DOSE is the same as attribute CHEMOTHERAPY ACTUAL DOSE.

    The actual Chemotherapy dose given in milligrams or other applicable unit, for example, 400 milligrams, 200 units, 1.5 grammes etc.For the Systemic Anti-Cancer Therapy Data Set, the actual Chemotherapy dose can be given in 'Milligrams (mg)' or other applicable units, for example, 400 milligrams, 200 units, 1.5 grams etc.

     

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    CHOLESTEROL HIGH DENSITY LIPOPROTEIN CONCENTRATION

    Change to Data Element: Changed Description

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    Default Codes: 

    Notes:
    CHOLESTEROL HIGH DENSITY LIPOPROTEIN CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's cholesterol high density lipoprotein (HDL) concentration in 'mmol/L'.CHOLESTEROL HIGH DENSITY LIPOPROTEIN CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's cholesterol high density lipoprotein (HDL) concentration in 'Millimoles per litre (mmol/L)'. 

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    CHOLESTEROL LOW DENSITY LIPOPROTEIN CONCENTRATION

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    Notes:
    CHOLESTEROL LOW DENSITY LIPOPROTEIN CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's cholesterol low density lipoprotein (LDL) concentration in 'mmol/L'.CHOLESTEROL LOW DENSITY LIPOPROTEIN CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's cholesterol low density lipoprotein (LDL) concentration in 'Millimoles per litre (mmol/L)'. 

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    CHOLESTEROL TOTAL CONCENTRATION

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    Format/Length:max n2.max n1
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    National Codes: 
    Default Codes: 

    Notes:
    CHOLESTEROL TOTAL CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's cholesterol total concentration in 'mmol/L'.CHOLESTEROL TOTAL CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's cholesterol total concentration in 'Millimoles per litre (mmol/L)'. 

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    DIALYSATE 24 HOUR CREATININE CONCENTRATION

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    Notes:
    DIALYSATE 24 HOUR CREATININE CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's dialysate 24 hour creatinine concentration in 'Litres'. DIALYSATE 24 HOUR CREATININE CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's dialysate 24 hour creatinine concentration in 'Litres (l)'. 

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    DIALYSATE 24 HOUR PROTEIN LOSS

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    Default Codes: 

    Notes:
    DIALYSATE 24 HOUR PROTEIN LOSS is the result of the Clinical Investigation which measures the PATIENT's 24 hour dialysate protein loss in 'grammes'.DIALYSATE 24 HOUR PROTEIN LOSS is the result of the Clinical Investigation which measures the PATIENT's 24 hour dialysate protein loss in 'Grams (g)'. 

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    DIALYSATE 24 HOUR UREA CONCENTRATION

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    Format/Length:max n3
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    Notes:
    DIALYSATE 24 HOUR UREA CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's dialysate 24 hour urea concentration in 'mmol/L'.DIALYSATE 24 HOUR UREA CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's dialysate 24 hour urea concentration in 'Millimoles per litre (mmol/L)'. 

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    DIALYSATE 24 HOUR VOLUME

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    Notes:
    DIALYSATE 24 HOUR VOLUME is the result of the Clinical Investigation which measures the PATIENT's dialysate total 24 hour volume in 'Litres'. DIALYSATE 24 HOUR VOLUME is the result of the Clinical Investigation which measures the PATIENT's dialysate total 24 hour volume in 'Litres (l)'. 

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    DIALYSATE EFFLUENT VOLUME (4 HOUR)

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    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    DIALYSATE EFFLUENT VOLUME (4 HOUR) is the result of the Clinical Investigation which measures the dialysate effulent volume (4 hours) in 'Litres'. DIALYSATE EFFLUENT VOLUME (4 HOUR) is the result of the Clinical Investigation which measures the PATIENT's dialysate effulent volume (4 hours) in 'Litres (l)'. 

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    DIALYSATE GLUCOSE END OF DWELL (4 HOUR)

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    Notes:
    DIALYSATE GLUCOSE END OF DWELL (4 HOUR) is the result of the Clinical Investigation which measures the dialysate glucose at the end of dwell (4 hours) in 'mmol/L'.DIALYSATE GLUCOSE END OF DWELL (4 HOUR) is the result of the Clinical Investigation which measures the PATIENT's dialysate glucose at the end of dwell (4 hours) in 'Millimoles per litre (mmol/L)'. 

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    DIALYSATE GLUCOSE START OF DWELL (4 HOUR)

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    Notes:
    DIALYSATE GLUCOSE START OF DWELL (4 HOUR) is the result of the Clinical Investigation which measures the dialysate glucose at the start of dwell (4 hours) in 'mmol/L'.DIALYSATE GLUCOSE START OF DWELL (4 HOUR) is the result of the Clinical Investigation which measures the PATIENT's dialysate glucose at the start of dwell (4 hours) in 'Millimoles per litre (mmol/L)'. 

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    DIASTOLIC BLOOD PRESSURE

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    Notes:
    DIASTOLIC BLOOD PRESSURE records Diastolic Blood Pressure.DIASTOLIC BLOOD PRESSURE is the Diastolic Blood Pressure of a PATIENT in 'Millilitres of mercury (mmHg)'. 

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    DISTANCE BEYOND MUSCULARIS PROPRIA

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    Format/Length:max n3.n1
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    Default Codes: 

    Notes:
    DISTANCE BEYOND MUSCULARIS PROPRIA is the maximum distance of spread of the Tumour beyond muscularis propria, measured in 'Millimetres (mm)', to the nearest 0.DISTANCE BEYOND MUSCULARIS PROPRIA is the maximum distance of spread of the Tumour beyond muscularis propria, in 'Millimetres (mm)', to the nearest 0.1mm.

    Note: if there is doubt about the sites of the muscularis propria, the distance should be estimated as accurately as possible.

     

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    DISTANCE FROM DENTATE LINE

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    Notes:
    DISTANCE FROM DENTATE LINE is the distance of the Tumour from the dentate line for Abdomino-Perineal Excision of Rectum (APER) specimens, measured in 'Millimetres (mm)', to the nearest 0.DISTANCE FROM DENTATE LINE is the distance of the Tumour from the dentate line for Abdomino-Perineal Excision of Rectum (APER) specimens, in 'Millimetres (mm)', to the nearest 0.1mm. 

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    DISTANCE TO CIRCUMFERENTIAL EXCISION MARGIN

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    Notes:
    DISTANCE TO CIRCUMFERENTIAL EXCISION MARGIN is the distance from the Tumour to the circumferential margin, measured in 'Millimetres (mm)', to the nearest 0.DISTANCE TO CIRCUMFERENTIAL EXCISION MARGIN is the distance from the Tumour to the circumferential margin, in 'Millimetres (mm)', to the nearest 0.1mm. 

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    DISTANCE TO CLOSEST NON PERITONEALISED RESECTION MARGIN

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    Notes:
    DISTANCE TO CLOSEST NON PERITONEALISED RESECTION MARGIN is the distance from the outer margin of the Tumour to the closest non peritonealised resection margin, measured in 'Millimetres (mm)', to the nearest 0.DISTANCE TO CLOSEST NON PERITONEALISED RESECTION MARGIN is the distance from the outer margin of the Tumour to the closest non peritonealised resection margin, in 'Millimetres (mm)', to the nearest 0.1mm. 

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    DISTANCE TO DISTAL RESECTION MARGIN

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    Notes:
    DISTANCE TO DISTAL RESECTION MARGIN is the distance between the lower end of the Tumour and the distal resection margin, measured in 'Millimetres (mm)', to the nearest 0.DISTANCE TO DISTAL RESECTION MARGIN is the distance between the lower end of the Tumour and the distal resection margin in 'Millimetres (mm)', to the nearest 0.1mm. 

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    DISTANCE TO MARGIN

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    Notes:
    DISTANCE TO MARGIN is the distance of the Tumour to the nearest margin (the rim of TISSUE around the Tumour or lesion which has been removed) whether the Tumour is invasive or non invasive, measured in 'Millimetres (mm)'.DISTANCE TO MARGIN is the distance of the Tumour to the nearest margin (the rim of TISSUE around the Tumour or lesion which has been removed) whether the Tumour is invasive or non invasive in 'Millimetres (mm)'. 

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    DISTANCE TO SEROSA

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    Notes:
    DISTANCE TO SEROSA is the Tumour-free distance from the Tumour to the serosa (a smooth membrane consisting of a thin layer of CELLS which secrete serous fluid), measured in 'Millimetres (mm)'.DISTANCE TO SEROSA is the Tumour-free distance from the Tumour to the serosa (a smooth membrane consisting of a thin layer of CELLS which secrete serous fluid), in 'Millimetres (mm)'. 

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    ESTIMATED ENERGY INTAKE

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    Notes:
    ESTIMATED ENERGY INTAKE is the same as attribute ESTIMATED ENERGY INTAKE.ESTIMATED ENERGY INTAKE is the same as attribute ESTIMATED ENERGY INTAKE in 'Kilocalories (kcal)'. 

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    ESTIMATED GLOMERULAR FILTRATION RATE

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    Notes:
    ESTIMATED GLOMERULAR FILTRATION RATE is the outcome of the Clinical Investigation to determine the PATIENT's Estimated Glomerular Filtration Rate (eGFR), a test that is used to assess how well the kidneys are working.ESTIMATED GLOMERULAR FILTRATION RATE is the result of the Clinical Investigation to determine the PATIENT's Estimated Glomerular Filtration Rate (eGFR), a test that is used to assess how well the kidneys are working.

    ESTIMATED GLOMERULAR FILTRATION RATE is a measurement of how many millilitres (ml) of waste fluid the kidneys can filter from the blood in a minute, measured in'Millilitres per Minute (ml/min/1.73m2)' for renal cancer only.ESTIMATED GLOMERULAR FILTRATION RATE is a measurement of how many millilitres (ml) of waste fluid the kidneys can filter from the blood in a minute, measured in 'Millilitres per Minute divided by 1.73 Square Metres (ml/min/1.73m2)'.

    For the Cancer Outcomes and Services Data Set: Urology, ESTIMATED GLOMERULAR FILTRATION RATE is collected once at PATIENT DIAGNOSIS.

     

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    ESTIMATED POTASSIUM INTAKE

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    Format/Length:max n2.max n1
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    ESTIMATED POTASSIUM INTAKE is the same as attribute ESTIMATED POTASSIUM INTAKE.ESTIMATED POTASSIUM INTAKE is the same as attribute ESTIMATED POTASSIUM INTAKE in 'Millimoles (mmol)'. 

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    ESTIMATED PROTEIN INTAKE

    Change to Data Element: Changed Description

    Format/Length:max n3.max n1
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    National Codes: 
    Default Codes: 

    Notes:
    ESTIMATED PROTEIN INTAKE is the same as attribute ESTIMATED PROTEIN INTAKE.ESTIMATED PROTEIN INTAKE is the same as attribute ESTIMATED PROTEIN INTAKE in 'Grams (g)'. 

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    FINAL EXCISION MARGIN AFTER WIDE LOCAL EXCISION

    Change to Data Element: Changed Description

    Format/Length:max n2
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    FINAL EXCISION MARGIN AFTER WIDE LOCAL EXCISION is the same as attribute FINAL EXCISION MARGIN AFTER WIDE LOCAL EXCISION.FINAL EXCISION MARGIN AFTER WIDE LOCAL EXCISION is the same as attribute FINAL EXCISION MARGIN AFTER WIDE LOCAL EXCISION, measured in 'Millimetres (mm)'. 

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    FORCED EXPIRATORY VOLUME IN 1 SECOND (ABSOLUTE AMOUNT)

    Change to Data Element: Changed Description

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    FORCED EXPIRATORY VOLUME IN 1 SECOND (PERCENTAGE)

    Change to Data Element: Changed Description

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    GLUCOSE CONCENTRATION (DONOR)

    Change to Data Element: Changed Description

    Format/Length:max n2.max n1
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    GLUCOSE CONCENTRATION (DONOR) is the result of the Clinical Investigation which measures the ORGAN OR TISSUE DONOR's glucose concentration in 'mmol/L'.GLUCOSE CONCENTRATION (DONOR) is the result of the Clinical Investigation which measures the ORGAN OR TISSUE DONOR's glucose concentration in 'Millimoles per litre (mmol/L)'. 

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    HAEMOGLOBIN CONCENTRATION

    Change to Data Element: Changed Description

    Format/Length:max n2.n1
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    HAEMOGLOBIN CONCENTRATION is the outcome of the Clinical Investigation which measures the PERSON's haemoglobin concentration, measured in 'Grammes per decilitre (g/dl)'.HAEMOGLOBIN CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's haemoglobin concentration in 'Grams per decilitre (g/dl)'.

    For the Cancer Outcomes and Services Data Set, the value is presented in the range 1.0-25.0

     

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    HAND GRIP STRENGTH

    Change to Data Element: Changed Description

    Format/Length:max n2.n1
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    HAND GRIP STRENGTH is the Hand Grip Strength of the PERSON in kilograms.HAND GRIP STRENGTH is the Hand Grip Strength of a PATIENT, where the MEASUREMENT VALUE TYPE CODE is 'Kilograms (kg)'. 

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    HBA1C CONCENTRATION (DCCT)

    Change to Data Element: Changed Description

    Format/Length:max n2.max n1
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    HbA1c CONCENTRATION (DCCT) is the result of the Clinical Investigation which measures the PATIENT's HbA1c concentration where the measurement is made using the Diabetes Control and Complications Trial (DCCT) reference method  in 'Percentage'. HbA1c CONCENTRATION (DCCT) is the result of the Clinical Investigation which measures the PATIENT's HbA1c concentration where the MEASUREMENT VALUE TYPE CODE is 'Percentage'using the Diabetes Control and Complications Trial (DCCT) reference method. 

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    HBA1C CONCENTRATION (IFCC)

    Change to Data Element: Changed Description

    Format/Length:n1.n1
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    HbA1c CONCENTRATION (IFCC) is the result of the Clinical Investigation which measures the PATIENT's HbA1c concentration where the measurement is made using the International Federation of Clinical Chemistry (IFCC) reference method in 'mmol/mol'. HbA1c CONCENTRATION (IFCC) is the result of the Clinical Investigation which measures the PATIENT's HbA1c concentration in 'Millimoles per mole (mmol/mol)', where the measurement is made using the International Federation of Clinical Chemistry (IFCC) reference method. 

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    HEAD CIRCUMFERENCE (RENAL PAEDIATRIC)

    Change to Data Element: Changed Description

    Format/Length:max n3
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    Default Codes: 


    Notes:
    HEAD CIRCUMFERENCE (RENAL PAEDIATRIC) is the Head Circumference of the PERSON in centimetres.

    HEAD CIRCUMFERENCE (RENAL PAEDIATRIC) is the Head Circumference of a PATIENT, where the MEASUREMENT VALUE TYPE CODE is 'Centimetres (cm)'. 

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    HEAD CIRCUMFERENCE (RENAL PAEDIATRIC)

    Change to Data Element: Changed Description

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    HEART RATE

    Change to Data Element: Changed Description

    Format/Length:max n3
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    HEART RATE is the Heart Rate of the PERSON.HEART RATE is the Heart Rate of the PATIENT, where the MEASUREMENT VALUE TYPE CODE is 'Beats per minute (bpm)'. 

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    HIP MEASUREMENT

    Change to Data Element: Changed Description

    Format/Length:max n3
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    HIP MEASUREMENT is the Hip Measurement of the PERSON in centimetres.HIP MEASUREMENT is the Hip Measurement of the PATIENT, where the MEASUREMENT VALUE TYPE CODE is 'Centimetres (cm)'. 

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    HUMAN CHORIONIC GONADOTROPIN

    Change to Data Element: Changed Description

    Format/Length:max n7
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    HUMAN CHORIONIC GONADOTROPIN is the outcome of the Clinical Investigation to determine the PATIENT's serum Tumour markers for human chorionic gonadotropin (HCG) (a glycoprotein found in abnormal amounts in the blood of PATIENTS with cancer).HUMAN CHORIONIC GONADOTROPIN is the result of the Clinical Investigation to determine the PATIENT's serum Tumour markers for human chorionic gonadotropin (HCG) (a glycoprotein found in abnormal amounts in the blood of PATIENTS with cancer). 

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    ISOTOPIC GLOMERULAR FILTRATION RATE (LIVING DONOR)

    Change to Data Element: Changed Description

    Format/Length:max n3
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    Notes:
    ISOTOPIC GLOMERULAR FILTRATION RATE (LIVING DONOR) is the result of the Clinical Investigation which measures the living ORGAN OR TISSUE DONOR's isotopic glomerular filtration rate in 'ml/min'. ISOTOPIC GLOMERULAR FILTRATION RATE (LIVING DONOR) is the result of the Clinical Investigation which measures the living ORGAN OR TISSUE DONOR's isotopic glomerular filtration rate in 'Millilitres per Minute (ml/min)'. 

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    LESION SIZE (RADIOLOGICAL)

    Change to Data Element: Changed Description

    Format/Length:max n3
    HES Item: 
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    Default Codes: 

    Notes:
    LESION SIZE (RADIOLOGICAL) is the same as attribute LESION SIZE.

    LESION SIZE (RADIOLOGICAL) is the radiological estimate size of the maximum diameter of the primary Lesion (or largest Lesion if there is more than one), measured in 'Millimetres (mm)'.LESION SIZE (RADIOLOGICAL) is the radiologically estimated size of the maximum diameter of the primary Lesion (or largest Lesion if there is more than one), measured in Millimetres (mm)'.

    For the Cancer Outcomes and Services Data Set: Central Nervous System:

    • The maximum size of the Tumour or Lesion will be 99 Millimetres
    • Record '00' to indicate the Tumour or Lesion is not assessable for diffuse Tumours (e.g. gliomatosis cerebri).
     

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    MEASURED 24HR CREATININE CLEARANCE

    Change to Data Element: Changed Description

    Format/Length:max n3.max n2
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    MEASURED 24HR CREATININE CLEARANCE is the result of the Clinical Investigation which measures the PATIENT's measured creatinine clearance in "ml/min".MEASURED 24HR CREATININE CLEARANCE is the result of the Clinical Investigation which measures the PATIENT's measured creatinine clearance in 'Millilitres per Minute (ml/min)', in a 24 hour period. 

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    MEASURED CREATININE CLEARANCE

    Change to Data Element: Changed Description

    Format/Length:max n3.max n2
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    Notes:
    MEASURED CREATININE CLEARANCE is the result of the Clinical Investigation which measures the  PERSON's measured creatinine clearance in "ml/min".MEASURED CREATININE CLEARANCE is the result of the Clinical Investigation which measures the PATIENT's measured creatinine clearance in 'Millilitres per Minute (ml/min)'. 

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    MEASURED GLOMERULAR FILTRATION RATE

    Change to Data Element: Changed Description

    Format/Length:max n3.max n2
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    MEASURED GLOMERULAR FILTRATION RATE is the result of the Clinical Investigation which measures the PATIENT's measured glomerular filtration rate in 'ml/min' where the measurement is uncorrected or in 'ml/min/1.73²' where the measurement is corrected.MEASURED GLOMERULAR FILTRATION RATE is the result of the Clinical Investigation which measures the PATIENT's measured glomerular filtration rate in: 
  • 'Millilitres per Minute (ml/min)' where the measurement is uncorrected or
  • 'Millilitres per Minute (ml/min/1.73m2)'  where the measurement is corrected.
  •  

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    MITOTIC RATE

    Change to Data Element: Changed Description

    Format/Length:max n2
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    MITOTIC RATE is the outcome of the Clinical Investigation which measures the PERSON's Mitotic Rate (MR), a measure of how fast cancer CELLS are dividing and growing, measured in 'Square Millimetre (mm2)'.MITOTIC RATE is the outcome of the Clinical Investigation which measures the PATIENT's Mitotic Rate (MR), a measure of how fast cancer CELLS are dividing and growing, in 'Square Millimetres (mm2)'. 

    The value is presented in the range 0-20.

     

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    MYCOPHENOLIC ACID TROUGH LEVEL (RECIPIENT)

    Change to Data Element: Changed Description

    Format/Length:max n2.max n1
    HES Item: 
    National Codes: 
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    Notes:
    MYCOPHENOLIC ACID TROUGH LEVEL (RECIPIENT) is the result of the Clinical Investigation which measures the PATIENT's mycophenolic acid (MPA) trough level in 'µg/ml'.MYCOPHENOLIC ACID TROUGH LEVEL (RECIPIENT) is the result of the Clinical Investigation which measures the PATIENT's mycophenolic acid (MPA) trough level in 'Micrograms per millilitre (µg/ml)'. 

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    NUMBER OF SENTINEL NODES POSITIVE

    Change to Data Element: Changed Description

    Format/Length:max n2
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    Default Codes: 

    Notes:
    NUMBER OF SENTINEL NODES POSITIVE is the outcome of the Clinical Investigation which measures the number of Sentinel Lymph Nodes tested as positive.NUMBER OF SENTINEL NODES POSITIVE is the result of the Clinical Investigation which measures the number of Sentinel Lymph Nodes tested as positive.

    Note: a positive result indicates that cancer is present in the sampled Sentinel Node(s).

     

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    NUMBER OF SENTINEL NODES POSITIVE (POST SENTINEL NODE COMPLETION LYMPHADENECTOMY)

    Change to Data Element: Changed Description

    Format/Length:max n2
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    NUMBER OF SENTINEL NODES POSITIVE is the outcome of the Clinical Investigation which measures the number of Sentinel Lymph Nodes tested as positive following a Sentinel Lymph Node Biopsy completion lymphadenectomy.NUMBER OF SENTINEL NODES POSITIVE is the result of the Clinical Investigation which measures the number of Sentinel Lymph Nodes tested as positive following a Sentinel Lymph Node Biopsy completion lymphadenectomy. 

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    NUMBER OF SENTINEL NODES SAMPLED

    Change to Data Element: Changed Description

    Format/Length:max n2
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    NUMBER OF SENTINEL NODES SAMPLED is the outcome of the Clinical Investigation which measures the number of Sentinel Lymph Nodes sampled.NUMBER OF SENTINEL NODES SAMPLED is the result of the Clinical Investigation which measures the number of Sentinel Lymph Nodes sampled. 

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    NUMBER OF SENTINEL NODES SAMPLED (POST SENTINEL NODE COMPLETION LYMPHADENECTOMY)

    Change to Data Element: Changed Description

    Format/Length:max n2
    HES item: 
    National Codes: 
    Default Codes: 

    Notes:
    NUMBER OF SENTINEL NODES SAMPLED (POST SENTINEL NODE COMPLETION LYMPHADENECTOMY) is the outcome of the Clinical Investigation which measures the number of Sentinel Lymph Nodes sampled following a Sentinel Lymph Node Biopsy completion lymphadenectomy.NUMBER OF SENTINEL NODES SAMPLED (POST SENTINEL NODE COMPLETION LYMPHADENECTOMY) is the result of the Clinical Investigation which measures the number of Sentinel Lymph Nodes sampled following a Sentinel Lymph Node Biopsy completion lymphadenectomy. 

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    OBSERVATION DATE (WAIST MEASUREMENT)

    Change to Data Element: Changed Description

    Format/Length:See DATE 
    HES Item: 
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    Default Codes: 

    Notes:
    OBSERVATION DATE (WAIST MEASUREMENT) is the same as attribute PERSON PROPERTY OBSERVED DATE.

    OBSERVATION DATE (WAIST MEASUREMENT) is the date when the PERSON's Waist Measurement was taken.OBSERVATION DATE (WAIST MEASUREMENT) is the date when the PATIENT's Waist Measurement was taken.

     

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    PERCENTAGE WEIGHT LOSS

    Change to Data Element: Changed Description

    Format/Length:max n2.max n1
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    PERCENTAGE WEIGHT LOSS corresponds to the MEASURED OBSERVATION VALUE:PERCENTAGE WEIGHT LOSS is a PATIENT's Percentage Weight Loss, where the MEASUREMENT VALUE TYPE CODE is 'Percentage'. 

    In a Nutritional Assessment for a renal PATIENT this would be measured over a 3 month period.

     

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    PERITONEAL DIALYSIS TOTAL WEEKLY FLUID VOLUME

    Change to Data Element: Changed Description

    Format/Length:max n3.max n2
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    PERITONEAL DIALYSIS TOTAL WEEKLY FLUID VOLUME is the result of the Clinical Investigation which measures the PATIENT's peritoneal dialysis total fluid volume per week in 'Litres'.PERITONEAL DIALYSIS TOTAL WEEKLY FLUID VOLUME is the result of the Clinical Investigation which measures the PATIENT's peritoneal dialysis total fluid volume per week in 'Litres (l)'. 

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    PERSON HEIGHT IN CENTIMETRES

    Change to Data Element: Changed Description

    Format/Length:max n3.n1
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    PERSON HEIGHT IN CENTIMETRES records the Height of the PERSON in centimetres.PERSON HEIGHT IN CENTIMETRES is the Height of the PATIENT, where the MEASUREMENT VALUE TYPE CODE is 'Centimetres (cm)'. 

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    PERSON HEIGHT IN METRES

    Change to Data Element: Changed Description

    Format/Length:n1.max n2
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    PERSON HEIGHT IN METRES records the Height of the PERSON in metres.PERSON HEIGHT IN METRES is the Height of the PATIENT, where the MEASUREMENT VALUE TYPE CODE is 'Metres (m)'.

    For the Systemic Anti-Cancer Therapy Data Set, PERSON HEIGHT IN METRES is the Height at the start of the Systemic Anti-Cancer Drug Regimen.

     

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    PERSON OBSERVATION (BMI)

    Change to Data Element: Changed Description

    Format/Length:nn.n
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    PERSON OBSERVATION (BMI) records the Body Mass Index of the PERSON.PERSON OBSERVATION (BMI) is the Body Mass Index of the PATIENT.

    This value is derived from Weight in kilograms divided by Height in metres squared (kg/m²).

    PERSON OBSERVATION (BMI) will be replaced with BODY MASS INDEX, which should be used for all new and developing data sets and for XML messages.

     

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    PERSON OBSERVATION (HBA1C LEVEL)

    Change to Data Element: Changed Description

    Format/Length:n3 nn.n
    Format/Length:n2.n1
    HES Item: 
    National Codes: 
    Default Codes: 


    Notes:
    PERSON OBSERVATION (HbA1c LEVEL) is the recorded Glycated Hemoglobin (HbA1c) of a PERSON.

    This corresponds to MEASURED OBSERVATION VALUE where the MEASURED PERSON OBSERVATION TYPE CODE is 'HbA1c' and the MEASUREMENT VALUE TYPE CODE is 'Number'. 

    PERSON OBSERVATION (HbA1c LEVEL) is the Glycated Hemoglobin (HbA1c) of a PATIENT, where the MEASUREMENT VALUE TYPE CODE is 'Millimoles per litre (mmol/L)'. 

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    PERSON OBSERVATION (SERUM CHOLESTEROL LEVEL)

    Change to Data Element: Changed Description

    Format/Length:n3 nn.n
    Format/Length:n3
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    PERSON OBSERVATION (SERUM CHOLESTEROL LEVEL) is the recorded cholesterol level (Serum Cholesterol Level in mmol/L) of a PATIENT.

    This corresponds to MEASURED OBSERVATION VALUE where the MEASURED PERSON OBSERVATION TYPE CODE is 'Serum Cholesterol Level' and the MEASUREMENT VALUE TYPE CODE is 'mmol/L'. 

    PERSON OBSERVATION (SERUM CHOLESTEROL LEVEL) is the Serum Cholesterol Level of a PATIENT, where the MEASUREMENT VALUE TYPE CODE is 'Millimoles per litre (mmol/L)'. 

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    PERSON OBSERVATION (SERUM CREATININE LEVEL)

    Change to Data Element: Changed Description

    Format/Length:n4 - nnnn
    Format/Length:n4
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    National Codes: 
    Default Codes: 


    Notes:
    PERSON OBSERVATION (SERUM CREATININE LEVEL) is the recorded Serum Creatinine Level (µmol/L) of a PERSON using laboratory assay.

    This corresponds to MEASURED OBSERVATION VALUE where the MEASURED PERSON OBSERVATION TYPE CODE is 'Serum Creatinine Level' and the MEASUREMENT VALUE TYPE CODE is 'µmol/L'. 

    PERSON OBSERVATION (SERUM CREATININE LEVEL) is the Serum Creatinine Level of a PATIENT using laboratory assay, where the MEASUREMENT VALUE TYPE CODE is 'Micromoles per litre (µmol/L)'. 

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    PERSON OBSERVATION (URINARY ALBUMIN LEVEL)

    Change to Data Element: Changed Description

    Format/Length:n3 - nnn
    Format/Length:n3
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    Default Codes: 


    Notes:
    PERSON OBSERVATION (URINARY ALBUMIN LEVEL) is the recorded result of the Urinary Albumin Level and must be accompanied by a recorded URINARY ALBUMIN LEVEL TESTING METHOD.

    PERSON OBSERVATION (URINARY ALBUMIN LEVEL) is the result of the Urinary Albumin Level test.

    PERSON OBSERVATION (URINARY ALBUMIN LEVEL) is derived from the MEASURED OBSERVATION VALUE recorded for the MEASURED PERSON OBSERVATION TYPE CODE 'Urinary Albumin Level'.For the Diabetes Data Set (Summary Core), PERSON OBSERVATION (URINARY ALBUMIN LEVEL) must be accompanied by a recorded URINARY ALBUMIN LEVEL TESTING METHOD.

     

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    PERSON WEIGHT

    Change to Data Element: Changed Description

    Format/Length:max n3.max n3
    HES Item: 
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    Default Codes: 

    Notes:
    PERSON WEIGHT records the Weight of the PERSON.PERSON WEIGHT is the Weight of the PATIENT, where the MEASUREMENT VALUE TYPE CODE is 'Kilograms (kg)'.

    PERSON WEIGHT corresponds to MEASURED OBSERVATION VALUE where the MEASURED PERSON OBSERVATION TYPE CODE is 'Weight' and the MEASUREMENT VALUE TYPE CODE is 'Kilograms'.

    Notes:

     

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    PERSON WEIGHT (POST DIALYSIS)

    Change to Data Element: Changed Description

    Format/Length:max n3.max n2
    HES Item: 
    National Codes: 
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    Notes:
    PERSON WEIGHT (POST DIALYSIS) records the PATIENT's Weight before a Haemodialysis session where the MEASURED PERSON OBSERVATION TYPE CODE is 'Kilograms'.PERSON WEIGHT (POST DIALYSIS) is a PATIENT's Weight following a Haemodialysis session, where the MEASUREMENT VALUE TYPE CODE is 'Kilograms (kg)'. 

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    PERSON WEIGHT (PRE-DIALYSIS)

    Change to Data Element: Changed Description

    Format/Length:max n3.max n2
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    Notes:
    PERSON WEIGHT (PRE-DIALYSIS) records the PATIENT's Weight before a Haemodialysis session where the MEASURED PERSON OBSERVATION TYPE CODE is 'Kilograms'.PERSON WEIGHT (PRE-DIALYSIS) is a PATIENT's Weight before a Haemodialysis session, where the MEASUREMENT VALUE TYPE CODE is 'Kilograms (kg)'. 

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    PERSON WEIGHT (RENAL CARE)

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    Notes:
    PERSON WEIGHT (RENAL CARE) is the record of a PERSON's Weight in 'Kilograms'.

    During a Nutritional Assessment the PERSON's Dry Weight will be recorded.

    PERSON WEIGHT (RENAL CARE) is a PATIENT's Weight, for the purpose of the National Renal Data Set, where the MEASUREMENT VALUE TYPE CODE is 'Kilograms (kg)'. 

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    PHOSPHATE CONCENTRATION

    Change to Data Element: Changed Description

    Format/Length:max n2.max n2
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    Notes:
    PHOSPHATE CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's phosphate concentration in 'mmol/L'.PHOSPHATE CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's phosphate concentration in 'Millimoles per litre (mmol/L)'. 

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    POSITIVE END-EXPIRATORY PRESSURE

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    Format/Length:max n2
    HES Item: 
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    Notes:
    POSITIVE END-EXPIRATORY PRESSURE is the outcome of the Clinical Investigation which measures the PERSON's positive end-expiratory pressure (PEEP) in 'mmH2O'.POSITIVE END-EXPIRATORY PRESSURE is the result of the Clinical Investigation which measures the PERSON's positive end-expiratory pressure (PEEP) in 'Millimetres of water (mmH2O)'. 

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    POTASSIUM CONCENTRATION (DONOR ON ADMISSION)

    Change to Data Element: Changed Description

    Format/Length:n1.n1
    HES Item: 
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    Default Codes: 

    Notes:
    POTASSIUM CONCENTRATION (DONOR ON ADMISSION) is the outcome of the Clinical Investigation which measures the ORGAN OR TISSUE DONOR's potassium concentration on admission in 'mmol/L'.POTASSIUM CONCENTRATION (DONOR ON ADMISSION) is the result of the Clinical Investigation which measures the ORGAN OR TISSUE DONOR's potassium concentration on admission in 'Millimoles per litre (mmol/L)'. 

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    POTASSIUM CONCENTRATION (DONOR ON RETRIEVAL)

    Change to Data Element: Changed Description

    Format/Length:n1.n1
    HES Item: 
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    Notes:
    POTASSIUM CONCENTRATION (DONOR ON RETRIEVAL) is the outcome of the Clinical Investigation which measures the ORGAN OR TISSUE DONOR's potassium concentration on retrieval in 'mmol/L'.POTASSIUM CONCENTRATION (DONOR ON RETRIEVAL) is the result of the Clinical Investigation which measures the ORGAN OR TISSUE DONOR's potassium concentration on retrieval in 'Millimoles per litre (mmol/L)'. 

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    PRESCRIBED DOSE

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    Notes:
    PRESCRIBED DOSE is the dose stated against the PRESCRIBED ITEM on the PRESCRIPTION for the PATIENT.

    The measurement for PRESCRIBED DOSE is in MEASUREMENT VALUE TYPE CODE National code  'milligrams (mg)'. 

     

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    PRESCRIBED DOSE (ALEMTUZUMAB)

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    Notes:
    PRESCRIBED DOSE (ALEMTUZUMAB) is the PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Alemtuzumab'.PRESCRIBED DOSE (ALEMTUZUMAB) is the PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Alemtuzumab' in 'Milligrams (mg)'. 

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    PRESCRIBED DOSE (ANTI-HUMAN T-LYMPHOCYTE GLOBULIN)

    Change to Data Element: Changed Description

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    Notes:
    PRESCRIBED DOSE (ANTI-HUMAN T-LYMPHOCYTE GLOBULIN) is the total PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Anti-human T-lymphocyte globulin'.PRESCRIBED DOSE (ANTI-HUMAN T-LYMPHOCYTE GLOBULIN) is the total PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Anti-human T-lymphocyte globulin' in 'Milligrams (mg)'. 

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    PRESCRIBED DOSE (ANTITHYMOCYTE GLOBULIN)

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    Default Codes: 

    Notes:
    PRESCRIBED DOSE (ANTITHYMOCYTE GLOBULIN) is the total PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Antithymocyte globulin'.PRESCRIBED DOSE (ANTITHYMOCYTE GLOBULIN) is the total PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Antithymocyte globulin' in 'Milligrams (mg)'. 

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    PRESCRIBED DOSE (AZATHIOPRINE)

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    Notes:
    PRESCRIBED DOSE (AZATHIOPRINE) is the PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Azathioprine'.PRESCRIBED DOSE (AZATHIOPRINE) is the PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Azathioprine' in 'Milligrams (mg)'. 

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    PRESCRIBED DOSE (BASILIXIMAB)

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    Default Codes: 

    Notes:
    PRESCRIBED DOSE (BASILIXIMAB) is the PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Basililximab'.PRESCRIBED DOSE (BASILIXIMAB) is the PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Basililximab' in 'Milligrams (mg)'. 

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    PRESCRIBED DOSE (CICLOSPORIN)

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    Default Codes: 

    Notes:
    PRESCRIBED DOSE (CICLOSPORIN) is the PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Ciclosporin'.PRESCRIBED DOSE (CICLOSPORIN) is the PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Ciclosporin' in 'Milligrams (mg)'. 

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    PRESCRIBED DOSE (DACLIZUMAB)

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    Default Codes: 

    Notes:
    PRESCRIBED DOSE (DACLIZUMAB) is the PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Daclizumab'.PRESCRIBED DOSE (DACLIZUMAB) is the PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Daclizumab' in 'Milligrams (mg)'. 

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    PRESCRIBED DOSE (GROWTH HORMONE)

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    Format/Length:max n2.n1
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    Notes:
    PRESCRIBED DOSE (GROWTH HORMONE) is the PATIENT's PRESCRIBED DOSE of growth hormone where the MEASUREMENT VALUE TYPE CODE = 'iu/kg'.PRESCRIBED DOSE (GROWTH HORMONE) is the PATIENT's PRESCRIBED DOSE of growth hormone in 'International Units per kilogram (IU/kg)'. 

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    PRESCRIBED DOSE (MUROMONAB-CD3)

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    Default Codes: 

    Notes:
    PRESCRIBED DOSE (MUROMONAB-CD3) is the total PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Muromonab-CD3'.PRESCRIBED DOSE (MUROMONAB-CD3) is the total PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Muromonab-CD3' in 'Milligrams (mg)'. 

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    PRESCRIBED DOSE (MYCOPHENOLATE MOFETIL)

    Change to Data Element: Changed Description

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    Default Codes: 

    Notes:
    PRESCRIBED DOSE (MYCOPHENOLATE MOFETIL) is the PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Mycophenolate mofetil'.PRESCRIBED DOSE (MYCOPHENOLATE MOFETIL) is the PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Mycophenolate mofetil' in 'Milligrams (mg)'. 

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    PRESCRIBED DOSE (MYCOPHENOLATE SODIUM)

    Change to Data Element: Changed Description

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    Default Codes: 

    Notes:
    PRESCRIBED DOSE (MYCOPHENOLATE SODIUM) is the PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Mycophenolate sodium'.PRESCRIBED DOSE (MYCOPHENOLATE SODIUM) is the PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Mycophenolate sodium' in 'Milligrams (mg)'. 

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    PRESCRIBED DOSE (PREDNISOLONE OR PREDNISONE)

    Change to Data Element: Changed Description

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    Default Codes: 

    Notes:
    PRESCRIBED DOSE (PREDNISOLONE OR PREDNISONE) is the PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Prednisolone or prednisone'.PRESCRIBED DOSE (PREDNISOLONE OR PREDNISONE) is the PRESCRIBED DOSE of the RENAL MEDICATION TYPE of 'Prednisolone or prednisone' in 'Milligrams (mg)'. 

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    PRESCRIBED ITEM (VOLUME OF 136 GLUCOSE FLUID)

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    Notes:
    PRESCRIBED ITEM (VOLUME OF 136 GLUCOSE FLUID) records the volume used per day of the RENAL DIALYSIS MEDICATION TYPE 'Volume of 1.36% glucose fluid' in ml.PRESCRIBED ITEM (VOLUME OF 136 GLUCOSE FLUID) is the volume used per day of the RENAL DIALYSIS MEDICATION TYPE '1.36% glucose' in 'Millilitres (ml)'. 

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    PRESCRIBED ITEM (VOLUME OF 227 GLUCOSE FLUID)

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    Notes:
    PRESCRIBED ITEM (VOLUME OF 227 GLUCOSE FLUID) records the volume used per day of the RENAL DIALYSIS MEDICATION TYPE 'Volume of 2.27% glucose fluid' in ml.PRESCRIBED ITEM (VOLUME OF 227 GLUCOSE FLUID) is the volume used per day of the RENAL DIALYSIS MEDICATION TYPE '2.27% glucose' in 'Millilitres (ml)'. 

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    PRESCRIBED ITEM (VOLUME OF 386 GLUCOSE FLUID)

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    Notes:
    PRESCRIBED ITEM (VOLUME OF 386 GLUCOSE FLUID) records the volume used per day of the RENAL DIALYSIS MEDICATION TYPE 'Volume of 3.86% glucose fluid' in ml.PRESCRIBED ITEM (VOLUME OF 386 GLUCOSE FLUID) is the volume used per day of the RENAL DIALYSIS MEDICATION TYPE '3.86% glucose' in 'Millilitres (ml)'. 

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    PRESCRIBED ITEM (VOLUME OF AMINO ACID DIALYSIS FLUID)

    Change to Data Element: Changed Description

    Format/Length:max n4
    HES Item: 
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    Default Codes: 

    Notes:
    PRESCRIBED ITEM (VOLUME OF AMINO ACID DIALYSIS FLUID) records the volume used per day of the RENAL DIALYSIS MEDICATION TYPE 'Volume of amino acid dialysis fluid' in ml.PRESCRIBED ITEM (VOLUME OF AMINO ACID DIALYSIS FLUID) is the volume used per day of the RENAL DIALYSIS MEDICATION TYPE 'Amino acid solution' in 'Millilitres (ml)'. 

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    PRESCRIBED ITEM (VOLUME OF ICODEXTRIN DIALYSIS FLUID)

    Change to Data Element: Changed Description

    Format/Length:max n4
    HES Item: 
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    Default Codes: 

    Notes:
    PRESCRIBED ITEM (VOLUME OF ICODEXTRIN DIALYSIS FLUID) records the volume used per day of the RENAL DIALYSIS MEDICATION TYPE 'Volume of icodextrin dialysis fluid' in ml.PRESCRIBED ITEM (VOLUME OF ICODEXTRIN DIALYSIS FLUID) is the volume used per day of the RENAL DIALYSIS MEDICATION TYPE 'Icodextrin peritoneal dialysis solution' in 'Millilitres (ml)'. 

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    PRESCRIBED ITEM SIZE (PERITONEAL BAG)

    Change to Data Element: Changed Description

    Format/Length:max n1.max n2
    HES Item: 
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    Default Codes: 

    Notes:
    PRESCRIBED ITEM SIZE (PERITONEAL BAG) is the peritoneal dialysis bag size in litres that was prescribed for the PATIENT.PRESCRIBED ITEM SIZE (PERITONEAL BAG) is the peritoneal dialysis bag size that was prescribed for the PATIENT in 'Litres (l)'. 

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    PRESCRIBED ITEM VOLUME USAGE PER OVERNIGHT (PERITONEAL DIALYSIS FLUID ON AUTOMATED PERITONEAL DIALYSIS)

    Change to Data Element: Changed Description

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    Default Codes: 

    Notes:
    PRESCRIBED ITEM VOLUME USAGE PER OVERNIGHT (PERITONEAL DIALYSIS FLUID ON AUTOMATED PERITONEAL DIALYSIS) is the overnight peritoneal dialysis volume in millilitres used on automated peritoneal dialysis (APD).PRESCRIBED ITEM VOLUME USAGE PER OVERNIGHT (PERITONEAL DIALYSIS FLUID ON AUTOMATED PERITONEAL DIALYSIS) is the overnight peritoneal dialysis volume used on automated peritoneal dialysis (APD) in 'Millilitres (ml)'. 

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    PRESCRIBED TOTAL DAILY DOSE (ALEMTUZUMAB)

    Change to Data Element: Changed Description

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    Default Codes: 

    Notes:
    PRESCRIBED TOTAL DAILY DOSE (ALEMTUZUMAB) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Alemtuzumab' being administered to the PATIENT at the time of the follow up assessment in mgs.PRESCRIBED TOTAL DAILY DOSE (ALEMTUZUMAB) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Alemtuzumab' in 'Milligrams (mg)'. For the National Renal Data Set, PRESCRIBED TOTAL DAILY DOSE (ALEMTUZUMAB) is the prescribed daily amount being administered to the PATIENT at the time of the follow up assessment.

     

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    PRESCRIBED TOTAL DAILY DOSE (AZATHIOPRINE)

    Change to Data Element: Changed Description

    Format/Length:max n3
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    Default Codes: 

    Notes:
    PRESCRIBED TOTAL DAILY DOSE (AZATHIOPRINE) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Azathioprine' being administered to the PATIENT at the time of the follow up assessment in mgs.PRESCRIBED TOTAL DAILY DOSE (AZATHIOPRINE) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Azathioprine' in 'Milligrams (mg)'. For the National Renal Data Set, PRESCRIBED TOTAL DAILY DOSE (AZATHIOPRINE) is the prescribed daily amount being administered to the PATIENT at the time of the follow up assessment.

     

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    PRESCRIBED TOTAL DAILY DOSE (BASILIXIMAB)

    Change to Data Element: Changed Description

    Format/Length:max n3
    HES Item: 
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    Default Codes: 

    Notes:
    PRESCRIBED TOTAL DAILY DOSE (BASILIXIMAB) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Basiliximab" being administered to the PATIENT at the time of the follow up assessment.PRESCRIBED TOTAL DAILY DOSE (BASILIXIMAB) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Basiliximab". For the National Renal Data Set, PRESCRIBED TOTAL DAILY DOSE (BASILIXIMAB) is the prescribed daily amount being administered to the PATIENT at the time of the follow up assessment.

     

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    PRESCRIBED TOTAL DAILY DOSE (CICLOSPORIN)

    Change to Data Element: Changed Description

    Format/Length:max n3
    HES Item: 
    National Codes: 
    Default Codes: 

    Notes:
    PRESCRIBED TOTAL DAILY DOSE (CICLOSPORIN) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Ciclosporine' being administered to the PATIENT at the time of the follow up assessment in mgs.PRESCRIBED TOTAL DAILY DOSE (CICLOSPORIN) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Ciclosporine' in 'Milligrams (mg)'. For the National Renal Data Set, PRESCRIBED TOTAL DAILY DOSE (CICLOSPORIN) is the prescribed daily amount being administered to the PATIENT at the time of the follow up assessment.

     

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    PRESCRIBED TOTAL DAILY DOSE (DACLIZUMAB)

    Change to Data Element: Changed Description

    Format/Length:max n3
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    National Codes: 
    Default Codes: 

    Notes:
    PRESCRIBED TOTAL DAILY DOSE (DACLIZUMAB) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Daclizumab' being administered to the PATIENT at the time of the follow up assessment in mgs.PRESCRIBED TOTAL DAILY DOSE (DACLIZUMAB) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Daclizumab' in 'Milligrams (mg)'. For the National Renal Data Set, PRESCRIBED TOTAL DAILY DOSE (DACLIZUMAB) is the prescribed daily amount being administered to the PATIENT at the time of the follow up assessment.

     

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    PRESCRIBED TOTAL DAILY DOSE (MYCOPHENOLATE MOFETIL)

    Change to Data Element: Changed Description

    Format/Length:max n3
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    Default Codes: 

    Notes:
    PRESCRIBED TOTAL DAILY DOSE (MYCOPHENOLATE MOFETIL) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Mycophenolate mofetil' being administered to the PATIENT at the time of the follow up assessment.PRESCRIBED TOTAL DAILY DOSE (MYCOPHENOLATE MOFETIL) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Mycophenolate mofetil'. For the National Renal Data Set, PRESCRIBED TOTAL DAILY DOSE (MYCOPHENOLATE MOFETIL) is the prescribed daily amount being administered to the PATIENT at the time of the follow up assessment

     

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    PRESCRIBED TOTAL DAILY DOSE (MYCOPHENOLATE SODIUM)

    Change to Data Element: Changed Description

    Format/Length:max n3
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    Notes:
    PRESCRIBED TOTAL DAILY DOSE (MYCOPHENOLATE SODIUM) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Mycophenolate sodium' being administered to the PATIENT at the time of the follow up assessment in mgs.PRESCRIBED TOTAL DAILY DOSE (MYCOPHENOLATE SODIUM) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Mycophenolate sodium' in 'Milligrams (mg)'. For the National Renal Data Set, PRESCRIBED TOTAL DAILY DOSE (MYCOPHENOLATE SODIUM) is the prescribed daily amount being administered to the PATIENT at the time of the follow up assessment.

     

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    PRESCRIBED TOTAL DAILY DOSE (PREDNISOLONE OR PREDNISONE)

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    Format/Length:max n3
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    Notes:
    PRESCRIBED TOTAL DAILY DOSE (PREDNISOLONE OR PREDNISONE) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Prednisolone or prednisone' being administered to the PATIENT at the time of the follow up assessment.PRESCRIBED TOTAL DAILY DOSE (PREDNISOLONE OR PREDNISONE) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Prednisolone or prednisone'. For the National Renal Data Set, PRESCRIBED TOTAL DAILY DOSE (PREDNISOLONE OR PREDNISONE) is the prescribed daily amount being administered to the PATIENT at the time of the follow up assessment.

     

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    PRESCRIBED TOTAL DAILY DOSE (SIROLIMUS)

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    Notes:
    PRESCRIBED TOTAL DAILY DOSE (SIROLIMUS) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Sirolimus' being administered to the PATIENT

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    PRESCRIBED TOTAL DAILY DOSE (TACROLIMUS)

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    Notes:
    PRESCRIBED TOTAL DAILY DOSE (TACROLIMUS) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Tacrolimus' being administered to the PATIENT at the time of the follow up assessment in mgs.PRESCRIBED TOTAL DAILY DOSE (TACROLIMUS) is the prescribed daily amount of the RENAL MEDICATION TYPE of 'Tacrolimus' in 'Milligrams (mg)'. For the National Renal Data Set, PRESCRIBED TOTAL DAILY DOSE (TACROLIMUS) is the prescribed daily amount being administered to the PATIENT at the time of the follow up assessment.

     

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    PRIMARY TUMOUR SIZE (RADIOLOGICAL)

    Change to Data Element: Changed Description

    Format/Length:max n3
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    Notes:
    PRIMARY TUMOUR SIZE (RADIOLOGICAL) is the same as attribute TUMOUR SIZE.

    PRIMARY TUMOUR SIZE (RADIOLOGICAL) is the maximum dimension the primary Tumour, measured in 'Millimetres (mm)', as agreed at the Multidisciplinary Team Meeting.PRIMARY TUMOUR SIZE (RADIOLOGICAL) is the maximum dimension of the primary Tumour, as agreed at the Multidisciplinary Team Meeting, in 'Millimetres (mm)'.

     

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    PROCEDURE (NET DAILY ULTRAFILTRATION)

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    Notes:
    PROCEDURE (NET DAILY ULTRAFILTRATION) records the net daily volume in 'ml', for peritoneal dialysis PATIENTS.PROCEDURE (NET DAILY ULTRAFILTRATION) is the net daily volume in 'Millilitres (ml)', for peritoneal dialysis PATIENTS. 

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    PROSTATE SPECIFIC ANTIGEN (DIAGNOSIS)

    Change to Data Element: Changed Description

    Format/Length:max n5.n1
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    Notes:
    PROSTATE SPECIFIC ANTIGEN (DIAGNOSIS) is the outcome of the Clinical Investigation to measure the Prostate Specific Antigen blood level (a protein made by the prostate gland and found in the blood) at the time of PATIENT DIAGNOSIS for prostate cancer, measured in 'Nanograms per millilitre (ng/ml)'.PROSTATE SPECIFIC ANTIGEN (DIAGNOSIS) is the result of the Clinical Investigation to measure the Prostate Specific Antigen blood level (a protein made by the prostate gland and found in the blood) at the time of PATIENT DIAGNOSIS for prostate cancer in 'Nanograms per millilitre (ng/ml)'. 

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    PROSTATE SPECIFIC ANTIGEN (PRE-TREATMENT)

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    Notes:
    PROSTATE SPECIFIC ANTIGEN (PRE-TREATMENT) is the outcome of the Clinical Investigation to measure the Prostate Specific Antigen blood level (a protein made by the prostate gland and found in the blood) before treatment (including second and subsequent treatments) for prostate cancer, measured in 'Nanograms per millilitre (ng/ml)'.PROSTATE SPECIFIC ANTIGEN (PRE-TREATMENT) is the result of the Clinical Investigation to measure the Prostate Specific Antigen blood level (a protein made by the prostate gland and found in the blood) before treatment (including second and subsequent treatments) for prostate cancer in 'Nanograms per millilitre (ng/ml)'. 

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    PROTEIN CREATININE RATIO

    Change to Data Element: Changed Description

    Format/Length:max n3.max n1
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    Notes:
    PROTEIN CREATININE RATIO records the outcome of the Clinical Investigation which measures the PERSON's protein:creatinine ratio in 'mg/mmol'.PROTEIN CREATININE RATIO is the result of the Clinical Investigation which measures the PATIENT's protein creatinine ratio in 'Milligrams per millimole (mg/mmol)'. 

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    RADIOTHERAPY ACTUAL DOSE

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    Format/Length:n4
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    Notes:
    RADIOTHERAPY ACTUAL DOSE is the same as attribute RADIOTHERAPY ACTUAL DOSE.RADIOTHERAPY ACTUAL DOSE is the same as attribute RADIOTHERAPY ACTUAL DOSE in 'Grays (Gy)'. 

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    RADIOTHERAPY PRESCRIBED DOSE

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    Format/Length:n4
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    Notes:
    RADIOTHERAPY PRESCRIBED DOSE is the same as attribute RADIOTHERAPY PRESCRIBED DOSE.RADIOTHERAPY PRESCRIBED DOSE is the same as attribute RADIOTHERAPY PRESCRIBED DOSE in 'Grays (Gy)'. 

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    RADIOTHERAPY TOTAL DOSE

    Change to Data Element: Changed Description

    Format/Length:max n3.n2
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    Notes:
    RADIOTHERAPY TOTAL DOSE is the same as attribute RADIOTHERAPY ACTUAL DOSE.RADIOTHERAPY TOTAL DOSE is the same as attribute RADIOTHERAPY ACTUAL DOSE in 'Grays (Gy)'.

    RADIOTHERAPY TOTAL DOSE is the total actual absorbed radiation dose given in Grays (Gy) as received during a course of treatment.RADIOTHERAPY TOTAL DOSE is the total actual absorbed radiation dose received during a course of treatment.

    For the Cancer Outcomes and Services Data Set: Core, RADIOTHERAPY TOTAL DOSE is derived from the Radiotherapy Data Set.

     

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    RED CELL FOLATE CONCENTRATION

    Change to Data Element: Changed Description

    Format/Length:n1.n1
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    Notes:
    RED CELL FOLATE CONCENTRATION records the outcome of the Clinical Investigation which measures the PATIENT's red cell folate concentration in 'µmol/L'.RED CELL FOLATE CONCENTRATION records the result of the Clinical Investigation which measures the PATIENT's red cell folate concentration in 'Micromoles per litre (µmol/L)'.  

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    S CATEGORY (LACTATE DEHYDROGENASE)

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    Format/Length:max n6
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    Notes:
    S CATEGORY (LACTATE DEHYDROGENASE) is the outcome of the Clinical Investigation to determine the PATIENT's serum Tumour markers for serum lactate dehydrogenase (LDH) (an enzyme found in abnormal amounts in the blood of PATIENTS with cancer).S CATEGORY (LACTATE DEHYDROGENASE) is the result of the Clinical Investigation to determine the PATIENT's serum Tumour markers for serum lactate dehydrogenase (LDH) (an enzyme found in abnormal amounts in the blood of PATIENTS with cancer).

    For the Cancer Outcomes and Services Data Set, S CATEGORY (LACTATE DEHYDROGENASE) is collected once at PATIENT DIAGNOSIS by a specialist Multidisciplinary Team for testicular cancer only.

     

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    SERUM ALBUMIN CONCENTRATION

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    Notes:
    SERUM ALBUMIN CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's serum albumin concentration in 'g/L'.SERUM ALBUMIN CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's serum albumin concentration in 'Grams per litre (g/l)'. 

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    SERUM ALUMINIUM CONCENTRATION

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    Notes:
    SERUM ALUMINIUM CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's  serum aluminium concentration in 'mg/L'.SERUM ALUMINIUM CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's serum aluminium concentration in 'Milligrammes per litre (mg/l)'. 

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    SERUM B12 CONCENTRATION

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    Notes:
    SERUM B12 CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's serum B12 concentration in 'ng/L'.SERUM B12 CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's serum B12 concentration in 'Nanograms per litre (ng/l)'. 

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    SERUM BICARBONATE CONCENTRATION

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    Format/Length:max n2.max n1
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    Notes:
    SERUM BICARBONATE CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's  serum bicarbonate concentration in 'mmol/L'.SERUM BICARBONATE CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's  serum bicarbonate concentration in 'Millimoles per litre (mmol/L)'. 

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    SERUM CALCIUM CONCENTRATION

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    Notes:
    SERUM CALCIUM CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's  serum calcium concentration in 'mmol/L'.SERUM CALCIUM CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's  serum calcium concentration in 'Millimoles per litre (mmol/L)'. 

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    SERUM C-REACTIVE PROTEIN CONCENTRATION

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    Notes:
    SERUM C-REACTIVE PROTEIN CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's serum C-reactive protein concentration in 'mg/L'.SERUM C-REACTIVE PROTEIN CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's serum C-reactive protein concentration in 'Milligrams per litre (mg/l)'. 

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    SERUM CREATININE CONCENTRATION

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    Notes:
    SERUM CREATININE CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's serum creatinine concentration in 'µmol/L'.SERUM CREATININE CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's serum creatinine concentration in 'Micromoles per litre (µmol/L)'. 

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    SERUM FERRITIN CONCENTRATION

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    Notes:
    SERUM FERRITIN CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's serum ferritin concentration in 'µg/L'.SERUM FERRITIN CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's serum ferritin concentration in 'Micrograms per litre µg/L'. 

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    SERUM INTACT PARATHYROID HORMOME CONCENTRATION

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    Notes:
    SERUM INTACT PARATHYROID HORMOME CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's serum intact parathyroid hormone concentration in 'pmol/L'.SERUM INTACT PARATHYROID HORMOME CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's serum intact parathyroid hormone concentration in 'Picomoles per litre (pmol/L)'. 

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    SERUM MAGNESIUM CONCENTRATION

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    Notes:
    SERUM MAGNESIUM CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's serum magnesium concentration in 'mmol/L'.SERUM MAGNESIUM CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's serum magnesium concentration in 'Millimoles per litre (mmol/L)'. 

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    SERUM POTASSIUM CONCENTRATION

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    Notes:
    The result of the Clinical Investigation which measures the PATIENT's serum potassium concentration in 'mmol/L'. SERUM POTASSIUM CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's serum potassium concentration in 'Millimoles per litre (mmol/L)'. 

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    SERUM UREA CONCENTRATION (POST DIALYSIS)

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    Notes:
    SERUM UREA CONCENTRATION (POST DIALYSIS) is the result of the Clinical Investigation which measures the PATIENT's post dialysis serum urea concentration in 'µmol/L'.SERUM UREA CONCENTRATION (POST DIALYSIS) is the result of the Clinical Investigation which measures the PATIENT's post dialysis serum urea concentration in 'Micromoles per litre (µmol/L'. 

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    SERUM UREA CONCENTRATION (PRE-DIALYSIS)

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    Notes:
    SERUM UREA CONCENTRATION (PRE-DIALYSIS) is the result of the Clinical Investigation which measures the PATIENT's pre-dialysis serum urea concentration in µmol/L.SERUM UREA CONCENTRATION (PRE-DIALYSIS) is the result of the Clinical Investigation which measures the PATIENT's pre-dialysis serum urea concentration in 'Micromoles per litre (µmol/L'. 

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    SIROLIMUS TROUGH LEVEL (RECIPIENT)

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    Notes:
    SIROLIMUS TROUGH LEVEL (RECIPIENT) is the result of the Clinical Investigation which measures the PATIENT's sirolimus trough level in 'ng/ml'.SIROLIMUS TROUGH LEVEL (RECIPIENT) is the result of the Clinical Investigation which measures the PATIENT's sirolimus trough level in 'Nanograms per millilitre (ng/ml)'. 

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    SODIUM CONCENTRATION

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    Notes:
    SODIUM CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's sodium concentration in 'mmol/L'.SODIUM CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's sodium concentration in 'Millimoles per litre (mmol/L)'. 

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    SYSTOLIC BLOOD PRESSURE

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    Notes:
    SYSTOLIC BLOOD PRESSURE records the Systolic Blood Pressure.SYSTOLIC BLOOD PRESSURE is the Systolic Blood Pressure of a PATIENT in 'Millilitres of mercury (mmHg)'. 

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    TACROLIMUS 12 HOUR TROUGH LEVEL (RECIPIENT)

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    Notes:
    TACROLIMUS 12 HOUR TROUGH LEVEL (RECIPIENT) is the result of the Clinical Investigation which measures the PATIENT's tacrolimus 12 hour trough level in 'µg/ml'.TACROLIMUS 12 HOUR TROUGH LEVEL (RECIPIENT) is the result of the Clinical Investigation which measures the PATIENT's tacrolimus 12 hour trough level in 'Micrograms per millilitre (µg/ml)'. 

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    TEMPERATURE

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    Notes:
    TEMPERATURE is the Temperature of the PERSON in 'celsius'. TEMPERATURE is the PATIENT's Temperature, where the MEASUREMENT VALUE TYPE CODE is 'Celsius (ºC)'. 

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    TOTAL CHOLESTEROL HIGH DENSITY LIPOPROTEIN RATIO

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    Notes:
    TOTAL CHOLESTEROL HIGH DENSITY LIPOPROTEIN RATIO is the outcome of the Clinical Investigation which measures the PATIENT's total cholesterol high density lipoprotein ratio.TOTAL CHOLESTEROL HIGH DENSITY LIPOPROTEIN RATIO is the result of the Clinical Investigation which measures the PATIENT's total cholesterol high density lipoprotein ratio.

    This value is calculated by dividing the total cholesterol value by the value of the High Density Lipoprotein cholesterol.

    This value is calculated by dividing the total cholesterol value by the value of the High Density Lipoprotein cholesterol.

     

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    TOTAL CHOLESTEROL LEVEL

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    Notes:
    TOTAL CHOLESTEROL LEVEL is the outcome of the Clinical Investigation which measures the PATIENT's total Cholesterol Level.

    TOTAL CHOLESTEROL LEVEL is the result of the Clinical Investigation which measures the PATIENT's total Cholesterol Level. 

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    TRIGLYCERIDES CONCENTRATION

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    Notes:
    TRIGLYCERIDES CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's triglycerides concentration in "mmol/L".

    TRIGLYCERIDES CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's triglycerides concentration in 'Millimoles per litre (mmol/L)'. 

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    URIC ACID CONCENTRATION

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    Notes:
    URIC ACID CONCENTRATION is the result of the  Clinical Investigation which measures the PATIENT's uric acid concentration in "mmol/L".URIC ACID CONCENTRATION is the result of the  Clinical Investigation which measures the PATIENT's uric acid concentration in 'Millimoles per litre (mmol/L)'. 

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    URINE CREATININE CONCENTRATION

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    Notes:
    URINE CREATININE CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's 24 hour urine creatinine concentration in "mmol/L". URINE CREATININE CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's 24 hour urine creatinine concentration in 'Millimoles per litre (mmol/L)'. 

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    URINE OUTPUT LAST 24 HOURS

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    Notes:
    URINE OUTPUT LAST 24 HOURS records the Urine Output of the PERSON in the last 24 hours where the MEASUREMENT VALUE TYPE CODE is 'Millimetres'.URINE OUTPUT LAST 24 HOURS is the Urine Output of a PATIENT in the last 24 hours, where the MEASUREMENT VALUE TYPE CODE is 'Millilitres (ml)'. 

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    URINE OUTPUT LAST HOUR

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    Notes:
    URINE OUTPUT LAST HOUR records the Urine Output of the PERSON in the last hour where the MEASUREMENT VALUE TYPE CODE is 'Millimetres'.URINE OUTPUT LAST HOUR is the Urine Output of a PATIENT in the last hour. 

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    URINE UREA CONCENTRATION

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    Notes:
    URINE UREA CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's 24 hour urine urea concentration in "mmol/L". URINE UREA CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's 24 hour urine urea concentration in 'Millimoles per litre (mmol/L)'. 

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    URINE VOLUME

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    Notes:
    URINE VOLUME is the result of the Clinical Investigation to measure the PATIENT's urine volume by 24 hour collection measured in "ml". URINE VOLUME is the result of the Clinical Investigation which measures the PATIENT's urine volume in 'Millilitres (ml)'.

    For the National Renal Data Set, URINE VOLUME is the PATIENT's urine volume by 24 hour collection.

     

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    VIRAL LOAD COUNT

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    Notes:
    VIRAL LOAD COUNT is the result of the Clinical Investigation which measures the PATIENT's viral load count in 'Millilitres (ml)', as recorded at the HIV Clinic Attendance.VIRAL LOAD COUNT is the result of the Clinical Investigation which measures the PATIENT's viral load count in 'Millilitres (ml)', as recorded at the HIV Clinic Attendance.

    If the PATIENT's viral load count has not been recorded, the field should be omitted.For the HIV and AIDS Reporting Data Set, VIRAL LOAD COUNT should be omitted if the PATIENT's viral load count has not been recorded.

     

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    VITAMIN D CONCENTRATION

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    Notes:
    VITAMIN D CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's vitamin D concentration in "ng/ml".VITAMIN D CONCENTRATION is the result of the Clinical Investigation which measures the PATIENT's vitamin D concentration in 'Nanograms per millilitre (ng/ml)'. 

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    WAIST MEASUREMENT

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    Notes:
    WAIST MEASUREMENT is the Waist Measurement of the PERSON in centimetres.

    WAIST MEASUREMENT is the Waist Measurement of the PATIENT, where the MEASUREMENT VALUE TYPE CODE is 'Centimetres (cm)'. 

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    WHITE BLOOD CELL COUNT

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    Notes:
    WHITE BLOOD CELL COUNT is the outcome of the Clinical Investigation which measures the PERSON's white CELL blood count measured as 'n x109/l (i.e. number times ten to the power 9 per litre).WHITE BLOOD CELL COUNT is the result of the Clinical Investigation which measures the PERSON's white CELL blood count measured as 'n x109/l (i.e. number times ten to the power 9 per litre).' 

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    For enquiries, please email information.standards@hscic.gov.uk