auto-id data work team hospital survey - gs1...auto-id data work team hospital survey berlin, 1...
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HUG
Auto-ID Data Work TeamHospital Survey
Berlin, 1 February 2007
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©2006 GS12GS1 HUG
A Hospital Survey
• Gather input from Hospitals, by using their language• English• French• German• Dutch• Italian• Spanish• Japanese• Chinese
• Be able to understand hospital’s voice regarding• 2 Groups of products (pharmaceuticals, biologics, vaccines & medical
devices)• Patient safety and data which automatic capture is needed• Ask to explain the business needs• Status is AutoID
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©2006 GS13GS1 HUG
A hospital Survey
• The survey is focused on the data requirement needs of Hospitals for supply chain items
• The questionnaire is structured as follow :
Categories Questions aboutMedical Devices UNIT OF USE package level
packaging containing more than one unit of use
Pharmaceuticals, biologics, vaccines
UNIT OF USE package level
packaging containing more than one unit of use
Data capture Barcodes
RFID
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©2006 GS14GS1 HUG
Responses to the survey
17 countries – 633 Hospital with ~ 244’000 beds – 117 Respondents110 Hospitals – 3 Health Authorities – 7 providers
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©2006 GS15GS1 HUG
Hospitals by number of bedsN
umbe
rof b
eds
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©2006 GS16GS1 HUG
Answers per department
Other : 26%
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©2006 GS17GS1 HUG
Answers per department (“other”)
9
9
8
3
ManagementITWard, OR, etc.Regulators
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©2006 GS18GS1 HUG
Area of interest
8475
8
MedicalDevices
Pharmaceuticals, Biologics,VaccinesNone
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HUG
Medical Devices
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©2006 GS110GS1 HUG
Data on Medical Devices on unit-of-use level
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©2006 GS111GS1 HUG
Data on Medical Devices on unit-of-use level -Product Identification
• Product Identification Number ↔ National Registration Number
• Understand the difference on the respondent point of view
• Both solution allow (unique) product identification• Product Identification Number and National Registration
Number can be a number allocated by “a third party”(Manufacturer, Registration Authority, etc.)
• Some respondents mention Product Identification allocated internally in the hospital
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©2006 GS112GS1 HUG
Data on Medical Devices on unit-of-use level -Product Identification Number
• Why do you need the Product Identification Number / National Registration Number?
• Stock Management, Logistics, Re-ordering, support the picking process
• Traceability, Transparency, Data Management, Documentation, access product information
• Avoid errors
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©2006 GS113GS1 HUG
Data on Medical Devices on unit-of-use level –Serial Number – Lot Number
• Why is the Serial Number required ?• To trace certain MD (surgical instruments, implants) to
the patient (document the patient file)• To identify pieces belonging to an equipment, link
reusable devices to sterilisation steps including process documentation
• For stock management, recalls, consignment
• Why is the Lot Number required ?• Traceability, recalls, vigilance, documentation,
accounting• To calibrate equipment with reagents• To fulfil regulatory requirements• For logistics and stock management purpose
Numbers in ( ) refere to the number of the respondant
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©2006 GS114GS1 HUG
Data on Medical Devices on unit-of-use level –Expiry Date
• Why is the Expiry Date required ?• Patient safety; traceability, security, duration
of sterility • Logistics and stock management (better use
of products before exp), including decentralised stocks
• For chemicals, reagents• Regulation requirement
Numbers in ( ) refere to the number of the respondant
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©2006 GS115GS1 HUG
Data on Medical Devices on unit-of-use level
• Why do you need these data on a data carrier?• Faster processes (incl recalls), reduction of errors (i.e.
picking)• Avoid key entries (traceability)• Safer key entries, simpler integration into database; data
accuracy• Accounting with mobile data capture• Possibility of logical controls• “Our system is built according to GS1 system, reading GS1-
128. We just utilize it” (*)• “in one scan, have all the necessary information”• Better patient file documentation with a thinner granularity (lot
/ serial, exp)
(*) = 118 hospitals, 37’000 beds
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©2006 GS116GS1 HUG
Data for Medical Devices on case/shipper
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©2006 GS117GS1 HUG
Data on Medical Devices on carton level
• Why is a Product Identification Number required?
• Same as for primary pack level• Allows stock management with different hierarchies
(primary / secondary pack levels)
• Why is the Serial Number required?• Serial number is needed to track maintenance• Traceability, Stock Management
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©2006 GS118GS1 HUG
Data on Medical Devices on carton level
• Why do you need these data on a data carrier?
• Faster processes, reliability of stock, accounting, document databases, support ordering processes (internal / external)
• Reliability of traceability
Numbers in ( ) refere to the number of the respondant
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HUG
Pharmaceuticals
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©2006 GS120GS1 HUG
Data for Pharmaceuticals on unit-of-use level
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©2006 GS121GS1 HUG
Data on Pharmaceutical unit-of-use level
• Why is Product Identification required ?• Same as for Medical Devices (traceability,
etc.)• Avoid errors (differentiation with colours not
reliable)• To notify narcotic trade (ex : Morphin
anhydrid, 7611746078005)• Internal ordering, documentation, accounting,
traceability• Blood derivate underlie the same regulatory
requirements as implants
Numbers in ( ) refere to the number of the respondant
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©2006 GS122GS1 HUG
Data on Pharmaceutical unit-of-use level
• Why is the Serial Number required ?• Same as for Medical Devices• Traceability and link to supplier• For biologics / blood derivates full traceability• For traceability to the patient (legal requirement)• Quality insurance, vigilance
• Why is the Lot Number required ?• Same as for Medical Devices• For blood derivates, biologics• Traceability, documentation of patient file
Numbers in ( ) refere to the number of the respondant
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©2006 GS123GS1 HUG
Data on Pharmaceutical unit-of-use level
• Why is the Exp Date required ?• Same as for Medical Devices• To check if date is not expired• Stock control at the ward• Overall control of the stock (especially for the
drugs with a low turnover)• Manual control of exp date is a long task with
a high degree of error risks• Reduce waist on stocks (react before exp
date)
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©2006 GS124GS1 HUG
Data on Pharmaceutical unit-of-use level
• Why do you need these data on a data carrier ?
• Same as for Medical Devices• Support picking, capture delivery at ward,
ward capturing administration to patient (document patient file), have a better traceability in the medication process
• Last check at the bed of the patient (bedside scanning), reduction of medication errors
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©2006 GS125GS1 HUG
Data for Pharmaceuticals on case/shipper level
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©2006 GS126GS1 HUG
Data on Pharmaceutical unit-of-use level
• Why do you need these data on a data carrier ?
• Same as for Medical Devices• Support stock management processes (deliveries,
picking, inventory)• Dispose of accurate data about stocked products in the
shortest time (also in decentralised stocks)• Real standardisation would allow the effective use of
data with barcodes in the administration process• Security of the drugs supply chain (manufacturer
patient)
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HUG
Data capture
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©2006 GS128GS1 HUG
Level of scanning in hospitals by respondent
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©2006 GS129GS1 HUG
Level of scanning in hospitals by Nb of beds
Barcodes – Does your area currently scan any Barcodes on Pharmaceuticals,
Biologics, Vaccines or Medical Devices?
0 20000 40000 60000 80000 100000
yes, we scan (patient safety)yes, we scan (no patient safety)No we don't scan (but is planed)No we don't scan (not planed)
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©2006 GS130GS1 HUG
Origin of barcodes on products by respondent
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©2006 GS131GS1 HUG
Origin of barcodes on products by number of beds
0 50000 100000 150000 200000
applied by supplierapplied by hospitalsome applied by supplier, some by hospitalskipped response
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©2006 GS132GS1 HUG
Manual key entries for patient safety by respondent
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©2006 GS133GS1 HUG
Manual key entries for patient safety by number of beds
0 50000 100000 150000 200000 250000
skipped response no yes
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©2006 GS134GS1 HUG
What patient safety issues could be prevented with AIDC?
• More efficiency in the internal supply chains (inclrecalls, decentralised stocks); vigilance
• Less errors by data capture, better (reliable) documentation; DRG calculation; avoid documenting the wrong patient file
• Bedside scanning (right product, right patient, etc.); barcode on the unit of use (pill, vial, etc.); alerts when allergies, interactions; also for nursing homes; for hospitals preparing patient daily doses
• Avoid wrong blood transfusion• Master data and software must be available to profit of
AIDC• More time for proactive quality measures with less
manual stock control systems• Simplify processes better patient safety
Numbers in ( ) refere to the number of the respondant
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©2006 GS135GS1 HUG
Use of RFID for patient safety by respondent
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©2006 GS136GS1 HUG
Use of RFID for patient safety by number of beds
0 50000 100000 150000 200000 250000
don't know no yes
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©2006 GS137GS1 HUG
Regulation and Data capture by respondent
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©2006 GS138GS1 HUG
Regulation and Data capture by number of beds
0 50000 100000 150000
don't know no yes
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©2006 GS139GS1 HUG
Christian HayDelegate Healthcare, GS1 Switzerland
Längassstrasse 213012 Berne
T. +41 21 825 32 19E. [email protected]