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A vision for the health service in Sweden for use of the GS1 system

A vision for the health service in Sweden for use of the GS1 system

A vision for the health service in Sweden for use of the GS1 system

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• patients do not <strong>use</strong> counterfeit medic<strong>in</strong>es or medical devices.• <strong>the</strong> products <strong>use</strong>d <strong>for</strong> patients can be traced to <strong>the</strong> orig<strong>in</strong>al manufacturer and itsproduction <strong>system</strong>.• <strong>in</strong>ternal processes such as sterilization <strong>of</strong> <strong>in</strong>struments, hazardous waste managementand handl<strong>in</strong>g and wash<strong>in</strong>g <strong>of</strong> clo<strong>the</strong>s can be improved, while ensur<strong>in</strong>g quality andfollow-up.• products that <strong>for</strong> some reason do not meet set quality requirements can be identifiedand withdrawn <strong>in</strong> an efficient manner.Basic possibilities with <strong>the</strong> <strong>GS1</strong> SystemValidation: Unique identification and mark<strong>in</strong>g with bar codes/RFID makes it possible to verify<strong>the</strong> identity <strong>of</strong> an object, person or procedure and l<strong>in</strong>k this with <strong>the</strong> person giv<strong>in</strong>g <strong>the</strong>treatment.Data capture: There are many situations where a serial number or reference number mustbe entered <strong>in</strong>to <strong>the</strong> electronic patient record. By read<strong>in</strong>g a barcode and automaticallyrecord<strong>in</strong>g <strong>the</strong> <strong>in</strong><strong>for</strong>mation, <strong>the</strong> risk <strong>of</strong> manual key<strong>in</strong>g errors is elim<strong>in</strong>ated.Care documentation: The <strong>health</strong> <strong>service</strong> spends considerable time on care documentation<strong>for</strong> each <strong>in</strong>dividual procedure. By verify<strong>in</strong>g drug or o<strong>the</strong>r product at <strong>the</strong> patient (so-called"bedside scann<strong>in</strong>g") <strong>the</strong> documentation can be structured and made searchable, while <strong>the</strong>total hours spent on care documentation, <strong>in</strong><strong>for</strong>mation retrieval, read<strong>in</strong>g, revocations, etc.,decreases.Supply cha<strong>in</strong>: The ability to track goods efficiently improves <strong>in</strong>ventory control, so that <strong>the</strong>right materials are <strong>in</strong> <strong>the</strong> right place at <strong>the</strong> right time.What does <strong>the</strong> <strong>vision</strong> mean <strong>for</strong> <strong>the</strong> patient?Patients should be able to ask five basic rights <strong>of</strong> care:• right patient• right product• right route• right dose/<strong>in</strong>strument• right timeBy mak<strong>in</strong>g <strong>the</strong> <strong>vision</strong> reality, safety <strong>in</strong> <strong>health</strong> care will be improved.The <strong>health</strong> <strong>service</strong> is prepar<strong>in</strong>g to achieve <strong>the</strong> <strong>vision</strong>To <strong>use</strong> <strong>the</strong> <strong>GS1</strong> <strong>system</strong>, <strong>the</strong> <strong>health</strong> <strong>service</strong> needs to <strong>in</strong>vest <strong>in</strong> equipment to read both l<strong>in</strong>earbar codes and 2D codes. Future <strong>use</strong> <strong>of</strong> automatic data capture us<strong>in</strong>g RFID <strong>in</strong> accordancewith <strong>GS1</strong> standards is also <strong>in</strong> l<strong>in</strong>e with <strong>the</strong> <strong>health</strong> <strong>service</strong> <strong>vision</strong> <strong>of</strong> improv<strong>in</strong>g patient safetyand efficiency.When request<strong>in</strong>g tenders, county councils and o<strong>the</strong>r public <strong>health</strong> care providers arebeg<strong>in</strong>n<strong>in</strong>g to require unique identification <strong>of</strong> items and sometimes <strong>service</strong>s. When tender<strong>in</strong>g<strong>for</strong> IT <strong>system</strong>s, global identification and automatic data capture will be <strong>in</strong>cluded <strong>in</strong> <strong>the</strong>technical specifications and requirements documents.This <strong>vision</strong> was developed by <strong>the</strong> <strong>use</strong>r group “identification, mark<strong>in</strong>g and classification", with participants from: ÖstergötlandCounty Council, Region Skåne, Västra Götalands Region, Stockholm County Council, Karol<strong>in</strong>ska University Hospital andNorrbotten County Council <strong>in</strong> collaboration with <strong>the</strong> County Councils <strong>of</strong> Uppsala, Dalarna, Västmanland, Örebro andSödermanland. Supplier representatives <strong>in</strong> <strong>the</strong> <strong>use</strong>r group are Swedish Medtech, Cook Medical, Mölnlycke Healthcare, OneMed<strong>Sweden</strong> AB, and MediCarrier. The <strong>use</strong>r group meets and comments on <strong>the</strong> implementation <strong>of</strong> <strong>GS1</strong> standards <strong>in</strong> <strong>health</strong>careunder <strong>the</strong> auspices <strong>of</strong> <strong>GS1</strong> <strong>Sweden</strong>.

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