226 research outputs found

    The need for best practice standards in electronic governance of patient medical records to facilitate innovation

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    Background : Optimising the use of electronic data offers many opportunities to health services, particularly in rural and remote areas. These include reducing the effect of distance on access to clinical information and sharing information where there are multiple service providers for a single patient. The increasing compilation of large electronic databases of patient information and the ease with which electronic information can be transferred has raised concerns about the privacy and confidentiality of such records.Aims &amp; rationale/Objectives : This review aims to identify legal and ethical standards for areas of electronic governance where a lack of clarity may currently impede innovation in health service delivery.Methods : This paper describes best practices for storage and transfer of electronic patient data based on an examination of Australian legislative requirements and a review of a number of current models. This will firstly allow us to identify basic legal requirements of electronic governance as well as areas of ambiguity not fully addressed by legislation. An examination of current models will suggest recommendations for best practice in areas lacking sufficient legal guidance.Principal findings : We have identified the following four areas of importance, and shall discuss relevant details:1) Patients\u27 right of ownership to electronic patient records. 2) Custodial issues with data stored in centralised health care institutions 3) IT Security, including hierarchical level access, data encryption, data transfer standards and physical security 4) Software applications usage.Discussion : Our examination of several models of best practice for the transfer of electronic patient data, both in Australia and internationally, identifies and clarifies many unresolved issues of electronic governance. This paper will also inform future policy in this area.Implications : Clarification will facilitate the future development of beneficial technology-based innovations by rural health services.Presentation type : Poster <br /

    Addressing podiatry shortages in Western Victoria

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    A dimolybdenum paddlewheel as a building block for heteromultimetallic structures

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    Diphenylphosphine functionalized propionic acid was applied for the synthesis of heteromultimetallic dimolybdenum(II) complexes. The ligand features both carboxylic acid and phosphine functionalities, allowing the selective synthesis of a tetracarboxylate bridged Mo2(II)-paddlewheel structure in a first step. Due to the symmetrically arranged phosphine functionalities, the dimolybdenum(II) complex was utilized as a metalloligand. Subsequent coordination of late transition metal ions, such as gold(I), rhodium(I), iridium(I) or ruthenium(II) to the phosphine moieties allowed the formation of heteromultimetallic structures. The flexibility of the diphenylphosphino propionate ligand system enabled intermolecular aurophilic interactions in the Au(I) functionalized dimolybdenum(II) complexes. Depending on the Au(I) species applied, either a dimeric structure or a 1D coordination polymer was formed in the solid state. These structures represent the first examples of heterometallic dimolybdenum(II) complexes, forming supramolecular structures via aurophilic interactions

    A cyclopentadienyl functionalized silylene-a flexible ligand for Si- And C-coordination

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    The synthesis of a 1,2,3,4-tetramethylcyclopentadienyl (Cp4^{4}) substituted four-membered N-heterocyclic silylene [{PhC(NtBu) 2_{2}}Si(C5_{5}Me4_{4}H)] is reported first. Then, selected reactions with transition metal and a calcium precursor are shown. The proton of the Cp4_{4}-unit is labile. This results in two different reaction pathways: (1) deprotonation and (2) rearrangement reactions. Deprotonation was achieved by the reaction of [{PhC(NtBu) 2_{2}}Si(C5_{5}Me4_{4}H)] with suitable zinc precursors. Rearrangement to [{PhC(NtBu) 2_{2}}(C5_{5}Me4_{4})SiH], featuring a formally tetravalent silicon R2_{2}CSi(R′)-H unit, was observed when the proton of the Cp4^{4} ring was shifted from the Cp4^{4}-ring to the silylene in the presence of a Lewis acid. This allows for the coordination of the Cp4^{4}-ring to a calcium compound. Furthermore, upon reaction with transition metal dimers [MCl(cod)] 2_{2} (M = Rh, Ir; cod = 1,5-cyclooctadiene) the proton stays at the Cp4^{4}-ring and the silylene reacts as a sigma donor, which breaks the dimeric structure of the precursors

    3d-4f heterometallic complexes by the reduction of transition metal carbonyls with bulky LnII^{II} amidinates

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    The redox chemistry between divalent lanthanide complexes bearing bulky amidinate ligands has been studied with 3d transition metal carbonyl complexes (iron and cobalt). The reaction of [(DippForm)2_{2}Smǁ^{ǁ}(thf)2_{2}] (DippForm = N,N′-bis(2,6-diisopropylphenyl)formamidinate) with [Co2_{2}(CO)8_{8}] resulted in the formation of a tetranuclear Sm–Co complex, [{(DippForm)2_{2}Smǁǀ^{ǁǀ}(thf)}2_{2}{(μ-CO)2_{2}Co(CO)2_{2}}2_{2}]. The product of the reaction of [(DippForm)2_{2}Ybǁ^{ǁ}(thf)2_{2}] and [Co2_{2}(CO)8_{8}] gives the dinuclear Yb–Co complex [{(DippForm)2_{2}Ybǁǀ^{ǁǀ}(thf)}{(μ-CO)Co(CO)3_{3}}] in toluene. The reaction of [(DippForm)2_{2}Smǁ^{ǁ}(thf)2_{2}] was also carried with the neighbouring group 8 carbonyl complexes [Fe2_{2}(CO)9_{9}] and [Fe3_{3}(CO)12_{12}], resulting in a pentanuclear Smǁǀ^{ǁǀ}–Fe complex, [{(DippForm)2_{2}Smǁǀ^{ǁǀ}}2_{2}{(μ3_{3}-CO)2_{2}Fe2_{2}(CO)9_{9}}], featuring a triangular iron carbonyl cluster core

    3d-4f heterometallic complexes by the reduction of transition metal carbonyls with bulky Ln(II) amidinates

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    The redox chemistry between divalent lanthanide complexes bearing bulky amidinate ligands has been studied with 3d transition metal carbonyl complexes (iron and cobalt). The reaction of [(DippForm)(2)Sm-II(thf)(2)] (DippForm = N,N '-bis(2,6-diisopropylphenyl)formamidinate) with [Co-2(CO)(8)] resulted in the formation of a tetranuclear Sm-Co complex, [{(DippForm)(2)Sm-III(thf)}(2){(mu-CO)(2)Co(CO)(2)}2]. The product of the reaction of [(DippForm)(2)Yb-II(thf)(2)] and [Co-2(CO)(8)] gives the dinuclear Yb-Co complex [{(DippForm)(2)Yb-III(thf)}{(mu-CO)Co(CO)(3)}] in toluene. The reaction of [(DippForm)(2)Sm-II(thf)(2)] was also carried with the neighbouring group 8 carbonyl complexes [Fe-2(CO)(9)] and [Fe-3(CO)(12)], resulting in a pentanuclear Sm-III-Fe complex, [{(DippForm)(2)Sm-III}(2){(mu(3)-CO)(2)Fe-3(CO)(9)}], featuring a triangular iron carbonyl cluster core
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