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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
21

Gestão da inovação em medicina diagnóstica: um estudo de caso / Innovation management in diagnostic medicine: a case study

Arnas, Edgard Rasquini 01 December 2017 (has links)
Este trabalho busca responder a pergunta de pesquisa: como ocorre a gestão da inovação em uma empresa de Medicina Diagnóstica? Para isso teve como objetivo aprofundar a compreensão sobre a gestão da inovação nesta empresa, entendendo as etapas do processo de inovação (ideação, conversão e difusão), entendendo como a estratégia da inovação se insere no processo de gestão da inovação, e entendendo como que pessoas e organização se inserem na gestão da inovação. Esta pesquisa fez uso de uma abordagem de natureza teórico-prática de enfoque qualitativo e objetivos de caráter exploratório por meio deum estudo de caso único em um centro de medicina diagnóstica de grande porte, reconhecido por práticas de gestão e inovação. Foram utilizadas as técnicas de entrevistas semiestruturadas, observação direta na empresa, e análise de documentos. Para a etapa de entrevista foi elaborado um protocolo semiestruturado com questões orientadoras conforme pesquisa bibliográfica a respeito de gestão da inovação, o setor de saúde e medicina diagnóstica.Foram entrevistados 12 líderes da empresa envolvidos com a gestão da inovação. Todas as fontes de dados foram analisadas e trianguladas chegando à apresentação e discussão de resultados do caso. Como resultados, a pesquisa evidenciou a importância da inovação em medicina diagnóstica, podendo reduzir custos e aumentar a qualidade, além de gerar valor para o restante da cadeia. A estratégia da inovação é alinhada à estratégia corporativa em diversos elementos e possui um processo de definição de drivers que direcionam a companhia no processo de inovação. O processo de inovação é influenciado por atores encontrados na literatura como órgãos reguladores, médicos, pacientes, fornecedores, universidades e operadoras. Além destes, outros foram citados, como órgãos representativos e o Ministério da Ciência e Tecnologia. Dois processos estruturados de inovação foram evidenciados: de novos produtos e de novos processos. O processo de novos produtos é alinhado ao modelo destagegates, enquanto que o processo de novos processos é mais amplo seguindo o modelo hegemônico. A etapa de ideação ocorre com geração de ideias tanto por fontes internas como externas, sendo as principais fontes os médicos e técnicos assessores, e os colaboradores. Técnicas como brainstorming, observação do comportamento dos clientes, e pesquisas acadêmicas são utilizadas. Na etapa de conversão, a seleção e avaliação é feita de maneira colegiada ou individual, por meio de fóruns presenciais ou virtuais. Os critérios de seleção são o alinhamento estratégico, as análises financeiras, técnicas e comerciais. No desenvolvimento e implantação, destaca-se a aplicação de pilotos e testes antes da efetiva implantação da inovação, treinamentos e acompanhamentos da implantação. Por fim, a etapa de difusão ocorre externamente, por meio da equipe comercial junto às operadoras, e com a equipe de médicos e técnicos assessores, junto aos clientes médicos, além dos canais de divulgação como eventos e congressos. A divulgação com clientes finais se dá por meio dos sites, redes sociais, e revistas. Já internamente, a comunicação ocorre principalmente na forma de murais e portais virtuais de comunicação, na atualização de documentos técnicos, e por meio de eventos internos de divulgação do conhecimento, premiação e reconhecimento. Em pessoas e organização, a pesquisa evidenciou que a cultura influencia o processo de gestão da inovação, sendo formada historicamente sobre os pilares de geração de conhecimento e relacionamento acadêmico nas universidades. Objetiva-se gerenciar os recursos humanos capturando pessoas alinhadas ao valor da inovação desde a fase de contratação, passando por treinamentos, avaliação anual de desempenho, premiação e reconhecimento. Não somente os colaboradores internos recebem incentivos e reconhecimentos, como também há incentivos a fornecedores, médicos e universitários por meio de programas específicos. / This master thesis seeks to answer the research question: how works the management of innovation in a case of Diagnostic Medicine? The purpose of this study was to deepen the understanding of innovation management in a diagnostic medicine company, understanding the stages of the innovation process (ideation, conversion and diffusion), understanding how the innovation strategy is embedded in the process of innovation management, and understanding how people and organizations are involved in managing innovation. This research made use of a theoretical-practical approach of qualitative approach and exploratory objectives through a case study in a large diagnostic medicine center, recognized by management and innovation practices. The techniques of semi-structured interviews, direct observation in the company, and document analysis were used. For the interview stage, a semistructured protocol was developed with orienting questions according to bibliographic research regarding innovation management, the health sector and diagnostic medicine. We interviewed 12 company leaders involved in innovation management. All data sources were analyzed and triangulated, arriving at the presentation and discussion of the results of the case. The research highlighted the importance of innovation in diagnostic medicine, which can reduce costs and increase quality, and generate value for the rest of the chain. The innovation strategy is aligned with the corporate strategy in several elements and has a process of definition of drivers that guide the company in the process of innovation. The innovation process is influenced by several stakeholders found in the literature. Besides these others were cited as representative bodies, and the ministry of science and technology. Two structured innovation processes were evidenced: process of new products and new processes. The process of new products is aligned with the stage gates model, while the process of new processes is broader following the hegemonic model. The stage of ideation occurs with the generation of ideas by both internal and external sources, the main sources being the doctors and technical advisors, and collaborators. Techniques such as brainstorming, customer behavior observation, and academic research are used. In the conversion stage, the selection and evaluation can be done collegially or individually, through forums that can be even virtual. The selection criteria are strategic alignment, financial, technical and commercial analysis. In the development and implementation, we highlight the application of pilots and tests before the effective implementation of the innovation, the training and follow-up of the implementation. Finally, the diffusion stage occurs externally, through the commercial team with the operators, and with the team of medical and technical advisors, with the medical clients, in addition to the channels of dissemination such as events, congresses. Publicity with end customers is through websites, social networks, and magazines. Already internally the communication occurs mainly in the form of virtual murals and portals of communication, in the updating of technical documents, and through internal events of dissemination of knowledge, awards and recognition. In people and organization, the research evidenced that culture influences the process of innovation management, being historically formed on the pillars of knowledge generation and academic relationship in universities. It aims to manage human resources by capturing people aligned with the value of innovation from the hiring stage, through training, annual performance evaluation, awards and recognition. Not only do internal collaborators receive incentives and recognition, but there are also incentives to suppliers, doctors and university students through specific programs.
22

Artidentifiering av mögelsvamp med MALDI-TOF MS / Species identification of filamentous fungi with MALDI-TOF MS

Leander, Ellinor January 2018 (has links)
Snabb och korrekt artidentifiering är avgörande för effektiv behandling av svampinfektioner, särskilt bland immunsupprimerade patienter. Matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) används rutinmässigt på kliniska laboratorier för identifiering av karaktäristiska proteinmönster hos bakterier och jästsvampar genom tolkning av proteinspektra i en masspektradatabas för korrekt artidentifiering. Mögelsvamparnas hårda cellvägg och heterogena växtsätt med varierande proteinuttryck beroende på mognadsstadie, försvårar identifiering med MALDI-TOF MS. Metodens tänkbara fördelar mot traditionella metoden mikroskopering är förkortade svarstider, säkrare artidentifiering av fler arter och mindre beroende av subjektiv morfologisk bedömning. Studiens syfte var att undersöka om MALDI-TOF MS kunde anpassas och användas för identifieringen av mögelsvamp i klinisk rutindiagnostik. Fyra referensstammar (Aspergillus niger, A. fumigatus, A.terreus, A.flavus) och ett kliniskt isolat (A.terreus) undersöktes. Preparationsmetoderna (I) fullständig myrsyraextraktion, (II) direktapplicering och (III) suspension i destillerat vatten användes för analys av sporer och frontmycel hos yngre och äldre mögelkulturer. Två olika masspektradatabaser för artidentifiering jämfördes; rutindatabasen BDAL och den specialiserade mögeldatabasen Filamentous Fungi Library. Även plocktekniken av mögelmaterial inför analys med MALDI-TOF MS utvärderades. Vid vissa tillfällen förbättrades artidentifieringen efter extraktion av mögelkulturerna, medan i andra fall var direktapplicering fullt tillräcklig. Mögelmaterial med mycket sporer tenderade ge något fler artidentifieringar i BDAL oavsett kulturernas ålder.  Filamentous Fungi Library tenderade i vissa fall ge bättre resultat jämfört med BDAL för yngre kulturer. Fler studier krävs för att utvärdera och optimera MALDI-TOF MS som metod för artidentifiering av mögelsvamp. / Rapid and accurate species identification is crucial for successful treatment of fungal infections, especially among immunosuppressed patients. Matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) is used routinely at clinical laboratories to identify characteristic protein patterns of bacteria and yeast by the interpretation of protein spectra in a database for accurate species identification. The hard cell wall of the mold and the heterogeneous growth with varying protein expression due to maturation, complicates identification with MALDI-TOF MS. The potential benefits of this method compared to microscopy as traditional method are shortened turn-around times, safer species identification of more species that is independent on subjective morphological assessment. The purpose of the study was to investigate whether MALDI-TOF MS could be adapted and used for the identification of molds in clinical routine diagnostics. Four reference strains (Aspergillus niger, A.fumigatus, A.terreus, A.flavus) and a clinical isolate (A.terreus) were examined. The preparation methods (I) complete formic acid extraction, (II) direct application and (III) suspension in distilled water were used for analysis of spores and frontmycelium from younger and older mold cultures. Two different masspektradatabases for species identification were compared; routine database BDAL and the specialized mold database, Filamentous Fungi Library. Also the collecting technique of mold prior to analysis with MALDI-TOF MS was evaluated. Sometimes, the species identification improved after extraction of mold cultures, while in other cases direct application was sufficient. Cultures with a lot of spores tended to give slightly more species identifications in BDAL regardless of the age of cultures. Filamentous Fungi Library, in some cases, tended to improve the performance compared to BDAL for younger cultures. More studies are required to evaluate and optimize MALDI-TOF MS as a method of mold identification.
23

Tendinosis in Trigger Finger

Lundin, Anna-Carin January 2017 (has links)
Trigger finger is one of the most common hand conditions, with a prevalence of almost 3%. The aetiology remains unclear even though many causes have been suggested. The prevailing paradigm is that the pathogenesis of trigger finger is ascribed to primary changes in the first fibrous condensation of the tendon sheath (A1-pulley). Several studies have investigated pathology in the pulley, but few have investigated the tendon. The general aim of this thesis was to find out if there is pathology in the trigger finger tendon and to define it. We first looked at trigger finger tendon biopsies in a light microscope, and found that they were histologically different from healthy tendons. They showed signs of micro-ruptures, collagen degradation, increased amounts of ground substance, both hyper- and hypo-cellular areas, round active cell nuclei and absence of inflammatory cells, all similar to tendinosis. The histological picture was further assessed by using a scoring system for Achilles tendinosis. The trigger finger tendons scored high, suggesting a similar histopathology. Next, we performed a quantitative real-time polymerase chain reaction (qPCR) on trigger finger tendons. We assessed the mRNA expression of 10 genes, which have been described to be differently expressed in Achilles tendinosis (collagen 1 and 3, versican, decorin, biglycan, aggrecan, MMP-2, MMP-3, ADAMTS-5, and TIMP-3). The overall expression pattern agreed with previous studies on Achilles tendinosis, suggesting that the cellular function in trigger finger tendons is disturbed in a similar way as in Achilles tendinosis. Recent experimental and observational research has suggested potential side effects of statin treatment on tendons, but firm evidence was lacking. We performed an epidemiological study on two large population-based cohorts. Statin use was found to increase the risk of both trigger finger and tendinosis in the shoulder and Achilles tendons, especially among men. This suggests a similar pathology in trigger finger and tendinosis. We have also studied the time to treatment effect after a single injection of glucocorticoid in trigger finger. Our results suggest that 60-80% of patients can expect resolution of the triggering within 14 days, and half of them within seven days. This result allows correct information to be given to the patient and proper planning of follow-ups. In conclusion, the pathology in trigger finger tendons is similar to tendinosis in other tendons.
24

Jämföra Protrombinkomplex International Normalized Ratio, PK (INR)- värdet, för plasma och helblod för kapillärt tagna PK-prover på instrumentet STA R Max (Stago) / Comparing Prothrombin International Normalized Ratio, PT (INR)- value, for plasma and whole blood for capillary PT samples on STA R Max instrument (Stago).

Olsson, Oskar January 2018 (has links)
Warfarin är ett läkemedel som används för att förhindra att högriskpatienter såsom de med förmaksflimmer får tromboembolism. Denna verkan uppnås genom att hämma de K-vitaminberoende faktorerna VII, X och protrombin och på så sätt minska blodets förmåga att koagulera. Att hitta rätt dosering av läkemedlet för warfarinbehandlade patienter har visat sig vara svårt eftersom det kräver regelbunden provtagning och påverkas av mat- och levnadsvanor. Det vanligaste sättet att mäta protrombinkomplexhalten är med venös plasma men det är även möjligt att använda sig av kapillär plasma. Helblod kan användas för mekaniska metoder som inte använder sig av optisk detektion. Fördelen är att helblod inte kräver centrifugering. Studiens syfte var att undersöka om det fanns en signifikant skillnad (p≤0,05) mellan helblod och plasma som används i den nuvarande metoden för kapillära prover och om det finns en skillnad i stabiliteten av dessa prov. Dubbla prover togs från 30 warfarinbehandlade patienter och 5 icke warfarinbehandlade individer. Ett av proven centrifugerades och analyserades på plasma, det andra analyserades på helblod. Resultaten visade att det fanns en signifikant skillnad (p≤0,05) mellan metoderna. Bland-Altman diagrammet visade att 95 % av helblodsproverna inte var högre än 0,25 INR och lägre än 0,14 INR. Detta har en låg klinisk inverkan. 4 Proverna förvarades i rumstemperatur i upp till 24 timmar och analyserades sedan om. Ingen förändring över 10 % kunde observeras i hållbarheten. Studien visade att trots att det finns en signifikant skillnad är det möjligt att ersätta den nuvarande metoden med plasma och använda helblod istället. / Warfarin is a drug used to prevent high-risk patients such as those with atrial fibrillation from thromboembolisms. This effect is achieved by suppressing vitamin-K dependent factors VII, X and prothrombin and therefore decreasing the bloods ability to clot. Finding the right dosage of the drug for warfarin treated patients has proven difficult, as it demands regular blood draws to monitor their prothrombin complex level, which is affected by dietary and living habits. The most common way to measure prothrombin complex levels is by using venous plasma but it is also possible to use capillary plasma. Whole blood can be used for mechanical methods, which don’t use optical detection. The benefit is that whole blood doesn’t require centrifugation. The aim of this study was to investigate if there was a significant difference (p≤0,05) between using whole blood and plasma which is the existing method for capillary sample and also if there is any differences between the stability of these samples. Double samples from 30 warfarin treated patients and 5 non-treated persons were taken. One of the samples were centrifuged and analyzed on plasma and the other analyzed on whole blood. The results showed that there was a significant difference (p≤0,05) between the methods. Bland-Altman plot comparison showed that 95 % of the whole blood samples would not be higher than 0,25 INR and lower than 0,14 INR. This has low clinical impact. The samples were stored at room temperature for up to 24 hours and reanalyzed. No changes over 10 % in INR values were observed. This study showed that even though there is a significant difference, it is possible to replace the existing method which using plasma with the whole blood instead.
25

Gestão da inovação em medicina diagnóstica: um estudo de caso / Innovation management in diagnostic medicine: a case study

Edgard Rasquini Arnas 01 December 2017 (has links)
Este trabalho busca responder a pergunta de pesquisa: como ocorre a gestão da inovação em uma empresa de Medicina Diagnóstica? Para isso teve como objetivo aprofundar a compreensão sobre a gestão da inovação nesta empresa, entendendo as etapas do processo de inovação (ideação, conversão e difusão), entendendo como a estratégia da inovação se insere no processo de gestão da inovação, e entendendo como que pessoas e organização se inserem na gestão da inovação. Esta pesquisa fez uso de uma abordagem de natureza teórico-prática de enfoque qualitativo e objetivos de caráter exploratório por meio deum estudo de caso único em um centro de medicina diagnóstica de grande porte, reconhecido por práticas de gestão e inovação. Foram utilizadas as técnicas de entrevistas semiestruturadas, observação direta na empresa, e análise de documentos. Para a etapa de entrevista foi elaborado um protocolo semiestruturado com questões orientadoras conforme pesquisa bibliográfica a respeito de gestão da inovação, o setor de saúde e medicina diagnóstica.Foram entrevistados 12 líderes da empresa envolvidos com a gestão da inovação. Todas as fontes de dados foram analisadas e trianguladas chegando à apresentação e discussão de resultados do caso. Como resultados, a pesquisa evidenciou a importância da inovação em medicina diagnóstica, podendo reduzir custos e aumentar a qualidade, além de gerar valor para o restante da cadeia. A estratégia da inovação é alinhada à estratégia corporativa em diversos elementos e possui um processo de definição de drivers que direcionam a companhia no processo de inovação. O processo de inovação é influenciado por atores encontrados na literatura como órgãos reguladores, médicos, pacientes, fornecedores, universidades e operadoras. Além destes, outros foram citados, como órgãos representativos e o Ministério da Ciência e Tecnologia. Dois processos estruturados de inovação foram evidenciados: de novos produtos e de novos processos. O processo de novos produtos é alinhado ao modelo destagegates, enquanto que o processo de novos processos é mais amplo seguindo o modelo hegemônico. A etapa de ideação ocorre com geração de ideias tanto por fontes internas como externas, sendo as principais fontes os médicos e técnicos assessores, e os colaboradores. Técnicas como brainstorming, observação do comportamento dos clientes, e pesquisas acadêmicas são utilizadas. Na etapa de conversão, a seleção e avaliação é feita de maneira colegiada ou individual, por meio de fóruns presenciais ou virtuais. Os critérios de seleção são o alinhamento estratégico, as análises financeiras, técnicas e comerciais. No desenvolvimento e implantação, destaca-se a aplicação de pilotos e testes antes da efetiva implantação da inovação, treinamentos e acompanhamentos da implantação. Por fim, a etapa de difusão ocorre externamente, por meio da equipe comercial junto às operadoras, e com a equipe de médicos e técnicos assessores, junto aos clientes médicos, além dos canais de divulgação como eventos e congressos. A divulgação com clientes finais se dá por meio dos sites, redes sociais, e revistas. Já internamente, a comunicação ocorre principalmente na forma de murais e portais virtuais de comunicação, na atualização de documentos técnicos, e por meio de eventos internos de divulgação do conhecimento, premiação e reconhecimento. Em pessoas e organização, a pesquisa evidenciou que a cultura influencia o processo de gestão da inovação, sendo formada historicamente sobre os pilares de geração de conhecimento e relacionamento acadêmico nas universidades. Objetiva-se gerenciar os recursos humanos capturando pessoas alinhadas ao valor da inovação desde a fase de contratação, passando por treinamentos, avaliação anual de desempenho, premiação e reconhecimento. Não somente os colaboradores internos recebem incentivos e reconhecimentos, como também há incentivos a fornecedores, médicos e universitários por meio de programas específicos. / This master thesis seeks to answer the research question: how works the management of innovation in a case of Diagnostic Medicine? The purpose of this study was to deepen the understanding of innovation management in a diagnostic medicine company, understanding the stages of the innovation process (ideation, conversion and diffusion), understanding how the innovation strategy is embedded in the process of innovation management, and understanding how people and organizations are involved in managing innovation. This research made use of a theoretical-practical approach of qualitative approach and exploratory objectives through a case study in a large diagnostic medicine center, recognized by management and innovation practices. The techniques of semi-structured interviews, direct observation in the company, and document analysis were used. For the interview stage, a semistructured protocol was developed with orienting questions according to bibliographic research regarding innovation management, the health sector and diagnostic medicine. We interviewed 12 company leaders involved in innovation management. All data sources were analyzed and triangulated, arriving at the presentation and discussion of the results of the case. The research highlighted the importance of innovation in diagnostic medicine, which can reduce costs and increase quality, and generate value for the rest of the chain. The innovation strategy is aligned with the corporate strategy in several elements and has a process of definition of drivers that guide the company in the process of innovation. The innovation process is influenced by several stakeholders found in the literature. Besides these others were cited as representative bodies, and the ministry of science and technology. Two structured innovation processes were evidenced: process of new products and new processes. The process of new products is aligned with the stage gates model, while the process of new processes is broader following the hegemonic model. The stage of ideation occurs with the generation of ideas by both internal and external sources, the main sources being the doctors and technical advisors, and collaborators. Techniques such as brainstorming, customer behavior observation, and academic research are used. In the conversion stage, the selection and evaluation can be done collegially or individually, through forums that can be even virtual. The selection criteria are strategic alignment, financial, technical and commercial analysis. In the development and implementation, we highlight the application of pilots and tests before the effective implementation of the innovation, the training and follow-up of the implementation. Finally, the diffusion stage occurs externally, through the commercial team with the operators, and with the team of medical and technical advisors, with the medical clients, in addition to the channels of dissemination such as events, congresses. Publicity with end customers is through websites, social networks, and magazines. Already internally the communication occurs mainly in the form of virtual murals and portals of communication, in the updating of technical documents, and through internal events of dissemination of knowledge, awards and recognition. In people and organization, the research evidenced that culture influences the process of innovation management, being historically formed on the pillars of knowledge generation and academic relationship in universities. It aims to manage human resources by capturing people aligned with the value of innovation from the hiring stage, through training, annual performance evaluation, awards and recognition. Not only do internal collaborators receive incentives and recognition, but there are also incentives to suppliers, doctors and university students through specific programs.
26

Method verification for homocysteine and a sustainability study on glucose, homocysteine and lactate in different sampling tubes

Bohjort, Emelie January 2016 (has links)
The pre-analytical phase is known for being the most important step in the laboratory process to reach reliable test results. If handling, transport or preparation of the sample is performed incorrectly the results can deviate from the true value. Today, sampling tubes contains various additives to stabilize concentration levels. The aim of this study was to test a new sampling tube containing fluoride/citrate for glucose, lactate and homocysteine. It was also of interest to evaluate the stability of those three analytes in lithium-heparin, sodium-fluoride/potassium oxalate and fluoride/citrate tubes. To perform the sustainability study, a method verification was done for homocysteine in plasma. The study was performed in a hospital laboratory on the routine instrument Roche Cobas 6000 analyzer. Blood was drawn from 20 patients and was analyzed at the hospital laboratory in Gävle. The blood samples were transported frozen to the laboratory in Hudiksvall and were used in the method verification. For the sustainability study, blood was drawn from 10 healthy volunteers in lithium-heparin, sodium-fluoride/potassium oxalate and fluoride/citrate tubes. The method verification was approved. The results showed that glucose was stable for up to 72 hours in Vacuette Glycaemia tube with fluoride/citrate and this tube also gave more accurate results. Lactate and homocysteine were also stable in fluoride/citrate, but needs further studies. All three analytes were more stable if the sample tubes were centrifuged as soon as possible after blood collection. Fluoride/citrate tubes were stable without centrifugation directly.
27

Detektion av ciprofloxacin-resistens hos Neisseria gonorrhoeae med PCR

Jensen Alas, Gabriel January 2020 (has links)
Neisseria gonorrhoeae (NG) har successivt utvecklat resistens mot många antimikrobiella medel och betraktas som ett av de tre reella hoten bland antibiotikaresistenta bakterier. Ciprofloxacin är ett bredspektrum-antibiotikum tillhörande gruppen kinoloner som, förutom att behandla urinvägsinfektioner, används mot NG och infektioner i mage och tarm. Dock har det rapporterats att ca 30 % av NG-isolat som samlats in genom gonokock-isolatövervakningsprojekt (GISP) under 2017 var resistenta mot ciprofloxacin. På molekylnivå är resistens mot ciprofloxacin starkt associerad med en enda mutation i kodon 91 i gyras-genen (gyrA). Detta projekt har undersökt om det går att använda molekylärbiologiska metoder för att detektera NG-isolat med gyrA mutationen. Analysen gjordes med två olika PCR-system, ”7500 Fast Real-Time PCR System” från Applied Biosystems (ABI) och Panther Fusion från Hologic. Proberna som användes designades för påvisning av vildtyp gyrA (ciprofloxacin-känslig) och mutant gyrA (ciprofloxacin-resistent) hos NG. I projektet analyserades 50 NG-positiva prov (analyserade med screeningtest APTIMA COMBO2 från Hologic), från 43 patienter som provtagits under januari-februari 2020 i Region Skåne. Några patienter testades flera gånger vid olika tillfällen. NG-odling hade utförts parallellt från motsvarande tagna prov från patienterna. ABI-metoden påvisade genen hos 90 % (45/50) av NG-positiva prover (APTIMA COMBO2) medan endast 24 av de 49 proven (49 %) kunde odlas med traditionell metodik för att därefter resistensbestämmas. Av de 45 prov där gyras-genen kunde detekteras med ABI-metoden, uppvisade 28 (62 %) av proven en muterad gen och därmed en potentiell resistens för ciprofloxacin. Panther Fusion-metoden påvisade genen hos 80 % (40/50) av NG-positiva prover (APTIMA COMBO2), och såsom tidigare nämnts, kunde endast 24 av de 49 proven (49 %) odlas med traditionell metodik för att därefter resistensbestämmas. Av de 40 prov där gyras-genen kunde detekteras med Panther Fusion-metoden, uppvisade 26 av proven (65 %) en muterad gen och därmed en potentiell resistens för ciprofloxacin. En jämförelse mellan resultaten från PCR-metoderna och odlingarna visar att av de 24 odlingarna som kunde resistensbestämmas fick ABI-metoden resultat för 23 och Panther Fusion för 22. PCR-metodernas resultat överensstämde perfekt med resultaten från odling med samma 8 känsliga och 15 respektive 14 resistenta NG-isolat som odling. De båda PCR-metoderna och traditionell odling uppvisade jämförbara resultat. Av de 24 prov som kunde odlas och därmed resistensbestämmas, detekterades med ABI-metoden gyras-genen i 23 av dessa prov och i 22 av proven med Panther Fusion-metoden. Resistens mot ciprofloxacin uppvisades genom odling i 16 av de 24 odlingsbara prov, och av dessa 24 odlingsbara prov uppvisade ABI-metoden en muterad gen i 15 av proven och Panther Fusion-metoden en muterad gen i 14 av proven. Traditionell odling kunde bara genomföras på 24 av proven och PCR-metoderna identifierade signifikant fler prov innehållande vildtyp eller muterad gyras-gen, 45 respektive 40 prov. Projektet visade tydligt att PCR-metoderna kan identifiera fler prov än genom traditionell odling och kan därmed upptäcka fler prov med förväntad ciprofloxacin-resistens än vad som kan bestämmas genom traditionell odling. / Neisseria gonorrhoeae (NG) has been developing a resistance towards several different antibiotics and is viewed as one of the three real threats among resistant bacteria. Ciprofloxacin is a broad-spectrum-antibiotic belonging to the group quinolone antibiotics which, in addition to being used to treat urinal infections, is used to treat NG and infections in the stomach and intestines. However, it has been reported that 30 % of NG-isolates that have been gathered through the Gonococcal Isolate Surveillance Project (GISP) throughout 2017 were resistant to ciprofloxacin. On a molecular level, resistance to ciprofloxacin is strongly associated with a single mutation in kodon 91 in the gyras-gene (gyrA). This project sought to examine if it is possible to use methods from molecular biology to detect which NG that have the gyrA-mutation. The test was done using two different PCR-systems, ”7500 Fast Real-Time PCR System” from Applied Biosystems (ABI) and Panther Fusion from Hologic. The probes used were designed to show wild type gyrA (ciprofloxacin sensitive), and mutated gyrA (ciprofloxacin resistant) in NG. In this project 50 NG-positive samples (analysed with screentest APTIMA COMBO2 from Hologic), from 43 patients that had been tested during January-February 2020 in Region Skåne, were analysed. Some patients were tested several times, within the time period. NG-cultivation had been done in parallel from corresponding samples taken from the patients. The ABI-method showed the gene in 90 % (45/50) of NG-positive samples (APTIMA COMBO2) while only 24 of the 49 samples (49 %) could be cultivated by traditional methodology, and then tested for resistance. Of the 45 samples where the gyras-gene could be detected with the ABI-method, 28 samples (62 %) exhibited a mutated gene and thus a potential resistance to ciprofloxacin. The Panther fusion-method showed the gene in 80 % (40/50) of NG-positive samples (APTIMA COMBO2), and as mentioned earlier, only 24 of the 49 samples (49 %) could be cultivated by traditional methodology to then be tested for resistance. Of the 40 samples where the gyras-gene could be detected with the Panther Fusion-method, 26 samples (65 %) exhibited a mutated gene and thus a potential resistance to ciprofloxacin. The two PCR-methods and traditional cultivation exhibited comparable results. Of the 24 samples that could be cultivated and thus tested for resistance, the ABI-method detected the gyras-gene in 23 of these samples and the Panther Fusion-method detected the gene in 22 of the samples. Cultivation exhibited resistance to ciprofloxacin in 16 of the 24 samples that could be cultivated, and of these 24 cultivatable samples the ABI method exhibited a mutated gene in 15 of the samples and the Panther Fusion-method exhibited a mutated gene in 14 of the samples. Traditional cultivation could only be done on 24 of the samples and the PCR-methods could identify significantly more samples containing either wild type or mutated gyras-gene, 45 and 40 samples, respectively. The project clearly showed that more samples can be identified with the PCR-methods than through traditional cultivation, and thereby discover more samples with expected ciprofloxacin-resistance, than can be determined through traditional cultivation.
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Sambandet mellan TAPSE och RVs´ vid bedömning av RV:s funktion med ekokardiografi hos hjärtfriska individer : En jämförande studie / The relationship between TAPSE and RVs' when assessing RV function with echocardiography in heart healthy individuals : A comparative study

Wafaa, Hamsho, Hosseinzadeh, Sousan January 2023 (has links)
Högerkammare (RV) har en komplex anatomi, spelar en viktig roll för blodsyresättning och kan påverkas av fler patofysiologiska tillstånd. Utvärdering av RV:s funktion är viktig för överlevnad och har prognostiskt värde vid hjärt-och lungsjukdomar. Transthorakal ekokardiografi (TTE) används för RV:s storlek- och funktionsbedömning. Tricuspid annular plane systolic excursion (TAPSE) och annulus tricuspid peak systolic velocity (RVs´) är två vanliga metoder för bedömning av RV:s funktion. Båda metoderna har bra reproducerbarhet och är enkla att utföra.  Syftet med detta arbete är att utreda interobservatörvariation, sambandet och överensstämmelse mellan TAPSE och RVs´. Studien är en tvärsnittsstudie av 53 friska testpersoner 18-60 åringar. Mätningen baserades på en blind dubbelbestämning av två biomedicinska analytiker studenter. Analysen genomfördes med programmet IBM SPSS Statistics.  Interobservatörvariationsanalys visade ingen signifikant skillnad i mätosäkerheten mellan studenterna, (PTAPSE=0,568 och PRVs´=0,548). Enligt regressionsanalysen hade RVs´ något mindre mätosäkerhet än TAPSE. Ett svagt positivt samband hittades mellan RVs´ och TAPSE och 100% överenstämmelse avseende utfall påvisades, Kappavärdet blev 1. Båda metoderna har bra interobservatörvariation hos oerfarna undersökare. Hos hjärt- och lungfriska ser sambandet svagt positivt ut mellan TAPSE och RVs´. Dock kunde tidigare studier identifiera starkare positivt samband. Skillnaden i resultatet kan bero på erfarenhetsbrist hos studenterna och lågt antal deltagare. / The Right ventricle (RV) has a complex anatomy, plays an important role in blood oxygenation and can be affected by several pathophysiological conditions. Evaluation of RV function has prognostic value in heart and lung diseases. Tricuspid annular plane systolic excursion (TAPSE) and annulus tricuspid peak systolic velocity (RVs´) are two common methods for assessing RV function in Transthoracic echocardiography.  The study aimed to investigate interobserver variation, the correlation and agreement between TAPSE and RVs´. The study is a cross-sectional study of 53 healthy participants aged 18-60. The measurement was based on a blind double determination by two biomedical analyst students. The analysis was implemented with the program IBM SPSS Statistics. Interobserver variation analysis showed no significant difference between the two students, (PTAPSE =0,568 and PRVs´=0,548). Regression analysis showed RVs´ had slightly less measurement uncertainty than TAPSE. A weak positive correlation was found between RVs´ and TAPSE and 100% agreement regarding outcome was demonstrated, Kappa value was 1. Both methods have good interobserver variation in inexperienced examiners. In people with healthy heart and lungs, the relationship between TAPSE and RVs looks weakly positive. Previous studies identified stronger positive association. Differences in the results may be due to a lack of experience on the part of the students and a low number of participants.
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En jämförelse mellan mättekniker för högerkammarbedömning vid ekokardiografi : Överensstämmelse mellan s´ och TAPSE / A comparison of measure techniques for right ventricular function assessment in echocardiography : Correlation between s´ and TAPSE

Göransson, Lizette, Fredlund, Filippa January 2017 (has links)
Bedömningen av höger kammares systoliska funktion kan med fördel göras med ekokardiografi, bl.a. med tekniker som tvådimensionell ekokardiografi, motion-mode (M-mode) och Tissue Doppler Imaging (TDI). Mätvärden som kan fås ut av dessa tekniker är Tricuspid Annular Plane Systolic Excursion (TAPSE) och s`. TAPSE beskriver annulus tricuspidalis longitudinella rörlighet. s´ beskriver den maximala systoliska hastigheten i annulus tricuspidalis. Syftet med examensarbetet var att undersöka sambandet mellan TAPSE och s´ vid högerkammarfunktionsbestämning. Studien är en retrospektiv tvärsnittsstudie och består av 99 deltagare i åldrarna 18–90 år. Både friska och hjärt-och kärlsjuka deltagare inkluderades, men inte patienter med förmaksflimmer eller individer som var yngre än 18 år. Deltagarna undersöktes med transthorakal ekokardiografi (TTE) vid Länssjukhuset Ryhov i Jönköping, vid undersökningen mättes TAPSE och s´. Det var samma biomedicinska analytiker (BMA) som utförde undersökningarna. McNemars test utfördes och ett Kappa-värde räknades ut. Resultatet visade signifikant skillnad och Kappa-värdet var lågt vilket talar för dåligt samband mellan de båda variablerna. Utfallet i studien visar att fler deltagare klassas med normal högerkammarfunktion mätt med TAPSE, medan samma individer klassas med högerkammardysfunktion mätt med s´. Orsaken till det dåliga sambandet mellan parametrarna är okänt och bör studeras vidare i kommande studier. / The assessment of right ventricular systolic function is done by echocardiography, with techniques as twodimensional echocardiography, motion-mode (M-mode) and Tissue Doppler Imaging (TDI). Measurements ​​obtained from these techniques are Tricuspid Annular Plane Systolic Excursion (TAPSE) and s`. TAPSE describes the longitudinal movement of annulus tricuspidalis. s´ describes annulus tricuspidalis maximal systolic velocity. The purpose of this essay was to explore the relationship between TAPSE and s´. The study consists of 99 participants between the ages of 18 and 90. The population was consisted of individuals with or without cardiovascular disease, but not individuals with atrial fibrillation. Participants were investigated with transthorakal echocardiography (TTE) at Länssjukhuset Ryhov in Jönköping. At the examination both TAPSE and s´ was measured. McNemar's test was performed and a Kappa value was calculated. The result showed a significant difference and the Kappa value was low which indicates a low relationship between the variables. The outcome of the study shows that several participants are classified with normal right ventricular function measured with TAPSE, but the same individuals are classified with right ventricular dysfunction measured by s'. The reason for the poor relationship between the parameters is unknown and should be studied further in future studies.
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Estudo do sistema de planejamento e controle de materiais no Laboratório de Hematologia do Hospital das Clínicas de Ribeirão Preto / Study of materials planning and control system on the Haematology Laboratory of the Clinical Hospital of Ribeirão Preto

Duarte, Nathalia Campos Moura 20 October 2015 (has links)
Diante do atual contexto econômico enfrentado pelas organizações, ações que visam a redução de custos e desperdícios são cada vez mais evidentes. No setor de saúde, em especial no ramo da medicina diagnóstica, a pressão financeira exercida tanto no âmbito público como privado, o aumento da demanda por exames, o avanço da tecnologia, e consequentemente, o aumento do investimento associado ao seu uso fizeram com que os custos aumentassem de forma crescente. Dessa forma, um dos maiores custos dos laboratórios se refere a materiais (insumos), inclusive equipamentos, sendo assim, os estoques representam importante quesito a ser administrado uma vez que a gestão de materiais tem o objetivo de conciliar os interesses entre as necessidades de suprimentos e a otimização dos recursos financeiros e operacionais das empresas. Nesse sentido o presente estudo objetivou o estudo e análise do sistema de planejamento e controle de materiais (mais especificamente os reagentes utilizados na realização dos e hemogramas e contagem de reticulócitos) do Laboratório de Hematologia do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto. A pesquisa caracterizou-se por ser uma pesquisa aplicada, qualitativa e quantitativa, bem como exploratória. Para tanto foram utilizadas como técnicas de coleta de dados observação in locco, entrevistas e análise documental de dados secundários. Os dados coletados foram relacionados ao processo de realização dos exames e da gestão e controle dos reagentes, além da gestão do contrato. Para realização das análises quantitativas foram levantadas informações sobre a quantidade de reagentes adquiridos bem como demanda de exames realizados ao longo dos anos de 2013 e 2014, período das análises compreendido durante o estudo. Os resultados analisados permitiram concluir que a forma de estruturação do contrato com fornecedor dificulta a gestão eficiente dos recursos. / According to the actual economic context faced by organizations, pressures for cost and waste reduction are increasingly evident. In the healthcare sector, especially in diagnostic medicine, the financial pressure, the increased demand for test, the advance of technology and the high investment associated to it use induced to an incrementally increase of the costs. Thus, one of the biggest costs of laboratories refers to materials (inputs), including equipment. Therefore, stocks represent an important issue to consider, once materials management aims to reconcile the interests of the supply needs and the optimization of financial and operational resources of the companies. In this sense, the present research aimed the study and analysis the materials and control system (specifically the reagents used in clinical blood count tests and reticulocyte count) on the Hematology Laboratory of the Ribeirão Preto School of Medicine Clinical Hospital. The study was considered an applied, exploratory, qualitative and quantitative research. It was used as data collection techniques in loco observation, interviews and document analysis of secondary data. The collected data were related to the process of the examinations and the management and control of reagents, as well as contract management. To perform the quantitative analyzes information about the amount of reagents purchased and demand for tests performed over the years 2013 and 2014 have been raised. Therefore, it was concluded that the form of contract suppliers structuring does not allow an efficient management of resources.

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