Dissertations / Theses on the topic 'Deep vein thrombosis'
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Warwick, David John. "Deep vein thrombosis after total hip replacement." Thesis, University of Bristol, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283969.
Full textHoward, Adam Quentin. "The prevention of post-operative deep vein thrombosis." Thesis, Imperial College London, 2007. http://hdl.handle.net/10044/1/8187.
Full textBaarslag, Hendrik Jan. "Diagnosis and management of upper extremity deep vein thrombosis." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2003. http://dare.uva.nl/document/86567.
Full textCate-Hoek, Arina Janna ten. "New developments in diagnosis and treatment of deep vein thrombosis." [Maastricht] : Maastricht : [Maastricht University] ; University Library, Universiteit Maastricht [host], 2008. http://arno.unimaas.nl/show.cgi?fid=13095.
Full textKahn, Susan Rebecca. "Clinical predictors of-deep vein thrombosis in patients with leg symptoms." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp04/mq29730.pdf.
Full textLindmarker, Per. "Treatment of deep vein thrombosis and risk of recurrent venous thromboembolism /." Stockholm, 1998. http://diss.kib.ki.se/1998/91-628-3211-5/.
Full textKahn, Susan Rebecca. "Clinical predictors of deep vein thrombosis in patients with leg symptoms." Thesis, McGill University, 1996. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=27355.
Full textPurpose. To determine, in patients presenting with leg symptoms, which clinical variables best predict (1) DVT and (2) proximal DVT. To estimate the probability of DVT in an individual presenting with a particular grouping of these variables.
Results. Male sex, orthopedic surgery, and warmth and superficial venous dilation on exam were independent predictors of DVT (adjusted odds ratios and 95% confidence intervals 2.8 (1.5, 5.1), 5.4 (2.2, 13.6), 2.1 (1.2, 3.9) and 2.9 (1.4, 5.7), respectively) and proximal DVT (adjusted odds ratios 2.4 (1.2, 4.8), 4.1 (1.4, 12.3), 2.3 (1.2, 4.7) and 3.4 (1.6, 7.0), respectively). A clinical prediction index that categorized patients into different levels of DVT risk was created, and its ROC curve showed moderate predictive ability. No single cutoff point was ideal in terms of desired sensitivity and specificity, however the index was useful in a strategy aimed to limit the need for contrast venography in patients with suspected DVT. Using this strategy, 78% of study patients could have avoided contrast venography. (Abstract shortened by UMI.)
Balendra, Padma Rani. "Deep vein thrombosis of the leg : natural history and haemostatic variables." Thesis, Queen's University Belfast, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334477.
Full textBrock, Sheila Anne. "Compression and Doppler ultrasound of deep vein thrombosis in patients on tuberculosis treatment." Thesis, Cape Peninsula University of Technology, 2013. http://hdl.handle.net/20.500.11838/1570.
Full textBackground. Ultrasound has until recently been regarded as a sophisticated examination reserved for tertiary health care. In reality it is well suited to the district or primary health-care situation. A DVT (deep vein thrombosis) is an important complication of the treatment of TB and this can lead to more devastating sequelae such as a pulmonary embolus. Many DVTs are clinically silent, making the diagnosis difficult. Method. This study was a prospective, longitudinal observational study. The study documented the incidence of DVTs and their onset, assessed certain aspects in an attempt to identify some risk factors, and noted the most common position of the DVT in a TB population. The feasibility of a sonographer-led ultrasound clinic for the diagnosis of DVTs was also assessed. This was achieved by screening the in-patient population at a district TB hospital. The participants received up to four routine duplex Doppler compression ultrasound examinations of the venous system of the lower extremities on week 0, week 4, week 8 and week 14. In addition a single abdominal ultrasound was performed at week 0. Results The incidence of DVTs in this TB population was 15.3%. A median of day 10 from commencing TB treatment was identified as the most common day to develop a DVT. The popliteal vein was the most frequent position for a DVT. Several statistically significant factors were identified, including a decreased ambulatory status, TB regimen and the use of anticoagulants. Only 52% of the DVTs were clinically symptomatic. The clinical evaluation for a DVT diagnosis in this study population had a sensitivity of 52.4% and a specificity of 65.3%. The positive predictive value (PPV) was 21.7%. Of the abdominal ultrasound reports there were 75.5% (281) abnormal reports, 22.5% (n = 90) normal reports and 4.5% (n = 18) with no report. Conclusion This body of work has shown how an effective ultrasound service can be provided at a district level TB hospital successfully administered by a trained ultrasonographer. This also facilitated a screening service to diagnose both symptomatic and asymptomatic deep vein thromboses in newly diagnosed tuberculosis patients. This study confirmed a higher rate of DVT in newly diagnosed TB patients than has been previously seen. It also provided detail on additional risk factors. The study illustrates the poor performance of clinical signs and symptoms as a trigger for further investigation for the confirmation of a DVT. Given the frequency and impact of the embolic complications of DVT, this study provides a strong justification for further research into routine serial ultrasonic screening and/or prophylactic antithrombolytics in newly diagnosed TB patients. As well as the DVT ultrasound scans there was the ancillary service offered by the research sonographers. This included an abdominal scan that detected abdominal pathology in 75% of the scans performed. An ultrasound scan is not pathognomonic but it does provide significant insight into the extent of some of the abdominal pathologies seen in TB patients. The information provided from this study gives a good indication of the problem that DVTs present in this population and the complexities of the disease TB. It is hoped that the results from this study will better equip the medical team in the non-tertiary situation to be vigilant for the presence of a DVT and educate them on the usefulness of the ultrasound scan.
Alshehri, Mohammed Faiez. "Risk factors for deep vein thrombosis in a South African public hospital." Master's thesis, University of Cape Town, 2013. http://hdl.handle.net/11427/2879.
Full textIncludes abstract.
The evidence suggests an association between HIV, TB and DVT. There are no studies of this link in the Southern African setting, where the incidence of both of these conditions (HIV and TB) is high. We therefore undertook a study to define the incidence of HIV and TB in patients with confirmed DVT in this setting. The aim of this study is to describe the incidence of HIV, TB and the more commonly accepted risk factors in patients with confirmed DVT in a South African public hospital.
Brandão, Gustavo Muçouçah Sampaio [UNESP]. "Pentasaccharides para o tratamento da trombose venosa profunda." Universidade Estadual Paulista (UNESP), 2016. http://hdl.handle.net/11449/141498.
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Pentasaccharides para o tratamento da trombose venosa profunda Questão da revisão: Os novos anticoagulantes da classe dos pentasaccharides podem ser uma alternativa eficaz e segura aos anticoagulantes convencionais utilizados na terapia padrão do tratamento da trombose venosa profunda? Visão geral: Trombose venosa profunda (TVP) é uma doença grave e potencialmente fatal que se caracteriza pela formação aguda de um coágulo de sangue nas veias profundas. Sua incidência aumenta exponencialmente com a idade e estima-se que na população geral, sua incidência seja de 5 casos em 10,000 habitantes. O tratamento padrão se faz por meio de medicamentos anticoagulantes, inicialmente pela administração de medicamentos injetáveis, as heparinas, por 5 a 7 dias e em seguida pelo uso prolongado de medicamentos de uso oral, os antagonistas da vitamina K. Entretanto, o alto risco de sangramento e a necessidade de um rigoroso controle laboratorial, permanecem como importantes limitações à terapia padrão. Os pentasaccharides são anticoagulantes sintéticos que podem apresentar vantagens em relação ao tratamento convencional como um efeito mais previsível, um regime de dosagem mais conveniente, a ausência da necessidade de controle laboratorial, ausência de interações com medicamentos e/ou alimentos, ausência da temida diminuição das plaquetas induzida pela heparina e em muitos casos melhor custo-benefício. Características chaves e resultados: Nossas buscas, realizadas até julho de 2015, identificaram 20 entre 730 registros que representavam 5 estudos elegíveis, compreendendo um total de 6981 pacientes. Os estudos compararam os pentasaccharides fondaparinux, idraparinux e idrabiotaparinux com a terapia padrão (heparina seguida por antagonista da vitamina K). O principal resultado de eficácia foi feito pela avaliação da incidência de qualquer episódio tromboembolismo venoso (novo episódio de TVP ou embolia pulmonar) durante o tratamento. E o principal resultado de danos foi incidência de sangramento. Esta revisão mostrou que os pentasaccharides (fondaparinux, e a dose de 2.5 mg de idraparinux e a dose equivalente de 3.0 mg de idrabiotaparinux) podem ser uma alternativa eficaz e segura a anticoagulação convencional para o tratamento da TVP. Qualidade da evidência: A qualidade da evidência foi considerada moderada a alta. Um único estudo incluído (Persist) poderia ser julgado potencialmente falho devido ao relevante número de pacientes que foram perdidos ou descontinuaram prematuramente o tratamento após a randomização. De forma geral, os estudos incluídos responderam diretamente as perguntas e foram considerados de boa qualidade. Os resultados dos estudos foram consistentes e os efeitos estimados foram precisos. Nós acreditamos que seja improvável que a maioria dos nossos principais resultados de eficácia e danos possam ser modificados por estudos adicionais. Entretanto, estudos futuros com os pentasaccharides de meia vida prolongada (idraparinux e idrabiotaparinux) em baixas doses podem confirmar nossas estimativas com relação a sua não inferioridade em comparação à terapia padrão.
Background: Deep vein thrombosis (DVT) is a severe disorder caused by acute formation of a clot or thrombus in the deep vein system. The incidence of DVT increases with age: from 2 to 3/10,000 in adults aged 30 to 49 years to 20/10,000 in adults aged 70 to 79 years. If left untreated, the clot can travel up to the lungs and cause a potentially life-threatening pulmonary embolism (PE). Standard treatment is based on antithrombotic therapy, initially with parenteral administration of unfractionated heparin or low molecular weight heparins (LMWH) for five to seven days, then subsequent long-term oral vitamin K antagonists (e.g. warfarin) therapy. However, hemorrhagic complications are a major concern associated with warfarin treatment. Indeed, the hemorrhagic risk of warfarin and the required laboratory control remain the Achilles’ heel of vitamin K antagonist management. The pentasaccharides have characteristics that may be favourable over conventional treatment, including a predictable effect, lack of frequent monitoring or re-dosing and few known drug interactions and absence of heparin-induced thrombocytopenia. To date, no systematic review has measured the effectiveness and safety of these drugs in the treatment of DVT. Objectives: To assess the efficacy and harms of pentasaccharides for the treatment of deep venous thrombosis. Search strategy: 1 The Cochrane Peripheral Vascular Diseases Group Trials Search Co-ordinator searched the Specialised Register (last searched July 2015) and the Cochrane Register of Studies (last searched July 2015). We searched clinical trials databases for details of ongoing or unpublished studies and the reference lists of relevant articles retrieved by electronic searches for additional citations. Selection criteria: We included randomised controlled trials in which people with a DVTconfirmed by standard imaging techniques, were allocated to receive a pentasaccharide (fondaparinux, idraparinux or idrabiotaparinux) for the treatment of DVT. Data collection and analysis: Three review authors (GB, DJ and MS) independently extracted the data and assessed the risk of bias in the trials. Any disagreements were resolved by discussion. We performed meta-analyses when we considered heterogeneity low. The two primary outcomes were recurrent VTE and major (and clinically non-major) bleeding. Other outcomes included all-cause mortality, recurrent DVT, PE, thrombocytopenia, heparin-induced thrombocytopenia syndrome and all other adverse effects induced by the treatments . We calculated all outcomes using a relative risk (RR) with a 95% confidence interval (CI). Main results: We included 5 randomised controlled trials of 6981 participants. Two studies tested fondaparinux, while three tested idraparinux (being one tested idrabiotaparinux). We deemed all included studies to be of high methodological quality and generally low risk of bias. The quality of the evidence was generally graded as high as the outcomes were direct and effect estimates were consistent and precise, as reflected in the narrow CIs around the RRs. Meta-analysis of two studies (2658 participants) comparing fondaparinux with standard anticoagulation groups showed no difference in the risk of recurrent VTE (RR 0.88, 95% CI 0.60 to 1.29). The RR of bleeding in the initial period of treatment (RR 0.94, 95% CI 0.73 to 1.22) and three months of follow up (RR 0.61, 95% CI 0.36 to 1.01) were similar comparing both interventions. Two studies comparing idraparinux with standard therapy showed no difference in the risk of recurrent VTE during three months (RR 1.51; 95% CI 0.26, 8.90) and (RR 0.79; 95% CI 0.21; 2.91). The treatment with idraparinux clearly showed a bleeding risk with a pattern dose-response. However, at a dose of 2.5 mg idraparinux, there was no significant difference in the risk of bleeding in patients receiving idrapaparinux in comparison to standard therapy during six months of follow up (RR 0.92, 95% CI 0.69 to 1.22). One study contributed with data for the analysis (n=741 participants) that there was no significant difference in the risk of recurrent VTE during six months follow-up between idrabiotaparinux compared with idraparinux (RR 0.71, 95% CI 0.30 to 1.66). The risk of bleeding was also similar comparing the two interventions (RR 0.71, 95% CI 0.49 to 1.04). Authors' conclusions: The pentasaccharides (fondaparinux, the dose of 2.5 mg idraparinux and equimolar dose of 3.0 mg idrabiotaparinux) may be an effective and safe alternative to conventional anticoagulation treatment for acute DVT.
Daniel, Öberg. "Clinical Assessment for Deep Vein Thrombosis using Support Vector Machines : A description of a clinical assessment and compression ultrasonography journaling system for deep vein thrombosis using support vector machines." Thesis, KTH, Skolan för datavetenskap och kommunikation (CSC), 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-178419.
Full textI denna rapport beskrivs ett journalsystem samt ett system för klinisk bedömning av djupvenstromboser.Vår modell baserar sig på en stödvektormaskin (eng. Support Vector Machine) med linjär och radial basfunktion för att fastställa förekomsten av djupa ventromboser samt att hjälpa till i skapandet av nya modeller för bedömning. 159 patientjournaler användes för att fastställa att Wells Score har en klinisk precision på 58%, 60% sensitivitet och specificitet på 57% somkan jämföras med våran modell som har en precision på 81%, 66% sensitivitet och specificitet på 84%. En 23 procentenheters ökning i precision.Den diagnostiska oddskvoten gick från 2.12 till 11.26. Det behövs dock en större datamängd för att rapportera något avgörande. Då vårt system både är för journalskapande och klinisk bedömning så kommer varje undersökt patient att bidra till högre precision i modellen.
Dalton, Edward J. "A Novel Manually Operated Compression Device for the Prevention of Deep Vein Thrombosis." Master's thesis, Temple University Libraries, 2018. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/503693.
Full textM.S.
Deep Vein Thrombosis, a potentially fatal event, occurs when a blood clot forms within the deep veins of the body. This most frequently manifests in the lower extremities. The goal of this research was to build an inexpensive device that could apply therapeutic compressive pressure to the lower leg to aid in the prevention of deep vein thrombosis using only mechanical input from the user. Several different prototypes were designed and built with varying degrees of success. Characterization of the final prototype required calibration of pressure and force measurement sensors. Additionally, a mathematical model was developed in order to predict how changes in the design of the device, as well as differing sizes and shapes of lower legs, would impact the amount of applied pressure. The predictions of this mathematical model were found to be substantially larger when compared against empirical data. However, there is evidence to indicate that the final prototype could be minimally altered to apply ample therapeutic pressure.
Temple University--Theses
Olakareem, Halima. "Prognostic factors associated with the development of post-thrombotic syndrome after a deep vein thrombosis of the lower limb." Thesis, University of Birmingham, 2016. http://etheses.bham.ac.uk//id/eprint/7002/.
Full textGuerrero, Julian. "System for vessel characterization : development and evaluation with application to deep vein thrombosis diagnosis." Thesis, University of British Columbia, 2008. http://hdl.handle.net/2429/1558.
Full text麥寶晶 and Po-ching Mak. "Evidence-based guidelines for deep vein thrombosis prophylaxis in a surgical intensive care unit." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2013. http://hdl.handle.net/10722/193031.
Full textpublished_or_final_version
Nursing Studies
Master
Master of Nursing
Horner, Daniel. "Isolated distal deep vein thrombosis in symptomatic ambulatory patients : a prospective data analysis and therapeutic feasibility study." Thesis, University of Manchester, 2013. https://www.research.manchester.ac.uk/portal/en/theses/isolated-distal-deep-vein-thrombosis-in-symptomatic-ambulatory-patients-a-prospective-data-analysis-and-therapeutic-feasibility-study(02979c49-ec26-4099-b0f8-3da2acbf0672).html.
Full textForgie, Melissa Anne. "Duration of oral anticoagulation in first-episode idiopathic deep vein thrombosis: A Markov decision analysis." Thesis, University of Ottawa (Canada), 2001. http://hdl.handle.net/10393/9288.
Full textJackson, Brandon Spencer. "Hypercoagulability using biophysical parameters in HIV positive versus HIV negative patients with deep vein thrombosis." Thesis, University of Pretoria, 2018. http://hdl.handle.net/2263/65529.
Full textThesis (PhD)--University of Pretoria, 2018.
Surgery
PhD
Unrestricted
Galanaud, Jean-Philippe. "Les thromboses veineuses méconnues des membres inferieurs : thromboses veineuses profondes distales et thromboses veineuses superficielles." Thesis, Montpellier 1, 2011. http://www.theses.fr/2011MON1T027.
Full textBackground: Though they represent the majority of all lower limbs thromboses, isolated distal deep-vein thrombosis (DVT) (without symptomatic pulmonary embolism (PE)) and isolated superficial vein thrombosis (SVT) (without DVT or PE) have been poorly studied. Their clinical significance and management are under debate.Methods: Data from epidemiological multicenter prospective studies OPTIMEV, POST, RIETEResults and comments: Isolated distal DVT: Distal and proximal DVTs exhibit a different risk factor profile, the latter being more associated with chronic risk factors. Three-month mortality of distal DVT patient is lower than that of proximal DVT ones but is higher than that of controls. This evidences that distal DVT is a clinically significant finding. Differences in population profile and outcomes suggests that the benefit/risk ratio of anticoagulant treatment is not similar. Data from proximal DVT clinical trials should no longer be extrapolated to distal DVT.Isolated SVT: In case of SVT the risk of concomitant DVT is high. A compression ultrasonographic exam should be performed and at least explore the whole deep venous system of the affected limb. Male gender and history of DVT/Pulmonary embolism are independent predicators of recurrence. Some SVT can be safely treated without anticoagulants. On contrary, in patients with cancer or a sapheno-femoral junction involvement, the risk of deep venous recurrence is high even upon full therapeutic dose of anticoagulants
Ikesaka, Rick. "The Risk of Upper Extremity Deep Vein Thrombosis and Primary Thromboprophylaxis with Low Dose Rivaroxaban in Oncology Patients with Central Venous Catheters." Thesis, Université d'Ottawa / University of Ottawa, 2021. http://hdl.handle.net/10393/41954.
Full textSobieraj, Diana M., Craig I. Coleman, Vinay Pasupuleti, Abhishek Deshpande, Roop Kaw, and Adrian V. Hernández. "Comparative efficacy and safety of anticoagulants and aspirin for extended treatment of venous thromboembolism: A network meta-analysis." Elsevier B.V, 2015. http://hdl.handle.net/10757/346496.
Full textObjective To systematically review the literature and to quantitatively evaluate the efficacy and safety of extended pharmacologic treatment of venous thromboembolism (VTE) through network meta-analysis (NMA). Methods A systematic literature search (MEDLINE, Embase, Cochrane CENTRAL, through September 2014) and searching of reference lists of included studies and relevant reviews was conducted to identify randomized controlled trials of patients who completed initial anticoagulant treatment for VTE and then randomized for the extension study; compared extension of anticoagulant treatment to placebo or active control; and reported at least one outcome of interest (VTE or a composite of major bleeding or clinically relevant non-major bleeding). A random-effects Frequentist approach to NMA was used to calculate relative risks with 95% confidence intervals. Results Ten trials (n=11,079) were included. Risk of bias (assessed with the Cochrane tool) was low in most domains assessed across the included trials. Apixaban (2.5mg and 5mg), dabigatran, rivaroxaban, idraparinux and vitamin K antagonists (VKA) each significantly reduced the risk of VTE recurrence compared to placebo, ranging from a 73% reduction with idraparinux to 86% with VKAs. With exception of idraparinux, all active therapies significantly reduced VTE recurrence risk versus aspirin, ranging from a 73% reduction with either apixaban 2.5mg or rivaroxaban to 80% with VKAs. Apixaban and aspirin were the only therapies that did not increase composite bleeding risk significantly compared to placebo. All active therapies except aspirin increased risk of composite bleeding by 2 to 4-fold compared to apixaban 2.5mg, with no difference found between the two apixaban doses. Conclusion Extended treatment of VTE is a reasonable approach to provide continued protection from VTE recurrence although bleeding risk is variable across therapeutic options. Our results indicate that apixaban, dabigatran, rivaroxaban, idraparinux and VKAs all reduced VTE recurrence when compared to placebo. Apixaban appears to have a more favorable safety profile compared to other therapies.
Revisión por pares
Prado, Lucas Bessa 1986. "Avaliação da atividade anticoagulante e antitrombótica de enoxaparina encapsulada em nanopartículas em modelo de trombose venosa profunda em ratos." [s.n.], 2013. http://repositorio.unicamp.br/jspui/handle/REPOSIP/310153.
Full textDissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas
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Resumo: A Trombose Venosa Profunda (TVP) é definida como uma oclusão parcial ou total da circulação venosa profunda. A heparina é um fármaco com ação anticoagulante e antitrombótica utilizado desde 1930. O custo, a via de administração (endovenosa ou subcutânea) e as doses repetidas são algumas das limitações do seu uso. Assim, o desenvolvimento de um produto que possa ser administrado por via subcutânea ou oral em um menor número de aplicações, torna-se um importante desafio e de grande aplicabilidade clínica. Sistemas de liberação sustentada permitem que o fármaco seja encapsulado e liberado gradativamente. Este estudo constituiu na preparação, caracterização e avaliação in vivo de nanopartículas de poli (?-caprolactona) (PCL) e quitosana como carreadores de heparina de baixo peso molecular (enoxaparina). As nanopartículas foram preparadas pelo método de dupla emulsão água/óleo/água e evaporação do solvente. A caracterização das nanopartículas foi realizada por microscopia eletrônica de varredura (MEV), onde foram observadas partículas esféricas e homogêneas. O diâmetro médio das nanopartículas foi de 512,8 ± 13,8 nm e o potencial zeta foi de +30,9 ± 1,3 mV. A eficiência de encapsulamento, analisada pelo método Azure II foi de 99,04 ± 0,001 %. A atividade anticoagulante in vivo da enoxaparina encapsulada foi avaliada pela atividade anti-Xa plasmática, através de método colorimétrico. Quando a enoxaparina livre foi administrada por via subcutânea observou-se um pico de atividade (0,5 UI/mL) em 1 hora, com um decréscimo gradual até 6 horas. A atividade anticoagulante da enoxaparina encapsulada em nanopartículas manteve-se por até 14 horas, quando foi administrada por via subcutânea, sugerindo que as nanopartículas podem permitir que a enoxaparina seja liberada de forma gradual, podendo ser uma vantagem na prática clínica. Após a administração das nanopartículas por via oral não se observou nenhuma atividade em até 14 horas, sugerindo que as nanopartículas não tenham sido absorvidas ou a enoxaparina tenha sido degradada no trato gastrointestinal. Para avaliação do efeito antitrombótico foi padronizado o modelo de TVP por estase e hipercoagulabilidade em ratos. Após administração subcutânea, houve uma significativa diminuição do tamanho do trombo formado tanto com o emprego de enoxaparina livre (p= 0,002) como após encapsulamento em nanopartículas (p= 0,0411) em comparação ao grupo controle. Quando foram administradas nanopartículas por via oral, os resultados mostraram que não houve diferença estatística em comparação ao grupo controle (p= 0,9476) e a um grupo de nanopartículas vazias (p= 0,9372). Em resumo, o método de dupla emulsão a/o/a mostrou-se eficiente para o encapsulamento de enoxaparina, proporcionando a obtenção de nanopartículas esféricas e com alta eficiência de encapsulamento. Pelos estudos in vivo, a enoxaparina encapsulada mostrou uma atividade anticoagulante com liberação sustentada, por um período superior ao obtido com a enoxaparina livre, com excelente efeito antitrombótico quando administrada por via subcutânea. Contudo, não se observou nenhum efeito anticoagulante ou antitrombótico quando as nanopartículas foram administradas por via oral. Novos experimentos com quitosanas de diferentes massas molares serão necessários na tentativa de possibilitar a absorção oral dessas nanopartículas
Abstract: Deep vein thrombosis (DVT) is defined as partial or total occlusion of the deep venous circulation. Heparin is a drug with anticoagulant and antithrombotic action used since 1930. The costs, administration vias (intravenous or subcutaneous) and the repeated doses are some limitations of its use. Thus, the development of a product that could be administered subcutaneous or orally in a smaller number of applications becomes a major challenge with huge clinical applicability. Sustained release systems allow the medication to be gradually encapsulated and released. This study was based on the preparation, characterization and in vivo evaluation of nanoparticles of poly (?-caprolactone) (PCL) and chitosan as carriers of low molecular weight heparin (enoxaparin). The nanoparticles were prepared by the double emulsion water/oil/water method and solvent evaporation. The nanoparticles characterization was performed by scanning electron microscopy (SEM), in which were observed spherical and homogeneous particles. The average diameter of the nanoparticles was 512.8 ± 13.8 nm and the zeta potential was +30.9 ± 1.3 mV. The encapsulation efficiency, analyzed by Azure II method, was 99.04 ± 0.001%. The in vivo anticoagulant activity of the encapsulated enoxaparin was evaluated by plasmatic anti-Xa activity performed by colorimetric method. When the free enoxaparin was subcutaneously administered a peak of activity was observed (0.5 IU/mL) in 1 hour with a gradual decrease until 6 hours. The anticoagulant activity of the nanoparticles encapsulated enoxaparin was kept until 14 hours when it was administered subcutaneously, suggesting that nanoparticles may allow the enoxaparin release by a gradual way, what could be an advantage on clinical practice. After the oral administration of the nanoparticles, any activity could be observed in until 14 hours, suggesting that or the nanoparticles might be not absorbed or the enoxaparin might be degraded on the gastrointestinal tract. In order to evaluate its antithrombotic effect, it was standardized a model of DVT by stasis and hypercoagulability in rats. After subcutaneous administration, there was a significative reduction on the thrombus size both with free enoxaparin (p= 0.002) and after encapsulation (p= 0.0411) in comparison with control group. When nanoparticles were administered orally, the results showed no statistical difference compared to the control group (p = 0.9476) and to a group of empty nanoparticles (p = 0.9372). In summary, the double emulsion method w/o/w was efficient for the enoxaparin encapsulation, providing the obtainment of spherical nanoparticles with high encapsulation efficiency. For in vivo studies, the encapsulated enoxaparin showed a sustained release anticoagulant activity for a higher period than that obtained with free enoxaparin, with an excellent antithrombotic effect when administered subcutaneously. However, there was no anticoagulant or antithrombotic effect when the nanoparticles were administered orally. Further experiments with chitosans of different molecular weights will be needed on the attempt to allow the oral absorption of these nanoparticles
Mestrado
Medicina Experimental
Mestre em Fisiopatologia Médica
Midha, Prem Anand. "Long-term patency of a polymer vein valve." Thesis, Atlanta, Ga. : Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/29721.
Full textCommittee Chair: Ku, David; Committee Member: Gleason, Rudolph; Committee Member: Milner, Ross. Part of the SMARTech Electronic Thesis and Dissertation Collection.
Smith, Sarah Faith. "Influences on the incidence of clinical deep vein thrombosis and pulmonary embolism in a prospectively collated population of 21,000 neurosurgical inpatients." University of Sydney. Public Health and Community Medicine, 2001. http://hdl.handle.net/2123/818.
Full textCheung, William Ka Wai. "Development and initial evaluation of wireless self-monitoring pneumatic compression sleeves for preventing deep vein thrombosis in surgical patients." Thesis, University of British Columbia, 2007. http://hdl.handle.net/2429/402.
Full textMatida, Caroline Kazue [UNESP]. "Trombose venosa profunda dos membros inferiores em crianças e adolescentes tratados em um único centro no Brasil: epidemiologia e evolução." Universidade Estadual Paulista (UNESP), 2010. http://hdl.handle.net/11449/103480.
Full textA importância do estudo da trombose venosa profunda (TVP) em crianças e adolescentes reside no impacto desta doença sobre a qualidade de vida desta população, tendo em vista sua longa expectativa de vida e a morbidade associada ao tromboembolismo venoso. Com o passar dos anos, a síndrome pós-trombótica e a recorrência podem deixar sequelas que vão desde dor crônica nos membros, edema e até úlceras de difícil cicatrização. A TVP em crianças está sendo melhor estudada nos últimos anos. Até então, seu diagnóstico e tratamento eram baseados em experiências individuais, pequenas séries de casos ou extrapolados das recomendações para adultos. Realizamos a presente revisão para melhor compreensão da epidemiologia, fisiopatologia, etiologia, diagnóstico, tratamento desta doença
The study of deep vein thrombosis (DVT) in children and adolescents assesses the important impact of this disease on the quality of life of this population considering its long life expectancy and morbidity associated to venous thromboembolism. Within the years, the pos-thrombotic syndrome and recurrence can cause sequelae including chronic lower limb pain, edema and even hard cicatrization ulcer. Recently, DVT in children has been studied more appropriately. Previously, its diagnosis and treatment were based on individual experience, some serial cases or comparisons with recommendations to the adult treatments. This present study has been presented to better comprehend the epidemiology, physiopathology, etiology, diagnosis, treatment and prophylaxis of the deep vein thrombosis
Tinkler, Kerry. "Setting up, piloting, implementing and reviewing a GP direct access service for the diagnosis of lower limb deep vein thrombosis." Thesis, University of Portsmouth, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.407268.
Full textFrappé, Paul. "Epidémiologie en soins primaires de la thrombose veineuse superficielle des membres inférieurs." Thesis, Saint-Etienne, 2015. http://www.theses.fr/2015STET004T/document.
Full textThe potential severity of superficial vein thrombosis (SVT) of the lower limbs has recently been shown by studies perfomed in secondary and tertiary care. The epidemiology of SVT remains unknown in primary care. The first objective of this study was to measure the prevalence of SVT in primary care, and the rate of concomitant thromboembolic events at diagnosis. A collaborative research network between general practitioners and vascular physicians from Saint-Etienne has been set up. A cross-sectional study has been conducted within this network during one year. The annual prevalence of SVT was measured to 0.64 per thousand inhabitants. At diagnosis, 24.6% of SVT were associated with symptomatic deep vein thrombosis and 4.7% with symptomatic pulmonary embolism. A second study was looking for a seasonal variation of SVT frequency by analyzing individual data from three studies with different designs; the STENOX study, the POST study and the STEPH study. A significant variation was found only in the POST study, and peak-to-low ratios were below 1.2 in the three studies. Thus, if other more powerful and exhaustive studies could find a seasonal variation, that variation would probably be of low magnitude and without clinical significance
Blecher, Gabriel E. "Diagnosing DVT in the Emergency Department: Combining Clinical Predictors, D-dimer and Bedside Ultrasound." Thèse, Université d'Ottawa / University of Ottawa, 2013. http://hdl.handle.net/10393/24003.
Full textMatida, Caroline Kazue. "Trombose venosa profunda dos membros inferiores em crianças e adolescentes tratados em um único centro no Brasil : epidemiologia e evolução /." Botucatu : [s.n.], 2010. http://hdl.handle.net/11449/103480.
Full textBanca: Hamilton de Almeida Rollo
Banca: José Roberto Fioretto
Banca: Fausto Miranda Junior
Banca: Jorge David Aivazoglou Carneiro
Resumo: A importância do estudo da trombose venosa profunda (TVP) em crianças e adolescentes reside no impacto desta doença sobre a qualidade de vida desta população, tendo em vista sua longa expectativa de vida e a morbidade associada ao tromboembolismo venoso. Com o passar dos anos, a síndrome pós-trombótica e a recorrência podem deixar sequelas que vão desde dor crônica nos membros, edema e até úlceras de difícil cicatrização. A TVP em crianças está sendo melhor estudada nos últimos anos. Até então, seu diagnóstico e tratamento eram baseados em experiências individuais, pequenas séries de casos ou extrapolados das recomendações para adultos. Realizamos a presente revisão para melhor compreensão da epidemiologia, fisiopatologia, etiologia, diagnóstico, tratamento desta doença
Abstract: The study of deep vein thrombosis (DVT) in children and adolescents assesses the important impact of this disease on the quality of life of this population considering its long life expectancy and morbidity associated to venous thromboembolism. Within the years, the pos-thrombotic syndrome and recurrence can cause sequelae including chronic lower limb pain, edema and even hard cicatrization ulcer. Recently, DVT in children has been studied more appropriately. Previously, its diagnosis and treatment were based on individual experience, some serial cases or comparisons with recommendations to the adult treatments. This present study has been presented to better comprehend the epidemiology, physiopathology, etiology, diagnosis, treatment and prophylaxis of the deep vein thrombosis
Doutor
Farrell, Laura-Lee Amelia Catherine. "Prosthetic Vein Valve: Delivery and In Vitro Evaluation." Thesis, Available online, Georgia Institute of Technology, 2007, 2007. http://etd.gatech.edu/theses/available/etd-04042007-180135/.
Full textTófano, Viviane Alessandra Capelluppi [UNESP]. "Avaliação clínica e ultrassonografia tardia de pacientes com trombose venosa profunda, portadores de trombofilia." Universidade Estadual Paulista (UNESP), 2008. http://hdl.handle.net/11449/103481.
Full textCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
A trombose venosa profunda (TVP) caracteriza-se pela formação aguda de um trombo no interior das veias profundas. É uma doença de alta incidência e de grande importância clínica e epidemiológica devido à sua morbimortalidade, sendo atualmente, considerada multifatorial. São vários os fatores de risco genéticos e/ou adquiridos relacionados à TVP e a compreensão da interação destes, permite melhor entender esta doença, não só devido aos seus sintomas de fase aguda mas, principalmente, por sua complicação mais temida, a embolia pulmonar e, a longo prazo, a síndrome pós-trombótica (SPT), que apresenta importante morbidade, inclusive com repercussões sócio-econômicas. A avaliação a longo prazo, clínica e ultrassonográfica, de pacientes com diagnóstico de TVP, visando verificar a incidência e gravidade da SPT é necessária para a compreensão da evolução destes pacientes. Desconhecemos a existência de trabalhos em nosso meio, que avaliem a evolução tardia da TVP. Objetivo: Determinar a evolução a longo prazo de pacientes com TVP de membros, portadores de trombofilia e verificar se existem diferenças na evolução de pacientes trombofílicos e não trombofílicos. Método: Num estudo coorte retrospectivo foram avaliados os prontuários de 275 pacientes atendidos no Hospital das Clínicas da Faculdade de Medicina de Botucatu-Unesp, dos quais foram identificados 60 pacientes trombofílicos, sendo possível contactar 40 deles para consulta, dos quais 39 pacientes aceitaram participar do estudo. Foram selecionados 25 pacientes com diagnóstico de TVP, não trombofílicos, pareados para sexo e idade, para comparação com o grupo trombofílico. Durante a consulta foi preenchido um protocolo que continha as seguintes variáveis: dados demográficos, profissão, antecedentes pessoais e antecedentes obstétricos (se mulher), antecedentes familiares com relação...
Deep vein thrombosis (DVT) is characterized by the acute formation of a thrombus in the interior of the deep veins. It is a disease of high incidence and great clinical and epidemiological importance due to its morbimortality, being presently considered multifactorial. The genetic and/or acquired risk factors related to DVT are various and understanding their interaction allows a better comprehension of this illness, due to both symptoms of the acute stage and, mainly, its most feared complication, the pulmonary embolism and, in long term, the post-thrombotic syndrome (PTS), which presents important morbidity, inclusively with social and economical repercussions. The long-term clinical and ultrasound evaluation of patients with DVT diagnosis, aiming to verify the incidence and seriousness of PTS, is necessary to understand the evolution of these patients. We are not aware of the existence of works in our area which evaluate the late evolution of DVT. Objective: To determine the long-term evolution of patients with DVT of limbs, carriers of thrombophilia, and verify the existence of differences in the evolution of thrombophilic and non-thrombophilic patients. Method: In a retrospective cohort study, the medical registers of 275 patients attended at the Clinics Hospital of the School of Medicine of the Paulista State University, in Botucatu, São Paulo, Brazil, were evaluated, from which 60 thrombophilic patients were identified. It was possible to contact 40 of them for appointment, from which 39 patients accepted to participate in the study. 25 non-thrombophilic patients, paired for sex and age, were selected with DVT diagnosis, for comparison with the thrombophilic group. During the appointment, a protocol was filled in, containing the following variables: demographic data, occupation, personal antecedents and obstetric antecedents (if woman), familiar antecedents concerning thrombosis... (Complete abstract click electronic access below)
Sathe, Rahul D. "Design and Development of a Novel Implantable Prosthetic Vein Valve." Thesis, Georgia Institute of Technology, 2006. http://hdl.handle.net/1853/14495.
Full textAutar, A. Ricky. "Advancing clinical practice in the management of deep vein thrombosis (DVT) : development, application and evaluation of the Autar DVT risk assessment scale." Thesis, De Montfort University, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.250780.
Full textDomberg, Asplund Jenny, and Stina Isaxon. "Prevention mot djup ventrombos : vad säger evidensen och hur arbetar sjuksköterskan kliniskt?" Thesis, Uppsala universitet, Institutionen för folkhälso- och vårdvetenskap, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-294573.
Full textBackground: Deep vein thrombosis is a serious complication during surgical and orthopaedic procedures. This leads to increased patient suffering, longer hospital stays and thereby also higher cost for society. To prevent DVT requires knowledge about preventive care measures that are effective, and how they will be used. Aim: The aim of this study was to examine the current state of knowledge about preventive care measures against DVT and how effective they are. The aim was also, by conducting a survey, to find out how nurses work clinically for the prevention of DVT. Study design: A literature study was conducted. The study was based on ten original articles. As a complement to the literature study a questionnaire was created and handed out to ten surgical and orthopaedic nurses. Results: Early mobilization in combination with mechanical prophylactics is seen as effective for preventing DVT. In many of the included studies patients were given low molecular weight heparin (LMH). However the frequency of DVT in these patients was not lower compared to those who did not get LMH. Instead it was at the introduction of prophylactic care measures such as early mobilization, compression stockings and compression pumps as the frequency of DVT fell. The questionnaires showed that clinical nurses worked actively with care measures. However, there were no specific guidelines for the measures in the organisation. Conclusion: The study shows that there is a need for developing methods for individual prophylactic care as patients from different risk groups have different needs. There should also be focus on developing and implementing guidelines for early mobilization as this study has shown it is effective in preventing DVT.
Bichsel, Leila Tièche Raphaël. "D-dimers, localization of first deep vein thrombosis and awareness of risk factors as independent predictors of the risk of recurrent thromboembolic events /." Bern : [s.n.], 2006. http://www.ub.unibe.ch/content/bibliotheken_sammlungen/sondersammlungen/dissen_bestellformular/index_ger.html.
Full textHebeshy, Mona Ibrahim. "ATTITUDE, SUBJECTIVE NORMS, PERCEIVED BEHAVIORAL CONTROL, AND INTENTION OF EGYPTIAN NURSES TOWARDS PREVENTION OF DEEP VEIN THROMBOSIS AMONG CRITICALLY ILL PATIENTS IN INTENSIVE CARE UNITS." Kent State University / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=kent1524226281287546.
Full textRowland, Denise Phi-Phoung. "Evaluation of soluble fibrin as an early marker of thrombosis." Thesis, Queensland University of Technology, 1997.
Find full textTófano, Viviane Alessandra Capelluppi. "Avaliação clínica e ultrassonografia tardia de pacientes com trombose venosa profunda, portadores de trombofilia /." Botucatu : [s.n.], 2008. http://hdl.handle.net/11449/103481.
Full textBanca: Hamilton Almeida Rollo
Banca: Adilson F. Paschôa
Banca: Newton Key Hokama
Banca: Cyrillo C. Filho
Resumo: A trombose venosa profunda (TVP) caracteriza-se pela formação aguda de um trombo no interior das veias profundas. É uma doença de alta incidência e de grande importância clínica e epidemiológica devido à sua morbimortalidade, sendo atualmente, considerada multifatorial. São vários os fatores de risco genéticos e/ou adquiridos relacionados à TVP e a compreensão da interação destes, permite melhor entender esta doença, não só devido aos seus sintomas de fase aguda mas, principalmente, por sua complicação mais temida, a embolia pulmonar e, a longo prazo, a síndrome pós-trombótica (SPT), que apresenta importante morbidade, inclusive com repercussões sócio-econômicas. A avaliação a longo prazo, clínica e ultrassonográfica, de pacientes com diagnóstico de TVP, visando verificar a incidência e gravidade da SPT é necessária para a compreensão da evolução destes pacientes. Desconhecemos a existência de trabalhos em nosso meio, que avaliem a evolução tardia da TVP. Objetivo: Determinar a evolução a longo prazo de pacientes com TVP de membros, portadores de trombofilia e verificar se existem diferenças na evolução de pacientes trombofílicos e não trombofílicos. Método: Num estudo coorte retrospectivo foram avaliados os prontuários de 275 pacientes atendidos no Hospital das Clínicas da Faculdade de Medicina de Botucatu-Unesp, dos quais foram identificados 60 pacientes trombofílicos, sendo possível contactar 40 deles para consulta, dos quais 39 pacientes aceitaram participar do estudo. Foram selecionados 25 pacientes com diagnóstico de TVP, não trombofílicos, pareados para sexo e idade, para comparação com o grupo trombofílico. Durante a consulta foi preenchido um protocolo que continha as seguintes variáveis: dados demográficos, profissão, antecedentes pessoais e antecedentes obstétricos (se mulher), antecedentes familiares com relação... (Resumo completo, clicar acesso eletrônico abaixo)
Abstract: Deep vein thrombosis (DVT) is characterized by the acute formation of a thrombus in the interior of the deep veins. It is a disease of high incidence and great clinical and epidemiological importance due to its morbimortality, being presently considered multifactorial. The genetic and/or acquired risk factors related to DVT are various and understanding their interaction allows a better comprehension of this illness, due to both symptoms of the acute stage and, mainly, its most feared complication, the pulmonary embolism and, in long term, the post-thrombotic syndrome (PTS), which presents important morbidity, inclusively with social and economical repercussions. The long-term clinical and ultrasound evaluation of patients with DVT diagnosis, aiming to verify the incidence and seriousness of PTS, is necessary to understand the evolution of these patients. We are not aware of the existence of works in our area which evaluate the late evolution of DVT. Objective: To determine the long-term evolution of patients with DVT of limbs, carriers of thrombophilia, and verify the existence of differences in the evolution of thrombophilic and non-thrombophilic patients. Method: In a retrospective cohort study, the medical registers of 275 patients attended at the Clinics Hospital of the School of Medicine of the Paulista State University, in Botucatu, São Paulo, Brazil, were evaluated, from which 60 thrombophilic patients were identified. It was possible to contact 40 of them for appointment, from which 39 patients accepted to participate in the study. 25 non-thrombophilic patients, paired for sex and age, were selected with DVT diagnosis, for comparison with the thrombophilic group. During the appointment, a protocol was filled in, containing the following variables: demographic data, occupation, personal antecedents and obstetric antecedents (if woman), familiar antecedents concerning thrombosis... (Complete abstract click electronic access below)
Doutor
Crawford, Yupin. "The cost-effectiveness of current practice of venous thromboembolism prophylaxis as compared to no prophylaxis or pharmaceuticals only prophylaxis." Thesis, Queensland University of Technology, 2018. https://eprints.qut.edu.au/120279/1/Yupin_Crawford_Thesis.pdf.
Full textGandara, Esteban. "Is an Intermediate Dose of LMWH Effective for Secondary Prevention of Recurrent Venous Thromboembolism in Pregnant Patients Diagnosed with Deep Vein Thrombosis or Pulmonary Embolism? Design of a Pilot Study." Thèse, Université d'Ottawa / University of Ottawa, 2012. http://hdl.handle.net/10393/23388.
Full textNilsson, Elin, and Linnéa Oskarsson. "Graderade kompressionsstrumpors preventiva effekt för djup ventrombos och posttrombotiskt syndrom." Thesis, Uppsala universitet, Institutionen för folkhälso- och vårdvetenskap, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-408302.
Full textABSTRACT Background: Deep vein thrombosis (DVT) is a serious complication postoperatively and can lead to a life threatening condition for the patient. Graded compression stockings (GCS) are used in many post-operative departments along with other prophylactic measures to prevent the development of DVT. Compression stockings are also used to prevent postthrombotic syndrome (PTS) after a DVT. PTS can develop because the venous valves are damaged by a DVT, as a result, the blood is stored and edema is formed, which leads to poor nutritional and oxygen supply to the tissues. Aim: The aim of the literature study was to investigate whether compression stockings had any effect in preventing DVT postoperatively, and also whether the compression stockings had any effect in preventing PTS after a DVT. Method: Literature study based on 11 RCT studies. Results: GCS without other prophylactic measures was found to have a good effect in avoiding the development of DVT in patients who underwent surgery. However, the use of GCS in combination with other proven prophylaxis was found to have no significant effect in further reducing the onset of DVT. The results regarding the GCS effect to avoid the development of PTS showed no unambiguity. Conclusion: GCS has a preventive effect to avoid the onset of DVT. However, the use of GCS in combination with other prophylaxis does not potentiate the effect of prevention for DVT. The effect of GCS in preventing the onset of PTS is not unambiguous and several studies are needed to see evidence of this.
Harrison, Jeffrey. "Deep vein thrombosis after total hip and knee replacement : a review of the incidence, prophylaxis, diagnosis and economic impact of thromboembolic disease in lower limb joint replacement. A comparison of low molecular weight heparin and pneumatic plantar." Thesis, University of Bristol, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311366.
Full textHuang, Wei. "A Population-Based Perspective on Clinically Recognized Venous Thromboembolism: Contemporary Trends in Clinical Epidemiology and Risk Assessment of Recurrent Events: A Dissertation." eScholarship@UMMS, 2014. https://escholarship.umassmed.edu/gsbs_diss/730.
Full textHuang, Wei. "A Population-Based Perspective on Clinically Recognized Venous Thromboembolism: Contemporary Trends in Clinical Epidemiology and Risk Assessment of Recurrent Events: A Dissertation." eScholarship@UMMS, 2011. http://escholarship.umassmed.edu/gsbs_diss/730.
Full textBrown, John Gordon. "A study of deep venous thrombosis." Thesis, Queen's University Belfast, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.303015.
Full textGoudot, Guillaume. "Applications innovantes des ultrasons en pathologie vasculaire : utilisation de l'imagerie ultrarapide dans l'analyse de la rigidité artérielle et des ultrasons pulsés en thérapie Arterial stiffening assessed by ultrafast ultrasound imaging gives new insight into arterial phenotype of vascular Ehlers–Danlos mouse models Aortic wall elastic properties in case of bicuspid aortic valve Segmental aortic stiffness in bicuspid aortic valve patients compared to first-degree relatives Wall shear stress measurement by ultrafast vector flow imaging for atherosclerotic carotid stenosis Pulsed cavitational therapy using high-frequency ultrasound for the treatment of deep vein thrombosis in an in vitro model of human blood clot." Thesis, Sorbonne Paris Cité, 2018. https://wo.app.u-paris.fr/cgi-bin/WebObjects/TheseWeb.woa/wa/show?t=2215&f=13951.
Full textMeng-Shan, Li, and 李孟珊. "Deep Vein Thrombosis in Acute Stroke Patients." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/07555884155882226575.
Full text大葉大學
生物資源學系碩士班
101
DVT (Deep Vein Thrombosis, DVT) referring to the leg vein thrombosis, is a common complication of acute stroke patients. Usually non-routine prophylaxis is associated with a high mortality rate of pulmonary embolism (Pulmonary embolism, PE). Both the D-dimer blood test and ultrasonography of the lower extremities were applied for the clinical diagnosis. In Asia there is no enough research and regular preventive approach for DVT, this research explored the ischemic and hemorrhagic acute stroke patients with deep vein thrombosis incidence from Changhua Christian Hospital. 19 of 136 acute stroke patients with deep vein thrombosis (14.0%), one-way anova analysis with and without deep vein thrombosis in two groups of patients, D-dimer (P = 0.025), age> 80 years (P = 0.041), anticoagulants (P = 0.041), showed significant statistical difference. The binary regression analysis showed that independent predictors of deep vein thrombosis are: age> 80 years (odds ratio = 4.23, P = 0.017) and D-dimer (odds ratio = 1.03 per 100 ng / mL, P = 0.041). The results showed that acute stroke patients had a significant risk of deep vein thrombosis rate, and age> 80 years and D-dimer can be considered as the independent predictors of deep vein thrombosis diagnosis.
"Arterial resistance changes in lower limb deep vein thrombosis." 1998. http://library.cuhk.edu.hk/record=b5889782.
Full textThesis submitted in: Dec, 1997.
Thesis (M.Phil.)--Chinese University of Hong Kong, 1998.
Includes bibliographical references (leaves 87-95).
Abstract also in Chinese.
Chapter 1 --- Introduction --- p.1
Chapter 2 --- Literature Review --- p.3
Chapter 2.1 --- Venous anatomy --- p.3
Chapter 2.2 --- Arterial anatomy --- p.6
Chapter 2.3 --- Deep vein thrombosis --- p.8
Chapter 2.3.1 --- Clinical Examination --- p.11
Chapter 2.3.2 --- Contrast Venogram --- p.12
Chapter 2.3.3 --- Color duplex ultrasound --- p.13
Chapter 2.4 --- Arterial resistance --- p.24
Chapter 2.5 --- Basis for study --- p.28
Chapter 3 --- Method --- p.30
Chapter 3.1 --- Subjects --- p.30
Chapter 3.2 --- Equipments --- p.30
Chapter 3.3 --- Procedure --- p.31
Chapter 3.4 --- Data analysis --- p.38
Chapter 4 --- Results --- p.40
Chapter 4.1 --- Arterial resistance changes in different groups --- p.40
Chapter 4.1.1 --- Symptomatic with no DVT versus asymtomatic with no DVT --- p.40
Chapter 4.1.2 --- Symptomatic with DVT versus symptomatic with no DVT --- p.43
Chapter 4.1.3 --- Symptomatic acute DVT versus symptomatic chronic DVT --- p.46
Chapter 4.1.4 --- Symptomatic proximal-DVT versus symptomatic calf-DVT --- p.49
Chapter 4.1.5 --- symptomatic occlusive DVT versus symptomatic non- occlusive DVT --- p.52
Chapter 4.2 --- Diagnosis of DVT by arterial resistance changes --- p.57
Chapter 4.2.1 --- Detection of presence of symptomatic DVT --- p.57
Chapter 4.2.2 --- Differentiation of characteristics of symptomatic DVT --- p.60
Chapter 5 --- Discussion --- p.64
Chapter 5.1 --- Investigation of arterial resistance changes --- p.64
Chapter 5.1.1 --- Symptomatic with no DVT versus asymtomatic with no DVT --- p.66
Chapter 5.1.2 --- Symptomatic with DVT versus symptomatic with no DVT --- p.69
Chapter 5.1.3 --- Symptomatic acute DVT versus symptomatic chronic DVT --- p.72
Chapter 5.1.4 --- Symptomatic proximal-DVT versus symptomatic calf-DVT --- p.74
Chapter 5.1.5 --- symptomatic occlusive DVT versus symptomatic non- occlusive DVT --- p.76
Chapter 5.2 --- Detection and differentiation of DVT by arterial resistance --- p.80
Chapter 5.2.1 --- Detection of symptomatic DVT --- p.80
Chapter 5.2.2 --- Differentiation of occlusive DVT from non-occlusive DVT --- p.82
Chapter 6 --- Conclusion --- p.85
Chapter 7 --- References --- p.87