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1.
EuroIntervention ; 8 Suppl P: P86-9, 2012 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-22917799

RESUMO

At the moment of signing the Stent for Life (SFL) Initiative on August 31st, 2009, it was shown that, in Serbia during 2008, 48% of patients with ST-elevation myocardial infarction (STEMI) did not receive any reperfusion and only 19% and 33% received primary percutaneous coronary intervention (p-PCI) or hospital thrombolysis, respectively. However, during 2009, there was a trend towards a substantial increase in p-PCI procedures. This was the result of the commitment of cardiologists, the contract signed by the Health Insurance Fund (HIF) for remuneration of catheterisation laboratory (cathlab) staff for each p-PCI procedure (2005), and the provision of new cathlabs by the Ministry of Health (MOH). The number of PCI centres and trained cardiologists has been rising simultaneously. Direct mobile telephone contact with interventional cardiologists has facilitated the transport of patients directly to cathlabs (from 7.5% before 2009 to 34.2% in 2010 and 2011). Although the number of patients treated with p-PCI is increasing (2006 - 647 p-PCIs; 2007 - 1,248 p-PCIs; 2008 -1,794 p-PCIs; 2009 - 2,468 p-PCIs; 2010 - 3,216 and 2011 - 3,498 p-PCIs), the percentage of patients who are treated within 120 minutes of establishing a diagnosis (first medical contact) is still not satisfactory (38%).


Assuntos
Angioplastia Coronária com Balão , Conhecimentos, Atitudes e Prática em Saúde , Acessibilidade aos Serviços de Saúde/organização & administração , Planejamento Hospitalar/organização & administração , Infarto do Miocárdio/terapia , Tempo para o Tratamento/organização & administração , Angioplastia Coronária com Balão/instrumentação , Angioplastia Coronária com Balão/normas , Atitude do Pessoal de Saúde , Fidelidade a Diretrizes , Acessibilidade aos Serviços de Saúde/normas , Planejamento Hospitalar/normas , Humanos , Modelos Organizacionais , Infarto do Miocárdio/diagnóstico , Objetivos Organizacionais , Equipe de Assistência ao Paciente/organização & administração , Educação de Pacientes como Assunto , Guias de Prática Clínica como Assunto , Sérvia , Stents , Fatores de Tempo , Tempo para o Tratamento/normas , Resultado do Tratamento
2.
J Vasc Surg ; 49(5): 1242-7, 2009 May.
Artigo em Inglês | MEDLINE | ID: mdl-19233601

RESUMO

BACKGROUND: Compression therapy is the most widely used treatment for venous leg ulcers and it was used in different forms for more than 400 years. Published healing rates of venous ulcers obtained with compression therapy vary widely from 40-95%. According to numerous studies, it has been suggested that the application of external pressure to the calf muscle raises the interstitial pressure resulting in improved venous return and reduction in the venous hypertension. Several risk factors have been identified to be correlated with the failure of venous leg ulcers to heal with compression therapy (longer ulcer duration; large surface area; fibrinous deposition present on >50% of the wound surface and an Ankle Brachial Pressure Index (ABPI) of <0.85. METHODS: An open prospective single-center study was performed in order to determine possible risk factors associated with the failure of venous ulcers to heal when treated with multi-layer high compression bandaging system for 52 weeks. In the study, 189 patients (101 women, 88 men; mean age 61 years) with venous leg ulcers (ulcer surface >5 cm(2); duration >3 months) were included. The study excluded patients with arterial disease (ABPI <0.8), heart insufficiency with ejection fraction (EF) <35, pregnancy, cancer disease, rheumatoid arthritis, and diabetes. Based on clinical opinion and available literature, the following were considered as potential risk factors: sex, age, ulceration surface, time since ulcer onset, previous operations, history of deep vein thrombosis, body mass index (BMI), reduction in calf circumference >3 cm during the first 50 days of treatment, walking distance during the day <200 meters, calf:ankle circumference ratio <1.3, fixed ankle joint, history of surgical wound debridement, >50% of wound covered with fibrin, depth of the wound >2 cm. RESULTS: Within 52 weeks of limb-compression therapy, 24 (12.7%) venous ulcers had failed to heal. A small ulceration surface (<20 cm(2)), the duration of the venous ulcer <12 months, a decrease in calf circumference of more than 3 cm, and emergence of new skin islets on >10% of wound surface during the first 50 days of treatment were favorable prognostic factors for ulcer healing. A large BMI (>33 kg/m(2)), short walking distance during the day (<200 m), a history of wound debridement, and ulcers with deepest presentation (>2 cm) were indicators of slow healing. Calf:ankle circumference ratio <1.3, fixed ankle joint, and reduced ankle range of motion were the only independent parameters associated with non-healing (P < .001). CONCLUSION: The results obtained in this study suggest that non-healing venous ulcers are related to the impairment of the calf muscle pump.


Assuntos
Dispositivos de Compressão Pneumática Intermitente , Úlcera Varicosa/terapia , Cicatrização , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Desbridamento , Feminino , Humanos , Perna (Membro) , Modelos Logísticos , Masculino , Pessoa de Meia-Idade , Contração Muscular , Músculo Esquelético/irrigação sanguínea , Músculo Esquelético/fisiopatologia , Razão de Chances , Estudos Prospectivos , Medição de Risco , Fatores de Risco , Fatores de Tempo , Falha de Tratamento , Úlcera Varicosa/fisiopatologia , Adulto Jovem
3.
Europace ; 7(4): 374-9, 2005 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15944096

RESUMO

AIM: The aim of our study was to establish the efficiency of fibrin sealant in the prevention of pocket related complications in patients undergoing pacemaker implantation who are receiving anticoagulant treatment. METHODS: The study was performed on 40 and 41 patients prospectively randomized into treatment and control groups who underwent pacemaker implantation procedure between January 2002 and July 2004 at the Pacemaker Center - Clinical Centre Nis, Serbia. Both groups of patients were receiving anticoagulant treatment with either heparin or warfarin. Surgical procedures between the groups differed only in the application of fibrin sealant prior to wound closure in the treatment group. RESULTS: In the treatment group, there were no pocket related complications while in the control group six patients (14.63%) had minor haematomas that required no treatment. Four patients (9.76%) had significant haematomas (two patients were treated conservatively while the other two needed reintervention). The INR in the treatment group was 2.76+/-0.85 and in the control group 2.65+/-0.79 (P=ns). In the follow-up period (2-27 months) no late complications were registered in either group. CONCLUSION: Fibrin sealant is an effective haemostatic agent. The results obtained in our study show that the administration of fibrin sealant in patients receiving anticoagulant treatment eliminates postoperative haematomas after pacemaker implantation.


Assuntos
Anticoagulantes/efeitos adversos , Adesivo Tecidual de Fibrina/uso terapêutico , Hemostáticos/uso terapêutico , Marca-Passo Artificial , Próteses e Implantes , Infecções Relacionadas à Prótese/prevenção & controle , Idoso , Feminino , Hematoma/induzido quimicamente , Hematoma/prevenção & controle , Heparina/efeitos adversos , Humanos , Masculino , Cuidados Pós-Operatórios , Estudos Prospectivos , Varfarina/efeitos adversos
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