Prosthesis-patient mismatch after surgical aortic valve replacement: neither uncommon nor harmless

Abstract Prosthesis-patient mismatch (PPM) after surgical aortic valve replacement (SAVR) is an issue that has been overlooked (not to say neglected). Cardiac surgeons must bear in mind that this is a real problem that we must tackle. The purpose of this paper is to be a wake-up call to the surgical community by giving a brief overview of what PPM is, its incidence and impact on the outcomes. We also discuss the increasing role played by imaging for predicting and assessing PPM after SAVR (with which surgeons must become more acquainted) and, finally, we present some options to avoid PPM after the surgical procedure.

Impact of prosthesis-patient mismatch on 1-year outcomes after transcatheter aortic valve implantation: meta-analysis of 71, 106 patients

Abstract Objectives: This study sought to evaluate the impact of prosthesis-patient mismatch (PPM) on the risk of early-term mortality after transcatheter aortic valve implantation (TAVI). Methods: Databases (Medical Literature Analysis and Retrieval System Online [MEDLINE], Excerpta Medica dataBASE [EMBASE], Cochrane Controlled Trials Register [CENTRAL/CCTR], ClinicalTrials.gov, Scientific Electronic Library Online [SciELO], Latin American and Caribbean Literature on Health Sciences [LILACS], and Google Scholar) were searched for studies published until February 2019. PPM after TAVI was defined as moderate if the indexed effective orifice area (iEOA) was between 0.85 cm2/m2 and 0.65 cm2/m2 and as severe if iEOA ≤ 0.65 cm2/m2. Results: The search yielded 1,092 studies for inclusion. Of these, 18 articles were analyzed, and their data extracted. The total number of patients included who underwent TAVI was 71,106. The incidence of PPM after TAVI was 36.3% (25,846 with PPM and 45,260 without PPM). One-year mortality was not increased in patients with any PPM (odds ratio [OR] 1.021, 95% confidence interval [CI] 0.979-1.065, P=0.338) neither in those with moderate PPM (OR 0.980, 95% CI 0.933-1.029, P=0.423). Severe PPM was separately associated with high risk (OR 1.109, 95% CI 1.041-1.181, P=0.001). Conclusion: The presence of severe PPM after TAVI increased early-term mortality. Although moderate PPM seemed harmless, the findings of this study cannot not rule out the possibility of it being detrimental, since there are other registries that did not address this issue yet.

Prosthesis-patient mismatch negatively affects outcomes after mitral valve replacement: meta-analysis of 10, 239 patients

Abstract Objective: This study sought to evaluate the impact of prosthesis-patient mismatch on the risk of perioperative and long-term mortality after mitral valve replacement. Methods: Databases were researched for studies published until December 2018. Main outcomes of interest were perioperative and 10-year mortality and echocardiographic parameters. Results: The research yielded 2,985 studies for inclusion. Of these, 16 articles were analyzed, and their data extracted. The total number of patients included was 10,239, who underwent mitral valve replacement. The incidence of prosthesis-patient mismatch after mitral valve replacement was 53.7% (5,499 with prosthesis-patient mismatch and 4,740 without prosthesis-patient mismatch). Perioperative (OR 1.519; 95%CI 1.194-1.931, P<0.001) and 10-year (OR 1.515; 95%CI 1.280-1.795, P<0.001) mortality was increased in patients with prosthesis-patient mismatch. Patients with prosthesis-patient mismatch after mitral valve replacement had higher systolic pulmonary artery pressure and transprosthethic gradient and lower indexed effective orifice area and left ventricle ejection fraction. Conclusion: Prosthesis-patient mismatch increases perioperative and long-term mortality. Prosthesis-patient mismatch is also associated with pulmonary hypertension and depressed left ventricle systolic function. The findings of this study support the implementation of surgical strategies to prevent prosthesis-patient mismatch in order to decrease mortality rates.

Current practice of state-of-the-art coronary revascularization in patients with heart failure

Abstract The best treatment for patients with ischemic heart failure (HF) is still on debate. There is growing evidence that coronary artery bypass graft (CABG) benefits these patients. The current recommendations for revascularization in this context are that CABG is reasonable when it comes to decreasing morbidity and mortality rates for patients with severe left ventricular dysfunction (ejection fraction <35%), and significant coronary artery disease (CAD) and should be considered in patients with operable coronary anatomy, regardless whether or not there is a viable myocardium (class IIb). Percutaneous coronary intervention (PCI) does not have enough data to allow the panels to reach a conclusion. The Korean Acute Heart Failure registry (KorAHF) had its data released recently, showing that patients with acute HF who underwent CABG had lower death rates, more complete revascularization and less adverse outcomes compared with patients treated with PCI. Recent ESC/EACTS guidelines on myocardial revascularization clearly recommended CABG as the first choice of revascularization strategy in patients with multivessel disease and acceptable surgical risk to improve prognosis in this scenario of left ventricular dysfunction. However, a high peri-procedural risk must be compared with the benefit of late mortality, and pros and cons of each strategy (either PCI or CABG) must be weighed in the decision-making process. Spurred on by the publication of the above-mentioned article and the release of new guidelines, we went on to write an overview of the current practice of state-of-the-art coronary revascularization options in patients with HF.

Updated meta-analysis on the closure of patent foramen ovale in reduction of stroke rates: the defense-pfo trial does not change the scenario

Abstract Objective: We aimed to analyze whether patent foramen ovale (PFO) closure reduces the risk of stroke, assessing also some safety outcomes after the publication of a new trial. Introduction: The clinical benefit of closing a PFO has been an open question, so it is necessary to review the current state of published medical data in regards to this subject. Methods: MEDLINE, EMBASE, CENTRAL/CCTR, SciELO, LILACS, Google Scholar and reference lists of relevant articles were used to search for randomized controlled trials (RCTs) that reported any of the following outcomes: stroke, death, major bleeding or atrial fibrillation. Six studies fulfilled our eligibility criteria and included 3560 patients (1889 for PFO closure and 1671 for medical therapy. Results: The risk ration (RR) for stroke in the "closure" group compared with the "medical therapy" showed a statistically significant difference between the groups, favouring the "closure" group (RR 0.366; 95%CI 0.171-0.782, P=0.010). There was no statistically significant difference between the groups regarding the safety outcomes, death and major bleeding, but we observed an increase in the risk of atrial fibrillation in the "closure" group (RR 4.131; 95%CI 2.293-7.443, P<0.001). We also observed that the larger the proportion of effective closure, the lower the risk of stroke. Conclusion: This meta-analysis found that stroke rates are lower with percutaneously implanted device closure than with medical therapy alone, being these rates modulated by the rates of hypertension, atrial septal aneurysm and effective closure. The publication of a new trial did not change the scenario in the medical literature.

Closure of patent foramen ovale versus medical therapy after cryptogenic stroke: meta-analysis of five randomized controlled trials with 3440 patients

Abstract Objective: We aimed to determine whether patent foramen ovale closure reduces the risk of stroke, also assessing some safety outcomes. Introduction: The clinical benefit of closing a patent foramen ovale after a cryptogenic stroke has been an open question for several decades, so that it is necessary to review the current state of published medical data in this regard. Methods: MEDLINE, EMBASE, CENTRAL/CCTR, SciELO, LI-LACS, Google Scholar and reference lists of relevant articles were searched for randomized controlled trials that reported any of the following outcomes: stroke, death, major bleeding or atrial fibrillation. Five studies fulfilled our eligibility criteria and included 3440 patients (1829 for patent foramen ovale closure and 1611 for medical therapy). Results: The risk ratio (RR) for stroke in the "device closure" group compared with the "medical therapy" showed a statistically significant difference between the groups, favouring the "device closure" group (RR 0.400; 95% CI 0.183-0.873, P=0.021). There was no statistically significant difference between the groups regarding the safety outcomes death and major bleeding, but we observed an increase in the risk of atrial fibrillation in the "device closure group (RR 4.000; 95% CI 2.262-7.092, P<0.001). We also observed that the larger the proportion of effective closure, the lower the risk of stroke. Conclusion: This meta-analysis found that stroke rates are lower with percutaneously implanted device closure than with medical therapy alone, being these rates modulated by the rates of effective closure.

CABG surgery remains the best option for patients with left main coronary disease in comparison with pci-des: meta-analysis of randomized controlled trials

Abstract Objective: To compare the safety and efficacy of coronary artery bypass grafting (CABG) with percutaneous coronary intervention (PCI) using drug-eluting stents (DES) in patients with unprotected left main coronary artery (ULMCA) disease. Methods: MEDLINE, EMBASE, CENTRAL/CCTR, SciELO, LILACS, Google Scholar and reference lists of relevant articles were searched for clinical studies that reported outcomes at 1-year follow-up after PCI with DES and CABG for the treatment of ULMCA stenosis. Five studies fulfilled our eligibility criteria and they included a total of 4.595 patients (2.298 for CABG and 2.297 for PCI with DES). Results: At 1-year follow-up, there was no significant difference between CABG and DES groups concerning the risk for death (risk ratio [RR] 0.973, P=0.830), myocardial infarction (RR 0.694, P=0.148), stroke (RR 1.224, P=0.598), and major adverse cerebrovascular and cardiovascular events (RR 0.948, P=0.680). The risk for target vessel revascularization (TVR) was significantly lower in the CABG group compared to the DES group (RR 0.583, P<0.001). It was observed no publication bias regarding the outcomes, but only the outcome TVR was free from substantial statistical heterogeneity of the effects. In the meta-regression, there was evidence that the factor "female gender" modulated the effect regarding myocardial infarction rates, favoring the CABG strategy. Conclusion: CABG surgery remains the best option of treatment for patients with ULMCA disease, with lower TVR rates.

A experiência brasileira com a implementação do 4: 1 dose fixa combinada para o tratamento da tuberculose / The brazilian experience of implementing RHZE fixed-dose combination for tuberculosis treatment / La experiencia brasileña con la implementación del 4:1 a dosis fija combinada para el tratamiento de la tuberculosis

Em 2009, o Programa Nacional de Controle da Tuberculose recomendou a mudança do regime para o tratamento da tuberculose sensível. As mudanças consistiram na inclusão do etambutol, a redução das dosagens de isoniazida e pirazinamida e a modificação da formulação de cápsula para comprimido em dose fixa combinada. O processo de mudança foi viabilizado por apoio técnico, político e financeiro, que garantiu o abastecimento interno e o treinamento dos profissionais de saúde. A presente análise do caso brasileiro permitiu elencar lições aprendidas com o processo e formular recomendações para a sustentabilidade desta e de futuras inovações tecnológicas no diagnóstico, prevenção e tratamento da tuberculose.

In 2009, the Brazilian National Tuberculosis Program recommended changing the regimen for the treatment of sensitive tuberculosis by replacing RHZE with RHZ, involving reduced doses of isoniazid and pyrazinamide in a fixed-dose combination formulation. The process of change was made possible by the financial, political and technical support that ensured national drug provision and the training of healthcare professionals. In this analysis of the Brazilian case, we present the lessons learned with the implementation process and we formulate recommendations for the sustainability of this and other future technological innovations in the diagnosis, prevention and treatment of tuberculosis.

En 2009, el Programa Nacional de Control de la Tuberculosis recomendó el cambio de régimen para el tratamiento de la tuberculosis sensible. Los cambios consistieron en la inclusión del etambutol, la reducción de las dosis de isoniazida y pirazinamida y la modificación de la formulación de cápsula para comprimido a dosis fija combinada. El proceso de cambio fue viable por el gracias al apoyo técnico, político y financiero, que garantizó el abastecimiento interno y la capacitación de los profesionales de salud. El presente análisis del caso brasileño permitió registrar las lecciones aprendidas con el proceso y formular recomendaciones para la sustentabilidad de esta y de futuras innovaciones tecnológicas en el diagnóstico, prevención y tratamiento de la tuberculosis.

Tratamento da fibrilação atrial com ablação por ultrassom, durante correção cirúrgica de doença valvar cardíaca / Treatment of atrial fibrillation using ultrasonic cardiac ablation, during valvular heart surgery

OBJETIVO: Este estudo visa avaliar a eficácia do tratamento cirúrgico da fibrilação atrial com ablação por ultrassom, concomitante à cirurgia valvar mitral, em pacientes do Pronto Socorro Cardiológico de Pernambuco (PROCAPE) portadores de fibrilação atrial permanente. MÉTODOS: De março 2008 até janeiro 2009, foi realizado no PROCAPE um estudo prospectivo com 44 pacientes consecutivos, portadores de fibrilação atrial permanente e indicação de cirurgia valvar mitral. Vinte e dois pacientes foram submetidos à ablação com ultrassom no epicárdio do átrio direito (AD) e no endocárdio do átrio esquerdo (AE) concomitantemente ao reparo valvar. Os outros 22 pacientes foram submetidos ao procedimento valvar sem ablação por ultrassom. Pacientes com doença coronária diagnosticada e outras enfermidades graves foram excluídos da pesquisa. RESULTADOS: Foi observada 90 por cento de reversão da FA a ritmo sinusal no pós-operatório imediato dos pacientes que receberam ablação por ultrassom concomitante ao reparo mitral. A evolução no pós-operatório tardio mostrou queda na permanência da reversão a sinusal, porém o grupo que recebeu intervenção ainda apresentou percentual superior a 27 por cento em relação ao grupo controle. Dos 22 pacientes submetidos à ablação com ultrassom, 86,40 por cento apresentaram melhora da classe funcional e não foi constatado neste grupo maior ocorrência de complicações do que no grupo que foi submetido à correção valvar sem ablação. CONCLUSÃO: Os resultados apresentados pelo estudo demonstraram que os pacientes submetidos a tratamento cirúrgico da FA, com aplicação de ultrassom concomitante à correção valvar, apresentaram vantagens em relação ao grupo controle.

OBJECTIVE: This study aims to evaluate the surgical treatment of atrial fibrillation with ultrasound ablation concomitant to mitral surgery in PROCAPE's patients with permanent atrial fibrillation. METHODS: From March 2008 through January 2009 a prospective study was performed at the Pernambuco Cardiology Emergency Facility on 44 consecutive patients with a permanent atrial fibrillation and concomitant cardiac valvular surgery indication, from March 2008 through January 2009 at Pernambuco Cardiology Emergency Facility Twenty two patients underwent epicardial ultrasonic ablation on the right atrium and had ultrasonic ablation performed in the left atrium endocardial concomitant with the valve procedure. The other 22 patients, the concurrent controls were submitted to valve procedure without ultrasonic ablation. Patients with serious diseases such as coronary and others were excluded of the research. RESULTS: It was observed 90 percent restoration to sinus rhythm immediately after surgery in patients submitted to treatment of atrial fibrillation with ultrasound ablation simultaneous a mitral surgery. The evolution in late post operation showed that the maintenance of sinus rhythm drops although it was still 27 percent higher in the group which received ablation compared with the control group. 86.40 percent of the patients who received ablation had improved in functional class; they also have fewer complications than patients in the control group. CONCLUSION: The results showed that the patients who received treatment for atrial fibrillation simultaneously with valvar surgery had advantages related to the control group.

Nova técnica cirúrgica de preparo da veia safena para revascularização do miocárdio sem manipulação direta - no-touch / Novel no-touch technique of harvesting the saphenous vein for coronary artery bypass grafting

FUNDAMENTO: Otimização da veia safena na revascularização miocárdica. OBJETIVO: Apresentar a técnica no-touch de preparo da veia safena. Essa técnica consiste na retirada da veia safena do seu leito, com um pedículo de tecido adiposo, protegendo-a contra espasmos, sendo desnecessário distendê-la. MÉTODOS: Estudo prospectivo e randomizado, incluindo 156 pacientes submetidos a cirurgia de revascularização miocárdica. Comparação da técnica no-touch com duas outras técnicas: convencional e intermediária. Procedeu-se à avaliação da morfologia endotelial, utilizando a microscopia. A perviabilidade das pontes foi determinada com exame angiográfico num período médio de 18 meses após a operação. A enzima óxido nítrico sintetase endotelial (eNOS) foi identificada por meio do estudo imunohistoquímico. RESULTADOS: A avaliação morfológica mostrou integridade endotelial de 97 por cento nas veias do grupo no-touch; enquanto quase metade da superfície endotelial das veias tratadas pelas outras técnicas exibiu ausência de células endoteliais. A angiografia revelou perviabilidade de 95,4 por cento para as pontes do grupo no-touch, 88,9 e 86,2 por cento para as pontes do grupo convencional e intermediária, respectivamente. O estudo imunohistoquímico revelou a presença da eNOS nas três camadas que compõem a parede da veia no grupo no-touch e redução dessa enzima no grupo convencional. CONCLUSÃO: A integridade endotelial e a atividade da eNOS foram melhor preservadas com o uso da técnica no-touch. A proteção mecânica fornecida pelo tecido gorduroso circundante à veia e a atividade vasodilatadora e bloqueadora da agregação plaquetária causada pelo óxido nítrico podem ser responsáveis pela proteção da veia contra o espasmo, como também por sua alta perviabilidade imediata.

BACKGROUND: Optimization of the saphenous vein for myocardial revascularization. OBJECTIVE: To present the no-touch technique of the saphenous vein preparation. This technique consists of harvesting the vein with a pedicle of surrounding tissue, which protects the vein from spasms, obviating the need for distension. METHODS: A prospective, randomized study with 156 patients who underwent artery bypass grafting was performed comparing three saphenous vein harvesting techniques: conventional, intermediate, and no-touch. A morphological study of the endothelium was carried out using scanning microscopy. An angiographic assessment of the vein graft patency was performed at a mean follow-up time of 18 months. Also, an immunohistochemical assessment was carried out to identify the endothelial enzyme nitric oxide synthase (eNOS) in the vein wall RESULTS: The preservation of the endothelial cell integrity was greater in the no-touch technique than in the other procedures. At angiographic follow-up, the patency for the no-touch group was 95.4 percent, 88.9 percent for the grafts of the conventional technique group, and 86.2 percent for the grafts performed in the intermediate technique group. The immunohistochemical assessment revealed eNOS in all three layers of the vein wall in the no-touch group and reduction of this enzyme in the conventional group. CONCLUSION: The endothelial integrity and eNOS activity were better preserved when using the no-touch technique for vein graft harvesting. The mechanical protection provided by the cushion of surrounding tissue in the no-touch group, the vasorelaxation and thromboresistant activities of nitric oxide may be responsible for the reduction of vasospasms and improved patency rate.

Aspectos técnicos na esqueletização da artéria torácica interna com bisturi ultra-sônico / Technical aspects in skeletonization of the internal thoracic artery using an ultrasonic scalpel

OBJETIVO: Descrever a técnica e avaliar os resultados imediatos da utilização do bisturi ultra-sônico nas esqueletizações da artéria torácica interna, na cirurgia de revascularização do miocárdio. MÉTODO: Foram operados com essa técnica 188 pacientes submetidos à cirurgia de revascularização do miocárdio, no período de janeiro de 2000 a outubro de 2006. Setenta e um (37,8 por cento) pacientes eram do sexo feminino. A idade variou de 28 a 81 anos. A técnica utilizada na dissecação consistiu em expor toda artéria torácica interna, abrindo-se a fáscia endotorácica com tesoura o mais próximo possível da adventícia da artéria. Com o bisturi ultra-sônico é feita a secção dos ramos colaterais e sua respectiva hemostasia, dispensando-se o uso de "clips" metálicos na artéria torácica interna. RESULTADOS: As artérias torácicas internas esqueletizadas com bisturi ultra-sônico apresentaram fluxos excelentes, não sendo necessárias manipulações intraluminais para vasodilatação. No pós-operatório imediato, dois pacientes apresentaram paralisia temporária da hemicúpula diafragmática esquerda. Não houve infecção do esterno nesta série. O tempo de dissecação foi de aproximadamente 33 minutos, mas com o aumento da experiência esse tempo pôde ser reduzido. CONCLUSÃO: Essa técnica facilita e abrevia o procedimento da esqueletização da artéria torácica interna, não promove espasmos e a cauterização dos ramos colaterais com o bisturi ultra-sônico é eficiente, dispensando o uso de "clips" metálicos. É um procedimento de fácil reprodução, podendo ser recomendado para sua realização de maneira preferencial.

OBJECTIVE: To describe the technique and evaluate the immediate results of using an ultrasonic scalpel in the skeletonization of the internal thoracic artery for coronary artery bypass grafting surgery. METHODS: From January 2000 to October 2006, 188 patients were submitted to coronary artery bypass grafting with the internal thoracic artery skeletonized using an ultrasonic scalpel. Seventy-one patients (37.8 percent) were women. The patients' ages varied from 28 to 81 years old. The entire internal thoracic artery was exposed opening the endothoracic fascia using scissors as close as possible to the arterial adventitia. An ultrasonic scalpel was used to transect and coagulate all the intercostal branches, thereby minimizing the use of metallic clips. RESULTS: The skeletonized internal thoracic arteries presented with excellent flow, obviating the need for intraluminal manipulation for vasodilatation. In the immediate postoperative period, two patients were found to have temporary left-sided diaphragmatic paralysis. There were no sternal wound infections in this series. The dissection can be performed in approximately 33 minutes however with more experience this time may be reduced. CONCLUSION: This technique facilitates and shortens the internal thoracic artery skeletonization procedure and does not cause arterial spasms. Cauterization of the collateral branches with an ultrasonic scalpel is efficient and the use of metallic clips is almost unnecessary. It is a procedure that is easy to reproduce and may be recommended as the first-choice technique for the dissection of the internal thoracic artery.

Variação temporal no desempenho em testes de memória em pacientes com doença vascular cerebral / Temporal variation in memory tests performance in cerebral vascular disease patients

Buscando adequar a avaliação neuropsicológica à organização temporal do organismo humano, avaliou-se o desempenho em testes de memória em 12 pacientes pós Doença Vascular Cerebral e 12 indivíduos controle, de ambos os sexos, com idade de 45 a 65 anos. Foram aplicados dois testes de memória com estímulos visuais (figuras) e dois com estímulos verbais (palavras), em 3 dias consecutivos por semana, às 08:00, 10:00 e 12:00 h na primeira semana e às 14:00 e 16:00 h na seguinte. Os pacientes apresentaram menor número de acertos do que os indivíduos controle em todos os testes aplicados (p<0,05). A sensibilidade foi maior às 14h00min para o teste de evocação livre e às 16h00min para os testes de reconhecimento. Diante dos resultados, conclui-se que a avaliação neuropsicológica deva ser realizada preferencialmente à tarde, tanto na avaliação inicial quanto nas reavaliações.

This study intended to investigate the performance in memory tests in order to adequate the neuropsychological evaluation to the temporal order of the human organism. Twelve cerebral vascular accident patients and 12 controls, of both sexes and 45-65 years old were studied. Two memory tests with visual stimuli (pictures) and two with verbal stimuli (words) were applied three times a day (08:00, 10:00 and 12:00 h) during the first week and twice a day (14:00 and 16:00 h) in the second week, during three consecutive days in two consecutive weeks. The patients showed lower scores than control subjects in all applied tests (p<0,05). The greater test sensitivity was at 14:00 h for the free recall test and at 16:00 h for recognition tests. According to these results, it is concluded that neuropsychological evaluations should be conducted preferably in the afternoon, as well for the first evaluation as for the re-evaluations.

Experiência clínica inicial na desmineralização química da valva aórtica: potencial aplicação como procedimento minimamente invasivo / Chemical demineralization of the aortic valve: a potential application and preliminary clinical experience

OBJETIVO: Utilização de nova tecnologia na desmineralização química da valva aórtica, em cirurgia cardíaca com circulação extracorpórea, avaliação de suas alterações hemodinâmicas e reportar eventos relacionados à técnica. MÉTODO: Cinco pacientes, submetidos à revascularização miocárdica e portadores de estenose aórtica leve a moderada, receberam tratamento químico na valva aórtica. A idade dos pacientes variou de 65 a 81 anos, com média de 73 anos; sendo todos do sexo masculino. Um paciente tinha doença uniarterial e quatro, multiarterial (quatro vasos). O gradiente médio variou de 13 a 49 mmHg, com média de 25 mmHg. A área média do orifício aórtico variou de 0,8 a 1,3 cm², com média de 1,1cm². Os antecedentes observados foram: hipertensão arterial, hipercolesterolemia, diabete melito e fumo. RESULTADOS: O período de pinçamento aórtico variou de 94 a 126 minutos, com média de 107 minutos. O tempo de "bypass" variou de 134 a 171 minutos, com média de 152 minutos. O tempo de tratamento variou de 13 a 33 minutos, com média de 28 minutos. Não foi observado nenhum óbito. Complicações pós-operatórias observadas foram: bloqueio atrioventricular total em três pacientes. Não foram observados eventos que comprometessem a integridade da valva aórtica ou provocassem insuficiência aórtica pós-tratamento. Também não se observaram eventos neurológicos, sistêmicos, metabólicos ou hematológicos. O gradiente transvalvar pós-operatório, determinado pelo ecocardiograma, demonstrou melhora no gradiente sistólico e médio. CONCLUSÕES: O tratamento demonstrou ser efetivo e seguro, não causando lesão à valva ou algum evento sistêmico. As alterações do sistema de condução parecem relacionadas com o equipamento e seu sistema de liberação da substância de lavagem. A utilização desta tecnologia poderá ser, no futuro, um importante coadjuvante na substituição da valva aórtica por via transcutânea.

OBJECTIVE: To discuss the use of new technology in the chemical demineralization of the aortic valve in coronary artery bypass surgery, together with its hemodynamic changes and to report events related to the technique. METHOD: Five patients with mild to moderate aortic stenosis submitted to myocardial revascularization underwent chemical treatment of the aortic valve. The patients' ages ranged from 65 to 81 years, with a mean of 73 years. All were men. One patient had the involvement of a single artery and four multiple arteries (four vessels). The gradient ranged from 13 to 49 mmHg, with a mean of 25 mmHg. The size of the aortic orifice ranged from 0.8 to 1.3 cm², with a mean of 1.1 cm². The following antecedents were observed: arterial hypertension, hypercholesterolemia, diabetes mellitus and smoking. RESULTS: The aorta clamping time ranged from 94 to 126 minutes, with a mean of 107 minutes and the bypass time was from 134 to 171 minutes, with a mean of 152 minutes. The time of surgery was from 13 to 33 minutes with a mean of 28 minutes. No deaths were recorded. The only postoperative complication noted was a total AV block in three patients. No events were observed that might impair the integrity of the aortic valve or cause aortic insufficiency following treatment. Likewise, no neurologic, systemic, metabolic or hematologic events were seen. The postoperative transvalvular gradient identified by echocardiography showed an improvement in the systolic gradient and in the mean gradient. CONCLUSIONS: The treatment proved to be effective and safe, causing no lesions of the valve or any systemic event. The changes in the conduction system appear to be related to the equipment and its system of releasing the lavage solution. The use of this technology may, in the future, be an important adjuvant in aorta valve replacement using percutaneous techniques.

Mitral-aortic annular enlargement: modification of Manouguian's technique

Apresentamos uma modificaçäo técnica para ampliaçäo anular mitro-aórtica. A prótese mitral é implantada pela via retrosseptal, evitando retalhos para fechar o teto atrial esquerdo. Relatamos um implante valvar mitro-aórtico em paciente cujos anéis originais impossibilitariam próteses adequadas. A ampliaçäo pode ser necessária para evitar a inadequaçäo prótese-paciente ou para reconstruir anéis mitral e aórtico destruídos. Esta técnica pode diminuir o risco de sangramento e de vazamento paravalvar, utilizando um acesso bem conhecido por cirurgiöes cardíacos.

Incontinência urinária em pacientes com mais de 60 anos: avaliaçäo da necessidade da realizaçäo de propedêutica diagnóstica específica / Urinary incontinence in patients over 60 years old: evaluation of specific diagnostic procedure necessity

Avaliar as causas da incontinência urinária em pacientes acima de 60 anos e estudar a necessidade de realizaçäo de propedêutica urinária nestas pacientes. De um total de 2633 urodinâmicas realizadas no período de janeiro de 1991 a março de 2000 dentro dos padröes da Sociedade Internacional de Continência (ICS), selecionamos 397 (15 por cento) exames de pacientes com queixa de incontinência urinária e idade superior a 60 anos. A partir da anamnese detalhada, exame uroginecológico, neurológico superficial, um diagnóstico clínico foi estabelecido e comparado ao diagnóstico urodinâmico obtido posteriormente. A média de idade foi 68 anos. Freqüência de diagnósticos urodinâmicos obtidos: Hiperatividade do detrusor=51 por cento (n=202); Incontinência Urinária de Esforço Genuína=21 por cento (n=84); Incontinência Urinária Mista=20 por cento (n=77); Normal=7,5 por cento (n=30). Das pacientes com diagnóstico de hiperatividade do detrusor, 167 (83 por cento) apresentaram instabilidade vesical, 35 (17 por cento) apresentaram hiperreflexia do detrusor e 2 (0,5 por cento) apresentaram urgência sensorial. O acerto entre diagnóstico clínico e urodinâmico foi de 58,4 por cento (n=232). O diagnóstico urodinâmico mais freqüentemente encontrado no grupo de pacientes estudado foi a hiperatividade do detrusor. Após avaliaçäo detalhada, o acerto no diagnóstico clínico da causa de incontinência urinária situa-se em torno de 41 a 72 por cento. Os autores consideram importante o erro diagnóstico encontrado, principalmente nessa faixa etária que possui alta incidência de cirurgias anteriores sobre o colo vesical e freqüente associaçäo com doenças neurológicas. O estudo urodinâmico dever ser realizado sempre que possível, exceto nos casos de incapacidade física, porque o tratamento adequado é diferente de acordo com a causa específica de incontinência urinária.

Abordagem farmacológica da síndrome do intestino irritável / Pharmacological approach to the Sll

Apesar das várias opções terapêuticas existentes para o Sll, as dificuldades em definir seus mecanismos fisiopatólogicos são ainda o principal obstátulo ao sucesso do tratamento desses pacientes. Os autores fazem uma revisão crítica dos medicamentos utilizados, reiterando que abordagem de cada caso individualmente ainda é a principal arma no alívio dos sintomas desses pacientes

Uraco permeavel / Patent urachus

O uraco permeavel e uma anomalia rara. Os autores apresentaram um caso em que e enfatizada a embriologia, sintomas clinicos, diagnostico e diagnostico diferencial do denominado "umbigo molhado".

Polipo da uretra posterior / Posterior urethral polyp

O polipo na uretra posterior e de origem congenita, podendo apresentar-se com sintomas obstrutivos ou sangramento. No entanto, sao relatados dois casos com sintomatologia clinica distinta.

Variaçäo cicardiana do efeito hipnótico do propofol em camundongos / Circadian variation of profofol sleeping time in mice

Camundongos sincronizados em ciclo claro/escuro de 12 h (repouso e atividade, respectivamente) foram submetidos a injeçåo intraperitoneal de propofol a 1 por cento no sentido de avaliar a curva dose/resposta para seu efeito hipnótico com doses cresentes (método de Litchifield-Wilcoxon), bem como sua eventual variaçäo circadiana. Os resultados demonstraram qua a dose hipnótica 50 por cento (DH50) do agente proporcionou menor latência hipnótica na administraçäo ao meio dia (fase de repouso) em relaçäo à meia-noite (fase de atividade); também a perda do reflexo postural à meia-noite foi mais curta em relaçäo às 18 horas e ao meio-dia (teste "t" de Student). Näo se observou variaçäo circadiana do efeito hipnótico para a DH80. Embora o teste Cosinor näo tenha demonstrado ritmicidade, ficou evidente a existência de uma variaçäo circadiana da ação hipnótica do propofol no animal (maior atividade no período de repouso).