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1.
Arq Bras Cardiol ; 120(3): e20220608, 2023 03.
Article de Anglais, Portugais | MEDLINE | ID: mdl-36946858

RÉSUMÉ

BACKGROUND: Infectious endocarditis (IE) refers to infection of the endocardial surface of the heart and usually occurs in native or prosthetic valves. OBJECTIVE: This study aimed to raise IE data reflecting the surgical therapy in a University Hospital in the interior of the State of Sao Paulo-Brazil. METHOD: Retrospective and observational approach of 328 patients with IE who underwent surgery between 1982 and 2020. RESULTS: The main data (n=121/37%), congestive heart failure (n=114/35%), valve disease (n=92/28%), diabetes mellitus (n=85/26%), chronic kidney disease (n=59/18%), and rheumatic fever (49/15%). Renal failure is one of the main and most relevant pre-surgical risk factors for a poor prognosis. CONCLUSION: For a better clinical and surgical outcome, an early syndromic and etiological diagnosis of IE is necessary, especially in patients with multiple comorbidities.


FUNDAMENTO: A endocardite infecciosa (EI) refere-se à infecção da superfície endocárdica do coração e geralmente ocorre em valvas nativas ou protéticas. OBJETIVO: Este estudo teve como objetivo levantar dados de EI refletindo a terapêutica cirúrgica, em um Hospital Universitário do interior do estado de São Paulo ­ Brasil. MÉTODO: Abordagem retrospectiva e observacional de 328 pacientes com EI operados entre 1982 e 2020. RESULTADOS: Os principais dados (n=121/37%), insuficiência cardíaca congestiva (n=114/35%), valvopatia (n=92/28%), diabetes mellitus (n=85/26%), doença renal crônica (n=59/18%) e febre reumática (49/15%). A insuficiência renal é um dos principais e mais relevantes fatores de risco pré-cirúrgicos para um mau prognóstico. CONCLUSÃO: Para um melhor resultado clínico e cirúrgico é necessário o diagnóstico sindrômico e etiológico precoce da EI, principalmente em pacientes com múltiplas comorbidades.


Sujet(s)
Endocardite bactérienne , Endocardite , Humains , Brésil/épidémiologie , Endocardite/chirurgie , Endocardite bactérienne/chirurgie , Endocardite bactérienne/complications , Endocardite bactérienne/diagnostic , Mortalité hospitalière , Études rétrospectives , Centres de soins tertiaires
2.
Arq. bras. cardiol ; 120(3): e20220608, 2023. tab, graf
Article de Portugais | LILACS-Express | LILACS | ID: biblio-1420200

RÉSUMÉ

Resumo Fundamento A endocardite infecciosa (EI) refere-se à infecção da superfície endocárdica do coração e geralmente ocorre em valvas nativas ou protéticas. Objetivo Este estudo teve como objetivo levantar dados de EI refletindo a terapêutica cirúrgica, em um Hospital Universitário do interior do estado de São Paulo - Brasil. Método Abordagem retrospectiva e observacional de 328 pacientes com EI operados entre 1982 e 2020 Resultados Os principais dados (n=121/37%), insuficiência cardíaca congestiva (n=114/35%), valvopatia (n=92/28%), diabetes mellitus (n=85/26%), doença renal crônica (n=59/18%) e febre reumática (49/15%). A insuficiência renal é um dos principais e mais relevantes fatores de risco pré-cirúrgicos para um mau prognóstico. Conclusão Para um melhor resultado clínico e cirúrgico é necessário o diagnóstico sindrômico e etiológico precoce da EI, principalmente em pacientes com múltiplas comorbidades.


Abstract Background Infectious endocarditis (IE) refers to infection of the endocardial surface of the heart and usually occurs in native or prosthetic valves. Objective This study aimed to raise IE data reflecting the surgical therapy in a University Hospital in the interior of the State of Sao Paulo-Brazil. Method Retrospective and observational approach of 328 patients with IE who underwent surgery between 1982 and 2020 Results The main data (n=121/37%), congestive heart failure (n=114/35%), valve disease (n=92/28%), diabetes mellitus (n=85/26%), chronic kidney disease (n=59/18%), and rheumatic fever (49/15%). Renal failure is one of the main and most relevant pre-surgical risk factors for a poor prognosis. Conclusion For a better clinical and surgical outcome, an early syndromic and etiological diagnosis of IE is necessary, especially in patients with multiple comorbidities.

3.
Neurología (Barc., Ed. impr.) ; 36(1): 50-60, ene.-feb. 2021. tab
Article de Espagnol | IBECS | ID: ibc-200446

RÉSUMÉ

ANTECEDENTES: La reciente aparición de terapias de alta efectividad para el tratamiento de la esclerosis múltiple (EM), con potencial riesgo de complicaciones infecciosas, obliga plantear estrategias de prevención y minimización de riesgos. La vacunación constituye una parte esencial del manejo de estos pacientes. Este consenso recoge una serie de pautas y escenarios prácticos de vacunación en pacientes adultos con EM candidatos a tratamiento inmunosupresor. METODOLOGÍA: Se llevó a cabo un consenso de tipo formal. Tras definir el alcance del documento, se realizó una búsqueda bibliográfica de vacunación en pacientes con EM, así como guías de vacunación específicas de pacientes inmunosuprimidos y en tratamiento biológico con otras enfermedades. Para la formulación de las recomendaciones se empleó la metodología de Modified Nominal Group Technique. DESARROLLO: La vacunación en pacientes candidatos a tratamiento inmunosupresor se debe plantear antes de iniciar un tratamiento inmunosupresor siempre que la situación clínica del paciente lo permita. Se recomendarán tanto aquellas indicadas en el calendario vacunal del adulto, como algunas específicas, en función de la inmunidad previa. Si ya está instaurado el tratamiento inmunosupresor las vacunas vivas atenuadas estarán contraindicadas. Para aquellas vacunas que dispongan de un correlato de protección se recomienda monitorizar la respuesta serológica transcurridos de uno a 2 meses de la última dosis


BACKGROUND: The recent development of highly effective treatments for multiple sclerosis (MS) and the potential risk of infectious complications require the development of prevention and risk minimisation strategies. Vaccination is an essential element of the management of these patients. This consensus statement includes a series of recommendations and practical scenarios for the vaccination of adult patients with MS who are eligible for highly effective immunosuppressive treatments. METHODOLOGY: A formal consensus procedure was followed. Having defined the scope of the statement, we conducted a literature search on recommendations for the vaccination of patients with MS and specific vaccination guidelines for immunosuppressed patients receiving biological therapy for other conditions. The modified nominal group technique methodology was used to formulate the recommendations. DEVELOPMENT: Vaccination in patients who are candidates for immunosuppressive therapy should be considered before starting immunosuppressive treatment providing the patient's clinical situation allows. Vaccines included in the routine adult vaccination schedule, as well as some specific ones, are recommended depending on the pre-existing immunity status. If immunosuppressive treatment is already established, live attenuated vaccines are contraindicated. For vaccines with a correlate of protection, it is recommended to monitor the serological response in an optimal interval of 1-2 months from the last dose


Sujet(s)
Humains , Consensus , Guides de bonnes pratiques cliniques comme sujet , Sclérose en plaques/prévention et contrôle , Sclérose en plaques/immunologie , Vaccination/normes , Immunosuppresseurs/usage thérapeutique , Vaccins/normes , Immunocompétence , Facteurs de risque , Vaccination/effets indésirables , Espagne , Vaccins/administration et posologie
4.
Neurologia (Engl Ed) ; 36(1): 50-60, 2021.
Article de Anglais, Espagnol | MEDLINE | ID: mdl-32561334

RÉSUMÉ

BACKGROUND: The recent development of highly effective treatments for multiple sclerosis (MS) and the potential risk of infectious complications require the development of prevention and risk minimisation strategies. Vaccination is an essential element of the management of these patients. This consensus statement includes a series of recommendations and practical scenarios for the vaccination of adult patients with MS who are eligible for highly effective immunosuppressive treatments. METHODOLOGY: A formal consensus procedure was followed. Having defined the scope of the statement, we conducted a literature search on recommendations for the vaccination of patients with MS and specific vaccination guidelines for immunosuppressed patients receiving biological therapy for other conditions. The modified nominal group technique methodology was used to formulate the recommendations. DEVELOPMENT: Vaccination in patients who are candidates for immunosuppressive therapy should be considered before starting immunosuppressive treatment providing the patient's clinical situation allows. Vaccines included in the routine adult vaccination schedule, as well as some specific ones, are recommended depending on the pre-existing immunity status. If immunosuppressive treatment is already established, live attenuated vaccines are contraindicated. For vaccines with a correlate of protection, it is recommended to monitor the serological response in an optimal interval of 1-2 months from the last dose.


Sujet(s)
Immunosuppression thérapeutique , Sclérose en plaques , Adulte , Consensus , Humains , Sclérose en plaques/traitement médicamenteux , Vaccination , Vaccins atténués
5.
Eur Heart J ; 41(22): 2092-2112, 2020 06 07.
Article de Anglais | MEDLINE | ID: mdl-32511724

RÉSUMÉ

The COVID-19 pandemic has greatly impacted the daily clinical practice of cardiologists and cardiovascular surgeons. Preparedness of health workers and health services is crucial to tackle the enormous challenge posed by SARS-CoV-2 in wards, operating theatres, intensive care units, and interventionist laboratories. This Clinical Review provides an overview of COVID-19 and focuses on relevant aspects on prevention and management for specialists within the cardiovascular field.


Sujet(s)
Betacoronavirus , Infections à coronavirus/épidémiologie , Infections à coronavirus/thérapie , Pandémies , Pneumopathie virale/épidémiologie , Pneumopathie virale/thérapie , Betacoronavirus/pathogénicité , Betacoronavirus/physiologie , COVID-19 , Infections à coronavirus/diagnostic , Infections à coronavirus/transmission , Endocardite/chirurgie , Humains , Mâle , Adulte d'âge moyen , Pneumopathie virale/diagnostic , Pneumopathie virale/transmission , Infections dues aux prothèses/chirurgie , SARS-CoV-2
6.
Braz J Cardiovasc Surg ; 31(3): 226-231, 2016.
Article de Anglais | MEDLINE | ID: mdl-27737405

RÉSUMÉ

Objective: To examine if methylene blue (MB) can counteract or prevent protamine (P) cardiovascular effects. Methods: The protocol included five heparinized pig groups: Group Sham -without any drug; Group MB - MB 3 mg/kg infusion; Group P - protamine; Group P/MB - MB after protamine; Group MB/P - MB before protamine. Nitric oxide levels were obtained by the nitric oxide/ozone chemiluminescence method, performed using the Nitric Oxide Analizer 280i (Sievers, Boulder, CO, USA). Malondialdehyde plasma levels were estimated using the thiobarbiturate technique. Results: 1) Groups Sham and MB presented unchanged parameters; 2) Group P - a) Intravenous protamine infusion caused mean arterial pressure decrease and recovery trend after 25-30 minutes, b) Cardiac output decreased and remained stable until the end of protamine injection, and c) Sustained systemic vascular resistance increased until the end of protamine injection; 3) Methylene blue infusion after protamine (Group P/MB) - a) Marked mean arterial pressure decreased after protamine, but recovery after methylene blue injection, b) Cardiac output decreased after protamine infusion, recovering after methylene blue infusion, and c) Sustained systemic vascular resistance increased after protamine infusion and methylene blue injections; 4) Methylene blue infusion before protamine (Group MB/P) - a) Mean arterial pressure decrease was less severe with rapid recovery, b) After methylene blue, there was a progressive cardiac output increase up to protamine injection, when cardiac output decreased, and c) Sustained systemic vascular resistance decreased after protamine, followed by immediate Sustained systemic vascular resistance increase; 5) Plasma nitrite/nitrate and malondialdehyde values did not differ among the experimental groups. Conclusion: Reviewing these experimental results and our clinical experience, we suggest methylene blue safely prevents and treats hemodynamic protamine complications, from the endothelium function point of view.


Sujet(s)
Antienzymes/pharmacologie , Hémodynamique/effets des médicaments et des substances chimiques , Antagonistes de l'héparine/administration et posologie , Bleu de méthylène/pharmacologie , Protamine/antagonistes et inhibiteurs , Anaphylaxie/étiologie , Anaphylaxie/prévention et contrôle , Animaux , Pression veineuse centrale/effets des médicaments et des substances chimiques , Endothélium vasculaire/effets des médicaments et des substances chimiques , Femelle , Antagonistes de l'héparine/effets indésirables , Malonaldéhyde/sang , Modèles animaux , Monoxyde d'azote/sang , Protamine/effets indésirables , Suidae
7.
Rev. bras. cir. cardiovasc ; 31(3): 226-231, May.-June 2016. tab, graf
Article de Anglais | LILACS | ID: lil-796123

RÉSUMÉ

ABSTRACT Objective: To examine if methylene blue (MB) can counteract or prevent protamine (P) cardiovascular effects. Methods: The protocol included five heparinized pig groups: Group Sham -without any drug; Group MB - MB 3 mg/kg infusion; Group P - protamine; Group P/MB - MB after protamine; Group MB/P - MB before protamine. Nitric oxide levels were obtained by the nitric oxide/ozone chemiluminescence method, performed using the Nitric Oxide Analizer 280i (Sievers, Boulder, CO, USA). Malondialdehyde plasma levels were estimated using the thiobarbiturate technique. Results: 1) Groups Sham and MB presented unchanged parameters; 2) Group P - a) Intravenous protamine infusion caused mean arterial pressure decrease and recovery trend after 25-30 minutes, b) Cardiac output decreased and remained stable until the end of protamine injection, and c) Sustained systemic vascular resistance increased until the end of protamine injection; 3) Methylene blue infusion after protamine (Group P/MB) - a) Marked mean arterial pressure decreased after protamine, but recovery after methylene blue injection, b) Cardiac output decreased after protamine infusion, recovering after methylene blue infusion, and c) Sustained systemic vascular resistance increased after protamine infusion and methylene blue injections; 4) Methylene blue infusion before protamine (Group MB/P) - a) Mean arterial pressure decrease was less severe with rapid recovery, b) After methylene blue, there was a progressive cardiac output increase up to protamine injection, when cardiac output decreased, and c) Sustained systemic vascular resistance decreased after protamine, followed by immediate Sustained systemic vascular resistance increase; 5) Plasma nitrite/nitrate and malondialdehyde values did not differ among the experimental groups. Conclusion: Reviewing these experimental results and our clinical experience, we suggest methylene blue safely prevents and treats hemodynamic protamine complications, from the endothelium function point of view.


Sujet(s)
Animaux , Femelle , Protamine/antagonistes et inhibiteurs , Antienzymes/pharmacologie , Hémodynamique/effets des médicaments et des substances chimiques , Antagonistes de l'héparine/administration et posologie , Bleu de méthylène/pharmacologie , Suidae , Endothélium vasculaire/effets des médicaments et des substances chimiques , Protamine/effets indésirables , Pression veineuse centrale/effets des médicaments et des substances chimiques , Modèles animaux , Antagonistes de l'héparine/effets indésirables , Anaphylaxie/étiologie , Anaphylaxie/prévention et contrôle , Malonaldéhyde/sang , Monoxyde d'azote/sang
8.
Mol Pharm ; 12(10): 3672-84, 2015 Oct 05.
Article de Anglais | MEDLINE | ID: mdl-26312414

RÉSUMÉ

Drugs can be targeted to the brain using polymeric nanoparticles (NPs) engineered on their surface with ligands able to allow crossing of the blood-brain barrier (BBB). This article aims to investigate the BBB crossing efficiency of polymeric poly lactide-co-glycolide (PLGA) NPs modified with a mutated form of diphtheria toxin (CRM197) in comparison with the results previously obtained using PLGA NPs modified with a glycopeptide (g7-NPs). Different kinds of NPs, covalently coupled PLGA with different fluorescent probes (DY405, rhodamine-B base and DY675) and different ligands (g7 and CRM197) were tested in vivo to assess their behavior and trafficking. The results highlighted the possibility to distinguish the different kinds of simultaneously administered NPs and to emphasize that CRM-197 modified NPs and g7-NPs can cross the BBB at a similar extent. The analysis of BBB crossing and of the neuronal tropism of CRM197 modified NPs, along with their BBB crossing pathways were also developed. In vivo pharmacological studies performed on CRM197 engineered NPs, loaded with loperamide, underlined their ability as drug carriers to the CNS.


Sujet(s)
Protéines bactériennes/métabolisme , Barrière hémato-encéphalique/métabolisme , Toxine diphtérique/métabolisme , Systèmes de délivrance de médicaments/méthodes , Nanoparticules/usage thérapeutique , Animaux , Protéines bactériennes/pharmacocinétique , Barrière hémato-encéphalique/microbiologie , Toxine diphtérique/génétique , Lopéramide/métabolisme , Souris , Microscopie confocale , Nanoparticules/métabolisme , Nociception/effets des médicaments et des substances chimiques
9.
Acta cir. bras ; 26(6): 481-489, Nov.-Dec. 2011. ilus
Article de Anglais | LILACS | ID: lil-604198

RÉSUMÉ

PURPOSE: To verify if the methylene blue (MB) administration prevents and/or reverses the compound 48/80 (C48/80)-induced anaphylactic shock in pigs. METHODS: Female Dalland pigs were anesthetized and had the hemodynamic parameters recorded during the necessary time to administer some drugs and observe their effect. The animals were randomly assigned to one of the five groups: 1) control; 2) MB: the animals received a bolus injection of MB (2 mg/kg) followed by continuous infusion of MB (2.66 mg/Kg/h delivered by syringe infusion pump); 3) C48/80: the animals received a bolus injection of C48/80 (4 mg/kg); 4) C48/80+MB: the animals received a bolus injection of C48/80 (4 mg/kg) and 10 minutes after the C48/80 administration the animals received a bolus injection of MB (2 mg/kg) followed by continuous infusion of MB (2.66 mg/Kg/h delivered by syringe infusion pump); 5) MB+C48/80: the animals received a bolus injection of MB (2 mg/kg) and 3 minutes later they received a bolus injection of C48/80 (4 mg/kg). RESULTS: The intravenous infusion of MB alone caused no changes in the mean arterial pressure (MAP) showing that the administered MB dose was safe in this experimental model. The C48/80 was effective in producing experimental anaphylactic shock since it was observed a decrease in both MAP and cardiac output (CO) after its administration. The MB did not prevent or reverse the C48/80-induced anaphylactic shock in this model. In fact, the MAP of the animals with anaphylactic shock treated with MB decreased even more than the MAP of the animals from the C48/80 group. On the other hand, the C48/80-induced epidermal alterations disappeared after the MB infusion. CONCLUSION: Despite our data, the clinical manifestations improvement brings some optimism and does not allow excluding the MB as a possible therapeutic option in the anaphylactic shock.


OBJETIVO: Verificar se a administração de azul de metileno (AM) previne e/ou reverte o choque anafilático induzido por composto 48/80 (C48/80) em suínos. MÉTODOS: Porcos fêmeas Dalland foram anestesiados e tiveram os parâmetros hemodinâmicos registados durante o tempo necessário para administrar algumas drogas e observar seu efeito. Os animais foram aleatoriamente destribuídos em um dos cinco grupos: 1) controle, 2) AM: os animais receberam uma injeção em bolus de AM (2mg/kg), seguido de infusão contínua de AM (2,66mg/Kg /h por bomba de infusão de seringa); 3) C48/80: os animais receberam uma injeção em bolus de C48/80 (4mg/kg); 4) C48/80 + AM: os animais receberam uma injeção em bolus de C48/80 (4mg/kg) e 10 minutos após a administração de C48/80 os animais receberam uma injeção em bolus de AM (2mg/kg), seguido de infusão contínua de AM (2,66mg/kg/h por bomba de infusão de seringa); 5) AM+C48/80: os animais receberam uma injeção em bolus de AM (2mg/kg) e três minutos depois, receberam uma injeção em bolus de C48/80 (4mg/kg). RESULTADOS: A infusão intravenosa de AM não causou mudanças na pressão arterial média (PAM), mostrando que a dose de AM administrada foi segura neste modelo experimental. O C48/80 foi eficaz na indução do choque anafilático experimental, uma vez que foi observada redução na PAM e débito cardíaco (DC), após a sua administração. O AM não preveniu ou reverte o choque anafilático induzido por C48/80 neste modelo. Na verdade, a PAM dos animais com choque anafilático tratados com AM diminuiu mais do que o PAM dos animais do grupo C48/80. Por outro lado, as alterações epidérmicas induzidas pelo C48/80 desapareceu após a infusão do AM. CONCLUSÃO: Apesar dos resultados a melhora clínica das manifestações anafiláticas permite considerar a possibilidade do azul de metileno como opção terapêutica no tratamento do choque anafilático.


Sujet(s)
Animaux , Femelle , Anaphylaxie/traitement médicamenteux , Hémodynamique/effets des médicaments et des substances chimiques , Bleu de méthylène/usage thérapeutique , 4-Méthoxyphénéthyl-méthyl-amine/toxicité , Anaphylaxie/induit chimiquement , Anaphylaxie/prévention et contrôle , Pression sanguine/effets des médicaments et des substances chimiques , Débit cardiaque/effets des médicaments et des substances chimiques , Modèles animaux de maladie humaine , Hémodynamique/physiologie , Répartition aléatoire , Suidae , Facteurs temps , Résistance vasculaire/effets des médicaments et des substances chimiques , 4-Méthoxyphénéthyl-méthyl-amine/antagonistes et inhibiteurs
10.
Acta Cir Bras ; 26(6): 481-9, 2011 Dec.
Article de Anglais | MEDLINE | ID: mdl-22042112

RÉSUMÉ

PURPOSE: To verify if the methylene blue (MB) administration prevents and/or reverses the compound 48/80 (C48/80)-induced anaphylactic shock in pigs. METHODS: Female Dalland pigs were anesthetized and had the hemodynamic parameters recorded during the necessary time to administer some drugs and observe their effect. The animals were randomly assigned to one of the five groups: 1) control; 2) MB: the animals received a bolus injection of MB (2 mg/kg) followed by continuous infusion of MB (2.66 mg/Kg/h delivered by syringe infusion pump); 3) C48/80: the animals received a bolus injection of C48/80 (4 mg/kg); 4) C48/80+MB: the animals received a bolus injection of C48/80 (4 mg/kg) and 10 minutes after the C48/80 administration the animals received a bolus injection of MB (2 mg/kg) followed by continuous infusion of MB (2.66 mg/Kg/h delivered by syringe infusion pump); 5) MB+C48/80: the animals received a bolus injection of MB (2 mg/kg) and 3 minutes later they received a bolus injection of C48/80 (4 mg/kg). RESULTS: The intravenous infusion of MB alone caused no changes in the mean arterial pressure (MAP) showing that the administered MB dose was safe in this experimental model. The C48/80 was effective in producing experimental anaphylactic shock since it was observed a decrease in both MAP and cardiac output (CO) after its administration. The MB did not prevent or reverse the C48/80-induced anaphylactic shock in this model. In fact, the MAP of the animals with anaphylactic shock treated with MB decreased even more than the MAP of the animals from the C48/80 group. On the other hand, the C48/80-induced epidermal alterations disappeared after the MB infusion. CONCLUSION: Despite our data, the clinical manifestations improvement brings some optimism and does not allow excluding the MB as a possible therapeutic option in the anaphylactic shock.


Sujet(s)
Anaphylaxie/traitement médicamenteux , Hémodynamique/effets des médicaments et des substances chimiques , Bleu de méthylène/usage thérapeutique , 4-Méthoxyphénéthyl-méthyl-amine/toxicité , Anaphylaxie/induit chimiquement , Anaphylaxie/prévention et contrôle , Animaux , Pression sanguine/effets des médicaments et des substances chimiques , Débit cardiaque/effets des médicaments et des substances chimiques , Modèles animaux de maladie humaine , Femelle , Hémodynamique/physiologie , Répartition aléatoire , Suidae , Facteurs temps , Résistance vasculaire/effets des médicaments et des substances chimiques , 4-Méthoxyphénéthyl-méthyl-amine/antagonistes et inhibiteurs
12.
Br J Cancer ; 105(6): 870-5, 2011 Sep 06.
Article de Anglais | MEDLINE | ID: mdl-21811255

RÉSUMÉ

BACKGROUND: Colorectal cancer (CRC) is the second cause of cancer-related death in the Western world. Much of the CRC genetic risk remains unidentified and may be attributable to a large number of common, low-penetrance genetic variants. Genetic linkage studies in CRC families have reported additional association with regions 9q22-31, 3q21-24, 7q31, 11q, 14q and 22q. There are several plausible candidate genes for CRC susceptibility within the aforementioned linkage regions including PTCH1, XPA and TGFBR1 in 9q22-31, and EPHB1 and MRAS in 3q21-q24. METHODS: CRC cases and matched controls were from EPICOLON, a prospective, multicentre, nationwide Spanish initiative, composed of two independent phases. Phase 1 corresponded to 515 CRC cases and 515 controls, whereas phase 2 consisted of 901 CRC cases and 909 controls. Genotyping was performed for 172 single-nucleotide polymorphisms (SNPs) in 84 genes located within regions 9q22-31 and 3q21-q24. RESULTS: None of the 172 SNPs analysed in our study could be formally associated with CRC risk. However, rs1444601 (TOPBP1) and rs13088006 (CDV3) in region 3q22 showed interesting results and may have an effect on CRC risk. CONCLUSIONS: TOPBP1 and CDV3 genetic variants on region 3q22 may modulate CRC risk. Further validation and meta-analysis should be undertaken in larger CRC cohorts.


Sujet(s)
Chromosomes humains de la paire 3 , Chromosomes humains de la paire 9 , Tumeurs colorectales/génétique , Prédisposition génétique à une maladie , Sujet âgé , Antigènes CD/génétique , Protéines de transport/génétique , Études cas-témoins , Protéines de liaison à l'ADN/génétique , Protéines liées au GPI/génétique , Études d'associations génétiques , Humains , Mâle , Protéines nucléaires/génétique , Polymorphisme de nucléotide simple , Sémaphorines/génétique
13.
Rev Esp Enferm Dig ; 103(1): 5-12, 2011 Jan.
Article de Anglais | MEDLINE | ID: mdl-21341931

RÉSUMÉ

OBJECTIVE: Analysis and evaluation of a multidisciplinary approach, postoperative results and survival of a group of patients with resected pancreatic cancer after a multimodal therapy. DESIGN: DESCRIPTIVE, prospective and observational study. PATIENTS: Between January 2004 and December 2004, 124 patients with pancreatic cancer were evaluated. In 30 patients pancreatic resection was performed, and they are the object of this study. Results of preoperative evaluation, postoperative morbidity and mortality, and long term survival were studied. RESULTS: Diagnostic evaluation was completed in ambulatory basis in 20% of the patients. In 63% of cases, admission was done in the same day of surgery. In 3 patients (9%), tumor resection was not achieved, therefore, concordance between radiological and surgical resectability rate was 91%. Resectability rate was 24.1%. Surgical Mortality was 3.3%, with a global morbidity rate of 56.6%. Survival at one, two, three and, four years was 76.2%, 56.3%, 43%, y 27.3% respectively. CONCLUSIONS: Technological development and coordination of efforts in multidisciplinary teams offer an accurate evaluation of tumor involvement, and may reduce the number of laparotomies without tumor resection. The application of a systematic and generalized multimodal treatment in pancreatic cancer is progressively showing a tendency of progressive increase in resectability and survival rates in pancreatic cancer.


Sujet(s)
Protocoles de polychimiothérapie antinéoplasique/usage thérapeutique , Carcinome du canal pancréatique/thérapie , Pancréatectomie/méthodes , Tumeurs du pancréas/thérapie , Équipe soignante , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Carcinomes/diagnostic , Carcinomes/imagerie diagnostique , Carcinomes/anatomopathologie , Carcinomes/thérapie , Carcinome du canal pancréatique/diagnostic , Carcinome du canal pancréatique/imagerie diagnostique , Carcinome du canal pancréatique/anatomopathologie , Carcinome du canal pancréatique/secondaire , Traitement médicamenteux adjuvant , Cholangiopancréatographie rétrograde endoscopique , Colectomie , Association thérapeutique , Désoxycytidine/administration et posologie , Désoxycytidine/analogues et dérivés , Imagerie diagnostique , Femelle , Hépatectomie/méthodes , Humains , Estimation de Kaplan-Meier , Tumeurs du foie/secondaire , Tumeurs du foie/chirurgie , Mâle , Adulte d'âge moyen , Traitement néoadjuvant , Composés organiques du platine/administration et posologie , Oxaliplatine , Pancréatectomie/mortalité , Tumeurs du pancréas/diagnostic , Tumeurs du pancréas/imagerie diagnostique , Tumeurs du pancréas/anatomopathologie , Duodénopancréatectomie , Études prospectives , Endoprothèses , Taux de survie ,
14.
HIV Med ; 12(4): 236-45, 2011 Apr.
Article de Anglais | MEDLINE | ID: mdl-21255221

RÉSUMÉ

OBJECTIVES: HIV-infected adults are considered to be at higher risk for influenza A H1N1 complications but data supporting this belief are lacking. We aimed to compare epidemiological data, clinical characteristics, and outcomes of influenza A H1N1 infection between HIV-infected and -uninfected adults. METHODS: From 26 April to 6 December 2009, each adult presenting with acute respiratory illness at the emergency department of our institution was considered for an influenza A H1N1 diagnosis by specific multiplex real-time polymerase chain reaction. For every HIV-infected adult diagnosed, three consecutive adults not known to be HIV-infected diagnosed in the same calendar week were randomly chosen as controls. RESULTS: Among 2106 adults tested, 623 (30%) had influenza A H1N1 infection confirmed. Fifty-six (9%) were HIV-positive and were compared with 168 HIV-negative controls. Relative to HIV-negative controls, HIV-positive patients were older, more frequently male, and more frequently smokers (P≤0.02). In the HIV-positive group, prior or current AIDS-defining events were reported for 30% of patients, 9% and 30% had CD4 counts of <200 and 200-500cells/µL, respectively, and 95% had HIV-1 RNA <50copies/mL. Pneumonia (9%vs. 25%, respectively, in the HIV-positive and HIV-negative groups; P=0.01) and respiratory failure (9%vs. 21%, respectively; P=0.04) were less common in the HIV-positive group. Oseltamivir (95%vs. 71% in the HIV-positive and HIV-negative groups, respectively; P=0.003) was administered more often in HIV-positive patients. Three patients (all HIV-negative) died. In the HIV-positive group, CD4 cell count and plasma HIV-1 RNA did not differ before and 4-6 weeks after influenza A H1N1 diagnosis (P>0.05). CONCLUSIONS: HIV infection did not increase the severity of influenza A H1N1 infection, and influenza A H1N1 infection did not have a major effect on HIV infection.


Sujet(s)
Infections opportunistes liées au SIDA/épidémiologie , Infections à VIH/complications , VIH-1 (Virus de l'Immunodéficience Humaine de type 1) , Sous-type H1N1 du virus de la grippe A , Grippe humaine/complications , Infections opportunistes liées au SIDA/traitement médicamenteux , Infections opportunistes liées au SIDA/immunologie , Adulte , Numération des lymphocytes CD4 , Femelle , Infections à VIH/épidémiologie , Infections à VIH/immunologie , VIH-1 (Virus de l'Immunodéficience Humaine de type 1)/immunologie , Humains , Sous-type H1N1 du virus de la grippe A/immunologie , Mâle , Études prospectives , Résultat thérapeutique
15.
Rev. esp. enferm. dig ; 103(1): 5-12, ene. 2011. tab, ilus
Article de Espagnol | IBECS | ID: ibc-84891

RÉSUMÉ

Objetivo: analizar la evaluación del abordaje multidisciplinario de un grupo de pacientes con cáncer de páncreas resecado, los resultados postoperatorios y la supervivencia tras la aplicación de un tratamiento multimodal. Diseño: estudio descriptivo prospectivo observacional. Pacientes: entre enero de 2004 y diciembre 2009 se evaluaron 124 pacientes con cáncer de páncreas. De ellos, se realizó la resección pancreática con intención curativa en 30 casos que constituyen el objeto del estudio. Se analizaron los resultados del estudio preoperatorio de extensión tumoral, la morbi-mortalidad postoperatoria, y la supervivencia. Resultados: la evaluación diagnóstica se hizo en régimen ambulatorio en el 20% de los pacientes. En el 63% de los casos, el ingreso fue el mismo día de la intervención. En 3 pacientes intervenidos no se consiguió realizar la resección del tumor (9%), por lo que la tasa de concordancia entre la resecabilidad radiológica y la quirúrgica fue del 91%. La tasa de resecabilidad quirúrgica fue del 24,1%. La mortalidad quirúrgica de la serie fue de un 3,3%, con una morbilidad global del 56,6%. La supervivencia al año, dos, tres y cuatro años fue del 76,2%, 56,3%, 43%, y 27,3% respectivamente. Conclusiones: el desarrollo tecnológico y la evaluación multidisciplinar coordinada, permite realizar una evaluación precisa de la extensión tumoral, y puede reducir el número de laparotomías sin resección del tumor. Con la aplicación de una terapia multimodal sistemática combinada, la resecabilidad quirúrgica y la supervivencia a medio y largo plazo parece que están aumentando de forma progresiva(AU)


Objective: analysis and evaluation of a multidisciplinary approach, postoperative results and survival of a group of patients with resected pancreatic cancer after a multimodal therapy. Design: descriptive, prospective and observational study. Patients: between January 2004 and December 2004, 124 patients with pancreatic cancer were evaluated. In 30 patients pancreatic resection was performed, and they are the object of this study. Results of preoperative evaluation, postoperative morbidity and mortality, and long term survival were studied. Results: diagnostic evaluation was completed in ambulatory basis in 20% of the patients. In 63% of cases, admission was done in the same day of surgery. In 3 patients (9%), tumor resection was not achieved, therefore, concordance between radiological and surgical resectability rate was 91%. Resectability rate was 24.1%. Surgical Mortality was 3.3%, with a global morbidity rate of 56.6%. Survival at one, two, three and, four years was 76.2%, 56.3%, 43%, y 27.3% respectively. Conclusions: technological development and coordination of efforts in multidisciplinary teams offer an accurate evaluation of tumor involvement, and may reduce the number of laparotomies without tumor resection. The application of a systematic and generalized multimodal treatment in pancreatic cancer is progressively showing a tendency of progressive increase in resectability and survival rates in pancreatic cancer(AU)


Sujet(s)
Humains , Mâle , Femelle , Adulte , Adulte d'âge moyen , Sujet âgé , Sujet âgé de 80 ans ou plus , Association thérapeutique/tendances , Association thérapeutique , Signes et symptômes , Tumeurs du pancréas/diagnostic , Tumeurs du pancréas/thérapie , /tendances , Lymphadénectomie , Adjuvants pharmaceutiques/usage thérapeutique , Pancréatectomie/méthodes , Protocoles de polychimiothérapie antinéoplasique/usage thérapeutique , Indicateurs de Morbidité et de Mortalité , Soins postopératoires/tendances , Fistule/thérapie , Pancréatectomie/tendances , Pancréatectomie
16.
HIV Med ; 11(8): 535-9, 2010 Sep.
Article de Anglais | MEDLINE | ID: mdl-20408890

RÉSUMÉ

OBJECTIVES: The acquisition of adequate vaccine-induced humoral immunity is especially important in HIV-infected individuals, who are at increased risk of infections. The aim of the study was to assess the safety of administering a complete vaccination programme to successfully treated HIV-infected adults and to evaluate specific humoral responses and the effect of highly active antiretroviral therapy (HAART) interruption on these responses. METHODS: A placebo-controlled, double-blind clinical trial was designed and 26 HIV-infected adults enrolled. Study participants were randomized to receive either a complete immunization schedule with commercial vaccines or placebo for 12 months. HAART was then discontinued for 6 months. Specific humoral responses were evaluated at baseline, at month 12 and after HAART interruption and compared between groups. RESULTS: There were neither local nor systemic secondary effects related to vaccination. Specific humoral responses to vaccines were adequate, but a loss of immunoglobulin G titres was observed after HAART interruption in 12 study participants. CONCLUSIONS: HAART interruption may cause impairment of previously acquired vaccine-induced immunity in HIV-infected adults.


Sujet(s)
Antirétroviraux/administration et posologie , Thérapie antirétrovirale hautement active , Infections à VIH/immunologie , VIH-1 (Virus de l'Immunodéficience Humaine de type 1) , Vaccins antiviraux/immunologie , Adulte , Antirétroviraux/immunologie , Anticorps antiviraux/immunologie , Numération des lymphocytes CD4 , Femelle , Infections à VIH/traitement médicamenteux , Humains , Immunoglobuline G/sang , Mâle , Adulte d'âge moyen , Placebo , Vaccination , Charge virale
17.
Nucleic Acids Res ; 38(Database issue): D563-9, 2010 Jan.
Article de Anglais | MEDLINE | ID: mdl-19884133

RÉSUMÉ

Ensembl Genomes (http://www.ensemblgenomes.org) is a new portal offering integrated access to genome-scale data from non-vertebrate species of scientific interest, developed using the Ensembl genome annotation and visualisation platform. Ensembl Genomes consists of five sub-portals (for bacteria, protists, fungi, plants and invertebrate metazoa) designed to complement the availability of vertebrate genomes in Ensembl. Many of the databases supporting the portal have been built in close collaboration with the scientific community, which we consider as essential for maintaining the accuracy and usefulness of the resource. A common set of user interfaces (which include a graphical genome browser, FTP, BLAST search, a query optimised data warehouse, programmatic access, and a Perl API) is provided for all domains. Data types incorporated include annotation of (protein and non-protein coding) genes, cross references to external resources, and high throughput experimental data (e.g. data from large scale studies of gene expression and polymorphism visualised in their genomic context). Additionally, extensive comparative analysis has been performed, both within defined clades and across the wider taxonomy, and sequence alignments and gene trees resulting from this can be accessed through the site.


Sujet(s)
Biologie informatique/méthodes , Bases de données génétiques , Bases de données d'acides nucléiques , Animaux , Biologie informatique/tendances , Expression des gènes , Génome bactérien , Génome fongique , Génome végétal , Mémorisation et recherche des informations/méthodes , Internet , Invertébrés/génétique , Polymorphisme génétique , Structure tertiaire des protéines , Logiciel
18.
Nucleic Acids Res ; 37(Database issue): D690-7, 2009 Jan.
Article de Anglais | MEDLINE | ID: mdl-19033362

RÉSUMÉ

The Ensembl project (http://www.ensembl.org) is a comprehensive genome information system featuring an integrated set of genome annotation, databases, and other information for chordate, selected model organism and disease vector genomes. As of release 51 (November 2008), Ensembl fully supports 45 species, and three additional species have preliminary support. New species in the past year include orangutan and six additional low coverage mammalian genomes. Major additions and improvements to Ensembl since our previous report include a major redesign of our website; generation of multiple genome alignments and ancestral sequences using the new Enredo-Pecan-Ortheus pipeline and development of our software infrastructure, particularly to support the Ensembl Genomes project (http://www.ensemblgenomes.org/).


Sujet(s)
Bases de données génétiques , Génomique , Animaux , Variation génétique , Humains , Internet , Alignement de séquences
19.
Rev Esp Enferm Dig ; 100(7): 411-5, 2008 Jul.
Article de Anglais | MEDLINE | ID: mdl-18808288

RÉSUMÉ

OBJECTIVE: to report on the first liver resection performed on a human being by a transvaginal NOTES approach combined with minilaparoscopy. PATIENTS AND METHODS: a sixty-one-year-old woman with a history of Wertheim s hysterectomy for endometrial carcinoma 10 years ago, and malignant melanoma correctly treated in 2006, had suspected segment-V liver metastasis near the gallbladder by CT-scan and MRI. The indication for a laparoscopic approach was made, and a combined transvaginal and minilaparoscopic resection was offered and accepted by the patient. The procedure was performed by a multidisciplinary team composed of surgeons and gastroenterologists. It involved creating a pneumoperitoneum by placing a Veres needle in the umbilical fundus, followed by the insertion of a 5-mm trocar. A second, 3-mm trocar was placed in the right upper quadrant. A lot of pelvic adhesions were found in the major pelvis, and it was necessary to place a third, 5-mm trocar in the left abdominal side. It was employed only for the adhesions, not for liver resection. Adhesions were removed to reveal the minor pelvis and the vaginal fornix. A colpotomy was performed with a 12-mm trocar placed inside the vagina, which allowed the insertion of the videogastroscope as far as the liver hilum. RESULTS: liver resection (segment-V partial resection) and cholecystectomy were performed by using a combination of working tools inserted through the entry port for the minilaparoscopy and the videogastroscope. The en bloc resection was removed transvaginally through the videogastroscope. There were no postoperative complications, and the patient was discharged after 48 hours. CONCLUSIONS: transvaginal liver resection is possible and safe when performed by a multidisciplinary team. Natural orifice transluminal endoscopic surgery (NOTES) is an emerging modality that seeks to be less invasive, better tolerated, and more respectful of esthetics. It will probably open the way for very important medical and technological innovations.


Sujet(s)
Hépatectomie/méthodes , Laparoscopie/méthodes , Femelle , Humains , Adulte d'âge moyen , Vagin
20.
Rev. esp. enferm. dig ; 100(7): 411-415, jul. 2008. ilus
Article de En | IBECS | ID: ibc-70996

RÉSUMÉ

Objetivo: comunicar la primera resección hepática realizadaen humanos mediante cirugía endoscópica transluminal con abordajetransvaginal combinada con minilaparoscopia.Pacientes y métodos: paciente de 61 años de edad con antecedentesde intervención de Wertheim por carcinoma endometriala los 50 años y melanoma maligno correctamente tratado alos 59 años, con sospecha por tomografía y resonancia de metástasishepática en segmento V próxima a la vesícula biliar. Se indicócirugía exerética mediante abordaje laparoscópico y se ofrecióa la paciente abordaje combinado NOTES transvaginal y minilaparoscópico,que aceptó. La intervención fue realizada por unequipo multidisciplinar compuesto por cirujanos y endoscopistas.Se creó el neumoperitoneo mediante aguja de Veres en el fondoumbilical y posteriormente se insertaron dos trócares en el abdomen,transumbilical de 5 mm y en hipocondrio derecho de 3 mm.Se hallaron numerosas adherencias pélvicas que obligaron a colocarun trócar accesorio en el cuadrante inferior izquierdo de 5mm, empleado exclusivamente para la adhesiolisis. Se liberó eidentificó el fondo de saco vaginal y se realizó la entrada vaginalcon trócar de 12 mm que permitió el paso del endoscopio hastael espacio subhepático.Resultados: la resección hepática (hepatectomía limitada ensegmento V) y colecistectomía se realizaron usando una combinaciónde instrumentos endoscópicos y laparoscópicos. La resecciónen bloque fue extraída por vía transvaginal mediante tracciónendoscópica. No existieron complicaciones postoperatorias y lapaciente fue dada de alta a las 48 horas del procedimiento.Conclusiones: la resección hepática transvaginal es posible ysegura cuando la realiza un equipo multidisciplinario con experienciaen estos campos. La cirugía endoscópica transluminal através de orificios naturales (NOTES) es una técnica emergenteque permite realizar el procedimiento con menor invasión en lapared abdominal, mejor tolerancia por el paciente y con un beneficioestético. Será, además, una vía de importantes avances parala medicina y la innovaciones tecnológicas


Objective: to report on the first liver resection performed ona human being by a transvaginal NOTES approach combinedwith minilaparoscopy.Patients and methods: a sixty-one-year-old woman with a historyof Wertheim’s hysterectomy for endometrial carcinoma 10years ago, and malignant melanoma correctly treated in 2006, hadsuspected segment-V liver metastasis near the gallbladder by CTscanand MRI. The indication for a laparoscopic approach wasmade, and a combined transvaginal and minilaparoscopic resectionwas offered and accepted by the patient. The procedure was performedby a multidisciplinary team composed of surgeons and gastroenterologists.It involved creating a pneumoperitoneum by placinga Veres needle in the umbilical fundus, followed by the insertionof a 5-mm trocar. A second, 3-mm trocar was placed in the rightupper quadrant. A lot of pelvic adhesions were found in the majorpelvis, and it was necessary to place a third, 5-mm trocar in the leftabdominal side. It was employed only for the adhesions, not for liverresection. Adhesions were removed to reveal the minor pelvisand the vaginal fornix. A colpotomy was performed with a 12-mmtrocar placed inside the vagina, which allowed the insertion of thevideogastroscope as far as the liver hilum.Results: liver resection (segment-V partial resection) and cholecystectomywere performed by using a combination of workingtools inserted through the entry port for the minilaparoscopy andthe videogastroscope. The en bloc resection was removed transvaginallythrough the videogastroscope. There were no postoperativecomplications, and the patient was discharged after 48 hours.Conclusions: transvaginal liver resection is possible and safewhen performed by a multidisciplinary team. Natural orifice transluminalendoscopic surgery (NOTES) is an emerging modality thatseeks to be less invasive, better tolerated, and more respectful ofesthetics. It will probably open the way for very important medicaland technological innovations


Sujet(s)
Humains , Femelle , Adulte d'âge moyen , Hépatectomie/méthodes , Laparoscopie , Vagin
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