The aim of this study was to test the influence of bleeding on the flesh quality of common carp. For the assessment of the influence of bleeding on the colour, spectrophotometrical measuring was used. The sensory quality was evaluated to an ISO 8529 standard by a trained staff member of the Institute of Aquaculture and Protection of Water. Both raw and cooked samples were evaluated. Microbiological analysis was done according to ISO 4833 standard and lipid oxidation measured by TBARS. The influence of the bleeding was observed in all colour parameters (L*, a* and b*). The average of L* values was 43.7 +- 1; 42.7 +- 1, a 43 +- 0.9 in bled group and 37.51 +- 0.54; 37.98 +- 0.79; 37.42 +- 0.6 in unbled. The average of a* values was -1.4 +- 0.2; -1.6 +- 0.2; -0.9 +- 0.4 in the bled group and 4.5 +- 2.3; 3.6 +- 1.6; 7.4 +- 1 in the unbled group. A significant difference (p < 0.05) between groups was observed in all days of study in the L* and a* parameter. In the b* parameter there was a difference observed just in the first nine days. A significant difference (p < 0.05) between the bled and the unbled groups was observed in all criteria on the raw sample on the 1st and 3rd days. Cooked samples were significantly different (p < 0.05) just on the 6th day of study. Microbiological results came up to 4 +- 0.2 log CFU.g-1 in the bled group and 6.3 +- 0.1 log CFU.g-1 in the unbled group. The influence of bleeding was shown in lipid oxidation too. At the end of the study TBARS values were 17.8 +- 8.8 ug.kg-1 of the sample in the bled group and 39.9 +- 6.4 ug.kg-1 of the sample in the unbled group. In both groups, exponential growth was shown. The influence of bleeding was observed in all parameters. It can be stated that the bleeding has a positive influence on the flesh quality of common carp. In order to convert these results into practice, further studies to optimize the bleeding process are needed.

A uremia é uma desordem sistêmica que pode estar associada à disfunção plaquetária adquirida, levando a alterações na hemostasia primária. Vários modelos de interferência entre a uremia e a falha na hemostasia já foram propostos, porém o mecanismo exato é desconhecido, e a tendência ao sangramento parece ser de origem multifatorial. O teste do tempo de sangramento da mucosa oral (TSMO) pode ser utilizado na avaliação da hemostasia primária em animais. O fator de von Willebrand (FvW:Ag) normal ou aumentado, observado na maioria dos cães urêmicos, contribui para o diagnóstico de uma alteração plaquetária adquirida. A contagem de plaquetas e os testes de coagulação normais associados a um aumento no TSMO dão suporte à suspeita de um defeito qualitativo. O objetivo deste trabalho foi investigar possíveis anormalidades na hemostasia, buscando estabelecer uma relação entre os resultados de exames laboratoriais e alterações no tempo de sangramento. A hemostasia foi avaliada em quarenta cães azotêmicos, urêmicos ou não. O aumento no TSMO foi observado em 35% dos cães azotêmicos. O teste de Spearman demonstrou haver correlação entre o TSMO e os valores de creatinina, uréia e hematócrito, porém, o ajuste pela Regressão Linear Múltipla evidenciou o hematócrito como única variável associada com o TSMO. Valores de hematócrito abaixo do intervalo de referência para a espécie foram observados em 92,86% dos pacientes que apresentaram aumento no TSMO. Esses valores reduzidos parecem contribuir para a tendência ao sangramento, embora não possam ser considerados como fator determinante preditivo, uma vez que sua ocorrência nem sempre se associou com interferências no TSMO. / Uremia is a systemic disorder that may be associated with acquired platelet dysfunction, leading to changes in primary hemostasis. Several interference models between uremia and hemostasis failure have been proposed, but the exact mechanism is unknown, and bleeding tendencies seem to have a multifactorial origin. The buccal mucosal bleeding time (BMBT) test can be used in the assessment of primary hemostasis in animals. Normal or increased von Willebrand factor (vWF:Ag), observed in most uremic dogs, contributes to the diagnosis of an acquired platelet alteration. Normal platelet counts and coagulation tests associated with BMBT raises support the suspicion of a qualitative defect. The aim of this study was to investigate possible hemostasis abnormalities, trying to establish a relation between the results of laboratory tests and changes in bleeding times. Hemostasis was evaluated in forty azotemic dogs, uremic or not. Increase in BMBTs was observed in 35% of the azotemic dogs. Spearman’s test showed a correlation between BMBT and the values of creatinine, urea and hematocrit; however, adjusting for Multiple Linear Regression showed hematocrit as the only variable associated with BMBT. Hematocrit values below reference range for the species was observed in 92,86% of the patients showed an increase in BMBT. These low values appear to contribute to the tendency to bleed, although they cannot be considered as a preditive determining factor, since their occurrence is not always associated with interference in BMBT.

Base teórica: O tratamento dos pacientes hemofílicos no Brasil apresentou avanços importantes nos últimos anos. Passamos de uma realidade de tratamento sob demanda, com quantitativos de fatores de coagulação insuficientes segundo o preconizado pela Federação Mundial de Hemofilia, para uma situação de programas de profilaxia primária, imunotolerância e fatores de coagulação recombinantes. A análise dos dados obtidos através do registro dos pacientes origina as informações imprescindíveis à concepção, gestão e avaliação de um programa público desta monta. O Ministério da Saúde, através do Perfil das Coagulopatias Hereditárias no Brasil, tem publicado de forma sistemática os resultados da compilação dos dados enviados pelos diferentes centros de tratamento do país. Nessas publicações ficam evidentes o sub-registro, ou a subavaliação, de dados clínicos imprescindíveis ao adequado tratamento destes pacientes. Objetivo: Avaliar as características epidemiológicas e clínicas dos pacientes portadores de hemofilia no estado do Rio Grande do Sul, no período de 01 de janeiro de 2003 a 31 de dezembro de 2007, uma vez que não foram encontrados estudos epidemiológicos publicados sobre a realidade nacional ou regional dos pacientes hemofílicos, anteriores ao acima descrito, em nosso país. Métodos: Este estudo avaliou de forma histórica os pacientes com diagnóstico de hemofilia no estado do Rio Grande do Sul. Foram consultados dois bancos de dados: o cadastro de portadores de coagulopatias hereditárias do Hemocentro do Estado do Rio Grande do Sul (HEMORGS), bem como seus registros de prontuário, e os arquivos do Laboratório de Hemostasia do Departamento de Genética da Universidade Federal do Rio Grande do Sul. Foram incluídos no estudo todos os pacientes cadastrados no HEMORGS até 31/12/2007 e aqueles cujo exame realizado no Laboratório de Hemostasia do Departamento de Genética da Universidade Federal do Rio Grande do Sul confirmou o diagnóstico de hemofilia e que ainda não haviam sido cadastrados. O registro constou de dados demográficos como data de nascimento, idade, raça/cor, sexo, data do diagnóstico, procedência e local de tratamento. Também foram levantados a prevalência de complicações crônicas da hemofilia como acometimento musculoesquelético, presença de inibidores e infecções relacionadas às transfusões ou infusões de fatores de coagulação e os produtos empregados na terapêutica, tais como fatores de coagulação liofilizados derivados de plasma humano e recombinantes, antifibrinolíticos, hemocomponentes e outros. Por fim, os óbitos ocorridos nos últimos cinco anos também foram analisados. Conclusão: Os recentes avanços no tratamento da hemofilia no Brasil são inegáveis. Entretanto, o impacto destes avanços na situação clínica e qualidade de vida dos pacientes hemofílicos serão de difícil avaliação, uma vez que são poucos os estudos que avaliam as condições clínicas e complicações relacionadas ao tratamento destes. Os dados obtidos através dos Perfis das Coagulopatias Hereditárias no Brasil, indicam claramente o sub-registro e a sub-avaliação nesta população de pacientes. Neste trabalho, realizamos um amplo perfil epidemiológico e clínico da população de pacientes portadores de hemofilia no estado do Rio Grande do Sul em um período não compreendido por estudos prévios. / Theoretical basis: The treatment of hemophilia patients in Brazil has made important advances in recent years. At first the treatment was on demand with insuficent clotting factors according to the World Federation of Hemophilia, than the reality changed improving considerably including primary prevention programs, immune tolerance and sufficient recombinant clotting factors. The analysis of data obtained from the patient record information are essential to the design, management and evaluation of a public health program. The Ministry of Health (MOH), through the Profile of Hereditary Coagulopathies in Brazil, has published systematically the data compilation, results reported by the country's different treatment centers. These publications demonstrate underreporting, or underdiagnosis, data essential to provide adequate treatment for these patients. Objective: To evaluate the epidemiological and clinical characteristics of patients with hemophilia in the state of Rio Grande do Sul, from January 1, 2003 to December 31, 2007, since there are no epidemiological studies on the national reality or regional of hemophiliacs, patients prior to the above, in our country. Methods: This study evaluated the medical records of patients diagnosed with hemophilia in the state of Rio Grande do Sul. Two databases were consulted: The registration of patients with hereditary the Blood Bank of the Rio Grande do Sul State coagulopathies (HEMORGS) and the Hemostasis Laboratory of the Department of Genetics of the Federal University of Rio Grande do Sul files. The study included all patients enrolled in HEMORGS until 31/12/2007 and those whose examination conducted in the Laboratory hemostasis of the Genetics Department of the Federal University of Rio Grande do Sul confirmed the diagnosis of hemophilia and who had not yet been registered. We retrieved data in regard to age, skin color, sex, date of diagnosis, origin and place of treatment, prevalence of chronic complications including musculoskeletal involvement, presence of inhibitors and infections related to transfusion or infusion of coagulation factors and products used in therapy, such as coagulation factors lyophilized derived from human and recombinant plasma antifibrinolytic agents, and other blood components. Also, the deaths in the past five years were also analyzed. Conclusion: Recent advances in the treatment of hemophilia in Brazil are undeniable. However, the impact of these advances in the clinical situation and quality of life of hemophilia patients are difficult to assess, since there are few studies evaluating the clinical conditions and treatment-related complications. The data obtained from the Hereditary Coagulopathies profiles in Brazil, clearly indicate underreporting and under-estimation in this patient population. We carried out an extensive clinical and epidemiological profile of the population of patients with hemophilia in Rio Grande do Sul state in a period not investigated by previous studies.

A uremia é uma desordem sistêmica que pode estar associada à disfunção plaquetária adquirida, levando a alterações na hemostasia primária. Vários modelos de interferência entre a uremia e a falha na hemostasia já foram propostos, porém o mecanismo exato é desconhecido, e a tendência ao sangramento parece ser de origem multifatorial. O teste do tempo de sangramento da mucosa oral (TSMO) pode ser utilizado na avaliação da hemostasia primária em animais. O fator de von Willebrand (FvW:Ag) normal ou aumentado, observado na maioria dos cães urêmicos, contribui para o diagnóstico de uma alteração plaquetária adquirida. A contagem de plaquetas e os testes de coagulação normais associados a um aumento no TSMO dão suporte à suspeita de um defeito qualitativo. O objetivo deste trabalho foi investigar possíveis anormalidades na hemostasia, buscando estabelecer uma relação entre os resultados de exames laboratoriais e alterações no tempo de sangramento. A hemostasia foi avaliada em quarenta cães azotêmicos, urêmicos ou não. O aumento no TSMO foi observado em 35% dos cães azotêmicos. O teste de Spearman demonstrou haver correlação entre o TSMO e os valores de creatinina, uréia e hematócrito, porém, o ajuste pela Regressão Linear Múltipla evidenciou o hematócrito como única variável associada com o TSMO. Valores de hematócrito abaixo do intervalo de referência para a espécie foram observados em 92,86% dos pacientes que apresentaram aumento no TSMO. Esses valores reduzidos parecem contribuir para a tendência ao sangramento, embora não possam ser considerados como fator determinante preditivo, uma vez que sua ocorrência nem sempre se associou com interferências no TSMO. / Uremia is a systemic disorder that may be associated with acquired platelet dysfunction, leading to changes in primary hemostasis. Several interference models between uremia and hemostasis failure have been proposed, but the exact mechanism is unknown, and bleeding tendencies seem to have a multifactorial origin. The buccal mucosal bleeding time (BMBT) test can be used in the assessment of primary hemostasis in animals. Normal or increased von Willebrand factor (vWF:Ag), observed in most uremic dogs, contributes to the diagnosis of an acquired platelet alteration. Normal platelet counts and coagulation tests associated with BMBT raises support the suspicion of a qualitative defect. The aim of this study was to investigate possible hemostasis abnormalities, trying to establish a relation between the results of laboratory tests and changes in bleeding times. Hemostasis was evaluated in forty azotemic dogs, uremic or not. Increase in BMBTs was observed in 35% of the azotemic dogs. Spearman’s test showed a correlation between BMBT and the values of creatinine, urea and hematocrit; however, adjusting for Multiple Linear Regression showed hematocrit as the only variable associated with BMBT. Hematocrit values below reference range for the species was observed in 92,86% of the patients showed an increase in BMBT. These low values appear to contribute to the tendency to bleed, although they cannot be considered as a preditive determining factor, since their occurrence is not always associated with interference in BMBT.

Introdução: Acretismo placentário é condição pouco frequente na qual há aderência anormal do tecido trofoblástico à parede uterina. É uma causa importante de hemorragia puerperal, associada a altas taxas de morbimortalidade maternofetal, grande necessidade de transfusão de hemoconcentrados. Os tratamentos propostos variam desde conduta conservadora até a histerectomia pós-parto, associada ou não a procedimentos endovasculares. Objetivo: O presente estudo visa descrever a técnica endovascular de balonamento temporário e embolização das artérias ilíacas internas durante o parto cesáreo, avaliar sua eficácia em reduzir o sangramento materno relacionado ao acretismo placentário, bem como relatar a segurança e o índice de complicações relacionadas ao tratamento endovascular. Materiais e métodos: Coorte retrospectiva de pacientes com diagnóstico pré-natal de acretismo placentário submetidas a tratamento endovascular de balonamento temporário e embolização das artérias ilíacas internas, seguido de histerectomia puerperal no nosso serviço, no período de janeiro de 2012 até novembro de 2016. Foram analisados dados relativos aos antecedentes gestacionais e cirúrgicos, achados de exames de imagem, achados histológicos, níveis de hemoglobina prévios, durante e após o parto, bem como volumes de hemoconcentrados administrados e taxa de complicações relacionadas ao procedimento endovascular. Resultados: Trinta e Siqueira FM 7 cinco pacientes foram submetidas ao manejo proposto durante o período estudado. Foi observado um volume médio de transfusão relacionado ao procedimento e perda sanguínea estimada de 540 ml e 1229 ml, respectivamente. Ocorreram complicações relacionadas ao procedimento endovascular em quatro pacientes, sendo um caso de necrose muscular glútea, um de lesão isquêmica cutânea superficial e dois casos de trombose arterial aguda de membros inferiores. Conclusão: O presente estudo demonstrou que o balonamento temporário e embolização das artérias ilíacas internas reduziu significativamente as necessidades transfusionais relacionadas ao parto nas pacientes com acretismo placentário, quando comparado com casos da literatura nos quais não foram realizadas intervenções endovasculares, com baixo índice de complicações relacionadas ao procedimento. / Introduction: Placenta accreta (PA) is the infrequent condition in which there is abnormal adherence of the trophoblastic tissue to the uterine wall. It\'s considered a major cause of puerperal bleeding, associated with high maternal morbimortality and need for blood products transfusion. Proposed treatments range from conservative to postpartum hysterectomy, combined or not to endovascular techniques. Objectives: to describe the detailed endovascular technique of temporary balloon occlusion followed by embolization of the internal iliac arteries (IIA) during cesarean section, evaluate the ability in reducing birth-related blood loss in patients with diagnosed PA and to assess safety and complications related to the endovascular procedure. Materials and methods: retrospective cohort of patients diagnosed with PA submitted to temporary balloting and embolization of the IAA followed by puerperal hysterectomy in our institution from January 2012 to November 2016. We recorded patient data such as gestational and surgical history, pre-natal radiological image findings, histopathological description, pre e postoperative hemoglobin levels and volume of blood products transfused in all patients. Follow up accounted for possible complications related to the procedure. Results: thirty-five patients were submitted to the approach during the study period. The median volume of packed red blood cells (RBC) and estimated blood loss were 540 ml and 1229 ml respectively. A total of 4 patients had complications attributed to the endovascular procedure - one case of Siqueira FM 9 deep glute tissue necrosis, one of superficial tissue necrosis and two cases of acute arterial thrombosis of the inferior limbs. Conclusion: the present study demonstrated that temporary ballooning and embolization of the IAA was able to significantly reduce birth-related blood loss and transfusion needs in patients with PA when compared to other literature series where no endovascular procedures were performed, with a low rate of procedure-related complications.

L’étude de l’identification des défauts moléculaires mis jeu dans les pathologies héréditaires plaquettaires est d’un apport considérable pour améliorer la compréhension des mécanismes physiologiques. Durant ma thèse, j’ai étudié les plaquettes d’individus appartenant à deux familles distinctes souffrant de dysfonctions plaquettaires à l’origine d’hémorragies sévères. Par séquençage entier des exons, nous avons identifié pour la première famille une mutation du gène RASGRP2 à l’origine de la substitution Gβ48W empêchant l’activation de CalDAG-GEFI. Les plaquettes des individus porteurs de la mutation à l’état homozygote ont une capacité réduite à activer Rap1 et l’intégrine αIIbß3 en réponse à de faibles doses d'agonistes. La présence d'un allèle non muté (hétérozygotie) est suffisante pour prévenir lessaignements mais ne permet pas de rétablir totalement une fonction plaquettaire normale. La deuxième famille est porteuse d’une mutation du gène FERMT3 (pN54RfsX142) conduisant à une absence complète de kindline-3. Les plaquettes homozygotes pour cette mutation sont incapables d’activer l’intégrine αIIbß3. Elles forment des filopodes et desnodules d’actine mais ne peuvent étendre des lamellipodes même en présence de Mn2+. La kindline-3 s’est révélée essentielle à la régulation de l’activité de Cdc4β et au réarrangement au cytosquelette d'actine lors de la signalisation «outside-in» de l’intégrineαIIbß3. Seule la kindline-3 a jusqu’ici été impliquée dans l'activation des intégrinesplaquettaires. Nous mettons en évidence la présence de kindline-2 dans les plaquettes et les mégacaryocytes humains. Des localisations différentes ont été mises en évidence pour ces deux kindlines. Dans le mégacaryocyte la kindline-2 se situe dans les zones d’adhérence focales et s’associe préférentiellement avec les intégrines ß3. Dans les plaquettes, seule la kindline-3 est présente dans nodules d’actine. Ces résultats sont en faveur de rôles non redondants des kindlines-2 et -γ et d’une implication potentielle de la kindline-2 dans la mégacaryopoïèse. / Inherited platelet disorders are rare diseases that give rise to severe bleeding when platelets fail to fulfill their hemostatic function upon vessel injury. Identifying the molecular mechanisms involved brings important insight into platelet pathophysiology. During my PhD, I studied platelets isolated from members of two families suffering severe bleedings among those one had no established diagnosis. In the first family, using whole exome sequencing, we identified a RASGRP2 mutation causing a G248W substitution leaving CalDAG-GEFI inactive. Platelets from individualscarrying the mutation exhibit a reduced ability to activate Rap1 and to perform proper Inherited platelet disorders are rare diseases that give rise to severe bleeding when platelets fail to fulfill their hemostatic function upon vessel injury. Identifying the molecular mechanisms involved brings important insight into platelet pathophysiology. During my PhD, I studied platelets isolated from members of two families suffering severe bleedings among those one had no established diagnosis. In the first family, using whole exome sequencing, we identified a RASGRP2 mutation causing a G248W substitution leaving CalDAG-GEFI inactive. Platelets from individuals carrying the mutation exhibit a reduced ability to activate Rap1 and to perform proper αIIbß3 integrin inside-out signaling in response to low doses agonists. The presence of a single normal allele is sufficient to prevent bleeding but does not allow normal platelet function. integrin inside-out signaling in response to low doses agonists. The presence of a single normal allele is sufficient to prevent bleeding but does not allow normal platelet function. Members of the second family carry a FERMT3 mutation leading to a completekindlin-3 deficiency (pN54RfsX142). Platelets from the homozygous patient are unable to perform proper integrin αIIbß3 activation. We now observe that kindlin-3 deficient platelets form filipodia and actin nodules but are unable to extend lamellipodia even in presence of Mn2+. We demonstrate that kindlin-3 is essential for Cdc42 activity regulation and actincytoskeleton remodeling during αIIbß3 integrin outside-in signaling To date, only the kindlin-3 has been involved in integrin activation. We show that kindlin-2 is present in human platelets and megakaryocytes. Both kindlins exhibit distinctlocalizations. In megakaryocytes, kindlin-2 specifically localizes within focal adhesion and associates preferentially with ß3 integrins. In platelets, unlike kindline-2, kindline-3 is located in actin nodule. All together these data argue in favor of specific roles played by each kindlins and a possible implication of kindlin-2 in megakaryocytopoiesis.

Severe congenital heart disease (CHD) is diagnosed in the United States 147.4 times per 100,000 live births, excluding still births and abortions^1. With the advancement of diagnostic methods, prenatal care, and screening modalities, the total CHD birth prevalence has increased substantially^2. In turn, this increases the number of cardiac surgery cases. With the advancement of technology and cardiac surgery, smaller and younger patients are undergoing more complex cardiac procedures that involve cardiopulmonary bypass (CPB). Neonates and infants undergoing CPB are susceptible to adverse effects of CPB on the coagulation cascade due to their smaller weight and hematologic immaturity^3,4. In addition to these physiological issues in neonates and infants, CPB decreases circulating coagulation factors and anti- thrombin III levels to 50% and platelet counts to 70%^5, which can contribute to the post-operative bleeding.During CPB, neonates' and infants' coagulation factors become extremely diluted causing multiple coagulation defects^6. Optimizing the CPB circuit volume and the use of anti-fibrinolytic, packed red blood cells (pRBCs), platelets, cryoprecipitate, and ultrafiltration are among the most widely used methods in preserving and aiding coagulation factors^3,7-9. Another method of improving hemodilution-related coagulation dysfunction bleeding is by transfusing Fresh Frozen Plasma (FFP)^10. However, there are only a small number of articles focusing on the effect of FFP in post-operative bleeding in neonates and infants following complex cardiac surgery with CPB. I postulate that adding FFP during CPB will lower the possibility of patients to experience post-operational bleeding, thus, shortening their length of stay (LOS).

Magister Curationis - MCur / Increasing numbers of unintended pregnancies are occurring due to contraceptive failure. Unsafe abortion remains one of the top five avoidable patient-related causes of maternal death in South Africa. There are much higher reported failure rates for short-acting methods of contraceptives than long-acting methods of contraceptives; the uptake of long-acting methods of contraception though remains low.

Introducción: La hemorragia digestiva alta (HDA) es una de las emergencias más frecuentes en medicina. Parte de su abordaje incluye la realización de una segunda endoscopia de control programada llamada “second look” (SL) con el propósito de reducir la incidencia de resangrado. No obstante, existe controversia en cuando su indicación y utilidad. Objetivo: Evaluar la efectividad del SL en la prevención del resangrado intrahospitalario en pacientes adultos con HDA no variceal. Métodos: Se llevó a cabo un estudio de cohorte retrospectivo sobre 1 144 pacientes con diagnóstico de HDA admitidos en la Unidad de Hemorragia Digestiva de un centro de referencia de la Seguridad Social en Lima, Perú; durante los años 2012 y 2014. La variable de respuesta fue el resangrado y la variable de exposición fue la programación a SL. Además se midió la hemoglobina al ingreso, comorbilidades, trasfusión de paquetes globulares y variables endoscópicas. Se calculó la incidencia acumulada (IA), riesgo relativo (RR), efectividad y mediante un modelo lineal generalizado de familia Poisson link log con errores estándar robustos se estimaron razones de tasas de incidencia (RTI). Resultados: La IA global de resangrado fue de 24,48% (n=280). Se encontró diferencia significativa entre las incidencias acumuladas (IA) entre el grupo de SL y el grupo de control (11,7 % vs 29,0 %, respectivamente, p<0,01). El RR fue 0,40 (IC95%:0,29-0,56) y la efectividad fue de 59,81% (IC95%: 44,17-71,08). En los modelos de regresión también se encontró una disminución de las tasas de incidencia tanto en el modelo crudo (RTI: 0,34 IC95%: 0,24-0,49), como en el modelo ajustado con diferencia estadística significativa entre los sometidos y no sometidos a SL (RTI: 0,12 IC95%: 0,08-0,18), por las variables asociadas con el resangrado (RTI: 0,21 IC95%: 0,15-0,30) y por las variables que cumplían los criterios clásicos de confusión (RTI: 0,12 IC95%: 0,08-0,18). Conclusiones: El SL es efectivo en la prevención de resangrado intrahospitalario en pacientes adultos con HDA en un hospital de referencia nacional. / Background: Upper gastrointestinal bleeding (UGIB) is one of the most common medical emergencies. Part of its approach includes performing a second endoscopy, known as second look (SL). However, its indications and usefulness are controversial. Objectives: To evaluate the effectiveness of SL in preventing nosocomial rebleeding in adult patients with non-variceal upper gastrointestinal bleeding. Methods: A retrospective cohort of 1144 patients diagnosed with UGIB admitted at a Digestive Bleeding Unit of a reference center for Social Security in Lima, Peru was performed; during the years 2012 and 2014. The response variable was rebleeding and the exposure variable was programmed SL. Besides hemoglobin on admission, comorbidities, blood transfusion and endoscopic variables were measured. The cumulative incidence, relative risk (RR) and effectiveness were calculated, and using a generalized linear model of the Poisson family link log with robust standard errors, incidence rate ratios (IRR) were estimated. Results: The cumulative incidence rebleeding overall was 24.48% (n = 280). Significant difference between the cumulative incidences (IA) between the SL group and the control group (11.7% vs 29.0%, respectively, p <0.01) was found. The RR was 0.40 (95% CI 0.29 - 0.56) .The calculated effectiveness was 59.81% (95% CI: 44.17 - 71.08). The regression models also found a decrease in incidence in both crude model (IRR: 0.34 95% CI 0.24 to 0.49) and in the adjusted models. The first model was adjusted for variables with statistically significant differences between exposed and unexposed (IRR: 0.12 95% CI 1.8 to 0.18), the second was adjusted for variables that were significantly associated with rebleeding (IRR 0.21 95% CI 0.15-0.30). The third model was adjusted for variables that met classical criteria of confusion (IRR: 0.12 95% CI 0.08 to 0.18). / Tesis

The principles of neurosurgical and neurointensive care liquorology We observed the development of the cerebrospinal fluid (CSF) patterns in 120 patients after bleeding in the CNS (central nervous system). We used our original cytological- energetic principle to investigate 1453 samples of the CSF from these patients. The principal aim of our investigation is the detection of immunocompetitive cells in the CSF and the specification of their activation via the coefficient of energy balance (KEB). Furthermore we evaluated the numbers of erythrocytes and leucocytes in the CSF and also the catalytic activities of the aspartate aminotranspherase (AST) in the CSF as biomarkers of structural disorder of the CNS. Our goal was to evaluate a three week long development of the CSF patterns to gain more accurate information for a more effective therapy and for a better prediction of further clinical development of these patients. We confirmed that following biomarkers were unfavourable for the development of the CSF compartment and probably the CNS as a whole: higher extent of bleeding in the CNS; higher frequency of the neutrophile granulocytes in the CSF compartment; higher extent of anaerobic metabolism in the CSF compartment; higher level of the catalytic activity of the AST in the CSF; higher age...