Bakgrund: Senior alert är ett nationellt kvalitetsregister som avser att förebygga trycksår, fall, undernäring, ohälsa i munnen och blåsdysfunktion hos patienter över 65 år. För att identifiera dessa riskområden används olika bedömningsinstrument och sjuksköterskor ansvarar för att registreringarna genomförs och att förebyggande åtgärder sätts in. Syfte: Studiens syfte var att studera sjuksköterskors upplevelse av att arbeta med kvalitetsregistret Senior alert samt hur sjuksköterskorna upplever att arbetet med kvalitetsregistret påverkar vården hos de äldre. Metod: Sex sjuksköterskor verksamma inom Uppsala kommun med erfarenhet av att arbeta med Senior alert intervjuades och en kvalitativ innehållsanalys användes för att bearbeta den insamlade datan.   Resultat: Utifrån den insamlade datan utformades fyra kategorier, Upplevelser av Senior alert som redskap, Senior alert kan förbättras, Tillämpandet av senior alert i praktiken och Arbetet med Senior alert bidrar till ökad vårdprevention och sju underkategorier. Slutsats: Senior alert upplevs som ett bra redskap för att arbeta förebyggande och främja teamarbete, men uppfattas som tidskrävande. Sjuksköterskorna i den här studien anser att vården av de äldre förbättras då identifiering av riskområden sker tidigt och åtgärder sätts in. För att kunna göra resultatet överförbart och veta på vilket sätt vården förbättras behövs ett större urval och frågor som är utformade för att kunna besvara syftet. / Background: Senior Alert is a quality registry which aims to prevent pressure ulcers, falling, malnutrition, bad oral health and urinary incontinence among patients over 65 years. To identify these areas different evaluation tools are used and nurses are responsible for the registrations and making sure preventive actions are made. Aim: The aim of this study was to describe how nurses experience working with the quality registry Senior Alert and how it affects the care of the elderly. Methods: Six nurses working in Uppsala county with experience of working with Senior Alert was interviewed. The interviews were analyzed using a qualitative content analysis. Results: Four categories, Senior Alert as a tool, Senior Alert needs improvement, Working with Senior Alert and Senior Alert contributes to a better health care and seven subcategories were identified. Conclusions: The respondents found Senior Alert to be a helpful tool for preventive work and that it promotes teamwork, but is perceived as time consuming. The nurses in this study think that the care of the elderly improves by early identification and preventive actions, but to do this, study-result transferability and knowing in what way the care will improve it will need a larger target group and more questions to answer the aim of the study.

Unicompartmental knee replacement (UKR) is the principal alternative to total knee replacement (TKR) in the treatment of end-stage knee osteoarthritis. It involves less tissue resection, resulting in lower rates of morbidity and faster recoveries compared to TKR. However, UKR has a significantly higher revision rate compared to TKR. As a result, whilst over a third of patients are eligible for UKR, only around 8% receive it. A comprehensive comparison of matched patients undergoing TKR and UKR was undertaken using a large dataset from the National Joint Registry for England and Wales (NJR). Failure rates (revision, reoperation, complications and mortality), length of stay and patient-reported outcomes (PROMs) were studied. Whilst patients undergoing TKR had lower reoperation and revision rates, they had higher rates of morbidity and mortality, longer hospital stays, and inferior PROMs compared to UKR. The main reason for revision in UKR was loosening. In view of the high revision rate in UKR, NJR data was studied to identify modifiable risk factors for failure in UKR. Important patient factors were identified including age, gender and pre-operative function. Surgeons with a higher UKR caseload had significantly lower revision rates and superior patient-reported outcomes. Increasing usage (offering UKR to a greater proportion of knee replacement patients) appears to be a viable method of increasing caseload and therefore of improving results. Surgeons with optimal usage (around 50% of patients, using appropriate implants) achieved revision/reoperation rates similar to matched patients undergoing TKR. Two clinical studies were conducted to establish whether the use of cementless fixation would improve fixation and reduce the revision rate of UKR. Cementless UKR was demonstrated to be safe and reliable, with PROMs similar or superior to those demonstrated in cemented UKR. Patients with suboptimal cementless fixation were examined and pre-disposing technical factors were identified. Finally, using NJR data, the effect of the introduction of cementless UKR on overall outcomes was examined. The number of cementless cases was small, and no significant effect on implant survival was demonstrated. However, patients undergoing cementless UKR demonstrated superior PROMs. These studies demonstrate that UKR has numerous advantages over TKR in terms of morbidity, mortality and PROMs. If surgeons perform high volumes of UKR (achievable by increasing their UKR usage), these advantages can be attained without the large difference in revision rates previously demonstrated. Cementless UKR is safe and provides superior fixation and outcomes in the hands of high-volume surgeons. Further work is needed to quantify the revision rate of cementless UKR, and to assess its results in the hands of less experienced surgeons.

"Mémoire présenté à la Faculté des études supérieures en vue de l'obtention du grade de Maîtrise en LL.M. Droit - Recherche option Droit, Biotechnologies et Sociétés" / Les registres médicaux sont des banques de données, ayant des caractéristiques spécifiques, rassemblant tous les cas d'une maladie sur un territoire précis. Ces informations permettent la mise en place de politiques de santé publique ainsi que l'étude de maladies afin de faire progresser la recherche médicale. La question se pose donc de savoir comment la réglementation concernant le respect de la vie privée s'applique aux particularités des registres. La législation actuellement en vigueur au Québec prévoit l'obligation d'obtenir le consentement du patient avant d'inclure les données le concernant dans le registre. Ces renseignements personnels de santé recueillis dans le registre doivent être protégés afin de respecter la vie privée des participants. Pour cela, des mesures concernant la confidentialité et la sécurité des données doivent être mises en place en vue de leur conservation et durant celle-ci. Après l'utilisation principale de ces données, il est possible de se servir à nouveau de ces renseignements personnels à d'autres fins, qu'il faille ou non les transférer vers une autre banque de données, nationale ou étrangère. Néanmoins cette utilisation secondaire ne peut se faire qu'à certaines conditions, sans porter atteinte au droit des participants concernant le respect de la vie privée. / Medical registries are databases which record aIl cases of a specifie disease found in a given area. Registries provide vital information for public health research and for the implementation of appropriate public policies. The question is : How does the regulation of privacy apply to registries? Legislation currently in force in the province of Quebec requires the consent of a patient in order to inc1ude personal information in the registry. Personal health data in a registry have to be protected to preserve the privacy of research subjects. To ensure data security and confidentiality sorne measures must be taken during their conservation. Secondary use of data is possible under certain conditions aimed at protecting the right to privacy. It is possible to use such personal information again for other purposes even if the data need to be transferred to another national or foreign database.

The aim of the diploma thesis is to give readers an idea of cadastral legislation. The main attention is paid to the importance of Land registry for the area of private law. The thesis is logically structured and consists of three separate chapters, subdivided into parts and sections. The first chapter is composed of three parts and contains a historical guide throught the development of real estate records since the perriod of land registry books to the current form of cadastre of real estates. Emphasis is placed on the legal institution of Land registry books, which is the main source of inspiration for the treatment of so-called public directories contained in the new Civil Code. Author of the work include a historical chapter for better understanding of the current form of the cadastre and its main weaknesses. The second chapter is divided into five parts. The first two sections explains the basic concepts (eg, land, plot, building, dwelling unit and non-residential premises unit), and the principles on which the modification of cadastre costs (eg the principle of priority, the principle of formal and material publicity). Remaining three parts of the second chapter deal with the private aspects of the cadastral proceedings. Special emphasis is placed on the entry of legal relations, which is from the...

This thesis analyzes the problem of real property selling in the legal sense under Act No. 89/2012 Coll. compared to Act No. 40/1964 Coll. and also contains their comparison. Firstly, the definition of real property and its transfer under Act 40/1964 Coll. is being examined. This paper deals particularly with new principle of superficies solo cedit and influence it has on real property selling, as well as with real property definition. Further issues covered are material publicity, note of disputability and requirement of written form upon transfer of real estate. At the end this thesis compares selected legal concepts and pros and cons brought by new legislation. title: Legal regulation of sale of property - comparison of current civil code and the proposed new wording of Civil Code keywords: real property, sale, legal concept of superficies solo cedit, material publicity, land registry

La ville d'Antioche fut parmi les villes qui aspiraient une prédominance à la culture, à l'éloquence, à l'enseignement, à l'art mais aussi à l'artisanat et au commerce. Un lieu privilégié de la rencontre avec le reste du monde hellénique et, en même temps, la porte de l'Asie profonde, une ville puissante du Proche-Orient, une base administrative et militaire de premier ordre.Le but est de décrire une ville ottomane formée de quelques quartiers, sa campagne, sa population hétérogène qui vivent essentiellement de l'agriculture, de l'artisanat et du commerce. Une situation décrite dans les registres ottomans conçus au départ pour recenser les foyers fiscaux, les lieux habités, les activités de la population et la production locale, afin de fixer les impôts à récolter. Ce travail est renforcé par des récits de voyage qui décrivent une situation différente, mélancolique et nostalgique à la fois. L'intérêt est de peindre un tableau de la ville tout en essayant de comprendre sa viabilité dans l'espace ottoman. Associés aux sources ottomanes, les textes des voyageurs sont précieux pour un rapprochement des éléments essentiels de l'histoire de la ville.Enfin, pour mieux comprendre la situation de la ville à l'époque ottomane, survoler l'époque mamelouk nous est indispensable. Nous avons ajouté un chapitre sur la chute de la Principauté latine d'Antioche, la division administrative de la Syrie du Nord, la description de la ville par les chroniques et récits de voyage, les bouleversements et la situation générale sous les Mamelouks. Ce chapitre sert de guide afin de tracer un tableau fidèle et jeter la lumière sur une foule de points demeurés obscurs. / The city of Antioch was among the cities that aspired to a predominance culture, eloquence, education, art, but also crafts and trade. A privileged place of encounter with the rest of the Hellenic world, and at the same time, the door of deep Asia, a powerful city of the Middle East, administrative and military order first base.Meanwhile, this work is enhanced by travel stories that describe a different, melancholic and nostalgic at the same time position. The advantage of this formula is to paint a picture of the city while trying to understand the viability of the Ottoman space. Associated with the Ottoman sources, the texts of travelers are valuable for a reconciliation of the essential elements of the history of the city.In this thesis, the goal is not to show again the saga of the metropolis, but to describe an Ottoman town consisted of a few neighborhoods, countryside, its heterogeneous population that lives mainly on agriculture, crafts and trade. A situation described in the Ottoman records originally designed to identify tax households, populated places, the activities of the local population and production, to set taxes to collect.Finally, to better understand the situation of the city in the Ottoman era, fly over the previous period, the Mamluk era, is indispensable. That is why we have added a chapter on the fall of the Latin Principality of Antioch, the administrative division of the northern Syria, the description of the city and tales from travel disruption and the general situation in the Mamluks. This chapter, we consider it useful and interesting to our thesis serves as a guide to draw a fair and shed light on a host of issues remained unclear.

Orientador: Cassiana Mendes Bertoncello Fontes / Resumo: Objetivo Geral: Elaborar um instrumento de registro da Sistematização da Assistência de Enfermagem (SAE) para a Sala de Recuperação Pós-anestésica (SRPA) com Diagnóstico de Enfermagem (DE), Intervenções de Enfermagem (IE) e Resultados de Enfermagem (RE). Objetivos específicos: Realizar o mapeamento cruzado entre a classificação de DE da NANDA-International (NANDA-I) e o conteúdo do registro de enfermagem utilizado na SRPA; Elencar os DE após o mapeamento cruzado; Propor para cada DE eleito as IE e respectivas atividades de enfermagem (AE) e RE e respectivos indicadores de resultados (IR) da Classificação das Intervenções de Enfermagem (NIC) e da Classificação dos Resultados de Enfermagem (NOC). Métodos: Trata-se de um estudo descritivo, exploratório e retrospectivo de análise documental, aprovado pelo Comitê de Ética e Pesquisa das instituições participantes, para a construção de um instrumento de registro manual do enfermeiro em uma SRPA de um hospital de referência em tratamento oncológico e realização de transplante de medula óssea no interior do Estado de São Paulo. O universo foi composto por 264 fichas pertencentes aos prontuários físicos com os dados: sinais vitais, necessidades afetas, prescrição médica e anotações de enfermagem. Os critérios de inclusão foram às fichas completas e preenchidas na SRPA entre 06h e 12h, de segunda-feira a sábado. A amostra constituiu-se por 187 fichas. A pesquisadora coletou os dados de junho a julho de 2018. A análise dos dados constit... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: General Objective: To elaborate a registry of the Systematization of Nursing Assistance (SAE) for the Post-Anesthesia Recovery Room (SRPA) with Nursing Diagnosis (DE), Nursing Interventions (IE) and Nursing Results (RE). Specific Objectives: Carry out the cross-mapping between the NANDA-International classification of ED (NANDA-I) and the content of the nursing record used in the PACU; List EDs after cross-mapping; To propose for each ED elected IH and respective nursing activities (AE) and RE and respective outcome indicators (IR) of the Nursing Interventions Classification (NIC) and the Nursing Results Classification (NOC). Methods: This is a descriptive, exploratory and retrospective study of documentary analysis, approved by the Ethics and Research Committee of the participating institutions, for the construction of a manual registry of nurses in a PACU of a reference hospital in cancer treatment and bone marrow transplantation in the interior of the State of São Paulo. The universe consisted of 264 records belonging to the physical records with the data: vital signs, needs, medical prescription and nursing notes. The inclusion criteria were the complete files completed in the PACU between 06h to 12h from Monday to Saturday. The sample was 187 files. The researcher collected the data from June to July 2018. Data analysis consisted of three steps: The first step was to transcribe data from the files analyzed that represented the signs and/or significant symptoms of nursing... (Complete abstract click electronic access below) / Mestre

The Cadastre of Real estate has relied on a principle of formal publicity for a long time since the Cadastre integrates functions of both land registry and land cadastre. According to some authors, unfettered access to information in the Cadastre is the only possible way to meet its purpose. Such idea is in a violation of a right to privacy and personal data protection that were accepted as fundamental human rights, therefore I am convinced that there exists a necessity to find an equity between the value of privacy and the principle of formal publicity. The diploma thesis deals with contemporary legislation of Cadastre's publicity as well as its prior regulation. Every single important amendment concerning publicity is followed by a comment where I try to criticize it objectively with regard to the personal data protection. The first part of the thesis consists of a description of what a cadastre is and what the word means, history of land registry and land cadastres in the context of predecessors of the Czech Republic and finally the Cadastre of Real estate of the Czech Republic. There is a short section categorizing the principle of formal publicity among other principles applied to the Cadastre at the end of the part as well. The second part explains in general the value of privacy along with...

Introdução - Quando se fala da epidemiologia do suicídio, é importante destacar que as estatísticas oficiais podem estar subestimadas em decorrência de possíveis falhas na identificação e classificação da causa de morte. Objetivo - Investigar a existência de suicídios de adolescentes da cidade de Recife, que tenham sido classificados como óbitos de intencionalidade indeterminada, dos anos de 2000 a 2014, e a percepção dos legistas sobre o fenômeno e sua subnotificação. Metodologia - No Sistema de Informação sobre Mortalidade (SIM) de Recife, foram coletados todos os dados dos óbitos de adolescentes com intencionalidade indeterminada. Em seguida, foi criado um banco de dados com essas informações e, a partir deste, foram localizados, no Instituto de Medicina Legal (IML) de Recife, os documentos (Boletim de Ocorrência, Guia de Remoção de Cadáver, Ofício Policial de Encaminhamento do Corpo ao IML, Livro de Registro de Entrada de Corpos no IML, Laudo Tanatoscópico, Laudo Toxicológico e a guia rosa da Declaração de Óbito) referentes ao percurso que o corpo de cada vítima fez até ter sua morte classificada como indeterminada. Após o exame de cada um desses documentos, foi possível reclassificar 43 (21 por cento ) dos 203 óbitos em questão, utilizando um escore baseado no Índice de Concordância entre as classificações da intencionalidade do óbito registradas nos documentos. Todos os óbitos que apresentaram um percentual de concordância acima de 50 por cento , a partir da consulta aos referidos documentos, tiveram sua intencionalidade reclassificada. Para a definição e reclassificação dos casos, foi utilizada a décima revisão da Classificação Internacional de Doenças (CID-10), na qual os suicídios correspondem aos códigos X60 a X84, sob a denominação de lesões autoprovocadas intencionalmente. Resultados - Dos casos inicialmente classificados como sendo de intencionalidade indeterminada (n=203), 9 por cento (n=19) foram reclassificados como suicídio. A estatística oficial do SIM reporta que, no período estudado, houve apenas 61 suicídios. Contudo, ao somar os 19 suicídios reclassificados ao quantitativo da estatística oficial, tem-se um total de 80 suicídios de adolescentes ocorridos de 2000 a 2014, o que indica um percentual geral de 23,7 por cento de subnotificação. Não houve mudança no perfil das vítimas quando comparamos os dados antes e depois da reclassificação dos casos. Em ambas as situações, o maior contingente de casos de suicídio se concentra no seguinte perfil: adolescentes do sexo masculino, com idades entre 15 e 19 anos e de raça/cor parda. De acordo com os legistas entrevistados, questões como a sobrecarga de trabalho e a quantidade reduzida de recursos humanos são fatores que podem interferir no processo de indeterminação da intencionalidade dos óbitos. Conclusões - A partir da recuperação de informações contidas nos documentos encontrados no IML, foi possível reclassificar a intencionalidade das mortes por causas externas, melhorando a qualidade dos dados do SIM e permitindo a elaboração de um perfil epidemiológico mais fidedigno e condizente com o que ocorre na realidade. Este estudo, portanto, dentre todas as conclusões obtidas, reafirma a necessidade de sensibilizar constantemente os profissionais envolvidos no registro do óbito, para que se tenha um aprimoramento na qualidade das informações em saúde / Introduction - Regarding suicide epidemiology, it is important to highlight that official statistics may be underestimated due to possible mistakes on the identification and classification of the cause of death. Objective - To investigate the existence of suicide cases among adolescents in the city of Recife, which had been classified as undetermined intentionality deaths, from the years 2000 to 2014, and the perception of the medical examiners on the phenomenon and its sub notification. Methodology - In the Mortality Information System (SIM) in Recife, all data from adolescent deaths with undetermined intentionality was collected. Afterward, a databank with all this information was created and, from there, the documents could be located in the Medico-Legal Institute (IML) in Recife: the Event bulletin, the Body Removal document, the Police document for Corpse Entry in IML, the Registry Book for Corpse Entry in IML, the Cause of Death and Toxicology reports and the pink version of the Death Certificate; all these documents refer to the path the body of each victim made until having its death classified as undetermined. After examination of each one of these documents, it was possible to reclassify 43 (21 per cent ) out of the 203 deaths in the case, using a score based on the index of agreement between classifications of death intentionality registered in the documents. All deaths which presented a percentage of agreement above 50 per cent from the consultation to the referred documents had their intentionality reclassified. For the definition and reclassification of such cases, the tenth review of the International Disease Classification (CID-10) was used, where suicides correspond to codes X60 to X84, under the name of intentionally self-inflicted lesions. Results - Out of the cases initially classified as having undetermined intentionality (n=203), 9 per cent (n=19) were reclassified as suicide. The official statistics from SIM report that, within the studied period of time, there were only 61 suicides. However, adding the 19 reclassified cases to the official statistics quantitative, there are a total of 80 suicides among adolescents from the year 2000 to 2014, which indicates a general percentage of 23.7 per cent of sub notification. There was no change in the profile of the victims when comparing data from before and after the reclassification of the cases. In both situations, the bigger contingent of suicide cases is concentrated in the following profile: male adolescents, brown-coloured, aging from 15 to 19 years. According to the interviewed medical examiners, issues such as work overload and reduced amount of human resources are factors that might interfere in the process of undetermining death intentionality. Conclusions - From the recuperation of information contained in the documents found in IML, it was possible to reclassify the intentionality of deaths by external causes, improving the quality of data in SIM and allowing the elaboration of a more reliable and compatible epidemiologic profile regarding reality. This study, in fact, among all the obtained conclusions, reaffirms the need for constant sensitization of professionals involved in the death registration process, so that there is an enhancement in the quality of information in healthcare

Registros de Câncer são sistemas padronizados, flexíveis e multicêntricos para coleta de dados de pacientes com neoplasias, permitindo a obtenção de dados epidemiológicos de alta qualidade a um baixo custo. Eles podem ser de base populacional, abrangendo todos os casos de uma área geográfica delimitada, possibilitando calcular sua incidência e sobrevida, quanto de base hospitalar, coletando dados sobre o paciente para uso em pesquisa, educação continuada e melhoria dos atendimentos. Essas abordagens, na Medicina Veterinária, tiveram início na década de 60 com o Kansas Animal Tumor Registry (1961) e com o California Animal Tumor Registry (1963). Desde então, outras iniciativas similares surgiram nos Estados Unidos, Canadá, Noruega, Dinamarca, Suécia e Reino Unido. Esses registros, concentrados no Hemisfério Norte, não existem ainda na América Latina. Este trabalho teve como objetivo avaliar a viabilidade de implantação de um Registro de Câncer Animal na cidade de São Paulo, SP, Brasil. Elaborou-se um registro piloto para permitir entender a sua viabilidade em larga escala quanto Sistema de Informação em Saúde. Foram desenvolvidos identidade, logotipo, formulários de admissão e seguimento, e um software especializado, o SIRCA-SP, para o funcionamento do Registro de Câncer Animal de São Paulo (RCA-SP). O fluxo de informação foi planejado para que a coleta pudesse ser realizada de forma multicêntrica, padronizada e sigilosa. A análise preliminar dos dados permite entender as características da distribuição local do câncer e o potencial do RCA-SP. O estudo de viabilidade foi realizado através de parâmetros definidos pelo Center for Diseases Control, Atlanta, EUA. O RCA-SP foi criado, em 2013, como um registro de base hospitalar que coleta informações sobre cães e gatos diagnosticados com câncer a partir de janeiro de 2012 em hospitais, clínicas e serviços autônomos veterinários sediados na cidade de São Paulo. O software SIRCA-SP foi desenvolvido para otimizar e garantir a qualidade dos dados coletados, consolidados e armazenados pelo RCA-SP. O sistema possui interface amigável e pode ser acessado via internet. Os formulários foram padronizados e geram dados comparáveis aos outros Registros de Câncer em animais e humanos. Avaliação preliminar dos dados demonstra predomínio, nos 645 casos registrados de cães (96,58%) e de fêmeas (80,15%). As localizações de câncer mais comuns foram em glândula mamária (63,88%), pele (17,98%) e em órgãos genitais (5,43%). O sistema demonstrou ser simples, flexível, bem aceito, oportuno e útil. A sua representatividade, por ser projeto piloto, é pequena, mas tenderá a aumentar com adesão de novas fontes notificadoras. O sistema não possui mecanismos de garantia de sua exaustividade. Algumas soluções como o sistema de pré-verificação de inclusão, projetado para evitar entrada duplicada de dados, e a integração entre prontuário eletrônico e os campos de interesse epidemiológico auxiliam na distribuição de responsabilidades do registro aos usuários e, consequente, diminuição de custos operacionais. A implantação de um Registro de Câncer Animal na cidade de São Paulo mostrou-se viável e a coleta multicêntrica é realizada de forma contínua e ininterrupta / Cancer Registries are flexible, multicentric and standardized systems to collect data from patients with neoplasia, allowing the epidemiological registry of high quality data, at low cost. They can be classified as population-based, covering all cases in a defined geographical area, allowing incidence and survival calculation, or, hospital-based, collecting data about the patient for research, continuing education and improvement of care. Those approaches started in Veterinary Medicine in the 60’s, with the Kansas Animal Tumor Registry (1961) and the California Animal Tumor Registry (1963). Since then, other similar initiatives have emerged in United States, Canada, Norway, Denmark, Sweden, Italy and United Kingdom. Those registries, concentrated in North Hemisphere, were absent in Latin America up to now. This study aimed to assess the feasibility of implementing an Animal Cancer Registry in Sao Paulo, SP, Brazil. A pilot cancer registry system was developed to allow understanding its feasibility, in large scale, as a Health Information System. An identity, logo, admission and follow-up forms were developed, and a specialized software, the SIRCA-SP, for Sao Paulo Animal Cancer Registry (RCA-SP) operation was standardized. An information flow was planned, so that the collection could be performed in a multicentric, standardized and confidential way. Preliminary analysis of the data allowed the understanding of local cancer distribution characteristics and the RCA-SP potential. The feasibility study was perform using parameters defined by the Centers for Disease Control, Atlanta, USA. The RCA-SP, created in 2013, is a hospital-based cancer registry, which collects information about dogs and cats diagnosed with cancer since January 2012 in hospitals, clinics and veterinary autonomous services in Sao Paulo, SP, Brazil. The SIRCA-SP was designed to optimize and ensure the quality of data collection, consolidation and storing by RCA-SP. The system has a friendly interface and can be access via Internet. The forms were standardized and generate data comparable to other cancer registries in animals and humans. Preliminary survey data shows predominance, in the 645 cases, of dogs (96.58%) and females (80.15%). The most common cancer location were mammary gland (63.88%), skin (17.98%) and genitals (5.43%). The system proved to be simple, flexible, well accepted, timely and useful. As a pilot study, its representativeness is still small, but tends to increase with the accession of new reporting sources. The system has no assurance mechanisms of their completeness. Some solutions such, as the pre-verification tool, designed to avoid duplicated entries, and the electronic medical records integration with the standard epidemiological fields, share the fields to assist in the distribution of registry responsibilities to users and, consequently, decrease operating costs. The implementation of an Animal Cancer Registry in São Paulo proved to be feasible, and the multicentric collection is ready to be carried out continuously and uninterruptedly