Abstract Malignant neoplasms are increasingly prevalent in the daily clinical practice. Up to 61% of patients with pelvic malignancies undergo pelvic radiotherapy in different doses, which may cause intestinal damage, and the rectum is the segment most frequently affected due to its fixed position in the pelvis. Currently, there are several strategies to minimize the effects of radiation on the tissues surrounding the neoplastic site; despite those strategies, radiotherapy can still result in serious damage to organs and structures, and these injuries accompany patients throughout their lives. One of the most common damages resulting from pelvic radiotherapy is acute proctitis.The diagnosis is confirmed by visualizing the rectal mucosa through rigid or flexible rectosigmoidoscopy and colonoscopy. The objective of the present study was to review the forms of radiation-induced proctopathytherapy, and to evaluate the results of each method to propose a standardization for the treatment of this pathology. Despite the prevalence of radiation-induced proctopathy, there is no definitive standardized treatment strategy so far. The first approach can be tried with local agents, such as mesalazine and formalin. For refractory cases, control can usually be achieved with argon plasma coagulation, hyperbaric oxygen, and radiofrequency ablation therapies. Regarding the study of radiation-induced proctopathy, there is a lack of robust studies with large samples and standardized therapies to be compared. There is a lack of double-blinded, randomized controlled studies to determine a definitive standard treatment algorithm.

ABSTRACT Purpose: The present study aimed at testing a new formulation of mesalazine linked to chondroitin sulfate and its components alone in the treatment of actinic proctitis in rats. Methods: Forty-seven female Wistar rats were submitted to pelvic radiation and divided into eight groups: control A, mesalazine A, chondroitin A, and conjugate A, gavage of the according substance two weeks after irradiation and sacrifice three weeks after oral treatment; control C, mesalazine C, chondroitin C, and conjugate C, sacrifice six weeks after oral treatment. The rectum was submitted to histological characterization for each of the findings: inflammatory infiltrate, epithelial degeneration, mucosal necrosis, and fibrosis. Results: The inflammatory infiltrate was more intense in chondroitin A, mesalazine A, and conjugate C. The collagen deposition was less intense in chondroitin A, and mesalazine A, and more intense in control C. Conclusions: Mesalazine and chondroitin alone were efficacious in inducing a delayed inflammatory response, hence reducing the late fibrosis. The conjugate was able to induce an ever more delayed inflammatory response.

Abstract Purpose: To describe a new model of actinic enteritis that does not use radiotherapy machines. Methods: Sixteen Wistar rats were divided into four groups, consisting of four animals each: control (group A), two weeks after irradiation (group B), five weeks after irradiation (group C) and eight weeks after irradiation (group D). Animals were given a 10Gy radiation from a Cobalt-60 natural source in a nuclear technology research center. Protections of the surrounding tissues were obtained through the usage of plumb devices with a hole in the center, which served as a collimator. We obtained irradiated and non-irradiated colons from each animal. Results: In group B we found an important inflammatory response in the irradiated colon, which appeared in a reduced way in group C and was minimal in group D, in which we found a relevant collagen submucosal deposition/fibrosis. In all groups, the non-irradiated colon had a lower pathological damage in comparison with the irradiated colon. Conclusion: We thus described an efficient and feasible technique for obtaining an animal model of actinic enteritis.

PURPOSE:To evaluate whether scintigraphy with technetium-99m-labeled ceftizoxime (99mTc-CFT) can differentiate mediastinitis from aseptic inflammation associated with sternotomy.METHODS:Twenty female Wistar rats were randomly distributed into four groups: S (control) -partial upper median sternotomy with no treatment; SW (control) - sternotomy and treatment of sternal wounds with bone wax; SB - sternotomy and infection with Staphylococcus aureus; SWB - sternotomy with bone wax treatment and bacterial infection. Scintigraphy with 99mTc-CFT was performed eight days after surgery and images were collected 210 and 360 min after infusion of the radiopharmaceutical.RESULTS: No animals exhibited clinical signs of wound infection at the end of the experiment, although histological data verified acute inflammatory response in those experimentally infected with bacteria. Scintigraphic images revealed that tropism of 99mTc-CFT to infected sternums was greater than to their non-infected counterparts. Mean counts of radioactivity in bacteria-infected sternal regions (SB and SWB) were significantly higher (p = 0.0007) than those of the respective controls (S and SW).CONCLUSION:Scintigraphy with technetium-99m-labeled ceftizoxime is a method that can potentially detect infection post sternotomy and differentiate from aseptic inflammation in animals experimentally inoculated with S. aureus.

OBJETIVO: Comparar os resultados clínicos e radiográficos da osteossíntese de fraturas do terço lateral da clavícula com dois métodos: placa T ou âncoras associadas aos fios de Kirschner.MÉTODOS: Foram avaliados 15 pacientes com média de idade de 34,3 anos (19-57) e seguimento médio de 22,7 meses (14-32). Em nove casos foi usada a placa T e em seis casos a fixação coracoclavicular com âncoras no processo coracoide e fios de Kirschner através da articulação acromioclavicular (AC). A avaliação incluiu o escore de Constant, satisfação pessoal e avaliação radiográfica.RESULTADOS: Ambas as modalidades de tratamento obtiveram consolidação em todos os casos. O Grupo 1 apresentou escore de Constant mais elevado (83,4) quando comparado com o Grupo 2 (76,4) p = 0,029. Nenhuma das técnicas apresentou complicações graves, embora complicações leves tenham sido observadas apenas no Grupo 2 (80%), a maioria delas a migração do fio de Kirschner e infecção superficial.CONCLUSÃO: O tratamento cirúrgico das fraturas da clavícula distal com placa T proporciona a mesma taxa de consolidação da fixação coracoclavicular com âncoras no coracoide e fios de Kirschner através da articulação AC e melhores resultados clínicos.NÍVEL DE EVIDÊNCIA: Nível III, estudo retrospectivo comparativo, estudo terapêutico.

OBJECTIVE: To compare the clinical and radiographic results from osteosynthesis of fractures of the lateral third of the clavicle, using two methods: T plates or anchors together with Kirschner wires.METHODS: Fifteen patients of mean age 34.3 years (range: 19-57) and mean follow-up 22.7 months (range: 14-32) were evaluated. In nine cases, a T plate was used; and in six cases, coracoclavicular fixation was used with anchors in the coracoid process and Kirschner wires through the acromioclavicular joint. The evaluation included the Constant score, personal satisfaction and radiographic assessment.RESULTS: Both types of treatment achieved consolidation in all cases. Group 1 presented a higher Constant score (83.4) than that of Group 2 (76.4) (p = 0.029). Neither of the techniques presented any severe complications, and mild complications were only observed in Group 2 (80%), mostly consisting of migration of the Kirschner wire and superficial infection.CONCLUSION: Surgical treatment of fractures of the distal clavicle using T plates provided the same consolidation rate as shown by coracoclavicular fixation with anchors in the coracoid process and Kirschner wires through the acromioclavicular joint, and better clinical results.LEVEL OF EVIDENCE: Level III evidence was obtained. Comparative retrospective study and therapeutic study were performed.

OBJETIVO: avaliar a eficácia da membrana amniótica usada com tela de polipropileno contra a formação de aderências e sua influência na cicatrização. MÉTODOS: vinte e cinco ratas Wistar foram anestesiadas para criação de um defeito parietal na parede abdominal anterior. Sua correção foi feita com tela de polipropileno isolada e associada à membrana amniótica. No grupo Controle (n=11), a tela foi inserida isoladamente intra-abdominal. No grupo A (n=7), interpôs-se a membrana amniótica entre a tela e a parede abdominal. No grupo B, a membrana amniótica foi colocada sobre a tela, recobrindo-a. Após sete dias, os animais foram eutanasiados para avaliação macroscópica e microscópica da cicatrização. RESULTADOS: aderências foram observadas em todos os animais, exceto em um do grupo Controle. Inflamação acentuada foi observada em todos os animais dos grupos A e B e em três do grupo Controle, com diferença significativa entre eles (A e B com p=0,01). Acentuada atividade angiogênica foi notada em um animal do grupo Controle, seis do grupo A e quatro do grupo B, com diferença significativa entre o grupo Controle e os grupos A (p=0,002) e B (p=0,05). O colágeno cicatricial foi predominantemente maduro, exceto em cinco animais do grupo Controle, com diferença significativa entre o grupo Controle e os grupos A (p=0,05) e B (p=0,05). CONCLUSÃO: a presença da membrana amniótica não alterou a formação de aderências na primeira semana de pós-operatório. Associou-se à inflamação acentuada, elevada atividade angiogênica e predomínio de fibras colágenas maduras, independente do plano anatômico em que foi inserida.

OBJECTIVE: to evaluate the efficacy of the amniotic membrane used with polypropylene mesh against the formation of adhesions and its influence on healing. METHODS: twenty five female Wistar rats were anesthetized for creating a parietal defect in the anterior abdominal wall. Its correction was made with polypropylene mesh alone and associated with amniotic membrane. In the control group (n=11), the screen was inserted alone. In group A (n=7) we interposed the amniotic membrane between the screen and the abdominal wall. In group B, the amniotic membrane was placed on the mesh, covering it. After seven days, the animals were euthanized for macroscopic and microscopic evaluation of healing. RESULTS: adhesions were observed in all animals except one in the control group. Severe inflammation was observed in all animals in groups A and B and in three of the control group, with significant difference between them (A and B with p=0.01). Pronounced angiogenic activity was noted in one animal in the control group, six in group A and four in group B, with a significant difference between the control group and group A (p=0.002) and group B (p=0.05). The scar collagen was predominantly mature, except in five animals of the control group, with significant difference between the control group and group A (p=0.05) and group B (p=0.05). CONCLUSION: The amniotic membrane did not alter the formation of adhesions in the first postoperative week. There were also pronounced inflammation, high angiogenic activity and predominance of mature collagen fibers, regardless of the anatomical plane that it was inserted in.

PURPOSE:To investigate amniotic membrane as a biological dressing in infected wound healing in rabbits.METHODS: The use of preserved amniotic membranes (AMs) was examined using 15 rabbits with experimentally induced wound infections on their backs. Healing was histologically evaluated during different phases including inflammation, granulation, epithelialization, and fibroplasia. The animals were distributed into three groups for histological study at seven, 14, 21, and 28 days post-wound induction. Group A did not receive treatment: the wound was left exposed and dry; Group B received a daily exposure treatment with collagenase; and Group C received one AM, which also remained exposed.RESULTS: A marked reduction of the inflammatory phase was observed in Group C at 21 days, and the granulation phase of this healing increased at 14 days. Epithelialization was similar among the three groups, and fibroplasia was more pronounced in Group C at 14 days. Furthermore, gradual collagen organization also began for the animals in Group B at 14 days.CONCLUSION:The amniotic membrane did not significantly alter the inflammation, epithelialization, or fibroplasia phases but did increase angiogenesis up to Day 14 compared with the dry dressing and collagenase treatments.

Racional: O uso de telas inorgânicas historicamente é contra-indicado em paciente com infecções. Objetivo : Avaliar o comportamento e cicatrização de paredes abdominais com uso de telas de polipropileno após infecções intra-cavitárias. Método : Foram estudadas 20 ratas Wistar aleatoriamente divididas nos grupos Estudo (com peritonite) e Controle (sem peritonite). Um defeito na parede abdominal foi criado em todos os animais, onde foi aplicada tela de polipropileno. Foi feita avaliação da força de tensão com uso de tensiômetro, além de análise histológica da área cicatricial. Resultados : Observou-se maior adesividade da tela às paredes dos animais do grupo Estudo quando comparado ao grupo Controle. A análise histopatológica mostrou prevalência de tecido de granulação de acentuado à moderado em ambos os grupos, sem diferença significativa. Conclusão : O uso de telas inorgânicas nos defeitos da parede abdominal em ratos com peritonite induzida não mostrou resultado pior do que aquele obtido de animais sem infecção, tanto em relação à sua integração quanto ao tecido cicatricial no defeito da parede abdominal.

Background : The use of alloplastic meshes has been historically contra-indicated in patients with infection. Aim : To evaluate the use of polypropylene meshes in the treatment of abdominal wall defects in rats with peritonitis. Methods : Twenty Wistar female rats were divided into two groups: induction of peritonitis (test group) and without peritonitis (control group). An abdominal wall defect was created in all animals, and polypropylene mesh was applied. The evaluation of the tensile strength of the mesh was carried out using tensiometer and microscopic analysis of the healing area was done. Results : More adhesion of the mesh to the rat abdominal wall was observed in test group. The histopathological analyses showed prevalence of moderate to accentuated granulation tissue in both groups, without significant differences. Conclusion : The use of the mesh coverage on abdominal wall defects of rats with induced peritonitis did not show worse results than its use in healthy animals, nor was its integration to the resident tissue any worse.

OBJETIVO: Avaliar a viabilidade de retalhos cutâneos de ratos à McFarlane após a administração de sildenafil. MÉTODOS: Vinte ratos Wistar foram distribuídos em dois grupos: Controle (confecção do retalho cutâneo dorsal, aplicação subdérmica de solução salina a 0,9%) e Estudo (confecção do retalho cutâneo dorsal, aplicação subdérmica de sildenafil). Sete dias após a operação, os retalhos foram fotografados e representados graficamente, para serem analisados com o programa AutoCad. Três biópsias (cranial, média e caudal) foram coletadas de cada retalho, para análise histológica. RESULTADOS: A análise macroscópica evidenciou que os animais do grupo Estudo apresentaram maiores áreas de necrose (p=0,003) nos retalhos cutâneos dorsais. Além disso, a análise histológica dos terços distais dos retalhos mostrou uma tendência à formação de menos tecido de granulação nos animais que receberam o sildenafil. CONCLUSÃO: O sildenafil subdérmico esteve associado com uma pior viabilidade tecidual dos retalhos cutâneos dorsais de ratos.

PURPOSE: To assess the viability of McFarlane skin flaps in rats with administration of sildenafil. METHODS: Twenty Wistar rats were distributed into two groups: Control (dorsal skin flap, subdermal application of saline solution at 0.9%) and Study (dorsal skin flap, subdermal application of sildenafil). Seven days after the surgery, flaps were photographed and graphically rendered. Then, they were analyzed with AutoCAD software. Three biopsies (proximal, medial and distal) of each flap were collected for histological analysis. RESULTS: Macroscopic analysis showed that animals of the study group had greater necrotic areas (p=0.003) in the dorsal skin flaps. Additionally, histological analysis of the distal third of these flaps showed a tendency to less granulated tissue formation in animals treated with sildenafil. CONCLUSION: Sildenafil subdermally was associated with lower viability of the random skin flap in rats.

OBJETIVO: Avaliar a eficácia do uso do polivinilpirrolidona-iodo (PVPI) acrescido ao líquido de lavagem da cavidade peritoneal na redução da absorção bacteriana e no remanescente bacteriano não fagocitado no sangue periférico de ratos. MÉTODOS: Estudou-se 34 ratos Wistar fêmeas, distribuídos aleatoriamente nos seguintes grupos: controle (n=10), nenhum tratamento; PVPI (n=9), lavagem da cavidade peritoneal com solução de PVPI a 10% em solução salina; salina (n=15), lavagem da cavidade com solução salina. Após anestesia, fez-se inoculação intraperitoneal de solução de Escherichia coli marcadas com 99mTc contendo 10(8) UFC/ml. Após 40 minutos, realizou-se o tratamento que foi, no grupo controle, manipulação das vísceras; no grupo PVPI, irrigação da cavidade peritoneal com solução de PVPI aquecido a 37,5ºC na concentração de 1%, e no grupo salina irrigação com solução salina aquecida a 37,5ºC. Após 15 minutos do tratamento, os animais foram mortos por secção da aorta abdominal e colhidas amostras do sangue, do fígado, do baço e do pulmão para contagem da radioatividade. Foram determinados o índice de absorção bacteriano e o índice de remanescente no sangue periférico. RESULTADOS: Do total de bactérias inoculadas no peritôneo, houve absorção de 0,92% (0,14% a 2,13%) nos animais do grupo controle, 0,49% (0,18% a 0,71%) após uso do PVPI tópico e 0,80% (0,04% a 3,8%) após lavagem com solução salina. Houve redução significativa da absorção quando comparados os animais tratados com o PVPI e os controles não tratados (p=0,03). Do total de bactérias absorvidas para a corrente circulatória, o percentual de bactérias não fagocitadas presentes no sangue periférico foi de 2,9% (1,1% a 17,7%) nos animais controle 15,2% (8,3% a 21,4%) naqueles tratados com PVPI e 6,9% (0,8% a 29,7%) após lavagem com solução salina, com diferença entre os animais controle e os tratados com PVPI (p=0,01). CONCLUSÃO: A lavagem da cavidade peritoneal de camundongos com solução contendo PVPI mostrou ser capaz de reduzir a absorção de bactérias pelo peritôneo de ratos, entretanto associou-se a aumento de bactérias viáveis no sangue periférico desses animais.

PURPOSE: To evaluate the effectiveness of the use of the povidone-iodine (PVI) added to the liquid of wash of the peritoneal cavity in the reduction of bacterial absorption and in the remainder non-phagocyted bacteria in the circulating blood of rat. METHODS: Thirty four Wistar females rats were used, distributed in the following groups: A (n=10), non-treated; B (n=9), wash of the peritoneal cavity with solution of PVI to 1% in saline solution; C (n=15), wash of the cavity with saline solution. After anesthesia, it was made intraperitoneal infusion of solution of Escherichia coli labeled with 99mTc containing 10(8) CFU/ml. After 40 minutes, it was made the treatment, in the group A, manipulation of the viscera; in the group B, irrigation of the peritoneal cavity with warm solution of 1% PVPI to 37,5ºC, and in the group C irrigation with warm saline (37,5ºC). After 15 minutes of the treatment, blood samples and fragments of liver, spleen and lung was obtained for count of the radioactivity, and animals killed by abdominal aorta section. There were determined the bacterial absorption index and the remainder index in the bloodstream. RESULTS: Of the total of bacteria infused in the peritoneum, there was absorption of 0,92% (0,14% to 2,13%) in the animals of the group A (controls), 0,49% (0,18% to 0,71%) after use of topical PVPI (group B) and 0,80% (0,04% to 3,8%) after wash with saline solution (group C). There was significant reduction of the absorption when compared the treated animals with PVPI and the controls (p=0,003). Of the total of bacteria absorbed for the circulatory current, the percentile amount of bacteria non-phagocyted in the outlying blood was of 2,9% (1,1% to 17,7%) in the control group, 15,2% (8,3% to 21,4%) in those treated with PVPI (group B) and 6,9% (0,8% to 29,7%) after wash with saline solution (group C), with difference among controls and treated with PVPI (p=0,01). CONCLUSION: The wash of the cavity peritoneal of mice with solution containing PVPI showed to be capable to reduce the absorption of bacteria by peritoneum of rat; however it seems to interfere with the function of the phagocytic cells for the observation of the increase of viable bacteria in the outlying blood of those animals.

OBJETIVO: Avaliar, experimentalmente, os efeitos da mucosectomia química sobre a cicatrização de anastomoses colônicas. METODOLOGIA: Estudou-se 17 ratos Wistar machos divididos nos seguintes grupos: A (n=12), anastomose colônica; B (n=13), anastomose colônica após mucosectomia. A mucosectomia foi realizada através da introdução de um bastão de nitrato de prata a 10%, durante um minuto, através das duas bocas a serem anastomosadas, e as anastomoses realizadas em plano único total, evertente, com fio polivicril 6-0 em pontos separados. Os animais foram estudados após 7 dias (6 do grupo A1 e 6 do grupo B1) e 14 dias (7 do grupo A2 e 6 do grupo B2) da cirurgia, e realizadas observações macroscópicas da presença de aderências, fístulas (saída de secreção através da anastomose ou teste da pressão de ruptura igual a zero), estenose (dilatação intestinal proximal à anastomose), abscessos peri-anastomóticos e peritonite. Foi também avaliada a pressão de ruptura das anastomoses e histologia das anastomoses. Os resultados qualitativos foram avaliados pelo teste do Qui-quadrado (com correção de Yates) e os quantitativos através do teste de Kruskall-Wallis, sendo considerados significativos valores de p<0,05. RESULTADOS: Nenhum dos animais estudados apresentou fístulas. A incidência de aderências peri-anastomóticas não foi diferente entre os grupos (A1=100%, B1=100%, p=N.S.; A2=75%, B2=50%, p=N.S.). Houve semi-obstrução da anastomose em 25% dos animais do grupo A1, 50% daqueles do grupo B1, 25% dos animais do grupo A2 e 50% dos animais do grupo B2, sem diferença significativa entre os grupos. A pressão de ruptura, em mmHg, foi de 27,0 ± 4,5 no grupo A1, 34,5 ± 2,0 no grupo B1, 28,9 ± 4,2 no grupo A2 e 24,0 ± 3,4 no grupo B2, com aumento significativo no grupo B1 quando comparados aos grupos A1 (p=0,03) e B2 (p=0,02). Concluindo, a mucosectomia química com o uso do nitrato de prata, ao contrário daquela realizada mecanicamente, não associou-se a maior incidência de complicações da anastomose no cólon direito de ratos. Houve, entretanto, aumento da força da anastomose no período inflamatório, sem influência no período de fibroplasia da cicatrização.

OBJECTIVE: To evaluate, experimentally, the effects of chemical mucosectomy on colon healing in rats. METHODS: We studied 17 male Wistar rats divided into following groups: A (n=12), colonic anastomosis; B (n=13), colonic anastomosis after use of 10% silver nitrate. The mucosectomy in group B was made by means introduction of 10% silver nitrate pencil into anastomotic surfaces during 1 minute in an extension of 0.5 cm. The anastomosis was made in single plane with evertent sutures of polyvicryl 6-0 in separated sutures. The animals were evaluated in the seventh postoperative day (A1, 6 of the group A and B1, 6 of the group B) and fourth postoperative day (A2, 7 of the group A and B2, 6 of the group B). The anastomosis was evaluated in macroscopic aspect (adherence, fistula, stenosis, perianastomotic abscesses, peritonitis), rupture pressure (mmHg) and histology (inflammatory infiltrate). The data were analysed by Chi-square test (qualitative data) and ANOVA (quantitative data), and considered significative values of p<0.05. RESULTS: None animal presented fistula. The incidence of adherence was no different among the groups. (A1=100%, B1=100%, p= NS; A2=75%, B2=50%, p= NS). There were anastomosis partial obstruction in 25% of group A1, 50% in B1, 25% in A2 and 50% in B2, without significant differences among the groups. The rupture pressure was 27,0 ± 4,5 in A1 group, 34,5 ± 2,0 in B1 group, 28,9 ± 4,2 in A2 group and 24,0 ± 3,4 in group. There was an significant increase in pressure rupture in B1 group when compared with A1 group (p=0,03) and B2 group (p=0,02). CONCLUSION: The chemical mucosectomy with silver nitrate was not associated with increase in postoperative cicatricial complications in wound colon healing in rats. There was, however, an increase in anastomosis strength in early period of the cicatricial process, without influence in latter period.

OBJETIVO: Avaliar a eficácia de induzir peritonite em ratos através da ligadura cecal laparoscópica (CL), por meio de banda elástica. MÉTODOS: Doze ratos Wistar foram submetidos a ligadura cecal com banda elástica aplicada com dispositivo especialmente construído para este fim. Em seis animais (grupo CL), a bolsa cecal foi mantida intacta, enquanto nos outros animais (grupo CLP), a bolsa foi perfurada com tesoura. Parâmetros clínicos, características da cavidade peritonial e ceco, e histologia do tecido cecal foram examinados em todos os animais 8 e 24 horas após a cirurgia. RESULTADOS: Os animais do grupo CLP apresentaram pelo menos um sinal clínico de sepses nas primeiras 8 h de observação. Líquido peritonial claro foi observado em quase todos os membros do grupo CLP. Leucócitos polimorfonucleares foram identificados na serosa do ceco dos animais do grupo CLP. Por outro lado, todos os animais do grupo CL estavam vivos após 24 h, e leucócitos polimorfonucleares estavam restritos à muscular própria. Presença de líquido peritonial não foi detectada nos animais do grupo CL. CONCLUSÃO: A ligadura elástica do ceco foi reprodutível e a secção da bolsa cecal foi essencial para a indução de sepse.

PURPOSE: To evaluate the efficacy of inducing peritonitis in rats through laparoscopic cecal ligation (CL), by means of an elastic band. METHODS: Twelve Wistar rats were subjected to cecal ligated with an elastic band applied using a specially constructed applicator. In six of the animals (the CL group) the cecal sac was preserved intact whilst in the remaining animals (the CLP group) the sac was perforated with scissors. Clinical parameters, characteristics of the peritoneal cavity and cecum, and histological features of the cecal tissue were observed in all experimental animals 8 and 24 h after surgery. RESULTS: CLP animals exhibited at least one clinical sign of sepsis within the first 8 h of observation. The peritoneal liquid was observed to be clear in almost all members of the CLP. Polymorphonucleated cells were detected in the tunica serosa of the cecum of CLP animals. In contrast, all members of the CL group were alive after 24h, and of polymorphonucleated cells in the muscle layer of the cecal wall were observed. The presence of peritoneal liquid was not detected in CL animals. CONCLUSION: Although elastic ligation of the cecum was reproducible, puncture of the cecal sac was essential for induction of sepsis.

As alterações qualitativas e quantitativas da flora ileal na obstrução biliar e o papel dos sais biliares foram avaliados em ratos. Em animais com obstrução biliar houve aumento da população ileal. Esse efeito é provavelmente causado pela ausência de sais biliares no lúmen ileal, uma vez que em animais cuja dieta foi suplementada com sais biliares houve redução da flora ileal.

Qualitative and quantitative alterations in ileal flora during obstructive jaundice and the role of bile salts were evaluated in rats. Obstructive jaundice was associated with bacterial overgrowth in the ileum. This effect may be due to the reduced concentration of bile salts, since dietary supplementation reduced the small bowel aerobic bacterial flora.

Avaliou-se, retrospectivamente, a evolução pós-operatória das varizes esofagogástricas em 40 pacientes submetidos a um dos seguintes procedimentos cirúrgicos: a (n=27) derivação esplenorrenal distal (ERD) e B (n=13) derivação esplenorrenal proximal (ERP). Todos os pacientes tinham hipertensão porta esquistossomótica com diagnóstico prévio de varizes do esôfago, presentes ou não no estômago, com um ou mais episódios de sangramento. Os pacientes foram submetidos a um dos procedimentos cirúrgicos de acordo com a preferência do cirurgião assistente. Foram realizadas, nesses pacientes, endoscopias no período pré-operatório e aos seis, 12 e 18 meses no pós-operatório. Os dados de cada endoscopia foram coletados e comparados entre os grupos, verificando-se a presença de varizes do esôfago e estômago nos diferentes períodos, comparando esses achados através do teste do qui-quadrado, com significância para p<0,05. Os resultados obtidos não mostraram casos de ressangramento até o 18º mês pós-operatório, nem casos de encefalopatia. Foram diagnosticadas varizes esofágicas, no pré-operatório, em 100% dos pacientes nos dois grupos. No período pós-operatório, houve redução significativa das varizes do esôfago, quando estudados os dois grupos conjuntamente, para 40% no sexto mês (p = 0,0002), 30% no 12º mês (p = 0,003) e 27,5% no 18º mês (p = 0,003). No sexto mês pós-operatório, a incidência de varizes do esôfago foi maior nos pacientes com ERD quando comparados àqueles com ERP (51,9% vs. 15,4%, p = 0,03). Quando estudadas as varizes aos 12 e 18 meses não foi observada diferença significativa entre pacientes submetidos a ERD ou ERP (12º mês, 37% vs. 15,4%; 18º mês, 25,9% vs. 30,8%). Foram vistas varizes gástricas em 37,5% dos pacientes, com redução significativa no sexto mês (2,5%, p = 0,005). Entretanto, quando comparada com a freqüência do sexto mês, houve aumento significativo no 12º mês (5%, p = 0,00001) e 18º mês (7,5%, p = 0,02). Quando comparados os grupos, no período pré-operatório, estas varizes estiveram presentes mais freqüentemente no grupo submetido a ERP (69,2% vs. 26%, p = 0,0005), sem diferença significativa no período pós-operatório (6º mês, 16,6% vs. 0%; 12º mês, 33,3% vs. 0%; 18º mês, 33,3% vs. 11,1%). Este trabalho demonstrou que os dois tipos de cirurgia têm resultado semelhante em relação à resolução das varizes do esôfago e estômago no 18º mês, mas os resultados indicam que a redução na incidência das varizes do esôfago se acompanha de aumento das varizes gástricas, provavelmente devido à abertura de novas vias colaterais de drenagem em casos de persistência de uma pressão porta aumentada ou mau funcionamento da derivação esplenorrenal.

Bleeding due to esophagogastric varices is the major cause of death in patients with hepatic disease. The most frequent treatment of these varices in elective conditions are based in mechanisms that interrupt the connection between splancnic and systemic venous bed. Surgical procedures are divided into portosystemic shunts (selective and non-selective) and disconnection. In portasystemic shunt, the purpose is to derive the splancnic flux, diminishing the esophagogastric varices and prevent re-bleeding. But literature is controversial about the index of re-bleeding and hepatic encephalophaty after proximal or distal splenorenal shunts. We performed this study to evaluate the evolution of esophagogastric varices after proximal splenorenal (PS) or distal splenorenal (DS) shunt. Postoperative outcome of oesophageal and gastric varices were retrospectively evaluated in forty patients submitted to one of two following procedures: A (n=27), distal splenorenal shunt (DS), and B (n=13), proximal splenorenal shunt (PS). All patients had portal hypertension with oesophageal or gastric varices due to schistosomiasis, and a pre-operative history of variceal bleeding. Patients were submitted to the surgical procedure according to personal preference of the assistant surgeon, and preoperatively and after endoscopy was performed six, twelve and eighteen months after surgery. Endoscopy data were collected and compared bet were the two groups according the presence or absence of gastric and oesophageal varices in pre and postoperative period. Results showed no rebleeding in this group, and no of encephalopathy. The incidence of oesophageal varices was 100% in pre-operative period in two groups. There was a significative decrease in oesophageal varices after six (40%, p = 0,0002), twelve (30%, p = 0,003) and eighteen months (27.5%, p = 0,003). In the six months period, the incidence of oesophageal varices was higher in DS group, when compared with PS group (51.9% vs. 15.4%, p = 0,03). In twelve and eighteen months periods, there was no difference among these two groups in relation to the presence of oesophageal varices (twelve months, 37% vs. 15.4%; eighteen months, 25.9 vs. 30.8%). In relation to the gastric varices, there was an higher incidence of this type of varices in PS group in preoperative period when compared with DS group (26% vs. 69.2%, p = 0,005). However, in the six months period there was no difference between the groups (16,6% vs. 0%), which is also observed in twelve months period (33.3% vs. 0%) or in the eighteen months period (33.3% vs. 11.1%). The overall incidence of gastric varices was 37.5%, with a significative reduction in the six month period (2.5%, p=0.005), but with an increase in twelve month period (5%, p=0.00001) and eighteen month period (7.5%, p=0.02). In conclusion we observed both surgical techniques make similar results in relation to resolution of oesophageal and gastric varices after 18 months, but the results suggest that the decrease in oesophageal varices in both groups is accompanied by an increase in gastric varices, probably due to overture of new collateral vessels in cases of persistence of a higher portal pressure or splenorenal shunt failure.