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1.
Endoscopy ; 43(8): 697-701, 2011 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-21611944

RESUMEN

BACKGROUND AND STUDY AIM: Chronic radiation coloproctopathy (CRCP) is a well-recognized complication of radiotherapy, with rectal bleeding the most common presentation. It is frequently refractory to conservative management, but the optimal endoscopic treatment of bleeding secondary to CRCP is still controversial. The efficacy and safety of bipolar eletrocoagulation (BEC) and argon plasma coagulation (APC) in the management of bleeding from CRCP were evaluated and compared. PATIENTS AND METHODS: 30 patients (mean age 67.4 years) with active and chronic bleeding from telangiectasias, were randomly allocated to BEC or APC and stratified by severity of CRCP according to clinical severity and endoscopic findings (Saunders score). Success was defined as eradication of all telangiectasias, and therapeutic failure as need for more than seven sessions or for other treatment. Complications were categorized as minor (e.g. fever, anal or abdominal pain) or major (hemorrhagic). RESULTS: Both treatments were equally effective for the treatment of CRCP rectal bleeding. Only one failure was observed in each group (P = 1.000). There was no significant difference between the two groups regarding number of sessions, minor or major complications, or relapse. However, overall complication rate was significantly higher in the BEC group (P = 0.003). CONCLUSIONS: BEC and APC are both effective for the therapy of bleeding telangiectasias from CRCP. There are probably no major differences between them. Although APC seemed safer than BEC in this investigation, further studies, involving a much larger population, are needed to assess the complication rates and determine the best management option.


Asunto(s)
Electrocoagulación/métodos , Hemorragia Gastrointestinal/cirugía , Traumatismos por Radiación/cirugía , Radioterapia/efectos adversos , Enfermedades del Recto/cirugía , Enfermedades del Sigmoide/cirugía , Telangiectasia/cirugía , Adulto , Anciano , Anciano de 80 o más Años , Coagulación con Plasma de Argón/efectos adversos , Enfermedad Crónica , Colon Sigmoide/efectos de la radiación , Electrocoagulación/efectos adversos , Neoplasias Endometriales/radioterapia , Femenino , Hemorragia Gastrointestinal/etiología , Humanos , Análisis de Intención de Tratar , Masculino , Persona de Mediana Edad , Neoplasias de la Próstata/radioterapia , Traumatismos por Radiación/complicaciones , Enfermedades del Recto/etiología , Recto/efectos de la radiación , Índice de Severidad de la Enfermedad , Enfermedades del Sigmoide/etiología , Telangiectasia/complicaciones , Resultado del Tratamiento , Neoplasias del Cuello Uterino/radioterapia
2.
Colorectal Dis ; 13(7): 823-5, 2011 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-20402735

RESUMEN

AIM: Argon plasma coagulation (APC) is considered a safe treatment for haemorrhagic chronic radiation proctocolitis (CRPC), but bacteraemia is a rare complication. The study aimed to evaluate the frequency of bacteraemia after APC. METHOD: A prospective study of 21 patients who underwent APC (30 procedures) for CRPC was carried out. Blood cultures (Bactec(®) ) were obtained before and 30 min after the procedure (60 samples total). Patients were monitored for 48 h after the procedure to detect signs of infection. RESULTS: None of the 21 patients had fever or any sign suggestive of infection after any of the 30 sessions. All baseline blood cultures were negative and two (7%) of the 30-min blood cultures were positive (Staphylococcus hominis n = 1; Streptococcus bovis and Rhodotorula sp n = 1). The first was likely to be a contaminant and the second patient had no evidence of any other colonic disease (neoplasia or polyps) beside CRPC. CONCLUSION: APC is a low-risk procedure regarding bacteraemia and does not warrant prophylactic antibiotic administration.


Asunto(s)
Coagulación con Plasma de Argón , Bacteriemia/etiología , Proctocolitis/cirugía , Traumatismos por Radiación/cirugía , Adulto , Anciano , Anciano de 80 o más Años , Enfermedad Crónica , Femenino , Humanos , Masculino , Persona de Mediana Edad , Proctocolitis/etiología , Estudios Prospectivos , Traumatismos por Radiación/etiología , Radioterapia/efectos adversos
4.
Dis Esophagus ; 16(1): 33-8, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-12581252

RESUMEN

According to the WHO, 16-18 million people in Central and South America are infected by Trypanosoma cruzi. Chagasic achalasia affects between 7.1% and 10.6% of the population. The aim of this study was to evaluate the effects of Botox injections in the clinical response and esophageal function of patients with dysphagia due to chagasic achalasia. In total, 24 symptomatic patients with chagasic achalasia were randomly chosen to receive Botulinum Toxin (BT) or saline injected by endoscopy in the lower esophageal sphincter (LES). Patients were monitored with a clinical score of dysphagia and an objective assessment (esophagograms, scintillography, manometry, and nutritional assessment) for a period of 6 months. Clinical improvement of dysphagia was statistically significant (P < 0.001) in patients receiving BT when compared with the placebo. There was no significant difference in the placebo group regarding clinical score, LES basal pressure and esophageal emptying time. Esophageal emptying time in the toxin group was significantly lower than in the placebo (P=0.04) after 90 days. There were non-significant increases in esophageal emptying of 25.36% and 17.39%, respectively, at 90 and 180 days, in the BT group (P=0.266). Gender, age, and baseline LES pressure did not influence the response to BT. Our data strongly suggests that intrasphincteric injection of BT in LES is clinically effective in the treatment of chagasic achalasia.


Asunto(s)
Antidiscinéticos/administración & dosificación , Toxinas Botulínicas/administración & dosificación , Enfermedad de Chagas/complicaciones , Acalasia del Esófago/tratamiento farmacológico , Acalasia del Esófago/etiología , Adolescente , Adulto , Anciano , Método Doble Ciego , Esquema de Medicación , Acalasia del Esófago/diagnóstico , Unión Esofagogástrica/efectos de los fármacos , Esofagoscopía , Femenino , Estudios de Seguimiento , Humanos , Inyecciones Intralesiones , Masculino , Persona de Mediana Edad , Probabilidad , Estudios Prospectivos , Recuperación de la Función , Valores de Referencia , Índice de Severidad de la Enfermedad , Resultado del Tratamiento
5.
Braz. j. med. biol. res ; 34(6): 753-7, Jun. 2001. tab, ilus
Artículo en Inglés | LILACS | ID: lil-285848

RESUMEN

Helicobacter pylori (HP) infection is endemic worldwide. The proposed treatment is expensive and there are few reports regarding reinfection rates in Brazil. The aim of this study was to compare the eradication rates obtained with two therapeutic options and to evaluate reinfection one year after treatment. This was a prospective randomized trial with 55 patients. Thirty-nine patients had active duodenal ulcer (DU) and 16 non-ulcer dyspepsia (NUD), and all tested positive for HP. Diagnosis was based on at least two positive tests: ultrarapid urease test, histology and/or culture. Patients were randomized to two groups: group OMC treated with 40 mg omeprazole (once a day), 500 mg metronidazole and 250 mg clarithromycin (twice daily) for 7 days, or group NA treated with 300 mg nizatidine (once a day) and 1000 mg amoxicillin (twice daily) for 14 days. Those patients in whom HP was eradicated were followed up for one year to evaluate reinfection. Twenty-five patients were randomized for OMC and 30 for NA. HP eradication occurred in 20/25 patients (80 per cent) treated with OMC and 13/30 (43 per cent) treated with NA (P = 0.01). After reallocation because of initial treatment failure, the overall eradication rate was 44/51 patients (86 per cent). After an average follow-up of one year, we evaluated 34 patients (23 with DU and 11 with NUD). Reinfection occurred in 3/34 patients (7.6 per cent). We conclude that OMC is effective for HP eradication, and that NA should not be used. Reinfection occurs in 7.6 per cent of the patients in the first year after eradication.


Asunto(s)
Humanos , Masculino , Femenino , Adolescente , Adulto , Persona de Mediana Edad , Úlcera Duodenal/tratamiento farmacológico , Dispepsia/tratamiento farmacológico , Infecciones por Helicobacter/tratamiento farmacológico , Helicobacter pylori , Amoxicilina/uso terapéutico , Antibacterianos/uso terapéutico , Antiinfecciosos/uso terapéutico , Antiulcerosos/uso terapéutico , Claritromicina/uso terapéutico , Quimioterapia Combinada , Úlcera Duodenal/microbiología , Dispepsia/microbiología , Metronidazol/uso terapéutico , Nizatidina/uso terapéutico , Omeprazol/uso terapéutico , Penicilinas/uso terapéutico , Estudios Prospectivos , Recurrencia , Factores de Tiempo , Resultado del Tratamiento
6.
Braz J Med Biol Res ; 34(6): 753-7, 2001 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-11378663

RESUMEN

Helicobacter pylori (HP) infection is endemic worldwide. The proposed treatment is expensive and there are few reports regarding reinfection rates in Brazil. The aim of this study was to compare the eradication rates obtained with two therapeutic options and to evaluate reinfection one year after treatment. This was a prospective randomized trial with 55 patients. Thirty-nine patients had active duodenal ulcer (DU) and 16 non-ulcer dyspepsia (NUD), and all tested positive for HP. Diagnosis was based on at least two positive tests: ultrarapid urease test, histology and/or culture. Patients were randomized to two groups: group OMC treated with 40 mg omeprazole (once a day), 500 mg metronidazole and 250 mg clarithromycin (twice daily) for 7 days, or group NA treated with 300 mg nizatidine (once a day) and 1000 mg amoxicillin (twice daily) for 14 days. Those patients in whom HP was eradicated were followed up for one year to evaluate reinfection. Twenty-five patients were randomized for OMC and 30 for NA. HP eradication occurred in 20/25 patients (80%) treated with OMC and 13/30 (43%) treated with NA (P = 0.01). After reallocation because of initial treatment failure, the overall eradication rate was 44/51 patients (86%). After an average follow-up of one year, we evaluated 34 patients (23 with DU and 11 with NUD). Reinfection occurred in 3/34 patients (7.6%). We conclude that OMC is effective for HP eradication, and that NA should not be used. Reinfection occurs in 7.6% of the patients in the first year after eradication.


Asunto(s)
Úlcera Duodenal/tratamiento farmacológico , Dispepsia/tratamiento farmacológico , Infecciones por Helicobacter/tratamiento farmacológico , Helicobacter pylori , Adolescente , Adulto , Anciano , Antibacterianos/uso terapéutico , Antiulcerosos/uso terapéutico , Quimioterapia Combinada , Úlcera Duodenal/microbiología , Dispepsia/microbiología , Femenino , Humanos , Macrólidos , Masculino , Metronidazol/uso terapéutico , Persona de Mediana Edad , Omeprazol/uso terapéutico , Penicilinas/uso terapéutico , Estudios Prospectivos , Recurrencia , Factores de Tiempo , Resultado del Tratamiento
7.
HPB Surg ; 11(5): 333-8, 2000.
Artículo en Inglés | MEDLINE | ID: mdl-10674749

RESUMEN

BACKGROUND: Pancreatic pseudocyst endoscopic drainage has been described as a good treatment option, with morbidity and mortality rates that are lower than surgery. The aim of our study is to describe the efficacy of different forms of endoscopic drainage and estimate pseudocyst recurrence rate after short follow up period. PATIENTS AND METHODS: We studied 30 patients with pancreatic pseudocyst that presented some indication for treatment: persistent abdominal pain, infection or cholestasis. Clinical evaluation was performed with a pain scale, 0 meaning absence of pain and 4 meaning continuous pain. Pseudocysts were first evaluated by abdominal CT scan, and after endoscopic retrograde pancreatography the patients were treated by transpapillary or transmural (cystduodenostomy or cystgastrostomy) drainage. Pseudocyst resolution was documented by serial CT scans. RESULTS: 25/30 patients could be treated. Drainage was successful in 21 (70% in an 'intention to treat' basis). After a mean follow-up of 42 +/- 35.82 weeks, there was only 1 (4.2%) recurrence. A total of 6 complications occurred in 37 procedures (16.2%), and all but 2 were managed clinically and/or endoscopically: there was no mortality related to the procedure. Patients submitted to combined drainage needed more procedures than the other groups. There was no difference in the efficacy when we compared the three different drainage methods. CONCLUSIONS: We concluded that pancreatic pseudocyst endoscopic drainage is possible in most patients, with high success rate and low morbidity.


Asunto(s)
Drenaje/métodos , Seudoquiste Pancreático/cirugía , Adulto , Colangiopancreatografia Retrógrada Endoscópica , Endoscopía del Sistema Digestivo , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Stents , Resultado del Tratamiento
8.
HPB Surg ; 11(1): 27-32, 1998.
Artículo en Inglés | MEDLINE | ID: mdl-9830578

RESUMEN

Endoscopic sclerotherapy and banding ligation are the two preferred methods to treat oesophageal variceal bleeding. There are many reports dealing with such treatment in cirrhotic patients but we do not know how good they are to treat varices secondary to other forms of portal hypertension. Schistosomiasis mansoni is the main cause of portal hypertension and oesophageal varices in Brazil. We performed a prospective randomised study to compare: 1) the efficacy of both treatments in eradicating oesophageal varices, and 2) complications secondary to both treatments. Forty patients were divided in two groups. Both sclerotherapy and banding ligation were performed until variceal eradication. There were no severe complications. Variceal eradication was faster obtained with banding ligation than sclerotherapy although there was no statistical difference (mean number of sessions 3.05 vs 3.72, p = 0.053). Benign complications were equally frequent in both groups, although additional sedation was more common in the sclerotherapy group. We concluded that both treatments are equally effective in the eradication of oesophageal varices, although banding ligation is better tolerated by the patient and probably faster.


Asunto(s)
Endoscopía/métodos , Várices Esofágicas y Gástricas/terapia , Esofagoplastia/métodos , Esofagoscopía/métodos , Hemorragia Gastrointestinal/terapia , Esquistosomiasis mansoni/terapia , Escleroterapia/métodos , Adulto , Anciano , Endoscopía/estadística & datos numéricos , Várices Esofágicas y Gástricas/etiología , Esofagoplastia/estadística & datos numéricos , Esofagoscopía/estadística & datos numéricos , Femenino , Hemorragia Gastrointestinal/etiología , Humanos , Ligadura/métodos , Ligadura/estadística & datos numéricos , Masculino , Persona de Mediana Edad , Ácidos Oléicos/administración & dosificación , Estudios Prospectivos , Esquistosomiasis mansoni/complicaciones , Soluciones Esclerosantes/administración & dosificación , Escleroterapia/estadística & datos numéricos , Estadísticas no Paramétricas
10.
Gastrointest Endosc ; 46(4): 321-3, 1997 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-9351034

RESUMEN

BACKGROUND: Esophageal band ligation is considered to be as efficient as endoscopic sclerotherapy, with a lower complication rate, including bacteremia. There are few studies comparing the two methods. The aim of this study was to compare the incidence of bacteremia after both treatments in patients with portal hypertension secondary to schistosomiasis. METHODS: Endoscopic sclerotherapy and band ligation were performed using standard techniques. Blood samples were obtained 5 and 30 minutes after endoscopic band ligation or sclerotherapy and cultured for aerobic and anaerobic organisms. RESULTS: In the sclerotherapy group 2 of 43 (4.6%) blood cultures were positive (Peptostreptococcus sp and Streptococcus mitis). A similar result was obtained in the band ligation group: 2 of 35 (5.7%) had positive cultures, both with Staphylococcus aureus. CONCLUSIONS: There is no difference in the frequency of bacteremia after treatment of esophageal varices with endoscopic sclerotherapy or endoscopic band ligation in patients with portal hypertension secondary to schistosomiasis.


Asunto(s)
Bacteriemia/epidemiología , Várices Esofágicas y Gástricas/terapia , Esofagoscopía/efectos adversos , Hipertensión Portal/complicaciones , Parasitosis Hepáticas/complicaciones , Esquistosomiasis/complicaciones , Escleroterapia/efectos adversos , Enfermedades del Bazo/complicaciones , Adulto , Anciano , Bacteriemia/microbiología , Sangre/microbiología , Várices Esofágicas y Gástricas/etiología , Esofagoscopía/métodos , Femenino , Humanos , Hipertensión Portal/sangre , Incidencia , Ligadura/efectos adversos , Ligadura/métodos , Parasitosis Hepáticas/parasitología , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Factores de Riesgo , Esquistosomiasis/parasitología , Escleroterapia/instrumentación , Enfermedades del Bazo/parasitología
12.
Arq Gastroenterol ; 34(4): 207-11, 1997.
Artículo en Portugués | MEDLINE | ID: mdl-9629313

RESUMEN

Helicobacter pylori is a Gram negative bacteria that colonizes gastric epithelial cells. It has been associated with several gastric disease including chronic gastritis and peptic ulcer. Helicobacter pylori infection diagnosis can be done with invasive and non-invasive methods. In invasive methods an endoscopic gastric mucosa biopsy specimen is used. In our study we compare the sensitivity, specificity, costs and applicability of four invasive diagnostic tests: culture, urease ultra-rapid test, histology (Giemsa and Hematoxilineosin stain) and fuchsin stained mucosal slides. Urease test was the easiest, fastest diagnostic test, with sensitivity of 86% and specificity of 100%, being also the cheapest test. We concluded that it should be the test of choice for Helicobacter pylori infection diagnosis.


Asunto(s)
Endoscopía del Sistema Digestivo , Mucosa Gástrica/microbiología , Infecciones por Helicobacter/diagnóstico , Helicobacter pylori/aislamiento & purificación , Adulto , Anciano , Biopsia , Femenino , Humanos , Masculino , Persona de Mediana Edad , Valor Predictivo de las Pruebas , Colorantes de Rosanilina , Sensibilidad y Especificidad , Ureasa/economía
13.
Minerva Cardioangiol ; 44(12): 669-73, 1996 Dec.
Artículo en Italiano | MEDLINE | ID: mdl-9053822

RESUMEN

The authors report the case of a severely vasculopathic patient with pulmonary mediastinal tumour who presented, probably on a paraneoplastic basis, the onset of severe thrombocytopenic purpura persisting for several months. The syndrome was not classifiable in any of the forms known to the authors and was completely resolved by treatment with PGE1 (alprostadil-alpha-cyclodextrine (Prostavasin, Schwarz Pharma).


Asunto(s)
Alprostadil/uso terapéutico , Síndromes Paraneoplásicos/tratamiento farmacológico , Inhibidores de Agregación Plaquetaria/uso terapéutico , Púrpura Trombocitopénica/tratamiento farmacológico , Anciano , Humanos , Masculino
14.
Arq Gastroenterol ; 32(3): 110-5, 1995.
Artículo en Portugués | MEDLINE | ID: mdl-8728785

RESUMEN

Endoscopy therapy of pancreatic pseudocyst has been described as an efficient method. We report six cases of pancreatic pseudocyst treated by pancreatic stenting (three cases), cystogastrostomy (three cases) and cystoduodenostomy (one case). Rapid symptomatic improvement and pseudocyst regression were noted in all cases, except one. Such patient needed pancreatic stenting even after cystogastrostomy due to main pancreatic duct stenosis. There were three complications: hemorrhage (one case) and pseudocyst infection (two cases), and all were treated clinically. Two patients had pseudocyst infection previous to endoscopic manipulation, and they were treated only with antibiotics and endoscopic drainage, without surgery (treatment suggested by most of the authors). We concluded that endoscopic therapy of pancreatic pseudocyst is efficient and safe, being responsible for rapid relief of symptoms in most of patients.


Asunto(s)
Endoscopía , Seudoquiste Pancreático/cirugía , Adulto , Estudios de Seguimiento , Humanos , Masculino , Persona de Mediana Edad , Seudoquiste Pancreático/diagnóstico , Seudoquiste Pancreático/diagnóstico por imagen , Complicaciones Posoperatorias , Ultrasonografía
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