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1.
J Gastroenterol ; 54(3): 261-270, 2019 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-30232597

RESUMO

BACKGROUND: Scientific literature shows a high prevalence of Small Intestinal Bacterial Overgrowth (SIBO) in patients with Cystic Fibrosis (CF). The role of SIBO in nutritional status and gastrointestinal symptoms in CF is not known. Our aim was to study epidemiology and clinical impact of SIBO while assessing the efficacy of rifaximin in eradicating SIBO in CF patients. METHODS: Symptoms questionnaire and Glucose Breath Test (GBT) were given to 79 CF patients (median age 19.6 years; 9.2-36.9). Subjects with a positive GBT were enrolled in a randomized controlled trial and received rifaximin 1200 mg for 14 days or no treatment. Questionnaire and GBT were repeated 1 month after the end of treatment or 45 days after the first negative GBT. RESULTS: Out of 79 patients, 25 were affected by SIBO (31.6%) with a significant correlation with lower BMI, SDS-BMI (p < 0.05) and serum albumin levels (p < 0.05), independently from pancreas insufficiency. Twenty-three patients took part in the randomized trial, 13 patients (56.5%) in rifaximin group and 10 patients (43.5%) in control group. Eradication rate of SIBO was 9/10 (90%) in rifaximin group and 2/6 (33.3%) in control group (p < 0.05). In the rifaximin group, gastrointestinal symptom improvement was observed in 4/5 patients aged ≤ 14 years and in 0/5 patients aged > 14 years (p < 0.05); in 2/6 patients in the control group. CONCLUSIONS: CF patients show a high prevalence of SIBO, related to a poorer nutritional status. Rifaximin therapy is well tolerated and the results are promising in terms of efficacy in eradicating small intestinal bacterial overgrowth in CF.


Assuntos
Síndrome da Alça Cega/tratamento farmacológico , Fibrose Cística/tratamento farmacológico , Intestino Delgado/microbiologia , Rifaximina/uso terapêutico , Adolescente , Adulto , Fatores Etários , Índice de Massa Corporal , Testes Respiratórios , Estudos de Casos e Controles , Criança , Correlação de Dados , Feminino , Humanos , Masculino , Albumina Sérica/metabolismo , Resultado do Tratamento , Adulto Jovem
2.
Clin Transl Gastroenterol ; 9(6): 162, 2018 06 19.
Artigo em Inglês | MEDLINE | ID: mdl-29915215

RESUMO

BACKGROUND: D-lactic acidosis is characterized by brain fogginess (BF) and elevated D-lactate and occurs in short bowel syndrome. Whether it occurs in patients with an intact gut and unexplained gas and bloating is unknown. We aimed to determine if BF, gas and bloating is associated with D-lactic acidosis and small intestinal bacterial overgrowth (SIBO). METHODS: Patients with gas, bloating, BF, intact gut, and negative endoscopic and radiological tests, and those without BF were evaluated. SIBO was assessed with glucose breath test (GBT) and duodenal aspiration/culture. Metabolic assessments included urinary D-lactic acid and blood L-lactic acid, and ammonia levels. Bowel symptoms, and gastrointestinal transit were assessed. RESULTS: Thirty patients with BF and 8 without BF were evaluated. Abdominal bloating, pain, distension and gas were the most severe symptoms and their prevalence was similar between groups. In BF group, all consumed probiotics. SIBO was more prevalent in BF than non-BF group (68 vs. 28%, p = 0.05). D-lactic acidosis was more prevalent in BF compared to non-BF group (77 vs. 25%, p = 0.006). BF was reproduced in 20/30 (66%) patients. Gastrointestinal transit was slow in 10/30 (33%) patients with BF and 2/8 (25%) without. Other metabolic tests were unremarkable. After discontinuation of probiotics and a course of antibiotics, BF resolved and gastrointestinal symptoms improved significantly (p = 0.005) in 23/30 (77%). CONCLUSIONS: We describe a syndrome of BF, gas and bloating, possibly related to probiotic use, SIBO, and D-lactic acidosis in a cohort without short bowel. Patients with BF exhibited higher prevalence of SIBO and D-lactic acidosis. Symptoms improved with antibiotics and stopping probiotics. Clinicians should recognize and treat this condition.


Assuntos
Acidose Láctica/fisiopatologia , Síndrome da Alça Cega/fisiopatologia , Transtornos Cognitivos/etiologia , Gases , Intestinos/fisiologia , Probióticos/efeitos adversos , Adulto , Idoso , Idoso de 80 Anos ou mais , Antibacterianos/uso terapêutico , Síndrome da Alça Cega/tratamento farmacológico , Síndrome da Alça Cega/microbiologia , Testes Respiratórios , Duodeno/microbiologia , Feminino , Seguimentos , Trânsito Gastrointestinal , Glucose/análise , Humanos , Ácido Láctico/sangue , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos
3.
BMJ Case Rep ; 20182018 Jan 11.
Artigo em Inglês | MEDLINE | ID: mdl-29326369

RESUMO

A patient with severe postural orthostatic tachycardia syndrome (POTS) and mast cell activation syndrome (MCAS) received immunotherapy with low-dose naltrexone (LDN) and intravenous immunoglobulin (IVIg) and antibiotic therapy for small intestinal bacterial overgrowth (SIBO). A dramatic and sustained response was documented. The utility of IVIg in autoimmune neuromuscular diseases has been published, but clinical experience with POTS is relatively unknown and has not been reported in MCAS. As a short-acting mu-opioid antagonist, LDN paradoxically increases endorphins which then bind to regulatory T cells which regulate T-lymphocyte and B-lymphocyte production and this reduces cytokine and antibody production. IVIg is emerging as a promising therapy for POTS. Diagnosis and treatment of SIBO in POTS is a new concept and appears to play an important role.


Assuntos
Antibacterianos/administração & dosagem , Síndrome da Alça Cega/tratamento farmacológico , Imunoglobulinas Intravenosas/administração & dosagem , Mastocitose/tratamento farmacológico , Naltrexona/administração & dosagem , Antagonistas de Entorpecentes/administração & dosagem , Síndrome da Taquicardia Postural Ortostática/tratamento farmacológico , Adulto , Quimioterapia Combinada , Feminino , Humanos , Intestino Delgado/microbiologia
5.
Ter Arkh ; 85(2): 21-6, 2013.
Artigo em Russo | MEDLINE | ID: mdl-23653934

RESUMO

AIM: To estimate the incidence of secondary lactase deficiency (SLD) in patients with postinfectious irritable bowel syndrome (PIBS) and the value of the small bowel microflora in its development and to elaborate treatment options for SLD. SUBJECTS AND METHODS: One hundred and thirty-eight patients with PIBS, including 112 (81.2%) women and 26 (18.8%) men, were examined. The patients' mean age was 33.9 +/- 9.1 years. The duration of the disease was 2.6 +/- 1.4 years. Lactase deficiency (LD) was diagnosed using the color scale to test biopsy specimens from the duodenal retrobulbar region. The bacterial overgrowth syndrome (BOS) was identified by a 2-hour lactulose (20 ml) hydrogen breath test. Sixty patients with moderate SLD were randomized to 2 groups: 1) 41 patients received basic therapy (mesim forte as one tablet t.i.d., no-spa, 40 mg, t.i.d.) and combined probiotic bifiform (Ferrosan) containing Bifidobacterium longum 107, Enterococcus faecium 107 as one capsule t.i.d. for 14 days. Group 2 patients (n = 19) had basic therapy in combination with placebo. RESULTS: SLD was detected in 59.4% of the patients with PIBS, including 43.5 and 15.9% with moderate and severe forms, respectively. In all cases, SLD was accompanied by BOS in the small bowel lumen, as confirmed by the results of a hydrogen breath test [101 +/- 37 ppm (a normal value of < 20 ppm)]. After a 14-day course of therapy with the combined probiotic bifiform, restoration of eubiosis in the small bowel lumen was achieved in 70.8% of the patients, as shown by the lesser degree of BOS (86.9 +/- 40.9 and 17.4 +/- 6.6 ppm before and after treatment, respectively; p < 0.01) and by normalization of the lactase test (p < 0.01). In the comparative placebo group, 68.4% showed no clear positive changes, SLD and BOS remained. CONCLUSION: The changes in the small bowel intraluminal microflora, which developed after prior intestinal infection, played a great role in the development of SLD. Bifiform belongs to the currently available probiotics and may be recommended to correct SLD in patients with PIBS resulting from the impaired microbiota of the small bowel and to prevent BOS.


Assuntos
Bifidobacterium , Síndrome da Alça Cega/tratamento farmacológico , Enterococcus faecium , Intestino Delgado/microbiologia , Síndrome do Intestino Irritável/tratamento farmacológico , Intolerância à Lactose/tratamento farmacológico , Adulto , Analgésicos/administração & dosagem , Síndrome da Alça Cega/enzimologia , Síndrome da Alça Cega/epidemiologia , Feminino , Humanos , Intestino Delgado/efeitos dos fármacos , Síndrome do Intestino Irritável/enzimologia , Síndrome do Intestino Irritável/epidemiologia , Lactase/deficiência , Intolerância à Lactose/enzimologia , Intolerância à Lactose/etiologia , Masculino , Papaverina/administração & dosagem , Papaverina/análogos & derivados , Probióticos , Resultado do Tratamento
7.
Nutrition ; 28(1): 108-11, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21996046

RESUMO

D-Lactic acidosis is a rare complication that occurs in patients with short bowel syndrome due to surgical intestine resection for treatment of obesity. The clinical presentation is characterized by neurologic symptoms and high anion gap metabolic acidosis. The incidence of this syndrome is unknown, probably because of misdiagnosis and sometimes symptoms may be incorrectly attributed to other causes. Therapy is based on low carbohydrate diet, sodium bicarbonate intravenous, rehydratation, antiobiotics, and probiotics that only produce L-lactate. In the case we describe, D-lactic acidosis encephalopathy occurred 25 y after bypass jejunoileal, due to Salmonella enteriditis infection.


Assuntos
Acidose Láctica/etiologia , Cirurgia Bariátrica/efeitos adversos , Síndrome da Alça Cega/microbiologia , Complicações Pós-Operatórias/microbiologia , Salmonella enteritidis/crescimento & desenvolvimento , Síndrome do Intestino Curto/fisiopatologia , Acidose Láctica/fisiopatologia , Síndrome da Alça Cega/tratamento farmacológico , Síndrome da Alça Cega/etiologia , Síndrome da Alça Cega/fisiopatologia , Confusão/etiologia , Fezes/microbiologia , Feminino , Humanos , Pessoa de Meia-Idade , Obesidade/cirurgia , Complicações Pós-Operatórias/tratamento farmacológico , Complicações Pós-Operatórias/fisiopatologia , Infecções por Salmonella/tratamento farmacológico , Infecções por Salmonella/microbiologia , Infecções por Salmonella/fisiopatologia , Salmonella enteritidis/isolamento & purificação , Resultado do Tratamento
8.
Can J Urol ; 18(4): 5826-30, 2011 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-21854715

RESUMO

INTRODUCTION: This pilot study determined the efficacy of rifaximin, a gut-directed antibiotic, in reducing chronic prostatitis (CP) and gastrointestinal (GI) symptoms in patients with CP type III. The prevalence of small intestinal bacterial overgrowth (SIBO) and irritable bowel syndrome (IBS) in patients with CP was also evaluated. MATERIALS AND METHODS: Chronic prostatitis patients were recruited and screened for SIBO and IBS using the lactulose breath test (LBT) and Rome II criteria, respectively. Patients with a positive LBT result and Chronic Prostatitis Symptom Index (CPSI) score ≥ 15 received rifaximin 550 mg three times daily for 10 days. The CPSI score and global improvement of CP and GI symptoms were ascertained at screening (ie, 7 days before therapy), at baseline immediately before therapy (ie, day 0), and on days 14 and 28. RESULTS: Fourteen of 16 CP patients (88%) had a positive LBT result and were included in this therapeutic study (mean age, 41 years). Mean CPSI score significantly decreased from screening to day 28 (ie, 18 days after rifaximin treatment; p = 0.043). Mean abdominal pain and bloating scores were also significantly reduced on day 28 versus baseline (p = 0.010 and p = 0.003, respectively). Chronic prostatitis patients with IBS and SIBO had a statistically significant response as well. CONCLUSION: Data from this pilot study suggest that SIBO and IBS are common in CP and that patients with CP and SIBO may benefit from rifaximin therapy. Further studies are warranted.


Assuntos
Síndrome da Alça Cega/tratamento farmacológico , Síndrome da Alça Cega/epidemiologia , Intestino Delgado/microbiologia , Síndrome do Intestino Irritável/epidemiologia , Prostatite/complicações , Rifamicinas/uso terapêutico , Adulto , Antibacterianos/uso terapêutico , Síndrome da Alça Cega/diagnóstico , Testes Respiratórios , Doença Crônica , Humanos , Síndrome do Intestino Irritável/diagnóstico , Síndrome do Intestino Irritável/tratamento farmacológico , Masculino , Programas de Rastreamento/métodos , Pessoa de Meia-Idade , Projetos Piloto , Prevalência , Rifaximina , Resultado do Tratamento
9.
Adv Perit Dial ; 26: 130-6, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-21348395

RESUMO

Bowel bacterial overgrowth syndrome (BBOS) is an important cause of gastrointestinal (GI) abnormalities. Proinflammatory cytokines (PICs) are excessively produced and accumulate because of kidney failure in dialysis patients who experience chronic infections such as BBOS. We explored the association between GL function, BBOS, and the malnutrition, inflammation, and atherosclerosis (MIA) syndrome. We studied GI malabsorption and maldigestion by analyzing fecal starch, sugar, fat, and nitrogen; intestinal protein permeability (alpha1-antitrypsin fecal clearance); and fecal chymotrypsin. We evaluated BBOS by breath hydrogen test (BHT) after a 3-day fat-and-carbohydrate-overload diet. Positive BHT was present in 10 patients, showing a high prevalence of GI macronutrient malabsorption and maldigestion, and compared with the other patients, the highest plasma levels of tumor necrosis factor alpha and interleukin 6 and lower levels of albumin and prealbumin. Those 10 patients were treated with a combination of several antibiotics, including neomycin, amoxicillin-clavulanate, and quinolones. Between 2 and 3 months later, the BHT, markers of nutrition, and PIC were re-tested. All treated patients showed an improvement in nutrition status and a lesser inflammatory pattern. The BBOS infectious process is found frequently in dialysis patients in association with GI malabsorption and maldigestion, malnutrition, and systemic inflammation. Hyperproduction of PIC because of BBOS induces MIA through a double pathway: GI disorders and deleterious systemic effects.


Assuntos
Aterosclerose/etiologia , Síndrome da Alça Cega/complicações , Gastroenteropatias/complicações , Desnutrição/etiologia , Diálise Peritoneal , Adulto , Idoso , Antibacterianos/uso terapêutico , Síndrome da Alça Cega/diagnóstico , Síndrome da Alça Cega/tratamento farmacológico , Testes Respiratórios , Proteína C-Reativa/análise , Feminino , Gastroenteropatias/diagnóstico , Gastroenteropatias/tratamento farmacológico , Humanos , Inflamação/etiologia , Interleucina-6/sangue , Absorção Intestinal , Masculino , Pessoa de Meia-Idade , Estado Nutricional , Diálise Peritoneal/efeitos adversos , Fator de Necrose Tumoral alfa/sangue
13.
J Rheumatol ; 6(1): 57-64, 1979.
Artigo em Inglês | MEDLINE | ID: mdl-439112

RESUMO

A young female with osteomalacia complicating a blind loop syndrome associated with congenital megaduodenum is described. In this case, the correction of vitamin D malabsorption by administration of antibiotics highlights the role of massive intraluminal bacterial overgrowth from destruction of vitamin D, or decreased unicellar solubilization due to deconjugation of biliary acids. The importance of cutaneous vitamin D synthesis in patients with osteomalacia of gastrointestinal origin is emphasized. The detection of megaduodenum and megaesophagus in the patient's father may be the first report of a familial association of these gastrointestinal abnormalities.


Assuntos
Síndrome da Alça Cega/complicações , Duodeno/anormalidades , Esôfago/anormalidades , Osteomalacia/etiologia , Anormalidades Múltiplas/complicações , Anormalidades Múltiplas/genética , Adulto , Síndrome da Alça Cega/diagnóstico por imagem , Síndrome da Alça Cega/tratamento farmacológico , Duodeno/diagnóstico por imagem , Esôfago/diagnóstico por imagem , Feminino , Humanos , Masculino , Osteomalacia/diagnóstico por imagem , Osteomalacia/tratamento farmacológico , Osteomalacia/genética , Radiografia , Vitamina D/uso terapêutico
14.
Major Probl Clin Surg ; 20: 129-46, 1976.
Artigo em Inglês | MEDLINE | ID: mdl-957777

RESUMO

We have tried to stress the complexity of the bacterial ecology that may exist in the intestine of patients and experimental animals with small intestinal bacterial overgrowth. The multiplicity of organisms often makes the management of these patients quite frustrating. A number of metabolic derangements of varying severity may occur in any given patient. Although many of the observed abnormalities are secondary to disturbed events with the luminal environment of the small intestine, the significance of direct damage to the small intestinal epithelium has been emphasized. Since intestinal cultures are both cumbersome and difficult to perform on a routine basis, the use of labeled substrate breath tests will allow guided, outpatient therapy more easily than in the past. Since full correction of the malabsorption is seldom achieved with antibiotic therapy, nutritional supplementation deserves more attention than it has previously received.


Assuntos
Síndromes de Malabsorção/etiologia , Síndromes Pós-Gastrectomia , Animais , Antibacterianos/uso terapêutico , Infecções Bacterianas/tratamento farmacológico , Infecções Bacterianas/etiologia , Síndrome da Alça Cega/complicações , Síndrome da Alça Cega/tratamento farmacológico , Humanos
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