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1.
J Physiol Pharmacol ; 72(4)2021 Aug.
Article in English | MEDLINE | ID: mdl-34987127

ABSTRACT

Ustekinumab (UST), a human anti-IL12/23p40 monoclonal antibody, was approved by FDA and EMA for the treatment of moderate to severe Crohn's disease (CD). Whether UST is effective in inducing deep remission, including mucosal healing and transmural healing, in patients with CD in a real life setting is not completely clear. This study was performed on 92 subjects with confirmed diagnosis of moderate to severe Crohn's disease and no neoplasia. Before inclusion, all patients had been exposed and had failed to respond to conventional and/or at least one biological therapy. All patients underwent endoscopic examination and bowel MRI and ultrasonography at baseline (T0). At week 52 (T52), patients underwent colonoscopy for assessment of mucosal healing and MRI or ultrasonography for assessment of transmural healing. CDAI was used for the assessment of clinical response and clinical remission. SES-CD was used to assess endoscopic response and remission. Incidence of treatment-related adverse events (TRAEs) was recorded during the study period. Clinical response at week 52 was achieved in 38 (50.5%) patients and clinical remission in 29 (39%). Twenty-six (34%) patients showed mucosal healing, 34 (45%) showed partial endoscopic response. We observed a reduction in SES-CD of at least 50% in 34 (45%) patients as well as an SES-CD ≤ 2 in 26 (35%) patients. All patients with mucosal healing also showed transmural healing. No major TRAEs were observed during treatment. In this multicenter, real life study, we show that UST was well tolerated and effective in inducing clinical response and clinical remission in patients with moderate to severe CD who had previously failed to respond to conventional or biologic therapy. UST showed limited efficacy in inducing deep remission (i.e. mucosal+transmural healing).


Subject(s)
Crohn Disease , Ustekinumab , Biological Therapy , Crohn Disease/drug therapy , Humans , Prospective Studies , Remission Induction , Treatment Outcome , Ustekinumab/therapeutic use
2.
Diabetes Res Clin Pract ; 108(2): e21-4, 2015 May.
Article in English | MEDLINE | ID: mdl-25773377

ABSTRACT

We investigated the usefulness of a new examiner-independent method based on the duration of vibration sensation following the placement of the Rydel-Seiffer tuning fork over the dorsum of the interphalangeal hallux joint. This method demonstrated the same diagnostic efficacy as the Rydel-Seiffer method coupled with greater ease of use.


Subject(s)
Diabetic Neuropathies/diagnosis , Diabetic Neuropathies/physiopathology , Diagnostic Techniques, Neurological , Sensation/physiology , Vibration , Adult , Aged , Case-Control Studies , Female , Hallux/innervation , Humans , Male , Mass Screening/methods , Middle Aged , Neural Conduction/physiology , Pilot Projects , Sensitivity and Specificity , Toe Joint/innervation
3.
G Chir ; 32(4): 188-93, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21554849

ABSTRACT

BACKGROUND: The ingestion of caustic substances is one of the most difficult conditions to be treated in Emergency Department. PATIENTS AND METHODS: The medical records of patients with caustic ingestion and hospitalized from 2003 to 2008 at the Division of General Emergency Surgery with Polyspecialistic Observation of AORN "A. Cardarelli "in Naples, have been revalued. RESULTS: From 2003 to 2008, 58 patients with caustic ingestion were admitted to our Division. Ten of these patients (17.24%) underwent surgery. Six patients underwent oesophageal and gastric resection with cervical esophagostomy and alimentary digiunostomy in emergency; two underwent exploratory laparotomy, two had gastroenteroanastomosis for antropyloric stenosis. One patient underwent new operation for a complication. In total, three reconstructions of oesophagus with colon were performed . Of the six patients undergoing esofagogastrectomy, two died in the first postoperative day, but four have passed the acute phase. CONCLUSIONS: There is no universally accepted diagnostic and therapeutic procedure for the management of these patients, who are often left - as it appears in literature - to the personal experience of the surgeon who is dealing with this situation.


Subject(s)
Burns, Chemical/surgery , Caustics/toxicity , Upper Gastrointestinal Tract/injuries , Upper Gastrointestinal Tract/surgery , Female , Humans , Male
4.
Minerva Endocrinol ; 36(4): 295-310, 2011 Dec.
Article in English | MEDLINE | ID: mdl-22322653

ABSTRACT

Gastrointestinal disorders are strictly related to the ovary function. In fact, it is noted that the prevalence of visceral pain disorders such as irritable bowel syndrome, gastroesophageal reflux disease, gallbladder and biliary tract diseases are significantly higher in women. Furthermore, symptom such as nausea, vomiting, abdominal pain, distension, satiety, bloating, diarrhoa or constipation, frequently appears in relation with pregnancy, luteal phase of the menstrual cycle or perimenopausal and menopausal states. Further support for the contribution of ovarian steroids to functional gastrointestinal disorders comes from studies demonstrating that pharmacological ovariectomy reduces abdominal pain symptoms. Therefore, addressing the influence of sex and sex hormones in the modulation of visceral pain appears critical to develop new strategies of diagnosis and therapy sex-directed for gastro-intestinal disorders.


Subject(s)
Gastrointestinal Diseases/physiopathology , Gastrointestinal Motility/physiology , Gonadal Steroid Hormones/physiology , Ovary/physiology , Amygdala/physiopathology , Animals , Combined Modality Therapy , Contraceptives, Oral, Hormonal/therapeutic use , Disease Susceptibility , Emotions , Esophageal Motility Disorders/epidemiology , Esophageal Motility Disorders/etiology , Esophageal Motility Disorders/physiopathology , Estradiol/pharmacology , Estradiol/toxicity , Female , Gallbladder Diseases/etiology , Gallbladder Diseases/physiopathology , Gastrointestinal Diseases/drug therapy , Gastrointestinal Diseases/epidemiology , Gastrointestinal Diseases/etiology , Gastrointestinal Diseases/psychology , Gastrointestinal Hormones/physiology , Gastrointestinal Motility/drug effects , Hormone Replacement Therapy/adverse effects , Humans , Menopause , Menstrual Cycle , Ovary/physiopathology , Pregnancy , Pregnancy Complications/physiopathology , Rats , Sex Distribution , Visceral Pain/etiology , Visceral Pain/physiopathology
5.
Reumatismo ; 61(1): 15-20, 2009.
Article in Italian | MEDLINE | ID: mdl-19370183

ABSTRACT

OBJECTIVE: To evaluate efficacy of methotrexate treatment in peripheral arthritis of ulcerative colitis. METHODS: We studied 18 patients (10/8 M/F; mean age: 38.90 yrs; range: 21-65 yrs), with peripheral arthritis (14 with polyarticular, 4 with oligoarticular subset) associate ulcerative colitis. Methotrexate 20 mg/week was administered in our patients, who were already receiving mesalazina for inflammatory bowel disease. At baseline, after 3 (T1), 6 (T2) and 12 months (T3) serological parameters (ESR and CRP), functional status (HAQ) and disease activity (VAS, GH, Ritchie articular index) were evaluated. RESULTS: During the therapy a significant improvement was observed in disease activity, functional status and serological parameters since T1. ESR and CRP did not change at T2 and T3. Instead VAS, GH, Ritchie articular index and HAQ had a significant and gradual improvement from T1 to T3. CONCLUSION: Methotrexate treatment was efficacious in the treatment of peripheral arthritis associate ulcerative colitis. This drug induced improvement in disease activity, functional status and serological parameters after 3 months of therapy.


Subject(s)
Antirheumatic Agents/therapeutic use , Colitis, Ulcerative/complications , Methotrexate/therapeutic use , Spondylarthropathies/drug therapy , Adult , Aged , Antirheumatic Agents/administration & dosage , Antirheumatic Agents/adverse effects , Female , Humans , Male , Methotrexate/administration & dosage , Methotrexate/adverse effects , Middle Aged , Randomized Controlled Trials as Topic , Spondylarthropathies/diagnosis , Surveys and Questionnaires , Time Factors , Treatment Outcome
6.
Allergy ; 62(7): 738-43, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17573720

ABSTRACT

BACKGROUND: Little is known about the diagnostic accuracy of atopy patch tests (APT) in the clinical practice of pediatric gastroenterology. Moreover, APTs containing purified food extracts have recently become available, but their diagnostic accuracy is largely undefined. PATIENTS AND METHODS: We evaluated the diagnostic accuracy of food challenge, skin prick test (SPT), serum specific IgE determination, and APT using fresh food and commercial food extracts in parallel in children referred for suspected food allergy-related gastrointestinal symptoms. RESULTS: Eighty-nine food challenges were performed in 60 patients (38 boys, median age 23 months, range 3-48 months): 31 tested positive for cow's milk (CM), 19 for hen's egg (HE), and two for wheat. Specific immunoglobulin E (IgE) determination, and SPT, respectively, were positive in 7/31 and 14/31 of patients with cow's milk allergy (CMA), and in 7/19 and 7/19 with HE allergy. The results of APT with fresh food vs a commercial assay were (1) CM: sensitivity: 64.5%vs 6.4%, specificity 95.8%vs 95.6%, positive predictive value (PPV) 95.2%vs 66.6% and negative predictive value (NPV) 67.6%vs 43.1%; (2) HE: sensitivity 84.2%vs 5.2%, specificity 100%vs 100%, PPV 100%vs 100% and NPV 75.0%vs 33.3%. CONCLUSIONS: Atopy patch test is a useful tool in the diagnostic work up of children with food-allergy-related gastrointestinal symptoms. The diagnostic accuracy of ATP was higher with fresh food than with commercial food extracts.


Subject(s)
Food Hypersensitivity/complications , Gastrointestinal Diseases/etiology , Patch Tests/standards , Animals , Child , Child, Preschool , Egg Hypersensitivity/diagnosis , Female , Food Preservation , Humans , Immunoglobulin E/immunology , Infant , Male , Milk Hypersensitivity/diagnosis , Predictive Value of Tests , Reproducibility of Results , Sensitivity and Specificity , Wheat Hypersensitivity/diagnosis
7.
Aliment Pharmacol Ther ; 26(1): 21-9, 2007 Jul 01.
Article in English | MEDLINE | ID: mdl-17555418

ABSTRACT

BACKGROUND: Beclomethasone dipropionate (BDP) is a second-generation steroid with topical effects and minimal systemic activity for patients with ulcerative colitis (UC). AIM: To review all available literature to assess the efficacy of enema/foam BDP compared with enema/foam 5-aminosalicylic acid (5-ASA) in the control of left-sided mild-moderate UC. METHODS: We selected randomized controlled trials of enema/foam BDP compared with enema/foam 5-ASA treatment in patients with UC. Two reviewers assessed trial quality and extracted data independently. RESULTS: Four trials involving 428 UC patients, 209 treated with 5-ASA (1-4 g o.d.) and 219 with BDP (3 mg o.d.), were included. Intention-to-treat analysis showed that 5-ASA induced improvement/remission of UC in 146 (69.9%) patients, while BDP in 143 (65.3%). The test for heterogeneity (Cochran Q) was not significant and Mantel-Haenszel pooled estimate of odds ratio was 1.23 (95% CI = 0.82-1.85). The results did not change when analysis was performed on a per-protocol basis. CONCLUSION: The randomized controlled trials identified in this review showed that rectal BDP has equal effect as 5-ASA to control symptoms in UC.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Anti-Inflammatory Agents/therapeutic use , Beclomethasone/therapeutic use , Mesalamine/therapeutic use , Administration, Rectal , Beclomethasone/economics , Female , Humans , Male , Mesalamine/economics , Treatment Outcome
8.
Dig Liver Dis ; 39(5): 466-72, 2007 May.
Article in English | MEDLINE | ID: mdl-17369113

ABSTRACT

OBJECTIVE: Both arterial hypertension and chronic hepatitis are common disorders. The relationship between arterial pressure and liver cirrhosis has been extensively studied, but no studies are available in chronic hepatitis (CH). Recently, a few studies have reported that treatment with angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin-receptor blockers (ARBs), commonly used in arterial hypertension, reduce hepatic fibrosis in patients with viral CH and in nonalcoholic steatohepatitis. This study was aimed at comparing the evolution of post-viral CH in patients with/without concomitant essential hypertension. METHODS: Two sets of observations were carried out: (a) a cross-sectional cohort study of 95 patients with viral CH, to compare the severity of histological and biochemical data at diagnosis, in relation to pharmacologically treated essential hypertension, and (b) a retrospective study with the observation of 254 patients with CH of viral etiology, followed up from 2 to 20 years, to establish the natural history of viral CH in relation to treated essential hypertension. RESULTS: In the cross-sectional analysis, patients with treated hypertension had a significantly older age at diagnosis of CH (51.4 +/- 8.4 years vs. 46.2 +/- 12.2 in normotensive; P < 0.001) and histological evidence of less severe necro-inflammatory liver damage. ALT levels were also lower (109.8 +/- 62.5 U/L vs. 166.0+/-169.5 in normotensive; P < 0.001) as were endothelin-1 levels (0.74 +/- 0.97 vs. 1.77 +/- 1.51 fmol/mL; P < 0.001). The retrospective study confirmed an older age at diagnosis in patients with treated hypertension (48.7 +/- 9.8 vs. 41.9 +/- 11.8 years; P < 0.001) and lower death rates (2.2% vs. 11%; P < 0.05). CONCLUSIONS: The evolution of post-viral CH seems to be less severe in subjects with essential hypertension, possibly in relation to treatment with antihypertensive drugs.


Subject(s)
Antihypertensive Agents/therapeutic use , Hepatitis, Chronic/complications , Hepatitis, Viral, Human/complications , Hypertension/complications , Adult , Angiotensin II Type 1 Receptor Blockers/therapeutic use , Angiotensin-Converting Enzyme Inhibitors/therapeutic use , Cross-Sectional Studies , Female , Hepatitis, Chronic/drug therapy , Hepatitis, Viral, Human/drug therapy , Humans , Hypertension/drug therapy , Male , Middle Aged , Retrospective Studies , Treatment Outcome
9.
Hum Reprod ; 22(2): 578-85, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17050549

ABSTRACT

BACKGROUND: During the childbearing years, the standard fertility-sparing treatment for bilateral borderline ovarian tumours (BOTs) is the unilateral oophorectomy plus controlateral cystectomy. The aim of the present study was to compare the effects of two laparoscopic fertility-sparing surgical procedures for the treatment of bilateral BOTs on recurrence and fertility in young women who desire to conceive as soon as possible. METHODS: Thirty-two women affected by bilateral early-stage BOTs who desired to conceive were randomized to receive bilateral cystectomy (experimental group, n=15) or oophorectomy plus controlateral cystectomy (control group, n=17). At the first recurrence after childbearing completion, each patient was treated with non-conservative standard treatment. Recurrences and reproductive events were recorded. RESULTS: After a follow-up period of 81 months (19 inter-quartile; 60-96 range), the cumulative pregnancy rate (CPR) (14/15 versus 9/17; P=0.003) and the cumulative probability of first pregnancy (P= 0.011) were significantly higher in the experimental than in control group. No significant (P=0.358) difference between groups was detected in cumulative probability of first recurrence. CONCLUSIONS: The laparoscopic bilateral cystectomy followed by non-conservative treatment performed at the first recurrence after the childbearing completion is an effective surgical strategy for patients with bilateral early-stage BOTs who desire to conceive as soon as possible.


Subject(s)
Infertility, Female/prevention & control , Ovarian Neoplasms/surgery , Pregnancy Rate , Adult , Cystectomy , Female , Humans , Laparoscopy , Neoplasm Recurrence, Local/surgery , Ovarian Neoplasms/pathology , Ovariectomy , Pregnancy
10.
Dig Liver Dis ; 38(6): 381-7, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16301010

ABSTRACT

BACKGROUND: Comparative data on the therapeutic efficacy of different enteral nutrition formulas and corticosteroids to obtain clinical remission and to induce mucosal healing influencing long-term disease course in paediatric Crohn's disease are still scarce. AIMS: To investigate the efficacy of nutritional therapy using three different formulas versus corticosteroids to achieve clinical remission as well as to induce intestinal mucosal healing in active Crohn's disease children. Duration of remission and effect on growth recovery were also assessed. PATIENTS AND METHODS: Clinical, laboratory, endoscopic and histological data of all new diagnosed active Crohn's disease paediatric cases were retrospectively recorded and reviewed. Thirty-seven children (median age 12.1 years) received nutritional therapy (12 polymeric; 13 semi-elemental; 12 elemental diet) and 10 subjects (median age 12.4 years) received corticosteroids. RESULTS: Similar clinical remission rate were observed after 8 weeks of treatment: 86.5% children receiving nutritional therapy versus 90% treated with corticosteroids. Improvement in mucosal inflammation occurred in 26 out of 37 (64.8%) patients on nutritional therapy and in 4 out of 10 (40%) children on steroids (p < 0.05). Finally, seven subjects on nutritional therapy and none on corticosteroids achieved complete mucosal healing (p < 0.005) at the end of the treatment. Nutritional therapy was more effective than corticosteroids in improving nutritional status and linear growth recovery. Compared to corticosteroids, the duration of clinical remission was longer in the nutritional therapy groups without differences among the three different formulas. CONCLUSIONS: In children with active Crohn's disease, nutritional therapy is more effective than corticosteroids to improve intestinal inflammation and to maintain a more sustained clinical remission.


Subject(s)
Adrenal Cortex Hormones/therapeutic use , Crohn Disease/therapy , Enteral Nutrition , Adolescent , Child , Crohn Disease/drug therapy , Enteral Nutrition/methods , Female , Food, Formulated , Humans , Male , Remission Induction , Retrospective Studies , Treatment Outcome
11.
Clin Nutr ; 24(5): 751-9, 2005 Oct.
Article in English | MEDLINE | ID: mdl-16182039

ABSTRACT

BACKGROUND AND AIMS: In patients with liver cirrhosis, protein-energy malnutrition is a frequent finding and a risk factor influencing survival. The aim was to estimate the effects of an adequate diet on malnutrition and clinical outcome in patients with Child A or B HCV-related liver cirrhosis. METHODS: We enrolled 90 consecutive outpatients (M/F=52/38) with liver cirrhosis, 30 in Child class A and 60 in class B. Patients were evaluated by anamnesis, clinical examination, estimation of daily caloric intake and measurement of anthropometrical and biochemical indexes. Patients were randomized into two groups: group 1 with a 3-month oral controlled diet started one week after the first examination and this was followed by a 3-month of spontaneous dietary intake, and group 2 which started a 3-month spontaneous dietary intake followed by a 3-month of controlled diet. The follow-up was performed every month. RESULTS: During the period of controlled diet in patients of both groups, protein malnutrition assessed by midarm muscle circumference, creatinine-height index and serum albumin significantly improved independently of the Child class. Lipid malnutrition, assessed by triceps skin fold thickness values, did not improve during the course of the study. The compliance to the prescribed diet was very high in both groups, and no carry over effect of the previous dietary intake was observed during the follow-up period. CONCLUSIONS: The results emphasize the importance of both nutritional status evaluation and improvement in the Child A and B cirrhotic patients with HCV-related disease. The proposed nutritional approach was able to influence their protein malnutrition positively.


Subject(s)
Anthropometry , Energy Intake/physiology , Liver Cirrhosis/physiopathology , Nutritional Status , Protein-Energy Malnutrition/diet therapy , Child , Creatinine/urine , Cross-Over Studies , Dietary Proteins/administration & dosage , Double-Blind Method , Female , Hepatitis C/complications , Humans , Liver Cirrhosis/complications , Male , Prospective Studies , Protein-Energy Malnutrition/etiology , Protein-Energy Malnutrition/prevention & control , Treatment Outcome
12.
Dig Liver Dis ; 36(9): 632-4, 2004 Sep.
Article in English | MEDLINE | ID: mdl-15460849

ABSTRACT

Pill oesophagitis is a frequent clinical entity that may induce dysphagia and exceptionally oesophageal occlusion. The mechanisms inducing mucosal inflammation are not completely defined, but oesophageal damage occurring when the caustic content of a drug remains in the oesophagus long enough to produce mucosal lesions seems to be a main factor. We report a case of a life-threatening stenosing pill hypopharynx-oesophagitis caused by the ingestion of a capsule of tamsulosin, a drug diffusely used for benign prostatic hyperplasia treatment.


Subject(s)
Esophageal Stenosis/chemically induced , Esophagitis/chemically induced , Sulfonamides/adverse effects , Adrenergic alpha-Antagonists/adverse effects , Aged , Esophageal Stenosis/diagnosis , Esophagitis/diagnosis , Humans , Hypophosphatasia/chemically induced , Male , Pharyngitis/chemically induced , Prostatic Hyperplasia/drug therapy , Tamsulosin , Tomography, X-Ray Computed
13.
Dig Liver Dis ; 36(7): 467-70, 2004 Jul.
Article in English | MEDLINE | ID: mdl-15285526

ABSTRACT

BACKGROUND: Faecal calprotectin (FC) is a new marker of intestinal inflammation. Data on FC in paediatric gastroenterology clinical practice are still scarce. AIMS: To assess FC values in different paediatric gastrointestinal diseases comparing them with those obtained in healthy children. PATIENTS: Two hundred and eighty-one children (age range 13-216 months) consecutively referred for gastrointestinal symptoms. Seventy-six healthy controls (age range 13-209 months). The exclusion criteria in healthy children were the following: any known underlying chronic disease or a history of abdominal pain, diarrhoea, acute respiratory tract infection, intake of non-steroidal anti-inflammatory drugs, gastric acidity inhibitors, antibiotics, drugs influencing gut motility, and menstrual or nasal bleeding in the last 3 weeks. METHODS: Stool samples stored, prepared and analyzed by an ELISA assay. RESULTS: In healthy children the median FC value was 28.0 microg/g (15-57 interquartile range) with a 95th percentile value of 95.3 microg/g. An increase in FC concentration was observed in all diseases characterized by gastrointestinal mucosa inflammation, and the active inflammatory bowel disease patients showed the higher FC values. All children affected by functional bowel disorders or by non-inflammatory diseases showed normal values. We calculated an optimized FC cut off value of 102.9266 microg/g (revealed by the receiver operating characteristic curve) to distinguish patients with active organic/inflammatory disorders from healthy subjects and from patients with functional bowel disorders. CONCLUSIONS: Calprotectin is a sensitive, but not disease specific, marker to easily detect inflammation throughout the whole gastrointestinal tract. It may help in identifying an organic disease characterized by intestinal mucosa inflammation and in the differential diagnosis of functional bowel disorders.


Subject(s)
Biomarkers/analysis , Feces/chemistry , Gastrointestinal Diseases/diagnosis , Leukocyte L1 Antigen Complex/analysis , Adolescent , Child , Child, Preschool , Enzyme-Linked Immunosorbent Assay , Female , Humans , Infant , Inflammation/diagnosis , Male
14.
Am J Gastroenterol ; 99(2): 327-34, 2004 Feb.
Article in English | MEDLINE | ID: mdl-15046225

ABSTRACT

OBJECTIVE: Two common factors, cigarette smoking and appendectomy, have been found to play a role in ulcerative colitis (UC). Data on their role in the development of extraintestinal manifestations (EIM) are scarce. METHODS: The relationship between cigarette smoking, appendectomy, and EIM was examined in a prospective study involving 535 (M/F = 319/216) consecutive UC patients followed up for 18 yr. We considered the major EIM: seronegative spondyloarthropathy, pyoderma gangrenosum/erythema nodosum, acute anterior uveitis, and primary sclerosing cholangitis. We excluded patients with a history of EIM or those colectomized before study entry, ex-smokers, and those who started to smoke during the course of UC. RESULTS: In UC patients, seronegative spondyloarthropathy and dermatologic complications were found increased in smokers (p < 0.0001; p = 0.001) or in subjects with appendectomy (p = 0.0003; p = 0.02), while acute anterior uveitis and primary sclerosing cholangitis did not differ. The Kaplan-Meier analysis showed 18-yr rates for EIM of 71% in smokers and 45% in nonsmokers (log-rank test, p = 0.0001), and of 85% in patients with appendectomy and 48% in those without (p = 0.0001). Cox proportional-hazard model showed that cigarette smoking and appendectomy are independent factors promoting EIM. In smokers with appendectomy the adjusted hazard ratio (3.197, 95% CI 1.529-6.684) was higher than in patients with appendectomy alone (2.617, 95% CI 1.542-4.442) or smoking alone (1.947, 95% CI 1.317-2.879). CONCLUSIONS: In UC patients, appendectomy and cigarette smoking are prognostic factors for the development of EIM. The unfavorable effect of cigarette smoking on EIM is additive to that of appendectomy.


Subject(s)
Appendectomy/adverse effects , Colitis, Ulcerative/complications , Smoking/adverse effects , Adolescent , Adult , Child , Cholangitis, Sclerosing/etiology , Female , Humans , Male , Middle Aged , Prognosis , Prospective Studies , Risk Factors , Skin Diseases/etiology , Spinal Osteophytosis/etiology , Uveitis, Anterior/etiology
15.
Aliment Pharmacol Ther ; 18(11-12): 1107-12, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14653830

ABSTRACT

BACKGROUND: Small bowel bacterial overgrowth is common in Crohn's disease but its treatment is not clearly defined. Metronidazole and ciprofloxacin are effective antibiotics in active Crohn's disease. AIM: To investigate the efficacy of metronidazole and ciprofloxacin in the treatment of bacterial overgrowth in patients with Crohn's disease. PATIENTS AND METHODS: We performed the lactulose breath test in 145 consecutive patients affected by Crohn's disease. Patients positive to the lactulose breath test underwent a glucose breath test to confirm the overgrowth. These patients were randomized in two treatment groups: metronidazole 250 mg t.d.s. (Group A) and ciprofloxacin 500 mg b.d. (Group B), both orally for 10 days. The glucose breath test was repeated at the end of treatment. The clinical outcome after therapy was also recorded. RESULTS: Bacterial overgrowth was present in 29 patients (20%). Breath test normalization occurred in 13 out of 15 patients treated by metronidazole and in all 14 patients treated by ciprofloxacin (P = ns). In both groups antibiotic treatment induced an improvement of intestinal symptoms: bloating (Group A 85% and Group B 83%), stool softness (44% and 50%), and abdominal pain (50% and 43%). CONCLUSIONS: Small bowel bacterial overgrowth is a frequent condition in Crohn's disease which can be effectively treated by metronidazole or ciprofloxacin.


Subject(s)
Anti-Infective Agents/therapeutic use , Bacterial Infections/drug therapy , Ciprofloxacin/therapeutic use , Crohn Disease/complications , Metronidazole/therapeutic use , Adult , Aged , Breath Tests/methods , Colonic Diseases/drug therapy , Female , Glucose/analysis , Humans , Ileal Diseases/drug therapy , Lactulose/analysis , Male , Middle Aged , Treatment Outcome
16.
Aliment Pharmacol Ther ; 17(12): 1471-80, 2003 Jun 15.
Article in English | MEDLINE | ID: mdl-12823149

ABSTRACT

AIM: To explore the efficacy and safety of the topically acting steroid beclometasone dipropionate (BDP) in an oral controlled release formulation in the treatment of extensive or left-sided ulcerative colitis. METHODS: In a multicentre, randomised, parallel-group, single-blind study, patients with active mild to moderate ulcerative colitis were randomised to a 4-week treatment with BDP 5 mg/day o.d. vs. 5-ASA 0.8 g t.d.s. The primary efficacy variable was the decrease of Disease Activity Index (DAI) (clinical symptoms and endoscopic appearance of mucosa). Safety was evaluated by monitoring adverse events, vital signs, haematochemical parameters and adrenal function. RESULTS: One hundred and seventy-seven patients were enrolled and randomly treated with BDP (n = 90) or 5-ASA (n = 87). Mean DAI score decreased in both treatments groups (P < 0.0001 vs. baseline for both groups). Clinical remission was achieved in 63.0% of patients in the BDP group vs. 62.5% in the 5-ASA group. A significant DAI score improvement (P < 0.05) in favour of BDP was observed in patients with extensive disease. Both treatments were well tolerated. Mean plasma cortisol levels were significantly reduced vs. baseline in BDP recipients, but without signs of pituitary-adrenal function depletion. CONCLUSION: Oral BDP gave an overall treatment result in patients with active ulcerative colitis without signs of systemic side-effects.


Subject(s)
Anti-Inflammatory Agents/administration & dosage , Beclomethasone/administration & dosage , Colitis, Ulcerative/drug therapy , Administration, Oral , Adolescent , Adult , Aged , Aged, 80 and over , Anti-Inflammatory Agents/adverse effects , Beclomethasone/adverse effects , Delayed-Action Preparations , Female , Humans , Male , Middle Aged , Single-Blind Method , Treatment Outcome
18.
Epidemiol Infect ; 131(3): 1111-5, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14959778

ABSTRACT

We investigated whether there are differences between the natural history of B and C chronic hepatitis in a southern Italian population, and whether the chronic viral hepatitis population was modified by the introduction of the anti-HCV test in 1989. We examined clinical charts of 1120 patients consecutively admitted to our division from January 1979 to December 1998 with the histological diagnosis of chronic viral hepatitis (304 from 1979 to 1988; 816 from 1989 to 1998). We found significant differences only in age at diagnosis (higher in the second decade, P = 0.001), and in aetiology (HBV decreased in the second decade, P < 0.0001). We were able to follow up 449 patients for 2-20 years (311 with HCV and 138 with HBV infection), and found that chronic HCV evolved to cirrhosis more frequently than did chronic HBV; but in both types time to development of cirrhosis and the incidence of death were similar. Our data confirm that a higher onset age of HBV and of HCV is frequently observed in those subjects who have a faster disease progression.


Subject(s)
Antibodies, Viral/analysis , Hepatitis B, Chronic/epidemiology , Hepatitis C, Chronic/epidemiology , Adult , Age of Onset , Aged , Disease Progression , Epidemiologic Studies , Female , Hepatitis B, Chronic/etiology , Hepatitis B, Chronic/pathology , Hepatitis C, Chronic/etiology , Hepatitis C, Chronic/pathology , Humans , Italy/epidemiology , Liver Cirrhosis/virology , Male , Middle Aged , Prognosis , Retrospective Studies
19.
Scand J Gastroenterol ; 37(10): 1156-63, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12408520

ABSTRACT

BACKGROUND: Allergic diseases and seronegative spondyloarthropathies are frequently observed in ulcerative colitis (UC). In this report we have investigated possible relationships between IgE-mediated allergic disease (AD), allergic contact dermatitis (ACD) and seronegative spondyloarthropathy (SpA) in UC patients at different grades and extensions of mucosa inflammation. METHODS: Forty-five UC consecutive outpatients were graded according to clinical, endoscopic and histologic activity scores. SpA was diagnosed according to the European Spondyloarthropathy Study Group criteria. AD was detected by skin prick tests and confirmed by specific provocation tests, while ACD was diagnosed using the European standard series of patch tests. Thirty-seven patients' spouses or partners served as controls. RESULTS: Fourteen patients and 1 control subject showed SpA (P = 0.001). Diagnosis of rhinitis, conjunctivitis or asthma was made in 19 patients and in 5 controls (P = 0.004), while ACD was found in 10 and in 4 (P = 0.17), respectively. In UC, AD coexisted with SpA in 2 cases (P = 0.01), AD with ACD in 1 case (P = 0.03) and ACD with SpA in 5 (P = 0.24). CONCLUSIONS: Notwithstanding the high frequency of AD and SpA found in UC, the concurrence of AD with SpA or ACD is an unusual finding, while SpA and ACD may coexist. These data suggest that, in UC, atopy and seronegative arthritis, as well as atopy and delayed-type allergy, are strongly polarized conditions tending to mutual exclusion. In UC, the presence of AD without SpA or ACD, and of SpA or ACD without AD may indicate subgroups of patients in which T-helper-2 cell or T-helper-1 cell responses predominate.


Subject(s)
Colitis, Ulcerative/complications , Dermatitis, Allergic Contact/complications , Hypersensitivity, Immediate/complications , Spondylarthropathies/complications , Adolescent , Adult , Aged , Colitis, Ulcerative/blood , Colitis, Ulcerative/immunology , Dermatitis, Allergic Contact/blood , Dermatitis, Allergic Contact/immunology , Female , Gastric Mucosa/physiopathology , HLA-B27 Antigen/blood , Humans , Hypersensitivity, Immediate/blood , Hypersensitivity, Immediate/immunology , Male , Middle Aged , Serologic Tests , Severity of Illness Index , Spondylarthropathies/blood , Spondylarthropathies/immunology
20.
Allergy ; 57(11): 1044-7, 2002 Nov.
Article in English | MEDLINE | ID: mdl-12359001

ABSTRACT

BACKGROUND: Clinical complaints in atopic subjects with asthma and rhinitis occur more frequently in the presence of high total and allergen-specific IgE serum levels. Here we report on the relationship between total and allergen-specific IgE serum levels and presence of symptoms in an unselected farmer population sensitized to Tetranychus urticae (TU). METHODS: Farmers were recruited as previously described. Total IgE and allergen-specific IgE were measured by immunoassay in TU-positive skin prick test (SPT) farmers (n = 58) and two control groups including Dermatophagoides pteronyssinus (Dp)-positive SPT subjects (n = 40) and non-atopic, TU-negative SPT healthy farmers (n = 25). RESULTS: Both TU+ and Dp+ subjects had significantly higher total IgE values (P < 0.001) than healthy non-atopic subjects. TU-specific IgE levels were significantly more elevated in symptomatic than non-symptomatic TU+ subjects (P = 0.028). Dp-specific IgE levels were higher in symptomatic than non-symptomatic Dp+ subjects (P = 0.003). Finally, total IgE levels were significantly higher in the symptomatic than non-symptomatic subgroups in both TU+ and Dp+ subjects (P < 0.0001 and P = 0.007, respectively). Logistic regression analysis showed that only total IgE concentrations were significant predictors of current symptoms in TU+ subjects. CONCLUSIONS: High total IgE and allergen-specific IgE levels are associated with symptoms in TU+ subjects. Definition of their predictive value requires further studies.


Subject(s)
Agricultural Workers' Diseases/immunology , Agricultural Workers' Diseases/therapy , Allergens/blood , Allergens/immunology , Epitopes/immunology , Hypersensitivity, Immediate/immunology , Hypersensitivity, Immediate/therapy , Immunoglobulin E/blood , Immunoglobulin E/immunology , Tetranychidae/immunology , Adult , Agricultural Workers' Diseases/blood , Cross Reactions/immunology , Female , Humans , Hypersensitivity, Immediate/blood , Immunization , Male , Predictive Value of Tests , Prevalence , Randomized Controlled Trials as Topic , Single-Blind Method , Skin Tests , Statistics as Topic
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