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1.
J Aerosol Med ; 13(1): 25-33, 2000.
Article in English | MEDLINE | ID: mdl-10947321

ABSTRACT

The aim of this study was to compare the immediate and long-term bronchodilator effect as well as the patient acceptability of a 2-week, multidrug, inhalation treatment delivered by a metered dose inhaler (MDI) versus a jet nebulizer in a group of elderly patients with chronic obstructive pulmonary disease (COPD) or asthma and an at least partially reversible airflow obstruction. Twenty elderly outpatients (17 men; mean +/- SD age, 67 +/- 2 years; mean +/- SD baseline forced expiratory volume in 1 second [FEV1], 46.5 +/- 14% of predicted value) with COPD or asthma participated in the study, which was of an open, randomized, crossover design. After a 1-day baseline evaluation, including patient history, clinical examination, and spirometry, participants were randomly assigned to receive a multidrug inhalation treatment (a combination of salbutamol, ipratropium, and flunisolide) with either an MDI or a jet nebulizer. Two weeks later, they were shifted to treatment with the alternative system for a further 2 weeks. FEV1 was measured on the first and fourteenth days of each treatment period, on each occasion both before and 30 minutes after the morning inhalation. At the end of the study, patients were asked to express a personal preference for one of the two inhalation treatments with regard to effectiveness and acceptability by filling out a simple questionnaire. Both the MDI and jet nebulizer had a significant immediate bronchodilator effect on the first and fourteenth days of treatment, with no differences between treatments. No long-term bronchodilator effect was seen with either aerosol delivery system. Patient preferences were clearly in favor of the jet nebulizer with regard to effectiveness and in favor of the MDI with regard to acceptability. In conclusion, in elderly patients with COPD or asthma and partially reversible airflow obstruction, a maintenance multidrug bronchodilator/anti-inflammatory inhalation treatment produced a statistically significant and clinically relevant bronchodilator effect without substantial differences between the two delivery systems. Most patients considered the MDI to be more acceptable and the jet nebulizer to be more effective. These preferences should be taken into consideration when prescribing a maintenance aerosol inhalation treatment.


Subject(s)
Anti-Asthmatic Agents/administration & dosage , Asthma/drug therapy , Bronchodilator Agents/administration & dosage , Lung Diseases, Obstructive/drug therapy , Nebulizers and Vaporizers , Respiratory Therapy/instrumentation , Administration, Inhalation , Aged , Albuterol/administration & dosage , Cross-Over Studies , Drug Therapy, Combination , Female , Fluocinolone Acetonide/administration & dosage , Fluocinolone Acetonide/analogs & derivatives , Forced Expiratory Volume , Humans , Ipratropium/administration & dosage , Male , Patient Satisfaction , Spirometry , Surveys and Questionnaires
2.
Tumori ; 65(1): 111-7, 1979 Feb 28.
Article in English | MEDLINE | ID: mdl-87046

ABSTRACT

The effectiveness of the cyclophosphamide + methotrexate + 5-fluorouracil schedule (CMF) in 28 patients with advanced gastrointestinal cancer has been studied. No complete remission was obtained; partial remission and objective improvement constituted 56%. The median response period is calculated at a minimum of 12 months, without significant differences between the group of patients previously subjected to palliative canalization surgery and the group of patients not subjected to this operation. The overall median survival time is 10.8 months. On the basis of the data given, the authors conclude by stressing that the CMF combination should be studied more fully in relation to its use in gastrointestinal forms of cancer.


Subject(s)
Cyclophosphamide/administration & dosage , Fluorouracil/administration & dosage , Gastrointestinal Neoplasms/drug therapy , Methotrexate/administration & dosage , Aged , Bone Marrow/drug effects , Cyclophosphamide/adverse effects , Drug Therapy, Combination , Female , Fluorouracil/adverse effects , Gastrointestinal Neoplasms/surgery , Humans , Male , Methotrexate/adverse effects , Middle Aged , Palliative Care , Remission, Spontaneous , Vomiting/chemically induced
3.
Tumori ; 63(2): 175-80, 1977.
Article in English | MEDLINE | ID: mdl-898288

ABSTRACT

Serum copper and ceruloplasmin levels were determined in patients with solid neoplasias in different sites (stomach, large intestine, lung). Statistical analysis showed that serum copper levels increased significantly in all the forms studied. The serum ceruloplasmin level, on the contrary, was high in gastric and pulmonary cancer, while in tumors localised in the large intestine the increase was not significant. In 58 cases, there was a correlation between copper and ceruloplasmin levels in the same subject; this correlation proved significant solely in gastric forms. Moreover, statistical analysis of the two parameters in question did not reveal any significant differences between localized and metastasized in forms.


Subject(s)
Ceruloplasmin/blood , Copper/blood , Gastrointestinal Neoplasms/blood , Lung Neoplasms/blood , Adult , Aged , Female , Humans , Intestinal Neoplasms/blood , Intestine, Large , Male , Middle Aged , Stomach Neoplasms/blood
4.
Tumori ; 65(3): 331-8, 1979 Jun 30.
Article in English | MEDLINE | ID: mdl-462583

ABSTRACT

Serum copper and ceruloplasmin levels (SCL, SCeL) in 57 patients with advanced cancer of the stomach (35 cases) or large intestine (22 cases) treated with polychemotherapy were studies. In gastroenteric cancer, SCL, which are already high in untreated patients, have a tendency to increase further in cases of progression of the disease, while they seem to significantly decrease in cases of remission. SCeL during the trial appeared to be correlated to the clinical evolution of the disease only in the case of stomach cancer. In large intestine cancer, SCeL did not show any significant variation in relation to the normal range. These observations, in particular on the behavior of SCL in the neoplasms of the digestive tract, are in accordance with the results of other studies. The authors are inclined to attach a diagnostic and prognostic value to the variation in SCL and SCeL in gastrointestinal cancer.


Subject(s)
Antineoplastic Agents/administration & dosage , Ceruloplasmin/metabolism , Copper/blood , Gastrointestinal Neoplasms/blood , Aged , Colonic Neoplasms/blood , Cyclophosphamide/administration & dosage , Drug Administration Schedule , Drug Therapy, Combination , Female , Fluorouracil/administration & dosage , Gastrointestinal Neoplasms/drug therapy , Humans , Male , Methotrexate/administration & dosage , Middle Aged , Prognosis , Stomach Neoplasms/blood
5.
Minerva Gastroenterol Dietol ; 45(4): 287-96, 1999 Dec.
Article in Italian | MEDLINE | ID: mdl-16498341

ABSTRACT

Fifty-nine patients with ulcerative colitis localised in the rectum, sigmoid and colon entered the trial. Thirty were treated with BDP and twenty-nine with 5-Aminosalicylic (enemas and suppositories) for 8 weeks, in a doubleblind, controlled study. Clinical, endoscopic and histological assessment was carried out before and after 4 and 8 weeks of treatment. It is concluded that BDP is a new important treatment for mild and moderate activity ulcerative colitis.

6.
Minerva Med ; 76(17-18): 851-7, 1985 Apr 28.
Article in Italian | MEDLINE | ID: mdl-3889721

ABSTRACT

29 patients affected by ovarian (9 cases), head and neck, and miscellaneous neoplasms were treated with Cisplatinum. Most cases had been previously treated with different drugs. Complete and partial remission achieved significative results in 4, 7 and 9 ovarian patients. In the patients with head and neck tumor no complete remission and 4 partial remissions were obtained. These observations confirm that Cisplatinum may be a useful drug in chemotherapy of cancer.


Subject(s)
Cisplatin/therapeutic use , Neoplasms/drug therapy , Adult , Aged , Antineoplastic Agents/therapeutic use , Clinical Trials as Topic , Drug Evaluation , Drug Therapy, Combination , Female , Head and Neck Neoplasms/drug therapy , Humans , Male , Middle Aged , Ovarian Neoplasms/drug therapy
7.
Minerva Med ; 83(12): 805-13, 1992 Dec.
Article in Italian | MEDLINE | ID: mdl-1491760

ABSTRACT

Intranasal desmopressin represents the treatment of choice in Central Diabetes Insipidus. Nevertheless, this route of administration bears some practical disadvantage, linked to either difficult delivering technique, or the status of nasal mucose. The antidiuretic effectiveness of oral desmopressin has been recently demonstrated, both in experimental animals and in man. In our study we compared oral vs. intranasal desmopressin efficacy in 13 patients affected by Central Diabetes Insipidus. The results show that the peroral administration of Desmopressin at a mean dose of 500-600 micrograms/die determines an antidiuretic effect comparable to that of intranasal route, without affecting body weight, arterial pressure and chemical analysis. Side effects, generally limited to the first week of treatment, were described (nausea, vomiting, headache, dizziness [corrected], bitter taste, epygastralgia, asthenia, epystassis), inducing 4/13 patients to withdrawal the trial.


Subject(s)
Deamino Arginine Vasopressin/administration & dosage , Diabetes Insipidus/drug therapy , Administration, Intranasal , Administration, Oral , Adult , Blood Pressure/drug effects , Body Weight/drug effects , Deamino Arginine Vasopressin/pharmacology , Deamino Arginine Vasopressin/therapeutic use , Diabetes Insipidus/blood , Diabetes Insipidus/urine , Diuresis/drug effects , Drug Administration Schedule , Female , Humans , Male , Osmolar Concentration , Specific Gravity/drug effects
8.
Minerva Gastroenterol Dietol ; 45(1): 59-73, 1999 Mar.
Article in Italian | MEDLINE | ID: mdl-16498317

ABSTRACT

The authors assessed the efficacy and tolerability of BDP in an open protocol using rectal enemas and suppositories and in a double-blind protocol vs mesalazine using rectal enemas. A total of 47 patients suffering from ulcerous rectocolitis were enrolled in the study and treated for 42 days while undergoing endoscopic, histologic and clinical controls. In conclusion, the authors affirm that BDP may represent a useful new therapeutic instrument in the treatment of slight to moderately severe forms of inflammatory intestinal disease.

9.
Minerva Chir ; 48(19): 1091-6, 1993 Oct 15.
Article in Italian | MEDLINE | ID: mdl-8309607

ABSTRACT

The efficacy and tolerability of both Terlipressin and Octreotide in the treatment of upper digestive haemorrhage (oesophagus, stomach and duodenum) have been compared, at random, on 30 adult patients. Terlipressin dosage was 2 mg/4 hours i.v. during the first 24 hours, 2 mg/6 hours during the following 24 hours. Octreotide dosage was 50 micrograms i.v. and infusional therapy, 25 micrograms/hours, followed. Haemostasis was obtained in 100% of patients treated with Terlipressin and in 73% of patients treated with Octreotide. Rebleeding occurred in 3 patients treated with Terlipressin and 4 patients treated with Octreotide. Side effects occurred in 4 patients treated with Terlipressin and 8 patients treated with Octreotide. Terlipressin proved to have a better efficacy in comparison with Octreotide, and had less side effects.


Subject(s)
Duodenal Diseases/drug therapy , Esophageal Diseases/drug therapy , Gastrointestinal Hemorrhage/drug therapy , Lypressin/analogs & derivatives , Octreotide/therapeutic use , Stomach Diseases/drug therapy , Adult , Aged , Female , Humans , Lypressin/therapeutic use , Male , Middle Aged , Terlipressin
10.
Minerva Chir ; 54(9): 635-44, 1999 Sep.
Article in Italian | MEDLINE | ID: mdl-10549210

ABSTRACT

BACKGROUND AND AIMS: The use of steroids was recently extended to the various forms of ulcerative rectocolitis by the introduction of topical formulations, above all steroids with an hepatic "first pass" devoid of systemic interference. The aim of this study was to evaluate the efficacy and tolerability of Beclomethasone dipropionate (BDP) in a rectal foam formulation, in the treatment of patients suffering from ulcerative colitis. METHODS: The experimental protocol took the form of a 28-day open prospective trial using BDP rectal foam in patients suffering from ulcerative colitis. Endoscopic, histological, clinical and tolerability parameters were evaluated. The centres taking part in the trial collected data for 60 cases out of a total of 80 patients enrolled in the study, of both sexes and aged between 20 and 81 years old, suffering from proctosigmoiditis (46.7%) and ulcerative rectocolitis (53.3%). RESULTS: Endoscopic parameters showed an improvement after 28 days of treatment in 74.5% of patients; a clinical improvement was achieved in 65.2% of cases. In percentage terms of the mean value of all the improved parameters, histological parameters were altered in 56.9% of patients. With regard to tolerability 82% of patients judged the treatment to be good/excellent. CONCLUSIONS: In conclusion, in line with recent reports regarding other pharmaceutical forms of BDP, including the use of rectal foam, these data confirm the efficacy and tolerability of this molecule and emphasise the validity of its use in the treatment of ulcerative colitis and proctosigmoiditis.


Subject(s)
Anti-Inflammatory Agents/administration & dosage , Beclomethasone/administration & dosage , Colitis, Ulcerative/drug therapy , Administration, Topical , Adult , Aged , Aged, 80 and over , Chi-Square Distribution , Colitis, Ulcerative/diagnosis , Colitis, Ulcerative/pathology , Colonoscopy , Female , Glucocorticoids , Humans , Italy , Male , Middle Aged , Prospective Studies , Remission Induction
11.
G Chir ; 10(9): 513-5, 1989 Sep.
Article in Italian | MEDLINE | ID: mdl-2577207

ABSTRACT

Authors' personal experience is reported in the use of somatostatin for the treatment of acute pancreatitis and after bilio-pancreatic surgery. The drug has proved to be highly effective in reducing the pain and in controlling the biohumoral balance. The preliminary results appear to confirm the opinion that somatostatin is a major therapeutic tool in the treatment of bilio-pancreatic diseases.


Subject(s)
Pancreatitis/drug therapy , Somatostatin/therapeutic use , Acute Disease , Adult , Aged , Aged, 80 and over , Drug Evaluation , Female , Humans , Male , Middle Aged , Pancreatitis/prevention & control , Postoperative Complications/prevention & control
12.
G Chir ; 11(7-8): 429-33, 1990.
Article in Italian | MEDLINE | ID: mdl-2282278

ABSTRACT

Transplenic decompression of esophageal varices by distal splenorenal shunt according to Warren (DSRS) aims to a selective detention of the esophago-gastric varices, also assuring an adequate portal perfusion and hypertensive state of the porto-mesenteric district. The DSRS though, should and must not be performed in emergency as a high mortality rate is registered in all cases of emergency porto-systemic derivations. A mortality risk is reported even during endoscopic sclerosis if performed in emergency compared to the elective procedure. The scope of our study was to test the validity of a new approach of the hemorrhagic cirrhotic patient: the end point was to stop the bleeding with Glypressin and deferred sclerotherapy, associating a selective shunt at 40-60 days. Out of 32 patients with esophago-gastric variceal bleeding, 8 were selected also for derivative surgery. Results show Glypressin as the first and best therapeutic approach. The drug in many cases stops bleeding or at least reduces the blood loss allowing an easier endoscopic sclerosis. Further sclerosis and/or surgical therapy may assure variceal eradication.


Subject(s)
Esophageal and Gastric Varices/complications , Gastrointestinal Hemorrhage/prevention & control , Lypressin/analogs & derivatives , Portasystemic Shunt, Surgical , Sclerotherapy , Adult , Aged , Emergencies , Female , Humans , Liver Cirrhosis/complications , Lypressin/therapeutic use , Male , Middle Aged , Portacaval Shunt, Surgical , Terlipressin
13.
Minerva Pediatr ; 64(3): 341-6, 2012 Jun.
Article in Italian | MEDLINE | ID: mdl-22555328

ABSTRACT

AIM: The duration of therapy represents a fundamental aspect in the compliance to the therapy of child pathologies, such as pharyngotonsillitis, treated with oral therapy. Although penicillin and amoxicillin are the first choice antibiotics in the case of a child suffering from pharyngotonsillitis with the proven presence of Group A Ɵ-hemolytic Streptococcus (GAS), the number of orally administered doses and 10 days of therapy, considerably lower the compliance. METHODS: An open phase IV randomized multicenter clinical trial was conducted in parallel groups, involving 49 family pediatrician (FP), distributed over the entire national territory, enrolling 435 children suffering from GAS-FT. 210 children received Cefaclor, 50 mg/kg/day, administered twice daily for five days, whilst 213 children received amoxicillin/clavulanate 40 mg/kg/day administered twice daily for 10 days. RESULTS: The results showed percentages of eradication of 88.4% for the Cefaclor group and 94.3% for the amoxicillin/clavulanate group, and a positive clinical judgement of 92.3% for the Cefaclor group and 96.6% for the amoxicillin/clavulanate group. The two arms of the study did not have any significant statistical differences, neither for the eradication, nor for the clinical judgement nor for the reduction of the Milano Score between the beginning and the end of treatment, with a P=0.042 for amoxicillin/clavulanate for eradication. CONCLUSION: This study confirms that the administration of Cefaclor for five days during GAS-FT has the same efficacy as a 10-day therapy with amoxicillin/clavulanate, with a clearly different compliance.


Subject(s)
Amoxicillin-Potassium Clavulanate Combination/therapeutic use , Anti-Bacterial Agents/therapeutic use , Cefaclor/therapeutic use , Pharyngitis/drug therapy , Streptococcal Infections/drug therapy , Streptococcus pyogenes , Adolescent , Algorithms , Amoxicillin-Potassium Clavulanate Combination/administration & dosage , Anti-Bacterial Agents/administration & dosage , Cefaclor/administration & dosage , Child , Child, Preschool , Drug Administration Schedule , Female , Humans , Male , Pharyngitis/microbiology , Sicily , Streptococcal Infections/complications , Streptococcus pyogenes/drug effects , Streptococcus pyogenes/isolation & purification , Time Factors , Treatment Outcome
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